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 AbstractIdentification of Bacillus velezensis SBB and Its Antifungal Effects against Verticillium dahliae    Next Abstract[Electroantennogram responses of Maruca testulalis (Lepidoptera: Pyralidae) to plant volatiles and sex pheromone] »

Biophys J


Title:"Bistability, stochasticity, and oscillations in the mitogen-activated protein kinase cascade"
Author(s):Wang X; Hao N; Dohlman HG; Elston TC;
Address:"Department of Statistics and Operations Research, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-7365, USA"
Journal Title:Biophys J
Year:2006
Volume:20051216
Issue:6
Page Number:1961 - 1978
DOI: 10.1529/biophysj.105.073874
ISSN/ISBN:0006-3495 (Print) 1542-0086 (Electronic) 0006-3495 (Linking)
Abstract:"Signaling pathways respond to stimuli in a variety of ways, depending on the magnitude of the input and the physiological status of the cell. For instance, yeast can respond to pheromone stimulation in either a binary or graded fashion. Here we present single cell transcription data indicating that a transient binary response in which all cells eventually become activated is typical. Stochastic modeling of the biochemical steps that regulate activation of the mitogen-activated protein kinase Fus3 reveals that this portion of the pathway can account for the graded-to-binary conversion. To test the validity of the model, genetic approaches are used to alter expression levels of Msg5 and Ste7, two of the proteins that negatively and positively regulate Fus3, respectively. Single cell measurements of the genetically altered cells are shown to be consistent with predictions of the model. Finally, computational modeling is used to investigate the effects of protein turnover on the response of the pathway. We demonstrate that the inclusion of protein turnover can lead to sustained oscillations of protein concentrations in the absence of feedback regulation. Thus, protein turnover can profoundly influence the output of a signaling pathway"
Keywords:"Biological Clocks/drug effects/*physiology Computer Simulation Gene Expression Regulation/drug effects/*physiology MAP Kinase Signaling System/drug effects/*physiology *Models, Biological Models, Statistical Pheromones/*pharmacology Saccharomyces cerevisi;"
Notes:"MedlineWang, Xiao Hao, Nan Dohlman, Henrik G Elston, Timothy C eng R01 GM059167/GM/NIGMS NIH HHS/ R01 GM073180/GM/NIGMS NIH HHS/ GM059167/GM/NIGMS NIH HHS/ GM073180/GM/NIGMS NIH HHS/ Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S. 2005/12/20 Biophys J. 2006 Mar 15; 90(6):1961-78. doi: 10.1529/biophysj.105.073874. Epub 2005 Dec 16"

 
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 27-12-2024