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« Previous Abstract"Multiple genes coding for precursors of rhodotorucine A, a farnesyl peptide mating pheromone of the basidiomycetous yeast Rhodosporidium toruloides"    Next AbstractA comparison of volatile components from the peel of Ohshima no. 1 with its parent cultivars »

Genetics


Title:"Genetic relationships between the G protein beta gamma complex, Ste5p, Ste20p and Cdc42p: investigation of effector roles in the yeast pheromone response pathway"
Author(s):Akada R; Kallal L; Johnson DI; Kurjan J;
Address:"Department of Microbiology and Molecular Genetics, University of Vermont, Burlington 05405, USA"
Journal Title:Genetics
Year:1996
Volume:143
Issue:1
Page Number:103 - 117
DOI: 10.1093/genetics/143.1.103
ISSN/ISBN:0016-6731 (Print) 0016-6731 (Linking)
Abstract:"The Saccharomyces cerevisiae G protein beta gamma dimer, Ste4p/Ste18p, acts downstream of the alpha subunit, Gpa1p, to activate the pheromone response pathway and therefore must interact with a downstream effector. Synthetic sterile mutants that exacerbate the phenotype of ste4-ts mutations were isolated to identify proteins that functionally interact with Ste4p. The identification of a ste18 mutant indicated that this screen could identify proteins that interact directly with Ste4p. The other mutations were in STE5 and the STE20 kinase gene, which act near Ste4p in the pathway, and a new gene called STE21. ste20 null mutants showed residual mating, suggesting that another kinase may provide some function. Overexpression of Ste5p under galactose control activated the pheromone response pathway. This activation was dependent on Ste4p and Ste18p and partially dependent on Ste20p. These results cannot be explained by the linear pathway of Ste4p-->Ste20p-->Ste5p. Overexpression of Cdc42p resulted in a slight increase in pheromone induction of a reporter gene, and overexpression of activated forms of Cdc42p resulted in a further twofold increase. Mutations in pheromone response pathway components did not suppress the lethality associated with the activated CDC42 mutations, suggesting that this effect is independent of the pheromone response pathway"
Keywords:"*Adaptor Proteins, Signal Transducing *Carrier Proteins Cell Cycle Proteins/genetics/*metabolism Cloning, Molecular Crosses, Genetic Fungal Proteins/genetics/*metabolism GTP-Binding Proteins/genetics/*metabolism *Genes, Fungal Genotype Intracellular Signa;"
Notes:"MedlineAkada, R Kallal, L Johnson, D I Kurjan, J eng GM-40585/GM/NIGMS NIH HHS/ Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S. 1996/05/01 Genetics. 1996 May; 143(1):103-17. doi: 10.1093/genetics/143.1.103"

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