Evidence map›Paper›PMID 26883014›Full record

ArticleGenome biology2016

Variation in 5-hydroxymethylcytosine across human cortex and cerebellum.

Katie Lunnon, Eilis Hannon, Rebecca G Smith, Emma Dempster, Chloe Wong, Joe Burrage, Claire Troakes, Safa Al-Sarraj, Agnieszka Kepa, Leonard Schalkwyk and 1 more

Erratum issuedAbstract read
In one paragraph

Article in Genome biology, 2016. 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 57 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

57 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Genome-wide methylomic regulation of multiscale gene networks in Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2023
    Article
  6. Epigenetics in psychiatry: Beyond DNA methylation.World journal of psychiatry · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Epigenetic age prediction.Aging cell · 2021 · on this map
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Katie LunnonUniversity of Exeter Medical School, RILD, University of Exeter, Barrack Road, Devon, UK. k.lunnon@exeter.ac.uk.
Eilis HannonUniversity of Exeter Medical School, RILD, University of Exeter, Barrack Road, Devon, UK.
Rebecca G SmithUniversity of Exeter Medical School, RILD, University of Exeter, Barrack Road, Devon, UK.
Emma DempsterUniversity of Exeter Medical School, RILD, University of Exeter, Barrack Road, Devon, UK.
Chloe WongInstitute of Psychiatry, Psychology and Neuroscience, King's College London, De Crespigny Park, London, UK.
Joe BurrageUniversity of Exeter Medical School, RILD, University of Exeter, Barrack Road, Devon, UK.
Claire TroakesInstitute of Psychiatry, Psychology and Neuroscience, King's College London, De Crespigny Park, London, UK.
Safa Al-SarrajInstitute of Psychiatry, Psychology and Neuroscience, King's College London, De Crespigny Park, London, UK.
Agnieszka KepaInstitute of Psychiatry, Psychology and Neuroscience, King's College London, De Crespigny Park, London, UK.
Leonard SchalkwykUniversity of Essex, Wivenhoe Park, Colchester, CO4 3SQ, UK.
Jonathan MillUniversity of Exeter Medical School, RILD, University of Exeter, Barrack Road, Devon, UK.

Funding

A multi-faceted approach to epigenomic profiling in Alzheimer's disorderR01AG036039 · NIA · KING'S COLLEGE LONDON · PI MILL, JONATHAN · 2009 to 2012
$1.7M
Medical Research Council G1100695Medical Research Council G9318379Medical Research Council MR/K013807/1Medical Research Council MR/L016397/1NIA NIH HHS AG036039NIA NIH HHS R01 AG036039
6 · The paper itself

Abstract

backgroundThe most widely utilized approaches for quantifying DNA methylation involve the treatment of genomic DNA with sodium bisulfite; however, this method cannot distinguish between 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC). Previous studies have shown that 5hmC is enriched in the brain, although little is known about its genomic distribution and how it differs between anatomical regions and individuals. In this study, we combine oxidative bisulfite (oxBS) treatment with the Illumina Infinium 450K BeadArray to quantify genome-wide patterns of 5hmC in two distinct anatomical regions of the brain from multiple individuals.

resultsWe identify 37,145 and 65,563 sites passing our threshold for detectable 5hmC in the prefrontal cortex and cerebellum respectively, with 23,445 loci common across both brain regions. Distinct patterns of 5hmC are identified in each brain region, with notable differences in the genomic location of the most hydroxymethylated loci between these brain regions. Tissue-specific patterns of 5hmC are subsequently confirmed in an independent set of prefrontal cortex and cerebellum samples.

conclusionsThis study represents the first systematic analysis of 5hmC in the human brain, identifying tissue-specific hydroxymethylated positions and genomic regions characterized by inter-individual variation in DNA hydroxymethylation. This study demonstrates the utility of combining oxBS-treatment with the Illumina 450k methylation array to systematically quantify 5hmC across the genome and the potential utility of this approach for epigenomic studies of brain disorders.

Indexed as

Genome, Human5-MethylcytosineCerebellar CortexCerebellumCytosineDNADNA MethylationEpigenesis, GeneticHumansSequence Analysis, DNASulfites5-hydroxymethylcytosine5-MethylcytosineCytosineDNAsodium bisulfiteSulfites

Identifiers

PMID26883014
PMCPMC4756397

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.