Evidence map›Paper›PMID 10611335›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1999

Varying the number of telomere-bound proteins does not alter telomere length in tel1Delta cells.

A Ray, K W Runge

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.6field-weighted citation impact, top 43% 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

19 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. The budding yeast nucleus.Cold Spring Harbor perspectives in biology · 2010
    Review
  6. Article
  7. Review
  8. Article
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  11. Ataxia telangiectasia mutated (Atm) is not required for telomerase-mediated elongation of short telomeres.Proceedings of the National Academy of Sciences of the United States of America · 2006
    Article
  12. Article
  13. Making the most of a little: dosage effects in eukaryotic telomere length maintenance.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2005
    Review
  14. Article
  15. Article
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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

2 authors at 1 institution in 1 country.

A RayLerner Research Institute, Cleveland Clinic Foundation, Department of Molecular Biology, NC20, 9500 Euclid Avenue, Cleveland, OH 44195, USA.
K W Runge
Cleveland Clinic · US

Funding

REGULATION OF TELOMERE LENGTHR01GM050752 · NIGMS · CLEVELAND CLINIC LERNER COM-CWRU · PI RUNGE, KURT W · 1994 to 2012
$3.2M
NIGMS NIH HHS GM50752NIGMS NIH HHS R01 GM050752
6 · The paper itself

Abstract

Yeast telomere DNA consists of a continuous, approximately 330-bp tract of the heterogeneous repeat TG(1-3) with irregularly spaced, high affinity sites for the protein Rap1p. Yeast monitor, or count, the number of telomeric Rap1p C termini in a negative feedback mechanism to modulate the length of the terminal TG(1-3) repeats, and synthetic telomeres that tether Rap1p molecules adjacent to the TG(1-3) tract cause wild-type cells to maintain a shorter TG(1-3) tract. To identify trans-acting proteins required to count Rap1p molecules, these same synthetic telomeres were placed in two short telomere mutants: yku70Delta (which lack the yeast Ku70 protein) and tel1Delta (which lack the yeast ortholog of ATM). Although both mutants maintain telomeres with approximately 100 bp of TG(1-3), only yku70Delta cells maintained shorter TG(1-3) repeats in response to internal Rap1p molecules. This distinct response to internal Rap1p molecules was not caused by a variation in Rap1p site density in the TG(1-3) repeats as sequencing of tel1Delta and yku70Delta telomeres showed that both strains have only five to six Rap1p sites per 100-bp telomere. In addition, the tel1Delta short telomere phenotype was epistatic to the unregulated telomere length caused by deletion of the Rap1p C-terminal domain. Thus, the length of the TG(1-3) repeats in tel1Delta cells was independent of the number of the Rap1p C termini at the telomere. These data indicate that tel1Delta cells use an alternative mechanism to regulate telomere length that is distinct from monitoring the number of telomere binding proteins.

Indexed as

MutationSaccharomyces cerevisiae ProteinsTelomere-Binding ProteinsTranscription FactorsBinding SitesCloning, MolecularDNA-Binding ProteinsMolecular Sequence DataProtein BindingSaccharomyces cerevisiaeSequence Analysis, DNAShelterin ComplexTelomeraseTelomereDNA-Binding ProteinsRAP1 protein, S cerevisiaeSaccharomyces cerevisiae ProteinsShelterin ComplexTelomeraseTelomere-Binding ProteinsTranscription Factors

Identifiers

PMID10611335
PMCPMC24770
OpenAlexW1980683278

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.