Evidence map›Paper›PMID 36175410›Full record

ArticleNature communications2022

Exploration of nuclear body-enhanced sumoylation reveals that PML represses 2-cell features of embryonic stem cells.

Sarah Tessier, Omar Ferhi, Marie-Claude Geoffroy, Román González-Prieto, Antoine Canat, Samuel Quentin, Marika Pla, Michiko Niwa-Kawakita, Pierre Bercier, Domitille Rérolle and 6 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

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  18. The PML hub: An emerging actor of leukemia therapies.The Journal of experimental medicine · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 4 countries.

Sarah Tessier *Center for Interdisciplinary Research in Biology (CIRB), Collège de France, PSL research university, Inserm, Cnrs, 11 place Marcelin Berthelot, 75005, Paris, France.ORCID http://orcid.org/0000-0003-2146-3031
Omar Ferhi *Center for Interdisciplinary Research in Biology (CIRB), Collège de France, PSL research university, Inserm, Cnrs, 11 place Marcelin Berthelot, 75005, Paris, France.
Marie-Claude Geoffroy *Center for Interdisciplinary Research in Biology (CIRB), Collège de France, PSL research university, Inserm, Cnrs, 11 place Marcelin Berthelot, 75005, Paris, France.ORCID http://orcid.org/0000-0001-8298-467X
Román González-PrietoDepartment of Cell and Chemical Biology, Leiden University Medical Center (LUMC), Einthovenweg 20, 2333, ZC, Leiden, The Netherlands.ORCID http://orcid.org/0000-0001-8997-2321
Antoine CanatUniversité Paris Cité, Inserm, CNRS, GenCellDis, Institut de Recherche Saint-Louis, F-75010, Paris, France.ORCID http://orcid.org/0000-0003-2080-9803
Samuel QuentinUniversité Paris Cité, Inserm, CNRS, GenCellDis, Institut de Recherche Saint-Louis, F-75010, Paris, France.
Marika PlaNormal and pathological hematopoiesis: Emergence, Environment and translational research, Université de Paris Cité, Inserm, IRSL, F-75010, Paris, France.
Michiko Niwa-KawakitaUniversité Paris Cité, Inserm, CNRS, GenCellDis, Institut de Recherche Saint-Louis, F-75010, Paris, France.ORCID http://orcid.org/0000-0002-9450-583X
Pierre BercierCenter for Interdisciplinary Research in Biology (CIRB), Collège de France, PSL research university, Inserm, Cnrs, 11 place Marcelin Berthelot, 75005, Paris, France.
Domitille RérolleCenter for Interdisciplinary Research in Biology (CIRB), Collège de France, PSL research university, Inserm, Cnrs, 11 place Marcelin Berthelot, 75005, Paris, France.
Marilyn TirardDepartment of Molecular Neurobiology, Max Planck Institute of Multidisciplinary Sciences, D-37075, Goettingen, Germany.
Pierre TherizolsUniversité Paris Cité, Inserm, CNRS, GenCellDis, Institut de Recherche Saint-Louis, F-75010, Paris, France.ORCID http://orcid.org/0000-0002-5916-0987
Emmanuelle FabreUniversité Paris Cité, Inserm, CNRS, GenCellDis, Institut de Recherche Saint-Louis, F-75010, Paris, France.ORCID http://orcid.org/0000-0002-0009-4604
Alfred C O VertegaalDepartment of Cell and Chemical Biology, Leiden University Medical Center (LUMC), Einthovenweg 20, 2333, ZC, Leiden, The Netherlands.
Hugues de ThéCenter for Interdisciplinary Research in Biology (CIRB), Collège de France, PSL research university, Inserm, Cnrs, 11 place Marcelin Berthelot, 75005, Paris, France. hugues.dethe@inserm.fr.ORCID http://orcid.org/0000-0002-1113-4472
Valérie Lallemand-BreitenbachCenter for Interdisciplinary Research in Biology (CIRB), Collège de France, PSL research university, Inserm, Cnrs, 11 place Marcelin Berthelot, 75005, Paris, France. valerie.lallemand@inserm.fr.ORCID http://orcid.org/0000-0001-9852-204X
Centre National de la Recherche Scientifique · FRLeiden University Medical Center · NLInserm · FRMax Planck Institute for Multidisciplinary Sciences

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Membrane-less organelles are condensates formed by phase separation whose functions often remain enigmatic. Upon oxidative stress, PML scaffolds Nuclear Bodies (NBs) to regulate senescence or metabolic adaptation. PML NBs recruit many partner proteins, but the actual biochemical mechanism underlying their pleiotropic functions remains elusive. Similarly, PML role in embryonic stem cell (ESC) and retro-element biology is unsettled. Here we demonstrate that PML is essential for oxidative stress-driven partner SUMO2/3 conjugation in mouse ESCs (mESCs) or leukemia, a process often followed by their poly-ubiquitination and degradation. Functionally, PML is required for stress responses in mESCs. Differential proteomics unravel the KAP1 complex as a PML NB-dependent SUMO2-target in arsenic-treated APL mice or mESCs. PML-driven KAP1 sumoylation enables activation of this key epigenetic repressor implicated in retro-element silencing. Accordingly, Pml

Indexed as

ArsenicSumoylationAnimalsDNA Transposable ElementsEmbryonic Stem CellsMiceNuclear BodiesTranscription FactorsArsenicDNA Transposable ElementsDppa2 protein, mouseTranscription Factors

Identifiers

PMID36175410
PMCPMC9522831
OpenAlexW4297997389

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.