De Lucca Fernando L, Sales Valeria S F, Souza Liliana R, Murad Joana M, Watanabe Maria Angelica E
Department of Biochemistry and Immunology, School of Medicine University of São Paulo, Ribeirão Preto, SP, Brazil.
Mol Cell Biochem. 2003 May;247(1-2):211-7. doi: 10.1023/a:1024107512419.
Previous results with p9-RNA, obtained from lymph nodes of animals immunized with the peptide p9 of HIV-1, suggested that its effects on lymphocytes could be mediated by RNA-dependent protein kinase (PKR). Here we report that p9-RNA activates PKR leading to the degradation of the inhibitor I-kappaB alpha and the concomitant nuclear factor kappa B (NF-kappaB) activation. The fractionation of p9-RNA by affinity chromatography indicates that the poly A(+) p9-RNA is the fraction responsible for PKR activation. We also found that p9-RNA induces the production of interferon-gamma (IFN-gamma), but not interleukin (IL-4) since only IFN-gamma gene promoter contains NF-kappaB binding site. This study provides the first evidence that transcriptional control of gene expression by regulatory RNAs can be mediated by PKR through NF-kappaB activation. A model for the mechanism of action of poly A(+) p9-RNA is proposed.
先前从用HIV-1肽p9免疫的动物淋巴结中获得的p9-RNA的研究结果表明,其对淋巴细胞的作用可能由RNA依赖性蛋白激酶(PKR)介导。在此我们报告,p9-RNA激活PKR,导致抑制剂I-κBα降解,并伴随核因子κB(NF-κB)激活。通过亲和层析对p9-RNA进行分级分离表明,聚腺苷酸(+)p9-RNA是负责PKR激活的部分。我们还发现,p9-RNA诱导干扰素-γ(IFN-γ)产生,但不诱导白细胞介素(IL-4)产生,因为只有IFN-γ基因启动子含有NF-κB结合位点。本研究首次证明,调节性RNA对基因表达的转录控制可由PKR通过NF-κB激活介导。提出了聚腺苷酸(+)p9-RNA作用机制的模型。