Cited by 68Fungal and yeast genetics researchBacterial Genetics and BiotechnologyRedox biology and oxidative stress

The Hog1 Mitogen-Activated Protein Kinase Mediates a Hypoxic Response in Saccharomyces cerevisiae

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Hickman, Mark J, Spatt, Dan, Winston, Fred·2011·Genetics

Abstract

We have studied hypoxic induction of transcription by studying the seripauperin (PAU) genes of Saccharomyces cerevisiae. Previous studies showed that PAU induction requires the depletion of heme and is dependent upon the transcription factor Upc2. We have now identified additional factors required for PAU induction during hypoxia, including Hog1, a mitogen-activated protein kinase (MAPK) whose signaling pathway originates at the membrane. Our results have led to a model in which heme and ergosterol depletion alters membrane fluidity, thereby activating Hog1 for hypoxic induction. Hypoxic activation of Hog1 is distinct from its previously characterized response to osmotic stress, as the two conditions cause different transcriptional consequences. Furthermore, Hog1-dependent hypoxic activation is independent of the S. cerevisiae general stress response. In addition to Hog1, specific components of the SAGA coactivator complex, including Spt20 and Sgf73, are also required for PAU induction. Interestingly, the mammalian ortholog of Spt20, p38IP, has been previously shown to interact with the mammalian ortholog of Hog1, p38. Taken together, our results have uncovered a previously unknown hypoxic-response pathway that may be conserved throughout eukaryotes.

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  • In addition to Upc2, the MAPK Hog1 and specific components of the SAGA co-activator complex also contribute to the induction of PAU genes in response to oxygen limitation.

    “In addition to Upc2, the mitogen-activated protein kinase (MAPK) Hog1 and specific components of the SAGA co-activator complex also contribute to the induction of PAU genes in response to oxygen limitation [96].”
  • Several genome-wide expression studies under low oxygen conditions have reflected that the pattern of expression differs among ERG genes, although some general trends can be extracted.

    “Several genome-wide expression studies based on microarray and RNA-Seq analyses under low oxygen conditions have reflected that the pattern of expression differs among ERG genes, although some general trends can be extracted [94,96,98,100,101,102,103].”
  • Conflicting results have been observed for the effect of Hap1 on the expression of ERG genes during anaerobic conditions.

    “However, conflicting results have been observed for the effect of Hap1 on the expression of ERG genes during anaerobic conditions [75,96,99,100].”

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References 124 · Cited by 68

Authors
Hickman, M. J., Spatt, D., & Winston, F.
Affiliations
Harvard University (US)
Corresponding author
Winston, Fred
Venue
Genetics
Published
2011-06-01
Volume
188
Issue
2
Pages
325-338
ISSN
  • 0016-6731 (ISSN-L)
  • 1943-2631
OpenAlex
W2063436167
Cited by
68
References
124
Citations by year
2026: 4 · 2025: 3 · 2024: 5 · 2023: 2 · 2022: 1 · 2021: 7 · 2020: 6 · 2019: 3 · 2018: 3 · 2017: 9 · 2016: 3 · 2015: 6 · 2014: 4 · 2013: 6 · 2012: 6
FWCI
2.08
Type
journal article
Language
en
Open access
Locations
  • Genetics (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Princeton University
  • National Institutes of Health (GM046406)
  • National Institute of General Medical Sciences (F32GM071102, R01GM045720, R37GM046406, R01GM046406, GM046406, F32GM71102, P50GM071508, GM 45720)
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 › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
Keywords
Hog1, mitogen-activated protein kinase, hypoxia response, ergosterol depletion, membrane fluidity, p38 MAPK, osmotic stress, Saccharomyces cerevisiae, transcriptional regulation
MeSH terms
p300-CBP-Associated Factor, Anaerobiosis, Ergosterol, Heme, Membrane Fluidity, Membrane Proteins, Mutation, Saccharomyces cerevisiae, Transcription Factors, Blotting, Northern, Blotting, Western, Trans-Activators, Gene Expression Regulation, Fungal, Gene Expression Regulation, Developmental, Reverse Transcriptase Polymerase Chain Reaction, Oligonucleotide Array Sequence Analysis, Gene Expression Profiling, Mitogen-Activated Protein Kinases, Saccharomyces cerevisiae Proteins, Histone Acetyltransferases

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