IRF-3-Dependent, NFκB- and JNK-Independent Activation of the 561 and IFN-β Genes in Response to Double-Stranded RNA

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 99; no. 9; pp. 6322 - 6327
• Main Authors: Peters, Kristi L., Smith, Heather L., Stark, George R., Sen, Ganes C.
• Format: Journal Article
• Language: English
• Published: National Academy of Sciences 30.04.2002; National Acad Sciences; The National Academy of Sciences
• Subjects: Actins; Biological Sciences; Cell culture techniques; Cell lines; Double stranded RNA; Gene induction; Genes; Inductive reasoning; IRF-3 protein; Messenger RNA; RNA; Transcription factors
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.092133199

Double-stranded (ds) RNA induces transcription of the 561 gene by activating IFN regulatory factor (IRF) transcription factors, whereas similar induction of the IFN-β gene is thought to require additional activation of NFκB and AP-1. In mutant P2.1 cells, dsRNA failed to activate NFκB, IRF-3, p38, or c-Jun N-terminal kinase, and transcription of neither 561 mRNA nor IFN-β mRNA was induced. The defect in the IRF-3 pathway was traced to a low cellular level of this protein because of its higher rate of degradation in P2.1 cells. As anticipated, in several clonal derivatives of P2.1 cells expressing different levels of transfected IRF-3, activation of IRF-3 and induction of 561 mRNA by dsRNA was restored fully, although the defects in other responses to dsRNA persisted. Surprisingly, IFN-β mRNA also was induced strongly in these cells in response to dsRNA, demonstrating that the activation of NFκB and AP-1 is not required. This conclusion was confirmed in wild-type cells overexpressing IRF-3 by blocking NFκB activation with the IκB superrepressor and AP-1 activation with a p38 inhibitor. Therefore, IRF-3 activation by dsRNA is sufficient to induce the transcription of genes with simple promoters such as 561 as well as complex promoters such as IFN-β.