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Nonrandom segregation of sister chromosomes by Escherichia coli MukBEF

Structural maintenance of chromosomes (SMC) complexes contribute to chromosome organization in all domains of life. In Escherichia coli, MukBEF, the functional SMC homolog, promotes spatiotemporal chromosome organization and faithful chromosome segregation. Here, we address the relative contribution...

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Autores principales: Mäkelä, Jarno, Uphoff, Stephan, Sherratt, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8379921/
https://www.ncbi.nlm.nih.gov/pubmed/34385314
http://dx.doi.org/10.1073/pnas.2022078118
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author Mäkelä, Jarno
Uphoff, Stephan
Sherratt, David J.
author_facet Mäkelä, Jarno
Uphoff, Stephan
Sherratt, David J.
author_sort Mäkelä, Jarno
collection PubMed
description Structural maintenance of chromosomes (SMC) complexes contribute to chromosome organization in all domains of life. In Escherichia coli, MukBEF, the functional SMC homolog, promotes spatiotemporal chromosome organization and faithful chromosome segregation. Here, we address the relative contributions of MukBEF and the replication terminus (ter) binding protein, MatP, to chromosome organization–segregation. We show that MukBEF, but not MatP, is required for the normal localization of the origin of replication to midcell and for the establishment of translational symmetry between newly replicated sister chromosomes. Overall, chromosome orientation is normally maintained through division from one generation to the next. Analysis of loci flanking the replication termination region (ter), which demark the ends of the linearly organized portion of the nucleoid, demonstrates that MatP is required for maintenance of chromosome orientation. We show that DNA-bound β(2)-processivity clamps, which mark the lagging strands at DNA replication forks, localize to the cell center, independent of replisome location but dependent on MukBEF action, and consistent with translational symmetry of sister chromosomes. Finally, we directly show that the older (“immortal”) template DNA strand, propagated from previous generations, is preferentially inherited by the cell forming at the old pole, dependent on MukBEF and MatP. The work further implicates MukBEF and MatP as central players in chromosome organization, segregation, and nonrandom inheritance of genetic material and suggests a general framework for understanding how chromosome conformation and dynamics shape subcellular organization.
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spelling pubmed-83799212021-08-30 Nonrandom segregation of sister chromosomes by Escherichia coli MukBEF Mäkelä, Jarno Uphoff, Stephan Sherratt, David J. Proc Natl Acad Sci U S A Biological Sciences Structural maintenance of chromosomes (SMC) complexes contribute to chromosome organization in all domains of life. In Escherichia coli, MukBEF, the functional SMC homolog, promotes spatiotemporal chromosome organization and faithful chromosome segregation. Here, we address the relative contributions of MukBEF and the replication terminus (ter) binding protein, MatP, to chromosome organization–segregation. We show that MukBEF, but not MatP, is required for the normal localization of the origin of replication to midcell and for the establishment of translational symmetry between newly replicated sister chromosomes. Overall, chromosome orientation is normally maintained through division from one generation to the next. Analysis of loci flanking the replication termination region (ter), which demark the ends of the linearly organized portion of the nucleoid, demonstrates that MatP is required for maintenance of chromosome orientation. We show that DNA-bound β(2)-processivity clamps, which mark the lagging strands at DNA replication forks, localize to the cell center, independent of replisome location but dependent on MukBEF action, and consistent with translational symmetry of sister chromosomes. Finally, we directly show that the older (“immortal”) template DNA strand, propagated from previous generations, is preferentially inherited by the cell forming at the old pole, dependent on MukBEF and MatP. The work further implicates MukBEF and MatP as central players in chromosome organization, segregation, and nonrandom inheritance of genetic material and suggests a general framework for understanding how chromosome conformation and dynamics shape subcellular organization. National Academy of Sciences 2021-08-17 2021-08-12 /pmc/articles/PMC8379921/ /pubmed/34385314 http://dx.doi.org/10.1073/pnas.2022078118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Biological Sciences
Mäkelä, Jarno
Uphoff, Stephan
Sherratt, David J.
Nonrandom segregation of sister chromosomes by Escherichia coli MukBEF
title Nonrandom segregation of sister chromosomes by Escherichia coli MukBEF
title_full Nonrandom segregation of sister chromosomes by Escherichia coli MukBEF
title_fullStr Nonrandom segregation of sister chromosomes by Escherichia coli MukBEF
title_full_unstemmed Nonrandom segregation of sister chromosomes by Escherichia coli MukBEF
title_short Nonrandom segregation of sister chromosomes by Escherichia coli MukBEF
title_sort nonrandom segregation of sister chromosomes by escherichia coli mukbef
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8379921/
https://www.ncbi.nlm.nih.gov/pubmed/34385314
http://dx.doi.org/10.1073/pnas.2022078118
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