Evidence map›Paper›PMID 34471108›Full record

ArticleNature communications2021

Defining the RBPome of primary T helper cells to elucidate higher-order Roquin-mediated mRNA regulation.

Kai P Hoefig, Alexander Reim, Christian Gallus, Elaine H Wong, Gesine Behrens, Christine Conrad, Meng Xu, Lisa Kifinger, Taku Ito-Kureha, Kyra A Y Defourny and 9 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

28 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Review
  3. IGF2BP3 regulates EMP1 stability in an mCell death & disease · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Review
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  11. Review
  12. Article
  13. Article
  14. RNA Metabolism Governs Immune Function and Response.Advances in experimental medicine and biology · 2024
    Review
  15. Article
  16. 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
  17. Review
  18. Article
  19. Post-transcriptional checkpoints in autoimmunity.Nature reviews. Rheumatology · 2023
    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

19 authors at 8 institutions in 4 countries.

Kai P Hoefig *Research Unit Molecular Immune Regulation, Helmholtz Center Munich, Munich, Germany.
Alexander Reim *Department of Proteomics and Signal Transduction, Max-Planck-Institute of Biochemistry, Munich, Germany.ORCID 0000-0001-8388-8620
Christian Gallus *Institute of Diabetes and Obesity, Helmholtz Center Munich, Munich, Germany.
Elaine H WongInstitute for Immunology, Biomedical Center, Ludwig Maximilians University Munich, Planegg-Martinsried, Germany.
Gesine BehrensResearch Unit Molecular Immune Regulation, Helmholtz Center Munich, Munich, Germany.
Christine ConradInstitute for Immunology, Biomedical Center, Ludwig Maximilians University Munich, Planegg-Martinsried, Germany.
Meng XuResearch Unit Molecular Immune Regulation, Helmholtz Center Munich, Munich, Germany.
Lisa KifingerInstitute for Immunology, Biomedical Center, Ludwig Maximilians University Munich, Planegg-Martinsried, Germany.ORCID 0000-0001-6422-057X
Taku Ito-KurehaInstitute for Immunology, Biomedical Center, Ludwig Maximilians University Munich, Planegg-Martinsried, Germany.
Kyra A Y DefournyInstitute for Immunology, Biomedical Center, Ludwig Maximilians University Munich, Planegg-Martinsried, Germany.
Arie GeerlofInstitute of Structural Biology, Helmholtz Center Munich, Neuherberg, Germany.
Josef MautnerResearch Unit Gene Vectors, Helmholtz Center Munich & Children's Hospital, TU Munich, Munich, Germany.
Stefanie M HauckResearch Unit Protein Science, Helmholtz Center Munich, Munich, Germany.ORCID 0000-0002-1630-6827
Dirk BaumjohannInstitute for Immunology, Biomedical Center, Ludwig Maximilians University Munich, Planegg-Martinsried, Germany.ORCID 0000-0001-8385-8288
Regina FeederleMonoclonal Antibody Core Facility and Research Group, Institute for Diabetes and Obesity, Helmholtz Center Munich, Neuherberg, Germany.ORCID 0000-0002-3981-367X
Matthias MannDepartment of Proteomics and Signal Transduction, Max-Planck-Institute of Biochemistry, Munich, Germany.ORCID 0000-0003-1292-4799
Michael WiererDepartment of Proteomics and Signal Transduction, Max-Planck-Institute of Biochemistry, Munich, Germany. wierer@biochem.mpg.de.ORCID 0000-0002-0356-5571
Elke GlasmacherInstitute of Diabetes and Obesity, Helmholtz Center Munich, Munich, Germany. elke.glasmacher@roche.com.ORCID 0000-0003-1265-2543
Vigo HeissmeyerResearch Unit Molecular Immune Regulation, Helmholtz Center Munich, Munich, Germany. vigo.heissmeyer@med.uni-muenchen.de.ORCID 0000-0002-2263-8545
Helmholtz Zentrum München · DELudwig-Maximilians-Universität München · DEMax Planck Institute of Biochemistry · DECenter for Integrated Protein Science Munich · DERoche (Switzerland) · CHUniversity of Bonn · DEUniversity of Copenhagen · DKUtrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Post-transcriptional gene regulation in T cells is dynamic and complex as targeted transcripts respond to various factors. This is evident for the Icos mRNA encoding an essential costimulatory receptor that is regulated by several RNA-binding proteins (RBP), including Roquin-1 and Roquin-2. Here, we identify a core RBPome of 798 mouse and 801 human T cell proteins by utilizing global RNA interactome capture (RNA-IC) and orthogonal organic phase separation (OOPS). The RBPome includes Stat1, Stat4 and Vav1 proteins suggesting unexpected functions for these transcription factors and signal transducers. Based on proximity to Roquin-1, we select ~50 RBPs for testing coregulation of Roquin-1/2 targets by induced expression in wild-type or Roquin-1/2-deficient T cells. Besides Roquin-independent contributions from Rbms1 and Cpeb4 we also show Roquin-1/2-dependent and target-specific coregulation of Icos by Celf1 and Igf2bp3. Connecting the cellular RBPome in a post-transcriptional context, we find contributions from multiple RBPs to the prototypic regulation of mRNA targets by individual trans-acting factors.

Indexed as

AnimalsDNA-Binding ProteinsGene Expression RegulationHEK293 CellsHumansInducible T-Cell Co-Stimulator ProteinMiceProto-Oncogene Proteins c-vavRNA-Binding ProteinsRNA, MessengerSignal TransductionSTAT1 Transcription FactorSTAT4 Transcription FactorT-Lymphocytes, Helper-InducerTrans-ActivatorsUbiquitin-Protein LigasesCPEB4 protein, humanDNA-Binding ProteinsICOS protein, humanIcos protein, mouseInducible T-Cell Co-Stimulator ProteinProto-Oncogene Proteins c-vavRBMS1 protein, humanRc3h1 protein, mouseRNA-Binding ProteinsRNA, MessengerSTAT1 Transcription FactorSTAT4 Transcription FactorTrans-ActivatorsUbiquitin-Protein LigasesVAV1 protein, human

Identifiers

PMID34471108
PMCPMC8410761
OpenAlexW3197899290

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Registered trials

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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.