Author
Listed:
- Jun Arii
(The Institute of Medical Science, The University of Tokyo, Minato-ku
The Institute of Medical Science, The University of Tokyo, Minato-ku)
- Mizuki Watanabe
(The Institute of Medical Science, The University of Tokyo, Minato-ku
The Institute of Medical Science, The University of Tokyo, Minato-ku)
- Fumio Maeda
(The Institute of Medical Science, The University of Tokyo, Minato-ku
The Institute of Medical Science, The University of Tokyo, Minato-ku)
- Noriko Tokai-Nishizumi
(The Institute of Medical Science, The University of Tokyo, Minato-ku)
- Takahiro Chihara
(The University of Tokyo
Hiroshima University, Higashi-Hiroshima)
- Masayuki Miura
(The University of Tokyo)
- Yuhei Maruzuru
(The Institute of Medical Science, The University of Tokyo, Minato-ku
The Institute of Medical Science, The University of Tokyo, Minato-ku)
- Naoto Koyanagi
(The Institute of Medical Science, The University of Tokyo, Minato-ku
The Institute of Medical Science, The University of Tokyo, Minato-ku)
- Akihisa Kato
(The Institute of Medical Science, The University of Tokyo, Minato-ku
The Institute of Medical Science, The University of Tokyo, Minato-ku)
- Yasushi Kawaguchi
(The Institute of Medical Science, The University of Tokyo, Minato-ku
The Institute of Medical Science, The University of Tokyo, Minato-ku)
Abstract
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.
Suggested Citation
Jun Arii & Mizuki Watanabe & Fumio Maeda & Noriko Tokai-Nishizumi & Takahiro Chihara & Masayuki Miura & Yuhei Maruzuru & Naoto Koyanagi & Akihisa Kato & Yasushi Kawaguchi, 2018.
"ESCRT-III mediates budding across the inner nuclear membrane and regulates its integrity,"
Nature Communications, Nature, vol. 9(1), pages 1-15, December.
Handle:
RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-05889-9
DOI: 10.1038/s41467-018-05889-9
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