Regulation of beta-catenin function by the IkappaB kinases

J Biol Chem. 2001 Nov 9;276(45):42276-86. doi: 10.1074/jbc.M104227200. Epub 2001 Aug 29.

Abstract

Both the beta-catenin and the nuclear factor kappaB (NF-kappaB) proteins are important regulators of gene expression and cellular proliferation. Two kinases, IKKalpha and IKKbeta, are critical activators of the NF-kappaB pathway. Here we present evidence that these kinases are also important in the regulation of beta-catenin function. IKKalpha- and IKKbeta-deficient mouse embryo fibroblasts exhibited different patterns of beta-catenin cellular localization. IKKbeta decreases beta-catenin-dependent transcriptional activation, while IKKalpha increases beta-catenin-dependent transcriptional activity. IKKalpha and IKKbeta interact with and phosphorylate beta-catenin using both in vitro and in vivo assays. Our results suggest that differential interactions of beta-catenin with IKKalpha and IKKbeta may in part be responsible for regulating beta-catenin protein levels and cellular localization and integrating signaling events between the NF-kappaB and Wingless pathways.

Publication types

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

MeSH terms

  • Animals
  • COS Cells
  • Cytoskeletal Proteins / analysis
  • Cytoskeletal Proteins / physiology*
  • I-kappa B Kinase
  • Mice
  • NF-kappa B / physiology
  • Phosphorylation
  • Protein Serine-Threonine Kinases / physiology*
  • Trans-Activators*
  • Transcriptional Activation
  • Tumor Necrosis Factor-alpha / pharmacology
  • beta Catenin

Substances

  • CTNNB1 protein, mouse
  • Cytoskeletal Proteins
  • NF-kappa B
  • Trans-Activators
  • Tumor Necrosis Factor-alpha
  • beta Catenin
  • Protein Serine-Threonine Kinases
  • Chuk protein, mouse
  • I-kappa B Kinase
  • Ikbkb protein, mouse
  • Ikbke protein, mouse