Evidence map›Paper›PMID 24013550›Full record

ArticleGenome research2013

DNA methylation profiling in human B cells reveals immune regulatory elements and epigenetic plasticity at Alu elements during B-cell activation.

Anne Y Lai, Deepak Mav, Ruchir Shah, Sara A Grimm, Dhiral Phadke, Katerina Hatzi, Ari Melnick, Cissy Geigerman, Steve E Sobol, David L Jaye and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed
–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

78 citing papers in PubMed, 107 citations in OpenAlex.

  1. Article
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  7. Article
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  12. Epigenomic insights into common human disease pathology.Cellular and molecular life sciences : CMLS · 2024
    Review
  13. Article
  14. Review
  15. Review
  16. L-methionine supplementation modulates IgMFrontiers in immunology · 2023
    Article
  17. Impact ofFrontiers in genetics · 2023
    Article
  18. Article
  19. Review
  20. Article

18 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

11 authors at 6 institutions in 1 country.

Anne Y LaiLaboratory of Molecular Carcinogenesis, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA;
Deepak Mav
Ruchir Shah
Sara A Grimm
Dhiral Phadke
Katerina Hatzi
Ari Melnick
Cissy Geigerman
Steve E Sobol
David L Jaye
Paul A Wade
SRA International (United States) · USCornell University · USEmory University Hospital · USNational Institutes of Health · USEmory University · USNational Institute of Environmental Health Sciences · US

Funding

Eukaryotic Transcriptional RegulationZIAES101965 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI WADE, PAUL A · 2009 to 2025
$40.9M
Eukaryotic Transcriptional RegulationZ01ES101965 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI WADE, PAUL A · 2005 to 2008
$3.5M
Transcriptional silencing by the BCL6 oncoproteinR01CA104348 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI MELNICK, ARI M. · 2004 to 2014
$2.6M
GI Inflammation: Novel G-Protein Coupled PMN ResponsesK08DK060647 · NIDDK · EMORY UNIVERSITY · PI JAYE, DAVID L. · 2002 to 2006
$634k
Intramural NIH HHS Z01 ES101965NCI NIH HHS R01 CA104348NIDDK NIH HHS DK60647NIDDK NIH HHS K08 DK060647NIEHS NIH HHS Z01ES101965PHS HHS HHSN291200555547
6 · The paper itself

Abstract

Memory is a hallmark of adaptive immunity, wherein lymphocytes mount a superior response to a previously encountered antigen. It has been speculated that epigenetic alterations in memory lymphocytes contribute to their functional distinction from their naive counterparts. However, the nature and extent of epigenetic alterations in memory compartments remain poorly characterized. Here we profile the DNA methylome and the transcriptome of B-lymphocyte subsets representing stages of the humoral immune response before and after antigen exposure in vivo from multiple humans. A significant percentage of activation-induced losses of DNA methylation mapped to transcription factor binding sites. An additional class of demethylated loci mapped to Alu elements across the genome and accompanied repression of DNA methyltransferase 3A. The activation-dependent DNA methylation changes were largely retained in the progeny of activated B cells, generating a similar epigenetic signature in downstream memory B cells and plasma cells with distinct transcriptional programs. These findings provide insights into the methylation dynamics of the genome during cellular differentiation in an immune response.

Indexed as

Alu ElementsDNA MethylationAdaptive ImmunityBinding SitesB-LymphocytesCell DifferentiationDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3AEpigenesis, GeneticGene Expression ProfilingGene Expression RegulationGenome, HumanHumansImmunologic MemoryLymphocyte ActivationPlasma CellsDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3ADNMT3A protein, humanTranscription Factors

Identifiers

PMID24013550
PMCPMC3847773
OpenAlexW2011730338

What OpenQuestion holds

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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.