Multi-Omics Analysis Reveals Adaptation Strategies of Marine Diatom to Long-Term Ocean Warming: Resource Allocation Trade-Offs and Epigenetic Regulation.

IF 6 1区 生物学 Q1 PLANT SCIENCES
Ting Hong, Jiezhang Mo, Tangcheng Li, Nan Huang, Wenhua Liu, Honghao Liang, Pengbing Pei, Ping Li, Jing Chen, Hong Du
{"title":"Multi-Omics Analysis Reveals Adaptation Strategies of Marine Diatom to Long-Term Ocean Warming: Resource Allocation Trade-Offs and Epigenetic Regulation.","authors":"Ting Hong, Jiezhang Mo, Tangcheng Li, Nan Huang, Wenhua Liu, Honghao Liang, Pengbing Pei, Ping Li, Jing Chen, Hong Du","doi":"10.1111/pce.15482","DOIUrl":null,"url":null,"abstract":"<p><p>High CO<sub>2</sub> emissions originating from anthropogenic sources have resulted in ocean warming (OW), posing a severe threat to marine organisms and ecosystems. Recent evidence has shown that marine phytoplankton may acclimate and adapt to long-term OW. Whether and how marine diatoms-a functional group of phytoplankton that contributes to 40% of marine primary production-can adapt to long-term OW remains virtually unknown. The model marine diatom Phaeodactylum tricornutum was subjected to thermal stress (25°C, compared to the Control at 20°C) for 400 days (~400 generations), and physiological, transcriptomic, genetic and epigenetic analyses were performed to reveal the adaptation mechanisms under long-term OW. During the adaptation, regulation of resource allocation (e.g., photosynthesis, nitrogen metabolism, ribosomal synthesis and translation, carbon metabolism and heat shock response) at the genetic and transcriptional levels was linked to accumulated proteins, carbohydrates and particulate organic carbon, reduced lipid content, and enlarged cell size. Integrated analyses of histone modification (H3K27me3) and transcriptome data sets revealed the potential role of transposable elements and epigenetic regulation of transposable elements via histone modification in the adaptation of P. tricornutum to long-term thermal stress. These mechanistic insights may facilitate the modelling and prediction of OW-induced impacts on marine phytoplankton in the future.</p>","PeriodicalId":222,"journal":{"name":"Plant, Cell & Environment","volume":" ","pages":""},"PeriodicalIF":6.0000,"publicationDate":"2025-03-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant, Cell & Environment","FirstCategoryId":"2","ListUrlMain":"https://doi.org/10.1111/pce.15482","RegionNum":1,"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

Abstract

High CO2 emissions originating from anthropogenic sources have resulted in ocean warming (OW), posing a severe threat to marine organisms and ecosystems. Recent evidence has shown that marine phytoplankton may acclimate and adapt to long-term OW. Whether and how marine diatoms-a functional group of phytoplankton that contributes to 40% of marine primary production-can adapt to long-term OW remains virtually unknown. The model marine diatom Phaeodactylum tricornutum was subjected to thermal stress (25°C, compared to the Control at 20°C) for 400 days (~400 generations), and physiological, transcriptomic, genetic and epigenetic analyses were performed to reveal the adaptation mechanisms under long-term OW. During the adaptation, regulation of resource allocation (e.g., photosynthesis, nitrogen metabolism, ribosomal synthesis and translation, carbon metabolism and heat shock response) at the genetic and transcriptional levels was linked to accumulated proteins, carbohydrates and particulate organic carbon, reduced lipid content, and enlarged cell size. Integrated analyses of histone modification (H3K27me3) and transcriptome data sets revealed the potential role of transposable elements and epigenetic regulation of transposable elements via histone modification in the adaptation of P. tricornutum to long-term thermal stress. These mechanistic insights may facilitate the modelling and prediction of OW-induced impacts on marine phytoplankton in the future.

求助全文
约1分钟内获得全文 求助全文
来源期刊
Plant, Cell & Environment
Plant, Cell & Environment 生物-植物科学
CiteScore
13.30
自引率
4.10%
发文量
253
审稿时长
1.8 months
期刊介绍: Plant, Cell & Environment is a premier plant science journal, offering valuable insights into plant responses to their environment. Committed to publishing high-quality theoretical and experimental research, the journal covers a broad spectrum of factors, spanning from molecular to community levels. Researchers exploring various aspects of plant biology, physiology, and ecology contribute to the journal's comprehensive understanding of plant-environment interactions.
×
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:481959085
Book学术官方微信