灰葡萄孢在不同寄主中宿主特异性和一般毒力的多基因策略。

IF 5.1 3区 生物学 Q2 GENETICS & HEREDITY
Genetics Pub Date : 2025-07-09 DOI:10.1093/genetics/iyaf079
Céline Caseys, Daniel J Kliebenstein
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引用次数: 0

摘要

不同的定性和定量遗传结构可以成功地确定真菌的毒力和宿主范围。为了模拟具有广泛寄主范围的多面手病原体的定量遗传结构,我们对8个寄主的灰霉病(Botrytis cinerea)病变区域进行了全基因组关联研究(GWAS)。这表明,根据病变区域的定义,可以将所有宿主共有的毒力从宿主特异性毒力中分离出来。所有性状都表明,很大比例的葡萄孢菌基因组可能对叶片上真菌损伤的发育有贡献,但效应量很小。候选基因均匀地分布在核心染色体上,没有二部基因组结构的迹象。gwas鉴定的多态性和基因表明,灰芽孢杆菌依靠数百个基因的遗传变异在不同的宿主上生长,大多数基因影响相对较少的宿主。当病原体基因与多个宿主相关时,它们与不相关的而不是相关的宿主物种相关。比较基因组学进一步表明,gwas鉴定的基因在很大程度上与其他特殊的葡萄孢菌属同源,而不是葡萄孢杆菌所特有的。总体而言,如拟南芥所示,拟南芥的通才行为源于基因网络中全基因组遗传变异的总和,这些基因网络以不同的方式协调与不同宿主的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Polygenic strategies for host-specific and general virulence of Botrytis cinerea across diverse eudicot hosts.

Diverse qualitative and quantitative genetic architectures can successfully enable fungal virulence and host range. To model the quantitative genetic architecture of a generalist pathogen with an extensive host range, we conducted a genome-wide association study (GWAS) of the lesion area of Botrytis cinerea across 8 hosts. This revealed that it was possible to partition the virulence, as defined by the lesion area, common across all hosts from host-specific virulence. All traits showed that a large proportion of the Botrytis genome likely contributes to fungal lesion development on leaves with small effect sizes. The candidate genes are evenly spread across the core chromosomes with no indication of bipartite genomic architecture. The GWAS-identified polymorphisms and genes show that B. cinerea relies on genetic variants across hundreds of genes for growing on diverse hosts, with most genes influencing relatively few hosts. When pathogen genes were associated with multiple hosts, they were associated with unrelated rather than related host species. Comparative genomics further suggested that the GWAS-identified genes are largely syntenic with other specialist Botrytis species and not unique to B. cinerea. Overall, as shown in Arabidopsis thaliana, B. cinerea's generalist behavior is derived from the sum of the genome-wide genetic variation acting within gene networks that differentially coordinate the interaction with diverse hosts.

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来源期刊
Genetics
Genetics GENETICS & HEREDITY-
CiteScore
6.90
自引率
6.10%
发文量
177
审稿时长
1.5 months
期刊介绍: GENETICS is published by the Genetics Society of America, a scholarly society that seeks to deepen our understanding of the living world by advancing our understanding of genetics. Since 1916, GENETICS has published high-quality, original research presenting novel findings bearing on genetics and genomics. The journal publishes empirical studies of organisms ranging from microbes to humans, as well as theoretical work. While it has an illustrious history, GENETICS has changed along with the communities it serves: it is not your mentor''s journal. The editors make decisions quickly – in around 30 days – without sacrificing the excellence and scholarship for which the journal has long been known. GENETICS is a peer reviewed, peer-edited journal, with an international reach and increasing visibility and impact. All editorial decisions are made through collaboration of at least two editors who are practicing scientists. GENETICS is constantly innovating: expanded types of content include Reviews, Commentary (current issues of interest to geneticists), Perspectives (historical), Primers (to introduce primary literature into the classroom), Toolbox Reviews, plus YeastBook, FlyBook, and WormBook (coming spring 2016). For particularly time-sensitive results, we publish Communications. As part of our mission to serve our communities, we''ve published thematic collections, including Genomic Selection, Multiparental Populations, Mouse Collaborative Cross, and the Genetics of Sex.
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