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 AbstractRecycling of the yeast a-factor receptor    Next AbstractPerformance evaluation of a wood-chip based biofilter using solid-phase microextraction and gas chromatography-mass spectroscopy-olfactometry »

Traffic


Title:Ubiquitin-independent entry into the yeast recycling pathway
Author(s):Chen L; Davis NG;
Address:"Department of Physiology, University of Michigan School of Medicine, Ann Arbor, MI 48109, USA"
Journal Title:Traffic
Year:2002
Volume:3
Issue:2
Page Number:110 - 123
DOI: 10.1034/j.1600-0854.2002.030204.x
ISSN/ISBN:1398-9219 (Print) 1398-9219 (Linking)
Abstract:"The yeast a-factor receptor (Ste3p) is subject to two mechanistically distinct modes of endocytosis: a constitutive, ligand-independent pathway links to vacuolar degradation of the receptor, while a ligand-dependent uptake pathway links primarily to recycling and thus, receptor reutilization. Ste3p ubiquitination triggers its uptake into the constitutive pathway. The present work considers the role of the receptor ubiquitination associated with the Ste3p ligand-dependent endocytosis mechanism. The doa4delta mutation which reduces the cellular availability of ubiquitin blocks the Ste3p constitutive uptake. Uptake into the Ste3p ligand-dependent recycling pathway, however, continues unimpaired. The ubiquitin independence of Ste3p ligand-dependent uptake was further indicated by analysis of receptor mutants having Lys-to-Arg substitutions at all possible ubiquitin acceptor sites. Again, the ligand-induced internalization was unimpaired. Furthermore, no discernible effect was seen on either recycling or on the slow PEP4-dependent turnover of the receptor (for receptor internalized via the ligand-dependent mechanism, trafficking to the vacuole/lysosome is the minor, alternate fate to recycling). However, one striking effect of the Lys-to-Arg mutations was noted. Following a prolonged exposure of the cells to the a-factor ligand, rather than being delivered to the vacuolar lumen, the Lys-to-Arg receptor was found to localize instead to the limiting membrane of the vacuole. Thus, while receptor ubiquitination clearly is not required for either the a-factor-dependent uptake into recycling pathway or for the recycling itself, it does affect the routing of receptor to the vacuole, likely by affecting the routing through the late endosomal, multivesicular body: ubiquitinated receptor may be selected into the internal, lumenal vesicles, while unmodified receptor may be left to reside at the limiting external membrane"
Keywords:"Alleles Arginine/chemistry Blotting, Western Cytoplasm/metabolism Cytosol/metabolism Endocytosis Endopeptidases/metabolism/physiology Endosomal Sorting Complexes Required for Transport Epitopes Fungal Proteins/metabolism/physiology Galactose/metabolism Ki;"
Notes:"MedlineChen, Linyi Davis, Nicholas G eng Research Support, U.S. Gov't, Non-P.H.S. England 2002/04/04 Traffic. 2002 Feb; 3(2):110-23. doi: 10.1034/j.1600-0854.2002.030204.x"

 
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 22-11-2024