Cdk2 is required for p53-independent G2/M checkpoint control

PLoS Genet. 2010 Feb 26;6(2):e1000863. doi: 10.1371/journal.pgen.1000863.

Abstract

The activation of phase-specific cyclin-dependent kinases (Cdks) is associated with ordered cell cycle transitions. Among the mammalian Cdks, only Cdk1 is essential for somatic cell proliferation. Cdk1 can apparently substitute for Cdk2, Cdk4, and Cdk6, which are individually dispensable in mice. It is unclear if all functions of non-essential Cdks are fully redundant with Cdk1. Using a genetic approach, we show that Cdk2, the S-phase Cdk, uniquely controls the G(2)/M checkpoint that prevents cells with damaged DNA from initiating mitosis. CDK2-nullizygous human cells exposed to ionizing radiation failed to exclude Cdk1 from the nucleus and exhibited a marked defect in G(2)/M arrest that was unmasked by the disruption of P53. The DNA replication licensing protein Cdc6, which is normally stabilized by Cdk2, was physically associated with the checkpoint regulator ATR and was required for efficient ATR-Chk1-Cdc25A signaling. These findings demonstrate that Cdk2 maintains a balance of S-phase regulatory proteins and thereby coordinates subsequent p53-independent G(2)/M checkpoint activation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Ataxia Telangiectasia Mutated Proteins
  • Cell Cycle Proteins / metabolism
  • Checkpoint Kinase 1
  • Cyclin-Dependent Kinase 2 / deficiency
  • Cyclin-Dependent Kinase 2 / metabolism*
  • Cytoplasm / metabolism
  • Cytoplasm / radiation effects
  • Enzyme Activation / radiation effects
  • Enzyme Stability / radiation effects
  • G2 Phase* / radiation effects
  • HCT116 Cells
  • Humans
  • Mice
  • Mitosis* / radiation effects
  • Models, Biological
  • Nuclear Proteins / metabolism
  • Phosphorylation / radiation effects
  • Protein Kinases / metabolism
  • Protein Processing, Post-Translational / radiation effects
  • Protein Transport / radiation effects
  • Protein-Serine-Threonine Kinases / metabolism
  • Radiation, Ionizing
  • Tumor Suppressor Protein p53 / metabolism*
  • cdc25 Phosphatases / metabolism

Substances

  • CDC6 protein, human
  • Cell Cycle Proteins
  • Nuclear Proteins
  • Tumor Suppressor Protein p53
  • Protein Kinases
  • ATR protein, human
  • Ataxia Telangiectasia Mutated Proteins
  • CHEK1 protein, human
  • Checkpoint Kinase 1
  • Chek1 protein, mouse
  • Protein-Serine-Threonine Kinases
  • CDK2 protein, human
  • Cyclin-Dependent Kinase 2
  • cdc25 Phosphatases