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Signal transduction in yeast upon stress conditions

Iwona Wojda 1Jan-Paul Bebelman 2Teresa J. Jakubowicz 1Marco Siderius 2

1. Maria Curie-Sklodowska University, Department of Invertebrate Immunology, Akademicka 19, Lublin 20-033, Poland
2. Vrije Universiteit Amsterdam, Department of Biochemistry and Molecular Biology, De Boelelaan 1083, Amsterdam 1081HV, Netherlands

Abstract

The natural environment of unicellular organisms like yeast does not provide constant growth conditions. Yeast cells are challenged by changes in e.g., temperature, osmolarity, pH, the presence of reactive oxygen intermediates, the availability of nutrients or a combination of these agents. In order to continue growth, cells have to sense and properly respond to these changes to adapt their growth potential. Adverse growth conditions induce the general stress response and specific responses. The former evoke common molecular responses such as expression of heat shock proteins (Hsp12, Hsp26, Hsp104), degradation of damaged proteins as a result of increased expression of polyubiquitin gene (UBI4), increase in trehalose synthesis (higher expression of TPS2 encoding trehalose phosphate phosphatase) etc. The general stress response is sometimes called methabolic stress and is regulated by Ras-cAMP signalling pathway. Apart from inducing general stress response differential extracellular conditions trigger also specific pathways regulating expression of genes necessary under certain circumstances. Sacharomyces cerevisiae posses at least five MAP kinase pathways (Mitogen Activating Protein) responding to different extra-or intracellular stimuli. Among them are: cell integrity (protein kinase C) pathway induced by elevated temperature, morphogenetic events, hypo-osmotic shock or cell wall perturbation, HOG (High Osmolarity Glycerol) pathway activated upon hyper-osmotic conditions, Filamentous/Invasive Growth - FG pathway and Sporulation pathway, activated upon starvation and Mating pathway, activated by mating pheromone. Our focus is on the interplay between signalling pathways activated by the osmotic stress and elevated temperature. We show that the osmosensitive phenotype of the hog1 strain is suppressed at elevated temperature and the same holds true for the other commonly used HOG pathway mutant strains pbs2 and sho1ssk2ssk22, but not for the ste11ssk2ssk22. Instead, the ste11ssk2ssk2 strain displayed a hyperosmosensitive phenotype at 370C, suggesting the additional role of Ste11p in the maintenance of cellular integrity. This phenotype can be suppressed by genes involved in cell wall maintenance and genes increasing internal glycerol level. Also we show that sensing and response to osmotic stress is temperature-dependent. For example activation Hog1p MAP kinase, which occurs under hyperosmotic condtions, is very transient at 370C in comparson to optimal growth temperature (280C), and activation of Mpk1p/Slt2p – the MAP kinase activated at elevated temperature is inhibited under hyperosmotic conditions and this phenomenon is independent of HOG-pathway activity. Additionally, accumulation of intracellular glycerol, the osmolyte in yeast, is different under the same osmotic stress at different temperatures. Finally we discuss the role of intracellular glycerol in the maintenance of cellular integrity in Saccharomyces cerevisiae.

 

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Related papers

Presentation: Wykład at Zjazd Polskiego Towarzystwa Biochemicznego, Sympozjum L, by Iwona Wojda
See On-line Journal of Zjazd Polskiego Towarzystwa Biochemicznego

Submitted: 2007-04-25 11:20
Revised:   2009-06-07 00:44