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Replication of the promiscuous plasmid pMV158 requires expression of the initiator repB gene, which is controlled by the repressor CopG. Genes repB and copG are co-transcribed from promoter P(cr). We have studied the interactions between RNA polymerase, CopG and the promoter to elucidate the mechanism of repression by CopG. Complexes formed at 0 degrees C and at 37 degrees C between RNA polymerase and P(cr) differed from each other in stability and in the extent of the DNA contacted. The 37 degrees C complex was very stable (half-life of about 3 h), and shared features with typical open complexes generated at a variety of promoters. CopG protein repressed transcription from P(cr) at two different stages in the process leading to the initiation complex. First, CopG hindered binding of RNA polymerase to the promoter. Second, CopG was able to displace RNA polymerase once the enzyme has formed a stable complex with P(cr). A model for the CopG-mediated disassembly of the stable RNA polymerase-P(cr) promoter complex is presented.
Binding Sites, Operator Regions, Genetic, Models, Genetic, DNA Footprinting, Temperature, DNA, DNA-Directed RNA Polymerases, Gene Regulation, Chromatin and Epigenetics, Binding, Competitive, Repressor Proteins, Kinetics, Promoter Regions, Genetic
Binding Sites, Operator Regions, Genetic, Models, Genetic, DNA Footprinting, Temperature, DNA, DNA-Directed RNA Polymerases, Gene Regulation, Chromatin and Epigenetics, Binding, Competitive, Repressor Proteins, Kinetics, Promoter Regions, Genetic
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