Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractDominant negative selection of heterologous genes: isolation of Candida albicans genes that interfere with Saccharomyces cerevisiae mating factor-induced cell cycle arrest    Next AbstractGenetic identification of residues involved in association of alpha and beta G-protein subunits »

Biochem Cell Biol


Title:"Mutagenesis of Ste18, a putative G gamma subunit in the Saccharomyces cerevisiae pheromone response pathway"
Author(s):Whiteway M; Dignard D; Thomas DY;
Address:"Biotechnology Research Institute, National Research Council of Canada, Montreal, Que"
Journal Title:Biochem Cell Biol
Year:1992
Volume:70
Issue:10-Nov
Page Number:1230 - 1237
DOI: 10.1139/o92-169
ISSN/ISBN:0829-8211 (Print) 0829-8211 (Linking)
Abstract:"The yeast STE18 gene product has sequence and functional similarity to the gamma subunits of G proteins. The cloned STE18 gene was subjected to a saturation mutagenesis using doped oligonucleotides. The populations of mutant genes were screened for two classes of STE18 mutations, those that allowed for increased mating of a strain containing a defective STE4 gene (compensators) and those that inhibited mating even in the presence of a functional STE18 gene (dominant negatives). Three amino acid substitutions that enhanced mating in a specific STE4 (G beta) point mutant background were identified. These compensatory mutations were allele specific and had no detectable phenotype of their own; they may define residues that mediate an association between the G beta and G gamma subunits or in the association of the G beta gamma subunit with other components of the signalling pathway. Several dominant negative mutations were also identified, including two C terminal truncations. These mutant proteins were unable to function in signal transduction by themselves, but they prevented signal transduction mediated by pheromone, as well as the constitutive signalling which is present in cells defective in the GPA1 (G alpha) gene. These mutant proteins may sequester G beta or some other component of the signalling machinery in a nonfunctional complex"
Keywords:"Fungal Proteins/*genetics/metabolism GTP-Binding Proteins/*genetics/physiology Gene Expression Regulation, Fungal Genes, Fungal Mating Factor Mutagenesis Peptides/*physiology Pheromones/*physiology Recombinant Fusion Proteins/metabolism Reproduction Sacch;"
Notes:"MedlineWhiteway, M Dignard, D Thomas, D Y eng Canada 1992/10/01 Biochem Cell Biol. 1992 Oct-Nov; 70(10-11):1230-7. doi: 10.1139/o92-169"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 27-12-2024