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。

Alvaro Soler-Garzón, Phillip E. McClean, Phillip N. Miklas
{"title":"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。","authors":"Alvaro Soler-Garzón, Phillip E. McClean, Phillip N. Miklas","doi":"10.1002/tpg2.20421","DOIUrl":null,"url":null,"abstract":"<i>Bean common mosaic virus</i> (BCMV) and <i>bean common mosaic necrosis virus</i> (BCMNV) have a damaging impact on global common bean (<i>Phaseolus vulgaris</i> 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 <i>bc-u</i><sup>d</sup> gene as revealed by long-read sequencing, develop an efficient DNA marker to assist selection of <i>bc-u</i><sup>d</sup> in snap and dry beans, and examine the interactions between the <i>bc-u</i><sup>d</sup> 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 <i>bc-u</i><sup>d</sup>. An 84-bp repetitive insertion variant within the gene, exhibited 100% co-segregation with the <i>bc-u</i><sup>d</sup> 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 <i>bc-u</i><sup>d</sup> allele across diverse germplasm. A different single nucleotide polymorphism variant within the same candidate gene was associated with the <i>bc-4</i> gene. Segregation in F<sub>2</sub> populations confirmed <i>bc-u</i><sup>d</sup> and <i>bc-4</i> were alleles, so <i>bc-4</i> was renamed <i>bc-u</i><sup>r</sup> to fit gene nomenclature guidelines. The interactions of <i>bc-u</i><sup>d</sup> and <i>bc-u</i><sup>r</sup> with other resistance genes, such as <i>bc-1</i> (receptor-like kinase on Pv03) and <i>bc-2</i> (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 <i>Bc-u</i> locus, and enhance our ability to develop more resilient bean varieties through marker-assisted selection, reducing the impact of BCMV and BCMNV.","PeriodicalId":501653,"journal":{"name":"The Plant Genome","volume":"38 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"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\",\"authors\":\"Alvaro Soler-Garzón, Phillip E. McClean, Phillip N. Miklas\",\"doi\":\"10.1002/tpg2.20421\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<i>Bean common mosaic virus</i> (BCMV) and <i>bean common mosaic necrosis virus</i> (BCMNV) have a damaging impact on global common bean (<i>Phaseolus vulgaris</i> 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 <i>bc-u</i><sup>d</sup> gene as revealed by long-read sequencing, develop an efficient DNA marker to assist selection of <i>bc-u</i><sup>d</sup> in snap and dry beans, and examine the interactions between the <i>bc-u</i><sup>d</sup> 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 <i>bc-u</i><sup>d</sup>. An 84-bp repetitive insertion variant within the gene, exhibited 100% co-segregation with the <i>bc-u</i><sup>d</sup> 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 <i>bc-u</i><sup>d</sup> allele across diverse germplasm. A different single nucleotide polymorphism variant within the same candidate gene was associated with the <i>bc-4</i> gene. Segregation in F<sub>2</sub> populations confirmed <i>bc-u</i><sup>d</sup> and <i>bc-4</i> were alleles, so <i>bc-4</i> was renamed <i>bc-u</i><sup>r</sup> to fit gene nomenclature guidelines. The interactions of <i>bc-u</i><sup>d</sup> and <i>bc-u</i><sup>r</sup> with other resistance genes, such as <i>bc-1</i> (receptor-like kinase on Pv03) and <i>bc-2</i> (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 <i>Bc-u</i> locus, and enhance our ability to develop more resilient bean varieties through marker-assisted selection, reducing the impact of BCMV and BCMNV.\",\"PeriodicalId\":501653,\"journal\":{\"name\":\"The Plant Genome\",\"volume\":\"38 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-12-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Plant Genome\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/tpg2.20421\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Plant Genome","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/tpg2.20421","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
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
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.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Deciphering the genetic basis of novel traits that discriminate useful and non-useful biomass to enhance harvest index in wheat. Functional characterization of protein SUMOylation in the miRNA transcription regulation during heat stress in Arabidopsis Genome‐wide association mapping reveals novel genes and genomic regions controlling root‐lesion nematode resistance in chickpea mini core collection Genomic prediction for potato (Solanum tuberosum) quality traits improved through image analysis Multi‐locus genome‐wide association study for grain yield and drought tolerance indices in sorghum accessions
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1