The interplay between epigenomic and transcriptomic variation during ecotype divergence in stickleback.

IF 4.5 1区 生物学 Q1 BIOLOGY BMC Biology Pub Date : 2025-03-05 DOI:10.1186/s12915-025-02176-0
Man Luo, Junjie Zhao, Juha Merilä, Rowan D H Barrett, Baocheng Guo, Juntao Hu
{"title":"The interplay between epigenomic and transcriptomic variation during ecotype divergence in stickleback.","authors":"Man Luo, Junjie Zhao, Juha Merilä, Rowan D H Barrett, Baocheng Guo, Juntao Hu","doi":"10.1186/s12915-025-02176-0","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Populations colonizing contrasting environments are likely to undergo adaptive divergence and evolve ecotypes with locally adapted phenotypes. While diverse molecular mechanisms underlying ecotype divergence have been identified, less is known about their interplay and degree of divergence.</p><p><strong>Results: </strong>Here we integrated epigenomic and transcriptomic data to explore the interactions among gene expression, alternative splicing, DNA methylation, and microRNA expression to gauge the extent to which patterns of divergence at the four molecular levels are aligned in a case of postglacial divergence between marine and freshwater ecotypes of nine-spined sticklebacks (Pungitius pungitius). Despite significant genome-wide associations between epigenomic and transcriptomic variation, we found largely non-parallel patterns of ecotype divergence across epigenomic and transcriptomic levels, with predominantly nonoverlapping (ranging from 43.40 to 87.98%) sets of differentially expressed, spliced and methylated genes, and candidate genes targeted by differentially expressed miRNA between the ecotypes. Furthermore, we found significant variation in the extent of ecotype divergence across different molecular mechanisms, with differential methylation and differential splicing showing the highest and lowest extent of divergence between ecotypes, respectively. Finally, we found a significant enrichment of genes associated with ecotype divergence in differential methylation.</p><p><strong>Conclusions: </strong>Our results suggest a nuanced relationship between epigenomic and transcriptomic processes, with alignment at the genome-wide level masking relatively independent effects of different molecular mechanisms on ecotype divergence at the gene level.</p>","PeriodicalId":9339,"journal":{"name":"BMC Biology","volume":"23 1","pages":"70"},"PeriodicalIF":4.5000,"publicationDate":"2025-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11881503/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s12915-025-02176-0","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Populations colonizing contrasting environments are likely to undergo adaptive divergence and evolve ecotypes with locally adapted phenotypes. While diverse molecular mechanisms underlying ecotype divergence have been identified, less is known about their interplay and degree of divergence.

Results: Here we integrated epigenomic and transcriptomic data to explore the interactions among gene expression, alternative splicing, DNA methylation, and microRNA expression to gauge the extent to which patterns of divergence at the four molecular levels are aligned in a case of postglacial divergence between marine and freshwater ecotypes of nine-spined sticklebacks (Pungitius pungitius). Despite significant genome-wide associations between epigenomic and transcriptomic variation, we found largely non-parallel patterns of ecotype divergence across epigenomic and transcriptomic levels, with predominantly nonoverlapping (ranging from 43.40 to 87.98%) sets of differentially expressed, spliced and methylated genes, and candidate genes targeted by differentially expressed miRNA between the ecotypes. Furthermore, we found significant variation in the extent of ecotype divergence across different molecular mechanisms, with differential methylation and differential splicing showing the highest and lowest extent of divergence between ecotypes, respectively. Finally, we found a significant enrichment of genes associated with ecotype divergence in differential methylation.

Conclusions: Our results suggest a nuanced relationship between epigenomic and transcriptomic processes, with alignment at the genome-wide level masking relatively independent effects of different molecular mechanisms on ecotype divergence at the gene level.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
棘鱼生态型分化过程中表观基因组和转录组变异的相互作用。
背景:在不同环境中定居的种群可能会经历适应性分化,并进化出具有局部适应表型的生态型。虽然已经确定了生态型分化的多种分子机制,但对它们的相互作用和分化程度知之甚少。结果:本研究整合了表观基因组学和转录组学数据,探讨了基因表达、选择性剪接、DNA甲基化和microRNA表达之间的相互作用,以衡量九刺棘鱼(Pungitius Pungitius)冰川后海洋和淡水生态型差异的四个分子水平上的差异模式在何种程度上一致。尽管表观基因组和转录组变异之间存在显著的全基因组关联,但我们发现表观基因组和转录组水平上的生态型差异在很大程度上是非平行的模式,主要是差异表达、剪接和甲基化基因的非重叠(范围从43.40%到87.98%),以及生态型之间差异表达的miRNA靶向的候选基因。此外,我们还发现不同分子机制的生态型分化程度存在显著差异,差异甲基化和差异剪接分别表现出生态型之间最高和最低的分化程度。最后,我们发现差异甲基化中与生态型差异相关的基因显著富集。结论:我们的研究结果表明表观基因组和转录组过程之间存在微妙的关系,在全基因组水平上的比对掩盖了不同分子机制在基因水平上对生态型差异的相对独立影响。
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 去求助
来源期刊
BMC Biology
BMC Biology 生物-生物学
CiteScore
7.80
自引率
1.90%
发文量
260
审稿时长
3 months
期刊介绍: BMC Biology is a broad scope journal covering all areas of biology. Our content includes research articles, new methods and tools. BMC Biology also publishes reviews, Q&A, and commentaries.
期刊最新文献
Identification of prospective PETases across prokaryotes using an in silico approach. Melatonin promotes embryonic development by enhancing tryptophan metabolism and NAD + synthesis. Axolotls retain fertility throughout lifespan. Chromosomal rearrangements and segmental deletions contribute to gene loss in squamates. Stretching inhibits tumor growth in MMTV-PYMT via a direct mechanical effect.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1