Association of the Yeast Pheromone Response G Protein βγ Subunits with the Map Kinase Scaffold Ste5p

Malcolm Whiteway(National Academies of Sciences, Engineering, and Medicine), Cunle Wu(National Academies of Sciences, Engineering, and Medicine), Thomas Leeuw(National Academies of Sciences, Engineering, and Medicine), Karen Clark(National Academies of Sciences, Engineering, and Medicine), Anne Fourest‐Lieuvin(National Academies of Sciences, Engineering, and Medicine), David Y. Thomas(National Academies of Sciences, Engineering, and Medicine), Ekkehard Leberer(National Academies of Sciences, Engineering, and Medicine)
Science
September 15, 1995
Cited by 172

Abstract

The mating response pathway of the yeast Saccharomyces cerevisiae includes a heterotrimeric guanine nucleotide-binding protein (G protein) that activates a mitogen-activated protein MAP kinase cascade by an unknown mechanism. An amino-terminal fragment of the MAP kinase scaffold protein Ste5p that interfered with pheromone-induced cell cycle arrest was identified. A haploid-specific interaction between the amino terminus of Ste5p and the G protein beta subunit Ste4p was also detected in a two-hybrid assay, and the product of a signaling-defective allele of STE4 was defective in this interaction. In cells with a constitutively activated pheromone response pathway, epitope-tagged Ste4p was coimmunoprecipitated with Ste5p. Thus, association of the G protein and the MAP kinase cassette via the scaffolding protein Ste5p may transmit the G protein signal.


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