Flexibility in Gene Coexpression at Developmental and Evolutionary Timescales.

IF 5.3 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Eva K Fischer, Youngseok Song, Wen Zhou, Kim L Hoke
{"title":"Flexibility in Gene Coexpression at Developmental and Evolutionary Timescales.","authors":"Eva K Fischer, Youngseok Song, Wen Zhou, Kim L Hoke","doi":"10.1093/molbev/msaf194","DOIUrl":null,"url":null,"abstract":"<p><p>The explosion of next-generation sequencing technologies has allowed researchers to move from studying single genes to studying thousands of genes, and thereby to also consider the relationships within gene networks. Like others, we are interested in understanding how developmental and evolutionary forces shape the expression of individual genes, as well as the interactions among genes. In pursuing these questions, we confronted the central challenge that standard approaches fail to control the Type I error and/or have low power in the presence of high dimensionality (i.e. large number of genes) and small sample size, as in many gene expression studies. To overcome these challenges, we used random projection tests and correlation network comparisons to characterize differences in network connectivity and density. We detail central challenges, discuss sample size guidelines, and provide rigorous statistical approaches for exploring coexpression differences with small sample sizes. We apply these approaches in a species known for rapid adaptation-the Trinidadian guppy (Poecilia reticulata)-and find evidence for coexpression network differences at developmental and evolutionary timescales. Our findings suggest that flexibility in gene coexpression relationships could promote evolvability.</p>","PeriodicalId":18730,"journal":{"name":"Molecular biology and evolution","volume":" ","pages":""},"PeriodicalIF":5.3000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12486243/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular biology and evolution","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/molbev/msaf194","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

The explosion of next-generation sequencing technologies has allowed researchers to move from studying single genes to studying thousands of genes, and thereby to also consider the relationships within gene networks. Like others, we are interested in understanding how developmental and evolutionary forces shape the expression of individual genes, as well as the interactions among genes. In pursuing these questions, we confronted the central challenge that standard approaches fail to control the Type I error and/or have low power in the presence of high dimensionality (i.e. large number of genes) and small sample size, as in many gene expression studies. To overcome these challenges, we used random projection tests and correlation network comparisons to characterize differences in network connectivity and density. We detail central challenges, discuss sample size guidelines, and provide rigorous statistical approaches for exploring coexpression differences with small sample sizes. We apply these approaches in a species known for rapid adaptation-the Trinidadian guppy (Poecilia reticulata)-and find evidence for coexpression network differences at developmental and evolutionary timescales. Our findings suggest that flexibility in gene coexpression relationships could promote evolvability.

基因共表达在发育和进化时间尺度上的灵活性。
下一代测序技术的爆炸式发展使研究人员能够从研究单个基因转向研究数千个基因,从而也可以考虑基因网络内部的关系。像其他人一样,我们对理解发育和进化力量如何塑造个体基因的表达以及基因之间的相互作用感兴趣。在追求这些问题的过程中,我们面临的核心挑战是,标准方法无法控制I型错误和/或在高维(即大量基因)和小样本量的情况下,如在许多基因表达研究中一样,效能较低。为了克服这些挑战,我们使用随机投影测试和相关网络比较来表征网络连通性和密度的差异。我们详细介绍了中心挑战,讨论了样本量指南,并提供了严格的统计方法来探索小样本量的共表达差异。我们将这些方法应用于一个以快速适应而闻名的物种——特立尼达孔雀鱼(Poecilia reticulata)——并在发育和进化的时间尺度上找到了共表达网络差异的证据。我们的研究结果表明,基因共表达关系的灵活性可以促进进化。
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