Evidence map›Paper›PMID 37650648›Full record

ArticleNucleic acids research2023

Different modification pathways for m1A58 incorporation in yeast elongator and initiator tRNAs.

Marcel-Joseph Yared, Yasemin Yoluç, Marjorie Catala, Carine Tisné, Stefanie Kaiser, Pierre Barraud

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Pseudouridylation landscape across 42bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Optimized tRNA structure-seq reveals robust tRNA secondary structures inbioRxiv : the preprint server for biology · 2026
    Article
  5. The highly conserved intron of tyrosine tRNA is critical forProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Review
  7. Article
  8. A primer on tRNAs, tRNA-mFrontiers in cell and developmental biology · 2025
    Review
  9. Imino chemical shift assignments of tRNABiomolecular NMR assignments · 2024
    Article
  10. Article
  11. RNA modifying enzymes shape tRNA biogenesis and function.The Journal of biological chemistry · 2024
    Review
  12. Review
  13. 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

6 authors at 3 institutions in 2 countries.

Marcel-Joseph YaredExpression génétique microbienne, Université Paris Cité, CNRS, Institut de biologie physico-chimique, Paris, France.ORCID 0000-0002-8473-9085
Yasemin YoluçDepartment of Chemistry, Ludwig Maximilians University, Munich, Germany.ORCID 0000-0001-9535-5020
Marjorie CatalaExpression génétique microbienne, Université Paris Cité, CNRS, Institut de biologie physico-chimique, Paris, France.
Carine TisnéExpression génétique microbienne, Université Paris Cité, CNRS, Institut de biologie physico-chimique, Paris, France.ORCID 0000-0001-5534-4650
Stefanie KaiserDepartment of Chemistry, Ludwig Maximilians University, Munich, Germany.ORCID 0000-0003-3224-7502
Pierre BarraudExpression génétique microbienne, Université Paris Cité, CNRS, Institut de biologie physico-chimique, Paris, France.ORCID 0000-0003-4460-8360
Centre National de la Recherche Scientifique · FRGoethe University Frankfurt · DELudwig-Maximilians-Universität München · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As essential components of the protein synthesis machinery, tRNAs undergo a tightly controlled biogenesis process, which include the incorporation of numerous posttranscriptional modifications. Defects in these tRNA maturation steps may lead to the degradation of hypomodified tRNAs by the rapid tRNA decay (RTD) and nuclear surveillance pathways. We previously identified m1A58 as a late modification introduced after modifications Ψ55 and T54 in yeast elongator tRNAPhe. However, previous reports suggested that m1A58 is introduced early during the tRNA modification process, in particular on primary transcripts of initiator tRNAiMet, which prevents its degradation by RNA decay pathways. Here, aiming to reconcile this apparent inconsistency on the temporality of m1A58 incorporation, we examined its introduction into yeast elongator and initiator tRNAs. We used specifically modified tRNAs to report on the molecular aspects controlling the Ψ55 → T54 → m1A58 modification circuit in elongator tRNAs. We also show that m1A58 is efficiently introduced on unmodified tRNAiMet, and does not depend on prior modifications. Finally, we show that m1A58 has major effects on the structural properties of initiator tRNAiMet, so that the tRNA elbow structure is only properly assembled when this modification is present. This observation provides a structural explanation for the degradation of hypomodified tRNAiMet lacking m1A58 by the nuclear surveillance and RTD pathways.

Indexed as

RNA, Transfer, MetSaccharomyces cerevisiaeProtein BiosynthesisRNA Processing, Post-TranscriptionalRNA, TransferRNA, TransferRNA, Transfer, Met

Identifiers

PMID37650648
PMCPMC10602860
OpenAlexW4386305415

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.