Multiple Functions of the IKK-Related Kinase IKKε in Interferon-Mediated Antiviral Immunity

Author:

tenOever Benjamin R.1234,Ng Sze-Ling1234,Chua Mark A.1234,McWhirter Sarah M.1234,García-Sastre Adolfo1234,Maniatis Tom1234

Affiliation:

1. Department of Molecular and Cellular Biology, Harvard University, 7 Divinity Avenue, Cambridge, MA02138, USA.

2. Department of Microbiology, Mount Sinai School of Medicine, One Gustave L. Levy Place, Box 1124, New York, NY 10029, USA.

3. Microbiology Graduate School Training Program, Mount Sinai School of Medicine, One Gustave L. Levy Place, Box 1124, New York, NY 10029, USA.

4. Emerging Pathogens Institute, Mount Sinai School of Medicine, One Gustave L. Levy Place, Box 1124, New York, NY 10029, USA.

Abstract

IKKϵ is an IKK (inhibitor of nuclear factor κBkinase)–related kinase implicated in virus induction of interferon-β (IFNβ). We report that, although mice lacking IKKϵ produce normal amounts of IFNβ, they are hypersusceptible to viral infection because of a defect in the IFN signaling pathway. Specifically, a subset of type I IFN-stimulated genes are not activated in the absence of IKKϵ because the interferon-stimulated gene factor 3 complex (ISGF3) does not bind to promoter elements of the affected genes. We demonstrate that IKKϵ is activated by IFNβ and that IKKϵ directly phosphorylates signal transducer and activator of transcription 1 (STAT1), a component of ISGF3. We conclude that IKKϵ plays a critical role in the IFN-inducible antiviral transcriptional response.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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