Evidence map›Paper›PMID 38658796›Full record

ArticleThe EMBO journal2024

Dynamic control of gene expression by ISGF3 and IRF1 during IFNβ and IFNγ signaling.

Aarathy Ravi Sundar Jose Geetha, Katrin Fischer, Olga Babadei, Georg Smesnik, Alex Vogt, Ekaterini Platanitis, Mathias Müller, Matthias Farlik, Thomas Decker

Open access · diamondAbstract read
In one paragraph

Article in The EMBO journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.3field-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

13 citing papers in PubMed, 14 citations in OpenAlex.

  1. Trial
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  7. Review
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  11. Article
  12. lncRNALife science alliance · 2025
    Article
  13. Transcriptional control of interferon-stimulated genes.The Journal of biological chemistry · 2024
    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

9 authors at 4 institutions in 2 countries.

Aarathy Ravi Sundar Jose Geetha *Max Perutz Labs, Vienna Biocenter Campus (VBC), Vienna, 1030, Austria.
Katrin Fischer *Max Perutz Labs, Vienna Biocenter Campus (VBC), Vienna, 1030, Austria.ORCID http://orcid.org/0000-0002-0445-7986
Olga BabadeiMax Perutz Labs, Vienna Biocenter Campus (VBC), Vienna, 1030, Austria.ORCID http://orcid.org/0009-0005-9992-0572
Georg SmesnikMax Perutz Labs, Vienna Biocenter Campus (VBC), Vienna, 1030, Austria.
Alex VogtEvotec, Hamburg, Germany.
Ekaterini PlatanitisMax Perutz Labs, Vienna Biocenter Campus (VBC), Vienna, 1030, Austria.
Mathias MüllerInstitute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, 1210, Austria.ORCID http://orcid.org/0000-0002-7879-3552
Matthias FarlikDepartment of Dermatology, Medical University of Vienna, Vienna, 1090, Austria.ORCID http://orcid.org/0000-0003-0698-2992
Thomas DeckerMax Perutz Labs, Vienna Biocenter Campus (VBC), Vienna, 1030, Austria. thomas.decker@univie.ac.at.ORCID http://orcid.org/0000-0001-9683-0620
University of Vienna · ATEvotec (Germany) · DEMedical University of Vienna · ATUniversity of Veterinary Medicine Vienna · AT

Funding

Austrian Science Fund (FWF) SFB 6106Austrian Science Fund (FWF) SFB 6107Austrian Science Fund (FWF) SFB F6101Austrian Science Fund (FWF) W1261Austrian Science Fund FWF W 1261
6 · The paper itself

Abstract

Type I interferons (IFN-I, including IFNβ) and IFNγ produce overlapping, yet clearly distinct immunological activities. Recent data show that the distinctness of global transcriptional responses to the two IFN types is not apparent when comparing their immediate effects. By analyzing nascent transcripts induced by IFN-I or IFNγ over a period of 48 h, we now show that the distinctiveness of the transcriptomes emerges over time and is based on differential employment of the ISGF3 complex as well as of the second-tier transcription factor IRF1. The distinct transcriptional properties of ISGF3 and IRF1 correspond with a largely diverse nuclear protein interactome. Mechanistically, we describe the specific input of ISGF3 and IRF1 into enhancer activation and the regulation of chromatin accessibility at interferon-stimulated genes (ISG). We further report differences between the IFN types in altering RNA polymerase II pausing at ISG 5' ends. Our data provide insight how transcriptional regulators create immunological identities of IFN-I and IFNγ.

Indexed as

Gene Expression RegulationInterferon-betaInterferon-gammaInterferon Regulatory Factor-1Signal TransductionAnimalsHumansInterferon-Stimulated Gene Factor 3MiceRNA Polymerase IIInterferon-betaInterferon-gammaInterferon Regulatory Factor-1Interferon-Stimulated Gene Factor 3IRF1 protein, humanRNA Polymerase IIInterferonsIRFMacrophageSTATTranscription

Identifiers

PMID38658796
PMCPMC11148166
OpenAlexW4395074721

What Socratic 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 Socratic graph.