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Conditional expression explains molecular evolution of social genes in a microbe
Conflict is thought to play a critical role in the evolution of social interactions by promoting diversity or driving accelerated evolution. However, despite our sophisticated understanding of how conflict shapes social traits, we have limited knowledge of how it impacts molecular evolution across t...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6650454/ https://www.ncbi.nlm.nih.gov/pubmed/31337766 http://dx.doi.org/10.1038/s41467-019-11237-2 |
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author | de Oliveira, Janaina Lima Morales, Atahualpa Castillo Stewart, Balint Gruenheit, Nicole Engelmoer, Jennifer Brown, Suzanne Battom de Brito, Reinaldo A. Hurst, Laurence D. Urrutia, Araxi O. Thompson, Christopher R. L. Wolf, Jason B. |
author_facet | de Oliveira, Janaina Lima Morales, Atahualpa Castillo Stewart, Balint Gruenheit, Nicole Engelmoer, Jennifer Brown, Suzanne Battom de Brito, Reinaldo A. Hurst, Laurence D. Urrutia, Araxi O. Thompson, Christopher R. L. Wolf, Jason B. |
author_sort | de Oliveira, Janaina Lima |
collection | PubMed |
description | Conflict is thought to play a critical role in the evolution of social interactions by promoting diversity or driving accelerated evolution. However, despite our sophisticated understanding of how conflict shapes social traits, we have limited knowledge of how it impacts molecular evolution across the underlying social genes. Here we address this problem by analyzing the genome-wide impact of social interactions using genome sequences from 67 Dictyostelium discoideum strains. We find that social genes tend to exhibit enhanced polymorphism and accelerated evolution. However, these patterns are not consistent with conflict driven processes, but instead reflect relaxed purifying selection. This pattern is most likely explained by the conditional nature of social interactions, whereby selection on genes expressed only in social interactions is diluted by generations of inactivity. This dilution of selection by inactivity enhances the role of drift, leading to increased polymorphism and accelerated evolution, which we call the Red King process. |
format | Online Article Text |
id | pubmed-6650454 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66504542019-07-25 Conditional expression explains molecular evolution of social genes in a microbe de Oliveira, Janaina Lima Morales, Atahualpa Castillo Stewart, Balint Gruenheit, Nicole Engelmoer, Jennifer Brown, Suzanne Battom de Brito, Reinaldo A. Hurst, Laurence D. Urrutia, Araxi O. Thompson, Christopher R. L. Wolf, Jason B. Nat Commun Article Conflict is thought to play a critical role in the evolution of social interactions by promoting diversity or driving accelerated evolution. However, despite our sophisticated understanding of how conflict shapes social traits, we have limited knowledge of how it impacts molecular evolution across the underlying social genes. Here we address this problem by analyzing the genome-wide impact of social interactions using genome sequences from 67 Dictyostelium discoideum strains. We find that social genes tend to exhibit enhanced polymorphism and accelerated evolution. However, these patterns are not consistent with conflict driven processes, but instead reflect relaxed purifying selection. This pattern is most likely explained by the conditional nature of social interactions, whereby selection on genes expressed only in social interactions is diluted by generations of inactivity. This dilution of selection by inactivity enhances the role of drift, leading to increased polymorphism and accelerated evolution, which we call the Red King process. Nature Publishing Group UK 2019-07-23 /pmc/articles/PMC6650454/ /pubmed/31337766 http://dx.doi.org/10.1038/s41467-019-11237-2 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article de Oliveira, Janaina Lima Morales, Atahualpa Castillo Stewart, Balint Gruenheit, Nicole Engelmoer, Jennifer Brown, Suzanne Battom de Brito, Reinaldo A. Hurst, Laurence D. Urrutia, Araxi O. Thompson, Christopher R. L. Wolf, Jason B. Conditional expression explains molecular evolution of social genes in a microbe |
title | Conditional expression explains molecular evolution of social genes in a microbe |
title_full | Conditional expression explains molecular evolution of social genes in a microbe |
title_fullStr | Conditional expression explains molecular evolution of social genes in a microbe |
title_full_unstemmed | Conditional expression explains molecular evolution of social genes in a microbe |
title_short | Conditional expression explains molecular evolution of social genes in a microbe |
title_sort | conditional expression explains molecular evolution of social genes in a microbe |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6650454/ https://www.ncbi.nlm.nih.gov/pubmed/31337766 http://dx.doi.org/10.1038/s41467-019-11237-2 |
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