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Genome-wide parallelism underlies contemporary adaptation in urban lizards

Urbanization drastically transforms landscapes, resulting in fragmentation, degradation, and the loss of local biodiversity. Yet, urban environments also offer opportunities to observe rapid evolutionary change in wild populations that survive and even thrive in these novel habitats. In many ways, c...

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Autores principales: Winchell, Kristin M., Campbell-Staton, Shane C., Losos, Jonathan B., Revell, Liam J., Verrelli, Brian C., Geneva, Anthony J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9934206/
https://www.ncbi.nlm.nih.gov/pubmed/36634133
http://dx.doi.org/10.1073/pnas.2216789120
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author Winchell, Kristin M.
Campbell-Staton, Shane C.
Losos, Jonathan B.
Revell, Liam J.
Verrelli, Brian C.
Geneva, Anthony J.
author_facet Winchell, Kristin M.
Campbell-Staton, Shane C.
Losos, Jonathan B.
Revell, Liam J.
Verrelli, Brian C.
Geneva, Anthony J.
author_sort Winchell, Kristin M.
collection PubMed
description Urbanization drastically transforms landscapes, resulting in fragmentation, degradation, and the loss of local biodiversity. Yet, urban environments also offer opportunities to observe rapid evolutionary change in wild populations that survive and even thrive in these novel habitats. In many ways, cities represent replicated “natural experiments” in which geographically separated populations adaptively respond to similar selection pressures over rapid evolutionary timescales. Little is known, however, about the genetic basis of adaptive phenotypic differentiation in urban populations nor the extent to which phenotypic parallelism is reflected at the genomic level with signatures of parallel selection. Here, we analyzed the genomic underpinnings of parallel urban-associated phenotypic change in Anolis cristatellus, a small-bodied neotropical lizard found abundantly in both urbanized and forested environments. We show that phenotypic parallelism in response to parallel urban environmental change is underlain by genomic parallelism and identify candidate loci across the Anolis genome associated with this adaptive morphological divergence. Our findings point to polygenic selection on standing genetic variation as a key process to effectuate rapid morphological adaptation. Identified candidate loci represent several functions associated with skeletomuscular development, morphology, and human disease. Taken together, these results shed light on the genomic basis of complex morphological adaptations, provide insight into the role of contingency and determinism in adaptation to novel environments, and underscore the value of urban environments to address fundamental evolutionary questions.
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spelling pubmed-99342062023-07-12 Genome-wide parallelism underlies contemporary adaptation in urban lizards Winchell, Kristin M. Campbell-Staton, Shane C. Losos, Jonathan B. Revell, Liam J. Verrelli, Brian C. Geneva, Anthony J. Proc Natl Acad Sci U S A Biological Sciences Urbanization drastically transforms landscapes, resulting in fragmentation, degradation, and the loss of local biodiversity. Yet, urban environments also offer opportunities to observe rapid evolutionary change in wild populations that survive and even thrive in these novel habitats. In many ways, cities represent replicated “natural experiments” in which geographically separated populations adaptively respond to similar selection pressures over rapid evolutionary timescales. Little is known, however, about the genetic basis of adaptive phenotypic differentiation in urban populations nor the extent to which phenotypic parallelism is reflected at the genomic level with signatures of parallel selection. Here, we analyzed the genomic underpinnings of parallel urban-associated phenotypic change in Anolis cristatellus, a small-bodied neotropical lizard found abundantly in both urbanized and forested environments. We show that phenotypic parallelism in response to parallel urban environmental change is underlain by genomic parallelism and identify candidate loci across the Anolis genome associated with this adaptive morphological divergence. Our findings point to polygenic selection on standing genetic variation as a key process to effectuate rapid morphological adaptation. Identified candidate loci represent several functions associated with skeletomuscular development, morphology, and human disease. Taken together, these results shed light on the genomic basis of complex morphological adaptations, provide insight into the role of contingency and determinism in adaptation to novel environments, and underscore the value of urban environments to address fundamental evolutionary questions. National Academy of Sciences 2023-01-12 2023-01-17 /pmc/articles/PMC9934206/ /pubmed/36634133 http://dx.doi.org/10.1073/pnas.2216789120 Text en Copyright © 2023 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Winchell, Kristin M.
Campbell-Staton, Shane C.
Losos, Jonathan B.
Revell, Liam J.
Verrelli, Brian C.
Geneva, Anthony J.
Genome-wide parallelism underlies contemporary adaptation in urban lizards
title Genome-wide parallelism underlies contemporary adaptation in urban lizards
title_full Genome-wide parallelism underlies contemporary adaptation in urban lizards
title_fullStr Genome-wide parallelism underlies contemporary adaptation in urban lizards
title_full_unstemmed Genome-wide parallelism underlies contemporary adaptation in urban lizards
title_short Genome-wide parallelism underlies contemporary adaptation in urban lizards
title_sort genome-wide parallelism underlies contemporary adaptation in urban lizards
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9934206/
https://www.ncbi.nlm.nih.gov/pubmed/36634133
http://dx.doi.org/10.1073/pnas.2216789120
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