Evidence map›Paper›PMID 37717009›Full record

ArticleNature communications2023

Phenylalanine-tRNA aminoacylation is compromised by ALS/FTD-associated C9orf72 C4G2 repeat RNA.

Mirjana Malnar Črnigoj, Urša Čerček, Xiaoke Yin, Manh Tin Ho, Barbka Repic Lampret, Manuela Neumann, Andreas Hermann, Guy Rouleau, Beat Suter, Manuel Mayr and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. LINE-1 Retrotransposons and Amyotrophic Lateral Sclerosis.International journal of molecular sciences · 2026
    Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. tRNAmicroPublication biology · 2024
    Article
  7. 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

11 authors at 6 institutions in 5 countries.

Mirjana Malnar Črnigoj *Department of Biotechnology, Jožef Stefan Institute, Ljubljana, 1000, Slovenia.ORCID http://orcid.org/0000-0002-6200-6251
Urša Čerček *Department of Biotechnology, Jožef Stefan Institute, Ljubljana, 1000, Slovenia.
Xiaoke YinKing's BHF Centre, King's College London, London, SE5 9NU, UK.ORCID http://orcid.org/0000-0002-5172-0935
Manh Tin HoInstitute of Cell Biology, University of Bern, Bern, 3012, Switzerland.
Barbka Repic LampretClinical Institute of Special Laboratory Diagnostics, University Children's Hospital, University Medical Centre Ljubljana, Ljubljana, 1000, Slovenia.
Manuela NeumannMolecular Neuropathology of Neurodegenerative Diseases, German Center for Neurodegenerative Diseases, Tübingen, 72076, Germany.
Andreas HermannTranslational Neurodegeneration Section "Albrecht-Kossel", Department of Neurology and Center for Transdisciplinary Neurosciences Rostock (CTNR), University Medical Center Rostock, University of Rostock, 18147, Rostock, Germany.ORCID http://orcid.org/0000-0002-7364-7791
Guy RouleauDepartment of Human Genetics, McGill University, Montréal, QC, H3A 0G4, Canada.ORCID http://orcid.org/0000-0001-8403-1418
Beat SuterInstitute of Cell Biology, University of Bern, Bern, 3012, Switzerland.
Manuel MayrKing's BHF Centre, King's College London, London, SE5 9NU, UK.ORCID http://orcid.org/0000-0002-0597-829X
Boris RogeljDepartment of Biotechnology, Jožef Stefan Institute, Ljubljana, 1000, Slovenia. boris.rogelj@ijs.si.ORCID http://orcid.org/0000-0003-3898-1943
University of Ljubljana · SIGerman Center for Neurodegenerative Diseases · DEKing's College London · GBUniversity of Bern · CHLjubljana University Medical Centre · SIMontreal Neurological Institute and Hospital · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The expanded hexanucleotide GGGGCC repeat mutation in the C9orf72 gene is the main genetic cause of amyotrophic lateral sclerosis and frontotemporal dementia. Under one disease mechanism, sense and antisense transcripts of the repeat are predicted to bind various RNA-binding proteins, compromise their function and cause cytotoxicity. Here we identify phenylalanine-tRNA synthetase (FARS) subunit alpha (FARSA) as the main interactor of the CCCCGG antisense repeat RNA in cytosol. The aminoacylation of tRNA

Indexed as

Amyotrophic Lateral SclerosisFrontotemporal DementiaAminoacylationC9orf72 ProteinHumansPhenylalanineRNA, AntisenseRNA, Transfer, PheTransfer RNA AminoacylationC9orf72 ProteinC9orf72 protein, humanPhenylalanineRNA, AntisenseRNA, Transfer, Phe

Identifiers

PMID37717009
PMCPMC10505166
OpenAlexW4386800822

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.