Syngenta Seeds Inc., 2369 330th St., Slater, IA 50224, USA.
Theor Appl Genet. 2011 Feb;122(2):445-57. doi: 10.1007/s00122-010-1459-6. Epub 2010 Oct 8.
Soybean mosaic virus (SMV) is one of the most destructive viral diseases in soybean (Glycine max). Three independent loci for SMV resistance have been identified in soybean germplasm. The use of genetic resistance is the most effective method of controlling this disease. Marker assisted selection (MAS) has become very important and useful in the effort of selecting genes for SMV resistance. Single nucleotide polymorphism (SNP), because of its abundance and high-throughput potential, is a powerful tool in genome mapping, association studies, diversity analysis, and tagging of important genes in plant genomics. In this study, a 10 SNPs plus one insert/deletion (InDel) multiplex assay was developed for SMV resistance: two SNPs were developed from the candidate gene 3gG2 at Rsv1 locus, two SNPs selected from the clone N11PF linked to Rsv1, one 'BARC' SNP screened from soybean chromosome 13 [linkage group (LG) F] near Rsv1, two 'BARC' SNPs from probe A519 linked to Rsv3, one 'BARC' SNP from chromosome 14 (LG B2) near Rsv3, and two 'BARC' SNPs from chromosome 2 (LG D1b) near Rsv4, plus one InDel marker from expressed sequence tag (EST) AW307114 linked to Rsv4. This 11 SNP/InDel multiplex assay showed polymorphism among 47 diverse soybean germplasm, indicating this assay can be used to investigate the mode of inheritance in a SMV resistant soybean line carrying Rsv1, Rsv3, and/or Rsv4 through a segregating population with phenotypic data, and to select a specific gene or pyramid two or three genes for SMV resistance through MAS in soybean breeding program. The presence of two SMV resistance genes (Rsv1 and Rsv3) in J05 soybean was confirmed by the SNP assay.
大豆花叶病毒(SMV)是大豆(Glycine max)最具破坏性的病毒性疾病之一。在大豆种质资源中已鉴定出三个独立的 SMV 抗性基因座。利用遗传抗性是控制这种疾病最有效的方法。标记辅助选择(MAS)已成为选择 SMV 抗性基因的非常重要和有用的方法。单核苷酸多态性(SNP)由于其丰富性和高通量潜力,是植物基因组学中基因组图谱、关联研究、多样性分析和重要基因标记的有力工具。在这项研究中,开发了一种用于 SMV 抗性的 10 个 SNP 加一个插入/缺失(InDel)多重检测方法:两个 SNP 是从候选基因 3gG2 在 Rsv1 基因座中开发的,两个 SNP 是从与 Rsv1 连锁的克隆 N11PF 中选择的,一个'BARC' SNP 是从大豆染色体 13 上 Rsv1 附近的[连锁群(LG)F]筛选出来的,两个'BARC' SNP 是从与 Rsv3 连锁的探针 A519 中筛选出来的,一个'BARC' SNP 是从染色体 14(LG B2)上 Rsv3 附近筛选出来的,两个'BARC' SNP 是从染色体 2(LG D1b)上 Rsv4 附近筛选出来的,以及一个来自表达序列标签(EST)AW307114 的 InDel 标记与 Rsv4 连锁。该 11 个 SNP/InDel 多重检测方法在 47 种不同的大豆种质资源中表现出多态性,表明该检测方法可用于通过具有表型数据的分离群体研究携带 Rsv1、Rsv3 和/或 Rsv4 的抗 SMV 大豆品系的遗传模式,并通过大豆 MAS 选择特定基因或三个基因的抗 SMV 性。通过 SNP 检测证实 J05 大豆中存在两个 SMV 抗性基因(Rsv1 和 Rsv3)。