| Literature DB >> 25486560 |
Nicolai B Larsen1, Ian D Hickson, Hocine W Mankouri.
Abstract
The high-affinity binding of the Tus protein to specific 21-bp sequences, called Ter, causes site-specific, and polar, DNA replication fork arrest in E coli. The Tus-Ter complex serves to coordinate DNA replication with chromosome segregation in this organism. A number of recent and ongoing studies have demonstrated that Tus-Ter can be used as a heterologous tool to generate site-specific perturbation of DNA replication when reconstituted in eukaryotes. Here, we review these recent findings and explore the molecular mechanism by which Tus-Ter mediates replication fork (RF) arrest in the budding yeast, S. cerevisiae. We propose that Tus-Ter is a versatile, genetically tractable, and regulatable RF blocking system that can be utilized for disrupting DNA replication in a diverse range of host cells.Entities:
Keywords: DnaB helicase; MCM helicase; RecQ helicase; homologous recombination repair; replication fork
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Year: 2014 PMID: 25486560 PMCID: PMC4614373 DOI: 10.4161/15384101.2014.958912
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534