Evidence map›Paper›PMID 37666988›Full record

ArticleNature genetics2023

Symmetric inheritance of parental histones governs epigenome maintenance and embryonic stem cell identity.

Alice Wenger, Alva Biran, Nicolas Alcaraz, Alba Redó-Riveiro, Annika Charlotte Sell, Robert Krautz, Valentin Flury, Nazaret Reverón-Gómez, Victor Solis-Mezarino, Moritz Völker-Albert and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Nature genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
10.9field-weighted citation impact, top 1% 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

51 citing papers in PubMed, 72 citations in OpenAlex.

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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

14 authors at 3 institutions in 3 countries.

Alice Wenger *Novo Nordisk Foundation Center for Protein Research (CPR), University of Copenhagen, Copenhagen, Denmark.ORCID http://orcid.org/0000-0001-5133-7074
Alva Biran *Novo Nordisk Foundation Center for Protein Research (CPR), University of Copenhagen, Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-0276-2004
Nicolas Alcaraz *Novo Nordisk Foundation Center for Protein Research (CPR), University of Copenhagen, Copenhagen, Denmark.
Alba Redó-Riveiro *Novo Nordisk Foundation Center for Stem Cell Medicine (reNEW), University of Copenhagen, Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-7015-2486
Annika Charlotte SellNovo Nordisk Foundation Center for Stem Cell Medicine (reNEW), University of Copenhagen, Copenhagen, Denmark.
Robert KrautzSection for Computational and RNA Biology, Department of Biology, University of Copenhagen, Copenhagen, Denmark.
Valentin FluryNovo Nordisk Foundation Center for Protein Research (CPR), University of Copenhagen, Copenhagen, Denmark.ORCID http://orcid.org/0000-0003-0476-4940
Nazaret Reverón-GómezNovo Nordisk Foundation Center for Protein Research (CPR), University of Copenhagen, Copenhagen, Denmark.
Victor Solis-MezarinoEpiQMAx GmbH, Planegg, Germany.
Moritz Völker-AlbertEpiQMAx GmbH, Planegg, Germany.
Axel ImhofFaculty of Medicine, Biomedical Center, Protein Analysis Unit, Ludwig-Maximilians-Universität München, Planegg, Germany.ORCID http://orcid.org/0000-0003-2993-8249
Robin AnderssonSection for Computational and RNA Biology, Department of Biology, University of Copenhagen, Copenhagen, Denmark. robin@bio.ku.dk.ORCID http://orcid.org/0000-0003-1516-879X
Joshua M BrickmanNovo Nordisk Foundation Center for Stem Cell Medicine (reNEW), University of Copenhagen, Copenhagen, Denmark. joshua.brickman@sund.ku.dk.ORCID http://orcid.org/0000-0003-1580-7491
Anja GrothNovo Nordisk Foundation Center for Protein Research (CPR), University of Copenhagen, Copenhagen, Denmark. anja.groth@cpr.ku.dk.ORCID http://orcid.org/0000-0003-0577-1771
University of Copenhagen · DKLudwig-Maximilians-Universität München · DEBroad Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Modified parental histones are segregated symmetrically to daughter DNA strands during replication and can be inherited through mitosis. How this may sustain the epigenome and cell identity remains unknown. Here we show that transmission of histone-based information during DNA replication maintains epigenome fidelity and embryonic stem cell plasticity. Asymmetric segregation of parental histones H3-H4 in MCM2-2A mutants compromised mitotic inheritance of histone modifications and globally altered the epigenome. This included widespread spurious deposition of repressive modifications, suggesting elevated epigenetic noise. Moreover, H3K9me3 loss at repeats caused derepression and H3K27me3 redistribution across bivalent promoters correlated with misexpression of developmental genes. MCM2-2A mutation challenged dynamic transitions in cellular states across the cell cycle, enhancing naïve pluripotency and reducing lineage priming in G1. Furthermore, developmental competence was diminished, correlating with impaired exit from pluripotency. Collectively, this argues that epigenetic inheritance of histone modifications maintains a correctly balanced and dynamic chromatin landscape able to support mammalian cell differentiation.

Indexed as

EpigenomeHistonesAnimalsChromatinEmbryonic Stem CellsMammalsMitosisChromatinHistones

Identifiers

PMID37666988
PMCPMC10484787
OpenAlexW4386415927

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.