Evidence map›Paper›PMID 31599722›Full record

ArticleeLife2019

CTCF confers local nucleosome resiliency after DNA replication and during mitosis.

Nick Owens, Thaleia Papadopoulou, Nicola Festuccia, Alexandra Tachtsidi, Inma Gonzalez, Agnes Dubois, Sandrine Vandormael-Pournin, Elphège P Nora, Benoit G Bruneau, Michel Cohen-Tannoudji and 1 more

Abstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing 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

58 citing papers in PubMed.

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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

11 authors.

Nick Owens *Epigenomics, Proliferation, and the Identity of Cells, Department of Developmental and Stem Cell Biology, Institut Pasteur, CNRS UMR3738, Paris, France.ORCID 0000-0002-2151-9923
Thaleia Papadopoulou *Epigenomics, Proliferation, and the Identity of Cells, Department of Developmental and Stem Cell Biology, Institut Pasteur, CNRS UMR3738, Paris, France.
Nicola FestucciaEpigenomics, Proliferation, and the Identity of Cells, Department of Developmental and Stem Cell Biology, Institut Pasteur, CNRS UMR3738, Paris, France.
Alexandra TachtsidiEpigenomics, Proliferation, and the Identity of Cells, Department of Developmental and Stem Cell Biology, Institut Pasteur, CNRS UMR3738, Paris, France.
Inma GonzalezEpigenomics, Proliferation, and the Identity of Cells, Department of Developmental and Stem Cell Biology, Institut Pasteur, CNRS UMR3738, Paris, France.
Agnes DuboisEpigenomics, Proliferation, and the Identity of Cells, Department of Developmental and Stem Cell Biology, Institut Pasteur, CNRS UMR3738, Paris, France.
Sandrine Vandormael-PourninEpigenomics, Proliferation, and the Identity of Cells, Department of Developmental and Stem Cell Biology, Institut Pasteur, CNRS UMR3738, Paris, France.
Elphège P NoraGladstone Institutes, San Francisco, United States.
Benoit G BruneauGladstone Institutes, San Francisco, United States.ORCID 0000-0002-0804-7597
Michel Cohen-TannoudjiEpigenomics, Proliferation, and the Identity of Cells, Department of Developmental and Stem Cell Biology, Institut Pasteur, CNRS UMR3738, Paris, France.ORCID 0000-0002-6405-2657
Pablo NavarroEpigenomics, Proliferation, and the Identity of Cells, Department of Developmental and Stem Cell Biology, Institut Pasteur, CNRS UMR3738, Paris, France.ORCID 0000-0002-2700-6598

Funding

Agence Nationale de la Recherche ANR 16 CE12 0004 01 MITMATAgence Nationale de la Recherche Investissement d'Avenir; Revive Labex; ANR-10-LABX-73European Molecular Biology Organization ALTF523-2013European Research Council ERC-CoG-2017 BINDFondation Schlumberger FRM FSER 2017Ligue Contre le Cancer LNCC EL2018 NAVARROSchlumberger Foundation FRM FSER 2017
6 · The paper itself

Abstract

The access of Transcription Factors (TFs) to their cognate DNA binding motifs requires a precise control over nucleosome positioning. This is especially important following DNA replication and during mitosis, both resulting in profound changes in nucleosome organization over TF binding regions. Using mouse Embryonic Stem (ES) cells, we show that the TF CTCF displaces nucleosomes from its binding site and locally organizes large and phased nucleosomal arrays, not only in interphase steady-state but also immediately after replication and during mitosis. Correlative analyses suggest this is associated with fast gene reactivation following replication and mitosis. While regions bound by other TFs (Oct4/Sox2), display major rearrangement, the post-replication and mitotic nucleosome positioning activity of CTCF is not unique: Esrrb binding regions are also characterized by persistent nucleosome positioning. Therefore, selected TFs such as CTCF and Esrrb act as resilient TFs governing the inheritance of nucleosome positioning at regulatory regions throughout the cell-cycle.

Indexed as

DNA ReplicationMitosisAnimalsCCCTC-Binding FactorCells, CulturedEmbryonic Stem CellsGene Expression RegulationMiceNucleosomesTranscriptional ActivationCCCTC-Binding FactorCtcf protein, mouseNucleosomeschromosomesCTCFgene expressionmitosismousenucleosome positioningpluripotencyreplicationtranscription factors

Identifiers

PMID31599722
PMCPMC6844645

What OpenQuestion holds

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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.