生物
先天免疫系统
泛素连接酶
干扰素
坦克结合激酶1
刺
泛素
DNA连接酶
基因敲除
细胞生物学
Ⅰ型干扰素
干扰素基因刺激剂
DNA
DNA病毒
免疫系统
分子生物学
激酶
基因
病毒学
蛋白激酶A
免疫学
生物化学
MAP激酶激酶激酶
航空航天工程
基因组
工程类
作者
Tetsuo Tsuchida,Jian Zou,Tatsuya Saitoh,Himanshu Kumar,Takayuki Abe,Yoshiharu Matsuura,Taro Kawai,Shizuo Akira
出处
期刊:Immunity
[Cell Press]
日期:2010-11-01
卷期号:33 (5): 765-776
被引量:449
标识
DOI:10.1016/j.immuni.2010.10.013
摘要
The innate immune system detects pathogen- and host-derived double-stranded DNA exposed to the cytosol and induces type I interferon (IFN) and other cytokines. Here, we identified interferon-inducible tripartite-motif (TRIM) 56 as a regulator of double-stranded DNA-mediated type I interferon induction. TRIM56 overexpression enhanced IFN-β promoter activation after double-stranded DNA stimulation whereas TRIM56 knockdown abrogated it. TRIM56 interacted with STING and targeted it for lysine 63-linked ubiquitination. This modification induced STING dimerization, which was a prerequisite for recruitment of the antiviral kinase TBK1 and subsequent induction of IFN-β. Taken together, these results indicate that TRIM56 is an interferon-inducible E3 ubiquitin ligase that modulates STING to confer double-stranded DNA-mediated innate immune responses.
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