Cdk phosphorylation triggers sequential intramolecular interactions that progressively block Rb functions as cells move through G1

  • Cell. 1999 Sep 17;98(6):859-69. doi: 10.1016/s0092-8674(00)81519-6.
J W Harbour  1 R X Luo A Dei Santi A A Postigo D C Dean
Affiliations
  • 1. Department of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Abstract

We present evidence that phosphorylation of the C-terminal region of Rb by CDK4/6 initiates successive intramolecular interactions between the C-terminal region and the central pocket. The initial interaction displaces histone deacetylase from the pocket, blocking active transcriptional repression by Rb. This facilitates a second interaction that leads to phosphorylation of the pocket by CDK2 and disruption of pocket structure. These intramolecular interactions provide a molecular basis for sequential phosphorylation of Rb by CDK4/6 and CDK2. CDK4/6 is activated early in G1, blocking active repression by Rb. However, it is not until near the end of G1, when cyclin E is expressed and CDK2 is activated, that Rb is prevented from binding and inactivating E2F.