Evidence map›Paper›PMID 30232334›Full record

ArticleNature communications2018

Roquin targets mRNAs in a 3'-UTR-specific manner by different modes of regulation.

Katharina Essig, Nina Kronbeck, Joao C Guimaraes, Claudia Lohs, Andreas Schlundt, Anne Hoffmann, Gesine Behrens, Sven Brenner, Joanna Kowalska, Cristina Lopez-Rodriguez and 7 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

40 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
  2. Article
  3. Serous Cavity Mast Cells Depend on the ROQUIN Paralogs.European journal of immunology · 2025
    Article
  4. Article
  5. Article
  6. Regulation and Function of the Atypical IκBs-Bcl-3, IκBEuropean journal of immunology · 2025
    Review
  7. Roquin exhibits opposing effects on RNA stem-loop stability through its two ROQ domain binding sites.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Review
  9. Comprehensive Profiling of Roquin Binding Preferences for RNA Stem-Loops.Angewandte Chemie (International ed. in English) · 2024
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. MALT1 substrate cleavage: what is it good for?Frontiers in immunology · 2024
    Review
  16. RNA Metabolism Governs Immune Function and Response.Advances in experimental medicine and biology · 2024
    Review
  17. Article
  18. Unrestrained cleavage of Roquin-1 by MALT1 induces spontaneous T cell activation and the development of autoimmunity.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  19. Review
  20. Article
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

17 authors at 8 institutions in 5 countries.

Katharina EssigInstitute for Immunology at the Biomedical Center, Ludwig-Maximilians-Universität München, 82152, Planegg-Martinsried, Germany.
Nina KronbeckInstitute for Immunology at the Biomedical Center, Ludwig-Maximilians-Universität München, 82152, Planegg-Martinsried, Germany.
Joao C GuimaraesComputational and Systems Biology, Biozentrum, University of Basel, 4056, Basel, Switzerland.ORCID http://orcid.org/0000-0002-1664-472X
Claudia LohsResearch Unit Molecular Immune Regulation, Helmholtz Zentrum München, 81377, München, Germany.
Andreas SchlundtInstitute of Structural Biology, Helmholtz Zentrum München, 85764, Neuherberg, Germany.ORCID http://orcid.org/0000-0003-2254-7560
Anne HoffmannYoung Investigators Group Bioinformatics and Transcriptomics, Department Molecular Systems Biology, Helmholtz Centre for Environmental Research-UFZ, Leipzig, Germany.
Gesine BehrensInstitute for Immunology at the Biomedical Center, Ludwig-Maximilians-Universität München, 82152, Planegg-Martinsried, Germany.
Sven BrennerResearch Unit Molecular Immune Regulation, Helmholtz Zentrum München, 81377, München, Germany.
Joanna KowalskaDivision of Biophysics, Institute of Experimental Physics, Faculty of Physics, University of Warsaw, 02-089, Warsaw, Poland.ORCID http://orcid.org/0000-0002-9174-7999
Cristina Lopez-RodriguezImmunology Unit, Department of Experimental and Health Sciences, Pompeu Fabra University, 08003, Barcelona, Spain.
Jacek JemielityCentre of New Technologies, University of Warsaw, 02-097, Warsaw, Poland.
Helmut HoltmannInstitute of Biochemistry, Hannover Medical School, 30623, Hannover, Germany.
Kristin ReicheYoung Investigators Group Bioinformatics and Transcriptomics, Department Molecular Systems Biology, Helmholtz Centre for Environmental Research-UFZ, Leipzig, Germany.
Jörg HackermüllerYoung Investigators Group Bioinformatics and Transcriptomics, Department Molecular Systems Biology, Helmholtz Centre for Environmental Research-UFZ, Leipzig, Germany.ORCID http://orcid.org/0000-0003-4920-7072
Michael SattlerInstitute of Structural Biology, Helmholtz Zentrum München, 85764, Neuherberg, Germany.ORCID http://orcid.org/0000-0002-1594-0527
Mihaela ZavolanComputational and Systems Biology, Biozentrum, University of Basel, 4056, Basel, Switzerland. mihaela.zavolan@unibas.ch.ORCID http://orcid.org/0000-0002-8832-2041
Vigo HeissmeyerInstitute for Immunology at the Biomedical Center, Ludwig-Maximilians-Universität München, 82152, Planegg-Martinsried, Germany. vigo.heissmeyer@med.uni-muenchen.de.
Helmholtz Centre for Environmental Research · DEHelmholtz Zentrum München · DELudwig-Maximilians-Universität München · DECenter for Integrated Protein Science Munich · DEUniversity of Basel · CHUniversity of Warsaw · PLMedizinische Hochschule Hannover · DEUniversitat Pompeu Fabra · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The RNA-binding proteins Roquin-1 and Roquin-2 redundantly control gene expression and cell-fate decisions. Here, we show that Roquin not only interacts with stem-loop structures, but also with a linear sequence element present in about half of its targets. Comprehensive analysis of a minimal response element of the Nfkbid 3'-UTR shows that six stem-loop structures cooperate to exert robust and profound post-transcriptional regulation. Only binding of multiple Roquin proteins to several stem-loops exerts full repression, which redundantly involved deadenylation and decapping, but also translational inhibition. Globally, most Roquin targets are regulated by mRNA decay, whereas a small subset, including the Nfat5 mRNA, with more binding sites in their 3'-UTRs, are also subject to translational inhibition. These findings provide insights into how the robustness and magnitude of Roquin-mediated regulation is encoded in complex cis-elements.

Indexed as

Gene Expression Regulation3' Untranslated RegionsAmino Acid MotifsAnimalsBase SequenceBinding SitesCross-Linking ReagentsHeLa CellsHumansMiceNucleic Acid ConformationProtein BindingProtein BiosynthesisResponse ElementsRibonucleosidesRNA, Messenger3' Untranslated RegionsCross-Linking ReagentsRc3h1 protein, mouseRibonucleosidesRNA, MessengerUbiquitin-Protein Ligases

Identifiers

PMID30232334
PMCPMC6145892
OpenAlexW2890742416

What OpenQuestion holds

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LicenceCC BY
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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.