Zhu Sheng-Li, Wang Li, Cao Zhong-Ying, Wang Jun, Jing Ming-Zhen, Xia Zhang-Chuan, Ao Fang, Ye Lin-Bai, Liu Shi, Zhu Ying
State Key Laboratory of Virology and College of Life Sciences, Wuhan University, Wuhan 430072, China.
Biochem Biophys Res Commun. 2016 Feb 26;471(1):95-102. doi: 10.1016/j.bbrc.2016.01.173. Epub 2016 Feb 1.
Hepatitis C virus (HCV) nonstructural protein 5B (NS5B) functions as an RNA-dependent RNA polymerase in the HCV replication complex derived from the endoplasmic reticulum in hepatic cells. In this study, NS5B was used as bait in a yeast two-hybrid assay to screen a human liver cDNA library. We confirmed that CYP4F12, a member of the cytochrome P450 superfamily, interacted with NS5B. Furthermore, overexpression of CYP4F12 facilitated HCV replication. In contrast, knockdown of CYP4F12 by specific shRNA decreased HCV replication and viral protein expression. Moreover, our results demonstrated that HCV infection increased the binding of the transcription factor SREBP1 to the CYP4F12 promoter and activated the promoter activity, which indicated that HCV infection increased the expression of CYP4F12 through the SREBP1 pathway. Our results showed that HCV infection induced expression of CYP4F12 protein, which bound to the HCV replication complex to facilitate viral replication.
丙型肝炎病毒(HCV)非结构蛋白5B(NS5B)在源自肝细胞内质网的HCV复制复合体中作为一种依赖RNA的RNA聚合酶发挥作用。在本研究中,NS5B在酵母双杂交试验中用作诱饵,以筛选人肝脏cDNA文库。我们证实,细胞色素P450超家族成员CYP4F12与NS5B相互作用。此外,CYP4F12的过表达促进了HCV复制。相反,通过特异性短发夹RNA(shRNA)敲低CYP4F12可降低HCV复制和病毒蛋白表达。此外,我们的结果表明,HCV感染增加了转录因子SREBP1与CYP4F12启动子的结合并激活了启动子活性,这表明HCV感染通过SREBP1途径增加了CYP4F12的表达。我们的结果表明,HCV感染诱导了CYP4F12蛋白的表达,该蛋白与HCV复制复合体结合以促进病毒复制。