Preparing your results

Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

Cyclin-dependent kinase 1 (CDK1)-mediated phosphorylation of enhancer of zeste 2 (Ezh2) regulates its stability.

The H3K27 histone methyltransferase, Ezh2 (enhancer of zeste 2), is a Polycomb group protein that plays important roles in many biological processes including cellular differentiation, stem cell biology, and cancer development. Up-regulation of Ezh2 is observed in various human cancers consistent with its role in cell proliferation. Thus, understanding the regulation of Ezh2 may reveal how it contributes to the cellular proliferation process. Here, we demonstrate that Ezh2 can be regulated by the cyclin-dependent kinase, CDK1, which phosphorylates Ezh2 at threonines 345 and 487. Consistent with the cell cycle phase during which CDK1 exhibits peak activity, Ezh2 phosphorylation is enriched in cells arrested in mitosis when compared with S-phase. Phosphorylation of Thr-345 and Thr-487 promotes Ezh2 ubiquitination and subsequent degradation by the proteasome. Furthermore, expression of T345A/T487A confers a proliferative disadvantage when compared with cells expressing wild-type Ezh2, which suggests that phosphorylation of Ezh2 is important for cell proliferation. Collectively, these results establish a novel function for CDK1-mediated Ezh2 phosphorylation and provide a mechanism by which Ezh2 protein levels can be regulated in cells.

Pubmed ID: 21659531


  • Wu SC
  • Zhang Y


The Journal of biological chemistry

Publication Data

August 12, 2011

Associated Grants

  • Agency: NIGMS NIH HHS, Id: GM68804
  • Agency: Howard Hughes Medical Institute, Id:

Mesh Terms

  • Amino Acid Substitution
  • Animals
  • CDC2 Protein Kinase
  • Cell Cycle Checkpoints
  • Cell Proliferation
  • DNA-Binding Proteins
  • Enzyme Stability
  • HEK293 Cells
  • HeLa Cells
  • Histone-Lysine N-Methyltransferase
  • Humans
  • Mice
  • Mutation, Missense
  • NIH 3T3 Cells
  • Phosphorylation
  • Polycomb Repressive Complex 2
  • Transcription Factors
  • Ubiquitination