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Divergence with gene flow across a speciation continuum of Heliconius butterflies

BACKGROUND: A key to understanding the origins of species is determining the evolutionary processes that drive the patterns of genomic divergence during speciation. New genomic technologies enable the study of high-resolution genomic patterns of divergence across natural speciation continua, where t...

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Autores principales: Supple, Megan A., Papa, Riccardo, Hines, Heather M., McMillan, W. Owen, Counterman, Brian A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4582928/
https://www.ncbi.nlm.nih.gov/pubmed/26403600
http://dx.doi.org/10.1186/s12862-015-0486-y
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author Supple, Megan A.
Papa, Riccardo
Hines, Heather M.
McMillan, W. Owen
Counterman, Brian A.
author_facet Supple, Megan A.
Papa, Riccardo
Hines, Heather M.
McMillan, W. Owen
Counterman, Brian A.
author_sort Supple, Megan A.
collection PubMed
description BACKGROUND: A key to understanding the origins of species is determining the evolutionary processes that drive the patterns of genomic divergence during speciation. New genomic technologies enable the study of high-resolution genomic patterns of divergence across natural speciation continua, where taxa pairs with different levels of reproductive isolation can be used as proxies for different stages of speciation. Empirical studies of these speciation continua can provide valuable insights into how genomes diverge during speciation. METHODS: We examine variation across a handful of genomic regions in parapatric and allopatric populations of Heliconius butterflies with varying levels of reproductive isolation. Genome sequences were mapped to 2.2-Mb of the H. erato genome, including 1-Mb across the red color pattern locus and multiple regions unlinked to color pattern variation. RESULTS: Phylogenetic analyses reveal a speciation continuum of pairs of hybridizing races and incipient species in the Heliconius erato clade. Comparisons of hybridizing pairs of divergently colored races and incipient species reveal that genomic divergence increases with ecological and reproductive isolation, not only across the locus responsible for adaptive variation in red wing coloration, but also at genomic regions unlinked to color pattern. DISCUSSION: We observe high levels of divergence between the incipient species H. erato and H. himera, suggesting that divergence may accumulate early in the speciation process. Comparisons of genomic divergence between the incipient species and allopatric races suggest that limited gene flow cannot account for the observed high levels of divergence between the incipient species. CONCLUSIONS: Our results provide a reconstruction of the speciation continuum across the H. erato clade and provide insights into the processes that drive genomic divergence during speciation, establishing the H. erato clade as a powerful framework for the study of speciation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-015-0486-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-45829282015-09-26 Divergence with gene flow across a speciation continuum of Heliconius butterflies Supple, Megan A. Papa, Riccardo Hines, Heather M. McMillan, W. Owen Counterman, Brian A. BMC Evol Biol Research Article BACKGROUND: A key to understanding the origins of species is determining the evolutionary processes that drive the patterns of genomic divergence during speciation. New genomic technologies enable the study of high-resolution genomic patterns of divergence across natural speciation continua, where taxa pairs with different levels of reproductive isolation can be used as proxies for different stages of speciation. Empirical studies of these speciation continua can provide valuable insights into how genomes diverge during speciation. METHODS: We examine variation across a handful of genomic regions in parapatric and allopatric populations of Heliconius butterflies with varying levels of reproductive isolation. Genome sequences were mapped to 2.2-Mb of the H. erato genome, including 1-Mb across the red color pattern locus and multiple regions unlinked to color pattern variation. RESULTS: Phylogenetic analyses reveal a speciation continuum of pairs of hybridizing races and incipient species in the Heliconius erato clade. Comparisons of hybridizing pairs of divergently colored races and incipient species reveal that genomic divergence increases with ecological and reproductive isolation, not only across the locus responsible for adaptive variation in red wing coloration, but also at genomic regions unlinked to color pattern. DISCUSSION: We observe high levels of divergence between the incipient species H. erato and H. himera, suggesting that divergence may accumulate early in the speciation process. Comparisons of genomic divergence between the incipient species and allopatric races suggest that limited gene flow cannot account for the observed high levels of divergence between the incipient species. CONCLUSIONS: Our results provide a reconstruction of the speciation continuum across the H. erato clade and provide insights into the processes that drive genomic divergence during speciation, establishing the H. erato clade as a powerful framework for the study of speciation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-015-0486-y) contains supplementary material, which is available to authorized users. BioMed Central 2015-09-24 /pmc/articles/PMC4582928/ /pubmed/26403600 http://dx.doi.org/10.1186/s12862-015-0486-y Text en © Supple et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Supple, Megan A.
Papa, Riccardo
Hines, Heather M.
McMillan, W. Owen
Counterman, Brian A.
Divergence with gene flow across a speciation continuum of Heliconius butterflies
title Divergence with gene flow across a speciation continuum of Heliconius butterflies
title_full Divergence with gene flow across a speciation continuum of Heliconius butterflies
title_fullStr Divergence with gene flow across a speciation continuum of Heliconius butterflies
title_full_unstemmed Divergence with gene flow across a speciation continuum of Heliconius butterflies
title_short Divergence with gene flow across a speciation continuum of Heliconius butterflies
title_sort divergence with gene flow across a speciation continuum of heliconius butterflies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4582928/
https://www.ncbi.nlm.nih.gov/pubmed/26403600
http://dx.doi.org/10.1186/s12862-015-0486-y
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