Expression and regulation of the RepA protein of the RepFIB replicon from plasmid P307

A. J. Spiers, P. L. Bergquist*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

11 Citations (Scopus)


The control of RepFIB replication appears to rely on the interaction between an initiator protein (RepA) and two sets of DNA repeat elements located on either side of the repA gene. Limited N-terminal sequence information obtained from a RepA:β-galactosidase fusion protein indicates that although the first residue of RepA is methionine, the initiation of translation of RepA occurs from a CTG codon rather than from the predicted GTG codon located further downstream. Overexpressed RepA in trans is capable of repressing a repA:lacZ fusion plasmid in which the expression of the fusion protein is under the control of the repA promoter. The repA promoter has been located functionally by testing a series of repA:lacZ fusion plasmids. Both in vivo genetic tests and in vitro DNA-binding studies indicate that repA autoregulation can be achieved by RepA binding to one or more repeat elements which overlap the repA promoter sequence.

Original languageEnglish
Pages (from-to)7533-7541
Number of pages9
JournalJournal of Bacteriology
Issue number23
Publication statusPublished - 1992
Externally publishedYes


Dive into the research topics of 'Expression and regulation of the RepA protein of the RepFIB replicon from plasmid P307'. Together they form a unique fingerprint.

Cite this