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Hybridization is a recurrent evolutionary stimulus in wild yeast speciation
Hybridization can result in reproductively isolated and phenotypically distinct lineages that evolve as independent hybrid species. How frequently hybridization leads to speciation remains largely unknown. Here we examine the potential recurrence of hybrid speciation in the wild yeast Saccharomyces...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389940/ https://www.ncbi.nlm.nih.gov/pubmed/30804385 http://dx.doi.org/10.1038/s41467-019-08809-7 |
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author | Eberlein, Chris Hénault, Mathieu Fijarczyk, Anna Charron, Guillaume Bouvier, Matteo Kohn, Linda M. Anderson, James B. Landry, Christian R. |
author_facet | Eberlein, Chris Hénault, Mathieu Fijarczyk, Anna Charron, Guillaume Bouvier, Matteo Kohn, Linda M. Anderson, James B. Landry, Christian R. |
author_sort | Eberlein, Chris |
collection | PubMed |
description | Hybridization can result in reproductively isolated and phenotypically distinct lineages that evolve as independent hybrid species. How frequently hybridization leads to speciation remains largely unknown. Here we examine the potential recurrence of hybrid speciation in the wild yeast Saccharomyces paradoxus in North America, which comprises two endemic lineages SpB and SpC, and an incipient hybrid species, SpC*. Using whole-genome sequences from more than 300 strains, we uncover the hybrid origin of another group, SpD, that emerged from hybridization between SpC* and one of its parental species, the widespread SpB. We show that SpD has the potential to evolve as a novel hybrid species, because it displays phenotypic novelties that include an intermediate transcriptome profile, and partial reproductive isolation with its most abundant sympatric parental species, SpB. Our findings show that repetitive cycles of divergence and hybridization quickly generate diversity and reproductive isolation, providing the raw material for speciation by hybridization. |
format | Online Article Text |
id | pubmed-6389940 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63899402019-02-27 Hybridization is a recurrent evolutionary stimulus in wild yeast speciation Eberlein, Chris Hénault, Mathieu Fijarczyk, Anna Charron, Guillaume Bouvier, Matteo Kohn, Linda M. Anderson, James B. Landry, Christian R. Nat Commun Article Hybridization can result in reproductively isolated and phenotypically distinct lineages that evolve as independent hybrid species. How frequently hybridization leads to speciation remains largely unknown. Here we examine the potential recurrence of hybrid speciation in the wild yeast Saccharomyces paradoxus in North America, which comprises two endemic lineages SpB and SpC, and an incipient hybrid species, SpC*. Using whole-genome sequences from more than 300 strains, we uncover the hybrid origin of another group, SpD, that emerged from hybridization between SpC* and one of its parental species, the widespread SpB. We show that SpD has the potential to evolve as a novel hybrid species, because it displays phenotypic novelties that include an intermediate transcriptome profile, and partial reproductive isolation with its most abundant sympatric parental species, SpB. Our findings show that repetitive cycles of divergence and hybridization quickly generate diversity and reproductive isolation, providing the raw material for speciation by hybridization. Nature Publishing Group UK 2019-02-25 /pmc/articles/PMC6389940/ /pubmed/30804385 http://dx.doi.org/10.1038/s41467-019-08809-7 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Eberlein, Chris Hénault, Mathieu Fijarczyk, Anna Charron, Guillaume Bouvier, Matteo Kohn, Linda M. Anderson, James B. Landry, Christian R. Hybridization is a recurrent evolutionary stimulus in wild yeast speciation |
title | Hybridization is a recurrent evolutionary stimulus in wild yeast speciation |
title_full | Hybridization is a recurrent evolutionary stimulus in wild yeast speciation |
title_fullStr | Hybridization is a recurrent evolutionary stimulus in wild yeast speciation |
title_full_unstemmed | Hybridization is a recurrent evolutionary stimulus in wild yeast speciation |
title_short | Hybridization is a recurrent evolutionary stimulus in wild yeast speciation |
title_sort | hybridization is a recurrent evolutionary stimulus in wild yeast speciation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389940/ https://www.ncbi.nlm.nih.gov/pubmed/30804385 http://dx.doi.org/10.1038/s41467-019-08809-7 |
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