Importin-7-dependent nuclear translocation of the Flavivirus core protein is required for infectious virus production

病毒学 生物 黄病毒 内输蛋白 核运输 黄病毒科 病毒 核蛋白 病毒生命周期 核定位序列 病毒复制 细胞核 细胞生物学 细胞质 丙型肝炎病毒 遗传学 基因 转录因子
作者
Yumi Itoh,Yoichi Miyamoto,Makoto Tokunaga,Tatsuya Suzuki,Akira Takada,Akinori Ninomiya,Tomomi Hishinuma,Mami Matsuda,Yoshihiro Yoneda,Masahiro Oka,Ryosuke Suzuki,Yoshiharu Matsuura,Toru Okamoto
出处
期刊:PLOS Pathogens [Public Library of Science]
卷期号:20 (8): e1012409-e1012409 被引量:6
标识
DOI:10.1371/journal.ppat.1012409
摘要

Flaviviridae is a family of positive-stranded RNA viruses, including human pathogens, such as Japanese encephalitis virus (JEV), dengue virus (DENV), Zika virus (ZIKV), and West Nile virus (WNV). Nuclear localization of the viral core protein is conserved among Flaviviridae , and this feature may be targeted for developing broad-ranging anti-flavivirus drugs. However, the mechanism of core protein translocation to the nucleus and the importance of nuclear translocation in the viral life cycle remain unknown. We aimed to identify the molecular mechanism underlying core protein nuclear translocation. We identified importin-7 (IPO7), an importin-β family protein, as a nuclear carrier for Flaviviridae core proteins. Nuclear import assays revealed that core protein was transported into the nucleus via IPO7, whereas IPO7 deletion by CRISPR/Cas9 impaired their nuclear translocation. To understand the importance of core protein nuclear translocation, we evaluated the production of infectious virus or single-round-infectious-particles in wild-type or IPO7-deficient cells; both processes were significantly impaired in IPO7-deficient cells, whereas intracellular infectious virus levels were equivalent in wild-type and IPO7-deficient cells. These results suggest that IPO7-mediated nuclear translocation of core proteins is involved in the release of infectious virus particles of flaviviruses.
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