The level of cAMP‐dependent protein kinase A activity strongly affects osmotolerance andosmo‐instigated gene expression changes in Saccharomyces cerevisiae

The influence of cAMP‐dependent protein kinase (PKA) on protein expression during exponential growth under osmotic stress was studied by two‐dimensional polyacrylamide gel electrophoresis (2D–PAGE). The responses of isogenic strains (tpk2Δtpk3Δ) with either constitutively low (tpk1w1), regulated (TPK1) or constitutively high (TPK1bcy1Δ) PKA activity were compared. The activity of cAMP‐dependent protein kinase (PKA) was shown to be a major determinant of osmotic shock tolerance. Proteins with increased expression during growth under sodium chloride stress could be grouped into three classes with respect to PKA activity, with the glycerol metabolic proteins GPD1, GPP2 and DAK1 standing out as independent of PKA. The other osmotically induced proteins displayed a variable dependence on PKA activity; fully PKA‐dependent genes were TPS1 and GCY1, partly PKA‐dependent genes were ENO1, TDH1, ALD3 and CTT1. The proteins repressed by osmotic stress also fell into distinct classes of PKA‐dependency. Ymr116c was PKA‐independent, while Pgi1p, Sam1p, Gdh1p and Vma1p were fully PKA‐dependent. Hxk2p, Pdc1p, Ssb1p, Met6p, Atp2p and Hsp60p displayed a partially PKA‐dependent repression. The promotors of all induced PKA‐dependent genes have STRE sites in their promotors suggestive of a mechanism acting via Msn2/4p. The mechanisms governing the expression of the other classes are unknown. From the protein expression data we conclude that a low PKA activity causes a protein expression resembling that of osmotically stressed cells, and furthermore makes cells tolerant to this type of stress. Copyright © 2000 John Wiley & Sons, Ltd.

[1]  J. Thevelein Signal transduction in yeast , 1994, Yeast.

[2]  A. Rodríguez-Navarro,et al.  A novel P‐type ATPase from yeast involved in sodium transport , 1991, FEBS letters.

[3]  V. Magdolen,et al.  Transcriptional control by galactose of a yeast gene encoding a protein homologous to mammalian aldo/keto reductases. , 1990, Gene.

[4]  A. Blomberg Metabolic surprises in Saccharomyces cerevisiae during adaptation to saline conditions: questions, some answers and a model. , 2000, FEMS microbiology letters.

[5]  Stefan Hohmann,et al.  Regulation of genes encoding subunits of the trehalose synthase complex in , 1996 .

[6]  D. Botstein,et al.  Cluster analysis and display of genome-wide expression patterns. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[7]  A. Blomberg,et al.  Global changes in protein synthesis during adaptation of the yeast Saccharomyces cerevisiae to 0.7 M NaCl , 1995, Journal of bacteriology.

[8]  G. Adam,et al.  A Saccharomyces cerevisiae UAS element controlled by protein kinase A activates transcription in response to a variety of stress conditions. , 1993, The EMBO journal.

[9]  Michael Wigler,et al.  Three different genes in S. cerevisiae encode the catalytic subunits of the cAMP-dependent protein kinase , 1987, Cell.

[10]  Bruce Futcher,et al.  Proteome studies of Saccharomyces cerevisiae: Identification and characterization of abundant proteins , 1997, Electrophoresis.

[11]  Anders Blomberg,et al.  Purification and Characterization of Two Isoenzymes of DL-Glycerol-3-phosphatase from Saccharomyces cerevisiae , 1996, The Journal of Biological Chemistry.

[12]  J. Buhler,et al.  The H2O2 Stimulon in Saccharomyces cerevisiae * , 1998, The Journal of Biological Chemistry.

[13]  Ramón Serrano,et al.  Multiple transduction pathways regulate the sodium‐extrusion gene PMR2/ENA1 during salt stress in yeast , 1996, FEBS letters.

[14]  M. Wigler,et al.  Cloning and characterization of BCY1, a locus encoding a regulatory subunit of the cyclic AMP-dependent protein kinase in Saccharomyces cerevisiae , 1987, Molecular and cellular biology.

[15]  H. Ruis,et al.  The HOG pathway controls osmotic regulation of transcription via the stress response element (STRE) of the Saccharomyces cerevisiae CTT1 gene. , 1994, The EMBO journal.

[16]  T. Maeda,et al.  Activation of yeast PBS2 MAPKK by MAPKKKs or by binding of an SH3-containing osmosensor. , 1995, Science.

[17]  M. Proft,et al.  The Ssn6–Tup1 repressor complex of Saccharomyces cerevisiae is involved in the osmotic induction of HOG‐dependent and ‐independent genes , 1998, The EMBO journal.

[18]  A. Blomberg,et al.  Two‐dimensional electrophoretic separation of yeast proteins using a non‐linear wide range (pH 3–10) immobilized pH gradient in the first dimension; reproducibility and evidence for isoelectric focusing of alkaline (pI >7) proteins , 1997, Yeast.

[19]  Ichiro Yahara,et al.  Yeast heat-shock protein of Mr 48,000 is an isoprotein of enolase , 1985, Nature.

[20]  R. Serrano,et al.  Repressors and Upstream Repressing Sequences of the Stress-Regulated ENA1 Gene in Saccharomyces cerevisiae: bZIP Protein Sko1p Confers HOG-Dependent Osmotic Regulation , 1999, Molecular and Cellular Biology.

[21]  M. Jacquet,et al.  Msn2p and Msn4p Control a Large Number of Genes Induced at the Diauxic Transition Which Are Repressed by Cyclic AMP inSaccharomyces cerevisiae , 1998, Journal of bacteriology.

[22]  B Hamilton,et al.  Nuclear localization of the C2H2 zinc finger protein Msn2p is regulated by stress and protein kinase A activity. , 1998, Genes & development.

[23]  A. Blomberg,et al.  Protein expression during exponential growth in 0.7 M NaCl medium of Saccharomyces cerevisiae. , 1996, FEMS microbiology letters.

[24]  I. Yahara,et al.  A heat shock-resistant mutant of Saccharomyces cerevisiae shows constitutive synthesis of two heat shock proteins and altered growth , 1984, The Journal of cell biology.

[25]  T. Maeda,et al.  Activation of Yeast PBS 2 MAPKK by MAPKKKs or by Binding of an SH 3-Containing Osmosensor , 2022 .

[26]  A. Blomberg,et al.  Metabolic and Regulatory Changes Associated with Growth of Saccharomyces cerevisiae in 1.4 M NaCl , 1997, The Journal of Biological Chemistry.

[27]  P. Brown,et al.  Exploring the metabolic and genetic control of gene expression on a genomic scale. , 1997, Science.

[28]  E. Winter,et al.  An osmosensing signal transduction pathway in yeast. , 1993, Science.

[29]  A. Blomberg,et al.  Cloning and characterization of GPD2, a second gene encoding sn‐glycerol 3‐phosphate dehydrogenase (NAD+) in Saccharomyces cerevisiae, and its comparison with GPD1 , 1995, Molecular microbiology.

[30]  H. W. Lee,et al.  Studies on compartmentation of S-adenosyl-L-methionine in Saccharomyces cerevisiae and isolated rat hepatocytes. , 1983, Biochimica et biophysica acta.

[31]  H. Feldmann,et al.  Molecular cloning of CIF1, a yeast gene necessary for growth on glucose , 1992, Yeast.

[32]  M. Wigler,et al.  cAMP-independent control of sporulation, glycogen metabolism, and heat shock resistance in S. cerevisiae , 1988, Cell.

[33]  Tatsuya Maeda,et al.  A two-component system that regulates an osmosensing MAP kinase cascade in yeast , 1994, Nature.

[34]  R. Serrano,et al.  A genomic locus in Saccharomyces cerevisiae with four genes up‐regulated by osmotic stress , 1995, Molecular microbiology.

[35]  J M Thevelein,et al.  Fps1, a yeast member of the MIP family of channel proteins, is a facilitator for glycerol uptake and efflux and is inactive under osmotic stress. , 1995, The EMBO journal.

[36]  A. Blomberg The Osmotic Hypersensitivity of the Yeast Saccharomyces cerevisiae is Strain and Growth Media Dependent: Quantitative Aspects of the Phenomenon , 1997, Yeast.

[37]  J M Thevelein,et al.  GPD1, which encodes glycerol-3-phosphate dehydrogenase, is essential for growth under osmotic stress in Saccharomyces cerevisiae, and its expression is regulated by the high-osmolarity glycerol response pathway , 1994, Molecular and cellular biology.

[38]  A. Blomberg,et al.  Osmoregulation and protein expression in a pbs2Δ mutant of Saccharomyces cerevisiae during adaptation to hypersaline stress , 1997, FEBS letters.

[39]  A. Marchler-Bauer,et al.  The Saccharomyces cerevisiae zinc finger proteins Msn2p and Msn4p are required for transcriptional induction through the stress response element (STRE). , 1996, The EMBO journal.

[40]  G. Boguslawski PBS2, a yeast gene encoding a putative protein kinase, interacts with the RAS2 pathway and affects osmotic sensitivity of Saccharomyces cerevisiae. , 1992, Journal of general microbiology.

[41]  H. Iida Multistress resistance of Saccharomyces cerevisiae is generated by insertion of retrotransposon Ty into the 5' coding region of the adenylate cyclase gene , 1988, Molecular and cellular biology.

[42]  W. H. Mager,et al.  High-osmolarity signalling in Saccharomyces cerevisiae is modulated in a carbon-source-dependent fashion. , 1997, Microbiology.

[43]  Fred Winston,et al.  Construction of a set of convenient saccharomyces cerevisiae strains that are isogenic to S288C , 1995, Yeast.

[44]  K. Larsson,et al.  A gene encoding sn‐glycerol 3‐phosphate dehydrogenase (NAD+) complements an osmosensitive mutant of Saccharomyces cerevisiae , 1993, Molecular microbiology.

[45]  W. H. Mager,et al.  General stress response: In search of a common denominator. , 1997 .

[46]  Anders Blomberg,et al.  Interlaboratory reproducibility of yeast protein patterns analyzed by immobilized pH gradient two‐dimensional gel electrophoresis , 1995, Electrophoresis.

[47]  W. H. Mager,et al.  The Saccharomyces cerevisiae HSP12 gene is activated by the high-osmolarity glycerol pathway and negatively regulated by protein kinase A , 1995, Molecular and cellular biology.