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The cellular environment shapes the nuclear pore complex architecture

Author

Listed:
  • Anthony P. Schuller

    (Massachusetts Institute of Technology)

  • Matthias Wojtynek

    (University of Zurich
    ETH Zurich)

  • David Mankus

    (Massachusetts Institute of Technology)

  • Meltem Tatli

    (University of Zurich)

  • Rafael Kronenberg-Tenga

    (University of Zurich)

  • Saroj G. Regmi

    (NIH)

  • Phat V. Dip

    (Massachusetts Institute of Technology
    Massachusetts Institute of Technology)

  • Abigail K. R. Lytton-Jean

    (Massachusetts Institute of Technology)

  • Edward J. Brignole

    (Massachusetts Institute of Technology
    Massachusetts Institute of Technology)

  • Mary Dasso

    (NIH)

  • Karsten Weis

    (ETH Zurich)

  • Ohad Medalia

    (University of Zurich)

  • Thomas U. Schwartz

    (Massachusetts Institute of Technology)

Abstract

Nuclear pore complexes (NPCs) create large conduits for cargo transport between the nucleus and cytoplasm across the nuclear envelope (NE)1–3. These multi-megadalton structures are composed of about thirty different nucleoporins that are distributed in three main substructures (the inner, cytoplasmic and nucleoplasmic rings) around the central transport channel4–6. Here we use cryo-electron tomography on DLD-1 cells that were prepared using cryo-focused-ion-beam milling to generate a structural model for the human NPC in its native environment. We show that—compared with previous human NPC models obtained from purified NEs—the inner ring in our model is substantially wider; the volume of the central channel is increased by 75% and the nucleoplasmic and cytoplasmic rings are reorganized. Moreover, the NPC membrane exhibits asymmetry around the inner-ring complex. Using targeted degradation of Nup96, a scaffold nucleoporin of the cytoplasmic and nucleoplasmic rings, we observe the interdependence of each ring in modulating the central channel and maintaining membrane asymmetry. Our findings highlight the inherent flexibility of the NPC and suggest that the cellular environment has a considerable influence on NPC dimensions and architecture.

Suggested Citation

  • Anthony P. Schuller & Matthias Wojtynek & David Mankus & Meltem Tatli & Rafael Kronenberg-Tenga & Saroj G. Regmi & Phat V. Dip & Abigail K. R. Lytton-Jean & Edward J. Brignole & Mary Dasso & Karsten W, 2021. "The cellular environment shapes the nuclear pore complex architecture," Nature, Nature, vol. 598(7882), pages 667-671, October.
  • Handle: RePEc:nat:nature:v:598:y:2021:i:7882:d:10.1038_s41586-021-03985-3
    DOI: 10.1038/s41586-021-03985-3
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    Citations

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    Cited by:

    1. Asaf Ashkenazy-Titelman & Mohammad Khaled Atrash & Alon Boocholez & Noa Kinor & Yaron Shav-Tal, 2022. "RNA export through the nuclear pore complex is directional," Nature Communications, Nature, vol. 13(1), pages 1-14, December.
    2. Sheung Chun Ng & Abin Biswas & Trevor Huyton & Jürgen Schünemann & Simone Reber & Dirk Görlich, 2023. "Barrier properties of Nup98 FG phases ruled by FG motif identity and inter-FG spacer length," Nature Communications, Nature, vol. 14(1), pages 1-17, December.
    3. Casper Berger & Maud Dumoux & Thomas Glen & Neville B.-y. Yee & John M. Mitchels & Zuzana Patáková & Michele C. Darrow & James H. Naismith & Michael Grange, 2023. "Plasma FIB milling for the determination of structures in situ," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    4. Patrick Bryant & Gabriele Pozzati & Wensi Zhu & Aditi Shenoy & Petras Kundrotas & Arne Elofsson, 2022. "Predicting the structure of large protein complexes using AlphaFold and Monte Carlo tree search," Nature Communications, Nature, vol. 13(1), pages 1-14, December.
    5. David Winogradoff & Han-Yi Chou & Christopher Maffeo & Aleksei Aksimentiev, 2022. "Percolation transition prescribes protein size-specific barrier to passive transport through the nuclear pore complex," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
    6. Fabrizio A. Pennacchio & Alessandro Poli & Francesca Michela Pramotton & Stefania Lavore & Ilaria Rancati & Mario Cinquanta & Daan Vorselen & Elisabetta Prina & Orso Maria Romano & Aldo Ferrari & Matt, 2024. "N2FXm, a method for joint nuclear and cytoplasmic volume measurements, unravels the osmo-mechanical regulation of nuclear volume in mammalian cells," Nature Communications, Nature, vol. 15(1), pages 1-10, December.

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