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 García‐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:326
标识
DOI:10.1126/science.1136567
摘要
IKKepsilon is an IKK (inhibitor of nuclear factor kappaBkinase)-related kinase implicated in virus induction of interferon-beta (IFNbeta). We report that, although mice lacking IKKepsilon produce normal amounts of IFNbeta, 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 IKKepsilon because the interferon-stimulated gene factor 3 complex (ISGF3) does not bind to promoter elements of the affected genes. We demonstrate that IKKepsilon is activated by IFNbeta and that IKKepsilon directly phosphorylates signal transducer and activator of transcription 1 (STAT1), a component of ISGF3. We conclude that IKKepsilon plays a critical role in the IFN-inducible antiviral transcriptional response.
科研通智能强力驱动
Strongly Powered by AbleSci AI