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狂犬病病毒P蛋白与LC8动力蛋白轻链的相互作用。

Interaction of the rabies virus P protein with the LC8 dynein light chain.

作者信息

Raux H, Flamand A, Blondel D

机构信息

Laboratoire de Génétique des Virus, CNRS, 91198 Gif sur Yvette, France.

出版信息

J Virol. 2000 Nov;74(21):10212-6. doi: 10.1128/jvi.74.21.10212-10216.2000.

Abstract

The rabies virus P protein is involved in viral transcription and replication but its precise function is not clear. We investigated the role of P (CVS strain) by searching for cellular partners by using a two-hybrid screening of a PC12 cDNA library. We isolated a cDNA encoding a 10-kDa dynein light chain (LC8). LC8 is a component of cytoplasmic dynein involved in the minus end-directed movement of organelles along microtubules. We confirmed that this molecule interacts with P by coimmunoprecipitation in infected cells and in cells transfected with a plasmid encoding P protein. LC8 was also detected in virus particles. Series of deletions from the N- and C-terminal ends of P protein were used to map the LC8-binding domain to the central part of P (residues 138 to 172). These results are relevant to speculate that dynein may be involved in the axonal transport of rabies virus along microtubules through neuron cells.

摘要

狂犬病病毒P蛋白参与病毒转录和复制,但其确切功能尚不清楚。我们通过对PC12 cDNA文库进行双杂交筛选寻找细胞伴侣,来研究P(CVS株)的作用。我们分离出一个编码10 kDa动力蛋白轻链(LC8)的cDNA。LC8是胞质动力蛋白的一个组成部分,参与细胞器沿微管向负端的移动。我们通过免疫共沉淀在感染细胞和转染了编码P蛋白质粒的细胞中证实了该分子与P相互作用。在病毒颗粒中也检测到了LC8。对P蛋白的N端和C端进行一系列缺失,将LC8结合域定位到P的中部(第138至172位氨基酸)。这些结果有助于推测动力蛋白可能通过神经元细胞参与狂犬病病毒沿微管的轴突运输。

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