Evidence map›Paper›PMID 10783163›Full record

ArticleGenes & development2000

Ku complex interacts with and stimulates the Werner protein.

M P Cooper, A Machwe, D K Orren, R M Brosh, D Ramsden, V A Bohr

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 132 papers.

0numbers the graph read from it
0cells of the map it votes in
132citing 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

132 citing papers in PubMed, 312 citations in OpenAlex.

  1. Article
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  15. Human RecQ Helicases in DNA Double-Strand Break Repair.Frontiers in cell and developmental biology · 2021
    Review
  16. Review
  17. Article
  18. Werner Syndrome Protein and DNA Replication.International journal of molecular sciences · 2018
    Review
  19. Article
  20. Serum vitamin C levels modulate the lifespan and endoplasmic reticulum stress response pathways in mice synthesizing a nonfunctional mutant WRN protein.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2018
    Article

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

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

6 authors at 3 institutions in 2 countries.

M P CooperLaboratory of Molecular Genetics, National Institute on Aging, National Institutes of Health, Baltimore, Maryland 21224, USA.
A Machwe
D K Orren
R M Brosh
D Ramsden
V A Bohr
Johns Hopkins University · USNational Institute on Aging · USNational Institutes of Health · US

Funding

Roles Of DNA Helicases In Pathways Required For Maintenance Of Genomic StabilityZIAAG000741 · NIA · NATIONAL INSTITUTE ON AGING · PI BROSH, ROBERT · 2009 to 2025
$7.6M
Roles Of Dna Helicases:Pathways Required For MaintenanceZ01AG000741 · NIA · NATIONAL INSTITUTE ON AGING · PI BROSH, ROBERT M · 2001 to 2008
$1.1M
6 · The paper itself

Abstract

Werner syndrome (WS) is the hallmark premature aging disorder in which affected humans appear older than their chronological age. The protein WRNp, defective in WS, has helicase function, DNA-dependent ATPase, and exonuclease activity. Although WRNp functions in nucleic acid metabolism, there is little or no information about the pathways or protein interactions in which it participates. Here we identify Ku70 and Ku86 as proteins that interact with WRNp. Although Ku proteins had no effect on ATPase or helicase activity, they strongly stimulated specific exonuclease activity. These results suggest that WRNp and the Ku complex participate in a common DNA metabolic pathway.

Indexed as

Antigens, NuclearAdenosine TriphosphatasesAnimalsBase SequenceBlotting, WesternCell LineCell NucleusChromatography, AffinityDNA-Binding ProteinsDNA HelicasesElectrophoresis, Polyacrylamide GelEnzyme ActivationExodeoxyribonucleasesExonucleasesHumansKu AutoantigenAdenosine TriphosphatasesAntigens, NuclearDNA-Binding ProteinsDNA HelicasesExodeoxyribonucleasesExonucleasesKu AutoantigenNuclear ProteinsRecQ HelicasesWerner Syndrome HelicaseWRN protein, humanXRCC5 protein, humanXrcc6 protein, human

Identifiers

PMID10783163
PMCPMC316545
OpenAlexW1940074648

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.