Cargando…

Atypical meiosis can be adaptive in outcrossed Schizosaccharomyces pombe due to wtf meiotic drivers

Killer meiotic drivers are genetic parasites that destroy ‘sibling’ gametes lacking the driver allele. The fitness costs of drive can lead to selection of unlinked suppressors. This suppression could involve evolutionary tradeoffs that compromise gametogenesis and contribute to infertility. Schizosa...

Descripción completa

Detalles Bibliográficos
Autores principales: Bravo Núñez, María Angélica, Sabbarini, Ibrahim M, Eide, Lauren E, Unckless, Robert L, Zanders, Sarah E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426094/
https://www.ncbi.nlm.nih.gov/pubmed/32790622
http://dx.doi.org/10.7554/eLife.57936
_version_ 1783570619384725504
author Bravo Núñez, María Angélica
Sabbarini, Ibrahim M
Eide, Lauren E
Unckless, Robert L
Zanders, Sarah E
author_facet Bravo Núñez, María Angélica
Sabbarini, Ibrahim M
Eide, Lauren E
Unckless, Robert L
Zanders, Sarah E
author_sort Bravo Núñez, María Angélica
collection PubMed
description Killer meiotic drivers are genetic parasites that destroy ‘sibling’ gametes lacking the driver allele. The fitness costs of drive can lead to selection of unlinked suppressors. This suppression could involve evolutionary tradeoffs that compromise gametogenesis and contribute to infertility. Schizosaccharomyces pombe, an organism containing numerous gamete (spore)-killing wtf drivers, offers a tractable system to test this hypothesis. Here, we demonstrate that in scenarios analogous to outcrossing, wtf drivers generate a fitness landscape in which atypical spores, such as aneuploids and diploids, are advantageous. In this context, wtf drivers can decrease the fitness costs of mutations that disrupt meiotic fidelity and, in some circumstances, can even make such mutations beneficial. Moreover, we find that S. pombe isolates vary greatly in their ability to make haploid spores, with some isolates generating up to 46% aneuploid or diploid spores. This work empirically demonstrates the potential for meiotic drivers to shape the evolution of gametogenesis.
format Online
Article
Text
id pubmed-7426094
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-74260942020-08-17 Atypical meiosis can be adaptive in outcrossed Schizosaccharomyces pombe due to wtf meiotic drivers Bravo Núñez, María Angélica Sabbarini, Ibrahim M Eide, Lauren E Unckless, Robert L Zanders, Sarah E eLife Evolutionary Biology Killer meiotic drivers are genetic parasites that destroy ‘sibling’ gametes lacking the driver allele. The fitness costs of drive can lead to selection of unlinked suppressors. This suppression could involve evolutionary tradeoffs that compromise gametogenesis and contribute to infertility. Schizosaccharomyces pombe, an organism containing numerous gamete (spore)-killing wtf drivers, offers a tractable system to test this hypothesis. Here, we demonstrate that in scenarios analogous to outcrossing, wtf drivers generate a fitness landscape in which atypical spores, such as aneuploids and diploids, are advantageous. In this context, wtf drivers can decrease the fitness costs of mutations that disrupt meiotic fidelity and, in some circumstances, can even make such mutations beneficial. Moreover, we find that S. pombe isolates vary greatly in their ability to make haploid spores, with some isolates generating up to 46% aneuploid or diploid spores. This work empirically demonstrates the potential for meiotic drivers to shape the evolution of gametogenesis. eLife Sciences Publications, Ltd 2020-08-13 /pmc/articles/PMC7426094/ /pubmed/32790622 http://dx.doi.org/10.7554/eLife.57936 Text en © 2020, Bravo Núñez et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Evolutionary Biology
Bravo Núñez, María Angélica
Sabbarini, Ibrahim M
Eide, Lauren E
Unckless, Robert L
Zanders, Sarah E
Atypical meiosis can be adaptive in outcrossed Schizosaccharomyces pombe due to wtf meiotic drivers
title Atypical meiosis can be adaptive in outcrossed Schizosaccharomyces pombe due to wtf meiotic drivers
title_full Atypical meiosis can be adaptive in outcrossed Schizosaccharomyces pombe due to wtf meiotic drivers
title_fullStr Atypical meiosis can be adaptive in outcrossed Schizosaccharomyces pombe due to wtf meiotic drivers
title_full_unstemmed Atypical meiosis can be adaptive in outcrossed Schizosaccharomyces pombe due to wtf meiotic drivers
title_short Atypical meiosis can be adaptive in outcrossed Schizosaccharomyces pombe due to wtf meiotic drivers
title_sort atypical meiosis can be adaptive in outcrossed schizosaccharomyces pombe due to wtf meiotic drivers
topic Evolutionary Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426094/
https://www.ncbi.nlm.nih.gov/pubmed/32790622
http://dx.doi.org/10.7554/eLife.57936
work_keys_str_mv AT bravonunezmariaangelica atypicalmeiosiscanbeadaptiveinoutcrossedschizosaccharomycespombeduetowtfmeioticdrivers
AT sabbariniibrahimm atypicalmeiosiscanbeadaptiveinoutcrossedschizosaccharomycespombeduetowtfmeioticdrivers
AT eidelaurene atypicalmeiosiscanbeadaptiveinoutcrossedschizosaccharomycespombeduetowtfmeioticdrivers
AT uncklessrobertl atypicalmeiosiscanbeadaptiveinoutcrossedschizosaccharomycespombeduetowtfmeioticdrivers
AT zanderssarahe atypicalmeiosiscanbeadaptiveinoutcrossedschizosaccharomycespombeduetowtfmeioticdrivers