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 AbstractPheromone induction promotes Ste11 degradation through a MAPK feedback and ubiquitin-dependent mechanism    Next AbstractOnline comprehensive two-dimensional characterization of puff-by-puff resolved cigarette smoke by hyphenation of fast gas chromatography to single-photon ionization time-of-flight mass spectrometry: quantification of hazardous volatile organic compounds »

Eukaryot Cell


Title:Pheromone-induced degradation of Ste12 contributes to signal attenuation and the specificity of developmental fate
Author(s):Esch RK; Wang Y; Errede B;
Address:"Department of Biochemistry and Biophysics, CB 7260 512 ME Jones, University of North Carolina, Chapel Hill, NC 27599-7260, USA"
Journal Title:Eukaryot Cell
Year:2006
Volume:20061013
Issue:12
Page Number:2147 - 2160
DOI: 10.1128/EC.00270-06
ISSN/ISBN:1535-9778 (Print) 1535-9786 (Electronic) 1535-9786 (Linking)
Abstract:"The Ste12 transcription factor of Saccharomyces cerevisiae regulates transcription programs controlling two different developmental fates. One is differentiation into a mating-competent form that occurs in response to mating pheromone. The other is the transition to a filamentous-growth form that occurs in response to nutrient deprivation. These two distinct roles for Ste12 make it a focus for studies into regulatory mechanisms that impart biological specificity. The transient signal characteristic of mating differentiation led us to test the hypothesis that regulation of Ste12 turnover might contribute to attenuation of the mating-specific transcription program and restrict activation of the filamentation program. We show that prolonged pheromone induction leads to ubiquitin-mediated destabilization and decreased amounts of Ste12. This depletion in pheromone-stimulated cultures is dependent on the mating-pathway-dedicated mitogen-activated protein kinase Fus3 and its target Cdc28 inhibitor, Far1. Attenuation of pheromone-induced mating-specific gene transcription (FUS1) temporally correlates with Ste12 depletion. This attenuation is abrogated in the deletion backgrounds (fus3Delta or far1Delta) where Ste12 is found to persist. Additionally, pheromone induces haploid invasion and filamentous-like growth instead of mating differentiation when Ste12 levels remain high. These observations indicate that loss of Ste12 reinforces the adaptive response to pheromone and contributes to the curtailing of a filamentation response"
Keywords:"Base Sequence Cell Cycle Proteins/genetics/metabolism Cyclin-Dependent Kinase Inhibitor Proteins DNA, Fungal/genetics Genes, Fungal Haploidy Mating Factor Mitogen-Activated Protein Kinases/genetics/metabolism Peptides/*pharmacology Repressor Proteins/gene;"
Notes:"MedlineEsch, R Keith Wang, Yuqi Errede, Beverly eng R01 GM067809/GM/NIGMS NIH HHS/ GM067809/GM/NIGMS NIH HHS/ GM39852/GM/NIGMS NIH HHS/ Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't 2006/10/17 Eukaryot Cell. 2006 Dec; 5(12):2147-60. doi: 10.1128/EC.00270-06. Epub 2006 Oct 13"

 
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 23-11-2024