The Rep protein binding elements of the plasmid ColE2-P9 replication origin

• Published in: Biochemical and biophysical research communications Vol. 345; no. 2; pp. 872 - 877
• Main Authors: Yagura, Masaru, Itoh, Tateo
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 30.06.2006
• Subjects: Amino Acid Sequence; Base Sequence; ColE2; DNA replication; DNA Replication - genetics; DNA–protein interaction; Escherichia coli Proteins - chemistry; Escherichia coli Proteins - genetics; Escherichia coli Proteins - metabolism; Fungal Proteins - chemistry; Fungal Proteins - metabolism; Gel mobility shift assay; Initiator protein; Molecular Sequence Data; Mutagenesis; Plasmid; Plasmids - genetics; Plasmids - metabolism; Protein Binding; Replication origin; Replication Origin - genetics; SELEX experiment; Trans-Activators - chemistry; Trans-Activators - genetics; Trans-Activators - metabolism; Plasmid; Replication origin; DNA replication; Mutagenesis; Initiator protein; SELEX experiment; ColE2; DNA–protein interaction; Gel mobility shift assay
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2006.04.168

The plasmid ColE2-P9 (ColE2) origin (32 bp) is specifically recognized by the plasmid-specified Rep protein that initiates DNA replication. The ColE2 origin is divided into at least three functional subregions (I, II, and III), and three sites (a, b, and c) found in subregions I and II play important roles in Rep protein binding. We performed SELEX experiments of plasmid ColE2 to determine the optimal sequences for specific binding of the Rep protein. From these experiments, we obtained a common 16-bp sequence (5′-TGAGACCANATAAGCC-3′), which corresponds to about one half of the minimal ColE2 origin and contains sites a and b. Gel mobility shift assays using single-point mutant origins and the Rep protein further indicated that high affinity sequence-specific recognition by the Rep protein requires sites a, b, and c, but that mutations in site c were less disruptive to this recognition than those in sites a and b.