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Identification of quantitative trait loci for flowering time by a combination of restriction site-associated DNA sequencing and bulked segregant analysis in soybean

机译:通过限制性位点相关的DNA测序组合鉴定开花时间的定量性状基因座在大豆中的组合和膨胀的偏分析分析

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摘要

Soybean (Glycine max) has a paleopolyploid genome, and many re-sequencing experiments to characterize soybean genotypes have been conducted using next-generation sequencing platforms. The accumulation of information about single nucleotide polymorphisms (SNPs) throughout the soybean genome has accelerated identification of genomic regions related to agronomically important traits through association studies. However, although many efficient mapping techniques that use next-generation sequencing are available, the number of practical approaches to identify genes/loci is still limited. In this study, we used a combination of restriction site associated DNA sequencing (RAD-seq) and bulk segregant analysis (BSA) to identify quantitative trait locus (QTLs) for flowering time in a segregating population derived from a cross between Japanese soybean cultivars. Despite the homogeneous genetic background of the parents, over 7000 SNPs were identified and can be used to detect QTLs by RAD-seq BSA analysis. By comparing genotype frequency between early and late-flowering bulks from the F-3 segregating population, we identified a QTL on Gm10, which corresponds to the previously identified E2 locus, and a QTL on Gm04, which is close to the E8 locus. Out of these SNPs, more than 2000 were easily converted to conventional DNA markers. Our approach would improve the efficiency of genetic mapping.
机译:大豆(MAX)具有古聚吡啶基因组,许多重新测序实验表征大豆基因型的使用下一代测序平台进行。整个大豆基因组中单核苷酸多态性(SNP)的累积积累了通过关联研究的基因组区域的鉴定。然而,尽管可以使用许多使用下一代测序的有效映射技术,但是识别基因/基因座的实际方法的数量仍然有限。在该研究中,我们使用限制性位点相关的DNA测序(Rad-SEQ)和批量分析分析(BSA)的组合来鉴定从日本大豆品种之间的交叉的分离群体中开花时间的定量性状基因座(QTLS)。尽管父母的均匀遗传背景,但鉴定了超过7000个SNP,并且可用于通过Rad-SEQ BSA分析检测QTL。通过比较来自F-3分离群体的早期和后期开花块之间的基因型频率,我们在GM10上识别了QTL,其对应于先前识别的E2基因座,以及GM04上的QTL,其接近E8基因座。在这些SNP中,超过2000年易于转化为常规DNA标记。我们的方法将提高遗传映射的效率。

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