Abstract
The OmpR binding sequence (OBS) in the upstream region of the ompF promoter of Escherichia coli was fused to 27 synthetic promoters. Transcription from a number of weak promoters, regardless of their sequences, was dramatically activated in the presence of OmpR, a transcriptional activator. In vivo DNA footprinting revealed that OmpR enhanced the binding of RNA polymerase to the promoters. This enhancement was essential for transcription of weak promoters, while OmpR binding to the OBS fused to a strong promoter was inhibitory for transcription. These results indicate that OmpR stabilizes the formation of an RNA polymerase-promoter complex, possibly a closed promoter complex, and that a transcription activator can serve not only as a positive but also as a negative regulator for gene expression.
MeSH Terms
Bacterial Outer Membrane Proteins/metabolism
Base Sequence
DNA-Directed RNA Polymerases/metabolism
Escherichia coli/enzymology,genetics
Molecular Sequence Data
Nucleotide Mapping
Oligonucleotide Probes/chemical synthesis
Promoter Regions, Genetic
Protein Binding
Restriction Mapping
Transcription, Genetic
Chemicals
Bacterial Outer Membrane Proteins
Oligonucleotide Probes
DNA-Directed RNA Polymerases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Tsung K
Department of Biochemistry, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey at Rutgers, Piscataway 08854.
Brissette R E
Inouye M
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