Evidence map›Paper›PMID 31157618›Full record

ArticleeLife2019

Age-dependent deterioration of nuclear pore assembly in mitotic cells decreases transport dynamics.

Irina L Rempel, Matthew M Crane, David J Thaller, Ankur Mishra, Daniel Pm Jansen, Georges Janssens, Petra Popken, Arman Akşit, Matt Kaeberlein, Erik van der Giessen and 4 more

Abstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

55 citing papers in PubMed.

  1. Review
  2. Review
  3. Chromatin Packing Domain Engineering Through the Manipulation of Nuclear Cationic States.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  4. Article
  5. Review
  6. Structure, function and assembly of nuclear pore complexes.Nature reviews. Molecular cell biology · 2026
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Irina L RempelEuropean Research Institute for the Biology of Ageing (ERIBA), University of Groningen, University Medical Center Groningen, Groningen, Netherlands.
Matthew M CraneDepartment of Pathology, University of Washington, Seattle, United States.ORCID 0000-0002-6234-0954
David J ThallerDepartment of Cell Biology, Yale School of Medicine, New Haven, United States.ORCID 0000-0003-3577-5562
Ankur MishraZernike Institute for Advanced Materials, University of Groningen, Groningen, Netherlands.
Daniel Pm JansenEuropean Research Institute for the Biology of Ageing (ERIBA), University of Groningen, University Medical Center Groningen, Groningen, Netherlands.
Georges JanssensEuropean Research Institute for the Biology of Ageing (ERIBA), University of Groningen, University Medical Center Groningen, Groningen, Netherlands.
Petra PopkenEuropean Research Institute for the Biology of Ageing (ERIBA), University of Groningen, University Medical Center Groningen, Groningen, Netherlands.
Arman AkşitEuropean Research Institute for the Biology of Ageing (ERIBA), University of Groningen, University Medical Center Groningen, Groningen, Netherlands.ORCID 0000-0001-9053-701X
Matt KaeberleinDepartment of Pathology, University of Washington, Seattle, United States.ORCID 0000-0002-1311-3421
Erik van der GiessenZernike Institute for Advanced Materials, University of Groningen, Groningen, Netherlands.ORCID 0000-0002-8369-2254
Anton SteenEuropean Research Institute for the Biology of Ageing (ERIBA), University of Groningen, University Medical Center Groningen, Groningen, Netherlands.
Patrick R OnckZernike Institute for Advanced Materials, University of Groningen, Groningen, Netherlands.
C Patrick LuskDepartment of Cell Biology, Yale School of Medicine, New Haven, United States.ORCID 0000-0003-4703-0533
Liesbeth M VeenhoffEuropean Research Institute for the Biology of Ageing (ERIBA), University of Groningen, University Medical Center Groningen, Groningen, Netherlands.ORCID 0000-0002-0158-4728

Funding

Skill Development for Diverse Scientific Careers: A New Course Predoctoral Program in Cellular and Molecular BiologyT32GM007223 · NIGMS · YALE UNIVERSITY · PI BASERGA, SUSAN J · 1985 to 2019
$31.0M
The mechanism of ESCRT-mediated surveillance of the nuclear envelope barrierR01GM105672 · NIGMS · YALE UNIVERSITY · PI LUSK, CHARLES PATRICK · 2013 to 2025
$4.6M
Nederlandse Organisatie voor Wetenschappelijk Onderzoek ALWOP.2015.053Nederlandse Organisatie voor Wetenschappelijk Onderzoek ECHO.711.013.008Nederlandse Organisatie voor Wetenschappelijk Onderzoek SURFsaraNetherlands Organization for Scientific Research ALWOP.2015.053Netherlands Organization for Scientific Research ECHO.711.013.008Netherlands Organization for Scientific Research SURFsaraNIGMS NIH HHS R01 GM105672NIGMS NIH HHS T32 GM007223NIH HHS NIH GM 105672NIH HHS T32GM007223University Medical Center Groningen Graduate Student FellowshipUniversity of Groningen Graduate Student FellowshipUniversity of Groningen Ubbo Emmius FundUniversity of Groningen and University Medical Center Groningen Graduate Student Fellowship
6 · The paper itself

Abstract

Nuclear transport is facilitated by the Nuclear Pore Complex (NPC) and is essential for life in eukaryotes. The NPC is a long-lived and exceptionally large structure. We asked whether NPC quality control is compromised in aging mitotic cells. Our images of single yeast cells during aging, show that the abundance of several NPC components and NPC assembly factors decreases. Additionally, the single-cell life histories reveal that cells that better maintain those components are longer lived. The presence of herniations at the nuclear envelope of aged cells suggests that misassembled NPCs are accumulated in aged cells. Aged cells show decreased dynamics of transcription factor shuttling and increased nuclear compartmentalization. These functional changes are likely caused by the presence of misassembled NPCs, as we find that two NPC assembly mutants show similar transport phenotypes as aged cells. We conclude that NPC interphase assembly is a major challenge for aging mitotic cells.

Indexed as

MitosisCell NucleusMutationNuclear EnvelopeNuclear PoreOxidative StressPermeabilityProtein TransportSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsTranscription FactorsSaccharomyces cerevisiae ProteinsTranscription Factorscell biologymicrofluidicsnuclear envelope herniationnuclear pore complex assemblynuclear transportprotein complex stoichiometryreplicative agingS. cerevisiae

Identifiers

PMID31157618
PMCPMC6579512

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.