Evidence map›Paper›PMID 22292019›Full record

ArticlePloS one2012

Persistence of cytosine methylation of DNA following fertilisation in the mouse.

Yan Li, Chris O'Neill

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 45 citations in OpenAlex.

  1. Epigenetic Modifications at the Center of the Barker Hypothesis and Their Transgenerational Implications.International journal of environmental research and public health · 2021
    Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Measurement of global DNA methylation levels by flow cytometry in mouse fibroblasts.In vitro cellular & developmental biology. Animal · 2017
    Article
  7. Article
  8. Article
  9. Article
  10. Glucocorticoids and fetal programming part 1: Outcomes.Nature reviews. Endocrinology · 2014
    Review
  11. Article
  12. The intergenerational effects of early adversity.Progress in molecular biology and translational science · 2014
    Review
  13. Article
  14. The maternal to zygotic transition in mammals.Molecular aspects of medicine · 2013
    Review
  15. Article
  16. What obesity research tells us about epigenetic mechanisms.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2013
    Review
  17. 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

2 authors at 1 institution in 1 country.

Yan LiSydney Medical School, Centre for Developmental and Regenerative Medicine, Kolling Institute for Medical Research, University of Sydney, Sydney, Australia.
Chris O'Neill
University of Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Normal development of the mammalian embryo requires epigenetic reprogramming of the genome. The level of cytosine methylation of CpG-rich (5meC) regions of the genome is a major epigenetic regulator and active global demethylation of 5meC throughout the genome is reported to occur within the first cell-cycle following fertilization. An enzyme or mechanism capable of catalysing such rapid global demethylation has not been identified. The mouse is a widely used model for studying developmental epigenetics. We have reassessed the evidence for this phenomenon of genome-wide demethylation following fertilisation in the mouse. We found when using conventional methods of immunolocalization that 5meC showed a progressive acid-resistant antigenic masking during zygotic maturation which gave the appearance of demethylation. Changing the unmasking strategy by also performing tryptic digestion revealed a persistence of a methylated state. Analysis of methyl binding domain 1 protein (MBD1) binding confirmed that the genome remained methylated following fertilisation. The maintenance of this methylated state over the first several cell-cycles required the actions of DNA methyltransferase activity. The study shows that any 5meC remodelling that occurs during early development is not explained by a global active loss of 5meC staining during the cleavage stage of development and global loss of methylation following fertilization is not a major component of epigenetic reprogramming in the mouse zygote.

Indexed as

AnimalsCells, CulturedCellular ReprogrammingCytosineDNA MethylationEmbryo, MammalianEpigenesis, GeneticFemaleFertilizationMiceMice, Inbred C57BLMice, Inbred CBAPregnancyTime FactorsZygoteCytosine

Identifiers

PMID22292019
PMCPMC3266909
OpenAlexW2100600153

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.