Evidence map›Paper›PMID 28605464›Full record

ArticleNucleic acids research2017

Strand-specific CpG hemimethylation, a novel epigenetic modification functional for genomic imprinting.

Iris Patiño-Parrado, Álvaro Gómez-Jiménez, Noelia López-Sánchez, José M Frade

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. A novel workflow for the qualitative analysis of DNA methylation data.Computational and structural biotechnology journal · 2022
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. 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

4 authors at 1 institution in 1 country.

Iris Patiño-ParradoDepartment of Molecular, Cellular, and Developmental Neurobiology, Cajal Institute, Consejo Superior de Investigaciones Científicas (IC-CSIC), Madrid E-28002, Spain.
Álvaro Gómez-JiménezDepartment of Molecular, Cellular, and Developmental Neurobiology, Cajal Institute, Consejo Superior de Investigaciones Científicas (IC-CSIC), Madrid E-28002, Spain.
Noelia López-SánchezDepartment of Molecular, Cellular, and Developmental Neurobiology, Cajal Institute, Consejo Superior de Investigaciones Científicas (IC-CSIC), Madrid E-28002, Spain.
José M FradeDepartment of Molecular, Cellular, and Developmental Neurobiology, Cajal Institute, Consejo Superior de Investigaciones Científicas (IC-CSIC), Madrid E-28002, Spain.
Consejo Superior de Investigaciones Científicas · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Imprinted genes are regulated by allele-specific differentially DNA-methylated regions (DMRs). Epigenetic methylation of the CpGs constituting these DMRs is established in the germline, resulting in a 5-methylcytosine-specific pattern that is tightly maintained in somatic tissues. Here, we show a novel epigenetic mark, characterized by strand-specific hemimethylation of contiguous CpG sites affecting the germline DMR of the murine Peg3, but not Snrpn, imprinted domain. This modification is enriched in tetraploid cortical neurons, a cell type where evidence for a small proportion of formylmethylated CpG sites within the Peg3-controlling DMR is also provided. Single nucleotide polymorphism (SNP)-based transcriptional analysis indicated that these epigenetic modifications participate in the maintainance of the monoallelic expression pattern of the Peg3 imprinted gene. Our results unexpectedly demonstrate that the methylation pattern observed in DMRs controlling defined imprinting regions can be modified in somatic cells, resulting in a novel epigenetic modification that gives rise to strand-specific hemimethylated domains functional for genomic imprinting. We anticipate the existence of a novel molecular mechanism regulating the transition from fully methylated CpGs to strand-specific hemimethylated CpGs.

Indexed as

DNA MethylationEpigenesis, GeneticGenomic Imprinting5-MethylcytosineAllelesAnimalsBase SequenceCell NucleusCerebral CortexCpG IslandsEmbryo, MammalianKruppel-Like Transcription FactorsMaleMiceMice, Inbred C57BLNeurons5-MethylcytosineKruppel-Like Transcription FactorsPeg3 protein, mouse

Identifiers

PMID28605464
PMCPMC5587773
OpenAlexW2624274374

What OpenQuestion holds

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LicenceCC BY-NC
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.