Comprehensive Mutational Landscape of Yeast Mutator Strains Reveals the Genetic Basis of Mutational Signatures in Cancer.

IF 5.3 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Lei Liu, Danyang Sun, Haoxuan Liu
{"title":"Comprehensive Mutational Landscape of Yeast Mutator Strains Reveals the Genetic Basis of Mutational Signatures in Cancer.","authors":"Lei Liu, Danyang Sun, Haoxuan Liu","doi":"10.1093/molbev/msaf252","DOIUrl":null,"url":null,"abstract":"<p><p>Spontaneous mutation rates and spectra are influenced by an intricate interplay of processes including DNA replication, proofreading, and diverse DNA damage repair pathways. Although significant progress has been made in characterizing the functions of individual genes involved in these processes, their direct effects on mutation rates and spectra remain unclear. In this study, we employed a systematic gene knockout approach coupled with mutation accumulation (MA) experiments and whole-genome sequencing (WGS) to investigate the mutational landscape of Saccharomyces cerevisiae. We targeted 136 gene-deletion strains encompassing nearly all known genes associated with DNA replication and repair. Analysis of 1,081 MA lines revealed that 114 of the 136 genes significantly influenced at least one type of mutation rate. Furthermore, deletions of specific genes led to marked shifts in mutational biases and spectra, with some deletions amplifying existing biases and others reversing them entirely. In contrast, mitochondrial mutation rates were notably less affected, with no significant impact detected. Importantly, comparative analysis revealed striking similarities between yeast mutational spectrum and those observed in human cancers with the same pathway deficiencies, suggesting conserved functional roles across species. In conclusion, our findings provided critical insights into the genetic underpinnings of these signatures and underscoring the utility of yeast as a model for studying the molecular basis of cancer-associated mutational processes.</p>","PeriodicalId":18730,"journal":{"name":"Molecular biology and evolution","volume":" ","pages":""},"PeriodicalIF":5.3000,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular biology and evolution","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/molbev/msaf252","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Spontaneous mutation rates and spectra are influenced by an intricate interplay of processes including DNA replication, proofreading, and diverse DNA damage repair pathways. Although significant progress has been made in characterizing the functions of individual genes involved in these processes, their direct effects on mutation rates and spectra remain unclear. In this study, we employed a systematic gene knockout approach coupled with mutation accumulation (MA) experiments and whole-genome sequencing (WGS) to investigate the mutational landscape of Saccharomyces cerevisiae. We targeted 136 gene-deletion strains encompassing nearly all known genes associated with DNA replication and repair. Analysis of 1,081 MA lines revealed that 114 of the 136 genes significantly influenced at least one type of mutation rate. Furthermore, deletions of specific genes led to marked shifts in mutational biases and spectra, with some deletions amplifying existing biases and others reversing them entirely. In contrast, mitochondrial mutation rates were notably less affected, with no significant impact detected. Importantly, comparative analysis revealed striking similarities between yeast mutational spectrum and those observed in human cancers with the same pathway deficiencies, suggesting conserved functional roles across species. In conclusion, our findings provided critical insights into the genetic underpinnings of these signatures and underscoring the utility of yeast as a model for studying the molecular basis of cancer-associated mutational processes.

酵母突变株的综合突变景观揭示了癌症突变特征的遗传基础。
自发突变率和谱受到包括DNA复制、校对和多种DNA损伤修复途径在内的过程的复杂相互作用的影响。尽管在描述参与这些过程的单个基因的功能方面取得了重大进展,但它们对突变率和谱的直接影响仍不清楚。在这项研究中,我们采用了系统的基因敲除方法,结合突变积累(MA)实验和全基因组测序(WGS)来研究酿酒酵母的突变景观。我们的目标是136个基因缺失菌株,几乎包含所有已知的与DNA复制和修复相关的基因。对1081个MA系的分析显示,136个基因中有114个显著影响至少一种类型的突变率。此外,特定基因的缺失导致突变偏差和谱的显著变化,一些缺失放大了现有的偏差,而另一些则完全逆转了它们。相比之下,线粒体突变率受到的影响较小,未检测到显著影响。重要的是,比较分析揭示了酵母突变谱与具有相同途径缺陷的人类癌症中观察到的突变谱之间惊人的相似性,表明物种之间存在保守的功能作用。总之,我们的发现为这些特征的遗传基础提供了重要的见解,并强调了酵母作为研究癌症相关突变过程分子基础的模型的实用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Molecular biology and evolution
Molecular biology and evolution 生物-进化生物学
CiteScore
19.70
自引率
3.70%
发文量
257
审稿时长
1 months
期刊介绍: Molecular Biology and Evolution Journal Overview: Publishes research at the interface of molecular (including genomics) and evolutionary biology Considers manuscripts containing patterns, processes, and predictions at all levels of organization: population, taxonomic, functional, and phenotypic Interested in fundamental discoveries, new and improved methods, resources, technologies, and theories advancing evolutionary research Publishes balanced reviews of recent developments in genome evolution and forward-looking perspectives suggesting future directions in molecular evolution applications.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信