Grandvaux Nathalie, Servant Marc J, tenOever Benjamin, Sen Ganes C, Balachandran Siddarth, Barber Glen N, Lin Rongtuan, Hiscott John
Terry Fox Molecular Oncology Group, Lady Davis Institute for Medical Research, McGill University, Montreal, Quebec H3T 1E2, Canada.
J Virol. 2002 Jun;76(11):5532-9. doi: 10.1128/jvi.76.11.5532-5539.2002.
Ubiquitously expressed interferon regulatory factor 3 (IRF-3) is directly activated after virus infection and functions as a key activator of the immediate-early alpha/beta interferon (IFN) genes, as well as the RANTES chemokine gene. In the present study, a tetracycline-inducible expression system expressing a constitutively active form of IRF-3 (IRF-3 5D) was combined with DNA microarray analysis to identify target genes regulated by IRF-3. Changes in mRNA expression profiles of 8,556 genes were monitored after Tet-inducible expression of IRF-3 5D. Among the genes upregulated by IRF-3 were transcripts for several known IFN-stimulated genes (ISGs). Subsequent analysis revealed that IRF-3 directly induced the expression of ISG56 in an IFN-independent manner through the IFN-stimulated responsive elements (ISREs) of the ISG56 promoter. These results demonstrate that, in addition to its role in the formation of a functional immediate-early IFN-beta enhanceosome, IRF-3 is able to discriminate among ISRE-containing genes involved in the establishment of the antiviral state as a direct response to virus infection.
普遍表达的干扰素调节因子3(IRF-3)在病毒感染后被直接激活,并作为即刻早期α/β干扰素(IFN)基因以及RANTES趋化因子基因的关键激活因子发挥作用。在本研究中,将表达组成型活性形式的IRF-3(IRF-3 5D)的四环素诱导表达系统与DNA微阵列分析相结合,以鉴定受IRF-3调控的靶基因。在四环素诱导表达IRF-3 5D后,监测了8556个基因的mRNA表达谱变化。在受IRF-3上调的基因中,有几个已知的干扰素刺激基因(ISG)的转录本。随后的分析表明,IRF-3通过ISG56启动子的干扰素刺激反应元件(ISRE)以不依赖干扰素的方式直接诱导ISG56的表达。这些结果表明,除了在功能性即刻早期IFN-β增强体形成中的作用外,IRF-3还能够区分参与建立抗病毒状态的含ISRE基因,作为对病毒感染的直接反应。