Evidence map›Paper›PMID 32601371›Full record

ArticleNature cell biology2020

Heterochromatin establishment during early mammalian development is regulated by pericentromeric RNA and characterized by non-repressive H3K9me3.

Adam Burton, Vincent Brochard, Carmen Galan, Elias R Ruiz-Morales, Quirze Rovira, Diego Rodriguez-Terrones, Kai Kruse, Stéphanie Le Gras, Vishnu S Udayakumar, Hang Gyeong Chin and 9 more

Open access · greenAbstract read
In one paragraph

Article in Nature cell biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 98 papers.

0numbers the graph read from it
0cells of the map it votes in
98citing papers in PubMed
7.9field-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

98 citing papers in PubMed, 145 citations in OpenAlex.

  1. Article
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  8. Article
  9. Histone Modifications in Mammalian Early Embryos.Advances in experimental medicine and biology · 2026
    Review
  10. Epigenetic remodeling during early embryonic development.Frontiers in cell and developmental biology · 2026
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
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  20. Review

38 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

19 authors at 11 institutions in 6 countries.

Adam BurtonInstitute of Epigenetics and Stem Cells, Helmholtz Zentrum München, München, Germany.
Vincent BrochardUniversité Paris-Saclay, INRAE, ENVA, BREED U1198, Jouy-en-Josas, France.ORCID http://orcid.org/0000-0002-2850-8821
Carmen GalanDepartment of Epigenetics, Max Planck Institute of Immunobiology and Epigenetics, Freiburg, Germany.
Elias R Ruiz-MoralesInstitute of Epigenetics and Stem Cells, Helmholtz Zentrum München, München, Germany.ORCID http://orcid.org/0000-0002-5801-6190
Quirze RoviraMax Planck Institute for Molecular Biomedicine, Münster, Germany.ORCID http://orcid.org/0000-0002-1472-1250
Diego Rodriguez-TerronesInstitute of Epigenetics and Stem Cells, Helmholtz Zentrum München, München, Germany.ORCID http://orcid.org/0000-0001-6306-5942
Kai KruseMax Planck Institute for Molecular Biomedicine, Münster, Germany.
Stéphanie Le GrasInstitut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS/INSERM U964, CU de Strasbourg, France.
Vishnu S UdayakumarNew England Biolabs, Ipswich, MA, USA.
Hang Gyeong ChinNew England Biolabs, Ipswich, MA, USA.
André EidInstitute of Epigenetics and Stem Cells, Helmholtz Zentrum München, München, Germany.ORCID http://orcid.org/0000-0003-1046-4119
Xiaoyu LiuClinical and Translational Research Center of Shanghai First Maternity and Infant Hospital, School of Life Sciences and Technology, Tongji University, Shanghai, China.
Chenfei WangClinical and Translational Research Center of Shanghai First Maternity and Infant Hospital, School of Life Sciences and Technology, Tongji University, Shanghai, China.ORCID http://orcid.org/0000-0001-7573-3768
Shaorong GaoClinical and Translational Research Center of Shanghai First Maternity and Infant Hospital, School of Life Sciences and Technology, Tongji University, Shanghai, China.ORCID http://orcid.org/0000-0003-1041-3928
Sriharsa PradhanNew England Biolabs, Ipswich, MA, USA.
Juan M VaquerizasMax Planck Institute for Molecular Biomedicine, Münster, Germany.ORCID http://orcid.org/0000-0002-6583-6541
Nathalie BeaujeanUniversité Paris-Saclay, INRAE, ENVA, BREED U1198, Jouy-en-Josas, France.ORCID http://orcid.org/0000-0003-0188-9190
Thomas JenuweinDepartment of Epigenetics, Max Planck Institute of Immunobiology and Epigenetics, Freiburg, Germany.
Maria-Elena Torres-PadillaInstitute of Epigenetics and Stem Cells, Helmholtz Zentrum München, München, Germany. torres-padilla@helmholtz-muenchen.de.ORCID http://orcid.org/0000-0002-1020-2074
Helmholtz Zentrum München · DENew England Biolabs (United States) · USShanghai First Maternity and Infant Hospital · CNCentre National de la Recherche Scientifique · FRÉcole Nationale Vétérinaire d'Alfort · FRInmunal (Spain) · ESJiangsu Agri-animal Husbandry Vocational College · CNMax Planck Institute for Molecular Biomedicine · DEMax Planck Institute of Immunobiology and Epigenetics · DEThe Francis Crick Institute · GBUniversité Claude Bernard Lyon 1 · FR

Funding

European Research Council 280840Medical Research Council MC_UP_1605/10
6 · The paper itself

Abstract

Following fertilization in mammals, the gametes are reprogrammed to create a totipotent zygote, a process that involves de novo establishment of chromatin domains. A major feature occurring during preimplantation development is the dramatic remodelling of constitutive heterochromatin, although the functional relevance of this is unknown. Here, we show that heterochromatin establishment relies on the stepwise expression and regulated activity of SUV39H enzymes. Enforcing precocious acquisition of constitutive heterochromatin results in compromised development and epigenetic reprogramming, which demonstrates that heterochromatin remodelling is essential for natural reprogramming at fertilization. We find that de novo H3K9 trimethylation (H3K9me3) in the paternal pronucleus after fertilization is catalysed by SUV39H2 and that pericentromeric RNAs inhibit SUV39H2 activity and reduce H3K9me3. De novo H3K9me3 is initially non-repressive for gene expression, but instead bookmarks promoters for compaction. Overall, we uncover the functional importance for the restricted transmission of constitutive heterochromatin during reprogramming and a non-repressive role for H3K9me3.

Indexed as

Embryonic DevelopmentAnimalsCell NucleusCentromereEmbryo, MammalianEpigenesis, GeneticFemaleHeterochromatinHistonesMaleMethylationMiceMice, Inbred C57BLMice, Inbred CBARNAHeterochromatinHistonesRNA

Identifiers

PMID32601371
PMCPMC7610380
OpenAlexW3037659659

What OpenQuestion holds

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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.