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Severe liver degeneration in mice lacking the IkappaB kinase 2 gene.

Phosphorylation of inhibitor of kappa B (IkappaB) proteins is an important step in the activation of the transcription nuclear factor kappa B (NF-kappaB) and requires two IkappaB kinases, IKK1 (IKKalpha) and IKK2 (IKKbeta). Mice that are devoid of the IKK2 gene had extensive liver damage from apoptosis and died as embryos, but these mice could be rescued by the inactivation of the gene encoding tumor necrosis factor receptor 1. Mouse embryonic fibroblast cells that were isolated from IKK2-/- embryos showed a marked reduction in tumor necrosis factor-alpha (TNF-alpha)- and interleukin-1alpha-induced NF-kappaB activity and an enhanced apoptosis in response to TNF-alpha. IKK1 associated with NF-kappaB essential modulator (IKKgamma/IKKAP1), another component of the IKK complex. These results show that IKK2 is essential for mouse development and cannot be substituted with IKK1.

Pubmed ID: 10195897

Authors

  • Li Q
  • Van Antwerp D
  • Mercurio F
  • Lee KF
  • Verma IM

Journal

Science (New York, N.Y.)

Publication Data

April 9, 1999

Associated Grants

None

Mesh Terms

  • Animals
  • Apoptosis
  • Cell Line
  • DNA-Binding Proteins
  • Embryonic and Fetal Development
  • Gene Targeting
  • I-kappa B Kinase
  • I-kappa B Proteins
  • Interleukin-1
  • Liver
  • Mice
  • NF-kappa B
  • Phosphorylation
  • Polymerase Chain Reaction
  • Protein-Serine-Threonine Kinases
  • Receptors, Tumor Necrosis Factor
  • Recombinant Fusion Proteins
  • Sequence Deletion
  • Signal Transduction
  • Transcription Factor RelA
  • Transcription Factors
  • Tumor Necrosis Factor-alpha