Evidence map›Paper›PMID 35852463›Full record

ArticleEMBO reports2022

Transient upregulation of IRF1 during exit from naive pluripotency confers viral protection.

Merrit Romeike, Stephanie Spach, Marie Huber, Songjie Feng, Gintautas Vainorius, Ulrich Elling, Gjis A Versteeg, Christa Buecker

Open access · hybridAbstract read
In one paragraph

Article in EMBO reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Merrit RomeikeMax Perutz Labs Vienna, Vienna Biocenter (VBC), University of Vienna, Vienna, Austria.ORCID 0000-0002-5890-2213
Stephanie SpachMax Perutz Labs Vienna, Vienna Biocenter (VBC), University of Vienna, Vienna, Austria.
Marie HuberMax Perutz Labs Vienna, Vienna Biocenter (VBC), University of Vienna, Vienna, Austria.
Songjie FengMax Perutz Labs Vienna, Vienna Biocenter (VBC), University of Vienna, Vienna, Austria.ORCID 0000-0003-0629-6896
Gintautas VainoriusVienna Biocenter PhD Program, A Doctoral School of the University of Vienna and Medical University of Vienna, Vienna, Austria.
Ulrich EllingInstitute of Molecular Biotechnology of the Austrian Academy of Science (IMBA), Vienna Biocenter (VBC), Vienna, Austria.
Gjis A VersteegMax Perutz Labs Vienna, Vienna Biocenter (VBC), University of Vienna, Vienna, Austria.
Christa BueckerMax Perutz Labs Vienna, Vienna Biocenter (VBC), University of Vienna, Vienna, Austria.ORCID 0000-0003-3055-2642
University of Vienna · ATInstitute of Molecular Biotechnology · AT

Funding

Austrian Science Fund FWF W 1261
6 · The paper itself

Abstract

Stem cells intrinsically express a subset of genes which are normally associated with interferon stimulation and the innate immune response. However, the expression of these interferon-stimulated genes (ISG) in stem cells is independent from external stimuli such as viral infection. Here, we show that the interferon regulatory factor 1, Irf1, is directly controlled by the murine formative pluripotency gene regulatory network and transiently upregulated during the transition from naive to formative pluripotency. IRF1 binds to regulatory regions of a conserved set of ISGs and is required for their faithful expression upon exit from naive pluripotency. We show that in the absence of IRF1, cells exiting the naive pluripotent stem cell state are more susceptible to viral infection. Irf1 therefore acts as a link between the formative pluripotency network, regulation of innate immunity genes, and defense against viral infections during formative pluripotency.

Indexed as

Pluripotent Stem CellsVirus DiseasesAnimalsAntiviral AgentsInterferon Regulatory Factor-1InterferonsMiceUp-RegulationAntiviral AgentsInterferon Regulatory Factor-1InterferonsIRF1 protein, humancell fate transitiongene regulatory networksISGpluripotencyviral infection

Identifiers

PMID35852463
PMCPMC9442322
OpenAlexW4286218908

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.