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首页> 外文期刊>Electronic Journal of Biotechnology >A real-time PCR genotyping assay to detect FAD2A SNPs in peanuts (Arachis hypogaea L.)
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A real-time PCR genotyping assay to detect FAD2A SNPs in peanuts (Arachis hypogaea L.)

机译:实时PCR基因分型测定法,检测花生中的FAD2A SNPs(花生)

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摘要

The high oleic (C18:1) phenotype in peanuts has been previously demonstrated to result from a homozygous recessive genotype (ol1ol1ol2ol2) in two homeologous fatty acid desaturase genes (FAD2A and FAD2B) with two key SNPs. These mutant SNPs, specifically G448A in FAD2A and 442insA in FAD2B, significantly limit the normal function of the desaturase enzyme activity which converts oleic acid into linoleic acid by the addition of a second double bond in the hydrocarbon chain. Previously, a genotyping assay was developed to detect wild type and mutant alleles in FAD2B. A real-time PCR assay has now been developed to detect wild type and mutant alleles (G448A) in FAD2A using either seed or leaf tissue. This assay was demonstrated to be applicable for the detection of homozygous and heterozygous samples. The FAD2A genotyping assay was validated by employing gas chromatography (GC) to determine total fatty acid composition and by genotyping peanut lines that have been well characterized. Overall, development of rapid assays such as real-time PCR which can identify key genotypes associated with important agronomic traits such as oleic acid, will improve breeding efficiency by targeting desirable genotypes at early stages of development.
机译:先前已证明花生中的高油酸(C18:1)表型是由两个具有两个关键SNP的同源脂肪酸去饱和酶基因(FAD2A和FAD2B)中的纯合性隐性基因型(ol1ol1ol2ol2)引起的。这些突变SNP,特别是FAD2A中的G448A和FAD2B中的442insA,极大地限制了去饱和酶活性的正常功能,该去饱和酶活性通过在烃链中添加第二个双键将油酸转化为亚油酸。以前,已开发出一种基因分型测定法来检测FAD2B中的野生型和突变等位基因。现在已经开发了一种实时PCR检测方法,可以使用种子或叶组织检测FAD2A中的野生型和突变等位基因(G448A)。已证明该测定法可用于检测纯合子和杂合子样品。通过使用气相色谱法(GC)确定总脂肪酸组成并通过对已经充分表征的花生品系进行基因分型,验证了FAD2A基因型分析的有效性。总体而言,快速测定法(例如实时PCR)的开发可以识别与重要农艺性状(例如油酸)相关的关键基因型,将通过在开发的早期阶段靶向所需的基因型来提高育种效率。

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