Activation in vitro of NF-kappa B by phosphorylation of its inhibitor I kappa B

Nature. 1990 Apr 12;344(6267):678-82. doi: 10.1038/344678a0.

Abstract

Nuclear factor kappa B (NF-kappa B), which was first detected by its binding to the kappa B site in the immunoglobulin kappa-gene enhancer, is important for the regulated expression of the kappa-gene and is partly responsible for the induction in appropriate cells of interleukin-2 (IL-2), IL-2 alpha receptor, beta-interferon and serum amyloid A protein. NF-kappa B is present as a nuclear DNA-binding protein in B lymphocytes and mature macrophages, but is found in the cytoplasm of many cells in a form unable to bind to DNA. The cytoplasmic form is bound to an inhibitor protein, I kappa B, from which it can be released in vitro by deoxycholate and other agents. Activation of cells by various agents, notably the phorbol esters that stimulate protein kinase C (PKC), leads to dissociation in vivo of the NF-kappa B/I kappa B complex and migration of NF-kappa B to the nucleus. Therefore, it acts as a second messenger system, transducing activation signals from the cytoplasm to the nucleus. To elucidate the mechanism of signal transfer, we have used an in vitro system in which addition of purified protein kinases to a partially purified NF-kappa B/I kappa B complex leads to the activation of the DNA-binding activity of NF-kappa B. Using gel retardation assays we found that PKC, cyclic AMP-dependent protein kinase (PKA) and a haem-regulated eIF-2 kinase (HRI) could activate NF-kappa B in vitro, whereas casein kinase II was ineffective. To determine the target for the protein kinases we purified and characterized both NF-kappa B and I kappa B and found that I kappa B is phosphorylated and inactivated in the presence of PKC and HRI but not PKA.

Publication types

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

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Animals
  • Casein Kinases
  • Cell Line
  • Cyclic AMP / pharmacology
  • DNA / metabolism
  • Electrophoresis, Polyacrylamide Gel
  • Mice
  • NF-kappa B
  • Phosphorylation
  • Protein Kinase C / metabolism
  • Protein Kinases / metabolism*
  • Rats
  • Second Messenger Systems
  • Signal Transduction
  • Transcription Factors / antagonists & inhibitors*
  • Transcription Factors / metabolism*
  • eIF-2 Kinase

Substances

  • NF-kappa B
  • Transcription Factors
  • Adenosine Triphosphate
  • DNA
  • Cyclic AMP
  • Protein Kinases
  • Casein Kinases
  • eIF-2 Kinase
  • Protein Kinase C