Evidence map›Paper›PMID 35243225›Full record

ArticleiScience2022

Interferons reshape the 3D conformation and accessibility of macrophage chromatin.

Ekaterini Platanitis, Stephan Gruener, Aarathy Ravi Sundar Jose Geetha, Laura Boccuni, Alexander Vogt, Maria Novatchkova, Andreas Sommer, Iros Barozzi, Mathias Müller, Thomas Decker

Open access · goldAbstract read
In one paragraph

Article in iScience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

30 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Regulation of immune signal integration and memory by inflammation-induced chromosome conformation.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Review
  4. Review
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  7. Review
  8. Article
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  13. Transcriptional control of interferon-stimulated genes.The Journal of biological chemistry · 2024
    Review
  14. Review
  15. Article
  16. Article
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  18. Review
  19. Article
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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

10 authors at 6 institutions in 1 country.

Ekaterini PlatanitisMax Perutz Labs, University of Vienna, Vienna, Austria.
Stephan GruenerMax Perutz Labs, University of Vienna, Vienna, Austria.
Aarathy Ravi Sundar Jose GeethaMax Perutz Labs, University of Vienna, Vienna, Austria.
Laura BoccuniMax Perutz Labs, University of Vienna, Vienna, Austria.
Alexander VogtVienna Biocenter Core Facilities GmbH (VBCF), Vienna, Austria.
Maria NovatchkovaInstitute of Molecular Biotechnology of the Austrian Academy of Sciences (IMBA), Vienna, Austria.
Andreas SommerVienna Biocenter Core Facilities GmbH (VBCF), Vienna, Austria.
Iros BarozziInstitute of Cancer Research, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Mathias MüllerInstitute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, Austria.
Thomas DeckerMax Perutz Labs, University of Vienna, Vienna, Austria.
University of Vienna · ATVienna BioCenter Core Facilities · ATInstitute of Molecular Biotechnology · ATMax Perutz Labs · ATMedical University of Vienna · ATUniversity of Veterinary Medicine Vienna · AT

Funding

Austrian Science Fund FWF P 25186Austrian Science Fund FWF P 30992Austrian Science Fund FWF W 1261
6 · The paper itself

Abstract

Engagement of macrophages in innate immune responses is directed by type I and type II interferons (IFN-I and IFN-γ, respectively). IFN triggers drastic changes in cellular transcriptomes, executed by JAK-STAT signal transduction and the transcriptional control of interferon-stimulated genes (ISG) by STAT transcription factors. Here, we study the immediate-early nuclear response to IFN-I and IFN-γ in murine macrophages. We show that the mechanism of gene control by both cytokines includes a rapid increase of DNA accessibility and rearrangement of the 3D chromatin contacts particularly between open chromatin of ISG loci. IFN-stimulated gene factor 3 (ISGF3), the major transcriptional regulator of ISG, controlled homeostatic and, most notably, induced-state DNA accessibility at a subset of ISG. Increases in DNA accessibility correlated with the appearance of activating histone marks at surrounding nucleosomes. Collectively our data emphasize changes in the three-dimensional nuclear space and epigenome as an important facet of transcriptional control by the IFN-induced JAK-STAT pathway.

Indexed as

Cell biologyEpigeneticsMolecular biologyMolecular mechanism of gene regulation

Identifiers

PMID35243225
PMCPMC8857492
OpenAlexW4220802683

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.