Evidence map›Paper›PMID 34326481›Full record

ArticleNature cell biology2021

CTCF chromatin residence time controls three-dimensional genome organization, gene expression and DNA methylation in pluripotent cells.

Widia Soochit, Frank Sleutels, Gregoire Stik, Marek Bartkuhn, Sreya Basu, Silvia C Hernandez, Sarra Merzouk, Enrique Vidal, Ruben Boers, Joachim Boers and 13 more

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Nature cell biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 4% 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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 64 citations in OpenAlex.

  1. An updated catalog ofFrontiers in molecular neuroscience · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 3 institutions in 3 countries.

Widia Soochit *Department of Cell Biology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Frank Sleutels *Department of Cell Biology, Erasmus University Medical Center, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0001-6813-5209
Gregoire Stik *Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.ORCID http://orcid.org/0000-0002-1404-1992
Marek BartkuhnInstitute for Genetics, Justus-Liebig-University Giessen, Giessen, Germany.
Sreya BasuDepartment of Cell Biology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Silvia C HernandezDepartment of Cell Biology, Erasmus University Medical Center, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0002-6525-5296
Sarra MerzoukDepartment of Developmental Biology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Enrique VidalCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.ORCID http://orcid.org/0000-0002-4217-1807
Ruben BoersDepartment of Developmental Biology, Erasmus University Medical Center, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0002-3377-2897
Joachim BoersDepartment of Developmental Biology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Michael van der ReijdenDepartment of Cell Biology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Bart GevertsDepartment of Pathology, Josephine Nefkens Institute, Erasmus University Medical Center, Rotterdam, The Netherlands.
Wiggert A van CappellenDepartment of Pathology, Josephine Nefkens Institute, Erasmus University Medical Center, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0001-9059-8365
Mirjam van den HoutDepartment of Cell Biology, Erasmus University Medical Center, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0003-2412-7631
Zeliha OzgurDepartment of Cell Biology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Wilfred F J van IJckenDepartment of Cell Biology, Erasmus University Medical Center, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0002-0421-8301
Joost GribnauDepartment of Developmental Biology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Rainer RenkawitzInstitute for Genetics, Justus-Liebig-University Giessen, Giessen, Germany.
Thomas GrafCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.ORCID http://orcid.org/0000-0003-2774-4117
Adriaan HoutsmullerDepartment of Pathology, Josephine Nefkens Institute, Erasmus University Medical Center, Rotterdam, The Netherlands.
Frank Grosveld *Department of Cell Biology, Erasmus University Medical Center, Rotterdam, The Netherlands. f.grosveld@erasmusmc.nl.ORCID http://orcid.org/0000-0002-7051-4715
Ralph Stadhouders *Department of Cell Biology, Erasmus University Medical Center, Rotterdam, The Netherlands. r.stadhouders@erasmusmc.nl.ORCID http://orcid.org/0000-0002-1060-5607
Niels Galjart *Department of Cell Biology, Erasmus University Medical Center, Rotterdam, The Netherlands. n.galjart@erasmusmc.nl.ORCID http://orcid.org/0000-0003-1964-3607
Erasmus MC · NLCentre for Genomic Regulation · ESJustus-Liebig-Universität Gießen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The 11 zinc finger (ZF) protein CTCF regulates topologically associating domain formation and transcription through selective binding to thousands of genomic sites. Here, we replaced endogenous CTCF in mouse embryonic stem cells with green-fluorescent-protein-tagged wild-type or mutant proteins lacking individual ZFs to identify additional determinants of CTCF positioning and function. While ZF1 and ZF8-ZF11 are not essential for cell survival, ZF8 deletion strikingly increases the DNA binding off-rate of mutant CTCF, resulting in reduced CTCF chromatin residence time. Loss of ZF8 results in widespread weakening of topologically associating domains, aberrant gene expression and increased genome-wide DNA methylation. Thus, important chromatin-templated processes rely on accurate CTCF chromatin residence time, which we propose depends on local sequence and chromatin context as well as global CTCF protein concentration.

Indexed as

DNA MethylationGene Expression RegulationGenomeAnimalsCCCTC-Binding FactorChromatinFemaleGreen Fluorescent ProteinsMaleMiceMitosisMouse Embryonic Stem CellsMutationPluripotent Stem CellsTime FactorsTranscription Elongation, GeneticCCCTC-Binding FactorChromatinCtcf protein, mouseGreen Fluorescent Proteins

Identifiers

PMID34326481
OpenAlexW3185409663

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.