The parasexual cycle in Candida albicans provides an alternative pathway to meiosis for the formation of recombinant strains.

Candida albicans has an elaborate, yet efficient, mating system that promotes conjugation between diploid a and alpha strains. The product of mating is a tetraploid a/alpha cell that must undergo a reductional division to return to the diploid state. Despite the presence of several "meiosis-spe...

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Main Authors: Anja Forche, Kevin Alby, Dana Schaefer, Alexander D Johnson, Judith Berman, Richard J Bennett
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2008-05-01
Series:PLoS Biology
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/18462019/?tool=EBI
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author Anja Forche
Kevin Alby
Dana Schaefer
Alexander D Johnson
Judith Berman
Richard J Bennett
author_facet Anja Forche
Kevin Alby
Dana Schaefer
Alexander D Johnson
Judith Berman
Richard J Bennett
author_sort Anja Forche
collection DOAJ
description Candida albicans has an elaborate, yet efficient, mating system that promotes conjugation between diploid a and alpha strains. The product of mating is a tetraploid a/alpha cell that must undergo a reductional division to return to the diploid state. Despite the presence of several "meiosis-specific" genes in the C. albicans genome, a meiotic program has not been observed. Instead, tetraploid products of mating can be induced to undergo efficient, random chromosome loss, often producing strains that are diploid, or close to diploid, in ploidy. Using SNP and comparative genome hybridization arrays we have now analyzed the genotypes of products from the C. albicans parasexual cycle. We show that the parasexual cycle generates progeny strains with shuffled combinations of the eight C. albicans chromosomes. In addition, several isolates had undergone extensive genetic recombination between homologous chromosomes, including multiple gene conversion events. Progeny strains exhibited altered colony morphologies on laboratory media, demonstrating that the parasexual cycle generates phenotypic variants of C. albicans. In several fungi, including Saccharomyces cerevisiae and Schizosaccharomyces pombe, the conserved Spo11 protein is integral to meiotic recombination, where it is required for the formation of DNA double-strand breaks. We show that deletion of SPO11 prevented genetic recombination between homologous chromosomes during the C. albicans parasexual cycle. These findings suggest that at least one meiosis-specific gene has been re-programmed to mediate genetic recombination during the alternative parasexual life cycle of C. albicans. We discuss, in light of the long association of C. albicans with warm-blooded animals, the potential advantages of a parasexual cycle over a conventional sexual cycle.
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spelling doaj.art-97c39029db9c40e3b4599c338a522ac22022-12-21T21:24:27ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852008-05-0165e11010.1371/journal.pbio.0060110The parasexual cycle in Candida albicans provides an alternative pathway to meiosis for the formation of recombinant strains.Anja ForcheKevin AlbyDana SchaeferAlexander D JohnsonJudith BermanRichard J BennettCandida albicans has an elaborate, yet efficient, mating system that promotes conjugation between diploid a and alpha strains. The product of mating is a tetraploid a/alpha cell that must undergo a reductional division to return to the diploid state. Despite the presence of several "meiosis-specific" genes in the C. albicans genome, a meiotic program has not been observed. Instead, tetraploid products of mating can be induced to undergo efficient, random chromosome loss, often producing strains that are diploid, or close to diploid, in ploidy. Using SNP and comparative genome hybridization arrays we have now analyzed the genotypes of products from the C. albicans parasexual cycle. We show that the parasexual cycle generates progeny strains with shuffled combinations of the eight C. albicans chromosomes. In addition, several isolates had undergone extensive genetic recombination between homologous chromosomes, including multiple gene conversion events. Progeny strains exhibited altered colony morphologies on laboratory media, demonstrating that the parasexual cycle generates phenotypic variants of C. albicans. In several fungi, including Saccharomyces cerevisiae and Schizosaccharomyces pombe, the conserved Spo11 protein is integral to meiotic recombination, where it is required for the formation of DNA double-strand breaks. We show that deletion of SPO11 prevented genetic recombination between homologous chromosomes during the C. albicans parasexual cycle. These findings suggest that at least one meiosis-specific gene has been re-programmed to mediate genetic recombination during the alternative parasexual life cycle of C. albicans. We discuss, in light of the long association of C. albicans with warm-blooded animals, the potential advantages of a parasexual cycle over a conventional sexual cycle.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/18462019/?tool=EBI
spellingShingle Anja Forche
Kevin Alby
Dana Schaefer
Alexander D Johnson
Judith Berman
Richard J Bennett
The parasexual cycle in Candida albicans provides an alternative pathway to meiosis for the formation of recombinant strains.
PLoS Biology
title The parasexual cycle in Candida albicans provides an alternative pathway to meiosis for the formation of recombinant strains.
title_full The parasexual cycle in Candida albicans provides an alternative pathway to meiosis for the formation of recombinant strains.
title_fullStr The parasexual cycle in Candida albicans provides an alternative pathway to meiosis for the formation of recombinant strains.
title_full_unstemmed The parasexual cycle in Candida albicans provides an alternative pathway to meiosis for the formation of recombinant strains.
title_short The parasexual cycle in Candida albicans provides an alternative pathway to meiosis for the formation of recombinant strains.
title_sort parasexual cycle in candida albicans provides an alternative pathway to meiosis for the formation of recombinant strains
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/18462019/?tool=EBI
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