对干旱的地上和地下表型反应的动态表观遗传学观点:来自黄牡丹全球DNA甲基化的见解。

IF 3.6 3区 生物学 Q1 PLANT SCIENCES
Plant Biology Pub Date : 2025-09-15 DOI:10.1111/plb.70110
C Alonso, M Medrano, C M Herrera
{"title":"对干旱的地上和地下表型反应的动态表观遗传学观点:来自黄牡丹全球DNA甲基化的见解。","authors":"C Alonso, M Medrano, C M Herrera","doi":"10.1111/plb.70110","DOIUrl":null,"url":null,"abstract":"<p><p>There is mounting evidence that plant responses to environmental stress are mediated by epigenetic factors, including DNA methylation. Understanding relationships between DNA methylation, plant development and individual fitness in contrasting environments is key to uncover potential impacts of epigenetic regulation on plant adaptation. Here, we used an experimental approach combining controlled alteration of epigenetic features with exposure to stress. Two provenances of Erodium cicutarium were exposed to a demethylating agent (5-azacytidine) and recurrent drought, and effects on above- and belowground phenotypic traits related to early development, phenology and fitness assessed. Application of 5-azacytidine significantly reduced DNA methylation in leaf and root tissues. This slowed plant development, delayed flowering, and reduced the number of inflorescences produced, independent of water regime. Recurrent drought reduced final above- and belowground biomass and inflorescence production, regardless of the 5-azacytidine exposure. Increased fruit and seed-set were the only adaptations to drought in E. cicutarium, together with an increased number of flowers per inflorescence in water-stressed plants previously treated with 5-azacytidine. Epigenetic effects can desynchronize plant growth, flowering and senescence in both favourable and adverse environments. Future studies should focus on understanding intraspecific variation in ability to change the plant methylome in response to stress, and transgenerational transmission of such responses.</p>","PeriodicalId":220,"journal":{"name":"Plant Biology","volume":" ","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2025-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A dynamic epigenetic perspective on above- and belowground phenotypic responses to drought: Insights from global DNA methylation in Erodium cicutarium.\",\"authors\":\"C Alonso, M Medrano, C M Herrera\",\"doi\":\"10.1111/plb.70110\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>There is mounting evidence that plant responses to environmental stress are mediated by epigenetic factors, including DNA methylation. Understanding relationships between DNA methylation, plant development and individual fitness in contrasting environments is key to uncover potential impacts of epigenetic regulation on plant adaptation. Here, we used an experimental approach combining controlled alteration of epigenetic features with exposure to stress. Two provenances of Erodium cicutarium were exposed to a demethylating agent (5-azacytidine) and recurrent drought, and effects on above- and belowground phenotypic traits related to early development, phenology and fitness assessed. Application of 5-azacytidine significantly reduced DNA methylation in leaf and root tissues. This slowed plant development, delayed flowering, and reduced the number of inflorescences produced, independent of water regime. Recurrent drought reduced final above- and belowground biomass and inflorescence production, regardless of the 5-azacytidine exposure. Increased fruit and seed-set were the only adaptations to drought in E. cicutarium, together with an increased number of flowers per inflorescence in water-stressed plants previously treated with 5-azacytidine. Epigenetic effects can desynchronize plant growth, flowering and senescence in both favourable and adverse environments. Future studies should focus on understanding intraspecific variation in ability to change the plant methylome in response to stress, and transgenerational transmission of such responses.</p>\",\"PeriodicalId\":220,\"journal\":{\"name\":\"Plant Biology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2025-09-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1111/plb.70110\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/plb.70110","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

摘要

越来越多的证据表明,植物对环境胁迫的反应是由表观遗传因素介导的,包括DNA甲基化。了解不同环境下DNA甲基化、植物发育和个体适应度之间的关系是揭示表观遗传调控对植物适应的潜在影响的关键。在这里,我们采用了一种实验方法,将表观遗传特征的受控改变与暴露于压力相结合。研究了两个种源黄牡丹在去甲基化剂(5-氮胞苷)和反复干旱条件下的早期发育、物候和适合度对其地上、地下表型性状的影响。施用5-氮杂胞苷显著降低了叶片和根组织的DNA甲基化。这减缓了植物的发育,延迟开花,减少了花序的数量,独立于水制度。不论是否暴露于5-氮胞苷,反复的干旱都减少了最终的地上和地下生物量和花序产量。增加的果实和结实率是金合春对干旱的唯一适应,同时在先前用5-氮胞苷处理过的缺水植物中,每花序的花数也增加了。无论在有利环境还是不利环境下,表观遗传效应都能使植物生长、开花和衰老失同步。未来的研究应侧重于了解植物甲基组在逆境下的种内变化,以及这种反应的跨代传递。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A dynamic epigenetic perspective on above- and belowground phenotypic responses to drought: Insights from global DNA methylation in Erodium cicutarium.

There is mounting evidence that plant responses to environmental stress are mediated by epigenetic factors, including DNA methylation. Understanding relationships between DNA methylation, plant development and individual fitness in contrasting environments is key to uncover potential impacts of epigenetic regulation on plant adaptation. Here, we used an experimental approach combining controlled alteration of epigenetic features with exposure to stress. Two provenances of Erodium cicutarium were exposed to a demethylating agent (5-azacytidine) and recurrent drought, and effects on above- and belowground phenotypic traits related to early development, phenology and fitness assessed. Application of 5-azacytidine significantly reduced DNA methylation in leaf and root tissues. This slowed plant development, delayed flowering, and reduced the number of inflorescences produced, independent of water regime. Recurrent drought reduced final above- and belowground biomass and inflorescence production, regardless of the 5-azacytidine exposure. Increased fruit and seed-set were the only adaptations to drought in E. cicutarium, together with an increased number of flowers per inflorescence in water-stressed plants previously treated with 5-azacytidine. Epigenetic effects can desynchronize plant growth, flowering and senescence in both favourable and adverse environments. Future studies should focus on understanding intraspecific variation in ability to change the plant methylome in response to stress, and transgenerational transmission of such responses.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Plant Biology
Plant Biology 生物-植物科学
CiteScore
8.20
自引率
2.60%
发文量
109
审稿时长
3 months
期刊介绍: Plant Biology is an international journal of broad scope bringing together the different subdisciplines, such as physiology, molecular biology, cell biology, development, genetics, systematics, ecology, evolution, ecophysiology, plant-microbe interactions, and mycology. Plant Biology publishes original problem-oriented full-length research papers, short research papers, and review articles. Discussion of hot topics and provocative opinion articles are published under the heading Acute Views. From a multidisciplinary perspective, Plant Biology will provide a platform for publication, information and debate, encompassing all areas which fall within the scope of plant science.
×
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