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 the thresholds for transcriptional activation by the yeast MAP kinases Fus3 and Kss1    Next AbstractApplying the electronic nose for pre-operative SARS-CoV-2 screening »

Mol Biol Cell


Title:MAPK modulation of yeast pheromone signaling output and the role of phosphorylation sites in the scaffold protein Ste5
Author(s):Winters MJ; Pryciak PM;
Address:"Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA 01605"
Journal Title:Mol Biol Cell
Year:2019
Volume:20190206
Issue:8
Page Number:1037 - 1049
DOI: 10.1091/mbc.E18-12-0793
ISSN/ISBN:1939-4586 (Electronic) 1059-1524 (Print) 1059-1524 (Linking)
Abstract:"Mitogen-activated protein kinases (MAPKs) mediate numerous eukaryotic signaling responses. They also can modulate their own signaling output via positive or negative feedback loops. In the yeast pheromone response pathway, the MAPK Fus3 triggers negative feedback that dampens its own activity. One target of this feedback is Ste5, a scaffold protein that promotes Fus3 activation. Binding of Fus3 to a docking motif (D motif) in Ste5 causes signal dampening, which was proposed to involve a central cluster of phosphorylation sites in Ste5. Here, we reanalyzed the role of these central sites. Contrary to prior claims, phosphorylation-mimicking mutations at these sites did not impair signaling. Also, the hyperactive signaling previously observed when these sites were mutated to nonphosphorylatable residues arose from their replacement with valine residues and was not observed with other substitutes. Instead, a cluster of N-terminal sites in Ste5, not the central sites, is required for the rapid dampening of initial responses. Further results suggest that the role of the Fus3 D motif is most simply explained by a tethering effect that promotes Ste5 phosphorylation, rather than an allosteric effect proposed to regulate Fus3 activity. These findings substantially revise our understanding of how MAPK feedback attenuates scaffold-mediated signaling in this model pathway"
Keywords:"Adaptor Proteins, Signal Transducing/genetics/*metabolism/*physiology Carrier Proteins/metabolism MAP Kinase Signaling System Mitogen-Activated Protein Kinase Kinases/metabolism Mitogen-Activated Protein Kinases/metabolism/physiology Nuclear Matrix-Associ;"
Notes:"MedlineWinters, Matthew J Pryciak, Peter M eng R01 GM057769/GM/NIGMS NIH HHS/ Research Support, N.I.H., Extramural 2019/02/07 Mol Biol Cell. 2019 Apr 1; 30(8):1037-1049. doi: 10.1091/mbc.E18-12-0793. Epub 2019 Feb 6"

 
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 23-11-2024