Evidence map›Paper›PMID 19000832›Full record

ArticleDevelopmental cell2008

Nucleoporin levels regulate cell cycle progression and phase-specific gene expression.

Papia Chakraborty, Yaming Wang, Jen-Hsuan Wei, Jan van Deursen, Hongtao Yu, Liviu Malureanu, Mary Dasso, Douglass J Forbes, David E Levy, Joachim Seemann and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
3.9field-weighted citation impact, top 6% of its field
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

61 citing papers in PubMed, 90 citations in OpenAlex.

  1. Article
  2. Advances in the understanding of nuclear pore complexes in human diseases.Journal of cancer research and clinical oncology · 2024
    Review
  3. Review
  4. Article
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  8. Article
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  18. Article
  19. The Ultrastructural Signature of Human Embryonic Stem Cells.Journal of cellular biochemistry · 2017
    Article
  20. Article

1 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 6 institutions in 1 country.

Papia ChakrabortyDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Yaming Wang
Jen-Hsuan Wei
Jan van Deursen
Hongtao Yu
Liviu Malureanu
Mary Dasso
Douglass J Forbes
David E Levy
Joachim Seemann
Beatriz M A Fontoura
The University of Texas Southwestern Medical Center · USNew York University · USMayo Clinic · USMayo Clinic in Florida · USNational Institutes of Health · USUniversity of California San Diego · US

Funding

Viral Pathogenesis and TherapeuticsU54AI057158 · NIAID · WADSWORTH CENTER · PI LEVY, DAVID E · 2003 to 2014
$100.8M
FUNCTIONAL STUDY OF NATIVE AND SYNTHETIC NUCLEIR01GM033279 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FORBES, DOUGLASS JANE · 1985 to 2015
$7.0M
SIGNAL TRANSDUCTION PATHWAY IN IFN INDUCED TRANSCRIPTIONR01AI028900 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI LEVY, DAVID E · 1990 to 2010
$5.6M
Mitotic roles of Nuclear Pore Complex (NPC) proteinsZIAHD008816 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI DASSO, MARY C. · 2009 to 2014
$3.3M
Regulation of Nucleoporins by InterferonR01GM067159 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI FONTOURA, BEATRIZ MA · 2003 to 2011
$2.9M
NIAID NIH HHS R01 AI028900NIAID NIH HHS R01AI28900NIAID NIH HHS U54AI5715801NIGMS NIH HHS R01 GM033279NIGMS NIH HHS R01 GM067159NIGMS NIH HHS R01GM07159-01
6 · The paper itself

Abstract

The Nup107-160 complex, the largest subunit of the nuclear pore, is multifunctional. It mediates mRNA export in interphase, and has roles in kinetochore function, spindle assembly, and postmitotic nuclear pore assembly. We report here that the levels of constituents of the Nup107-160 complex are coordinately cell cycle-regulated. At mitosis, however, a member of the complex, Nup96, is preferentially downregulated. This occurs via the ubiquitin-proteasome pathway. When the levels of Nup96 are kept high, a significant delay in G1/S progression occurs. Conversely, in cells of Nup96(+/-) mice, which express low levels of Nup96, cell cycle progression is accelerated. These lowered levels of Nup96 yield specific defects in nuclear export of certain mRNAs and protein expression, among which are key cell cycle regulators. Thus, Nup96 levels regulate differential gene expression in a phase-specific manner, setting the stage for proper cell cycle progression.

Indexed as

Cell CycleDown-RegulationAnimalsCell LineGene ExpressionHeLa CellsHumansMiceMitosisNuclear PoreNuclear Pore Complex ProteinsRNA, Messengernuclear pore complex protein 96Nuclear Pore Complex ProteinsRNA, Messenger

Identifiers

PMID19000832
PMCPMC2835575
OpenAlexW2024160864

What OpenQuestion holds

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Registered trials

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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.