| Literature DB >> 31829498 |
Bocun Shen1, Yanmeng Chen1, Jie Hu1, Miao Qiao1, Jihua Ren1, Jieli Hu1, Juan Chen1, Ni Tang1, Ailong Huang1, Yuan Hu1.
Abstract
Hepatitis B virus (HBV) infection is a major cause of acute and chronic liver diseases. During the HBV life cycle, HBV hijacks various host factors to assist viral replication. In this research, we find that the HBV regulatory protein X (HBx) can induce the upregulation of DExH-box RNA helicase 9 (DHX9) expression by repressing proteasome-dependent degradation mediated by MDM2. Furthermore, we demonstrate that DHX9 contributes to viral DNA replication in dependence on its helicase activity and nuclear localization. In addition, the promotion of viral DNA replication by DHX9 is dependent on its interaction with Nup98. Our findings reveal that HBx-mediated DHX9 upregulation is essential for HBV DNA replication.Entities:
Keywords: DHX9; HBx protein; Nup98; hepatitis B Virus; ubiquitylation
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Year: 2019 PMID: 31829498 DOI: 10.1111/cmi.13148
Source DB: PubMed Journal: Cell Microbiol ISSN: 1462-5814 Impact factor: 3.715