Transcriptional Profiling of Interferon Regulatory Factor 3 Target Genes: Direct Involvement in the Regulation of Interferon-Stimulated Genes

Nathalie Grandvaux(Molecular Oncology (United States)), Marc J. Servant(Molecular Oncology (United States)), Benjamin R. tenOever(Molecular Oncology (United States)), Ganes C. Sen(Cleveland Clinic), Siddarth Balachandran(University of Miami), Glen N. Barber(University of Miami), Rongtuan Lin(Molecular Oncology (United States)), John Hiscott(Molecular Oncology (United States))
Journal of Virology
June 1, 2002
Cited by 522Open Access
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Abstract

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.


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