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Origins Left, Right, and Centre: Increasing the Number of Initiation Sites in the Chromosome

Overview
Journal Genes (Basel)
Publisher MDPI
Date 2018 Aug 1
PMID 30060465
Citations 17
Authors
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Abstract

The bacterium contains a single circular chromosome with a defined architecture. DNA replication initiates at a single origin called Two replication forks are assembled and proceed in opposite directions until they fuse in a specialised zone opposite the origin. This termination area is flanked by polar replication fork pause sites that allow forks to enter, but not to leave. Thus, the chromosome is divided into two replichores, each replicated by a single replication fork. Recently, we analysed the replication parameters in cells, in which an ectopic origin termed was integrated in the right-hand replichore. Two major obstacles to replication were identified: (1) head-on replication⁻transcription conflicts at highly transcribed operons, and (2) the replication fork trap. Here, we describe replication parameters in cells with ectopic origins, termed and , integrated into the left-hand replichore, and a triple origin construct with integrated in the left-hand and in the right-hand replichore. Our data again highlight both replication⁻transcription conflicts and the replication fork trap as important obstacles to DNA replication, and we describe a number of spontaneous large genomic rearrangements which successfully alleviate some of the problems arising from having an additional origin in an ectopic location. However, our data reveal additional factors that impact efficient chromosome duplication, highlighting the complexity of chromosomal architecture.

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References
1.
Babu V, Itsko M, Baxter J, Schaaper R, Sutton M . Insufficient levels of the nrdAB-encoded ribonucleotide reductase underlie the severe growth defect of the Δhda E. coli strain. Mol Microbiol. 2017; 104(3):377-399. PMC: 5397354. DOI: 10.1111/mmi.13632. View

2.
Dimude J, Stockum A, Midgley-Smith S, Upton A, Foster H, Khan A . The Consequences of Replicating in the Wrong Orientation: Bacterial Chromosome Duplication without an Active Replication Origin. mBio. 2015; 6(6):e01294-15. PMC: 4631800. DOI: 10.1128/mBio.01294-15. View

3.
Wendel B, Courcelle C, Courcelle J . Completion of DNA replication in Escherichia coli. Proc Natl Acad Sci U S A. 2014; 111(46):16454-9. PMC: 4246274. DOI: 10.1073/pnas.1415025111. View

4.
Roth A, Messer W . High-affinity binding sites for the initiator protein DnaA on the chromosome of Escherichia coli. Mol Microbiol. 1998; 28(2):395-401. DOI: 10.1046/j.1365-2958.1998.00813.x. View

5.
Neylon C, Kralicek A, Hill T, Dixon N . Replication termination in Escherichia coli: structure and antihelicase activity of the Tus-Ter complex. Microbiol Mol Biol Rev. 2005; 69(3):501-26. PMC: 1197808. DOI: 10.1128/MMBR.69.3.501-526.2005. View