Interaction of the Initiator Protein of an IncB Plasmid with Its Origin of DNA Replication
Open Access
- 1 April 2003
- journal article
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 185 (7), 2210-2218
- https://doi.org/10.1128/jb.185.7.2210-2218.2003
Abstract
The replication initiator protein RepA of the IncB plasmid pMU720 was purified and used in DNase I protection assays in vitro. RepA protected a 68-bp region of the origin of replication of pMU720. This region, which lies immediately downstream of the DnaA box, contains four copies of the sequence motif 5′AANCNGCAA3′. Mutational analyses identified this sequence as the binding site specifically recognized by RepA (the RepA box). Binding of RepA to the RepA boxes was ordered and sequential, with the box closest to the DnaA binding site (box 1) occupied first and the most distant boxes (boxes 3 and 4) occupied last. However, only boxes 1, 2, and 4 were essential for origin activity, with box 3 playing a lesser role. Changing the spacing between box 1 and the other three boxes affected binding of RepA in vitro and origin activity in vivo, indicating that the RepA molecules bound to ori B interact with one another.Keywords
This publication has 42 references indexed in Scilit:
- The Plasmid ColIb-P9 Antisense Inc RNA Controls Expression of the RepZ Replication Protein and Its Positive Regulator repYwith Different MechanismsPublished by Elsevier ,1999
- An RNA Pseudoknot as the Molecular Switch for Translation of therepZ Gene Encoding the Replication Initiator of IncIα Plasmid ColIb-P9Journal of Biological Chemistry, 1998
- A comprehensive set of DnaA‐box mutations in the replication origin, oriC, of Escherichia coliMolecular Microbiology, 1996
- A transcription terminator signal necessary for plasmid Collb-P9 replicationMolecular Microbiology, 1995
- Differential binding of wild-type and a mutant RepA protein to oriR sequence suggests a model for the initiation of plasmid R1 replicationJournal of Molecular Biology, 1992
- ColE1-type vectors with fully repressible replicationGene, 1991
- Synergy between Escherichia coli CAP protein and RNA polymerase in the lac promoter open complexJournal of Molecular Biology, 1989
- A simple and rapid method for the selection of oligodeoxynucleotide-directed mutantsGene, 1988
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976
- Sur la biosynthese de la β-galactosidase (lactase) chez Escherichia coli. La specificite de l'inductionBiochimica et Biophysica Acta, 1951