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 AbstractThe light chain subunit is required for clathrin function in Saccharomyces cerevisiae    Next AbstractAdsorption of toluene with water on zeolitic imidazolate framework-8/graphene oxide hybrid nanocomposites in a humid atmosphere »

Mol Biol Cell


Title:A modulatory role for clathrin light chain phosphorylation in Golgi membrane protein localization during vegetative growth and during the mating response of Saccharomyces cerevisiae
Author(s):Chu DS; Pishvaee B; Payne GS;
Address:"Department of Biological Chemistry, University of California Los Angeles, Los Angeles, California 90095-3717, USA"
Journal Title:Mol Biol Cell
Year:1999
Volume:10
Issue:3
Page Number:713 - 726
DOI: 10.1091/mbc.10.3.713
ISSN/ISBN:1059-1524 (Print) 1059-1524 (Linking)
Abstract:"The role of clathrin light chain phosphorylation in regulating clathrin function has been examined in Saccharomyces cerevisiae. The phosphorylation state of yeast clathrin light chain (Clc1p) in vivo was monitored by [32P]phosphate labeling and immunoprecipitation. Clc1p was phosphorylated in growing cells and also hyperphosphorylated upon activation of the mating response signal transduction pathway. Mating pheromone-stimulated hyperphosphorylation of Clc1p was dependent on the mating response signal transduction pathway MAP kinase Fus3p. Both basal and stimulated phosphorylation occurred exclusively on serines. Mutagenesis of Clc1p was used to map major phosphorylation sites to serines 52 and 112, but conversion of all 14 serines in Clc1p to alanines [S(all)A] was necessary to eliminate phosphorylation. Cells expressing the S(all)A mutant Clc1p displayed no defects in Clc1p binding to clathrin heavy chain, clathrin trimer stability, sorting of a soluble vacuolar protein, or receptor-mediated endocytosis of mating pheromone. However, the trans-Golgi network membrane protein Kex2p was not optimally localized in mutant cells. Furthermore, pheromone treatment exacerbated the Kex2p localization defect and caused a corresponding defect in Kex2p-mediated maturation of the alpha-factor precursor. The results reveal a novel requirement for clathrin during the mating response and suggest that phosphorylation of the light chain subunit modulates the activity of clathrin at the trans-Golgi network"
Keywords:Amino Acid Sequence Animals Base Sequence Casein Kinase II Cell Cycle/physiology Clathrin/genetics/*metabolism Fungal Proteins/metabolism Golgi Apparatus/*metabolism Intracellular Membranes/*metabolism *Mitogen-Activated Protein Kinases Molecular Sequence;
Notes:"MedlineChu, D S Pishvaee, B Payne, G S eng R01 GM039040/GM/NIGMS NIH HHS/ T32 GM007185/GM/NIGMS NIH HHS/ GM-07185/GM/NIGMS NIH HHS/ GM-39040/GM/NIGMS NIH HHS/ Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. 1999/03/09 Mol Biol Cell. 1999 Mar; 10(3):713-26. doi: 10.1091/mbc.10.3.713"

 
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 29-06-2024