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A ‘parameiosis’ drives depolyploidization and homologous recombination in Candida albicans

Meiosis is a conserved tenet of sexual reproduction in eukaryotes, yet this program is seemingly absent from many extant species. In the human fungal pathogen Candida albicans, mating of diploid cells generates tetraploid products that return to the diploid state via a non-meiotic process of depolyp...

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Autores principales: Anderson, Matthew Z., Thomson, Gregory J., Hirakawa, Matthew P., Bennett, Richard J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6763455/
https://www.ncbi.nlm.nih.gov/pubmed/31558727
http://dx.doi.org/10.1038/s41467-019-12376-2
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author Anderson, Matthew Z.
Thomson, Gregory J.
Hirakawa, Matthew P.
Bennett, Richard J.
author_facet Anderson, Matthew Z.
Thomson, Gregory J.
Hirakawa, Matthew P.
Bennett, Richard J.
author_sort Anderson, Matthew Z.
collection PubMed
description Meiosis is a conserved tenet of sexual reproduction in eukaryotes, yet this program is seemingly absent from many extant species. In the human fungal pathogen Candida albicans, mating of diploid cells generates tetraploid products that return to the diploid state via a non-meiotic process of depolyploidization known as concerted chromosome loss (CCL). Here, we report that recombination rates are more than three orders of magnitude higher during CCL than during normal mitotic growth. Furthermore, two conserved ‘meiosis-specific’ factors play central roles in CCL as SPO11 mediates DNA double-strand break formation while both SPO11 and REC8 regulate chromosome stability and promote inter-homolog recombination. Unexpectedly, SPO11 also promotes DNA repair and recombination during normal mitotic divisions. These results indicate that C. albicans CCL represents a ‘parameiosis’ that blurs the conventional boundaries between mitosis and meiosis. They also reveal parallels with depolyploidization in mammalian cells and provide potential insights into the evolution of meiosis.
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spelling pubmed-67634552019-09-30 A ‘parameiosis’ drives depolyploidization and homologous recombination in Candida albicans Anderson, Matthew Z. Thomson, Gregory J. Hirakawa, Matthew P. Bennett, Richard J. Nat Commun Article Meiosis is a conserved tenet of sexual reproduction in eukaryotes, yet this program is seemingly absent from many extant species. In the human fungal pathogen Candida albicans, mating of diploid cells generates tetraploid products that return to the diploid state via a non-meiotic process of depolyploidization known as concerted chromosome loss (CCL). Here, we report that recombination rates are more than three orders of magnitude higher during CCL than during normal mitotic growth. Furthermore, two conserved ‘meiosis-specific’ factors play central roles in CCL as SPO11 mediates DNA double-strand break formation while both SPO11 and REC8 regulate chromosome stability and promote inter-homolog recombination. Unexpectedly, SPO11 also promotes DNA repair and recombination during normal mitotic divisions. These results indicate that C. albicans CCL represents a ‘parameiosis’ that blurs the conventional boundaries between mitosis and meiosis. They also reveal parallels with depolyploidization in mammalian cells and provide potential insights into the evolution of meiosis. Nature Publishing Group UK 2019-09-26 /pmc/articles/PMC6763455/ /pubmed/31558727 http://dx.doi.org/10.1038/s41467-019-12376-2 Text en © The Author(s) 2019 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/.
spellingShingle Article
Anderson, Matthew Z.
Thomson, Gregory J.
Hirakawa, Matthew P.
Bennett, Richard J.
A ‘parameiosis’ drives depolyploidization and homologous recombination in Candida albicans
title A ‘parameiosis’ drives depolyploidization and homologous recombination in Candida albicans
title_full A ‘parameiosis’ drives depolyploidization and homologous recombination in Candida albicans
title_fullStr A ‘parameiosis’ drives depolyploidization and homologous recombination in Candida albicans
title_full_unstemmed A ‘parameiosis’ drives depolyploidization and homologous recombination in Candida albicans
title_short A ‘parameiosis’ drives depolyploidization and homologous recombination in Candida albicans
title_sort ‘parameiosis’ drives depolyploidization and homologous recombination in candida albicans
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6763455/
https://www.ncbi.nlm.nih.gov/pubmed/31558727
http://dx.doi.org/10.1038/s41467-019-12376-2
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