{"title":"Network Properties Influence Covariance Between Gene Expression and Fecundity Fitness of Caenorhabditis elegans in a Novel Laboratory Environment.","authors":"Tyler R Inskeep, Simon C Groen","doi":"10.1093/gbe/evag180","DOIUrl":null,"url":null,"abstract":"<p><p>Gene expression bridges genotype and phenotype, shaping how organisms respond to their environments. Yet, it remains difficult to untangle how the architecture of gene regulatory networks (GRNs) influences the relationship between gene expression and fitness-especially in structured populations where genetic variants affecting both types of traits are inherited together. Here, we use publicly available data from wild Caenorhabditis elegans strains to link genome-wide gene expression levels to lifetime fecundity upon cultivation in a novel laboratory environment. Despite strong population structure caused by self-fertilization, selective sweeps, and hyperdivergent haplotypes, we find that a small subset of genes show significant covariance between their expression levels and fecundity fitness in laboratory cultivation conditions. These associations persist even after controlling for underlying genomic features. Genes that are older, show more tissue-specific expression patterns, and are particularly enriched in the germline and nervous system exhibit stronger covariance with fecundity in the new laboratory environment, consistent with known patterns of genetic divergence between wild and \"domesticated\" laboratory strains. Moreover, genes that are centrally positioned within GRNs, or are regulated downstream of certain transcription factors, show stronger associations with fitness. Together, these results suggest that genome structure and network topology jointly shape how variation in gene expression translates into fitness, shedding light on the early stages of adaptation to novel environments.</p>","PeriodicalId":12779,"journal":{"name":"Genome Biology and Evolution","volume":" ","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2026-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13429268/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genome Biology and Evolution","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/gbe/evag180","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"EVOLUTIONARY BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Gene expression bridges genotype and phenotype, shaping how organisms respond to their environments. Yet, it remains difficult to untangle how the architecture of gene regulatory networks (GRNs) influences the relationship between gene expression and fitness-especially in structured populations where genetic variants affecting both types of traits are inherited together. Here, we use publicly available data from wild Caenorhabditis elegans strains to link genome-wide gene expression levels to lifetime fecundity upon cultivation in a novel laboratory environment. Despite strong population structure caused by self-fertilization, selective sweeps, and hyperdivergent haplotypes, we find that a small subset of genes show significant covariance between their expression levels and fecundity fitness in laboratory cultivation conditions. These associations persist even after controlling for underlying genomic features. Genes that are older, show more tissue-specific expression patterns, and are particularly enriched in the germline and nervous system exhibit stronger covariance with fecundity in the new laboratory environment, consistent with known patterns of genetic divergence between wild and "domesticated" laboratory strains. Moreover, genes that are centrally positioned within GRNs, or are regulated downstream of certain transcription factors, show stronger associations with fitness. Together, these results suggest that genome structure and network topology jointly shape how variation in gene expression translates into fitness, shedding light on the early stages of adaptation to novel environments.
期刊介绍:
About the journal
Genome Biology and Evolution (GBE) publishes leading original research at the interface between evolutionary biology and genomics. Papers considered for publication report novel evolutionary findings that concern natural genome diversity, population genomics, the structure, function, organisation and expression of genomes, comparative genomics, proteomics, and environmental genomic interactions. Major evolutionary insights from the fields of computational biology, structural biology, developmental biology, and cell biology are also considered, as are theoretical advances in the field of genome evolution. GBE’s scope embraces genome-wide evolutionary investigations at all taxonomic levels and for all forms of life — within populations or across domains. Its aims are to further the understanding of genomes in their evolutionary context and further the understanding of evolution from a genome-wide perspective.