Postmitotic nuclear pore assembly proceeds by radial dilation of small membrane openings
Postmitotic nuclear pore assembly proceeds by radial dilation of small membrane openings
The nuclear envelope has to be reformed after mitosis to create viable daughter cells with closed nuclei. How membrane sealing of DNA and assembly of nuclear pore complexes (NPCs) are achieved and coordinated is poorly understood. Here, we reconstructed nuclear membrane topology and the structures of assembling NPCs in a correlative 3D EM time course of dividing human cells. Our quantitative ultrastructural analysis shows that nuclear membranes form from highly fenestrated ER sheets whose holes progressively shrink. NPC precursors are found in small membrane holes and dilate radially during assembly of the inner ring complex, forming thousands of transport channels within minutes. This mechanism is fundamentally different from that of interphase NPC assembly and explains how mitotic cells can rapidly establish a closed nuclear compartment while making it transport competent.
21-28
Otsuka, Shotaro
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Steyer, Anna M.
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Schorb, Martin
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Hériché, Jean-Karim
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Hossain, M. Julius
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Sethi, Suruchi
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Kueblbeck, Moritz
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Schwab, Yannick
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Beck, Martin
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Ellenberg, Jan
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1 January 2018
Otsuka, Shotaro
bd4a044c-b56e-4a10-9297-9b87b1fea825
Steyer, Anna M.
afbe6fec-995e-49a2-9b82-dddf2377602e
Schorb, Martin
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Hériché, Jean-Karim
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Hossain, M. Julius
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Sethi, Suruchi
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Kueblbeck, Moritz
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Schwab, Yannick
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Beck, Martin
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Ellenberg, Jan
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Otsuka, Shotaro, Steyer, Anna M., Schorb, Martin, Hériché, Jean-Karim, Hossain, M. Julius, Sethi, Suruchi, Kueblbeck, Moritz, Schwab, Yannick, Beck, Martin and Ellenberg, Jan
(2018)
Postmitotic nuclear pore assembly proceeds by radial dilation of small membrane openings.
Nature Structural & Molecular Biology, 25, .
(doi:10.1038/s41594-017-0001-9).
Abstract
The nuclear envelope has to be reformed after mitosis to create viable daughter cells with closed nuclei. How membrane sealing of DNA and assembly of nuclear pore complexes (NPCs) are achieved and coordinated is poorly understood. Here, we reconstructed nuclear membrane topology and the structures of assembling NPCs in a correlative 3D EM time course of dividing human cells. Our quantitative ultrastructural analysis shows that nuclear membranes form from highly fenestrated ER sheets whose holes progressively shrink. NPC precursors are found in small membrane holes and dilate radially during assembly of the inner ring complex, forming thousands of transport channels within minutes. This mechanism is fundamentally different from that of interphase NPC assembly and explains how mitotic cells can rapidly establish a closed nuclear compartment while making it transport competent.
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e-pub ahead of print date: 27 November 2017
Published date: 1 January 2018
Additional Information:
© 2018 Nature America Inc., part of Springer Nature. All rights reserved.
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Local EPrints ID: 458229
URI: http://eprints.soton.ac.uk/id/eprint/458229
ISSN: 1545-9993
PURE UUID: f0469f9f-ffd5-44a0-9b91-3b5662e41dd1
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Date deposited: 01 Jul 2022 16:36
Last modified: 17 Mar 2024 04:12
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Contributors
Author:
Shotaro Otsuka
Author:
Anna M. Steyer
Author:
Martin Schorb
Author:
Jean-Karim Hériché
Author:
M. Julius Hossain
Author:
Suruchi Sethi
Author:
Moritz Kueblbeck
Author:
Yannick Schwab
Author:
Martin Beck
Author:
Jan Ellenberg
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