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 AbstractHow does pollination mutualism affect the evolution of prior self-fertilization? A model    Next AbstractDetoxification and elimination of nicotine by nectar-feeding birds »

Eur J Biochem


Title:Neurotensin induces mating in Saccharomyces cerevisiae cells that express human neurotensin receptor type 1 in place of the endogenous pheromone receptor
Author(s):Leplatois P; Josse A; Guillemot M; Febvre M; Vita N; Ferrara P; Loison G;
Address:"Molecular and Functional Genomics Department, Sanofi-Synthelabo Recherche, Labege, France"
Journal Title:Eur J Biochem
Year:2001
Volume:268
Issue:18
Page Number:4860 - 4867
DOI: 10.1046/j.0014-2956.2001.02407.x
ISSN/ISBN:0014-2956 (Print) 0014-2956 (Linking)
Abstract:"Heterologous expression of the human neurotensin receptor type I (hNT1-R) has been achieved in the yeast Saccharomyces cerevisiae. Immunoanalysis of membranes prepared from cells expressing a c-myc-tagged version of hNT1-R revealed multiple c-myc cross-reacting polypeptides of high molecular mass, suggesting that hNT1-R was glycosylated in yeast. High-affinity binding sites for 125I-labeled-[monoiodo-Tyr3]neurotensin ([125I-Tyr3]NT) were detected on hNT1-R-expressing cells with Kd and Bmax values of 3.2 nM and of 500 receptors per cell, respectively. Competition binding studies of neurotensin with SR142948 and SR48692, two nonpeptidic antagonists of hNT1-R, indicated that the yeast-produced recombinant receptor displayed the same pharmacological properties as hNT1-R expressed in mammalian cells. Interestingly, neurotensin activated the pheromone pathway in hNT1-R-expressing cells in a dose-dependent fashion, as revealed by a beta-galactosidase activity assay with a pheromone-responsive Fus1:lacZ construct. Mutational inactivation of the SST2 and STE2 genes increased the level of beta-galactosidase activity in response to neurotensin by twofold. Recombinant hNT1-R-producing cells, which lacked the endogenous G-protein-coupled receptor for the alpha pheromone, mated with wild-type MATalpha haploid cells in response to neurotensin, leading to bona fide diploid zygote formation. This is the first report of a mammalian receptor that can replace the endogenous pheromone receptor when produced in yeast, by signaling a fully effective, agonist-induced, mating process"
Keywords:"Binding, Competitive Blotting, Western *Diploidy *Gene Deletion Gene Expression Regulation, Fungal/drug effects Genes, Reporter/genetics Heterotrimeric GTP-Binding Proteins/chemistry/metabolism Humans Mating Factor Neurotensin/antagonists & inhibitors/met;"
Notes:"MedlineLeplatois, P Josse, A Guillemot, M Febvre, M Vita, N Ferrara, P Loison, G eng England 2001/09/18 Eur J Biochem. 2001 Sep; 268(18):4860-7. doi: 10.1046/j.0014-2956.2001.02407.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 23-11-2024