| Literature DB >> 17855521 |
Yasuo Ariumi1, Misao Kuroki, Ken-ichi Abe, Hiromichi Dansako, Masanori Ikeda, Takaji Wakita, Nobuyuki Kato.
Abstract
DDX3, a DEAD-box RNA helicase, binds to the hepatitis C virus (HCV) core protein. However, the role(s) of DDX3 in HCV replication is still not understood. Here we demonstrate that the accumulation of both genome-length HCV RNA (HCV-O, genotype 1b) and its replicon RNA were significantly suppressed in HuH-7-derived cells expressing short hairpin RNA targeted to DDX3 by lentivirus vector transduction. As well, RNA replication of JFH1 (genotype 2a) and release of the core into the culture supernatants were suppressed in DDX3 knockdown cells after inoculation of the cell culture-generated HCVcc. Thus, DDX3 is required for HCV RNA replication.Entities:
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Year: 2007 PMID: 17855521 PMCID: PMC2168844 DOI: 10.1128/JVI.01517-07
Source DB: PubMed Journal: J Virol ISSN: 0022-538X Impact factor: 5.103