Multiple functions of DDX3 RNA helicase in gene regulation, tumorigenesis, and viral infection

被引:108
作者
Ariumi, Yasuo [1 ]
机构
[1] Kumamoto Univ, Int Res Ctr Med Sci, Ctr AIDS Res, Ariumi Project Lab, Kumamoto 8600811, Japan
基金
日本学术振兴会;
关键词
HEPATITIS-C-VIRUS; HUMAN-IMMUNODEFICIENCY-VIRUS; JAPANESE ENCEPHALITIS-VIRUS; CORE PROTEIN INTERACTS; DEAD-BOX PROTEIN-3; RIG-I; HIV-1; REV; TRANSCRIPTIONAL REGULATION; TRANSLATION INITIATION; ADAPTER PROTEIN;
D O I
10.3389/fgene.2014.00423
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
The DEAD-box RNA helicase DDX3 is a multifunctional protein involved in all aspects of RNA metabolism, including transcription, splicing, mRNA nuclear export, translation, RNA decay and ribosome biogenesis. In addition, DDX3 is also implicated in cell cycle regulation, apoptosis, Wnt-beta-catenin signaling, tumorigenesis, and viral infection. Notably, recent studies suggest that DDX3 is a component of anti-viral innate immune signaling pathways. Indeed, DDX3 contributes to enhance the induction of anti-viral mediators, interferon (IFN) regulatory factor 3 and type I IFN. However, DDX3 seems to be an important target for several viruses, such as human immunodeficiency virus type 1 (HIV-1), hepatitis C virus (HCV), hepatitis B virus (HBV), and poxvirus. DDX3 interacts with HIV-1 Rev or HCV Core protein and modulates its function. At least, DDX3 is required for both HIV-1 and HCV replication. Therefore, DDX3 could be a novel therapeutic target for the development of drug against HIV-1 and HCV.
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页数:10
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