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 AbstractIncidence of antibiotic resistance and sex pheromone response among enterococci isolated from clinical human samples and from municipal waste water    Next AbstractBoron and Coumaphos Residues in Hive Materials Following Treatments for the Control of Aethina tumida Murray »

Mol Cell Biol


Title:FAR1 is required for posttranscriptional regulation of CLN2 gene expression in response to mating pheromone
Author(s):Valdivieso MH; Sugimoto K; Jahng KY; Fernandes PM; Wittenberg C;
Address:"Department of Molecular Biology, Scripps Research Institute, La Jolla, California 92037"
Journal Title:Mol Cell Biol
Year:1993
Volume:13
Issue:2
Page Number:1013 - 1022
DOI: 10.1128/mcb.13.2.1013-1022.1993
ISSN/ISBN:0270-7306 (Print) 1098-5549 (Electronic) 0270-7306 (Linking)
Abstract:"Yeast cells arrest during the G1 interval of the cell cycle in response to peptide mating pheromones. The FAR1 gene is required for cell cycle arrest but not for a number of other aspects of the pheromone response. Genetic evidence suggests that FAR1 is required specifically for inactivation of the G1 cyclin CLN2. From these observations, the FAR1 gene has been proposed to encode an element of the interface between the mating pheromone signal transduction pathway and the cell cycle regulatory apparatus. We show here that FAR1 is necessary for the decrease in CLN1 and CLN2 transcript accumulation observed in response to mating pheromone but is unnecessary for regulation of the same transcripts during vegetative growth. However, the defect in regulation of CLN1 expression is dependent upon CLN2. We show that pheromone regulates the abundance of Cln2 at a posttranscriptional level and that FAR1 is required for that regulation. From these observations, we suggest that FAR1 function is limited to posttranscriptional regulation of CLN2 expression by mating pheromone. The failure of mating pheromone to repress CLN2 transcript levels in far1 mutants can be explained by the stimulatory effect of the persistent Cln2 protein on CLN2 transcription via the CLN/CDC28-dependent feedback pathway"
Keywords:"Cell Cycle Cyclins/*genetics/metabolism Fungal Proteins/*genetics/metabolism *Gene Expression Regulation, Fungal Genes, Fungal Kinetics Mating Factor Mutation Peptides/*physiology Pheromones/*physiology Saccharomyces cerevisiae/cytology/*genetics/physiolo;"
Notes:"MedlineValdivieso, M H Sugimoto, K Jahng, K Y Fernandes, P M Wittenberg, C eng GM43487/GM/NIGMS NIH HHS/ GM46006/GM/NIGMS NIH HHS/ Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. 1993/02/01 Mol Cell Biol. 1993 Feb; 13(2):1013-22. doi: 10.1128/mcb.13.2.1013-1022.1993"

 
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 26-12-2024