Transcriptional Profiling of Biofilm Regulators Identified by an Overexpression Screen in Saccharomyces cerevisiae

Biofilm formation by microorganisms is a major cause of recurring infections and removal of biofilms has proven to be extremely difficult given their inherent drug resistance . Understanding the biological processes that underlie biofilm formation is thus extremely important and could lead to the de...

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Main Authors: Gareth A. Cromie, Zhihao Tan, Michelle Hays, Amy Sirr, Eric W. Jeffery, Aimée M. Dudley
Format: Article
Language:English
Published: Oxford University Press 2017-08-01
Series:G3: Genes, Genomes, Genetics
Subjects:
Online Access:http://g3journal.org/lookup/doi/10.1534/g3.117.042440
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spelling doaj-f8def44de937413d83e3cb51a10d65282021-07-02T14:11:03ZengOxford University PressG3: Genes, Genomes, Genetics2160-18362017-08-01782845285410.1534/g3.117.04244038Transcriptional Profiling of Biofilm Regulators Identified by an Overexpression Screen in Saccharomyces cerevisiaeGareth A. CromieZhihao TanMichelle HaysAmy SirrEric W. JefferyAimée M. DudleyBiofilm formation by microorganisms is a major cause of recurring infections and removal of biofilms has proven to be extremely difficult given their inherent drug resistance . Understanding the biological processes that underlie biofilm formation is thus extremely important and could lead to the development of more effective drug therapies, resulting in better infection outcomes. Using the yeast Saccharomyces cerevisiae as a biofilm model, overexpression screens identified DIG1, SFL1, HEK2, TOS8, SAN1, and ROF1/YHR177W as regulators of biofilm formation. Subsequent RNA-seq analysis of biofilm and nonbiofilm-forming strains revealed that all of the overexpression strains, other than DIG1 and TOS8, were adopting a single differential expression profile, although induced to varying degrees. TOS8 adopted a separate profile, while the expression profile of DIG1 reflected the common pattern seen in most of the strains, plus substantial DIG1-specific expression changes. We interpret the existence of the common transcriptional pattern seen across multiple, unrelated overexpression strains as reflecting a transcriptional state, that the yeast cell can access through regulatory signaling mechanisms, allowing an adaptive morphological change between biofilm-forming and nonbiofilm states.http://g3journal.org/lookup/doi/10.1534/g3.117.042440biofilmtranscriptional regulationoverexpressioncolony morphology
collection DOAJ
language English
format Article
sources DOAJ
author Gareth A. Cromie
Zhihao Tan
Michelle Hays
Amy Sirr
Eric W. Jeffery
Aimée M. Dudley
spellingShingle Gareth A. Cromie
Zhihao Tan
Michelle Hays
Amy Sirr
Eric W. Jeffery
Aimée M. Dudley
Transcriptional Profiling of Biofilm Regulators Identified by an Overexpression Screen in Saccharomyces cerevisiae
G3: Genes, Genomes, Genetics
biofilm
transcriptional regulation
overexpression
colony morphology
author_facet Gareth A. Cromie
Zhihao Tan
Michelle Hays
Amy Sirr
Eric W. Jeffery
Aimée M. Dudley
author_sort Gareth A. Cromie
title Transcriptional Profiling of Biofilm Regulators Identified by an Overexpression Screen in Saccharomyces cerevisiae
title_short Transcriptional Profiling of Biofilm Regulators Identified by an Overexpression Screen in Saccharomyces cerevisiae
title_full Transcriptional Profiling of Biofilm Regulators Identified by an Overexpression Screen in Saccharomyces cerevisiae
title_fullStr Transcriptional Profiling of Biofilm Regulators Identified by an Overexpression Screen in Saccharomyces cerevisiae
title_full_unstemmed Transcriptional Profiling of Biofilm Regulators Identified by an Overexpression Screen in Saccharomyces cerevisiae
title_sort transcriptional profiling of biofilm regulators identified by an overexpression screen in saccharomyces cerevisiae
publisher Oxford University Press
series G3: Genes, Genomes, Genetics
issn 2160-1836
publishDate 2017-08-01
description Biofilm formation by microorganisms is a major cause of recurring infections and removal of biofilms has proven to be extremely difficult given their inherent drug resistance . Understanding the biological processes that underlie biofilm formation is thus extremely important and could lead to the development of more effective drug therapies, resulting in better infection outcomes. Using the yeast Saccharomyces cerevisiae as a biofilm model, overexpression screens identified DIG1, SFL1, HEK2, TOS8, SAN1, and ROF1/YHR177W as regulators of biofilm formation. Subsequent RNA-seq analysis of biofilm and nonbiofilm-forming strains revealed that all of the overexpression strains, other than DIG1 and TOS8, were adopting a single differential expression profile, although induced to varying degrees. TOS8 adopted a separate profile, while the expression profile of DIG1 reflected the common pattern seen in most of the strains, plus substantial DIG1-specific expression changes. We interpret the existence of the common transcriptional pattern seen across multiple, unrelated overexpression strains as reflecting a transcriptional state, that the yeast cell can access through regulatory signaling mechanisms, allowing an adaptive morphological change between biofilm-forming and nonbiofilm states.
topic biofilm
transcriptional regulation
overexpression
colony morphology
url http://g3journal.org/lookup/doi/10.1534/g3.117.042440
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