ESCRT-III mediates budding across the inner nuclear membrane and regulates its integrity

被引:85
作者
Arii, Jun [1 ,2 ]
Watanabe, Mizuki [1 ,2 ]
Maeda, Fumio [1 ,2 ]
Tokai-Nishizumi, Noriko [3 ]
Chihara, Takahiro [4 ,5 ]
Miura, Masayuki [4 ]
Maruzuru, Yuhei [1 ,2 ]
Koyanagi, Naoto [1 ,2 ]
Kato, Akihisa [1 ,2 ]
Kawaguchi, Yasushi [1 ,2 ]
机构
[1] Univ Tokyo, Inst Med Sci, Div Mol Virol, Dept Microbiol & Immunol,Minato Ku, Tokyo 1088639, Japan
[2] Univ Tokyo, Inst Med Sci, Dept Infect Dis Control, Int Res Ctr Infect Dis,Minato Ku, Tokyo 1088639, Japan
[3] Univ Tokyo, Inst Med Sci, Microscope Core Lab, Minato Ku, Tokyo 1088639, Japan
[4] Univ Tokyo, Grad Sch Pharmaceut Sci, Dept Genet, Tokyo 1130033, Japan
[5] Hiroshima Univ, Grad Sch Sci, Hiroshima 7398526, Japan
基金
日本学术振兴会;
关键词
SIMPLEX-VIRUS; 1; IN-VITRO; PRIMARY ENVELOPMENT; STRUCTURAL BASIS; CELL-MIGRATION; DE-ENVELOPMENT; INFECTED-CELLS; LAMIN-B; PROTEIN; EGRESS;
D O I
10.1038/s41467-018-05889-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Vesicle-mediated nucleocytoplasmic transport is a nuclear pore-independent mechanism for the nuclear export of macromolecular complexes, but the molecular basis for this transport remains largely unknown. Here we show that endosomal sorting complex required for transport-III (ESCRT-III) is recruited to the inner nuclear membrane (INM) during the nuclear export of herpes simplex virus 1 (HSV-1). Scission during HSV-1 budding through the INM is prevented by depletion of ESCRT-III proteins. Interestingly, in uninfected human cells, the depletion of ESCRT-III proteins induces aberrant INM proliferation. Our results show that HSV-1 expropriates the ESCRT-III machinery in infected cells for scission of the INM to produce vesicles containing progeny virus nucleocapsids. In uninfected cells, ESCRT-III regulates INM integrity by downregulating excess INM.
引用
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页数:15
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