Evidence map›Paper›PMID 26928226›Full record

ArticleNature genetics2016

Active DNA demethylation at enhancers during the vertebrate phylotypic period.

Ozren Bogdanović, Arne H Smits, Elisa de la Calle Mustienes, Juan J Tena, Ethan Ford, Ruth Williams, Upeka Senanayake, Matthew D Schultz, Saartje Hontelez, Ila van Kruijsbergen and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in Nature genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 139 papers.

0numbers the graph read from it
0cells of the map it votes in
139citing papers in PubMed
18.1field-weighted citation impact, top 1% 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

139 citing papers in PubMed, 267 citations in OpenAlex.

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79 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 7 institutions in 6 countries.

Ozren BogdanovićAustralian Research Council Centre of Excellence in Plant Energy Biology, University of Western Australia, Perth, Western Australia, Australia.
Arne H SmitsDepartment of Molecular Biology, Faculty of Science, Radboud Institute for Molecular Life Sciences, Radboud University, Nijmegen, the Netherlands.
Elisa de la Calle MustienesCentro Andaluz de Biología del Desarrollo, Consejo Superior de Investigaciones Científicas, Universidad Pablo de Olavide, Seville, Spain.
Juan J TenaCentro Andaluz de Biología del Desarrollo, Consejo Superior de Investigaciones Científicas, Universidad Pablo de Olavide, Seville, Spain.
Ethan FordAustralian Research Council Centre of Excellence in Plant Energy Biology, University of Western Australia, Perth, Western Australia, Australia.
Ruth WilliamsWeatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
Upeka SenanayakeWeatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
Matthew D SchultzGenomic Analysis Laboratory, Salk Institute for Biological Studies, La Jolla, California, USA.
Saartje HontelezDepartment of Molecular Developmental Biology, Faculty of Science, Radboud Institute for Molecular Life Sciences, Radboud University, Nijmegen, the Netherlands.ORCID http://orcid.org/0000-0002-5286-7859
Ila van KruijsbergenDepartment of Molecular Developmental Biology, Faculty of Science, Radboud Institute for Molecular Life Sciences, Radboud University, Nijmegen, the Netherlands.
Teresa RayonCentro Nacional de Investigaciones Cardiovasculares, Madrid, Spain.
Felix GnerlichCentre for Integrated Protein Science, Ludwig Maximilians Universität München, Munich, Germany.
Thomas CarellCentre for Integrated Protein Science, Ludwig Maximilians Universität München, Munich, Germany.
Gert Jan C VeenstraDepartment of Molecular Developmental Biology, Faculty of Science, Radboud Institute for Molecular Life Sciences, Radboud University, Nijmegen, the Netherlands.ORCID http://orcid.org/0000-0002-7787-4940
Miguel ManzanaresCentro Nacional de Investigaciones Cardiovasculares, Madrid, Spain.
Tatjana Sauka-SpenglerWeatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
Joseph R EckerGenomic Analysis Laboratory, Salk Institute for Biological Studies, La Jolla, California, USA.
Michiel VermeulenDepartment of Molecular Biology, Faculty of Science, Radboud Institute for Molecular Life Sciences, Radboud University, Nijmegen, the Netherlands.
José Luis Gómez-SkarmetaCentro Andaluz de Biología del Desarrollo, Consejo Superior de Investigaciones Científicas, Universidad Pablo de Olavide, Seville, Spain.
Ryan ListerAustralian Research Council Centre of Excellence in Plant Energy Biology, University of Western Australia, Perth, Western Australia, Australia.ORCID http://orcid.org/0000-0001-6637-7239
Radboud University Nijmegen · NLAustralian Research Council · AUConsejo Superior de Investigaciones Científicas · ESUniversity of Oxford · GBCenter for Integrated Protein Science Munich · DESalk Institute for Biological Studies · USSpanish National Centre for Cardiovascular Research · ES

Funding

Epigenomic mapping approaches for cell-type classification in the brainU01MH105985 · NIMH · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI BEHRENS, M MARGARITA, ECKER, JOSEPH R · 2014 to 2016
$3.3M
Epigenome maps of regulatory activity in Xenopus tropicalis embryosR01HD069344 · NICHD · STICHTING RADBOUD UNIVERSITEIT · PI VEENSTRA, GERT JAN C. · 2011 to 2015
$1.4M
European Research Council 309384Howard Hughes Medical InstituteMedical Research Council G0902418Medical Research Council G1000801NICHD NIH HHS R01 HD069344NICHD NIH HHS R01HD069344NIMH NIH HHS U01 MH105985
6 · The paper itself

Abstract

The vertebrate body plan and organs are shaped during a conserved embryonic phase called the phylotypic stage. However, the mechanisms that guide the epigenome through this transition and their evolutionary conservation remain elusive. Here we report widespread DNA demethylation of enhancers during the phylotypic period in zebrafish, Xenopus tropicalis and mouse. These enhancers are linked to developmental genes that display coordinated transcriptional and epigenomic changes in the diverse vertebrates during embryogenesis. Binding of Tet proteins to (hydroxy)methylated DNA and enrichment of 5-hydroxymethylcytosine in these regions implicated active DNA demethylation in this process. Furthermore, loss of function of Tet1, Tet2 and Tet3 in zebrafish reduced chromatin accessibility and increased methylation levels specifically at these enhancers, indicative of DNA methylation being an upstream regulator of phylotypic enhancer function. Overall, our study highlights a regulatory module associated with the most conserved phase of vertebrate embryogenesis and suggests an ancient developmental role for Tet dioxygenases.

Indexed as

DNA MethylationEnhancer Elements, GeneticAnimalsBody PatterningEpigenesis, GeneticGene Expression Regulation, DevelopmentalMiceXenopusZebrafishZebrafish ProteinsZebrafish Proteins

Identifiers

PMID26928226
PMCPMC5912259
OpenAlexW2290125147

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.