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Clinal genomic analysis reveals strong reproductive isolation across a steep habitat transition in stickleback fish

How ecological divergence causes strong reproductive isolation between populations in close geographic contact remains poorly understood at the genomic level. We here study this question in a stickleback fish population pair adapted to contiguous, ecologically different lake and stream habitats. Cli...

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Autores principales: Haenel, Quiterie, Oke, Krista B., Laurentino, Telma G., Hendry, Andrew P., Berner, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8358029/
https://www.ncbi.nlm.nih.gov/pubmed/34381033
http://dx.doi.org/10.1038/s41467-021-25039-y
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author Haenel, Quiterie
Oke, Krista B.
Laurentino, Telma G.
Hendry, Andrew P.
Berner, Daniel
author_facet Haenel, Quiterie
Oke, Krista B.
Laurentino, Telma G.
Hendry, Andrew P.
Berner, Daniel
author_sort Haenel, Quiterie
collection PubMed
description How ecological divergence causes strong reproductive isolation between populations in close geographic contact remains poorly understood at the genomic level. We here study this question in a stickleback fish population pair adapted to contiguous, ecologically different lake and stream habitats. Clinal whole-genome sequence data reveal numerous genome regions (nearly) fixed for alternative alleles over a distance of just a few hundred meters. This strong polygenic adaptive divergence must constitute a genome-wide barrier to gene flow because a steep cline in allele frequencies is observed across the entire genome, and because the cline center closely matches the habitat transition. Simulations confirm that such strong divergence can be maintained by polygenic selection despite high dispersal and small per-locus selection coefficients. Finally, comparing samples from near the habitat transition before and after an unusual ecological perturbation demonstrates the fragility of the balance between gene flow and selection. Overall, our study highlights the efficacy of divergent selection in maintaining reproductive isolation without physical isolation, and the analytical power of studying speciation at a fine eco-geographic and genomic scale.
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spelling pubmed-83580292021-08-30 Clinal genomic analysis reveals strong reproductive isolation across a steep habitat transition in stickleback fish Haenel, Quiterie Oke, Krista B. Laurentino, Telma G. Hendry, Andrew P. Berner, Daniel Nat Commun Article How ecological divergence causes strong reproductive isolation between populations in close geographic contact remains poorly understood at the genomic level. We here study this question in a stickleback fish population pair adapted to contiguous, ecologically different lake and stream habitats. Clinal whole-genome sequence data reveal numerous genome regions (nearly) fixed for alternative alleles over a distance of just a few hundred meters. This strong polygenic adaptive divergence must constitute a genome-wide barrier to gene flow because a steep cline in allele frequencies is observed across the entire genome, and because the cline center closely matches the habitat transition. Simulations confirm that such strong divergence can be maintained by polygenic selection despite high dispersal and small per-locus selection coefficients. Finally, comparing samples from near the habitat transition before and after an unusual ecological perturbation demonstrates the fragility of the balance between gene flow and selection. Overall, our study highlights the efficacy of divergent selection in maintaining reproductive isolation without physical isolation, and the analytical power of studying speciation at a fine eco-geographic and genomic scale. Nature Publishing Group UK 2021-08-11 /pmc/articles/PMC8358029/ /pubmed/34381033 http://dx.doi.org/10.1038/s41467-021-25039-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Haenel, Quiterie
Oke, Krista B.
Laurentino, Telma G.
Hendry, Andrew P.
Berner, Daniel
Clinal genomic analysis reveals strong reproductive isolation across a steep habitat transition in stickleback fish
title Clinal genomic analysis reveals strong reproductive isolation across a steep habitat transition in stickleback fish
title_full Clinal genomic analysis reveals strong reproductive isolation across a steep habitat transition in stickleback fish
title_fullStr Clinal genomic analysis reveals strong reproductive isolation across a steep habitat transition in stickleback fish
title_full_unstemmed Clinal genomic analysis reveals strong reproductive isolation across a steep habitat transition in stickleback fish
title_short Clinal genomic analysis reveals strong reproductive isolation across a steep habitat transition in stickleback fish
title_sort clinal genomic analysis reveals strong reproductive isolation across a steep habitat transition in stickleback fish
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8358029/
https://www.ncbi.nlm.nih.gov/pubmed/34381033
http://dx.doi.org/10.1038/s41467-021-25039-y
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