A Topology-Centric View on Mitotic Chromosome Architecture

Int J Mol Sci. 2017 Dec 18;18(12):2751. doi: 10.3390/ijms18122751.

Abstract

Mitotic chromosomes are long-known structures, but their internal organization and the exact process by which they are assembled are still a great mystery in biology. Topoisomerase II is crucial for various aspects of mitotic chromosome organization. The unique ability of this enzyme to untangle topologically intertwined DNA molecules (catenations) is of utmost importance for the resolution of sister chromatid intertwines. Although still controversial, topoisomerase II has also been proposed to directly contribute to chromosome compaction, possibly by promoting chromosome self-entanglements. These two functions raise a strong directionality issue towards topoisomerase II reactions that are able to disentangle sister DNA molecules (in trans) while compacting the same DNA molecule (in cis). Here, we review the current knowledge on topoisomerase II role specifically during mitosis, and the mechanisms that directly or indirectly regulate its activity to ensure faithful chromosome segregation. In particular, we discuss how the activity or directionality of this enzyme could be regulated by the SMC (structural maintenance of chromosomes) complexes, predominantly cohesin and condensin, throughout mitosis.

Keywords: catenation; chromosome condensation; cohesin; condensin; mitosis; mitotic chromosomes; sister chromatid intertwines; sister chromatid resolution; topoisomerase II; ultra-fine bridges.

Publication types

  • Review

MeSH terms

  • Adenosine Triphosphatases / metabolism
  • Animals
  • Cell Cycle Proteins / metabolism
  • Chromosomal Proteins, Non-Histone / metabolism
  • Chromosome Segregation / physiology
  • Chromosomes / genetics
  • Chromosomes / metabolism*
  • Cohesins
  • DNA Topoisomerases, Type II / metabolism
  • DNA-Binding Proteins / metabolism
  • Humans
  • Mitosis / genetics
  • Mitosis / physiology*
  • Multiprotein Complexes / metabolism

Substances

  • Cell Cycle Proteins
  • Chromosomal Proteins, Non-Histone
  • DNA-Binding Proteins
  • Multiprotein Complexes
  • condensin complexes
  • Adenosine Triphosphatases
  • DNA Topoisomerases, Type II