Evidence map›Paper›PMID 32442533›Full record

ArticleStem cell reports2020

TET1 and 5-Hydroxymethylation Preserve the Stem Cell State of Mouse Trophoblast.

Claire E Senner, Stephanie Chrysanthou, Sarah Burge, Hai-Yan Lin, Miguel R Branco, Myriam Hemberger

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  11. Cells · 2022
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  13. Review
  14. Integrating High-Throughput Approaches andFrontiers in cell and developmental biology · 2021
    Review
  15. Article
  16. 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 4 institutions in 4 countries.

Claire E SennerEpigenetics Programme, Babraham Institute, Cambridge CB22 3AT, UK; Centre for Trophoblast Research, Department of Physiology, Development and Neuroscience, University of Cambridge, Tennis Court Road, Cambridge CB2 3EG, UK. Electronic address: ces207@cam.ac.uk.
Stephanie ChrysanthouEpigenetics Programme, Babraham Institute, Cambridge CB22 3AT, UK; Department of Genetics, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA.
Sarah BurgeEpigenetics Programme, Babraham Institute, Cambridge CB22 3AT, UK.
Hai-Yan LinKey Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.
Miguel R BrancoBlizard Institute, Barts and the London School of Medicine and Dentistry, QMUL, London E1 2AT, UK.
Myriam HembergerEpigenetics Programme, Babraham Institute, Cambridge CB22 3AT, UK; Centre for Trophoblast Research, Department of Physiology, Development and Neuroscience, University of Cambridge, Tennis Court Road, Cambridge CB2 3EG, UK; Departments of Biochemistry & Molecular Biology and Medical Genetics, Cumming School of Medicine, University of Calgary, 3330 Hospital Drive N.W., Calgary, Alberta T2N 4N1, Canada; Alberta Children's Hospital Research Institute, University of Calgary, 3330 Hospital Drive N.W., Calgary, Alberta, T2N 4N1, Canada. Electronic address: myriam.hemberger@ucalgary.ca.
Babraham Institute · GBAlbert Einstein College of Medicine · USChinese Academy of Sciences · CNQueen Mary University of London · GB

Funding

Biotechnology and Biological Sciences Research CouncilMedical Research Council
6 · The paper itself

Abstract

The ten-eleven translocation factor TET1 and its conferred epigenetic modification 5-hydroxymethylcytosine (5hmC) have important roles in maintaining the pluripotent state of embryonic stem cells (ESCs). We previously showed that TET1 is also essential to maintain the stem cell state of trophoblast stem cells (TSCs). Here, we establish an integrated panel of absolute 5hmC levels, genome-wide DNA methylation and hydroxymethylation patterns, transcriptomes, and TET1 chromatin occupancy in TSCs and differentiated trophoblast cells. We show that the combined presence of 5-methylcytosine (5mC) and 5hmC correlates with transcriptional activity of associated genes. Hypoxia can slow down the global loss of 5hmC that occurs upon differentiation of TSCs. Notably, unlike in ESCs and epiblast cells, most TET1-bound regions overlap with active chromatin marks and TFAP2C binding sites and demarcate putative trophoblast enhancer regions. These chromatin modification and occupancy patterns are highly informative to identify novel candidate regulators of the TSC state.

Indexed as

DNA MethylationAnimalsCell HypoxiaDNA-Binding ProteinsEnhancer Elements, GeneticMiceProto-Oncogene ProteinsStem CellsTranscription Factor AP-2TrophoblastsDNA-Binding ProteinsProto-Oncogene ProteinsTET1 protein, mouseTfap2c protein, mouseTranscription Factor AP-2chromatin interactionsDNA hydroxymethylationDNA methylationembryonic stem cellsenhancersepigeneticsgene regulationTET1trophoblast stem cells

Identifiers

PMID32442533
PMCPMC7724466
OpenAlexW3028277731

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.