Difference between revisions of "Qsw5"

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Expression
 
Expression
As Darwin (1857) noted, crop domestication resembles a rapid evolutionary process that results from artificial selection but that otherwise has all the characteristics of evolution by means of natural selection. With increasing availability of crop genome information, the accumulation of knowledge about domestication-related genes, and the identification of functional nucleotide polymorphisms (FNPs), the crop domestication process is being increasingly elucidated (Doebley et al. 2006). In maize, for example, extensive genome analysis to find genes with reduced natural variation among cultivars, landraces and their wild relatives has suggested that thousands of genes might have been subjected to selection during domestication (Gaut et al. 2000, Matsuoka et al. 2002, Yamasaki et al. 2005). In wheat, archeological analysis of plant remains has revealed that the domestication process took a few thousand years (Tanno and Willcox 2006, Dubcovsky and Dvorak 2007). In barley, natural variation among landraces from Europe to Asia has been examined to reveal how barley cultivation propagated throughout these regions, with some genome changes detected and two distinct domestication processes proposed for European and Asian barley (Morrell and Clegg 2007, Pourkheirandish and Komatsuda 2007, Saisho and Purugganan 2007). In addition, some domestication-related genes have been cloned, and key natural variations in these genes (i.e. FNPs) have been examined to elucidate the domestication process in several crops, including maize, wheat and barley (Wang et al. 2005, Doebley et al. 2006, Simons et al. 2006, Komatsuda et al. 2007), even though the domestication process itself remains largely unknown.  
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Qsw5 can be involved in the expression of rice seed colors .
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Variation in the colors of the rice seed pericarp of the previous ‘heritage landraces’. These landraces retain all functional alleles of three domestication-related genes (qSW5, Wx and qSH1) at the three FNP positions (Shomura et al. 2008).  
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Use japonica rice  Nipponbare with  indica rice Kasalath hybrid to biuld  F2 population,In the fifth chromosome location to a control grain width of main effect QTL, it ie the Qsw5.Through positional cloning puting qSW5 finly positioning into 2263 bp, Finally,through gene expression analysis, and a complementary experiment to determine which one ORF (open reading frame) of qSW5.
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Qsw5 can be involved in the expression of rice seed width.
 
Evolution
 
Evolution
We can express the OsSUT gene in yeast to test whether it's functional. Choose the yeast strain which is unable to hydrolyse exogenous sucrose but if transformed with a functional SUT, can import sucrose and hydrolyse it internally , allowing it to grow on media containing sucrose as the sole carbon source.
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By combining qSW5, wx and qSH1 variation of these three genes form the current "Nipponbare."
 
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Rice seed size is an important agronomic trait in determining the yield potential, and four seed size related genes (GS3, GW2, qSW5/GW5 and GIF1) have been cloned in rice so far. However, the relationship among these four genes is still unclear, which will impede the process of gene pyramiding breeding program to some extent. To shade light on the relationship of above four genes, gene expression analysis was performed with GS3-RNAi, GW2-RNAi lines and CSSL of qSW5 at the transcriptional level. The results clearly showed that qSW5 and GW2 positively regulate the expression of GS3. Meanwhile, qSW5 can be down-regulated by repression of GW2 transcription. Additionally, GIF1 expression was found to be positively regulated by qSW5 but negatively by GW2 and GS3. Moreover, the allelic effects of qSW5 and GS3 were detailedly characterized based on a natural population consisting of 180 rice cultivars. It was indicated that mutual interactions exist between the two genes, in which, qSW5 affecting seed length is masked by GS3 alleles, and GS3 affecting seed width is masked by qSW5 alleles. These findings provide more insights into the molecular mechanisms underlying seed size development in rice and are likely to be useful for improving rice grain yield.
 
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[1]. Alonso-Blanco C, Aarts MG, Bentsink L, Keurentjes JJ, Reymond M, Vreugdenhil D, et al. What has natural variation taught us about plant development, physiology, and adaptation?[J]. The Plant cell. 2009,21(7):1877-96.
" Test function in yeast(from reference [2]).. "
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[2]. Kitagawa K, Kurinami S, Oki K, Abe Y, Ando T, Kono I, et al. A novel kinesin 13 protein regulating rice seed length[J]. Plant & cell physiology. 2010,51(8):1315-29.
There is also a novel fluorescent assay for sucrose transporter activity based on the ability of type I SUTs to transport the highly fluorescent molecule esculin (6,7-dihydroxycoumarin β-D-glucoside). Using fluorescence microscopy, we can do the research conveniently.
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[3]. Konishi S, Ebana K, Izawa T. Inference of the japonica rice domestication process from the distribution of six functional nucleotide polymorphisms of domestication-related genes in various landraces and modern cultivars[J]. Plant & cell physiology. 2008,49(9):1283-93.
 
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[4]. Tanabata T, Shibaya T, Hori K, Ebana K, Yano M. SmartGrain: high-throughput phenotyping software for measuring seed shape through image analysis[J]. Plant physiology. 2012,160(4):1871-80.
 
 
" Esculin uptake by yeast cells expressing StSUT1 was detected using FACS.(from reference [5]).. "Labs working on this gene
 
 
 
Univ Minnesota, Dept Plant Biol, Biol Sci Ctr 250, 1445 Gortner Ave, St Paul, MN 55108 USA.
 
CSIRO Plant Ind, Canberra, ACT 2601, Australia.
 
Chinese Acad Sci, Inst Genet & Dev Biol, Natl Key Lab Plant Genom, Beijing 100101, Peoples R China
 
Natl Agr Res Ctr, Dept Rice Res, Niigata 9430193, Japan
 
National Key Laboratory of Plant Molecular Genetics, Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences,Peoples R China
 
Department of Rice Research, National Agricultural Research Center, Joetsu, Niigata, 943-0193 JapanReferences
 
 
 
↑ Lu J M-Y. and Bush D R.(1998) His-65 in the proton-sucrose symporter is an essential amino acid whose modification with site-directed mutagenesis increases transport activity. Proc Natl Acad 95: 9025–9030.
 
2.0 2.1 2.2 Aoki N, Hirose T, Scofield G N, et al.(2003)The Sucrose Transporter Gene Family in Rice. Plant and Cell Physiology 44:223-232.
 
↑ Furbank R T, Scofield G N, Hirose T, et al. (2001) Cellular localisation and function of a sucrose transporter OsSUT1 in developing rice grains. Aust. J. Plant Physiol 28: 1187–1196.
 
↑ Hirose T, Imaizumi N, Scofield G N, et al. (1997) cDNA cloning and tissue-specific expression of a gene for sucrose transporter from rice (Oryza sativa L.). Plant Cell Physiol 38: 1389–1396.
 
↑ Gora P J, Reinders A, Ward J M, et al.(2012)A novel fluorescent assay for sucrose transporters. Plant Methods 8:13.
 

Latest revision as of 14:51, 7 June 2014

Function

The biological function of gene Qsw5 is that it through increasing the number of cells in rice flowers lemma,then increaseing the capacity of rice husk, and ultimately increase the grain width.Pets the gene loci of  Kasalath qSW5,  the grain width lines into smaller, field production decreased by 10%.But through the gene RNAi regulate ORF1's expression down  (ORF1 is one sets of Kasalath qSW5) ,then can make larger grain width and increase output.Therefore, loss of function qSW5 sites have value in breeding.


Expression Qsw5 can be involved in the expression of rice seed colors . Variation in the colors of the rice seed pericarp of the previous ‘heritage landraces’. These landraces retain all functional alleles of three domestication-related genes (qSW5, Wx and qSH1) at the three FNP positions (Shomura et al. 2008). Use japonica rice Nipponbare with indica rice Kasalath hybrid to biuld F2 population,In the fifth chromosome location to a control grain width of main effect QTL, it ie the Qsw5.Through positional cloning puting qSW5 finly positioning into 2263 bp, Finally,through gene expression analysis, and a complementary experiment to determine which one ORF (open reading frame) of qSW5. Qsw5 can be involved in the expression of rice seed width. Evolution By combining qSW5, wx and qSH1 variation of these three genes form the current "Nipponbare." Rice seed size is an important agronomic trait in determining the yield potential, and four seed size related genes (GS3, GW2, qSW5/GW5 and GIF1) have been cloned in rice so far. However, the relationship among these four genes is still unclear, which will impede the process of gene pyramiding breeding program to some extent. To shade light on the relationship of above four genes, gene expression analysis was performed with GS3-RNAi, GW2-RNAi lines and CSSL of qSW5 at the transcriptional level. The results clearly showed that qSW5 and GW2 positively regulate the expression of GS3. Meanwhile, qSW5 can be down-regulated by repression of GW2 transcription. Additionally, GIF1 expression was found to be positively regulated by qSW5 but negatively by GW2 and GS3. Moreover, the allelic effects of qSW5 and GS3 were detailedly characterized based on a natural population consisting of 180 rice cultivars. It was indicated that mutual interactions exist between the two genes, in which, qSW5 affecting seed length is masked by GS3 alleles, and GS3 affecting seed width is masked by qSW5 alleles. These findings provide more insights into the molecular mechanisms underlying seed size development in rice and are likely to be useful for improving rice grain yield. [1]. Alonso-Blanco C, Aarts MG, Bentsink L, Keurentjes JJ, Reymond M, Vreugdenhil D, et al. What has natural variation taught us about plant development, physiology, and adaptation?[J]. The Plant cell. 2009,21(7):1877-96. [2]. Kitagawa K, Kurinami S, Oki K, Abe Y, Ando T, Kono I, et al. A novel kinesin 13 protein regulating rice seed length[J]. Plant & cell physiology. 2010,51(8):1315-29. [3]. Konishi S, Ebana K, Izawa T. Inference of the japonica rice domestication process from the distribution of six functional nucleotide polymorphisms of domestication-related genes in various landraces and modern cultivars[J]. Plant & cell physiology. 2008,49(9):1283-93. [4]. Tanabata T, Shibaya T, Hori K, Ebana K, Yano M. SmartGrain: high-throughput phenotyping software for measuring seed shape through image analysis[J]. Plant physiology. 2012,160(4):1871-80.