Lai Chao-Kuen, Jeng King-Song, Machida Keigo, Lai Michael M C
Institute of Molecular Biology, Academia Sinica, Taipei, Taiwan.
J Virol. 2008 Sep;82(17):8838-48. doi: 10.1128/JVI.00398-08. Epub 2008 Jun 18.
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.
丙型肝炎病毒(HCV)RNA复制复合体(RC)由病毒非结构(NS)蛋白和宿主细胞蛋白组成,与细胞内膜结合复制病毒RNA基因组。两种病毒NS蛋白,即NS3和NS5A,是RC的关键组成部分。在此,我们通过免疫沉淀和荧光共振能量转移分析证明,NS3和NS5A与微管蛋白和肌动蛋白相互作用。此外,免疫荧光显微镜和电子显微镜显示,在HCV复制子细胞和HCV感染细胞中,HCV RC均沿微管和肌动蛋白丝排列。另外,当微管或肌动蛋白丝分别被秋水仙碱和细胞松弛素B解聚时,RC的移动受到抑制。基于我们的观察结果,我们提出微管和肌动蛋白丝为HCV RC向细胞其他区域移动提供了轨道,并且RC与微管或RC与肌动蛋白丝之间的分子相互作用是由NS3和NS5A介导的。