Evidence map›Paper›PMID 32240642›Full record

ArticleDevelopmental biology2020

DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain.

Yasuhiro Kyono, Samhitha Raj, Christopher J Sifuentes, Nicolas Buisine, Laurent Sachs, Robert J Denver

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Developmental biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

10 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Yasuhiro KyonoNeuroscience Graduate Program, The University of Michigan, Ann Arbor, MI, 48109, USA.
Samhitha RajDepartment of Molecular, Cellular and Developmental Biology, The University of Michigan, Ann Arbor, MI, 48109, USA.
Christopher J SifuentesDepartment of Molecular, Cellular and Developmental Biology, The University of Michigan, Ann Arbor, MI, 48109, USA.
Nicolas BuisineUMR-7221, Centre National de la recherche scientifique (CNRS), Muséum National d'Histoire Naturelle, 75005, Paris, France.
Laurent SachsUMR-7221, Centre National de la recherche scientifique (CNRS), Muséum National d'Histoire Naturelle, 75005, Paris, France.
Robert J DenverDepartment of Molecular, Cellular and Developmental Biology, The University of Michigan, Ann Arbor, MI, 48109, USA. Electronic address: rdenver@umich.edu.
University of Michigan · USCentre National de la Recherche Scientifique · FR

Funding

Thyroid hormone-dependent DNA methylation in the developing brainF31NS073294 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KYONO, YASUHIRO · 2011 to 2012
$64k
NINDS NIH HHS F31 NS073294
6 · The paper itself

Abstract

Methylation of cytosine residues in DNA influences chromatin structure and gene transcription, and its regulation is crucial for brain development. There is mounting evidence that DNA methylation can be modulated by hormone signaling. We analyzed genome-wide changes in DNA methylation and their relationship to gene regulation in the brain of Xenopus tadpoles during metamorphosis, a thyroid hormone-dependent developmental process. We studied the region of the tadpole brain containing neurosecretory neurons that control pituitary hormone secretion, a region that is highly responsive to thyroid hormone action. Using Methylated DNA Capture sequencing (MethylCap-seq) we discovered a diverse landscape of DNA methylation across the tadpole neural cell genome, and pairwise stage comparisons identified several thousand differentially methylated regions (DMRs). During the pre-to pro-metamorphic period, the number of DMRs was lowest (1,163), with demethylation predominating. From pre-metamorphosis to metamorphic climax DMRs nearly doubled (2,204), with methylation predominating. The largest changes in DNA methylation were seen from metamorphic climax to the completion of metamorphosis (2960 DMRs), with 80% of the DMRs representing demethylation. Using RNA sequencing, we found negative correlations between differentially expressed genes and DMRs localized to gene bodies and regions upstream of transcription start sites. DNA demethylation at metamorphosis revealed by MethylCap-seq was corroborated by increased immunoreactivity for the DNA demethylation intermediates 5-hydroxymethylcytosine and 5-carboxymethylcytosine, and the methylcytosine dioxygenase ten eleven translocation 3 that catalyzes DNA demethylation. Our findings show that the genome of tadpole neural cells undergoes significant changes in DNA methylation during metamorphosis, and these changes likely influence chromatin architecture, and gene regulation programs occurring during this developmental period.

Indexed as

DNA MethylationGene Expression Regulation, DevelopmentalAnimalsBrainCysteine DioxygenaseDemethylationDNAGene ExpressionLarvaMetamorphosis, BiologicalRNA, MessengerXenopus laevisXenopus ProteinsCysteine DioxygenaseDNARNA, MessengerXenopus ProteinsBrain developmentDNA methylationMetamorphosisTET enzymesTranscriptionXenopus

Identifiers

PMID32240642
PMCPMC7251973
OpenAlexW3015153080

What OpenQuestion holds

Textmetadata
LicenceTDM
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.