ACBD3-mediated recruitment of PI4KB to picornavirus RNA replication sites

被引:159
作者
Sasaki, Jun [1 ]
Ishikawa, Kumiko [1 ]
Arita, Minetaro [2 ]
Taniguchi, Koki [1 ]
机构
[1] Fujita Hlth Univ, Dept Virol & Parasitol, Sch Med, Toyoake, Aichi 4701192, Japan
[2] Natl Inst Infect Dis, Dept Virol 2, Tokyo, Japan
关键词
ACBD3; Aichi virus; PI4KB; picornavirus; RNA replication; MOUTH-DISEASE VIRUS; ACYL-COENZYME-A; AICHI-VIRUS; SECRETORY PATHWAY; BREFELDIN-A; MOLECULAR CHARACTERIZATION; NONSTRUCTURAL PROTEINS; ENDOPLASMIC-RETICULUM; MEMBRANE ASSOCIATION; TRANSPORT VESICLES;
D O I
10.1038/emboj.2011.429
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Phosphatidylinositol 4-kinase III beta (PI4KB) is a host factor required for genome RNA replication of enteroviruses, small non-enveloped viruses belonging to the family Picornaviridae. Here, we demonstrated that PI4KB is also essential for genome replication of another picornavirus, Aichi virus (AiV), but is recruited to the genome replication sites by a different strategy from that utilized by enteroviruses. AiV non-structural proteins, 2B, 2BC, 2C, 3A, and 3AB, interacted with a Golgi protein, acylcoenzyme A binding domain containing 3 (ACBD3). Furthermore, we identified previously unknown interaction between ACBD3 and PI4KB, which provides a novel manner of Golgi recruitment of PI4KB. Knockdown of ACBD3 or PI4KB suppressed AiV RNA replication. The viral proteins, ACBD3, PI4KB, and phophatidylinositol-4-phosphate (PI4P) localized to the viral RNA replication sites. AiV replication and recruitment of PI4KB to the RNA replication sites were not affected by brefeldin A, in contrast to those in enterovirus infection. These results indicate that a viral protein/ACBD3/PI4KB complex is formed to synthesize PI4P at the AiV RNA replication sites and plays an essential role in viral RNA replication. The EMBO Journal (2012) 31, 754-766. doi: 10.1038/emboj.2011.429; Published online 29 November 2011
引用
收藏
页码:754 / 766
页数:13
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