MatP regulates the coordinated action of topoisomerase IV and MukBEF in chromosome segregation

The Escherichia coli SMC complex, MukBEF, forms clusters of molecules that interact with the decatenase topisomerase IV and which are normally associated with the chromosome replication origin region (ori). Here we demonstrate an additional ATP-hydrolysis-dependent association of MukBEF with the rep...

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Main Authors: Nolivos, Sophie, Upton, Amy L., Badrinarayanan, Anjana, Zawadzka, Katarzyna, Wiktor, Jakub, Gill, Amber, Arciszewska, Lidia, Nicolas, Emilien, Sherratt, David, Muller, Julius
Other Authors: Massachusetts Institute of Technology. Department of Biology
Format: Article
Language:en_US
Published: Nature Publishing Group 2016
Online Access:http://hdl.handle.net/1721.1/101744
https://orcid.org/0000-0002-6807-6576
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author Nolivos, Sophie
Upton, Amy L.
Badrinarayanan, Anjana
Zawadzka, Katarzyna
Wiktor, Jakub
Gill, Amber
Arciszewska, Lidia
Nicolas, Emilien
Sherratt, David
Muller, Julius
author2 Massachusetts Institute of Technology. Department of Biology
author_facet Massachusetts Institute of Technology. Department of Biology
Nolivos, Sophie
Upton, Amy L.
Badrinarayanan, Anjana
Zawadzka, Katarzyna
Wiktor, Jakub
Gill, Amber
Arciszewska, Lidia
Nicolas, Emilien
Sherratt, David
Muller, Julius
author_sort Nolivos, Sophie
collection MIT
description The Escherichia coli SMC complex, MukBEF, forms clusters of molecules that interact with the decatenase topisomerase IV and which are normally associated with the chromosome replication origin region (ori). Here we demonstrate an additional ATP-hydrolysis-dependent association of MukBEF with the replication termination region (ter). Consistent with this, MukBEF interacts with MatP, which binds matS sites in ter. MatP displaces wild-type MukBEF complexes from ter, thereby facilitating their association with ori, and limiting the availability of topoisomerase IV (TopoIV) at ter. Displacement of MukBEF is impaired when MukB ATP hydrolysis is compromised and when MatP is absent, leading to a stable association of ter and MukBEF. Impairing the TopoIV-MukBEF interaction delays sister ter segregation in cells lacking MatP. We propose that the interplay between MukBEF and MatP directs chromosome organization in relation to MukBEF clusters and associated topisomerase IV, thereby ensuring timely chromosome unlinking and segregation.
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spelling mit-1721.1/1017442022-09-27T15:05:29Z MatP regulates the coordinated action of topoisomerase IV and MukBEF in chromosome segregation Nolivos, Sophie Upton, Amy L. Badrinarayanan, Anjana Zawadzka, Katarzyna Wiktor, Jakub Gill, Amber Arciszewska, Lidia Nicolas, Emilien Sherratt, David Muller, Julius Massachusetts Institute of Technology. Department of Biology Badrinarayanan, Anjana The Escherichia coli SMC complex, MukBEF, forms clusters of molecules that interact with the decatenase topisomerase IV and which are normally associated with the chromosome replication origin region (ori). Here we demonstrate an additional ATP-hydrolysis-dependent association of MukBEF with the replication termination region (ter). Consistent with this, MukBEF interacts with MatP, which binds matS sites in ter. MatP displaces wild-type MukBEF complexes from ter, thereby facilitating their association with ori, and limiting the availability of topoisomerase IV (TopoIV) at ter. Displacement of MukBEF is impaired when MukB ATP hydrolysis is compromised and when MatP is absent, leading to a stable association of ter and MukBEF. Impairing the TopoIV-MukBEF interaction delays sister ter segregation in cells lacking MatP. We propose that the interplay between MukBEF and MatP directs chromosome organization in relation to MukBEF clusters and associated topisomerase IV, thereby ensuring timely chromosome unlinking and segregation. 2016-03-18T17:14:33Z 2016-03-18T17:14:33Z 2016-01 2015-08 Article http://purl.org/eprint/type/JournalArticle 2041-1723 http://hdl.handle.net/1721.1/101744 Nolivos, Sophie, Amy L. Upton, Anjana Badrinarayanan, Julius Müller, Katarzyna Zawadzka, Jakub Wiktor, Amber Gill, Lidia Arciszewska, Emilien Nicolas, and David Sherratt. “MatP Regulates the Coordinated Action of Topoisomerase IV and MukBEF in Chromosome Segregation.” Nat Comms 7 (January 28, 2016): 10466. https://orcid.org/0000-0002-6807-6576 en_US http://dx.doi.org/10.1038/ncomms10466 Nature Communications Creative Commons Attribution http://creativecommons.org/licenses/by/4.0/ application/pdf Nature Publishing Group Nature Publishing Group
spellingShingle Nolivos, Sophie
Upton, Amy L.
Badrinarayanan, Anjana
Zawadzka, Katarzyna
Wiktor, Jakub
Gill, Amber
Arciszewska, Lidia
Nicolas, Emilien
Sherratt, David
Muller, Julius
MatP regulates the coordinated action of topoisomerase IV and MukBEF in chromosome segregation
title MatP regulates the coordinated action of topoisomerase IV and MukBEF in chromosome segregation
title_full MatP regulates the coordinated action of topoisomerase IV and MukBEF in chromosome segregation
title_fullStr MatP regulates the coordinated action of topoisomerase IV and MukBEF in chromosome segregation
title_full_unstemmed MatP regulates the coordinated action of topoisomerase IV and MukBEF in chromosome segregation
title_short MatP regulates the coordinated action of topoisomerase IV and MukBEF in chromosome segregation
title_sort matp regulates the coordinated action of topoisomerase iv and mukbef in chromosome segregation
url http://hdl.handle.net/1721.1/101744
https://orcid.org/0000-0002-6807-6576
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