The alleles bc-ud and bc-ur (previously bc-4 gene), representing coding mutations within Vps4 AAA+ ATPase ESCRT protein, interact with other genes to condition resistance to BCMV and BCMNV in common bean

Alvaro Soler-Garzón, Phillip E. McClean, Phillip N. Miklas
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Abstract

Bean common mosaic virus (BCMV) and bean common mosaic necrosis virus (BCMNV) have a damaging impact on global common bean (Phaseolus vulgaris L.) cultivation, causing potential yield losses of over 80%. The primary strategy for controlling these viruses is through host plant resistance. This research aimed to identify and validate structural variations for the bc-ud gene as revealed by long-read sequencing, develop an efficient DNA marker to assist selection of bc-ud in snap and dry beans, and examine the interactions between the bc-ud allele and other BCMV resistance genes. A gene (Phvul.005G125100) model on chromosome Pv05, encoding a vacuolar protein-sorting 4 (Vps4) AAA+ ATPase endosomal sorting complexes required for transport (ESCRT) protein, was identified as the best candidate gene for bc-ud. An 84-bp repetitive insertion variant within the gene, exhibited 100% co-segregation with the bc-ud resistance allele across 264 common bean accessions. The 84-bp repetitive insertion was labeled with an indel marker IND_05_36225873 which was useful for tracking the bc-ud allele across diverse germplasm. A different single nucleotide polymorphism variant within the same candidate gene was associated with the bc-4 gene. Segregation in F2 populations confirmed bc-ud and bc-4 were alleles, so bc-4 was renamed bc-ur to fit gene nomenclature guidelines. The interactions of bc-ud and bc-ur with other resistance genes, such as bc-1 (receptor-like kinase on Pv03) and bc-2 (Vps4 AAA+ ATPase ESCRT protein on Pv11), validated gene combinations in the differential “host groups” effective against specific BCMV/BCMNV “pathogroups.” These findings increase our understanding of the Bc-u locus, and enhance our ability to develop more resilient bean varieties through marker-assisted selection, reducing the impact of BCMV and BCMNV.
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代表 Vps4 AAA+ ATPase ESCRT 蛋白编码突变的等位基因 bc-ud 和 bc-ur(以前的 bc-4 基因)与其他基因相互作用,对普通豆类的 BCMV 和 BCMNV 产生抗性。
大豆普通花叶病毒(BCMV)和大豆普通花叶坏死病毒(BCMNV)对全球普通豆(Phaseolus vulgaris L.)种植造成破坏性影响,造成80%以上的潜在产量损失。控制这些病毒的主要策略是通过寄主植物的抗性。本研究旨在通过长读测序鉴定和验证bc-ud基因的结构变异,开发一种高效的DNA标记来辅助速食和干豆中bc-ud基因的选择,并研究bc-ud等位基因与其他BCMV抗性基因之间的相互作用。染色体Pv05上的一个编码空泡蛋白-分选4 (Vps4) AAA+ atp酶内体转运所需分选复合物(ESCRT)蛋白的基因(phvull . 005g125100)模型被确定为bc-ud的最佳候选基因。该基因中的一个84 bp重复插入变异在264份普通豆材料中与bc-ud抗性等位基因表现出100%的共分离。将84 bp重复插入片段用indel标记IND_05_36225873进行标记,该标记可用于在不同种质间追踪bc-ud等位基因。bc-4基因与同一候选基因内不同的单核苷酸多态性变异相关。在F2个群体中分离证实bc-ud和bc-4为等位基因,因此bc-4被重新命名为bc-ur,以符合基因命名指南。bc-ud和bc-ur与其他耐药基因,如bc-1 (Pv03上的受体样激酶)和bc-2 (Pv11上的Vps4 AAA+ ATPase ESCRT蛋白)的相互作用,证实了差异“宿主组”中的基因组合对特定BCMV/BCMNV“病理组”有效。这些发现增加了我们对Bc-u基因座的理解,并增强了我们通过标记辅助选择开发更具抗逆性的豆类品种的能力,减少了BCMV和BCMNV的影响。
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