Tenoever Benjamin R, Ng Sze-Ling, Chua Mark A, McWhirter Sarah M, García-Sastre Adolfo, Maniatis Tom
Department of Molecular and Cellular Biology, Harvard University, 7 Divinity Avenue, Cambridge, MA 02138, USA.
Science. 2007 Mar 2;315(5816):1274-8. doi: 10.1126/science.1136567.
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.
IKKε是一种与核因子κB激酶(IKK)相关的激酶,参与病毒诱导的β干扰素(IFNβ)产生。我们报告,尽管缺乏IKKε的小鼠产生正常量的IFNβ,但由于IFN信号通路存在缺陷,它们对病毒感染高度敏感。具体而言,在缺乏IKKε的情况下,一部分I型IFN刺激基因未被激活,因为干扰素刺激基因因子3复合物(ISGF3)不与受影响基因的启动子元件结合。我们证明IKKε被IFNβ激活,并且IKKε直接磷酸化ISGF3的一个组成部分——信号转导和转录激活因子1(STAT1)。我们得出结论,IKKε在IFN诱导的抗病毒转录反应中起关键作用。