Tracking of controlled Escherichia coli replication fork stalling and restart at repressor-bound DNA in vivo.

Journal article

We report an efficient, controllable, site-specific replication roadblock that blocks cell proliferation, but which can be rapidly and efficiently reversed, leading to recovery of viability. Escherichia coli replication forks of both polarities stalled in vivo within the first 500 bp of a 10 kb repressor-bound array of operator DNA-binding sites. Controlled release of repressor binding led to rapid restart of the blocked replication fork without the participation of homologous recombination. Cytological tracking of fork stalling and restart showed that the replisome-associated SSB protein remains associated with the blocked fork for extended periods and that duplication of the fluorescent foci associated with the blocked operator array occurs immediately after restart, thereby demonstrating a lack of sister cohesion in the region of the array. Roadblocks positioned near oriC or the dif site did not prevent replication and segregation of the rest of the chromosome.

Authors: Possoz, C; Filipe, SR; Grainge, I; Sherratt, D

• Publication status: Published
• Journal: EMBO journal
• Volume: 25
• Issue: 11
• Pages: 2596-2604
• Publication date: 2006-06-01
• DOI: 10.1038/sj.emboj.7601155
• EISSN: 1460-2075
• ISSN: 0261-4189
• Language: English
• Keywords: DNA Replication; Operator Regions, Genetic; Escherichia coli; Recombinant Fusion Proteins; Cell Survival; Terminator Regions, Genetic; Replication Origin; Cell Proliferation; Tetracyclines; Nucleic Acid Conformation; Repressor Proteins; Exodeoxyribonuclease V; Escherichia coli Proteins; Recombination, Genetic; DNA, Bacterial; Rec A Recombinases