Evidence map›Paper›PMID 32395866›Full record

ArticleThe EMBO journal2020

SUMOylated PRC1 controls histone H3.3 deposition and genome integrity of embryonic heterochromatin.

Zichuan Liu, Mathieu Tardat, Mark E Gill, Helene Royo, Raphael Thierry, Evgeniy A Ozonov, Antoine Hfm Peters

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

21 citing papers in PubMed, 29 citations in OpenAlex.

  1. Cross-species incompatibilities offer new insights into the functional consequences of satellite DNA evolution.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2026
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  12. Reduced histone gene copy number disruptsbioRxiv : the preprint server for biology · 2023
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  16. Chromatin role in early programming of embryos.Animal frontiers : the review magazine of animal agriculture · 2021
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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

7 authors at 2 institutions in 1 country.

Zichuan Liu *Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
Mathieu Tardat *Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
Mark E GillFriedrich Miescher Institute for Biomedical Research, Basel, Switzerland.ORCID 0000-0002-2069-958X
Helene RoyoFriedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
Raphael ThierryFriedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
Evgeniy A OzonovFriedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
Antoine Hfm PetersFriedrich Miescher Institute for Biomedical Research, Basel, Switzerland.ORCID 0000-0002-0311-1887
Friedrich Miescher Institute · CHUniversity of Basel · CH

Funding

EC | H2020 | H2020 Priority Excellent Science | H2020 European Research Council (ERC) 695288Novartis Research FoundationSchweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (SNF) 31003A_146293Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (SNF) 406340_128131
6 · The paper itself

Abstract

Chromatin integrity is essential for cellular homeostasis. Polycomb group proteins modulate chromatin states and transcriptionally repress developmental genes to maintain cell identity. They also repress repetitive sequences such as major satellites and constitute an alternative state of pericentromeric constitutive heterochromatin at paternal chromosomes (pat-PCH) in mouse pre-implantation embryos. Remarkably, pat-PCH contains the histone H3.3 variant, which is absent from canonical PCH at maternal chromosomes, which is marked by histone H3 lysine 9 trimethylation (H3K9me3), HP1, and ATRX proteins. Here, we show that SUMO2-modified CBX2-containing Polycomb Repressive Complex 1 (PRC1) recruits the H3.3-specific chaperone DAXX to pat-PCH, enabling H3.3 incorporation at these loci. Deficiency of Daxx or PRC1 components Ring1 and Rnf2 abrogates H3.3 incorporation, induces chromatin decompaction and breakage at PCH of exclusively paternal chromosomes, and causes their mis-segregation. Complementation assays show that DAXX-mediated H3.3 deposition is required for chromosome stability in early embryos. DAXX also regulates repression of PRC1 target genes during oogenesis and early embryogenesis. The study identifies a novel critical role for Polycomb in ensuring heterochromatin integrity and chromosome stability in mouse early development.

Indexed as

Genomic InstabilitySumoylationAnimalsCo-Repressor ProteinsEmbryo, MammalianFemaleHeterochromatinHistonesMaleMiceMolecular ChaperonesPolycomb Repressive Complex 1Small Ubiquitin-Related Modifier ProteinsCo-Repressor ProteinsDaxx protein, mouseHeterochromatinHistonesMolecular ChaperonesPolycomb Repressive Complex 1Small Ubiquitin-Related Modifier ProteinsSUMO2 protein, mousechromosome stabilityconstitutive heterochromatinhistone variantPRC1SUMOylation

Identifiers

PMID32395866
PMCPMC7327501
OpenAlexW3024885938

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.