Human kinome analysis reveals novel kinases contributing to virus infection and retinoic-acid inducible gene I-induced type I and type III IFN gene expression

Innate Immun. 2013 Oct;19(5):516-30. doi: 10.1177/1753425912473345. Epub 2013 Feb 12.

Abstract

Activation of host innate antiviral responses are mediated by retinoic-acid inducible gene I (RIG-I)-like receptors, RIG-I and melanoma differentiation-associated gene 5, and TLRs 3, 7, 8 and 9, recognising different types of viral nucleic acids. The major components of the RIG-I- and TLR pathways have putatively been identified, but previously unrecognised kinases may contribute to virus infection-induced activation of the IFN response. Here, we screened a human kinase cDNA library, termed the kinome, using an IFN-λ1 promoter-driven luciferase reporter assay in HEK293 cells during Sendai virus infection. Of the 568 kinases analysed, nearly 50 enhanced IFN-λ1 gene expression at least twofold in response to Sendai virus infection. The best activators were FYN (FYN oncogene related to SRC, FGR, YES), serine/threonine kinase 24, activin A receptor type 1 and SRPK1 (SFRS protein kinase 1). These kinases enhanced RIG-I-dependent IFN-λ1 promoter activation via IFN-stimulated response and NF-κB elements, as confirmed using mutant IFN-λ1 promoter constructs. FYN and SRPK1 enhanced IFN-λ1 and CXCL10 protein production via the RIG-I pathway, and stimulated RIG-I and MyD88-dependent phosphorylation of IRF3 and IRF7 transcription factors, respectively. We conclude that several previously unrecognised kinases, particularly FYN and SRPK1, positively regulate IFN-λ1 and similarly regulated cytokine and chemokine genes during viral infection.

Keywords: Viral infection; innate immunity; interferon regulatory factor; kinase signalling; type III interferon.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Activin Receptors, Type I / metabolism
  • DEAD Box Protein 58
  • DEAD-box RNA Helicases / genetics
  • DEAD-box RNA Helicases / metabolism*
  • Gene Library
  • HEK293 Cells
  • Humans
  • Immunity, Innate / genetics
  • Interferon-Induced Helicase, IFIH1
  • Interferons
  • Interleukins / genetics
  • Interleukins / metabolism*
  • Mutagenesis, Site-Directed
  • Protein Serine-Threonine Kinases / metabolism*
  • Proto-Oncogene Proteins c-fyn / metabolism*
  • Receptors, Immunologic
  • Respirovirus Infections / immunology
  • Respirovirus Infections / metabolism*
  • Sendai virus / immunology*
  • Signal Transduction / genetics
  • Toll-Like Receptors / metabolism
  • Up-Regulation

Substances

  • interferon-lambda, human
  • Interleukins
  • Receptors, Immunologic
  • Toll-Like Receptors
  • Interferons
  • SRPK1 protein, human
  • Proto-Oncogene Proteins c-fyn
  • Protein Serine-Threonine Kinases
  • ACVR1 protein, human
  • Activin Receptors, Type I
  • RIGI protein, human
  • IFIH1 protein, human
  • DEAD Box Protein 58
  • DEAD-box RNA Helicases
  • Interferon-Induced Helicase, IFIH1