Evidence map›Paper›PMID 29507242›Full record

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

hnRNP R and its main interactor, the noncoding RNA 7SK, coregulate the axonal transcriptome of motoneurons.

Michael Briese, Lena Saal-Bauernschubert, Changhe Ji, Mehri Moradi, Hanaa Ghanawi, Michael Uhl, Silke Appenzeller, Rolf Backofen, Michael Sendtner

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 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

39 citing papers in PubMed, 61 citations in OpenAlex.

  1. RNArchitects: how hnRNPs shape neuronal landscapes.Brain : a journal of neurology · 2026
    Review
  2. Quantifying MgbioRxiv : the preprint server for biology · 2026
    Article
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  9. Contributions of Folded and Disordered Domains to RNA Binding by HNRNPR.bioRxiv : the preprint server for biology · 2025
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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

9 authors at 2 institutions in 1 country.

Michael BrieseInstitute for Clinical Neurobiology, University of Wuerzburg, 97078 Wuerzburg, Germany.
Lena Saal-BauernschubertInstitute for Clinical Neurobiology, University of Wuerzburg, 97078 Wuerzburg, Germany.
Changhe JiInstitute for Clinical Neurobiology, University of Wuerzburg, 97078 Wuerzburg, Germany.
Mehri MoradiInstitute for Clinical Neurobiology, University of Wuerzburg, 97078 Wuerzburg, Germany.
Hanaa GhanawiInstitute for Clinical Neurobiology, University of Wuerzburg, 97078 Wuerzburg, Germany.
Michael UhlDepartment of Computer Science, Albert-Ludwigs-Universität Freiburg, 79110 Freiburg, Germany.
Silke AppenzellerCore Unit Systems Medicine, University of Wuerzburg, 97078 Wuerzburg, Germany.
Rolf BackofenDepartment of Computer Science, Albert-Ludwigs-Universität Freiburg, 79110 Freiburg, Germany.
Michael SendtnerInstitute for Clinical Neurobiology, University of Wuerzburg, 97078 Wuerzburg, Germany; Sendtner_M@ukw.de.
University of Würzburg · DEUniversity of Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Disturbed RNA processing and subcellular transport contribute to the pathomechanisms of motoneuron diseases such as amyotrophic lateral sclerosis and spinal muscular atrophy. RNA-binding proteins are involved in these processes, but the mechanisms by which they regulate the subcellular diversity of transcriptomes, particularly in axons, are not understood. Heterogeneous nuclear ribonucleoprotein R (hnRNP R) interacts with several proteins involved in motoneuron diseases. It is located in axons of developing motoneurons, and its depletion causes defects in axon growth. Here, we used individual nucleotide-resolution cross-linking and immunoprecipitation (iCLIP) to determine the RNA interactome of hnRNP R in motoneurons. We identified ∼3,500 RNA targets, predominantly with functions in synaptic transmission and axon guidance. Among the RNA targets identified by iCLIP, the noncoding RNA 7SK was the top interactor of hnRNP R. We detected 7SK in the nucleus and also in the cytosol of motoneurons. In axons, 7SK localized in close proximity to hnRNP R, and depletion of hnRNP R reduced axonal 7SK. Furthermore, suppression of 7SK led to defective axon growth that was accompanied by axonal transcriptome alterations similar to those caused by hnRNP R depletion. Using a series of 7SK-deletion mutants, we show that the function of 7SK in axon elongation depends on its interaction with hnRNP R but not with the PTEF-B complex involved in transcriptional regulation. These results propose a role for 7SK as an essential interactor of hnRNP R to regulate its function in axon maintenance.

Indexed as

3' Untranslated RegionsAnimalsAxonsCell NucleusCytosolGene Expression RegulationGene Knockdown TechniquesHeterogeneous-Nuclear RibonucleoproteinsImmunoprecipitationMiceMotor NeuronsRNA, MessengerRNA, Small NuclearTranscriptome3' Untranslated RegionsHeterogeneous-Nuclear RibonucleoproteinsHnrpr protein, mouseRNA, MessengerRNA, Small Nuclear7SKaxonhnRNP RiCLIPmotoneuron

Identifiers

PMID29507242
PMCPMC5866599
OpenAlexW2789940080

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.