SCF(beta)(-TrCP) ubiquitin ligase-mediated processing of NF-kappaB p105 requires phosphorylation of its C-terminus by IkappaB kinase

EMBO J. 2000 Jun 1;19(11):2580-91. doi: 10.1093/emboj/19.11.2580.

Abstract

Processing of the p105 precursor to form the active subunit p50 of the NF-kappaB transcription factor is a unique case in which the ubiquitin system is involved in limited processing rather than in complete destruction of the target substrate. A glycine-rich region along with a downstream acidic domain have been demonstrated to be essential for processing. Here we demonstrate that following IkappaB kinase (IkappaK)-mediated phosphorylation, the C-terminal domain of p105 (residues 918-934) serves as a recognition motif for the SCF(beta)(-TrCP) ubiquitin ligase. Expression of IkappaKbeta dramatically increases processing of wild-type p105, but not of p105-Delta918-934. Dominant-negative beta-TrCP inhibits IkappaK-dependent processing. Furthermore, the ligase and wild-type p105 but not p105-Delta918-934 associate physically following phosphorylation. In vitro, SCF(beta)(-TrCP) specifically conjugates and promotes processing of phosphorylated p105. Importantly, the TrCP recognition motif in p105 is different from that described for IkappaBs, beta-catenin and human immunodeficiency virus type 1 Vpu. Since p105-Delta918-934 is also conjugated and processed, it appears that p105 can be recognized under different physiological conditions by two different ligases, targeting two distinct recognition motifs.

Publication types

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

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Amino Acid Motifs
  • Animals
  • COS Cells
  • Chlorocebus aethiops
  • HeLa Cells
  • Humans
  • I-kappa B Kinase
  • I-kappa B Proteins / metabolism
  • Macromolecular Substances
  • NF-kappa B / metabolism*
  • NF-kappa B p50 Subunit
  • Peptide Synthases / physiology*
  • Phosphorylation
  • Protein Precursors / metabolism*
  • Protein Processing, Post-Translational*
  • Protein Serine-Threonine Kinases / physiology*
  • Protein Structure, Tertiary
  • SKP Cullin F-Box Protein Ligases
  • Transcription, Genetic

Substances

  • I-kappa B Proteins
  • Macromolecular Substances
  • NF-kappa B
  • NF-kappa B p50 Subunit
  • Protein Precursors
  • Adenosine Triphosphate
  • SKP Cullin F-Box Protein Ligases
  • Protein Serine-Threonine Kinases
  • CHUK protein, human
  • I-kappa B Kinase
  • IKBKB protein, human
  • IKBKE protein, human
  • Peptide Synthases