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}
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.