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Genetic accommodation via modified endocrine signalling explains phenotypic divergence among spadefoot toad species
Phenotypic differences among species may evolve through genetic accommodation, but mechanisms accounting for this process are poorly understood. Here we compare hormonal variation underlying differences in the timing of metamorphosis among three spadefoot toads with different larval periods and resp...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5648835/ https://www.ncbi.nlm.nih.gov/pubmed/29051478 http://dx.doi.org/10.1038/s41467-017-00996-5 |
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author | Kulkarni, Saurabh S. Denver, Robert J. Gomez-Mestre, Ivan Buchholz, Daniel R. |
author_facet | Kulkarni, Saurabh S. Denver, Robert J. Gomez-Mestre, Ivan Buchholz, Daniel R. |
author_sort | Kulkarni, Saurabh S. |
collection | PubMed |
description | Phenotypic differences among species may evolve through genetic accommodation, but mechanisms accounting for this process are poorly understood. Here we compare hormonal variation underlying differences in the timing of metamorphosis among three spadefoot toads with different larval periods and responsiveness to pond drying. We find that, in response to pond drying, Pelobates cultripes and Spea multiplicata accelerate metamorphosis, increase standard metabolic rate (SMR), and elevate whole-body content of thyroid hormone (the primary morphogen controlling metamorphosis) and corticosterone (a stress hormone acting synergistically with thyroid hormone to accelerate metamorphosis). In contrast, Scaphiopus couchii has the shortest larval period, highest whole-body thyroid hormone and corticosterone content, and highest SMR, and these trait values are least affected by pond drying among the three species. Our findings support that the atypically rapid and canalized development of S. couchii evolved by genetic accommodation of endocrine pathways controlling metamorphosis, showing how phenotypic plasticity within species may evolve into trait variation among species. |
format | Online Article Text |
id | pubmed-5648835 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56488352017-10-23 Genetic accommodation via modified endocrine signalling explains phenotypic divergence among spadefoot toad species Kulkarni, Saurabh S. Denver, Robert J. Gomez-Mestre, Ivan Buchholz, Daniel R. Nat Commun Article Phenotypic differences among species may evolve through genetic accommodation, but mechanisms accounting for this process are poorly understood. Here we compare hormonal variation underlying differences in the timing of metamorphosis among three spadefoot toads with different larval periods and responsiveness to pond drying. We find that, in response to pond drying, Pelobates cultripes and Spea multiplicata accelerate metamorphosis, increase standard metabolic rate (SMR), and elevate whole-body content of thyroid hormone (the primary morphogen controlling metamorphosis) and corticosterone (a stress hormone acting synergistically with thyroid hormone to accelerate metamorphosis). In contrast, Scaphiopus couchii has the shortest larval period, highest whole-body thyroid hormone and corticosterone content, and highest SMR, and these trait values are least affected by pond drying among the three species. Our findings support that the atypically rapid and canalized development of S. couchii evolved by genetic accommodation of endocrine pathways controlling metamorphosis, showing how phenotypic plasticity within species may evolve into trait variation among species. Nature Publishing Group UK 2017-10-19 /pmc/articles/PMC5648835/ /pubmed/29051478 http://dx.doi.org/10.1038/s41467-017-00996-5 Text en © The Author(s) 2017 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 Kulkarni, Saurabh S. Denver, Robert J. Gomez-Mestre, Ivan Buchholz, Daniel R. Genetic accommodation via modified endocrine signalling explains phenotypic divergence among spadefoot toad species |
title | Genetic accommodation via modified endocrine signalling explains phenotypic divergence among spadefoot toad species |
title_full | Genetic accommodation via modified endocrine signalling explains phenotypic divergence among spadefoot toad species |
title_fullStr | Genetic accommodation via modified endocrine signalling explains phenotypic divergence among spadefoot toad species |
title_full_unstemmed | Genetic accommodation via modified endocrine signalling explains phenotypic divergence among spadefoot toad species |
title_short | Genetic accommodation via modified endocrine signalling explains phenotypic divergence among spadefoot toad species |
title_sort | genetic accommodation via modified endocrine signalling explains phenotypic divergence among spadefoot toad species |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5648835/ https://www.ncbi.nlm.nih.gov/pubmed/29051478 http://dx.doi.org/10.1038/s41467-017-00996-5 |
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