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Recurring adaptive introgression of a supergene variant that determines social organization
Introgression has been proposed as an essential source of adaptive genetic variation. However, a key barrier to adaptive introgression is that recombination can break down combinations of alleles that underpin many traits. This barrier might be overcome in supergene regions, where suppressed recombi...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8917144/ https://www.ncbi.nlm.nih.gov/pubmed/35277489 http://dx.doi.org/10.1038/s41467-022-28806-7 |
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author | Stolle, Eckart Pracana, Rodrigo López-Osorio, Federico Priebe, Marian K. Hernández, Gabriel Luis Castillo-Carrillo, Claudia Arias, Maria Cristina Paris, Carolina Ivon Bollazzi, Martin Priyam, Anurag Wurm, Yannick |
author_facet | Stolle, Eckart Pracana, Rodrigo López-Osorio, Federico Priebe, Marian K. Hernández, Gabriel Luis Castillo-Carrillo, Claudia Arias, Maria Cristina Paris, Carolina Ivon Bollazzi, Martin Priyam, Anurag Wurm, Yannick |
author_sort | Stolle, Eckart |
collection | PubMed |
description | Introgression has been proposed as an essential source of adaptive genetic variation. However, a key barrier to adaptive introgression is that recombination can break down combinations of alleles that underpin many traits. This barrier might be overcome in supergene regions, where suppressed recombination leads to joint inheritance across many loci. Here, we study the evolution of a large supergene region that determines a major social and ecological trait in Solenopsis fire ants: whether colonies have one queen or multiple queens. Using coalescent-based phylogenies built from the genomes of 365 haploid fire ant males, we show that the supergene variant responsible for multiple-queen colonies evolved in one species and repeatedly spread to other species through introgressive hybridization. This finding highlights how supergene architecture can enable a complex adaptive phenotype to recurrently permeate species boundaries. |
format | Online Article Text |
id | pubmed-8917144 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89171442022-04-01 Recurring adaptive introgression of a supergene variant that determines social organization Stolle, Eckart Pracana, Rodrigo López-Osorio, Federico Priebe, Marian K. Hernández, Gabriel Luis Castillo-Carrillo, Claudia Arias, Maria Cristina Paris, Carolina Ivon Bollazzi, Martin Priyam, Anurag Wurm, Yannick Nat Commun Article Introgression has been proposed as an essential source of adaptive genetic variation. However, a key barrier to adaptive introgression is that recombination can break down combinations of alleles that underpin many traits. This barrier might be overcome in supergene regions, where suppressed recombination leads to joint inheritance across many loci. Here, we study the evolution of a large supergene region that determines a major social and ecological trait in Solenopsis fire ants: whether colonies have one queen or multiple queens. Using coalescent-based phylogenies built from the genomes of 365 haploid fire ant males, we show that the supergene variant responsible for multiple-queen colonies evolved in one species and repeatedly spread to other species through introgressive hybridization. This finding highlights how supergene architecture can enable a complex adaptive phenotype to recurrently permeate species boundaries. Nature Publishing Group UK 2022-03-11 /pmc/articles/PMC8917144/ /pubmed/35277489 http://dx.doi.org/10.1038/s41467-022-28806-7 Text en © The Author(s) 2022 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 Stolle, Eckart Pracana, Rodrigo López-Osorio, Federico Priebe, Marian K. Hernández, Gabriel Luis Castillo-Carrillo, Claudia Arias, Maria Cristina Paris, Carolina Ivon Bollazzi, Martin Priyam, Anurag Wurm, Yannick Recurring adaptive introgression of a supergene variant that determines social organization |
title | Recurring adaptive introgression of a supergene variant that determines social organization |
title_full | Recurring adaptive introgression of a supergene variant that determines social organization |
title_fullStr | Recurring adaptive introgression of a supergene variant that determines social organization |
title_full_unstemmed | Recurring adaptive introgression of a supergene variant that determines social organization |
title_short | Recurring adaptive introgression of a supergene variant that determines social organization |
title_sort | recurring adaptive introgression of a supergene variant that determines social organization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8917144/ https://www.ncbi.nlm.nih.gov/pubmed/35277489 http://dx.doi.org/10.1038/s41467-022-28806-7 |
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