Evidence map›Paper›PMID 21407207›Full record

ArticleNature communications2011

5-Hydroxymethylcytosine in the mammalian zygote is linked with epigenetic reprogramming.

Mark Wossidlo, Toshinobu Nakamura, Konstantin Lepikhov, C Joana Marques, Valeri Zakhartchenko, Michele Boiani, Julia Arand, Toru Nakano, Wolf Reik, Jörn Walter

Open access · bronzeAbstract read
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In one paragraph

Article in Nature communications, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 382 papers.

0numbers the graph read from it
0cells of the map it votes in
382citing papers in PubMed
42.6field-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

382 citing papers in PubMed, 778 citations in OpenAlex.

  1. Review
  2. Maternal O-GlcNAc Transferase Is Required for the Asymmetry of Epigenetic Modifications in Mouse Zygotes.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  3. Review
  4. Article
  5. Epigenetic remodeling during early embryonic development.Frontiers in cell and developmental biology · 2026
    Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Perturbing nuclear glycosylation in the mouse preimplantation embryo slows down embryonic development.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  12. Review
  13. Article
  14. Review
  15. Mouse and human embryonic genome activation initiate at the one-cell stage.Frontiers in cell and developmental biology · 2025
    Article
  16. Article
  17. Article
  18. 5-Formylcytosine: a new epigenetic player.Signal transduction and targeted therapy · 2024
    Article
  19. Article
  20. Review

322 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

10 authors at 6 institutions in 3 countries.

Mark WossidloDepartment of Genetics/Epigenetics, Saarland University, Saarbrücken 66123, Germany.
Toshinobu Nakamura
Konstantin Lepikhov
C Joana Marques
Valeri Zakhartchenko
Michele Boiani
Julia Arand
Toru Nakano
Wolf Reik
Jörn Walter
Saarland University · DEOsaka University · JPBabraham Institute · GBLudwig-Maximilians-Universität München · DEMax Planck Institute for Molecular Biomedicine · DEUniversity of Cambridge · GB

Funding

Biotechnology and Biological Sciences Research Council BBS/E/B/0000Q192Medical Research Council G0700098
6 · The paper itself

Abstract

The epigenomes of early mammalian embryos are extensively reprogrammed to acquire a totipotent developmental potential. A major initial event in this reprogramming is the active loss/demethylation of 5-methylcytosine (5mC) in the zygote. Here, we report on findings that link this active demethylation to molecular mechanisms. We detect 5-hydroxymethylcytosine (5hmC) as a novel modification in mouse, bovine and rabbit zygotes. On zygotic development 5hmC accumulates in the paternal pronucleus along with a reduction of 5mC. A knockdown of the 5hmC generating dioxygenase Tet3 simultaneously affects the patterns of 5hmC and 5mC in the paternal pronucleus. This finding links the loss of 5mC to its conversion into 5hmC. The maternal pronucleus seems to be largely protected against this mechanism by PGC7/Dppa3/Stella, as in PGC7 knockout zygotes 5mC also becomes accessible to oxidation into 5hmC. In summary, our data suggest an important role of 5hmC and Tet3 for DNA methylation reprogramming processes in the mammalian zygote.

Indexed as

Epigenomics5-MethylcytosineAnimalsCattleCell NucleusChromosomal Proteins, Non-HistoneCytosineDioxygenasesDNA-Binding ProteinsDNA MethylationEmbryo, MammalianFemaleFertilization in VitroGene Expression Regulation, DevelopmentalGene Knockdown TechniquesMammals5-hydroxymethylcytosine5-MethylcytosineChromosomal Proteins, Non-HistoneCytosineDioxygenasesDNA-Binding ProteinsDppa3 protein, mouseProto-Oncogene ProteinsRepressor ProteinsTet3 protein, mouse

Identifiers

PMID21407207
OpenAlexW1971157495

What OpenQuestion holds

Textmetadata
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.