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大豆GmTFIIB基因的克隆及其功能预测分析

Functional prediction analysis and cloning of GmTFIIB gene in soybean

中文摘要英文摘要

大豆花叶病毒病(SMV)是我国大豆主产区黑龙江省分布最广的病毒性病害,其严重影响大豆的产量和品质。采用抗病基因工程育种方法是解除该病对黑龙江省大豆生产威胁的有效途径之一。本研究以前人精细定位后获得抗病候选区域为基础,选取GmTFIIB基因作为大豆抗病候选基因。根据已知片段序列克隆了GmTFIIB基因,其完整的CDS序列全长为573bp,同源序列比较发现该基因与Glyma09g11870、Glyma13g25410、Glyma13g25430和Glyma13g25765等基因同源性较高,这表明该基因在大豆进化过程中没有发生明显的功能分化。组织特异性表达分析结果表明该基因在根、茎、叶、荚、未成熟果实、成熟果实等不同组织中均有表达,而在茎、叶和未成熟果实中具有较高的表达量;并且该基因可受大豆花叶病毒病N1株系诱导而表达,这表明该基因可能参与抗大豆花叶病毒病反应。

Soybean mosaic virus (SMV) is a prevalent virus disease in Chinese main soybean producting region(Heilongjiang Province),which seriously impacts on yield and quality of soybean. Resistance disease gene engineering breeding is one of the effective ways to control the threat to soybean production in Heilongjiang province. In the present study, the GmTFIIB gene was selected as the candidate gene with resistance to soybean mosaic virus, which was based on the fine mapping result of the previous studies. Based on the known CDS sequences of this gene, the complete CDS was clonin, which was 573bp. The homologous sequences of this gene were analyzed, the result showed that Glyma09g11870, Glyma13g25410, Glyma13g25765 and Glyma13g25430 have higher homology with this gene. It suggested that this gene in soybean evolution didn't occur in obvious functional differentiation. The result of tissue specific expression analysis showed that this gene could express in different tissues including roots, stems, leaves, pods, immature fruit, and mature fruit. And this gene could express higher in stems, leaves and immature fruits than that in other tissues. Expression of this gene could be induced by soybean mosaic virus strain N1, which suggested that this gene may be involved in resistance to soybean mosaic virus.

孙晶、赵雪、李海燕、韩英鹏

植物保护农作物生物科学研究方法、生物科学研究技术

作物遗传育种大豆花叶病毒病抗病基因克隆生物信息学分析

rop Genetics and BreedingSoybean Mosaic VirusResistance Gene CloningBioinfomatical Analysis

孙晶,赵雪,李海燕,韩英鹏.大豆GmTFIIB基因的克隆及其功能预测分析[EB/OL].(2016-05-18)[2025-08-11].http://www.paper.edu.cn/releasepaper/content/201605-558.点此复制

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