A coupled process of same- and opposite-sex mating generates polyploidy and genetic diversity in Candida tropicalis.

Sexual reproduction is a universal mechanism for generating genetic diversity in eukaryotes. Fungi exhibit diverse strategies for sexual reproduction both in nature and in the laboratory. In this study, we report the discovery of same-sex (homothallic) mating in the human fungal pathogen Candida tro...

Full description

Bibliographic Details
Main Authors: Han Du, Qiushi Zheng, Jian Bing, Richard J Bennett, Guanghua Huang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-05-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC5957450?pdf=render
id doaj-22e24ed9934847919d0c7cf7e83732c4
record_format Article
spelling doaj-22e24ed9934847919d0c7cf7e83732c42020-11-24T21:56:17ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042018-05-01145e100737710.1371/journal.pgen.1007377A coupled process of same- and opposite-sex mating generates polyploidy and genetic diversity in Candida tropicalis.Han DuQiushi ZhengJian BingRichard J BennettGuanghua HuangSexual reproduction is a universal mechanism for generating genetic diversity in eukaryotes. Fungi exhibit diverse strategies for sexual reproduction both in nature and in the laboratory. In this study, we report the discovery of same-sex (homothallic) mating in the human fungal pathogen Candida tropicalis. We show that same-sex mating occurs between two cells carrying the same mating type (MTLa/a or α/α) and requires the presence of pheromone from the opposite mating type as well as the receptor for this pheromone. In ménage à trois mating mixes (i.e., "a x a + α helper" or "α x α + a helper" mixes), pheromone secreted by helper strains promotes diploid C. tropicalis cells to undergo same-sex mating and form tetraploid products. Surprisingly, however, the tetraploid mating products can then efficiently mate with cells of the opposite mating type to generate hexaploid products. The unstable hexaploid progeny generated from this coupled process of same- and opposite-sex mating undergo rapid chromosome loss and generate extensive genetic variation. Phenotypic analysis demonstrated that the mating progeny-derived strains exhibit diverse morphologies and phenotypes, including differences in secreted aspartic proteinase (Sap) activity and susceptibility to the antifungal drugs. Thus, the coupling of same- and opposite-sex mating represents a novel mode to generate polyploidy and genetic diversity, which may facilitate the evolution of new traits in C. tropicalis and adaptation to changing environments.http://europepmc.org/articles/PMC5957450?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Han Du
Qiushi Zheng
Jian Bing
Richard J Bennett
Guanghua Huang
spellingShingle Han Du
Qiushi Zheng
Jian Bing
Richard J Bennett
Guanghua Huang
A coupled process of same- and opposite-sex mating generates polyploidy and genetic diversity in Candida tropicalis.
PLoS Genetics
author_facet Han Du
Qiushi Zheng
Jian Bing
Richard J Bennett
Guanghua Huang
author_sort Han Du
title A coupled process of same- and opposite-sex mating generates polyploidy and genetic diversity in Candida tropicalis.
title_short A coupled process of same- and opposite-sex mating generates polyploidy and genetic diversity in Candida tropicalis.
title_full A coupled process of same- and opposite-sex mating generates polyploidy and genetic diversity in Candida tropicalis.
title_fullStr A coupled process of same- and opposite-sex mating generates polyploidy and genetic diversity in Candida tropicalis.
title_full_unstemmed A coupled process of same- and opposite-sex mating generates polyploidy and genetic diversity in Candida tropicalis.
title_sort coupled process of same- and opposite-sex mating generates polyploidy and genetic diversity in candida tropicalis.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2018-05-01
description Sexual reproduction is a universal mechanism for generating genetic diversity in eukaryotes. Fungi exhibit diverse strategies for sexual reproduction both in nature and in the laboratory. In this study, we report the discovery of same-sex (homothallic) mating in the human fungal pathogen Candida tropicalis. We show that same-sex mating occurs between two cells carrying the same mating type (MTLa/a or α/α) and requires the presence of pheromone from the opposite mating type as well as the receptor for this pheromone. In ménage à trois mating mixes (i.e., "a x a + α helper" or "α x α + a helper" mixes), pheromone secreted by helper strains promotes diploid C. tropicalis cells to undergo same-sex mating and form tetraploid products. Surprisingly, however, the tetraploid mating products can then efficiently mate with cells of the opposite mating type to generate hexaploid products. The unstable hexaploid progeny generated from this coupled process of same- and opposite-sex mating undergo rapid chromosome loss and generate extensive genetic variation. Phenotypic analysis demonstrated that the mating progeny-derived strains exhibit diverse morphologies and phenotypes, including differences in secreted aspartic proteinase (Sap) activity and susceptibility to the antifungal drugs. Thus, the coupling of same- and opposite-sex mating represents a novel mode to generate polyploidy and genetic diversity, which may facilitate the evolution of new traits in C. tropicalis and adaptation to changing environments.
url http://europepmc.org/articles/PMC5957450?pdf=render
work_keys_str_mv AT handu acoupledprocessofsameandoppositesexmatinggeneratespolyploidyandgeneticdiversityincandidatropicalis
AT qiushizheng acoupledprocessofsameandoppositesexmatinggeneratespolyploidyandgeneticdiversityincandidatropicalis
AT jianbing acoupledprocessofsameandoppositesexmatinggeneratespolyploidyandgeneticdiversityincandidatropicalis
AT richardjbennett acoupledprocessofsameandoppositesexmatinggeneratespolyploidyandgeneticdiversityincandidatropicalis
AT guanghuahuang acoupledprocessofsameandoppositesexmatinggeneratespolyploidyandgeneticdiversityincandidatropicalis
AT handu coupledprocessofsameandoppositesexmatinggeneratespolyploidyandgeneticdiversityincandidatropicalis
AT qiushizheng coupledprocessofsameandoppositesexmatinggeneratespolyploidyandgeneticdiversityincandidatropicalis
AT jianbing coupledprocessofsameandoppositesexmatinggeneratespolyploidyandgeneticdiversityincandidatropicalis
AT richardjbennett coupledprocessofsameandoppositesexmatinggeneratespolyploidyandgeneticdiversityincandidatropicalis
AT guanghuahuang coupledprocessofsameandoppositesexmatinggeneratespolyploidyandgeneticdiversityincandidatropicalis
_version_ 1725858719594446848