Literature DB >> 1629213

Upstream sequence elements required for NarL-mediated activation of transcription from the narGHJI promoter of Escherichia coli.

X R Dong1, S F Li, J A DeMoss.   

Abstract

Transcription of the narGHJI operon (encoding nitrate reductase) in Escherichia coli is primarily dependent on the activation of the pleiotropic transacting factor Fnr, which interacts with the promoter through a cis element (Fnr box) located near the transcription start site. Further stimulation of transcription occurs in the presence of nitrate and is dependent on activation of the transacting factor NarL and a cis-acting sequence (NarL box) located approximately 200 base pairs upstream from the transcription start site. To define the structure of the NarL box, alterations in the NarL box region, generated by saturation mutagenesis of the sequence from positions -184 to -202 in the narGHJI promoter of a narG::lacZ fusion-bearing plasmid, were analyzed for their effects on NarL-mediated stimulation of transcription. Single base substitutions that significantly reduced the NarL-mediated stimulation were restricted to a 6-base sequence, TACTCC, located at positions -193 to -198 in the narGHJI promoter. When 2 bases were modified, NarL-mediated stimulation was severely reduced when one or both alterations were located within the 6-base sequence. Attempts to restore NarL-mediated stimulation with an inverted NarL box were not successful. Although previous studies suggested that NarL-mediated stimulation of transcription may occur by a DNA looping mechanism, the results presented here demonstrate that it does not involve the passive formation of a simple DNA loop. Replacement of 94 or 108 bases of the approximately 150 base sequence between the Fnr box and the NarL box with an unrelated sequence resulted in elimination of NarL-mediated stimulation of transcription. Furthermore, shifting of most of the intervening sequence or defined segments of the sequence by 4 bases while maintaining the position of the NarL box relative to sequences required for Fnr-dependent, anaerobic transcription also eliminated the NarL-mediated stimulation. We conclude that in addition to the 6-base NarL box located on a specific face of the promoter DNA, the stimulation of transcription by NarL requires some specific sequences and/or higher order structure specified by the DNA that separates the NarL box from the Fnr box.

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Year:  1992        PMID: 1629213

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  20 in total

1.  Mutational scanning and affinity cleavage analysis of UhpA-binding sites in the Escherichia coli uhpT promoter.

Authors:  Igor N Olekhnovich; Robert J Kadner
Journal:  J Bacteriol       Date:  2002-05       Impact factor: 3.490

2.  Synthetic lac operator substitutions for studying the nitrate- and nitrite-responsive NarX-NarL and NarQ-NarP two-component regulatory systems of Escherichia coli K-12.

Authors:  Valley Stewart; Peggy J Bledsoe
Journal:  J Bacteriol       Date:  2003-04       Impact factor: 3.490

3.  Regulation of narK gene expression in Escherichia coli in response to anaerobiosis, nitrate, iron, and molybdenum.

Authors:  T Kolesnikow; I Schröder; R P Gunsalus
Journal:  J Bacteriol       Date:  1992-11       Impact factor: 3.490

4.  In vivo requirement of integration host factor for nar (nitrate reductase) operon expression in Escherichia coli K-12.

Authors:  R S Rabin; L A Collins; V Stewart
Journal:  Proc Natl Acad Sci U S A       Date:  1992-09-15       Impact factor: 11.205

5.  Structure modification induced in the narG promoter by binding of integration host factor and NARL-P.

Authors:  X Zhang; J A DeMoss
Journal:  J Bacteriol       Date:  1996-07       Impact factor: 3.490

6.  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

7.  Characterization of CorR, a transcriptional activator which is required for biosynthesis of the phytotoxin coronatine.

Authors:  A Peñaloza-Vázquez; C L Bender
Journal:  J Bacteriol       Date:  1998-12       Impact factor: 3.490

8.  cis- and trans-acting elements involved in regulation of aniA, the gene encoding the major anaerobically induced outer membrane protein in Neisseria gonorrhoeae.

Authors:  T C Householder; W A Belli; S Lissenden; J A Cole; V L Clark
Journal:  J Bacteriol       Date:  1999-01       Impact factor: 3.490

9.  Integration host factor is required for anaerobic pyruvate induction of pfl operon expression in Escherichia coli.

Authors:  A Sirko; E Zehelein; M Freundlich; G Sawers
Journal:  J Bacteriol       Date:  1993-09       Impact factor: 3.490

10.  Compensatory periplasmic nitrate reductase activity supports anaerobic growth of Pseudomonas aeruginosa PAO1 in the absence of membrane nitrate reductase.

Authors:  Nadine E Van Alst; Lani A Sherrill; Barbara H Iglewski; Constantine G Haidaris
Journal:  Can J Microbiol       Date:  2009-10       Impact factor: 2.419

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