p27KIP1, an inhibitor of cyclin-dependent kinases

Prog Cell Cycle Res. 1995:1:141-7. doi: 10.1007/978-1-4615-1809-9_11.

Abstract

The identification of a family of proteins that stoichiometrically regulate the activation of the G1 cyclin-dependent kinases has added to our understanding of the process of commitment to the mitotic cycle. The properties of p27 as a CDK binding protein, the ability of environmental signals to regulate the expression of p27, and the observation that p27 may link the accumulation of G1 CDK complexes with activation of the CDK2 kinase, suggest it may have a critical role in establishing a threshold for G1 cyclin/CDK accumulation prior to activation of CDK2 kinase and entry into the mitotic cycle.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Cell Cycle
  • Cell Cycle Proteins*
  • Cyclin-Dependent Kinase Inhibitor p27
  • Cyclin-Dependent Kinases / antagonists & inhibitors*
  • Cyclins / physiology
  • Enzyme Activation
  • Microtubule-Associated Proteins / physiology*
  • Mitosis
  • Tumor Suppressor Proteins*

Substances

  • Cell Cycle Proteins
  • Cyclins
  • Microtubule-Associated Proteins
  • Tumor Suppressor Proteins
  • Cyclin-Dependent Kinase Inhibitor p27
  • Cyclin-Dependent Kinases