Key Laboratory of Molecular Biology on Infectious Diseases, Ministry of Education, Second Affiliated Hospital, Chongqing Medical University, Chongqing 400016, China.
Antiviral Res. 2012 Jun;94(3):225-31. doi: 10.1016/j.antiviral.2012.04.004. Epub 2012 Apr 24.
Drosha regulates the biogenesis of microRNAs (miRNAs) and plays an essential role in the regulation of gene expression. Infection with hepatitis B virus (HBV) causes chronic hepatitis and liver cirrhosis. It is also a major risk factor for hepatocellular carcinoma. Emerging evidence suggests that HBV alters miRNA expression profiles, but the mechanisms underlying this process have not yet been fully elucidated. We therefore examined how HBV affected the production of miRNAs. We found that Drosha mRNA and protein expression were downregulated in cells expressing the HBV genome. This was associated with a reduction in the activity of the Drosha gene promoter. Gene silencing of HBx by RNA interference significantly restored the expression of Drosha. In conclusion, our data show that HBV could downregulate Drosha expression by inhibiting promoter activity, and the transcription factors SP1 and AP-2α may be involved in this process. This provides a new understanding of the mechanism of HBV-induced miRNAs dysregulation.
Drosha 调控 microRNAs (miRNAs) 的生物发生,在基因表达调控中发挥重要作用。乙型肝炎病毒 (HBV) 感染可导致慢性肝炎和肝硬化,也是肝细胞癌的主要危险因素。新出现的证据表明,HBV 改变了 miRNA 的表达谱,但这一过程的机制尚未完全阐明。因此,我们研究了 HBV 如何影响 miRNA 的产生。我们发现,表达 HBV 基因组的细胞中 Drosha mRNA 和蛋白表达下调,这与 Drosha 基因启动子活性降低有关。通过 RNA 干扰沉默 HBx 可显著恢复 Drosha 的表达。总之,我们的数据表明,HBV 通过抑制启动子活性下调 Drosha 表达,转录因子 SP1 和 AP-2α 可能参与这一过程。这为 HBV 诱导的 miRNAs 失调的机制提供了新的认识。