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Adaptation, chance, and history in experimental evolution reversals to unicellularity

Evolution is often deemed irreversible. The evolution of complex traits that require many mutations makes their reversal unlikely. Even in simpler traits, reversals might become less likely as neutral or beneficial mutations, with deleterious effects in the ancestral context, become fixed in the nov...

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Detalles Bibliográficos
Autores principales: Rebolleda‐Gómez, María, Travisano, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6590667/
https://www.ncbi.nlm.nih.gov/pubmed/30520011
http://dx.doi.org/10.1111/evo.13654
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author Rebolleda‐Gómez, María
Travisano, Michael
author_facet Rebolleda‐Gómez, María
Travisano, Michael
author_sort Rebolleda‐Gómez, María
collection PubMed
description Evolution is often deemed irreversible. The evolution of complex traits that require many mutations makes their reversal unlikely. Even in simpler traits, reversals might become less likely as neutral or beneficial mutations, with deleterious effects in the ancestral context, become fixed in the novel background. This is especially true in changes that involve large reorganizations of the organism and its interactions with the environment. The evolution of multicellularity involves the reorganization of previously autonomous cells into a more complex organism; despite the complexity of this change, single cells have repeatedly evolved from multicellular ancestors. These repeated reversals to unicellularity undermine the generality of Dollo's law. In this article, we evaluated the dynamics of reversals to unicellularity from recently evolved multicellular phenotypes of the brewers yeast Saccharomyces cerevisae. Even though multicellularity in this system evolved recently, it involves the evolution of new levels of selection. Strong selective pressures against multicellularity lead to rapid reversibility to single cells in all of our replicate lines, whereas counterselection favoring multicellularity led to minimal reductions to the rates of reversal. History and chance played an important role in the tempo and mode of reversibility, highlighting the interplay of deterministic and stochastic events in evolutionary reversals.
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spelling pubmed-65906672019-07-08 Adaptation, chance, and history in experimental evolution reversals to unicellularity Rebolleda‐Gómez, María Travisano, Michael Evolution Original Articles Evolution is often deemed irreversible. The evolution of complex traits that require many mutations makes their reversal unlikely. Even in simpler traits, reversals might become less likely as neutral or beneficial mutations, with deleterious effects in the ancestral context, become fixed in the novel background. This is especially true in changes that involve large reorganizations of the organism and its interactions with the environment. The evolution of multicellularity involves the reorganization of previously autonomous cells into a more complex organism; despite the complexity of this change, single cells have repeatedly evolved from multicellular ancestors. These repeated reversals to unicellularity undermine the generality of Dollo's law. In this article, we evaluated the dynamics of reversals to unicellularity from recently evolved multicellular phenotypes of the brewers yeast Saccharomyces cerevisae. Even though multicellularity in this system evolved recently, it involves the evolution of new levels of selection. Strong selective pressures against multicellularity lead to rapid reversibility to single cells in all of our replicate lines, whereas counterselection favoring multicellularity led to minimal reductions to the rates of reversal. History and chance played an important role in the tempo and mode of reversibility, highlighting the interplay of deterministic and stochastic events in evolutionary reversals. John Wiley and Sons Inc. 2018-12-14 2019-01 /pmc/articles/PMC6590667/ /pubmed/30520011 http://dx.doi.org/10.1111/evo.13654 Text en © 2018 The Author(s). Evolution published by Wiley Periodicals, Inc. on behalf of The Society for the Study of Evolution. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Rebolleda‐Gómez, María
Travisano, Michael
Adaptation, chance, and history in experimental evolution reversals to unicellularity
title Adaptation, chance, and history in experimental evolution reversals to unicellularity
title_full Adaptation, chance, and history in experimental evolution reversals to unicellularity
title_fullStr Adaptation, chance, and history in experimental evolution reversals to unicellularity
title_full_unstemmed Adaptation, chance, and history in experimental evolution reversals to unicellularity
title_short Adaptation, chance, and history in experimental evolution reversals to unicellularity
title_sort adaptation, chance, and history in experimental evolution reversals to unicellularity
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6590667/
https://www.ncbi.nlm.nih.gov/pubmed/30520011
http://dx.doi.org/10.1111/evo.13654
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