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. 1992 Jul;174(14):4777–4782. doi: 10.1128/jb.174.14.4777-4782.1992

Identification of a novel promoter in the replication control region of plasmid R6K.

P Mukerji 1, A Greener 1, M Filutowicz 1
PMCID: PMC206275  PMID: 1624464

Abstract

A novel source of transcription has been detected in the replication region of plasmid R6K by using fusions involving the galK reporter gene. The -35 and -10 consensus RNA polymerase binding sites were identified in the region overlapping the binding sites for the R6K-encoded replication protein pi. Transcription from this promoter, designated P2, is repressed in vivo by pi-protein levels that are inhibitory for replication. Promoter-down mutations in P2 induced in vitro by bisulfite mutagenesis result in a reduced copy number of a beta-replicon but not of a gamma-replicon. Implications of the role of P2 in R6K replication are discussed.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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