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对来自野生大豆85-32的大豆蚜抗性基因Rag6和Rag3c进行精细定位。

Fine mapping of the soybean aphid-resistance genes Rag6 and Rag3c from Glycine soja 85-32.

作者信息

Zhang Shichen, Zhang Zhongnan, Wen Zixiang, Gu Cuihua, An Yong-Qiang Charles, Bales Carmille, DiFonzo Chris, Song Qijian, Wang Dechun

机构信息

Department of Plant, Soil and Microbial Sciences, Michigan State University, 1066 Bogue St., Rm. A384E, East Lansing, MI, 48824-1325, USA.

Plant Genetic Research Unit, Agricultural Research Service, United States Department of Agriculture, at Danforth Plant Science Center, St. Louis, MO, 63132, USA.

出版信息

Theor Appl Genet. 2017 Dec;130(12):2601-2615. doi: 10.1007/s00122-017-2979-0. Epub 2017 Sep 8.

Abstract

Rag6 and Rag3c were delimited to a 49-kb interval on chromosome 8 and a 150-kb interval on chromosome 16, respectively. Structural variants in the exons of candidate genes were identified. The soybean aphid, an invasive species, has significantly threatened soybean production in North America since 2000. Host-plant resistance is known as an ideal management strategy for aphids. Two novel aphid-resistance loci, Rag6 and Rag3c, from Glycine soja 85-32, were previously detected in a 10.5-cM interval on chromosome 8 and a 7.5-cM interval on chromosome 16, respectively. Defining the exact genomic position of these two genes is critical for improving the effectiveness of marker-assisted selection for aphid resistance and for identification of the functional genes. To pinpoint the locations of Rag6 and Rag3c, four populations segregating for Rag6 and Rag3c were used to fine map these two genes. The availability of the Illumina Infinium SoySNP50K/8K iSelect BeadChip, combined with single-nucleotide polymorphism (SNP) markers discovered through the whole-genome re-sequencing of E12901, facilitated the fine mapping process. Rag6 was refined to a 49-kb interval on chromosome 8 with four candidate genes, including three clustered nucleotide-binding site leucine-rich repeat (NBS-LRR) genes and an amine oxidase encoding gene. Rag3c was refined to a 150-kb interval on chromosome 16 with 11 candidate genes, two of which are a LRR gene and a lipase gene. Moreover, by sequencing the whole-genome exome-capture of the resistant source (E12901), structural variants were identified in the exons of the candidate genes of Rag6 and Rag3c. The closely linked SNP markers and the candidate gene information presented in this study will be significant resources for integrating Rag6 and Rag3c into elite cultivars and for future functional genetics studies.

摘要

Rag6和Rag3c分别被定位到8号染色体上一个49千碱基对的区间和16号染色体上一个150千碱基对的区间。鉴定了候选基因外显子中的结构变异。大豆蚜是一种入侵物种,自2000年以来已对北美大豆生产造成严重威胁。寄主植物抗性是防治蚜虫的理想策略。先前从野生大豆85 - 32中检测到两个新的抗蚜位点Rag6和Rag3c,分别位于8号染色体上一个10.5厘摩的区间和16号染色体上一个7.5厘摩的区间。确定这两个基因的确切基因组位置对于提高抗蚜性标记辅助选择的有效性以及鉴定功能基因至关重要。为了精确确定Rag6和Rag3c的位置,利用四个分离Rag6和Rag3c的群体对这两个基因进行精细定位。Illumina Infinium SoySNP50K/8K iSelect BeadChip的可用性,结合通过E12901全基因组重测序发现的单核苷酸多态性(SNP)标记,促进了精细定位过程。Rag6被精细定位到8号染色体上一个49千碱基对的区间,有四个候选基因,包括三个成簇的核苷酸结合位点富含亮氨酸重复序列(NBS - LRR)基因和一个胺氧化酶编码基因。Rag3c被精细定位到16号染色体上一个150千碱基对的区间,有11个候选基因,其中两个是LRR基因和一个脂肪酶基因。此外,通过对抗性来源(E12901)的全基因组外显子捕获进行测序,在Rag6和Rag3c的候选基因外显子中鉴定到了结构变异。本研究中呈现的紧密连锁SNP标记和候选基因信息将是把Rag6和Rag3c整合到优良品种中以及未来功能遗传学研究的重要资源。

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