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 AbstractEnhancement of the deposition of ultrafine secondary organic aerosols by the negative air ion and the effect of relative humidity    Next Abstract[Competition and allelopathy of rice isogenic lines having similar genetic background but different plant morphology against weed] »

J Biol Chem


Title:Functional expression of the yeast alpha-factor receptor in Xenopus oocytes
Author(s):Yu L; Blumer KJ; Davidson N; Lester HA; Thorner J;
Address:"Division of Biology, California Institute of Technology, Pasadena 91125"
Journal Title:J Biol Chem
Year:1989
Volume:264
Issue:35
Page Number:20847 - 20850
DOI:
ISSN/ISBN:0021-9258 (Print) 0021-9258 (Linking)
Abstract:"The STE2 gene of the yeast Saccharomyces cerevisiae encodes a 431-residue polypeptide that has been shown by chemical cross-linking and genetic studies to be a component of the receptor for the peptide mating pheromone, alpha-factor. To demonstrate directly that the ligand binding site of the alpha-factor receptor is comprised solely of the STE2 gene product, the STE2 protein was expressed in Xenopus oocytes. Oocytes microinjected with synthetic STE2 mRNA displayed specific surface binding for 35S-labeled alpha-factor (up to 40 sites/micron2/ng RNA). Oocytes injected with either STE2 antisense RNA or heterologous receptor mRNA (nicotinic acetylcholine receptor alpha, beta, gamma, and delta subunit mRNAs) showed no binding activity (indistinguishable from uninjected control oocytes). The apparent KD (7 nM) of the alpha-factor binding sites expressed on the oocyte surface, determined by competition binding studies, agreed with the values reported for intact yeast cells and yeast plasma membrane fractions. These findings demonstrate that the STE2 gene product is the only yeast polypeptide required for biogenesis of a functional alpha-factor receptor. Electrophysiological measurements indicated that the membrane conductance of oocytes injected with STE2 mRNA, or with both STE2 and GPA1 (encoding a yeast G protein alpha-subunit) mRNAs, did not change and was not affected by pheromone binding. Thus, the alpha-factor receptor, like mammalian G protein-coupled receptors, apparently lacks activity as an intrinsic or ligand-gated ion channel. This report is the first instance in which a membrane-bound receptor from a unicellular eukaryote has been expressed in a vertebrate cell"
Keywords:"Animals Female *Gene Expression *Genes, Fungal Kinetics Mating Factor Oocytes/*metabolism Peptides/metabolism Pheromones/metabolism Plasmids RNA, Messenger/genetics Receptors, Cell Surface/biosynthesis/*genetics Receptors, Mating Factor *Receptors, Peptid;"
Notes:"MedlineYu, L Blumer, K J Davidson, N Lester, H A Thorner, J eng GM10991/GM/NIGMS NIH HHS/ GM21841/GM/NIGMS NIH HHS/ NS11756/NS/NINDS NIH HHS/ Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. 1989/12/15 J Biol Chem. 1989 Dec 15; 264(35):20847-50"

 
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 28-12-2024