Evidence map›Paper›PMID 21924933›Full record

ArticleMolecular cell2011

Directional DNA methylation changes and complex intermediate states accompany lineage specificity in the adult hematopoietic compartment.

Emily Hodges, Antoine Molaro, Camila O Dos Santos, Pramod Thekkat, Qiang Song, Philip J Uren, Jin Park, Jason Butler, Shahin Rafii, W Richard McCombie and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 172 papers.

0numbers the graph read from it
0cells of the map it votes in
172citing papers in PubMed
13.3field-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

172 citing papers in PubMed, 320 citations in OpenAlex.

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  12. Epigenomic insights into common human disease pathology.Cellular and molecular life sciences : CMLS · 2024
    Review
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112 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

12 authors at 3 institutions in 1 country.

Emily HodgesWatson School of Biological Sciences, Cold Spring Harbor Laboratory, 1 Bungtown Road, Cold Spring Harbor, NY 11724, USA.
Antoine Molaro
Camila O Dos Santos
Pramod Thekkat
Qiang Song
Philip J Uren
Jin Park
Jason Butler
Shahin Rafii
W Richard McCombie
Andrew D Smith
Gregory J Hannon
Howard Hughes Medical Institute · USUniversity of Southern California · USCold Spring Harbor Laboratory · US

Funding

Analytic tools to examine high-resolution and genome-scale DNA methylation dataR01HG005238 · NHGRI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI SMITH, ANDREW DAVID · 2010 to 2013
$1.5M
NHGRI NIH HHS R01 HG005238
6 · The paper itself

Abstract

DNA methylation has been implicated as an epigenetic component of mechanisms that stabilize cell-fate decisions. Here, we have characterized the methylomes of human female hematopoietic stem/progenitor cells (HSPCs) and mature cells from the myeloid and lymphoid lineages. Hypomethylated regions (HMRs) associated with lineage-specific genes were often methylated in the opposing lineage. In HSPCs, these sites tended to show intermediate, complex patterns that resolve to uniformity upon differentiation, by increased or decreased methylation. Promoter HMRs shared across diverse cell types typically display a constitutive core that expands and contracts in a lineage-specific manner to fine-tune the expression of associated genes. Many newly identified intergenic HMRs, both constitutive and lineage specific, were enriched for factor binding sites with an implied role in genome organization and regulation of gene expression, respectively. Overall, our studies represent an important reference data set and provide insights into directional changes in DNA methylation as cells adopt terminal fates.

Indexed as

DNA MethylationAdultBinding SitesCell DifferentiationCell LineageComparative Genomic HybridizationEpigenesis, GeneticFemaleGene Expression RegulationGenome, HumanHematopoietic Stem CellsHematopoietic SystemHumansModels, BiologicalPromoter Regions, Genetic

Identifiers

PMID21924933
PMCPMC3412369
OpenAlexW2004729058

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.