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Open AccessJournal ArticleDOI

Organization and segregation of bacterial chromosomes

Xindan Wang, +2 more
- 01 Mar 2013 - 
- Vol. 14, Iss: 3, pp 191-203
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TLDR
It is argued that the key feature of compaction is the orderly folding of DNA along adjacent segments and that this organization provides easy and efficient access for protein–DNA transactions and has a central role in driving segregation.
Abstract
The bacterial chromosome must be compacted more than 1,000-fold to fit into the compartment in which it resides. How it is condensed, organized and ultimately segregated has been a puzzle for over half a century. Recent advances in live-cell imaging and genome-scale analyses have led to new insights into these problems. We argue that the key feature of compaction is the orderly folding of DNA along adjacent segments and that this organization provides easy and efficient access for protein-DNA transactions and has a central role in driving segregation. Similar principles and common proteins are used in eukaryotes to condense and to resolve sister chromatids at metaphase.

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How to get (a)round: mechanisms controlling growth and division of coccoid bacteria

TL;DR: Recent progress that has advanced knowledge of the complex mechanisms for chromosome segregation and cell division in bacteria which have, deceptively, the simplest possible shape: the cocci are discussed.
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Multiscale Structuring of the E. coli Chromosome by Nucleoid-Associated and Condensin Proteins

TL;DR: This work investigates the higher-order architecture of the Escherichia coli genome, showing its partition into two structurally distinct entities by a complex and intertwined network of contacts: the replication terminus (ter) region and the rest of the chromosome.
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Exploring bacterial cell biology with single-molecule tracking and super-resolution imaging

TL;DR: This Review considers what single-molecule fluorescence tracking and super-resolution imaging have taught us about the bacterial cytoskeleton, nucleoid organization and the dynamic processes of transcription and translation, and highlights the methodological improvements that are needed to address a number of experimental challenges.
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Broken detailed balance and non-equilibrium dynamics in living systems: a review

TL;DR: A more recent approach to detect actively driven dynamics, which is based on inferring broken detailed balance constitutes a non-invasive method that uses time-lapse microscopy data, and can be applied to a broad range of systems in cells and tissue.
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Evidence for a DNA-relay mechanism in ParABS-mediated chromosome segregation

TL;DR: This work combines biochemical approaches, quantitative imaging and mathematical modeling to examine the mechanism by which ParA drives the translocation of the ParB/parS partition complex in Caulobacter crescentus, suggesting a novel 'DNA-relay' mechanism in which the chromosome plays a mechanical function.
References
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Journal ArticleDOI

Capturing Chromosome Conformation

TL;DR: Using the yeast Saccharomyces cerevisiae, this work could confirm known qualitative features of chromosome organization within the nucleus and dynamic changes in that organization during meiosis and found that chromatin is highly flexible throughout.
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Macromolecular Crowding and Confinement: Biochemical, Biophysical, and Potential Physiological Consequences*

TL;DR: Theoretical and experimental approaches to the characterization of crowding- and confinement-induced effects in systems approaching the complexity of living organisms are suggested.
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Cohesins: chromosomal proteins that prevent premature separation of sister chromatids

TL;DR: Three chromosmal proteins that prevent premature separation of sister chromatids in yeast are described, two of which are members of the SMC family, which are putative ATPases with coiled-coil domains.
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