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 AbstractAnalysis of RGSZ1 protein interaction with Galphai subunits    Next AbstractCharacterization of hydrocarbon emissions from green sand foundry core binders by analytical pyrolysis »

J Biol Chem


Title:Cdc24 regulates nuclear shuttling and recruitment of the Ste5 scaffold to a heterotrimeric G protein in Saccharomyces cerevisiae
Author(s):Wang Y; Chen W; Simpson DM; Elion EA;
Address:"Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, USA"
Journal Title:J Biol Chem
Year:2005
Volume:20050118
Issue:13
Page Number:13084 - 13096
DOI: 10.1074/jbc.M410461200
ISSN/ISBN:0021-9258 (Print) 0021-9258 (Linking)
Abstract:"The Saccharomyces cerevisiae guanine nucleotide exchange factor Cdc24 regulates polarized growth by binding to Cdc42, a Rho-type GTPase that has many effectors, including Ste20 kinase, which activates multiple MAPK cascades. Here, we show that Cdc24 promotes MAPK signaling during mating through interactions with Ste5, a scaffold that must shuttle through the nucleus and bind to the beta subunit (Ste4) of a G protein for Ste20 to activate the tethered MAPK cascade. Ste5 was basally recruited to growth sites of G1 phase cells independently of Ste4. Loss of Cdc24 inhibited nuclear import and blocked basal and pheromone-induced recruitment of Ste5. Ste5 was not basally recruited and the MAPK Fus3 was not basally activated in the presence of a Cdc24 mutant (G168D) that still activates Cdc42, suggesting that Cdc24 regulates Ste5 and the associated MAPK cascade through a function that is not dependent on its guanine nucleotide exchange factor activity. Consistent with this, Cdc24 bound Ste5 and coprecipitated with Ste4 independently of Far1 and Ste5. Loss of Cdc24 decreased Ste5-Ste4 complex formation, and loss of Ste4 stimulated Cdc24-Ste5 complex formation. Collectively, these findings suggest that Cdc24 mediates site-specific localization of Ste5 to a heterotrimeric G protein and may therefore ensure localized activation of the associated MAPK cascade"
Keywords:"Actins/chemistry Active Transport, Cell Nucleus Adaptor Proteins, Signal Transducing/*chemistry/metabolism Bridged Bicyclo Compounds, Heterocyclic/pharmacology Cell Cycle Proteins/metabolism/*physiology Cell Membrane/metabolism Cell Nucleus/metabolism Cyc;"
Notes:"MedlineWang, Yunmei Chen, Weidong Simpson, David M Elion, Elaine A eng GM69462/GM/NIGMS NIH HHS/ Research Support, U.S. Gov't, P.H.S. 2005/01/20 J Biol Chem. 2005 Apr 1; 280(13):13084-96. doi: 10.1074/jbc.M410461200. Epub 2005 Jan 18"

 
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