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The ensemble of gene regulatory networks at mutation–selection balance
The evolution of diverse phenotypes both involves and is constrained by molecular interaction networks. When these networks influence patterns of expression, we refer to them as gene regulatory networks (GRNs). Here, we develop a model of GRN evolution analogous to work from quasi-species theory, wh...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9810427/ https://www.ncbi.nlm.nih.gov/pubmed/36596452 http://dx.doi.org/10.1098/rsif.2022.0075 |
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author | Yang, Chia-Hung Scarpino, Samuel V. |
author_facet | Yang, Chia-Hung Scarpino, Samuel V. |
author_sort | Yang, Chia-Hung |
collection | PubMed |
description | The evolution of diverse phenotypes both involves and is constrained by molecular interaction networks. When these networks influence patterns of expression, we refer to them as gene regulatory networks (GRNs). Here, we develop a model of GRN evolution analogous to work from quasi-species theory, which is itself essentially the mutation–selection balance model from classical population genetics extended to multiple loci. With this GRN model, we prove that—across a broad spectrum of selection pressures—the dynamics converge to a stationary distribution over GRNs. Next, we show from first principles how the frequency of GRNs at equilibrium is related to the topology of the genotype network, in particular, via a specific network centrality measure termed the eigenvector centrality. Finally, we determine the structural characteristics of GRNs that are favoured in response to a range of selective environments and mutational constraints. Our work connects GRN evolution to quasi-species theory—and thus to classical populations genetics—providing a mechanistic explanation for the observed distribution of GRNs evolving in response to various evolutionary forces, and shows how complex fitness landscapes can emerge from simple evolutionary rules. |
format | Online Article Text |
id | pubmed-9810427 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-98104272023-01-11 The ensemble of gene regulatory networks at mutation–selection balance Yang, Chia-Hung Scarpino, Samuel V. J R Soc Interface Life Sciences–Mathematics interface The evolution of diverse phenotypes both involves and is constrained by molecular interaction networks. When these networks influence patterns of expression, we refer to them as gene regulatory networks (GRNs). Here, we develop a model of GRN evolution analogous to work from quasi-species theory, which is itself essentially the mutation–selection balance model from classical population genetics extended to multiple loci. With this GRN model, we prove that—across a broad spectrum of selection pressures—the dynamics converge to a stationary distribution over GRNs. Next, we show from first principles how the frequency of GRNs at equilibrium is related to the topology of the genotype network, in particular, via a specific network centrality measure termed the eigenvector centrality. Finally, we determine the structural characteristics of GRNs that are favoured in response to a range of selective environments and mutational constraints. Our work connects GRN evolution to quasi-species theory—and thus to classical populations genetics—providing a mechanistic explanation for the observed distribution of GRNs evolving in response to various evolutionary forces, and shows how complex fitness landscapes can emerge from simple evolutionary rules. The Royal Society 2023-01-04 /pmc/articles/PMC9810427/ /pubmed/36596452 http://dx.doi.org/10.1098/rsif.2022.0075 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Life Sciences–Mathematics interface Yang, Chia-Hung Scarpino, Samuel V. The ensemble of gene regulatory networks at mutation–selection balance |
title | The ensemble of gene regulatory networks at mutation–selection balance |
title_full | The ensemble of gene regulatory networks at mutation–selection balance |
title_fullStr | The ensemble of gene regulatory networks at mutation–selection balance |
title_full_unstemmed | The ensemble of gene regulatory networks at mutation–selection balance |
title_short | The ensemble of gene regulatory networks at mutation–selection balance |
title_sort | ensemble of gene regulatory networks at mutation–selection balance |
topic | Life Sciences–Mathematics interface |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9810427/ https://www.ncbi.nlm.nih.gov/pubmed/36596452 http://dx.doi.org/10.1098/rsif.2022.0075 |
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