Department of Plant Breeding and Genetics, Cornell University, New York State Agricultural Experiment Station, Geneva, NY, 14456, USA.
Theor Appl Genet. 2013 Nov;126(11):2849-63. doi: 10.1007/s00122-013-2176-8. Epub 2013 Aug 11.
Clover yellow vein virus (ClYVV) is capable of causing severe damage to common bean (Phaseolus vulgaris L.) production worldwide. The snap bean market class is particularly vulnerable because infection may lead to distortion and necrosis of the fresh green pods and rejection of the harvest. Three putatively independent recessive genes (cyv, desc, bc-3) have been reported to condition resistance to ClYVV; however, their allelic relationships have not been resolved. We identified, evaluated, and characterized the phenotypic and molecular genetic variation present in 21 informative common bean genotypes for resistance to ClYVV. Allelism testing phenotypes from multiple populations provided clear evidence that the three genes were a series of recessive alleles at the Bc-3 locus that condition unique potyvirus strain- and species-specific resistance spectra. Candidate gene analysis revealed complete association between the recessive resistance alleles and unique patterns of predicted amino acid substitutions in P. vulgaris eukaryotic translation initiation factor 4E (PveIF4E). This led to the discovery and characterization of two novel PveIF4E alleles associated with resistance to ClYVV, PveIF4E (3) , and PveIF4E (4) . We developed KASPar allele-specific SNP genotyping assays and demonstrated their ability to accurately detect and differentiate all of the PveIF4E haplotypes present in the germplasm, allelism testing, and in three separate segregating populations. The results contribute to an enhanced understanding and accessibility of the important potyvirus resistance conditioned by recessive alleles at Bc-3. The KASPar assays should be useful to further enable germplasm exploration, allelic discrimination, and marker-assisted introgression of bc-3 alleles in common bean.
三叶草黄脉病毒(ClYVV)能够在全球范围内对普通菜豆(Phaseolus vulgaris L.)的生产造成严重损害。青刀豆市场品种特别容易受到感染,因为感染可能导致新鲜绿色豆荚的扭曲和坏死,以及拒收。已经报道了三个独立的隐性基因(cyv、desc、bc-3)条件对 ClYVV 的抗性;然而,它们的等位基因关系尚未解决。我们鉴定、评估和表征了 21 个信息丰富的普通菜豆基因型对 ClYVV 的抗性表型和分子遗传变异。来自多个群体的等位基因测试表型提供了明确的证据,证明这三个基因是 Bc-3 位点的一系列隐性等位基因,决定了独特的马铃薯 Y 病毒株系和种特异性抗性谱。候选基因分析显示,隐性抗性等位基因与 P. vulgaris 真核翻译起始因子 4E(PveIF4E)中独特的预测氨基酸取代模式完全相关。这导致了两个与 ClYVV 抗性相关的新型 PveIF4E 等位基因的发现和表征,PveIF4E(3)和 PveIF4E(4)。我们开发了 KASPar 等位基因特异性 SNP 基因分型检测,并证明它们能够准确检测和区分种质、等位基因测试和三个分离群体中存在的所有 PveIF4E 单倍型。这些结果有助于深入了解和获得 Bc-3 条件下重要的马铃薯 Y 病毒抗性。KASPar 检测应该有助于进一步探索种质资源、等位基因鉴别以及 bc-3 等位基因在普通菜豆中的标记辅助导入。