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A novel chromatin tether domain controls topoisomerase IIα dynamics and mitotic chromosome formation

DNA topoisomerase IIα (Topo IIα) is the target of an important class of anticancer drugs, but tumor cells can become resistant by reducing the association of the enzyme with chromosomes. Here we describe a critical mechanism of chromatin recruitment and exchange that relies on a novel chromatin teth...

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Detalles Bibliográficos
Autores principales: Lane, Andrew B., Giménez-Abián, Juan F., Clarke, Duncan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3824022/
https://www.ncbi.nlm.nih.gov/pubmed/24217621
http://dx.doi.org/10.1083/jcb.201303045
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author Lane, Andrew B.
Giménez-Abián, Juan F.
Clarke, Duncan J.
author_facet Lane, Andrew B.
Giménez-Abián, Juan F.
Clarke, Duncan J.
author_sort Lane, Andrew B.
collection PubMed
description DNA topoisomerase IIα (Topo IIα) is the target of an important class of anticancer drugs, but tumor cells can become resistant by reducing the association of the enzyme with chromosomes. Here we describe a critical mechanism of chromatin recruitment and exchange that relies on a novel chromatin tether (ChT) domain and mediates interaction with histone H3 and DNA. We show that the ChT domain controls the residence time of Topo IIα on chromatin in mitosis and is necessary for the formation of mitotic chromosomes. Our data suggest that the dynamics of Topo IIα on chromosomes are important for successful mitosis and implicate histone tail posttranslational modifications in regulating Topo IIα.
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spelling pubmed-38240222014-05-11 A novel chromatin tether domain controls topoisomerase IIα dynamics and mitotic chromosome formation Lane, Andrew B. Giménez-Abián, Juan F. Clarke, Duncan J. J Cell Biol Research Articles DNA topoisomerase IIα (Topo IIα) is the target of an important class of anticancer drugs, but tumor cells can become resistant by reducing the association of the enzyme with chromosomes. Here we describe a critical mechanism of chromatin recruitment and exchange that relies on a novel chromatin tether (ChT) domain and mediates interaction with histone H3 and DNA. We show that the ChT domain controls the residence time of Topo IIα on chromatin in mitosis and is necessary for the formation of mitotic chromosomes. Our data suggest that the dynamics of Topo IIα on chromosomes are important for successful mitosis and implicate histone tail posttranslational modifications in regulating Topo IIα. The Rockefeller University Press 2013-11-11 /pmc/articles/PMC3824022/ /pubmed/24217621 http://dx.doi.org/10.1083/jcb.201303045 Text en © 2013 Lane et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Articles
Lane, Andrew B.
Giménez-Abián, Juan F.
Clarke, Duncan J.
A novel chromatin tether domain controls topoisomerase IIα dynamics and mitotic chromosome formation
title A novel chromatin tether domain controls topoisomerase IIα dynamics and mitotic chromosome formation
title_full A novel chromatin tether domain controls topoisomerase IIα dynamics and mitotic chromosome formation
title_fullStr A novel chromatin tether domain controls topoisomerase IIα dynamics and mitotic chromosome formation
title_full_unstemmed A novel chromatin tether domain controls topoisomerase IIα dynamics and mitotic chromosome formation
title_short A novel chromatin tether domain controls topoisomerase IIα dynamics and mitotic chromosome formation
title_sort novel chromatin tether domain controls topoisomerase iiα dynamics and mitotic chromosome formation
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3824022/
https://www.ncbi.nlm.nih.gov/pubmed/24217621
http://dx.doi.org/10.1083/jcb.201303045
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