Regulation of sister chromatid cohesion between chromosome arms

Curr Biol. 2004 Jul 13;14(13):1187-93. doi: 10.1016/j.cub.2004.06.052.

Abstract

Sister chromatid separation in anaphase depends on the removal of cohesin complexes from chromosomes. In vertebrates, the bulk of cohesin is already removed from chromosome arms during prophase and prometaphase, whereas cohesin remains at centromeres until metaphase, when cohesin is cleaved by the protease separase. In unperturbed mitoses, arm cohesion nevertheless persists throughout metaphase and is principally sufficient to maintain sister chromatid cohesion. How arm cohesion is maintained until metaphase is unknown. Here we show that small amounts of cohesin can be detected in the interchromatid region of metaphase chromosome arms. If prometaphase is prolonged by treatment of cells with microtubule poisons, these cohesin complexes dissociate from chromosome arms, and arm cohesion is dissolved. If cohesin dissociation in prometaphase-arrested cells is prevented by depletion of Plk1 or inhibition of Aurora B, arm cohesion is maintained. These observations imply that, in unperturbed mitoses, small amounts of cohesin maintain arm cohesion until metaphase. When cells lacking Plk1 and Aurora B activity enter anaphase, chromatids lose cohesin. This loss is prevented by proteasome inhibitors, implying that it depends on separase activation. Separase may therefore be able to cleave cohesin at centromeres and on chromosome arms.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aurora Kinase B
  • Aurora Kinases
  • Cell Cycle Proteins / metabolism
  • Cells, Cultured / cytology
  • Chromatids / physiology*
  • Chromosomal Proteins, Non-Histone
  • Chromosomes, Human / physiology*
  • Cohesins
  • Endopeptidases / metabolism
  • Fungal Proteins
  • HeLa Cells / cytology
  • Humans
  • Immunoblotting
  • Metaphase / physiology
  • Microscopy, Fluorescence
  • Mitosis / physiology*
  • Models, Biological*
  • Nuclear Proteins / metabolism*
  • Nuclear Proteins / physiology
  • Polo-Like Kinase 1
  • Protein Kinases
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins
  • RNA Interference
  • Rats
  • Separase

Substances

  • Cell Cycle Proteins
  • Chromosomal Proteins, Non-Histone
  • Fungal Proteins
  • Nuclear Proteins
  • Proto-Oncogene Proteins
  • Protein Kinases
  • AURKB protein, human
  • Aurkb protein, rat
  • Aurora Kinase B
  • Aurora Kinases
  • Protein Serine-Threonine Kinases
  • Endopeptidases
  • ESPL1 protein, human
  • Separase