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 AbstractPreparation of Carbotrap/silica composite for needle trap field sampling of halogenated volatile organic compounds followed by gas chromatography/mass spectrometry determination    Next AbstractPheromone-binding proteins contribute to the activation of olfactory receptor neurons in the silkmoths antheraea polyphemus and Bombyx mori »

Curr Biol


Title:Regulation of cyclin-substrate docking by a G1 arrest signaling pathway and the Cdk inhibitor Far1
Author(s):Pope PA; Bhaduri S; Pryciak PM;
Address:"Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA 01605, USA. Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA 01605, USA. Electronic address: peter.pryciak@umassmed.edu"
Journal Title:Curr Biol
Year:2014
Volume:20140605
Issue:12
Page Number:1390 - 1396
DOI: 10.1016/j.cub.2014.05.002
ISSN/ISBN:1879-0445 (Electronic) 0960-9822 (Print) 0960-9822 (Linking)
Abstract:"Eukaryotic cell division is often regulated by extracellular signals. In budding yeast, signaling from mating pheromones arrests the cell cycle in G1 phase. This arrest requires the protein Far1, which is thought to antagonize the G1/S transition by acting as a Cdk inhibitor (CKI), although the mechanisms remain unresolved. Recent studies found that G1/S cyclins (Cln1 and Cln2) recognize Cdk substrates via specific docking motifs, which promote substrate phosphorylation in vivo. Here, we show that these docking interactions are inhibited by pheromone signaling and that this inhibition requires Far1. Moreover, Far1 mutants that cannot inhibit docking are defective at cell-cycle arrest. Consistent with this arrest function, Far1 outcompetes substrates for association with G1/S cyclins in vivo, and it is present in large excess over G1/S cyclins during the precommitment period where pheromone can impose G1 arrest. Finally, a comparison of substrates that do and do not require docking suggests that Far1 acts as a multimode inhibitor that antagonizes both kinase activity and substrate recognition by Cln1/2-Cdk complexes. Our findings uncover a novel mechanism of Cdk regulation by external signals and shed new light on Far1 function to provide a revised view of cell-cycle arrest in this model system"
Keywords:"Adaptor Proteins, Signal Transducing/genetics/metabolism Cell Cycle Proteins/genetics/metabolism Cyclin-Dependent Kinase Inhibitor Proteins/*genetics/metabolism Cyclin-Dependent Kinases/genetics/metabolism Cyclins/genetics/metabolism *G1 Phase *Gene Expre;"
Notes:"MedlinePope, Patricia A Bhaduri, Samyabrata Pryciak, Peter M eng R01 GM057769/GM/NIGMS NIH HHS/ GM57769/GM/NIGMS NIH HHS/ Research Support, N.I.H., Extramural England 2014/06/10 Curr Biol. 2014 Jun 16; 24(12):1390-1396. doi: 10.1016/j.cub.2014.05.002. Epub 2014 Jun 5"

 
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