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 AbstractEmission strength validation using four-dimensional data assimilation: application to primary aerosol and precursors to ozone and secondary aerosol    Next Abstract"Biogenetic study of the emissions of species: Pinus radiata, Eucalyptus globulus Labill and Alnus acuminata in Riobamba canton, Ecuador" »

Mol Microbiol


Title:Hap2 regulates the pheromone response transcription factor prf1 in Ustilago maydis
Author(s):Mendoza-Mendoza A; Eskova A; Weise C; Czajkowski R; Kahmann R;
Address:"Max-Planck-Institute for Terrestrial Microbiology, Karl-von-Frisch-Str., Marburg, Germany"
Journal Title:Mol Microbiol
Year:2009
Volume:72
Issue:3
Page Number:683 - 698
DOI: 10.1111/j.1365-2958.2009.06676.x
ISSN/ISBN:1365-2958 (Electronic) 0950-382X (Linking)
Abstract:"In Ustilago maydis the pheromone signal is transmitted via a mitogen-activated protein kinase (MAP kinase) module to the transcription factor Prf1. Prf1 activates transcription of a and b mating type genes by binding to pheromone response elements (PREs) located in regulatory regions of these genes. Here we show that the CCAAT-box binding protein Hap2 from U. maydis regulates prf1 expression. Hap2 was initially identified as a potential interaction partner of the MAP kinase Kpp6 in yeast two-hybrid screens and was subsequently also shown to interact with the MAPK Kpp2. Deletion of hap2 in haploid cells abolished mating, resulting from a defect in pheromone-induced gene expression. Crosses of haploid hap2 deletion strains were completely impaired in pathogenicity. Constitutive expression of prf1 complemented the pheromone response defect in Deltahap2 strains. Chromatin immunoprecipitation assays indicated that Hap2 binds directly to CCAAT motifs in the prf1 promoter. Point mutations in two putative MAPK phosphorylation sites in Hap2 attenuated the pheromone response. In a solopathogenic strain hap2 deletion affected filamentation and the mutants showed reduced pathogenicity symptoms. These data suggest that Hap2 is a novel regulator of prf1 with additional functions after cell fusion"
Keywords:"Chromatin Immunoprecipitation Gene Deletion Gene Expression Regulation, Fungal Genes, Mating Type, Fungal Genes, Regulator Genetic Complementation Test High Mobility Group Proteins/genetics/*metabolism Pheromones/metabolism Plant Proteins/genetics/*metabo;"
Notes:"MedlineMendoza-Mendoza, Artemio Eskova, Anastasia Weise, Carolin Czajkowski, Robert Kahmann, Regine eng Research Support, Non-U.S. Gov't England 2009/04/30 Mol Microbiol. 2009 May; 72(3):683-98. doi: 10.1111/j.1365-2958.2009.06676.x"

 
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