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...
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
eLife Sciences Publications Ltd
2019-08-01
|
Series: | eLife |
Subjects: | |
Online Access: | https://elifesciences.org/articles/46564 |
id |
doaj-0357fa893dde4fb7beaefa07439f4a25 |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT andreashofmann selforganisedsegregationofbacterialchromosomalorigins AT jarnomakela selforganisedsegregationofbacterialchromosomalorigins AT davidjsherratt selforganisedsegregationofbacterialchromosomalorigins AT dieterheermann selforganisedsegregationofbacterialchromosomalorigins AT seanmmurray selforganisedsegregationofbacterialchromosomalorigins |
_version_ |
1721458933580693504 |