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 AbstractSpatial dynamics of receptor-mediated endocytic trafficking in budding yeast revealed by using fluorescent alpha-factor derivatives    Next AbstractPolydimethylsiloxane Droplets Exhibit Extraordinarily High Antioxidative Effects in Deep-Frying »

Mol Biol Cell


Title:Requirements for recruitment of a G protein-coupled receptor to clathrin-coated pits in budding yeast
Author(s):Toshima JY; Nakanishi J; Mizuno K; Toshima J; Drubin DG;
Address:"Department of Biological Science and Technology, Tokyo University of Science, Yamazaki 2641, Noda, Chiba 278-8510, Japan"
Journal Title:Mol Biol Cell
Year:2009
Volume:20
Issue:24
Page Number:5039 - 5050
DOI: 10.1091/mbc.e09-07-0541
ISSN/ISBN:1939-4586 (Electronic) 1059-1524 (Print) 1059-1524 (Linking)
Abstract:"Endocytic internalization of G protein-coupled receptors (GPCRs) plays a critical role in down-regulation of GPCR signaling. The yeast mating pheromone receptor Ste2p has been used as a model to investigate mechanisms of signal transduction, modification, and endocytic internalization of GPCRs. We previously used a fluorescently labeled mating pheromone derivative to reveal unappreciated molecular and spatiotemporal features of GPCR endocytosis in budding yeast. Here, we identify recruitment of Ste2p to preexisting clathrin-coated pits (CCPs) as a key step regulated by receptor phosphorylation and subsequent ubiquitination upon ligand binding. The yeast casein kinase I homologue Yck2p directly phosphorylates six serine residues located in the C-terminal tail of Ste2p, and mutation of these serine residues to alanine significantly decreased recruitment of Ste2p to CCPs. We also found that the clathrin adaptors Ent1p, Ent2p, and Ede1p work cooperatively to recruit ubiquitinated Ste2p to CCPs. In addition, ubiquitination has a role in ligand-independent constitutive recruitment of Ste2p to CCPs, although this process is much slower than ligand-induced recruitment. These results suggest that ubiquitination of Ste2p is indispensable for recruiting Ste2p to CCPs in both ligand-dependent and ligand-independent endocytosis"
Keywords:"Amino Acid Motifs Amino Acid Sequence Clathrin/*metabolism Coated Pits, Cell-Membrane/*metabolism Endocytosis Ligands Molecular Sequence Data Phosphorylation Protein Binding Protein Precursors/metabolism Protein Structure, Tertiary Protein Transport Recep;"
Notes:"MedlineToshima, Junko Y Nakanishi, Jun-ichi Mizuno, Kensaku Toshima, Jiro Drubin, David G eng GM-R0150399/GM/NIGMS NIH HHS/ Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't 2009/10/16 Mol Biol Cell. 2009 Dec; 20(24):5039-50. doi: 10.1091/mbc.e09-07-0541"

 
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 27-12-2024