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The evolution of mating type switching
Predictions about the evolution of sex determination mechanisms have mainly focused on animals and plants, whereas unicellular eukaryotes such as fungi and ciliates have received little attention. Many taxa within the latter groups can stochastically switch their mating type identity during vegetati...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008120/ https://www.ncbi.nlm.nih.gov/pubmed/27271362 http://dx.doi.org/10.1111/evo.12959 |
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author | Hadjivasiliou, Zena Pomiankowski, Andrew Kuijper, Bram |
author_facet | Hadjivasiliou, Zena Pomiankowski, Andrew Kuijper, Bram |
author_sort | Hadjivasiliou, Zena |
collection | PubMed |
description | Predictions about the evolution of sex determination mechanisms have mainly focused on animals and plants, whereas unicellular eukaryotes such as fungi and ciliates have received little attention. Many taxa within the latter groups can stochastically switch their mating type identity during vegetative growth. Here, we investigate the hypothesis that mating type switching overcomes distortions in the distribution of mating types due to drift during asexual growth. Using a computational model, we show that smaller population size, longer vegetative periods and more mating types lead to greater distortions in the distribution of mating types. However, the impact of these parameters on optimal switching rates is not straightforward. We find that longer vegetative periods cause reductions and considerable fluctuations in the switching rate over time. Smaller population size increases the strength of selection for switching but has little impact on the switching rate itself. The number of mating types decreases switching rates when gametes can freely sample each other, but increases switching rates when there is selection for speedy mating. We discuss our results in light of empirical work and propose new experiments that could further our understanding of sexuality in isogamous eukaryotes. |
format | Online Article Text |
id | pubmed-5008120 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50081202016-09-16 The evolution of mating type switching Hadjivasiliou, Zena Pomiankowski, Andrew Kuijper, Bram Evolution Original Articles Predictions about the evolution of sex determination mechanisms have mainly focused on animals and plants, whereas unicellular eukaryotes such as fungi and ciliates have received little attention. Many taxa within the latter groups can stochastically switch their mating type identity during vegetative growth. Here, we investigate the hypothesis that mating type switching overcomes distortions in the distribution of mating types due to drift during asexual growth. Using a computational model, we show that smaller population size, longer vegetative periods and more mating types lead to greater distortions in the distribution of mating types. However, the impact of these parameters on optimal switching rates is not straightforward. We find that longer vegetative periods cause reductions and considerable fluctuations in the switching rate over time. Smaller population size increases the strength of selection for switching but has little impact on the switching rate itself. The number of mating types decreases switching rates when gametes can freely sample each other, but increases switching rates when there is selection for speedy mating. We discuss our results in light of empirical work and propose new experiments that could further our understanding of sexuality in isogamous eukaryotes. John Wiley and Sons Inc. 2016-06-17 2016-07 /pmc/articles/PMC5008120/ /pubmed/27271362 http://dx.doi.org/10.1111/evo.12959 Text en © 2016 The Author(s). Evolution published by Wiley Periodicals, Inc. on behalf of The Society for the Study of Evolution. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Hadjivasiliou, Zena Pomiankowski, Andrew Kuijper, Bram The evolution of mating type switching |
title | The evolution of mating type switching |
title_full | The evolution of mating type switching |
title_fullStr | The evolution of mating type switching |
title_full_unstemmed | The evolution of mating type switching |
title_short | The evolution of mating type switching |
title_sort | evolution of mating type switching |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008120/ https://www.ncbi.nlm.nih.gov/pubmed/27271362 http://dx.doi.org/10.1111/evo.12959 |
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