Terenzi Fulvia, White Christine, Pal Srabani, Williams Bryan R G, Sen Ganes C
Department of Molecular Genetics/NE20, The Lewrnert research Institute, Cleveland Clinic, 9500 Euclid Avenue, Cleveland, OH 44195, USA.
J Virol. 2007 Aug;81(16):8656-65. doi: 10.1128/JVI.00322-07. Epub 2007 Jun 6.
The interferon-stimulated genes (ISGs) ISG56 and ISG54 are strongly induced in cultured cells by type I interferons (IFNs), viruses, and double-stranded RNA (dsRNA), which activate their transcription by various signaling pathways. Here we studied the stimulus-dependent induction of both genes in vivo. dsRNA, which is generated during virus infection, induced the expression of both genes in all organs examined. Induction was not seen in STAT1-deficient mice, indicating that dsRNA-induced gene expression requires endogenous IFN. We further examined the regulation of these ISGs in several organs from mice injected with dsRNA or IFN-beta. Both ISG56 and ISG54 were widely expressed and at comparable levels. However, in organs isolated from mice injected with IFN-alpha the expression of ISG54 was reduced and more restricted in distribution compared with the expression level and distribution of ISG56. When we began to study specific cell types, splenic B cells showed ISG54 but not ISG56 expression in response to all agonists. Finally, in livers isolated from mice infected with vesicular stomatitis virus, the expression of ISG56, but not ISG54, was induced; this difference was observed at both protein and mRNA levels. These studies have revealed unexpected complexity in IFN-stimulated gene induction in vivo. For the first time we showed that the two closely related genes are expressed in a tissue-specific and inducer-specific manner. Furthermore, our findings provide the first evidence of a differential pattern of expression of ISG54 and ISG56 genes by IFN-alpha and IFN-beta.
干扰素刺激基因(ISGs)ISG56和ISG54在培养细胞中可被I型干扰素(IFNs)、病毒和双链RNA(dsRNA)强烈诱导,这些物质通过各种信号通路激活它们的转录。在此,我们研究了这两种基因在体内的刺激依赖性诱导情况。病毒感染期间产生的dsRNA可诱导所检测的所有器官中这两种基因的表达。在STAT1缺陷小鼠中未观察到诱导现象,这表明dsRNA诱导的基因表达需要内源性IFN。我们进一步研究了在注射dsRNA或IFN-β的小鼠的多个器官中这些ISGs的调控情况。ISG56和ISG54均广泛表达且水平相当。然而,与ISG56的表达水平和分布相比,在从注射IFN-α的小鼠分离出的器官中,ISG54的表达降低且分布更受限。当我们开始研究特定细胞类型时,脾B细胞对所有激动剂的反应显示出ISG54的表达,但未显示ISG56的表达。最后,在从感染水疱性口炎病毒的小鼠分离出的肝脏中,诱导了ISG56的表达,但未诱导ISG54的表达;在蛋白质和mRNA水平均观察到了这种差异。这些研究揭示了体内干扰素刺激基因诱导中意想不到的复杂性。我们首次表明这两个密切相关的基因以组织特异性和诱导剂特异性的方式表达。此外,我们的发现首次提供了IFN-α和IFN-β对ISG54和ISG56基因表达差异模式的证据。