Shaping the landscape of theEscherichia colichromosome: replication-transcription encounters in cells with an ectopic replication origin
Author(s) -
Darja Ivanova,
Toni S. Taylor,
Sarah Smith,
Juachi U. Dimude,
Amy L. Upton,
Mana M. Mehrjouy,
Ole Skovgaard,
David J. Sherratt,
Renata Retkutė,
Christian Rudolph
Publication year - 2015
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gkv704
Subject(s) - biology , transcription (linguistics) , dna replication , genetics , origin of replication , origin recognition complex , control of chromosome duplication , pre replication complex , eukaryotic dna replication , gene , philosophy , linguistics
Each cell division requires the unwinding of millions of DNA base pairs to allow chromosome duplication and gene transcription. As DNA replication and transcription share the same template, conflicts between both processes are unavoidable and head-on collisions are thought to be particularly problematic. Surprisingly, a recent study reported unperturbed cell cycle progression in Escherichia coli cells with an ectopic replication origin in which highly transcribed rrn operons were forced to be replicated opposite to normal. In this study we have re-generated a similar strain and found the doubling time to be twice that of normal cells. Replication profiles of this background revealed significant deviations in comparison to wild-type profiles, particularly in highly transcribed regions and the termination area. These deviations were alleviated by mutations that either inactivate the termination area or destabilise RNA polymerase complexes and allow their easier displacement by replication forks. Our data demonstrate that head-on replication-transcription conflicts are highly problematic. Indeed, analysis of the replication profile of the previously published E. coli construct revealed a chromosomal rearrangement that alleviates replication-transcription conflicts in an intriguingly simple way. Our data support the idea that avoiding head-on collisions has significantly contributed to shaping the distinct architecture of bacterial chromosomes.
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