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Coevolutionary transitions from antagonism to mutualism explained by the Co-Opted Antagonist Hypothesis
There is now good evidence that many mutualisms evolved from antagonism; why or how, however, remains unclear. We advance the Co-Opted Antagonist (COA) Hypothesis as a general mechanism explaining evolutionary transitions from antagonism to mutualism. COA involves an eco-coevolutionary process where...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8129128/ https://www.ncbi.nlm.nih.gov/pubmed/34001894 http://dx.doi.org/10.1038/s41467-021-23177-x |
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author | Johnson, Christopher A. Smith, Gordon P. Yule, Kelsey Davidowitz, Goggy Bronstein, Judith L. Ferrière, Régis |
author_facet | Johnson, Christopher A. Smith, Gordon P. Yule, Kelsey Davidowitz, Goggy Bronstein, Judith L. Ferrière, Régis |
author_sort | Johnson, Christopher A. |
collection | PubMed |
description | There is now good evidence that many mutualisms evolved from antagonism; why or how, however, remains unclear. We advance the Co-Opted Antagonist (COA) Hypothesis as a general mechanism explaining evolutionary transitions from antagonism to mutualism. COA involves an eco-coevolutionary process whereby natural selection favors co-option of an antagonist to perform a beneficial function and the interacting species coevolve a suite of phenotypic traits that drive the interaction from antagonism to mutualism. To evaluate the COA hypothesis, we present a generalized eco-coevolutionary framework of evolutionary transitions from antagonism to mutualism and develop a data-based, fully ecologically-parameterized model of a small community in which a lepidopteran insect pollinates some of its larval host plant species. More generally, our theory helps to reconcile several major challenges concerning the mechanisms of mutualism evolution, such as how mutualisms evolve without extremely tight host fidelity (vertical transmission) and how ecological context influences evolutionary outcomes, and vice-versa. |
format | Online Article Text |
id | pubmed-8129128 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81291282021-06-01 Coevolutionary transitions from antagonism to mutualism explained by the Co-Opted Antagonist Hypothesis Johnson, Christopher A. Smith, Gordon P. Yule, Kelsey Davidowitz, Goggy Bronstein, Judith L. Ferrière, Régis Nat Commun Article There is now good evidence that many mutualisms evolved from antagonism; why or how, however, remains unclear. We advance the Co-Opted Antagonist (COA) Hypothesis as a general mechanism explaining evolutionary transitions from antagonism to mutualism. COA involves an eco-coevolutionary process whereby natural selection favors co-option of an antagonist to perform a beneficial function and the interacting species coevolve a suite of phenotypic traits that drive the interaction from antagonism to mutualism. To evaluate the COA hypothesis, we present a generalized eco-coevolutionary framework of evolutionary transitions from antagonism to mutualism and develop a data-based, fully ecologically-parameterized model of a small community in which a lepidopteran insect pollinates some of its larval host plant species. More generally, our theory helps to reconcile several major challenges concerning the mechanisms of mutualism evolution, such as how mutualisms evolve without extremely tight host fidelity (vertical transmission) and how ecological context influences evolutionary outcomes, and vice-versa. Nature Publishing Group UK 2021-05-17 /pmc/articles/PMC8129128/ /pubmed/34001894 http://dx.doi.org/10.1038/s41467-021-23177-x Text en © The Author(s) 2021 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 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Johnson, Christopher A. Smith, Gordon P. Yule, Kelsey Davidowitz, Goggy Bronstein, Judith L. Ferrière, Régis Coevolutionary transitions from antagonism to mutualism explained by the Co-Opted Antagonist Hypothesis |
title | Coevolutionary transitions from antagonism to mutualism explained by the Co-Opted Antagonist Hypothesis |
title_full | Coevolutionary transitions from antagonism to mutualism explained by the Co-Opted Antagonist Hypothesis |
title_fullStr | Coevolutionary transitions from antagonism to mutualism explained by the Co-Opted Antagonist Hypothesis |
title_full_unstemmed | Coevolutionary transitions from antagonism to mutualism explained by the Co-Opted Antagonist Hypothesis |
title_short | Coevolutionary transitions from antagonism to mutualism explained by the Co-Opted Antagonist Hypothesis |
title_sort | coevolutionary transitions from antagonism to mutualism explained by the co-opted antagonist hypothesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8129128/ https://www.ncbi.nlm.nih.gov/pubmed/34001894 http://dx.doi.org/10.1038/s41467-021-23177-x |
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