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Mitotic chromosomes are self-entangled and disentangle through a topoisomerase-II-dependent two-stage exit from mitosis.
Hildebrand, Erica M; Polovnikov, Kirill; Dekker, Bastiaan; Liu, Yu; Lafontaine, Denis L; Fox, A Nicole; Li, Ying; Venev, Sergey V; Mirny, Leonid A; Dekker, Job.
Afiliação
  • Hildebrand EM; Department of Systems Biology, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA.
  • Polovnikov K; Independent Researcher, Moscow, Russia.
  • Dekker B; Department of Systems Biology, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA.
  • Liu Y; Department of Systems Biology, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA; Nuclear Dynamics and Cancer Program, Cancer Epigenetics Institute, Fox Chase Cancer Center, Temple Health, Philadelphia, PA 19111, USA.
  • Lafontaine DL; Department of Systems Biology, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA.
  • Fox AN; Department of Systems Biology, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA.
  • Li Y; Department of Systems Biology, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA.
  • Venev SV; Department of Systems Biology, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA.
  • Mirny LA; Institute for Medical Engineering and Science and Department of Physics, Massachusetts Institute of Technology, Cambridge, MA 02139, USA. Electronic address: leonid@mit.edu.
  • Dekker J; Department of Systems Biology, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA. Electronic address: job.dekker@umassmed.edu.
Mol Cell ; 84(8): 1422-1441.e14, 2024 Apr 18.
Article em En | MEDLINE | ID: mdl-38521067
ABSTRACT
The topological state of chromosomes determines their mechanical properties, dynamics, and function. Recent work indicated that interphase chromosomes are largely free of entanglements. Here, we use Hi-C, polymer simulations, and multi-contact 3C and find that, by contrast, mitotic chromosomes are self-entangled. We explore how a mitotic self-entangled state is converted into an unentangled interphase state during mitotic exit. Most mitotic entanglements are removed during anaphase/telophase, with remaining ones removed during early G1, in a topoisomerase-II-dependent process. Polymer models suggest a two-stage disentanglement pathway first, decondensation of mitotic chromosomes with remaining condensin loops produces entropic forces that bias topoisomerase II activity toward decatenation. At the second stage, the loops are released, and the formation of new entanglements is prevented by lower topoisomerase II activity, allowing the establishment of unentangled and territorial G1 chromosomes. When mitotic entanglements are not removed in experiments and models, a normal interphase state cannot be acquired.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromossomos / DNA Topoisomerases Tipo II Idioma: En Revista: Mol Cell Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromossomos / DNA Topoisomerases Tipo II Idioma: En Revista: Mol Cell Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos