Development of a genome-wide marker design workflow for onions and its application in target amplicon sequencing-based genotyping.

Daisuke Sekine, Satoshi Oku, Tsukasa Nunome, Hideki Hirakawa, Mai Tsujimura, Toru Terachi, Atsushi Toyoda, Masayoshi Shigyo, Shusei Sato, Hikaru Tsukazaki
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引用次数: 2

Abstract

Onions are one of the most widely cultivated vegetables worldwide; however, the development and utilization of molecular markers have been limited because of the large genome of this plant. We present a genome-wide marker design workflow for onions and its application in a high-throughput genotyping method based on target amplicon sequencing. The efficiency of the method was evaluated by genotyping of F2 populations. In the marker design workflow, unigene and genomic sequence data sets were constructed, and polymorphisms between parental lines were detected through transcriptome sequence analysis. The positions of polymorphisms detected in the unigenes were mapped onto the genome sequence, and primer sets were designed. In total, 480 markers covering the whole genome were selected. By genotyping an F2 population, 329 polymorphic sites were obtained from the estimated positions or the flanking sequences. However, missing or sparse marker regions were observed in the resulting genetic linkage map. We modified the markers to cover these regions by genotyping the other F2 populations. The grouping and order of markers on the linkages were similar across the genetic maps. Our marker design workflow and target amplicon sequencing are useful for genome-wide genotyping of onions owing to their reliability, cost effectiveness, and flexibility.

Abstract Image

Abstract Image

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洋葱全基因组标记设计流程的建立及其在基于靶扩增子测序的基因分型中的应用。
洋葱是世界上种植最广泛的蔬菜之一;然而,由于该植物基因组大,限制了分子标记的开发和利用。我们提出了洋葱全基因组标记设计工作流程及其在基于靶扩增子测序的高通量基因分型方法中的应用。通过对F2群体进行基因分型,评价了该方法的有效性。在标记设计流程中,构建了单基因和基因组序列数据集,并通过转录组序列分析检测亲本间的多态性。将检测到的单基因多态性定位到基因组序列上,设计引物集。总共选择了覆盖整个基因组的480个标记。通过对F2群体进行基因分型,从估计的位置或侧翼序列中获得了329个多态性位点。然而,在所得到的遗传连锁图中观察到缺失或稀疏的标记区域。我们通过对其他F2群体进行基因分型来修改标记以覆盖这些区域。在整个遗传图谱中,连锁标记的分组和顺序是相似的。我们的标记设计工作流程和目标扩增子测序因其可靠性、成本效益和灵活性而适用于洋葱全基因组基因分型。
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