Yeast osmoregulation – glycerol still in pole position

Author:

Blomberg Anders1ORCID

Affiliation:

1. Department of Chemistry and Molecular Biology, University of Gothenburg , 405 30 Gothenburg, Sweden

Abstract

ABSTRACT In response to osmotic dehydration cells sense, signal, alter gene expression, and metabolically counterbalance osmotic differences. The main compatible solute/osmolyte that accumulates in yeast cells is glycerol, which is produced from the glycolytic intermediate dihydroxyacetone phosphate. This review covers recent advancements in understanding mechanisms involved in sensing, signaling, cell-cycle delays, transcriptional responses as well as post-translational modifications on key proteins in osmoregulation. The protein kinase Hog1 is a key-player in many of these events, however, there is also a growing body of evidence for important Hog1-independent mechanisms playing vital roles. Several missing links in our understanding of osmoregulation will be discussed and future avenues for research proposed. The review highlights that this rather simple experimental system—salt/sorbitol and yeast—has developed into an enormously potent model system unravelling important fundamental aspects in biology.

Funder

Swedish Research Council

European Commission

Publisher

Oxford University Press (OUP)

Subject

Applied Microbiology and Biotechnology,General Medicine,Microbiology

Reference131 articles.

1. Glycerol metabolism and osmoregulation in the salt-tolerant yeast Debaryomyces hansenii;Adler;J Bacteriol,1985

2. Yeast reveals unexpected roles and regulatory features of aquaporins and aquaglyceroporins;Ahmadpour;Biochim Biophys Acta,2014

3. Osmoregulation and protein expression in a pbs2∆ mutant of Saccharomyces cerevisiae during adaptation to hypersaline stress;Akhtar;FEBS Lett,1997

4. GPD1, which encodes glycerol-3-phosphate dehydrogenase, is essential for growth under osmotic stress in Saccharomycescerevisiae, and its expression is regulated by the high osmolarity glycerol response pathway;Albertyn;Mol Cell Biol,1994

5. Osmostress-induced transcription by hot1 depends on a Hog1-mediated recruitment of the RNA pol iI;Alepuz;EMBO J,2003

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