Evidence map›Paper›PMID 25197097›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Transcription factor EKLF (KLF1) recruitment of the histone chaperone HIRA is essential for β-globin gene expression.

Shefali Soni, Nikolay Pchelintsev, Peter D Adams, James J Bieker

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

27 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. New Gene Therapy Strategy for β-Thalassemia.Stem cell reviews and reports · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Histone Chaperones as Cardinal Players in Development.Frontiers in cell and developmental biology · 2022
    Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. AMolecular and cellular biology · 2020
    Article
  18. Article
  19. Article
  20. Article
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

4 authors at 3 institutions in 3 countries.

Shefali SoniDepartment of Developmental and Regenerative Biology, Mount Sinai School of Medicine, New York, NY 10029;
Nikolay PchelintsevInstitute of Cancer Sciences, University of Glasgow, Glasgow G61 1BD, Scotland;
Peter D AdamsInstitute of Cancer Sciences, University of Glasgow, Glasgow G61 1BD, Scotland; Beatson Institute for Cancer Research, Glasgow G61 1BD, Scotland; and.
James J BiekerDepartment of Developmental and Regenerative Biology, Mount Sinai School of Medicine, New York, NY 10029; Black Family Stem Cell Institute, Tisch Cancer Institute, Mount Sinai School of Medicine, New York, NY 10029 james.bieker@mssm.edu.
Icahn School of Medicine at Mount Sinai · USCancer Research UK Scotland Institute · GBUniversity of Glasgow · GB

Funding

Function of Putative Determinant in HematopoiesisR01DK046865 · NIDDK · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI JAMES J BIEKER · 1993 to 2026
$11.2M
Medical Research Council G1100054NIDDK NIH HHS R01 DK046865NIDDK NIH HHS R01 DK46865
6 · The paper itself

Abstract

The binding of chromatin-associated proteins and incorporation of histone variants correlates with alterations in gene expression. These changes have been particularly well analyzed at the mammalian β-globin locus, where transcription factors such as erythroid Krüppel-like factor (EKLF), which is also known as Krüppel-like factor 1 (KLF1), play a coordinating role in establishing the proper chromatin structure and inducing high-level expression of adult β-globin. We had previously shown that EKLF preferentially interacts with histone H3 and that the H3.3 variant is differentially recruited to the β-globin promoter. We now find that a novel interaction between EKLF and the histone cell cycle regulation defective homolog A (HIRA) histone chaperone accounts for these effects. HIRA is not only critical for β-globin expression but is also required for activation of the erythropoietic regulators EKLF and GATA binding protein 1 (GATA1). Our results provide a mechanism by which transcription factor-directed recruitment of a generally expressed histone chaperone can lead to tissue-restricted changes in chromatin components, structure, and transcription at specific genomic sites during differentiation.

Indexed as

Gene Expression RegulationAnimalsbeta-GlobinsCell Cycle ProteinsCell DifferentiationEmbryonic Stem CellsErythroid CellsErythropoiesisHistone ChaperonesKruppel-Like Transcription FactorsMicePromoter Regions, GeneticProtein BindingProtein Structure, TertiarySequence DeletionTranscriptional Activationbeta-GlobinsCell Cycle Proteinserythroid Kruppel-like factorHira protein, mouseHistone ChaperonesKruppel-Like Transcription FactorsTranscription Factors

Identifiers

PMID25197097
PMCPMC4169976
OpenAlexW2079794644

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.