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首页> 外文期刊>Molecular Breeding >A PCR-based method to test for the presence or absence of /J-conglycinin a'- and a-subunits in soybean
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A PCR-based method to test for the presence or absence of /J-conglycinin a'- and a-subunits in soybean

机译:一种基于PCR的方法来检测大豆中J-伴大豆球蛋白a'和a亚基的存在与否

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摘要

The soybean cultivar Yumeminori, which lacks the alpha'- and a-subunits of beta-conglycinin, carries both naturally occurring and induced mutations. While the cause of the natural mutation resulting in the alpha'-subunit deficiency has been determined, the induced mutation in the CG-2 gene encoding the a-subunit has not been characterized at the molecular level. In this study, we identified a four base pair insertion in the first exon of CG-2, which introduced a premature stop codon. The insertion co-segregated with the lack of alpha-subunit, indicating that this mutation is the cause of the a-subunit deficiency. A multiplex PCR method of testing for the presence or absence of alpha'- and a-subunits was developed based on the sequences of mutated and wild-type alleles. This PCR-based test was also capable of detecting the presence of wild-type genes when Yumeminori DNA samples were contaminated with wild-type DNA at levels of 0.2% or greater. Thus, this method will be useful both for marker-assisted selection in soybean breeding programs, and for seed purity tests in food industries.
机译:缺乏β-伴大豆球蛋白的α'-和α-亚基的大豆栽培品种梦me,具有自然发生的突变和诱导的突变。虽然已经确定了导致α'-亚基缺乏的自然突变的原因,但尚未在分子水平上表征编码α-亚基的CG-2基因中的诱导突变。在这项研究中,我们在CG-2的第一个外显子中发现了一个4个碱基对的插入,这引入了一个过早的终止密码子。插入与缺少α-亚基共分离,表明该突变是α-亚基缺乏的原因。基于突变等位基因和野生型等位基因的序列,开发了一种用于检测α'和α亚基是否存在的多重PCR方法。当Yumeminori DNA样品被0.2%或更高水平的野生型DNA污染时,这种基于PCR的测试还能够检测野生型基因的存在。因此,该方法对于大豆育种计划中的标记辅助选择以及食品工业中的种子纯度测试都将是有用的。

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