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Identification of candidate loci for adaptive phenotypic plasticity in natural populations of spadefoot toads

Phenotypic plasticity allows organisms to alter their phenotype in direct response to changes in the environment. Despite growing recognition of plasticity's role in ecology and evolution, few studies have probed plasticity's molecular bases—especially using natural populations. We investi...

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Autores principales: Levis, Nicholas A., Reed, Emily M. X., Pfennig, David W., Burford Reiskind, Martha O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7452772/
https://www.ncbi.nlm.nih.gov/pubmed/32884672
http://dx.doi.org/10.1002/ece3.6602
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author Levis, Nicholas A.
Reed, Emily M. X.
Pfennig, David W.
Burford Reiskind, Martha O.
author_facet Levis, Nicholas A.
Reed, Emily M. X.
Pfennig, David W.
Burford Reiskind, Martha O.
author_sort Levis, Nicholas A.
collection PubMed
description Phenotypic plasticity allows organisms to alter their phenotype in direct response to changes in the environment. Despite growing recognition of plasticity's role in ecology and evolution, few studies have probed plasticity's molecular bases—especially using natural populations. We investigated the genetic basis of phenotypic plasticity in natural populations of spadefoot toads (Spea multiplicata). Spea tadpoles normally develop into an “omnivore” morph that is favored in long‐lasting, low‐density ponds. However, if tadpoles consume freshwater shrimp or other tadpoles, they can alternatively develop (via plasticity) into a “carnivore” morph that is favored in ephemeral, high‐density ponds. By combining natural variation in pond ecology and morph production with population genetic approaches, we identified candidate loci associated with each morph (carnivores vs. omnivores) and loci associated with adaptive phenotypic plasticity (adaptive vs. maladaptive morph choice). Our candidate morph loci mapped to two genes, whereas our candidate plasticity loci mapped to 14 genes. In both cases, the identified genes tended to have functions related to their putative role in spadefoot tadpole biology. Our results thereby form the basis for future studies into the molecular mechanisms that mediate plasticity in spadefoots. More generally, these results illustrate how diverse loci might mediate adaptive plasticity.
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spelling pubmed-74527722020-09-02 Identification of candidate loci for adaptive phenotypic plasticity in natural populations of spadefoot toads Levis, Nicholas A. Reed, Emily M. X. Pfennig, David W. Burford Reiskind, Martha O. Ecol Evol Original Research Phenotypic plasticity allows organisms to alter their phenotype in direct response to changes in the environment. Despite growing recognition of plasticity's role in ecology and evolution, few studies have probed plasticity's molecular bases—especially using natural populations. We investigated the genetic basis of phenotypic plasticity in natural populations of spadefoot toads (Spea multiplicata). Spea tadpoles normally develop into an “omnivore” morph that is favored in long‐lasting, low‐density ponds. However, if tadpoles consume freshwater shrimp or other tadpoles, they can alternatively develop (via plasticity) into a “carnivore” morph that is favored in ephemeral, high‐density ponds. By combining natural variation in pond ecology and morph production with population genetic approaches, we identified candidate loci associated with each morph (carnivores vs. omnivores) and loci associated with adaptive phenotypic plasticity (adaptive vs. maladaptive morph choice). Our candidate morph loci mapped to two genes, whereas our candidate plasticity loci mapped to 14 genes. In both cases, the identified genes tended to have functions related to their putative role in spadefoot tadpole biology. Our results thereby form the basis for future studies into the molecular mechanisms that mediate plasticity in spadefoots. More generally, these results illustrate how diverse loci might mediate adaptive plasticity. John Wiley and Sons Inc. 2020-07-24 /pmc/articles/PMC7452772/ /pubmed/32884672 http://dx.doi.org/10.1002/ece3.6602 Text en © 2020 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Levis, Nicholas A.
Reed, Emily M. X.
Pfennig, David W.
Burford Reiskind, Martha O.
Identification of candidate loci for adaptive phenotypic plasticity in natural populations of spadefoot toads
title Identification of candidate loci for adaptive phenotypic plasticity in natural populations of spadefoot toads
title_full Identification of candidate loci for adaptive phenotypic plasticity in natural populations of spadefoot toads
title_fullStr Identification of candidate loci for adaptive phenotypic plasticity in natural populations of spadefoot toads
title_full_unstemmed Identification of candidate loci for adaptive phenotypic plasticity in natural populations of spadefoot toads
title_short Identification of candidate loci for adaptive phenotypic plasticity in natural populations of spadefoot toads
title_sort identification of candidate loci for adaptive phenotypic plasticity in natural populations of spadefoot toads
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7452772/
https://www.ncbi.nlm.nih.gov/pubmed/32884672
http://dx.doi.org/10.1002/ece3.6602
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