Mitotic chromosomes are self-entangled and disentangle through a topoisomerase-II-dependent two-stage exit from mitosis

Erica M Hildebrand, Kirill Polovnikov, Bastiaan Dekker, Yu Liu, Denis L Lafontaine, A Nicole Fox, Ying Li, Sergey V Venev, Leonid A Mirny, Job Dekker

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

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.

Original languageEnglish
Pages (from-to)1422-1441.e14
JournalMolecular Cell
Volume84
Issue number8
DOIs
StatePublished - Apr 18 2024

Keywords

  • DNA Topoisomerases, Type II/genetics
  • Chromosomes/genetics
  • Mitosis/genetics
  • Interphase/genetics
  • Polymers
  • G1
  • mitosis
  • genome architecture
  • chromosome folding
  • topoisomerase II
  • cohesin
  • genome topology
  • chromosome entanglement
  • fractal globule
  • self-catenation

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