CARMA3 deficiency abrogates G protein-coupled receptor-induced NF-{kappa}B activation

Genes Dev. 2007 Apr 15;21(8):984-96. doi: 10.1101/gad.1502507.

Abstract

G protein-coupled receptors (GPCRs) play pivotal roles in regulating various cellular functions. Although many GPCRs induce NF-kappaB activation, the molecular mechanism of GPCR-induced NF-kappaB activation remains largely unknown. CARMA3 (CARD and MAGUK domain-containing protein 3) is a scaffold molecule with unknown biological functions. By generating CARMA3 knockout mice using the gene targeting approach, here we show CARMA3 is required for GPCR-induced NF-kappaB activation. Mechanistically, we found that CARMA3 deficiency impairs GPCR-induced IkappaB kinase (IKK) activation, although it does not affect GPCR-induced IKKalpha/beta phosphorylation, indicating that inducible phosphorylation of IKKalpha/beta alone is not sufficient to induce its kinase activity. We also found that CARMA3 is physically associated with NEMO/IKKgamma, and induces polyubiquitination of an unknown protein(s) that associates with NEMO, likely by linking NEMO to TRAF6. Consistently, we found TRAF6 deficiency also abrogates GPCR-induced NF-kappaB activation. Together, our results provide the genetic evidence that CARMA3 is required for GPCR-induced NF-kappaB activation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism
  • Animals
  • Apoptosis Regulatory Proteins / genetics
  • Apoptosis Regulatory Proteins / metabolism*
  • B-Cell CLL-Lymphoma 10 Protein
  • CARD Signaling Adaptor Proteins / genetics
  • CARD Signaling Adaptor Proteins / metabolism*
  • Embryo, Mammalian / cytology
  • Female
  • Fibroblasts
  • I-kappa B Kinase / metabolism
  • Lysophospholipids / metabolism
  • Mice
  • Mice, Knockout
  • NF-kappa B / metabolism*
  • Phosphorylation
  • Pregnancy
  • Receptors, G-Protein-Coupled / metabolism*
  • Signal Transduction
  • TNF Receptor-Associated Factor 6 / metabolism

Substances

  • Adaptor Proteins, Signal Transducing
  • Apoptosis Regulatory Proteins
  • B-Cell CLL-Lymphoma 10 Protein
  • Bcl10 protein, mouse
  • CARD Signaling Adaptor Proteins
  • Card10 protein, mouse
  • Lysophospholipids
  • NF-kappa B
  • Receptors, G-Protein-Coupled
  • TNF Receptor-Associated Factor 6
  • Chuk protein, mouse
  • I-kappa B Kinase
  • lysophosphatidic acid