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		<updated>2026-05-07T14:04:05Z</updated>
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	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os01g0703600&amp;diff=175171</id>
		<title>Os01g0703600</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os01g0703600&amp;diff=175171"/>
				<updated>2014-05-31T15:04:39Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;''SPL28'' encodes a clathrin-associated adaptor protein complex 1, medium subunit μ1 (AP1M1) and is responsible for spotted leaf and early senescence in rice.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File: QiaoFig1.gif|right|thumb|100px|Fig 1. Phenotype of the ''spotted leaf 28'' (''spl28'') mutant &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File: QiaoFig6.gif|right|thumb|100px|Fig 6. Map-based cloning and identification of ''SPOTTED LEAF 28'' (''SPL28'') &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
A novel rice (''Oryza sativa'') spotted leaf mutant (''spl28'') that displays a lesion mimic phenotype in the absence of pathogen attack was isolated through treatment of Hwacheongbyeo (an elite Korean japonica cultivar) with N-methyl-N-nitrosourea (MNU). Early stage development of the ''spl28'' mutant was normal. However, after flowering, spl28 mutants exhibited a significant decrease in chlorophyll content, soluble protein content, and photosystem II efficiency, and high concentrations of reactive oxygen species (ROS), phytoalexin, callose, and autofluorescent phenolic compounds that localized in or around the lesions. The ''spl28'' mutant also exhibited significantly enhanced resistance to rice blast and bacterial blight. Using a map-based cloning approach, ''SPL28'' was determined to encode a clathrin-associated adaptor protein complex 1, medium subunit μ1 (AP1M1), which is involved in the post-Golgi trafficking pathway. A green fluorescent protein (GFP) fusion protein of ''SPL28'' (SPL28::GFP) localized to the Golgi apparatus, and expression of ''SPL28'' complemented the membrane trafficking defect of apm1-1Δ yeast mutants. ''SPL28'' was ubiquitously expressed and contained a highly conserved adaptor complex medium subunit (ACMS) family domain. ''SPL28'' appears to be involved in the regulation of vesicular trafficking, and ''SPL28'' dysfunction causes the formation of hypersensitive response (HR)-like lesions, leading to the initiation of leaf senescence &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
[[File: QiaoFig9.gif|right|thumb|100px|Fig 9. Subcellular localization of SPOTTED LEAF 28 (SPL28)-green fluorescent protein (GFP) fusion protein in onion epidermal cells &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
''SPL28'' was expressed in all organs examined. In wild-type plants, ''SPL28'' mRNA was most abundant in the root, leaf and panicle, and was weakly detected in the stem, which indicated that ''SPL28'' is expressed in a tissue-specific manner. ''SPL28'' transcripts exhibited the opposite trend in ''spl28'' mutant plants. The ''spl28'' phenotype was reminiscent of mutants in which defense signaling pathways are constitutively active. The expression of two defense signaling-related genes, PR1 and PR2, was also examined in wild-type and spl28 mutant plants. Based on RT-PCR analysis, PR1 and PR2 in the ''spl28'' mutant were strongly expressed. In addition, ''SAG12'', a gene that encodes a cysteine protease that accumulates during leaf senescence, was strongly expressed in ''spl28'' mutants.&lt;br /&gt;
&lt;br /&gt;
The subcellular localization of ''SPL28'' was in  the Golgi apparatus (Fig. 9), which indicated that ''SPL28'' might be involved in the regulation of clathrin-associated adaptor prtein complex 1 (AP-1) membrane-cytoplasm recycling, together with clathrin, during transport vesicle formation and vesicle uncoating in rice.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
Please input evolution information here.&lt;br /&gt;
&lt;br /&gt;
You can also add sub-section(s) at will.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Department of Plant Science, Research Institute for Agriculture and Life Sciences, and Plant Genomics and Breeding Institute, Seoul National University, Seoul, 151-921, Republic of Korea;&lt;br /&gt;
*Crop Environment and Biotechnology Division, National Institute of Crop Science, RDA, Suwon, 441-857, Republic of Korea;&lt;br /&gt;
*Key Laboratory of Crop Germplasm Resources and Biotechnology, Ministry of Agriculture, Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing 100081, China&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Qiao YL, et al. (2010) ''SPL28'' encodes a clathrin‐associated adaptor protein complex 1, medium subunit μ1 (AP1M1) and is responsible for spotted leaf and early senescence in rice (''Oryza sativa''). New phytologist 185: 258-274.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&amp;lt;/references&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os01g0703600|&lt;br /&gt;
Description = Similar to Mu1 adaptin|&lt;br /&gt;
Version = NM_001050536.1 GI:115439442 GeneID:4324247|&lt;br /&gt;
Length = 3941 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os01g0703600, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 1|Chromosome 1]]|&lt;br /&gt;
AP = Chromosome 1:30922266..30926206|&lt;br /&gt;
CDS = 30922506..30922634,30922736..30922885,30922973..30923035,30923128..30923304,30923384..30923487&amp;lt;br&amp;gt;,30924730..30924837,30924924..30925020,30925128..30925225,30925306..30925447&amp;lt;br&amp;gt;,30925529..30925651,30925749..30925847|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008394:30922266..30926206&lt;br /&gt;
source=RiceChromosome01&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008394:30922266..30926206&lt;br /&gt;
source=RiceChromosome01&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggcgggcgcggtgtcggcgctgttccttctggacatcaagggccgcgtcctcgtctggcgcgactaccgcggcgacgtctccgccctccaggctgagcgcttcttcaccaagctcctcgacaaggagggcgactcggaggcgcactcgccggtggtctacgacgatgccggggtcacctacatgttcatccagcacaacaacgtgttcctactaaccgcctcccgccagaactgcaacgccgccagcatcctcctcttcctccaccgcgtcgttgatgtgttcaagcactatttcgaagagttggaggaagagtcgctgagggataactttgtcgttgtgtatgagttgcttgatgaaatgatggattttgggtacccacaatacacggaggcgaaaatcttaagtgaattcattaagacggatgcgtacaggatggaggtatcacagaggccacctatggcagtgacaaatgccgtgtcatggcggagtgagggtattcggtacaagaagaatgaagtgttcttggatgttgtggagagtgttaacattcttgttaacagcaatgggcagattgtgagatcagatgttgttggggcactgaagatgcggacatatttgagtggaatgcctgagtgcaaacttggattgaacgatagggttcttttggaggctcaaggccgagctactaaaggaaaagcaatagatcttgatgatattaaatttcaccagtgcgtgaggttggctagatttgagaatgatagaactatatccttcatacctcctgacggatctttcgatctaatgacatacagacttagcacccaggtaaaaccacttatctgggtggaagcacaaattgagaaacattcaagaagccgaatagaacttatggtgaaagcaagaagtcagtttaaggaaaggagcacagcaacaaatgttgaaattgaagtgcctgttccttcagatgctacgaaccctaatataagaacttcaatgggctctgctgcatatgcacctgagagagatgcaatggtctggaaagtaaaatcatttcctggtggcaaggattacatgtgcagagctgaatttagtcttccaagtataactgcagaagaagcagctcctgaaaagaaggcaccaatacgagtgaaatttgagataccatatttcactgtgtcgggtattcaggttcgctatctgaagatcattgaaaagagtgggtaccaggcgcttccttgggttagatacattacaatggctggtgaatacgaactgagacttatatga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MAGAVSALFLLDIKGRVLVWRDYRGDVSALQAERFFTKLLDKEG                     DSEAHSPVVYDDAGVTYMFIQHNNVFLLTASRQNCNAASILLFLHRVVDVFKHYFEEL                     EEESLRDNFVVVYELLDEMMDFGYPQYTEAKILSEFIKTDAYRMEVSQRPPMAVTNAV                     SWRSEGIRYKKNEVFLDVVESVNILVNSNGQIVRSDVVGALKMRTYLSGMPECKLGLN                     DRVLLEAQGRATKGKAIDLDDIKFHQCVRLARFENDRTISFIPPDGSFDLMTYRLSTQ                     VKPLIWVEAQIEKHSRSRIELMVKARSQFKERSTATNVEIEVPVPSDATNPNIRTSMG                     SAAYAPERDAMVWKVKSFPGGKDYMCRAEFSLPSITAEEAAPEKKAPIRVKFEIPYFT                     VSGIQVRYLKIIEKSGYQALPWVRYITMAGEYELRLI&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;241..369#471..620#708..770#863..1039#1119..1222#2465..2572#2659..2755#2863..2960#3041..3182#3264..3386#3484..3582#cgtctccactcccgatctccccgctccccgcgtcccgtctccgatccacccaaacacccgcaccgccgcgctacgcgagcacggcaccgcggcgcggcgcgactccgcaggcgacaagccgaggagaatcccgcgcccgcccgcccgcatcaccgccggatggccgccggccgtcgccggtagggcgataggcgggtagatccagatccggcggggcgggatcatatacaccccgcgccgatggcgggcgcggtgtcggcgctgttccttctggacatcaagggccgcgtcctcgtctggcgcgactaccgcggcgacgtctccgccctccaggctgagcgcttcttcaccaagctcctcgacaaggaggtaagcgctcgcgcatcccggcctctctctatctcctcgtcctcgtaggatctatgtggctcgccggtggcgttgcgcgctaagctgatgtgaaccaacagggcgactcggaggcgcactcgccggtggtctacgacgatgccggggtcacctacatgttcatccagcacaacaacgtgttcctactaaccgcctcccgccagaactgcaacgccgccagcatcctcctcttcctccaccgcgtcgttgatgtacgtatacccaccctggatcctgggacgcagatgacatgttcagcgttcagtttgttcacgaagttggtttgtgcatgagtgcaggtgttcaagcactatttcgaagagttggaggaagagtcgctgagggataactttgtcgttgtggtaagtaatggtgcaagcagctaagcatcactctggtttgctgcacaatctactggatttgacacaagatggtgtttgatttgtgcctgcagtatgagttgcttgatgaaatgatggattttgggtacccacaatacacggaggcgaaaatcttaagtgaattcattaagacggatgcgtacaggatggaggtatcacagaggccacctatggcagtgacaaatgccgtgtcatggcggagtgagggtattcggtacaagaagaatgaagtaagatacaggctcactctgttattttgggtagttttgtgatggtgctttccaaattatctaaccgatgtgtttccaggtgttcttggatgttgtggagagtgttaacattcttgttaacagcaatgggcagattgtgagatcagatgttgttggggcactgaagatgcggacatatttgaggtgagcctacaatgttattgtggaactagtagtatgatatctggatctgtaattcaatagggatcacatttatatgagtgaacattcagggtaccttcaatcggatctcaccaatagatgaagtgtccaacctaattgcccatttagaagaccatttatcagaaaattgaactgtttaagtgatggcctaagcaaacttttttactttctttatttgtgaagtaaacgcgtcatcttacttgctggttcatatgctcatttttcctgtaatcatgcatttaatatgtatttgtattccaattgttccattcttatgtgtgtcaaactaagtattatactaccgcttcacttctgaaatttcatgattttatcatgtagccatagtgtttcattgaccttttgcctttgaaagttttcaggaagtcttattctagaaacctcttcgtctctaacagattactgcttgtagattcttctgttatgcaactagatctatcataaatcttggacaaagaaatgaaagcatgctgaatgtcttttgagctagatcaatttccatgcaatactatctgacgactttagaattggttcaaagttcaaacgtcaactattgttatatgaatttgatttgccaaggctatcacgtatttgtataaagaactgctattgccacacattaaatcatcaaggaatttgatcaaggtagaaattcactctgtaagcactacctgggagatgtgccgcaccgtttttttctaatttttaaaatgtctatgcatcttttatatcccatattcagaaagaatggtggtctctcatatgatcataaagtgacttgcagttgaaagatggacatacaatttatgacctgggaacatcgatactgcatttcaagtgtttgatgttggccatacccatcacaaaatgttagcaaatacctctaaatgtcaattatagcttcggagcctacaaattaagattattaggatataagcaatgagagtgctttgcagattaccagaatttgggagtattccgtttaatttgtttcagatgtctaccttttagcagacattctgaactgatcatctgatgatgctcatgcgccatgctccccatcgaattatgttttccatctatgtttcaaagttcaaattatttgtgttatgctgtcaccccaaccatttatgttttcctgcacatctctgacccccactaatactgaacaatattgtgaatcagtggaatgcctgagtgcaaacttggattgaacgatagggttcttttggaggctcaaggccgagctactaaaggaaaagcaatagatcttgatgatattaaatttcaccagtaagtaaacagtttagcatttttttcaagtcactttgacaatttgagcagggccatatatgacctctctcttctgttattactaggtgcgtgaggttggctagatttgagaatgatagaactatatccttcatacctcctgacggatctttcgatctaatgacatacagacttagcacccaggttttctctactgcttgtgatttacagctattggatgctttagatacctgaaatgcactgccttgctccgctattctcatgcctgtctttttttatatatccttaaggtaaaaccacttatctgggtggaagcacaaattgagaaacattcaagaagccgaatagaacttatggtgaaagcaagaagtcagtttaaggaaaggaggtgagcattttacaagagcaatgtttgctgttacactaatgcctcttggaaggtgacatatttcctattttcacctgcagcacagcaacaaatgttgaaattgaagtgcctgttccttcagatgctacgaaccctaatataagaacttcaatgggctctgctgcatatgcacctgagagagatgcaatggtctggaaagtaaaatcatttcctggtggcaaggtaagtttcaagccaagtcatctttgccttctacttcatgctacctagaagtgtgctaatatatgtgagtttttctgttaggattacatgtgcagagctgaatttagtcttccaagtataactgcagaagaagcagctcctgaaaagaaggcaccaatacgagtgaaatttgagataccatatttcactgtgtcgggtattcaggtaatcaaattactattgcaaatatgtacttgattgctcttatggtacttctttgctatcttcactcaaaatgtatgccatcttgtattttctgcaggttcgctatctgaagatcattgaaaagagtgggtaccaggcgcttccttgggttagatacattacaatggctggtgaatacgaactgagacttatatgagttatctctgatatggctgctcaaagattttgatgctaaatttcaactcccaagatacatgtttgatgctcgatatacaacatatagttggcattgggacgttgccatggaagtctttgaaaagctcaaccatgcaaggtttttctgtctcgttgttcatcttgttagtgttactttaccatggttactgtaagttacccatcaagtatagctttgaaaaaaactttttttttgttcacttgtatcattattgatttatttttgtgggtgtcgaactttcccccttttgtactacacaaaaatcttgagctgaattggtataaatgaaatacctgggcggtgcttttgaagtccagatt&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001050536.1 RefSeq:Os01g0703600]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 1]]&lt;br /&gt;
[[Category:Chromosome 1]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:QiaoFig9.gif&amp;diff=175170</id>
		<title>File:QiaoFig9.gif</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:QiaoFig9.gif&amp;diff=175170"/>
				<updated>2014-05-31T15:02:53Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:QiaoFig6.gif&amp;diff=175169</id>
		<title>File:QiaoFig6.gif</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:QiaoFig6.gif&amp;diff=175169"/>
				<updated>2014-05-31T15:02:41Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os01g0703600&amp;diff=175168</id>
		<title>Os01g0703600</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os01g0703600&amp;diff=175168"/>
				<updated>2014-05-31T15:02:13Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;''SPL28'' encodes a clathrin-associated adaptor protein complex 1, medium subunit μ1 (AP1M1) and is responsible for spotted leaf and early senescence in rice.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File: QiaoFig1.gif|right|thumb|100px|Fig 1. Phenotype of the ''spotted leaf 28'' (''spl28'') mutant &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
A novel rice (''Oryza sativa'') spotted leaf mutant (''spl28'') that displays a lesion mimic phenotype in the absence of pathogen attack was isolated through treatment of Hwacheongbyeo (an elite Korean japonica cultivar) with N-methyl-N-nitrosourea (MNU). Early stage development of the ''spl28'' mutant was normal. However, after flowering, spl28 mutants exhibited a significant decrease in chlorophyll content, soluble protein content, and photosystem II efficiency, and high concentrations of reactive oxygen species (ROS), phytoalexin, callose, and autofluorescent phenolic compounds that localized in or around the lesions. The ''spl28'' mutant also exhibited significantly enhanced resistance to rice blast and bacterial blight. Using a map-based cloning approach, ''SPL28'' was determined to encode a clathrin-associated adaptor protein complex 1, medium subunit μ1 (AP1M1), which is involved in the post-Golgi trafficking pathway. A green fluorescent protein (GFP) fusion protein of ''SPL28'' (SPL28::GFP) localized to the Golgi apparatus, and expression of ''SPL28'' complemented the membrane trafficking defect of apm1-1Δ yeast mutants. ''SPL28'' was ubiquitously expressed and contained a highly conserved adaptor complex medium subunit (ACMS) family domain. ''SPL28'' appears to be involved in the regulation of vesicular trafficking, and ''SPL28'' dysfunction causes the formation of hypersensitive response (HR)-like lesions, leading to the initiation of leaf senescence &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
''SPL28'' was expressed in all organs examined. In wild-type plants, ''SPL28'' mRNA was most abundant in the root, leaf and panicle, and was weakly detected in the stem, which indicated that ''SPL28'' is expressed in a tissue-specific manner. ''SPL28'' transcripts exhibited the opposite trend in ''spl28'' mutant plants. The ''spl28'' phenotype was reminiscent of mutants in which defense signaling pathways are constitutively active. The expression of two defense signaling-related genes, PR1 and PR2, was also examined in wild-type and spl28 mutant plants. Based on RT-PCR analysis, PR1 and PR2 in the ''spl28'' mutant were strongly expressed. In addition, ''SAG12'', a gene that encodes a cysteine protease that accumulates during leaf senescence, was strongly expressed in ''spl28'' mutants.&lt;br /&gt;
&lt;br /&gt;
The subcellular localization of ''SPL28'' was in  the Golgi apparatus (Fig. 9), which indicated that ''SPL28'' might be involved in the regulation of clathrin-associated adaptor prtein complex 1 (AP-1) membrane-cytoplasm recycling, together with clathrin, during transport vesicle formation and vesicle uncoating in rice.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
Please input evolution information here.&lt;br /&gt;
&lt;br /&gt;
You can also add sub-section(s) at will.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Department of Plant Science, Research Institute for Agriculture and Life Sciences, and Plant Genomics and Breeding Institute, Seoul National University, Seoul, 151-921, Republic of Korea;&lt;br /&gt;
*Crop Environment and Biotechnology Division, National Institute of Crop Science, RDA, Suwon, 441-857, Republic of Korea;&lt;br /&gt;
*Key Laboratory of Crop Germplasm Resources and Biotechnology, Ministry of Agriculture, Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing 100081, China&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Qiao YL, et al. (2010) ''SPL28'' encodes a clathrin‐associated adaptor protein complex 1, medium subunit μ1 (AP1M1) and is responsible for spotted leaf and early senescence in rice (''Oryza sativa''). New phytologist 185: 258-274.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&amp;lt;/references&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os01g0703600|&lt;br /&gt;
Description = Similar to Mu1 adaptin|&lt;br /&gt;
Version = NM_001050536.1 GI:115439442 GeneID:4324247|&lt;br /&gt;
Length = 3941 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os01g0703600, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 1|Chromosome 1]]|&lt;br /&gt;
AP = Chromosome 1:30922266..30926206|&lt;br /&gt;
CDS = 30922506..30922634,30922736..30922885,30922973..30923035,30923128..30923304,30923384..30923487&amp;lt;br&amp;gt;,30924730..30924837,30924924..30925020,30925128..30925225,30925306..30925447&amp;lt;br&amp;gt;,30925529..30925651,30925749..30925847|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008394:30922266..30926206&lt;br /&gt;
source=RiceChromosome01&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008394:30922266..30926206&lt;br /&gt;
source=RiceChromosome01&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggcgggcgcggtgtcggcgctgttccttctggacatcaagggccgcgtcctcgtctggcgcgactaccgcggcgacgtctccgccctccaggctgagcgcttcttcaccaagctcctcgacaaggagggcgactcggaggcgcactcgccggtggtctacgacgatgccggggtcacctacatgttcatccagcacaacaacgtgttcctactaaccgcctcccgccagaactgcaacgccgccagcatcctcctcttcctccaccgcgtcgttgatgtgttcaagcactatttcgaagagttggaggaagagtcgctgagggataactttgtcgttgtgtatgagttgcttgatgaaatgatggattttgggtacccacaatacacggaggcgaaaatcttaagtgaattcattaagacggatgcgtacaggatggaggtatcacagaggccacctatggcagtgacaaatgccgtgtcatggcggagtgagggtattcggtacaagaagaatgaagtgttcttggatgttgtggagagtgttaacattcttgttaacagcaatgggcagattgtgagatcagatgttgttggggcactgaagatgcggacatatttgagtggaatgcctgagtgcaaacttggattgaacgatagggttcttttggaggctcaaggccgagctactaaaggaaaagcaatagatcttgatgatattaaatttcaccagtgcgtgaggttggctagatttgagaatgatagaactatatccttcatacctcctgacggatctttcgatctaatgacatacagacttagcacccaggtaaaaccacttatctgggtggaagcacaaattgagaaacattcaagaagccgaatagaacttatggtgaaagcaagaagtcagtttaaggaaaggagcacagcaacaaatgttgaaattgaagtgcctgttccttcagatgctacgaaccctaatataagaacttcaatgggctctgctgcatatgcacctgagagagatgcaatggtctggaaagtaaaatcatttcctggtggcaaggattacatgtgcagagctgaatttagtcttccaagtataactgcagaagaagcagctcctgaaaagaaggcaccaatacgagtgaaatttgagataccatatttcactgtgtcgggtattcaggttcgctatctgaagatcattgaaaagagtgggtaccaggcgcttccttgggttagatacattacaatggctggtgaatacgaactgagacttatatga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MAGAVSALFLLDIKGRVLVWRDYRGDVSALQAERFFTKLLDKEG                     DSEAHSPVVYDDAGVTYMFIQHNNVFLLTASRQNCNAASILLFLHRVVDVFKHYFEEL                     EEESLRDNFVVVYELLDEMMDFGYPQYTEAKILSEFIKTDAYRMEVSQRPPMAVTNAV                     SWRSEGIRYKKNEVFLDVVESVNILVNSNGQIVRSDVVGALKMRTYLSGMPECKLGLN                     DRVLLEAQGRATKGKAIDLDDIKFHQCVRLARFENDRTISFIPPDGSFDLMTYRLSTQ                     VKPLIWVEAQIEKHSRSRIELMVKARSQFKERSTATNVEIEVPVPSDATNPNIRTSMG                     SAAYAPERDAMVWKVKSFPGGKDYMCRAEFSLPSITAEEAAPEKKAPIRVKFEIPYFT                     VSGIQVRYLKIIEKSGYQALPWVRYITMAGEYELRLI&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;241..369#471..620#708..770#863..1039#1119..1222#2465..2572#2659..2755#2863..2960#3041..3182#3264..3386#3484..3582#cgtctccactcccgatctccccgctccccgcgtcccgtctccgatccacccaaacacccgcaccgccgcgctacgcgagcacggcaccgcggcgcggcgcgactccgcaggcgacaagccgaggagaatcccgcgcccgcccgcccgcatcaccgccggatggccgccggccgtcgccggtagggcgataggcgggtagatccagatccggcggggcgggatcatatacaccccgcgccgatggcgggcgcggtgtcggcgctgttccttctggacatcaagggccgcgtcctcgtctggcgcgactaccgcggcgacgtctccgccctccaggctgagcgcttcttcaccaagctcctcgacaaggaggtaagcgctcgcgcatcccggcctctctctatctcctcgtcctcgtaggatctatgtggctcgccggtggcgttgcgcgctaagctgatgtgaaccaacagggcgactcggaggcgcactcgccggtggtctacgacgatgccggggtcacctacatgttcatccagcacaacaacgtgttcctactaaccgcctcccgccagaactgcaacgccgccagcatcctcctcttcctccaccgcgtcgttgatgtacgtatacccaccctggatcctgggacgcagatgacatgttcagcgttcagtttgttcacgaagttggtttgtgcatgagtgcaggtgttcaagcactatttcgaagagttggaggaagagtcgctgagggataactttgtcgttgtggtaagtaatggtgcaagcagctaagcatcactctggtttgctgcacaatctactggatttgacacaagatggtgtttgatttgtgcctgcagtatgagttgcttgatgaaatgatggattttgggtacccacaatacacggaggcgaaaatcttaagtgaattcattaagacggatgcgtacaggatggaggtatcacagaggccacctatggcagtgacaaatgccgtgtcatggcggagtgagggtattcggtacaagaagaatgaagtaagatacaggctcactctgttattttgggtagttttgtgatggtgctttccaaattatctaaccgatgtgtttccaggtgttcttggatgttgtggagagtgttaacattcttgttaacagcaatgggcagattgtgagatcagatgttgttggggcactgaagatgcggacatatttgaggtgagcctacaatgttattgtggaactagtagtatgatatctggatctgtaattcaatagggatcacatttatatgagtgaacattcagggtaccttcaatcggatctcaccaatagatgaagtgtccaacctaattgcccatttagaagaccatttatcagaaaattgaactgtttaagtgatggcctaagcaaacttttttactttctttatttgtgaagtaaacgcgtcatcttacttgctggttcatatgctcatttttcctgtaatcatgcatttaatatgtatttgtattccaattgttccattcttatgtgtgtcaaactaagtattatactaccgcttcacttctgaaatttcatgattttatcatgtagccatagtgtttcattgaccttttgcctttgaaagttttcaggaagtcttattctagaaacctcttcgtctctaacagattactgcttgtagattcttctgttatgcaactagatctatcataaatcttggacaaagaaatgaaagcatgctgaatgtcttttgagctagatcaatttccatgcaatactatctgacgactttagaattggttcaaagttcaaacgtcaactattgttatatgaatttgatttgccaaggctatcacgtatttgtataaagaactgctattgccacacattaaatcatcaaggaatttgatcaaggtagaaattcactctgtaagcactacctgggagatgtgccgcaccgtttttttctaatttttaaaatgtctatgcatcttttatatcccatattcagaaagaatggtggtctctcatatgatcataaagtgacttgcagttgaaagatggacatacaatttatgacctgggaacatcgatactgcatttcaagtgtttgatgttggccatacccatcacaaaatgttagcaaatacctctaaatgtcaattatagcttcggagcctacaaattaagattattaggatataagcaatgagagtgctttgcagattaccagaatttgggagtattccgtttaatttgtttcagatgtctaccttttagcagacattctgaactgatcatctgatgatgctcatgcgccatgctccccatcgaattatgttttccatctatgtttcaaagttcaaattatttgtgttatgctgtcaccccaaccatttatgttttcctgcacatctctgacccccactaatactgaacaatattgtgaatcagtggaatgcctgagtgcaaacttggattgaacgatagggttcttttggaggctcaaggccgagctactaaaggaaaagcaatagatcttgatgatattaaatttcaccagtaagtaaacagtttagcatttttttcaagtcactttgacaatttgagcagggccatatatgacctctctcttctgttattactaggtgcgtgaggttggctagatttgagaatgatagaactatatccttcatacctcctgacggatctttcgatctaatgacatacagacttagcacccaggttttctctactgcttgtgatttacagctattggatgctttagatacctgaaatgcactgccttgctccgctattctcatgcctgtctttttttatatatccttaaggtaaaaccacttatctgggtggaagcacaaattgagaaacattcaagaagccgaatagaacttatggtgaaagcaagaagtcagtttaaggaaaggaggtgagcattttacaagagcaatgtttgctgttacactaatgcctcttggaaggtgacatatttcctattttcacctgcagcacagcaacaaatgttgaaattgaagtgcctgttccttcagatgctacgaaccctaatataagaacttcaatgggctctgctgcatatgcacctgagagagatgcaatggtctggaaagtaaaatcatttcctggtggcaaggtaagtttcaagccaagtcatctttgccttctacttcatgctacctagaagtgtgctaatatatgtgagtttttctgttaggattacatgtgcagagctgaatttagtcttccaagtataactgcagaagaagcagctcctgaaaagaaggcaccaatacgagtgaaatttgagataccatatttcactgtgtcgggtattcaggtaatcaaattactattgcaaatatgtacttgattgctcttatggtacttctttgctatcttcactcaaaatgtatgccatcttgtattttctgcaggttcgctatctgaagatcattgaaaagagtgggtaccaggcgcttccttgggttagatacattacaatggctggtgaatacgaactgagacttatatgagttatctctgatatggctgctcaaagattttgatgctaaatttcaactcccaagatacatgtttgatgctcgatatacaacatatagttggcattgggacgttgccatggaagtctttgaaaagctcaaccatgcaaggtttttctgtctcgttgttcatcttgttagtgttactttaccatggttactgtaagttacccatcaagtatagctttgaaaaaaactttttttttgttcacttgtatcattattgatttatttttgtgggtgtcgaactttcccccttttgtactacacaaaaatcttgagctgaattggtataaatgaaatacctgggcggtgcttttgaagtccagatt&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001050536.1 RefSeq:Os01g0703600]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 1]]&lt;br /&gt;
[[Category:Chromosome 1]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os01g0703600&amp;diff=175166</id>
		<title>Os01g0703600</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os01g0703600&amp;diff=175166"/>
				<updated>2014-05-31T14:51:39Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;''SPL28'' encodes a clathrin-associated adaptor protein complex 1, medium subunit μ1 (AP1M1) and is responsible for spotted leaf and early senescence in rice.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File: QiaoFig1.gif|right|thumb|100px|Fig 1. Phenotype of the ''spotted leaf 28'' (''spl28'') mutant &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
A novel rice (''Oryza sativa'') spotted leaf mutant (''spl28'') that displays a lesion mimic phenotype in the absence of pathogen attack was isolated through treatment of Hwacheongbyeo (an elite Korean japonica cultivar) with N-methyl-N-nitrosourea (MNU). Early stage development of the ''spl28'' mutant was normal. However, after flowering, spl28 mutants exhibited a significant decrease in chlorophyll content, soluble protein content, and photosystem II efficiency, and high concentrations of reactive oxygen species (ROS), phytoalexin, callose, and autofluorescent phenolic compounds that localized in or around the lesions. The ''spl28'' mutant also exhibited significantly enhanced resistance to rice blast and bacterial blight. Using a map-based cloning approach, ''SPL28'' was determined to encode a clathrin-associated adaptor protein complex 1, medium subunit μ1 (AP1M1), which is involved in the post-Golgi trafficking pathway. A green fluorescent protein (GFP) fusion protein of ''SPL28'' (SPL28::GFP) localized to the Golgi apparatus, and expression of ''SPL28'' complemented the membrane trafficking defect of apm1-1Δ yeast mutants. ''SPL28'' was ubiquitously expressed and contained a highly conserved adaptor complex medium subunit (ACMS) family domain. ''SPL28'' appears to be involved in the regulation of vesicular trafficking, and ''SPL28'' dysfunction causes the formation of hypersensitive response (HR)-like lesions, leading to the initiation of leaf senescence &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
Please input expression information here.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
Please input evolution information here.&lt;br /&gt;
&lt;br /&gt;
You can also add sub-section(s) at will.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Department of Plant Science, Research Institute for Agriculture and Life Sciences, and Plant Genomics and Breeding Institute, Seoul National University, Seoul, 151-921, Republic of Korea;&lt;br /&gt;
*Crop Environment and Biotechnology Division, National Institute of Crop Science, RDA, Suwon, 441-857, Republic of Korea;&lt;br /&gt;
*Key Laboratory of Crop Germplasm Resources and Biotechnology, Ministry of Agriculture, Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing 100081, China&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Qiao YL, et al. (2010) ''SPL28'' encodes a clathrin‐associated adaptor protein complex 1, medium subunit μ1 (AP1M1) and is responsible for spotted leaf and early senescence in rice (''Oryza sativa''). New phytologist 185: 258-274.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&amp;lt;/references&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os01g0703600|&lt;br /&gt;
Description = Similar to Mu1 adaptin|&lt;br /&gt;
Version = NM_001050536.1 GI:115439442 GeneID:4324247|&lt;br /&gt;
Length = 3941 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os01g0703600, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 1|Chromosome 1]]|&lt;br /&gt;
AP = Chromosome 1:30922266..30926206|&lt;br /&gt;
CDS = 30922506..30922634,30922736..30922885,30922973..30923035,30923128..30923304,30923384..30923487&amp;lt;br&amp;gt;,30924730..30924837,30924924..30925020,30925128..30925225,30925306..30925447&amp;lt;br&amp;gt;,30925529..30925651,30925749..30925847|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008394:30922266..30926206&lt;br /&gt;
source=RiceChromosome01&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008394:30922266..30926206&lt;br /&gt;
source=RiceChromosome01&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggcgggcgcggtgtcggcgctgttccttctggacatcaagggccgcgtcctcgtctggcgcgactaccgcggcgacgtctccgccctccaggctgagcgcttcttcaccaagctcctcgacaaggagggcgactcggaggcgcactcgccggtggtctacgacgatgccggggtcacctacatgttcatccagcacaacaacgtgttcctactaaccgcctcccgccagaactgcaacgccgccagcatcctcctcttcctccaccgcgtcgttgatgtgttcaagcactatttcgaagagttggaggaagagtcgctgagggataactttgtcgttgtgtatgagttgcttgatgaaatgatggattttgggtacccacaatacacggaggcgaaaatcttaagtgaattcattaagacggatgcgtacaggatggaggtatcacagaggccacctatggcagtgacaaatgccgtgtcatggcggagtgagggtattcggtacaagaagaatgaagtgttcttggatgttgtggagagtgttaacattcttgttaacagcaatgggcagattgtgagatcagatgttgttggggcactgaagatgcggacatatttgagtggaatgcctgagtgcaaacttggattgaacgatagggttcttttggaggctcaaggccgagctactaaaggaaaagcaatagatcttgatgatattaaatttcaccagtgcgtgaggttggctagatttgagaatgatagaactatatccttcatacctcctgacggatctttcgatctaatgacatacagacttagcacccaggtaaaaccacttatctgggtggaagcacaaattgagaaacattcaagaagccgaatagaacttatggtgaaagcaagaagtcagtttaaggaaaggagcacagcaacaaatgttgaaattgaagtgcctgttccttcagatgctacgaaccctaatataagaacttcaatgggctctgctgcatatgcacctgagagagatgcaatggtctggaaagtaaaatcatttcctggtggcaaggattacatgtgcagagctgaatttagtcttccaagtataactgcagaagaagcagctcctgaaaagaaggcaccaatacgagtgaaatttgagataccatatttcactgtgtcgggtattcaggttcgctatctgaagatcattgaaaagagtgggtaccaggcgcttccttgggttagatacattacaatggctggtgaatacgaactgagacttatatga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MAGAVSALFLLDIKGRVLVWRDYRGDVSALQAERFFTKLLDKEG                     DSEAHSPVVYDDAGVTYMFIQHNNVFLLTASRQNCNAASILLFLHRVVDVFKHYFEEL                     EEESLRDNFVVVYELLDEMMDFGYPQYTEAKILSEFIKTDAYRMEVSQRPPMAVTNAV                     SWRSEGIRYKKNEVFLDVVESVNILVNSNGQIVRSDVVGALKMRTYLSGMPECKLGLN                     DRVLLEAQGRATKGKAIDLDDIKFHQCVRLARFENDRTISFIPPDGSFDLMTYRLSTQ                     VKPLIWVEAQIEKHSRSRIELMVKARSQFKERSTATNVEIEVPVPSDATNPNIRTSMG                     SAAYAPERDAMVWKVKSFPGGKDYMCRAEFSLPSITAEEAAPEKKAPIRVKFEIPYFT                     VSGIQVRYLKIIEKSGYQALPWVRYITMAGEYELRLI&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;241..369#471..620#708..770#863..1039#1119..1222#2465..2572#2659..2755#2863..2960#3041..3182#3264..3386#3484..3582#cgtctccactcccgatctccccgctccccgcgtcccgtctccgatccacccaaacacccgcaccgccgcgctacgcgagcacggcaccgcggcgcggcgcgactccgcaggcgacaagccgaggagaatcccgcgcccgcccgcccgcatcaccgccggatggccgccggccgtcgccggtagggcgataggcgggtagatccagatccggcggggcgggatcatatacaccccgcgccgatggcgggcgcggtgtcggcgctgttccttctggacatcaagggccgcgtcctcgtctggcgcgactaccgcggcgacgtctccgccctccaggctgagcgcttcttcaccaagctcctcgacaaggaggtaagcgctcgcgcatcccggcctctctctatctcctcgtcctcgtaggatctatgtggctcgccggtggcgttgcgcgctaagctgatgtgaaccaacagggcgactcggaggcgcactcgccggtggtctacgacgatgccggggtcacctacatgttcatccagcacaacaacgtgttcctactaaccgcctcccgccagaactgcaacgccgccagcatcctcctcttcctccaccgcgtcgttgatgtacgtatacccaccctggatcctgggacgcagatgacatgttcagcgttcagtttgttcacgaagttggtttgtgcatgagtgcaggtgttcaagcactatttcgaagagttggaggaagagtcgctgagggataactttgtcgttgtggtaagtaatggtgcaagcagctaagcatcactctggtttgctgcacaatctactggatttgacacaagatggtgtttgatttgtgcctgcagtatgagttgcttgatgaaatgatggattttgggtacccacaatacacggaggcgaaaatcttaagtgaattcattaagacggatgcgtacaggatggaggtatcacagaggccacctatggcagtgacaaatgccgtgtcatggcggagtgagggtattcggtacaagaagaatgaagtaagatacaggctcactctgttattttgggtagttttgtgatggtgctttccaaattatctaaccgatgtgtttccaggtgttcttggatgttgtggagagtgttaacattcttgttaacagcaatgggcagattgtgagatcagatgttgttggggcactgaagatgcggacatatttgaggtgagcctacaatgttattgtggaactagtagtatgatatctggatctgtaattcaatagggatcacatttatatgagtgaacattcagggtaccttcaatcggatctcaccaatagatgaagtgtccaacctaattgcccatttagaagaccatttatcagaaaattgaactgtttaagtgatggcctaagcaaacttttttactttctttatttgtgaagtaaacgcgtcatcttacttgctggttcatatgctcatttttcctgtaatcatgcatttaatatgtatttgtattccaattgttccattcttatgtgtgtcaaactaagtattatactaccgcttcacttctgaaatttcatgattttatcatgtagccatagtgtttcattgaccttttgcctttgaaagttttcaggaagtcttattctagaaacctcttcgtctctaacagattactgcttgtagattcttctgttatgcaactagatctatcataaatcttggacaaagaaatgaaagcatgctgaatgtcttttgagctagatcaatttccatgcaatactatctgacgactttagaattggttcaaagttcaaacgtcaactattgttatatgaatttgatttgccaaggctatcacgtatttgtataaagaactgctattgccacacattaaatcatcaaggaatttgatcaaggtagaaattcactctgtaagcactacctgggagatgtgccgcaccgtttttttctaatttttaaaatgtctatgcatcttttatatcccatattcagaaagaatggtggtctctcatatgatcataaagtgacttgcagttgaaagatggacatacaatttatgacctgggaacatcgatactgcatttcaagtgtttgatgttggccatacccatcacaaaatgttagcaaatacctctaaatgtcaattatagcttcggagcctacaaattaagattattaggatataagcaatgagagtgctttgcagattaccagaatttgggagtattccgtttaatttgtttcagatgtctaccttttagcagacattctgaactgatcatctgatgatgctcatgcgccatgctccccatcgaattatgttttccatctatgtttcaaagttcaaattatttgtgttatgctgtcaccccaaccatttatgttttcctgcacatctctgacccccactaatactgaacaatattgtgaatcagtggaatgcctgagtgcaaacttggattgaacgatagggttcttttggaggctcaaggccgagctactaaaggaaaagcaatagatcttgatgatattaaatttcaccagtaagtaaacagtttagcatttttttcaagtcactttgacaatttgagcagggccatatatgacctctctcttctgttattactaggtgcgtgaggttggctagatttgagaatgatagaactatatccttcatacctcctgacggatctttcgatctaatgacatacagacttagcacccaggttttctctactgcttgtgatttacagctattggatgctttagatacctgaaatgcactgccttgctccgctattctcatgcctgtctttttttatatatccttaaggtaaaaccacttatctgggtggaagcacaaattgagaaacattcaagaagccgaatagaacttatggtgaaagcaagaagtcagtttaaggaaaggaggtgagcattttacaagagcaatgtttgctgttacactaatgcctcttggaaggtgacatatttcctattttcacctgcagcacagcaacaaatgttgaaattgaagtgcctgttccttcagatgctacgaaccctaatataagaacttcaatgggctctgctgcatatgcacctgagagagatgcaatggtctggaaagtaaaatcatttcctggtggcaaggtaagtttcaagccaagtcatctttgccttctacttcatgctacctagaagtgtgctaatatatgtgagtttttctgttaggattacatgtgcagagctgaatttagtcttccaagtataactgcagaagaagcagctcctgaaaagaaggcaccaatacgagtgaaatttgagataccatatttcactgtgtcgggtattcaggtaatcaaattactattgcaaatatgtacttgattgctcttatggtacttctttgctatcttcactcaaaatgtatgccatcttgtattttctgcaggttcgctatctgaagatcattgaaaagagtgggtaccaggcgcttccttgggttagatacattacaatggctggtgaatacgaactgagacttatatgagttatctctgatatggctgctcaaagattttgatgctaaatttcaactcccaagatacatgtttgatgctcgatatacaacatatagttggcattgggacgttgccatggaagtctttgaaaagctcaaccatgcaaggtttttctgtctcgttgttcatcttgttagtgttactttaccatggttactgtaagttacccatcaagtatagctttgaaaaaaactttttttttgttcacttgtatcattattgatttatttttgtgggtgtcgaactttcccccttttgtactacacaaaaatcttgagctgaattggtataaatgaaatacctgggcggtgcttttgaagtccagatt&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001050536.1 RefSeq:Os01g0703600]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 1]]&lt;br /&gt;
[[Category:Chromosome 1]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:QiaoFig1.gif&amp;diff=175165</id>
		<title>File:QiaoFig1.gif</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:QiaoFig1.gif&amp;diff=175165"/>
				<updated>2014-05-31T14:50:14Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os01g0703600&amp;diff=174779</id>
		<title>Os01g0703600</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os01g0703600&amp;diff=174779"/>
				<updated>2014-05-31T01:45:55Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;''SPL28'' encodes a clathrin-associated adaptor protein complex 1, medium subunit μ1 (AP1M1) and is responsible for spotted leaf and early senescence in rice.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
A novel rice (''Oryza sativa'') spotted leaf mutant (''spl28'') that displays a lesion mimic phenotype in the absence of pathogen attack was isolated through treatment of Hwacheongbyeo (an elite Korean japonica cultivar) with N-methyl-N-nitrosourea (MNU). Early stage development of the ''spl28'' mutant was normal. However, after flowering, spl28 mutants exhibited a significant decrease in chlorophyll content, soluble protein content, and photosystem II efficiency, and high concentrations of reactive oxygen species (ROS), phytoalexin, callose, and autofluorescent phenolic compounds that localized in or around the lesions. The ''spl28'' mutant also exhibited significantly enhanced resistance to rice blast and bacterial blight. Using a map-based cloning approach, ''SPL28'' was determined to encode a clathrin-associated adaptor protein complex 1, medium subunit μ1 (AP1M1), which is involved in the post-Golgi trafficking pathway. A green fluorescent protein (GFP) fusion protein of ''SPL28'' (SPL28::GFP) localized to the Golgi apparatus, and expression of ''SPL28'' complemented the membrane trafficking defect of apm1-1Δ yeast mutants. ''SPL28'' was ubiquitously expressed and contained a highly conserved adaptor complex medium subunit (ACMS) family domain. ''SPL28'' appears to be involved in the regulation of vesicular trafficking, and ''SPL28'' dysfunction causes the formation of hypersensitive response (HR)-like lesions, leading to the initiation of leaf senescence &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
Please input expression information here.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
Please input evolution information here.&lt;br /&gt;
&lt;br /&gt;
You can also add sub-section(s) at will.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Department of Plant Science, Research Institute for Agriculture and Life Sciences, and Plant Genomics and Breeding Institute, Seoul National University, Seoul, 151-921, Republic of Korea;&lt;br /&gt;
*Crop Environment and Biotechnology Division, National Institute of Crop Science, RDA, Suwon, 441-857, Republic of Korea;&lt;br /&gt;
*Key Laboratory of Crop Germplasm Resources and Biotechnology, Ministry of Agriculture, Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing 100081, China&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Qiao YL, et al. (2010) ''SPL28'' encodes a clathrin‐associated adaptor protein complex 1, medium subunit μ1 (AP1M1) and is responsible for spotted leaf and early senescence in rice (''Oryza sativa''). New phytologist 185: 258-274.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&amp;lt;/references&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os01g0703600|&lt;br /&gt;
Description = Similar to Mu1 adaptin|&lt;br /&gt;
Version = NM_001050536.1 GI:115439442 GeneID:4324247|&lt;br /&gt;
Length = 3941 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os01g0703600, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 1|Chromosome 1]]|&lt;br /&gt;
AP = Chromosome 1:30922266..30926206|&lt;br /&gt;
CDS = 30922506..30922634,30922736..30922885,30922973..30923035,30923128..30923304,30923384..30923487&amp;lt;br&amp;gt;,30924730..30924837,30924924..30925020,30925128..30925225,30925306..30925447&amp;lt;br&amp;gt;,30925529..30925651,30925749..30925847|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008394:30922266..30926206&lt;br /&gt;
source=RiceChromosome01&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008394:30922266..30926206&lt;br /&gt;
source=RiceChromosome01&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggcgggcgcggtgtcggcgctgttccttctggacatcaagggccgcgtcctcgtctggcgcgactaccgcggcgacgtctccgccctccaggctgagcgcttcttcaccaagctcctcgacaaggagggcgactcggaggcgcactcgccggtggtctacgacgatgccggggtcacctacatgttcatccagcacaacaacgtgttcctactaaccgcctcccgccagaactgcaacgccgccagcatcctcctcttcctccaccgcgtcgttgatgtgttcaagcactatttcgaagagttggaggaagagtcgctgagggataactttgtcgttgtgtatgagttgcttgatgaaatgatggattttgggtacccacaatacacggaggcgaaaatcttaagtgaattcattaagacggatgcgtacaggatggaggtatcacagaggccacctatggcagtgacaaatgccgtgtcatggcggagtgagggtattcggtacaagaagaatgaagtgttcttggatgttgtggagagtgttaacattcttgttaacagcaatgggcagattgtgagatcagatgttgttggggcactgaagatgcggacatatttgagtggaatgcctgagtgcaaacttggattgaacgatagggttcttttggaggctcaaggccgagctactaaaggaaaagcaatagatcttgatgatattaaatttcaccagtgcgtgaggttggctagatttgagaatgatagaactatatccttcatacctcctgacggatctttcgatctaatgacatacagacttagcacccaggtaaaaccacttatctgggtggaagcacaaattgagaaacattcaagaagccgaatagaacttatggtgaaagcaagaagtcagtttaaggaaaggagcacagcaacaaatgttgaaattgaagtgcctgttccttcagatgctacgaaccctaatataagaacttcaatgggctctgctgcatatgcacctgagagagatgcaatggtctggaaagtaaaatcatttcctggtggcaaggattacatgtgcagagctgaatttagtcttccaagtataactgcagaagaagcagctcctgaaaagaaggcaccaatacgagtgaaatttgagataccatatttcactgtgtcgggtattcaggttcgctatctgaagatcattgaaaagagtgggtaccaggcgcttccttgggttagatacattacaatggctggtgaatacgaactgagacttatatga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MAGAVSALFLLDIKGRVLVWRDYRGDVSALQAERFFTKLLDKEG                     DSEAHSPVVYDDAGVTYMFIQHNNVFLLTASRQNCNAASILLFLHRVVDVFKHYFEEL                     EEESLRDNFVVVYELLDEMMDFGYPQYTEAKILSEFIKTDAYRMEVSQRPPMAVTNAV                     SWRSEGIRYKKNEVFLDVVESVNILVNSNGQIVRSDVVGALKMRTYLSGMPECKLGLN                     DRVLLEAQGRATKGKAIDLDDIKFHQCVRLARFENDRTISFIPPDGSFDLMTYRLSTQ                     VKPLIWVEAQIEKHSRSRIELMVKARSQFKERSTATNVEIEVPVPSDATNPNIRTSMG                     SAAYAPERDAMVWKVKSFPGGKDYMCRAEFSLPSITAEEAAPEKKAPIRVKFEIPYFT                     VSGIQVRYLKIIEKSGYQALPWVRYITMAGEYELRLI&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;241..369#471..620#708..770#863..1039#1119..1222#2465..2572#2659..2755#2863..2960#3041..3182#3264..3386#3484..3582#cgtctccactcccgatctccccgctccccgcgtcccgtctccgatccacccaaacacccgcaccgccgcgctacgcgagcacggcaccgcggcgcggcgcgactccgcaggcgacaagccgaggagaatcccgcgcccgcccgcccgcatcaccgccggatggccgccggccgtcgccggtagggcgataggcgggtagatccagatccggcggggcgggatcatatacaccccgcgccgatggcgggcgcggtgtcggcgctgttccttctggacatcaagggccgcgtcctcgtctggcgcgactaccgcggcgacgtctccgccctccaggctgagcgcttcttcaccaagctcctcgacaaggaggtaagcgctcgcgcatcccggcctctctctatctcctcgtcctcgtaggatctatgtggctcgccggtggcgttgcgcgctaagctgatgtgaaccaacagggcgactcggaggcgcactcgccggtggtctacgacgatgccggggtcacctacatgttcatccagcacaacaacgtgttcctactaaccgcctcccgccagaactgcaacgccgccagcatcctcctcttcctccaccgcgtcgttgatgtacgtatacccaccctggatcctgggacgcagatgacatgttcagcgttcagtttgttcacgaagttggtttgtgcatgagtgcaggtgttcaagcactatttcgaagagttggaggaagagtcgctgagggataactttgtcgttgtggtaagtaatggtgcaagcagctaagcatcactctggtttgctgcacaatctactggatttgacacaagatggtgtttgatttgtgcctgcagtatgagttgcttgatgaaatgatggattttgggtacccacaatacacggaggcgaaaatcttaagtgaattcattaagacggatgcgtacaggatggaggtatcacagaggccacctatggcagtgacaaatgccgtgtcatggcggagtgagggtattcggtacaagaagaatgaagtaagatacaggctcactctgttattttgggtagttttgtgatggtgctttccaaattatctaaccgatgtgtttccaggtgttcttggatgttgtggagagtgttaacattcttgttaacagcaatgggcagattgtgagatcagatgttgttggggcactgaagatgcggacatatttgaggtgagcctacaatgttattgtggaactagtagtatgatatctggatctgtaattcaatagggatcacatttatatgagtgaacattcagggtaccttcaatcggatctcaccaatagatgaagtgtccaacctaattgcccatttagaagaccatttatcagaaaattgaactgtttaagtgatggcctaagcaaacttttttactttctttatttgtgaagtaaacgcgtcatcttacttgctggttcatatgctcatttttcctgtaatcatgcatttaatatgtatttgtattccaattgttccattcttatgtgtgtcaaactaagtattatactaccgcttcacttctgaaatttcatgattttatcatgtagccatagtgtttcattgaccttttgcctttgaaagttttcaggaagtcttattctagaaacctcttcgtctctaacagattactgcttgtagattcttctgttatgcaactagatctatcataaatcttggacaaagaaatgaaagcatgctgaatgtcttttgagctagatcaatttccatgcaatactatctgacgactttagaattggttcaaagttcaaacgtcaactattgttatatgaatttgatttgccaaggctatcacgtatttgtataaagaactgctattgccacacattaaatcatcaaggaatttgatcaaggtagaaattcactctgtaagcactacctgggagatgtgccgcaccgtttttttctaatttttaaaatgtctatgcatcttttatatcccatattcagaaagaatggtggtctctcatatgatcataaagtgacttgcagttgaaagatggacatacaatttatgacctgggaacatcgatactgcatttcaagtgtttgatgttggccatacccatcacaaaatgttagcaaatacctctaaatgtcaattatagcttcggagcctacaaattaagattattaggatataagcaatgagagtgctttgcagattaccagaatttgggagtattccgtttaatttgtttcagatgtctaccttttagcagacattctgaactgatcatctgatgatgctcatgcgccatgctccccatcgaattatgttttccatctatgtttcaaagttcaaattatttgtgttatgctgtcaccccaaccatttatgttttcctgcacatctctgacccccactaatactgaacaatattgtgaatcagtggaatgcctgagtgcaaacttggattgaacgatagggttcttttggaggctcaaggccgagctactaaaggaaaagcaatagatcttgatgatattaaatttcaccagtaagtaaacagtttagcatttttttcaagtcactttgacaatttgagcagggccatatatgacctctctcttctgttattactaggtgcgtgaggttggctagatttgagaatgatagaactatatccttcatacctcctgacggatctttcgatctaatgacatacagacttagcacccaggttttctctactgcttgtgatttacagctattggatgctttagatacctgaaatgcactgccttgctccgctattctcatgcctgtctttttttatatatccttaaggtaaaaccacttatctgggtggaagcacaaattgagaaacattcaagaagccgaatagaacttatggtgaaagcaagaagtcagtttaaggaaaggaggtgagcattttacaagagcaatgtttgctgttacactaatgcctcttggaaggtgacatatttcctattttcacctgcagcacagcaacaaatgttgaaattgaagtgcctgttccttcagatgctacgaaccctaatataagaacttcaatgggctctgctgcatatgcacctgagagagatgcaatggtctggaaagtaaaatcatttcctggtggcaaggtaagtttcaagccaagtcatctttgccttctacttcatgctacctagaagtgtgctaatatatgtgagtttttctgttaggattacatgtgcagagctgaatttagtcttccaagtataactgcagaagaagcagctcctgaaaagaaggcaccaatacgagtgaaatttgagataccatatttcactgtgtcgggtattcaggtaatcaaattactattgcaaatatgtacttgattgctcttatggtacttctttgctatcttcactcaaaatgtatgccatcttgtattttctgcaggttcgctatctgaagatcattgaaaagagtgggtaccaggcgcttccttgggttagatacattacaatggctggtgaatacgaactgagacttatatgagttatctctgatatggctgctcaaagattttgatgctaaatttcaactcccaagatacatgtttgatgctcgatatacaacatatagttggcattgggacgttgccatggaagtctttgaaaagctcaaccatgcaaggtttttctgtctcgttgttcatcttgttagtgttactttaccatggttactgtaagttacccatcaagtatagctttgaaaaaaactttttttttgttcacttgtatcattattgatttatttttgtgggtgtcgaactttcccccttttgtactacacaaaaatcttgagctgaattggtataaatgaaatacctgggcggtgcttttgaagtccagatt&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001050536.1 RefSeq:Os01g0703600]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 1]]&lt;br /&gt;
[[Category:Chromosome 1]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174769</id>
		<title>Os10g0478000</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174769"/>
				<updated>2014-05-31T01:24:34Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; The rice ''TAWAWA1'' (''TAW1'') gene, a member of ALOG family, was identified as a  regulator of rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:YoshidaF1.jpg|right|thumb|100px|Fig 1. Characterization of ''taw1'' dominant mutants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF2.jpg|right|thumb|100px|Fig 2. Isolation of the ''TAW1'' gene &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF3.jpg|right|thumb|100px|Fig 3. Expression pattern of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF4.jpg|right|thumb|100px|Fig 4. ''SVP'' subfamily MADS-box genes work downstream of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF5.jpg|right|thumb|100px|Fig 5. Phenotype of ''taw1-D2''–introgressed Koshihikari BC5F2 plants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
In the dominant gain-of-function mutant ''tawawa1-D'' (Fig. 1), the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in ''TAWAWA1'' (''TAW1'') activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. ''TAW1'' encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the branch meristem (BMs). ''TAW1'' expression disappears from incipient spikelet meristems (SMs). It is demonstrated that members of the ''SHORT VEGETATIVE PHASE'' subfamily of MADS-box genes function downstream of ''TAW1''. Thus, ''TAW1'' is proposed as a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
To understand the molecular links between the control of meristem phase transition and inflorescence structure, mutants were identified with altered inflorescence branching patterns &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;. Two lines with increased branching phenotypes were isolated from a screening population in which nDart1, an endogenous rice transposon, actively transposes (Fig. 1C). The mutation was inherited in a semidominant manner in both lines, and subsequent analyses revealed mutations in the same gene. The gene was named ''TAWAWA1'' (''TAW1''), from a traditional Japanese word meaning “very fruitful.” ''taw1-D1'' exhibits more severe defects than those of ''taw1-D2''. Both mutant lines show normal growth patterns during the vegetative phase, for example, meristem size, date of leaf initiation, and number of leaves produced. However, in ''taw1-D1'' homozygous plants, stem elongation is suppressed after the transition to reproductive growth, and the inflorescence does not emerge from the leaves. In both mutant lines, the number of lateral meristems produced on each primary branch is comparable to that of wild-type plants; however, a higher percentage of lateral meristems grows as secondary branches (Fig. 1D). Reiteration of this pattern results in the production of tertiary branches, which are not formed on wild-type plants (Fig. 1E).&lt;br /&gt;
&lt;br /&gt;
In homozygous ''taw1-D1'' mutants (carrying the more severe allele), the increase in inflorescence branching is so extreme that the inflorescence forms an agglomerate with a massive number of undifferentiated meristems (Fig. 1 F and G). Such aggregated meristems are also frequently observed in the inflorescences of ''taw1-D1'' heterozygous and ''taw1-D2'' homozygous plants (Fig. 1 H and I). Observations using a scanning electron microscope confirmed that these structures are formed from the repeated production of undifferentiated meristems (Fig. S2). The meristems in ''taw1-D1'' homozygous inflorescences were analyzed for expression of two SM marker genes, ''FRIZZY PANICLE'' (''FZP'') and ''LEAFY HULL STERILE1'' (''LHS1'')/''OsMADS1'', by in situ hybridization. The lack of expression of these genes indicated that the meristems in the homozygous mutants do not acquire SM identity (Fig. 1 J–M).&lt;br /&gt;
&lt;br /&gt;
Grain number per panicle is one of the four major determinants of rice yield. To test the usefulness of ''TAW1'' mutations for increasing grain yield, the moderate ''taw1-D2'' allele was introgressed into Koshihikari, which is a leading commercial rice cultivar in Japan (Fig. 5 A and B). Field-grown selfed progeny of fifth backcross (BC5F2)-generation plants showed ∼45% increases in grain weight per plant (Fig. 5C). These increases were mainly due to extensive increases in grain number per panicle (Fig. 5D), resulting from increases in the numbers of primary, secondary, and tertiary branches. Slight decreases in fertility and grain weight were also observed (Fig. 5E). Despite the increase in panicle size, the total plant height was slightly reduced in BC5F2 plants. Increases in grain number are often linked to decreases in the numbers of branch shoots, called “tillers,” in rice. However, this tradeoff effect was not observed in the ''taw1-D2'' introgression line.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
''TAW1'' contains a conserved domain and a nuclear localization signal. Indeed, ''TAW1'' localizes to the nucleus and shows slight but significant activity as a transcriptional activator (Fig. 3 A and B). The spatiotemporal pattern of ''TAW1'' mRNA accumulation was examined by in situ hybridization. During the vegetative phase of development, ''TAW1'' was predominantly expressed in meristems, including the SAM, axillary meristems, and young leaves (Fig. 3 A and C). After transition to the reproductive phase, ''TAW1'' mRNA continued to accumulate in the IM (Fig. 3D). The strongest signal was observed in BMs in the growing inflorescence (Fig. 3E). After initiation of the primary BMs, ''TAW1'' expression gradually disappeared from the IM as it degenerated (Fig. 3F). In wild-type inflorescences, the signal intensity in the meristem gradually decreased and became undetectable at SM initiation (Fig. 3G). On the other hand, in ''taw1-D'' inflorescences, stronger TAW1 signals were detected, even at the stage when the SMs were formed in the wild-type plants (Fig. 3 H and I). Quantitative PCR analysis indicated that the levels of ''TAW1'' expression in the mutant inflorescences roughly coincided with the severity of their phenotypes (Fig. 3J). These results imply that ''TAW1'' functions to suppress SM identity and that its activity must be below a certain threshold level to allow SM specification. Interestingly, ''TAW1'' expression is reduced in the vegetative shoot apices, leaves, and roots of ''taw1-D'' mutants compared with wild-type plants. These results suggest that the sequence surrounding the ''nDart1'' insertion sites is necessary for fine-tuning the spatial and quantitative expression pattern of ''TAW1''. It may be that positive regulators of SM identity interact with this sequence, which is located downstream of the transcribed region. It is also possible that ''nDart1'' carries a sequence that functions as a transcriptional enhancer; however, this is unlikely because not all ''nDart1'' insertions activate transcription. Unraveling the molecular mechanisms that regulate ''TAW1'' transcription will shed light on the regulatory networks controlling rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
The rice genes ''G1'' and ''TH1'' are ALOG family members that are expressed in the lemma, palea, and floral organs and control their identity and development. On the other hand, the ''Arabidopsis'' ALOG family genes ''LSH3/OBO1'' and ''LSH4'' are expressed in shoot organ boundary cells. The functions of ''LSH3/OBO1'' and ''LSH4'' are unknown; however, they induce the overproliferation of shoot meristems and the formation of extra organs when ectopically expressed. A plausible scenario is that at least some of the ALOG family proteins share conserved functions, but it may be that their distinctive expression patterns have led to divergent functions. The establishment of the machinery for meristem-specific expression may be a primary reason for the evolution of ''TAW1'' as a major regulator of meristem activity and phase transition &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
''TAW1'' function might have evolved to ensure the production of sufficient numbers of spikelets. Unraveling the molecular function of ''TAW1'' will provide an opportunity for a greater understanding of meristem activity and identity, which is a fundamental issue in plant biology. Furthermore, such knowledge could be exploited to further increase crop yields. In addition, ''TAW1'' is of great interest with respect to the evolution of inflorescence architecture. ''TAW1'' function may be essential for the development of compound inflorescences, in which the branching pattern is crucial &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Yoshida A, Sasao M, Yasuno N, et al. (2013) ''TAWAWA1'', a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition. Proceedings of the National Academy of Sciences 110: 767-772.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&amp;lt;/references&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os10g0478000|&lt;br /&gt;
Description = Protein of unknown function DUF640 domain containing protein|&lt;br /&gt;
Version = NM_001189280.1 GI:297727690 GeneID:9266624|&lt;br /&gt;
Length = 1426 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os10g0478000, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 10|Chromosome 10]]|&lt;br /&gt;
AP = Chromosome 10:18345508..18346933|&lt;br /&gt;
CDS = 18345710..18346324|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MEFVAHAAAPDSPHSDSGGGGGGMATGATSASAAGASPSRYESQ                     KRRDWNTFGQYLRNHRPPLSLARCSGAHVLEFLRYLDQFGKTKVHAPACPFFGHPAPP                     APCPCPLRQAWGSLDALVGRLRAAYEENGGRPENNPFGARAVRLYLREVREHQARARG                     VSYEKKKRKKPPHPSSAAAAHDDAANGALHHHHHMPPPPPGAAA&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;610..1224#tatcggctccttctcgcccagcttttgctcacgtcacatcaccttccacctccacccctccactcgctcgctcgcttgcttgctccaattaatacctcttctccttctcccccagcaactagcttccttctccgcttttgcagctcgccgccgccgccgccgccgccgccgcgacacggcgcgcatatggtcgtcgtcgtcgtcgtcgtcgtcgctggagaagacgaagaaagatagtagacctgagctgggggggcggtgaattcgccggagagctagctaaggtgagtttcgttttcggtttcggtttcgatcgatttgttggtgcagatgcatctgggagctagagaactatttatagtggctgcggtgcggtgcggcgtcgccacgccgcgcacgcgctcgcccacgtcgcgcgcgcgcgggcgcgcgtccactctctctctctcttggaccactgcgcgcgcgggcgcgcgtcggcgtcgccacggcttctcaagaacgcgcgcgcgcgcactgattcccagatagatagatctatatctgttcgtcttcctcagctatggtgtggtggtggtggtggtgtttgtggtgttgtgcagatcgacgatggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctgagccgagccgagcttgctccaagatcgccggaaaacgagctgctagcctcctacgcatgcactagttactccactccactccactccactatgatccctagctaggctgctcttgctactagcaaaactacggattaatctccatgcttgctactgctgctgctgctgctactgcatctaattaattaggttgattatttcct&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001189280.1 RefSeq:Os10g0478000]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 10]]&lt;br /&gt;
[[Category:Chromosome 10]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os09g0395300&amp;diff=174681</id>
		<title>Os09g0395300</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os09g0395300&amp;diff=174681"/>
				<updated>2014-05-30T15:23:14Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;The rice ''SHALLOT-LIKE1'' (''SLL1'') gene, a member of KANADI family, is a key gene controlling rice leaf rolling.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File: ZhangF1.jpg|right|thumb|100px|Fig 1. ''sll1'' has extremely incurved leaves, with deficiency of sclerenchymatous cells at the abaxial side &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File: ZhangF3.jpg|right|thumb|100px|Fig 3. Map-based cloning of ''SLL1'', which encodes an MYB transcription factor &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File: ZhangF8.jpg|right|thumb|100px|Fig 8. ''Sll1'' alters adaxial-abaxial pattern formation &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File: ZhangF10.jpg|right|thumb|100px|Fig 10. ''SLL1'' Affected multiple developmental processes in rice &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
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''SLL1'' arrests normal sclerenchymatous cell formation and controls leaf rolling, controls the establishment of rice leaf polarity, and modulates ohotosynthesis by regulating cell fate &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
To investigate the molecular mechanisms of rice leaf rolling, a rice mutant population (''Oryza sativa'' L. ssp. ''japonica'' variety Nipponbare) generated by ethyl methanesulphonate mutagenesis was screened. Two allelic mutants with extremely incurved leaves were identified, designated as ''sll1-1'' and ''sll1-2'' (Fig. 1A ). ''sll1'', a rice mutant with shallot-like Leaves, displays abnormal sclerenchymatous cell development in the abaxial cell layers, altered mesophyll cell distribution, increased amounts of chlorophyll, and enhanced photosynthesis.&lt;br /&gt;
&lt;br /&gt;
Genetic analysis revealed that the abnormal character of ''sll1'' was controlled by a single recessive gene. To isolate the relevant mutant gene, ''SLL1'' was mapped to the long arm of rice chromosome 9 between markers RM1896 and RM3700. A large F2 mapping population was then generated, allowing the fine-mapping of ''SLL1'' to a 29.57-kb region, using the sequence tagged site and simple sequence repeat markers (Fig. 3A). Three annotated candidate genes, encoding a hypothetical protein, an En/Spm-like transposon, and a transcription factor containing a MYB-like domain, respectively, were located in this region. Further amplification of the relevant DNA fragments and sequence comparison revealed differences in ''sll1-1'' and ''sll1-2'' alleles in the gene encoding the transcription factor containing the MYB-like domain. Comparison with the corresponding genomic sequence revealed that the ''SLL1'' gene consists of six exons and five introns. The gene encodes a 377–amino acid MYB family transcription factor (Fig. 3B). Homologous analysis showed that ''SLL1'' shares high similarity with the KANADI family members in ''Arabidopsis''.&lt;br /&gt;
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A distinguishing characteristic of the monocot leaf is that microhairs or ligules are present only at the adaxial surface. In ''sll1-1'', the microhairs can be observed on both epidermal surfaces of some plants (Fig. 8A ), and the ligules exist on the abaxial side of the joint (Fig. 8B). This suggests an adaxialized trend in the abaxial epidermis of ''sll1-1'' and indicates the involvement of ''SLL1'' in the development of polarity throughout the leaf abaxial epidermis. ''SLL1'' overexpression resulted in dwarf plants with twisted and abnormal inner rolled leaves. We also observed enlarged phloem in the midrib as well as large and small veins, revealing the enhanced abaxial features of leaves following ''SLL1'' overexpression.&lt;br /&gt;
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''SLL1'' affected developmental processes in multiple developmental stages, in accordance with its expression patterns. Aside from altered leaf morphology, other tissues, including seeds, anthers, and roots, displayed abnormal development in ''sll1'' mutants (Fig. 10).&lt;br /&gt;
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===Expression===&lt;br /&gt;
[[File: ZhangF5.jpg|right|thumb|100px|Fig 5. ''SLL1'' expression pattern analysis &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
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Quantitative real-time RT-PCR (qRT-PCR) analysis revealed the expression of ''SLL1'' in various tissues, including roots, stems, leaves, flowers, and seedlings, with relatively high expression in leaf and seedlings (Fig. 5A , top panel). With an emphasis on the leaf, analysis by qRT-PCR showed that ''SLL1'' is ubiquitously expressed in shoot apical meristem (SAM), leaf blade, or leaf sheath at different developmental stages (Figure 5A, bottom panel) &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
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To assess the expression pattern comprehensively, β-glucuronidase (GUS) activity was examined histochemically in transgenic plants carrying an ''SLL1'' promoter-GUS reporter gene. Results showed that ''SLL1'' was transcribed in stem (Fig. 5B, panels 1 and 2), anthers of young or mature flowers (Fig. 5B, panels 3 to 5), pistil tip (Fig. 5B, panel 6), glume (Fig. 5B, panel 7), vascular tissues of mature seeds (Fig. 5B, panels 8 and 9), coleoptile and embryonic root of germinating seedlings (Fig. 5B, panel 10), and root vascular tissues (Fig. 5B, panel 11). In addition, ''SLL1'' is highly transcribed in leaf veins and leaf sheath (Fig. 5C, panels 1 to 3), guard cells, and tracheal elements (Fig. 5C, panels 4 and 5).&lt;br /&gt;
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The spatial and temporal localization of ''SLL1'' during leaf development was further examined by in situ hybridization analysis. The mRNA expression of ''SLL1'' was detected throughout the young leaf primordium (plastochrons 1 to 3) and was more intense in abaxial cell layer through leaf development (plastochrons 4 and 5) (Fig. 5D, panel 2). However, the ''SLL1'' transcript did not demonstrate apical/basal polarity and did not accumulate at the apex of the meristem (Fig.e 5D, panel 3). Cross-section analysis of the shoot apex showed that ''SLL1'' was more highly expressed in the abaxial cell layer, including the epidermis and vasculature of the early leaf blade (Fig. 5D, panels 5 and 6). In the mature leaf, ''SLL1'' mainly accumulated at the abaxial epidermis, abaxial mesophyll cells, and vasculature (Fig. 5D, panels 8 and 9). In contrast with the sense probe (Fig. 5D, panels 4 and 7), ''SLL1'' was transcribed at a relatively low level throughout other leaf positions including the adaxial epidermis (Fig. 5D, panels 5 and 6).&lt;br /&gt;
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===Evolution===&lt;br /&gt;
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==Labs working on this gene==&lt;br /&gt;
*State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou 310006, Zhejiang, China&lt;br /&gt;
*National Key Laboratory of Plant Molecular Genetics, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China&lt;br /&gt;
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==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Zhang GH, et al. (2009) ''SHALLOT-LIKE1'' is a KANADI transcription factor that modulates rice leaf rolling by regulating leaf abaxial cell development. The Plant Cell Online 21: 719-735.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&amp;lt;/references&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os09g0395300|&lt;br /&gt;
Description = Similar to CDPK substrate protein 1|&lt;br /&gt;
Version = NM_001069632.1 GI:115479006 GeneID:4346973|&lt;br /&gt;
Length = 7672 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os09g0395300, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 9|Chromosome 9]]|&lt;br /&gt;
AP = Chromosome 9:14411926..14419597|&lt;br /&gt;
CDS = 14411926..14412128,14413047..14413888,14413990..14414066,14414656..14414701,14414841..14415084&amp;lt;br&amp;gt;,14418440..14418512,14419481..14419597|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008402:14411926..14419597&lt;br /&gt;
source=RiceChromosome09&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008402:14411926..14419597&lt;br /&gt;
source=RiceChromosome09&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggcaatggtgcgggagctcgagttgatgacgagctggagcaacagcatggggcgacaccgctacccaacgcgcatcctcgtcgattccttcgggcataagtgcagtgcctctgacaagggtgtgtggacctcctgcagcattcgcgcacccttgcaaggacgcggctccttccgacgtggcgcgaatattcgctttgggagcttgccgagcagcgcggcggtggcgacgtcggggggagggcgtggcggcggcggggtggtggtgggaggaggaggaggggacccgtggcggaggctggatgggtccacggcgtcgacggagttgtcgctgtcgccgccgccggcgcaggcggcgggtgggggaggtggtggtggtggagcggacgcgctgccgtggcggcaccgaccttcgccgccgtcgtcggcggtggccaccacgtctgccgccgccgcggcggcgctgatggcgccgatgatgctgcagccgctcgacgccggcggcggcgcgtcggcgccgccgccgccgatccgcgggatacctatctacaacggccccggcgggttcccgttcctgcagccgtcgcccaccgccggcgacgtcggccaccaccaccaccaccaccccaagatgggattctacagctcgtaccaccacccatccacgtggccctccacgtcgccgtccccgctcgcggcgccgccgggcgccgcgtcgtcgccgctcgaccccacggcggcgttcctctcctccccccaccaccggatgctgtccgccgcctcggggaggctcaacggcatgctctccgtctccgacaccctccgcagctacggcgtccccggcgccgccgcccccggcgtcatcggcggcgcgcaccaccaccaccaccacctccacggcggccagccgttcgtcggcgccctcgcgtcccgcttcatgcccaagctccccgccaagcgcagcatgcgcgcgccgcgcatgcgctggacgagcaccctccacgcccgcttcgtccacgccgtcgagctcctcggcggccacgagagggcgacgcccaagtcggtgctggagctcatggacgtcaaggatctgacgctagcgcatgtcaagagccacctccagatgtatcgcaccgtgaagagcactgacaagcctgcagcctcttcagggccggcggacggcggctccggcgacgaggagttcgccggcggcgggcaggcggcgtcgggcggcggcgacagcatgtgcctgaggggtggcggcggcggcggggtggccgcggcggcgttcgcggagcacggccggtcggcgtcggagggcgccgccagctcggtcggcggcggcggcggcggcgacatggaccagtcgtcggccggcaacaccagcaccaccaggtggagcaactcctcaagggacccatggctgtcgtccaattcttgcaacatggacgcccatcgctccgtaggattgtcttctcctattgaggttcttgcacttcctttagcctcattgatcatgtcagatactgcctacctgttcttttccagcaaccatggccggtgtgaaccggcctctcttgaccagaaactagcagatatctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MAMVRELELMTSWSNSMGRHRYPTRILVDSFGHKCSASDKGVWT                     SCSIRAPLQGRGSFRRGANIRFGSLPSSAAVATSGGGRGGGGVVVGGGGGDPWRRLDG                     STASTELSLSPPPAQAAGGGGGGGGADALPWRHRPSPPSSAVATTSAAAAAALMAPMM                     LQPLDAGGGASAPPPPIRGIPIYNGPGGFPFLQPSPTAGDVGHHHHHHPKMGFYSSYH                     HPSTWPSTSPSPLAAPPGAASSPLDPTAAFLSSPHHRMLSAASGRLNGMLSVSDTLRS                     YGVPGAAAPGVIGGAHHHHHHLHGGQPFVGALASRFMPKLPAKRSMRAPRMRWTSTLH                     ARFVHAVELLGGHERATPKSVLELMDVKDLTLAHVKSHLQMYRTVKSTDKPAASSGPA                     DGGSGDEEFAGGGQAASGGGDSMCLRGGGGGGVAAAAFAEHGRSASEGAASSVGGGGG                     GDMDQSSAGNTSTTRWSNSSRDPWLSSNSCNMDAHRSVGLSSPIEVLALPLASLIMSD                     TAYLFFSSNHGRCEPASLDQKLADI&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;1..203#1122..1963#2065..2141#2731..2776#2916..3159#6515..6587#7556..7672#atggcaatggtgcgggagctcgagttgatgacgagctggagcaacagcatggggcgacaccgctacccaacgcgcatcctcgtcgattccttcgggcataagtgcagtgcctctgacaagggtgtgtggacctcctgcagcattcgcgcacccttgcaaggacgcggctccttccgacgtggcgcgaatattcgctttgggaggtatgagactacgctccatggtggagcgttgggcgtgaccttagtgtgcgcatatgtaagctgtatgcgtacgtataaatgttgagcttgcagtacatgtatacttgtttttttcttcttttttatgaggtcctttaattccattgtctgtattatttatgctagtatggaggatgatggtggcagtgacataaagtatacaaaaagcatagtatagtatacgtatggaaacaaaagcatgctacctttgactccacttgcattgcctgctaactgccattatttaaggaatacatggttgaatgcctgcctaaacatcaagataacctcacattctcctctctctctctcctaccttgcaattaagggtagcagcagtactctcctcactgctggctgactgctcccattttctctctctactctctctctctctctctcctctattccttttatacttgttgttggtagctaggagtatagcaggacagcacaaggaaccaattcatgcatatatccctggtgtctctcatgcatgttagtgtgaagaaagaagaagcttgagagagaagagagagttagagagagaaagtagagtgtttgtagagagagaaagtggtgtgtgtactagtagtaactccaagccagtgctagagacagagatacaaaaaggagacatcatccttctcttggccaaagcaagcaaccaagcaaagcttcctcttcttctccaagaactccaagaaccttctccttcatcttctccaccatgattccttccatcgcatgagctccatctccggcgtgtcgatcgagatcaccgttgctgctgccgaggtggagaaggaggtgtttgatcgatcggtcgatggaggcgagctcggcggcgacgccaccggacctgtcgctgcacatcagcttgccgagcagcgcggcggtggcgacgtcggggggagggcgtggcggcggcggggtggtggtgggaggaggaggaggggacccgtggcggaggctggatgggtccacggcgtcgacggagttgtcgctgtcgccgccgccggcgcaggcggcgggtgggggaggtggtggtggtggagcggacgcgctgccgtggcggcaccgaccttcgccgccgtcgtcggcggtggccaccacgtctgccgccgccgcggcggcgctgatggcgccgatgatgctgcagccgctcgacgccggcggcggcgcgtcggcgccgccgccgccgatccgcgggatacctatctacaacggccccggcgggttcccgttcctgcagccgtcgcccaccgccggcgacgtcggccaccaccaccaccaccaccccaagatgggattctacagctcgtaccaccacccatccacgtggccctccacgtcgccgtccccgctcgcggcgccgccgggcgccgcgtcgtcgccgctcgaccccacggcggcgttcctctcctccccccaccaccggatgctgtccgccgcctcggggaggctcaacggcatgctctccgtctccgacaccctccgcagctacggcgtccccggcgccgccgcccccggcgtcatcggcggcgcgcaccaccaccaccaccacctccacggcggccagccgttcgtcggcgccctcgcgtcccgcttcatgcccaagctccccgccaagcgcagcatgcgcgcgccgcgcatgcgctggacgagcaccctccacgcccgcttcgtccacgccgtcgagctcctcggcggccacgagagtacgcccccgccatcatcgtcgtcgtcctcctcctccttctcaccaccatcatcaacgagctcgatcaatctgatgagaatccaatcttgttcttggcaggggcgacgcccaagtcggtgctggagctcatggacgtcaaggatctgacgctagcgcatgtcaagagccacctccaggtatcccgccattgccgaccaattctcacagctcgatcgatcgatcaaacaccactcaccactgcaccatctctctctttctctctctcgatttcgattccattcagcttctgttcttgatcatcttgtttgggtgagacaaagatgccaatgcagtaactcctgagttagtgaagaaactgccattcttgggagcagagagagagagtgtgtgtgtgacatgtttggggatgtgtgtgcaagagagaagagagagagagaggggaaaaaagttgccatcattacacaataatgcattgcatctgcatctgtgctactagctccttccttagctctagtcatactagcgtatatgtgcacggcccaaagcactctcacacacaaacacaagagagagagagagagagagaagaagaagatgagagatgagagagagtaggacatattttgtgtgtgtttctttgctgcttgtcttttgcaatggcttcaacctcctggtttcattttgatctcacaaaaaatgtgtgtgtgtgtgtaaatatatatattgatcttctttttgttggacttttgtgttttattactgcagatgtatcgcaccgtgaagagcactgacaagcctgcagcctcttcaggtgattttttttaccatggcagctactagtagtagtagtagtagctaatttagctaagctccattttgcttttctttttttttggcgttgtgcattgcgttttacattacattgttgctatggtttttttgacgtgtagggccggcggacggcggctccggcgacgaggagttcgccggcggcgggcaggcggcgtcgggcggcggcgacagcatgtgcctgaggggtggcggcggcggcggggtggccgcggcggcgttcgcggagcacggccggtcggcgtcggagggcgccgccagctcggtcggcggcggcggcggcggcgacatggaccagtcgtcggccggcaacaccagcaccaccaggtggagcaactcctcaaggtacacacatggcagagttgcatttcaagtctttcagattaattatatatctacattgttatgccatctttaattaattaaaaatgaaattaatcaatcagaatgtcatgagatgatgatgatgatgataataatactaggataggaagaggatgatatgatggatgggtgtgctatgtgtgtttttaagtgtgttttagcttagaaccaaaggcaacaccaacaaactttggcatgcattgatgatgtatctaaatatgagttagtgacatgcaaaattaacctgccaagtacaacctctatttattaattcccaaaaaaatctcatggaggagaagggagagagagagatagtagtaatgtgtggtgatgcatggctaaaaaagcttagcaaaagaatgttttgggggcacacacacacacacctggagagggagttgcctatgtttaggtggccaatgttgttatgtcacacaaaagaccaaaaagtcacacaccccatggcttggcctcctcctccccccttgacctgtgcagttagctaggcttcttctcttctctccctctgtgtttggtttttgtggagctaaaaacattttaaaaatcttgcaaacattgtgtgtaaaaataggttcttgggctctgcccattgtcctctagcttctctcaaatctctctctctctctctctctctctctctctctttctcaaacctagggaggggagggttactcaggcagggctccattatcatttcttatcaatgcatggctctgattccagggggatggggctttgacctgacatgccctattgcctaggaatatgtaaccaaggacttgctgcattcttggttctttctccctctctcaccagtctcttcaatgcccttttcttccacctcttgggcaattattagcatggatggagctcaccttttcactctaccctctagctgtgattaaatcattgactaatcctaattcataaatataagggattcaactatgtaactagatgtactagatcctagtattactagtgtgttttgattctgttaggaggagtgattagcgtttgtcgtaagtactagtattaaactataggggattagtgtagatcatttttttaaaaattagtgagtgtgcttgggcagattttactccagccattggcgtgaaaactttgatctttgggcagcttggaagcaagtacagttcaacctgtccttggctgcattcgctgctttttctttctcaggactcactgcaactttcttgccatccccaacacctccctttcggtcgtgtttgatcagttgcattgctggtttcttcgccgctttaatttctccatctttcttctgttccttattggctaagtaaaaaatcattctcagcaatcaagttttgaaattcaaattagcttcaggttttatctatctaataattctctgactagttctctttctttcaagacctgttcttgttcagaactcttatgcagttgagagttcagttgttcatggaagtaatggcaatgcctggtctagtctttgagcagtatcctccttatgctcttgattttccttcactttagccgtttcagtcaaactttggggacaaattaaagtcagctggtcaagtgcatacataccacgtcatattttttagatgaatccattgtagtattaaatactagtgacaaaaaaatataactaaatggcattaaattgcaaccttcttccccaaaataattgggcacaactaccttgcttgcatatgctttatagtactcctacttattacttccttgaatccatgaggattccaggaatttggtcaggtcaaatgtccaggaggaattaggctatctttttttatcttcttctttttcttctaggtagtaggatcgttgtgcacatataaacaaaacaaaatagaaatttaagaggaaaccctcccaaaaaaaatacgactatcaattatgagtgattttacagttcttgaggaggtacaatgatacattttctattttaaaattcagtaactttgatactatgaggtacagaaatttgcacaaaaaaaatttggtacctctcaagtacttaaaatatcttatcaattatatttcagcaatgttgtcgttgctcgagttgtgcaaaaacatttctgatgaacaagtggagatgtatgcatatttagagagggaaacacatgcattttttaatatacattctcatgacaaattttggtgttctcgtctcattttagtctagcttagattaatggcatccatatattggtgaactgaaacagattgtatatgtccagtcttgaacaaacttcattatacaatgcataatcagaaaagatacagacatatattggcagatcacataaagtggtgtatctatgattgggtggtattttggacatacaaagtctactggtccctcatttgttaacagcatacatttgttcctatcaagacaaaagcactttacaacagtttggtagtaagttggtgttatgtgcgtgtctatttagatagagtggtagtaaaggaaggacactttttcttgatataccaaaatcacacataaaaaagaagtgtcattttcatgatcaacatgtggggtatgaacaaaaatgttctcccccctccaaccaacattgaagtcatcacacataaaaagcaaaaacatttaacaataatacatgcagacacatgtgcatgcatgtgtggatcacgcaaggacatactaattcaattaggtattcacaattaattagtgcaggaaatgacatgtaattacaattatatatgcacaacgatccttgtgtatttgtgtgacccattgtagtagcatttgattcctttcttgtgcctttctctacattgaattcgatctttgccaacagcggcttgctgatgagctcctgtgccattgcactgctgagctgcaccaaacagggacatcttttaagagcttgttgcctggaaatgatccatgtaaccaactgttcaggaagagcacactgtttgctgctcactttagctaaagcaaaactgtgtgcattatgcaatgcatatgcatccttccatctacccctgtgtcctttgccccccaaactgtgtaactacagtttaccatgcacatacatacaatgcacatctacccaattgtagcattgttgcaaggcctacttcagaattcagttagtccccaattgatccaactgcacacatatacatttacatatacatatacacaaacataccagcttggagaaaaggttgtaacaactttgctaaatgtgagatgtgtaatgtgtgttcttcctcttttcagggacccatggctgtcgtccaattcttgcaacatggacgcccatcgctccgtaggattgtcttctcctattgaggtatatatccttacattgttcaaagcttctttcgattcctagctaactgcatatccatgcagaaattcattagctcgcattcattctgaacatgatgtctgaaactctgaattttttttcgtttgtgcgtgtttcagaacttggaaccgtgcagatcgagcagctcgcaggtgtccaaccatgagctgagtagccctagtctcgagttcactctagggaggcctgactggcacggtgcagatcatgattagatggcaatcacagaggctaatgatcaaaaaaaaatttctcctgagatgtgaaatatatatgtgatatacaccaacctggtgctgatcatctttcgccaaccccagcttagccagagccagttcgtctgaagcttgtcatggcgaagaatgatcagcagcaatggcttgaaacgcacatcatatccactgcgtcgtcgtcatcgtcgtcgcaatcgatcggagaagagatatatatttcgcgtctcgatctcatcatcacaatttgggttttcttgattccttcttcttcttctttttgcaattaatatcatggatgcagctagagtttccttgtctgatctccatatttatttagttttgttcgccgtgccgggatcgatttacagtgtagttcagtggtgagctagctagctagagagtgagtgagtgagtgtcagctaggcagctggagatcgagagtgtgagtttggtgatgagttggttgtgtgtttgtcagtgtgtgtgaaagtgtgtgtgccattagcacatggaaagttggaaaggagagaaaggaagaaagaaaagggaattgagttcaggtgaagcaatctgccaatctatctagctacctatctatccatctacttagctcagttgctcagatgatgatctcagatttccatggcccttttttgtgtgcatgcatgccgcatatgcttctttctttaatccctgcaggttcttgcacttcctttagcctcattgatcatgtcagatactgcctacctgttcttttccagcaaccatggccggtgtgaaccggcctctcttgaccagaaactagcagatatctga&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001069632.1 RefSeq:Os09g0395300]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 9]]&lt;br /&gt;
[[Category:Chromosome 9]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174628</id>
		<title>Os10g0478000</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174628"/>
				<updated>2014-05-30T12:09:29Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; The rice ''TAWAWA1'' (''TAW1'') gene, a member of ALOG family, was identified as a  regulator of rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:YoshidaF1.jpg|right|thumb|200px|Fig 1. Characterization of ''taw1'' dominant mutants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF2.jpg|right|thumb|200px|Fig 2. Isolation of the ''TAW1'' gene &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF3.jpg|right|thumb|200px|Fig 3. Expression pattern of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF4.jpg|right|thumb|200px|Fig 4. ''SVP'' subfamily MADS-box genes work downstream of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF5.jpg|right|thumb|200px|Fig 5. Phenotype of ''taw1-D2''–introgressed Koshihikari BC5F2 plants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
In the dominant gain-of-function mutant ''tawawa1-D'' (Fig. 1), the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in ''TAWAWA1'' (''TAW1'') activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. ''TAW1'' encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the branch meristem (BMs). ''TAW1'' expression disappears from incipient spikelet meristems (SMs). It is demonstrated that members of the ''SHORT VEGETATIVE PHASE'' subfamily of MADS-box genes function downstream of ''TAW1''. Thus, ''TAW1'' is proposed as a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
To understand the molecular links between the control of meristem phase transition and inflorescence structure, mutants were identified with altered inflorescence branching patterns &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;. Two lines with increased branching phenotypes were isolated from a screening population in which nDart1, an endogenous rice transposon, actively transposes (Fig. 1C). The mutation was inherited in a semidominant manner in both lines, and subsequent analyses revealed mutations in the same gene. The gene was named ''TAWAWA1'' (''TAW1''), from a traditional Japanese word meaning “very fruitful.” ''taw1-D1'' exhibits more severe defects than those of ''taw1-D2''. Both mutant lines show normal growth patterns during the vegetative phase, for example, meristem size, date of leaf initiation, and number of leaves produced. However, in ''taw1-D1'' homozygous plants, stem elongation is suppressed after the transition to reproductive growth, and the inflorescence does not emerge from the leaves. In both mutant lines, the number of lateral meristems produced on each primary branch is comparable to that of wild-type plants; however, a higher percentage of lateral meristems grows as secondary branches (Fig. 1D). Reiteration of this pattern results in the production of tertiary branches, which are not formed on wild-type plants (Fig. 1E).&lt;br /&gt;
&lt;br /&gt;
In homozygous ''taw1-D1'' mutants (carrying the more severe allele), the increase in inflorescence branching is so extreme that the inflorescence forms an agglomerate with a massive number of undifferentiated meristems (Fig. 1 F and G). Such aggregated meristems are also frequently observed in the inflorescences of ''taw1-D1'' heterozygous and ''taw1-D2'' homozygous plants (Fig. 1 H and I). Observations using a scanning electron microscope confirmed that these structures are formed from the repeated production of undifferentiated meristems (Fig. S2). The meristems in ''taw1-D1'' homozygous inflorescences were analyzed for expression of two SM marker genes, ''FRIZZY PANICLE'' (''FZP'') and ''LEAFY HULL STERILE1'' (''LHS1'')/''OsMADS1'', by in situ hybridization. The lack of expression of these genes indicated that the meristems in the homozygous mutants do not acquire SM identity (Fig. 1 J–M).&lt;br /&gt;
&lt;br /&gt;
Grain number per panicle is one of the four major determinants of rice yield. To test the usefulness of ''TAW1'' mutations for increasing grain yield, the moderate ''taw1-D2'' allele was introgressed into Koshihikari, which is a leading commercial rice cultivar in Japan (Fig. 5 A and B). Field-grown selfed progeny of fifth backcross (BC5F2)-generation plants showed ∼45% increases in grain weight per plant (Fig. 5C). These increases were mainly due to extensive increases in grain number per panicle (Fig. 5D), resulting from increases in the numbers of primary, secondary, and tertiary branches. Slight decreases in fertility and grain weight were also observed (Fig. 5E). Despite the increase in panicle size, the total plant height was slightly reduced in BC5F2 plants. Increases in grain number are often linked to decreases in the numbers of branch shoots, called “tillers,” in rice. However, this tradeoff effect was not observed in the ''taw1-D2'' introgression line.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
''TAW1'' contains a conserved domain and a nuclear localization signal. Indeed, ''TAW1'' localizes to the nucleus and shows slight but significant activity as a transcriptional activator (Fig. 3 A and B). The spatiotemporal pattern of ''TAW1'' mRNA accumulation was examined by in situ hybridization. During the vegetative phase of development, ''TAW1'' was predominantly expressed in meristems, including the SAM, axillary meristems, and young leaves (Fig. 3 A and C). After transition to the reproductive phase, ''TAW1'' mRNA continued to accumulate in the IM (Fig. 3D). The strongest signal was observed in BMs in the growing inflorescence (Fig. 3E). After initiation of the primary BMs, ''TAW1'' expression gradually disappeared from the IM as it degenerated (Fig. 3F). In wild-type inflorescences, the signal intensity in the meristem gradually decreased and became undetectable at SM initiation (Fig. 3G). On the other hand, in ''taw1-D'' inflorescences, stronger TAW1 signals were detected, even at the stage when the SMs were formed in the wild-type plants (Fig. 3 H and I). Quantitative PCR analysis indicated that the levels of ''TAW1'' expression in the mutant inflorescences roughly coincided with the severity of their phenotypes (Fig. 3J). These results imply that ''TAW1'' functions to suppress SM identity and that its activity must be below a certain threshold level to allow SM specification. Interestingly, ''TAW1'' expression is reduced in the vegetative shoot apices, leaves, and roots of ''taw1-D'' mutants compared with wild-type plants. These results suggest that the sequence surrounding the ''nDart1'' insertion sites is necessary for fine-tuning the spatial and quantitative expression pattern of ''TAW1''. It may be that positive regulators of SM identity interact with this sequence, which is located downstream of the transcribed region. It is also possible that ''nDart1'' carries a sequence that functions as a transcriptional enhancer; however, this is unlikely because not all ''nDart1'' insertions activate transcription. Unraveling the molecular mechanisms that regulate ''TAW1'' transcription will shed light on the regulatory networks controlling rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
The rice genes ''G1'' and ''TH1'' are ALOG family members that are expressed in the lemma, palea, and floral organs and control their identity and development. On the other hand, the ''Arabidopsis'' ALOG family genes ''LSH3/OBO1'' and ''LSH4'' are expressed in shoot organ boundary cells. The functions of ''LSH3/OBO1'' and ''LSH4'' are unknown; however, they induce the overproliferation of shoot meristems and the formation of extra organs when ectopically expressed. A plausible scenario is that at least some of the ALOG family proteins share conserved functions, but it may be that their distinctive expression patterns have led to divergent functions. The establishment of the machinery for meristem-specific expression may be a primary reason for the evolution of ''TAW1'' as a major regulator of meristem activity and phase transition &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
''TAW1'' function might have evolved to ensure the production of sufficient numbers of spikelets. Unraveling the molecular function of ''TAW1'' will provide an opportunity for a greater understanding of meristem activity and identity, which is a fundamental issue in plant biology. Furthermore, such knowledge could be exploited to further increase crop yields. In addition, ''TAW1'' is of great interest with respect to the evolution of inflorescence architecture. ''TAW1'' function may be essential for the development of compound inflorescences, in which the branching pattern is crucial &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
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==Labs working on this gene==&lt;br /&gt;
*Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Yoshida A, Sasao M, Yasuno N, et al. (2013) ''TAWAWA1'', a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition. Proceedings of the National Academy of Sciences 110: 767-772.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os10g0478000|&lt;br /&gt;
Description = Protein of unknown function DUF640 domain containing protein|&lt;br /&gt;
Version = NM_001189280.1 GI:297727690 GeneID:9266624|&lt;br /&gt;
Length = 1426 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os10g0478000, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 10|Chromosome 10]]|&lt;br /&gt;
AP = Chromosome 10:18345508..18346933|&lt;br /&gt;
CDS = 18345710..18346324|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MEFVAHAAAPDSPHSDSGGGGGGMATGATSASAAGASPSRYESQ                     KRRDWNTFGQYLRNHRPPLSLARCSGAHVLEFLRYLDQFGKTKVHAPACPFFGHPAPP                     APCPCPLRQAWGSLDALVGRLRAAYEENGGRPENNPFGARAVRLYLREVREHQARARG                     VSYEKKKRKKPPHPSSAAAAHDDAANGALHHHHHMPPPPPGAAA&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;610..1224#tatcggctccttctcgcccagcttttgctcacgtcacatcaccttccacctccacccctccactcgctcgctcgcttgcttgctccaattaatacctcttctccttctcccccagcaactagcttccttctccgcttttgcagctcgccgccgccgccgccgccgccgccgcgacacggcgcgcatatggtcgtcgtcgtcgtcgtcgtcgtcgctggagaagacgaagaaagatagtagacctgagctgggggggcggtgaattcgccggagagctagctaaggtgagtttcgttttcggtttcggtttcgatcgatttgttggtgcagatgcatctgggagctagagaactatttatagtggctgcggtgcggtgcggcgtcgccacgccgcgcacgcgctcgcccacgtcgcgcgcgcgcgggcgcgcgtccactctctctctctcttggaccactgcgcgcgcgggcgcgcgtcggcgtcgccacggcttctcaagaacgcgcgcgcgcgcactgattcccagatagatagatctatatctgttcgtcttcctcagctatggtgtggtggtggtggtggtgtttgtggtgttgtgcagatcgacgatggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctgagccgagccgagcttgctccaagatcgccggaaaacgagctgctagcctcctacgcatgcactagttactccactccactccactccactatgatccctagctaggctgctcttgctactagcaaaactacggattaatctccatgcttgctactgctgctgctgctgctactgcatctaattaattaggttgattatttcct&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001189280.1 RefSeq:Os10g0478000]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 10]]&lt;br /&gt;
[[Category:Chromosome 10]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os09g0395300&amp;diff=174627</id>
		<title>Os09g0395300</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os09g0395300&amp;diff=174627"/>
				<updated>2014-05-30T12:03:11Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;The rice ''SHALLOT-LIKE1'' (''SLL1'') gene, a member of KANADI family, is a key gene controlling rice leaf rolling.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File: ZhangF1.jpg|right|thumb|100px|Fig 1. ''sll1'' has extremely incurved leaves, with deficiency of sclerenchymatous cells at the abaxial side &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File: ZhangF3.jpg|right|thumb|100px|Fig 3. Map-based cloning of ''SLL1'', which encodes an MYB transcription factor &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File: ZhangF8.jpg|right|thumb|100px|Fig 8. ''Sll1'' alters adaxial-abaxial pattern formation &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File: ZhangF10.jpg|right|thumb|100px|Fig 10. ''SLL1'' Affected multiple developmental processes in rice &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
''SLL1'' arrests normal sclerenchymatous cell formation and controls leaf rolling, controls the establishment of rice leaf polarity, and modulates ohotosynthesis by regulating cell fate &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
To investigate the molecular mechanisms of rice leaf rolling, a rice mutant population (''Oryza sativa'' L. ssp. ''japonica'' variety Nipponbare) generated by ethyl methanesulphonate mutagenesis was screened. Two allelic mutants with extremely incurved leaves were identified, designated as ''sll1-1'' and ''sll1-2'' (Fig. 1A ). ''sll1'', a rice mutant with shallot-like Leaves, displays abnormal sclerenchymatous cell development in the abaxial cell layers, altered mesophyll cell distribution, increased amounts of chlorophyll, and enhanced photosynthesis.&lt;br /&gt;
&lt;br /&gt;
Genetic analysis revealed that the abnormal character of ''sll1'' was controlled by a single recessive gene. To isolate the relevant mutant gene, ''SLL1'' was mapped to the long arm of rice chromosome 9 between markers RM1896 and RM3700. A large F2 mapping population was then generated, allowing the fine-mapping of ''SLL1'' to a 29.57-kb region, using the sequence tagged site and simple sequence repeat markers (Fig. 3A). Three annotated candidate genes, encoding a hypothetical protein, an En/Spm-like transposon, and a transcription factor containing a MYB-like domain, respectively, were located in this region. Further amplification of the relevant DNA fragments and sequence comparison revealed differences in ''sll1-1'' and ''sll1-2'' alleles in the gene encoding the transcription factor containing the MYB-like domain. Comparison with the corresponding genomic sequence revealed that the ''SLL1'' gene consists of six exons and five introns. The gene encodes a 377–amino acid MYB family transcription factor (Fig. 3B). Homologous analysis showed that ''SLL1'' shares high similarity with the KANADI family members in ''Arabidopsis''.&lt;br /&gt;
&lt;br /&gt;
A distinguishing characteristic of the monocot leaf is that microhairs or ligules are present only at the adaxial surface. In ''sll1-1'', the microhairs can be observed on both epidermal surfaces of some plants (Fig. 8A ), and the ligules exist on the abaxial side of the joint (Fig. 8B). This suggests an adaxialized trend in the abaxial epidermis of ''sll1-1'' and indicates the involvement of ''SLL1'' in the development of polarity throughout the leaf abaxial epidermis. ''SLL1'' overexpression resulted in dwarf plants with twisted and abnormal inner rolled leaves. We also observed enlarged phloem in the midrib as well as large and small veins, revealing the enhanced abaxial features of leaves following ''SLL1'' overexpression.&lt;br /&gt;
&lt;br /&gt;
''SLL1'' affected developmental processes in multiple developmental stages, in accordance with its expression patterns. Aside from altered leaf morphology, other tissues, including seeds, anthers, and roots, displayed abnormal development in ''sll1'' mutants (Fig. 10).&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
[[File: ZhangF5.jpg|right|thumb|100px|Fig 5. ''SLL1'' expression pattern analysis &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
Quantitative real-time RT-PCR (qRT-PCR) analysis revealed the expression of ''SLL1'' in various tissues, including roots, stems, leaves, flowers, and seedlings, with relatively high expression in leaf and seedlings (Fig. 5A , top panel). With an emphasis on the leaf, analysis by qRT-PCR showed that ''SLL1'' is ubiquitously expressed in shoot apical meristem (SAM), leaf blade, or leaf sheath at different developmental stages (Figure 5A, bottom panel) &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
To assess the expression pattern comprehensively, β-glucuronidase (GUS) activity was examined histochemically in transgenic plants carrying an ''SLL1'' promoter-GUS reporter gene. Results showed that ''SLL1'' was transcribed in stem (Fig. 5B, panels 1 and 2), anthers of young or mature flowers (Fig. 5B, panels 3 to 5), pistil tip (Fig. 5B, panel 6), glume (Fig. 5B, panel 7), vascular tissues of mature seeds (Fig. 5B, panels 8 and 9), coleoptile and embryonic root of germinating seedlings (Fig. 5B, panel 10), and root vascular tissues (Fig. 5B, panel 11). In addition, ''SLL1'' is highly transcribed in leaf veins and leaf sheath (Fig. 5C, panels 1 to 3), guard cells, and tracheal elements (Fig. 5C, panels 4 and 5).&lt;br /&gt;
&lt;br /&gt;
The spatial and temporal localization of ''SLL1'' during leaf development was further examined by in situ hybridization analysis. The mRNA expression of ''SLL1'' was detected throughout the young leaf primordium (plastochrons 1 to 3) and was more intense in abaxial cell layer through leaf development (plastochrons 4 and 5) (Fig. 5D, panel 2). However, the ''SLL1'' transcript did not demonstrate apical/basal polarity and did not accumulate at the apex of the meristem (Fig.e 5D, panel 3). Cross-section analysis of the shoot apex showed that ''SLL1'' was more highly expressed in the abaxial cell layer, including the epidermis and vasculature of the early leaf blade (Fig. 5D, panels 5 and 6). In the mature leaf, ''SLL1'' mainly accumulated at the abaxial epidermis, abaxial mesophyll cells, and vasculature (Fig. 5D, panels 8 and 9). In contrast with the sense probe (Fig. 5D, panels 4 and 7), ''SLL1'' was transcribed at a relatively low level throughout other leaf positions including the adaxial epidermis (Fig. 5D, panels 5 and 6).&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou 310006, Zhejiang, China&lt;br /&gt;
*National Key Laboratory of Plant Molecular Genetics, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Zhang GH, et al. (2009) ''SHALLOT-LIKE1'' is a KANADI transcription factor that modulates rice leaf rolling by regulating leaf abaxial cell development. The Plant Cell Online 21: 719-735.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os09g0395300|&lt;br /&gt;
Description = Similar to CDPK substrate protein 1|&lt;br /&gt;
Version = NM_001069632.1 GI:115479006 GeneID:4346973|&lt;br /&gt;
Length = 7672 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os09g0395300, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 9|Chromosome 9]]|&lt;br /&gt;
AP = Chromosome 9:14411926..14419597|&lt;br /&gt;
CDS = 14411926..14412128,14413047..14413888,14413990..14414066,14414656..14414701,14414841..14415084&amp;lt;br&amp;gt;,14418440..14418512,14419481..14419597|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008402:14411926..14419597&lt;br /&gt;
source=RiceChromosome09&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008402:14411926..14419597&lt;br /&gt;
source=RiceChromosome09&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggcaatggtgcgggagctcgagttgatgacgagctggagcaacagcatggggcgacaccgctacccaacgcgcatcctcgtcgattccttcgggcataagtgcagtgcctctgacaagggtgtgtggacctcctgcagcattcgcgcacccttgcaaggacgcggctccttccgacgtggcgcgaatattcgctttgggagcttgccgagcagcgcggcggtggcgacgtcggggggagggcgtggcggcggcggggtggtggtgggaggaggaggaggggacccgtggcggaggctggatgggtccacggcgtcgacggagttgtcgctgtcgccgccgccggcgcaggcggcgggtgggggaggtggtggtggtggagcggacgcgctgccgtggcggcaccgaccttcgccgccgtcgtcggcggtggccaccacgtctgccgccgccgcggcggcgctgatggcgccgatgatgctgcagccgctcgacgccggcggcggcgcgtcggcgccgccgccgccgatccgcgggatacctatctacaacggccccggcgggttcccgttcctgcagccgtcgcccaccgccggcgacgtcggccaccaccaccaccaccaccccaagatgggattctacagctcgtaccaccacccatccacgtggccctccacgtcgccgtccccgctcgcggcgccgccgggcgccgcgtcgtcgccgctcgaccccacggcggcgttcctctcctccccccaccaccggatgctgtccgccgcctcggggaggctcaacggcatgctctccgtctccgacaccctccgcagctacggcgtccccggcgccgccgcccccggcgtcatcggcggcgcgcaccaccaccaccaccacctccacggcggccagccgttcgtcggcgccctcgcgtcccgcttcatgcccaagctccccgccaagcgcagcatgcgcgcgccgcgcatgcgctggacgagcaccctccacgcccgcttcgtccacgccgtcgagctcctcggcggccacgagagggcgacgcccaagtcggtgctggagctcatggacgtcaaggatctgacgctagcgcatgtcaagagccacctccagatgtatcgcaccgtgaagagcactgacaagcctgcagcctcttcagggccggcggacggcggctccggcgacgaggagttcgccggcggcgggcaggcggcgtcgggcggcggcgacagcatgtgcctgaggggtggcggcggcggcggggtggccgcggcggcgttcgcggagcacggccggtcggcgtcggagggcgccgccagctcggtcggcggcggcggcggcggcgacatggaccagtcgtcggccggcaacaccagcaccaccaggtggagcaactcctcaagggacccatggctgtcgtccaattcttgcaacatggacgcccatcgctccgtaggattgtcttctcctattgaggttcttgcacttcctttagcctcattgatcatgtcagatactgcctacctgttcttttccagcaaccatggccggtgtgaaccggcctctcttgaccagaaactagcagatatctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MAMVRELELMTSWSNSMGRHRYPTRILVDSFGHKCSASDKGVWT                     SCSIRAPLQGRGSFRRGANIRFGSLPSSAAVATSGGGRGGGGVVVGGGGGDPWRRLDG                     STASTELSLSPPPAQAAGGGGGGGGADALPWRHRPSPPSSAVATTSAAAAAALMAPMM                     LQPLDAGGGASAPPPPIRGIPIYNGPGGFPFLQPSPTAGDVGHHHHHHPKMGFYSSYH                     HPSTWPSTSPSPLAAPPGAASSPLDPTAAFLSSPHHRMLSAASGRLNGMLSVSDTLRS                     YGVPGAAAPGVIGGAHHHHHHLHGGQPFVGALASRFMPKLPAKRSMRAPRMRWTSTLH                     ARFVHAVELLGGHERATPKSVLELMDVKDLTLAHVKSHLQMYRTVKSTDKPAASSGPA                     DGGSGDEEFAGGGQAASGGGDSMCLRGGGGGGVAAAAFAEHGRSASEGAASSVGGGGG                     GDMDQSSAGNTSTTRWSNSSRDPWLSSNSCNMDAHRSVGLSSPIEVLALPLASLIMSD                     TAYLFFSSNHGRCEPASLDQKLADI&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;1..203#1122..1963#2065..2141#2731..2776#2916..3159#6515..6587#7556..7672#atggcaatggtgcgggagctcgagttgatgacgagctggagcaacagcatggggcgacaccgctacccaacgcgcatcctcgtcgattccttcgggcataagtgcagtgcctctgacaagggtgtgtggacctcctgcagcattcgcgcacccttgcaaggacgcggctccttccgacgtggcgcgaatattcgctttgggaggtatgagactacgctccatggtggagcgttgggcgtgaccttagtgtgcgcatatgtaagctgtatgcgtacgtataaatgttgagcttgcagtacatgtatacttgtttttttcttcttttttatgaggtcctttaattccattgtctgtattatttatgctagtatggaggatgatggtggcagtgacataaagtatacaaaaagcatagtatagtatacgtatggaaacaaaagcatgctacctttgactccacttgcattgcctgctaactgccattatttaaggaatacatggttgaatgcctgcctaaacatcaagataacctcacattctcctctctctctctcctaccttgcaattaagggtagcagcagtactctcctcactgctggctgactgctcccattttctctctctactctctctctctctctctcctctattccttttatacttgttgttggtagctaggagtatagcaggacagcacaaggaaccaattcatgcatatatccctggtgtctctcatgcatgttagtgtgaagaaagaagaagcttgagagagaagagagagttagagagagaaagtagagtgtttgtagagagagaaagtggtgtgtgtactagtagtaactccaagccagtgctagagacagagatacaaaaaggagacatcatccttctcttggccaaagcaagcaaccaagcaaagcttcctcttcttctccaagaactccaagaaccttctccttcatcttctccaccatgattccttccatcgcatgagctccatctccggcgtgtcgatcgagatcaccgttgctgctgccgaggtggagaaggaggtgtttgatcgatcggtcgatggaggcgagctcggcggcgacgccaccggacctgtcgctgcacatcagcttgccgagcagcgcggcggtggcgacgtcggggggagggcgtggcggcggcggggtggtggtgggaggaggaggaggggacccgtggcggaggctggatgggtccacggcgtcgacggagttgtcgctgtcgccgccgccggcgcaggcggcgggtgggggaggtggtggtggtggagcggacgcgctgccgtggcggcaccgaccttcgccgccgtcgtcggcggtggccaccacgtctgccgccgccgcggcggcgctgatggcgccgatgatgctgcagccgctcgacgccggcggcggcgcgtcggcgccgccgccgccgatccgcgggatacctatctacaacggccccggcgggttcccgttcctgcagccgtcgcccaccgccggcgacgtcggccaccaccaccaccaccaccccaagatgggattctacagctcgtaccaccacccatccacgtggccctccacgtcgccgtccccgctcgcggcgccgccgggcgccgcgtcgtcgccgctcgaccccacggcggcgttcctctcctccccccaccaccggatgctgtccgccgcctcggggaggctcaacggcatgctctccgtctccgacaccctccgcagctacggcgtccccggcgccgccgcccccggcgtcatcggcggcgcgcaccaccaccaccaccacctccacggcggccagccgttcgtcggcgccctcgcgtcccgcttcatgcccaagctccccgccaagcgcagcatgcgcgcgccgcgcatgcgctggacgagcaccctccacgcccgcttcgtccacgccgtcgagctcctcggcggccacgagagtacgcccccgccatcatcgtcgtcgtcctcctcctccttctcaccaccatcatcaacgagctcgatcaatctgatgagaatccaatcttgttcttggcaggggcgacgcccaagtcggtgctggagctcatggacgtcaaggatctgacgctagcgcatgtcaagagccacctccaggtatcccgccattgccgaccaattctcacagctcgatcgatcgatcaaacaccactcaccactgcaccatctctctctttctctctctcgatttcgattccattcagcttctgttcttgatcatcttgtttgggtgagacaaagatgccaatgcagtaactcctgagttagtgaagaaactgccattcttgggagcagagagagagagtgtgtgtgtgacatgtttggggatgtgtgtgcaagagagaagagagagagagaggggaaaaaagttgccatcattacacaataatgcattgcatctgcatctgtgctactagctccttccttagctctagtcatactagcgtatatgtgcacggcccaaagcactctcacacacaaacacaagagagagagagagagagagaagaagaagatgagagatgagagagagtaggacatattttgtgtgtgtttctttgctgcttgtcttttgcaatggcttcaacctcctggtttcattttgatctcacaaaaaatgtgtgtgtgtgtgtaaatatatatattgatcttctttttgttggacttttgtgttttattactgcagatgtatcgcaccgtgaagagcactgacaagcctgcagcctcttcaggtgattttttttaccatggcagctactagtagtagtagtagtagctaatttagctaagctccattttgcttttctttttttttggcgttgtgcattgcgttttacattacattgttgctatggtttttttgacgtgtagggccggcggacggcggctccggcgacgaggagttcgccggcggcgggcaggcggcgtcgggcggcggcgacagcatgtgcctgaggggtggcggcggcggcggggtggccgcggcggcgttcgcggagcacggccggtcggcgtcggagggcgccgccagctcggtcggcggcggcggcggcggcgacatggaccagtcgtcggccggcaacaccagcaccaccaggtggagcaactcctcaaggtacacacatggcagagttgcatttcaagtctttcagattaattatatatctacattgttatgccatctttaattaattaaaaatgaaattaatcaatcagaatgtcatgagatgatgatgatgatgataataatactaggataggaagaggatgatatgatggatgggtgtgctatgtgtgtttttaagtgtgttttagcttagaaccaaaggcaacaccaacaaactttggcatgcattgatgatgtatctaaatatgagttagtgacatgcaaaattaacctgccaagtacaacctctatttattaattcccaaaaaaatctcatggaggagaagggagagagagagatagtagtaatgtgtggtgatgcatggctaaaaaagcttagcaaaagaatgttttgggggcacacacacacacacctggagagggagttgcctatgtttaggtggccaatgttgttatgtcacacaaaagaccaaaaagtcacacaccccatggcttggcctcctcctccccccttgacctgtgcagttagctaggcttcttctcttctctccctctgtgtttggtttttgtggagctaaaaacattttaaaaatcttgcaaacattgtgtgtaaaaataggttcttgggctctgcccattgtcctctagcttctctcaaatctctctctctctctctctctctctctctctctttctcaaacctagggaggggagggttactcaggcagggctccattatcatttcttatcaatgcatggctctgattccagggggatggggctttgacctgacatgccctattgcctaggaatatgtaaccaaggacttgctgcattcttggttctttctccctctctcaccagtctcttcaatgcccttttcttccacctcttgggcaattattagcatggatggagctcaccttttcactctaccctctagctgtgattaaatcattgactaatcctaattcataaatataagggattcaactatgtaactagatgtactagatcctagtattactagtgtgttttgattctgttaggaggagtgattagcgtttgtcgtaagtactagtattaaactataggggattagtgtagatcatttttttaaaaattagtgagtgtgcttgggcagattttactccagccattggcgtgaaaactttgatctttgggcagcttggaagcaagtacagttcaacctgtccttggctgcattcgctgctttttctttctcaggactcactgcaactttcttgccatccccaacacctccctttcggtcgtgtttgatcagttgcattgctggtttcttcgccgctttaatttctccatctttcttctgttccttattggctaagtaaaaaatcattctcagcaatcaagttttgaaattcaaattagcttcaggttttatctatctaataattctctgactagttctctttctttcaagacctgttcttgttcagaactcttatgcagttgagagttcagttgttcatggaagtaatggcaatgcctggtctagtctttgagcagtatcctccttatgctcttgattttccttcactttagccgtttcagtcaaactttggggacaaattaaagtcagctggtcaagtgcatacataccacgtcatattttttagatgaatccattgtagtattaaatactagtgacaaaaaaatataactaaatggcattaaattgcaaccttcttccccaaaataattgggcacaactaccttgcttgcatatgctttatagtactcctacttattacttccttgaatccatgaggattccaggaatttggtcaggtcaaatgtccaggaggaattaggctatctttttttatcttcttctttttcttctaggtagtaggatcgttgtgcacatataaacaaaacaaaatagaaatttaagaggaaaccctcccaaaaaaaatacgactatcaattatgagtgattttacagttcttgaggaggtacaatgatacattttctattttaaaattcagtaactttgatactatgaggtacagaaatttgcacaaaaaaaatttggtacctctcaagtacttaaaatatcttatcaattatatttcagcaatgttgtcgttgctcgagttgtgcaaaaacatttctgatgaacaagtggagatgtatgcatatttagagagggaaacacatgcattttttaatatacattctcatgacaaattttggtgttctcgtctcattttagtctagcttagattaatggcatccatatattggtgaactgaaacagattgtatatgtccagtcttgaacaaacttcattatacaatgcataatcagaaaagatacagacatatattggcagatcacataaagtggtgtatctatgattgggtggtattttggacatacaaagtctactggtccctcatttgttaacagcatacatttgttcctatcaagacaaaagcactttacaacagtttggtagtaagttggtgttatgtgcgtgtctatttagatagagtggtagtaaaggaaggacactttttcttgatataccaaaatcacacataaaaaagaagtgtcattttcatgatcaacatgtggggtatgaacaaaaatgttctcccccctccaaccaacattgaagtcatcacacataaaaagcaaaaacatttaacaataatacatgcagacacatgtgcatgcatgtgtggatcacgcaaggacatactaattcaattaggtattcacaattaattagtgcaggaaatgacatgtaattacaattatatatgcacaacgatccttgtgtatttgtgtgacccattgtagtagcatttgattcctttcttgtgcctttctctacattgaattcgatctttgccaacagcggcttgctgatgagctcctgtgccattgcactgctgagctgcaccaaacagggacatcttttaagagcttgttgcctggaaatgatccatgtaaccaactgttcaggaagagcacactgtttgctgctcactttagctaaagcaaaactgtgtgcattatgcaatgcatatgcatccttccatctacccctgtgtcctttgccccccaaactgtgtaactacagtttaccatgcacatacatacaatgcacatctacccaattgtagcattgttgcaaggcctacttcagaattcagttagtccccaattgatccaactgcacacatatacatttacatatacatatacacaaacataccagcttggagaaaaggttgtaacaactttgctaaatgtgagatgtgtaatgtgtgttcttcctcttttcagggacccatggctgtcgtccaattcttgcaacatggacgcccatcgctccgtaggattgtcttctcctattgaggtatatatccttacattgttcaaagcttctttcgattcctagctaactgcatatccatgcagaaattcattagctcgcattcattctgaacatgatgtctgaaactctgaattttttttcgtttgtgcgtgtttcagaacttggaaccgtgcagatcgagcagctcgcaggtgtccaaccatgagctgagtagccctagtctcgagttcactctagggaggcctgactggcacggtgcagatcatgattagatggcaatcacagaggctaatgatcaaaaaaaaatttctcctgagatgtgaaatatatatgtgatatacaccaacctggtgctgatcatctttcgccaaccccagcttagccagagccagttcgtctgaagcttgtcatggcgaagaatgatcagcagcaatggcttgaaacgcacatcatatccactgcgtcgtcgtcatcgtcgtcgcaatcgatcggagaagagatatatatttcgcgtctcgatctcatcatcacaatttgggttttcttgattccttcttcttcttctttttgcaattaatatcatggatgcagctagagtttccttgtctgatctccatatttatttagttttgttcgccgtgccgggatcgatttacagtgtagttcagtggtgagctagctagctagagagtgagtgagtgagtgtcagctaggcagctggagatcgagagtgtgagtttggtgatgagttggttgtgtgtttgtcagtgtgtgtgaaagtgtgtgtgccattagcacatggaaagttggaaaggagagaaaggaagaaagaaaagggaattgagttcaggtgaagcaatctgccaatctatctagctacctatctatccatctacttagctcagttgctcagatgatgatctcagatttccatggcccttttttgtgtgcatgcatgccgcatatgcttctttctttaatccctgcaggttcttgcacttcctttagcctcattgatcatgtcagatactgcctacctgttcttttccagcaaccatggccggtgtgaaccggcctctcttgaccagaaactagcagatatctga&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001069632.1 RefSeq:Os09g0395300]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 9]]&lt;br /&gt;
[[Category:Chromosome 9]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os09g0395300&amp;diff=174626</id>
		<title>Os09g0395300</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os09g0395300&amp;diff=174626"/>
				<updated>2014-05-30T12:02:32Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;The rice ''SHALLOT-LIKE1'' ('' SLL1'') gene, a member of KANADI family, is a key gene controlling rice leaf rolling.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File: ZhangF1.jpg|right|thumb|100px|Fig 1. ''sll1'' has extremely incurved leaves, with deficiency of sclerenchymatous cells at the abaxial side &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File: ZhangF3.jpg|right|thumb|100px|Fig 3. Map-based cloning of ''SLL1'', which encodes an MYB transcription factor &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File: ZhangF8.jpg|right|thumb|100px|Fig 8. ''Sll1'' alters adaxial-abaxial pattern formation &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File: ZhangF10.jpg|right|thumb|100px|Fig 10. ''SLL1'' Affected multiple developmental processes in rice &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
''SLL1'' arrests normal sclerenchymatous cell formation and controls leaf rolling, controls the establishment of rice leaf polarity, and modulates ohotosynthesis by regulating cell fate &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
To investigate the molecular mechanisms of rice leaf rolling, a rice mutant population (''Oryza sativa'' L. ssp. ''japonica'' variety Nipponbare) generated by ethyl methanesulphonate mutagenesis was screened. Two allelic mutants with extremely incurved leaves were identified, designated as ''sll1-1'' and ''sll1-2'' (Fig. 1A ). ''sll1'', a rice mutant with shallot-like Leaves, displays abnormal sclerenchymatous cell development in the abaxial cell layers, altered mesophyll cell distribution, increased amounts of chlorophyll, and enhanced photosynthesis.&lt;br /&gt;
&lt;br /&gt;
Genetic analysis revealed that the abnormal character of ''sll1'' was controlled by a single recessive gene. To isolate the relevant mutant gene, ''SLL1'' was mapped to the long arm of rice chromosome 9 between markers RM1896 and RM3700. A large F2 mapping population was then generated, allowing the fine-mapping of ''SLL1'' to a 29.57-kb region, using the sequence tagged site and simple sequence repeat markers (Fig. 3A). Three annotated candidate genes, encoding a hypothetical protein, an En/Spm-like transposon, and a transcription factor containing a MYB-like domain, respectively, were located in this region. Further amplification of the relevant DNA fragments and sequence comparison revealed differences in ''sll1-1'' and ''sll1-2'' alleles in the gene encoding the transcription factor containing the MYB-like domain. Comparison with the corresponding genomic sequence revealed that the ''SLL1'' gene consists of six exons and five introns. The gene encodes a 377–amino acid MYB family transcription factor (Fig. 3B). Homologous analysis showed that ''SLL1'' shares high similarity with the KANADI family members in ''Arabidopsis''.&lt;br /&gt;
&lt;br /&gt;
A distinguishing characteristic of the monocot leaf is that microhairs or ligules are present only at the adaxial surface. In ''sll1-1'', the microhairs can be observed on both epidermal surfaces of some plants (Fig. 8A ), and the ligules exist on the abaxial side of the joint (Fig. 8B). This suggests an adaxialized trend in the abaxial epidermis of ''sll1-1'' and indicates the involvement of ''SLL1'' in the development of polarity throughout the leaf abaxial epidermis. ''SLL1'' overexpression resulted in dwarf plants with twisted and abnormal inner rolled leaves. We also observed enlarged phloem in the midrib as well as large and small veins, revealing the enhanced abaxial features of leaves following ''SLL1'' overexpression.&lt;br /&gt;
&lt;br /&gt;
''SLL1'' affected developmental processes in multiple developmental stages, in accordance with its expression patterns. Aside from altered leaf morphology, other tissues, including seeds, anthers, and roots, displayed abnormal development in ''sll1'' mutants (Fig. 10).&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
[[File: ZhangF5.jpg|right|thumb|100px|Fig 5. ''SLL1'' expression pattern analysis &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
Quantitative real-time RT-PCR (qRT-PCR) analysis revealed the expression of ''SLL1'' in various tissues, including roots, stems, leaves, flowers, and seedlings, with relatively high expression in leaf and seedlings (Fig. 5A , top panel). With an emphasis on the leaf, analysis by qRT-PCR showed that ''SLL1'' is ubiquitously expressed in shoot apical meristem (SAM), leaf blade, or leaf sheath at different developmental stages (Figure 5A, bottom panel) &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
To assess the expression pattern comprehensively, β-glucuronidase (GUS) activity was examined histochemically in transgenic plants carrying an ''SLL1'' promoter-GUS reporter gene. Results showed that ''SLL1'' was transcribed in stem (Fig. 5B, panels 1 and 2), anthers of young or mature flowers (Fig. 5B, panels 3 to 5), pistil tip (Fig. 5B, panel 6), glume (Fig. 5B, panel 7), vascular tissues of mature seeds (Fig. 5B, panels 8 and 9), coleoptile and embryonic root of germinating seedlings (Fig. 5B, panel 10), and root vascular tissues (Fig. 5B, panel 11). In addition, ''SLL1'' is highly transcribed in leaf veins and leaf sheath (Fig. 5C, panels 1 to 3), guard cells, and tracheal elements (Fig. 5C, panels 4 and 5).&lt;br /&gt;
&lt;br /&gt;
The spatial and temporal localization of ''SLL1'' during leaf development was further examined by in situ hybridization analysis. The mRNA expression of ''SLL1'' was detected throughout the young leaf primordium (plastochrons 1 to 3) and was more intense in abaxial cell layer through leaf development (plastochrons 4 and 5) (Fig. 5D, panel 2). However, the ''SLL1'' transcript did not demonstrate apical/basal polarity and did not accumulate at the apex of the meristem (Fig.e 5D, panel 3). Cross-section analysis of the shoot apex showed that ''SLL1'' was more highly expressed in the abaxial cell layer, including the epidermis and vasculature of the early leaf blade (Fig. 5D, panels 5 and 6). In the mature leaf, ''SLL1'' mainly accumulated at the abaxial epidermis, abaxial mesophyll cells, and vasculature (Fig. 5D, panels 8 and 9). In contrast with the sense probe (Fig. 5D, panels 4 and 7), ''SLL1'' was transcribed at a relatively low level throughout other leaf positions including the adaxial epidermis (Fig. 5D, panels 5 and 6).&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou 310006, Zhejiang, China&lt;br /&gt;
*National Key Laboratory of Plant Molecular Genetics, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Zhang GH, et al. (2009) ''SHALLOT-LIKE1'' is a KANADI transcription factor that modulates rice leaf rolling by regulating leaf abaxial cell development. The Plant Cell Online 21: 719-735.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os09g0395300|&lt;br /&gt;
Description = Similar to CDPK substrate protein 1|&lt;br /&gt;
Version = NM_001069632.1 GI:115479006 GeneID:4346973|&lt;br /&gt;
Length = 7672 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os09g0395300, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 9|Chromosome 9]]|&lt;br /&gt;
AP = Chromosome 9:14411926..14419597|&lt;br /&gt;
CDS = 14411926..14412128,14413047..14413888,14413990..14414066,14414656..14414701,14414841..14415084&amp;lt;br&amp;gt;,14418440..14418512,14419481..14419597|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008402:14411926..14419597&lt;br /&gt;
source=RiceChromosome09&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008402:14411926..14419597&lt;br /&gt;
source=RiceChromosome09&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggcaatggtgcgggagctcgagttgatgacgagctggagcaacagcatggggcgacaccgctacccaacgcgcatcctcgtcgattccttcgggcataagtgcagtgcctctgacaagggtgtgtggacctcctgcagcattcgcgcacccttgcaaggacgcggctccttccgacgtggcgcgaatattcgctttgggagcttgccgagcagcgcggcggtggcgacgtcggggggagggcgtggcggcggcggggtggtggtgggaggaggaggaggggacccgtggcggaggctggatgggtccacggcgtcgacggagttgtcgctgtcgccgccgccggcgcaggcggcgggtgggggaggtggtggtggtggagcggacgcgctgccgtggcggcaccgaccttcgccgccgtcgtcggcggtggccaccacgtctgccgccgccgcggcggcgctgatggcgccgatgatgctgcagccgctcgacgccggcggcggcgcgtcggcgccgccgccgccgatccgcgggatacctatctacaacggccccggcgggttcccgttcctgcagccgtcgcccaccgccggcgacgtcggccaccaccaccaccaccaccccaagatgggattctacagctcgtaccaccacccatccacgtggccctccacgtcgccgtccccgctcgcggcgccgccgggcgccgcgtcgtcgccgctcgaccccacggcggcgttcctctcctccccccaccaccggatgctgtccgccgcctcggggaggctcaacggcatgctctccgtctccgacaccctccgcagctacggcgtccccggcgccgccgcccccggcgtcatcggcggcgcgcaccaccaccaccaccacctccacggcggccagccgttcgtcggcgccctcgcgtcccgcttcatgcccaagctccccgccaagcgcagcatgcgcgcgccgcgcatgcgctggacgagcaccctccacgcccgcttcgtccacgccgtcgagctcctcggcggccacgagagggcgacgcccaagtcggtgctggagctcatggacgtcaaggatctgacgctagcgcatgtcaagagccacctccagatgtatcgcaccgtgaagagcactgacaagcctgcagcctcttcagggccggcggacggcggctccggcgacgaggagttcgccggcggcgggcaggcggcgtcgggcggcggcgacagcatgtgcctgaggggtggcggcggcggcggggtggccgcggcggcgttcgcggagcacggccggtcggcgtcggagggcgccgccagctcggtcggcggcggcggcggcggcgacatggaccagtcgtcggccggcaacaccagcaccaccaggtggagcaactcctcaagggacccatggctgtcgtccaattcttgcaacatggacgcccatcgctccgtaggattgtcttctcctattgaggttcttgcacttcctttagcctcattgatcatgtcagatactgcctacctgttcttttccagcaaccatggccggtgtgaaccggcctctcttgaccagaaactagcagatatctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MAMVRELELMTSWSNSMGRHRYPTRILVDSFGHKCSASDKGVWT                     SCSIRAPLQGRGSFRRGANIRFGSLPSSAAVATSGGGRGGGGVVVGGGGGDPWRRLDG                     STASTELSLSPPPAQAAGGGGGGGGADALPWRHRPSPPSSAVATTSAAAAAALMAPMM                     LQPLDAGGGASAPPPPIRGIPIYNGPGGFPFLQPSPTAGDVGHHHHHHPKMGFYSSYH                     HPSTWPSTSPSPLAAPPGAASSPLDPTAAFLSSPHHRMLSAASGRLNGMLSVSDTLRS                     YGVPGAAAPGVIGGAHHHHHHLHGGQPFVGALASRFMPKLPAKRSMRAPRMRWTSTLH                     ARFVHAVELLGGHERATPKSVLELMDVKDLTLAHVKSHLQMYRTVKSTDKPAASSGPA                     DGGSGDEEFAGGGQAASGGGDSMCLRGGGGGGVAAAAFAEHGRSASEGAASSVGGGGG                     GDMDQSSAGNTSTTRWSNSSRDPWLSSNSCNMDAHRSVGLSSPIEVLALPLASLIMSD                     TAYLFFSSNHGRCEPASLDQKLADI&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;1..203#1122..1963#2065..2141#2731..2776#2916..3159#6515..6587#7556..7672#atggcaatggtgcgggagctcgagttgatgacgagctggagcaacagcatggggcgacaccgctacccaacgcgcatcctcgtcgattccttcgggcataagtgcagtgcctctgacaagggtgtgtggacctcctgcagcattcgcgcacccttgcaaggacgcggctccttccgacgtggcgcgaatattcgctttgggaggtatgagactacgctccatggtggagcgttgggcgtgaccttagtgtgcgcatatgtaagctgtatgcgtacgtataaatgttgagcttgcagtacatgtatacttgtttttttcttcttttttatgaggtcctttaattccattgtctgtattatttatgctagtatggaggatgatggtggcagtgacataaagtatacaaaaagcatagtatagtatacgtatggaaacaaaagcatgctacctttgactccacttgcattgcctgctaactgccattatttaaggaatacatggttgaatgcctgcctaaacatcaagataacctcacattctcctctctctctctcctaccttgcaattaagggtagcagcagtactctcctcactgctggctgactgctcccattttctctctctactctctctctctctctctcctctattccttttatacttgttgttggtagctaggagtatagcaggacagcacaaggaaccaattcatgcatatatccctggtgtctctcatgcatgttagtgtgaagaaagaagaagcttgagagagaagagagagttagagagagaaagtagagtgtttgtagagagagaaagtggtgtgtgtactagtagtaactccaagccagtgctagagacagagatacaaaaaggagacatcatccttctcttggccaaagcaagcaaccaagcaaagcttcctcttcttctccaagaactccaagaaccttctccttcatcttctccaccatgattccttccatcgcatgagctccatctccggcgtgtcgatcgagatcaccgttgctgctgccgaggtggagaaggaggtgtttgatcgatcggtcgatggaggcgagctcggcggcgacgccaccggacctgtcgctgcacatcagcttgccgagcagcgcggcggtggcgacgtcggggggagggcgtggcggcggcggggtggtggtgggaggaggaggaggggacccgtggcggaggctggatgggtccacggcgtcgacggagttgtcgctgtcgccgccgccggcgcaggcggcgggtgggggaggtggtggtggtggagcggacgcgctgccgtggcggcaccgaccttcgccgccgtcgtcggcggtggccaccacgtctgccgccgccgcggcggcgctgatggcgccgatgatgctgcagccgctcgacgccggcggcggcgcgtcggcgccgccgccgccgatccgcgggatacctatctacaacggccccggcgggttcccgttcctgcagccgtcgcccaccgccggcgacgtcggccaccaccaccaccaccaccccaagatgggattctacagctcgtaccaccacccatccacgtggccctccacgtcgccgtccccgctcgcggcgccgccgggcgccgcgtcgtcgccgctcgaccccacggcggcgttcctctcctccccccaccaccggatgctgtccgccgcctcggggaggctcaacggcatgctctccgtctccgacaccctccgcagctacggcgtccccggcgccgccgcccccggcgtcatcggcggcgcgcaccaccaccaccaccacctccacggcggccagccgttcgtcggcgccctcgcgtcccgcttcatgcccaagctccccgccaagcgcagcatgcgcgcgccgcgcatgcgctggacgagcaccctccacgcccgcttcgtccacgccgtcgagctcctcggcggccacgagagtacgcccccgccatcatcgtcgtcgtcctcctcctccttctcaccaccatcatcaacgagctcgatcaatctgatgagaatccaatcttgttcttggcaggggcgacgcccaagtcggtgctggagctcatggacgtcaaggatctgacgctagcgcatgtcaagagccacctccaggtatcccgccattgccgaccaattctcacagctcgatcgatcgatcaaacaccactcaccactgcaccatctctctctttctctctctcgatttcgattccattcagcttctgttcttgatcatcttgtttgggtgagacaaagatgccaatgcagtaactcctgagttagtgaagaaactgccattcttgggagcagagagagagagtgtgtgtgtgacatgtttggggatgtgtgtgcaagagagaagagagagagagaggggaaaaaagttgccatcattacacaataatgcattgcatctgcatctgtgctactagctccttccttagctctagtcatactagcgtatatgtgcacggcccaaagcactctcacacacaaacacaagagagagagagagagagagaagaagaagatgagagatgagagagagtaggacatattttgtgtgtgtttctttgctgcttgtcttttgcaatggcttcaacctcctggtttcattttgatctcacaaaaaatgtgtgtgtgtgtgtaaatatatatattgatcttctttttgttggacttttgtgttttattactgcagatgtatcgcaccgtgaagagcactgacaagcctgcagcctcttcaggtgattttttttaccatggcagctactagtagtagtagtagtagctaatttagctaagctccattttgcttttctttttttttggcgttgtgcattgcgttttacattacattgttgctatggtttttttgacgtgtagggccggcggacggcggctccggcgacgaggagttcgccggcggcgggcaggcggcgtcgggcggcggcgacagcatgtgcctgaggggtggcggcggcggcggggtggccgcggcggcgttcgcggagcacggccggtcggcgtcggagggcgccgccagctcggtcggcggcggcggcggcggcgacatggaccagtcgtcggccggcaacaccagcaccaccaggtggagcaactcctcaaggtacacacatggcagagttgcatttcaagtctttcagattaattatatatctacattgttatgccatctttaattaattaaaaatgaaattaatcaatcagaatgtcatgagatgatgatgatgatgataataatactaggataggaagaggatgatatgatggatgggtgtgctatgtgtgtttttaagtgtgttttagcttagaaccaaaggcaacaccaacaaactttggcatgcattgatgatgtatctaaatatgagttagtgacatgcaaaattaacctgccaagtacaacctctatttattaattcccaaaaaaatctcatggaggagaagggagagagagagatagtagtaatgtgtggtgatgcatggctaaaaaagcttagcaaaagaatgttttgggggcacacacacacacacctggagagggagttgcctatgtttaggtggccaatgttgttatgtcacacaaaagaccaaaaagtcacacaccccatggcttggcctcctcctccccccttgacctgtgcagttagctaggcttcttctcttctctccctctgtgtttggtttttgtggagctaaaaacattttaaaaatcttgcaaacattgtgtgtaaaaataggttcttgggctctgcccattgtcctctagcttctctcaaatctctctctctctctctctctctctctctctctttctcaaacctagggaggggagggttactcaggcagggctccattatcatttcttatcaatgcatggctctgattccagggggatggggctttgacctgacatgccctattgcctaggaatatgtaaccaaggacttgctgcattcttggttctttctccctctctcaccagtctcttcaatgcccttttcttccacctcttgggcaattattagcatggatggagctcaccttttcactctaccctctagctgtgattaaatcattgactaatcctaattcataaatataagggattcaactatgtaactagatgtactagatcctagtattactagtgtgttttgattctgttaggaggagtgattagcgtttgtcgtaagtactagtattaaactataggggattagtgtagatcatttttttaaaaattagtgagtgtgcttgggcagattttactccagccattggcgtgaaaactttgatctttgggcagcttggaagcaagtacagttcaacctgtccttggctgcattcgctgctttttctttctcaggactcactgcaactttcttgccatccccaacacctccctttcggtcgtgtttgatcagttgcattgctggtttcttcgccgctttaatttctccatctttcttctgttccttattggctaagtaaaaaatcattctcagcaatcaagttttgaaattcaaattagcttcaggttttatctatctaataattctctgactagttctctttctttcaagacctgttcttgttcagaactcttatgcagttgagagttcagttgttcatggaagtaatggcaatgcctggtctagtctttgagcagtatcctccttatgctcttgattttccttcactttagccgtttcagtcaaactttggggacaaattaaagtcagctggtcaagtgcatacataccacgtcatattttttagatgaatccattgtagtattaaatactagtgacaaaaaaatataactaaatggcattaaattgcaaccttcttccccaaaataattgggcacaactaccttgcttgcatatgctttatagtactcctacttattacttccttgaatccatgaggattccaggaatttggtcaggtcaaatgtccaggaggaattaggctatctttttttatcttcttctttttcttctaggtagtaggatcgttgtgcacatataaacaaaacaaaatagaaatttaagaggaaaccctcccaaaaaaaatacgactatcaattatgagtgattttacagttcttgaggaggtacaatgatacattttctattttaaaattcagtaactttgatactatgaggtacagaaatttgcacaaaaaaaatttggtacctctcaagtacttaaaatatcttatcaattatatttcagcaatgttgtcgttgctcgagttgtgcaaaaacatttctgatgaacaagtggagatgtatgcatatttagagagggaaacacatgcattttttaatatacattctcatgacaaattttggtgttctcgtctcattttagtctagcttagattaatggcatccatatattggtgaactgaaacagattgtatatgtccagtcttgaacaaacttcattatacaatgcataatcagaaaagatacagacatatattggcagatcacataaagtggtgtatctatgattgggtggtattttggacatacaaagtctactggtccctcatttgttaacagcatacatttgttcctatcaagacaaaagcactttacaacagtttggtagtaagttggtgttatgtgcgtgtctatttagatagagtggtagtaaaggaaggacactttttcttgatataccaaaatcacacataaaaaagaagtgtcattttcatgatcaacatgtggggtatgaacaaaaatgttctcccccctccaaccaacattgaagtcatcacacataaaaagcaaaaacatttaacaataatacatgcagacacatgtgcatgcatgtgtggatcacgcaaggacatactaattcaattaggtattcacaattaattagtgcaggaaatgacatgtaattacaattatatatgcacaacgatccttgtgtatttgtgtgacccattgtagtagcatttgattcctttcttgtgcctttctctacattgaattcgatctttgccaacagcggcttgctgatgagctcctgtgccattgcactgctgagctgcaccaaacagggacatcttttaagagcttgttgcctggaaatgatccatgtaaccaactgttcaggaagagcacactgtttgctgctcactttagctaaagcaaaactgtgtgcattatgcaatgcatatgcatccttccatctacccctgtgtcctttgccccccaaactgtgtaactacagtttaccatgcacatacatacaatgcacatctacccaattgtagcattgttgcaaggcctacttcagaattcagttagtccccaattgatccaactgcacacatatacatttacatatacatatacacaaacataccagcttggagaaaaggttgtaacaactttgctaaatgtgagatgtgtaatgtgtgttcttcctcttttcagggacccatggctgtcgtccaattcttgcaacatggacgcccatcgctccgtaggattgtcttctcctattgaggtatatatccttacattgttcaaagcttctttcgattcctagctaactgcatatccatgcagaaattcattagctcgcattcattctgaacatgatgtctgaaactctgaattttttttcgtttgtgcgtgtttcagaacttggaaccgtgcagatcgagcagctcgcaggtgtccaaccatgagctgagtagccctagtctcgagttcactctagggaggcctgactggcacggtgcagatcatgattagatggcaatcacagaggctaatgatcaaaaaaaaatttctcctgagatgtgaaatatatatgtgatatacaccaacctggtgctgatcatctttcgccaaccccagcttagccagagccagttcgtctgaagcttgtcatggcgaagaatgatcagcagcaatggcttgaaacgcacatcatatccactgcgtcgtcgtcatcgtcgtcgcaatcgatcggagaagagatatatatttcgcgtctcgatctcatcatcacaatttgggttttcttgattccttcttcttcttctttttgcaattaatatcatggatgcagctagagtttccttgtctgatctccatatttatttagttttgttcgccgtgccgggatcgatttacagtgtagttcagtggtgagctagctagctagagagtgagtgagtgagtgtcagctaggcagctggagatcgagagtgtgagtttggtgatgagttggttgtgtgtttgtcagtgtgtgtgaaagtgtgtgtgccattagcacatggaaagttggaaaggagagaaaggaagaaagaaaagggaattgagttcaggtgaagcaatctgccaatctatctagctacctatctatccatctacttagctcagttgctcagatgatgatctcagatttccatggcccttttttgtgtgcatgcatgccgcatatgcttctttctttaatccctgcaggttcttgcacttcctttagcctcattgatcatgtcagatactgcctacctgttcttttccagcaaccatggccggtgtgaaccggcctctcttgaccagaaactagcagatatctga&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001069632.1 RefSeq:Os09g0395300]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 9]]&lt;br /&gt;
[[Category:Chromosome 9]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os09g0395300&amp;diff=174625</id>
		<title>Os09g0395300</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os09g0395300&amp;diff=174625"/>
				<updated>2014-05-30T11:55:41Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;The rice ''SHALLOT-LIKE1'' ('' SLL1'') gene, a member of KANADI family, is a key gene controlling rice leaf rolling.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File: ZhangF1.jpg|right|thumb|100px|Fig 1. ''sll1'' has extremely incurved leaves, with deficiency of sclerenchymatous cells at the abaxial side &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File: ZhangF3.jpg|right|thumb|100px|Fig 3. Map-based cloning of ''SLL1'', which encodes an MYB transcription factor &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File: ZhangF8.jpg|right|thumb|100px|Fig 8. ''Sll1'' alters adaxial-abaxial pattern formation &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File: ZhangF10.jpg|right|thumb|100px|Fig 10. ''SLL1'' Affected multiple developmental processes in rice &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
To investigate the molecular mechanisms of rice leaf rolling, a rice mutant population (''Oryza sativa'' L. ssp. ''japonica'' variety Nipponbare) generated by ethyl methanesulphonate mutagenesis was screened. Two allelic mutants with extremely incurved leaves were identified, designated as ''sll1-1'' and ''sll1-2'' (Fig. 1A ). ''sll1'', a rice mutant with shallot-like Leaves, displays abnormal sclerenchymatous cell development in the abaxial cell layers, altered mesophyll cell distribution, increased amounts of chlorophyll, and enhanced photosynthesis &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
Genetic analysis revealed that the abnormal character of ''sll1'' was controlled by a single recessive gene. To isolate the relevant mutant gene, ''SLL1'' was mapped to the long arm of rice chromosome 9 between markers RM1896 and RM3700. A large F2 mapping population was then generated, allowing the fine-mapping of ''SLL1'' to a 29.57-kb region, using the sequence tagged site and simple sequence repeat markers (Fig. 3A). Three annotated candidate genes, encoding a hypothetical protein, an En/Spm-like transposon, and a transcription factor containing a MYB-like domain, respectively, were located in this region. Further amplification of the relevant DNA fragments and sequence comparison revealed differences in ''sll1-1'' and ''sll1-2'' alleles in the gene encoding the transcription factor containing the MYB-like domain. Comparison with the corresponding genomic sequence revealed that the ''SLL1'' gene consists of six exons and five introns. The gene encodes a 377–amino acid MYB family transcription factor (Fig. 3B). Homologous analysis showed that ''SLL1'' shares high similarity with the KANADI family members in ''Arabidopsis''.&lt;br /&gt;
&lt;br /&gt;
A distinguishing characteristic of the monocot leaf is that microhairs or ligules are present only at the adaxial surface. In ''sll1-1'', the microhairs can be observed on both epidermal surfaces of some plants (Fig. 8A ), and the ligules exist on the abaxial side of the joint (Fig. 8B). This suggests an adaxialized trend in the abaxial epidermis of ''sll1-1'' and indicates the involvement of ''SLL1'' in the development of polarity throughout the leaf abaxial epidermis. ''SLL1'' overexpression resulted in dwarf plants with twisted and abnormal inner rolled leaves. We also observed enlarged phloem in the midrib as well as large and small veins, revealing the enhanced abaxial features of leaves following ''SLL1'' overexpression.&lt;br /&gt;
&lt;br /&gt;
''SLL1'' affected developmental processes in multiple developmental stages, in accordance with its expression patterns. Aside from altered leaf morphology, other tissues, including seeds, anthers, and roots, displayed abnormal development in ''sll1'' mutants (Fig. 10).&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
[[File: ZhangF5.jpg|right|thumb|100px|Fig 5. ''SLL1'' expression pattern analysis &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
Quantitative real-time RT-PCR (qRT-PCR) analysis revealed the expression of ''SLL1'' in various tissues, including roots, stems, leaves, flowers, and seedlings, with relatively high expression in leaf and seedlings (Fig. 5A , top panel). With an emphasis on the leaf, analysis by qRT-PCR showed that ''SLL1'' is ubiquitously expressed in shoot apical meristem (SAM), leaf blade, or leaf sheath at different developmental stages (Figure 5A, bottom panel).&lt;br /&gt;
&lt;br /&gt;
To assess the expression pattern comprehensively, β-glucuronidase (GUS) activity was examined histochemically in transgenic plants carrying an ''SLL1'' promoter-GUS reporter gene. Results showed that ''SLL1'' was transcribed in stem (Fig. 5B, panels 1 and 2), anthers of young or mature flowers (Fig. 5B, panels 3 to 5), pistil tip (Fig. 5B, panel 6), glume (Fig. 5B, panel 7), vascular tissues of mature seeds (Fig. 5B, panels 8 and 9), coleoptile and embryonic root of germinating seedlings (Fig. 5B, panel 10), and root vascular tissues (Fig. 5B, panel 11). In addition, ''SLL1'' is highly transcribed in leaf veins and leaf sheath (Fig. 5C, panels 1 to 3), guard cells, and tracheal elements (Fig. 5C, panels 4 and 5).&lt;br /&gt;
&lt;br /&gt;
The spatial and temporal localization of ''SLL1'' during leaf development was further examined by in situ hybridization analysis. The mRNA expression of ''SLL1'' was detected throughout the young leaf primordium (plastochrons 1 to 3) and was more intense in abaxial cell layer through leaf development (plastochrons 4 and 5) (Fig. 5D, panel 2). However, the ''SLL1'' transcript did not demonstrate apical/basal polarity and did not accumulate at the apex of the meristem (Fig.e 5D, panel 3). Cross-section analysis of the shoot apex showed that ''SLL1'' was more highly expressed in the abaxial cell layer, including the epidermis and vasculature of the early leaf blade (Fig. 5D, panels 5 and 6). In the mature leaf, ''SLL1'' mainly accumulated at the abaxial epidermis, abaxial mesophyll cells, and vasculature (Fig. 5D, panels 8 and 9). In contrast with the sense probe (Fig. 5D, panels 4 and 7), ''SLL1'' was transcribed at a relatively low level throughout other leaf positions including the adaxial epidermis (Fig. 5D, panels 5 and 6).&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
Please input evolution information here.&lt;br /&gt;
&lt;br /&gt;
You can also add sub-section(s) at will.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou 310006, Zhejiang, China&lt;br /&gt;
*National Key Laboratory of Plant Molecular Genetics, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Zhang GH, et al. (2009) ''SHALLOT-LIKE1'' is a KANADI transcription factor that modulates rice leaf rolling by regulating leaf abaxial cell development. The Plant Cell Online 21: 719-735.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os09g0395300|&lt;br /&gt;
Description = Similar to CDPK substrate protein 1|&lt;br /&gt;
Version = NM_001069632.1 GI:115479006 GeneID:4346973|&lt;br /&gt;
Length = 7672 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os09g0395300, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 9|Chromosome 9]]|&lt;br /&gt;
AP = Chromosome 9:14411926..14419597|&lt;br /&gt;
CDS = 14411926..14412128,14413047..14413888,14413990..14414066,14414656..14414701,14414841..14415084&amp;lt;br&amp;gt;,14418440..14418512,14419481..14419597|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008402:14411926..14419597&lt;br /&gt;
source=RiceChromosome09&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008402:14411926..14419597&lt;br /&gt;
source=RiceChromosome09&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggcaatggtgcgggagctcgagttgatgacgagctggagcaacagcatggggcgacaccgctacccaacgcgcatcctcgtcgattccttcgggcataagtgcagtgcctctgacaagggtgtgtggacctcctgcagcattcgcgcacccttgcaaggacgcggctccttccgacgtggcgcgaatattcgctttgggagcttgccgagcagcgcggcggtggcgacgtcggggggagggcgtggcggcggcggggtggtggtgggaggaggaggaggggacccgtggcggaggctggatgggtccacggcgtcgacggagttgtcgctgtcgccgccgccggcgcaggcggcgggtgggggaggtggtggtggtggagcggacgcgctgccgtggcggcaccgaccttcgccgccgtcgtcggcggtggccaccacgtctgccgccgccgcggcggcgctgatggcgccgatgatgctgcagccgctcgacgccggcggcggcgcgtcggcgccgccgccgccgatccgcgggatacctatctacaacggccccggcgggttcccgttcctgcagccgtcgcccaccgccggcgacgtcggccaccaccaccaccaccaccccaagatgggattctacagctcgtaccaccacccatccacgtggccctccacgtcgccgtccccgctcgcggcgccgccgggcgccgcgtcgtcgccgctcgaccccacggcggcgttcctctcctccccccaccaccggatgctgtccgccgcctcggggaggctcaacggcatgctctccgtctccgacaccctccgcagctacggcgtccccggcgccgccgcccccggcgtcatcggcggcgcgcaccaccaccaccaccacctccacggcggccagccgttcgtcggcgccctcgcgtcccgcttcatgcccaagctccccgccaagcgcagcatgcgcgcgccgcgcatgcgctggacgagcaccctccacgcccgcttcgtccacgccgtcgagctcctcggcggccacgagagggcgacgcccaagtcggtgctggagctcatggacgtcaaggatctgacgctagcgcatgtcaagagccacctccagatgtatcgcaccgtgaagagcactgacaagcctgcagcctcttcagggccggcggacggcggctccggcgacgaggagttcgccggcggcgggcaggcggcgtcgggcggcggcgacagcatgtgcctgaggggtggcggcggcggcggggtggccgcggcggcgttcgcggagcacggccggtcggcgtcggagggcgccgccagctcggtcggcggcggcggcggcggcgacatggaccagtcgtcggccggcaacaccagcaccaccaggtggagcaactcctcaagggacccatggctgtcgtccaattcttgcaacatggacgcccatcgctccgtaggattgtcttctcctattgaggttcttgcacttcctttagcctcattgatcatgtcagatactgcctacctgttcttttccagcaaccatggccggtgtgaaccggcctctcttgaccagaaactagcagatatctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MAMVRELELMTSWSNSMGRHRYPTRILVDSFGHKCSASDKGVWT                     SCSIRAPLQGRGSFRRGANIRFGSLPSSAAVATSGGGRGGGGVVVGGGGGDPWRRLDG                     STASTELSLSPPPAQAAGGGGGGGGADALPWRHRPSPPSSAVATTSAAAAAALMAPMM                     LQPLDAGGGASAPPPPIRGIPIYNGPGGFPFLQPSPTAGDVGHHHHHHPKMGFYSSYH                     HPSTWPSTSPSPLAAPPGAASSPLDPTAAFLSSPHHRMLSAASGRLNGMLSVSDTLRS                     YGVPGAAAPGVIGGAHHHHHHLHGGQPFVGALASRFMPKLPAKRSMRAPRMRWTSTLH                     ARFVHAVELLGGHERATPKSVLELMDVKDLTLAHVKSHLQMYRTVKSTDKPAASSGPA                     DGGSGDEEFAGGGQAASGGGDSMCLRGGGGGGVAAAAFAEHGRSASEGAASSVGGGGG                     GDMDQSSAGNTSTTRWSNSSRDPWLSSNSCNMDAHRSVGLSSPIEVLALPLASLIMSD                     TAYLFFSSNHGRCEPASLDQKLADI&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;1..203#1122..1963#2065..2141#2731..2776#2916..3159#6515..6587#7556..7672#atggcaatggtgcgggagctcgagttgatgacgagctggagcaacagcatggggcgacaccgctacccaacgcgcatcctcgtcgattccttcgggcataagtgcagtgcctctgacaagggtgtgtggacctcctgcagcattcgcgcacccttgcaaggacgcggctccttccgacgtggcgcgaatattcgctttgggaggtatgagactacgctccatggtggagcgttgggcgtgaccttagtgtgcgcatatgtaagctgtatgcgtacgtataaatgttgagcttgcagtacatgtatacttgtttttttcttcttttttatgaggtcctttaattccattgtctgtattatttatgctagtatggaggatgatggtggcagtgacataaagtatacaaaaagcatagtatagtatacgtatggaaacaaaagcatgctacctttgactccacttgcattgcctgctaactgccattatttaaggaatacatggttgaatgcctgcctaaacatcaagataacctcacattctcctctctctctctcctaccttgcaattaagggtagcagcagtactctcctcactgctggctgactgctcccattttctctctctactctctctctctctctctcctctattccttttatacttgttgttggtagctaggagtatagcaggacagcacaaggaaccaattcatgcatatatccctggtgtctctcatgcatgttagtgtgaagaaagaagaagcttgagagagaagagagagttagagagagaaagtagagtgtttgtagagagagaaagtggtgtgtgtactagtagtaactccaagccagtgctagagacagagatacaaaaaggagacatcatccttctcttggccaaagcaagcaaccaagcaaagcttcctcttcttctccaagaactccaagaaccttctccttcatcttctccaccatgattccttccatcgcatgagctccatctccggcgtgtcgatcgagatcaccgttgctgctgccgaggtggagaaggaggtgtttgatcgatcggtcgatggaggcgagctcggcggcgacgccaccggacctgtcgctgcacatcagcttgccgagcagcgcggcggtggcgacgtcggggggagggcgtggcggcggcggggtggtggtgggaggaggaggaggggacccgtggcggaggctggatgggtccacggcgtcgacggagttgtcgctgtcgccgccgccggcgcaggcggcgggtgggggaggtggtggtggtggagcggacgcgctgccgtggcggcaccgaccttcgccgccgtcgtcggcggtggccaccacgtctgccgccgccgcggcggcgctgatggcgccgatgatgctgcagccgctcgacgccggcggcggcgcgtcggcgccgccgccgccgatccgcgggatacctatctacaacggccccggcgggttcccgttcctgcagccgtcgcccaccgccggcgacgtcggccaccaccaccaccaccaccccaagatgggattctacagctcgtaccaccacccatccacgtggccctccacgtcgccgtccccgctcgcggcgccgccgggcgccgcgtcgtcgccgctcgaccccacggcggcgttcctctcctccccccaccaccggatgctgtccgccgcctcggggaggctcaacggcatgctctccgtctccgacaccctccgcagctacggcgtccccggcgccgccgcccccggcgtcatcggcggcgcgcaccaccaccaccaccacctccacggcggccagccgttcgtcggcgccctcgcgtcccgcttcatgcccaagctccccgccaagcgcagcatgcgcgcgccgcgcatgcgctggacgagcaccctccacgcccgcttcgtccacgccgtcgagctcctcggcggccacgagagtacgcccccgccatcatcgtcgtcgtcctcctcctccttctcaccaccatcatcaacgagctcgatcaatctgatgagaatccaatcttgttcttggcaggggcgacgcccaagtcggtgctggagctcatggacgtcaaggatctgacgctagcgcatgtcaagagccacctccaggtatcccgccattgccgaccaattctcacagctcgatcgatcgatcaaacaccactcaccactgcaccatctctctctttctctctctcgatttcgattccattcagcttctgttcttgatcatcttgtttgggtgagacaaagatgccaatgcagtaactcctgagttagtgaagaaactgccattcttgggagcagagagagagagtgtgtgtgtgacatgtttggggatgtgtgtgcaagagagaagagagagagagaggggaaaaaagttgccatcattacacaataatgcattgcatctgcatctgtgctactagctccttccttagctctagtcatactagcgtatatgtgcacggcccaaagcactctcacacacaaacacaagagagagagagagagagagaagaagaagatgagagatgagagagagtaggacatattttgtgtgtgtttctttgctgcttgtcttttgcaatggcttcaacctcctggtttcattttgatctcacaaaaaatgtgtgtgtgtgtgtaaatatatatattgatcttctttttgttggacttttgtgttttattactgcagatgtatcgcaccgtgaagagcactgacaagcctgcagcctcttcaggtgattttttttaccatggcagctactagtagtagtagtagtagctaatttagctaagctccattttgcttttctttttttttggcgttgtgcattgcgttttacattacattgttgctatggtttttttgacgtgtagggccggcggacggcggctccggcgacgaggagttcgccggcggcgggcaggcggcgtcgggcggcggcgacagcatgtgcctgaggggtggcggcggcggcggggtggccgcggcggcgttcgcggagcacggccggtcggcgtcggagggcgccgccagctcggtcggcggcggcggcggcggcgacatggaccagtcgtcggccggcaacaccagcaccaccaggtggagcaactcctcaaggtacacacatggcagagttgcatttcaagtctttcagattaattatatatctacattgttatgccatctttaattaattaaaaatgaaattaatcaatcagaatgtcatgagatgatgatgatgatgataataatactaggataggaagaggatgatatgatggatgggtgtgctatgtgtgtttttaagtgtgttttagcttagaaccaaaggcaacaccaacaaactttggcatgcattgatgatgtatctaaatatgagttagtgacatgcaaaattaacctgccaagtacaacctctatttattaattcccaaaaaaatctcatggaggagaagggagagagagagatagtagtaatgtgtggtgatgcatggctaaaaaagcttagcaaaagaatgttttgggggcacacacacacacacctggagagggagttgcctatgtttaggtggccaatgttgttatgtcacacaaaagaccaaaaagtcacacaccccatggcttggcctcctcctccccccttgacctgtgcagttagctaggcttcttctcttctctccctctgtgtttggtttttgtggagctaaaaacattttaaaaatcttgcaaacattgtgtgtaaaaataggttcttgggctctgcccattgtcctctagcttctctcaaatctctctctctctctctctctctctctctctctttctcaaacctagggaggggagggttactcaggcagggctccattatcatttcttatcaatgcatggctctgattccagggggatggggctttgacctgacatgccctattgcctaggaatatgtaaccaaggacttgctgcattcttggttctttctccctctctcaccagtctcttcaatgcccttttcttccacctcttgggcaattattagcatggatggagctcaccttttcactctaccctctagctgtgattaaatcattgactaatcctaattcataaatataagggattcaactatgtaactagatgtactagatcctagtattactagtgtgttttgattctgttaggaggagtgattagcgtttgtcgtaagtactagtattaaactataggggattagtgtagatcatttttttaaaaattagtgagtgtgcttgggcagattttactccagccattggcgtgaaaactttgatctttgggcagcttggaagcaagtacagttcaacctgtccttggctgcattcgctgctttttctttctcaggactcactgcaactttcttgccatccccaacacctccctttcggtcgtgtttgatcagttgcattgctggtttcttcgccgctttaatttctccatctttcttctgttccttattggctaagtaaaaaatcattctcagcaatcaagttttgaaattcaaattagcttcaggttttatctatctaataattctctgactagttctctttctttcaagacctgttcttgttcagaactcttatgcagttgagagttcagttgttcatggaagtaatggcaatgcctggtctagtctttgagcagtatcctccttatgctcttgattttccttcactttagccgtttcagtcaaactttggggacaaattaaagtcagctggtcaagtgcatacataccacgtcatattttttagatgaatccattgtagtattaaatactagtgacaaaaaaatataactaaatggcattaaattgcaaccttcttccccaaaataattgggcacaactaccttgcttgcatatgctttatagtactcctacttattacttccttgaatccatgaggattccaggaatttggtcaggtcaaatgtccaggaggaattaggctatctttttttatcttcttctttttcttctaggtagtaggatcgttgtgcacatataaacaaaacaaaatagaaatttaagaggaaaccctcccaaaaaaaatacgactatcaattatgagtgattttacagttcttgaggaggtacaatgatacattttctattttaaaattcagtaactttgatactatgaggtacagaaatttgcacaaaaaaaatttggtacctctcaagtacttaaaatatcttatcaattatatttcagcaatgttgtcgttgctcgagttgtgcaaaaacatttctgatgaacaagtggagatgtatgcatatttagagagggaaacacatgcattttttaatatacattctcatgacaaattttggtgttctcgtctcattttagtctagcttagattaatggcatccatatattggtgaactgaaacagattgtatatgtccagtcttgaacaaacttcattatacaatgcataatcagaaaagatacagacatatattggcagatcacataaagtggtgtatctatgattgggtggtattttggacatacaaagtctactggtccctcatttgttaacagcatacatttgttcctatcaagacaaaagcactttacaacagtttggtagtaagttggtgttatgtgcgtgtctatttagatagagtggtagtaaaggaaggacactttttcttgatataccaaaatcacacataaaaaagaagtgtcattttcatgatcaacatgtggggtatgaacaaaaatgttctcccccctccaaccaacattgaagtcatcacacataaaaagcaaaaacatttaacaataatacatgcagacacatgtgcatgcatgtgtggatcacgcaaggacatactaattcaattaggtattcacaattaattagtgcaggaaatgacatgtaattacaattatatatgcacaacgatccttgtgtatttgtgtgacccattgtagtagcatttgattcctttcttgtgcctttctctacattgaattcgatctttgccaacagcggcttgctgatgagctcctgtgccattgcactgctgagctgcaccaaacagggacatcttttaagagcttgttgcctggaaatgatccatgtaaccaactgttcaggaagagcacactgtttgctgctcactttagctaaagcaaaactgtgtgcattatgcaatgcatatgcatccttccatctacccctgtgtcctttgccccccaaactgtgtaactacagtttaccatgcacatacatacaatgcacatctacccaattgtagcattgttgcaaggcctacttcagaattcagttagtccccaattgatccaactgcacacatatacatttacatatacatatacacaaacataccagcttggagaaaaggttgtaacaactttgctaaatgtgagatgtgtaatgtgtgttcttcctcttttcagggacccatggctgtcgtccaattcttgcaacatggacgcccatcgctccgtaggattgtcttctcctattgaggtatatatccttacattgttcaaagcttctttcgattcctagctaactgcatatccatgcagaaattcattagctcgcattcattctgaacatgatgtctgaaactctgaattttttttcgtttgtgcgtgtttcagaacttggaaccgtgcagatcgagcagctcgcaggtgtccaaccatgagctgagtagccctagtctcgagttcactctagggaggcctgactggcacggtgcagatcatgattagatggcaatcacagaggctaatgatcaaaaaaaaatttctcctgagatgtgaaatatatatgtgatatacaccaacctggtgctgatcatctttcgccaaccccagcttagccagagccagttcgtctgaagcttgtcatggcgaagaatgatcagcagcaatggcttgaaacgcacatcatatccactgcgtcgtcgtcatcgtcgtcgcaatcgatcggagaagagatatatatttcgcgtctcgatctcatcatcacaatttgggttttcttgattccttcttcttcttctttttgcaattaatatcatggatgcagctagagtttccttgtctgatctccatatttatttagttttgttcgccgtgccgggatcgatttacagtgtagttcagtggtgagctagctagctagagagtgagtgagtgagtgtcagctaggcagctggagatcgagagtgtgagtttggtgatgagttggttgtgtgtttgtcagtgtgtgtgaaagtgtgtgtgccattagcacatggaaagttggaaaggagagaaaggaagaaagaaaagggaattgagttcaggtgaagcaatctgccaatctatctagctacctatctatccatctacttagctcagttgctcagatgatgatctcagatttccatggcccttttttgtgtgcatgcatgccgcatatgcttctttctttaatccctgcaggttcttgcacttcctttagcctcattgatcatgtcagatactgcctacctgttcttttccagcaaccatggccggtgtgaaccggcctctcttgaccagaaactagcagatatctga&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001069632.1 RefSeq:Os09g0395300]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 9]]&lt;br /&gt;
[[Category:Chromosome 9]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os09g0395300&amp;diff=174624</id>
		<title>Os09g0395300</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os09g0395300&amp;diff=174624"/>
				<updated>2014-05-30T11:51:45Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;The rice ''SHALLOT-LIKE1'' ('' SLL1'') gene, a member of KANADI family, is a key gene controlling rice leaf rolling.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File: ZhangF1.jpg|right|thumb|200px|Fig 1. ''sll1'' has extremely incurved leaves, with deficiency of sclerenchymatous cells at the abaxial side &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File: ZhangF3.jpg|right|thumb|200px|Fig 3. Map-based cloning of ''SLL1'', which encodes an MYB transcription factor &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File: ZhangF8.jpg|right|thumb|200px|Fig 8. ''Sll1'' alters adaxial-abaxial pattern formation &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File: ZhangF10.jpg|right|thumb|200px|Fig 10. ''SLL1'' Affected multiple developmental processes in rice &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
To investigate the molecular mechanisms of rice leaf rolling, a rice mutant population (''Oryza sativa'' L. ssp. ''japonica'' variety Nipponbare) generated by ethyl methanesulphonate mutagenesis was screened. Two allelic mutants with extremely incurved leaves were identified, designated as ''sll1-1'' and ''sll1-2'' (Fig. 1A ). ''sll1'', a rice mutant with shallot-like Leaves, displays abnormal sclerenchymatous cell development in the abaxial cell layers, altered mesophyll cell distribution, increased amounts of chlorophyll, and enhanced photosynthesis &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
Genetic analysis revealed that the abnormal character of ''sll1'' was controlled by a single recessive gene. To isolate the relevant mutant gene, ''SLL1'' was mapped to the long arm of rice chromosome 9 between markers RM1896 and RM3700. A large F2 mapping population was then generated, allowing the fine-mapping of ''SLL1'' to a 29.57-kb region, using the sequence tagged site and simple sequence repeat markers (Fig. 3A). Three annotated candidate genes, encoding a hypothetical protein, an En/Spm-like transposon, and a transcription factor containing a MYB-like domain, respectively, were located in this region. Further amplification of the relevant DNA fragments and sequence comparison revealed differences in ''sll1-1'' and ''sll1-2'' alleles in the gene encoding the transcription factor containing the MYB-like domain. Comparison with the corresponding genomic sequence revealed that the ''SLL1'' gene consists of six exons and five introns. The gene encodes a 377–amino acid MYB family transcription factor (Fig. 3B). Homologous analysis showed that ''SLL1'' shares high similarity with the KANADI family members in ''Arabidopsis''.&lt;br /&gt;
&lt;br /&gt;
A distinguishing characteristic of the monocot leaf is that microhairs or ligules are present only at the adaxial surface. In ''sll1-1'', the microhairs can be observed on both epidermal surfaces of some plants (Fig. 8A ), and the ligules exist on the abaxial side of the joint (Fig. 8B). This suggests an adaxialized trend in the abaxial epidermis of ''sll1-1'' and indicates the involvement of ''SLL1'' in the development of polarity throughout the leaf abaxial epidermis. ''SLL1'' overexpression resulted in dwarf plants with twisted and abnormal inner rolled leaves. We also observed enlarged phloem in the midrib as well as large and small veins, revealing the enhanced abaxial features of leaves following ''SLL1'' overexpression.&lt;br /&gt;
&lt;br /&gt;
''SLL1'' affected developmental processes in multiple developmental stages, in accordance with its expression patterns. Aside from altered leaf morphology, other tissues, including seeds, anthers, and roots, displayed abnormal development in ''sll1'' mutants (Fig. 10).&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
[[File: ZhangF5.jpg|right|thumb|200px|Fig 5. ''SLL1'' expression pattern analysis &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
Quantitative real-time RT-PCR (qRT-PCR) analysis revealed the expression of ''SLL1'' in various tissues, including roots, stems, leaves, flowers, and seedlings, with relatively high expression in leaf and seedlings (Fig. 5A , top panel). With an emphasis on the leaf, analysis by qRT-PCR showed that ''SLL1'' is ubiquitously expressed in shoot apical meristem (SAM), leaf blade, or leaf sheath at different developmental stages (Figure 5A, bottom panel).&lt;br /&gt;
&lt;br /&gt;
To assess the expression pattern comprehensively, β-glucuronidase (GUS) activity was examined histochemically in transgenic plants carrying an ''SLL1'' promoter-GUS reporter gene. Results showed that ''SLL1'' was transcribed in stem (Fig. 5B, panels 1 and 2), anthers of young or mature flowers (Fig. 5B, panels 3 to 5), pistil tip (Fig. 5B, panel 6), glume (Fig. 5B, panel 7), vascular tissues of mature seeds (Fig. 5B, panels 8 and 9), coleoptile and embryonic root of germinating seedlings (Fig. 5B, panel 10), and root vascular tissues (Fig. 5B, panel 11). In addition, ''SLL1'' is highly transcribed in leaf veins and leaf sheath (Fig. 5C, panels 1 to 3), guard cells, and tracheal elements (Fig. 5C, panels 4 and 5).&lt;br /&gt;
&lt;br /&gt;
The spatial and temporal localization of ''SLL1'' during leaf development was further examined by in situ hybridization analysis. The mRNA expression of ''SLL1'' was detected throughout the young leaf primordium (plastochrons 1 to 3) and was more intense in abaxial cell layer through leaf development (plastochrons 4 and 5) (Fig. 5D, panel 2). However, the ''SLL1'' transcript did not demonstrate apical/basal polarity and did not accumulate at the apex of the meristem (Fig.e 5D, panel 3). Cross-section analysis of the shoot apex showed that ''SLL1'' was more highly expressed in the abaxial cell layer, including the epidermis and vasculature of the early leaf blade (Fig. 5D, panels 5 and 6). In the mature leaf, ''SLL1'' mainly accumulated at the abaxial epidermis, abaxial mesophyll cells, and vasculature (Fig. 5D, panels 8 and 9). In contrast with the sense probe (Fig. 5D, panels 4 and 7), ''SLL1'' was transcribed at a relatively low level throughout other leaf positions including the adaxial epidermis (Fig. 5D, panels 5 and 6).&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
Please input evolution information here.&lt;br /&gt;
&lt;br /&gt;
You can also add sub-section(s) at will.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou 310006, Zhejiang, China&lt;br /&gt;
*National Key Laboratory of Plant Molecular Genetics, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Zhang GH, et al. (2009) ''SHALLOT-LIKE1'' is a KANADI transcription factor that modulates rice leaf rolling by regulating leaf abaxial cell development. The Plant Cell Online 21: 719-735.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os09g0395300|&lt;br /&gt;
Description = Similar to CDPK substrate protein 1|&lt;br /&gt;
Version = NM_001069632.1 GI:115479006 GeneID:4346973|&lt;br /&gt;
Length = 7672 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os09g0395300, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 9|Chromosome 9]]|&lt;br /&gt;
AP = Chromosome 9:14411926..14419597|&lt;br /&gt;
CDS = 14411926..14412128,14413047..14413888,14413990..14414066,14414656..14414701,14414841..14415084&amp;lt;br&amp;gt;,14418440..14418512,14419481..14419597|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008402:14411926..14419597&lt;br /&gt;
source=RiceChromosome09&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008402:14411926..14419597&lt;br /&gt;
source=RiceChromosome09&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggcaatggtgcgggagctcgagttgatgacgagctggagcaacagcatggggcgacaccgctacccaacgcgcatcctcgtcgattccttcgggcataagtgcagtgcctctgacaagggtgtgtggacctcctgcagcattcgcgcacccttgcaaggacgcggctccttccgacgtggcgcgaatattcgctttgggagcttgccgagcagcgcggcggtggcgacgtcggggggagggcgtggcggcggcggggtggtggtgggaggaggaggaggggacccgtggcggaggctggatgggtccacggcgtcgacggagttgtcgctgtcgccgccgccggcgcaggcggcgggtgggggaggtggtggtggtggagcggacgcgctgccgtggcggcaccgaccttcgccgccgtcgtcggcggtggccaccacgtctgccgccgccgcggcggcgctgatggcgccgatgatgctgcagccgctcgacgccggcggcggcgcgtcggcgccgccgccgccgatccgcgggatacctatctacaacggccccggcgggttcccgttcctgcagccgtcgcccaccgccggcgacgtcggccaccaccaccaccaccaccccaagatgggattctacagctcgtaccaccacccatccacgtggccctccacgtcgccgtccccgctcgcggcgccgccgggcgccgcgtcgtcgccgctcgaccccacggcggcgttcctctcctccccccaccaccggatgctgtccgccgcctcggggaggctcaacggcatgctctccgtctccgacaccctccgcagctacggcgtccccggcgccgccgcccccggcgtcatcggcggcgcgcaccaccaccaccaccacctccacggcggccagccgttcgtcggcgccctcgcgtcccgcttcatgcccaagctccccgccaagcgcagcatgcgcgcgccgcgcatgcgctggacgagcaccctccacgcccgcttcgtccacgccgtcgagctcctcggcggccacgagagggcgacgcccaagtcggtgctggagctcatggacgtcaaggatctgacgctagcgcatgtcaagagccacctccagatgtatcgcaccgtgaagagcactgacaagcctgcagcctcttcagggccggcggacggcggctccggcgacgaggagttcgccggcggcgggcaggcggcgtcgggcggcggcgacagcatgtgcctgaggggtggcggcggcggcggggtggccgcggcggcgttcgcggagcacggccggtcggcgtcggagggcgccgccagctcggtcggcggcggcggcggcggcgacatggaccagtcgtcggccggcaacaccagcaccaccaggtggagcaactcctcaagggacccatggctgtcgtccaattcttgcaacatggacgcccatcgctccgtaggattgtcttctcctattgaggttcttgcacttcctttagcctcattgatcatgtcagatactgcctacctgttcttttccagcaaccatggccggtgtgaaccggcctctcttgaccagaaactagcagatatctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MAMVRELELMTSWSNSMGRHRYPTRILVDSFGHKCSASDKGVWT                     SCSIRAPLQGRGSFRRGANIRFGSLPSSAAVATSGGGRGGGGVVVGGGGGDPWRRLDG                     STASTELSLSPPPAQAAGGGGGGGGADALPWRHRPSPPSSAVATTSAAAAAALMAPMM                     LQPLDAGGGASAPPPPIRGIPIYNGPGGFPFLQPSPTAGDVGHHHHHHPKMGFYSSYH                     HPSTWPSTSPSPLAAPPGAASSPLDPTAAFLSSPHHRMLSAASGRLNGMLSVSDTLRS                     YGVPGAAAPGVIGGAHHHHHHLHGGQPFVGALASRFMPKLPAKRSMRAPRMRWTSTLH                     ARFVHAVELLGGHERATPKSVLELMDVKDLTLAHVKSHLQMYRTVKSTDKPAASSGPA                     DGGSGDEEFAGGGQAASGGGDSMCLRGGGGGGVAAAAFAEHGRSASEGAASSVGGGGG                     GDMDQSSAGNTSTTRWSNSSRDPWLSSNSCNMDAHRSVGLSSPIEVLALPLASLIMSD                     TAYLFFSSNHGRCEPASLDQKLADI&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;1..203#1122..1963#2065..2141#2731..2776#2916..3159#6515..6587#7556..7672#atggcaatggtgcgggagctcgagttgatgacgagctggagcaacagcatggggcgacaccgctacccaacgcgcatcctcgtcgattccttcgggcataagtgcagtgcctctgacaagggtgtgtggacctcctgcagcattcgcgcacccttgcaaggacgcggctccttccgacgtggcgcgaatattcgctttgggaggtatgagactacgctccatggtggagcgttgggcgtgaccttagtgtgcgcatatgtaagctgtatgcgtacgtataaatgttgagcttgcagtacatgtatacttgtttttttcttcttttttatgaggtcctttaattccattgtctgtattatttatgctagtatggaggatgatggtggcagtgacataaagtatacaaaaagcatagtatagtatacgtatggaaacaaaagcatgctacctttgactccacttgcattgcctgctaactgccattatttaaggaatacatggttgaatgcctgcctaaacatcaagataacctcacattctcctctctctctctcctaccttgcaattaagggtagcagcagtactctcctcactgctggctgactgctcccattttctctctctactctctctctctctctctcctctattccttttatacttgttgttggtagctaggagtatagcaggacagcacaaggaaccaattcatgcatatatccctggtgtctctcatgcatgttagtgtgaagaaagaagaagcttgagagagaagagagagttagagagagaaagtagagtgtttgtagagagagaaagtggtgtgtgtactagtagtaactccaagccagtgctagagacagagatacaaaaaggagacatcatccttctcttggccaaagcaagcaaccaagcaaagcttcctcttcttctccaagaactccaagaaccttctccttcatcttctccaccatgattccttccatcgcatgagctccatctccggcgtgtcgatcgagatcaccgttgctgctgccgaggtggagaaggaggtgtttgatcgatcggtcgatggaggcgagctcggcggcgacgccaccggacctgtcgctgcacatcagcttgccgagcagcgcggcggtggcgacgtcggggggagggcgtggcggcggcggggtggtggtgggaggaggaggaggggacccgtggcggaggctggatgggtccacggcgtcgacggagttgtcgctgtcgccgccgccggcgcaggcggcgggtgggggaggtggtggtggtggagcggacgcgctgccgtggcggcaccgaccttcgccgccgtcgtcggcggtggccaccacgtctgccgccgccgcggcggcgctgatggcgccgatgatgctgcagccgctcgacgccggcggcggcgcgtcggcgccgccgccgccgatccgcgggatacctatctacaacggccccggcgggttcccgttcctgcagccgtcgcccaccgccggcgacgtcggccaccaccaccaccaccaccccaagatgggattctacagctcgtaccaccacccatccacgtggccctccacgtcgccgtccccgctcgcggcgccgccgggcgccgcgtcgtcgccgctcgaccccacggcggcgttcctctcctccccccaccaccggatgctgtccgccgcctcggggaggctcaacggcatgctctccgtctccgacaccctccgcagctacggcgtccccggcgccgccgcccccggcgtcatcggcggcgcgcaccaccaccaccaccacctccacggcggccagccgttcgtcggcgccctcgcgtcccgcttcatgcccaagctccccgccaagcgcagcatgcgcgcgccgcgcatgcgctggacgagcaccctccacgcccgcttcgtccacgccgtcgagctcctcggcggccacgagagtacgcccccgccatcatcgtcgtcgtcctcctcctccttctcaccaccatcatcaacgagctcgatcaatctgatgagaatccaatcttgttcttggcaggggcgacgcccaagtcggtgctggagctcatggacgtcaaggatctgacgctagcgcatgtcaagagccacctccaggtatcccgccattgccgaccaattctcacagctcgatcgatcgatcaaacaccactcaccactgcaccatctctctctttctctctctcgatttcgattccattcagcttctgttcttgatcatcttgtttgggtgagacaaagatgccaatgcagtaactcctgagttagtgaagaaactgccattcttgggagcagagagagagagtgtgtgtgtgacatgtttggggatgtgtgtgcaagagagaagagagagagagaggggaaaaaagttgccatcattacacaataatgcattgcatctgcatctgtgctactagctccttccttagctctagtcatactagcgtatatgtgcacggcccaaagcactctcacacacaaacacaagagagagagagagagagagaagaagaagatgagagatgagagagagtaggacatattttgtgtgtgtttctttgctgcttgtcttttgcaatggcttcaacctcctggtttcattttgatctcacaaaaaatgtgtgtgtgtgtgtaaatatatatattgatcttctttttgttggacttttgtgttttattactgcagatgtatcgcaccgtgaagagcactgacaagcctgcagcctcttcaggtgattttttttaccatggcagctactagtagtagtagtagtagctaatttagctaagctccattttgcttttctttttttttggcgttgtgcattgcgttttacattacattgttgctatggtttttttgacgtgtagggccggcggacggcggctccggcgacgaggagttcgccggcggcgggcaggcggcgtcgggcggcggcgacagcatgtgcctgaggggtggcggcggcggcggggtggccgcggcggcgttcgcggagcacggccggtcggcgtcggagggcgccgccagctcggtcggcggcggcggcggcggcgacatggaccagtcgtcggccggcaacaccagcaccaccaggtggagcaactcctcaaggtacacacatggcagagttgcatttcaagtctttcagattaattatatatctacattgttatgccatctttaattaattaaaaatgaaattaatcaatcagaatgtcatgagatgatgatgatgatgataataatactaggataggaagaggatgatatgatggatgggtgtgctatgtgtgtttttaagtgtgttttagcttagaaccaaaggcaacaccaacaaactttggcatgcattgatgatgtatctaaatatgagttagtgacatgcaaaattaacctgccaagtacaacctctatttattaattcccaaaaaaatctcatggaggagaagggagagagagagatagtagtaatgtgtggtgatgcatggctaaaaaagcttagcaaaagaatgttttgggggcacacacacacacacctggagagggagttgcctatgtttaggtggccaatgttgttatgtcacacaaaagaccaaaaagtcacacaccccatggcttggcctcctcctccccccttgacctgtgcagttagctaggcttcttctcttctctccctctgtgtttggtttttgtggagctaaaaacattttaaaaatcttgcaaacattgtgtgtaaaaataggttcttgggctctgcccattgtcctctagcttctctcaaatctctctctctctctctctctctctctctctctttctcaaacctagggaggggagggttactcaggcagggctccattatcatttcttatcaatgcatggctctgattccagggggatggggctttgacctgacatgccctattgcctaggaatatgtaaccaaggacttgctgcattcttggttctttctccctctctcaccagtctcttcaatgcccttttcttccacctcttgggcaattattagcatggatggagctcaccttttcactctaccctctagctgtgattaaatcattgactaatcctaattcataaatataagggattcaactatgtaactagatgtactagatcctagtattactagtgtgttttgattctgttaggaggagtgattagcgtttgtcgtaagtactagtattaaactataggggattagtgtagatcatttttttaaaaattagtgagtgtgcttgggcagattttactccagccattggcgtgaaaactttgatctttgggcagcttggaagcaagtacagttcaacctgtccttggctgcattcgctgctttttctttctcaggactcactgcaactttcttgccatccccaacacctccctttcggtcgtgtttgatcagttgcattgctggtttcttcgccgctttaatttctccatctttcttctgttccttattggctaagtaaaaaatcattctcagcaatcaagttttgaaattcaaattagcttcaggttttatctatctaataattctctgactagttctctttctttcaagacctgttcttgttcagaactcttatgcagttgagagttcagttgttcatggaagtaatggcaatgcctggtctagtctttgagcagtatcctccttatgctcttgattttccttcactttagccgtttcagtcaaactttggggacaaattaaagtcagctggtcaagtgcatacataccacgtcatattttttagatgaatccattgtagtattaaatactagtgacaaaaaaatataactaaatggcattaaattgcaaccttcttccccaaaataattgggcacaactaccttgcttgcatatgctttatagtactcctacttattacttccttgaatccatgaggattccaggaatttggtcaggtcaaatgtccaggaggaattaggctatctttttttatcttcttctttttcttctaggtagtaggatcgttgtgcacatataaacaaaacaaaatagaaatttaagaggaaaccctcccaaaaaaaatacgactatcaattatgagtgattttacagttcttgaggaggtacaatgatacattttctattttaaaattcagtaactttgatactatgaggtacagaaatttgcacaaaaaaaatttggtacctctcaagtacttaaaatatcttatcaattatatttcagcaatgttgtcgttgctcgagttgtgcaaaaacatttctgatgaacaagtggagatgtatgcatatttagagagggaaacacatgcattttttaatatacattctcatgacaaattttggtgttctcgtctcattttagtctagcttagattaatggcatccatatattggtgaactgaaacagattgtatatgtccagtcttgaacaaacttcattatacaatgcataatcagaaaagatacagacatatattggcagatcacataaagtggtgtatctatgattgggtggtattttggacatacaaagtctactggtccctcatttgttaacagcatacatttgttcctatcaagacaaaagcactttacaacagtttggtagtaagttggtgttatgtgcgtgtctatttagatagagtggtagtaaaggaaggacactttttcttgatataccaaaatcacacataaaaaagaagtgtcattttcatgatcaacatgtggggtatgaacaaaaatgttctcccccctccaaccaacattgaagtcatcacacataaaaagcaaaaacatttaacaataatacatgcagacacatgtgcatgcatgtgtggatcacgcaaggacatactaattcaattaggtattcacaattaattagtgcaggaaatgacatgtaattacaattatatatgcacaacgatccttgtgtatttgtgtgacccattgtagtagcatttgattcctttcttgtgcctttctctacattgaattcgatctttgccaacagcggcttgctgatgagctcctgtgccattgcactgctgagctgcaccaaacagggacatcttttaagagcttgttgcctggaaatgatccatgtaaccaactgttcaggaagagcacactgtttgctgctcactttagctaaagcaaaactgtgtgcattatgcaatgcatatgcatccttccatctacccctgtgtcctttgccccccaaactgtgtaactacagtttaccatgcacatacatacaatgcacatctacccaattgtagcattgttgcaaggcctacttcagaattcagttagtccccaattgatccaactgcacacatatacatttacatatacatatacacaaacataccagcttggagaaaaggttgtaacaactttgctaaatgtgagatgtgtaatgtgtgttcttcctcttttcagggacccatggctgtcgtccaattcttgcaacatggacgcccatcgctccgtaggattgtcttctcctattgaggtatatatccttacattgttcaaagcttctttcgattcctagctaactgcatatccatgcagaaattcattagctcgcattcattctgaacatgatgtctgaaactctgaattttttttcgtttgtgcgtgtttcagaacttggaaccgtgcagatcgagcagctcgcaggtgtccaaccatgagctgagtagccctagtctcgagttcactctagggaggcctgactggcacggtgcagatcatgattagatggcaatcacagaggctaatgatcaaaaaaaaatttctcctgagatgtgaaatatatatgtgatatacaccaacctggtgctgatcatctttcgccaaccccagcttagccagagccagttcgtctgaagcttgtcatggcgaagaatgatcagcagcaatggcttgaaacgcacatcatatccactgcgtcgtcgtcatcgtcgtcgcaatcgatcggagaagagatatatatttcgcgtctcgatctcatcatcacaatttgggttttcttgattccttcttcttcttctttttgcaattaatatcatggatgcagctagagtttccttgtctgatctccatatttatttagttttgttcgccgtgccgggatcgatttacagtgtagttcagtggtgagctagctagctagagagtgagtgagtgagtgtcagctaggcagctggagatcgagagtgtgagtttggtgatgagttggttgtgtgtttgtcagtgtgtgtgaaagtgtgtgtgccattagcacatggaaagttggaaaggagagaaaggaagaaagaaaagggaattgagttcaggtgaagcaatctgccaatctatctagctacctatctatccatctacttagctcagttgctcagatgatgatctcagatttccatggcccttttttgtgtgcatgcatgccgcatatgcttctttctttaatccctgcaggttcttgcacttcctttagcctcattgatcatgtcagatactgcctacctgttcttttccagcaaccatggccggtgtgaaccggcctctcttgaccagaaactagcagatatctga&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001069632.1 RefSeq:Os09g0395300]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 9]]&lt;br /&gt;
[[Category:Chromosome 9]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:ZhangF10.jpg&amp;diff=174623</id>
		<title>File:ZhangF10.jpg</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:ZhangF10.jpg&amp;diff=174623"/>
				<updated>2014-05-30T11:49:09Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:ZhangF8.jpg&amp;diff=174622</id>
		<title>File:ZhangF8.jpg</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:ZhangF8.jpg&amp;diff=174622"/>
				<updated>2014-05-30T11:48:47Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os09g0395300&amp;diff=174621</id>
		<title>Os09g0395300</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os09g0395300&amp;diff=174621"/>
				<updated>2014-05-30T11:47:39Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;The rice ''SHALLOT-LIKE1'' ('' SLL1'') gene, a member of KANADI family, is a key gene controlling rice leaf rolling.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:ZhangF1.jpg|right|thumb|200px|Fig 1. ''sll1'' has extremely incurved leaves, with deficiency of sclerenchymatous cells at the abaxial side &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:ZhangF3.jpg|right|thumb|200px|Fig 3. Map-based cloning of ''SLL1'', which encodes an MYB transcription factor &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
To investigate the molecular mechanisms of rice leaf rolling, a rice mutant population (''Oryza sativa'' L. ssp. ''japonica'' variety Nipponbare) generated by ethyl methanesulphonate mutagenesis was screened. Two allelic mutants with extremely incurved leaves were identified, designated as ''sll1-1'' and ''sll1-2'' (Fig. 1A ). ''sll1'', a rice mutant with shallot-like Leaves, displays abnormal sclerenchymatous cell development in the abaxial cell layers, altered mesophyll cell distribution, increased amounts of chlorophyll, and enhanced photosynthesis &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
Genetic analysis revealed that the abnormal character of ''sll1'' was controlled by a single recessive gene. To isolate the relevant mutant gene, ''SLL1'' was mapped to the long arm of rice chromosome 9 between markers RM1896 and RM3700. A large F2 mapping population was then generated, allowing the fine-mapping of ''SLL1'' to a 29.57-kb region, using the sequence tagged site and simple sequence repeat markers (Fig. 3A). Three annotated candidate genes, encoding a hypothetical protein, an En/Spm-like transposon, and a transcription factor containing a MYB-like domain, respectively, were located in this region. Further amplification of the relevant DNA fragments and sequence comparison revealed differences in ''sll1-1'' and ''sll1-2'' alleles in the gene encoding the transcription factor containing the MYB-like domain. Comparison with the corresponding genomic sequence revealed that the ''SLL1'' gene consists of six exons and five introns. The gene encodes a 377–amino acid MYB family transcription factor (Fig. 3B). Homologous analysis showed that ''SLL1'' shares high similarity with the KANADI family members in ''Arabidopsis''.&lt;br /&gt;
&lt;br /&gt;
A distinguishing characteristic of the monocot leaf is that microhairs or ligules are present only at the adaxial surface. In ''sll1-1'', the microhairs can be observed on both epidermal surfaces of some plants (Fig. 8A ), and the ligules exist on the abaxial side of the joint (Fig. 8B). This suggests an adaxialized trend in the abaxial epidermis of ''sll1-1'' and indicates the involvement of ''SLL1'' in the development of polarity throughout the leaf abaxial epidermis. ''SLL1'' overexpression resulted in dwarf plants with twisted and abnormal inner rolled leaves. We also observed enlarged phloem in the midrib as well as large and small veins, revealing the enhanced abaxial features of leaves following ''SLL1'' overexpression.&lt;br /&gt;
&lt;br /&gt;
''SLL1'' affected developmental processes in multiple developmental stages, in accordance with its expression patterns. Aside from altered leaf morphology, other tissues, including seeds, anthers, and roots, displayed abnormal development in ''sll1'' mutants.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
[[File:ZhangF5.jpg|right|thumb|200px|Fig 5. ''SLL1'' Expression Pattern Analysis &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
Quantitative real-time RT-PCR (qRT-PCR) analysis revealed the expression of ''SLL1'' in various tissues, including roots, stems, leaves, flowers, and seedlings, with relatively high expression in leaf and seedlings (Fig. 5A , top panel). With an emphasis on the leaf, analysis by qRT-PCR showed that ''SLL1'' is ubiquitously expressed in shoot apical meristem (SAM), leaf blade, or leaf sheath at different developmental stages (Figure 5A, bottom panel).&lt;br /&gt;
&lt;br /&gt;
To assess the expression pattern comprehensively, β-glucuronidase (GUS) activity was examined histochemically in transgenic plants carrying an ''SLL1'' promoter-GUS reporter gene. Results showed that ''SLL1'' was transcribed in stem (Fig. 5B, panels 1 and 2), anthers of young or mature flowers (Fig. 5B, panels 3 to 5), pistil tip (Fig. 5B, panel 6), glume (Fig. 5B, panel 7), vascular tissues of mature seeds (Fig. 5B, panels 8 and 9), coleoptile and embryonic root of germinating seedlings (Fig. 5B, panel 10), and root vascular tissues (Fig. 5B, panel 11). In addition, ''SLL1'' is highly transcribed in leaf veins and leaf sheath (Fig. 5C, panels 1 to 3), guard cells, and tracheal elements (Fig. 5C, panels 4 and 5).&lt;br /&gt;
&lt;br /&gt;
The spatial and temporal localization of ''SLL1'' during leaf development was further examined by in situ hybridization analysis. The mRNA expression of ''SLL1'' was detected throughout the young leaf primordium (plastochrons 1 to 3) and was more intense in abaxial cell layer through leaf development (plastochrons 4 and 5) (Fig. 5D, panel 2). However, the ''SLL1'' transcript did not demonstrate apical/basal polarity and did not accumulate at the apex of the meristem (Fig.e 5D, panel 3). Cross-section analysis of the shoot apex showed that ''SLL1'' was more highly expressed in the abaxial cell layer, including the epidermis and vasculature of the early leaf blade (Fig. 5D, panels 5 and 6). In the mature leaf, ''SLL1'' mainly accumulated at the abaxial epidermis, abaxial mesophyll cells, and vasculature (Fig. 5D, panels 8 and 9). In contrast with the sense probe (Fig. 5D, panels 4 and 7), ''SLL1'' was transcribed at a relatively low level throughout other leaf positions including the adaxial epidermis (Fig. 5D, panels 5 and 6).&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
Please input evolution information here.&lt;br /&gt;
&lt;br /&gt;
You can also add sub-section(s) at will.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou 310006, Zhejiang, China&lt;br /&gt;
*National Key Laboratory of Plant Molecular Genetics, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Zhang GH, et al. (2009) ''SHALLOT-LIKE1'' is a KANADI transcription factor that modulates rice leaf rolling by regulating leaf abaxial cell development. The Plant Cell Online 21: 719-735.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os09g0395300|&lt;br /&gt;
Description = Similar to CDPK substrate protein 1|&lt;br /&gt;
Version = NM_001069632.1 GI:115479006 GeneID:4346973|&lt;br /&gt;
Length = 7672 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os09g0395300, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 9|Chromosome 9]]|&lt;br /&gt;
AP = Chromosome 9:14411926..14419597|&lt;br /&gt;
CDS = 14411926..14412128,14413047..14413888,14413990..14414066,14414656..14414701,14414841..14415084&amp;lt;br&amp;gt;,14418440..14418512,14419481..14419597|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008402:14411926..14419597&lt;br /&gt;
source=RiceChromosome09&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008402:14411926..14419597&lt;br /&gt;
source=RiceChromosome09&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggcaatggtgcgggagctcgagttgatgacgagctggagcaacagcatggggcgacaccgctacccaacgcgcatcctcgtcgattccttcgggcataagtgcagtgcctctgacaagggtgtgtggacctcctgcagcattcgcgcacccttgcaaggacgcggctccttccgacgtggcgcgaatattcgctttgggagcttgccgagcagcgcggcggtggcgacgtcggggggagggcgtggcggcggcggggtggtggtgggaggaggaggaggggacccgtggcggaggctggatgggtccacggcgtcgacggagttgtcgctgtcgccgccgccggcgcaggcggcgggtgggggaggtggtggtggtggagcggacgcgctgccgtggcggcaccgaccttcgccgccgtcgtcggcggtggccaccacgtctgccgccgccgcggcggcgctgatggcgccgatgatgctgcagccgctcgacgccggcggcggcgcgtcggcgccgccgccgccgatccgcgggatacctatctacaacggccccggcgggttcccgttcctgcagccgtcgcccaccgccggcgacgtcggccaccaccaccaccaccaccccaagatgggattctacagctcgtaccaccacccatccacgtggccctccacgtcgccgtccccgctcgcggcgccgccgggcgccgcgtcgtcgccgctcgaccccacggcggcgttcctctcctccccccaccaccggatgctgtccgccgcctcggggaggctcaacggcatgctctccgtctccgacaccctccgcagctacggcgtccccggcgccgccgcccccggcgtcatcggcggcgcgcaccaccaccaccaccacctccacggcggccagccgttcgtcggcgccctcgcgtcccgcttcatgcccaagctccccgccaagcgcagcatgcgcgcgccgcgcatgcgctggacgagcaccctccacgcccgcttcgtccacgccgtcgagctcctcggcggccacgagagggcgacgcccaagtcggtgctggagctcatggacgtcaaggatctgacgctagcgcatgtcaagagccacctccagatgtatcgcaccgtgaagagcactgacaagcctgcagcctcttcagggccggcggacggcggctccggcgacgaggagttcgccggcggcgggcaggcggcgtcgggcggcggcgacagcatgtgcctgaggggtggcggcggcggcggggtggccgcggcggcgttcgcggagcacggccggtcggcgtcggagggcgccgccagctcggtcggcggcggcggcggcggcgacatggaccagtcgtcggccggcaacaccagcaccaccaggtggagcaactcctcaagggacccatggctgtcgtccaattcttgcaacatggacgcccatcgctccgtaggattgtcttctcctattgaggttcttgcacttcctttagcctcattgatcatgtcagatactgcctacctgttcttttccagcaaccatggccggtgtgaaccggcctctcttgaccagaaactagcagatatctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MAMVRELELMTSWSNSMGRHRYPTRILVDSFGHKCSASDKGVWT                     SCSIRAPLQGRGSFRRGANIRFGSLPSSAAVATSGGGRGGGGVVVGGGGGDPWRRLDG                     STASTELSLSPPPAQAAGGGGGGGGADALPWRHRPSPPSSAVATTSAAAAAALMAPMM                     LQPLDAGGGASAPPPPIRGIPIYNGPGGFPFLQPSPTAGDVGHHHHHHPKMGFYSSYH                     HPSTWPSTSPSPLAAPPGAASSPLDPTAAFLSSPHHRMLSAASGRLNGMLSVSDTLRS                     YGVPGAAAPGVIGGAHHHHHHLHGGQPFVGALASRFMPKLPAKRSMRAPRMRWTSTLH                     ARFVHAVELLGGHERATPKSVLELMDVKDLTLAHVKSHLQMYRTVKSTDKPAASSGPA                     DGGSGDEEFAGGGQAASGGGDSMCLRGGGGGGVAAAAFAEHGRSASEGAASSVGGGGG                     GDMDQSSAGNTSTTRWSNSSRDPWLSSNSCNMDAHRSVGLSSPIEVLALPLASLIMSD                     TAYLFFSSNHGRCEPASLDQKLADI&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;1..203#1122..1963#2065..2141#2731..2776#2916..3159#6515..6587#7556..7672#atggcaatggtgcgggagctcgagttgatgacgagctggagcaacagcatggggcgacaccgctacccaacgcgcatcctcgtcgattccttcgggcataagtgcagtgcctctgacaagggtgtgtggacctcctgcagcattcgcgcacccttgcaaggacgcggctccttccgacgtggcgcgaatattcgctttgggaggtatgagactacgctccatggtggagcgttgggcgtgaccttagtgtgcgcatatgtaagctgtatgcgtacgtataaatgttgagcttgcagtacatgtatacttgtttttttcttcttttttatgaggtcctttaattccattgtctgtattatttatgctagtatggaggatgatggtggcagtgacataaagtatacaaaaagcatagtatagtatacgtatggaaacaaaagcatgctacctttgactccacttgcattgcctgctaactgccattatttaaggaatacatggttgaatgcctgcctaaacatcaagataacctcacattctcctctctctctctcctaccttgcaattaagggtagcagcagtactctcctcactgctggctgactgctcccattttctctctctactctctctctctctctctcctctattccttttatacttgttgttggtagctaggagtatagcaggacagcacaaggaaccaattcatgcatatatccctggtgtctctcatgcatgttagtgtgaagaaagaagaagcttgagagagaagagagagttagagagagaaagtagagtgtttgtagagagagaaagtggtgtgtgtactagtagtaactccaagccagtgctagagacagagatacaaaaaggagacatcatccttctcttggccaaagcaagcaaccaagcaaagcttcctcttcttctccaagaactccaagaaccttctccttcatcttctccaccatgattccttccatcgcatgagctccatctccggcgtgtcgatcgagatcaccgttgctgctgccgaggtggagaaggaggtgtttgatcgatcggtcgatggaggcgagctcggcggcgacgccaccggacctgtcgctgcacatcagcttgccgagcagcgcggcggtggcgacgtcggggggagggcgtggcggcggcggggtggtggtgggaggaggaggaggggacccgtggcggaggctggatgggtccacggcgtcgacggagttgtcgctgtcgccgccgccggcgcaggcggcgggtgggggaggtggtggtggtggagcggacgcgctgccgtggcggcaccgaccttcgccgccgtcgtcggcggtggccaccacgtctgccgccgccgcggcggcgctgatggcgccgatgatgctgcagccgctcgacgccggcggcggcgcgtcggcgccgccgccgccgatccgcgggatacctatctacaacggccccggcgggttcccgttcctgcagccgtcgcccaccgccggcgacgtcggccaccaccaccaccaccaccccaagatgggattctacagctcgtaccaccacccatccacgtggccctccacgtcgccgtccccgctcgcggcgccgccgggcgccgcgtcgtcgccgctcgaccccacggcggcgttcctctcctccccccaccaccggatgctgtccgccgcctcggggaggctcaacggcatgctctccgtctccgacaccctccgcagctacggcgtccccggcgccgccgcccccggcgtcatcggcggcgcgcaccaccaccaccaccacctccacggcggccagccgttcgtcggcgccctcgcgtcccgcttcatgcccaagctccccgccaagcgcagcatgcgcgcgccgcgcatgcgctggacgagcaccctccacgcccgcttcgtccacgccgtcgagctcctcggcggccacgagagtacgcccccgccatcatcgtcgtcgtcctcctcctccttctcaccaccatcatcaacgagctcgatcaatctgatgagaatccaatcttgttcttggcaggggcgacgcccaagtcggtgctggagctcatggacgtcaaggatctgacgctagcgcatgtcaagagccacctccaggtatcccgccattgccgaccaattctcacagctcgatcgatcgatcaaacaccactcaccactgcaccatctctctctttctctctctcgatttcgattccattcagcttctgttcttgatcatcttgtttgggtgagacaaagatgccaatgcagtaactcctgagttagtgaagaaactgccattcttgggagcagagagagagagtgtgtgtgtgacatgtttggggatgtgtgtgcaagagagaagagagagagagaggggaaaaaagttgccatcattacacaataatgcattgcatctgcatctgtgctactagctccttccttagctctagtcatactagcgtatatgtgcacggcccaaagcactctcacacacaaacacaagagagagagagagagagagaagaagaagatgagagatgagagagagtaggacatattttgtgtgtgtttctttgctgcttgtcttttgcaatggcttcaacctcctggtttcattttgatctcacaaaaaatgtgtgtgtgtgtgtaaatatatatattgatcttctttttgttggacttttgtgttttattactgcagatgtatcgcaccgtgaagagcactgacaagcctgcagcctcttcaggtgattttttttaccatggcagctactagtagtagtagtagtagctaatttagctaagctccattttgcttttctttttttttggcgttgtgcattgcgttttacattacattgttgctatggtttttttgacgtgtagggccggcggacggcggctccggcgacgaggagttcgccggcggcgggcaggcggcgtcgggcggcggcgacagcatgtgcctgaggggtggcggcggcggcggggtggccgcggcggcgttcgcggagcacggccggtcggcgtcggagggcgccgccagctcggtcggcggcggcggcggcggcgacatggaccagtcgtcggccggcaacaccagcaccaccaggtggagcaactcctcaaggtacacacatggcagagttgcatttcaagtctttcagattaattatatatctacattgttatgccatctttaattaattaaaaatgaaattaatcaatcagaatgtcatgagatgatgatgatgatgataataatactaggataggaagaggatgatatgatggatgggtgtgctatgtgtgtttttaagtgtgttttagcttagaaccaaaggcaacaccaacaaactttggcatgcattgatgatgtatctaaatatgagttagtgacatgcaaaattaacctgccaagtacaacctctatttattaattcccaaaaaaatctcatggaggagaagggagagagagagatagtagtaatgtgtggtgatgcatggctaaaaaagcttagcaaaagaatgttttgggggcacacacacacacacctggagagggagttgcctatgtttaggtggccaatgttgttatgtcacacaaaagaccaaaaagtcacacaccccatggcttggcctcctcctccccccttgacctgtgcagttagctaggcttcttctcttctctccctctgtgtttggtttttgtggagctaaaaacattttaaaaatcttgcaaacattgtgtgtaaaaataggttcttgggctctgcccattgtcctctagcttctctcaaatctctctctctctctctctctctctctctctctttctcaaacctagggaggggagggttactcaggcagggctccattatcatttcttatcaatgcatggctctgattccagggggatggggctttgacctgacatgccctattgcctaggaatatgtaaccaaggacttgctgcattcttggttctttctccctctctcaccagtctcttcaatgcccttttcttccacctcttgggcaattattagcatggatggagctcaccttttcactctaccctctagctgtgattaaatcattgactaatcctaattcataaatataagggattcaactatgtaactagatgtactagatcctagtattactagtgtgttttgattctgttaggaggagtgattagcgtttgtcgtaagtactagtattaaactataggggattagtgtagatcatttttttaaaaattagtgagtgtgcttgggcagattttactccagccattggcgtgaaaactttgatctttgggcagcttggaagcaagtacagttcaacctgtccttggctgcattcgctgctttttctttctcaggactcactgcaactttcttgccatccccaacacctccctttcggtcgtgtttgatcagttgcattgctggtttcttcgccgctttaatttctccatctttcttctgttccttattggctaagtaaaaaatcattctcagcaatcaagttttgaaattcaaattagcttcaggttttatctatctaataattctctgactagttctctttctttcaagacctgttcttgttcagaactcttatgcagttgagagttcagttgttcatggaagtaatggcaatgcctggtctagtctttgagcagtatcctccttatgctcttgattttccttcactttagccgtttcagtcaaactttggggacaaattaaagtcagctggtcaagtgcatacataccacgtcatattttttagatgaatccattgtagtattaaatactagtgacaaaaaaatataactaaatggcattaaattgcaaccttcttccccaaaataattgggcacaactaccttgcttgcatatgctttatagtactcctacttattacttccttgaatccatgaggattccaggaatttggtcaggtcaaatgtccaggaggaattaggctatctttttttatcttcttctttttcttctaggtagtaggatcgttgtgcacatataaacaaaacaaaatagaaatttaagaggaaaccctcccaaaaaaaatacgactatcaattatgagtgattttacagttcttgaggaggtacaatgatacattttctattttaaaattcagtaactttgatactatgaggtacagaaatttgcacaaaaaaaatttggtacctctcaagtacttaaaatatcttatcaattatatttcagcaatgttgtcgttgctcgagttgtgcaaaaacatttctgatgaacaagtggagatgtatgcatatttagagagggaaacacatgcattttttaatatacattctcatgacaaattttggtgttctcgtctcattttagtctagcttagattaatggcatccatatattggtgaactgaaacagattgtatatgtccagtcttgaacaaacttcattatacaatgcataatcagaaaagatacagacatatattggcagatcacataaagtggtgtatctatgattgggtggtattttggacatacaaagtctactggtccctcatttgttaacagcatacatttgttcctatcaagacaaaagcactttacaacagtttggtagtaagttggtgttatgtgcgtgtctatttagatagagtggtagtaaaggaaggacactttttcttgatataccaaaatcacacataaaaaagaagtgtcattttcatgatcaacatgtggggtatgaacaaaaatgttctcccccctccaaccaacattgaagtcatcacacataaaaagcaaaaacatttaacaataatacatgcagacacatgtgcatgcatgtgtggatcacgcaaggacatactaattcaattaggtattcacaattaattagtgcaggaaatgacatgtaattacaattatatatgcacaacgatccttgtgtatttgtgtgacccattgtagtagcatttgattcctttcttgtgcctttctctacattgaattcgatctttgccaacagcggcttgctgatgagctcctgtgccattgcactgctgagctgcaccaaacagggacatcttttaagagcttgttgcctggaaatgatccatgtaaccaactgttcaggaagagcacactgtttgctgctcactttagctaaagcaaaactgtgtgcattatgcaatgcatatgcatccttccatctacccctgtgtcctttgccccccaaactgtgtaactacagtttaccatgcacatacatacaatgcacatctacccaattgtagcattgttgcaaggcctacttcagaattcagttagtccccaattgatccaactgcacacatatacatttacatatacatatacacaaacataccagcttggagaaaaggttgtaacaactttgctaaatgtgagatgtgtaatgtgtgttcttcctcttttcagggacccatggctgtcgtccaattcttgcaacatggacgcccatcgctccgtaggattgtcttctcctattgaggtatatatccttacattgttcaaagcttctttcgattcctagctaactgcatatccatgcagaaattcattagctcgcattcattctgaacatgatgtctgaaactctgaattttttttcgtttgtgcgtgtttcagaacttggaaccgtgcagatcgagcagctcgcaggtgtccaaccatgagctgagtagccctagtctcgagttcactctagggaggcctgactggcacggtgcagatcatgattagatggcaatcacagaggctaatgatcaaaaaaaaatttctcctgagatgtgaaatatatatgtgatatacaccaacctggtgctgatcatctttcgccaaccccagcttagccagagccagttcgtctgaagcttgtcatggcgaagaatgatcagcagcaatggcttgaaacgcacatcatatccactgcgtcgtcgtcatcgtcgtcgcaatcgatcggagaagagatatatatttcgcgtctcgatctcatcatcacaatttgggttttcttgattccttcttcttcttctttttgcaattaatatcatggatgcagctagagtttccttgtctgatctccatatttatttagttttgttcgccgtgccgggatcgatttacagtgtagttcagtggtgagctagctagctagagagtgagtgagtgagtgtcagctaggcagctggagatcgagagtgtgagtttggtgatgagttggttgtgtgtttgtcagtgtgtgtgaaagtgtgtgtgccattagcacatggaaagttggaaaggagagaaaggaagaaagaaaagggaattgagttcaggtgaagcaatctgccaatctatctagctacctatctatccatctacttagctcagttgctcagatgatgatctcagatttccatggcccttttttgtgtgcatgcatgccgcatatgcttctttctttaatccctgcaggttcttgcacttcctttagcctcattgatcatgtcagatactgcctacctgttcttttccagcaaccatggccggtgtgaaccggcctctcttgaccagaaactagcagatatctga&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001069632.1 RefSeq:Os09g0395300]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 9]]&lt;br /&gt;
[[Category:Chromosome 9]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:ZhangF3.jpg&amp;diff=174619</id>
		<title>File:ZhangF3.jpg</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:ZhangF3.jpg&amp;diff=174619"/>
				<updated>2014-05-30T11:33:26Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os09g0395300&amp;diff=174618</id>
		<title>Os09g0395300</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os09g0395300&amp;diff=174618"/>
				<updated>2014-05-30T11:32:24Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: /* Annotated Information */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;The rice ''SHALLOT-LIKE1'' ('' SLL1'') gene, a member of KANADI family, is a key gene controlling rice leaf rolling.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:ZhangF1.jpg|right|thumb|200px|Fig 1.''sll1'' has extremely incurved leaves, with deficiency of sclerenchymatous cells at the abaxial side &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
To investigate the molecular mechanisms of rice leaf rolling, a rice mutant population (''Oryza sativa'' L. ssp. ''japonica'' variety Nipponbare) generated by ethyl methanesulphonate mutagenesis was screened. Two allelic mutants with extremely incurved leaves were identified, designated as ''sll1-1'' and ''sll1-2'' (Fig. 1A ). ''sll1'', a rice mutant with shallot-like Leaves, displays abnormal sclerenchymatous cell development in the abaxial cell layers, altered mesophyll cell distribution, increased amounts of chlorophyll, and enhanced photosynthesis &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
Genetic analysis revealed that the abnormal character of ''sll1'' was controlled by a single recessive gene. To isolate the relevant mutant gene, ''SLL1'' was mapped to the long arm of rice chromosome 9 between markers RM1896 and RM3700. A large F2 mapping population was then generated, allowing the fine-mapping of ''SLL1'' to a 29.57-kb region, using the sequence tagged site and simple sequence repeat markers (Fig. 3A). Three annotated candidate genes, encoding a hypothetical protein, an En/Spm-like transposon, and a transcription factor containing a MYB-like domain, respectively, were located in this region. Further amplification of the relevant DNA fragments and sequence comparison revealed differences in ''sll1-1'' and ''sll1-2'' alleles in the gene encoding the transcription factor containing the MYB-like domain. Comparison with the corresponding genomic sequence revealed that the ''SLL1'' gene consists of six exons and five introns. The gene encodes a 377–amino acid MYB family transcription factor (Fig. 3B). Homologous analysis showed that ''SLL1'' shares high similarity with the KANADI family members in ''Arabidopsis''.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
[[File:ZhangF5.jpg|right|thumb|200px|Fig 5. ''SLL1'' Expression Pattern Analysis &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
Quantitative real-time RT-PCR (qRT-PCR) analysis revealed the expression of ''SLL1'' in various tissues, including roots, stems, leaves, flowers, and seedlings, with relatively high expression in leaf and seedlings (Fig. 5A , top panel). With an emphasis on the leaf, analysis by qRT-PCR showed that ''SLL1'' is ubiquitously expressed in shoot apical meristem (SAM), leaf blade, or leaf sheath at different developmental stages (Figure 5A, bottom panel).&lt;br /&gt;
&lt;br /&gt;
To assess the expression pattern comprehensively, β-glucuronidase (GUS) activity was examined histochemically in transgenic plants carrying an ''SLL1'' promoter-GUS reporter gene. Results showed that ''SLL1'' was transcribed in stem (Fig. 5B, panels 1 and 2), anthers of young or mature flowers (Fig. 5B, panels 3 to 5), pistil tip (Fig. 5B, panel 6), glume (Fig. 5B, panel 7), vascular tissues of mature seeds (Fig. 5B, panels 8 and 9), coleoptile and embryonic root of germinating seedlings (Fig. 5B, panel 10), and root vascular tissues (Fig. 5B, panel 11). In addition, ''SLL1'' is highly transcribed in leaf veins and leaf sheath (Fig. 5C, panels 1 to 3), guard cells, and tracheal elements (Fig. 5C, panels 4 and 5).&lt;br /&gt;
&lt;br /&gt;
The spatial and temporal localization of ''SLL1'' during leaf development was further examined by in situ hybridization analysis. The mRNA expression of ''SLL1'' was detected throughout the young leaf primordium (plastochrons 1 to 3) and was more intense in abaxial cell layer through leaf development (plastochrons 4 and 5) (Fig. 5D, panel 2). However, the ''SLL1'' transcript did not demonstrate apical/basal polarity and did not accumulate at the apex of the meristem (Fig.e 5D, panel 3). Cross-section analysis of the shoot apex showed that ''SLL1'' was more highly expressed in the abaxial cell layer, including the epidermis and vasculature of the early leaf blade (Fig. 5D, panels 5 and 6). In the mature leaf, ''SLL1'' mainly accumulated at the abaxial epidermis, abaxial mesophyll cells, and vasculature (Fig. 5D, panels 8 and 9). In contrast with the sense probe (Fig. 5D, panels 4 and 7), ''SLL1'' was transcribed at a relatively low level throughout other leaf positions including the adaxial epidermis (Fig. 5D, panels 5 and 6).&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
Please input evolution information here.&lt;br /&gt;
&lt;br /&gt;
You can also add sub-section(s) at will.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou 310006, Zhejiang, China&lt;br /&gt;
*National Key Laboratory of Plant Molecular Genetics, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Zhang GH, et al. (2009) ''SHALLOT-LIKE1'' is a KANADI transcription factor that modulates rice leaf rolling by regulating leaf abaxial cell development. The Plant Cell Online 21: 719-735.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os09g0395300|&lt;br /&gt;
Description = Similar to CDPK substrate protein 1|&lt;br /&gt;
Version = NM_001069632.1 GI:115479006 GeneID:4346973|&lt;br /&gt;
Length = 7672 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os09g0395300, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 9|Chromosome 9]]|&lt;br /&gt;
AP = Chromosome 9:14411926..14419597|&lt;br /&gt;
CDS = 14411926..14412128,14413047..14413888,14413990..14414066,14414656..14414701,14414841..14415084&amp;lt;br&amp;gt;,14418440..14418512,14419481..14419597|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008402:14411926..14419597&lt;br /&gt;
source=RiceChromosome09&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008402:14411926..14419597&lt;br /&gt;
source=RiceChromosome09&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggcaatggtgcgggagctcgagttgatgacgagctggagcaacagcatggggcgacaccgctacccaacgcgcatcctcgtcgattccttcgggcataagtgcagtgcctctgacaagggtgtgtggacctcctgcagcattcgcgcacccttgcaaggacgcggctccttccgacgtggcgcgaatattcgctttgggagcttgccgagcagcgcggcggtggcgacgtcggggggagggcgtggcggcggcggggtggtggtgggaggaggaggaggggacccgtggcggaggctggatgggtccacggcgtcgacggagttgtcgctgtcgccgccgccggcgcaggcggcgggtgggggaggtggtggtggtggagcggacgcgctgccgtggcggcaccgaccttcgccgccgtcgtcggcggtggccaccacgtctgccgccgccgcggcggcgctgatggcgccgatgatgctgcagccgctcgacgccggcggcggcgcgtcggcgccgccgccgccgatccgcgggatacctatctacaacggccccggcgggttcccgttcctgcagccgtcgcccaccgccggcgacgtcggccaccaccaccaccaccaccccaagatgggattctacagctcgtaccaccacccatccacgtggccctccacgtcgccgtccccgctcgcggcgccgccgggcgccgcgtcgtcgccgctcgaccccacggcggcgttcctctcctccccccaccaccggatgctgtccgccgcctcggggaggctcaacggcatgctctccgtctccgacaccctccgcagctacggcgtccccggcgccgccgcccccggcgtcatcggcggcgcgcaccaccaccaccaccacctccacggcggccagccgttcgtcggcgccctcgcgtcccgcttcatgcccaagctccccgccaagcgcagcatgcgcgcgccgcgcatgcgctggacgagcaccctccacgcccgcttcgtccacgccgtcgagctcctcggcggccacgagagggcgacgcccaagtcggtgctggagctcatggacgtcaaggatctgacgctagcgcatgtcaagagccacctccagatgtatcgcaccgtgaagagcactgacaagcctgcagcctcttcagggccggcggacggcggctccggcgacgaggagttcgccggcggcgggcaggcggcgtcgggcggcggcgacagcatgtgcctgaggggtggcggcggcggcggggtggccgcggcggcgttcgcggagcacggccggtcggcgtcggagggcgccgccagctcggtcggcggcggcggcggcggcgacatggaccagtcgtcggccggcaacaccagcaccaccaggtggagcaactcctcaagggacccatggctgtcgtccaattcttgcaacatggacgcccatcgctccgtaggattgtcttctcctattgaggttcttgcacttcctttagcctcattgatcatgtcagatactgcctacctgttcttttccagcaaccatggccggtgtgaaccggcctctcttgaccagaaactagcagatatctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MAMVRELELMTSWSNSMGRHRYPTRILVDSFGHKCSASDKGVWT                     SCSIRAPLQGRGSFRRGANIRFGSLPSSAAVATSGGGRGGGGVVVGGGGGDPWRRLDG                     STASTELSLSPPPAQAAGGGGGGGGADALPWRHRPSPPSSAVATTSAAAAAALMAPMM                     LQPLDAGGGASAPPPPIRGIPIYNGPGGFPFLQPSPTAGDVGHHHHHHPKMGFYSSYH                     HPSTWPSTSPSPLAAPPGAASSPLDPTAAFLSSPHHRMLSAASGRLNGMLSVSDTLRS                     YGVPGAAAPGVIGGAHHHHHHLHGGQPFVGALASRFMPKLPAKRSMRAPRMRWTSTLH                     ARFVHAVELLGGHERATPKSVLELMDVKDLTLAHVKSHLQMYRTVKSTDKPAASSGPA                     DGGSGDEEFAGGGQAASGGGDSMCLRGGGGGGVAAAAFAEHGRSASEGAASSVGGGGG                     GDMDQSSAGNTSTTRWSNSSRDPWLSSNSCNMDAHRSVGLSSPIEVLALPLASLIMSD                     TAYLFFSSNHGRCEPASLDQKLADI&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;1..203#1122..1963#2065..2141#2731..2776#2916..3159#6515..6587#7556..7672#atggcaatggtgcgggagctcgagttgatgacgagctggagcaacagcatggggcgacaccgctacccaacgcgcatcctcgtcgattccttcgggcataagtgcagtgcctctgacaagggtgtgtggacctcctgcagcattcgcgcacccttgcaaggacgcggctccttccgacgtggcgcgaatattcgctttgggaggtatgagactacgctccatggtggagcgttgggcgtgaccttagtgtgcgcatatgtaagctgtatgcgtacgtataaatgttgagcttgcagtacatgtatacttgtttttttcttcttttttatgaggtcctttaattccattgtctgtattatttatgctagtatggaggatgatggtggcagtgacataaagtatacaaaaagcatagtatagtatacgtatggaaacaaaagcatgctacctttgactccacttgcattgcctgctaactgccattatttaaggaatacatggttgaatgcctgcctaaacatcaagataacctcacattctcctctctctctctcctaccttgcaattaagggtagcagcagtactctcctcactgctggctgactgctcccattttctctctctactctctctctctctctctcctctattccttttatacttgttgttggtagctaggagtatagcaggacagcacaaggaaccaattcatgcatatatccctggtgtctctcatgcatgttagtgtgaagaaagaagaagcttgagagagaagagagagttagagagagaaagtagagtgtttgtagagagagaaagtggtgtgtgtactagtagtaactccaagccagtgctagagacagagatacaaaaaggagacatcatccttctcttggccaaagcaagcaaccaagcaaagcttcctcttcttctccaagaactccaagaaccttctccttcatcttctccaccatgattccttccatcgcatgagctccatctccggcgtgtcgatcgagatcaccgttgctgctgccgaggtggagaaggaggtgtttgatcgatcggtcgatggaggcgagctcggcggcgacgccaccggacctgtcgctgcacatcagcttgccgagcagcgcggcggtggcgacgtcggggggagggcgtggcggcggcggggtggtggtgggaggaggaggaggggacccgtggcggaggctggatgggtccacggcgtcgacggagttgtcgctgtcgccgccgccggcgcaggcggcgggtgggggaggtggtggtggtggagcggacgcgctgccgtggcggcaccgaccttcgccgccgtcgtcggcggtggccaccacgtctgccgccgccgcggcggcgctgatggcgccgatgatgctgcagccgctcgacgccggcggcggcgcgtcggcgccgccgccgccgatccgcgggatacctatctacaacggccccggcgggttcccgttcctgcagccgtcgcccaccgccggcgacgtcggccaccaccaccaccaccaccccaagatgggattctacagctcgtaccaccacccatccacgtggccctccacgtcgccgtccccgctcgcggcgccgccgggcgccgcgtcgtcgccgctcgaccccacggcggcgttcctctcctccccccaccaccggatgctgtccgccgcctcggggaggctcaacggcatgctctccgtctccgacaccctccgcagctacggcgtccccggcgccgccgcccccggcgtcatcggcggcgcgcaccaccaccaccaccacctccacggcggccagccgttcgtcggcgccctcgcgtcccgcttcatgcccaagctccccgccaagcgcagcatgcgcgcgccgcgcatgcgctggacgagcaccctccacgcccgcttcgtccacgccgtcgagctcctcggcggccacgagagtacgcccccgccatcatcgtcgtcgtcctcctcctccttctcaccaccatcatcaacgagctcgatcaatctgatgagaatccaatcttgttcttggcaggggcgacgcccaagtcggtgctggagctcatggacgtcaaggatctgacgctagcgcatgtcaagagccacctccaggtatcccgccattgccgaccaattctcacagctcgatcgatcgatcaaacaccactcaccactgcaccatctctctctttctctctctcgatttcgattccattcagcttctgttcttgatcatcttgtttgggtgagacaaagatgccaatgcagtaactcctgagttagtgaagaaactgccattcttgggagcagagagagagagtgtgtgtgtgacatgtttggggatgtgtgtgcaagagagaagagagagagagaggggaaaaaagttgccatcattacacaataatgcattgcatctgcatctgtgctactagctccttccttagctctagtcatactagcgtatatgtgcacggcccaaagcactctcacacacaaacacaagagagagagagagagagagaagaagaagatgagagatgagagagagtaggacatattttgtgtgtgtttctttgctgcttgtcttttgcaatggcttcaacctcctggtttcattttgatctcacaaaaaatgtgtgtgtgtgtgtaaatatatatattgatcttctttttgttggacttttgtgttttattactgcagatgtatcgcaccgtgaagagcactgacaagcctgcagcctcttcaggtgattttttttaccatggcagctactagtagtagtagtagtagctaatttagctaagctccattttgcttttctttttttttggcgttgtgcattgcgttttacattacattgttgctatggtttttttgacgtgtagggccggcggacggcggctccggcgacgaggagttcgccggcggcgggcaggcggcgtcgggcggcggcgacagcatgtgcctgaggggtggcggcggcggcggggtggccgcggcggcgttcgcggagcacggccggtcggcgtcggagggcgccgccagctcggtcggcggcggcggcggcggcgacatggaccagtcgtcggccggcaacaccagcaccaccaggtggagcaactcctcaaggtacacacatggcagagttgcatttcaagtctttcagattaattatatatctacattgttatgccatctttaattaattaaaaatgaaattaatcaatcagaatgtcatgagatgatgatgatgatgataataatactaggataggaagaggatgatatgatggatgggtgtgctatgtgtgtttttaagtgtgttttagcttagaaccaaaggcaacaccaacaaactttggcatgcattgatgatgtatctaaatatgagttagtgacatgcaaaattaacctgccaagtacaacctctatttattaattcccaaaaaaatctcatggaggagaagggagagagagagatagtagtaatgtgtggtgatgcatggctaaaaaagcttagcaaaagaatgttttgggggcacacacacacacacctggagagggagttgcctatgtttaggtggccaatgttgttatgtcacacaaaagaccaaaaagtcacacaccccatggcttggcctcctcctccccccttgacctgtgcagttagctaggcttcttctcttctctccctctgtgtttggtttttgtggagctaaaaacattttaaaaatcttgcaaacattgtgtgtaaaaataggttcttgggctctgcccattgtcctctagcttctctcaaatctctctctctctctctctctctctctctctctttctcaaacctagggaggggagggttactcaggcagggctccattatcatttcttatcaatgcatggctctgattccagggggatggggctttgacctgacatgccctattgcctaggaatatgtaaccaaggacttgctgcattcttggttctttctccctctctcaccagtctcttcaatgcccttttcttccacctcttgggcaattattagcatggatggagctcaccttttcactctaccctctagctgtgattaaatcattgactaatcctaattcataaatataagggattcaactatgtaactagatgtactagatcctagtattactagtgtgttttgattctgttaggaggagtgattagcgtttgtcgtaagtactagtattaaactataggggattagtgtagatcatttttttaaaaattagtgagtgtgcttgggcagattttactccagccattggcgtgaaaactttgatctttgggcagcttggaagcaagtacagttcaacctgtccttggctgcattcgctgctttttctttctcaggactcactgcaactttcttgccatccccaacacctccctttcggtcgtgtttgatcagttgcattgctggtttcttcgccgctttaatttctccatctttcttctgttccttattggctaagtaaaaaatcattctcagcaatcaagttttgaaattcaaattagcttcaggttttatctatctaataattctctgactagttctctttctttcaagacctgttcttgttcagaactcttatgcagttgagagttcagttgttcatggaagtaatggcaatgcctggtctagtctttgagcagtatcctccttatgctcttgattttccttcactttagccgtttcagtcaaactttggggacaaattaaagtcagctggtcaagtgcatacataccacgtcatattttttagatgaatccattgtagtattaaatactagtgacaaaaaaatataactaaatggcattaaattgcaaccttcttccccaaaataattgggcacaactaccttgcttgcatatgctttatagtactcctacttattacttccttgaatccatgaggattccaggaatttggtcaggtcaaatgtccaggaggaattaggctatctttttttatcttcttctttttcttctaggtagtaggatcgttgtgcacatataaacaaaacaaaatagaaatttaagaggaaaccctcccaaaaaaaatacgactatcaattatgagtgattttacagttcttgaggaggtacaatgatacattttctattttaaaattcagtaactttgatactatgaggtacagaaatttgcacaaaaaaaatttggtacctctcaagtacttaaaatatcttatcaattatatttcagcaatgttgtcgttgctcgagttgtgcaaaaacatttctgatgaacaagtggagatgtatgcatatttagagagggaaacacatgcattttttaatatacattctcatgacaaattttggtgttctcgtctcattttagtctagcttagattaatggcatccatatattggtgaactgaaacagattgtatatgtccagtcttgaacaaacttcattatacaatgcataatcagaaaagatacagacatatattggcagatcacataaagtggtgtatctatgattgggtggtattttggacatacaaagtctactggtccctcatttgttaacagcatacatttgttcctatcaagacaaaagcactttacaacagtttggtagtaagttggtgttatgtgcgtgtctatttagatagagtggtagtaaaggaaggacactttttcttgatataccaaaatcacacataaaaaagaagtgtcattttcatgatcaacatgtggggtatgaacaaaaatgttctcccccctccaaccaacattgaagtcatcacacataaaaagcaaaaacatttaacaataatacatgcagacacatgtgcatgcatgtgtggatcacgcaaggacatactaattcaattaggtattcacaattaattagtgcaggaaatgacatgtaattacaattatatatgcacaacgatccttgtgtatttgtgtgacccattgtagtagcatttgattcctttcttgtgcctttctctacattgaattcgatctttgccaacagcggcttgctgatgagctcctgtgccattgcactgctgagctgcaccaaacagggacatcttttaagagcttgttgcctggaaatgatccatgtaaccaactgttcaggaagagcacactgtttgctgctcactttagctaaagcaaaactgtgtgcattatgcaatgcatatgcatccttccatctacccctgtgtcctttgccccccaaactgtgtaactacagtttaccatgcacatacatacaatgcacatctacccaattgtagcattgttgcaaggcctacttcagaattcagttagtccccaattgatccaactgcacacatatacatttacatatacatatacacaaacataccagcttggagaaaaggttgtaacaactttgctaaatgtgagatgtgtaatgtgtgttcttcctcttttcagggacccatggctgtcgtccaattcttgcaacatggacgcccatcgctccgtaggattgtcttctcctattgaggtatatatccttacattgttcaaagcttctttcgattcctagctaactgcatatccatgcagaaattcattagctcgcattcattctgaacatgatgtctgaaactctgaattttttttcgtttgtgcgtgtttcagaacttggaaccgtgcagatcgagcagctcgcaggtgtccaaccatgagctgagtagccctagtctcgagttcactctagggaggcctgactggcacggtgcagatcatgattagatggcaatcacagaggctaatgatcaaaaaaaaatttctcctgagatgtgaaatatatatgtgatatacaccaacctggtgctgatcatctttcgccaaccccagcttagccagagccagttcgtctgaagcttgtcatggcgaagaatgatcagcagcaatggcttgaaacgcacatcatatccactgcgtcgtcgtcatcgtcgtcgcaatcgatcggagaagagatatatatttcgcgtctcgatctcatcatcacaatttgggttttcttgattccttcttcttcttctttttgcaattaatatcatggatgcagctagagtttccttgtctgatctccatatttatttagttttgttcgccgtgccgggatcgatttacagtgtagttcagtggtgagctagctagctagagagtgagtgagtgagtgtcagctaggcagctggagatcgagagtgtgagtttggtgatgagttggttgtgtgtttgtcagtgtgtgtgaaagtgtgtgtgccattagcacatggaaagttggaaaggagagaaaggaagaaagaaaagggaattgagttcaggtgaagcaatctgccaatctatctagctacctatctatccatctacttagctcagttgctcagatgatgatctcagatttccatggcccttttttgtgtgcatgcatgccgcatatgcttctttctttaatccctgcaggttcttgcacttcctttagcctcattgatcatgtcagatactgcctacctgttcttttccagcaaccatggccggtgtgaaccggcctctcttgaccagaaactagcagatatctga&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001069632.1 RefSeq:Os09g0395300]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 9]]&lt;br /&gt;
[[Category:Chromosome 9]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os09g0395300&amp;diff=174615</id>
		<title>Os09g0395300</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os09g0395300&amp;diff=174615"/>
				<updated>2014-05-30T11:15:14Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;The rice ''SHALLOT-LIKE1'' ('' SLL1'') gene, a member of KANADI family, is a key gene controlling rice leaf rolling.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:ZhangF1.jpg|right|thumb|200px|Fig 1.''sll1'' has extremely incurved leaves, with deficiency of sclerenchymatous cells at the abaxial side &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:ZhangF2.jpg|right|thumb|200px|Fig 2. ''SLL1'' deficiency results in increased chlorophyll content &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
''sll1'', a rice mutant with shallot-like Leaves, displays abnormal sclerenchymatous cell development in the abaxial cell layers, altered mesophyll cell distribution, increased amounts of chlorophyll, and enhanced photosynthesis (Fig. 1&amp;amp;2) &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
[[File:ZhangF5.jpg|right|thumb|200px|Fig 5. ''SLL1'' Expression Pattern Analysis &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
Quantitative real-time RT-PCR (qRT-PCR) analysis revealed the expression of ''SLL1'' in various tissues, including roots, stems, leaves, flowers, and seedlings, with relatively high expression in leaf and seedlings (Figure 5A , top panel). With an emphasis on the leaf, analysis by qRT-PCR showed that ''SLL1'' is ubiquitously expressed in shoot apical meristem (SAM), leaf blade, or leaf sheath at different developmental stages (Figure 5A, bottom panel).&lt;br /&gt;
&lt;br /&gt;
To assess the expression pattern comprehensively, β-glucuronidase (GUS) activity was examined histochemically in transgenic plants carrying an ''SLL1'' promoter-GUS reporter gene. Results showed that ''SLL1'' was transcribed in stem (Figure 5B, panels 1 and 2), anthers of young or mature flowers (Figure 5B, panels 3 to 5), pistil tip (Figure 5B, panel 6), glume (Figure 5B, panel 7), vascular tissues of mature seeds (Figure 5B, panels 8 and 9), coleoptile and embryonic root of germinating seedlings (Figure 5B, panel 10), and root vascular tissues (Figure 5B, panel 11). In addition, ''SLL1'' is highly transcribed in leaf veins and leaf sheath (Figure 5C, panels 1 to 3), guard cells, and tracheal elements (Figure 5C, panels 4 and 5).&lt;br /&gt;
&lt;br /&gt;
The spatial and temporal localization of ''SLL1'' during leaf development was further examined by in situ hybridization analysis. The mRNA expression of ''SLL1'' was detected throughout the young leaf primordium (plastochrons 1 to 3) and was more intense in abaxial cell layer through leaf development (plastochrons 4 and 5) (Figure 5D, panel 2). However, the ''SLL1'' transcript did not demonstrate apical/basal polarity and did not accumulate at the apex of the meristem (Figure 5D, panel 3). Cross-section analysis of the shoot apex showed that ''SLL1'' was more highly expressed in the abaxial cell layer, including the epidermis and vasculature of the early leaf blade (Figure 5D, panels 5 and 6). In the mature leaf, ''SLL1'' mainly accumulated at the abaxial epidermis, abaxial mesophyll cells, and vasculature (Figure 5D, panels 8 and 9). In contrast with the sense probe (Figure 5D, panels 4 and 7), ''SLL1'' was transcribed at a relatively low level throughout other leaf positions including the adaxial epidermis (Figure 5D, panels 5 and 6).&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
Please input evolution information here.&lt;br /&gt;
&lt;br /&gt;
You can also add sub-section(s) at will.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou 310006, Zhejiang, China&lt;br /&gt;
*National Key Laboratory of Plant Molecular Genetics, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Zhang GH, et al. (2009) ''SHALLOT-LIKE1'' is a KANADI transcription factor that modulates rice leaf rolling by regulating leaf abaxial cell development. The Plant Cell Online 21: 719-735.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os09g0395300|&lt;br /&gt;
Description = Similar to CDPK substrate protein 1|&lt;br /&gt;
Version = NM_001069632.1 GI:115479006 GeneID:4346973|&lt;br /&gt;
Length = 7672 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os09g0395300, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 9|Chromosome 9]]|&lt;br /&gt;
AP = Chromosome 9:14411926..14419597|&lt;br /&gt;
CDS = 14411926..14412128,14413047..14413888,14413990..14414066,14414656..14414701,14414841..14415084&amp;lt;br&amp;gt;,14418440..14418512,14419481..14419597|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008402:14411926..14419597&lt;br /&gt;
source=RiceChromosome09&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008402:14411926..14419597&lt;br /&gt;
source=RiceChromosome09&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggcaatggtgcgggagctcgagttgatgacgagctggagcaacagcatggggcgacaccgctacccaacgcgcatcctcgtcgattccttcgggcataagtgcagtgcctctgacaagggtgtgtggacctcctgcagcattcgcgcacccttgcaaggacgcggctccttccgacgtggcgcgaatattcgctttgggagcttgccgagcagcgcggcggtggcgacgtcggggggagggcgtggcggcggcggggtggtggtgggaggaggaggaggggacccgtggcggaggctggatgggtccacggcgtcgacggagttgtcgctgtcgccgccgccggcgcaggcggcgggtgggggaggtggtggtggtggagcggacgcgctgccgtggcggcaccgaccttcgccgccgtcgtcggcggtggccaccacgtctgccgccgccgcggcggcgctgatggcgccgatgatgctgcagccgctcgacgccggcggcggcgcgtcggcgccgccgccgccgatccgcgggatacctatctacaacggccccggcgggttcccgttcctgcagccgtcgcccaccgccggcgacgtcggccaccaccaccaccaccaccccaagatgggattctacagctcgtaccaccacccatccacgtggccctccacgtcgccgtccccgctcgcggcgccgccgggcgccgcgtcgtcgccgctcgaccccacggcggcgttcctctcctccccccaccaccggatgctgtccgccgcctcggggaggctcaacggcatgctctccgtctccgacaccctccgcagctacggcgtccccggcgccgccgcccccggcgtcatcggcggcgcgcaccaccaccaccaccacctccacggcggccagccgttcgtcggcgccctcgcgtcccgcttcatgcccaagctccccgccaagcgcagcatgcgcgcgccgcgcatgcgctggacgagcaccctccacgcccgcttcgtccacgccgtcgagctcctcggcggccacgagagggcgacgcccaagtcggtgctggagctcatggacgtcaaggatctgacgctagcgcatgtcaagagccacctccagatgtatcgcaccgtgaagagcactgacaagcctgcagcctcttcagggccggcggacggcggctccggcgacgaggagttcgccggcggcgggcaggcggcgtcgggcggcggcgacagcatgtgcctgaggggtggcggcggcggcggggtggccgcggcggcgttcgcggagcacggccggtcggcgtcggagggcgccgccagctcggtcggcggcggcggcggcggcgacatggaccagtcgtcggccggcaacaccagcaccaccaggtggagcaactcctcaagggacccatggctgtcgtccaattcttgcaacatggacgcccatcgctccgtaggattgtcttctcctattgaggttcttgcacttcctttagcctcattgatcatgtcagatactgcctacctgttcttttccagcaaccatggccggtgtgaaccggcctctcttgaccagaaactagcagatatctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MAMVRELELMTSWSNSMGRHRYPTRILVDSFGHKCSASDKGVWT                     SCSIRAPLQGRGSFRRGANIRFGSLPSSAAVATSGGGRGGGGVVVGGGGGDPWRRLDG                     STASTELSLSPPPAQAAGGGGGGGGADALPWRHRPSPPSSAVATTSAAAAAALMAPMM                     LQPLDAGGGASAPPPPIRGIPIYNGPGGFPFLQPSPTAGDVGHHHHHHPKMGFYSSYH                     HPSTWPSTSPSPLAAPPGAASSPLDPTAAFLSSPHHRMLSAASGRLNGMLSVSDTLRS                     YGVPGAAAPGVIGGAHHHHHHLHGGQPFVGALASRFMPKLPAKRSMRAPRMRWTSTLH                     ARFVHAVELLGGHERATPKSVLELMDVKDLTLAHVKSHLQMYRTVKSTDKPAASSGPA                     DGGSGDEEFAGGGQAASGGGDSMCLRGGGGGGVAAAAFAEHGRSASEGAASSVGGGGG                     GDMDQSSAGNTSTTRWSNSSRDPWLSSNSCNMDAHRSVGLSSPIEVLALPLASLIMSD                     TAYLFFSSNHGRCEPASLDQKLADI&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;1..203#1122..1963#2065..2141#2731..2776#2916..3159#6515..6587#7556..7672#atggcaatggtgcgggagctcgagttgatgacgagctggagcaacagcatggggcgacaccgctacccaacgcgcatcctcgtcgattccttcgggcataagtgcagtgcctctgacaagggtgtgtggacctcctgcagcattcgcgcacccttgcaaggacgcggctccttccgacgtggcgcgaatattcgctttgggaggtatgagactacgctccatggtggagcgttgggcgtgaccttagtgtgcgcatatgtaagctgtatgcgtacgtataaatgttgagcttgcagtacatgtatacttgtttttttcttcttttttatgaggtcctttaattccattgtctgtattatttatgctagtatggaggatgatggtggcagtgacataaagtatacaaaaagcatagtatagtatacgtatggaaacaaaagcatgctacctttgactccacttgcattgcctgctaactgccattatttaaggaatacatggttgaatgcctgcctaaacatcaagataacctcacattctcctctctctctctcctaccttgcaattaagggtagcagcagtactctcctcactgctggctgactgctcccattttctctctctactctctctctctctctctcctctattccttttatacttgttgttggtagctaggagtatagcaggacagcacaaggaaccaattcatgcatatatccctggtgtctctcatgcatgttagtgtgaagaaagaagaagcttgagagagaagagagagttagagagagaaagtagagtgtttgtagagagagaaagtggtgtgtgtactagtagtaactccaagccagtgctagagacagagatacaaaaaggagacatcatccttctcttggccaaagcaagcaaccaagcaaagcttcctcttcttctccaagaactccaagaaccttctccttcatcttctccaccatgattccttccatcgcatgagctccatctccggcgtgtcgatcgagatcaccgttgctgctgccgaggtggagaaggaggtgtttgatcgatcggtcgatggaggcgagctcggcggcgacgccaccggacctgtcgctgcacatcagcttgccgagcagcgcggcggtggcgacgtcggggggagggcgtggcggcggcggggtggtggtgggaggaggaggaggggacccgtggcggaggctggatgggtccacggcgtcgacggagttgtcgctgtcgccgccgccggcgcaggcggcgggtgggggaggtggtggtggtggagcggacgcgctgccgtggcggcaccgaccttcgccgccgtcgtcggcggtggccaccacgtctgccgccgccgcggcggcgctgatggcgccgatgatgctgcagccgctcgacgccggcggcggcgcgtcggcgccgccgccgccgatccgcgggatacctatctacaacggccccggcgggttcccgttcctgcagccgtcgcccaccgccggcgacgtcggccaccaccaccaccaccaccccaagatgggattctacagctcgtaccaccacccatccacgtggccctccacgtcgccgtccccgctcgcggcgccgccgggcgccgcgtcgtcgccgctcgaccccacggcggcgttcctctcctccccccaccaccggatgctgtccgccgcctcggggaggctcaacggcatgctctccgtctccgacaccctccgcagctacggcgtccccggcgccgccgcccccggcgtcatcggcggcgcgcaccaccaccaccaccacctccacggcggccagccgttcgtcggcgccctcgcgtcccgcttcatgcccaagctccccgccaagcgcagcatgcgcgcgccgcgcatgcgctggacgagcaccctccacgcccgcttcgtccacgccgtcgagctcctcggcggccacgagagtacgcccccgccatcatcgtcgtcgtcctcctcctccttctcaccaccatcatcaacgagctcgatcaatctgatgagaatccaatcttgttcttggcaggggcgacgcccaagtcggtgctggagctcatggacgtcaaggatctgacgctagcgcatgtcaagagccacctccaggtatcccgccattgccgaccaattctcacagctcgatcgatcgatcaaacaccactcaccactgcaccatctctctctttctctctctcgatttcgattccattcagcttctgttcttgatcatcttgtttgggtgagacaaagatgccaatgcagtaactcctgagttagtgaagaaactgccattcttgggagcagagagagagagtgtgtgtgtgacatgtttggggatgtgtgtgcaagagagaagagagagagagaggggaaaaaagttgccatcattacacaataatgcattgcatctgcatctgtgctactagctccttccttagctctagtcatactagcgtatatgtgcacggcccaaagcactctcacacacaaacacaagagagagagagagagagagaagaagaagatgagagatgagagagagtaggacatattttgtgtgtgtttctttgctgcttgtcttttgcaatggcttcaacctcctggtttcattttgatctcacaaaaaatgtgtgtgtgtgtgtaaatatatatattgatcttctttttgttggacttttgtgttttattactgcagatgtatcgcaccgtgaagagcactgacaagcctgcagcctcttcaggtgattttttttaccatggcagctactagtagtagtagtagtagctaatttagctaagctccattttgcttttctttttttttggcgttgtgcattgcgttttacattacattgttgctatggtttttttgacgtgtagggccggcggacggcggctccggcgacgaggagttcgccggcggcgggcaggcggcgtcgggcggcggcgacagcatgtgcctgaggggtggcggcggcggcggggtggccgcggcggcgttcgcggagcacggccggtcggcgtcggagggcgccgccagctcggtcggcggcggcggcggcggcgacatggaccagtcgtcggccggcaacaccagcaccaccaggtggagcaactcctcaaggtacacacatggcagagttgcatttcaagtctttcagattaattatatatctacattgttatgccatctttaattaattaaaaatgaaattaatcaatcagaatgtcatgagatgatgatgatgatgataataatactaggataggaagaggatgatatgatggatgggtgtgctatgtgtgtttttaagtgtgttttagcttagaaccaaaggcaacaccaacaaactttggcatgcattgatgatgtatctaaatatgagttagtgacatgcaaaattaacctgccaagtacaacctctatttattaattcccaaaaaaatctcatggaggagaagggagagagagagatagtagtaatgtgtggtgatgcatggctaaaaaagcttagcaaaagaatgttttgggggcacacacacacacacctggagagggagttgcctatgtttaggtggccaatgttgttatgtcacacaaaagaccaaaaagtcacacaccccatggcttggcctcctcctccccccttgacctgtgcagttagctaggcttcttctcttctctccctctgtgtttggtttttgtggagctaaaaacattttaaaaatcttgcaaacattgtgtgtaaaaataggttcttgggctctgcccattgtcctctagcttctctcaaatctctctctctctctctctctctctctctctctttctcaaacctagggaggggagggttactcaggcagggctccattatcatttcttatcaatgcatggctctgattccagggggatggggctttgacctgacatgccctattgcctaggaatatgtaaccaaggacttgctgcattcttggttctttctccctctctcaccagtctcttcaatgcccttttcttccacctcttgggcaattattagcatggatggagctcaccttttcactctaccctctagctgtgattaaatcattgactaatcctaattcataaatataagggattcaactatgtaactagatgtactagatcctagtattactagtgtgttttgattctgttaggaggagtgattagcgtttgtcgtaagtactagtattaaactataggggattagtgtagatcatttttttaaaaattagtgagtgtgcttgggcagattttactccagccattggcgtgaaaactttgatctttgggcagcttggaagcaagtacagttcaacctgtccttggctgcattcgctgctttttctttctcaggactcactgcaactttcttgccatccccaacacctccctttcggtcgtgtttgatcagttgcattgctggtttcttcgccgctttaatttctccatctttcttctgttccttattggctaagtaaaaaatcattctcagcaatcaagttttgaaattcaaattagcttcaggttttatctatctaataattctctgactagttctctttctttcaagacctgttcttgttcagaactcttatgcagttgagagttcagttgttcatggaagtaatggcaatgcctggtctagtctttgagcagtatcctccttatgctcttgattttccttcactttagccgtttcagtcaaactttggggacaaattaaagtcagctggtcaagtgcatacataccacgtcatattttttagatgaatccattgtagtattaaatactagtgacaaaaaaatataactaaatggcattaaattgcaaccttcttccccaaaataattgggcacaactaccttgcttgcatatgctttatagtactcctacttattacttccttgaatccatgaggattccaggaatttggtcaggtcaaatgtccaggaggaattaggctatctttttttatcttcttctttttcttctaggtagtaggatcgttgtgcacatataaacaaaacaaaatagaaatttaagaggaaaccctcccaaaaaaaatacgactatcaattatgagtgattttacagttcttgaggaggtacaatgatacattttctattttaaaattcagtaactttgatactatgaggtacagaaatttgcacaaaaaaaatttggtacctctcaagtacttaaaatatcttatcaattatatttcagcaatgttgtcgttgctcgagttgtgcaaaaacatttctgatgaacaagtggagatgtatgcatatttagagagggaaacacatgcattttttaatatacattctcatgacaaattttggtgttctcgtctcattttagtctagcttagattaatggcatccatatattggtgaactgaaacagattgtatatgtccagtcttgaacaaacttcattatacaatgcataatcagaaaagatacagacatatattggcagatcacataaagtggtgtatctatgattgggtggtattttggacatacaaagtctactggtccctcatttgttaacagcatacatttgttcctatcaagacaaaagcactttacaacagtttggtagtaagttggtgttatgtgcgtgtctatttagatagagtggtagtaaaggaaggacactttttcttgatataccaaaatcacacataaaaaagaagtgtcattttcatgatcaacatgtggggtatgaacaaaaatgttctcccccctccaaccaacattgaagtcatcacacataaaaagcaaaaacatttaacaataatacatgcagacacatgtgcatgcatgtgtggatcacgcaaggacatactaattcaattaggtattcacaattaattagtgcaggaaatgacatgtaattacaattatatatgcacaacgatccttgtgtatttgtgtgacccattgtagtagcatttgattcctttcttgtgcctttctctacattgaattcgatctttgccaacagcggcttgctgatgagctcctgtgccattgcactgctgagctgcaccaaacagggacatcttttaagagcttgttgcctggaaatgatccatgtaaccaactgttcaggaagagcacactgtttgctgctcactttagctaaagcaaaactgtgtgcattatgcaatgcatatgcatccttccatctacccctgtgtcctttgccccccaaactgtgtaactacagtttaccatgcacatacatacaatgcacatctacccaattgtagcattgttgcaaggcctacttcagaattcagttagtccccaattgatccaactgcacacatatacatttacatatacatatacacaaacataccagcttggagaaaaggttgtaacaactttgctaaatgtgagatgtgtaatgtgtgttcttcctcttttcagggacccatggctgtcgtccaattcttgcaacatggacgcccatcgctccgtaggattgtcttctcctattgaggtatatatccttacattgttcaaagcttctttcgattcctagctaactgcatatccatgcagaaattcattagctcgcattcattctgaacatgatgtctgaaactctgaattttttttcgtttgtgcgtgtttcagaacttggaaccgtgcagatcgagcagctcgcaggtgtccaaccatgagctgagtagccctagtctcgagttcactctagggaggcctgactggcacggtgcagatcatgattagatggcaatcacagaggctaatgatcaaaaaaaaatttctcctgagatgtgaaatatatatgtgatatacaccaacctggtgctgatcatctttcgccaaccccagcttagccagagccagttcgtctgaagcttgtcatggcgaagaatgatcagcagcaatggcttgaaacgcacatcatatccactgcgtcgtcgtcatcgtcgtcgcaatcgatcggagaagagatatatatttcgcgtctcgatctcatcatcacaatttgggttttcttgattccttcttcttcttctttttgcaattaatatcatggatgcagctagagtttccttgtctgatctccatatttatttagttttgttcgccgtgccgggatcgatttacagtgtagttcagtggtgagctagctagctagagagtgagtgagtgagtgtcagctaggcagctggagatcgagagtgtgagtttggtgatgagttggttgtgtgtttgtcagtgtgtgtgaaagtgtgtgtgccattagcacatggaaagttggaaaggagagaaaggaagaaagaaaagggaattgagttcaggtgaagcaatctgccaatctatctagctacctatctatccatctacttagctcagttgctcagatgatgatctcagatttccatggcccttttttgtgtgcatgcatgccgcatatgcttctttctttaatccctgcaggttcttgcacttcctttagcctcattgatcatgtcagatactgcctacctgttcttttccagcaaccatggccggtgtgaaccggcctctcttgaccagaaactagcagatatctga&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001069632.1 RefSeq:Os09g0395300]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 9]]&lt;br /&gt;
[[Category:Chromosome 9]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os09g0395300&amp;diff=174607</id>
		<title>Os09g0395300</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os09g0395300&amp;diff=174607"/>
				<updated>2014-05-30T11:03:14Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;The rice ''SHALLOT-LIKE1'' ('' SLL1'') gene, a member of KANADI family, is a key gene controlling rice leaf rolling.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:ZhangF1.jpg|right|thumb|200px|Fig 1.''sll1'' has extremely incurved leaves, with deficiency of sclerenchymatous cells at the abaxial side &amp;lt;ref name=''ref1'' /&amp;gt;.]]  [[File:ZhangF2.jpg|right|thumb|200px|Fig 2. ''SLL1'' deficiency results in increased chlorophyll content &amp;lt;ref name=''ref1'' /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
''sll1'', a rice mutant with shallot-like Leaves, displays abnormal sclerenchymatous cell development in the abaxial cell layers, altered mesophyll cell distribution, increased amounts of chlorophyll, and enhanced photosynthesis (Fig. 1&amp;amp;2) &amp;lt;ref name=''ref1'' /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
[[File:ZhangF5.jpg|right|thumb|200px|Fig 5. ''SLL1'' Expression Pattern Analysis &amp;lt;ref name=''ref1'' /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
Quantitative real-time RT-PCR (qRT-PCR) analysis revealed the expression of ''SLL1'' in various tissues, including roots, stems, leaves, flowers, and seedlings, with relatively high expression in leaf and seedlings (Figure 5A , top panel). With an emphasis on the leaf, analysis by qRT-PCR showed that ''SLL1'' is ubiquitously expressed in shoot apical meristem (SAM), leaf blade, or leaf sheath at different developmental stages (Figure 5A, bottom panel).&lt;br /&gt;
&lt;br /&gt;
To assess the expression pattern comprehensively, β-glucuronidase (GUS) activity was examined histochemically in transgenic plants carrying an ''SLL1'' promoter-GUS reporter gene. Results showed that ''SLL1'' was transcribed in stem (Figure 5B, panels 1 and 2), anthers of young or mature flowers (Figure 5B, panels 3 to 5), pistil tip (Figure 5B, panel 6), glume (Figure 5B, panel 7), vascular tissues of mature seeds (Figure 5B, panels 8 and 9), coleoptile and embryonic root of germinating seedlings (Figure 5B, panel 10), and root vascular tissues (Figure 5B, panel 11). In addition, ''SLL1'' is highly transcribed in leaf veins and leaf sheath (Figure 5C, panels 1 to 3), guard cells, and tracheal elements (Figure 5C, panels 4 and 5).&lt;br /&gt;
&lt;br /&gt;
The spatial and temporal localization of ''SLL1'' during leaf development was further examined by in situ hybridization analysis. The mRNA expression of ''SLL1'' was detected throughout the young leaf primordium (plastochrons 1 to 3) and was more intense in abaxial cell layer through leaf development (plastochrons 4 and 5) (Figure 5D, panel 2). However, the ''SLL1'' transcript did not demonstrate apical/basal polarity and did not accumulate at the apex of the meristem (Figure 5D, panel 3). Cross-section analysis of the shoot apex showed that ''SLL1'' was more highly expressed in the abaxial cell layer, including the epidermis and vasculature of the early leaf blade (Figure 5D, panels 5 and 6). In the mature leaf, ''SLL1'' mainly accumulated at the abaxial epidermis, abaxial mesophyll cells, and vasculature (Figure 5D, panels 8 and 9). In contrast with the sense probe (Figure 5D, panels 4 and 7), ''SLL1'' was transcribed at a relatively low level throughout other leaf positions including the adaxial epidermis (Figure 5D, panels 5 and 6).&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
Please input evolution information here.&lt;br /&gt;
&lt;br /&gt;
You can also add sub-section(s) at will.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou 310006, Zhejiang, China&lt;br /&gt;
*National Key Laboratory of Plant Molecular Genetics, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Zhang GH, et al. (2009) ''SHALLOT-LIKE1''is a KANADI transcription factor that modulates rice leaf rolling by regulating leaf abaxial cell development. The Plant Cell Online 21: 719-735.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os09g0395300|&lt;br /&gt;
Description = Similar to CDPK substrate protein 1|&lt;br /&gt;
Version = NM_001069632.1 GI:115479006 GeneID:4346973|&lt;br /&gt;
Length = 7672 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os09g0395300, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 9|Chromosome 9]]|&lt;br /&gt;
AP = Chromosome 9:14411926..14419597|&lt;br /&gt;
CDS = 14411926..14412128,14413047..14413888,14413990..14414066,14414656..14414701,14414841..14415084&amp;lt;br&amp;gt;,14418440..14418512,14419481..14419597|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008402:14411926..14419597&lt;br /&gt;
source=RiceChromosome09&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008402:14411926..14419597&lt;br /&gt;
source=RiceChromosome09&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggcaatggtgcgggagctcgagttgatgacgagctggagcaacagcatggggcgacaccgctacccaacgcgcatcctcgtcgattccttcgggcataagtgcagtgcctctgacaagggtgtgtggacctcctgcagcattcgcgcacccttgcaaggacgcggctccttccgacgtggcgcgaatattcgctttgggagcttgccgagcagcgcggcggtggcgacgtcggggggagggcgtggcggcggcggggtggtggtgggaggaggaggaggggacccgtggcggaggctggatgggtccacggcgtcgacggagttgtcgctgtcgccgccgccggcgcaggcggcgggtgggggaggtggtggtggtggagcggacgcgctgccgtggcggcaccgaccttcgccgccgtcgtcggcggtggccaccacgtctgccgccgccgcggcggcgctgatggcgccgatgatgctgcagccgctcgacgccggcggcggcgcgtcggcgccgccgccgccgatccgcgggatacctatctacaacggccccggcgggttcccgttcctgcagccgtcgcccaccgccggcgacgtcggccaccaccaccaccaccaccccaagatgggattctacagctcgtaccaccacccatccacgtggccctccacgtcgccgtccccgctcgcggcgccgccgggcgccgcgtcgtcgccgctcgaccccacggcggcgttcctctcctccccccaccaccggatgctgtccgccgcctcggggaggctcaacggcatgctctccgtctccgacaccctccgcagctacggcgtccccggcgccgccgcccccggcgtcatcggcggcgcgcaccaccaccaccaccacctccacggcggccagccgttcgtcggcgccctcgcgtcccgcttcatgcccaagctccccgccaagcgcagcatgcgcgcgccgcgcatgcgctggacgagcaccctccacgcccgcttcgtccacgccgtcgagctcctcggcggccacgagagggcgacgcccaagtcggtgctggagctcatggacgtcaaggatctgacgctagcgcatgtcaagagccacctccagatgtatcgcaccgtgaagagcactgacaagcctgcagcctcttcagggccggcggacggcggctccggcgacgaggagttcgccggcggcgggcaggcggcgtcgggcggcggcgacagcatgtgcctgaggggtggcggcggcggcggggtggccgcggcggcgttcgcggagcacggccggtcggcgtcggagggcgccgccagctcggtcggcggcggcggcggcggcgacatggaccagtcgtcggccggcaacaccagcaccaccaggtggagcaactcctcaagggacccatggctgtcgtccaattcttgcaacatggacgcccatcgctccgtaggattgtcttctcctattgaggttcttgcacttcctttagcctcattgatcatgtcagatactgcctacctgttcttttccagcaaccatggccggtgtgaaccggcctctcttgaccagaaactagcagatatctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MAMVRELELMTSWSNSMGRHRYPTRILVDSFGHKCSASDKGVWT                     SCSIRAPLQGRGSFRRGANIRFGSLPSSAAVATSGGGRGGGGVVVGGGGGDPWRRLDG                     STASTELSLSPPPAQAAGGGGGGGGADALPWRHRPSPPSSAVATTSAAAAAALMAPMM                     LQPLDAGGGASAPPPPIRGIPIYNGPGGFPFLQPSPTAGDVGHHHHHHPKMGFYSSYH                     HPSTWPSTSPSPLAAPPGAASSPLDPTAAFLSSPHHRMLSAASGRLNGMLSVSDTLRS                     YGVPGAAAPGVIGGAHHHHHHLHGGQPFVGALASRFMPKLPAKRSMRAPRMRWTSTLH                     ARFVHAVELLGGHERATPKSVLELMDVKDLTLAHVKSHLQMYRTVKSTDKPAASSGPA                     DGGSGDEEFAGGGQAASGGGDSMCLRGGGGGGVAAAAFAEHGRSASEGAASSVGGGGG                     GDMDQSSAGNTSTTRWSNSSRDPWLSSNSCNMDAHRSVGLSSPIEVLALPLASLIMSD                     TAYLFFSSNHGRCEPASLDQKLADI&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;1..203#1122..1963#2065..2141#2731..2776#2916..3159#6515..6587#7556..7672#atggcaatggtgcgggagctcgagttgatgacgagctggagcaacagcatggggcgacaccgctacccaacgcgcatcctcgtcgattccttcgggcataagtgcagtgcctctgacaagggtgtgtggacctcctgcagcattcgcgcacccttgcaaggacgcggctccttccgacgtggcgcgaatattcgctttgggaggtatgagactacgctccatggtggagcgttgggcgtgaccttagtgtgcgcatatgtaagctgtatgcgtacgtataaatgttgagcttgcagtacatgtatacttgtttttttcttcttttttatgaggtcctttaattccattgtctgtattatttatgctagtatggaggatgatggtggcagtgacataaagtatacaaaaagcatagtatagtatacgtatggaaacaaaagcatgctacctttgactccacttgcattgcctgctaactgccattatttaaggaatacatggttgaatgcctgcctaaacatcaagataacctcacattctcctctctctctctcctaccttgcaattaagggtagcagcagtactctcctcactgctggctgactgctcccattttctctctctactctctctctctctctctcctctattccttttatacttgttgttggtagctaggagtatagcaggacagcacaaggaaccaattcatgcatatatccctggtgtctctcatgcatgttagtgtgaagaaagaagaagcttgagagagaagagagagttagagagagaaagtagagtgtttgtagagagagaaagtggtgtgtgtactagtagtaactccaagccagtgctagagacagagatacaaaaaggagacatcatccttctcttggccaaagcaagcaaccaagcaaagcttcctcttcttctccaagaactccaagaaccttctccttcatcttctccaccatgattccttccatcgcatgagctccatctccggcgtgtcgatcgagatcaccgttgctgctgccgaggtggagaaggaggtgtttgatcgatcggtcgatggaggcgagctcggcggcgacgccaccggacctgtcgctgcacatcagcttgccgagcagcgcggcggtggcgacgtcggggggagggcgtggcggcggcggggtggtggtgggaggaggaggaggggacccgtggcggaggctggatgggtccacggcgtcgacggagttgtcgctgtcgccgccgccggcgcaggcggcgggtgggggaggtggtggtggtggagcggacgcgctgccgtggcggcaccgaccttcgccgccgtcgtcggcggtggccaccacgtctgccgccgccgcggcggcgctgatggcgccgatgatgctgcagccgctcgacgccggcggcggcgcgtcggcgccgccgccgccgatccgcgggatacctatctacaacggccccggcgggttcccgttcctgcagccgtcgcccaccgccggcgacgtcggccaccaccaccaccaccaccccaagatgggattctacagctcgtaccaccacccatccacgtggccctccacgtcgccgtccccgctcgcggcgccgccgggcgccgcgtcgtcgccgctcgaccccacggcggcgttcctctcctccccccaccaccggatgctgtccgccgcctcggggaggctcaacggcatgctctccgtctccgacaccctccgcagctacggcgtccccggcgccgccgcccccggcgtcatcggcggcgcgcaccaccaccaccaccacctccacggcggccagccgttcgtcggcgccctcgcgtcccgcttcatgcccaagctccccgccaagcgcagcatgcgcgcgccgcgcatgcgctggacgagcaccctccacgcccgcttcgtccacgccgtcgagctcctcggcggccacgagagtacgcccccgccatcatcgtcgtcgtcctcctcctccttctcaccaccatcatcaacgagctcgatcaatctgatgagaatccaatcttgttcttggcaggggcgacgcccaagtcggtgctggagctcatggacgtcaaggatctgacgctagcgcatgtcaagagccacctccaggtatcccgccattgccgaccaattctcacagctcgatcgatcgatcaaacaccactcaccactgcaccatctctctctttctctctctcgatttcgattccattcagcttctgttcttgatcatcttgtttgggtgagacaaagatgccaatgcagtaactcctgagttagtgaagaaactgccattcttgggagcagagagagagagtgtgtgtgtgacatgtttggggatgtgtgtgcaagagagaagagagagagagaggggaaaaaagttgccatcattacacaataatgcattgcatctgcatctgtgctactagctccttccttagctctagtcatactagcgtatatgtgcacggcccaaagcactctcacacacaaacacaagagagagagagagagagagaagaagaagatgagagatgagagagagtaggacatattttgtgtgtgtttctttgctgcttgtcttttgcaatggcttcaacctcctggtttcattttgatctcacaaaaaatgtgtgtgtgtgtgtaaatatatatattgatcttctttttgttggacttttgtgttttattactgcagatgtatcgcaccgtgaagagcactgacaagcctgcagcctcttcaggtgattttttttaccatggcagctactagtagtagtagtagtagctaatttagctaagctccattttgcttttctttttttttggcgttgtgcattgcgttttacattacattgttgctatggtttttttgacgtgtagggccggcggacggcggctccggcgacgaggagttcgccggcggcgggcaggcggcgtcgggcggcggcgacagcatgtgcctgaggggtggcggcggcggcggggtggccgcggcggcgttcgcggagcacggccggtcggcgtcggagggcgccgccagctcggtcggcggcggcggcggcggcgacatggaccagtcgtcggccggcaacaccagcaccaccaggtggagcaactcctcaaggtacacacatggcagagttgcatttcaagtctttcagattaattatatatctacattgttatgccatctttaattaattaaaaatgaaattaatcaatcagaatgtcatgagatgatgatgatgatgataataatactaggataggaagaggatgatatgatggatgggtgtgctatgtgtgtttttaagtgtgttttagcttagaaccaaaggcaacaccaacaaactttggcatgcattgatgatgtatctaaatatgagttagtgacatgcaaaattaacctgccaagtacaacctctatttattaattcccaaaaaaatctcatggaggagaagggagagagagagatagtagtaatgtgtggtgatgcatggctaaaaaagcttagcaaaagaatgttttgggggcacacacacacacacctggagagggagttgcctatgtttaggtggccaatgttgttatgtcacacaaaagaccaaaaagtcacacaccccatggcttggcctcctcctccccccttgacctgtgcagttagctaggcttcttctcttctctccctctgtgtttggtttttgtggagctaaaaacattttaaaaatcttgcaaacattgtgtgtaaaaataggttcttgggctctgcccattgtcctctagcttctctcaaatctctctctctctctctctctctctctctctctttctcaaacctagggaggggagggttactcaggcagggctccattatcatttcttatcaatgcatggctctgattccagggggatggggctttgacctgacatgccctattgcctaggaatatgtaaccaaggacttgctgcattcttggttctttctccctctctcaccagtctcttcaatgcccttttcttccacctcttgggcaattattagcatggatggagctcaccttttcactctaccctctagctgtgattaaatcattgactaatcctaattcataaatataagggattcaactatgtaactagatgtactagatcctagtattactagtgtgttttgattctgttaggaggagtgattagcgtttgtcgtaagtactagtattaaactataggggattagtgtagatcatttttttaaaaattagtgagtgtgcttgggcagattttactccagccattggcgtgaaaactttgatctttgggcagcttggaagcaagtacagttcaacctgtccttggctgcattcgctgctttttctttctcaggactcactgcaactttcttgccatccccaacacctccctttcggtcgtgtttgatcagttgcattgctggtttcttcgccgctttaatttctccatctttcttctgttccttattggctaagtaaaaaatcattctcagcaatcaagttttgaaattcaaattagcttcaggttttatctatctaataattctctgactagttctctttctttcaagacctgttcttgttcagaactcttatgcagttgagagttcagttgttcatggaagtaatggcaatgcctggtctagtctttgagcagtatcctccttatgctcttgattttccttcactttagccgtttcagtcaaactttggggacaaattaaagtcagctggtcaagtgcatacataccacgtcatattttttagatgaatccattgtagtattaaatactagtgacaaaaaaatataactaaatggcattaaattgcaaccttcttccccaaaataattgggcacaactaccttgcttgcatatgctttatagtactcctacttattacttccttgaatccatgaggattccaggaatttggtcaggtcaaatgtccaggaggaattaggctatctttttttatcttcttctttttcttctaggtagtaggatcgttgtgcacatataaacaaaacaaaatagaaatttaagaggaaaccctcccaaaaaaaatacgactatcaattatgagtgattttacagttcttgaggaggtacaatgatacattttctattttaaaattcagtaactttgatactatgaggtacagaaatttgcacaaaaaaaatttggtacctctcaagtacttaaaatatcttatcaattatatttcagcaatgttgtcgttgctcgagttgtgcaaaaacatttctgatgaacaagtggagatgtatgcatatttagagagggaaacacatgcattttttaatatacattctcatgacaaattttggtgttctcgtctcattttagtctagcttagattaatggcatccatatattggtgaactgaaacagattgtatatgtccagtcttgaacaaacttcattatacaatgcataatcagaaaagatacagacatatattggcagatcacataaagtggtgtatctatgattgggtggtattttggacatacaaagtctactggtccctcatttgttaacagcatacatttgttcctatcaagacaaaagcactttacaacagtttggtagtaagttggtgttatgtgcgtgtctatttagatagagtggtagtaaaggaaggacactttttcttgatataccaaaatcacacataaaaaagaagtgtcattttcatgatcaacatgtggggtatgaacaaaaatgttctcccccctccaaccaacattgaagtcatcacacataaaaagcaaaaacatttaacaataatacatgcagacacatgtgcatgcatgtgtggatcacgcaaggacatactaattcaattaggtattcacaattaattagtgcaggaaatgacatgtaattacaattatatatgcacaacgatccttgtgtatttgtgtgacccattgtagtagcatttgattcctttcttgtgcctttctctacattgaattcgatctttgccaacagcggcttgctgatgagctcctgtgccattgcactgctgagctgcaccaaacagggacatcttttaagagcttgttgcctggaaatgatccatgtaaccaactgttcaggaagagcacactgtttgctgctcactttagctaaagcaaaactgtgtgcattatgcaatgcatatgcatccttccatctacccctgtgtcctttgccccccaaactgtgtaactacagtttaccatgcacatacatacaatgcacatctacccaattgtagcattgttgcaaggcctacttcagaattcagttagtccccaattgatccaactgcacacatatacatttacatatacatatacacaaacataccagcttggagaaaaggttgtaacaactttgctaaatgtgagatgtgtaatgtgtgttcttcctcttttcagggacccatggctgtcgtccaattcttgcaacatggacgcccatcgctccgtaggattgtcttctcctattgaggtatatatccttacattgttcaaagcttctttcgattcctagctaactgcatatccatgcagaaattcattagctcgcattcattctgaacatgatgtctgaaactctgaattttttttcgtttgtgcgtgtttcagaacttggaaccgtgcagatcgagcagctcgcaggtgtccaaccatgagctgagtagccctagtctcgagttcactctagggaggcctgactggcacggtgcagatcatgattagatggcaatcacagaggctaatgatcaaaaaaaaatttctcctgagatgtgaaatatatatgtgatatacaccaacctggtgctgatcatctttcgccaaccccagcttagccagagccagttcgtctgaagcttgtcatggcgaagaatgatcagcagcaatggcttgaaacgcacatcatatccactgcgtcgtcgtcatcgtcgtcgcaatcgatcggagaagagatatatatttcgcgtctcgatctcatcatcacaatttgggttttcttgattccttcttcttcttctttttgcaattaatatcatggatgcagctagagtttccttgtctgatctccatatttatttagttttgttcgccgtgccgggatcgatttacagtgtagttcagtggtgagctagctagctagagagtgagtgagtgagtgtcagctaggcagctggagatcgagagtgtgagtttggtgatgagttggttgtgtgtttgtcagtgtgtgtgaaagtgtgtgtgccattagcacatggaaagttggaaaggagagaaaggaagaaagaaaagggaattgagttcaggtgaagcaatctgccaatctatctagctacctatctatccatctacttagctcagttgctcagatgatgatctcagatttccatggcccttttttgtgtgcatgcatgccgcatatgcttctttctttaatccctgcaggttcttgcacttcctttagcctcattgatcatgtcagatactgcctacctgttcttttccagcaaccatggccggtgtgaaccggcctctcttgaccagaaactagcagatatctga&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001069632.1 RefSeq:Os09g0395300]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 9]]&lt;br /&gt;
[[Category:Chromosome 9]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os09g0395300&amp;diff=174605</id>
		<title>Os09g0395300</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os09g0395300&amp;diff=174605"/>
				<updated>2014-05-30T11:02:11Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;The rice ''SHALLOT-LIKE1'' ('' SLL1'') gene, a member of KANADI family, is a key gene controlling rice leaf rolling.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:ZhangF1.jpg|right|thumb|200px|Fig 1.''sll1'' has extremely incurved leaves, with deficiency of sclerenchymatous cells at the abaxial side &amp;lt;ref name=''ref1'' /&amp;gt;.]]  [[File:ZhangF2.jpg|right|thumb|200px|Fig 2. ''SLL1'' deficiency results in increased chlorophyll content &amp;lt;ref name=''ref1'' /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
''sll1'', a rice mutant with shallot-like Leaves, displays abnormal sclerenchymatous cell development in the abaxial cell layers, altered mesophyll cell distribution, increased amounts of chlorophyll, and enhanced photosynthesis (Fig. 1&amp;amp;2).&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
[[File:ZhangF5.jpg|right|thumb|200px|Fig 5. ''SLL1'' Expression Pattern Analysis &amp;lt;ref name=''ref1'' /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
Quantitative real-time RT-PCR (qRT-PCR) analysis revealed the expression of ''SLL1'' in various tissues, including roots, stems, leaves, flowers, and seedlings, with relatively high expression in leaf and seedlings (Figure 5A , top panel). With an emphasis on the leaf, analysis by qRT-PCR showed that ''SLL1'' is ubiquitously expressed in shoot apical meristem (SAM), leaf blade, or leaf sheath at different developmental stages (Figure 5A, bottom panel).&lt;br /&gt;
&lt;br /&gt;
To assess the expression pattern comprehensively, β-glucuronidase (GUS) activity was examined histochemically in transgenic plants carrying an ''SLL1'' promoter-GUS reporter gene. Results showed that ''SLL1'' was transcribed in stem (Figure 5B, panels 1 and 2), anthers of young or mature flowers (Figure 5B, panels 3 to 5), pistil tip (Figure 5B, panel 6), glume (Figure 5B, panel 7), vascular tissues of mature seeds (Figure 5B, panels 8 and 9), coleoptile and embryonic root of germinating seedlings (Figure 5B, panel 10), and root vascular tissues (Figure 5B, panel 11). In addition, ''SLL1'' is highly transcribed in leaf veins and leaf sheath (Figure 5C, panels 1 to 3), guard cells, and tracheal elements (Figure 5C, panels 4 and 5).&lt;br /&gt;
&lt;br /&gt;
The spatial and temporal localization of ''SLL1'' during leaf development was further examined by in situ hybridization analysis. The mRNA expression of ''SLL1'' was detected throughout the young leaf primordium (plastochrons 1 to 3) and was more intense in abaxial cell layer through leaf development (plastochrons 4 and 5) (Figure 5D, panel 2). However, the ''SLL1'' transcript did not demonstrate apical/basal polarity and did not accumulate at the apex of the meristem (Figure 5D, panel 3). Cross-section analysis of the shoot apex showed that ''SLL1'' was more highly expressed in the abaxial cell layer, including the epidermis and vasculature of the early leaf blade (Figure 5D, panels 5 and 6). In the mature leaf, ''SLL1'' mainly accumulated at the abaxial epidermis, abaxial mesophyll cells, and vasculature (Figure 5D, panels 8 and 9). In contrast with the sense probe (Figure 5D, panels 4 and 7), ''SLL1'' was transcribed at a relatively low level throughout other leaf positions including the adaxial epidermis (Figure 5D, panels 5 and 6).&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
Please input evolution information here.&lt;br /&gt;
&lt;br /&gt;
You can also add sub-section(s) at will.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou 310006, Zhejiang, China&lt;br /&gt;
*National Key Laboratory of Plant Molecular Genetics, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Zhang GH, et al. (2009) ''SHALLOT-LIKE1''is a KANADI transcription factor that modulates rice leaf rolling by regulating leaf abaxial cell development. The Plant Cell Online 21: 719-735.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os09g0395300|&lt;br /&gt;
Description = Similar to CDPK substrate protein 1|&lt;br /&gt;
Version = NM_001069632.1 GI:115479006 GeneID:4346973|&lt;br /&gt;
Length = 7672 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os09g0395300, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 9|Chromosome 9]]|&lt;br /&gt;
AP = Chromosome 9:14411926..14419597|&lt;br /&gt;
CDS = 14411926..14412128,14413047..14413888,14413990..14414066,14414656..14414701,14414841..14415084&amp;lt;br&amp;gt;,14418440..14418512,14419481..14419597|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008402:14411926..14419597&lt;br /&gt;
source=RiceChromosome09&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008402:14411926..14419597&lt;br /&gt;
source=RiceChromosome09&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggcaatggtgcgggagctcgagttgatgacgagctggagcaacagcatggggcgacaccgctacccaacgcgcatcctcgtcgattccttcgggcataagtgcagtgcctctgacaagggtgtgtggacctcctgcagcattcgcgcacccttgcaaggacgcggctccttccgacgtggcgcgaatattcgctttgggagcttgccgagcagcgcggcggtggcgacgtcggggggagggcgtggcggcggcggggtggtggtgggaggaggaggaggggacccgtggcggaggctggatgggtccacggcgtcgacggagttgtcgctgtcgccgccgccggcgcaggcggcgggtgggggaggtggtggtggtggagcggacgcgctgccgtggcggcaccgaccttcgccgccgtcgtcggcggtggccaccacgtctgccgccgccgcggcggcgctgatggcgccgatgatgctgcagccgctcgacgccggcggcggcgcgtcggcgccgccgccgccgatccgcgggatacctatctacaacggccccggcgggttcccgttcctgcagccgtcgcccaccgccggcgacgtcggccaccaccaccaccaccaccccaagatgggattctacagctcgtaccaccacccatccacgtggccctccacgtcgccgtccccgctcgcggcgccgccgggcgccgcgtcgtcgccgctcgaccccacggcggcgttcctctcctccccccaccaccggatgctgtccgccgcctcggggaggctcaacggcatgctctccgtctccgacaccctccgcagctacggcgtccccggcgccgccgcccccggcgtcatcggcggcgcgcaccaccaccaccaccacctccacggcggccagccgttcgtcggcgccctcgcgtcccgcttcatgcccaagctccccgccaagcgcagcatgcgcgcgccgcgcatgcgctggacgagcaccctccacgcccgcttcgtccacgccgtcgagctcctcggcggccacgagagggcgacgcccaagtcggtgctggagctcatggacgtcaaggatctgacgctagcgcatgtcaagagccacctccagatgtatcgcaccgtgaagagcactgacaagcctgcagcctcttcagggccggcggacggcggctccggcgacgaggagttcgccggcggcgggcaggcggcgtcgggcggcggcgacagcatgtgcctgaggggtggcggcggcggcggggtggccgcggcggcgttcgcggagcacggccggtcggcgtcggagggcgccgccagctcggtcggcggcggcggcggcggcgacatggaccagtcgtcggccggcaacaccagcaccaccaggtggagcaactcctcaagggacccatggctgtcgtccaattcttgcaacatggacgcccatcgctccgtaggattgtcttctcctattgaggttcttgcacttcctttagcctcattgatcatgtcagatactgcctacctgttcttttccagcaaccatggccggtgtgaaccggcctctcttgaccagaaactagcagatatctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MAMVRELELMTSWSNSMGRHRYPTRILVDSFGHKCSASDKGVWT                     SCSIRAPLQGRGSFRRGANIRFGSLPSSAAVATSGGGRGGGGVVVGGGGGDPWRRLDG                     STASTELSLSPPPAQAAGGGGGGGGADALPWRHRPSPPSSAVATTSAAAAAALMAPMM                     LQPLDAGGGASAPPPPIRGIPIYNGPGGFPFLQPSPTAGDVGHHHHHHPKMGFYSSYH                     HPSTWPSTSPSPLAAPPGAASSPLDPTAAFLSSPHHRMLSAASGRLNGMLSVSDTLRS                     YGVPGAAAPGVIGGAHHHHHHLHGGQPFVGALASRFMPKLPAKRSMRAPRMRWTSTLH                     ARFVHAVELLGGHERATPKSVLELMDVKDLTLAHVKSHLQMYRTVKSTDKPAASSGPA                     DGGSGDEEFAGGGQAASGGGDSMCLRGGGGGGVAAAAFAEHGRSASEGAASSVGGGGG                     GDMDQSSAGNTSTTRWSNSSRDPWLSSNSCNMDAHRSVGLSSPIEVLALPLASLIMSD                     TAYLFFSSNHGRCEPASLDQKLADI&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;1..203#1122..1963#2065..2141#2731..2776#2916..3159#6515..6587#7556..7672#atggcaatggtgcgggagctcgagttgatgacgagctggagcaacagcatggggcgacaccgctacccaacgcgcatcctcgtcgattccttcgggcataagtgcagtgcctctgacaagggtgtgtggacctcctgcagcattcgcgcacccttgcaaggacgcggctccttccgacgtggcgcgaatattcgctttgggaggtatgagactacgctccatggtggagcgttgggcgtgaccttagtgtgcgcatatgtaagctgtatgcgtacgtataaatgttgagcttgcagtacatgtatacttgtttttttcttcttttttatgaggtcctttaattccattgtctgtattatttatgctagtatggaggatgatggtggcagtgacataaagtatacaaaaagcatagtatagtatacgtatggaaacaaaagcatgctacctttgactccacttgcattgcctgctaactgccattatttaaggaatacatggttgaatgcctgcctaaacatcaagataacctcacattctcctctctctctctcctaccttgcaattaagggtagcagcagtactctcctcactgctggctgactgctcccattttctctctctactctctctctctctctctcctctattccttttatacttgttgttggtagctaggagtatagcaggacagcacaaggaaccaattcatgcatatatccctggtgtctctcatgcatgttagtgtgaagaaagaagaagcttgagagagaagagagagttagagagagaaagtagagtgtttgtagagagagaaagtggtgtgtgtactagtagtaactccaagccagtgctagagacagagatacaaaaaggagacatcatccttctcttggccaaagcaagcaaccaagcaaagcttcctcttcttctccaagaactccaagaaccttctccttcatcttctccaccatgattccttccatcgcatgagctccatctccggcgtgtcgatcgagatcaccgttgctgctgccgaggtggagaaggaggtgtttgatcgatcggtcgatggaggcgagctcggcggcgacgccaccggacctgtcgctgcacatcagcttgccgagcagcgcggcggtggcgacgtcggggggagggcgtggcggcggcggggtggtggtgggaggaggaggaggggacccgtggcggaggctggatgggtccacggcgtcgacggagttgtcgctgtcgccgccgccggcgcaggcggcgggtgggggaggtggtggtggtggagcggacgcgctgccgtggcggcaccgaccttcgccgccgtcgtcggcggtggccaccacgtctgccgccgccgcggcggcgctgatggcgccgatgatgctgcagccgctcgacgccggcggcggcgcgtcggcgccgccgccgccgatccgcgggatacctatctacaacggccccggcgggttcccgttcctgcagccgtcgcccaccgccggcgacgtcggccaccaccaccaccaccaccccaagatgggattctacagctcgtaccaccacccatccacgtggccctccacgtcgccgtccccgctcgcggcgccgccgggcgccgcgtcgtcgccgctcgaccccacggcggcgttcctctcctccccccaccaccggatgctgtccgccgcctcggggaggctcaacggcatgctctccgtctccgacaccctccgcagctacggcgtccccggcgccgccgcccccggcgtcatcggcggcgcgcaccaccaccaccaccacctccacggcggccagccgttcgtcggcgccctcgcgtcccgcttcatgcccaagctccccgccaagcgcagcatgcgcgcgccgcgcatgcgctggacgagcaccctccacgcccgcttcgtccacgccgtcgagctcctcggcggccacgagagtacgcccccgccatcatcgtcgtcgtcctcctcctccttctcaccaccatcatcaacgagctcgatcaatctgatgagaatccaatcttgttcttggcaggggcgacgcccaagtcggtgctggagctcatggacgtcaaggatctgacgctagcgcatgtcaagagccacctccaggtatcccgccattgccgaccaattctcacagctcgatcgatcgatcaaacaccactcaccactgcaccatctctctctttctctctctcgatttcgattccattcagcttctgttcttgatcatcttgtttgggtgagacaaagatgccaatgcagtaactcctgagttagtgaagaaactgccattcttgggagcagagagagagagtgtgtgtgtgacatgtttggggatgtgtgtgcaagagagaagagagagagagaggggaaaaaagttgccatcattacacaataatgcattgcatctgcatctgtgctactagctccttccttagctctagtcatactagcgtatatgtgcacggcccaaagcactctcacacacaaacacaagagagagagagagagagagaagaagaagatgagagatgagagagagtaggacatattttgtgtgtgtttctttgctgcttgtcttttgcaatggcttcaacctcctggtttcattttgatctcacaaaaaatgtgtgtgtgtgtgtaaatatatatattgatcttctttttgttggacttttgtgttttattactgcagatgtatcgcaccgtgaagagcactgacaagcctgcagcctcttcaggtgattttttttaccatggcagctactagtagtagtagtagtagctaatttagctaagctccattttgcttttctttttttttggcgttgtgcattgcgttttacattacattgttgctatggtttttttgacgtgtagggccggcggacggcggctccggcgacgaggagttcgccggcggcgggcaggcggcgtcgggcggcggcgacagcatgtgcctgaggggtggcggcggcggcggggtggccgcggcggcgttcgcggagcacggccggtcggcgtcggagggcgccgccagctcggtcggcggcggcggcggcggcgacatggaccagtcgtcggccggcaacaccagcaccaccaggtggagcaactcctcaaggtacacacatggcagagttgcatttcaagtctttcagattaattatatatctacattgttatgccatctttaattaattaaaaatgaaattaatcaatcagaatgtcatgagatgatgatgatgatgataataatactaggataggaagaggatgatatgatggatgggtgtgctatgtgtgtttttaagtgtgttttagcttagaaccaaaggcaacaccaacaaactttggcatgcattgatgatgtatctaaatatgagttagtgacatgcaaaattaacctgccaagtacaacctctatttattaattcccaaaaaaatctcatggaggagaagggagagagagagatagtagtaatgtgtggtgatgcatggctaaaaaagcttagcaaaagaatgttttgggggcacacacacacacacctggagagggagttgcctatgtttaggtggccaatgttgttatgtcacacaaaagaccaaaaagtcacacaccccatggcttggcctcctcctccccccttgacctgtgcagttagctaggcttcttctcttctctccctctgtgtttggtttttgtggagctaaaaacattttaaaaatcttgcaaacattgtgtgtaaaaataggttcttgggctctgcccattgtcctctagcttctctcaaatctctctctctctctctctctctctctctctctttctcaaacctagggaggggagggttactcaggcagggctccattatcatttcttatcaatgcatggctctgattccagggggatggggctttgacctgacatgccctattgcctaggaatatgtaaccaaggacttgctgcattcttggttctttctccctctctcaccagtctcttcaatgcccttttcttccacctcttgggcaattattagcatggatggagctcaccttttcactctaccctctagctgtgattaaatcattgactaatcctaattcataaatataagggattcaactatgtaactagatgtactagatcctagtattactagtgtgttttgattctgttaggaggagtgattagcgtttgtcgtaagtactagtattaaactataggggattagtgtagatcatttttttaaaaattagtgagtgtgcttgggcagattttactccagccattggcgtgaaaactttgatctttgggcagcttggaagcaagtacagttcaacctgtccttggctgcattcgctgctttttctttctcaggactcactgcaactttcttgccatccccaacacctccctttcggtcgtgtttgatcagttgcattgctggtttcttcgccgctttaatttctccatctttcttctgttccttattggctaagtaaaaaatcattctcagcaatcaagttttgaaattcaaattagcttcaggttttatctatctaataattctctgactagttctctttctttcaagacctgttcttgttcagaactcttatgcagttgagagttcagttgttcatggaagtaatggcaatgcctggtctagtctttgagcagtatcctccttatgctcttgattttccttcactttagccgtttcagtcaaactttggggacaaattaaagtcagctggtcaagtgcatacataccacgtcatattttttagatgaatccattgtagtattaaatactagtgacaaaaaaatataactaaatggcattaaattgcaaccttcttccccaaaataattgggcacaactaccttgcttgcatatgctttatagtactcctacttattacttccttgaatccatgaggattccaggaatttggtcaggtcaaatgtccaggaggaattaggctatctttttttatcttcttctttttcttctaggtagtaggatcgttgtgcacatataaacaaaacaaaatagaaatttaagaggaaaccctcccaaaaaaaatacgactatcaattatgagtgattttacagttcttgaggaggtacaatgatacattttctattttaaaattcagtaactttgatactatgaggtacagaaatttgcacaaaaaaaatttggtacctctcaagtacttaaaatatcttatcaattatatttcagcaatgttgtcgttgctcgagttgtgcaaaaacatttctgatgaacaagtggagatgtatgcatatttagagagggaaacacatgcattttttaatatacattctcatgacaaattttggtgttctcgtctcattttagtctagcttagattaatggcatccatatattggtgaactgaaacagattgtatatgtccagtcttgaacaaacttcattatacaatgcataatcagaaaagatacagacatatattggcagatcacataaagtggtgtatctatgattgggtggtattttggacatacaaagtctactggtccctcatttgttaacagcatacatttgttcctatcaagacaaaagcactttacaacagtttggtagtaagttggtgttatgtgcgtgtctatttagatagagtggtagtaaaggaaggacactttttcttgatataccaaaatcacacataaaaaagaagtgtcattttcatgatcaacatgtggggtatgaacaaaaatgttctcccccctccaaccaacattgaagtcatcacacataaaaagcaaaaacatttaacaataatacatgcagacacatgtgcatgcatgtgtggatcacgcaaggacatactaattcaattaggtattcacaattaattagtgcaggaaatgacatgtaattacaattatatatgcacaacgatccttgtgtatttgtgtgacccattgtagtagcatttgattcctttcttgtgcctttctctacattgaattcgatctttgccaacagcggcttgctgatgagctcctgtgccattgcactgctgagctgcaccaaacagggacatcttttaagagcttgttgcctggaaatgatccatgtaaccaactgttcaggaagagcacactgtttgctgctcactttagctaaagcaaaactgtgtgcattatgcaatgcatatgcatccttccatctacccctgtgtcctttgccccccaaactgtgtaactacagtttaccatgcacatacatacaatgcacatctacccaattgtagcattgttgcaaggcctacttcagaattcagttagtccccaattgatccaactgcacacatatacatttacatatacatatacacaaacataccagcttggagaaaaggttgtaacaactttgctaaatgtgagatgtgtaatgtgtgttcttcctcttttcagggacccatggctgtcgtccaattcttgcaacatggacgcccatcgctccgtaggattgtcttctcctattgaggtatatatccttacattgttcaaagcttctttcgattcctagctaactgcatatccatgcagaaattcattagctcgcattcattctgaacatgatgtctgaaactctgaattttttttcgtttgtgcgtgtttcagaacttggaaccgtgcagatcgagcagctcgcaggtgtccaaccatgagctgagtagccctagtctcgagttcactctagggaggcctgactggcacggtgcagatcatgattagatggcaatcacagaggctaatgatcaaaaaaaaatttctcctgagatgtgaaatatatatgtgatatacaccaacctggtgctgatcatctttcgccaaccccagcttagccagagccagttcgtctgaagcttgtcatggcgaagaatgatcagcagcaatggcttgaaacgcacatcatatccactgcgtcgtcgtcatcgtcgtcgcaatcgatcggagaagagatatatatttcgcgtctcgatctcatcatcacaatttgggttttcttgattccttcttcttcttctttttgcaattaatatcatggatgcagctagagtttccttgtctgatctccatatttatttagttttgttcgccgtgccgggatcgatttacagtgtagttcagtggtgagctagctagctagagagtgagtgagtgagtgtcagctaggcagctggagatcgagagtgtgagtttggtgatgagttggttgtgtgtttgtcagtgtgtgtgaaagtgtgtgtgccattagcacatggaaagttggaaaggagagaaaggaagaaagaaaagggaattgagttcaggtgaagcaatctgccaatctatctagctacctatctatccatctacttagctcagttgctcagatgatgatctcagatttccatggcccttttttgtgtgcatgcatgccgcatatgcttctttctttaatccctgcaggttcttgcacttcctttagcctcattgatcatgtcagatactgcctacctgttcttttccagcaaccatggccggtgtgaaccggcctctcttgaccagaaactagcagatatctga&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001069632.1 RefSeq:Os09g0395300]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 9]]&lt;br /&gt;
[[Category:Chromosome 9]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:ZhangF5.jpg&amp;diff=174582</id>
		<title>File:ZhangF5.jpg</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:ZhangF5.jpg&amp;diff=174582"/>
				<updated>2014-05-30T10:17:59Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os09g0395300&amp;diff=174581</id>
		<title>Os09g0395300</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os09g0395300&amp;diff=174581"/>
				<updated>2014-05-30T10:17:44Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;The rice ''SHALLOT-LIKE1'' ('' SLL1'') gene, a member of KANADI family, is a key gene controlling rice leaf rolling.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:ZhangF1.jpg|right|thumb|200px|Fig 1.''sll1'' has extremely incurved leaves, with deficiency of sclerenchymatous cells at the abaxial side &amp;lt;ref name=''ref1'' /&amp;gt;.]]  [[File:ZhangF2.jpg|right|thumb|200px|Fig 2. ''SLL1'' deficiency results in increased chlorophyll content &amp;lt;ref name=''ref1'' /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
''sll1'', a rice mutant with shallot-like Leaves, displays abnormal sclerenchymatous cell development in the abaxial cell layers, altered mesophyll cell distribution, increased amounts of chlorophyll, and enhanced photosynthesis (Fig. 1&amp;amp;2).&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
Quantitative real-time RT-PCR (qRT-PCR) analysis revealed the expression of SLL1 in various tissues, including roots, stems, leaves, flowers, and seedlings, with relatively high expression in leaf and seedlings (Figure 5A , top panel). With an emphasis on the leaf, analysis by qRT-PCR showed that SLL1 is ubiquitously expressed in shoot apical meristem (SAM), leaf blade, or leaf sheath at different developmental stages (Figure 5A, bottom panel).&lt;br /&gt;
&lt;br /&gt;
To assess the expression pattern comprehensively, β-glucuronidase (GUS) activity was examined histochemically in transgenic plants carrying an SLL1 promoter-GUS reporter gene. Results showed that SLL1 was transcribed in stem (Figure 5B, panels 1 and 2), anthers of young or mature flowers (Figure 5B, panels 3 to 5), pistil tip (Figure 5B, panel 6), glume (Figure 5B, panel 7), vascular tissues of mature seeds (Figure 5B, panels 8 and 9), coleoptile and embryonic root of germinating seedlings (Figure 5B, panel 10), and root vascular tissues (Figure 5B, panel 11). In addition, SLL1 is highly transcribed in leaf veins and leaf sheath (Figure 5C, panels 1 to 3), guard cells, and tracheal elements (Figure 5C, panels 4 and 5).&lt;br /&gt;
&lt;br /&gt;
The spatial and temporal localization of SLL1 during leaf development was further examined by in situ hybridization analysis. The mRNA expression of SLL1 was detected throughout the young leaf primordium (plastochrons 1 to 3) and was more intense in abaxial cell layer through leaf development (plastochrons 4 and 5) (Figure 5D, panel 2). However, the SLL1 transcript did not demonstrate apical/basal polarity and did not accumulate at the apex of the meristem (Figure 5D, panel 3). Cross-section analysis of the shoot apex showed that SLL1 was more highly expressed in the abaxial cell layer, including the epidermis and vasculature of the early leaf blade (Figure 5D, panels 5 and 6). In the mature leaf, SLL1 mainly accumulated at the abaxial epidermis, abaxial mesophyll cells, and vasculature (Figure 5D, panels 8 and 9). In contrast with the sense probe (Figure 5D, panels 4 and 7), SLL1 was transcribed at a relatively low level throughout other leaf positions including the adaxial epidermis (Figure 5D, panels 5 and 6).&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
Please input evolution information here.&lt;br /&gt;
&lt;br /&gt;
You can also add sub-section(s) at will.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou 310006, Zhejiang, China&lt;br /&gt;
*National Key Laboratory of Plant Molecular Genetics, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Zhang GH, et al. (2009) ''SHALLOT-LIKE1''is a KANADI transcription factor that modulates rice leaf rolling by regulating leaf abaxial cell development. The Plant Cell Online 21: 719-735.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os09g0395300|&lt;br /&gt;
Description = Similar to CDPK substrate protein 1|&lt;br /&gt;
Version = NM_001069632.1 GI:115479006 GeneID:4346973|&lt;br /&gt;
Length = 7672 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os09g0395300, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 9|Chromosome 9]]|&lt;br /&gt;
AP = Chromosome 9:14411926..14419597|&lt;br /&gt;
CDS = 14411926..14412128,14413047..14413888,14413990..14414066,14414656..14414701,14414841..14415084&amp;lt;br&amp;gt;,14418440..14418512,14419481..14419597|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008402:14411926..14419597&lt;br /&gt;
source=RiceChromosome09&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008402:14411926..14419597&lt;br /&gt;
source=RiceChromosome09&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggcaatggtgcgggagctcgagttgatgacgagctggagcaacagcatggggcgacaccgctacccaacgcgcatcctcgtcgattccttcgggcataagtgcagtgcctctgacaagggtgtgtggacctcctgcagcattcgcgcacccttgcaaggacgcggctccttccgacgtggcgcgaatattcgctttgggagcttgccgagcagcgcggcggtggcgacgtcggggggagggcgtggcggcggcggggtggtggtgggaggaggaggaggggacccgtggcggaggctggatgggtccacggcgtcgacggagttgtcgctgtcgccgccgccggcgcaggcggcgggtgggggaggtggtggtggtggagcggacgcgctgccgtggcggcaccgaccttcgccgccgtcgtcggcggtggccaccacgtctgccgccgccgcggcggcgctgatggcgccgatgatgctgcagccgctcgacgccggcggcggcgcgtcggcgccgccgccgccgatccgcgggatacctatctacaacggccccggcgggttcccgttcctgcagccgtcgcccaccgccggcgacgtcggccaccaccaccaccaccaccccaagatgggattctacagctcgtaccaccacccatccacgtggccctccacgtcgccgtccccgctcgcggcgccgccgggcgccgcgtcgtcgccgctcgaccccacggcggcgttcctctcctccccccaccaccggatgctgtccgccgcctcggggaggctcaacggcatgctctccgtctccgacaccctccgcagctacggcgtccccggcgccgccgcccccggcgtcatcggcggcgcgcaccaccaccaccaccacctccacggcggccagccgttcgtcggcgccctcgcgtcccgcttcatgcccaagctccccgccaagcgcagcatgcgcgcgccgcgcatgcgctggacgagcaccctccacgcccgcttcgtccacgccgtcgagctcctcggcggccacgagagggcgacgcccaagtcggtgctggagctcatggacgtcaaggatctgacgctagcgcatgtcaagagccacctccagatgtatcgcaccgtgaagagcactgacaagcctgcagcctcttcagggccggcggacggcggctccggcgacgaggagttcgccggcggcgggcaggcggcgtcgggcggcggcgacagcatgtgcctgaggggtggcggcggcggcggggtggccgcggcggcgttcgcggagcacggccggtcggcgtcggagggcgccgccagctcggtcggcggcggcggcggcggcgacatggaccagtcgtcggccggcaacaccagcaccaccaggtggagcaactcctcaagggacccatggctgtcgtccaattcttgcaacatggacgcccatcgctccgtaggattgtcttctcctattgaggttcttgcacttcctttagcctcattgatcatgtcagatactgcctacctgttcttttccagcaaccatggccggtgtgaaccggcctctcttgaccagaaactagcagatatctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MAMVRELELMTSWSNSMGRHRYPTRILVDSFGHKCSASDKGVWT                     SCSIRAPLQGRGSFRRGANIRFGSLPSSAAVATSGGGRGGGGVVVGGGGGDPWRRLDG                     STASTELSLSPPPAQAAGGGGGGGGADALPWRHRPSPPSSAVATTSAAAAAALMAPMM                     LQPLDAGGGASAPPPPIRGIPIYNGPGGFPFLQPSPTAGDVGHHHHHHPKMGFYSSYH                     HPSTWPSTSPSPLAAPPGAASSPLDPTAAFLSSPHHRMLSAASGRLNGMLSVSDTLRS                     YGVPGAAAPGVIGGAHHHHHHLHGGQPFVGALASRFMPKLPAKRSMRAPRMRWTSTLH                     ARFVHAVELLGGHERATPKSVLELMDVKDLTLAHVKSHLQMYRTVKSTDKPAASSGPA                     DGGSGDEEFAGGGQAASGGGDSMCLRGGGGGGVAAAAFAEHGRSASEGAASSVGGGGG                     GDMDQSSAGNTSTTRWSNSSRDPWLSSNSCNMDAHRSVGLSSPIEVLALPLASLIMSD                     TAYLFFSSNHGRCEPASLDQKLADI&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;1..203#1122..1963#2065..2141#2731..2776#2916..3159#6515..6587#7556..7672#atggcaatggtgcgggagctcgagttgatgacgagctggagcaacagcatggggcgacaccgctacccaacgcgcatcctcgtcgattccttcgggcataagtgcagtgcctctgacaagggtgtgtggacctcctgcagcattcgcgcacccttgcaaggacgcggctccttccgacgtggcgcgaatattcgctttgggaggtatgagactacgctccatggtggagcgttgggcgtgaccttagtgtgcgcatatgtaagctgtatgcgtacgtataaatgttgagcttgcagtacatgtatacttgtttttttcttcttttttatgaggtcctttaattccattgtctgtattatttatgctagtatggaggatgatggtggcagtgacataaagtatacaaaaagcatagtatagtatacgtatggaaacaaaagcatgctacctttgactccacttgcattgcctgctaactgccattatttaaggaatacatggttgaatgcctgcctaaacatcaagataacctcacattctcctctctctctctcctaccttgcaattaagggtagcagcagtactctcctcactgctggctgactgctcccattttctctctctactctctctctctctctctcctctattccttttatacttgttgttggtagctaggagtatagcaggacagcacaaggaaccaattcatgcatatatccctggtgtctctcatgcatgttagtgtgaagaaagaagaagcttgagagagaagagagagttagagagagaaagtagagtgtttgtagagagagaaagtggtgtgtgtactagtagtaactccaagccagtgctagagacagagatacaaaaaggagacatcatccttctcttggccaaagcaagcaaccaagcaaagcttcctcttcttctccaagaactccaagaaccttctccttcatcttctccaccatgattccttccatcgcatgagctccatctccggcgtgtcgatcgagatcaccgttgctgctgccgaggtggagaaggaggtgtttgatcgatcggtcgatggaggcgagctcggcggcgacgccaccggacctgtcgctgcacatcagcttgccgagcagcgcggcggtggcgacgtcggggggagggcgtggcggcggcggggtggtggtgggaggaggaggaggggacccgtggcggaggctggatgggtccacggcgtcgacggagttgtcgctgtcgccgccgccggcgcaggcggcgggtgggggaggtggtggtggtggagcggacgcgctgccgtggcggcaccgaccttcgccgccgtcgtcggcggtggccaccacgtctgccgccgccgcggcggcgctgatggcgccgatgatgctgcagccgctcgacgccggcggcggcgcgtcggcgccgccgccgccgatccgcgggatacctatctacaacggccccggcgggttcccgttcctgcagccgtcgcccaccgccggcgacgtcggccaccaccaccaccaccaccccaagatgggattctacagctcgtaccaccacccatccacgtggccctccacgtcgccgtccccgctcgcggcgccgccgggcgccgcgtcgtcgccgctcgaccccacggcggcgttcctctcctccccccaccaccggatgctgtccgccgcctcggggaggctcaacggcatgctctccgtctccgacaccctccgcagctacggcgtccccggcgccgccgcccccggcgtcatcggcggcgcgcaccaccaccaccaccacctccacggcggccagccgttcgtcggcgccctcgcgtcccgcttcatgcccaagctccccgccaagcgcagcatgcgcgcgccgcgcatgcgctggacgagcaccctccacgcccgcttcgtccacgccgtcgagctcctcggcggccacgagagtacgcccccgccatcatcgtcgtcgtcctcctcctccttctcaccaccatcatcaacgagctcgatcaatctgatgagaatccaatcttgttcttggcaggggcgacgcccaagtcggtgctggagctcatggacgtcaaggatctgacgctagcgcatgtcaagagccacctccaggtatcccgccattgccgaccaattctcacagctcgatcgatcgatcaaacaccactcaccactgcaccatctctctctttctctctctcgatttcgattccattcagcttctgttcttgatcatcttgtttgggtgagacaaagatgccaatgcagtaactcctgagttagtgaagaaactgccattcttgggagcagagagagagagtgtgtgtgtgacatgtttggggatgtgtgtgcaagagagaagagagagagagaggggaaaaaagttgccatcattacacaataatgcattgcatctgcatctgtgctactagctccttccttagctctagtcatactagcgtatatgtgcacggcccaaagcactctcacacacaaacacaagagagagagagagagagagaagaagaagatgagagatgagagagagtaggacatattttgtgtgtgtttctttgctgcttgtcttttgcaatggcttcaacctcctggtttcattttgatctcacaaaaaatgtgtgtgtgtgtgtaaatatatatattgatcttctttttgttggacttttgtgttttattactgcagatgtatcgcaccgtgaagagcactgacaagcctgcagcctcttcaggtgattttttttaccatggcagctactagtagtagtagtagtagctaatttagctaagctccattttgcttttctttttttttggcgttgtgcattgcgttttacattacattgttgctatggtttttttgacgtgtagggccggcggacggcggctccggcgacgaggagttcgccggcggcgggcaggcggcgtcgggcggcggcgacagcatgtgcctgaggggtggcggcggcggcggggtggccgcggcggcgttcgcggagcacggccggtcggcgtcggagggcgccgccagctcggtcggcggcggcggcggcggcgacatggaccagtcgtcggccggcaacaccagcaccaccaggtggagcaactcctcaaggtacacacatggcagagttgcatttcaagtctttcagattaattatatatctacattgttatgccatctttaattaattaaaaatgaaattaatcaatcagaatgtcatgagatgatgatgatgatgataataatactaggataggaagaggatgatatgatggatgggtgtgctatgtgtgtttttaagtgtgttttagcttagaaccaaaggcaacaccaacaaactttggcatgcattgatgatgtatctaaatatgagttagtgacatgcaaaattaacctgccaagtacaacctctatttattaattcccaaaaaaatctcatggaggagaagggagagagagagatagtagtaatgtgtggtgatgcatggctaaaaaagcttagcaaaagaatgttttgggggcacacacacacacacctggagagggagttgcctatgtttaggtggccaatgttgttatgtcacacaaaagaccaaaaagtcacacaccccatggcttggcctcctcctccccccttgacctgtgcagttagctaggcttcttctcttctctccctctgtgtttggtttttgtggagctaaaaacattttaaaaatcttgcaaacattgtgtgtaaaaataggttcttgggctctgcccattgtcctctagcttctctcaaatctctctctctctctctctctctctctctctctttctcaaacctagggaggggagggttactcaggcagggctccattatcatttcttatcaatgcatggctctgattccagggggatggggctttgacctgacatgccctattgcctaggaatatgtaaccaaggacttgctgcattcttggttctttctccctctctcaccagtctcttcaatgcccttttcttccacctcttgggcaattattagcatggatggagctcaccttttcactctaccctctagctgtgattaaatcattgactaatcctaattcataaatataagggattcaactatgtaactagatgtactagatcctagtattactagtgtgttttgattctgttaggaggagtgattagcgtttgtcgtaagtactagtattaaactataggggattagtgtagatcatttttttaaaaattagtgagtgtgcttgggcagattttactccagccattggcgtgaaaactttgatctttgggcagcttggaagcaagtacagttcaacctgtccttggctgcattcgctgctttttctttctcaggactcactgcaactttcttgccatccccaacacctccctttcggtcgtgtttgatcagttgcattgctggtttcttcgccgctttaatttctccatctttcttctgttccttattggctaagtaaaaaatcattctcagcaatcaagttttgaaattcaaattagcttcaggttttatctatctaataattctctgactagttctctttctttcaagacctgttcttgttcagaactcttatgcagttgagagttcagttgttcatggaagtaatggcaatgcctggtctagtctttgagcagtatcctccttatgctcttgattttccttcactttagccgtttcagtcaaactttggggacaaattaaagtcagctggtcaagtgcatacataccacgtcatattttttagatgaatccattgtagtattaaatactagtgacaaaaaaatataactaaatggcattaaattgcaaccttcttccccaaaataattgggcacaactaccttgcttgcatatgctttatagtactcctacttattacttccttgaatccatgaggattccaggaatttggtcaggtcaaatgtccaggaggaattaggctatctttttttatcttcttctttttcttctaggtagtaggatcgttgtgcacatataaacaaaacaaaatagaaatttaagaggaaaccctcccaaaaaaaatacgactatcaattatgagtgattttacagttcttgaggaggtacaatgatacattttctattttaaaattcagtaactttgatactatgaggtacagaaatttgcacaaaaaaaatttggtacctctcaagtacttaaaatatcttatcaattatatttcagcaatgttgtcgttgctcgagttgtgcaaaaacatttctgatgaacaagtggagatgtatgcatatttagagagggaaacacatgcattttttaatatacattctcatgacaaattttggtgttctcgtctcattttagtctagcttagattaatggcatccatatattggtgaactgaaacagattgtatatgtccagtcttgaacaaacttcattatacaatgcataatcagaaaagatacagacatatattggcagatcacataaagtggtgtatctatgattgggtggtattttggacatacaaagtctactggtccctcatttgttaacagcatacatttgttcctatcaagacaaaagcactttacaacagtttggtagtaagttggtgttatgtgcgtgtctatttagatagagtggtagtaaaggaaggacactttttcttgatataccaaaatcacacataaaaaagaagtgtcattttcatgatcaacatgtggggtatgaacaaaaatgttctcccccctccaaccaacattgaagtcatcacacataaaaagcaaaaacatttaacaataatacatgcagacacatgtgcatgcatgtgtggatcacgcaaggacatactaattcaattaggtattcacaattaattagtgcaggaaatgacatgtaattacaattatatatgcacaacgatccttgtgtatttgtgtgacccattgtagtagcatttgattcctttcttgtgcctttctctacattgaattcgatctttgccaacagcggcttgctgatgagctcctgtgccattgcactgctgagctgcaccaaacagggacatcttttaagagcttgttgcctggaaatgatccatgtaaccaactgttcaggaagagcacactgtttgctgctcactttagctaaagcaaaactgtgtgcattatgcaatgcatatgcatccttccatctacccctgtgtcctttgccccccaaactgtgtaactacagtttaccatgcacatacatacaatgcacatctacccaattgtagcattgttgcaaggcctacttcagaattcagttagtccccaattgatccaactgcacacatatacatttacatatacatatacacaaacataccagcttggagaaaaggttgtaacaactttgctaaatgtgagatgtgtaatgtgtgttcttcctcttttcagggacccatggctgtcgtccaattcttgcaacatggacgcccatcgctccgtaggattgtcttctcctattgaggtatatatccttacattgttcaaagcttctttcgattcctagctaactgcatatccatgcagaaattcattagctcgcattcattctgaacatgatgtctgaaactctgaattttttttcgtttgtgcgtgtttcagaacttggaaccgtgcagatcgagcagctcgcaggtgtccaaccatgagctgagtagccctagtctcgagttcactctagggaggcctgactggcacggtgcagatcatgattagatggcaatcacagaggctaatgatcaaaaaaaaatttctcctgagatgtgaaatatatatgtgatatacaccaacctggtgctgatcatctttcgccaaccccagcttagccagagccagttcgtctgaagcttgtcatggcgaagaatgatcagcagcaatggcttgaaacgcacatcatatccactgcgtcgtcgtcatcgtcgtcgcaatcgatcggagaagagatatatatttcgcgtctcgatctcatcatcacaatttgggttttcttgattccttcttcttcttctttttgcaattaatatcatggatgcagctagagtttccttgtctgatctccatatttatttagttttgttcgccgtgccgggatcgatttacagtgtagttcagtggtgagctagctagctagagagtgagtgagtgagtgtcagctaggcagctggagatcgagagtgtgagtttggtgatgagttggttgtgtgtttgtcagtgtgtgtgaaagtgtgtgtgccattagcacatggaaagttggaaaggagagaaaggaagaaagaaaagggaattgagttcaggtgaagcaatctgccaatctatctagctacctatctatccatctacttagctcagttgctcagatgatgatctcagatttccatggcccttttttgtgtgcatgcatgccgcatatgcttctttctttaatccctgcaggttcttgcacttcctttagcctcattgatcatgtcagatactgcctacctgttcttttccagcaaccatggccggtgtgaaccggcctctcttgaccagaaactagcagatatctga&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001069632.1 RefSeq:Os09g0395300]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 9]]&lt;br /&gt;
[[Category:Chromosome 9]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174444</id>
		<title>Os10g0478000</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174444"/>
				<updated>2014-05-30T04:59:59Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: /* Function */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; The rice ''TAWAWA1'' (''TAW1'') gene, a member of ALOG family, was identified as a  regulator of rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:YoshidaF1.jpg|right|thumb|200px|Fig 1. Characterization of ''taw1'' dominant mutants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF2.jpg|right|thumb|200px|Fig 2. Isolation of the ''TAW1'' gene &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF3.jpg|right|thumb|200px|Fig 3. Expression pattern of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF4.jpg|right|thumb|200px|Fig 4. ''SVP'' subfamily MADS-box genes work downstream of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF5.jpg|right|thumb|200px|Fig 5. Phenotype of ''taw1-D2''–introgressed Koshihikari BC5F2 plants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
In the dominant gain-of-function mutant ''tawawa1-D''(Fig. 1), the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in ''TAWAWA1'' (''TAW1'') activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. ''TAW1'' encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the branch meristem (BMs). ''TAW1'' expression disappears from incipient spikelet meristems (SMs). It is demonstrated that members of the ''SHORT VEGETATIVE PHASE'' subfamily of MADS-box genes function downstream of ''TAW1''. Thus, ''TAW1'' is proposed as a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
To understand the molecular links between the control of meristem phase transition and inflorescence structure, mutants were identified with altered inflorescence branching patterns &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;. Two lines with increased branching phenotypes were isolated from a screening population in which nDart1, an endogenous rice transposon, actively transposes (Fig. 1C). The mutation was inherited in a semidominant manner in both lines, and subsequent analyses revealed mutations in the same gene. The gene was named ''TAWAWA1'' (''TAW1''), from a traditional Japanese word meaning “very fruitful.” ''taw1-D1'' exhibits more severe defects than those of ''taw1-D2''. Both mutant lines show normal growth patterns during the vegetative phase, for example, meristem size, date of leaf initiation, and number of leaves produced. However, in ''taw1-D1'' homozygous plants, stem elongation is suppressed after the transition to reproductive growth, and the inflorescence does not emerge from the leaves. In both mutant lines, the number of lateral meristems produced on each primary branch is comparable to that of wild-type plants; however, a higher percentage of lateral meristems grows as secondary branches (Fig. 1D). Reiteration of this pattern results in the production of tertiary branches, which are not formed on wild-type plants (Fig. 1E).&lt;br /&gt;
&lt;br /&gt;
In homozygous ''taw1-D1'' mutants (carrying the more severe allele), the increase in inflorescence branching is so extreme that the inflorescence forms an agglomerate with a massive number of undifferentiated meristems (Fig. 1 F and G). Such aggregated meristems are also frequently observed in the inflorescences of ''taw1-D1'' heterozygous and ''taw1-D2'' homozygous plants (Fig. 1 H and I). Observations using a scanning electron microscope confirmed that these structures are formed from the repeated production of undifferentiated meristems (Fig. S2). The meristems in ''taw1-D1'' homozygous inflorescences were analyzed for expression of two SM marker genes, ''FRIZZY PANICLE'' (''FZP'') and ''LEAFY HULL STERILE1'' (''LHS1'')/''OsMADS1'', by in situ hybridization. The lack of expression of these genes indicated that the meristems in the homozygous mutants do not acquire SM identity (Fig. 1 J–M).&lt;br /&gt;
&lt;br /&gt;
Grain number per panicle is one of the four major determinants of rice yield. To test the usefulness of ''TAW1'' mutations for increasing grain yield, the moderate ''taw1-D2'' allele was introgressed into Koshihikari, which is a leading commercial rice cultivar in Japan (Fig. 5 A and B). Field-grown selfed progeny of fifth backcross (BC5F2)-generation plants showed ∼45% increases in grain weight per plant (Fig. 5C). These increases were mainly due to extensive increases in grain number per panicle (Fig. 5D), resulting from increases in the numbers of primary, secondary, and tertiary branches. Slight decreases in fertility and grain weight were also observed (Fig. 5E). Despite the increase in panicle size, the total plant height was slightly reduced in BC5F2 plants. Increases in grain number are often linked to decreases in the numbers of branch shoots, called “tillers,” in rice. However, this tradeoff effect was not observed in the ''taw1-D2'' introgression line.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
''TAW1'' contains a conserved domain and a nuclear localization signal. Indeed, ''TAW1'' localizes to the nucleus and shows slight but significant activity as a transcriptional activator (Fig. 3 A and B). The spatiotemporal pattern of ''TAW1'' mRNA accumulation was examined by in situ hybridization. During the vegetative phase of development, ''TAW1'' was predominantly expressed in meristems, including the SAM, axillary meristems, and young leaves (Fig. 3 A and C). After transition to the reproductive phase, ''TAW1'' mRNA continued to accumulate in the IM (Fig. 3D). The strongest signal was observed in BMs in the growing inflorescence (Fig. 3E). After initiation of the primary BMs, ''TAW1'' expression gradually disappeared from the IM as it degenerated (Fig. 3F). In wild-type inflorescences, the signal intensity in the meristem gradually decreased and became undetectable at SM initiation (Fig. 3G). On the other hand, in ''taw1-D'' inflorescences, stronger TAW1 signals were detected, even at the stage when the SMs were formed in the wild-type plants (Fig. 3 H and I). Quantitative PCR analysis indicated that the levels of ''TAW1'' expression in the mutant inflorescences roughly coincided with the severity of their phenotypes (Fig. 3J). These results imply that ''TAW1'' functions to suppress SM identity and that its activity must be below a certain threshold level to allow SM specification. Interestingly, ''TAW1'' expression is reduced in the vegetative shoot apices, leaves, and roots of ''taw1-D'' mutants compared with wild-type plants. These results suggest that the sequence surrounding the ''nDart1'' insertion sites is necessary for fine-tuning the spatial and quantitative expression pattern of ''TAW1''. It may be that positive regulators of SM identity interact with this sequence, which is located downstream of the transcribed region. It is also possible that ''nDart1'' carries a sequence that functions as a transcriptional enhancer; however, this is unlikely because not all ''nDart1'' insertions activate transcription. Unraveling the molecular mechanisms that regulate ''TAW1'' transcription will shed light on the regulatory networks controlling rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
The rice genes ''G1'' and ''TH1'' are ALOG family members that are expressed in the lemma, palea, and floral organs and control their identity and development. On the other hand, the ''Arabidopsis'' ALOG family genes ''LSH3/OBO1'' and ''LSH4'' are expressed in shoot organ boundary cells. The functions of ''LSH3/OBO1'' and ''LSH4'' are unknown; however, they induce the overproliferation of shoot meristems and the formation of extra organs when ectopically expressed. A plausible scenario is that at least some of the ALOG family proteins share conserved functions, but it may be that their distinctive expression patterns have led to divergent functions. The establishment of the machinery for meristem-specific expression may be a primary reason for the evolution of ''TAW1'' as a major regulator of meristem activity and phase transition &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
''TAW1'' function might have evolved to ensure the production of sufficient numbers of spikelets. Unraveling the molecular function of ''TAW1'' will provide an opportunity for a greater understanding of meristem activity and identity, which is a fundamental issue in plant biology. Furthermore, such knowledge could be exploited to further increase crop yields. In addition, ''TAW1'' is of great interest with respect to the evolution of inflorescence architecture. ''TAW1'' function may be essential for the development of compound inflorescences, in which the branching pattern is crucial &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan&lt;br /&gt;
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==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Yoshida A, Sasao M, Yasuno N, et al. (2013) ''TAWAWA1'', a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition. Proceedings of the National Academy of Sciences 110: 767-772.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os10g0478000|&lt;br /&gt;
Description = Protein of unknown function DUF640 domain containing protein|&lt;br /&gt;
Version = NM_001189280.1 GI:297727690 GeneID:9266624|&lt;br /&gt;
Length = 1426 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os10g0478000, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 10|Chromosome 10]]|&lt;br /&gt;
AP = Chromosome 10:18345508..18346933|&lt;br /&gt;
CDS = 18345710..18346324|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MEFVAHAAAPDSPHSDSGGGGGGMATGATSASAAGASPSRYESQ                     KRRDWNTFGQYLRNHRPPLSLARCSGAHVLEFLRYLDQFGKTKVHAPACPFFGHPAPP                     APCPCPLRQAWGSLDALVGRLRAAYEENGGRPENNPFGARAVRLYLREVREHQARARG                     VSYEKKKRKKPPHPSSAAAAHDDAANGALHHHHHMPPPPPGAAA&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;610..1224#tatcggctccttctcgcccagcttttgctcacgtcacatcaccttccacctccacccctccactcgctcgctcgcttgcttgctccaattaatacctcttctccttctcccccagcaactagcttccttctccgcttttgcagctcgccgccgccgccgccgccgccgccgcgacacggcgcgcatatggtcgtcgtcgtcgtcgtcgtcgtcgctggagaagacgaagaaagatagtagacctgagctgggggggcggtgaattcgccggagagctagctaaggtgagtttcgttttcggtttcggtttcgatcgatttgttggtgcagatgcatctgggagctagagaactatttatagtggctgcggtgcggtgcggcgtcgccacgccgcgcacgcgctcgcccacgtcgcgcgcgcgcgggcgcgcgtccactctctctctctcttggaccactgcgcgcgcgggcgcgcgtcggcgtcgccacggcttctcaagaacgcgcgcgcgcgcactgattcccagatagatagatctatatctgttcgtcttcctcagctatggtgtggtggtggtggtggtgtttgtggtgttgtgcagatcgacgatggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctgagccgagccgagcttgctccaagatcgccggaaaacgagctgctagcctcctacgcatgcactagttactccactccactccactccactatgatccctagctaggctgctcttgctactagcaaaactacggattaatctccatgcttgctactgctgctgctgctgctactgcatctaattaattaggttgattatttcct&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001189280.1 RefSeq:Os10g0478000]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 10]]&lt;br /&gt;
[[Category:Chromosome 10]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174441</id>
		<title>Os10g0478000</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174441"/>
				<updated>2014-05-30T04:55:04Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: /* Annotated Information */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; The rice ''TAWAWA1'' (''TAW1'') gene, a member of ALOG family, was identified as a  regulator of rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:YoshidaF1.jpg|right|thumb|200px|Fig 1. Characterization of ''taw1'' dominant mutants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF2.jpg|right|thumb|200px|Fig 2. Isolation of the ''TAW1'' gene &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF3.jpg|right|thumb|200px|Fig 3. Expression pattern of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF4.jpg|right|thumb|200px|Fig 4. ''SVP'' subfamily MADS-box genes work downstream of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF5.jpg|right|thumb|200px|Fig 5. Phenotype of ''taw1-D2''–introgressed Koshihikari BC5F2 plants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
In the dominant gain-of-function mutant ''tawawa1-D''(Fig. 1), the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in ''TAWAWA1'' (''TAW1'') activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. ''TAW1'' encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the branch meristem (BMs). ''TAW1'' expression disappears from incipient spikelet meristems (SMs). It is demonstrated that members of the ''SHORT VEGETATIVE PHASE'' subfamily of MADS-box genes function downstream of ''TAW1''. Thus, ''TAW1'' is proposed as a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
To understand the molecular links between the control of meristem phase transition and inflorescence structure, mutants were identified with altered inflorescence branching patterns &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;. Two lines with increased branching phenotypes were isolated from a screening population in which nDart1, an endogenous rice transposon, actively transposes (Fig. 1C). The mutation was inherited in a semidominant manner in both lines, and subsequent analyses revealed mutations in the same gene. The gene was named ''TAWAWA1'' (''TAW1''), from a traditional Japanese word meaning “very fruitful.” ''taw1-D1'' exhibits more severe defects than those of ''taw1-D2''. Both mutant lines show normal growth patterns during the vegetative phase, for example, meristem size, date of leaf initiation, and number of leaves produced. However, in ''taw1-D1'' homozygous plants, stem elongation is suppressed after the transition to reproductive growth, and the inflorescence does not emerge from the leaves. In both mutant lines, the number of lateral meristems produced on each primary branch is comparable to that of wild-type plants; however, a higher percentage of lateral meristems grows as secondary branches (Fig. 1D). Reiteration of this pattern results in the production of tertiary branches, which are not formed on wild-type plants (Fig. 1E).&lt;br /&gt;
&lt;br /&gt;
In homozygous ''taw1-D1'' mutants (carrying the more severe allele), the increase in inflorescence branching is so extreme that the inflorescence forms an agglomerate with a massive number of undifferentiated meristems (Fig. 1 F and G). Such aggregated meristems are also frequently observed in the inflorescences of ''taw1-D1'' heterozygous and ''taw1-D2'' homozygous plants (Fig. 1 H and I). Observations using a scanning electron microscope confirmed that these structures are formed from the repeated production of undifferentiated meristems (Fig. S2). The meristems in ''taw1-D1'' homozygous inflorescences were analyzed for expression of two SM marker genes, ''FRIZZY PANICLE'' (''FZP'') and ''LEAFY HULL STERILE1'' (''LHS1'')/''OsMADS1'', by in situ hybridization. The lack of expression of these genes indicated that the meristems in the homozygous mutants do not acquire SM identity (Fig. 1 J–M).&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
''TAW1'' contains a conserved domain and a nuclear localization signal. Indeed, ''TAW1'' localizes to the nucleus and shows slight but significant activity as a transcriptional activator (Fig. 3 A and B). The spatiotemporal pattern of ''TAW1'' mRNA accumulation was examined by in situ hybridization. During the vegetative phase of development, ''TAW1'' was predominantly expressed in meristems, including the SAM, axillary meristems, and young leaves (Fig. 3 A and C). After transition to the reproductive phase, ''TAW1'' mRNA continued to accumulate in the IM (Fig. 3D). The strongest signal was observed in BMs in the growing inflorescence (Fig. 3E). After initiation of the primary BMs, ''TAW1'' expression gradually disappeared from the IM as it degenerated (Fig. 3F). In wild-type inflorescences, the signal intensity in the meristem gradually decreased and became undetectable at SM initiation (Fig. 3G). On the other hand, in ''taw1-D'' inflorescences, stronger TAW1 signals were detected, even at the stage when the SMs were formed in the wild-type plants (Fig. 3 H and I). Quantitative PCR analysis indicated that the levels of ''TAW1'' expression in the mutant inflorescences roughly coincided with the severity of their phenotypes (Fig. 3J). These results imply that ''TAW1'' functions to suppress SM identity and that its activity must be below a certain threshold level to allow SM specification. Interestingly, ''TAW1'' expression is reduced in the vegetative shoot apices, leaves, and roots of ''taw1-D'' mutants compared with wild-type plants. These results suggest that the sequence surrounding the ''nDart1'' insertion sites is necessary for fine-tuning the spatial and quantitative expression pattern of ''TAW1''. It may be that positive regulators of SM identity interact with this sequence, which is located downstream of the transcribed region. It is also possible that ''nDart1'' carries a sequence that functions as a transcriptional enhancer; however, this is unlikely because not all ''nDart1'' insertions activate transcription. Unraveling the molecular mechanisms that regulate ''TAW1'' transcription will shed light on the regulatory networks controlling rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
The rice genes ''G1'' and ''TH1'' are ALOG family members that are expressed in the lemma, palea, and floral organs and control their identity and development. On the other hand, the ''Arabidopsis'' ALOG family genes ''LSH3/OBO1'' and ''LSH4'' are expressed in shoot organ boundary cells. The functions of ''LSH3/OBO1'' and ''LSH4'' are unknown; however, they induce the overproliferation of shoot meristems and the formation of extra organs when ectopically expressed. A plausible scenario is that at least some of the ALOG family proteins share conserved functions, but it may be that their distinctive expression patterns have led to divergent functions. The establishment of the machinery for meristem-specific expression may be a primary reason for the evolution of ''TAW1'' as a major regulator of meristem activity and phase transition &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
''TAW1'' function might have evolved to ensure the production of sufficient numbers of spikelets. Unraveling the molecular function of ''TAW1'' will provide an opportunity for a greater understanding of meristem activity and identity, which is a fundamental issue in plant biology. Furthermore, such knowledge could be exploited to further increase crop yields. In addition, ''TAW1'' is of great interest with respect to the evolution of inflorescence architecture. ''TAW1'' function may be essential for the development of compound inflorescences, in which the branching pattern is crucial &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Yoshida A, Sasao M, Yasuno N, et al. (2013) ''TAWAWA1'', a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition. Proceedings of the National Academy of Sciences 110: 767-772.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os10g0478000|&lt;br /&gt;
Description = Protein of unknown function DUF640 domain containing protein|&lt;br /&gt;
Version = NM_001189280.1 GI:297727690 GeneID:9266624|&lt;br /&gt;
Length = 1426 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os10g0478000, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 10|Chromosome 10]]|&lt;br /&gt;
AP = Chromosome 10:18345508..18346933|&lt;br /&gt;
CDS = 18345710..18346324|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MEFVAHAAAPDSPHSDSGGGGGGMATGATSASAAGASPSRYESQ                     KRRDWNTFGQYLRNHRPPLSLARCSGAHVLEFLRYLDQFGKTKVHAPACPFFGHPAPP                     APCPCPLRQAWGSLDALVGRLRAAYEENGGRPENNPFGARAVRLYLREVREHQARARG                     VSYEKKKRKKPPHPSSAAAAHDDAANGALHHHHHMPPPPPGAAA&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;610..1224#tatcggctccttctcgcccagcttttgctcacgtcacatcaccttccacctccacccctccactcgctcgctcgcttgcttgctccaattaatacctcttctccttctcccccagcaactagcttccttctccgcttttgcagctcgccgccgccgccgccgccgccgccgcgacacggcgcgcatatggtcgtcgtcgtcgtcgtcgtcgtcgctggagaagacgaagaaagatagtagacctgagctgggggggcggtgaattcgccggagagctagctaaggtgagtttcgttttcggtttcggtttcgatcgatttgttggtgcagatgcatctgggagctagagaactatttatagtggctgcggtgcggtgcggcgtcgccacgccgcgcacgcgctcgcccacgtcgcgcgcgcgcgggcgcgcgtccactctctctctctcttggaccactgcgcgcgcgggcgcgcgtcggcgtcgccacggcttctcaagaacgcgcgcgcgcgcactgattcccagatagatagatctatatctgttcgtcttcctcagctatggtgtggtggtggtggtggtgtttgtggtgttgtgcagatcgacgatggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctgagccgagccgagcttgctccaagatcgccggaaaacgagctgctagcctcctacgcatgcactagttactccactccactccactccactatgatccctagctaggctgctcttgctactagcaaaactacggattaatctccatgcttgctactgctgctgctgctgctactgcatctaattaattaggttgattatttcct&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001189280.1 RefSeq:Os10g0478000]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 10]]&lt;br /&gt;
[[Category:Chromosome 10]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174432</id>
		<title>Os10g0478000</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174432"/>
				<updated>2014-05-30T04:46:51Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; The rice ''TAWAWA1'' (''TAW1'') gene, a member of ALOG family, was identified as a  regulator of rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:YoshidaF1.jpg|right|thumb|200px|Fig 1. Characterization of ''taw1'' dominant mutants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF2.jpg|right|thumb|200px|Fig 2. Isolation of the ''TAW1'' gene &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF3.jpg|right|thumb|200px|Fig 3. Expression pattern of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF4.jpg|right|thumb|200px|Fig 4. ''SVP'' subfamily MADS-box genes work downstream of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF5.jpg|right|thumb|200px|Fig 5. Phenotype of ''taw1-D2''–introgressed Koshihikari BC5F2 plants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
In the dominant gain-of-function mutant ''tawawa1-D''(Fig. 1), the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in ''TAWAWA1'' (''TAW1'') activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. ''TAW1'' encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the branch meristem (BMs). ''TAW1'' expression disappears from incipient spikelet meristems (SMs). It is demonstrated that members of the ''SHORT VEGETATIVE PHASE'' subfamily of MADS-box genes function downstream of ''TAW1''. Thus, ''TAW1'' is proposed as a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
''TAW1'' contains a conserved domain and a nuclear localization signal. Indeed, ''TAW1'' localizes to the nucleus and shows slight but significant activity as a transcriptional activator (Fig. 3 A and B). The spatiotemporal pattern of ''TAW1'' mRNA accumulation was examined by in situ hybridization. During the vegetative phase of development, ''TAW1'' was predominantly expressed in meristems, including the SAM, axillary meristems, and young leaves (Fig. 3 A and C). After transition to the reproductive phase, ''TAW1'' mRNA continued to accumulate in the IM (Fig. 3D). The strongest signal was observed in BMs in the growing inflorescence (Fig. 3E). After initiation of the primary BMs, ''TAW1'' expression gradually disappeared from the IM as it degenerated (Fig. 3F). In wild-type inflorescences, the signal intensity in the meristem gradually decreased and became undetectable at SM initiation (Fig. 3G). On the other hand, in ''taw1-D'' inflorescences, stronger TAW1 signals were detected, even at the stage when the SMs were formed in the wild-type plants (Fig. 3 H and I). Quantitative PCR analysis indicated that the levels of ''TAW1'' expression in the mutant inflorescences roughly coincided with the severity of their phenotypes (Fig. 3J). These results imply that ''TAW1'' functions to suppress SM identity and that its activity must be below a certain threshold level to allow SM specification. Interestingly, ''TAW1'' expression is reduced in the vegetative shoot apices, leaves, and roots of ''taw1-D'' mutants compared with wild-type plants. These results suggest that the sequence surrounding the ''nDart1'' insertion sites is necessary for fine-tuning the spatial and quantitative expression pattern of ''TAW1''. It may be that positive regulators of SM identity interact with this sequence, which is located downstream of the transcribed region. It is also possible that ''nDart1'' carries a sequence that functions as a transcriptional enhancer; however, this is unlikely because not all ''nDart1'' insertions activate transcription. Unraveling the molecular mechanisms that regulate ''TAW1'' transcription will shed light on the regulatory networks controlling rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
The rice genes ''G1'' and ''TH1'' are ALOG family members that are expressed in the lemma, palea, and floral organs and control their identity and development. On the other hand, the ''Arabidopsis'' ALOG family genes ''LSH3/OBO1'' and ''LSH4'' are expressed in shoot organ boundary cells. The functions of ''LSH3/OBO1'' and ''LSH4'' are unknown; however, they induce the overproliferation of shoot meristems and the formation of extra organs when ectopically expressed. A plausible scenario is that at least some of the ALOG family proteins share conserved functions, but it may be that their distinctive expression patterns have led to divergent functions. The establishment of the machinery for meristem-specific expression may be a primary reason for the evolution of ''TAW1'' as a major regulator of meristem activity and phase transition &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
''TAW1'' function might have evolved to ensure the production of sufficient numbers of spikelets. Unraveling the molecular function of ''TAW1'' will provide an opportunity for a greater understanding of meristem activity and identity, which is a fundamental issue in plant biology. Furthermore, such knowledge could be exploited to further increase crop yields. In addition, ''TAW1'' is of great interest with respect to the evolution of inflorescence architecture. ''TAW1'' function may be essential for the development of compound inflorescences, in which the branching pattern is crucial &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Yoshida A, Sasao M, Yasuno N, et al. (2013) ''TAWAWA1'', a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition. Proceedings of the National Academy of Sciences 110: 767-772.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os10g0478000|&lt;br /&gt;
Description = Protein of unknown function DUF640 domain containing protein|&lt;br /&gt;
Version = NM_001189280.1 GI:297727690 GeneID:9266624|&lt;br /&gt;
Length = 1426 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os10g0478000, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 10|Chromosome 10]]|&lt;br /&gt;
AP = Chromosome 10:18345508..18346933|&lt;br /&gt;
CDS = 18345710..18346324|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MEFVAHAAAPDSPHSDSGGGGGGMATGATSASAAGASPSRYESQ                     KRRDWNTFGQYLRNHRPPLSLARCSGAHVLEFLRYLDQFGKTKVHAPACPFFGHPAPP                     APCPCPLRQAWGSLDALVGRLRAAYEENGGRPENNPFGARAVRLYLREVREHQARARG                     VSYEKKKRKKPPHPSSAAAAHDDAANGALHHHHHMPPPPPGAAA&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;610..1224#tatcggctccttctcgcccagcttttgctcacgtcacatcaccttccacctccacccctccactcgctcgctcgcttgcttgctccaattaatacctcttctccttctcccccagcaactagcttccttctccgcttttgcagctcgccgccgccgccgccgccgccgccgcgacacggcgcgcatatggtcgtcgtcgtcgtcgtcgtcgtcgctggagaagacgaagaaagatagtagacctgagctgggggggcggtgaattcgccggagagctagctaaggtgagtttcgttttcggtttcggtttcgatcgatttgttggtgcagatgcatctgggagctagagaactatttatagtggctgcggtgcggtgcggcgtcgccacgccgcgcacgcgctcgcccacgtcgcgcgcgcgcgggcgcgcgtccactctctctctctcttggaccactgcgcgcgcgggcgcgcgtcggcgtcgccacggcttctcaagaacgcgcgcgcgcgcactgattcccagatagatagatctatatctgttcgtcttcctcagctatggtgtggtggtggtggtggtgtttgtggtgttgtgcagatcgacgatggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctgagccgagccgagcttgctccaagatcgccggaaaacgagctgctagcctcctacgcatgcactagttactccactccactccactccactatgatccctagctaggctgctcttgctactagcaaaactacggattaatctccatgcttgctactgctgctgctgctgctactgcatctaattaattaggttgattatttcct&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001189280.1 RefSeq:Os10g0478000]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 10]]&lt;br /&gt;
[[Category:Chromosome 10]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174429</id>
		<title>Os10g0478000</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174429"/>
				<updated>2014-05-30T04:43:27Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: /* Annotated Information */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; The rice ''TAWAWA1'' (''TAW1'') gene, a member of ALOG family, was identified as a  regulator of rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:YoshidaF1.jpg|right|thumb|200px|Fig 1. Characterization of ''taw1'' dominant mutants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF2.jpg|right|thumb|250px|Fig 2. Isolation of the ''TAW1'' gene &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF3.jpg|right|thumb|250px|Fig 3. Expression pattern of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF4.jpg|right|thumb|250px|Fig 4. ''SVP'' subfamily MADS-box genes work downstream of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF5.jpg|right|thumb|250px|Fig 5. Phenotype of ''taw1-D2''–introgressed Koshihikari BC5F2 plants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
In the dominant gain-of-function mutant ''tawawa1-D''(Fig. 1), the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in ''TAWAWA1'' (''TAW1'') activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. ''TAW1'' encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the branch meristem (BMs). ''TAW1'' expression disappears from incipient spikelet meristems (SMs). It is demonstrated that members of the ''SHORT VEGETATIVE PHASE'' subfamily of MADS-box genes function downstream of ''TAW1''. Thus, ''TAW1'' is proposed as a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
''TAW1'' contains a conserved domain and a nuclear localization signal. Indeed, ''TAW1'' localizes to the nucleus and shows slight but significant activity as a transcriptional activator (Fig. 3 A and B). The spatiotemporal pattern of ''TAW1'' mRNA accumulation was examined by in situ hybridization. During the vegetative phase of development, ''TAW1'' was predominantly expressed in meristems, including the SAM, axillary meristems, and young leaves (Fig. 3 A and C). After transition to the reproductive phase, ''TAW1'' mRNA continued to accumulate in the IM (Fig. 3D). The strongest signal was observed in BMs in the growing inflorescence (Fig. 3E). After initiation of the primary BMs, ''TAW1'' expression gradually disappeared from the IM as it degenerated (Fig. 3F). In wild-type inflorescences, the signal intensity in the meristem gradually decreased and became undetectable at SM initiation (Fig. 3G). On the other hand, in ''taw1-D'' inflorescences, stronger TAW1 signals were detected, even at the stage when the SMs were formed in the wild-type plants (Fig. 3 H and I). Quantitative PCR analysis indicated that the levels of ''TAW1'' expression in the mutant inflorescences roughly coincided with the severity of their phenotypes (Fig. 3J). These results imply that ''TAW1'' functions to suppress SM identity and that its activity must be below a certain threshold level to allow SM specification. Interestingly, ''TAW1'' expression is reduced in the vegetative shoot apices, leaves, and roots of ''taw1-D'' mutants compared with wild-type plants. These results suggest that the sequence surrounding the ''nDart1'' insertion sites is necessary for fine-tuning the spatial and quantitative expression pattern of ''TAW1''. It may be that positive regulators of SM identity interact with this sequence, which is located downstream of the transcribed region. It is also possible that ''nDart1'' carries a sequence that functions as a transcriptional enhancer; however, this is unlikely because not all ''nDart1'' insertions activate transcription. Unraveling the molecular mechanisms that regulate ''TAW1'' transcription will shed light on the regulatory networks controlling rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
The rice genes ''G1'' and ''TH1'' are ALOG family members that are expressed in the lemma, palea, and floral organs and control their identity and development. On the other hand, the ''Arabidopsis'' ALOG family genes ''LSH3/OBO1'' and ''LSH4'' are expressed in shoot organ boundary cells. The functions of ''LSH3/OBO1'' and ''LSH4'' are unknown; however, they induce the overproliferation of shoot meristems and the formation of extra organs when ectopically expressed. A plausible scenario is that at least some of the ALOG family proteins share conserved functions, but it may be that their distinctive expression patterns have led to divergent functions. The establishment of the machinery for meristem-specific expression may be a primary reason for the evolution of ''TAW1'' as a major regulator of meristem activity and phase transition &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
''TAW1'' function might have evolved to ensure the production of sufficient numbers of spikelets. Unraveling the molecular function of ''TAW1'' will provide an opportunity for a greater understanding of meristem activity and identity, which is a fundamental issue in plant biology. Furthermore, such knowledge could be exploited to further increase crop yields. In addition, ''TAW1'' is of great interest with respect to the evolution of inflorescence architecture. ''TAW1'' function may be essential for the development of compound inflorescences, in which the branching pattern is crucial &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Yoshida A, Sasao M, Yasuno N, et al. (2013) ''TAWAWA1'', a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition. Proceedings of the National Academy of Sciences 110: 767-772.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os10g0478000|&lt;br /&gt;
Description = Protein of unknown function DUF640 domain containing protein|&lt;br /&gt;
Version = NM_001189280.1 GI:297727690 GeneID:9266624|&lt;br /&gt;
Length = 1426 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os10g0478000, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 10|Chromosome 10]]|&lt;br /&gt;
AP = Chromosome 10:18345508..18346933|&lt;br /&gt;
CDS = 18345710..18346324|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MEFVAHAAAPDSPHSDSGGGGGGMATGATSASAAGASPSRYESQ                     KRRDWNTFGQYLRNHRPPLSLARCSGAHVLEFLRYLDQFGKTKVHAPACPFFGHPAPP                     APCPCPLRQAWGSLDALVGRLRAAYEENGGRPENNPFGARAVRLYLREVREHQARARG                     VSYEKKKRKKPPHPSSAAAAHDDAANGALHHHHHMPPPPPGAAA&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;610..1224#tatcggctccttctcgcccagcttttgctcacgtcacatcaccttccacctccacccctccactcgctcgctcgcttgcttgctccaattaatacctcttctccttctcccccagcaactagcttccttctccgcttttgcagctcgccgccgccgccgccgccgccgccgcgacacggcgcgcatatggtcgtcgtcgtcgtcgtcgtcgtcgctggagaagacgaagaaagatagtagacctgagctgggggggcggtgaattcgccggagagctagctaaggtgagtttcgttttcggtttcggtttcgatcgatttgttggtgcagatgcatctgggagctagagaactatttatagtggctgcggtgcggtgcggcgtcgccacgccgcgcacgcgctcgcccacgtcgcgcgcgcgcgggcgcgcgtccactctctctctctcttggaccactgcgcgcgcgggcgcgcgtcggcgtcgccacggcttctcaagaacgcgcgcgcgcgcactgattcccagatagatagatctatatctgttcgtcttcctcagctatggtgtggtggtggtggtggtgtttgtggtgttgtgcagatcgacgatggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctgagccgagccgagcttgctccaagatcgccggaaaacgagctgctagcctcctacgcatgcactagttactccactccactccactccactatgatccctagctaggctgctcttgctactagcaaaactacggattaatctccatgcttgctactgctgctgctgctgctactgcatctaattaattaggttgattatttcct&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001189280.1 RefSeq:Os10g0478000]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 10]]&lt;br /&gt;
[[Category:Chromosome 10]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174428</id>
		<title>Os10g0478000</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174428"/>
				<updated>2014-05-30T04:41:52Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; The rice ''TAWAWA1'' (''TAW1'') gene, a member of ALOG family, was identified as a  regulator of rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:YoshidaF1.jpg|right|thumb|200px|Fig 1. Characterization of ''taw1'' dominant mutants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF2.jpg|right|thumb|250px|Fig 2. Isolation of the ''TAW1'' gene &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF3.jpg|right|thumb|250px|Fig 3. Expression pattern of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF4.jpg|right|thumb|250px|Fig 4. ''SVP'' subfamily MADS-box genes work downstream of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF5.jpg|right|thumb|250px|Fig 5. Phenotype of ''taw1-D2''–introgressed Koshihikari BC5F2 plants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
In the dominant gain-of-function mutant ''tawawa1-D''(Fig. 1), the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in ''TAWAWA1'' (''TAW1'') activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. ''TAW1'' encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the branch meristem (BMs). ''TAW1'' expression disappears from incipient spikelet meristems (SMs). It is demonstrated that members of the ''SHORT VEGETATIVE PHASE'' subfamily of MADS-box genes function downstream of ''TAW1''. Thus, ''TAW1'' is proposed as a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
''TAW1'' contains a conserved domain and a nuclear localization signal. Indeed, ''TAW1'' localizes to the nucleus and shows slight but significant activity as a transcriptional activator (Fig. 3 A and B). The spatiotemporal pattern of ''TAW1'' mRNA accumulation was examined by in situ hybridization. During the vegetative phase of development, ''TAW1'' was predominantly expressed in meristems, including the SAM, axillary meristems, and young leaves (Fig. 3 A and C). After transition to the reproductive phase, ''TAW1'' mRNA continued to accumulate in the IM (Fig. 3D). The strongest signal was observed in BMs in the growing inflorescence (Fig. 3E). After initiation of the primary BMs, ''TAW1'' expression gradually disappeared from the IM as it degenerated (Fig. 3F). In wild-type inflorescences, the signal intensity in the meristem gradually decreased and became undetectable at SM initiation (Fig. 3G). On the other hand, in ''taw1-D'' inflorescences, stronger TAW1 signals were detected, even at the stage when the SMs were formed in the wild-type plants (Fig. 3 H and I). Quantitative PCR analysis indicated that the levels of ''TAW1'' expression in the mutant inflorescences roughly coincided with the severity of their phenotypes (Fig. 3J). These results imply that ''TAW1'' functions to suppress SM identity and that its activity must be below a certain threshold level to allow SM specification. Interestingly, ''TAW1'' expression is reduced in the vegetative shoot apices, leaves, and roots of ''taw1-D'' mutants compared with wild-type plants. These results suggest that the sequence surrounding the ''nDart1'' insertion sites is necessary for fine-tuning the spatial and quantitative expression pattern of ''TAW1''. It may be that positive regulators of SM identity interact with this sequence, which is located downstream of the transcribed region. It is also possible that ''nDart1'' carries a sequence that functions as a transcriptional enhancer; however, this is unlikely because not all ''nDart1'' insertions activate transcription. Unraveling the molecular mechanisms that regulate ''TAW1'' transcription will shed light on the regulatory networks controlling rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
The rice genes ''G1'' and ''TH1'' are ALOG family members that are expressed in the lemma, palea, and floral organs and control their identity and development. On the other hand, the ''Arabidopsis'' ALOG family genes ''LSH3/OBO1'' and ''LSH4'' are expressed in shoot organ boundary cells. The functions of ''LSH3/OBO1'' and ''LSH4'' are unknown; however, they induce the overproliferation of shoot meristems and the formation of extra organs when ectopically expressed. A plausible scenario is that at least some of the ALOG family proteins share conserved functions, but it may be that their distinctive expression patterns have led to divergent functions. The establishment of the machinery for meristem-specific expression may be a primary reason for the evolution of ''TAW1'' as a major regulator of meristem activity and phase transition.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
''TAW1'' function might have evolved to ensure the production of sufficient numbers of spikelets. Unraveling the molecular function of ''TAW1'' will provide an opportunity for a greater understanding of meristem activity and identity, which is a fundamental issue in plant biology. Furthermore, such knowledge could be exploited to further increase crop yields. In addition, ''TAW1'' is of great interest with respect to the evolution of inflorescence architecture. ''TAW1'' function may be essential for the development of compound inflorescences, in which the branching pattern is crucial &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Yoshida A, Sasao M, Yasuno N, et al. (2013) ''TAWAWA1'', a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition. Proceedings of the National Academy of Sciences 110: 767-772.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os10g0478000|&lt;br /&gt;
Description = Protein of unknown function DUF640 domain containing protein|&lt;br /&gt;
Version = NM_001189280.1 GI:297727690 GeneID:9266624|&lt;br /&gt;
Length = 1426 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os10g0478000, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 10|Chromosome 10]]|&lt;br /&gt;
AP = Chromosome 10:18345508..18346933|&lt;br /&gt;
CDS = 18345710..18346324|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MEFVAHAAAPDSPHSDSGGGGGGMATGATSASAAGASPSRYESQ                     KRRDWNTFGQYLRNHRPPLSLARCSGAHVLEFLRYLDQFGKTKVHAPACPFFGHPAPP                     APCPCPLRQAWGSLDALVGRLRAAYEENGGRPENNPFGARAVRLYLREVREHQARARG                     VSYEKKKRKKPPHPSSAAAAHDDAANGALHHHHHMPPPPPGAAA&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;610..1224#tatcggctccttctcgcccagcttttgctcacgtcacatcaccttccacctccacccctccactcgctcgctcgcttgcttgctccaattaatacctcttctccttctcccccagcaactagcttccttctccgcttttgcagctcgccgccgccgccgccgccgccgccgcgacacggcgcgcatatggtcgtcgtcgtcgtcgtcgtcgtcgctggagaagacgaagaaagatagtagacctgagctgggggggcggtgaattcgccggagagctagctaaggtgagtttcgttttcggtttcggtttcgatcgatttgttggtgcagatgcatctgggagctagagaactatttatagtggctgcggtgcggtgcggcgtcgccacgccgcgcacgcgctcgcccacgtcgcgcgcgcgcgggcgcgcgtccactctctctctctcttggaccactgcgcgcgcgggcgcgcgtcggcgtcgccacggcttctcaagaacgcgcgcgcgcgcactgattcccagatagatagatctatatctgttcgtcttcctcagctatggtgtggtggtggtggtggtgtttgtggtgttgtgcagatcgacgatggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctgagccgagccgagcttgctccaagatcgccggaaaacgagctgctagcctcctacgcatgcactagttactccactccactccactccactatgatccctagctaggctgctcttgctactagcaaaactacggattaatctccatgcttgctactgctgctgctgctgctactgcatctaattaattaggttgattatttcct&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001189280.1 RefSeq:Os10g0478000]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 10]]&lt;br /&gt;
[[Category:Chromosome 10]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174426</id>
		<title>Os10g0478000</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174426"/>
				<updated>2014-05-30T04:40:22Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; The rice ''TAWAWA1'' (''TAW1'') gene, a member of ALOG family, was identified as a  regulator of rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:YoshidaF1.jpg|right|thumb|200px|Fig 1. Characterization of ''taw1'' dominant mutants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF2.jpg|right|thumb|250px|Fig 2. Isolation of the ''TAW1'' gene &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF3.jpg|right|thumb|250px|Fig 3. Expression pattern of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF4.jpg|right|thumb|250px|Fig 4. ''SVP'' subfamily MADS-box genes work downstream of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF5.jpg|right|thumb|250px|Fig 5. Phenotype of ''taw1-D2''–introgressed Koshihikari BC5F2 plants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
In the dominant gain-of-function mutant ''tawawa1-D''(Fig. 1), the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in ''TAWAWA1'' (''TAW1'') activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. ''TAW1'' encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the branch meristem (BMs). ''TAW1'' expression disappears from incipient spikelet meristems (SMs). It is demonstrated that members of the ''SHORT VEGETATIVE PHASE'' subfamily of MADS-box genes function downstream of ''TAW1''. Thus, ''TAW1'' is proposed as a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
''TAW1'' contains a conserved domain and a nuclear localization signal. Indeed, ''TAW1'' localizes to the nucleus and shows slight but significant activity as a transcriptional activator (Fig. 3 A and B). The spatiotemporal pattern of ''TAW1'' mRNA accumulation was examined by in situ hybridization. During the vegetative phase of development, ''TAW1'' was predominantly expressed in meristems, including the SAM, axillary meristems, and young leaves (Fig. 3 A and C). After transition to the reproductive phase, ''TAW1'' mRNA continued to accumulate in the IM (Fig. 3D). The strongest signal was observed in BMs in the growing inflorescence (Fig. 3E). After initiation of the primary BMs, ''TAW1'' expression gradually disappeared from the IM as it degenerated (Fig. 3F). In wild-type inflorescences, the signal intensity in the meristem gradually decreased and became undetectable at SM initiation (Fig. 3G). On the other hand, in ''taw1-D'' inflorescences, stronger TAW1 signals were detected, even at the stage when the SMs were formed in the wild-type plants (Fig. 3 H and I). Quantitative PCR analysis indicated that the levels of ''TAW1'' expression in the mutant inflorescences roughly coincided with the severity of their phenotypes (Fig. 3J). These results imply that ''TAW1'' functions to suppress SM identity and that its activity must be below a certain threshold level to allow SM specification. Interestingly, ''TAW1'' expression is reduced in the vegetative shoot apices, leaves, and roots of ''taw1-D'' mutants compared with wild-type plants. These results suggest that the sequence surrounding the ''nDart1'' insertion sites is necessary for fine-tuning the spatial and quantitative expression pattern of ''TAW1''. It may be that positive regulators of SM identity interact with this sequence, which is located downstream of the transcribed region. It is also possible that ''nDart1'' carries a sequence that functions as a transcriptional enhancer; however, this is unlikely because not all ''nDart1'' insertions activate transcription. Unraveling the molecular mechanisms that regulate ''TAW1'' transcription will shed light on the regulatory networks controlling rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
The rice genes ''G1'' and ''TH1'' are ALOG family members that are expressed in the lemma, palea, and floral organs and control their identity and development. On the other hand, the ''Arabidopsis'' ALOG family genes ''LSH3/OBO1'' and ''LSH4'' are expressed in shoot organ boundary cells. The functions of ''LSH3/OBO1'' and ''LSH4'' are unknown; however, they induce the overproliferation of shoot meristems and the formation of extra organs when ectopically expressed. A plausible scenario is that at least some of the ALOG family proteins share conserved functions, but it may be that their distinctive expression patterns have led to divergent functions. The establishment of the machinery for meristem-specific expression may be a primary reason for the evolution of ''TAW1'' as a major regulator of meristem activity and phase transition.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
''TAW1'' function might have evolved to ensure the production of sufficient numbers of spikelets. Unraveling the molecular function of ''TAW1'' will provide an opportunity for a greater understanding of meristem activity and identity, which is a fundamental issue in plant biology. Furthermore, such knowledge could be exploited to further increase crop yields. In addition, ''TAW1'' is of great interest with respect to the evolution of inflorescence architecture. ''TAW1'' function may be essential for the development of compound inflorescences, in which the branching pattern is crucial &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Yoshida A, Sasao M, Yasuno N, et al. (2013) TAWAWA1, a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition. Proceedings of the National Academy of Sciences 110: 767-772.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os10g0478000|&lt;br /&gt;
Description = Protein of unknown function DUF640 domain containing protein|&lt;br /&gt;
Version = NM_001189280.1 GI:297727690 GeneID:9266624|&lt;br /&gt;
Length = 1426 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os10g0478000, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 10|Chromosome 10]]|&lt;br /&gt;
AP = Chromosome 10:18345508..18346933|&lt;br /&gt;
CDS = 18345710..18346324|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MEFVAHAAAPDSPHSDSGGGGGGMATGATSASAAGASPSRYESQ                     KRRDWNTFGQYLRNHRPPLSLARCSGAHVLEFLRYLDQFGKTKVHAPACPFFGHPAPP                     APCPCPLRQAWGSLDALVGRLRAAYEENGGRPENNPFGARAVRLYLREVREHQARARG                     VSYEKKKRKKPPHPSSAAAAHDDAANGALHHHHHMPPPPPGAAA&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;610..1224#tatcggctccttctcgcccagcttttgctcacgtcacatcaccttccacctccacccctccactcgctcgctcgcttgcttgctccaattaatacctcttctccttctcccccagcaactagcttccttctccgcttttgcagctcgccgccgccgccgccgccgccgccgcgacacggcgcgcatatggtcgtcgtcgtcgtcgtcgtcgtcgctggagaagacgaagaaagatagtagacctgagctgggggggcggtgaattcgccggagagctagctaaggtgagtttcgttttcggtttcggtttcgatcgatttgttggtgcagatgcatctgggagctagagaactatttatagtggctgcggtgcggtgcggcgtcgccacgccgcgcacgcgctcgcccacgtcgcgcgcgcgcgggcgcgcgtccactctctctctctcttggaccactgcgcgcgcgggcgcgcgtcggcgtcgccacggcttctcaagaacgcgcgcgcgcgcactgattcccagatagatagatctatatctgttcgtcttcctcagctatggtgtggtggtggtggtggtgtttgtggtgttgtgcagatcgacgatggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctgagccgagccgagcttgctccaagatcgccggaaaacgagctgctagcctcctacgcatgcactagttactccactccactccactccactatgatccctagctaggctgctcttgctactagcaaaactacggattaatctccatgcttgctactgctgctgctgctgctactgcatctaattaattaggttgattatttcct&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001189280.1 RefSeq:Os10g0478000]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 10]]&lt;br /&gt;
[[Category:Chromosome 10]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174422</id>
		<title>Os10g0478000</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174422"/>
				<updated>2014-05-30T04:35:09Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: /* Annotated Information */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; The rice ''TAWAWA1'' (''TAW1'') gene, a member of ALOG family, was identified as a  regulator of rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:YoshidaF1.jpg|right|thumb|200px|Fig 1. Characterization of ''taw1'' dominant mutants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF2.jpg|right|thumb|250px|Fig 2. Isolation of the ''TAW1'' gene &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF3.jpg|right|thumb|250px|Fig 3. Expression pattern of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF4.jpg|right|thumb|250px|Fig 4. ''SVP'' subfamily MADS-box genes work downstream of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF5.jpg|right|thumb|250px|Fig 5. Phenotype of ''taw1-D2''–introgressed Koshihikari BC5F2 plants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
In the dominant gain-of-function mutant ''tawawa1-D'', the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in ''TAWAWA1'' (''TAW1'') activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. ''TAW1'' encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the branch meristem (BMs). ''TAW1'' expression disappears from incipient spikelet meristems (SMs). It is demonstrated that members of the ''SHORT VEGETATIVE PHASE'' subfamily of MADS-box genes function downstream of ''TAW1''. Thus, ''TAW1'' is proposed as a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
''TAW1'' contains a conserved domain and a nuclear localization signal. Indeed, ''TAW1'' localizes to the nucleus and shows slight but significant activity as a transcriptional activator (Fig. 3 A and B). The spatiotemporal pattern of ''TAW1'' mRNA accumulation was examined by in situ hybridization. During the vegetative phase of development, ''TAW1'' was predominantly expressed in meristems, including the SAM, axillary meristems, and young leaves (Fig. 3 A and C). After transition to the reproductive phase, ''TAW1'' mRNA continued to accumulate in the IM (Fig. 3D). The strongest signal was observed in BMs in the growing inflorescence (Fig. 3E). After initiation of the primary BMs, ''TAW1'' expression gradually disappeared from the IM as it degenerated (Fig. 3F). In wild-type inflorescences, the signal intensity in the meristem gradually decreased and became undetectable at SM initiation (Fig. 3G). On the other hand, in ''taw1-D'' inflorescences, stronger TAW1 signals were detected, even at the stage when the SMs were formed in the wild-type plants (Fig. 3 H and I). Quantitative PCR analysis indicated that the levels of ''TAW1'' expression in the mutant inflorescences roughly coincided with the severity of their phenotypes (Fig. 3J). These results imply that ''TAW1'' functions to suppress SM identity and that its activity must be below a certain threshold level to allow SM specification. Interestingly, ''TAW1'' expression is reduced in the vegetative shoot apices, leaves, and roots of ''taw1-D'' mutants compared with wild-type plants. These results suggest that the sequence surrounding the ''nDart1'' insertion sites is necessary for fine-tuning the spatial and quantitative expression pattern of ''TAW1''. It may be that positive regulators of SM identity interact with this sequence, which is located downstream of the transcribed region. It is also possible that ''nDart1'' carries a sequence that functions as a transcriptional enhancer; however, this is unlikely because not all ''nDart1'' insertions activate transcription. Unraveling the molecular mechanisms that regulate ''TAW1'' transcription will shed light on the regulatory networks controlling rice inflorescence architecture.&lt;br /&gt;
The rice genes ''G1'' and ''TH1'' are ALOG family members that are expressed in the lemma, palea, and floral organs and control their identity and development. On the other hand, the ''Arabidopsis'' ALOG family genes ''LSH3/OBO1'' and ''LSH4'' are expressed in shoot organ boundary cells. The functions of ''LSH3/OBO1'' and ''LSH4'' are unknown; however, they induce the overproliferation of shoot meristems and the formation of extra organs when ectopically expressed. A plausible scenario is that at least some of the ALOG family proteins share conserved functions, but it may be that their distinctive expression patterns have led to divergent functions. The establishment of the machinery for meristem-specific expression may be a primary reason for the evolution of ''TAW1'' as a major regulator of meristem activity and phase transition.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
''TAW1'' function might have evolved to ensure the production of sufficient numbers of spikelets. Unraveling the molecular function of ''TAW1'' will provide an opportunity for a greater understanding of meristem activity and identity, which is a fundamental issue in plant biology. Furthermore, such knowledge could be exploited to further increase crop yields. In addition, ''TAW1'' is of great interest with respect to the evolution of inflorescence architecture. ''TAW1'' function may be essential for the development of compound inflorescences, in which the branching pattern is crucial &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Yoshida A, Sasao M, Yasuno N, et al. (2013) TAWAWA1, a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition. Proceedings of the National Academy of Sciences 110: 767-772.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os10g0478000|&lt;br /&gt;
Description = Protein of unknown function DUF640 domain containing protein|&lt;br /&gt;
Version = NM_001189280.1 GI:297727690 GeneID:9266624|&lt;br /&gt;
Length = 1426 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os10g0478000, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 10|Chromosome 10]]|&lt;br /&gt;
AP = Chromosome 10:18345508..18346933|&lt;br /&gt;
CDS = 18345710..18346324|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MEFVAHAAAPDSPHSDSGGGGGGMATGATSASAAGASPSRYESQ                     KRRDWNTFGQYLRNHRPPLSLARCSGAHVLEFLRYLDQFGKTKVHAPACPFFGHPAPP                     APCPCPLRQAWGSLDALVGRLRAAYEENGGRPENNPFGARAVRLYLREVREHQARARG                     VSYEKKKRKKPPHPSSAAAAHDDAANGALHHHHHMPPPPPGAAA&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;610..1224#tatcggctccttctcgcccagcttttgctcacgtcacatcaccttccacctccacccctccactcgctcgctcgcttgcttgctccaattaatacctcttctccttctcccccagcaactagcttccttctccgcttttgcagctcgccgccgccgccgccgccgccgccgcgacacggcgcgcatatggtcgtcgtcgtcgtcgtcgtcgtcgctggagaagacgaagaaagatagtagacctgagctgggggggcggtgaattcgccggagagctagctaaggtgagtttcgttttcggtttcggtttcgatcgatttgttggtgcagatgcatctgggagctagagaactatttatagtggctgcggtgcggtgcggcgtcgccacgccgcgcacgcgctcgcccacgtcgcgcgcgcgcgggcgcgcgtccactctctctctctcttggaccactgcgcgcgcgggcgcgcgtcggcgtcgccacggcttctcaagaacgcgcgcgcgcgcactgattcccagatagatagatctatatctgttcgtcttcctcagctatggtgtggtggtggtggtggtgtttgtggtgttgtgcagatcgacgatggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctgagccgagccgagcttgctccaagatcgccggaaaacgagctgctagcctcctacgcatgcactagttactccactccactccactccactatgatccctagctaggctgctcttgctactagcaaaactacggattaatctccatgcttgctactgctgctgctgctgctactgcatctaattaattaggttgattatttcct&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001189280.1 RefSeq:Os10g0478000]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 10]]&lt;br /&gt;
[[Category:Chromosome 10]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174421</id>
		<title>Os10g0478000</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174421"/>
				<updated>2014-05-30T04:30:04Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: /* Expression */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; The rice ''TAWAWA1'' (''TAW1'') gene, a member of ALOG family, was identified as a  regulator of rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:YoshidaF1.jpg|right|thumb|200px|Fig 1. Characterization of ''taw1'' dominant mutants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF2.jpg|right|thumb|250px|Fig 2. Isolation of the ''TAW1'' gene &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF3.jpg|right|thumb|250px|Fig 3. Expression pattern of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF4.jpg|right|thumb|250px|Fig 4. ''SVP'' subfamily MADS-box genes work downstream of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF5.jpg|right|thumb|250px|Fig 5. Phenotype of ''taw1-D2''–introgressed Koshihikari BC5F2 plants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
In the dominant gain-of-function mutant ''tawawa1-D'', the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in ''TAWAWA1'' (''TAW1'') activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. ''TAW1'' encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the branch meristem (BMs). ''TAW1'' expression disappears from incipient spikelet meristems (SMs). It is demonstrated that members of the ''SHORT VEGETATIVE PHASE'' subfamily of MADS-box genes function downstream of ''TAW1''. Thus, ''TAW1'' is proposed as a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
TAW1 contains a conserved domain and a nuclear localization signal (Fig. S5A). Indeed, TAW1 localizes to the nucleus and shows slight but significant activity as a transcriptional activator (Fig. 3 A and B). The spatiotemporal pattern of TAW1 mRNA accumulation was examined by in situ hybridization. During the vegetative phase of development, TAW1 was predominantly expressed in meristems, including the SAM, axillary meristems, and young leaves (Fig. 3 A and C). After transition to the reproductive phase, TAW1 mRNA continued to accumulate in the IM (Fig. 3D). The strongest signal was observed in BMs in the growing inflorescence (Fig. 3E). After initiation of the primary BMs, TAW1 expression gradually disappeared from the IM as it degenerated (Fig. 3F). In wild-type inflorescences, the signal intensity in the meristem gradually decreased and became undetectable at SM initiation (Fig. 3G). On the other hand, in taw1-D inflorescences, stronger TAW1 signals were detected, even at the stage when the SMs were formed in the wild-type plants (Fig. 3 H and I). Quantitative PCR analysis indicated that the levels of TAW1 expression in the mutant inflorescences roughly coincided with the severity of their phenotypes (Fig. 3J). These results imply that TAW1 functions to suppress SM identity and that its activity must be below a certain threshold level to allow SM specification. Interestingly, TAW1 expression is reduced in the vegetative shoot apices, leaves, and roots of taw1-D mutants compared with wild-type plants. These results suggest that the sequence surrounding the nDart1 insertion sites is necessary for fine-tuning the spatial and quantitative expression pattern of TAW1. It may be that positive regulators of SM identity interact with this sequence, which is located downstream of the transcribed region. It is also possible that nDart1 carries a sequence that functions as a transcriptional enhancer; however, this is unlikely because not all nDart1 insertions activate transcription. Unraveling the molecular mechanisms that regulate TAW1 transcription will shed light on the regulatory networks controlling rice inflorescence architecture.&lt;br /&gt;
The rice genes G1 and TH1 are ALOG family members that are expressed in the lemma, palea, and floral organs and control their identity and development. On the other hand, the Arabidopsis ALOG family genes LSH3/OBO1 and LSH4 are expressed in shoot organ boundary cells. The functions of LSH3/OBO1 and LSH4 are unknown; however, they induce the overproliferation of shoot meristems and the formation of extra organs when ectopically expressed. A plausible scenario is that at least some of the ALOG family proteins share conserved functions, but it may be that their distinctive expression patterns have led to divergent functions. The establishment of the machinery for meristem-specific expression may be a primary reason for the evolution of TAW1 as a major regulator of meristem activity and phase transition.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
''TAW1'' function might have evolved to ensure the production of sufficient numbers of spikelets. Unraveling the molecular function of ''TAW1'' will provide an opportunity for a greater understanding of meristem activity and identity, which is a fundamental issue in plant biology. Furthermore, such knowledge could be exploited to further increase crop yields. In addition, ''TAW1'' is of great interest with respect to the evolution of inflorescence architecture. ''TAW1'' function may be essential for the development of compound inflorescences, in which the branching pattern is crucial &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Yoshida A, Sasao M, Yasuno N, et al. (2013) TAWAWA1, a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition. Proceedings of the National Academy of Sciences 110: 767-772.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os10g0478000|&lt;br /&gt;
Description = Protein of unknown function DUF640 domain containing protein|&lt;br /&gt;
Version = NM_001189280.1 GI:297727690 GeneID:9266624|&lt;br /&gt;
Length = 1426 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os10g0478000, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 10|Chromosome 10]]|&lt;br /&gt;
AP = Chromosome 10:18345508..18346933|&lt;br /&gt;
CDS = 18345710..18346324|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MEFVAHAAAPDSPHSDSGGGGGGMATGATSASAAGASPSRYESQ                     KRRDWNTFGQYLRNHRPPLSLARCSGAHVLEFLRYLDQFGKTKVHAPACPFFGHPAPP                     APCPCPLRQAWGSLDALVGRLRAAYEENGGRPENNPFGARAVRLYLREVREHQARARG                     VSYEKKKRKKPPHPSSAAAAHDDAANGALHHHHHMPPPPPGAAA&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;610..1224#tatcggctccttctcgcccagcttttgctcacgtcacatcaccttccacctccacccctccactcgctcgctcgcttgcttgctccaattaatacctcttctccttctcccccagcaactagcttccttctccgcttttgcagctcgccgccgccgccgccgccgccgccgcgacacggcgcgcatatggtcgtcgtcgtcgtcgtcgtcgtcgctggagaagacgaagaaagatagtagacctgagctgggggggcggtgaattcgccggagagctagctaaggtgagtttcgttttcggtttcggtttcgatcgatttgttggtgcagatgcatctgggagctagagaactatttatagtggctgcggtgcggtgcggcgtcgccacgccgcgcacgcgctcgcccacgtcgcgcgcgcgcgggcgcgcgtccactctctctctctcttggaccactgcgcgcgcgggcgcgcgtcggcgtcgccacggcttctcaagaacgcgcgcgcgcgcactgattcccagatagatagatctatatctgttcgtcttcctcagctatggtgtggtggtggtggtggtgtttgtggtgttgtgcagatcgacgatggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctgagccgagccgagcttgctccaagatcgccggaaaacgagctgctagcctcctacgcatgcactagttactccactccactccactccactatgatccctagctaggctgctcttgctactagcaaaactacggattaatctccatgcttgctactgctgctgctgctgctactgcatctaattaattaggttgattatttcct&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001189280.1 RefSeq:Os10g0478000]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 10]]&lt;br /&gt;
[[Category:Chromosome 10]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174418</id>
		<title>Os10g0478000</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174418"/>
				<updated>2014-05-30T04:25:54Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: /* Function */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; The rice ''TAWAWA1'' (''TAW1'') gene, a member of ALOG family, was identified as a  regulator of rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:YoshidaF1.jpg|right|thumb|200px|Fig 1. Characterization of ''taw1'' dominant mutants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF2.jpg|right|thumb|250px|Fig 2. Isolation of the ''TAW1'' gene &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF3.jpg|right|thumb|250px|Fig 3. Expression pattern of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF4.jpg|right|thumb|250px|Fig 4. ''SVP'' subfamily MADS-box genes work downstream of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF5.jpg|right|thumb|250px|Fig 5. Phenotype of ''taw1-D2''–introgressed Koshihikari BC5F2 plants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
In the dominant gain-of-function mutant ''tawawa1-D'', the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in ''TAWAWA1'' (''TAW1'') activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. ''TAW1'' encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the branch meristem (BMs). ''TAW1'' expression disappears from incipient spikelet meristems (SMs). It is demonstrated that members of the ''SHORT VEGETATIVE PHASE'' subfamily of MADS-box genes function downstream of ''TAW1''. Thus, ''TAW1'' is proposed as a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
Please input expression information here.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
''TAW1'' function might have evolved to ensure the production of sufficient numbers of spikelets. Unraveling the molecular function of ''TAW1'' will provide an opportunity for a greater understanding of meristem activity and identity, which is a fundamental issue in plant biology. Furthermore, such knowledge could be exploited to further increase crop yields. In addition, ''TAW1'' is of great interest with respect to the evolution of inflorescence architecture. ''TAW1'' function may be essential for the development of compound inflorescences, in which the branching pattern is crucial &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Yoshida A, Sasao M, Yasuno N, et al. (2013) TAWAWA1, a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition. Proceedings of the National Academy of Sciences 110: 767-772.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os10g0478000|&lt;br /&gt;
Description = Protein of unknown function DUF640 domain containing protein|&lt;br /&gt;
Version = NM_001189280.1 GI:297727690 GeneID:9266624|&lt;br /&gt;
Length = 1426 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os10g0478000, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 10|Chromosome 10]]|&lt;br /&gt;
AP = Chromosome 10:18345508..18346933|&lt;br /&gt;
CDS = 18345710..18346324|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MEFVAHAAAPDSPHSDSGGGGGGMATGATSASAAGASPSRYESQ                     KRRDWNTFGQYLRNHRPPLSLARCSGAHVLEFLRYLDQFGKTKVHAPACPFFGHPAPP                     APCPCPLRQAWGSLDALVGRLRAAYEENGGRPENNPFGARAVRLYLREVREHQARARG                     VSYEKKKRKKPPHPSSAAAAHDDAANGALHHHHHMPPPPPGAAA&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;610..1224#tatcggctccttctcgcccagcttttgctcacgtcacatcaccttccacctccacccctccactcgctcgctcgcttgcttgctccaattaatacctcttctccttctcccccagcaactagcttccttctccgcttttgcagctcgccgccgccgccgccgccgccgccgcgacacggcgcgcatatggtcgtcgtcgtcgtcgtcgtcgtcgctggagaagacgaagaaagatagtagacctgagctgggggggcggtgaattcgccggagagctagctaaggtgagtttcgttttcggtttcggtttcgatcgatttgttggtgcagatgcatctgggagctagagaactatttatagtggctgcggtgcggtgcggcgtcgccacgccgcgcacgcgctcgcccacgtcgcgcgcgcgcgggcgcgcgtccactctctctctctcttggaccactgcgcgcgcgggcgcgcgtcggcgtcgccacggcttctcaagaacgcgcgcgcgcgcactgattcccagatagatagatctatatctgttcgtcttcctcagctatggtgtggtggtggtggtggtgtttgtggtgttgtgcagatcgacgatggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctgagccgagccgagcttgctccaagatcgccggaaaacgagctgctagcctcctacgcatgcactagttactccactccactccactccactatgatccctagctaggctgctcttgctactagcaaaactacggattaatctccatgcttgctactgctgctgctgctgctactgcatctaattaattaggttgattatttcct&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001189280.1 RefSeq:Os10g0478000]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 10]]&lt;br /&gt;
[[Category:Chromosome 10]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174408</id>
		<title>Os10g0478000</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174408"/>
				<updated>2014-05-30T04:18:32Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: /* Function */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; The rice ''TAWAWA1'' (''TAW1'') gene, a member of ALOG family, was identified as a  regulator of rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:YoshidaF1.jpg|right|thumb|200px|Fig 1. Characterization of ''taw1'' dominant mutants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF2.jpg|right|thumb|250px|Fig 2. Isolation of the ''TAW1'' gene &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF3.jpg|right|thumb|250px|Fig 3. Expression pattern of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF4.jpg|right|thumb|250px|Fig 4. ''SVP'' subfamily MADS-box genes work downstream of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF5.jpg|right|thumb|250px|Fig 5. Phenotype of ''taw1-D2''–introgressed Koshihikari BC5F2 plants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
In the dominant gain-of-function mutant ''tawawa1-D'', the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in ''TAWAWA1'' (''TAW1'') activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. ''TAW1'' encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the branch meristem (BMs). ''TAW1'' expression disappears from incipient spikelet meristems (SMs). It is demonstrated that members of the ''SHORT VEGETATIVE PHASE'' subfamily of MADS-box genes function downstream of ''TAW1''.Thus, ''TAW1'' is proposed as a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
Please input expression information here.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
''TAW1'' function might have evolved to ensure the production of sufficient numbers of spikelets. Unraveling the molecular function of ''TAW1'' will provide an opportunity for a greater understanding of meristem activity and identity, which is a fundamental issue in plant biology. Furthermore, such knowledge could be exploited to further increase crop yields. In addition, ''TAW1'' is of great interest with respect to the evolution of inflorescence architecture. ''TAW1'' function may be essential for the development of compound inflorescences, in which the branching pattern is crucial &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Yoshida A, Sasao M, Yasuno N, et al. (2013) TAWAWA1, a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition. Proceedings of the National Academy of Sciences 110: 767-772.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os10g0478000|&lt;br /&gt;
Description = Protein of unknown function DUF640 domain containing protein|&lt;br /&gt;
Version = NM_001189280.1 GI:297727690 GeneID:9266624|&lt;br /&gt;
Length = 1426 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os10g0478000, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 10|Chromosome 10]]|&lt;br /&gt;
AP = Chromosome 10:18345508..18346933|&lt;br /&gt;
CDS = 18345710..18346324|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MEFVAHAAAPDSPHSDSGGGGGGMATGATSASAAGASPSRYESQ                     KRRDWNTFGQYLRNHRPPLSLARCSGAHVLEFLRYLDQFGKTKVHAPACPFFGHPAPP                     APCPCPLRQAWGSLDALVGRLRAAYEENGGRPENNPFGARAVRLYLREVREHQARARG                     VSYEKKKRKKPPHPSSAAAAHDDAANGALHHHHHMPPPPPGAAA&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;610..1224#tatcggctccttctcgcccagcttttgctcacgtcacatcaccttccacctccacccctccactcgctcgctcgcttgcttgctccaattaatacctcttctccttctcccccagcaactagcttccttctccgcttttgcagctcgccgccgccgccgccgccgccgccgcgacacggcgcgcatatggtcgtcgtcgtcgtcgtcgtcgtcgctggagaagacgaagaaagatagtagacctgagctgggggggcggtgaattcgccggagagctagctaaggtgagtttcgttttcggtttcggtttcgatcgatttgttggtgcagatgcatctgggagctagagaactatttatagtggctgcggtgcggtgcggcgtcgccacgccgcgcacgcgctcgcccacgtcgcgcgcgcgcgggcgcgcgtccactctctctctctcttggaccactgcgcgcgcgggcgcgcgtcggcgtcgccacggcttctcaagaacgcgcgcgcgcgcactgattcccagatagatagatctatatctgttcgtcttcctcagctatggtgtggtggtggtggtggtgtttgtggtgttgtgcagatcgacgatggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctgagccgagccgagcttgctccaagatcgccggaaaacgagctgctagcctcctacgcatgcactagttactccactccactccactccactatgatccctagctaggctgctcttgctactagcaaaactacggattaatctccatgcttgctactgctgctgctgctgctactgcatctaattaattaggttgattatttcct&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001189280.1 RefSeq:Os10g0478000]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 10]]&lt;br /&gt;
[[Category:Chromosome 10]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174407</id>
		<title>Os10g0478000</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174407"/>
				<updated>2014-05-30T04:17:50Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: /* Function */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; The rice ''TAWAWA1'' (''TAW1'') gene, a member of ALOG family, was identified as a  regulator of rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:YoshidaF1.jpg|right|thumb|200px|Fig 1. Characterization of ''taw1'' dominant mutants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF2.jpg|right|thumb|200px|Fig 2. Isolation of the ''TAW1'' gene &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF3.jpg|right|thumb|200px|Fig 3. Expression pattern of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF4.jpg|right|thumb|200px|Fig 4. ''SVP'' subfamily MADS-box genes work downstream of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF5.jpg|right|thumb|200px|Fig 5. Phenotype of ''taw1-D2''–introgressed Koshihikari BC5F2 plants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
In the dominant gain-of-function mutant ''tawawa1-D'', the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in ''TAWAWA1'' (''TAW1'') activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. ''TAW1'' encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the branch meristem (BMs). ''TAW1'' expression disappears from incipient spikelet meristems (SMs). It is demonstrated that members of the ''SHORT VEGETATIVE PHASE'' subfamily of MADS-box genes function downstream of ''TAW1''.Thus, ''TAW1'' is proposed as a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
Please input expression information here.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
''TAW1'' function might have evolved to ensure the production of sufficient numbers of spikelets. Unraveling the molecular function of ''TAW1'' will provide an opportunity for a greater understanding of meristem activity and identity, which is a fundamental issue in plant biology. Furthermore, such knowledge could be exploited to further increase crop yields. In addition, ''TAW1'' is of great interest with respect to the evolution of inflorescence architecture. ''TAW1'' function may be essential for the development of compound inflorescences, in which the branching pattern is crucial &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Yoshida A, Sasao M, Yasuno N, et al. (2013) TAWAWA1, a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition. Proceedings of the National Academy of Sciences 110: 767-772.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os10g0478000|&lt;br /&gt;
Description = Protein of unknown function DUF640 domain containing protein|&lt;br /&gt;
Version = NM_001189280.1 GI:297727690 GeneID:9266624|&lt;br /&gt;
Length = 1426 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os10g0478000, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 10|Chromosome 10]]|&lt;br /&gt;
AP = Chromosome 10:18345508..18346933|&lt;br /&gt;
CDS = 18345710..18346324|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MEFVAHAAAPDSPHSDSGGGGGGMATGATSASAAGASPSRYESQ                     KRRDWNTFGQYLRNHRPPLSLARCSGAHVLEFLRYLDQFGKTKVHAPACPFFGHPAPP                     APCPCPLRQAWGSLDALVGRLRAAYEENGGRPENNPFGARAVRLYLREVREHQARARG                     VSYEKKKRKKPPHPSSAAAAHDDAANGALHHHHHMPPPPPGAAA&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;610..1224#tatcggctccttctcgcccagcttttgctcacgtcacatcaccttccacctccacccctccactcgctcgctcgcttgcttgctccaattaatacctcttctccttctcccccagcaactagcttccttctccgcttttgcagctcgccgccgccgccgccgccgccgccgcgacacggcgcgcatatggtcgtcgtcgtcgtcgtcgtcgtcgctggagaagacgaagaaagatagtagacctgagctgggggggcggtgaattcgccggagagctagctaaggtgagtttcgttttcggtttcggtttcgatcgatttgttggtgcagatgcatctgggagctagagaactatttatagtggctgcggtgcggtgcggcgtcgccacgccgcgcacgcgctcgcccacgtcgcgcgcgcgcgggcgcgcgtccactctctctctctcttggaccactgcgcgcgcgggcgcgcgtcggcgtcgccacggcttctcaagaacgcgcgcgcgcgcactgattcccagatagatagatctatatctgttcgtcttcctcagctatggtgtggtggtggtggtggtgtttgtggtgttgtgcagatcgacgatggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctgagccgagccgagcttgctccaagatcgccggaaaacgagctgctagcctcctacgcatgcactagttactccactccactccactccactatgatccctagctaggctgctcttgctactagcaaaactacggattaatctccatgcttgctactgctgctgctgctgctactgcatctaattaattaggttgattatttcct&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001189280.1 RefSeq:Os10g0478000]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 10]]&lt;br /&gt;
[[Category:Chromosome 10]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174405</id>
		<title>Os10g0478000</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174405"/>
				<updated>2014-05-30T04:16:19Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: /* Function */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; The rice ''TAWAWA1'' (''TAW1'') gene, a member of ALOG family, was identified as a  regulator of rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:YoshidaF1.jpg|right|thumb|100px|Fig 1. Characterization of ''taw1'' dominant mutants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF2.jpg|right|thumb|100px|Fig 2. Isolation of the ''TAW1'' gene &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF3.jpg|right|thumb|100px|Fig 3. Expression pattern of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF4.jpg|right|thumb|100px|Fig 4. ''SVP'' subfamily MADS-box genes work downstream of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF5.jpg|right|thumb|100px|Fig 5. Phenotype of ''taw1-D2''–introgressed Koshihikari BC5F2 plants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
In the dominant gain-of-function mutant ''tawawa1-D'', the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in ''TAWAWA1'' (''TAW1'') activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. ''TAW1'' encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the branch meristem (BMs). ''TAW1'' expression disappears from incipient spikelet meristems (SMs). It is demonstrated that members of the ''SHORT VEGETATIVE PHASE'' subfamily of MADS-box genes function downstream of ''TAW1''.Thus, ''TAW1'' is proposed as a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
Please input expression information here.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
''TAW1'' function might have evolved to ensure the production of sufficient numbers of spikelets. Unraveling the molecular function of ''TAW1'' will provide an opportunity for a greater understanding of meristem activity and identity, which is a fundamental issue in plant biology. Furthermore, such knowledge could be exploited to further increase crop yields. In addition, ''TAW1'' is of great interest with respect to the evolution of inflorescence architecture. ''TAW1'' function may be essential for the development of compound inflorescences, in which the branching pattern is crucial &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Yoshida A, Sasao M, Yasuno N, et al. (2013) TAWAWA1, a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition. Proceedings of the National Academy of Sciences 110: 767-772.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os10g0478000|&lt;br /&gt;
Description = Protein of unknown function DUF640 domain containing protein|&lt;br /&gt;
Version = NM_001189280.1 GI:297727690 GeneID:9266624|&lt;br /&gt;
Length = 1426 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os10g0478000, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 10|Chromosome 10]]|&lt;br /&gt;
AP = Chromosome 10:18345508..18346933|&lt;br /&gt;
CDS = 18345710..18346324|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MEFVAHAAAPDSPHSDSGGGGGGMATGATSASAAGASPSRYESQ                     KRRDWNTFGQYLRNHRPPLSLARCSGAHVLEFLRYLDQFGKTKVHAPACPFFGHPAPP                     APCPCPLRQAWGSLDALVGRLRAAYEENGGRPENNPFGARAVRLYLREVREHQARARG                     VSYEKKKRKKPPHPSSAAAAHDDAANGALHHHHHMPPPPPGAAA&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;610..1224#tatcggctccttctcgcccagcttttgctcacgtcacatcaccttccacctccacccctccactcgctcgctcgcttgcttgctccaattaatacctcttctccttctcccccagcaactagcttccttctccgcttttgcagctcgccgccgccgccgccgccgccgccgcgacacggcgcgcatatggtcgtcgtcgtcgtcgtcgtcgtcgctggagaagacgaagaaagatagtagacctgagctgggggggcggtgaattcgccggagagctagctaaggtgagtttcgttttcggtttcggtttcgatcgatttgttggtgcagatgcatctgggagctagagaactatttatagtggctgcggtgcggtgcggcgtcgccacgccgcgcacgcgctcgcccacgtcgcgcgcgcgcgggcgcgcgtccactctctctctctcttggaccactgcgcgcgcgggcgcgcgtcggcgtcgccacggcttctcaagaacgcgcgcgcgcgcactgattcccagatagatagatctatatctgttcgtcttcctcagctatggtgtggtggtggtggtggtgtttgtggtgttgtgcagatcgacgatggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctgagccgagccgagcttgctccaagatcgccggaaaacgagctgctagcctcctacgcatgcactagttactccactccactccactccactatgatccctagctaggctgctcttgctactagcaaaactacggattaatctccatgcttgctactgctgctgctgctgctactgcatctaattaattaggttgattatttcct&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001189280.1 RefSeq:Os10g0478000]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 10]]&lt;br /&gt;
[[Category:Chromosome 10]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174404</id>
		<title>Os10g0478000</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174404"/>
				<updated>2014-05-30T04:14:41Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: /* Function */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; The rice ''TAWAWA1'' (''TAW1'') gene, a member of ALOG family, was identified as a  regulator of rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:YoshidaF1.jpg|right|thumb|100px|Fig 1. Characterization of taw1 dominant mutants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF2.jpg|right|thumb|100px|Fig 2. Isolation of the ''TAW1'' gene &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF3.jpg|right|thumb|100px|Fig 3. Expression pattern of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF4.jpg|right|thumb|100px|Fig 4. SVP subfamily MADS-box genes work downstream of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF5.jpg|right|thumb|100px|Fig 5. Phenotype of ''taw1-D2''–introgressed Koshihikari BC5F2 plants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
In the dominant gain-of-function mutant ''tawawa1-D'', the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in ''TAWAWA1'' (''TAW1'') activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. ''TAW1'' encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the branch meristem (BMs). ''TAW1'' expression disappears from incipient spikelet meristems (SMs). It is demonstrated that members of the ''SHORT VEGETATIVE PHASE'' subfamily of MADS-box genes function downstream of ''TAW1''.Thus, ''TAW1'' is proposed as a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
Please input expression information here.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
''TAW1'' function might have evolved to ensure the production of sufficient numbers of spikelets. Unraveling the molecular function of ''TAW1'' will provide an opportunity for a greater understanding of meristem activity and identity, which is a fundamental issue in plant biology. Furthermore, such knowledge could be exploited to further increase crop yields. In addition, ''TAW1'' is of great interest with respect to the evolution of inflorescence architecture. ''TAW1'' function may be essential for the development of compound inflorescences, in which the branching pattern is crucial &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Yoshida A, Sasao M, Yasuno N, et al. (2013) TAWAWA1, a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition. Proceedings of the National Academy of Sciences 110: 767-772.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os10g0478000|&lt;br /&gt;
Description = Protein of unknown function DUF640 domain containing protein|&lt;br /&gt;
Version = NM_001189280.1 GI:297727690 GeneID:9266624|&lt;br /&gt;
Length = 1426 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os10g0478000, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 10|Chromosome 10]]|&lt;br /&gt;
AP = Chromosome 10:18345508..18346933|&lt;br /&gt;
CDS = 18345710..18346324|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MEFVAHAAAPDSPHSDSGGGGGGMATGATSASAAGASPSRYESQ                     KRRDWNTFGQYLRNHRPPLSLARCSGAHVLEFLRYLDQFGKTKVHAPACPFFGHPAPP                     APCPCPLRQAWGSLDALVGRLRAAYEENGGRPENNPFGARAVRLYLREVREHQARARG                     VSYEKKKRKKPPHPSSAAAAHDDAANGALHHHHHMPPPPPGAAA&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;610..1224#tatcggctccttctcgcccagcttttgctcacgtcacatcaccttccacctccacccctccactcgctcgctcgcttgcttgctccaattaatacctcttctccttctcccccagcaactagcttccttctccgcttttgcagctcgccgccgccgccgccgccgccgccgcgacacggcgcgcatatggtcgtcgtcgtcgtcgtcgtcgtcgctggagaagacgaagaaagatagtagacctgagctgggggggcggtgaattcgccggagagctagctaaggtgagtttcgttttcggtttcggtttcgatcgatttgttggtgcagatgcatctgggagctagagaactatttatagtggctgcggtgcggtgcggcgtcgccacgccgcgcacgcgctcgcccacgtcgcgcgcgcgcgggcgcgcgtccactctctctctctcttggaccactgcgcgcgcgggcgcgcgtcggcgtcgccacggcttctcaagaacgcgcgcgcgcgcactgattcccagatagatagatctatatctgttcgtcttcctcagctatggtgtggtggtggtggtggtgtttgtggtgttgtgcagatcgacgatggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctgagccgagccgagcttgctccaagatcgccggaaaacgagctgctagcctcctacgcatgcactagttactccactccactccactccactatgatccctagctaggctgctcttgctactagcaaaactacggattaatctccatgcttgctactgctgctgctgctgctactgcatctaattaattaggttgattatttcct&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001189280.1 RefSeq:Os10g0478000]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 10]]&lt;br /&gt;
[[Category:Chromosome 10]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174403</id>
		<title>Os10g0478000</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174403"/>
				<updated>2014-05-30T04:13:51Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; The rice ''TAWAWA1'' (''TAW1'') gene, a member of ALOG family, was identified as a  regulator of rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:YoshidaF1.jpg|right|thumb|100px|Fig 1. Characterization of taw1 dominant mutants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF2.jpg|right|thumb|150px|Fig 2. Isolation of the ''TAW1'' gene &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF3.jpg|right|thumb|150px|Fig 3. Expression pattern of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF4.jpg|right|thumb|100px|Fig 4. SVP subfamily MADS-box genes work downstream of ''TAW1'' &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]  [[File:YoshidaF5.jpg|right|thumb|150px|Fig 5. Phenotype of ''taw1-D2''–introgressed Koshihikari BC5F2 plants &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.]]&lt;br /&gt;
&lt;br /&gt;
In the dominant gain-of-function mutant ''tawawa1-D'', the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in ''TAWAWA1'' (''TAW1'') activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. ''TAW1'' encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the branch meristem (BMs). ''TAW1'' expression disappears from incipient spikelet meristems (SMs). It is demonstrated that members of the ''SHORT VEGETATIVE PHASE'' subfamily of MADS-box genes function downstream of ''TAW1''.Thus, ''TAW1'' is proposed as a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
Please input expression information here.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
''TAW1'' function might have evolved to ensure the production of sufficient numbers of spikelets. Unraveling the molecular function of ''TAW1'' will provide an opportunity for a greater understanding of meristem activity and identity, which is a fundamental issue in plant biology. Furthermore, such knowledge could be exploited to further increase crop yields. In addition, ''TAW1'' is of great interest with respect to the evolution of inflorescence architecture. ''TAW1'' function may be essential for the development of compound inflorescences, in which the branching pattern is crucial &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Yoshida A, Sasao M, Yasuno N, et al. (2013) TAWAWA1, a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition. Proceedings of the National Academy of Sciences 110: 767-772.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os10g0478000|&lt;br /&gt;
Description = Protein of unknown function DUF640 domain containing protein|&lt;br /&gt;
Version = NM_001189280.1 GI:297727690 GeneID:9266624|&lt;br /&gt;
Length = 1426 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os10g0478000, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 10|Chromosome 10]]|&lt;br /&gt;
AP = Chromosome 10:18345508..18346933|&lt;br /&gt;
CDS = 18345710..18346324|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MEFVAHAAAPDSPHSDSGGGGGGMATGATSASAAGASPSRYESQ                     KRRDWNTFGQYLRNHRPPLSLARCSGAHVLEFLRYLDQFGKTKVHAPACPFFGHPAPP                     APCPCPLRQAWGSLDALVGRLRAAYEENGGRPENNPFGARAVRLYLREVREHQARARG                     VSYEKKKRKKPPHPSSAAAAHDDAANGALHHHHHMPPPPPGAAA&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;610..1224#tatcggctccttctcgcccagcttttgctcacgtcacatcaccttccacctccacccctccactcgctcgctcgcttgcttgctccaattaatacctcttctccttctcccccagcaactagcttccttctccgcttttgcagctcgccgccgccgccgccgccgccgccgcgacacggcgcgcatatggtcgtcgtcgtcgtcgtcgtcgtcgctggagaagacgaagaaagatagtagacctgagctgggggggcggtgaattcgccggagagctagctaaggtgagtttcgttttcggtttcggtttcgatcgatttgttggtgcagatgcatctgggagctagagaactatttatagtggctgcggtgcggtgcggcgtcgccacgccgcgcacgcgctcgcccacgtcgcgcgcgcgcgggcgcgcgtccactctctctctctcttggaccactgcgcgcgcgggcgcgcgtcggcgtcgccacggcttctcaagaacgcgcgcgcgcgcactgattcccagatagatagatctatatctgttcgtcttcctcagctatggtgtggtggtggtggtggtgtttgtggtgttgtgcagatcgacgatggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctgagccgagccgagcttgctccaagatcgccggaaaacgagctgctagcctcctacgcatgcactagttactccactccactccactccactatgatccctagctaggctgctcttgctactagcaaaactacggattaatctccatgcttgctactgctgctgctgctgctactgcatctaattaattaggttgattatttcct&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001189280.1 RefSeq:Os10g0478000]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 10]]&lt;br /&gt;
[[Category:Chromosome 10]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174402</id>
		<title>Os10g0478000</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174402"/>
				<updated>2014-05-30T04:12:19Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; The rice ''TAWAWA1'' (''TAW1'') gene, a member of ALOG family, was identified as a  regulator of rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:YoshidaF1.jpg|right|thumb|100px|Fig 1. Characterization of taw1 dominant mutants. (from reference &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;).]]  [[File:YoshidaF2.jpg|right|thumb|150px|Fig 2. Isolation of the ''TAW1'' gene. (from reference &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;).]]  [[File:YoshidaF3.jpg|right|thumb|150px|Fig 3. Expression pattern of ''TAW1''. (from reference &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;).]]  [[File:YoshidaF4.jpg|right|thumb|100px|Fig 4. SVP subfamily MADS-box genes work downstream of ''TAW1''. (from reference &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;).]]  [[File:YoshidaF5.jpg|right|thumb|150px|Fig 5. Phenotype of ''taw1-D2''–introgressed Koshihikari BC5F2 plants. (from reference &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;).]]&lt;br /&gt;
&lt;br /&gt;
In the dominant gain-of-function mutant ''tawawa1-D'', the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in ''TAWAWA1'' (''TAW1'') activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. ''TAW1'' encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the branch meristem (BMs). ''TAW1'' expression disappears from incipient spikelet meristems (SMs). It is demonstrated that members of the ''SHORT VEGETATIVE PHASE'' subfamily of MADS-box genes function downstream of ''TAW1''.Thus, ''TAW1'' is proposed as a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
Please input expression information here.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
''TAW1'' function might have evolved to ensure the production of sufficient numbers of spikelets. Unraveling the molecular function of ''TAW1'' will provide an opportunity for a greater understanding of meristem activity and identity, which is a fundamental issue in plant biology. Furthermore, such knowledge could be exploited to further increase crop yields. In addition, ''TAW1'' is of great interest with respect to the evolution of inflorescence architecture. ''TAW1'' function may be essential for the development of compound inflorescences, in which the branching pattern is crucial &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Yoshida A, Sasao M, Yasuno N, et al. (2013) TAWAWA1, a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition. Proceedings of the National Academy of Sciences 110: 767-772.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os10g0478000|&lt;br /&gt;
Description = Protein of unknown function DUF640 domain containing protein|&lt;br /&gt;
Version = NM_001189280.1 GI:297727690 GeneID:9266624|&lt;br /&gt;
Length = 1426 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os10g0478000, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 10|Chromosome 10]]|&lt;br /&gt;
AP = Chromosome 10:18345508..18346933|&lt;br /&gt;
CDS = 18345710..18346324|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MEFVAHAAAPDSPHSDSGGGGGGMATGATSASAAGASPSRYESQ                     KRRDWNTFGQYLRNHRPPLSLARCSGAHVLEFLRYLDQFGKTKVHAPACPFFGHPAPP                     APCPCPLRQAWGSLDALVGRLRAAYEENGGRPENNPFGARAVRLYLREVREHQARARG                     VSYEKKKRKKPPHPSSAAAAHDDAANGALHHHHHMPPPPPGAAA&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;610..1224#tatcggctccttctcgcccagcttttgctcacgtcacatcaccttccacctccacccctccactcgctcgctcgcttgcttgctccaattaatacctcttctccttctcccccagcaactagcttccttctccgcttttgcagctcgccgccgccgccgccgccgccgccgcgacacggcgcgcatatggtcgtcgtcgtcgtcgtcgtcgtcgctggagaagacgaagaaagatagtagacctgagctgggggggcggtgaattcgccggagagctagctaaggtgagtttcgttttcggtttcggtttcgatcgatttgttggtgcagatgcatctgggagctagagaactatttatagtggctgcggtgcggtgcggcgtcgccacgccgcgcacgcgctcgcccacgtcgcgcgcgcgcgggcgcgcgtccactctctctctctcttggaccactgcgcgcgcgggcgcgcgtcggcgtcgccacggcttctcaagaacgcgcgcgcgcgcactgattcccagatagatagatctatatctgttcgtcttcctcagctatggtgtggtggtggtggtggtgtttgtggtgttgtgcagatcgacgatggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctgagccgagccgagcttgctccaagatcgccggaaaacgagctgctagcctcctacgcatgcactagttactccactccactccactccactatgatccctagctaggctgctcttgctactagcaaaactacggattaatctccatgcttgctactgctgctgctgctgctactgcatctaattaattaggttgattatttcct&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001189280.1 RefSeq:Os10g0478000]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 10]]&lt;br /&gt;
[[Category:Chromosome 10]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174401</id>
		<title>Os10g0478000</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174401"/>
				<updated>2014-05-30T04:11:29Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: /* Function */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; The rice ''TAWAWA1'' (''TAW1'') gene, a member of ALOG family, was identified as a  regulator of rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:YoshidaF1.jpg|right|thumb|100px|Fig 1. Characterization of taw1 dominant mutants. (from reference &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;).]]  [[File:YoshidaF2.jpg|right|thumb|100px|Fig 2. Isolation of the ''TAW1'' gene. (from reference &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;).]]  [[File:YoshidaF3.jpg|right|thumb|100px|Fig 3. Expression pattern of ''TAW1''. (from reference &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;).]]  [[File:YoshidaF4.jpg|right|thumb|100px|Fig 4. SVP subfamily MADS-box genes work downstream of ''TAW1''. (from reference &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;).]]  [[File:YoshidaF5.jpg|right|thumb|100px|Fig 5. Phenotype of ''taw1-D2''–introgressed Koshihikari BC5F2 plants. (from reference &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;).]]&lt;br /&gt;
&lt;br /&gt;
In the dominant gain-of-function mutant ''tawawa1-D'', the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in ''TAWAWA1'' (''TAW1'') activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. ''TAW1'' encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the branch meristem (BMs). ''TAW1'' expression disappears from incipient spikelet meristems (SMs). It is demonstrated that members of the ''SHORT VEGETATIVE PHASE'' subfamily of MADS-box genes function downstream of ''TAW1''.Thus, ''TAW1'' is proposed as a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
Please input expression information here.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
''TAW1'' function might have evolved to ensure the production of sufficient numbers of spikelets. Unraveling the molecular function of ''TAW1'' will provide an opportunity for a greater understanding of meristem activity and identity, which is a fundamental issue in plant biology. Furthermore, such knowledge could be exploited to further increase crop yields. In addition, ''TAW1'' is of great interest with respect to the evolution of inflorescence architecture. ''TAW1'' function may be essential for the development of compound inflorescences, in which the branching pattern is crucial &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Yoshida A, Sasao M, Yasuno N, et al. (2013) TAWAWA1, a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition. Proceedings of the National Academy of Sciences 110: 767-772.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os10g0478000|&lt;br /&gt;
Description = Protein of unknown function DUF640 domain containing protein|&lt;br /&gt;
Version = NM_001189280.1 GI:297727690 GeneID:9266624|&lt;br /&gt;
Length = 1426 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os10g0478000, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 10|Chromosome 10]]|&lt;br /&gt;
AP = Chromosome 10:18345508..18346933|&lt;br /&gt;
CDS = 18345710..18346324|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MEFVAHAAAPDSPHSDSGGGGGGMATGATSASAAGASPSRYESQ                     KRRDWNTFGQYLRNHRPPLSLARCSGAHVLEFLRYLDQFGKTKVHAPACPFFGHPAPP                     APCPCPLRQAWGSLDALVGRLRAAYEENGGRPENNPFGARAVRLYLREVREHQARARG                     VSYEKKKRKKPPHPSSAAAAHDDAANGALHHHHHMPPPPPGAAA&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;610..1224#tatcggctccttctcgcccagcttttgctcacgtcacatcaccttccacctccacccctccactcgctcgctcgcttgcttgctccaattaatacctcttctccttctcccccagcaactagcttccttctccgcttttgcagctcgccgccgccgccgccgccgccgccgcgacacggcgcgcatatggtcgtcgtcgtcgtcgtcgtcgtcgctggagaagacgaagaaagatagtagacctgagctgggggggcggtgaattcgccggagagctagctaaggtgagtttcgttttcggtttcggtttcgatcgatttgttggtgcagatgcatctgggagctagagaactatttatagtggctgcggtgcggtgcggcgtcgccacgccgcgcacgcgctcgcccacgtcgcgcgcgcgcgggcgcgcgtccactctctctctctcttggaccactgcgcgcgcgggcgcgcgtcggcgtcgccacggcttctcaagaacgcgcgcgcgcgcactgattcccagatagatagatctatatctgttcgtcttcctcagctatggtgtggtggtggtggtggtgtttgtggtgttgtgcagatcgacgatggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctgagccgagccgagcttgctccaagatcgccggaaaacgagctgctagcctcctacgcatgcactagttactccactccactccactccactatgatccctagctaggctgctcttgctactagcaaaactacggattaatctccatgcttgctactgctgctgctgctgctactgcatctaattaattaggttgattatttcct&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001189280.1 RefSeq:Os10g0478000]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 10]]&lt;br /&gt;
[[Category:Chromosome 10]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174397</id>
		<title>Os10g0478000</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174397"/>
				<updated>2014-05-30T04:06:27Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: /* Function */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; The rice ''TAWAWA1'' (''TAW1'') gene, a member of ALOG family, was identified as a  regulator of rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:YoshidaF1.jpg|right|thumb|100px|''Characterization of taw1 dominant mutants. (from reference &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;).'']]&lt;br /&gt;
&lt;br /&gt;
In the dominant gain-of-function mutant ''tawawa1-D'', the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in ''TAWAWA1'' (''TAW1'') activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. ''TAW1'' encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the branch meristem (BMs). ''TAW1'' expression disappears from incipient spikelet meristems (SMs). It is demonstrated that members of the ''SHORT VEGETATIVE PHASE'' subfamily of MADS-box genes function downstream of ''TAW1''.Thus, ''TAW1'' is proposed as a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
Please input expression information here.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
''TAW1'' function might have evolved to ensure the production of sufficient numbers of spikelets. Unraveling the molecular function of ''TAW1'' will provide an opportunity for a greater understanding of meristem activity and identity, which is a fundamental issue in plant biology. Furthermore, such knowledge could be exploited to further increase crop yields. In addition, ''TAW1'' is of great interest with respect to the evolution of inflorescence architecture. ''TAW1'' function may be essential for the development of compound inflorescences, in which the branching pattern is crucial &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Yoshida A, Sasao M, Yasuno N, et al. (2013) TAWAWA1, a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition. Proceedings of the National Academy of Sciences 110: 767-772.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os10g0478000|&lt;br /&gt;
Description = Protein of unknown function DUF640 domain containing protein|&lt;br /&gt;
Version = NM_001189280.1 GI:297727690 GeneID:9266624|&lt;br /&gt;
Length = 1426 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os10g0478000, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 10|Chromosome 10]]|&lt;br /&gt;
AP = Chromosome 10:18345508..18346933|&lt;br /&gt;
CDS = 18345710..18346324|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MEFVAHAAAPDSPHSDSGGGGGGMATGATSASAAGASPSRYESQ                     KRRDWNTFGQYLRNHRPPLSLARCSGAHVLEFLRYLDQFGKTKVHAPACPFFGHPAPP                     APCPCPLRQAWGSLDALVGRLRAAYEENGGRPENNPFGARAVRLYLREVREHQARARG                     VSYEKKKRKKPPHPSSAAAAHDDAANGALHHHHHMPPPPPGAAA&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;610..1224#tatcggctccttctcgcccagcttttgctcacgtcacatcaccttccacctccacccctccactcgctcgctcgcttgcttgctccaattaatacctcttctccttctcccccagcaactagcttccttctccgcttttgcagctcgccgccgccgccgccgccgccgccgcgacacggcgcgcatatggtcgtcgtcgtcgtcgtcgtcgtcgctggagaagacgaagaaagatagtagacctgagctgggggggcggtgaattcgccggagagctagctaaggtgagtttcgttttcggtttcggtttcgatcgatttgttggtgcagatgcatctgggagctagagaactatttatagtggctgcggtgcggtgcggcgtcgccacgccgcgcacgcgctcgcccacgtcgcgcgcgcgcgggcgcgcgtccactctctctctctcttggaccactgcgcgcgcgggcgcgcgtcggcgtcgccacggcttctcaagaacgcgcgcgcgcgcactgattcccagatagatagatctatatctgttcgtcttcctcagctatggtgtggtggtggtggtggtgtttgtggtgttgtgcagatcgacgatggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctgagccgagccgagcttgctccaagatcgccggaaaacgagctgctagcctcctacgcatgcactagttactccactccactccactccactatgatccctagctaggctgctcttgctactagcaaaactacggattaatctccatgcttgctactgctgctgctgctgctactgcatctaattaattaggttgattatttcct&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001189280.1 RefSeq:Os10g0478000]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 10]]&lt;br /&gt;
[[Category:Chromosome 10]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:YoshidaF5.jpg&amp;diff=174395</id>
		<title>File:YoshidaF5.jpg</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:YoshidaF5.jpg&amp;diff=174395"/>
				<updated>2014-05-30T04:05:40Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:YoshidaF4.jpg&amp;diff=174394</id>
		<title>File:YoshidaF4.jpg</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:YoshidaF4.jpg&amp;diff=174394"/>
				<updated>2014-05-30T04:05:25Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:YoshidaF3.jpg&amp;diff=174393</id>
		<title>File:YoshidaF3.jpg</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:YoshidaF3.jpg&amp;diff=174393"/>
				<updated>2014-05-30T04:05:11Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:YoshidaF2.jpg&amp;diff=174391</id>
		<title>File:YoshidaF2.jpg</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:YoshidaF2.jpg&amp;diff=174391"/>
				<updated>2014-05-30T04:04:55Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174387</id>
		<title>Os10g0478000</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174387"/>
				<updated>2014-05-30T04:02:41Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; The rice ''TAWAWA1'' (''TAW1'') gene, a member of ALOG family, was identified as a  regulator of rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:YoshidaF1.jpg|right|thumb|50px|''Characterization of taw1 dominant mutants. (from reference &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;).'']]&lt;br /&gt;
&lt;br /&gt;
In the dominant gain-of-function mutant ''tawawa1-D'', the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in ''TAWAWA1'' (''TAW1'') activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. ''TAW1'' encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the branch meristem (BMs). ''TAW1'' expression disappears from incipient spikelet meristems (SMs). It is demonstrated that members of the ''SHORT VEGETATIVE PHASE'' subfamily of MADS-box genes function downstream of ''TAW1''.Thus, ''TAW1'' is proposed as a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
Please input expression information here.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
''TAW1'' function might have evolved to ensure the production of sufficient numbers of spikelets. Unraveling the molecular function of ''TAW1'' will provide an opportunity for a greater understanding of meristem activity and identity, which is a fundamental issue in plant biology. Furthermore, such knowledge could be exploited to further increase crop yields. In addition, ''TAW1'' is of great interest with respect to the evolution of inflorescence architecture. ''TAW1'' function may be essential for the development of compound inflorescences, in which the branching pattern is crucial &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Yoshida A, Sasao M, Yasuno N, et al. (2013) TAWAWA1, a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition. Proceedings of the National Academy of Sciences 110: 767-772.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os10g0478000|&lt;br /&gt;
Description = Protein of unknown function DUF640 domain containing protein|&lt;br /&gt;
Version = NM_001189280.1 GI:297727690 GeneID:9266624|&lt;br /&gt;
Length = 1426 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os10g0478000, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 10|Chromosome 10]]|&lt;br /&gt;
AP = Chromosome 10:18345508..18346933|&lt;br /&gt;
CDS = 18345710..18346324|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MEFVAHAAAPDSPHSDSGGGGGGMATGATSASAAGASPSRYESQ                     KRRDWNTFGQYLRNHRPPLSLARCSGAHVLEFLRYLDQFGKTKVHAPACPFFGHPAPP                     APCPCPLRQAWGSLDALVGRLRAAYEENGGRPENNPFGARAVRLYLREVREHQARARG                     VSYEKKKRKKPPHPSSAAAAHDDAANGALHHHHHMPPPPPGAAA&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;610..1224#tatcggctccttctcgcccagcttttgctcacgtcacatcaccttccacctccacccctccactcgctcgctcgcttgcttgctccaattaatacctcttctccttctcccccagcaactagcttccttctccgcttttgcagctcgccgccgccgccgccgccgccgccgcgacacggcgcgcatatggtcgtcgtcgtcgtcgtcgtcgtcgctggagaagacgaagaaagatagtagacctgagctgggggggcggtgaattcgccggagagctagctaaggtgagtttcgttttcggtttcggtttcgatcgatttgttggtgcagatgcatctgggagctagagaactatttatagtggctgcggtgcggtgcggcgtcgccacgccgcgcacgcgctcgcccacgtcgcgcgcgcgcgggcgcgcgtccactctctctctctcttggaccactgcgcgcgcgggcgcgcgtcggcgtcgccacggcttctcaagaacgcgcgcgcgcgcactgattcccagatagatagatctatatctgttcgtcttcctcagctatggtgtggtggtggtggtggtgtttgtggtgttgtgcagatcgacgatggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctgagccgagccgagcttgctccaagatcgccggaaaacgagctgctagcctcctacgcatgcactagttactccactccactccactccactatgatccctagctaggctgctcttgctactagcaaaactacggattaatctccatgcttgctactgctgctgctgctgctactgcatctaattaattaggttgattatttcct&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001189280.1 RefSeq:Os10g0478000]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 10]]&lt;br /&gt;
[[Category:Chromosome 10]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174386</id>
		<title>Os10g0478000</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174386"/>
				<updated>2014-05-30T04:02:14Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; The rice ''TAWAWA1'' (''TAW1'') gene, a member of ALOG family, was identified as a  regulator of rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
[[File:YoshidaF1.jpg|right|thumb|300px|''Characterization of taw1 dominant mutants. (from reference &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;).'']]&lt;br /&gt;
&lt;br /&gt;
In the dominant gain-of-function mutant ''tawawa1-D'', the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in ''TAWAWA1'' (''TAW1'') activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. ''TAW1'' encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the branch meristem (BMs). ''TAW1'' expression disappears from incipient spikelet meristems (SMs). It is demonstrated that members of the ''SHORT VEGETATIVE PHASE'' subfamily of MADS-box genes function downstream of ''TAW1''.Thus, ''TAW1'' is proposed as a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
Please input expression information here.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
''TAW1'' function might have evolved to ensure the production of sufficient numbers of spikelets. Unraveling the molecular function of ''TAW1'' will provide an opportunity for a greater understanding of meristem activity and identity, which is a fundamental issue in plant biology. Furthermore, such knowledge could be exploited to further increase crop yields. In addition, ''TAW1'' is of great interest with respect to the evolution of inflorescence architecture. ''TAW1'' function may be essential for the development of compound inflorescences, in which the branching pattern is crucial &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Yoshida A, Sasao M, Yasuno N, et al. (2013) TAWAWA1, a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition. Proceedings of the National Academy of Sciences 110: 767-772.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os10g0478000|&lt;br /&gt;
Description = Protein of unknown function DUF640 domain containing protein|&lt;br /&gt;
Version = NM_001189280.1 GI:297727690 GeneID:9266624|&lt;br /&gt;
Length = 1426 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os10g0478000, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 10|Chromosome 10]]|&lt;br /&gt;
AP = Chromosome 10:18345508..18346933|&lt;br /&gt;
CDS = 18345710..18346324|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MEFVAHAAAPDSPHSDSGGGGGGMATGATSASAAGASPSRYESQ                     KRRDWNTFGQYLRNHRPPLSLARCSGAHVLEFLRYLDQFGKTKVHAPACPFFGHPAPP                     APCPCPLRQAWGSLDALVGRLRAAYEENGGRPENNPFGARAVRLYLREVREHQARARG                     VSYEKKKRKKPPHPSSAAAAHDDAANGALHHHHHMPPPPPGAAA&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;610..1224#tatcggctccttctcgcccagcttttgctcacgtcacatcaccttccacctccacccctccactcgctcgctcgcttgcttgctccaattaatacctcttctccttctcccccagcaactagcttccttctccgcttttgcagctcgccgccgccgccgccgccgccgccgcgacacggcgcgcatatggtcgtcgtcgtcgtcgtcgtcgtcgctggagaagacgaagaaagatagtagacctgagctgggggggcggtgaattcgccggagagctagctaaggtgagtttcgttttcggtttcggtttcgatcgatttgttggtgcagatgcatctgggagctagagaactatttatagtggctgcggtgcggtgcggcgtcgccacgccgcgcacgcgctcgcccacgtcgcgcgcgcgcgggcgcgcgtccactctctctctctcttggaccactgcgcgcgcgggcgcgcgtcggcgtcgccacggcttctcaagaacgcgcgcgcgcgcactgattcccagatagatagatctatatctgttcgtcttcctcagctatggtgtggtggtggtggtggtgtttgtggtgttgtgcagatcgacgatggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctgagccgagccgagcttgctccaagatcgccggaaaacgagctgctagcctcctacgcatgcactagttactccactccactccactccactatgatccctagctaggctgctcttgctactagcaaaactacggattaatctccatgcttgctactgctgctgctgctgctactgcatctaattaattaggttgattatttcct&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001189280.1 RefSeq:Os10g0478000]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 10]]&lt;br /&gt;
[[Category:Chromosome 10]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:YoshidaF1.jpg&amp;diff=174376</id>
		<title>File:YoshidaF1.jpg</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:YoshidaF1.jpg&amp;diff=174376"/>
				<updated>2014-05-30T03:52:58Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174358</id>
		<title>Os10g0478000</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174358"/>
				<updated>2014-05-30T03:37:52Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: /* Evolution */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; The rice ''TAWAWA1'' (''TAW1'') gene, a member of ALOG family, was identified as a  regulator of rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
In the dominant gain-of-function mutant ''tawawa1-D'', the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in ''TAWAWA1'' (''TAW1'') activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. ''TAW1'' encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the branch meristem (BMs). ''TAW1'' expression disappears from incipient spikelet meristems (SMs). It is demonstrated that members of the ''SHORT VEGETATIVE PHASE'' subfamily of MADS-box genes function downstream of ''TAW1''.Thus, ''TAW1'' is proposed as a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
Please input expression information here.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
''TAW1'' function might have evolved to ensure the production of sufficient numbers of spikelets. Unraveling the molecular function of ''TAW1'' will provide an opportunity for a greater understanding of meristem activity and identity, which is a fundamental issue in plant biology. Furthermore, such knowledge could be exploited to further increase crop yields. In addition, ''TAW1'' is of great interest with respect to the evolution of inflorescence architecture. ''TAW1'' function may be essential for the development of compound inflorescences, in which the branching pattern is crucial &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Yoshida A, Sasao M, Yasuno N, et al. (2013) TAWAWA1, a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition. Proceedings of the National Academy of Sciences 110: 767-772.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os10g0478000|&lt;br /&gt;
Description = Protein of unknown function DUF640 domain containing protein|&lt;br /&gt;
Version = NM_001189280.1 GI:297727690 GeneID:9266624|&lt;br /&gt;
Length = 1426 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os10g0478000, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 10|Chromosome 10]]|&lt;br /&gt;
AP = Chromosome 10:18345508..18346933|&lt;br /&gt;
CDS = 18345710..18346324|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MEFVAHAAAPDSPHSDSGGGGGGMATGATSASAAGASPSRYESQ                     KRRDWNTFGQYLRNHRPPLSLARCSGAHVLEFLRYLDQFGKTKVHAPACPFFGHPAPP                     APCPCPLRQAWGSLDALVGRLRAAYEENGGRPENNPFGARAVRLYLREVREHQARARG                     VSYEKKKRKKPPHPSSAAAAHDDAANGALHHHHHMPPPPPGAAA&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;610..1224#tatcggctccttctcgcccagcttttgctcacgtcacatcaccttccacctccacccctccactcgctcgctcgcttgcttgctccaattaatacctcttctccttctcccccagcaactagcttccttctccgcttttgcagctcgccgccgccgccgccgccgccgccgcgacacggcgcgcatatggtcgtcgtcgtcgtcgtcgtcgtcgctggagaagacgaagaaagatagtagacctgagctgggggggcggtgaattcgccggagagctagctaaggtgagtttcgttttcggtttcggtttcgatcgatttgttggtgcagatgcatctgggagctagagaactatttatagtggctgcggtgcggtgcggcgtcgccacgccgcgcacgcgctcgcccacgtcgcgcgcgcgcgggcgcgcgtccactctctctctctcttggaccactgcgcgcgcgggcgcgcgtcggcgtcgccacggcttctcaagaacgcgcgcgcgcgcactgattcccagatagatagatctatatctgttcgtcttcctcagctatggtgtggtggtggtggtggtgtttgtggtgttgtgcagatcgacgatggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctgagccgagccgagcttgctccaagatcgccggaaaacgagctgctagcctcctacgcatgcactagttactccactccactccactccactatgatccctagctaggctgctcttgctactagcaaaactacggattaatctccatgcttgctactgctgctgctgctgctactgcatctaattaattaggttgattatttcct&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001189280.1 RefSeq:Os10g0478000]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 10]]&lt;br /&gt;
[[Category:Chromosome 10]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174326</id>
		<title>Os10g0478000</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Os10g0478000&amp;diff=174326"/>
				<updated>2014-05-30T03:11:38Z</updated>
		
		<summary type="html">&lt;p&gt;Chenyaping: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; The rice ''TAWAWA1'' (''TAW1'') gene, a member of ALOG family, was identified as a  regulator of rice inflorescence architecture.&lt;br /&gt;
&lt;br /&gt;
==Annotated Information==&lt;br /&gt;
===Function===&lt;br /&gt;
In the dominant gain-of-function mutant ''tawawa1-D'', the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in ''TAWAWA1'' (''TAW1'') activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. ''TAW1'' encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the branch meristem (BMs). ''TAW1'' expression disappears from incipient spikelet meristems (SMs). It is demonstrated that members of the ''SHORT VEGETATIVE PHASE'' subfamily of MADS-box genes function downstream of ''TAW1''.Thus, ''TAW1'' is proposed as a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity &amp;lt;ref name=&amp;quot;ref1&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
===Expression===&lt;br /&gt;
Please input expression information here.&lt;br /&gt;
&lt;br /&gt;
===Evolution===&lt;br /&gt;
Please input evolution information here.&lt;br /&gt;
&lt;br /&gt;
You can also add sub-section(s) at will.&lt;br /&gt;
&lt;br /&gt;
==Labs working on this gene==&lt;br /&gt;
*Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references&amp;gt;&lt;br /&gt;
&amp;lt;ref name=&amp;quot;ref1&amp;quot;&amp;gt;Yoshida A, Sasao M, Yasuno N, et al. (2013) TAWAWA1, a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition. Proceedings of the National Academy of Sciences 110: 767-772.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structured Information==&lt;br /&gt;
{{JaponicaGene|&lt;br /&gt;
GeneName = Os10g0478000|&lt;br /&gt;
Description = Protein of unknown function DUF640 domain containing protein|&lt;br /&gt;
Version = NM_001189280.1 GI:297727690 GeneID:9266624|&lt;br /&gt;
Length = 1426 bp|&lt;br /&gt;
Definition = Oryza sativa Japonica Group Os10g0478000, complete gene.|&lt;br /&gt;
Source = Oryza sativa Japonica Group&lt;br /&gt;
&lt;br /&gt;
  ORGANISM  Oryza sativa Japonica Group&lt;br /&gt;
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;&lt;br /&gt;
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP&lt;br /&gt;
            clade; Ehrhartoideae; Oryzeae; Oryza.&lt;br /&gt;
|&lt;br /&gt;
Chromosome = [[:category:Japonica Chromosome 10|Chromosome 10]]|&lt;br /&gt;
AP = Chromosome 10:18345508..18346933|&lt;br /&gt;
CDS = 18345710..18346324|&lt;br /&gt;
GCID = &amp;lt;gbrowseImage1&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage1&amp;gt;|&lt;br /&gt;
GSID = &amp;lt;gbrowseImage2&amp;gt;&lt;br /&gt;
name=NC_008403:18345508..18346933&lt;br /&gt;
source=RiceChromosome10&lt;br /&gt;
preset=GeneLocation&lt;br /&gt;
&amp;lt;/gbrowseImage2&amp;gt;|&lt;br /&gt;
CDNA = &amp;lt;cdnaseq&amp;gt;atggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctga&amp;lt;/cdnaseq&amp;gt;|&lt;br /&gt;
AA = &amp;lt;aaseq&amp;gt;MEFVAHAAAPDSPHSDSGGGGGGMATGATSASAAGASPSRYESQ                     KRRDWNTFGQYLRNHRPPLSLARCSGAHVLEFLRYLDQFGKTKVHAPACPFFGHPAPP                     APCPCPLRQAWGSLDALVGRLRAAYEENGGRPENNPFGARAVRLYLREVREHQARARG                     VSYEKKKRKKPPHPSSAAAAHDDAANGALHHHHHMPPPPPGAAA&amp;lt;/aaseq&amp;gt;|&lt;br /&gt;
DNA = &amp;lt;dnaseqindica&amp;gt;610..1224#tatcggctccttctcgcccagcttttgctcacgtcacatcaccttccacctccacccctccactcgctcgctcgcttgcttgctccaattaatacctcttctccttctcccccagcaactagcttccttctccgcttttgcagctcgccgccgccgccgccgccgccgccgcgacacggcgcgcatatggtcgtcgtcgtcgtcgtcgtcgtcgctggagaagacgaagaaagatagtagacctgagctgggggggcggtgaattcgccggagagctagctaaggtgagtttcgttttcggtttcggtttcgatcgatttgttggtgcagatgcatctgggagctagagaactatttatagtggctgcggtgcggtgcggcgtcgccacgccgcgcacgcgctcgcccacgtcgcgcgcgcgcgggcgcgcgtccactctctctctctcttggaccactgcgcgcgcgggcgcgcgtcggcgtcgccacggcttctcaagaacgcgcgcgcgcgcactgattcccagatagatagatctatatctgttcgtcttcctcagctatggtgtggtggtggtggtggtgtttgtggtgttgtgcagatcgacgatggagttcgtggcgcacgcggcggcgccggacagcccgcactcggacagcggcggaggaggagggggaatggcgacgggggcgacgtcggcgtcggcggcgggggcgtcgccgagcaggtacgagtcgcagaagcggcgggactggaacacgttcgggcagtacctccgcaaccaccggccgccgctgtcgctggcgcggtgcagcggcgcgcacgtcctggagttcctccgctacctggaccagttcggcaagaccaaggtgcacgcgccggcgtgccccttcttcggccacccggcgccgccggcgccgtgcccgtgcccgcttcgccaggcgtggggcagcctcgacgccctcgtcggccgcctccgcgccgcctacgaggagaacggcggccgccccgagaacaaccccttcggcgcccgcgccgtccgcctctacctccgcgaggtccgcgagcaccaggcgcgcgcacgcggcgtcagctacgagaagaagaagcgcaagaagccaccccacccctcctccgccgccgccgcgcacgacgacgccgccaacggcgccctccaccaccaccaccacatgccgccgcctcctcccggcgccgccgcctgagccgagccgagcttgctccaagatcgccggaaaacgagctgctagcctcctacgcatgcactagttactccactccactccactccactatgatccctagctaggctgctcttgctactagcaaaactacggattaatctccatgcttgctactgctgctgctgctgctactgcatctaattaattaggttgattatttcct&amp;lt;/dnaseqindica&amp;gt;|&lt;br /&gt;
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001189280.1 RefSeq:Os10g0478000]|&lt;br /&gt;
}}&lt;br /&gt;
[[Category:Genes]]&lt;br /&gt;
[[Category:Japonica mRNA]]&lt;br /&gt;
[[Category:Oryza Sativa Japonica Group]]&lt;br /&gt;
[[Category:Japonica Genes]]&lt;br /&gt;
[[Category:Japonica Chromosome 10]]&lt;br /&gt;
[[Category:Chromosome 10]]&lt;/div&gt;</summary>
		<author><name>Chenyaping</name></author>	</entry>

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