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 AbstractGas-Phase Ozone Reaction Kinetics of C(5)-C(8) Unsaturated Alcohols of Biogenic Interest    Next AbstractControl of adaptation to mating pheromone by G protein beta subunits of Saccharomyces cerevisiae »

Mol Cell Biol


Title:Biochemical and genetic analysis of dominant-negative mutations affecting a yeast G-protein gamma subunit
Author(s):Grishin AV; Weiner JL; Blumer KJ;
Address:"Department of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, Missouri 63110"
Journal Title:Mol Cell Biol
Year:1994
Volume:14
Issue:7
Page Number:4571 - 4578
DOI: 10.1128/mcb.14.7.4571-4578.1994
ISSN/ISBN:0270-7306 (Print) 1098-5549 (Electronic) 0270-7306 (Linking)
Abstract:"Heterotrimeric guanine nucleotide-binding proteins (G proteins) consisting of alpha, beta, and gamma subunits mediate signalling between cell surface receptors and intracellular effectors in eukaryotic cells. To define signalling functions of G gamma subunits (STE18 gene product) involved in pheromone response and mating in the yeast Saccharomyces cerevisiae, we isolated and characterized dominant-negative STE18 alleles. We obtained dominant-negative mutations that disrupt C-terminal sequences required for prenylation of G gamma precursors (CAAX box) and that affect residues in the N-terminal half of Ste18p. Overexpression of mutant G gamma subunits in wild-type cells blocked signal transduction; this effect was suppressed upon overexpression of G beta subunits. Mutant G gamma subunits may therefore sequester G beta subunits into nonproductive G beta gamma dimers. Because mutant G gamma subunits blocked the constitutive signal resulting from disruption of the G alpha subunit gene (GPA1), they are defective in functions required for downstream signalling. Ste18p bearing a C107Y substitution in the CAAX box displayed reduced electrophoretic mobility, consistent with a prenylation defect. G gamma subunits carrying N-terminal substitutions had normal electrophoretic mobilities, suggesting that these proteins were prenylated. G gamma subunits bearing substitutions in their N-terminal region or C-terminal CAAX box (C107Y) supported receptor-G protein coupling in vitro, whereas C-terminal truncations caused partial defects in receptor coupling"
Keywords:"Alleles Amino Acid Sequence *GTP-Binding Protein gamma Subunits GTP-Binding Proteins/biosynthesis/*genetics Gene Expression/drug effects *Genes, Dominant *Genes, Fungal *Heterotrimeric GTP-Binding Proteins Kinetics Macromolecular Substances Molecular Sequ;"
Notes:"MedlineGrishin, A V Weiner, J L Blumer, K J eng GM44592/GM/NIGMS NIH HHS/ Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. 1994/07/01 Mol Cell Biol. 1994 Jul; 14(7):4571-8. doi: 10.1128/mcb.14.7.4571-4578.1994"

 
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 23-09-2024