共 53 条
Suppression of hepatitis C virus replicon by RNA interference directed against the NS3 and NS5B regions of the viral genome
被引:59
作者:

Takigawa, Y
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机构:
Kobe Univ, Grad Sch Med, Dept Microbiol, Chuo Ku, Kobe, Hyogo 6500017, Japan Kobe Univ, Grad Sch Med, Dept Microbiol, Chuo Ku, Kobe, Hyogo 6500017, Japan

Nagano-Fujii, M
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h-index: 0
机构:
Kobe Univ, Grad Sch Med, Dept Microbiol, Chuo Ku, Kobe, Hyogo 6500017, Japan Kobe Univ, Grad Sch Med, Dept Microbiol, Chuo Ku, Kobe, Hyogo 6500017, Japan

Deng, L
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h-index: 0
机构:
Kobe Univ, Grad Sch Med, Dept Microbiol, Chuo Ku, Kobe, Hyogo 6500017, Japan Kobe Univ, Grad Sch Med, Dept Microbiol, Chuo Ku, Kobe, Hyogo 6500017, Japan

Hidajat, R
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h-index: 0
机构:
Kobe Univ, Grad Sch Med, Dept Microbiol, Chuo Ku, Kobe, Hyogo 6500017, Japan Kobe Univ, Grad Sch Med, Dept Microbiol, Chuo Ku, Kobe, Hyogo 6500017, Japan

Tanaka, M
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h-index: 0
机构:
Kobe Univ, Grad Sch Med, Dept Microbiol, Chuo Ku, Kobe, Hyogo 6500017, Japan Kobe Univ, Grad Sch Med, Dept Microbiol, Chuo Ku, Kobe, Hyogo 6500017, Japan

Mizuta, H
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机构:
Kobe Univ, Grad Sch Med, Dept Microbiol, Chuo Ku, Kobe, Hyogo 6500017, Japan Kobe Univ, Grad Sch Med, Dept Microbiol, Chuo Ku, Kobe, Hyogo 6500017, Japan

Hotta, H
论文数: 0 引用数: 0
h-index: 0
机构:
Kobe Univ, Grad Sch Med, Dept Microbiol, Chuo Ku, Kobe, Hyogo 6500017, Japan Kobe Univ, Grad Sch Med, Dept Microbiol, Chuo Ku, Kobe, Hyogo 6500017, Japan
机构:
[1] Kobe Univ, Grad Sch Med, Dept Microbiol, Chuo Ku, Kobe, Hyogo 6500017, Japan
关键词:
hepatitis C virus;
nonstructural regions;
RNA interference;
lentivirus vector;
D O I:
10.1111/j.1348-0421.2004.tb03556.x
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
RNA interference (RNAi) is a phenomenon in which small interfering RNA (siRNA), an RNA duplex 21 to 23 nucleotides (nt) long, or short hairpin RNA (shRNA) resembling siRNA, mediates degradation of the target RNA molecule in a sequence-specific manner. RNAi is now expected to be a useful therapeutic strategy for hepatitis C virus (HCV) infection. In the present study we compared the efficacy of a number of shRNAs directed against different target regions of the HCV genome, such as 5'-untranslated region (5'UTR) (nt 286 to 304), Core (nt 371 to 389), NS3-1 (nt 2052 to 2060), NS3-2 (nt 2104 to 2122), and NS5B (nt 7326 to 7344), all of which except for NS5B are conserved among most, if not all, HCV subtype 1b (HCV-1b) isolates in Japan. We utilized two methods to express shRNAs, one utilizing an expression plasmid (pAVU6+27) and the other utilizing a recombinant lentivirus harboring the pAVU6+27-derived expression cassette. Although 5'UTR has been considered to be the most suitable region for therapeutic siRNA and/or shRNA because of its extremely high degree of sequence conservation, we observed only a faint suppression of an HCV subgenomic replicon by shRNA against 5'UTR. In both plasmid- and lentivirus-mediated expression systems, shRNAs against NS3-1 and NS5B suppressed most efficiently the replication of the HCV replicon without suppressing host cellular gene expression. Synthetic siRNA against NS3-1 also inhibited replication of the HCV replicon in a dose-dependent manner. Taken together, the present results imply the possibility that the recombinant lentivirus expressing shRNA against NS3-1 would be a useful tool to inhibit HCV-1b infection.
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收藏
页码:591 / 598
页数:8
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Lendeckel, W
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Max Planck Inst Biophys Chem, Dept Cellular Biochem, D-37077 Gottingen, Germany Max Planck Inst Biophys Chem, Dept Cellular Biochem, D-37077 Gottingen, Germany

Tuschl, T
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Max Planck Inst Biophys Chem, Dept Cellular Biochem, D-37077 Gottingen, Germany Max Planck Inst Biophys Chem, Dept Cellular Biochem, D-37077 Gottingen, Germany