Cargando…

Uniparental nuclear inheritance following bisexual mating in fungi

Some remarkable animal species require an opposite-sex partner for their sexual development but discard the partner’s genome before gamete formation, generating hemi-clonal progeny in a process called hybridogenesis. Here, we discovered a similar phenomenon, termed pseudosexual reproduction, in a ba...

Descripción completa

Detalles Bibliográficos
Autores principales: Yadav, Vikas, Sun, Sheng, Heitman, Joseph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8412948/
https://www.ncbi.nlm.nih.gov/pubmed/34338631
http://dx.doi.org/10.7554/eLife.66234
_version_ 1783747561284173824
author Yadav, Vikas
Sun, Sheng
Heitman, Joseph
author_facet Yadav, Vikas
Sun, Sheng
Heitman, Joseph
author_sort Yadav, Vikas
collection PubMed
description Some remarkable animal species require an opposite-sex partner for their sexual development but discard the partner’s genome before gamete formation, generating hemi-clonal progeny in a process called hybridogenesis. Here, we discovered a similar phenomenon, termed pseudosexual reproduction, in a basidiomycete human fungal pathogen, Cryptococcus neoformans, where exclusive uniparental inheritance of nuclear genetic material was observed during bisexual reproduction. Analysis of strains expressing fluorescent reporter proteins revealed instances where only one of the parental nuclei was present in the terminal sporulating basidium. Whole-genome sequencing revealed that the nuclear genome of the progeny was identical with one or the other parental genome. Pseudosexual reproduction was also detected in natural isolate crosses where it resulted in mainly MATα progeny, a bias observed in Cryptococcus ecological distribution as well. The mitochondria in these progeny were inherited from the MATa parent, resulting in nuclear-mitochondrial genome exchange. The meiotic recombinase Dmc1 was found to be critical for pseudosexual reproduction. These findings reveal a novel, and potentially ecologically significant, mode of eukaryotic microbial reproduction that shares features with hybridogenesis in animals.
format Online
Article
Text
id pubmed-8412948
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-84129482021-09-09 Uniparental nuclear inheritance following bisexual mating in fungi Yadav, Vikas Sun, Sheng Heitman, Joseph eLife Genetics and Genomics Some remarkable animal species require an opposite-sex partner for their sexual development but discard the partner’s genome before gamete formation, generating hemi-clonal progeny in a process called hybridogenesis. Here, we discovered a similar phenomenon, termed pseudosexual reproduction, in a basidiomycete human fungal pathogen, Cryptococcus neoformans, where exclusive uniparental inheritance of nuclear genetic material was observed during bisexual reproduction. Analysis of strains expressing fluorescent reporter proteins revealed instances where only one of the parental nuclei was present in the terminal sporulating basidium. Whole-genome sequencing revealed that the nuclear genome of the progeny was identical with one or the other parental genome. Pseudosexual reproduction was also detected in natural isolate crosses where it resulted in mainly MATα progeny, a bias observed in Cryptococcus ecological distribution as well. The mitochondria in these progeny were inherited from the MATa parent, resulting in nuclear-mitochondrial genome exchange. The meiotic recombinase Dmc1 was found to be critical for pseudosexual reproduction. These findings reveal a novel, and potentially ecologically significant, mode of eukaryotic microbial reproduction that shares features with hybridogenesis in animals. eLife Sciences Publications, Ltd 2021-08-02 /pmc/articles/PMC8412948/ /pubmed/34338631 http://dx.doi.org/10.7554/eLife.66234 Text en © 2021, Yadav et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Genetics and Genomics
Yadav, Vikas
Sun, Sheng
Heitman, Joseph
Uniparental nuclear inheritance following bisexual mating in fungi
title Uniparental nuclear inheritance following bisexual mating in fungi
title_full Uniparental nuclear inheritance following bisexual mating in fungi
title_fullStr Uniparental nuclear inheritance following bisexual mating in fungi
title_full_unstemmed Uniparental nuclear inheritance following bisexual mating in fungi
title_short Uniparental nuclear inheritance following bisexual mating in fungi
title_sort uniparental nuclear inheritance following bisexual mating in fungi
topic Genetics and Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8412948/
https://www.ncbi.nlm.nih.gov/pubmed/34338631
http://dx.doi.org/10.7554/eLife.66234
work_keys_str_mv AT yadavvikas uniparentalnuclearinheritancefollowingbisexualmatinginfungi
AT sunsheng uniparentalnuclearinheritancefollowingbisexualmatinginfungi
AT heitmanjoseph uniparentalnuclearinheritancefollowingbisexualmatinginfungi