Evidence map›Paper›PMID 21441303›Full record

ArticleMolecular biology of the cell2011

The effect of Ku on telomere replication time is mediated by telomere length but is independent of histone tail acetylation.

Hui-Yong Lian, E Douglas Robertson, Shin-ichiro Hiraga, Gina M Alvino, David Collingwood, Heather J McCune, Akila Sridhar, Bonita J Brewer, M K Raghuraman, Anne D Donaldson

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing 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

43 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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  5. Review
  6. Article
  7. Review
  8. Review
  9. The Protective Role of Dormant Origins in Response to Replicative Stress.International journal of molecular sciences · 2018
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. How and why multiple MCMs are loaded at origins of DNA replication.BioEssays : news and reviews in molecular, cellular and developmental biology · 2016
    Review
  19. Article
  20. 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

10 authors.

Hui-Yong LianInstitute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen AB25 2ZD, Scotland, UK.
E Douglas Robertson
Shin-ichiro Hiraga
Gina M Alvino
David Collingwood
Heather J McCune
Akila Sridhar
Bonita J Brewer
M K Raghuraman
Anne D Donaldson

Funding

Cancer Research UK C1445/A10817Cancer Research UK C1445/A2571Medical Research Council G0600774PHS HHS 18926
6 · The paper itself

Abstract

DNA replication in Saccharomyces cerevisiae proceeds according to a temporal program. We have investigated the role of the telomere-binding Ku complex in specifying late replication of telomere-proximal sequences. Genome-wide analysis shows that regions extending up to 80 kb from telomeres replicate abnormally early in a yku70 mutant. We find that Ku does not appear to regulate replication time by binding replication origins directly, nor is its effect on telomere replication timing mediated by histone tail acetylation. We show that Ku instead regulates replication timing through its effect on telomere length, because deletion of the telomerase regulator Pif1 largely reverses the short telomere defect of a yku70 mutant and simultaneously rescues its replication timing defect. Consistent with this conclusion, deleting the genome integrity component Elg1 partially rescued both length and replication timing of yku70 telomeres. Telomere length-mediated control of replication timing requires the TG(1-3) repeat-counting component Rif1, because a rif1 mutant replicates telomeric regions early, despite having extended TG(1-3) tracts. Overall, our results suggest that the effect of Ku on telomere replication timing results from its impact on TG(1-3) repeat length and support a model in which Rif1 measures telomere repeat length to ensure that telomere replication timing is correctly programmed.

Indexed as

DNA ReplicationAcetylationAcetyltransferasesBase SequenceCell CycleCell Cycle ProteinsChromosomes, FungalDNA-Binding ProteinsHistonesProtein Processing, Post-TranslationalProtein Serine-Threonine KinasesReplication OriginRepressor ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSequence DeletionAcetyltransferasesCDC7 protein, S cerevisiaeCell Cycle ProteinsDNA-Binding Proteinshigh affinity DNA-binding factor, S cerevisiaeHistonesProtein Serine-Threonine KinasesRepressor ProteinsRIF1 protein, S cerevisiaeSaccharomyces cerevisiae ProteinsTelomere-Binding ProteinsYKU70 protein, S cerevisiae

Identifiers

PMID21441303
PMCPMC3093326

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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.