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 AbstractIs Anopheles gambiae attraction to floral and human skin-based odours and their combination modulated by previous blood meal experience?    Next AbstractMeasuring and modelling VOC biotransformation rates »

Mol Cell Biol


Title:Far3 and five interacting proteins prevent premature recovery from pheromone arrest in the budding yeast Saccharomyces cerevisiae
Author(s):Kemp HA; Sprague GF;
Address:"Institute of Molecular Biology and Department of Biology, University of Oregon, Eugene, Oregon 97403-1229, USA"
Journal Title:Mol Cell Biol
Year:2003
Volume:23
Issue:5
Page Number:1750 - 1763
DOI: 10.1128/MCB.23.5.1750-1763.2003
ISSN/ISBN:0270-7306 (Print) 1098-5549 (Electronic) 0270-7306 (Linking)
Abstract:"In budding yeast, diffusible mating pheromones initiate a signaling pathway that culminates in several responses, including cell cycle arrest. Only a handful of genes required for the interface between pheromone response and the cell cycle have been identified, among them FAR1 and FAR3; of these, only FAR1 has been extensively characterized. In an effort to learn about the mechanism by which Far3 acts, we used the two-hybrid method to identify interacting proteins. We identified five previously uncharacterized open reading frames, dubbed FAR7, FAR8, FAR9, FAR10, and FAR11, that cause a far3-like pheromone arrest defect when disrupted. Using two-hybrid and coimmunoprecipitation analysis, we found that all six Far proteins interact with each other. Moreover, velocity sedimentation experiments suggest that Far3 and Far7 to Far11 form a complex. The phenotype of a sextuple far3far7-far11 mutant is no more severe than any single mutant. Thus, FAR3 and FAR7 to FAR11 all participate in the same pathway leading to G1 arrest. These mutants initially arrest in response to pheromone but resume budding after 10 h. Under these conditions, wild-type cells fail to resume budding even after several days whereas far1 mutant cells resume budding within 1 h. We conclude that the FAR3-dependent arrest pathway is functionally distinct from that which employs FAR1"
Keywords:"Amino Acid Sequence Blotting, Western Cell Cycle Cell Cycle Proteins/*metabolism Centrifugation, Density Gradient Electrophoresis, Polyacrylamide Gel G1 Phase Genotype Kinetics Models, Biological Molecular Sequence Data Mutation Phenotype Pheromones/metab;"
Notes:"MedlineKemp, Hilary A Sprague, George F Jr eng R01 GM030027/GM/NIGMS NIH HHS/ GM-30027/GM/NIGMS NIH HHS/ Research Support, U.S. Gov't, P.H.S. 2003/02/18 Mol Cell Biol. 2003 Mar; 23(5):1750-63. doi: 10.1128/MCB.23.5.1750-1763.2003"

 
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 06-07-2024