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Targeted enrichment by solution-based hybrid capture to identify genetic sequence variants in barley

机译:通过基于溶液的杂交捕获进行靶向富集以鉴定大麦中的遗传序列变异

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摘要

In barley and other cereal crops, phenological diversity drives adaptation to different cultivation areas. Improvement of barley yield and quality traits requires adaptation to specific production areas with introgression of favorable alleles dependent upon precise identification of the underlying genes. Combining targeted sequence capture systems with next-generation sequencing provides an efficient approach to explore target genetic regions at high resolution, and allows rapid discovery of thousands of genetic polymorphisms. Here, we apply a versatile target-capture method to detect genome-wide polymorphisms in 174 flowering time-related genes, chosen based on prior knowledge from barley, rice, and Arabidopsis thaliana. Sequences were generated across a phenologically diverse panel of 895 barley varieties, resulting a high mean depth coverage of ~25x allowing reliable discovery and calling of insertion-deletion (InDel) and single nucleotide polymorphisms (SNPs). Sequences of InDel and SNPs from the targeted enrichment were utilized to develop 67 Kompetitive Allele Specific PCR (KASP) markers for validation. This work provides researchers and breeders a comprehensive molecular toolkit for the selection of phenology-related traits in barley.
机译:在大麦和其他谷类作物中,物候学差异促使人们适应不同的种植区域。大麦产量和品质性状的提高需要适应特定生产区域,而有利的等位基因的渗入取决于对潜在基因的精确鉴定。将目标序列捕获系统与下一代测序相结合,可以提供一种有效的方法来高分辨率地探索目标遗传区域,并可以快速发现数千种遗传多态性。在这里,我们应用一种通用的目标捕获方法来检测174个与开花时间相关的基因中的全基因组多态性,该基因是基于从大麦,水稻和拟南芥中获得的先验知识而选择的。序列在895个大麦品种的物候学上多样化的面板上生成,导致〜25x的高平均深度覆盖,从而可以可靠地发现和调用插入缺失(InDel)和单核苷酸多态性(SNP)。来自目标富集的InDel和SNP序列被用于开发67个竞争性等位基因特异性PCR(KASP)标记以进行验证。这项工作为研究人员和育种人员提供了一个用于选择大麦物候相关性状的综合分子工具包。

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