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Great tits and the city: Distribution of genomic diversity and gene–environment associations along an urbanization gradient

Urbanization is a growing concern challenging the evolutionary potential of wild populations by reducing genetic diversity and imposing new selection regimes affecting many key fitness traits. However, genomic footprints of urbanization have received little attention so far. Using RAD sequencing, we...

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Autores principales: Perrier, Charles, Lozano del Campo, Ana, Szulkin, Marta, Demeyrier, Virginie, Gregoire, Arnaud, Charmantier, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5979639/
https://www.ncbi.nlm.nih.gov/pubmed/29875805
http://dx.doi.org/10.1111/eva.12580
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author Perrier, Charles
Lozano del Campo, Ana
Szulkin, Marta
Demeyrier, Virginie
Gregoire, Arnaud
Charmantier, Anne
author_facet Perrier, Charles
Lozano del Campo, Ana
Szulkin, Marta
Demeyrier, Virginie
Gregoire, Arnaud
Charmantier, Anne
author_sort Perrier, Charles
collection PubMed
description Urbanization is a growing concern challenging the evolutionary potential of wild populations by reducing genetic diversity and imposing new selection regimes affecting many key fitness traits. However, genomic footprints of urbanization have received little attention so far. Using RAD sequencing, we investigated the genomewide effects of urbanization on neutral and adaptive genomic diversity in 140 adult great tits Parus major collected in locations with contrasted urbanization levels (from a natural forest to highly urbanized areas of a city; Montpellier, France). Heterozygosity was slightly lower in the more urbanized sites compared to the more rural ones. Low but significant effect of urbanization on genetic differentiation was found, at the site level but not at the nest level, indicative of the geographic scale of urbanization impact and of the potential for local adaptation despite gene flow. Gene–environment association tests identified numerous SNPs with small association scores to urbanization, distributed across the genome, from which a subset of 97 SNPs explained up to 81% of the variance in urbanization, overall suggesting a polygenic response to selection in the urban environment. These findings open stimulating perspectives for broader applications of high‐resolution genomic tools on other cities and larger sample sizes to investigate the consistency of the effects of urbanization on the spatial distribution of genetic diversity and the polygenic nature of gene–urbanization association.
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spelling pubmed-59796392018-06-06 Great tits and the city: Distribution of genomic diversity and gene–environment associations along an urbanization gradient Perrier, Charles Lozano del Campo, Ana Szulkin, Marta Demeyrier, Virginie Gregoire, Arnaud Charmantier, Anne Evol Appl Original Articles Urbanization is a growing concern challenging the evolutionary potential of wild populations by reducing genetic diversity and imposing new selection regimes affecting many key fitness traits. However, genomic footprints of urbanization have received little attention so far. Using RAD sequencing, we investigated the genomewide effects of urbanization on neutral and adaptive genomic diversity in 140 adult great tits Parus major collected in locations with contrasted urbanization levels (from a natural forest to highly urbanized areas of a city; Montpellier, France). Heterozygosity was slightly lower in the more urbanized sites compared to the more rural ones. Low but significant effect of urbanization on genetic differentiation was found, at the site level but not at the nest level, indicative of the geographic scale of urbanization impact and of the potential for local adaptation despite gene flow. Gene–environment association tests identified numerous SNPs with small association scores to urbanization, distributed across the genome, from which a subset of 97 SNPs explained up to 81% of the variance in urbanization, overall suggesting a polygenic response to selection in the urban environment. These findings open stimulating perspectives for broader applications of high‐resolution genomic tools on other cities and larger sample sizes to investigate the consistency of the effects of urbanization on the spatial distribution of genetic diversity and the polygenic nature of gene–urbanization association. John Wiley and Sons Inc. 2017-12-20 /pmc/articles/PMC5979639/ /pubmed/29875805 http://dx.doi.org/10.1111/eva.12580 Text en © 2017 The Authors. Evolutionary Applications 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 Articles
Perrier, Charles
Lozano del Campo, Ana
Szulkin, Marta
Demeyrier, Virginie
Gregoire, Arnaud
Charmantier, Anne
Great tits and the city: Distribution of genomic diversity and gene–environment associations along an urbanization gradient
title Great tits and the city: Distribution of genomic diversity and gene–environment associations along an urbanization gradient
title_full Great tits and the city: Distribution of genomic diversity and gene–environment associations along an urbanization gradient
title_fullStr Great tits and the city: Distribution of genomic diversity and gene–environment associations along an urbanization gradient
title_full_unstemmed Great tits and the city: Distribution of genomic diversity and gene–environment associations along an urbanization gradient
title_short Great tits and the city: Distribution of genomic diversity and gene–environment associations along an urbanization gradient
title_sort great tits and the city: distribution of genomic diversity and gene–environment associations along an urbanization gradient
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5979639/
https://www.ncbi.nlm.nih.gov/pubmed/29875805
http://dx.doi.org/10.1111/eva.12580
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