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

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...

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Detalles Bibliográficos
Autores principales: Arii, Jun, Watanabe, Mizuki, Maeda, Fumio, Tokai-Nishizumi, Noriko, Chihara, Takahiro, Miura, Masayuki, Maruzuru, Yuhei, Koyanagi, Naoto, Kato, Akihisa, Kawaguchi, Yasushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107581/
https://www.ncbi.nlm.nih.gov/pubmed/30139939
http://dx.doi.org/10.1038/s41467-018-05889-9
Descripción
Sumario: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.