中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
TanK-Binding Kinase 1 (TBK1) Isoforms Negatively Regulate Type I Interferon Induction by Inhibiting TBK1-IRF3 Interaction and IRF3 Phosphorylation

文献类型:期刊论文

作者Cao, Lu1; Hu, Yi Wei1,2; Zhang, Jie1; Wu, Xiao Man1; Nie, Pin1,3; Chang, Ming Xian1,3
刊名FRONTIERS IN IMMUNOLOGY
出版日期2018-01-30
卷号9页码:17
关键词alternative splicing spring viremia of carp virus TANK-binding kinase 1 spliced isoforms TANK-binding kinase 1 IRF3 type I interferon signaling immune homeostasis
ISSN号1664-3224
DOI10.3389/fimmu.2018.00084
英文摘要TANK-binding kinase 1 (TBK1) is an important serine/threonine-protein kinase that mediates phosphorylation and nuclear translocation of IRF3, which contributes to induction of type I interferons (IFNs) in the innate antiviral response. In mammals, TBK1 spliced isoform negatively regulates the virus-triggered IFN-beta signaling pathway by disrupting the interaction between retinoic acid-inducible gene I (RIG-I) and mitochondria antiviral-signaling protein (MAVS). However, it is still unclear whether alternative splicing patterns and the function of TBK1 isoform(s) exist in teleost fish. In this study, we identify two alternatively spliced isoforms of TBK1 from zebrafish, termed TBK1_tv1 and TBK1_tv2. Both TBK1_tv1 and TBK1_tv2 contain an incomplete STKc_TBK1 domain. Moreover, the UBL_TBK1_like domain is also missing for TBK1_tv2. TBK1_tv1 and TBK1_tv2 are expressed in zebrafish larvae. Overexpression of TBK1_tv1 and TBK1_tv2 inhibits RIG-I-, MAVS-, TBK1-, and IRF3-mediated activation of IFN promoters in response to spring viremia of carp virus infection. Also, TBK1_tv1 and TBK1_tv2 inhibit expression of IFNs and IFN-stimulated genes induced by MAVS and TBK1. Mechanistically, TBK1_tv1 and TBK1_tv2 competitively associate with TBK1 and IRF3 to disrupt the formation of a functional TBK1-IRF3 complex, impeding the phosphorylation of IRF3 mediated by TBK1. Collectively, these results demonstrate that TBK1 spliced isoforms are dominant negative regulators in the RIG-I/MAVS/TBK1/IRF3 antiviral pathway by targeting the functional TBK1-IRF3 complex formation. Identification and functional characterization of piscine TBK1 spliced isoforms may contribute to understanding the role of TBK1 expression in innate antiviral response.
资助项目National Natural Science Foundation of China[31372531] ; National Natural Science Foundation of China[31672687]
WOS研究方向Immunology
语种英语
WOS记录号WOS:000423556800001
出版者FRONTIERS MEDIA SA
源URL[http://202.127.146.157/handle/2RYDP1HH/4620]  
专题中国科学院武汉植物园
通讯作者Chang, Ming Xian
作者单位1.Chinese Acad Sci, Inst Hydrobiol, State Key Lab Freshwater Ecol & Biotechnol, Wuhan, Hubei, Peoples R China
2.Univ Chinese Acad Sci, Beijing, Peoples R China
3.Minist Agr, Key Lab Aquaculture Dis Control, Wuhan, Hubei, Peoples R China
推荐引用方式
GB/T 7714
Cao, Lu,Hu, Yi Wei,Zhang, Jie,et al. TanK-Binding Kinase 1 (TBK1) Isoforms Negatively Regulate Type I Interferon Induction by Inhibiting TBK1-IRF3 Interaction and IRF3 Phosphorylation[J]. FRONTIERS IN IMMUNOLOGY,2018,9:17.
APA Cao, Lu,Hu, Yi Wei,Zhang, Jie,Wu, Xiao Man,Nie, Pin,&Chang, Ming Xian.(2018).TanK-Binding Kinase 1 (TBK1) Isoforms Negatively Regulate Type I Interferon Induction by Inhibiting TBK1-IRF3 Interaction and IRF3 Phosphorylation.FRONTIERS IN IMMUNOLOGY,9,17.
MLA Cao, Lu,et al."TanK-Binding Kinase 1 (TBK1) Isoforms Negatively Regulate Type I Interferon Induction by Inhibiting TBK1-IRF3 Interaction and IRF3 Phosphorylation".FRONTIERS IN IMMUNOLOGY 9(2018):17.

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来源:武汉植物园

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