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首页> 外文期刊>Plant Omics >Identification of a co-segregative protein associated with the tillering trait in rice (Oryza sativa L.)
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Identification of a co-segregative protein associated with the tillering trait in rice (Oryza sativa L.)

机译:鉴定与水稻中的分蘖性有关的共同分离蛋白(Oryza sativa L.)

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Tillering is an important trait for grain production in rice. To understand the mechanism underlying tillering regulation in rice, a combined proteomic and genetic approach was taken to analyze potential protein markers associated with the high-tillering dwarf phenotype. Total proteins were extracted from basal internodes of rice plants and subjected to 2-dimensional gel electrophoresis. Proteomes were compared between control rice cultivars and tillering mutant lines that are known to have a reduced number of culms or contain the d10 allele. A total of 33 polymorphic protein markers were identified between the wild-type cultivar GLA4 and the mutant line JHCA with dwarf and high tillering phenotype. A protein spot was found to behave as a qualitative trait, cosegregating with the normal-tillering phenotype in the F2 population. This protein was present in the wild-type plants, but was undetectable in the mutant line JHCA and the high-tillering dwarf F2 plants. Mass spectrometry analysis identified the protein as putative carboxyvinyl-carboxyphosphonate phosphorylmutase (CPPM; EC 2.7.8.23), which may catalyze the formation of a unique C-P bond from phosphoenolpyruvate and may participate in the biosynthesis of unidentified compounds with an inhibitory effect on tillering in rice. Real-time PCR analysis revealed that the mRNA level of CPPM was down-regulated in the high-tillering d10 dwarf plants, suggesting that the expression of the CPPM gene requires the function of D10. We propose that CPPM may play a role that is related to the tillering regulation in rice.Pages 36-45|
机译:分蘖是大米籽粒生产的重要特征。为了了解水稻中突出的调节机制,采用组合的蛋白质组学和遗传方法来分析与高耕作矮化表型相关的潜在蛋白质标志物。从水稻植物的基底间提取总蛋白质并进行二维凝胶电泳。在对照水稻品种和分蘖突变线之间比较蛋白质蛋白质,其已知具有减少数量的秆或含有D10等位基因。在野生型品种GLA4和突变线JHCA之间鉴定了33种多态性蛋白标记物,具有矮化和高分蘖表型。发现蛋白质点表现为与F2人群中的正常分蘖表型有关的性状。该蛋白质存在于野生型植物中,但在突变线JHCA和高分蘖性矮化F2植物中不可检测到。质谱分析将蛋白质鉴定为推定的羧乙烯基 - 羧基磷酸磷酸酶(CPPM; EC 2.7.8.23),其可以催化从磷酸丙酮替代品中形成独特的CP键,并且可以参与未识别的化合物的生物合成,并在水稻中具有抑制作用对未识别的化合物的生物合成。实时PCR分析显示,CPPM的mRNA水平在高耕作D10矮化植物中受到抑制,表明CPPM基因的表达需要D10的功能。我们建议CPPM可能发挥与稻米分蘖调节有关的作用。页面36-45 |

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    《Plant Omics》 |2013年第1期|共10页
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