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Transcriptomic and macroevolutionary evidence for phenotypic uncoupling between frog life history phases
Anuran amphibians undergo major morphological transitions during development, but the contribution of their markedly different life-history phases to macroevolution has rarely been analysed. Here we generate testable predictions for coupling versus uncoupling of phenotypic evolution of tadpole and a...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5440664/ https://www.ncbi.nlm.nih.gov/pubmed/28504275 http://dx.doi.org/10.1038/ncomms15213 |
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author | Wollenberg Valero, Katharina C. Garcia-Porta, Joan Rodríguez, Ariel Arias, Mónica Shah, Abhijeet Randrianiaina, Roger Daniel Brown, Jason L. Glaw, Frank Amat, Felix Künzel, Sven Metzler, Dirk Isokpehi, Raphael D. Vences, Miguel |
author_facet | Wollenberg Valero, Katharina C. Garcia-Porta, Joan Rodríguez, Ariel Arias, Mónica Shah, Abhijeet Randrianiaina, Roger Daniel Brown, Jason L. Glaw, Frank Amat, Felix Künzel, Sven Metzler, Dirk Isokpehi, Raphael D. Vences, Miguel |
author_sort | Wollenberg Valero, Katharina C. |
collection | PubMed |
description | Anuran amphibians undergo major morphological transitions during development, but the contribution of their markedly different life-history phases to macroevolution has rarely been analysed. Here we generate testable predictions for coupling versus uncoupling of phenotypic evolution of tadpole and adult life-history phases, and for the underlying expression of genes related to morphological feature formation. We test these predictions by combining evidence from gene expression in two distantly related frogs, Xenopus laevis and Mantidactylus betsileanus, with patterns of morphological evolution in the entire radiation of Madagascan mantellid frogs. Genes linked to morphological structure formation are expressed in a highly phase-specific pattern, suggesting uncoupling of phenotypic evolution across life-history phases. This gene expression pattern agrees with uncoupled rates of trait evolution among life-history phases in the mantellids, which we show to have undergone an adaptive radiation. Our results validate a prevalence of uncoupling in the evolution of tadpole and adult phenotypes of frogs. |
format | Online Article Text |
id | pubmed-5440664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-54406642017-06-02 Transcriptomic and macroevolutionary evidence for phenotypic uncoupling between frog life history phases Wollenberg Valero, Katharina C. Garcia-Porta, Joan Rodríguez, Ariel Arias, Mónica Shah, Abhijeet Randrianiaina, Roger Daniel Brown, Jason L. Glaw, Frank Amat, Felix Künzel, Sven Metzler, Dirk Isokpehi, Raphael D. Vences, Miguel Nat Commun Article Anuran amphibians undergo major morphological transitions during development, but the contribution of their markedly different life-history phases to macroevolution has rarely been analysed. Here we generate testable predictions for coupling versus uncoupling of phenotypic evolution of tadpole and adult life-history phases, and for the underlying expression of genes related to morphological feature formation. We test these predictions by combining evidence from gene expression in two distantly related frogs, Xenopus laevis and Mantidactylus betsileanus, with patterns of morphological evolution in the entire radiation of Madagascan mantellid frogs. Genes linked to morphological structure formation are expressed in a highly phase-specific pattern, suggesting uncoupling of phenotypic evolution across life-history phases. This gene expression pattern agrees with uncoupled rates of trait evolution among life-history phases in the mantellids, which we show to have undergone an adaptive radiation. Our results validate a prevalence of uncoupling in the evolution of tadpole and adult phenotypes of frogs. Nature Publishing Group 2017-05-15 /pmc/articles/PMC5440664/ /pubmed/28504275 http://dx.doi.org/10.1038/ncomms15213 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Wollenberg Valero, Katharina C. Garcia-Porta, Joan Rodríguez, Ariel Arias, Mónica Shah, Abhijeet Randrianiaina, Roger Daniel Brown, Jason L. Glaw, Frank Amat, Felix Künzel, Sven Metzler, Dirk Isokpehi, Raphael D. Vences, Miguel Transcriptomic and macroevolutionary evidence for phenotypic uncoupling between frog life history phases |
title | Transcriptomic and macroevolutionary evidence for phenotypic uncoupling between frog life history phases |
title_full | Transcriptomic and macroevolutionary evidence for phenotypic uncoupling between frog life history phases |
title_fullStr | Transcriptomic and macroevolutionary evidence for phenotypic uncoupling between frog life history phases |
title_full_unstemmed | Transcriptomic and macroevolutionary evidence for phenotypic uncoupling between frog life history phases |
title_short | Transcriptomic and macroevolutionary evidence for phenotypic uncoupling between frog life history phases |
title_sort | transcriptomic and macroevolutionary evidence for phenotypic uncoupling between frog life history phases |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5440664/ https://www.ncbi.nlm.nih.gov/pubmed/28504275 http://dx.doi.org/10.1038/ncomms15213 |
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