Department of Crop Sciences, University of Illinois, Urbana, IL 61801, USA.
Theor Appl Genet. 2010 Aug;121(3):599-610. doi: 10.1007/s00122-010-1333-6. Epub 2010 May 8.
The discovery of biotype diversity of soybean aphid (SA: Aphis glycines Matsumura) in North America emphasizes the necessity to identify new aphid-resistance genes. The soybean [Glycine max (L.) Merr.] plant introduction (PI) 200538 is a promising source of SA resistance because it shows a high level of resistance to a SA biotype that can overcome the SA-resistance gene Rag1 from 'Dowling'. The SA-resistance gene Rag2 was previously mapped from PI 200538 to a 10-cM marker interval on soybean chromosome 13 [formerly linkage group (LG) F]. The objective of this study was to fine map Rag2. This fine mapping was carried out using lines derived from 5,783 F(2) plants at different levels of backcrossing that were screened with flanking genetic markers for the presence of recombination in the Rag2 interval. Fifteen single nucleotide polymorphism (SNP) markers and two dominant polymerase chain reaction-based markers near Rag2 were developed by re-sequencing target intervals and sequence-tagged sites. These efforts resulted in the mapping of Rag2 to a 54-kb interval on the Williams 82 8x assembly (Glyma1). This Williams 82 interval contains seven predicted genes, which includes one nucleotide-binding site-leucine-rich repeat gene. SNP marker and candidate gene information identified in this study will be an important resource in marker-assisted selection for aphid resistance and for cloning the gene.
大豆蚜(SA:Aphis glycines Matsumura)在北美的生物型多样性的发现强调了鉴定新的蚜虫抗性基因的必要性。大豆[Glycine max(L.)Merr.]植物引种(PI)200538 是 SA 抗性的一个很有前途的来源,因为它对一种能够克服来自'Dowling'的 SA 抗性基因 Rag1 的 SA 生物型表现出高水平的抗性。先前已经将 SA 抗性基因 Rag2 从 PI 200538 映射到大豆染色体 13[以前的连锁群(LG)F]上的 10-cM 标记区间。本研究的目的是精细定位 Rag2。这项精细定位是使用来自不同回交水平的 5783 个 F2 植物系进行的,这些植物系通过侧翼遗传标记筛选 Rag2 区间是否存在重组。在 Rag2 附近开发了 15 个单核苷酸多态性(SNP)标记和两个基于显性聚合酶链反应的标记,通过重新测序目标间隔和序列标记位点。这些努力将 Rag2 映射到 Williams 82 8x 组装(Glyma1)上的 54-kb 区间。这个 Williams 82 区间包含七个预测基因,其中包括一个核苷酸结合位点-亮氨酸丰富重复基因。在这项研究中确定的 SNP 标记和候选基因信息将是蚜虫抗性辅助选择和基因克隆的重要资源。