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Fine mapping the soybean aphid resistance gene Rag1 in soybean

机译:精细定位大豆中的大豆抗蚜基因Rag1

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The soybean aphid (Aphis glycines Matsumura) is an important soybean [Glycine max (L.) Merr.] pest in North America. The dominant aphid resistance gene Rag1 was previously mapped from the cultivar Dowling' to a 12 cM marker interval on soybean chromosome 7 (formerly linkage group M). The development of additional genetic markers mapping closer to Rag1 was needed to accurately position the gene to improve the effectiveness of marker-assisted selection (MAS) and to eventually clone it. The objectives of this study were to identify single nucleotide polymorphisms (SNPs) near Rag1 and to position these SNPs relative to Rag1. To generate a fine map of the Rag1 interval, 824 BCF and 1,000 BCF plants segregating for the gene were screened with markers flanking Rag1. Plants with recombination events close to the gene were tested with SNPs identified in previous studies along with new SNPs identified from the preliminary Williams 82 draft soybean genome shotgun sequence using direct re-sequencing and gene-scanning melt-curve analysis. Progeny of these recombinant plants were evaluated for aphid resistance. These efforts resulted in the mapping of Rag1 between the two SNP markers 46169.7 and 21A, which corresponds to a physical distance on the Williams 82 8c draft assembly (Glyma1.01) of 115 kilobase pair (kb). Several candidate genes for Rag1 are present within the 115-kb interval. The markers identified in this study that are closely linked to Rag1 will be a useful resource in MAS for this important aphid resistance gene.
机译:大豆蚜虫(Aphis glycines Matsumura)是北美的一种重要大豆害虫[Glycine max(L.)Merr。]。先前将优势蚜虫抗性基因Rag1从品种Dowling'定位到大豆7号染色体(原连锁群M)的12 cM标记区间。需要开发更接近Rag1的其他遗传标记来精确定位基因,以提高标记辅助选择(MAS)的效率并最终克隆它。这项研究的目的是确定Rag1附近的单核苷酸多态性(SNP),并将这些SNP相对于Rag1定位。为了生成Rag1间隔的精细图,使用位于Rag1侧翼的标记筛选了针对该基因分离的824 BCF和1,000 BCF植物。使用直接重新测序和基因扫描熔解曲线分析,使用在先前研究中鉴定出的SNP以及从初步Williams 82大豆基因组shot弹枪序列鉴定出的新SNP,测试了具有接近基因重组事件的植物。评价这些重组植物的子代的蚜虫抗性。这些努力导致了Rag1在两个SNP标记46169.7和21A之间的映射,这对应于115碱基对(kb)的Williams 82 8c牵伸组件(Glyma1.01)上的物理距离。 115 kb间隔内存在Rag1的几个候选基因。在这项研究中确定的与Rag1密切相关的标记物将是MAS中重要的蚜虫抗性基因的有用资源。

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