![]()
|
|
||||||||
J. Biol. Chem., Vol. 268, Issue 23, 16907-16916, Aug, 1993
P Sander, W Langert and K Mueller
The rrn promoter regions of Escherichia coli contain a stretch of DNA, rich
in An and Tn homopolymer sequences, which is located upstream of the tandem
promoters P1 and P2. We have studied the effects of the upstream sequence
of the rrnD operon on promoter function, using deletion variants for in
vitro transcription. The presence of the upstream activating sequence (UAS)
was found to increase P1 promoter strength without influencing P2. Two
modes of P1 activation could be distinguished: a stimulation of P1
depending on the interaction of the factor of inversion stimulation (FIS)
with the UAS (within the deletion boundaries of -50 and -112) and second, a
factor-independent activation requiring the proximal part of the UAS
(within the boundaries of -50 and -89). Both modes of activation were
previously observed in the case of the rrnB operon and were ascribed to
increased constants of RNA polymerase binding to P1 (Leirmo, S., and
Gourse, R. L. (1991) J. Mol. Biol. 220, 555-568; Zacharias, M., Theissen,
G., Bradaczek, C., and Wagner, R. (1991) Biochimie 73, 699-712). Our
results show, however, that the mechanisms of upstream activation may vary
with the reaction conditions. In a complex transcription system, originally
designed for the use of cell extracts, FIS enhances first-order reactions
that convert binary (open) complexes to transcribing complexes. Initiated
complexes are stabilized by FIS. The factor-independent mode of P1
activation involves influences of the UAS on complex isomerizations as well
as on binary complex formation. The results show that low molecular weight
components of the complex transcription system change the function of the
RNA polymerase at the rrn promoters (not at the reference promoter Ptac),
so that the conversion of open to transcribing P1-complexes becomes
dependent on the UAS and FIS.
Mechanisms of upstream activation of the rrnD promoter P1 of Escherichia coli
Institut fur Allgemeine Zoologie und Genetik, Munster, Germany.
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?
This article has been cited by other articles:
![]() |
H. Zhi, X. Wang, J. E. Cabrera, R. C. Johnson, and D. J. Jin Fis Stabilizes the Interaction between RNA Polymerase and the Ribosomal Promoter rrnB P1, Leading to Transcriptional Activation J. Biol. Chem., November 21, 2003; 278(47): 47340 - 47349. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. A. Hirvonen, W. Ross, C. E. Wozniak, E. Marasco, J. R. Anthony, S. E. Aiyar, V. H. Newburn, and R. L. Gourse Contributions of UP Elements and the Transcription Factor FIS to Expression from the Seven rrn P1 Promoters in Escherichia coli J. Bacteriol., November 1, 2001; 183(21): 6305 - 6314. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. S. Bartlett, T. Gaal, W. Ross, and R. L. Gourse Regulation of rRNA Transcription Is Remarkably Robust: FIS Compensates for Altered Nucleoside Triphosphate Sensing by Mutant RNA Polymerases at Escherichia coli rrn P1 Promoters J. Bacteriol., April 1, 2000; 182(7): 1969 - 1977. [Abstract] [Full Text] |
||||
![]() |
W. Ross, S. E. Aiyar, J. Salomon, and R. L. Gourse Escherichia coli Promoters with UP Elements of Different Strengths: Modular Structure of Bacterial Promoters J. Bacteriol., October 15, 1998; 180(20): 5375 - 5383. [Abstract] [Full Text] |
||||
![]() |
K. Fredrick and J. D. Helmann RNA polymerase sigma factor determines start-site selection but is not required for upstream promoter element activation on heteroduplex (bubble) templates PNAS, May 13, 1997; 94(10): 4982 - 4987. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| All ASBMB Journals | Molecular and Cellular Proteomics |
| Journal of Lipid Research | ASBMB Today |