Functionally distinct effects of the C-terminal regions of IKKε and TBK1 on type I IFN production

• Published in: PloS one Vol. 9; no. 4; p. e94999
• Main Authors: Nakatsu, Yuichiro, Matsuoka, Mayumi, Chang, Tsung-Hsien, Otsuki, Noriyuki, Noda, Masahiro, Kimura, Hirokazu, Sakai, Kouji, Kato, Hiroshi, Takeda, Makoto, Kubota, Toru
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 10.04.2014; Public Library of Science (PLoS)
• Subjects: Activation; Animals; Biology and Life Sciences; Enzyme inhibitors; Gene expression; HEK293 Cells; Humans; I-kappa B Kinase - genetics; I-kappa B Kinase - metabolism; Immune response; Immune system; Immunity; Immunoglobulins; Infections; Infectious diseases; Innate immunity; Interferon; Interferon regulatory factor 3; Interferon regulatory factor 7; Interferon Type I - genetics; Interferon Type I - metabolism; Kinases; L Cells (Cell Line); Mice; Phosphorylation; Plasmids; Promoter Regions, Genetic; Protein-Serine-Threonine Kinases - genetics; Protein-Serine-Threonine Kinases - metabolism; Residues; Rodents; Signal Transduction - physiology; Signaling; Studies; Surveillance; Transcription factors; Viral infections; Virology; Japan
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0094999

Inhibitor of κB kinase ε (IKKε) and TANK binding kinase 1 (TBK1), so-called non-canonical IKKs or IKK-related kinases, are involved in the cellular innate immunity by inducing type I IFNs. Two kinases commonly phosphorylate transcription factors IRF3 and IRF7 in type I IFN production pathway. In contrast to TBK1, underlying mechanisms of IKKε activation and regions required for activation of downstream molecules are poorly understood. In this study, we investigated regions of IKKε required for the activation of type I IFN promoter specially, by focusing on the C-terminal region. To show the functional significance of the IKKε C-terminal region on type I IFN production, we employed various mutant forms of IKKε and compared to corresponding region of TBK1. We identified the specific regions and residues of IKKε involved in the activation of downstream signaling. Interestingly, corresponding region and residues are not required for activation of downstream signaling by TBK1. The results highlight the importance of the C-terminal region in the functional activity of IKKε in innate immune response and also the difference in activation mechanisms between IKKε and the closely related TBK1.