Cited by 137Fungal and yeast genetics researchBacterial Genetics and BiotechnologyPlant Stress Responses and Tolerance

Repression of ergosterol biosynthesis is essential for stress resistance and is mediated by the Hog1 MAP kinase and the Mot3 and Rox1 transcription factors

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Montañés, Fernando Martínez, Pascual‐Ahuir, Amparo, Proft, Markus·2011·Molecular Microbiology

Abstract

Hyperosmotic stress triggers a complex adaptive response that is dominantly regulated by the Hog1 MAP kinase in yeast. Here we characterize a novel physiological determinant of osmostress tolerance, which involves the Hog1-dependent transcriptional downregulation of ergosterol biosynthesis genes (ERG). Yeast cells considerably lower their sterol content in response to high osmolarity. The transcriptional repressors Mot3 and Rox1 are essential for this response. Both factors together with Hog1 are required to rapidly and transiently shut down transcription of ERG2 and ERG11 upon osmoshock. Mot3 abundance and its binding to the ERG2 promoter is stimulated by osmostress in a Hog1-dependent manner. As an additional layer of control, the expression of the main transcriptional activator of ERG gene expression, Ecm22, is negatively regulated by Hog1 and Mot3/Rox1 upon salt shock. Oxidative stress also triggers repression of ERG2, 11 transcription and a profound decrease in total sterol levels. However, this response was only partially dependent on Mot3/Rox1 and Hog1. Finally, we show that the upc2-1 mutation confers stress insensitive hyperaccumulation of ergosterol, overexpression of ERG2, 11 and severe sensitivity to salt and oxidative stress. Our results indicate that transcriptional control of ergosterol biosynthesis is an important physiological target of stress signalling.

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Crossref · 10.1111/j.1365-2958.2010.07502.x

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  • Hyperosmotic stress adaptation (such as salt or sorbitol treatment) leads to the decrease in ergosterol abundance.

    “Conversely, hyperosmotic stress adaptation (such as salt or sorbitol treatment) leads to the decrease in ergosterol abundance [6,7].”

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Authors
Montañés, F. M., Pascual‐Ahuir, A., & Proft, M.
Affiliations
  • Consejo Superior de Investigaciones Científicas (ES)
  • Instituto de Biología Molecular y Celular de Plantas (ES)
Corresponding author
Proft, Markus
Venue
Molecular Microbiology
Publisher
Wiley
Published
2010-12-28
Volume
79
Issue
4
Pages
1008-1023
ISSN
  • 0950-382X (ISSN-L)
  • 1365-2958
OpenAlex
W1952627112
Cited by
137
References
58
Citations by year
2026: 8 · 2025: 13 · 2024: 14 · 2023: 6 · 2022: 16 · 2021: 9 · 2020: 9 · 2019: 10 · 2018: 11 · 2017: 9 · 2016: 5 · 2015: 6 · 2014: 3 · 2013: 9 · 2012: 7
FWCI
2.34
Type
journal article
Language
en
Open access
Locations
  • Molecular Microbiology (publishedVersion)
  • PubMed (publishedVersion)
  • RiuNet (Universitat Politècnica de València) (submittedVersion, cc-by-nc-nd)
  • Zenodo (CERN European Organization for Nuclear Research) (cc-by)
Funders
  • Ministerio de Ciencia e Innovación
  • National Institutes of Health
  • Weill Cornell Medical College
  • Consejo Superior de Investigaciones Científicas
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Stress Responses and Tolerance
Keywords
ergosterol biosynthesis, Hog1 MAP kinase, hyperosmotic stress, salt stress, oxidative stress, sterol homeostasis, ERG2, ERG11, transcriptional repression, stress signaling, Saccharomyces cerevisiae, UPC2
MeSH terms
Ergosterol, Repressor Proteins, Saccharomyces cerevisiae, Sodium Chloride, Transcription Factors, Gene Expression Regulation, Fungal, Oxidative Stress, Oligonucleotide Array Sequence Analysis, Gene Expression Profiling, Mitogen-Activated Protein Kinases, Saccharomyces cerevisiae Proteins

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