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Microbiology 155 (2009), 3070-3082; DOI  10.1099/mic.0.030080-0
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Microbiology 155 (2009), 3070-3082; DOI  10.1099/mic.0.030080-0
© 2009 Society for General Microbiology

Effects of oriC relocation on control of replication initiation in Bacillus subtilis

Shigeki Moriya1, Yoshikazu Kawai2, Sakiko Kaji3, Adrian Smith4, Elizabeth J. Harry1 and Jeffery Errington2

1 Institute for the Biotechnology of Infectious Diseases, University of Technology Sydney, PO Box 123, Broadway, NSW 2007, Australia
2 Institute for Cell and Molecular Biosciences, University of Newcastle, Framlington Place, Newcastle NE2 4HH, UK
3 Graduate School of Biological Sciences, Nara Institute of Science and Technology, 8916-5 Takayama, Ikoma, Nara 630-0192, Japan
4 Centenary Institute of Cancer Medicine and Cell Biology, University of Sydney, Locked Bag No. 6, Newtown, NSW 2042, Australia

In bacteria, DNA replication initiation is tightly regulated in order to coordinate chromosome replication with cell growth. In Escherichia coli, positive factors and negative regulatory mechanisms playing important roles in the strict control of DNA replication initiation have been reported. However, it remains unclear how bacterial cells recognize the right time for replication initiation during the cell cycle. In the Gram-positive bacterium Bacillus subtilis, much less is known about the regulation of replication initiation, specifically, regarding negative control mechanisms which ensure replication initiation only once per cell cycle. Here we report that replication initiation was greatly enhanced in strains that had the origin of replication (oriC) relocated to various loci on the chromosome. When oriC was relocated to new loci further than 250 kb counterclockwise from the native locus, replication initiation became asynchronous and earlier than in the wild-type cells. In two oriC-relocated strains (oriC at argG or pnbA, 25 ° or 30 ° on the 36 ° chromosome map, respectively), DnaA levels were higher than in the wild-type but not enough to cause earlier initiation of replication. Our results suggest that the initiation capacity of replication is accumulated well before the actual time of initiation, and its release may be suppressed by a unique DNA structure formed near the native oriC locus.

Correspondence
Shigeki Moriya
shigeki.moriya{at}y8.dion.ne.jp


Abbreviations: DAPI, 4',6-diamidino-2-phenylindole; PLR, polar localization region

A supplementary table, listing nucleotide sequences of primers used in this study, is available with the online version of this paper.







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