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MukBEF-dependent chromosomal organization in widened Escherichia coli

The bacterial chromosome is spatially organized through protein-mediated compaction, supercoiling, and cell-boundary confinement. Structural Maintenance of Chromosomes (SMC) complexes are a major class of chromosome-organizing proteins present throughout all domains of life. Here, we study the role...

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Autores principales: Japaridze, Aleksandre, van Wee, Raman, Gogou, Christos, Kerssemakers, Jacob W. J., van den Berg, Daan F., Dekker, Cees
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10020239/
https://www.ncbi.nlm.nih.gov/pubmed/36937278
http://dx.doi.org/10.3389/fmicb.2023.1107093
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author Japaridze, Aleksandre
van Wee, Raman
Gogou, Christos
Kerssemakers, Jacob W. J.
van den Berg, Daan F.
Dekker, Cees
author_facet Japaridze, Aleksandre
van Wee, Raman
Gogou, Christos
Kerssemakers, Jacob W. J.
van den Berg, Daan F.
Dekker, Cees
author_sort Japaridze, Aleksandre
collection PubMed
description The bacterial chromosome is spatially organized through protein-mediated compaction, supercoiling, and cell-boundary confinement. Structural Maintenance of Chromosomes (SMC) complexes are a major class of chromosome-organizing proteins present throughout all domains of life. Here, we study the role of the Escherichia coli SMC complex MukBEF in chromosome architecture and segregation. Using quantitative live-cell imaging of shape-manipulated cells, we show that MukBEF is crucial to preserve the toroidal topology of the Escherichia coli chromosome and that it is non-uniformly distributed along the chromosome: it prefers locations toward the origin and away from the terminus of replication, and it is unevenly distributed over the origin of replication along the two chromosome arms. Using an ATP hydrolysis-deficient MukB mutant, we confirm that MukBEF translocation along the chromosome is ATP-dependent, in contrast to its loading onto DNA. MukBEF and MatP are furthermore found to be essential for sister chromosome decatenation. We propose a model that explains how MukBEF, MatP, and their interacting partners organize the chromosome and contribute to sister segregation. The combination of bacterial cell-shape modification and quantitative fluorescence microscopy paves way to investigating chromosome-organization factors in vivo.
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spelling pubmed-100202392023-03-18 MukBEF-dependent chromosomal organization in widened Escherichia coli Japaridze, Aleksandre van Wee, Raman Gogou, Christos Kerssemakers, Jacob W. J. van den Berg, Daan F. Dekker, Cees Front Microbiol Microbiology The bacterial chromosome is spatially organized through protein-mediated compaction, supercoiling, and cell-boundary confinement. Structural Maintenance of Chromosomes (SMC) complexes are a major class of chromosome-organizing proteins present throughout all domains of life. Here, we study the role of the Escherichia coli SMC complex MukBEF in chromosome architecture and segregation. Using quantitative live-cell imaging of shape-manipulated cells, we show that MukBEF is crucial to preserve the toroidal topology of the Escherichia coli chromosome and that it is non-uniformly distributed along the chromosome: it prefers locations toward the origin and away from the terminus of replication, and it is unevenly distributed over the origin of replication along the two chromosome arms. Using an ATP hydrolysis-deficient MukB mutant, we confirm that MukBEF translocation along the chromosome is ATP-dependent, in contrast to its loading onto DNA. MukBEF and MatP are furthermore found to be essential for sister chromosome decatenation. We propose a model that explains how MukBEF, MatP, and their interacting partners organize the chromosome and contribute to sister segregation. The combination of bacterial cell-shape modification and quantitative fluorescence microscopy paves way to investigating chromosome-organization factors in vivo. Frontiers Media S.A. 2023-03-03 /pmc/articles/PMC10020239/ /pubmed/36937278 http://dx.doi.org/10.3389/fmicb.2023.1107093 Text en Copyright © 2023 Japaridze, van Wee, Gogou, Kerssemakers, van den Berg and Dekker. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Japaridze, Aleksandre
van Wee, Raman
Gogou, Christos
Kerssemakers, Jacob W. J.
van den Berg, Daan F.
Dekker, Cees
MukBEF-dependent chromosomal organization in widened Escherichia coli
title MukBEF-dependent chromosomal organization in widened Escherichia coli
title_full MukBEF-dependent chromosomal organization in widened Escherichia coli
title_fullStr MukBEF-dependent chromosomal organization in widened Escherichia coli
title_full_unstemmed MukBEF-dependent chromosomal organization in widened Escherichia coli
title_short MukBEF-dependent chromosomal organization in widened Escherichia coli
title_sort mukbef-dependent chromosomal organization in widened escherichia coli
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10020239/
https://www.ncbi.nlm.nih.gov/pubmed/36937278
http://dx.doi.org/10.3389/fmicb.2023.1107093
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