Sha Fushen, Wu Shuangxing, Zhang Hui, Guo Xuemin
Zhongshan School of Medicine, Institute of Human Virology, Sun Yat-Sen University, Guangzhou 510080, China Key Laboratory of Tropical Disease Control, Sun Yat-Sen University, Ministry of Education, Guangzhou 510080, China.
Zhongshan School of Medicine, Institute of Human Virology, Sun Yat-Sen University, Guangzhou 510080, China Key Laboratory of Tropical Disease Control, Sun Yat-Sen University, Ministry of Education, Guangzhou 510080, China
Acta Biochim Biophys Sin (Shanghai). 2014 Nov;46(11):991-6. doi: 10.1093/abbs/gmu088. Epub 2014 Oct 1.
Nuclear factor-κB (NF-κB) is an important transcription factor. While the NF-κB signaling pathway is modulated by many microRNAs (miRNAs), very few have been reported to target NF-κB1 gene directly. In this study, we used multiple miRNA target prediction programs to predict miRNAs with putative NF-κB1 3'-untranslated region (UTR) binding sites. miR-183 was strongly implicated and experimentally validated by reporter assays. The results showed a reduced expression of the NF-κB1 3'UTR containing luciferase vector by ∼30%, which was comparable to the reduction by miR-9 (the only known miRNA targeting the NF-κB1 3'UTR). Mutagenesis of the miR-183 seed region binding sequence in the NF-κB1 3'UTR abolished the inhibitory effect of miR-183, as noted by the NF-κB1 3'UTR-containing reporter. Moreover, similar to miR-9, miR-183 could down-regulate the expression of the reporter driven by NF-κB promoter to some degree, suggesting that miR-183 might negatively regulate the endogenous NF-κB1. Overall, our data provide computational and experimental evidence that NF-κB1 is a potential target of miR-183.
核因子-κB(NF-κB)是一种重要的转录因子。虽然NF-κB信号通路受到许多微小RNA(miRNA)的调节,但据报道,直接靶向NF-κB1基因的miRNA却非常少。在本研究中,我们使用了多个miRNA靶标预测程序来预测具有假定的NF-κB1 3'-非翻译区(UTR)结合位点的miRNA。miR-183被强烈认为是候选对象,并通过报告基因检测进行了实验验证。结果显示,含有荧光素酶载体的NF-κB1 3'UTR的表达降低了约30%,这与miR-9(唯一已知的靶向NF-κB1 3'UTR的miRNA)导致的降低程度相当。NF-κB1 3'UTR中miR-183种子区域结合序列的诱变消除了miR-183的抑制作用,这在含有NF-κB1 3'UTR的报告基因中得到了证实。此外,与miR-9类似,miR-183在一定程度上可以下调由NF-κB启动子驱动的报告基因的表达,这表明miR-183可能对内源性NF-κB1产生负调控作用。总体而言,我们的数据提供了计算和实验证据,表明NF-κB1是miR-183的潜在靶标。