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Target Amplicon Sequencing for Genotyping Genome-Wide Single Nucleotide Polymorphisms Identified by Whole-Genome Resequencing in Peanut

机译:通过花生全基因组重测序鉴定基因组全基因组单核苷酸多态性的目标扩增子测序。

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Genome-wide genotyping data regarding breeding materials are essential resources for improving breeding efficiency, especially in plants with complex genomes with a high degree of polyploidy. Several current breeding efforts in cultivated peanut (Arachis hypogaea?L.), which has a tetraploid genome, are devoted to developing high oleic acid cultivars. Genetic maps for such breeding programs have been developed using simple-sequence repeat (SSR) markers, the use of which requires time-consuming electrophoretic analyses. Next-generation sequencing (NGS) technology can overcome this technical hurdle. Initially, we attempted double-digest restriction site-associated DNA sequencing on peanut breeding materials used to develop high oleic acid cultivars. However, this method was not effective because few single nucleotide polymorphism (SNPs) were available because of low genetic diversity of the lines. The genome sequences of the probable diploid ancestors of cultivated peanut,?A. duranensis?Krapov. & W. C. Greg. and?A. ipa?nsis?Krapov. & W. C. Greg., are available. Therefore, we next employed whole-genome resequencing analysis to obtain genome-wide SNP data. In this analysis, we observed large biases in the numbers and genomic positions of interspecific and intraspecific SNPs. For genome-wide genotyping, we selected a subset of SNPs covering the peanut genome as the targets of amplicon sequencing analysis. Using this technique, genome-wide genotypes of the breeding materials were easily and rapidly determined. The SNP information and analytic methods developed in this study should accelerate genetics, genomics, and breeding in peanut.
机译:关于育种材料的全基因组基因分型数据是提高育种效率的重要资源,特别是在具有高度多倍体的复杂基因组的植物中。当前在具有四倍体基因组的栽培花生(花生)中的几种育种工作致力于开发高油酸品种。已经使用简单序列重复(SSR)标记物开发了此类育种程序的遗传图谱,其使用需要耗时的电泳分析。下一代测序(NGS)技术可以克服这一技术障碍。最初,我们尝试对用于开发高油酸品种的花生育种材料进行双消化酶切位点相关的DNA测序。然而,该方法是无效的,因为由于品系的遗传多样性低,几乎没有单核苷酸多态性(SNP)。栽培花生的可能二倍体祖先的基因组序列。杜兰松?克拉波夫&W. C. Greg。和? ipa?nsis?Krapov。 &W. C. Greg。,可用。因此,我们接下来采用全基因组重测序分析来获得全基因组SNP数据。在此分析中,我们观察到种间和种内SNP的数量和基因组位置存在较大偏差。对于全基因组基因分型,我们选择了覆盖花生基因组的SNP子集作为扩增子测序分析的目标。使用这种技术,可以轻松,快速地确定育种材料的全基因组基因型。在这项研究中开发的SNP信息和分析方法应加快花生的遗传学,基因组学和育种工作。

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