Mutation of RGA1, which encodes a putative GTPase-activating protein for the polarity - Establishment protein Cdc42p, activates the pheromone-response pathway in the yeast Saccharomyces cerevisiae

Brian J. Stevenson, Betsy Ferguson, Claudio De Virgilio, Erfei Bi, John R. Pringle, Gustav Ammerer, George F. Sprague

    Research output: Contribution to journalArticle

    100 Citations (Scopus)

    Abstract

    We have selected yeast mutants that exhibit a constitutively active pheromone-response pathway in the absence of the β subunit of the trimeric G protein. Genetic analysis of one such mutant revealed that it contained recessive mutations in two distinct genes, both of which contributed to the constitutive phenotype. One mutation identifies the RGA1 locus (Rho GTPase activating protein), which encodes a protein with homology to GAP domains and to LIM domains. Deletion of RGA1 is sufficient to activate the pathway in strains lacking the Gβ subunit. Moreover, in wild-type strains, deletion of RGA1 increases signaling in the pheromone pathway, whereas over-expression of RGA1 dampens signaling, demonstrating that Rgalp functions as a negative regulator of the pheromone response pathway. The second mutation present in the original mutant proved to be an allele of a known gene, PBS2, which encodes a putative protein kinase that functions in the high osmolarity stress pathway. The pbs2 mutation enhanced the rga1 mutant phenotype, but by itself did not activate the pheromone pathway. Genetic and two-hybrid analyses indicate that an important target of Rga1p is Cdc42p, a p21 GTPase required for polarity establishment and bud emergence. This finding coupled with recent experiments with mammalian and yeast cells indicating that Cdc42p can interact with and activate Ste20p, a protein kinase that operates in the pheromone pathway, leads us to suggest that Rga1p controls the activity of Cdc42p, which in turn controls the magnitude of signaling in the pheromone pathway via Ste20p.

    Original languageEnglish (US)
    Pages (from-to)2949-2963
    Number of pages15
    JournalGenes and Development
    Volume9
    Issue number23
    StatePublished - Dec 1 1995

    Fingerprint

    GTPase-Activating Proteins
    Pheromones
    Saccharomyces cerevisiae
    Yeasts
    Mutation
    Proteins
    Protein Kinases
    Phenotype
    GTP Phosphohydrolases
    GTP-Binding Proteins
    Osmolar Concentration
    Genes
    Alleles

    Keywords

    • Cdc42p
    • GAPs
    • Pheromone-response pathway
    • RGA1
    • Saccharomyces cerevisiae

    ASJC Scopus subject areas

    • Developmental Biology
    • Genetics

    Cite this

    Mutation of RGA1, which encodes a putative GTPase-activating protein for the polarity - Establishment protein Cdc42p, activates the pheromone-response pathway in the yeast Saccharomyces cerevisiae. / Stevenson, Brian J.; Ferguson, Betsy; De Virgilio, Claudio; Bi, Erfei; Pringle, John R.; Ammerer, Gustav; Sprague, George F.

    In: Genes and Development, Vol. 9, No. 23, 01.12.1995, p. 2949-2963.

    Research output: Contribution to journalArticle

    Stevenson, Brian J. ; Ferguson, Betsy ; De Virgilio, Claudio ; Bi, Erfei ; Pringle, John R. ; Ammerer, Gustav ; Sprague, George F. / Mutation of RGA1, which encodes a putative GTPase-activating protein for the polarity - Establishment protein Cdc42p, activates the pheromone-response pathway in the yeast Saccharomyces cerevisiae. In: Genes and Development. 1995 ; Vol. 9, No. 23. pp. 2949-2963.
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    abstract = "We have selected yeast mutants that exhibit a constitutively active pheromone-response pathway in the absence of the β subunit of the trimeric G protein. Genetic analysis of one such mutant revealed that it contained recessive mutations in two distinct genes, both of which contributed to the constitutive phenotype. One mutation identifies the RGA1 locus (Rho GTPase activating protein), which encodes a protein with homology to GAP domains and to LIM domains. Deletion of RGA1 is sufficient to activate the pathway in strains lacking the Gβ subunit. Moreover, in wild-type strains, deletion of RGA1 increases signaling in the pheromone pathway, whereas over-expression of RGA1 dampens signaling, demonstrating that Rgalp functions as a negative regulator of the pheromone response pathway. The second mutation present in the original mutant proved to be an allele of a known gene, PBS2, which encodes a putative protein kinase that functions in the high osmolarity stress pathway. The pbs2 mutation enhanced the rga1 mutant phenotype, but by itself did not activate the pheromone pathway. Genetic and two-hybrid analyses indicate that an important target of Rga1p is Cdc42p, a p21 GTPase required for polarity establishment and bud emergence. This finding coupled with recent experiments with mammalian and yeast cells indicating that Cdc42p can interact with and activate Ste20p, a protein kinase that operates in the pheromone pathway, leads us to suggest that Rga1p controls the activity of Cdc42p, which in turn controls the magnitude of signaling in the pheromone pathway via Ste20p.",
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    AU - De Virgilio, Claudio

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