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 AbstractInferring the origin of rare fruit distillates from compositional data using multivariate statistical analyses and the identification of new flavour constituents    Next AbstractAnalysis of the GC-MS of volatile compounds and the phytochemical profile and antioxidant activities of some Bulgarian medicinal plants »

Int J Biochem Cell Biol


Title:Endocytosis of the AT1A angiotensin receptor is independent of ubiquitylation of its cytoplasmic serine/threonine-rich region
Author(s):Mihalik B; Gaborik Z; Varnai P; Clark AJ; Catt KJ; Hunyady L;
Address:"Department of Physiology, Faculty of Medicine, Semmelweis University, P.O. Box 259, H-1444 Budapest, Hungary"
Journal Title:Int J Biochem Cell Biol
Year:2003
Volume:35
Issue:6
Page Number:992 - 1002
DOI: 10.1016/s1357-2725(02)00277-7
ISSN/ISBN:1357-2725 (Print) 1357-2725 (Linking)
Abstract:"Agonist-induced internalisation of the rat type 1A (AT(1A)) angiotensin II receptor is associated with phosphorylation of a serine/threonine-rich region in its cytoplasmic tail. In yeast, hyperphosphorylation of the alpha-factor pheromone receptor regulates endocytosis of the receptor by facilitating the monoubiquitylation of its cytoplasmic tail on lysine residues. The role of receptor ubiquitylation in AT(1A) receptor internalisation was evaluated by deletion or replacement of lysine residues in its agonist-sensitive serine/threonine-rich region. Expression of such receptor mutants in CHO cells showed that these modifications had no detectable effect on the angiotensin II-induced endocytosis of the AT(1A) receptor. Furthermore, fusion of ubiquitin in-frame to an internalisation-deficient AT(1A) receptor mutant with a truncated carboxyl-terminal tail did not restore the endocytosis of the resulting chimeric receptor. No impairment of receptor internalisation was observed after substitution of all lysine residues in the serine/threonine-rich region at saturating angiotensin II concentrations, where endocytosis occurs by a beta-arrestin and dynamin independent mechanism. Taken together, these data demonstrate that ubiquitylation of the cytoplasmic serine/threonine-rich region of the AT(1A) receptor on lysine residues is not required for its agonist-induced internalisation, and suggest that endocytosis of mammalian G protein-coupled receptors (GPCRs) occurs by a different mechanism than that of yeast GPCRs"
Keywords:"Amino Acid Sequence Angiotensin II/*metabolism Animals CHO Cells Cricetinae Endocytosis/*physiology Molecular Sequence Data Mutagenesis Receptor, Angiotensin, Type 1 Receptors, Angiotensin/genetics/*metabolism Serine/genetics/*metabolism Threonine/genetic;"
Notes:"MedlineMihalik, Balazs Gaborik, Zsuzsanna Varnai, Peter Clark, Adrian J L Catt, Kevin J Hunyady, Laszlo eng Research Support, Non-U.S. Gov't Netherlands 2003/04/05 Int J Biochem Cell Biol. 2003 Jun; 35(6):992-1002. doi: 10.1016/s1357-2725(02)00277-7"

 
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