Evidence map›Paper›PMID 34214172›Full record

ArticleNucleic acids research2021

GGGCTA repeats can fold into hairpins poorly unfolded by replication protein A: a possible origin of the length-dependent instability of GGGCTA variant repeats in human telomeres.

Jean Chatain, Alain Blond, Anh Tuân Phan, Carole Saintomé, Patrizia Alberti

Abstract read
In one paragraph

Article in Nucleic acids research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Protection of the Telomeric Junction by the Shelterin Complex.Journal of the American Chemical Society · 2024
    Article
  3. Protection of the Telomeric Junction by the Shelterin Complex.bioRxiv : the preprint server for biology · 2024
    Article
  4. 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

5 authors.

Jean ChatainLaboratoire Structure et Instabilité des Génomes (StrInG), Muséum national d'Histoire naturelle, CNRS, Inserm, Paris 75005, France.
Alain BlondLaboratoire Molécules de Communication et Adaptation des Microorganismes (MCAM), Muséum national d'Histoire naturelle, CNRS, Paris 75005, France.
Anh Tuân PhanSchool of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371, Singapore.ORCID 0000-0002-4970-3861
Carole SaintoméLaboratoire Structure et Instabilité des Génomes (StrInG), Muséum national d'Histoire naturelle, CNRS, Inserm, Paris 75005, France.ORCID 0000-0002-7609-6913
Patrizia AlbertiLaboratoire Structure et Instabilité des Génomes (StrInG), Muséum national d'Histoire naturelle, CNRS, Inserm, Paris 75005, France.ORCID 0000-0002-5231-3768

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human telomeres are composed of GGGTTA repeats and interspersed with variant repeats. The GGGCTA variant motif was identified in the proximal regions of human telomeres about 10 years ago and was shown to display a length-dependent instability. In parallel, a structural study showed that four GGGCTA repeats folded into a non-canonical G-quadruplex (G4) comprising a Watson-Crick GCGC tetrad. It was proposed that this non-canonical G4 might be an additional obstacle for telomere replication. In the present study, we demonstrate that longer GGGCTA arrays fold into G4 and into hairpins. We also demonstrate that replication protein A (RPA) efficiently binds to GGGCTA repeats structured into G4 but poorly binds to GGGCTA repeats structured into hairpins. Our results (along with results obtained with a more stable variant motif) suggest that GGGCTA hairpins are at the origin of GGGCTA length-dependent instability. They also suggest, as working hypothesis, that failure of efficient binding of RPA to GGGCTA structured into hairpins might be involved in the mechanism of GGGCTA array instability. On the basis of our present and past studies about telomeric G4 and their interaction with RPA, we propose an original point of view about telomeric G4 and the evolution of telomeric motifs.

Indexed as

DNAG-QuadruplexesHumansNucleic Acid ConformationNucleotide MotifsOligonucleotidesRepetitive Sequences, Nucleic AcidReplication Protein AShelterin ComplexTelomereTelomere-Binding ProteinsDNAOligonucleotidesPOT1 protein, humanReplication Protein AShelterin ComplexTelomere-Binding Proteins

Identifiers

PMID34214172
PMCPMC8287962

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Registered trials

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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.