鉴定与小麦茎锈病(Puccinia graminis f. sp. tritici)抗性基因相对应的候选抗性基因和病毒基因

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-08-01 Epub Date: 2024-08-27 DOI:10.1094/MPMI-05-24-0056-R
Arjun Upadhaya, Sudha G C Upadhaya, Robert Brueggeman
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引用次数: 0

摘要

由生物营养真菌病原体 Puccinia graminis f. sp. tritici(Pgt)引起的茎锈病是小麦的一种重要病害。然而,由于开发这种强制性生物营养体的双亲种群的限制,大多数 Pgt 毒力/病毒位点和潜在基因仍未定性。利用主要从美国西北太平洋地区收集的有性 Pgt 群体进行的全基因组关联研究(GWAS),确定了与六个小麦 Sr 基因(Sr5、Sr21、Sr8a、Sr17、Sr9a 和 Sr9d)相对应的候选毒力/病毒力效应基因。利用全基因组枪式测序对 Pgt 分离物进行了基因分型,确定了约 120 万个单核苷酸多态性 (SNP),并在苗期对六个 Sr 基因差异品系进行了表型分析。关联图谱分析在六个 Pgt 抗性基因上发现了 17 个与毒力或无毒表型相关的 Pgt 基因位点。在这些基因座中,16 个与特定的 Sr 基因相互作用,表明 Sr 基因具有特异性相互作用。然而,一个无毒基因座与两个不同的 Sr 基因(Sr9a 和 Sr17)相互作用,表明两个不同的 Sr 基因识别了一个无毒效应因子。共鉴定出 24 个独特的候选效应基因,单倍型分析表明,在该种群中,AvrSr5、AvrSr21、AvrSr8a、AvrSr17 和 AvrSr9a 是显性无毒基因,而 avrSr9d 是显性毒力基因。推测的效应基因将是未来效应基因克隆工作的基础,有助于进一步了解锈病效应生物学以及 Pgt 中种族特异性 R 基因的毒力进化机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of Candidate Avirulence and Virulence Genes Corresponding to Stem Rust (Puccinia graminis f. sp. tritici) Resistance Genes in Wheat.

Stem rust, caused by the biotrophic fungal pathogen Puccinia graminis f. sp. tritici (Pgt), is an important disease of wheat. However, the majority of Pgt virulence/avirulence loci and underlying genes remain uncharacterized due to the constraints of developing bi-parental populations with this obligate biotroph. Genome-wide association studies (GWAS) using a sexual Pgt population mainly collected from the Pacific Northwestern United States were used to identify candidate virulence/avirulence effector genes corresponding to the six wheat Sr genes: Sr5, Sr21, Sr8a, Sr17, Sr9a, and Sr9d. The Pgt isolates were genotyped using whole-genome shotgun sequencing that identified approximately 1.2 million single nucleotide polymorphisms (SNPs) and were phenotyped at the seedling stage on six Sr gene differential lines. Association mapping analyses identified 17 Pgt loci associated with virulence or avirulence phenotypes on six Pgt resistance genes. Among these loci, 16 interacted with a specific Sr gene, indicating Sr-gene specific interactions. However, one avirulence locus interacted with two separate Sr genes (Sr9a and Sr17), suggesting two distinct Sr genes identifying a single avirulence effector. A total of 24 unique effector gene candidates were identified, and haplotype analysis suggests that within this population, AvrSr5, AvrSr21, AvrSr8a, AvrSr17, and AvrSr9a are dominant avirulence genes, while avrSr9d is a dominant virulence gene. The putative effector genes will be fundamental for future effector gene cloning efforts, allowing for further understanding of rust effector biology and the mechanisms underlying virulence evolution in Pgt with respect to race-specific R-genes. [Formula: see text] Copyright © 2024 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license.

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CiteScore
7.20
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