Evidence map›Paper›PMID 33268382›Full record

ArticleThe Journal of biological chemistry

YAP contributes to DNA methylation remodeling upon mouse embryonic stem cell differentiation.

Fabiana Passaro, Ilaria De Martino, Federico Zambelli, Giorgia Di Benedetto, Matteo Barbato, Anna Maria D'Erchia, Caterina Manzari, Graziano Pesole, Margherita Mutarelli, Davide Cacchiarelli and 3 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

23 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Article
  3. The Hippo pathway and p27Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. DNMT3A Cooperates with YAP/TAZ to Drive Gallbladder Cancer Metastasis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. IBtkα Activates the β-Catenin-Dependent Transcription ofInternational journal of molecular sciences · 2022
    Article
  17. Article
  18. Review
  19. Review
  20. Article
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

13 authors at 4 institutions in 1 country.

Fabiana PassaroDepartment of Molecular Medicine and Medical Biotechnology, University of Napoli Federico II, Italy. Electronic address: fabiana.passaro@unina.it.
Ilaria De MartinoDepartment of Molecular Medicine and Medical Biotechnology, University of Napoli Federico II, Italy.
Federico ZambelliDepartment of Biosciences, University of Milano, Italy; Institute of Biomembranes, Bioenergetics and Molecular Biotechnologies, National Research Council, Italy.
Giorgia Di BenedettoDepartment of Molecular Medicine and Medical Biotechnology, University of Napoli Federico II, Italy.
Matteo BarbatoDepartment of Molecular Medicine and Medical Biotechnology, University of Napoli Federico II, Italy.
Anna Maria D'ErchiaInstitute of Biomembranes, Bioenergetics and Molecular Biotechnologies, National Research Council, Italy; Department of Biosciences, Biotechnology and Biopharmaceutics, University of Bari, Italy.
Caterina ManzariInstitute of Biomembranes, Bioenergetics and Molecular Biotechnologies, National Research Council, Italy.
Graziano PesoleInstitute of Biomembranes, Bioenergetics and Molecular Biotechnologies, National Research Council, Italy; Department of Biosciences, Biotechnology and Biopharmaceutics, University of Bari, Italy.
Margherita MutarelliTigem and Department of Translational Medicine, University of Napoli Federico II, Italy.
Davide CacchiarelliTigem and Department of Translational Medicine, University of Napoli Federico II, Italy.
Dario AntoniniDepartment of Biology, University of Napoli Federico II, Italy.
Silvia ParisiDepartment of Molecular Medicine and Medical Biotechnology, University of Napoli Federico II, Italy.
Tommaso RussoDepartment of Molecular Medicine and Medical Biotechnology, University of Napoli Federico II, Italy. Electronic address: tommaso.russo@unina.it.
Institute of Biomembranes, Bioenergetics and Molecular Biotechnologies · ITUniversity of Naples Federico II · ITFederico II University Hospital · ITUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Yes-associated protein (YAP), one of the major effectors of the Hippo pathway together with its related protein WW-domain-containing transcription regulator 1 (WWTR1; also known as TAZ), mediates a range of cellular processes from proliferation and death to morphogenesis. YAP and WW-domain-containing transcription regulator 1 (WWTR1; also known as TAZ) regulate a large number of target genes, acting as coactivators of DNA-binding transcription factors or as negative regulators of transcription by interacting with the nucleosome remodeling and histone deacetylase complexes. YAP is expressed in self-renewing embryonic stem cells (ESCs), although it is still debated whether it plays any crucial roles in the control of either stemness or differentiation. Here we show that the transient downregulation of YAP in mouse ESCs perturbs cellular homeostasis, leading to the inability to differentiate properly. Bisulfite genomic sequencing revealed that this transient knockdown caused a genome-wide alteration of the DNA methylation remodeling that takes place during the early steps of differentiation, suggesting that the phenotype we observed might be due to the dysregulation of some of the mechanisms involved in regulation of ESC exit from pluripotency. By gene expression analysis, we identified two molecules that could have a role in the altered genome-wide methylation profile: the long noncoding RNA ephemeron, whose rapid upregulation is crucial for the transition of ESCs into epiblast, and the methyltransferase-like protein Dnmt3l, which, during the embryo development, cooperates with Dnmt3a and Dnmt3b to contribute to the de novo DNA methylation that governs early steps of ESC differentiation. These data suggest a new role for YAP in the governance of the epigenetic dynamics of exit from pluripotency.

Indexed as

Cell DifferentiationDNA MethylationAdaptor Proteins, Signal TransducingAnimalsDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3BMiceMouse Embryonic Stem CellsSignal TransductionYAP-Signaling ProteinsAdaptor Proteins, Signal TransducingDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3BYap1 protein, mouseYAP-Signaling ProteinsdifferentiationDNA methyltransferasesDnmt3lembryonic stem cellsephemeronepiblast-like stem cellspluripotencystemnessYes-associated protein

Identifiers

PMID33268382
PMCPMC7948423
OpenAlexW3107701424

What OpenQuestion holds

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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.