Evidence map›Paper›PMID 37580596›Full record

ArticleNature genetics2023

In vivo screening characterizes chromatin factor functions during normal and malignant hematopoiesis.

David Lara-Astiaso, Ainhoa Goñi-Salaverri, Julen Mendieta-Esteban, Nisha Narayan, Cynthia Del Valle, Torsten Gross, George Giotopoulos, Tumas Beinortas, Mar Navarro-Alonso, Laura Pilar Aguado-Alvaro and 12 more

Open access · hybridAbstract read
In one paragraph

Article in Nature genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
8.3field-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

38 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Article
  3. Genetic influences on haematopoiesis.Nature reviews. Genetics · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Why in vivo models of disease remain indispensable.Disease models & mechanisms · 2026
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
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  16. Article
  17. Article
  18. Review
  19. Article
  20. Hematopoietic Stem Cell Hierarchies as Novel Biomarkers of Drug Response in Myelodysplastic Syndromes and Acute Myeloid Leukemia.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Review
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

22 authors at 3 institutions in 3 countries.

David Lara-Astiaso *Department of Haematology, University of Cambridge, Cambridge, UK. dl627@cam.ac.uk.
Ainhoa Goñi-Salaverri *Centre for Applied Medical Research, University of Navarra, Pamplona, Spain.
Julen Mendieta-Esteban *Centre for Applied Medical Research, University of Navarra, Pamplona, Spain.ORCID http://orcid.org/0000-0002-5834-7643
Nisha NarayanDepartment of Haematology, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-4106-2166
Cynthia Del ValleCentre for Applied Medical Research, University of Navarra, Pamplona, Spain.
Torsten GrossRelation Therapeutics, London, UK.
George GiotopoulosDepartment of Haematology, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0003-1390-6592
Tumas BeinortasDepartment of Haematology, University of Cambridge, Cambridge, UK.
Mar Navarro-AlonsoCentre for Applied Medical Research, University of Navarra, Pamplona, Spain.
Laura Pilar Aguado-AlvaroCentre for Applied Medical Research, University of Navarra, Pamplona, Spain.
Jon ZazpeCentre for Applied Medical Research, University of Navarra, Pamplona, Spain.
Francesco MarcheseCentre for Applied Medical Research, University of Navarra, Pamplona, Spain.
Natalia TorreaCentre for Applied Medical Research, University of Navarra, Pamplona, Spain.
Isabel A CalvoCentre for Applied Medical Research, University of Navarra, Pamplona, Spain.ORCID http://orcid.org/0000-0001-6619-4571
Cecile K LopezDepartment of Haematology, University of Cambridge, Cambridge, UK.
Diego AlignaniCentre for Applied Medical Research, University of Navarra, Pamplona, Spain.
Aitziber LopezCentre for Applied Medical Research, University of Navarra, Pamplona, Spain.
Borja SaezCentre for Applied Medical Research, University of Navarra, Pamplona, Spain.
Jake P Taylor-KingRelation Therapeutics, London, UK.ORCID http://orcid.org/0000-0002-1025-0041
Felipe ProsperCentre for Applied Medical Research, University of Navarra, Pamplona, Spain.ORCID http://orcid.org/0000-0001-6115-8790
Nikolaus FortelnyDepartment of Biosciences & Medical Biology, University of Salzburg, Salzburg, Austria. nikolaus.fortelny@plus.ac.at.ORCID http://orcid.org/0000-0003-4025-9968
Brian J P HuntlyDepartment of Haematology, University of Cambridge, Cambridge, UK. bjph2@cam.ac.uk.ORCID http://orcid.org/0000-0003-0312-161X
Universidad de Navarra · ESWellcome/MRC Cambridge Stem Cell Institute · GBUniversity of Salzburg · AT

Funding

Cancer Research UK 25508Cancer Research UK DRCRPG-NOV22/100014Medical Research Council MC_PC_17230Medical Research Council MR/X008371/1Wellcome Trust
6 · The paper itself

Abstract

Cellular differentiation requires extensive alterations in chromatin structure and function, which is elicited by the coordinated action of chromatin and transcription factors. By contrast with transcription factors, the roles of chromatin factors in differentiation have not been systematically characterized. Here, we combine bulk ex vivo and single-cell in vivo CRISPR screens to characterize the role of chromatin factor families in hematopoiesis. We uncover marked lineage specificities for 142 chromatin factors, revealing functional diversity among related chromatin factors (i.e. barrier-to-autointegration factor subcomplexes) as well as shared roles for unrelated repressive complexes that restrain excessive myeloid differentiation. Using epigenetic profiling, we identify functional interactions between lineage-determining transcription factors and several chromatin factors that explain their lineage dependencies. Studying chromatin factor functions in leukemia, we show that leukemia cells engage homeostatic chromatin factor functions to block differentiation, generating specific chromatin factor-transcription factor interactions that might be therapeutically targeted. Together, our work elucidates the lineage-determining properties of chromatin factors across normal and malignant hematopoiesis.

Indexed as

ChromatinLeukemiaCell DifferentiationCell LineageHematopoiesisHumansTranscription FactorsChromatinTranscription Factors

Identifiers

PMID37580596
PMCPMC10484791
OpenAlexW4385812770

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.