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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
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.
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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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