Evidence map›Paper›PMID 42559688›Full record

ArticleNucleic acids research2026

Comprehensive post-transcriptional modification profiles in individual Staphylococcus aureus tRNA species.

Jose R Jaramillo-Ponce, Philippe Wolff, Virginie Marchand, Yuri Motorin, Maximilian Kohl, Béatrice Chane-Woon-Ming, Hiroki Kanazawa, Aila Ruiz-Paterson, Caroline Paulus, Johana Chicher and 8 more

Abstract read
In one paragraph

Article in Nucleic acids research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Compendium of RNA modifications for bacterial stress adaptation.Microbiology and molecular biology reviews : MMBR · 2026
    Review
  2. 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

18 authors.

Jose R Jaramillo-PonceUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, Strasbourg 67084, France.ORCID 0000-0002-9273-5922
Philippe WolffUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, Strasbourg 67084, France.
Virginie MarchandUniversité de Lorraine, SMP IBSLor, EpiRNA-Seq Core Facility, and IMoPA UMR7365 CNRS, Nancy F-54000, France.
Yuri MotorinUniversité de Lorraine, SMP IBSLor, EpiRNA-Seq Core Facility, and IMoPA UMR7365 CNRS, Nancy F-54000, France.ORCID 0000-0002-8018-334X
Maximilian KohlUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, Strasbourg 67084, France.
Béatrice Chane-Woon-MingUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, Strasbourg 67084, France.
Hiroki KanazawaUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, Strasbourg 67084, France.
Aila Ruiz-PatersonUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, Strasbourg 67084, France.
Caroline PaulusUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, Strasbourg 67084, France.
Johana ChicherStrasbourg-Esplanade Proteomics Facility, CNRS UAR1589, Université de Strasbourg, Strasbourg 67084, France.ORCID 0000-0002-4403-7484
Marine LenonUniversité de Lorraine, SMP IBSLor, EpiRNA-Seq Core Facility, and IMoPA UMR7365 CNRS, Nancy F-54000, France.
Martina KrämerInstitute for Pharmaceutical and Biomedical Sciences, Johannes Gutenberg University Mainz, Mainz 55128, Germany.
Anne-Sophie Gribling-BurrerUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, Strasbourg 67084, France.ORCID 0000-0003-2297-3244
Constantinos StathopoulosDepartment of Biochemistry, School of Medicine, University of Patras, Patras 26504, Greece.ORCID 0000-0002-5699-4118
Redmond SmythUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, Strasbourg 67084, France.ORCID 0000-0002-1580-0671
Mark HelmInstitute for Pharmaceutical and Biomedical Sciences, Johannes Gutenberg University Mainz, Mainz 55128, Germany.ORCID 0000-0002-0154-0928
Pascale RombyUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, Strasbourg 67084, France.ORCID 0000-0002-4250-6048
Stefano MarziUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, Strasbourg 67084, France.ORCID 0000-0003-0399-4613

Funding

French Investments for the Future ProgramFrench National Research Agency ANR-10-IDEX-0002French National Research Agency ANR-17-EURE-0023French National Research Agency ANR 20-SFRI-0012French National Research Agency ANR-21-CE12-0030-01French National Research Agency ANR-23-CE12-0041-01French National Research Agency ANR-24-CE11-7652Hellenic Foundation for Research and Innovation ANR-21-CE12-0030-01Hellenic Foundation for Research and Innovation ANR-24-CE11-7652Interdisciplinary Thematic InstituteUniversity of StrasbourgUniversity of Strasbourg Institute for Advanced ANR-10-IDEX-0002University of Strasbourg Institute for Advanced ANR-11-EQPX-0022University of Strasbourg Institute for Advanced CPER 2021-2027
6 · The paper itself

Abstract

Post-transcriptional modifications modulate transfer RNA (tRNA) structure, stability, and codon decoding properties, contributing to translation regulation and adaptation across diverse organisms, including bacterial pathogens. We provide a comprehensive analysis of tRNA modifications in Staphylococcus aureus using extensive oligonucleotide mass spectrometry and deep-sequencing methods, generating a high-confidence modification map for each individual tRNA species, including non-proteogenic tRNAGly. While the overall tRNA modification landscape is conserved among Gram-positive bacteria, our data uncovered unexpected S. aureus-specific features. These include the absence of m2A37 in tRNAs despite the presence of the methyltransferase RlmN, a single multi-site DusB2 enzyme catalyzing all tRNA dihydrouridylation, and evidence suggesting a dedicated pseudouridine synthase responsible for Ψ32. Besides, heterogeneous modification patterns were observed in tRNALeu(UAA) and tRNALys(UUU), highlighting a complex interplay in anticodon hypermodification. Time-course proteomics revealed dynamic expression of tRNA modifying enzymes during growth. Integration of ribosome profiling and Nanopore tRNA sequencing offered a global view of S. aureus decoding properties, revealing efficient four-way wobble recognition, slower translation of rare codons by low abundant tRNAs, and distinctive decoding dynamics of Gly codons potentially influenced by the unusual modification status of tRNAGly(UCC). This work establishes a framework to dissect the role of tRNA modifications in S. aureus physiology and pathogenesis.

Indexed as

RNA Processing, Post-TranscriptionalRNA, TransferStaphylococcus aureusIntramolecular TransferasesRibosome ProfilingRNA, BacterialRNA, Transfer, GlyRNA, Transfer, LeutRNA MethyltransferasesIntramolecular Transferasespseudouridine synthasesRNA, BacterialRNA, TransferRNA, Transfer, GlyRNA, Transfer, LeutRNA Methyltransferases

Identifiers

PMID42559688
PMCPMC13443448

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.