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Plasticity-led evolution as an intrinsic property of developmental gene regulatory networks
The modern evolutionary synthesis seemingly fails to explain how a population can survive a large environmental change: the pre-existence of heritable variants adapted to the novel environment is too opportunistic, whereas the search for new adaptive mutations after the environmental change is so sl...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10645858/ https://www.ncbi.nlm.nih.gov/pubmed/37963964 http://dx.doi.org/10.1038/s41598-023-47165-x |
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author | Ng, Eden Tian Hwa Kinjo, Akira R. |
author_facet | Ng, Eden Tian Hwa Kinjo, Akira R. |
author_sort | Ng, Eden Tian Hwa |
collection | PubMed |
description | The modern evolutionary synthesis seemingly fails to explain how a population can survive a large environmental change: the pre-existence of heritable variants adapted to the novel environment is too opportunistic, whereas the search for new adaptive mutations after the environmental change is so slow that the population may go extinct. Plasticity-led evolution, the initial environmental induction of a novel adaptive phenotype followed by genetic accommodation, has been proposed to solve this problem. However, the mechanism enabling plasticity-led evolution remains unclear. Here, we present computational models that exhibit behaviors compatible with plasticity-led evolution by extending the Wagner model of gene regulatory networks. The models show adaptive plastic response and the uncovering of cryptic mutations under large environmental changes, followed by genetic accommodation. Moreover, these behaviors are consistently observed over distinct novel environments. We further show that environmental cues, developmental processes, and hierarchical regulation cooperatively amplify the above behaviors and accelerate evolution. These observations suggest plasticity-led evolution is a universal property of complex developmental systems independent of particular mutations. |
format | Online Article Text |
id | pubmed-10645858 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106458582023-11-14 Plasticity-led evolution as an intrinsic property of developmental gene regulatory networks Ng, Eden Tian Hwa Kinjo, Akira R. Sci Rep Article The modern evolutionary synthesis seemingly fails to explain how a population can survive a large environmental change: the pre-existence of heritable variants adapted to the novel environment is too opportunistic, whereas the search for new adaptive mutations after the environmental change is so slow that the population may go extinct. Plasticity-led evolution, the initial environmental induction of a novel adaptive phenotype followed by genetic accommodation, has been proposed to solve this problem. However, the mechanism enabling plasticity-led evolution remains unclear. Here, we present computational models that exhibit behaviors compatible with plasticity-led evolution by extending the Wagner model of gene regulatory networks. The models show adaptive plastic response and the uncovering of cryptic mutations under large environmental changes, followed by genetic accommodation. Moreover, these behaviors are consistently observed over distinct novel environments. We further show that environmental cues, developmental processes, and hierarchical regulation cooperatively amplify the above behaviors and accelerate evolution. These observations suggest plasticity-led evolution is a universal property of complex developmental systems independent of particular mutations. Nature Publishing Group UK 2023-11-14 /pmc/articles/PMC10645858/ /pubmed/37963964 http://dx.doi.org/10.1038/s41598-023-47165-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ng, Eden Tian Hwa Kinjo, Akira R. Plasticity-led evolution as an intrinsic property of developmental gene regulatory networks |
title | Plasticity-led evolution as an intrinsic property of developmental gene regulatory networks |
title_full | Plasticity-led evolution as an intrinsic property of developmental gene regulatory networks |
title_fullStr | Plasticity-led evolution as an intrinsic property of developmental gene regulatory networks |
title_full_unstemmed | Plasticity-led evolution as an intrinsic property of developmental gene regulatory networks |
title_short | Plasticity-led evolution as an intrinsic property of developmental gene regulatory networks |
title_sort | plasticity-led evolution as an intrinsic property of developmental gene regulatory networks |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10645858/ https://www.ncbi.nlm.nih.gov/pubmed/37963964 http://dx.doi.org/10.1038/s41598-023-47165-x |
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