Cyclin D1-cdk4 induce runx2 ubiquitination and degradation

J Biol Chem. 2006 Jun 16;281(24):16347-53. doi: 10.1074/jbc.M603439200. Epub 2006 Apr 13.

Abstract

Runx2 is a Runt domain transcription factor involved in the activation of genes encoding osteoblast and chondrocyte-specific proteins. Runx2 activity is regulated by transcriptional and post-transcriptional mechanisms. The functional significance of the post-translational modification of Runx2 has not been fully defined. We show that cyclin D1-Cdk4 induce Runx2 degradation in an ubiquitination-proteasome-dependent manner. Mutagenesis of Runx2 serine-472, a consensus Cdk site, to alanine increases the half-life of Runx2 and causes loss of sensitivity to cyclin D1-induced Runx2 degradation. The targeted Runx2 degradation by cyclin D1 identifies a novel mechanism through which Runx2 activity is regulated coordinately with the cell cycle machinery in bone cells.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • COS Cells
  • Cell Cycle
  • Chlorocebus aethiops
  • Core Binding Factor Alpha 1 Subunit / physiology*
  • Cyclin D1 / metabolism
  • Cyclin D1 / physiology*
  • Cyclin-Dependent Kinase 4 / physiology*
  • Mice
  • Mice, Inbred C3H
  • Mutagenesis, Site-Directed
  • Proteasome Endopeptidase Complex / metabolism
  • Protein Binding
  • Serine / chemistry
  • Ubiquitin / chemistry*

Substances

  • Core Binding Factor Alpha 1 Subunit
  • Ubiquitin
  • Cyclin D1
  • Serine
  • Cyclin-Dependent Kinase 4
  • Proteasome Endopeptidase Complex