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 AbstractDominant-negative mutants of prgX: evidence for a role for PrgX dimerization in negative regulation of pheromone-inducible conjugation    Next Abstract"Intersexual chemo-sensation in a 'visually-oriented' lizard, Anolis sagrei" »

Mol Microbiol


Title:Characterization of cis-acting prgQ mutants: evidence for two distinct repression mechanisms by Qa RNA and PrgX protein in pheromone-inducible enterococcal plasmid pCF10
Author(s):Bae T; Kozlowicz BK; Dunny GM;
Address:"Department of Microbiology, University of Minnesota, Minneapolis, MN 55455, USA"
Journal Title:Mol Microbiol
Year:2004
Volume:51
Issue:1
Page Number:271 - 281
DOI: 10.1046/j.1365-2958.2003.03832.x
ISSN/ISBN:0950-382X (Print) 0950-382X (Linking)
Abstract:"The pCF10-encoded negative regulators PrgX and Qa (prgQ antisense) RNA inhibit pCF10 transfer by blocking prgQ transcription extension past a potential transcription terminator sequence IRS1. To identify potential target sites for negative regulation, we isolated and analysed 13 cis-acting mutations in the prgXQ region. Determination of the 3' end of Qa RNA showed that eight mutations mapped in the region encoding Qa RNA. Four mutations were in the Qa promoter region and one was in IRS1. Three mutations in Qa greatly reduced the intracellular level of this RNA but did not affect that of PrgX. However, both Qa RNA and PrgX protein were reduced in three Qa promoter region mutants and the expression of prgQ transcripts extending 3' from IRS1 became constitutive. Qa RNA could mediate its negative regulatory activity in the absence of PrgX, and this activity was not abolished by cCF10, the peptide pheromone that induces pCF10 transfer. RNA analysis showed that Qa RNA abolished transcription readthrough. Based on the experimental data as well as computer analysis of predicted secondary structures of prgQ mRNA in the presence or absence of Qa, we concluded that Qa RNA is a pheromone-insensitive effector of prgQ mRNA termination or degradation at IRS1. In cells lacking a Qa target sequence, expression of PrgX repressed transcription from the prgQ promoter, and this repression was relieved by addition of exogenous cCF10. Thus, even though the synthesis of these negative regulators is coupled, they each act independently on separate targets to regulate expression of conjugation functions"
Keywords:"Bacterial Proteins/*genetics Base Sequence Enterococcus faecalis/*genetics/growth & development/physiology *Gene Expression Regulation, Bacterial Models, Molecular Molecular Sequence Data Mutagenesis Nucleic Acid Conformation Pheromones/physiology Plasmid;"
Notes:"MedlineBae, Taeok Kozlowicz, Briana K Dunny, Gary M eng GM49530/GM/NIGMS NIH HHS/ T32 GM08347/GM/NIGMS NIH HHS/ Research Support, U.S. Gov't, P.H.S. England 2003/12/04 Mol Microbiol. 2004 Jan; 51(1):271-81. doi: 10.1046/j.1365-2958.2003.03832.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