Literature DB >> 9000616

On the role of the multiple regulatory elements involved in the activation of the Escherichia coli malEp promoter.

E Richet1.   

Abstract

Activation of malEp and malKp, two divergent promoters from Escherichia coli, depends on the synergistic action of MalT and CRP. The reaction involves a common regulatory region located in between and comprising multiple binding elements for both regulatory proteins. The binding of MalT and CRP to this region is known to result in the formation of a higher-order structure that is responsible for malKp activation. This paper presents genetic data which together with previous results, provide compelling evidence that this higher-order structure is also responsible for malEp activation. The role(s) that this structure or elements thereof play in the activation of malEp is analysed by monitoring both the occupancy of the proximal MalT sites (sites 1 and 2) and the activity of different malEp variants in strains containing increasing amounts of active MalT. A truncated malEp promoter comprising only MalT sites 1 and 2 forms a minimal MalT-dependent promoter whose activity is limited by the occupancy of these sites. One role of the higher-order structure formed by MalT and CRP when bound to the entire regulatory region is to ensure high occupation of MalT sites 1 and 2, but it is not its only function. Some elements of this structure, namely the CRP site 1, located at -76.5, and the distal MalT sites, seem to play a direct role in malEp activation besides their participation in the assembly of the higher-order structure.

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Year:  1996        PMID: 9000616     DOI: 10.1006/jmbi.1996.0682

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  14 in total

1.  The N terminus of the Escherichia coli transcription activator MalT is the domain of interaction with MalY.

Authors:  Anja Schlegel; Olivier Danot; Evelyne Richet; Thomas Ferenci; Winfried Boos
Journal:  J Bacteriol       Date:  2002-06       Impact factor: 3.490

2.  Synergistic transcription activation: a dual role for CRP in the activation of an Escherichia coli promoter depending on MalT and CRP.

Authors:  E Richet
Journal:  EMBO J       Date:  2000-10-02       Impact factor: 11.598

3.  Genome-wide transcriptional profiling of the Escherichia coli response to a proline-rich antimicrobial peptide.

Authors:  Linda Tomasinsig; Marco Scocchi; Romina Mettulio; Margherita Zanetti
Journal:  Antimicrob Agents Chemother       Date:  2004-09       Impact factor: 5.191

4.  Physical limits on cooperative protein-DNA binding and the kinetics of combinatorial transcription regulation.

Authors:  Nico Geisel; Ulrich Gerland
Journal:  Biophys J       Date:  2011-10-05       Impact factor: 4.033

5.  Conserved motifs involved in ATP hydrolysis by MalT, a signal transduction ATPase with numerous domains from Escherichia coli.

Authors:  Emélie Marquenet; Evelyne Richet
Journal:  J Bacteriol       Date:  2010-08-06       Impact factor: 3.490

6.  Constitutive expression of the maltoporin LamB in the absence of OmpR damages the cell envelope.

Authors:  Sylvia A Reimann; Alan J Wolfe
Journal:  J Bacteriol       Date:  2010-12-03       Impact factor: 3.490

7.  Fnr, NarP, and NarL regulation of Escherichia coli K-12 napF (periplasmic nitrate reductase) operon transcription in vitro.

Authors:  A J Darwin; E C Ziegelhoffer; P J Kiley; V Stewart
Journal:  J Bacteriol       Date:  1998-08       Impact factor: 3.490

8.  H-NS and StpA proteins stimulate expression of the maltose regulon in Escherichia coli.

Authors:  J Johansson; B Dagberg; E Richet; B E Uhlin
Journal:  J Bacteriol       Date:  1998-12       Impact factor: 3.490

Review 9.  Linkage map of Escherichia coli K-12, edition 10: the traditional map.

Authors:  M K Berlyn
Journal:  Microbiol Mol Biol Rev       Date:  1998-09       Impact factor: 11.056

10.  Glycerol-3-phosphate-induced catabolite repression in Escherichia coli.

Authors:  Tanja Eppler; Pieter Postma; Alexandra Schütz; Uwe Völker; Winfried Boos
Journal:  J Bacteriol       Date:  2002-06       Impact factor: 3.490

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