Sobecki Michal, Mrouj Karim, Camasses Alain, Parisis Nikolaos, Nicolas Emilien, Llères David, Gerbe François, Prieto Susana, Krasinska Liliana, David Alexandre, Eguren Manuel, Birling Marie-Christine, Urbach Serge, Hem Sonia, Déjardin Jérôme, Malumbres Marcos, Jay Philippe, Dulic Vjekoslav, Lafontaine Denis Lj, Feil Robert, Fisher Daniel
Montpellier Institute of Molecular Genetics (IGMM) CNRS UMR 5535, Centre National de la Recherche Scientifique (CNRS), Montpellier, France.
Faculty of Sciences, University of Montpellier, Montpellier, France.
Elife. 2016 Mar 7;5:e13722. doi: 10.7554/eLife.13722.
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.
抗原Ki-67是一种在增殖的哺乳动物细胞中表达的核蛋白。它在癌症组织病理学中被广泛应用,但其功能仍不清楚。在此,我们表明Ki-67控制异染色质的组织。改变Ki-67的表达水平在体内对细胞增殖没有显著影响。Ki-67突变小鼠正常发育,缺乏Ki-67的细胞能有效增殖。相反,在分化组织中上调Ki-67的表达并不能阻止细胞周期停滞。Ki-67相互作用蛋白包括参与核仁过程的蛋白质和染色质调节因子。Ki-67的缺失破坏了核仁形成,但不抑制前体rRNA加工。相反,它改变了基因表达。Ki-67的沉默对染色质组织也有广泛影响,破坏了异染色质的压缩和长程基因组相互作用。组蛋白H3K9和H4K20的三甲基化在细胞核内重新定位。最后,人或非洲爪蟾Ki-67的过表达诱导了异位异染色质的形成。总之,我们的结果表明增殖细胞中Ki-67的表达在空间上组织异染色质,从而控制基因表达。