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辣椒(Capsicum annuum L.)中辣椒脉斑驳病毒抗性4(cvr4)基因的精细定位

Fine mapping of the Chilli veinal mottle virus resistance 4 (cvr4) gene in pepper (Capsicum annuum L.).

作者信息

Lee Joung-Ho, Kim Jung-Min, Kwon Jin-Kyung, Kang Byoung-Cheorl

机构信息

Department of Agriculture, Forestry and Bioresources, Research Institute of Agriculture and Life Sciences, Plant Genomics and Breeding Institute, College of Agriculture and Life Sciences, Seoul National University, Seoul, 08826, Republic of Korea.

Interdisciplinary Program in Agricultural Biotechnology, College of Agriculture and Life Sciences, Seoul National University, Seoul, 08826, Republic of Korea.

出版信息

Theor Appl Genet. 2025 Jan 7;138(1):19. doi: 10.1007/s00122-024-04805-8.

DOI:10.1007/s00122-024-04805-8
PMID:39777543
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11706928/
Abstract

The single recessive Chilli veinal mottle virus resistance locus, cvr4, was fine-mapped in pepper through bulked segregant RNA sequencing combined with gene silencing analysis. Chilli veinal mottle virus (ChiVMV) is a widespread pathogen affecting the production of peppers (Capsicum annuum L.) in Asia and Africa. Few loci conferring resistance to ChiVMV have been identified, severely limiting the development of resistant cultivars. To identify ChiVMV resistance genes, we constructed an F segregating population derived from a cross between the ChiVMV-resistant cultivar 'CV9' and the susceptible cultivar 'Jeju'. The inheritance study of F populations showed a 1:3 ratio of resistant to susceptible individuals, demonstrating the existence of a single recessive ChiVMV resistance gene in CV9; we named this gene cvr4. To map the cvr4 locus, we employed bulked segregant analysis by RNA sequencing (BSR-seq) of pools from resistant and susceptible F individuals. We mapped cvr4 to the telomeric region of pepper chromosome 11. To narrow down the cvr4 locus, we developed additional molecular markers in the cvr4 target region, leading to a 2-Mb region of chromosome 11 showing complete co-segregation with the ChiVMV resistance phenotype. Using the polymorphisms identified during BSR-seq, we defined a list of 15 candidate genes for cvr4, which we tested through virus-induced gene silencing analysis for ChiVMV resistance. Of these, the silencing of several genes (DEM.v1.00021323, DEM.v1.00021336, and DEM.v1.00021337) restricted virus spread. Although DEM.v1.00021323 transcript levels were similar between the resistant and susceptible bulks, its alternative spliced isoforms differed in abundance, suggesting that the splicing variants of DEM.v1.00021323 might affect viral infection. These findings may facilitate the breeding of ChiVMV-resistant cultivars in pepper.

摘要

通过混合分组分离RNA测序结合基因沉默分析,在辣椒中对单隐性辣椒脉斑驳病毒抗性基因座cvr4进行了精细定位。辣椒脉斑驳病毒(ChiVMV)是一种广泛传播的病原体,影响亚洲和非洲辣椒(Capsicum annuum L.)的生产。已鉴定出的对ChiVMV具有抗性的基因座很少,这严重限制了抗性品种的培育。为了鉴定ChiVMV抗性基因,我们构建了一个F分离群体,该群体来自抗ChiVMV品种‘CV9’与感病品种‘济州’的杂交。F群体的遗传研究表明,抗性个体与感病个体的比例为1:3,这表明CV9中存在一个单隐性ChiVMV抗性基因;我们将该基因命名为cvr4。为了定位cvr4基因座,我们通过对来自抗性和感病F个体的池进行RNA测序的混合分组分离分析(BSR-seq)。我们将cvr4定位到辣椒11号染色体的端粒区域。为了缩小cvr4基因座的范围,我们在cvr4目标区域开发了额外的分子标记,从而确定11号染色体上一个2 Mb的区域与ChiVMV抗性表型完全共分离。利用在BSR-seq过程中鉴定出的多态性,我们确定了15个cvr4候选基因列表,并通过病毒诱导的基因沉默分析对它们进行ChiVMV抗性测试。其中,几个基因(DEM.v1.00021323、DEM.v1.00021336和DEM.v1.00021337)的沉默限制了病毒传播。尽管抗性和感病混合群体之间DEM.v1.00021323的转录水平相似,但其可变剪接异构体的丰度不同,这表明DEM.v1.00021323的剪接变体可能影响病毒感染。这些发现可能有助于辣椒抗ChiVMV品种的培育。

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A natural substitution of a conserved amino acid in eIF4E confers resistance against multiple potyviruses.
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