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Association of Hepatitis C Virus Replication Complexes with Microtubules and Actin Filaments Is Dependent on the Interaction of NS3 and NS5A

Association of Hepatitis C Virus Replication Complexes with Microtubules and Actin Filaments Is Dependent on the Interaction of NS3 and NS5A
ABSTRACT The hepatitis C virus (HCV) RNA replication complex (RC), which is composed of viral nonstructural (NS) proteins and host cellular proteins, replicates the viral RNA genome in association with intracellular membranes. Two viral NS proteins, NS3 and NS5A, are essential elements of the RC. Here, by using immunoprecipitation and fluorescence resonance energy transfer assays, we demonstrated that NS3 and NS5A interact with tubulin and actin. Furthermore, immunofluorescence microscopy and electron microscopy revealed that HCV RCs were aligned along microtubules and actin filaments in both HCV replicon cells and HCV-infected cells. In addition, the movement of RCs was inhibited when microtubules or actin filaments were depolymerized by colchicine and cytochalasin B, respectively. Based on our observations, we propose that microtubules and actin filaments provide the tracks for the movement of HCV RCs to other regions in the cell, and the molecular interactions between RCs and microtubules, or RCs and actin filaments, are mediated by NS3 and NS5A.
- National Cheng Kung University Taiwan
- Academia Sinica Taiwan
- University of California System United States
Carcinoma, Hepatocellular, Indoles, Cytochalasin B, Liver Neoplasms, Antibodies, Monoclonal, Hepacivirus, Carbocyanines, Kidney, Microtubules, Cell Line, Actin Cytoskeleton, Fluorescent Antibody Technique, Direct, Cell Line, Tumor, Fluorescence Resonance Energy Transfer, Humans, RNA, Viral, Colchicine, Fluorescein-5-isothiocyanate, RNA Helicases, Fluorescent Dyes
Carcinoma, Hepatocellular, Indoles, Cytochalasin B, Liver Neoplasms, Antibodies, Monoclonal, Hepacivirus, Carbocyanines, Kidney, Microtubules, Cell Line, Actin Cytoskeleton, Fluorescent Antibody Technique, Direct, Cell Line, Tumor, Fluorescence Resonance Energy Transfer, Humans, RNA, Viral, Colchicine, Fluorescein-5-isothiocyanate, RNA Helicases, Fluorescent Dyes
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