Evidence map›Paper›PMID 28827334›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

DNA methylation of intragenic CpG islands depends on their transcriptional activity during differentiation and disease.

Danuta M Jeziorska, Robert J S Murray, Marco De Gobbi, Ricarda Gaentzsch, David Garrick, Helena Ayyub, Taiping Chen, En Li, Jelena Telenius, Magnus Lynch and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

97 citing papers in PubMed, 171 citations in OpenAlex.

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  18. Epigenetic alterations inJournal of research in medical sciences : the official journal of Isfahan University of Medical Sciences · 2025
    Review
  19. Beyond the "Dominant" and "Recessive" Patterns of Inheritance.International journal of molecular sciences · 2024
    Article
  20. Article

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

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

16 authors at 4 institutions in 3 countries.

Danuta M JeziorskaMedical Research Council Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, Oxford University, Oxford OX3 9DS, United Kingdom.
Robert J S MurrayDepartment of Genetics, University of Leicester, Leicester LE1 7RH, United Kingdom.
Marco De GobbiMedical Research Council Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, Oxford University, Oxford OX3 9DS, United Kingdom.
Ricarda GaentzschMedical Research Council Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, Oxford University, Oxford OX3 9DS, United Kingdom.
David GarrickMedical Research Council Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, Oxford University, Oxford OX3 9DS, United Kingdom.
Helena AyyubMedical Research Council Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, Oxford University, Oxford OX3 9DS, United Kingdom.
Taiping ChenDepartment of Epigenetics and Molecular Carcinogenesis, Division of Basic Science Research, The University of Texas M. D. Anderson Cancer Center, Smithville, TX 78957.
En LiChina Novartis Institutes for BioMedical Research, Shanghai 201203, China.
Jelena TeleniusMedical Research Council Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, Oxford University, Oxford OX3 9DS, United Kingdom.
Magnus LynchMedical Research Council Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, Oxford University, Oxford OX3 9DS, United Kingdom.
Bryony GrahamMedical Research Council Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, Oxford University, Oxford OX3 9DS, United Kingdom.
Andrew J H SmithMedical Research Council Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, Oxford University, Oxford OX3 9DS, United Kingdom.
Jonathan N LundDivision of Medical Sciences and Graduate Entry Medicine, School of Medicine, University of Nottingham, Royal Derby Hospital, Derby DE22 3DT, United Kingdom.
Jim R HughesMedical Research Council Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, Oxford University, Oxford OX3 9DS, United Kingdom.
Douglas R HiggsMedical Research Council Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, Oxford University, Oxford OX3 9DS, United Kingdom; cristina.tufarelli@nottingham.ac.uk doug.higgs@imm.ox.ac.uk.
Cristina TufarelliDivision of Medical Sciences and Graduate Entry Medicine, School of Medicine, University of Nottingham, Royal Derby Hospital, Derby DE22 3DT, United Kingdom; cristina.tufarelli@nottingham.ac.uk doug.higgs@imm.ox.ac.uk.ORCID 0000-0002-1053-4618
University of Oxford · GBUniversity of Nottingham · GBNovartis (China) · CNThe University of Texas MD Anderson Cancer Center · US

Funding

Medical Research Council G1000801Medical Research Council MC_U137961144Medical Research Council MC_U137961145Medical Research Council MC_UU_00016/14Medical Research Council MC_UU_00016/4Medical Research Council MC_UU_12009/10Medical Research Council MC_UU_12009/15Medical Research Council MC_UU_12009/4
6 · The paper itself

Abstract

The human genome contains ∼30,000 CpG islands (CGIs). While CGIs associated with promoters nearly always remain unmethylated, many of the ∼9,000 CGIs lying within gene bodies become methylated during development and differentiation. Both promoter and intragenic CGIs may also become abnormally methylated as a result of genome rearrangements and in malignancy. The epigenetic mechanisms by which some CGIs become methylated but others, in the same cell, remain unmethylated in these situations are poorly understood. Analyzing specific loci and using a genome-wide analysis, we show that transcription running across CGIs, associated with specific chromatin modifications, is required for DNA methyltransferase 3B (DNMT3B)-mediated DNA methylation of many naturally occurring intragenic CGIs. Importantly, we also show that a subgroup of intragenic CGIs is not sensitive to this process of transcription-mediated methylation and that this correlates with their individual intrinsic capacity to initiate transcription in vivo. We propose a general model of how transcription could act as a primary determinant of the patterns of CGI methylation in normal development and differentiation, and in human disease.

Indexed as

AnimalsCell DifferentiationCell LineCpG IslandsDNA MethylationEpigenesis, GeneticGenome, HumanHumansMicePromoter Regions, GeneticSequence Analysis, DNATranscription, GeneticCGI methylationCGI transcriptionDNA methylationH3K36me3intragenic CGIs

Identifiers

PMID28827334
PMCPMC5594649
OpenAlexW2748203881

What OpenQuestion holds

Textmetadata
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.