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Intralocus conflicts associated with a supergene
Chromosomal inversions frequently underlie major phenotypic variation maintained by divergent selection within and between sexes. Here we examine whether and how intralocus conflicts contribute to balancing selection stabilizing an autosomal inversion polymorphism in the ruff Calidris pugnax. In thi...
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/PMC8927407/ https://www.ncbi.nlm.nih.gov/pubmed/35296671 http://dx.doi.org/10.1038/s41467-022-29033-w |
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author | Giraldo-Deck, Lina M. Loveland, Jasmine L. Goymann, Wolfgang Tschirren, Barbara Burke, Terry Kempenaers, Bart Lank, David B. Küpper, Clemens |
author_facet | Giraldo-Deck, Lina M. Loveland, Jasmine L. Goymann, Wolfgang Tschirren, Barbara Burke, Terry Kempenaers, Bart Lank, David B. Küpper, Clemens |
author_sort | Giraldo-Deck, Lina M. |
collection | PubMed |
description | Chromosomal inversions frequently underlie major phenotypic variation maintained by divergent selection within and between sexes. Here we examine whether and how intralocus conflicts contribute to balancing selection stabilizing an autosomal inversion polymorphism in the ruff Calidris pugnax. In this lekking shorebird, three male mating morphs (Independents, Satellites and Faeders) are controlled by an inversion-based supergene. We show that in a captive population, Faeder females, who are smaller and whose inversion haplotype has not undergone recombination, have lower average reproductive success in terms of laying rate, egg size, and offspring survival than Independent females, who lack the inversion. Satellite females, who carry a recombined inversion haplotype and have intermediate body size, more closely resemble Independent than Faeder females in reproductive performance. We inferred that the lower reproductive output of Faeder females is most likely balanced by higher than average reproductive success of individual Faeder males. These findings suggest that intralocus conflicts may play a major role in the evolution and maintenance of supergene variants. |
format | Online Article Text |
id | pubmed-8927407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89274072022-04-01 Intralocus conflicts associated with a supergene Giraldo-Deck, Lina M. Loveland, Jasmine L. Goymann, Wolfgang Tschirren, Barbara Burke, Terry Kempenaers, Bart Lank, David B. Küpper, Clemens Nat Commun Article Chromosomal inversions frequently underlie major phenotypic variation maintained by divergent selection within and between sexes. Here we examine whether and how intralocus conflicts contribute to balancing selection stabilizing an autosomal inversion polymorphism in the ruff Calidris pugnax. In this lekking shorebird, three male mating morphs (Independents, Satellites and Faeders) are controlled by an inversion-based supergene. We show that in a captive population, Faeder females, who are smaller and whose inversion haplotype has not undergone recombination, have lower average reproductive success in terms of laying rate, egg size, and offspring survival than Independent females, who lack the inversion. Satellite females, who carry a recombined inversion haplotype and have intermediate body size, more closely resemble Independent than Faeder females in reproductive performance. We inferred that the lower reproductive output of Faeder females is most likely balanced by higher than average reproductive success of individual Faeder males. These findings suggest that intralocus conflicts may play a major role in the evolution and maintenance of supergene variants. Nature Publishing Group UK 2022-03-16 /pmc/articles/PMC8927407/ /pubmed/35296671 http://dx.doi.org/10.1038/s41467-022-29033-w 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 Giraldo-Deck, Lina M. Loveland, Jasmine L. Goymann, Wolfgang Tschirren, Barbara Burke, Terry Kempenaers, Bart Lank, David B. Küpper, Clemens Intralocus conflicts associated with a supergene |
title | Intralocus conflicts associated with a supergene |
title_full | Intralocus conflicts associated with a supergene |
title_fullStr | Intralocus conflicts associated with a supergene |
title_full_unstemmed | Intralocus conflicts associated with a supergene |
title_short | Intralocus conflicts associated with a supergene |
title_sort | intralocus conflicts associated with a supergene |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8927407/ https://www.ncbi.nlm.nih.gov/pubmed/35296671 http://dx.doi.org/10.1038/s41467-022-29033-w |
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