A Conserved Stress-activated Protein Kinase Regulates a Core Stress Response in the Human Pathogen Candida albicans
Open accessAbstract
Previous work has implicated the Hog1 stress-activated protein kinase (SAPK) in osmotic and oxidative stress responses in the human pathogen Candida albicans. In this study, we have characterized the role of Hog1 in mediating these and other stress responses in C. albicans. We provide evidence that a SAPK-dependent core stress response exists in this pathogen. The Hog1 SAPK is phosphorylated and it accumulates in the nucleus in response to diverse stress conditions. In addition, we have identified Hog1-regulated genes that are induced in response to stress conditions that activate Hog1. These analyses reveal both activator and repressor functions for the Hog1 SAPK. Our results also demonstrate that stress cross-protection, a classical hallmark of the core stress response, occurs in C. albicans between stresses that activate the Hog1 SAPK. Importantly, we find that the core stress response in C. albicans has adapted to the environmental niche of this human pathogen. This niche specificity is reflected by the specific environmental conditions that drive the Hog1-regulated core stress response in C. albicans and by differences in the molecular circuitry that control this response.
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In C. albicans, Hog1 MAPK is a major regulator of fungal stress response, morphogenesis, and virulence.
“In C. albicans, Hog1 MAPK is a major regulator of fungal stress response, morphogenesis, and virulence (32–34, 36, 61).”
From The <i>Candida auris</i> Hog1 MAP kinase is essential for the colonization of murine skin and intradermal persistence (2024) · cites this paper as [33]
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References 59 · Cited by 263
- Authors
- Smith, D. A., Nicholls, S., Morgan, B. A., Brown, A. J. P., & Quinn, J.
- Affiliations
- Newcastle University (GB)
- University of Aberdeen (GB)
- Venue
- Molecular Biology of the Cell
- Published
- 2004-09
- Volume
- 15
- Issue
- 9
- Pages
- 4179-4190
- ISSN
- 1059-1524 (ISSN-L)
- 1939-4586
- PMC
- PMC515350
- OpenAlex
- W2104880204
- Cited by
- 263
- References
- 59
- Citations by year
- 2026: 5 · 2025: 5 · 2024: 6 · 2023: 6 · 2022: 5 · 2021: 8 · 2020: 20 · 2019: 11 · 2018: 8 · 2017: 19 · 2016: 14 · 2015: 13 · 2014: 23 · 2013: 8 · 2012: 20
- FWCI
- 4.63
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Molecular Biology of the Cell (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Aberdeen University Research Archive (Aberdeen University) (submittedVersion)
- Newcastle University ePrints (Newcastle Univesity)
- Funders
- Wellcome Trust (055015, 063204)
- European Commission
- Directorate for Biological Sciences
- Medical Research Council
- Biotechnology and Biological Sciences Research Council (BB/C510391/1)
- 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
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Keywords
- Hog1, c-Jun N-terminal kinase, Candida albicans, osmotic stress, oxidative stress, nuclear accumulation, fungal pathogens
- MeSH terms
- Base Sequence, Candida albicans, Cell Nucleus, DNA, Fungal, Enzyme Activation, Genes, Fungal, Genetic Complementation Test, Humans, Models, Biological, Molecular Sequence Data, Osmotic Pressure, Phenotype, Phosphorylation, Saccharomyces cerevisiae, Schizosaccharomyces, Species Specificity, Gene Expression Regulation, Fungal, Oxidative Stress, Mitogen-Activated Protein Kinases, MAP Kinase Signaling System, Schizosaccharomyces pombe Proteins
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