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Tuning Hsf1 levels drives distinct fungal morphogenetic programs with depletion impairing Hsp90 function and overexpression expanding the target space
Veri, Amanda O.1; Miao, Zhengqiang2; Shapiro, Rebecca S.3; Tebbji, Faiza4; O'Meara, Teresa R.1; Kim, Sang Hu1; Colazo, Juan5; Tan, Kaeling2; Vyas, Valmik K.6; Whiteway, Malcolm7; Robbins, Nicole1; Wong, Koon Ho2; Cowen, Leah E.1
2018-03
Source PublicationPLOS GENETICS
ISSN1553-7404
Volume14Issue:3
Abstract

The capacity to respond to temperature fluctuations is critical for microorganisms to survive within mammalian hosts, and temperature modulates virulence traits of diverse pathogens. One key temperature-dependent virulence trait of the fungal pathogen Candida albicans is its ability to transition from yeast to filamentous growth, which is induced by environmental cues at host physiological temperature. A key regulator of temperature-dependent morphogenesis is the molecular chaperone Hsp90, which has complex functional relationships with the transcription factor Hsf1. Although Hsf1 controls global transcriptional remodeling in response to heat shock, its impact on morphogenesis remains unknown. Here, we establish an intriguing paradigm whereby overexpression or depletion of C. albicans HSF1 induces morphogenesis in the absence of external cues. HSF1 depletion compromises Hsp90 function, thereby driving filamentation. HSF1 overexpression does not impact Hsp90 function, but rather induces a dose-dependent expansion of Hsf1 direct targets that drives overexpression of positive regulators of filamentation, including Brg1 and Ume6, thereby bypassing the requirement for elevated temperature during morphogenesis. This work provides new insight into Hsf1-mediated environmentally contingent transcriptional control, implicates Hsf1 in regulation of a key virulence trait, and highlights fascinating biology whereby either overexpression or depletion of a single cellular regulator induces a profound developmental transition.

DOI10.1371/journal.pgen.1007270
URLView the original
Indexed BySCI
Language英语
WOS Research AreaGenetics & Heredity
WOS SubjectGenetics & Heredity
WOS IDWOS:000428840600033
PublisherPUBLIC LIBRARY SCIENCE
The Source to ArticleWOS
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Citation statistics
Cited Times [WOS]:11   [WOS Record]     [Related Records in WOS]
Document TypeJournal article
CollectionFaculty of Health Sciences
Affiliation1.Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada
2.Faculty of Health Sciences, University of Macau, Macau SAR, China
3.Department of Molecular and Cellular Biology, University of Guelph, Guelph, Ontario, Canada
4.Infectious Disease Research Centre, Universite´ Laval, Quebec City, Quebec, Canada
5.Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America
6.Whitehead Institute for Biomedical Research, Cambridge, Massachusetts, United States of America
7.Department of Biology, Concordia University, Montre´al, Quebec, Canada
Recommended Citation
GB/T 7714
Veri, Amanda O.,Miao, Zhengqiang,Shapiro, Rebecca S.,et al. Tuning Hsf1 levels drives distinct fungal morphogenetic programs with depletion impairing Hsp90 function and overexpression expanding the target space[J]. PLOS GENETICS,2018,14(3).
APA Veri, Amanda O..,Miao, Zhengqiang.,Shapiro, Rebecca S..,Tebbji, Faiza.,O'Meara, Teresa R..,...&Cowen, Leah E..(2018).Tuning Hsf1 levels drives distinct fungal morphogenetic programs with depletion impairing Hsp90 function and overexpression expanding the target space.PLOS GENETICS,14(3).
MLA Veri, Amanda O.,et al."Tuning Hsf1 levels drives distinct fungal morphogenetic programs with depletion impairing Hsp90 function and overexpression expanding the target space".PLOS GENETICS 14.3(2018).
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