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Interspecific introgression mediates adaptation to whole genome duplication

Adaptive gene flow is a consequential phenomenon across all kingdoms. Although recognition is increasing, there is no study showing that bidirectional gene flow mediates adaptation at loci that manage core processes. We previously discovered concerted molecular changes among interacting members of t...

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Autores principales: Marburger, Sarah, Monnahan, Patrick, Seear, Paul J., Martin, Simon H., Koch, Jordan, Paajanen, Pirita, Bohutínská, Magdalena, Higgins, James D., Schmickl, Roswitha, Yant, Levi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6861236/
https://www.ncbi.nlm.nih.gov/pubmed/31740675
http://dx.doi.org/10.1038/s41467-019-13159-5
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author Marburger, Sarah
Monnahan, Patrick
Seear, Paul J.
Martin, Simon H.
Koch, Jordan
Paajanen, Pirita
Bohutínská, Magdalena
Higgins, James D.
Schmickl, Roswitha
Yant, Levi
author_facet Marburger, Sarah
Monnahan, Patrick
Seear, Paul J.
Martin, Simon H.
Koch, Jordan
Paajanen, Pirita
Bohutínská, Magdalena
Higgins, James D.
Schmickl, Roswitha
Yant, Levi
author_sort Marburger, Sarah
collection PubMed
description Adaptive gene flow is a consequential phenomenon across all kingdoms. Although recognition is increasing, there is no study showing that bidirectional gene flow mediates adaptation at loci that manage core processes. We previously discovered concerted molecular changes among interacting members of the meiotic machinery controlling crossover number upon adaptation to whole-genome duplication (WGD) in Arabidopsis arenosa. Here we conduct a population genomic study to test the hypothesis that adaptation to WGD has been mediated by adaptive gene flow between A. arenosa and A. lyrata. We find that A. lyrata underwent WGD more recently than A. arenosa, suggesting that pre-adapted alleles have rescued nascent A. lyrata, but we also detect gene flow in the opposite direction at functionally interacting loci under the most extreme levels of selection. These data indicate that bidirectional gene flow allowed for survival after WGD, and that the merger of these species is greater than the sum of their parts.
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spelling pubmed-68612362019-11-20 Interspecific introgression mediates adaptation to whole genome duplication Marburger, Sarah Monnahan, Patrick Seear, Paul J. Martin, Simon H. Koch, Jordan Paajanen, Pirita Bohutínská, Magdalena Higgins, James D. Schmickl, Roswitha Yant, Levi Nat Commun Article Adaptive gene flow is a consequential phenomenon across all kingdoms. Although recognition is increasing, there is no study showing that bidirectional gene flow mediates adaptation at loci that manage core processes. We previously discovered concerted molecular changes among interacting members of the meiotic machinery controlling crossover number upon adaptation to whole-genome duplication (WGD) in Arabidopsis arenosa. Here we conduct a population genomic study to test the hypothesis that adaptation to WGD has been mediated by adaptive gene flow between A. arenosa and A. lyrata. We find that A. lyrata underwent WGD more recently than A. arenosa, suggesting that pre-adapted alleles have rescued nascent A. lyrata, but we also detect gene flow in the opposite direction at functionally interacting loci under the most extreme levels of selection. These data indicate that bidirectional gene flow allowed for survival after WGD, and that the merger of these species is greater than the sum of their parts. Nature Publishing Group UK 2019-11-18 /pmc/articles/PMC6861236/ /pubmed/31740675 http://dx.doi.org/10.1038/s41467-019-13159-5 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
Marburger, Sarah
Monnahan, Patrick
Seear, Paul J.
Martin, Simon H.
Koch, Jordan
Paajanen, Pirita
Bohutínská, Magdalena
Higgins, James D.
Schmickl, Roswitha
Yant, Levi
Interspecific introgression mediates adaptation to whole genome duplication
title Interspecific introgression mediates adaptation to whole genome duplication
title_full Interspecific introgression mediates adaptation to whole genome duplication
title_fullStr Interspecific introgression mediates adaptation to whole genome duplication
title_full_unstemmed Interspecific introgression mediates adaptation to whole genome duplication
title_short Interspecific introgression mediates adaptation to whole genome duplication
title_sort interspecific introgression mediates adaptation to whole genome duplication
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6861236/
https://www.ncbi.nlm.nih.gov/pubmed/31740675
http://dx.doi.org/10.1038/s41467-019-13159-5
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