Evidence map›Paper›PMID 10891500›Full record

ArticleMolecular and cellular biology2000

Characterization and targeted disruption of murine Nup50, a p27(Kip1)-interacting component of the nuclear pore complex.

M Smitherman, K Lee, J Swanger, R Kapur, B E Clurman

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

58 citing papers in PubMed, 112 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Advances in the understanding of nuclear pore complexes in human diseases.Journal of cancer research and clinical oncology · 2024
    Review
  5. Ablation of ZC3H11A causes early embryonic lethality and dysregulation of metabolic processes.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  6. Article
  7. Case report: Compound heterozygousFrontiers in neurology · 2023
    Article
  8. Article
  9. Nup50 plays more than one instrument.Cell cycle (Georgetown, Tex.) · 2022
    Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. The Role of CDKs and CDKIs in Murine Development.International journal of molecular sciences · 2020
    Review
  20. Review
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

5 authors at 2 institutions in 2 countries.

M SmithermanClinical Research, Fred Hutchinson Cancer Research Center, Seattle, Washington, 98109, USA.
K Lee
J Swanger
R Kapur
B E Clurman
Clinical Research Management · USFred Hutch Cancer Center · US

Funding

Tumor Suppression by the Fbw7 Ubiquitin LigaseR01CA084069 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI CLURMAN, BRUCE E · 2000 to 2015
$5.1M
INTERCELLULAR SIGNALS AND INTESTINAL AGANGLIONOSISR01DK052530 · NIDDK · UNIVERSITY OF WASHINGTON · PI KAPUR, RAJ P. · 1997 to 2000
$241k
NCI NIH HHS R01 CA084069NCI NIH HHS R01 CA 84069NIDDK NIH HHS R01 DK52530
6 · The paper itself

Abstract

p27(Kip1) is a member of the Cip-Kip family of cyclin-dependent kinase (Cdk) inhibitors that binds to cyclin-Cdk complexes and inhibits their catalytic activity in response to antiproliferative stimuli. p27(Kip1) is regulated by several posttranscriptional mechanisms, including subcellular localization. We have identified a component of the nuclear pore complex (NPC), termed Nup50, through its two-hybrid interactions with p27(Kip1). Nup50 is a nucleoplasmically oriented component of the nuclear pore complex with a role in protein export (T. Guan, R. H. Kehlenbach, E. C. Schirmer, A. Kehlenbach, F. Fan, B. E. Clurman, N. Arnheim, and L. Gerace, Mol. Cell. Biol. 20:5619-5630, 2000). We found that murine Nup50 is a widely expressed nucleoporin and that Nup50 expression is highest in the developing neural tube and adult testes. We have also examined interactions between Nup50 and the NPC and found specific two-hybrid interactions between Nup50 and several well-defined components of the NPC, as well as coimmunoprecipitation of Nup50 with the nucleoporin Nup153 from transfected mammalian cells. In order to study Nup50 function in vivo, we cloned the mouse Nup50 genomic locus and created a targeted Nup50 deletion in the mouse germ line. Nup50 disruption resulted in a complex phenotype characterized by late embryonic lethality, neural tube defects, and intrauterine growth retardation. Although Nup50-null mouse embryo fibroblasts exhibited no defects in either cell cycle control or p27(Kip1) regulation, Nup50 deletion was associated with abnormalities in p27(Kip1) expression and cell proliferation in the developing neuroepithelium. We conclude that Nup50 is a nucleoporin with essential functions during mouse development.

Indexed as

Cell Cycle ProteinsNuclear Pore Complex ProteinsTumor Suppressor ProteinsAmino Acid SequenceAnimalsCell NucleusCloning, MolecularCyclin-Dependent Kinase Inhibitor p27Fetal DeathFetal Growth RetardationFibroblastsGene DeletionGene Expression Regulation, DevelopmentalMiceMice, Inbred C57BLMice, Mutant StrainsCdkn1b protein, mouseCell Cycle ProteinsCyclin-Dependent Kinase Inhibitor p27Microtubule-Associated ProteinsNuclear Pore Complex ProteinsNuclear ProteinsNup153 protein, mouseNup50 protein, mousePorinsTumor Suppressor Proteins

Identifiers

PMID10891500
PMCPMC86029
OpenAlexW2122565957

What OpenQuestion holds

Textmetadata
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.