Evidence map›Paper›PMID 21900194›Full record

ArticleBlood2011

Genome-wide ChIP-Seq reveals a dramatic shift in the binding of the transcription factor erythroid Kruppel-like factor during erythrocyte differentiation.

Andre M Pilon, Subramanian S Ajay, Swathi Ashok Kumar, Laurie A Steiner, Praveen F Cherukuri, Stephen Wincovitch, Stacie M Anderson, NISC Comparative Sequencing Center, James C Mullikin, Patrick G Gallagher and 3 more

Open access · bronzeAbstract readValidation Study
In one paragraph

Article in Blood, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
6.4field-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

80 citing papers in PubMed, 107 citations in OpenAlex.

  1. Trial
  2. Article
  3. Evidence for vitellogenin DNA-binding in honey bees.Protein science : a publication of the Protein Society · 2025
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  8. Review
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  10. Article
  11. Article
  12. Article
  13. What do Transcription Factors Interact With?Journal of molecular biology · 2021
    Review
  14. Review
  15. Negative Regulation of the Differentiation of Flk2International journal of molecular sciences · 2020
    Article
  16. Article
  17. Article
  18. Functional genomic approaches to elucidate the role of enhancers during development.Wiley interdisciplinary reviews. Systems biology and medicine · 2020
    Review
  19. AMolecular and cellular biology · 2020
    Article
  20. Article

20 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

13 authors at 3 institutions in 1 country.

Andre M PilonNational Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
Subramanian S Ajay
Swathi Ashok Kumar
Laurie A Steiner
Praveen F Cherukuri
Stephen Wincovitch
Stacie M Anderson
NISC Comparative Sequencing Center
James C Mullikin
Patrick G Gallagher
Ross C Hardison
Elliott H Margulies
David M Bodine
National Human Genome Research Institute · USPediatrics and Genetics · USPennsylvania State University · US

Funding

Inter- and Intra-Species Comparative SequencingZIBHG000196 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI THOMAS, JAMES · 2009 to 2025
$177.6M
NHGRI/DIR Cytogenetics and Microscopy CoreZICHG200348 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI WINCOVITCH, STEPHEN · 2010 to 2025
$20.3M
Comparative Genomics Unit ResearchZIAHG200330 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI MULLIKIN, JAMES C · 2009 to 2022
$17.9M
NHGRI/DIR Flow Cytometry CoreZICHG200350 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI ANDERSON, STACIE · 2010 to 2025
$16.3M
Red Cell BiologyZIAHG200339 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI BODINE, DAVID M. · 2009 to 2022
$11.8M
Global Predictions and Tests of Erythroid RegulationR01DK065806 · NIDDK · PENNSYLVANIA STATE UNIVERSITY-UNIV PARK · PI BLOBEL, GERD A, CHIAROMONTE, FRANCESCA · 2004 to 2013
$5.3M
MOLECULAR BIOLOGY OF HUMAN ERYTHROCYTE ALPHA-SPECTRINR01HL065448 · NHLBI · YALE UNIVERSITY · PI GALLAGHER, PATRICK G · 2000 to 2013
$4.4M
Molecular Biology of Erythrocyte AnkyrinR01DK062039 · NIDDK · YALE UNIVERSITY · PI GALLAGHER, PATRICK G · 2002 to 2010
$3.3M
Identifying and Characterizing Functional Elements in the Human GenomeZIAHG200341 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI MARGULIES, ELLIOTT · 2009 to 2011
$2.8M
Enhance human ENCODE by function comparisons to mouseRC2HG005573 · NHGRI · PENNSYLVANIA STATE UNIVERSITY, THE · PI HARDISON, ROSS C · 2009 to 2011
$2.2M
Identification of a Molecular Signature for Barrier InsulatorsK08DK090153 · NIDDK · YALE UNIVERSITY · PI STEINER, LAURIE A. · 2011 to 2013
$450k
Intramural NIH HHSNHGRI NIH HHS RC2 HG005573NHGRI NIH HHS RC2HG005573NHLBI NIH HHS R01 HL065448NHLBI NIH HHS R01HL65448NIDDK NIH HHS K08 DK090153NIDDK NIH HHS R01 DK062039NIDDK NIH HHS R01 DK065806NIDDK NIH HHS R01DK065806NIDDK NIH HHS R01DK62039
6 · The paper itself

Abstract

Erythropoiesis is dependent on the activity of transcription factors, including the erythroid-specific erythroid Kruppel-like factor (EKLF). ChIP followed by massively parallel sequencing (ChIP-Seq) is a powerful, unbiased method to map trans-factor occupancy. We used ChIP-Seq to study the interactome of EKLF in mouse erythroid progenitor cells and more differentiated erythroblasts. We correlated these results with the nuclear distribution of EKLF, RNA-Seq analysis of the transcriptome, and the occupancy of other erythroid transcription factors. In progenitor cells, EKLF is found predominantly at the periphery of the nucleus, where EKLF primarily occupies the promoter regions of genes and acts as a transcriptional activator. In erythroblasts, EKLF is distributed throughout the nucleus, and erythroblast-specific EKLF occupancy is predominantly in intragenic regions. In progenitor cells, EKLF modulates general cell growth and cell cycle regulatory pathways, whereas in erythroblasts EKLF is associated with repression of these pathways. The EKLF interactome shows very little overlap with the interactomes of GATA1, GATA2, or TAL1, leading to a model in which EKLF directs programs that are independent of those regulated by the GATA factors or TAL1.

Indexed as

Chromatin ImmunoprecipitationAnimalsBinding SitesCells, CulturedChromosome MappingEmbryo, MammalianErythrocytesErythroid Precursor CellsErythropoiesisKruppel-Like Transcription FactorsMiceMice, TransgenicProtein BindingSequence Analysis, DNATranscription Factorserythroid Kruppel-like factorKruppel-Like Transcription FactorsTranscription Factors

Identifiers

PMID21900194
PMCPMC3208289
OpenAlexW2074781142

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.