Skip Navigation

This Article
Right arrow Print PDF (1257K)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (15)
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Slany, R. K.
Right arrow Articles by Kersten, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Slany, R. K.
Right arrow Articles by Kersten, H.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1992, Vol. 20, No. 16 4193-4198
© 1992


MOLECULAR BIOLOGY

The promoter of the tgt/sec operon in Escherichia coli is preceded by an upstream activation sequence that contains a high affinity FIS binding site

Robert K. Slany and Helga Kersten*

Institut für Biochemie, Universität Erlangen-Nürnberg Fahrstrasse 17, D–8520 Erlangen, Germany

*To whom correspondence should be addressed

Received May 28, 1992. Revised July 17, 1992. Accepted July 17, 1992.

The tgt/sec operon in E.coll consists of five genes: queA, tgt, ORF12, SecD, and SecF. QueA and Tgt participate in the biosynthesis of the hypermodifled t-RNA nucleoside Queuosine, whereas SecD and SecF are involved in protein secretion. Examination of the promoter region of the operon showed structural similarity to promoter regions of the rrn-operons. An upstream activation sequence (UAS) containing a potential binding site for the factor of inversion stimulation (FIS) was found. Gel retardation assays and DNasel footprinting Indicated, that FIS binds specifically and with high affinity to a site centred at position –58. Binding of FIS caused bending of the DNA, as deduced from circular permutation analysis. Various 5' deletion mutants of the promoter region were constructed and fused to a lacZ reporter gene to determine the influence of the UAS element on the promoter strength. An approximately two-fold activation of the promoter by the UAS element was observed.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
MicrobiologyHome page
M. D. Bradley, M. B. Beach, A. P. J. de Koning, T. S. Pratt, and R. Osuna
Effects of Fis on Escherichia coli gene expression during different growth stages
Microbiology, September 1, 2007; 153(9): 2922 - 2940.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
R. K. Shultzaberger, L. R. Roberts, I. G. Lyakhov, I. A. Sidorov, A. G. Stephen, R. J. Fisher, and T. D. Schneider
Correlation between binding rate constants and individual information of E. coli Fis binding sites
Nucleic Acids Res., August 13, 2007; 35(16): 5275 - 5283.
[Abstract] [Full Text] [PDF]


Home page
J. Bacteriol.Home page
B. Esberg, H.-C. E. Leung, H.-C. T. Tsui, G. R. Björk, and M. E. Winkler
Identification of the miaB Gene, Involved in Methylthiolation of Isopentenylated A37 Derivatives in the tRNA of Salmonella typhimurium and Escherichia coli
J. Bacteriol., December 1, 1999; 181(23): 7256 - 7265.
[Abstract] [Full Text]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.