Involvement of zebrafish RIG-I in NF-κB and IFN signaling pathways: Insights into functional conservation of RIG-I in antiviral innate immunity

被引:35
作者
Nie, Li [1 ,2 ]
Zhang, Ying-sheng [1 ,2 ]
Dong, Wei-ren [1 ,2 ]
Xiang, Li-xin [1 ,2 ]
Shao, Jian-zhong [1 ,2 ]
机构
[1] Zhejiang Univ, Coll Life Sci, Hangzhou 310058, Zhejiang, Peoples R China
[2] Key Lab Cell & Gene Engn Zhejiang Prov, Hangzhou 310058, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Zebrafish RIG-I; NF-kappa B signaling pathway; IFN signaling pathway; TRIM25; regulation; HEPATITIS-C VIRUS; STRUCTURAL BASIS; RNA RECOGNITION; ACTIVATION; GENE; RECEPTORS; INDUCTION; HELICASE; PROTEIN; MECHANISM;
D O I
10.1016/j.dci.2014.09.008
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
The retinoic acid-inducible gene I (RIG-I) is a critical sensor for host recognition of RNA virus infection and initiation of antiviral signaling pathways in mammals. However, data on the occurrence and functions of this molecule in lower vertebrates are limited. In this study, we characterized an RIG-I homolog (DrRIG-I) from zebrafish. Structurally, this DrRIG-I shares a number of conserved functional domains/motifs with its mammalian counterparts, namely, caspase activation and recruitment domain, DExD/H box, a helicase domain, and a C-terminal domain. Functionally, stimulation with DrRIG-I CARD in zebrafish embryos significantly activated the NF-kappa B and IFN signaling pathways, leading to the expression of TNF-alpha, IL-8 and IFN-induced Mx, ISG15, and viperin. However, knockdown of TRIM25 (a pivotal activator for RIG-I receptors) significantly suppressed the induced activation of IFN signaling. Results suggested the functional conservation of RIG-I receptors in the NF-kappa B and IFN signaling pathways between teleosts and mammals, providing a perspective into the evolutionary history of RIG-I-mediated antiviral innate immunity. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:95 / 101
页数:7
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