Evidence map›Paper›PMID 25274733›Full record

ArticleNucleic acids research2014

Telomere stability and development of ctc1 mutants are rescued by inhibition of EJ recombination pathways in a telomerase-dependent manner.

Simon Amiard, Margaux Olivier, Elisabeth Allain, Kyuha Choi, Richard Smith-Unna, Ian R Henderson, Charles I White, Maria Eugenia Gallego

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Review
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

8 authors at 5 institutions in 2 countries.

Simon AmiardGénétique, Reproduction et Développement, UMR CNRS 6293, Clermont Université, INSERM U1103, Aubière, France megalleg@univ-bpclermont.fr.
Margaux OlivierGénétique, Reproduction et Développement, UMR CNRS 6293, Clermont Université, INSERM U1103, Aubière, France.
Elisabeth AllainGénétique, Reproduction et Développement, UMR CNRS 6293, Clermont Université, INSERM U1103, Aubière, France Department of Plant Sciences, University of Cambridge, Cambridge, UK.
Kyuha ChoiDepartment of Plant Sciences, University of Cambridge, Cambridge, UK.
Richard Smith-UnnaDepartment of Plant Sciences, University of Cambridge, Cambridge, UK.
Ian R HendersonDepartment of Plant Sciences, University of Cambridge, Cambridge, UK.
Charles I WhiteGénétique, Reproduction et Développement, UMR CNRS 6293, Clermont Université, INSERM U1103, Aubière, France.
Maria Eugenia GallegoGénétique, Reproduction et Développement, UMR CNRS 6293, Clermont Université, INSERM U1103, Aubière, France megalleg@univ-bpclermont.fr.
University of Cambridge · GBCentre National de la Recherche Scientifique · FRClermont Université · FRGenetique Reproduction and Developpement · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The telomeres of linear eukaryotic chromosomes are protected by caps consisting of evolutionarily conserved nucleoprotein complexes. Telomere dysfunction leads to recombination of chromosome ends and this can result in fusions which initiate chromosomal breakage-fusion-bridge cycles, causing genomic instability and potentially cell death or cancer. We hypothesize that in the absence of the recombination pathways implicated in these fusions, deprotected chromosome ends will instead be eroded by nucleases, also leading to the loss of genes and cell death. In this work, we set out to specifically test this hypothesis in the plant, Arabidopsis. Telomere protection in Arabidopsis implicates KU and CST and their absence leads to chromosome fusions, severe genomic instability and dramatic developmental defects. We have analysed the involvement of end-joining recombination pathways in telomere fusions and the consequences of this on genomic instability and growth. Strikingly, the absence of the multiple end-joining pathways eliminates chromosome fusion and restores normal growth and development to cst ku80 mutant plants. It is thus the chromosomal fusions, per se, which are the underlying cause of the severe developmental defects. This rescue is mediated by telomerase-dependent telomere extension, revealing a competition between telomerase and end-joining recombination proteins for access to deprotected telomeres.

Indexed as

DNA End-Joining RepairRecombination, GeneticTelomere HomeostasisArabidopsisArabidopsis ProteinsDNA HelicasesDNA RepairMutationRepetitive Sequences, Nucleic AcidTelomeraseTelomereTelomere-Binding ProteinsTelomere ShorteningArabidopsis ProteinsCTC1 protein, ArabidopsisDNA HelicasesKu80 protein, ArabidopsisTelomeraseTelomere-Binding ProteinsTERT protein, Arabidopsis

Identifiers

PMID25274733
PMCPMC4231758
OpenAlexW2107971326

What OpenQuestion holds

Textmetadata
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.