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Replication and segregation of an Escherichia coli chromosome with two replication origins

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TLDR
In all strains, spatial separation of sister loci adjacent to active origins occurred shortly after their replication, independently of whether replication initiated at the normal origin, the ectopic origin, or both origins.
Abstract
Characterized bacteria, unlike eukaryotes and some archaea, initiate replication bidirectionally from a single replication origin contained within a circular or linear chromosome. We constructed Escherichia coli cells with two WT origins separated by 1 Mb in their 4.64-Mb chromosome. Productive bidirectional replication initiated synchronously at both spatially separate origins. Newly replicated DNA from both origins was segregated sequentially as replication progressed, with two temporally and spatially separate replication termination events. Replication initiation occurred at a cell volume identical to that of cells with a single WT origin, showing that initiation control is independent of cellular and chromosomal oriC concentration. Cells containing just the ectopic origin initiated bidirectional replication at the expected cell mass and at the normal cellular location of that region. In all strains, spatial separation of sister loci adjacent to active origins occurred shortly after their replication, independently of whether replication initiated at the normal origin, the ectopic origin, or both origins.

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All tangled up: how cells direct, manage and exploit topoisomerase function

TL;DR: It is shown that topoisomerase activity is indispensible to cells, but requires the transient breakage of DNA strands, which has been exploited, often for significant clinical benefit, by various exogenous agents that interfere with cell proliferation.
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Chromosome Replication and Segregation in Bacteria

TL;DR: The strategies used by chromosomes and plasmids to ensure their accurate duplication and segregation are compared and discussed and how these processes are coordinated spatially and temporally with growth and cell division are compared.
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RecA bundles mediate homology pairing between distant sisters during DNA break repair

TL;DR: An unanticipated role of RecA bundles is revealed in channelling the movement of the DNA DSB ends, thereby facilitating the long-range homology search that occurs before the strand invasion and transfer reactions.
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Emergence of antibiotic resistance from multinucleated bacterial filaments

TL;DR: The data provide a better understanding of the processes underlying the origin of resistance at the single-cell level and suggest an analogous role to the eukaryotic aneuploidy condition in cancer.
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Sizing up the bacterial cell cycle

TL;DR: This Review summarizes recent findings, presents simple classic models for cell size control, introduces high-throughput data-collection techniques, and explores the mechanisms that coordinate cell size with essential growth and cell cycle processes.
References
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Journal ArticleDOI

One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products

TL;DR: A simple and highly efficient method to disrupt chromosomal genes in Escherichia coli in which PCR primers provide the homology to the targeted gene(s), which should be widely useful, especially in genome analysis of E. coli and other bacteria.
Journal ArticleDOI

Feature point tracking and trajectory analysis for video imaging in cell biology

TL;DR: A computationally efficient, two-dimensional, feature point tracking algorithm for the automated detection and quantitative analysis of particle trajectories as recorded by video imaging in cell biology.
Journal ArticleDOI

Chromosome replication and the division cycle of Escherichia coli B/r

TL;DR: It is suggested that the replication of the bacterial genome during the division cycle of Escherichia coli Br growing with doubling times between approximately 20 and 60 minutes can be described by two constants: C and D, the time for a replication point to traverse the genome.
Journal ArticleDOI

Relationship between Cell Size and Time of Initiation of DNA Replication

TL;DR: It is calculated that the initiation of a round of DNA replication always takes place at a time when the cell mass/chromosome origin reaches a particular critical value, which provides an explanation for the increase in size of cells with increase in the rate of growth.
Journal ArticleDOI

Chromosome Replication and the Division Cycle of Escherichia coli B/r

TL;DR: Within experimental errors, DNA content was dependent only on growth rate and independent of the type of culture, the carbon source, or the addition of growth factors.
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