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Human microRNA hsa-miR-125a-5p interferes with expression of hepatitis B virus surface antigen

机译:人类microRNA hsa-miR-125a-5p干扰乙型肝炎病毒表面抗原的表达

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摘要

MicroRNAs are small non-coding RNAs that modulate gene expression at post-transcriptional level, playing a crucial role in cell differentiation and development. Recently, some reports have shown that a limited number of mammalian microRNAs are also involved in anti-viral defense. In this study, the analysis of the hepatitis B virus (HBV) genome by the computer program MiRanda led to the identification of seven sites that are potential targets for human liver microRNAs. These sites were found to be clustered in a 995-bp segment within the viral polymerase ORF and the overlapping surface antigen ORF, and conserved among the most common HBV subtypes. The HBV genomic targets were then subjected to a validation test based on cultured hepatic cells (HepG2, HuH-7 and PLC/PRF/5) and luciferase reporter genes. In this test, one of the selected microRNAs, hsa-miR-125a-5p, was found to interact with the viral sequence and to suppress the reporter activity markedly. The microRNA was then shown to interfere with the viral translation, down-regulating the expression of the surface antigen. Overall, these results support the emerging concept that some mammalian microRNAs play a role in virus-host interaction. Furthermore, they provide the basis for the development of new strategies for anti-HBV intervention.
机译:MicroRNA是小的非编码RNA,可在转录后水平调节基因表达,在细胞分化和发育中起关键作用。最近,一些报道表明,有限数量的哺乳动物microRNA也参与了抗病毒防御。在这项研究中,通过计算机程序MiRanda对乙型肝炎病毒(HBV)基因组的分析导致确定了七个可能成为人类肝脏microRNA潜在靶点的位点。发现这些位点聚集在病毒聚合酶ORF和重叠表面抗原ORF的995 bp片段中,并且在最常见的HBV亚型中保守。然后,基于培养的肝细胞(HepG2,HuH-7和PLC / PRF / 5)和荧光素酶报道基因对HBV基因组靶标进行验证测试。在该测试中,发现一种选定的微RNA hsa-miR-125a-5p与病毒序列相互作用,并显着抑制了报道分子的活性。然后显示了microRNA干扰病毒翻译,下调了表面抗原的表达。总体而言,这些结果支持了一些哺乳动物microRNA在病毒-宿主相互作用中发挥作用的新概念。此外,它们为开发抗-HBV干预新策略提供了基础。

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