Evidence map›Paper›PMID 21552279›Full record

ArticleNature2011

Genome-wide mapping of 5-hydroxymethylcytosine in embryonic stem cells.

William A Pastor, Utz J Pape, Yun Huang, Hope R Henderson, Ryan Lister, Myunggon Ko, Erin M McLoughlin, Yevgeny Brudno, Sahasransu Mahapatra, Philipp Kapranov and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Nature, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 443 papers.

0numbers the graph read from it
0cells of the map it votes in
443citing papers in PubMed
47.2field-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

443 citing papers in PubMed, 800 citations in OpenAlex.

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  18. Review
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  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 6 institutions in 1 country.

William A PastorHarvard Medical School, Immune Disease Institute and Program in Cellular and Molecular Medicine, Children's Hospital Boston, Boston, Massachusetts 02115, USA.
Utz J Pape
Yun Huang
Hope R Henderson
Ryan Lister
Myunggon Ko
Erin M McLoughlin
Yevgeny Brudno
Sahasransu Mahapatra
Philipp Kapranov
Mamta Tahiliani
George Q Daley
X Shirley Liu
Joseph R Ecker
Patrice M Milos
Suneet Agarwal
Anjana Rao
Dana-Farber Cancer Institute · USHarvard University · USLa Jolla Institute for Immunology · USBoston Children's Hospital · USHelicos Biosciences (United States) · USSalk Institute for Biological Studies · US

Funding

HARVARD CLINICAL AND TRANSLATIONAL SCIENCE CENTER (UL1)UL1RR025758 · NCRR · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2008 to 2011
$91.4M
REGULATED ACCESSIBILITY OF A CYTOKINE GENE LOCUSR01AI044432 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI RAO, ANJANA · 1999 to 2014
$7.7M
Role of TET Proteins in ES Cell Pluripotency and FunctionR01HD065812 · NICHD · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI RAO, ANJANA · 2011 to 2015
$1.8M
Chemical modulators of Tet-family proteinsRC1DA028422 · NIDA · IMMUNE DISEASE INSTITUTE, INC. · PI RAO, ANJANA · 2009 to 2010
$1.0M
Molecular mechanisms of nuclear reprogrammingK08HL089150 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI AGARWAL, SUNEET · 2008 to 2012
$662k
NCRR NIH HHS 1 UL1 RR 025758-02NCRR NIH HHS UL1 RR025758NHLBI NIH HHS K08 HL089150NIAID NIH HHS R01 AI044432NIAID NIH HHS R01 AI44432NICHD NIH HHS 1 R01 HD065812-01A1NICHD NIH HHS R01 HD065812NIDA NIH HHS RC1 DA028422
6 · The paper itself

Abstract

5-hydroxymethylcytosine (5hmC) is a modified base present at low levels in diverse cell types in mammals. 5hmC is generated by the TET family of Fe(II) and 2-oxoglutarate-dependent enzymes through oxidation of 5-methylcytosine (5mC). 5hmC and TET proteins have been implicated in stem cell biology and cancer, but information on the genome-wide distribution of 5hmC is limited. Here we describe two novel and specific approaches to profile the genomic localization of 5hmC. The first approach, termed GLIB (glucosylation, periodate oxidation, biotinylation) uses a combination of enzymatic and chemical steps to isolate DNA fragments containing as few as a single 5hmC. The second approach involves conversion of 5hmC to cytosine 5-methylenesulphonate (CMS) by treatment of genomic DNA with sodium bisulphite, followed by immunoprecipitation of CMS-containing DNA with a specific antiserum to CMS. High-throughput sequencing of 5hmC-containing DNA from mouse embryonic stem (ES) cells showed strong enrichment within exons and near transcriptional start sites. 5hmC was especially enriched at the start sites of genes whose promoters bear dual histone 3 lysine 27 trimethylation (H3K27me3) and histone 3 lysine 4 trimethylation (H3K4me3) marks. Our results indicate that 5hmC has a probable role in transcriptional regulation, and suggest a model in which 5hmC contributes to the 'poised' chromatin signature found at developmentally-regulated genes in ES cells.

Indexed as

5-MethylcytosineAnimalsBiotinylationCell LineCytosineDNA MethylationEmbryonic Stem CellsExonsGene Expression Regulation, DevelopmentalGenomeGlucoseMicePeriodic AcidPromoter Regions, GeneticSequence Analysis, DNATranscription, Genetic5-hydroxymethylcytosine5-MethylcytosineCytosineGlucosemetaperiodatePeriodic Acid

Identifiers

PMID21552279
PMCPMC3124347
OpenAlexW1981543052

What OpenQuestion holds

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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.