Self-organised segregation of bacterial chromosomal origins

The chromosomal replication origin region (ori) of characterised bacteria is dynamically positioned throughout the cell cycle. In slowly growing Escherichia coli, ori is maintained at mid-cell from birth until its replication, after which newly replicated sister oris move to opposite quarter positio...

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Main Authors: Andreas Hofmann, Jarno Mäkelä, David J Sherratt, Dieter Heermann, Seán M Murray
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2019-08-01
Series:eLife
Subjects:
SMC
Online Access:https://elifesciences.org/articles/46564
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spelling doaj-0357fa893dde4fb7beaefa07439f4a252021-05-05T17:49:58ZengeLife Sciences Publications LtdeLife2050-084X2019-08-01810.7554/eLife.46564Self-organised segregation of bacterial chromosomal originsAndreas Hofmann0https://orcid.org/0000-0002-4800-8429Jarno Mäkelä1https://orcid.org/0000-0003-1844-2619David J Sherratt2https://orcid.org/0000-0002-2104-5430Dieter Heermann3Seán M Murray4https://orcid.org/0000-0002-2260-0774Institute for Theoretical Physics, Heidelberg University, Heidelberg, GermanyDepartment of Biochemistry, University of Oxford, Oxford, United KingdomDepartment of Biochemistry, University of Oxford, Oxford, United KingdomInstitute for Theoretical Physics, Heidelberg University, Heidelberg, GermanyMax Planck Institute for Terrestrial Microbiology, LOEWE Centre for Synthetic Microbiology (SYNMIKRO), Marburg, GermanyThe chromosomal replication origin region (ori) of characterised bacteria is dynamically positioned throughout the cell cycle. In slowly growing Escherichia coli, ori is maintained at mid-cell from birth until its replication, after which newly replicated sister oris move to opposite quarter positions. Here, we provide an explanation for ori positioning based on the self-organisation of the Structural Maintenance of Chromosomes complex, MukBEF, which forms dynamically positioned clusters on the chromosome. We propose that a non-trivial feedback between the self-organising gradient of MukBEF complexes and the oris leads to accurate ori positioning. We find excellent agreement with quantitative experimental measurements and confirm key predictions. Specifically, we show that oris exhibit biased motion towards MukBEF clusters, rather than mid-cell. Our findings suggest that MukBEF and oris act together as a self-organising system in chromosome organisation-segregation and introduces protein self-organisation as an important consideration for future studies of chromosome dynamics.https://elifesciences.org/articles/46564self-organisationSMCchromosome organisationTuring patterning
collection DOAJ
language English
format Article
sources DOAJ
author Andreas Hofmann
Jarno Mäkelä
David J Sherratt
Dieter Heermann
Seán M Murray
spellingShingle Andreas Hofmann
Jarno Mäkelä
David J Sherratt
Dieter Heermann
Seán M Murray
Self-organised segregation of bacterial chromosomal origins
eLife
self-organisation
SMC
chromosome organisation
Turing patterning
author_facet Andreas Hofmann
Jarno Mäkelä
David J Sherratt
Dieter Heermann
Seán M Murray
author_sort Andreas Hofmann
title Self-organised segregation of bacterial chromosomal origins
title_short Self-organised segregation of bacterial chromosomal origins
title_full Self-organised segregation of bacterial chromosomal origins
title_fullStr Self-organised segregation of bacterial chromosomal origins
title_full_unstemmed Self-organised segregation of bacterial chromosomal origins
title_sort self-organised segregation of bacterial chromosomal origins
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2019-08-01
description The chromosomal replication origin region (ori) of characterised bacteria is dynamically positioned throughout the cell cycle. In slowly growing Escherichia coli, ori is maintained at mid-cell from birth until its replication, after which newly replicated sister oris move to opposite quarter positions. Here, we provide an explanation for ori positioning based on the self-organisation of the Structural Maintenance of Chromosomes complex, MukBEF, which forms dynamically positioned clusters on the chromosome. We propose that a non-trivial feedback between the self-organising gradient of MukBEF complexes and the oris leads to accurate ori positioning. We find excellent agreement with quantitative experimental measurements and confirm key predictions. Specifically, we show that oris exhibit biased motion towards MukBEF clusters, rather than mid-cell. Our findings suggest that MukBEF and oris act together as a self-organising system in chromosome organisation-segregation and introduces protein self-organisation as an important consideration for future studies of chromosome dynamics.
topic self-organisation
SMC
chromosome organisation
Turing patterning
url https://elifesciences.org/articles/46564
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AT dieterheermann selforganisedsegregationofbacterialchromosomalorigins
AT seanmmurray selforganisedsegregationofbacterialchromosomalorigins
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