Evidence map›Paper›PMID 33555502›Full record

ArticleGenes & genomics2021

Evidence for divergence of DNA methylation maintenance and a conserved inhibitory mechanism from DNA demethylation in chickens and mammals.

Masako Tada, Ayaka Hayashi, Yumi Asano, Musashi Kubiura-Ichimaru, Takamasa Ito, Miho Yoshii, Hiroshi Kimura, Yoichi Matsuda, Mitsuo Oshimura

Open access · hybridAbstract read
In one paragraph

Article in Genes & genomics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 49% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Chicken Erythrocyte: Epigenomic Regulation of Gene Activity.International journal of molecular sciences · 2023
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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

9 authors at 4 institutions in 1 country.

Masako Tada *Stem Cells and Reprogramming Laboratory, Department of Biology, Faculty of Science, Toho University, Miyama 2-2-1, Funabashi, Chiba, 274-8510, Japan. masako.tada@sci.toho-u.ac.jp.ORCID 0000-0003-3641-3520
Ayaka Hayashi *Chromosome Engineering Research Center, Tottori University, Yonago, 683-8503, Japan.
Yumi AsanoChromosome Engineering Research Center, Tottori University, Yonago, 683-8503, Japan.
Musashi Kubiura-IchimaruStem Cells and Reprogramming Laboratory, Department of Biology, Faculty of Science, Toho University, Miyama 2-2-1, Funabashi, Chiba, 274-8510, Japan.
Takamasa ItoStem Cells and Reprogramming Laboratory, Department of Biology, Faculty of Science, Toho University, Miyama 2-2-1, Funabashi, Chiba, 274-8510, Japan.
Miho YoshiiStem Cells and Reprogramming Laboratory, Department of Biology, Faculty of Science, Toho University, Miyama 2-2-1, Funabashi, Chiba, 274-8510, Japan.
Hiroshi KimuraCell Biology Unit, Institute of Innovative Research, Tokyo Institute of Technology, Tokyo, 226-8501, Japan.
Yoichi MatsudaDepartment of Animal Sciences, Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya, 464-8601, Japan.
Mitsuo OshimuraChromosome Engineering Research Center, Tottori University, Yonago, 683-8503, Japan.
Toho University · JPTottori University · JPNagoya University · JPTokyo Institute of Technology · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDNA methylation is a significant epigenetic modification that is evolutionarily conserved in various species and often serves as a repressive mark for transcription. DNA methylation levels and patterns are regulated by a balance of opposing enzyme functions, DNA methyltransferases, DNMT1/3A/3B and methylcytosine dioxygenases, TET1/2/3. In mice, the TET enzyme converts DNA cytosine methylation (5mC) to 5-hydroxymethylcytosine (5hmC) at the beginning of fertilisation and gastrulation and initiates a global loss of 5mC, while the 5mC level is increased on the onset of cell differentiation during early embryonic development.

objectiveGlobal loss and gain of DNA methylation may be differently regulated in diverged species.

methodsChicken B-cell lymphoma DT40 cells were used as an avian model to compare differences in the overall regulation of DNA modification with mammals.

resultsWe found that DNA methylation is maintained at high levels in DT40 cells through compact chromatin formation, which inhibits TET-mediated demethylation. Human and mouse chromosomes introduced into DT40 cells by cell fusion lost the majority of 5mC, except for human subtelomeric repeats.

conclusionOur attempt to elucidate the differences in the epigenetic regulatory mechanisms between birds and mammals explored the evidence that they share a common chromatin-based regulation of TET-DNA access, while chicken DNMT1 is involved in different target sequence recognition systems, suggesting that factors inducing DNMT-DNA association have already diverged.

Indexed as

DNA DemethylationDNA MethylationAnimalsCell Line, TumorCells, CulturedChickensChromatinDioxygenasesDNA Modification MethylasesFemaleHumansInduced Pluripotent Stem CellsMiceMouse Embryonic Stem CellsChromatinDioxygenasesDNA Modification MethylasesChickenDivergenceDNA methylationMammalian chromosome

Identifiers

PMID33555502
PMCPMC7966644
OpenAlexW3127162456

What OpenQuestion holds

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Registered trials

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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.