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« Previous AbstractConstitutive mutants of the protein kinase STE11 activate the yeast pheromone response pathway in the absence of the G protein    Next AbstractDetermining circadian response of adult male Acrobasis nuxvorella (Lepidoptera: Pyralidae) to synthetic sex attractant pheromone through time-segregated trapping with a new clockwork timing trap »

Genes Dev


Title:"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"
Author(s):Stevenson BJ; Ferguson B; De Virgilio C; Bi E; Pringle JR; Ammerer G; Sprague GF;
Address:"Department of Biology and Institute of Molecular Biology, University of Oregon, Eugene 97403, USA"
Journal Title:Genes Dev
Year:1995
Volume:9
Issue:23
Page Number:2949 - 2963
DOI: 10.1101/gad.9.23.2949
ISSN/ISBN:0890-9369 (Print) 0890-9369 (Linking)
Abstract:"We have selected yeast mutants that exhibit a constitutively active pheromone-response pathway in the absence of the beta 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 G beta subunit. Moreover, in wild-type strains, deletion of RGA1 increases signaling in the pheromone pathway, whereas over-expression of RGA1 dampens signaling, demonstrating that Rga1p 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"
Keywords:"Amino Acid Sequence Base Sequence Cell Cycle Proteins/*metabolism Cell Polarity/genetics Drosophila Proteins GTP-Binding Proteins/biosynthesis/*genetics/*metabolism GTPase-Activating Proteins Gene Expression Regulation, Fungal *Insect Proteins Molecular S;"
Notes:"MedlineStevenson, B J Ferguson, B De Virgilio, C Bi, E Pringle, J R Ammerer, G Sprague, G F Jr eng GM30027/GM/NIGMS NIH HHS/ GM31006/GM/NIGMS NIH HHS/ Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. 1995/12/01 Genes Dev. 1995 Dec 1; 9(23):2949-63. doi: 10.1101/gad.9.23.2949"

 
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Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
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