{"title":"基因网络拓扑驱动基因表达的突变景观。","authors":"Sylvain Pouzet, Arnaud Le Rouzic","doi":"10.1093/evolut/qpaf068","DOIUrl":null,"url":null,"abstract":"<p><p>Regulatory mutations, coding sequence variations, and gene deletions and duplica- tions are generally expected to have qualitatively different effects on fitness during adaptation. We aim to ground this expectation within a theoretical framework using evolutionary simulations of gene regulatory networks (GRNs) controlling the expression of fitness-related genes. We examined the distribution of fitness effects as a function of the type of mutation and the topology of the gene network. Contrary to our expectation, the GRN topology had more influence on the effect of mutations than the type of mutation itself. In particular, the topology conditioned (i) the speed of adaptation, (ii) the distribution of fitness effects, and (iii) the degree of pleiotropy which acts as explanatory factor for all mutation types. All mutations had the potential to participate in adaptation, although their propensity to generate beneficial variants differed according to the net- work topology. In scale-free networks, arguably the most common topology for biological networks, coding mutations were more pleiotropic and overrepresented in both beneficial and deleterious mu- tations, while regulatory mutations were more often neutral. However, this observation was not general, as this pattern was reversed in the other network topologies. These results highlight the critical role of gene interactions in defining mutations' contributions to adaptation.</p>","PeriodicalId":12082,"journal":{"name":"Evolution","volume":" ","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Gene network topology drives the mutational landscape of gene expression.\",\"authors\":\"Sylvain Pouzet, Arnaud Le Rouzic\",\"doi\":\"10.1093/evolut/qpaf068\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Regulatory mutations, coding sequence variations, and gene deletions and duplica- tions are generally expected to have qualitatively different effects on fitness during adaptation. We aim to ground this expectation within a theoretical framework using evolutionary simulations of gene regulatory networks (GRNs) controlling the expression of fitness-related genes. We examined the distribution of fitness effects as a function of the type of mutation and the topology of the gene network. Contrary to our expectation, the GRN topology had more influence on the effect of mutations than the type of mutation itself. In particular, the topology conditioned (i) the speed of adaptation, (ii) the distribution of fitness effects, and (iii) the degree of pleiotropy which acts as explanatory factor for all mutation types. All mutations had the potential to participate in adaptation, although their propensity to generate beneficial variants differed according to the net- work topology. In scale-free networks, arguably the most common topology for biological networks, coding mutations were more pleiotropic and overrepresented in both beneficial and deleterious mu- tations, while regulatory mutations were more often neutral. However, this observation was not general, as this pattern was reversed in the other network topologies. These results highlight the critical role of gene interactions in defining mutations' contributions to adaptation.</p>\",\"PeriodicalId\":12082,\"journal\":{\"name\":\"Evolution\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2025-05-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Evolution\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://doi.org/10.1093/evolut/qpaf068\",\"RegionNum\":2,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ECOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Evolution","FirstCategoryId":"93","ListUrlMain":"https://doi.org/10.1093/evolut/qpaf068","RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ECOLOGY","Score":null,"Total":0}
Gene network topology drives the mutational landscape of gene expression.
Regulatory mutations, coding sequence variations, and gene deletions and duplica- tions are generally expected to have qualitatively different effects on fitness during adaptation. We aim to ground this expectation within a theoretical framework using evolutionary simulations of gene regulatory networks (GRNs) controlling the expression of fitness-related genes. We examined the distribution of fitness effects as a function of the type of mutation and the topology of the gene network. Contrary to our expectation, the GRN topology had more influence on the effect of mutations than the type of mutation itself. In particular, the topology conditioned (i) the speed of adaptation, (ii) the distribution of fitness effects, and (iii) the degree of pleiotropy which acts as explanatory factor for all mutation types. All mutations had the potential to participate in adaptation, although their propensity to generate beneficial variants differed according to the net- work topology. In scale-free networks, arguably the most common topology for biological networks, coding mutations were more pleiotropic and overrepresented in both beneficial and deleterious mu- tations, while regulatory mutations were more often neutral. However, this observation was not general, as this pattern was reversed in the other network topologies. These results highlight the critical role of gene interactions in defining mutations' contributions to adaptation.
期刊介绍:
Evolution, published for the Society for the Study of Evolution, is the premier publication devoted to the study of organic evolution and the integration of the various fields of science concerned with evolution. The journal presents significant and original results that extend our understanding of evolutionary phenomena and processes.