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 AbstractCompetent but complex communication: The phenomena of pheromone-responsive plasmids    Next AbstractCyclin B proteolysis and the cyclin-dependent kinase inhibitor rum1p are required for pheromone-induced G1 arrest in fission yeast »

EMBO J


Title:Fission yeast pheromone blocks S-phase by inhibiting the G1 cyclin B-p34cdc2 kinase
Author(s):Stern B; Nurse P;
Address:"Cell Cycle Laboratory, Imperial Cancer Research Fund, London, UK"
Journal Title:EMBO J
Year:1997
Volume:16
Issue:3
Page Number:534 - 544
DOI: 10.1093/emboj/16.3.534
ISSN/ISBN:0261-4189 (Print) 1460-2075 (Electronic) 0261-4189 (Linking)
Abstract:"Yeast pheromones block cell cycle progression in G1 in order to prepare mating partners for conjugation. We have investigated the mechanism underlying pheromone-induced G1 arrest in the fission yeast Schizosaccharomyces pombe. We find that the G1-specific transcription factor p65cdc10-p72res1/sct1 which controls the expression of S-phase genes is fully activated in pheromone, unlike the analogous control in budding yeast. In contrast, the G1 function of p34cdc2 acting after activation of the G1-specific transcription is blocked. Pheromone inhibits the p34cdc2 kinase associated with both the G1-specific B-type cyclin p45cig2 and the B-type cyclin p56cdc13 and overexpression of p45cig2 or p47cdc13delta90 overcomes the pheromone-induced G1 arrest. G1 arrest is compromised in enlarged cells. We suggest that onset of S-phase is controlled by pheromone inhibiting the B-cyclin-associated kinase in G1, and that increasing cell size contributes to the mechanism for pheromone adaptation. Thus, pheromone in fission and budding yeast acts similarly in inhibiting the G1 cyclin-dependent kinase (CDK), but differs in its effects on the G1/S transcriptional control, suggesting that inhibition of CDKs may be a more general mechanism for the control of G1 progression compared with G1/S transcriptional control"
Keywords:"Blotting, Northern CDC2 Protein Kinase/*metabolism Cell Count/drug effects Cell Cycle/drug effects/physiology Cell Size/drug effects Cyclin B Cyclin-Dependent Kinases/*antagonists & inhibitors/metabolism Cyclins/*metabolism DNA/analysis Enzyme Inhibitors/;"
Notes:"MedlineStern, B Nurse, P eng Research Support, Non-U.S. Gov't England 1997/02/03 EMBO J. 1997 Feb 3; 16(3):534-44. doi: 10.1093/emboj/16.3.534"

 
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 22-11-2024