Cargando…

Transcriptional Regulation on Aneuploid Chromosomes in Diverse Candida albicans Mutants

Candida albicans is a diploid fungus and a predominant opportunistic human pathogen. Notably, C. albicans employs reversible chromosomal aneuploidies as a means of survival in adverse environments. We previously characterized transcription on the monosomic chromosome 5 (Ch5) that arises with adaptat...

Descripción completa

Detalles Bibliográficos
Autores principales: Tucker, Christopher, Bhattacharya, Soumyaroop, Wakabayashi, Hironao, Bellaousov, Stanislav, Kravets, Anatoliy, Welle, Stephen L., Myers, Jason, Hayes, Jeffrey J., Bulger, Michael, Rustchenko, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786073/
https://www.ncbi.nlm.nih.gov/pubmed/29374238
http://dx.doi.org/10.1038/s41598-018-20106-9
_version_ 1783295728565616640
author Tucker, Christopher
Bhattacharya, Soumyaroop
Wakabayashi, Hironao
Bellaousov, Stanislav
Kravets, Anatoliy
Welle, Stephen L.
Myers, Jason
Hayes, Jeffrey J.
Bulger, Michael
Rustchenko, Elena
author_facet Tucker, Christopher
Bhattacharya, Soumyaroop
Wakabayashi, Hironao
Bellaousov, Stanislav
Kravets, Anatoliy
Welle, Stephen L.
Myers, Jason
Hayes, Jeffrey J.
Bulger, Michael
Rustchenko, Elena
author_sort Tucker, Christopher
collection PubMed
description Candida albicans is a diploid fungus and a predominant opportunistic human pathogen. Notably, C. albicans employs reversible chromosomal aneuploidies as a means of survival in adverse environments. We previously characterized transcription on the monosomic chromosome 5 (Ch5) that arises with adaptation to growth on the toxic sugar sorbose in the mutant Sor125(55). We now extend this analysis to the trisomic hybrid Ch4/7 within Sor125(55) and a diverse group of three mutants harboring a single Ch5. We find a similar pattern of transcriptional changes on either type of aneuploid chromosome within these mutants wherein expression of many genes follows chromosome ploidy, consistent with a direct mechanism to regulate genes important for adaptation to growth. In contrast, a significant number of genes are expressed at the disomic level, implying distinct mechanisms compensating for gene dose on monosomic or trisomic chromosomes consistent with maintaining cell homeostasis. Finally, we find evidence for an additional mechanism that elevates expression of genes on normal disomic Ch4 and Ch7 in mutants to levels commensurate with that found on the trisomic Ch4/7b in Sor125(55). Several of these genes are similarly differentially regulated among mutants, suggesting they play key functions in either maintaining aneuploidy or adaptation to growth conditions.
format Online
Article
Text
id pubmed-5786073
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-57860732018-02-07 Transcriptional Regulation on Aneuploid Chromosomes in Diverse Candida albicans Mutants Tucker, Christopher Bhattacharya, Soumyaroop Wakabayashi, Hironao Bellaousov, Stanislav Kravets, Anatoliy Welle, Stephen L. Myers, Jason Hayes, Jeffrey J. Bulger, Michael Rustchenko, Elena Sci Rep Article Candida albicans is a diploid fungus and a predominant opportunistic human pathogen. Notably, C. albicans employs reversible chromosomal aneuploidies as a means of survival in adverse environments. We previously characterized transcription on the monosomic chromosome 5 (Ch5) that arises with adaptation to growth on the toxic sugar sorbose in the mutant Sor125(55). We now extend this analysis to the trisomic hybrid Ch4/7 within Sor125(55) and a diverse group of three mutants harboring a single Ch5. We find a similar pattern of transcriptional changes on either type of aneuploid chromosome within these mutants wherein expression of many genes follows chromosome ploidy, consistent with a direct mechanism to regulate genes important for adaptation to growth. In contrast, a significant number of genes are expressed at the disomic level, implying distinct mechanisms compensating for gene dose on monosomic or trisomic chromosomes consistent with maintaining cell homeostasis. Finally, we find evidence for an additional mechanism that elevates expression of genes on normal disomic Ch4 and Ch7 in mutants to levels commensurate with that found on the trisomic Ch4/7b in Sor125(55). Several of these genes are similarly differentially regulated among mutants, suggesting they play key functions in either maintaining aneuploidy or adaptation to growth conditions. Nature Publishing Group UK 2018-01-26 /pmc/articles/PMC5786073/ /pubmed/29374238 http://dx.doi.org/10.1038/s41598-018-20106-9 Text en © The Author(s) 2018 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
Tucker, Christopher
Bhattacharya, Soumyaroop
Wakabayashi, Hironao
Bellaousov, Stanislav
Kravets, Anatoliy
Welle, Stephen L.
Myers, Jason
Hayes, Jeffrey J.
Bulger, Michael
Rustchenko, Elena
Transcriptional Regulation on Aneuploid Chromosomes in Diverse Candida albicans Mutants
title Transcriptional Regulation on Aneuploid Chromosomes in Diverse Candida albicans Mutants
title_full Transcriptional Regulation on Aneuploid Chromosomes in Diverse Candida albicans Mutants
title_fullStr Transcriptional Regulation on Aneuploid Chromosomes in Diverse Candida albicans Mutants
title_full_unstemmed Transcriptional Regulation on Aneuploid Chromosomes in Diverse Candida albicans Mutants
title_short Transcriptional Regulation on Aneuploid Chromosomes in Diverse Candida albicans Mutants
title_sort transcriptional regulation on aneuploid chromosomes in diverse candida albicans mutants
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786073/
https://www.ncbi.nlm.nih.gov/pubmed/29374238
http://dx.doi.org/10.1038/s41598-018-20106-9
work_keys_str_mv AT tuckerchristopher transcriptionalregulationonaneuploidchromosomesindiversecandidaalbicansmutants
AT bhattacharyasoumyaroop transcriptionalregulationonaneuploidchromosomesindiversecandidaalbicansmutants
AT wakabayashihironao transcriptionalregulationonaneuploidchromosomesindiversecandidaalbicansmutants
AT bellaousovstanislav transcriptionalregulationonaneuploidchromosomesindiversecandidaalbicansmutants
AT kravetsanatoliy transcriptionalregulationonaneuploidchromosomesindiversecandidaalbicansmutants
AT wellestephenl transcriptionalregulationonaneuploidchromosomesindiversecandidaalbicansmutants
AT myersjason transcriptionalregulationonaneuploidchromosomesindiversecandidaalbicansmutants
AT hayesjeffreyj transcriptionalregulationonaneuploidchromosomesindiversecandidaalbicansmutants
AT bulgermichael transcriptionalregulationonaneuploidchromosomesindiversecandidaalbicansmutants
AT rustchenkoelena transcriptionalregulationonaneuploidchromosomesindiversecandidaalbicansmutants