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Nonadaptive Amino Acid Convergence Rates Decrease over Time
Convergence is a central concept in evolutionary studies because it provides strong evidence for adaptation. It also provides information about the nature of the fitness landscape and the repeatability of evolution, and can mislead phylogenetic inference. To understand the role of adaptive convergen...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4572784/ https://www.ncbi.nlm.nih.gov/pubmed/25737491 http://dx.doi.org/10.1093/molbev/msv041 |
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author | Goldstein, Richard A. Pollard, Stephen T. Shah, Seena D. Pollock, David D. |
author_facet | Goldstein, Richard A. Pollard, Stephen T. Shah, Seena D. Pollock, David D. |
author_sort | Goldstein, Richard A. |
collection | PubMed |
description | Convergence is a central concept in evolutionary studies because it provides strong evidence for adaptation. It also provides information about the nature of the fitness landscape and the repeatability of evolution, and can mislead phylogenetic inference. To understand the role of adaptive convergence, we need to understand the patterns of nonadaptive convergence. Here, we consider the relationship between nonadaptive convergence and divergence in mitochondrial and model proteins. Surprisingly, nonadaptive convergence is much more common than expected in closely related organisms, falling off as organisms diverge. The extent of the convergent drop-off in mitochondrial proteins is well predicted by epistatic or coevolutionary effects in our “evolutionary Stokes shift” models and poorly predicted by conventional evolutionary models. Convergence probabilities decrease dramatically if the ancestral amino acids of branches being compared have diverged, but also drop slowly over evolutionary time even if the ancestral amino acids have not substituted. Convergence probabilities drop-off rapidly for quickly evolving sites, but much more slowly for slowly evolving sites. Furthermore, once sites have diverged their convergence probabilities are extremely low and indistinguishable from convergence levels at randomized sites. These results indicate that we cannot assume that excessive convergence early on is necessarily adaptive. This new understanding should help us to better discriminate adaptive from nonadaptive convergence and develop more relevant evolutionary models with improved validity for phylogenetic inference. |
format | Online Article Text |
id | pubmed-4572784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-45727842015-09-18 Nonadaptive Amino Acid Convergence Rates Decrease over Time Goldstein, Richard A. Pollard, Stephen T. Shah, Seena D. Pollock, David D. Mol Biol Evol Fast Tracks Convergence is a central concept in evolutionary studies because it provides strong evidence for adaptation. It also provides information about the nature of the fitness landscape and the repeatability of evolution, and can mislead phylogenetic inference. To understand the role of adaptive convergence, we need to understand the patterns of nonadaptive convergence. Here, we consider the relationship between nonadaptive convergence and divergence in mitochondrial and model proteins. Surprisingly, nonadaptive convergence is much more common than expected in closely related organisms, falling off as organisms diverge. The extent of the convergent drop-off in mitochondrial proteins is well predicted by epistatic or coevolutionary effects in our “evolutionary Stokes shift” models and poorly predicted by conventional evolutionary models. Convergence probabilities decrease dramatically if the ancestral amino acids of branches being compared have diverged, but also drop slowly over evolutionary time even if the ancestral amino acids have not substituted. Convergence probabilities drop-off rapidly for quickly evolving sites, but much more slowly for slowly evolving sites. Furthermore, once sites have diverged their convergence probabilities are extremely low and indistinguishable from convergence levels at randomized sites. These results indicate that we cannot assume that excessive convergence early on is necessarily adaptive. This new understanding should help us to better discriminate adaptive from nonadaptive convergence and develop more relevant evolutionary models with improved validity for phylogenetic inference. Oxford University Press 2015-06 2015-03-03 /pmc/articles/PMC4572784/ /pubmed/25737491 http://dx.doi.org/10.1093/molbev/msv041 Text en © The Author 2015. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/),which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Fast Tracks Goldstein, Richard A. Pollard, Stephen T. Shah, Seena D. Pollock, David D. Nonadaptive Amino Acid Convergence Rates Decrease over Time |
title | Nonadaptive Amino Acid Convergence Rates Decrease over Time |
title_full | Nonadaptive Amino Acid Convergence Rates Decrease over Time |
title_fullStr | Nonadaptive Amino Acid Convergence Rates Decrease over Time |
title_full_unstemmed | Nonadaptive Amino Acid Convergence Rates Decrease over Time |
title_short | Nonadaptive Amino Acid Convergence Rates Decrease over Time |
title_sort | nonadaptive amino acid convergence rates decrease over time |
topic | Fast Tracks |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4572784/ https://www.ncbi.nlm.nih.gov/pubmed/25737491 http://dx.doi.org/10.1093/molbev/msv041 |
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