The regulatory architecture of gene expression variation in C. elegans revealed by multi-strain allele-specific analysis.

IF 3.3 3区 生物学 Q2 GENETICS & HEREDITY
Genetics Pub Date : 2025-06-10 DOI:10.1093/genetics/iyaf110
Avery Davis Bell, Francisco Valencia, Annalise B Paaby
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Abstract

An outstanding question in the evolution of gene expression is the composition of the underlying regulatory architecture and the processes that shape it. Mutations affecting a gene's expression may reside locally in cis or distally in trans; the accumulation of these changes, their interactions, and their modes of inheritance influence how traits are expressed and how they evolve. Here, we interrogated gene expression variation in C. elegans, including the first allele-specific expression analysis in this system, capturing effects in cis and in trans that govern gene expression differences between the reference strain N2 and seven wild strains. We observed extensive compensatory regulation, in which opposite effects in cis and trans at individual genes mitigate expression differences among strains, and that genes with expression differences exhibit strain specificity. As the genomic distance increased between N2 and each wild strain, the number of genes with expression differences also increased. We also report for the first time that expression-variable genes are lower expressed on average than genes without expression differences, a trend that may extend to humans and Drosophila melanogaster and may reflect the selection constraints that govern the universal anticorrelation between gene expression and rate of protein evolution. Together, these and other observed trends support the conclusion that many C. elegans genes are under stabilizing selection for expression level, but we also highlight outliers that may be biologically significant. To provide community access to our data, we introduce an easily accessible, interactive web application for gene-based queries: https://wildworm.biosci.gatech.edu/ase/.

多菌株等位基因特异性分析揭示秀丽隐杆线虫基因表达变异的调控结构。
在基因表达的进化中,一个突出的问题是潜在的调控结构的组成和形成它的过程。影响基因表达的突变可能存在于局部的顺式或远端的反式;这些变化的积累、它们之间的相互作用以及它们的遗传模式影响着性状的表达和演化方式。在这里,我们研究了秀丽隐杆线虫的基因表达变化,包括该系统中第一个等位基因特异性表达分析,捕获了控制参考菌株N2和7个野生菌株之间基因表达差异的顺式和反式效应。我们观察到广泛的代偿调节,其中顺式和反式个体基因的相反作用减轻了菌株之间的表达差异,并且表达差异的基因表现出菌株特异性。随着N2与各野生菌株基因组距离的增加,表达差异基因的数量也在增加。我们还首次报道了表达可变基因的平均表达量低于无表达差异的基因,这一趋势可能延伸到人类和黑胃果蝇,并可能反映了控制基因表达与蛋白质进化速率之间普遍反相关的选择约束。总之,这些和其他观察到的趋势支持了许多秀丽隐杆线虫基因在表达水平上处于稳定选择的结论,但我们也强调了可能具有生物学意义的异常值。为了让社区能够访问我们的数据,我们为基于基因的查询引入了一个易于访问的交互式web应用程序:https://wildworm.biosci.gatech.edu/ase/。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Genetics
Genetics GENETICS & HEREDITY-
CiteScore
6.90
自引率
6.10%
发文量
177
审稿时长
1.5 months
期刊介绍: GENETICS is published by the Genetics Society of America, a scholarly society that seeks to deepen our understanding of the living world by advancing our understanding of genetics. Since 1916, GENETICS has published high-quality, original research presenting novel findings bearing on genetics and genomics. The journal publishes empirical studies of organisms ranging from microbes to humans, as well as theoretical work. While it has an illustrious history, GENETICS has changed along with the communities it serves: it is not your mentor''s journal. The editors make decisions quickly – in around 30 days – without sacrificing the excellence and scholarship for which the journal has long been known. GENETICS is a peer reviewed, peer-edited journal, with an international reach and increasing visibility and impact. All editorial decisions are made through collaboration of at least two editors who are practicing scientists. GENETICS is constantly innovating: expanded types of content include Reviews, Commentary (current issues of interest to geneticists), Perspectives (historical), Primers (to introduce primary literature into the classroom), Toolbox Reviews, plus YeastBook, FlyBook, and WormBook (coming spring 2016). For particularly time-sensitive results, we publish Communications. As part of our mission to serve our communities, we''ve published thematic collections, including Genomic Selection, Multiparental Populations, Mouse Collaborative Cross, and the Genetics of Sex.
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