Pellino1 Is Required for Interferon Production by Viral Double-stranded RNA

Viral double-stranded RNA, a ligand for Toll-like Receptor 3 (TLR3) and the cytoplasmic RNA receptors RIG1 and MDA5, activate a signaling network in which the IKK-related protein kinase TBK1 phosphorylates the transcription factor Interferon Regulatory Factor 3 (IRF3) and the E3 ubiquitin ligase Pel...

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Veröffentlicht in:The Journal of biological chemistry 2012-10, Vol.287 (41), p.34825-34835
Hauptverfasser: Enesa, Karine, Ordureau, Alban, Smith, Hilary, Barford, David, Cheung, Peter C.F., Patterson-Kane, Janet, Arthur, J.Simon C., Cohen, Philip
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Sprache:eng
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Zusammenfassung:Viral double-stranded RNA, a ligand for Toll-like Receptor 3 (TLR3) and the cytoplasmic RNA receptors RIG1 and MDA5, activate a signaling network in which the IKK-related protein kinase TBK1 phosphorylates the transcription factor Interferon Regulatory Factor 3 (IRF3) and the E3 ubiquitin ligase Pellino1. IRF3 then translocates to the nucleus where it stimulates transcription of the interferonβ (IFNβ) gene, but the function of Pellino1 in this pathway is unknown. Here, we report that myeloid cells and embryonic fibroblasts from knock-in mice expressing an E3 ligase-deficient mutant of Pellino1 produce reduced levels of IFNβ mRNA and secrete much less IFNβ in response to viral double-stranded RNA because the interaction of IRF3 with the IFNβ promoter is impaired. These results identify Pellino1 as a novel component of the signal transduction network by which viral double-stranded RNA stimulates IFNβ gene transcription. Background: Signaling networks activated by viral double-stranded (ds) RNA stimulate interferonβ (IFNβ) production. Results: Myeloid cells and fibroblasts from mice expressing an E3 ligase-deficient mutant of Pellino1 produce less IFNβ in response to viral dsRNA due to impaired interaction of IRF3 with the IFNβ promoter. Conclusion: Pellino1 is needed to stimulate IFNβ gene transcription. Significance: Pellino1 is a new component required to combat viral infection.
ISSN:0021-9258
1083-351X
DOI:10.1074/jbc.M112.367557