Nuclear pore assembly proceeds by an inside-out extrusion of the nuclear envelope

The nuclear pore complex (NPC) mediates nucleocytoplasmic transport through the nuclear envelope. How the NPC assembles into this double membrane boundary has remained enigmatic. Here, we captured temporally staged assembly intermediates by correlating live cell imaging with high-resolution electron...

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Main Authors: Shotaro Otsuka, Khanh Huy Bui, Martin Schorb, M Julius Hossain, Antonio Z Politi, Birgit Koch, Mikhail Eltsov, Martin Beck, Jan Ellenberg
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2016-09-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/19071
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spelling doaj-e7d3ccf9ec384e3e9334a9fd703446892021-05-05T00:34:53ZengeLife Sciences Publications LtdeLife2050-084X2016-09-01510.7554/eLife.19071Nuclear pore assembly proceeds by an inside-out extrusion of the nuclear envelopeShotaro Otsuka0https://orcid.org/0000-0003-3976-0843Khanh Huy Bui1Martin Schorb2M Julius Hossain3https://orcid.org/0000-0003-3303-5755Antonio Z Politi4Birgit Koch5Mikhail Eltsov6Martin Beck7Jan Ellenberg8https://orcid.org/0000-0001-5909-701XCell Biology and Biophysics Unit, European Molecular Biology Laboratory, Heidelberg, GermanyStructural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg, GermanyStructural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany; Electron Microscopy Core Facility, European Molecular Biology Laboratory, Heidelberg, GermanyCell Biology and Biophysics Unit, European Molecular Biology Laboratory, Heidelberg, GermanyCell Biology and Biophysics Unit, European Molecular Biology Laboratory, Heidelberg, GermanyCell Biology and Biophysics Unit, European Molecular Biology Laboratory, Heidelberg, GermanyCell Biology and Biophysics Unit, European Molecular Biology Laboratory, Heidelberg, GermanyStructural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg, GermanyCell Biology and Biophysics Unit, European Molecular Biology Laboratory, Heidelberg, GermanyThe nuclear pore complex (NPC) mediates nucleocytoplasmic transport through the nuclear envelope. How the NPC assembles into this double membrane boundary has remained enigmatic. Here, we captured temporally staged assembly intermediates by correlating live cell imaging with high-resolution electron tomography and super-resolution microscopy. Intermediates were dome-shaped evaginations of the inner nuclear membrane (INM), that grew in diameter and depth until they fused with the flat outer nuclear membrane. Live and super-resolved fluorescence microscopy revealed the molecular maturation of the intermediates, which initially contained the nuclear and cytoplasmic ring component Nup107, and only later the cytoplasmic filament component Nup358. EM particle averaging showed that the evagination base was surrounded by an 8-fold rotationally symmetric ring structure from the beginning and that a growing mushroom-shaped density was continuously associated with the deforming membrane. Quantitative structural analysis revealed that interphase NPC assembly proceeds by an asymmetric inside-out extrusion of the INM.https://elifesciences.org/articles/19071correlative light-electron microscopyelectron tomographylive cell imagingnuclear envelopenuclear pore complexsuper-resolution microscopy
collection DOAJ
language English
format Article
sources DOAJ
author Shotaro Otsuka
Khanh Huy Bui
Martin Schorb
M Julius Hossain
Antonio Z Politi
Birgit Koch
Mikhail Eltsov
Martin Beck
Jan Ellenberg
spellingShingle Shotaro Otsuka
Khanh Huy Bui
Martin Schorb
M Julius Hossain
Antonio Z Politi
Birgit Koch
Mikhail Eltsov
Martin Beck
Jan Ellenberg
Nuclear pore assembly proceeds by an inside-out extrusion of the nuclear envelope
eLife
correlative light-electron microscopy
electron tomography
live cell imaging
nuclear envelope
nuclear pore complex
super-resolution microscopy
author_facet Shotaro Otsuka
Khanh Huy Bui
Martin Schorb
M Julius Hossain
Antonio Z Politi
Birgit Koch
Mikhail Eltsov
Martin Beck
Jan Ellenberg
author_sort Shotaro Otsuka
title Nuclear pore assembly proceeds by an inside-out extrusion of the nuclear envelope
title_short Nuclear pore assembly proceeds by an inside-out extrusion of the nuclear envelope
title_full Nuclear pore assembly proceeds by an inside-out extrusion of the nuclear envelope
title_fullStr Nuclear pore assembly proceeds by an inside-out extrusion of the nuclear envelope
title_full_unstemmed Nuclear pore assembly proceeds by an inside-out extrusion of the nuclear envelope
title_sort nuclear pore assembly proceeds by an inside-out extrusion of the nuclear envelope
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2016-09-01
description The nuclear pore complex (NPC) mediates nucleocytoplasmic transport through the nuclear envelope. How the NPC assembles into this double membrane boundary has remained enigmatic. Here, we captured temporally staged assembly intermediates by correlating live cell imaging with high-resolution electron tomography and super-resolution microscopy. Intermediates were dome-shaped evaginations of the inner nuclear membrane (INM), that grew in diameter and depth until they fused with the flat outer nuclear membrane. Live and super-resolved fluorescence microscopy revealed the molecular maturation of the intermediates, which initially contained the nuclear and cytoplasmic ring component Nup107, and only later the cytoplasmic filament component Nup358. EM particle averaging showed that the evagination base was surrounded by an 8-fold rotationally symmetric ring structure from the beginning and that a growing mushroom-shaped density was continuously associated with the deforming membrane. Quantitative structural analysis revealed that interphase NPC assembly proceeds by an asymmetric inside-out extrusion of the INM.
topic correlative light-electron microscopy
electron tomography
live cell imaging
nuclear envelope
nuclear pore complex
super-resolution microscopy
url https://elifesciences.org/articles/19071
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