Evidence map›Paper›PMID 26098813›Full record

ReviewEpigenetics2015

Local chromatin microenvironment determines DNMT activity: from DNA methyltransferase to DNA demethylase or DNA dehydroxymethylase.

Monique G P van der Wijst, Muralidhar Venkiteswaran, Hui Chen, Guo-Liang Xu, Torsten Plösch, Marianne G Rots

Open access · bronzeAbstract readReview
In one paragraph

Review in Epigenetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
4.2field-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

50 citing papers in PubMed, 91 citations in OpenAlex.

  1. Trial
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  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. DNA Hydroxymethylation in Smoking-Associated Cancers.International journal of molecular sciences · 2022
    Review
  15. Review
  16. Review
  17. Structure and Function of TET Enzymes.Advances in experimental medicine and biology · 2022
    Article
  18. Review
  19. Article
  20. Review
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

6 authors at 3 institutions in 4 countries.

Monique G P van der Wijsta Epigenetic Editing; Department of Pathology and Medical Biology; University Medical Center Groningen; University of Groningen ; Groningen , The Netherlands.
Muralidhar Venkiteswaran
Hui Chen
Guo-Liang Xu
Torsten Plösch
Marianne G Rots
University of Groningen · NLUniversity Medical Center Groningen · NLChinese Academy of Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Insights on active DNA demethylation disproved the original assumption that DNA methylation is a stable epigenetic modification. Interestingly, mammalian DNA methyltransferases 3A and 3B (DNMT-3A and -3B) have also been reported to induce active DNA demethylation, in addition to their well-known function in catalyzing methylation. In situations of extremely low levels of S-adenosyl methionine (SAM), DNMT-3A and -3B might demethylate C-5 methyl cytosine (5mC) via deamination to thymine, which is subsequently replaced by an unmodified cytosine through the base excision repair (BER) pathway. Alternatively, 5mC when converted to 5- hydroxymethylcytosine (5hmC) by TET enzymes, might be further modified to an unmodified cytosine by DNMT-3A and -3B under oxidized redox conditions, although exact pathways are yet to be elucidated. Interestingly, even direct conversion of 5mC to cytosine might be catalyzed by DNMTs. Here, we summarize the evidence on the DNA dehydroxymethylase and demethylase activity of DNMT-3A and -3B. Although physiological relevance needs to be demonstrated, the current indications on the 5mC- and 5hmC-modifying activities of de novo DNA C-5 methyltransferases shed a new light on these enzymes. Despite the extreme circumstances required for such unexpected reactions to occur, we here put forward that the chromatin microenvironment can be locally exposed to extreme conditions, and hypothesize that such waves of extremes allow enzymes to act in differential ways.

Indexed as

AnimalsChromatinDNA (Cytosine-5-)-MethyltransferasesDNA MethylationDNA Methyltransferase 3ADNA Methyltransferase 3BDNA RepairEpigenesis, GeneticGene Expression RegulationHumansS-AdenosylmethionineChromatinDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3ADNA Methyltransferase 3BDNMT3A protein, humanS-Adenosylmethionine5caC, 5-carboxylcytosine5fC, 5-formylcytosine5hmC, 5 hydroxymethylcytosine5mC, 5-methylcytosineAID, activation-induced cytidine deaminaseAPOBEC, apolipoprotein B mRNA editing enzyme catalytic polypeptide-likeBER, base excision and repairC, cytosineCGI, CpG islandschromatin microenvironmentDNA dehydroxymethylationDNA demethylationDNMT, DNA methyltransferaseDNMTsGADD45, growth arrest and DNA-damage-inducible protein 45oxidizing redox stateRARE, retinoic acid response elementS-adenosyl methionine (SAM)SAM, S-adenosyl methionineTDG, thymine DNA glycosylaseTET, ten-eleven translocation.

Identifiers

PMID26098813
PMCPMC4622917
OpenAlexW1578724377

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.