| Literature DB >> 26845356 |
Sheng-Li Zhu1, Li Wang2, Zhong-Ying Cao3, Jun Wang4, Ming-Zhen Jing5, Zhang-Chuan Xia6, Fang Ao7, Lin-Bai Ye8, Shi Liu9, Ying Zhu10.
Abstract
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.Entities:
Keywords: CYP4F12; Hepatitis C virus; Viral replication
Mesh:
Substances:
Year: 2016 PMID: 26845356 DOI: 10.1016/j.bbrc.2016.01.173
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575