Evidence map›Paper›PMID 32514123›Full record

ArticleNature genetics2020

TETs compete with DNMT3 activity in pluripotent cells at thousands of methylated somatic enhancers.

Jocelyn Charlton, Eunmi J Jung, Alexandra L Mattei, Nina Bailly, Jing Liao, Eric J Martin, Pay Giesselmann, Björn Brändl, Elena K Stamenova, Franz-Josef Müller and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Nature genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed
6.3field-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

83 citing papers in PubMed, 116 citations in OpenAlex.

  1. Article
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  3. Review
  4. A cross-talk between p16High senescence and cellular reprogramming.Clinical science (London, England : 1979) · 2026
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  7. Epigenetic regulation in a high-sugar environment (Review).International journal of molecular medicine · 2026
    Review
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  12. Mechanisms of human germ cell development.Nature reviews. Molecular cell biology · 2026
    Review
  13. Epigenetic remodeling during early embryonic development.Frontiers in cell and developmental biology · 2026
    Review
  14. Article
  15. Article
  16. Epigenetic networks coordinate DNA methylation across the genome.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  17. Review
  18. Article
  19. Article
  20. Article

23 more citing papers are in PubMed but not listed here.

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

14 authors at 5 institutions in 2 countries.

Jocelyn CharltonDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, USA.
Eunmi J JungDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, USA.
Alexandra L MatteiDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, USA.ORCID http://orcid.org/0000-0003-1450-8924
Nina BaillyDepartment of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany.
Jing LiaoDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, USA.
Eric J MartinThe Ken & Ruth Davee Department of Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Pay GiesselmannDepartment of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany.ORCID http://orcid.org/0000-0002-1227-897X
Björn BrändlDepartment of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany.
Elena K StamenovaBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Franz-Josef MüllerDepartment of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany.
Evangelos KiskinisThe Ken & Ruth Davee Department of Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.ORCID http://orcid.org/0000-0001-8342-8616
Andreas GnirkeBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Zachary D SmithDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, USA.
Alexander MeissnerDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, USA. meissner@molgen.mpg.de.
Broad Institute · USHarvard University · USMax Planck Institute for Molecular Genetics · DENorthwestern University · USUniversitäts Hautklinik Kiel · DE

Funding

Regulatory Roles and Dynamics of Nuclear long-noncoding RNAs in PluripotencyP01GM099117 · NIGMS · HARVARD UNIVERSITY · PI MEISSNER, ALEXANDER · 2011 to 2021
$21.2M
Determining How Defective Nucleo-Cytoplasmic Trafficking Leads To Neurodegeneration In C9orf72-Related ALS And FTDR01NS104219 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI KISKINIS, EVANGELOS · 2018 to 2022
$2.3M
NIGMS NIH HHS P01 GM099117NINDS NIH HHS R01 NS104219
6 · The paper itself

Abstract

Mammalian cells stably maintain high levels of DNA methylation despite expressing both positive (DNMT3A/B) and negative (TET1-3) regulators. Here, we analyzed the independent and combined effects of these regulators on the DNA methylation landscape using a panel of knockout human embryonic stem cell (ESC) lines. The greatest impact on global methylation levels was observed in DNMT3-deficient cells, including reproducible focal demethylation at thousands of normally methylated loci. Demethylation depends on TET expression and occurs only when both DNMT3s are absent. Dynamic loci are enriched for hydroxymethylcytosine and overlap with subsets of putative somatic enhancers that are methylated in ESCs and can be activated upon differentiation. We observe similar dynamics in mouse ESCs that were less frequent in epiblast stem cells (EpiSCs) and scarce in somatic tissues, suggesting a conserved pluripotency-linked mechanism. Taken together, our data reveal tightly regulated competition between DNMT3s and TETs at thousands of somatic regulatory sequences within pluripotent cells.

Indexed as

AnimalsCell DifferentiationCell LineDNA (Cytosine-5-)-MethyltransferasesDNA MethylationDNA Methyltransferase 3AEmbryonic Stem CellsEnhancer Elements, GeneticEpigenesis, GeneticGene Expression Regulation, DevelopmentalGerm LayersHumansMiceMice, KnockoutMixed Function OxygenasesPluripotent Stem CellsDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3ADNMT3A protein, humanDnmt3a protein, mouseMixed Function OxygenasesProto-Oncogene Proteins

Identifiers

PMID32514123
PMCPMC7415576
OpenAlexW3033596656

What OpenQuestion holds

Textmetadata
LicenceTDM
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.