Evidence map›Paper›PMID 29317535›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Structural basis of STAT2 recognition by IRF9 reveals molecular insights into ISGF3 function.

Srinivasan Rengachari, Silvia Groiss, Juliette M Devos, Elise Caron, Nathalie Grandvaux, Daniel Panne

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
3.5field-weighted citation impact, top 5% 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

60 citing papers in PubMed, 86 citations in OpenAlex.

  1. Article
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  9. Functions of Tomato (International journal of molecular sciences · 2025
    Article
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  15. Transcriptional control of interferon-stimulated genes.The Journal of biological chemistry · 2024
    Review
  16. Article
  17. Article
  18. The JAK-STAT pathway: from structural biology to cytokine engineering.Signal transduction and targeted therapy · 2024
    Review
  19. Review
  20. 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

6 authors at 2 institutions in 2 countries.

Srinivasan RengachariEuropean Molecular Biology Laboratory, 38042 Grenoble, France.
Silvia GroissEuropean Molecular Biology Laboratory, 38042 Grenoble, France.
Juliette M DevosEuropean Molecular Biology Laboratory, 38042 Grenoble, France.
Elise CaronCRCHUM-Research Center, Centre Hospitalier de l'Université de Montréal, Montréal, H2X0A9, QC, Canada.
Nathalie GrandvauxCRCHUM-Research Center, Centre Hospitalier de l'Université de Montréal, Montréal, H2X0A9, QC, Canada.
Daniel PanneEuropean Molecular Biology Laboratory, 38042 Grenoble, France; panne@embl.fr.ORCID 0000-0001-9158-5507
European Molecular Biology Laboratory · FRCentre Hospitalier de l’Université de Montréal · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytokine signaling through the JAK/STAT pathway controls multiple cellular responses including growth, survival, differentiation, and pathogen resistance. An expansion in the gene regulatory repertoire controlled by JAK/STAT signaling occurs through the interaction of STATs with IRF transcription factors to form ISGF3, a complex that contains STAT1, STAT2, and IRF9 and regulates expression of IFN-stimulated genes. ISGF3 function depends on selective interaction between IRF9, through its IRF-association domain (IAD), with the coiled-coil domain (CCD) of STAT2. Here, we report the crystal structures of the IRF9-IAD alone and in a complex with STAT2-CCD. Despite similarity in the overall structure among respective paralogs, the surface features of the IRF9-IAD and STAT2-CCD have diverged to enable specific interaction between these family members. We derive a model for the ISGF3 complex bound to an ISRE DNA element and demonstrate that the observed interface between STAT2 and IRF9 is required for ISGF3 function in cells.

Indexed as

AnimalsGene Expression RegulationHEK293 CellsHumansInterferon-Stimulated Gene Factor 3, gamma SubunitJanus KinasesMicePoint MutationProtein DomainsSignal TransductionSTAT2 Transcription FactorInterferon-Stimulated Gene Factor 3, gamma SubunitIRF9 protein, humanIsgf3g protein, mouseJanus KinasesSTAT2 Transcription Factorcrystal structureinnate immunityIRF transcription factorJAK/STAT signalingSTAT2

Identifiers

PMID29317535
PMCPMC5789952
OpenAlexW2611222371

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.