Evidence map›Paper›PMID 36333500›Full record

ArticleNature genetics2022

DNA sequence and chromatin modifiers cooperate to confer epigenetic bistability at imprinting control regions.

Stefan Butz, Nina Schmolka, Ino D Karemaker, Rodrigo Villaseñor, Isabel Schwarz, Silvia Domcke, Esther C H Uijttewaal, Julian Jude, Florian Lienert, Arnaud R Krebs and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Nature genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

29 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
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  13. Review
  14. Article
  15. Overview and Prospects of DNA Sequence Visualization.International journal of molecular sciences · 2025
    Review
  16. Article
  17. Article
  18. Mechanistic drivers of chromatin organization into compartments.Current opinion in genetics & development · 2024
    Review
  19. Article
  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

16 authors at 6 institutions in 5 countries.

Stefan ButzDepartment of Molecular Mechanisms of Disease, University of Zurich, Zurich, Switzerland.
Nina SchmolkaDepartment of Molecular Mechanisms of Disease, University of Zurich, Zurich, Switzerland.
Ino D KaremakerDepartment of Molecular Mechanisms of Disease, University of Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0002-6528-9330
Rodrigo VillaseñorDepartment of Molecular Mechanisms of Disease, University of Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0002-3644-9817
Isabel SchwarzDepartment of Molecular Mechanisms of Disease, University of Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0003-4717-422X
Silvia DomckeFriedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
Esther C H UijttewaalInstitute of Molecular Biotechnology Austria (IMBA), Vienna BioCenter (VBC), Vienna, Austria.
Julian JudeResearch Institute of Molecular Pathology (IMP), Vienna BioCenter (VBC), Vienna, Austria.
Florian LienertFriedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
Arnaud R KrebsFriedrich Miescher Institute for Biomedical Research, Basel, Switzerland.ORCID http://orcid.org/0000-0001-7999-6127
Nathalie P de WagenaarDivision of Genome Biology and Epigenetics, Institute of Biodynamics and Biocomplexity, Department of Biology, Science Faculty, Utrecht University, Utrecht, the Netherlands.
Xue BaoDivision of Genome Biology and Epigenetics, Institute of Biodynamics and Biocomplexity, Department of Biology, Science Faculty, Utrecht University, Utrecht, the Netherlands.
Johannes ZuberResearch Institute of Molecular Pathology (IMP), Vienna BioCenter (VBC), Vienna, Austria.ORCID http://orcid.org/0000-0001-8810-6835
Ulrich EllingInstitute of Molecular Biotechnology Austria (IMBA), Vienna BioCenter (VBC), Vienna, Austria.ORCID http://orcid.org/0000-0002-4514-2809
Dirk SchübelerFriedrich Miescher Institute for Biomedical Research, Basel, Switzerland.ORCID http://orcid.org/0000-0002-9229-2228
Tuncay BaubecDepartment of Molecular Mechanisms of Disease, University of Zurich, Zurich, Switzerland. t.baubec@uu.nl.ORCID http://orcid.org/0000-0001-8474-6587
University of Zurich · CHUniversity of Basel · CHUtrecht University · NLInstitute of Molecular Biotechnology · ATResearch Institute of Molecular Pathology · ATEuropean Molecular Biology Laboratory · DE

Funding

European Research Council 865094Swiss National Science Foundation 157488
6 · The paper itself

Abstract

Genomic imprinting is regulated by parental-specific DNA methylation of imprinting control regions (ICRs). Despite an identical DNA sequence, ICRs can exist in two distinct epigenetic states that are memorized throughout unlimited cell divisions and reset during germline formation. Here, we systematically study the genetic and epigenetic determinants of this epigenetic bistability. By iterative integration of ICRs and related DNA sequences to an ectopic location in the mouse genome, we first identify the DNA sequence features required for maintenance of epigenetic states in embryonic stem cells. The autonomous regulatory properties of ICRs further enabled us to create DNA-methylation-sensitive reporters and to screen for key components involved in regulating their epigenetic memory. Besides DNMT1, UHRF1 and ZFP57, we identify factors that prevent switching from methylated to unmethylated states and show that two of these candidates, ATF7IP and ZMYM2, are important for the stability of DNA and H3K9 methylation at ICRs in embryonic stem cells.

Indexed as

DNA MethylationGenomic ImprintingAnimalsBase SequenceChromatinEpigenomicsMiceRepressor ProteinsAtf7ip protein, mouseChromatinRepressor Proteins

Identifiers

PMID36333500
PMCPMC9649441
OpenAlexW4308210326

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.