p21WAF1/CIP1 interacts with protein kinase CK2

Oncogene. 1996 Jul 18;13(2):391-8.

Abstract

p21WAF1/CIP1 which belongs to a class of regulatory proteins that interact with cyclin dependent kinases is a potent inhibitor of these kinases. The inhibition of the cyclin dependent kinases induces an arrest of cells in the G phase of the cell cycle. In addition p21WAF1/CIP1 associates with PCNA and inhibits DNA replication. Here, we show that p21WAF1/CIP1 binds to the regulatory beta-subunit of protein kinase CK2 but not to the catalytic alpha-subunit. Binding of p21WAF1/CIP1 down regulates the kinase activity of CK2 with respect to the phosphorylation of the beta-subunit of CK2, casein and the C-terminus of p53. This study demonstrates a new binding partner for the regulatory beta-subunit of protein kinase CK2 which regulates the activity of the holoenzyme.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Binding, Competitive
  • Casein Kinase II
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins / isolation & purification
  • Cyclins / metabolism*
  • Cyclins / pharmacology*
  • DNA, Complementary / genetics
  • Humans
  • Macromolecular Substances
  • Molecular Sequence Data
  • Phosphoric Monoester Hydrolases / metabolism
  • Phosphorylation
  • Protein Serine-Threonine Kinases / antagonists & inhibitors*
  • Protein Serine-Threonine Kinases / isolation & purification
  • Protein Serine-Threonine Kinases / metabolism*

Substances

  • CDKN1A protein, human
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins
  • DNA, Complementary
  • Macromolecular Substances
  • Casein Kinase II
  • Protein Serine-Threonine Kinases
  • Phosphoric Monoester Hydrolases