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Allorecognition genes drive reproductive isolation in Podospora anserina

Allorecognition, the capacity to discriminate self from conspecific non-self, is a ubiquitous organismal feature typically governed by genes evolving under balancing selection. Here, we show that in the fungus Podospora anserina, allorecognition loci controlling vegetative incompatibility (het genes...

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Autores principales: Ament-Velásquez, S. Lorena, Vogan, Aaron A., Granger-Farbos, Alexandra, Bastiaans, Eric, Martinossi-Allibert, Ivain, Saupe, Sven J., de Groot, Suzette, Lascoux, Martin, Debets, Alfons J. M., Clavé, Corinne, Johannesson, Hanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9262711/
https://www.ncbi.nlm.nih.gov/pubmed/35551248
http://dx.doi.org/10.1038/s41559-022-01734-x
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author Ament-Velásquez, S. Lorena
Vogan, Aaron A.
Granger-Farbos, Alexandra
Bastiaans, Eric
Martinossi-Allibert, Ivain
Saupe, Sven J.
de Groot, Suzette
Lascoux, Martin
Debets, Alfons J. M.
Clavé, Corinne
Johannesson, Hanna
author_facet Ament-Velásquez, S. Lorena
Vogan, Aaron A.
Granger-Farbos, Alexandra
Bastiaans, Eric
Martinossi-Allibert, Ivain
Saupe, Sven J.
de Groot, Suzette
Lascoux, Martin
Debets, Alfons J. M.
Clavé, Corinne
Johannesson, Hanna
author_sort Ament-Velásquez, S. Lorena
collection PubMed
description Allorecognition, the capacity to discriminate self from conspecific non-self, is a ubiquitous organismal feature typically governed by genes evolving under balancing selection. Here, we show that in the fungus Podospora anserina, allorecognition loci controlling vegetative incompatibility (het genes), define two reproductively isolated groups through pleiotropic effects on sexual compatibility. These two groups emerge from the antagonistic interactions of the unlinked loci het-r (encoding a NOD-like receptor) and het-v (encoding a methyltransferase and an MLKL/HeLo domain protein). Using a combination of genetic and ecological data, supported by simulations, we provide a concrete and molecularly defined example whereby the origin and coexistence of reproductively isolated groups in sympatry is driven by pleiotropic genes under balancing selection.
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spelling pubmed-92627112022-07-09 Allorecognition genes drive reproductive isolation in Podospora anserina Ament-Velásquez, S. Lorena Vogan, Aaron A. Granger-Farbos, Alexandra Bastiaans, Eric Martinossi-Allibert, Ivain Saupe, Sven J. de Groot, Suzette Lascoux, Martin Debets, Alfons J. M. Clavé, Corinne Johannesson, Hanna Nat Ecol Evol Article Allorecognition, the capacity to discriminate self from conspecific non-self, is a ubiquitous organismal feature typically governed by genes evolving under balancing selection. Here, we show that in the fungus Podospora anserina, allorecognition loci controlling vegetative incompatibility (het genes), define two reproductively isolated groups through pleiotropic effects on sexual compatibility. These two groups emerge from the antagonistic interactions of the unlinked loci het-r (encoding a NOD-like receptor) and het-v (encoding a methyltransferase and an MLKL/HeLo domain protein). Using a combination of genetic and ecological data, supported by simulations, we provide a concrete and molecularly defined example whereby the origin and coexistence of reproductively isolated groups in sympatry is driven by pleiotropic genes under balancing selection. Nature Publishing Group UK 2022-05-12 2022 /pmc/articles/PMC9262711/ /pubmed/35551248 http://dx.doi.org/10.1038/s41559-022-01734-x 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
Ament-Velásquez, S. Lorena
Vogan, Aaron A.
Granger-Farbos, Alexandra
Bastiaans, Eric
Martinossi-Allibert, Ivain
Saupe, Sven J.
de Groot, Suzette
Lascoux, Martin
Debets, Alfons J. M.
Clavé, Corinne
Johannesson, Hanna
Allorecognition genes drive reproductive isolation in Podospora anserina
title Allorecognition genes drive reproductive isolation in Podospora anserina
title_full Allorecognition genes drive reproductive isolation in Podospora anserina
title_fullStr Allorecognition genes drive reproductive isolation in Podospora anserina
title_full_unstemmed Allorecognition genes drive reproductive isolation in Podospora anserina
title_short Allorecognition genes drive reproductive isolation in Podospora anserina
title_sort allorecognition genes drive reproductive isolation in podospora anserina
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9262711/
https://www.ncbi.nlm.nih.gov/pubmed/35551248
http://dx.doi.org/10.1038/s41559-022-01734-x
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