Pharmaceutical Research, Global Preclinical Safety (PRN), F. Hoffmann-La Roche Ltd., 4070 Basel, Switzerland.
Biol Proced Online. 2009 Jul 23;11:113-29. doi: 10.1007/s12575-009-9012-1.
MicroRNAs are positive and negative regulators of eukaryotic gene expression that modulate transcript abundance by specific binding to sequence motifs located prevalently in the 3' untranslated regions of target messenger RNAs (mRNA). Interferon-alpha-2a (IFNα) induces a large set of protein coding genes mediating antiproliferative and antiviral responses. Here we use a global microarray-based microRNA detection platform to identify genes that are induced by IFNα in hepatoma- or melanoma-derived human tumor cell lines. Despite the enormous differences in expression levels between these models, we were able to identify microRNAs that are upregulated by IFNα in both lines suggesting the possibility that interferon-regulated microRNAs are involved in the transcriptional repression of mRNA relevant to cytokine responses.
microRNAs 是真核生物基因表达的正、负调控因子,通过特异性结合靶信使 RNA(mRNA)3'非翻译区中普遍存在的序列基序来调节转录物丰度。干扰素-α-2a(IFNα)诱导一大组编码蛋白的基因,介导抗增殖和抗病毒反应。在这里,我们使用基于全基因组的 microRNA 检测平台来鉴定 IFNα 在肝癌或黑色素瘤来源的人肿瘤细胞系中诱导的基因。尽管这些模型之间的表达水平存在巨大差异,但我们能够鉴定出 IFNα 在两条线中上调的 microRNAs,这表明干扰素调节的 microRNAs 可能参与与细胞因子反应相关的 mRNA 的转录抑制。