Evidence map›Paper›PMID 10930457›Full record

ArticleMolecular biology of the cell2000

The yeast TEL1 gene partially substitutes for human ATM in suppressing hyperrecombination, radiation-induced apoptosis and telomere shortening in A-T cells.

E Fritz, A A Friedl, R M Zwacka, F Eckardt-Schupp, M S Meyn

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

7 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Contribution of yeast models to neurodegeneration research.Journal of biomedicine & biotechnology · 2012
    Review
  5. Article
  6. Article
  7. 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

5 authors at 2 institutions in 2 countries.

E FritzGSF, National Research Center for Environment and Health, Institute of Radiobiology, Neuherberg, Germany. efritz@gsf.de
A A Friedl
R M Zwacka
F Eckardt-Schupp
M S Meyn
Hospital for Sick Children · CAUniversity of Edinburgh · GB

Funding

MOLECULAR ANALYSIS OF CHROMOSOME INSTABILITY SYNDROMESR01CA060592 · NCI · YALE UNIVERSITY · PI MEYN, M STEPHEN · 1994 to 1998
–
NCI NIH HHS R01 CA60592
6 · The paper itself

Abstract

Homozygous mutations in the human ATM gene lead to a pleiotropic clinical phenotype of ataxia-telangiectasia (A-T) patients and correlating cellular deficiencies in cells derived from A-T donors. Saccharomyces cerevisiae tel1 mutants lacking Tel1p, which is the closest sequence homologue to the ATM protein, share some of the cellular defects with A-T. Through genetic complementation of A-T cells with the yeast TEL1 gene, we provide evidence that Tel1p can partially compensate for ATM in suppressing hyperrecombination, radiation-induced apoptosis, and telomere shortening. Complementation appears to be independent of p53 activation. The data provided suggest that TEL1 is a functional homologue of human ATM in yeast, and they help to elucidate different cellular and biochemical pathways in human cells regulated by the ATM protein.

Indexed as

Recombination, GeneticApoptosisAtaxia Telangiectasia Mutated ProteinsCell Cycle ProteinsCell Line, TransformedDNA-Binding ProteinsFibroblastsFungal ProteinsGamma RaysGenetic Complementation TestHumansIntracellular Signaling Peptides and ProteinsMutationProtein Serine-Threonine KinasesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsAtaxia Telangiectasia Mutated ProteinsATM protein, humanCell Cycle ProteinsDNA-Binding ProteinsFungal ProteinsIntracellular Signaling Peptides and ProteinsProtein Serine-Threonine KinasesSaccharomyces cerevisiae ProteinsTEL1 protein, S cerevisiaeTumor Suppressor Protein p53Tumor Suppressor Proteins

Identifiers

PMID10930457
PMCPMC14943
OpenAlexW2081106264

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.