Evidence map›Paper›PMID 29727617›Full record

ArticleMolecular cell2018

Genome-wide Control of Heterochromatin Replication by the Telomere Capping Protein TRF2.

Aaron Mendez-Bermudez, Liudmyla Lototska, Serge Bauwens, Marie-Josèphe Giraud-Panis, Olivier Croce, Karine Jamet, Agurtzane Irizar, Macarena Mowinckel, Stephane Koundrioukoff, Nicolas Nottet and 8 more

Open access · bronzeAbstract read
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In one paragraph

Article in Molecular cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
12.5field-weighted citation impact, top 2% 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

45 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
  2. Article
  3. Molecular evolution of animal aging.The EMBO journal · 2026
    Review
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  6. G-quadruplex stabilization induces DNA breaks in pericentromeric repetitive DNA sequences in B lymphocytes.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. Article
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  12. Article
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  14. Article
  15. The landscape of aging.Science China. Life sciences · 2022
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 3 institutions in 2 countries.

Aaron Mendez-BermudezShanghai Ruijin Hospital, Shanghai Ruijin Hospital North, Shanghai Jiao Tong University School of Medicine, Université Côte d'Azur, CNRS, Inserm, "Laboratoire International Associé" (LIA) Hematology and Cancer, State Key Laboratory of Medical Genomics, "Pôle Sino-Français de Recherche en Sciences du Vivant et Génomique," Shanghai, P.R. China; Université Côte d'Azur, CNRS, Inserm, IRCAN, Faculty of Medicine Nice, France.
Liudmyla LototskaUniversité Côte d'Azur, CNRS, Inserm, IRCAN, Faculty of Medicine Nice, France.
Serge BauwensUniversité Côte d'Azur, CNRS, Inserm, IRCAN, Faculty of Medicine Nice, France.
Marie-Josèphe Giraud-PanisUniversité Côte d'Azur, CNRS, Inserm, IRCAN, Faculty of Medicine Nice, France.
Olivier CroceUniversité Côte d'Azur, CNRS, Inserm, IRCAN, Faculty of Medicine Nice, France.
Karine JametUniversité Côte d'Azur, CNRS, Inserm, IRCAN, Faculty of Medicine Nice, France.
Agurtzane IrizarUniversité Côte d'Azur, CNRS, Inserm, IRCAN, Faculty of Medicine Nice, France.
Macarena MowinckelUniversité Côte d'Azur, CNRS, Inserm, IRCAN, Faculty of Medicine Nice, France.
Stephane KoundrioukoffInstitut Gustave Roussy, Sorbonne Universités, UPMC University, Paris, France; CNRS, UMR 8200, Villejuif, France.
Nicolas NottetUniversité Côte d'Azur, CNRS, IPMC, France.
Genevieve AlmouzniInstitut Curie, PSL University, Sorbonne Universités, UPMC University, CNRS, UMR3664, Paris, France.
Mare-Paule Teulade-FichouInstitut Curie, PSL University, Sorbonne Universités, UPMC, CNRS, Inserm, UMR9187/U1196, Orsay, France.
Michael SchertzerInstitut Curie, PSL Research University, Sorbonne Universités, CNRS UMR3244 Telomere and Cancer Lab, Paris, France.
Mylène PerderisetInstitut Curie, PSL Research University, Sorbonne Universités, CNRS UMR3244 Telomere and Cancer Lab, Paris, France.
Arturo Londoño-VallejoInstitut Curie, PSL Research University, Sorbonne Universités, CNRS UMR3244 Telomere and Cancer Lab, Paris, France.
Michelle DebatisseInstitut Gustave Roussy, Sorbonne Universités, UPMC University, Paris, France.
Eric GilsonShanghai Ruijin Hospital, Shanghai Ruijin Hospital North, Shanghai Jiao Tong University School of Medicine, Université Côte d'Azur, CNRS, Inserm, "Laboratoire International Associé" (LIA) Hematology and Cancer, State Key Laboratory of Medical Genomics, "Pôle Sino-Français de Recherche en Sciences du Vivant et Génomique," Shanghai, P.R. China; Université Côte d'Azur, CNRS, Inserm, IRCAN, Faculty of Medicine Nice, France; Department of Genetics, CHU, Nice, France. Electronic address: eric.gilson@unice.fr.
Jing YeShanghai Ruijin Hospital, Shanghai Ruijin Hospital North, Shanghai Jiao Tong University School of Medicine, Université Côte d'Azur, CNRS, Inserm, "Laboratoire International Associé" (LIA) Hematology and Cancer, State Key Laboratory of Medical Genomics, "Pôle Sino-Français de Recherche en Sciences du Vivant et Génomique," Shanghai, P.R. China. Electronic address: yj11254@rjh.com.cn.
Centre National de la Recherche Scientifique · FRInstitut Gustave Roussy · FRRuijin Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hard-to-replicate regions of chromosomes (e.g., pericentromeres, centromeres, and telomeres) impede replication fork progression, eventually leading, in the event of replication stress, to chromosome fragility, aging, and cancer. Our knowledge of the mechanisms controlling the stability of these regions is essentially limited to telomeres, where fragility is counteracted by the shelterin proteins. Here we show that the shelterin subunit TRF2 ensures progression of the replication fork through pericentromeric heterochromatin, but not centromeric chromatin. In a process involving its N-terminal basic domain, TRF2 binds to pericentromeric Satellite III sequences during S phase, allowing the recruitment of the G-quadruplex-resolving helicase RTEL1 to facilitate fork progression. We also show that TRF2 is required for the stability of other heterochromatic regions localized throughout the genome, paving the way for future research on heterochromatic replication and its relationship with aging and cancer.

Indexed as

Cell Line, TumorCentromereChromatinDNA HelicasesDNA ReplicationGenomeG-QuadruplexesHeLa CellsHeterochromatinHumansS PhaseTelomereTelomeric Repeat Binding Protein 2ChromatinDNA HelicasesHeterochromatinTelomeric Repeat Binding Protein 2TERF2 protein, humancentromeresDNA combingDNA topologyG-quadruplexheterochromatinpericentromerereplicationRTEL1telomereTRF2

Identifiers

PMID29727617
OpenAlexW2802240298

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.