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 AbstractTrail following by gliding bacteria    Next Abstract"Terpenes, Phenylpropanoids, Sulfur and Other Essential Oil Constituents as Inhibitors of Cholinesterases" »

J Biol Chem


Title:"Regulation of stress response signaling by the N-terminal dishevelled/EGL-10/pleckstrin domain of Sst2, a regulator of G protein signaling in Saccharomyces cerevisiae"
Author(s):Burchett SA; Flanary P; Aston C; Jiang L; Young KH; Uetz P; Fields S; Dohlman HG;
Address:"Department of Pharmacology, Yale University School of Medicine, New Haven, Connecticut 06536, USA"
Journal Title:J Biol Chem
Year:2002
Volume:20020408
Issue:25
Page Number:22156 - 22167
DOI: 10.1074/jbc.M202254200
ISSN/ISBN:0021-9258 (Print) 0021-9258 (Linking)
Abstract:"All members of the regulator of G protein signaling (RGS) family contain a conserved core domain that can accelerate G protein GTPase activity. The RGS in yeast, Sst2, can inhibit a G protein signal leading to mating. In addition, some RGS proteins contain an N-terminal domain of unknown function. Here we use complementary whole genome analysis methods to investigate the function of the N-terminal Sst2 domain. To identify a signaling pathway regulated by N-Sst2, we performed genome-wide transcription profiling of cells expressing this fragment alone and found differences in 53 transcripts. Of these, 40 are induced by N-Sst2, and nearly all contain a stress response element (STRE) in the promoter region. To identify components of a signaling pathway leading from N-Sst2 to STREs, we performed a genome-wide two-hybrid analysis using N-Sst2 as bait and found 17 interacting proteins. To identify the functionally relevant interacting proteins, we analyzed all of the available gene deletion mutants and found three (vps36 Delta, pep12 Delta, and tlg2 Delta) that induce STRE and also repress pheromone-dependent transcription. We selected VPS36 for further characterization. A vps36 Delta mutation diminishes signaling by pheromone as well as by downstream components including the G protein, effector kinase (Ste11), and transcription factor (Ste12). Conversely, overexpression of Vps36 enhances the pheromone response in sst2 Delta cells but not in wild type. These findings indicate that Vps36 and Sst2 have opposite and opposing effects on the pheromone and stress response pathways, with Vps36 acting downstream of the G protein and independently of Sst2 RGS activity"
Keywords:"Adaptor Proteins, Signal Transducing Blood Proteins/*chemistry *Caenorhabditis elegans Proteins Cell Division Dishevelled Proteins Dose-Response Relationship, Drug Fungal Proteins/*genetics/*metabolism *GTPase-Activating Proteins Gene Expression Regulatio;"
Notes:"MedlineBurchett, Scott A Flanary, Paul Aston, Christopher Jiang, Lixin Young, Kathleen H Uetz, Peter Fields, Stanley Dohlman, Henrik G eng R01 GM055316/GM/NIGMS NIH HHS/ R01 GM059167/GM/NIGMS NIH HHS/ Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. 2002/04/10 J Biol Chem. 2002 Jun 21; 277(25):22156-67. doi: 10.1074/jbc.M202254200. Epub 2002 Apr 8"

 
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 19-12-2024