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Exploiting the Repetitive Fraction of the Wheat Genome for High-Throughput Single-Nucleotide Polymorphism Discovery and Genotyping

机译:利用小麦基因组的重复片段进行高通量单核苷酸多态性发现和基因分型

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Transposable elements (TEs) account for more than 80% of the wheat genome. Although they represent a major obstacle for genomic studies, TEs are also a source of polymorphism and consequently of molecular markers such as insertion site-based polymorphism (ISBP) markers. Insertion site-based polymorphisms have been found to be a great source of genome-specific single-nucleotide polymorphism (SNPs) in the hexaploid wheat (Triticum aestivum L.) genome. Here, we report on the development of a high-throughput SNP discovery approach based on sequence capture of ISBP markers. By applying this approach to the reference sequence of chromosome 3B from hexaploid wheat, we designed 39,077 SNPs that are evenly distributed along the chromosome. We demonstrate that these SNPs can be efficiently scored with the KASPar (Kompetitive allele-specific polymerase chain reaction) genotyping technology. Finally, through genetic diversity and genome-wide association studies, we also demonstrate that ISBP-derived SNPs can be used in marker-assisted breeding programs.
机译:转座因子(TEs)占小麦基因组的80%以上。尽管TEs代表了基因组研究的主要障碍,但TE还是多态性的来源,因此也是诸如基于插入位点的多态性(ISBP)标记等分子标记的来源。已经发现基于插入位点的多态性是六倍体小麦(Triticum aestivum L.)基因组中基因组特异性单核苷酸多态性(SNP)的重要来源。在这里,我们报告基于ISBP标记序列捕获的高通量SNP发现方法的发展。通过将此方法应用于六倍体小麦的3B染色体参考序列,我们设计了39,077个SNP,它们沿染色体均匀分布。我们证明,可以使用KASPar(竞争性等位基因特异性聚合酶链反应)基因分型技术对这些SNP进行有效评分。最后,通过遗传多样性和全基因组关联研究,我们还证明了ISBP衍生的SNP可用于标记辅助育种程序。

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