Difference between revisions of "Os02g0120500"

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[[File:OsTDR_1.jpg|right|thumb|390px|'''Figure 1.''' ''OsTDR Mutant VS. Wild-type(from reference)(from reference<ref name="ref1" />).'']]
 
[[File:OsTDR_1.jpg|right|thumb|390px|'''Figure 1.''' ''OsTDR Mutant VS. Wild-type(from reference)(from reference<ref name="ref1" />).'']]
 
===Function===
 
===Function===
Please input function information here.
+
* ''OsTDR'' is a key component of the molecular network regulating rice tapetum development and degeneration <ref name="ref1" /><ref name="ref2" />. As a member of [[bHLH]] family, ''OsTDR'' is a tapetal cell death regulator<ref name="ref1" /><ref name="ref2" /><ref name="ref3" /><ref name="ref4" />. It positively triggers programmed cell death (PCD) of tapetal cells and loss of ''OsTDR'' function could cause aborted tapetal PCD during pollen development<ref name="ref1" /><ref name="ref2" /><ref name="ref3" />.
 +
* In addition to its function in promoting tapetum PCD, ''OsTDR'' possibly plays some other crucial regulatory roles in several basic biological processes during rice pollen development, for example, aliphatic metabolism<ref name="ref2" /><ref name="ref3" />. It can regulate the synthesis of lipidic precursors during rice pollen wall development which might indirectly affect anther epidermis wax formation<ref name="ref2" />.
 +
'''GO assignment(s):''' GO:0005634, GO:0030528, GO:0045449
 +
===Wild Type & Mutations===
 +
* The phenotype analysis made by ''Na Li'' et al. showed that there was no obvious difference between the ''OsTDR'' mutant plant and wild-type plant in vegetative and floral development (Figures 1A to 1D).  However, the ''tdr'' mutant plant failed to produce any viable pollen (Figures 1A to 1D). Compared with wild-type anthers, the mutant anthers were small and white, without any mature pollen grains (Figures 1E to 1H)<ref name="ref1" />.
 +
[[File:OsTDR_2.jpg|right|thumb|390px|'''Figure 2.''' ''The expression of OsTDR by RT-PCR(from reference<ref name="ref1" />).'']]
 +
* Their further anther transverse sections study and transmission electron microscopy study suggested that the ''OsTDR'' mutation resulted in the defects in tapetum degeneration, then affecting microspore development, particularly exine formation<ref name="ref1" />.
  
 
===Expression===
 
===Expression===
Please input expression information here.
+
* The RT-PCR analysis made by ''Na Li'' et al. in 2006 showed that developing anther is the only organs that the expression of ''TDR'' can be detected, no vegetative organs or any other reproductive organs <ref name="ref1" /> (Figure 2). Their further ''RNA in situ hybridization'' showed that ''OsTDR'' expression is associated with the differentiation of tapetal cells during rice anther development.
 +
* The ''microarray analysis'' made by ''Da-Sheng Zhang'' et al. showed that 236 genes exhibited significantly different expression levels in ''tdr'' mutant compared with wild-type, including 154 up-regulated genes and 82 down-regulated gene, ssuggesting a regulatory role of ''OsTDR'' during rice pollen development<ref name="ref2" />.
 +
===Gene Structure===
 +
[[File:OsTDR_3.png|center|thumb|727px|'''Figure 3.''' ''Structure of OsTDR (from NCBI BLASTP).'']]
  
 
===Evolution===
 
===Evolution===
Please input evolution information here.
+
[[File:OsTDR_4.jpg|right|thumb|390px|'''Figure 4.''' ''The phylogenetic analysis of ''OsTDR''(from reference<ref name="ref1" />).'']]
 
+
* The phylogenetic analysis of ''OsTDR'' and its 12 related proteins made by ''Na Li'' et al. in 2006 showed that the most closest gene is ''  AMS'' in ''Arabidopsis''. ''OsTDR'' shares 32% identity with ''AtAMS'' which is also related with tapetum degeneration<ref name="ref1" />.
You can also add sub-section(s) at will.
 
  
 
==Labs working on this gene==
 
==Labs working on this gene==
Please input related labs here.
+
* Shanghai Jiao Tong University–Shanghai Institutes for Biological Sciences–Pennsylvania State University Joint Center for Life Sciences, School of Life Science and Biotechnology, Key Laboratory of Microbial Metabolism, Ministry of Education, Shanghai Jiao Tong University, Shanghai 200240, China
 +
* School of Life Sciences, Shanghai University, Shanghai 200240, China
 +
* School of Life Science and Biotechnology, Shanghai Jiao Tong University, Shanghai 200240, China
 +
* Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China
 +
* Department of Biology, Huck Institutes of the Life Sciences, Pennsylvania State University, University Park, Pennsylvania 16082
 +
* Instrumental Analysis Center of Shanghai Jiao Tong University, Shanghai 200240, China
 +
* State Key Laboratory of Hybrid Rice, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
 +
* Division of Plant Sciences, School of Biosciences, University of Nottingham, Loughborough, Leics, UK
 +
* Department of Energy Plant Research Laboratory, Michigan State University, East Lansing, Michigan, USA
  
 
==References==
 
==References==
Please input cited references here.
+
<references>
 
+
* <ref name="ref1">
 +
Li N, Zhang D S, Liu H S, et al. The rice tapetum degeneration retardation gene is required for tapetum degradation and anther development[J]. The Plant Cell Online, 2006, 18(11): 2999-3014.
 +
</ref>
 +
* <ref name="ref2">
 +
Zhang D S, Liang W Q, Yuan Z, et al. Tapetum degeneration retardation is critical for aliphatic metabolism and gene regulation during rice pollen development[J]. Molecular plant, 2008, 1(4): 599-610.
 +
</ref>
 +
* <ref name="ref3">
 +
Liu Z, Bao W, Liang W, et al. Identification of gamyb‐4 and Analysis of the Regulatory Role of GAMYB in Rice Anther Development[J]. Journal of Integrative Plant Biology, 2010, 52(7): 670-678.
 +
</ref>
 +
* <ref name="ref4">
 +
Niu N, Liang W, Yang X, et al. EAT1 promotes tapetal cell death by regulating aspartic proteases during male reproductive development in rice[J]. Nature communications, 2013, 4: 1445.
 +
</ref>
 +
</references>
 
==Structured Information==
 
==Structured Information==
{{JaponicaGene|
 
GeneName = Os02g0120500|
 
Description = Basic helix-loop-helix dimerisation region bHLH domain containing protein|
 
Version = NM_001052245.1 GI:115443860 GeneID:4328113|
 
Length = 3152 bp|
 
Definition = Oryza sativa Japonica Group Os02g0120500, complete gene.|
 
Source = Oryza sativa Japonica Group
 
  
  ORGANISM  Oryza sativa Japonica Group
 
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;
 
            Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP
 
            clade; Ehrhartoideae; Oryzeae; Oryza.
 
|
 
Chromosome = [[:category:Japonica Chromosome 2|Chromosome 2]]|
 
AP = Chromosome 2:1073625..1076776|
 
CDS = 1073790..1074026,1074113..1074595,1074686..1075213,1075421..1075513,1075620..1075671<br>,1075800..1075904,1076020..1076180|
 
GCID = <gbrowseImage1>
 
name=NC_008395:1073625..1076776
 
source=RiceChromosome02
 
preset=GeneLocation
 
</gbrowseImage1>|
 
GSID = <gbrowseImage2>
 
name=NC_008395:1073625..1076776
 
source=RiceChromosome02
 
preset=GeneLocation
 
</gbrowseImage2>|
 
CDNA = <cdnaseq>atgggaagaggagaccacctgctgatgaagaacagcaatgctgctgcagctgcagctgctgtcaatggaggtggcaccagtttggatgctgcattgaggcctctagttggttcagatggctgggattactgcatctactggaggctctctcctgatcagaggttcttggagatgacaggattctgctgcagcagtgagcttgaagcacaggtctcagcactgctggacctgccttcttcaatcccactggactcctcctccatagggatgcatgcgcaggcattgctgtcgaaccagccgatctggcagagcagcagtgaggaggaggaggctgatggcggcggtggcgccaagacgcggctgctggtccccgtcgccggcggcctcgtcgagctcttcgcgtcgagatatatggcggaggagcagcagatggcggagcttgtcatggcgcagtgcggcggcggcggcgccggggacgacggtggggggcaggcgtggccgccgccggagacgcccagcttccagtgggacggaggcgccgacgcgcagaggctgatgtacggcggctcgtcgctgaacctgttcgacgccgccgccgccgacgacgacccgttcttgggtggtggtggtggtgacgccgtgggcgacgaggcggcggcggcgggcgcgtggccgtacgcggggatggcggtgagcgagccgtcggtggcggtggcgcaggagcagatgcagcacgcggcgggcggcggcgtggcggagtccgggtcggaggggaggaagctgcatggcggtgacccggaggacgacggcgacggcgaggggcgctccggcggcgccaagaggcagcagtgcaagaacctcgaggcggagaggaagcggaggaagaagctcaatggccacctctacaagctccgctcgctcgtcccaaacatcaccaagatggatcgcgcgtcgattcttggagacgcgatcgactacatcgtggggttgcagaagcaggtgaaggagctgcaggacgagctggaagacaaccatgtccaccataagccgcccgacgtgctcatcgaccacccgccgccggcgagcctcgtcgggctcgacaacgacgacgcctcgccgcccaacagccaccaacagcagccgccgctcgccgtttccggcagcagcagcaggaggagtaacaaggacccagcaatgaccgacgacaaggtcggcggcggcggcggcggtgggcaccggatggagccgcagctggaggtgcgtcaggtgcaggggaacgagctgttcgtccaggtgctctgggagcacaagcccggcgggttcgtccgcctcatggacgccatgaacgcgctcggcctcgaggtcatcaacgtcaacgtcaccacctacaagaccctcgtcctcaacgtcttccgcgtcatggtgagggacagcgaggtggcggtgcaggcggacagggtgagggactcgctgctggaggtgacgcgggagacgtaccccggcgtgtggccgtcgccgcaggaggaggacgacgccaagttcgacggcggcgacggcgggcaggctgcggcggcggcggcggcggccggtggagagcactaccacgacgaagtcggcggcggataccatcagcacctgcattacctcgcgtttgattga</cdnaseq>|
 
AA = <aaseq>MGRGDHLLMKNSNAAAAAAAVNGGGTSLDAALRPLVGSDGWDYC                    IYWRLSPDQRFLEMTGFCCSSELEAQVSALLDLPSSIPLDSSSIGMHAQALLSNQPIW                    QSSSEEEEADGGGGAKTRLLVPVAGGLVELFASRYMAEEQQMAELVMAQCGGGGAGDD                    GGGQAWPPPETPSFQWDGGADAQRLMYGGSSLNLFDAAAADDDPFLGGGGGDAVGDEA                    AAAGAWPYAGMAVSEPSVAVAQEQMQHAAGGGVAESGSEGRKLHGGDPEDDGDGEGRS                    GGAKRQQCKNLEAERKRRKKLNGHLYKLRSLVPNITKMDRASILGDAIDYIVGLQKQV                    KELQDELEDNHVHHKPPDVLIDHPPPASLVGLDNDDASPPNSHQQQPPLAVSGSSSRR                    SNKDPAMTDDKVGGGGGGGHRMEPQLEVRQVQGNELFVQVLWEHKPGGFVRLMDAMNA                    LGLEVINVNVTTYKTLVLNVFRVMVRDSEVAVQADRVRDSLLEVTRETYPGVWPSPQE                    EDDAKFDGGDGGQAAAAAAAAGGEHYHDEVGGGYHQHLHYLAFD</aaseq>|
 
DNA = <dnaseqindica>2751..2987#2182..2664#1564..2091#1264..1356#1106..1157#873..977#597..757#agtatcatacataatttgacagccatttccgaagacttggtatcaatacatcatcagatagccatggctaaattcagaggaacacacacatgtgaactatatatatgcatgatgcaatagtccttctgtacaaaatgattcttcagttaccaatagctatcagctgatgcctctctcttccatctgttgatcactgccacagttcgtcagttagtttgaagcgatctcaggaagacagaaggtatctttctttctctgcttaattccaaaaattcactagaaaagatttcacatacaatcctgatgagccagaagaatgcagctttgatctctgtctctttaagttactgaaaatttgattcaacatagactgaattttcagactaaatctgtctctttagtctgatgaatattcagactgaatctgattgttcccttgctgtgatcataccctgaattttcgctgtatccttggtgacatcaacttatcctgtcctgacagcaagaaaaagcaggccttgtgaatgctgcaactgacacttgcatccattcttcttgctttcatgtgtcactgctagggcaagggtgatcaccacatgggaagaggagaccacctgctgatgaagaacagcaatgctgctgcagctgcagctgctgtcaatggaggtggcaccagtttggatgctgcattgaggcctctagttggttcagatggctgggattactgcatctactggaggctctctcctgatcagaggtatgtgattgattacttggcatatcatatcatatcatgcatgcaaagtagcaattacggtgtgatttattatctctgtagtgatatacaaccattaacacaaaattaatggcaggttcttggagatgacaggattctgctgcagcagtgagcttgaagcacaggtctcagcactgctggacctgccttcttcaatcccactggactcctcctccatagggtaaattgaatgattaatcaatcaatcgatacgtgttctgattacctgcaaaattgatggtttcttgtctagtaactctgaacatttgtatgcttggtgaatctgaatctctgtcactatccatcaaggatgcatgcgcaggcattgctgtcgaaccagccgatctggcagagcagcagtgtaagcaagattcatcactgaacccagtagctgaatctgaatctgaatctgaatctgaatatgaatctctgtcactgatgaggtgtgttgcttggatgcgtggcaggaggaggaggaggctgatggcggcggtggcgccaagacgcggctgctggtccccgtcgccggcggcctcgtcgagctcttcgcgtcgagatatgtgagtggtcggtcgttcgattggttagaggagtagtagttagagaggatgcggctgcggctgcggcggcggcggtggtggcggcggctcacgccatccgcgtgagccaacgaacgccggagagcttgcggttagctgcacgcaacggcctttgcgttttgcatggatgggttatatagatttgtgggttgatcggtgttggtgcagatggcggaggagcagcagatggcggagcttgtcatggcgcagtgcggcggcggcggcgccggggacgacggtggggggcaggcgtggccgccgccggagacgcccagcttccagtgggacggaggcgccgacgcgcagaggctgatgtacggcggctcgtcgctgaacctgttcgacgccgccgccgccgacgacgacccgttcttgggtggtggtggtggtgacgccgtgggcgacgaggcggcggcggcgggcgcgtggccgtacgcggggatggcggtgagcgagccgtcggtggcggtggcgcaggagcagatgcagcacgcggcgggcggcggcgtggcggagtccgggtcggaggggaggaagctgcatggcggtgacccggaggacgacggcgacggcgaggggcgctccggcggcgccaagaggcagcagtgcaagaacctcgaggcggagaggaagcggaggaagaagctcaatggccacctctacaagctccgctcgctcgtcccaaacatcaccaaggtatcttacctcctcgtcgatcgccatggccatgaacggatcaaaagcttcttcaaatcgatttccgtttgattttgcaacgaatcgtagatggatcgcgcgtcgattcttggagacgcgatcgactacatcgtggggttgcagaagcaggtgaaggagctgcaggacgagctggaagacaaccatgtccaccataagccgcccgacgtgctcatcgaccacccgccgccggcgagcctcgtcgggctcgacaacgacgacgcctcgccgcccaacagccaccaacagcagccgccgctcgccgtttccggcagcagcagcaggaggagtaacaaggacccagcaatgaccgacgacaaggtcggcggcggcggcggcggtgggcaccggatggagccgcagctggaggtgcgtcaggtgcaggggaacgagctgttcgtccaggtgctctgggagcacaagcccggcgggttcgtccgcctcatggacgccatgaacgcgctcggcctcgaggtcatcaacgtcaacgtcaccacctacaagaccctcgtcctcaacgtcttccgcgtcatggtagtacgccccgctcgccgccgccatggccatgaacgcgagctcgcgagctgactactccgagctggttggtttctgcattgcaggtgagggacagcgaggtggcggtgcaggcggacagggtgagggactcgctgctggaggtgacgcgggagacgtaccccggcgtgtggccgtcgccgcaggaggaggacgacgccaagttcgacggcggcgacggcgggcaggctgcggcggcggcggcggcggccggtggagagcactaccacgacgaagtcggcggcggataccatcagcacctgcattacctcgcgtttgattgatgatgatgattgattttaccatctacgtctcactactagtgtatacacactcgaattattcgagaaagaaacataatgctacgtactagtaataatggatttgataagtagttgtctagtatttgtgattaatggcatatatgcataatgacttgatgactgaaa</dnaseqindica>|
 
Link = [http://www.ncbi.nlm.nih.gov/nuccore/NM_001052245.1 RefSeq:Os02g0120500]|
 
}}
 
 
[[Category:Genes]]
 
[[Category:Genes]]
 
[[Category:Japonica mRNA]]
 
[[Category:Japonica mRNA]]

Latest revision as of 05:19, 14 May 2015

The rice Os02g0120500 was reported as OsTDR since the year 2006 . It is involved with pollen development in rice[1][2][3][4].

Annotated Information

Figure 1. OsTDR Mutant VS. Wild-type(from reference)(from reference[1]).

Function

  • OsTDR is a key component of the molecular network regulating rice tapetum development and degeneration [1][2]. As a member of bHLH family, OsTDR is a tapetal cell death regulator[1][2][3][4]. It positively triggers programmed cell death (PCD) of tapetal cells and loss of OsTDR function could cause aborted tapetal PCD during pollen development[1][2][3].
  • In addition to its function in promoting tapetum PCD, OsTDR possibly plays some other crucial regulatory roles in several basic biological processes during rice pollen development, for example, aliphatic metabolism[2][3]. It can regulate the synthesis of lipidic precursors during rice pollen wall development which might indirectly affect anther epidermis wax formation[2].

GO assignment(s): GO:0005634, GO:0030528, GO:0045449

Wild Type & Mutations

  • The phenotype analysis made by Na Li et al. showed that there was no obvious difference between the OsTDR mutant plant and wild-type plant in vegetative and floral development (Figures 1A to 1D). However, the tdr mutant plant failed to produce any viable pollen (Figures 1A to 1D). Compared with wild-type anthers, the mutant anthers were small and white, without any mature pollen grains (Figures 1E to 1H)[1].
Figure 2. The expression of OsTDR by RT-PCR(from reference[1]).
  • Their further anther transverse sections study and transmission electron microscopy study suggested that the OsTDR mutation resulted in the defects in tapetum degeneration, then affecting microspore development, particularly exine formation[1].

Expression

  • The RT-PCR analysis made by Na Li et al. in 2006 showed that developing anther is the only organs that the expression of TDR can be detected, no vegetative organs or any other reproductive organs [1] (Figure 2). Their further RNA in situ hybridization showed that OsTDR expression is associated with the differentiation of tapetal cells during rice anther development.
  • The microarray analysis made by Da-Sheng Zhang et al. showed that 236 genes exhibited significantly different expression levels in tdr mutant compared with wild-type, including 154 up-regulated genes and 82 down-regulated gene, ssuggesting a regulatory role of OsTDR during rice pollen development[2].

Gene Structure

Figure 3. Structure of OsTDR (from NCBI BLASTP).

Evolution

Figure 4. The phylogenetic analysis of OsTDR(from reference[1]).
  • The phylogenetic analysis of OsTDR and its 12 related proteins made by Na Li et al. in 2006 showed that the most closest gene is AMS in Arabidopsis. OsTDR shares 32% identity with AtAMS which is also related with tapetum degeneration[1].

Labs working on this gene

  • Shanghai Jiao Tong University–Shanghai Institutes for Biological Sciences–Pennsylvania State University Joint Center for Life Sciences, School of Life Science and Biotechnology, Key Laboratory of Microbial Metabolism, Ministry of Education, Shanghai Jiao Tong University, Shanghai 200240, China
  • School of Life Sciences, Shanghai University, Shanghai 200240, China
  • School of Life Science and Biotechnology, Shanghai Jiao Tong University, Shanghai 200240, China
  • Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China
  • Department of Biology, Huck Institutes of the Life Sciences, Pennsylvania State University, University Park, Pennsylvania 16082
  • Instrumental Analysis Center of Shanghai Jiao Tong University, Shanghai 200240, China
  • State Key Laboratory of Hybrid Rice, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
  • Division of Plant Sciences, School of Biosciences, University of Nottingham, Loughborough, Leics, UK
  • Department of Energy Plant Research Laboratory, Michigan State University, East Lansing, Michigan, USA

References

  1. 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 Li N, Zhang D S, Liu H S, et al. The rice tapetum degeneration retardation gene is required for tapetum degradation and anther development[J]. The Plant Cell Online, 2006, 18(11): 2999-3014.
  2. 2.0 2.1 2.2 2.3 2.4 2.5 2.6 Zhang D S, Liang W Q, Yuan Z, et al. Tapetum degeneration retardation is critical for aliphatic metabolism and gene regulation during rice pollen development[J]. Molecular plant, 2008, 1(4): 599-610.
  3. 3.0 3.1 3.2 3.3 Liu Z, Bao W, Liang W, et al. Identification of gamyb‐4 and Analysis of the Regulatory Role of GAMYB in Rice Anther Development[J]. Journal of Integrative Plant Biology, 2010, 52(7): 670-678.
  4. 4.0 4.1 Niu N, Liang W, Yang X, et al. EAT1 promotes tapetal cell death by regulating aspartic proteases during male reproductive development in rice[J]. Nature communications, 2013, 4: 1445.

Structured Information