Cutting Edge: NF-κB-Activating Kinase-Associated Protein 1 Participates in TLR3/Toll-IL-1 Homology Domain-Containing Adapter Molecule-1-Mediated IFN Regulatory Factor 3 Activation

Abstract

TLRs signal the presence of microbial patterns and activate transcription factors. In TLR3 and TLR4, the adapter Toll-IL-1R homology domain-containing adapter molecule (TICAM-1) (also called Toll/IL-1R domain-containing adapter inducing IFN-β (TRIF)) mediates IFN regulatory factor 3 (IRF3) phosphorylation followed by IFN-β production. The regulatory subunit TNFR-associated factor family member-associated NF-κB activator (TANK) couples with the kinase complex IκB kinase-related kinase ε/NF-κB-activating kinase (NAK) (TANK-binding kinase 1 (TBK1)) that involveTICAM-1-dependent IFN-β induction. There are several TANK-homologous proteins. We tested whether TICAM-1 binds and coprecipitates with TANK or its family proteins. The results are: 1) the TANK family protein NAK-associated protein 1 (NAP1), but not TANK, coprecipitates withTICAM-1; 2) NAP1 overexpression markedly enhances TBK1-mediated IFN-β promoter activation; 3) a dominant-negative form, NAP (158–270), suppresses IRF3 activation in response to poly(I:C) or LPS; 4) RNA interference targeting of the NAP1 message results in a failure of poly(I:C)-mediated IRF3 polymerization and IFN-β production. Thus, NAP1 is the kinase subunit responsible for TLR3/4-mediated IFN-β induction in the TICAM-1 pathway.