Evidence map›Paper›PMID 22989712›Full record

ArticleNucleic acids research2012

The roles of WRN and BLM RecQ helicases in the Alternative Lengthening of Telomeres.

Aaron Mendez-Bermudez, Alberto Hidalgo-Bravo, Victoria E Cotton, Athanasia Gravani, Jennie N Jeyapalan, Nicola J Royle

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

30 citing papers in PubMed, 75 citations in OpenAlex.

  1. Trial
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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

6 authors at 1 institution in 1 country.

Aaron Mendez-BermudezDepartment of Genetics, University of Leicester, University Road, Leicester LE1 7RH, UK.
Alberto Hidalgo-Bravo
Victoria E Cotton
Athanasia Gravani
Jennie N Jeyapalan
Nicola J Royle
University of Leicester · GB

Funding

Cancer Research UK C17992/A8641Medical Research Council G0500336
6 · The paper itself

Abstract

Approximately 10% of all cancers, but a higher proportion of sarcomas, use the recombination-based alternative lengthening of telomeres (ALT) to maintain telomeres. Two RecQ helicase genes, BLM and WRN, play important roles in homologous recombination repair and they have been implicated in telomeric recombination activity, but their precise roles in ALT are unclear. Using analysis of sequence variation present in human telomeres, we found that a WRN- ALT+ cell line lacks the class of complex telomere mutations attributed to inter-telomeric recombination in other ALT+ cell lines. This suggests that WRN facilitates inter-telomeric recombination when there are sequence differences between the donor and recipient molecules or that sister-telomere interactions are suppressed in the presence of WRN and this promotes inter-telomeric recombination. Depleting BLM in the WRN- ALT+ cell line increased the mutation frequency at telomeres and at the MS32 minisatellite, which is a marker of ALT. The absence of complex telomere mutations persisted in BLM-depleted clones, and there was a clear increase in sequence homogenization across the telomere and MS32 repeat arrays. These data indicate that BLM suppresses unequal sister chromatid interactions that result in excessive homogenization at MS32 and at telomeres in ALT+ cells.

Indexed as

Telomere HomeostasisBase SequenceCell LineDown-RegulationExodeoxyribonucleasesHumansMaleMiddle AgedMinisatellite RepeatsMolecular Sequence DataMutationRecQ HelicasesTelomereWerner Syndrome HelicaseBloom syndrome proteinExodeoxyribonucleasesRecQ HelicasesWerner Syndrome HelicaseWRN protein, human

Identifiers

PMID22989712
PMCPMC3510502
OpenAlexW2001703646

What OpenQuestion holds

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LicenceCC BY
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.