Phase-specific protein expression in the dimorphic yeast Saccharomyces cerevisiae.

In oxygen-limited continuous culture, Saccharomyces cerevisiae formed pseudohyphae by unipolar budding. We developed a continuous cultivation sequence to discriminate phase-specific from metabolically regulated proteins during dimorphism. Computer-aided substractive analysis of 2D-PAGE protein patterns allowed the detection of proteins specifically expressed during yeast and pseudohyphal phases. Image analysis resolved 3 spots that were specific to the pseudohyphal phase and 2 spots that were specific to yeast phase. In addition to phase-specific proteins, important regulation of protein expression took place. A group of 9 proteins was highly over-expressed during the yeast phase when another group of 12 was underexpressed. This phenomenon was reversed during the pseudohyphal phase. These experiments showed that dimorphism in S. cerevisiae is associated with the expression of specific proteins and suggest that yeast phase-specific proteins maintain the yeast form or repress pseudohyphae formation.

[1]  U. K. Laemmli,et al.  Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.

[2]  M. Bölker,et al.  The pheromone response factor coordinates filamentous growth and pathogenicity in Ustilago maydis. , 1996, The EMBO journal.

[3]  I. S. Pretorius,et al.  Muc1, a mucin-like protein that is regulated by Mss10, is critical for pseudohyphal differentiation in yeast. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[4]  Gerald R. Fink,et al.  Unipolar cell divisions in the yeast S. cerevisiae lead to filamentous growth: Regulation by starvation and RAS , 1992, Cell.

[5]  M. Shepherd Morphogenetic transformation of fungi. , 1988, Current topics in medical mycology.

[6]  G. Fink,et al.  Elements of the yeast pheromone response pathway required for filamentous growth of diploids. , 1993, Science.

[7]  Differential profiles of soluble proteins during the initiation of morphogenesis in Candida albicans , 1996, Archives of Microbiology.

[8]  J. Cutler,et al.  Putative virulence factors of Candida albicans. , 1991, Annual review of microbiology.

[9]  H. Kuriyama,et al.  Oscillatory metabolism of Saccharomyces cerevisiae in continuous culture. , 1992, FEMS microbiology letters.

[10]  G. Phillips,et al.  Effect of oxygen on morphogenesis and polypeptide expression by Mucor racemosus , 1985, Journal of bacteriology.

[11]  H. Kuriyama,et al.  Control of cell morphology of the yeast Saccharomyces cerevisiae by nutrient limitation in continuous culture , 1995, Letters in applied microbiology.

[12]  Byron F. Johnson,et al.  Cell Division: a Separable Cellular Sub-cycle in the Fission Yeast Schizosaccharomyces pombe , 1983 .

[13]  L. Daneo-Moore,et al.  Differential Protein Synthesis in Candida albicans during Blastospore Formation at 24.5 °C and during Germ Tube Formation at 37 °C , 1983 .

[14]  G. Fink,et al.  Saccharomyces cerevisiae S288C has a mutation in FLO8, a gene required for filamentous growth. , 1996, Genetics.

[15]  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.

[16]  S. H. Lillie,et al.  Reserve carbohydrate metabolism in Saccharomyces cerevisiae: responses to nutrient limitation , 1980, Journal of bacteriology.

[17]  P. O’Farrell High resolution two-dimensional electrophoresis of proteins. , 1975, The Journal of biological chemistry.

[18]  G. Phillips,et al.  Respiratory-competent conditional developmental mutant of Mucor racemosus , 1985, Journal of bacteriology.

[19]  James I. Garrels,et al.  YPD-A database for the proteins of Saccharomyces cerevisiae , 1996, Nucleic Acids Res..