Hui Eric Ka-Wai, Barman Subrata, Tang Dominic Ho-Ping, France Bryan, Nayak Debi P
Department of Microbiology, Immunology and Molecular Genetics, Jonsson Comprehensive Cancer Center, Molecular Biology Institute, David Geffen School of Medicine, UCLA, Los Angeles, 90095, USA.
J Virol. 2006 Mar;80(5):2291-308. doi: 10.1128/JVI.80.5.2291-2308.2006.
Earlier studies have shown that the C-terminal half of helix 6 (H6) of the influenza A virus matrix protein (M1) containing the YRKL sequence is involved in virus budding (E. K.-W. Hui, S. Barman, T. Y. Yang, and D. P. Nayak, J. Virol. 77:7078-7092, 2003). In this report, we show that the YRKL sequence is the L domain motif of influenza virus. Like other L domains, YRKL can be inserted at different locations on the mutant M1 protein and can restore virus budding in a position-independent manner. Although YRKL is a part of the nuclear localization signal (NLS), the function of YRKL was independent of the NLS activity and the NLS function of M1 was not required for influenza virus replication. Some mutations in YRKL and the adjacent region caused a reduction in the virus titer by blocking virus release, and some affected virus morphology, producing elongated particles. Coimmunoprecipitation and Western blotting analyses showed that VPS28, a component of the ESCRT-I complex, and Cdc42, a member of the Rho family GTP-binding proteins, interacted with the M1 protein via the YRKL motif. In addition, depletion of VPS28 and Cdc42 by small interfering RNA resulted in reduction of influenza virus production. Moreover, overexpression of dominant-negative Cdc42 inhibited influenza virus replication, whereas a constitutively active Cdc42 mutant enhanced virus production in infected cells. These results indicated that VPS28, a component of ESCRT-I, and Cdc42, a small G protein, are associated with the M1 protein and involved in the influenza virus life cycle.
早期研究表明,甲型流感病毒基质蛋白(M1)的螺旋6(H6)的C端含有YRKL序列,参与病毒出芽(E.K.-W.许、S.巴尔曼、T.Y.杨和D.P.纳亚克,《病毒学杂志》77:7078 - 7092,2003年)。在本报告中,我们表明YRKL序列是流感病毒的L结构域基序。与其他L结构域一样,YRKL可以插入突变M1蛋白的不同位置,并能以位置独立的方式恢复病毒出芽。尽管YRKL是核定位信号(NLS)的一部分,但其功能独立于NLS活性,且M1的NLS功能对流感病毒复制并非必需。YRKL及其相邻区域的一些突变通过阻断病毒释放导致病毒滴度降低,一些突变影响病毒形态,产生拉长的颗粒。免疫共沉淀和蛋白质印迹分析表明,ESCRT - I复合物的一个组分VPS28和Rho家族GTP结合蛋白成员Cdc42通过YRKL基序与M1蛋白相互作用。此外,小干扰RNA使VPS28和Cdc42缺失导致流感病毒产生减少。而且,显性负性Cdc42的过表达抑制流感病毒复制,而组成型活性Cdc42突变体增强感染细胞中的病毒产生。这些结果表明,ESCRT - I的一个组分VPS28和小G蛋白Cdc42与M1蛋白相关,并参与流感病毒的生命周期。