Pellino 3b negatively regulates interleukin-1-induced TAK1-dependent NF kappaB activation

J Biol Chem. 2008 May 23;283(21):14654-64. doi: 10.1074/jbc.M706931200. Epub 2008 Mar 7.

Abstract

IL-1 receptor-associated kinase (IRAK) is phosphorylated, ubiquitinated, and degraded upon interleukin-1 (IL-1) stimulation. In this study, we showed that IRAK can be ubiquitinated through both Lys-48- and Lys-63-linked polyubiquitin chains upon IL-1 induction. Pellino 3b is the RING-like motif ubiquitin protein ligase that promotes the Lys-63-linked polyubiquitination on IRAK. Pellino 3b-mediated Lys-63-linked IRAK polyubiquitination competed with Lys-48-linked IRAK polyubiquitination for the same ubiquitination site, Lys-134 of IRAK, thereby blocking IL-1-induced IRAK degradation. Importantly, the negative impact of Pellino 3b on IL-1-induced IRAK degradation correlated with the inhibitory effect of Pellino 3b on the IL-1-induced TAK1-dependent pathway, suggesting that a positive role of IRAK degradation in IL-1 induced TAK1 activation. Taken together, our results suggest that Pellino 3b acts as a negative regulator for IL-1 signaling by regulating IRAK degradation through its ubiquitin protein ligase activity.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Cell Line
  • Humans
  • Interleukin-1 / pharmacology*
  • Interleukin-1 Receptor-Associated Kinases / metabolism
  • MAP Kinase Kinase Kinases / metabolism*
  • NF-kappa B / metabolism*
  • Protein Binding
  • Signal Transduction / drug effects
  • Ubiquitin-Protein Ligases / metabolism
  • Ubiquitination

Substances

  • Interleukin-1
  • NF-kappa B
  • Ubiquitin-Protein Ligases
  • Interleukin-1 Receptor-Associated Kinases
  • MAP Kinase Kinase Kinases
  • MAP kinase kinase kinase 7