eLife (Mar 2016)

The cell proliferation antigen Ki-67 organises heterochromatin

  • Michal Sobecki,
  • Karim Mrouj,
  • Alain Camasses,
  • Nikolaos Parisis,
  • Emilien Nicolas,
  • David Llères,
  • François Gerbe,
  • Susana Prieto,
  • Liliana Krasinska,
  • Alexandre David,
  • Manuel Eguren,
  • Marie-Christine Birling,
  • Serge Urbach,
  • Sonia Hem,
  • Jérôme Déjardin,
  • Marcos Malumbres,
  • Philippe Jay,
  • Vjekoslav Dulic,
  • Denis LJ Lafontaine,
  • Robert Feil,
  • Daniel Fisher

DOI
https://doi.org/10.7554/eLife.13722
Journal volume & issue
Vol. 5

Abstract

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Antigen Ki-67 is a nuclear protein expressed in proliferating mammalian cells. It is widely used in cancer histopathology but its functions remain unclear. Here, we show that Ki-67 controls heterochromatin organisation. Altering Ki-67 expression levels did not significantly affect cell proliferation in vivo. Ki-67 mutant mice developed normally and cells lacking Ki-67 proliferated efficiently. Conversely, upregulation of Ki-67 expression in differentiated tissues did not prevent cell cycle arrest. Ki-67 interactors included proteins involved in nucleolar processes and chromatin regulators. Ki-67 depletion disrupted nucleologenesis but did not inhibit pre-rRNA processing. In contrast, it altered gene expression. Ki-67 silencing also had wide-ranging effects on chromatin organisation, disrupting heterochromatin compaction and long-range genomic interactions. Trimethylation of histone H3K9 and H4K20 was relocalised within the nucleus. Finally, overexpression of human or Xenopus Ki-67 induced ectopic heterochromatin formation. Altogether, our results suggest that Ki-67 expression in proliferating cells spatially organises heterochromatin, thereby controlling gene expression.

Keywords