Inhibition of HCV Replication in HCV Replicon by shRNAs |
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Authors: | Hiroyuki Hamazaki Hitoshi Takahashi Kunitada Shimotohno Naoko Miyano-Kurosaki Hiroshi Takaku |
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Affiliation: | 1. Department of Life and Environmental Sciences , Chiba Institute of Technology , Chiba, Japan;2. Department of Viral Oncology , Institute for Virus Research, Kyoto University , Kyoto, Japan;3. Department of Life and Environmental Sciences, and High Technology Research Center , Chiba Institute of Technology , Chiba, Japan |
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Abstract: | We show that the vector-derived long dsRNA specifically inhibits the replication of HCV RNA in HCV replicon. We designed a long dsRNA targeted to the full-length HCV IRES/core elements (1-to 377-nt). Our results revealed that the replication of HCV RNA was reduced to near background levels in a sequence-specific manner by the long dsRNAs in the HCV replicon. We also designed four shRNAs against several regions (120- to 139-nt, 260- to 279-nt, 330- to 349-nt, and 340- to 359-nt) of the HCV IRES/Core elements. The two HCV IRES/core-specific shRNAs, 330- to 349-nt and 340- to 359-nt, containing the AUG initiation codon sequence showed stronger HCV inhibitory effects than the other two shRNAs, 120- to 139-nt and 260- to 279-nt. |
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Keywords: | RNAi Long dsRNA shRNA HCV IRES/Core HCV replicon Anti-HCV |
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