DNA repair under heat: DNA polymerase λ modulates heat stress-induced mutagenesis in plants.

IF 11.6 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Plant Cell Pub Date : 2026-04-03 DOI:10.1093/plcell/koag090
Clair M Wootan, John Lutterman, Nathan Springer, Xiaosa Xu, Feng Zhang
{"title":"DNA repair under heat: DNA polymerase λ modulates heat stress-induced mutagenesis in plants.","authors":"Clair M Wootan, John Lutterman, Nathan Springer, Xiaosa Xu, Feng Zhang","doi":"10.1093/plcell/koag090","DOIUrl":null,"url":null,"abstract":"<p><p>Mutation rates often rise under environmental stress, a process known as stress-induced mutagenesis. Among abiotic factors, heat stress is a potent driver that elevates mutation rates and enhances genetic variation, yet the underlying mechanisms in eukaryotes remain unclear. Here, we investigated how heat stress influences DNA repair and mutagenesis both locally and globally in Arabidopsis thaliana using CRISPR-Cas9-induced DNA breaks, whole genome sequencing, and single-cell transcriptomic analysis. Heat stress greatly enhanced CRISPR editing efficiency across different chromatin contexts, reaching up to a 29.9-fold increase in heterochromatic regions. Moreover, heat stress consistently shifted repair outcomes toward one base pair insertions, independent of chromatin state. We identified a heat-inducible, error-prone DNA polymerase, DNA polymerase λ (DNA Polλ), as the key mediator of these repair profile changes. Genome-wide analyses of somatic mutations further revealed that the heat-induced increase in mutagenesis also depends on DNA Polλ. Single-cell transcriptomic profiling showed that DNA Polλ expression is tightly regulated and enriched in the central zone of the shoot apical meristem. Such tissue-specific patterns suggest that DNA Polλ serves dual functions: maintaining genome integrity in essential stem cell populations while also enabling stress-induced mutagenesis that can be transmitted to progeny.</p>","PeriodicalId":20186,"journal":{"name":"Plant Cell","volume":" ","pages":""},"PeriodicalIF":11.6000,"publicationDate":"2026-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13089500/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Cell","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/plcell/koag090","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

Mutation rates often rise under environmental stress, a process known as stress-induced mutagenesis. Among abiotic factors, heat stress is a potent driver that elevates mutation rates and enhances genetic variation, yet the underlying mechanisms in eukaryotes remain unclear. Here, we investigated how heat stress influences DNA repair and mutagenesis both locally and globally in Arabidopsis thaliana using CRISPR-Cas9-induced DNA breaks, whole genome sequencing, and single-cell transcriptomic analysis. Heat stress greatly enhanced CRISPR editing efficiency across different chromatin contexts, reaching up to a 29.9-fold increase in heterochromatic regions. Moreover, heat stress consistently shifted repair outcomes toward one base pair insertions, independent of chromatin state. We identified a heat-inducible, error-prone DNA polymerase, DNA polymerase λ (DNA Polλ), as the key mediator of these repair profile changes. Genome-wide analyses of somatic mutations further revealed that the heat-induced increase in mutagenesis also depends on DNA Polλ. Single-cell transcriptomic profiling showed that DNA Polλ expression is tightly regulated and enriched in the central zone of the shoot apical meristem. Such tissue-specific patterns suggest that DNA Polλ serves dual functions: maintaining genome integrity in essential stem cell populations while also enabling stress-induced mutagenesis that can be transmitted to progeny.

高温下的DNA修复:DNA聚合酶λ调节植物热胁迫诱导的诱变。
在环境压力下,突变率通常会上升,这一过程被称为压力诱导诱变。在非生物因素中,热应激是提高突变率和增强遗传变异的有力驱动因素,但真核生物的潜在机制尚不清楚。在这里,我们利用CRISPR-Cas9诱导的DNA断裂、全基因组测序和单细胞转录组分析,研究了热应激如何影响拟南芥局部和全局的DNA修复和突变。热应激极大地提高了CRISPR在不同染色质背景下的编辑效率,在异染色质区域的编辑效率提高了29.9倍。此外,热应激持续地将修复结果转向一个碱基对插入,独立于染色质状态。我们发现了一种热诱导的,容易出错的DNA聚合酶,DNA聚合酶λ (DNA Polλ),作为这些修复谱变化的关键介质。体细胞突变的全基因组分析进一步表明,热诱导的诱变增加也取决于DNA Polλ。单细胞转录组学分析表明,DNA Polλ的表达受到严格调控,并在茎尖分生组织中心区域富集。这种组织特异性模式表明,DNA Polλ具有双重功能:维持基本干细胞群体的基因组完整性,同时也使胁迫诱导的突变能够传递给后代。
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
Plant Cell
Plant Cell 生物-生化与分子生物学
CiteScore
16.90
自引率
5.20%
发文量
337
审稿时长
2.4 months
期刊介绍: Title: Plant Cell Publisher: Published monthly by the American Society of Plant Biologists (ASPB) Produced by Sheridan Journal Services, Waterbury, VT History and Impact: Established in 1989 Within three years of publication, ranked first in impact among journals in plant sciences Maintains high standard of excellence Scope: Publishes novel research of special significance in plant biology Focus areas include cellular biology, molecular biology, biochemistry, genetics, development, and evolution Primary criteria: articles provide new insight of broad interest to plant biologists and are suitable for a wide audience Tenets: Publish the most exciting, cutting-edge research in plant cellular and molecular biology Provide rapid turnaround time for reviewing and publishing research papers Ensure highest quality reproduction of data Feature interactive format for commentaries, opinion pieces, and exchange of information in review articles, meeting reports, and insightful overviews.
×
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
小红书