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Bottleneck‐associated changes in the genomic landscape of genetic diversity in wild lynx populations

Demographic bottlenecks generally reduce genetic diversity through more intense genetic drift, but their net effect may vary along the genome due to the random nature of genetic drift and to local effects of recombination, mutation, and selection. Here, we analyzed the changes in genetic diversity f...

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Autores principales: Lucena‐Perez, Maria, Kleinman‐Ruiz, Daniel, Marmesat, Elena, Saveljev, Alexander P., Schmidt, Krzysztof, Godoy, José A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8591332/
https://www.ncbi.nlm.nih.gov/pubmed/34815746
http://dx.doi.org/10.1111/eva.13302
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author Lucena‐Perez, Maria
Kleinman‐Ruiz, Daniel
Marmesat, Elena
Saveljev, Alexander P.
Schmidt, Krzysztof
Godoy, José A.
author_facet Lucena‐Perez, Maria
Kleinman‐Ruiz, Daniel
Marmesat, Elena
Saveljev, Alexander P.
Schmidt, Krzysztof
Godoy, José A.
author_sort Lucena‐Perez, Maria
collection PubMed
description Demographic bottlenecks generally reduce genetic diversity through more intense genetic drift, but their net effect may vary along the genome due to the random nature of genetic drift and to local effects of recombination, mutation, and selection. Here, we analyzed the changes in genetic diversity following a bottleneck by comparing whole‐genome diversity patterns in populations with and without severe recent documented declines of Iberian (Lynx pardinus, n = 31) and Eurasian lynx (Lynx lynx, n = 29). As expected, overall genomic diversity correlated negatively with bottleneck intensity and/or duration. Correlations of genetic diversity with divergence, chromosome size, gene or functional site content, GC content, or recombination were observed in nonbottlenecked populations, but were weaker in bottlenecked populations. Also, functional features under intense purifying selection and the X chromosome showed an increase in the observed density of variants, even resulting in higher θ (W) diversity than in nonbottlenecked populations. Increased diversity seems to be related to both a higher mutational input in those regions creating a large collection of low‐frequency variants, a few of which increase in frequency during the bottleneck to the point they become detectable with our limited sample, and the reduced efficacy of purifying selection, which affects not only protein structure and function but also the regulation of gene expression. The results of this study alert to the possible reduction of fitness and adaptive potential associated with the genomic erosion in regulatory elements. Further, the detection of a gain of diversity in ultra‐conserved elements can be used as a sensitive and easy‐to‐apply signature of genetic erosion in wild populations.
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spelling pubmed-85913322021-11-22 Bottleneck‐associated changes in the genomic landscape of genetic diversity in wild lynx populations Lucena‐Perez, Maria Kleinman‐Ruiz, Daniel Marmesat, Elena Saveljev, Alexander P. Schmidt, Krzysztof Godoy, José A. Evol Appl Original Articles Demographic bottlenecks generally reduce genetic diversity through more intense genetic drift, but their net effect may vary along the genome due to the random nature of genetic drift and to local effects of recombination, mutation, and selection. Here, we analyzed the changes in genetic diversity following a bottleneck by comparing whole‐genome diversity patterns in populations with and without severe recent documented declines of Iberian (Lynx pardinus, n = 31) and Eurasian lynx (Lynx lynx, n = 29). As expected, overall genomic diversity correlated negatively with bottleneck intensity and/or duration. Correlations of genetic diversity with divergence, chromosome size, gene or functional site content, GC content, or recombination were observed in nonbottlenecked populations, but were weaker in bottlenecked populations. Also, functional features under intense purifying selection and the X chromosome showed an increase in the observed density of variants, even resulting in higher θ (W) diversity than in nonbottlenecked populations. Increased diversity seems to be related to both a higher mutational input in those regions creating a large collection of low‐frequency variants, a few of which increase in frequency during the bottleneck to the point they become detectable with our limited sample, and the reduced efficacy of purifying selection, which affects not only protein structure and function but also the regulation of gene expression. The results of this study alert to the possible reduction of fitness and adaptive potential associated with the genomic erosion in regulatory elements. Further, the detection of a gain of diversity in ultra‐conserved elements can be used as a sensitive and easy‐to‐apply signature of genetic erosion in wild populations. John Wiley and Sons Inc. 2021-10-08 /pmc/articles/PMC8591332/ /pubmed/34815746 http://dx.doi.org/10.1111/eva.13302 Text en © 2021 The Authors. Evolutionary Applications published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://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
Lucena‐Perez, Maria
Kleinman‐Ruiz, Daniel
Marmesat, Elena
Saveljev, Alexander P.
Schmidt, Krzysztof
Godoy, José A.
Bottleneck‐associated changes in the genomic landscape of genetic diversity in wild lynx populations
title Bottleneck‐associated changes in the genomic landscape of genetic diversity in wild lynx populations
title_full Bottleneck‐associated changes in the genomic landscape of genetic diversity in wild lynx populations
title_fullStr Bottleneck‐associated changes in the genomic landscape of genetic diversity in wild lynx populations
title_full_unstemmed Bottleneck‐associated changes in the genomic landscape of genetic diversity in wild lynx populations
title_short Bottleneck‐associated changes in the genomic landscape of genetic diversity in wild lynx populations
title_sort bottleneck‐associated changes in the genomic landscape of genetic diversity in wild lynx populations
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8591332/
https://www.ncbi.nlm.nih.gov/pubmed/34815746
http://dx.doi.org/10.1111/eva.13302
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