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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...
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/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. |
format | Online Article Text |
id | pubmed-9262711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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