Evidence map›Paper›PMID 17640913›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

Epigenetic characterization of hematopoietic stem cell differentiation using miniChIP and bisulfite sequencing analysis.

Joanne L Attema, Peter Papathanasiou, E Camilla Forsberg, Jian Xu, Stephen T Smale, Irving L Weissman

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed, 1 pooled it
7.9field-weighted citation impact, top 2% 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

72 citing papers in PubMed, 1 synthesis or guideline pooled it, 137 citations in OpenAlex.

  1. Pooled it
  2. Review
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  5. Article
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  7. Article
  8. The eroding chromatin landscape of aging stem cells.Translational medicine of aging · 2020
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  15. The Regulatory Capacity of Bivalent Genes-A Theoretical Approach.International journal of molecular sciences · 2017
    Article
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  18. Review
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  20. Article

12 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

6 authors at 2 institutions in 2 countries.

Joanne L AttemaInstitute of Stem Cell Biology and Regenerative Medicine, Departments of Pathology and Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA. joattema@stanford.edu
Peter Papathanasiou
E Camilla Forsberg
Jian Xu
Stephen T Smale
Irving L Weissman
Stanford University · USHoward Hughes Medical Institute · US

Funding

STEM CELL DETRMINATION GENES IN HSC AND HEMATOLYMPHOID CELLS IN MICEP01DK053074 · NIDDK · STANFORD UNIVERSITY · PI CLARKE, MICHAEL F · 1997 to 2007
$8.3M
REGULATION OF TDT EXPRESSION DURING LYMPHOPOIESISR01DK043726 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SMALE, STEPHEN T · 1996 to 2014
$4.2M
Hematopoietic stem cell interactions with the nicheF32DK072620 · NIDDK · STANFORD UNIVERSITY · PI FORSBERG, CAMILLA · 2006 to 2007
$66k
NIDDK NIH HHS 1F32DK72620-01A1NIDDK NIH HHS 5P01DK053074NIDDK NIH HHS F32 DK072620NIDDK NIH HHS P01 DK053074NIDDK NIH HHS R01 DK043726NIDDK NIH HHS R01DK43726
6 · The paper itself

Abstract

Hematopoietic stem cells (HSC) produce all blood cell lineages by virtue of their capacity to self-renew and differentiate into progenitors with decreasing cellular potential. Recent studies suggest that epigenetic mechanisms play an important role in controlling stem cell potency and cell fate decisions. To investigate this hypothesis in HSC, we have modified the conventional chromatin immunoprecipitation assay allowing for the analysis of 50,000 prospectively purified stem and progenitor cells. Together with bisulfite sequencing analysis, we found that methylated H3K4 and AcH3 and unmethylated CpG dinucleotides colocalize across defined regulatory regions of lineage-affiliated genes in HSC. These active epigenetic histone modifications either accumulated or were replaced by increased DNA methylation and H3K27 trimethylation in committed progenitors consistent with gene expression. We also observed bivalent histone modifications at a lymphoid-affiliated gene in HSC and downstream transit-amplifying progenitors. Together, these data support a model in which epigenetic modifications serve as an important mechanism to control HSC multipotency.

Indexed as

Base SequenceCell DifferentiationCell LineageChromatin ImmunoprecipitationDNA MethylationEpigenesis, GeneticHematopoietic Stem CellsHistonesSequence Analysis, DNASulfitesHistonesSulfites

Identifiers

PMID17640913
PMCPMC1924790
OpenAlexW1983409497

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.