STAT1
干扰素
STAT蛋白
IκB激酶
干扰素调节因子
激活剂(遗传学)
激酶
生物
转录因子
信号转导
内部收益率1
免疫
磷酸化
基因
癌症研究
病毒学
细胞生物学
免疫系统
免疫学
NF-κB
车站3
遗传学
作者
Benjamin R. tenOever,Sze‐Ling Ng,Mark A. Chua,Sarah M. McWhirter,Adolfo Garcı́a-Sastre,Tom Maniatis
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2007-03-02
卷期号:315 (5816): 1274-1278
被引量:334
标识
DOI:10.1126/science.1136567
摘要
IKKϵ is an IKK (inhibitor of nuclear factor κBkinase)–related kinase implicated in virus induction of interferon-β (IFNβ). We report that, although mice lacking IKKϵ produce normal amounts of IFNβ, they are hypersusceptible to viral infection because of a defect in the IFN signaling pathway. Specifically, a subset of type I IFN-stimulated genes are not activated in the absence of IKKϵ because the interferon-stimulated gene factor 3 complex (ISGF3) does not bind to promoter elements of the affected genes. We demonstrate that IKKϵ is activated by IFNβ and that IKKϵ directly phosphorylates signal transducer and activator of transcription 1 (STAT1), a component of ISGF3. We conclude that IKKϵ plays a critical role in the IFN-inducible antiviral transcriptional response.
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