Abstract

The bacterium Escherichia coli contains a single circular chromosome with a defined architecture. DNA replication initiates at a single origin called oriC. 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 E. coli cells, in which an ectopic origin termed oriZ was integrated in the right-hand replichore. Two major obstacles to replication were identified: (1) head-on replication–transcription conflicts at highly transcribed rrn operons, and (2) the replication fork trap. Here, we describe replication parameters in cells with ectopic origins, termed oriX and oriY, integrated into the left-hand replichore, and a triple origin construct with oriX integrated in the left-hand and oriZ 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.

Highlights

  • The ability to accurately duplicate the genetic material and faithfully transmit it to daughter cells is a fundamental necessity of life

  • In Escherichia coli, initiation of DNA replication at origin per chromosome (oriC) is tightly controlled by the main initiator protein DnaA, which facilitates recruitment of two replisomes [2,5,6,7]

  • Our previous study had identified rrn operons C, A, B, E, and H as major obstacles to the progression of replication forks coming from the ectopic origin [18]

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Summary

Introduction

The ability to accurately duplicate the genetic material and faithfully transmit it to daughter cells is a fundamental necessity of life. An important regulatory step for the initiation of the DNA duplication process in all organisms is the assembly of fully functional replisomes at defined origin sequences [1,2]. In Escherichia coli, initiation of DNA replication at oriC is tightly controlled by the main initiator protein DnaA, which facilitates recruitment of two replisomes [2,5,6,7]. These replisomes proceed in opposite directions around the circular chromosome with very high speed and accuracy until they eventually fuse within a specialised termination area opposite the origin (Figure 1A) [8,9].

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