Evidence map›Paper›PMID 33275131›Full record

ArticleNucleic acids research2020

Bacterial tRNA 2'-O-methylation is dynamically regulated under stress conditions and modulates innate immune response.

Adeline Galvanin, Lea-Marie Vogt, Antonia Grober, Isabel Freund, Lilia Ayadi, Valerie Bourguignon-Igel, Larissa Bessler, Dominik Jacob, Tatjana Eigenbrod, Virginie Marchand and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

32 citing papers in PubMed, 52 citations in OpenAlex.

  1. Review
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  4. Unlocking the role of tRNA-derived fragments in shaping breast cancer signaling.Naunyn-Schmiedeberg's archives of pharmacology · 2025
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  19. Human TRMT1 catalyzes mScience China. Life sciences · 2023
    Article
  20. 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

13 authors at 4 institutions in 2 countries.

Adeline GalvaninUniversité de Lorraine, CNRS, IMoPA (UMR7365), F54000 Nancy, France.
Lea-Marie VogtInstitute of Pharmaceutical and Biomedical Science, Johannes Gutenberg-University Mainz, 55128 Mainz, Germany.
Antonia GroberInstitute of Medical Microbiology and Hygiene, Technische Universität Dresden, 01307 Dresden, Germany.
Isabel FreundDepartment of Infectious Diseases, Medical Microbiology and Hygiene, Ruprecht-Karls University Heidelberg, 69117 Heidelberg, Germany.
Lilia AyadiUniversité de Lorraine, CNRS, IMoPA (UMR7365), F54000 Nancy, France.
Valerie Bourguignon-IgelUniversité de Lorraine, CNRS, IMoPA (UMR7365), F54000 Nancy, France.
Larissa BesslerInstitute of Pharmaceutical and Biomedical Science, Johannes Gutenberg-University Mainz, 55128 Mainz, Germany.
Dominik JacobInstitute of Pharmaceutical and Biomedical Science, Johannes Gutenberg-University Mainz, 55128 Mainz, Germany.
Tatjana EigenbrodDepartment of Infectious Diseases, Medical Microbiology and Hygiene, Ruprecht-Karls University Heidelberg, 69117 Heidelberg, Germany.
Virginie MarchandUniversité de Lorraine, CNRS, INSERM, IBSLor (UMS2008/US40), Epitranscriptomics and RNA Sequencing Core Facility, F54000 Nancy, France.
Alexander DalpkeInstitute of Medical Microbiology and Hygiene, Technische Universität Dresden, 01307 Dresden, Germany.
Mark HelmInstitute of Pharmaceutical and Biomedical Science, Johannes Gutenberg-University Mainz, 55128 Mainz, Germany.
Yuri MotorinUniversité de Lorraine, CNRS, IMoPA (UMR7365), F54000 Nancy, France.
Centre National de la Recherche Scientifique · FRJohannes Gutenberg University Mainz · DEHeidelberg University · DEInstitute of Medical Microbiology and Hygiene · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RNA modifications are a well-recognized way of gene expression regulation at the post-transcriptional level. Despite the importance of this level of regulation, current knowledge on modulation of tRNA modification status in response to stress conditions is far from being complete. While it is widely accepted that tRNA modifications are rather dynamic, such variations are mostly assessed in terms of total tRNA, with only a few instances where changes could be traced to single isoacceptor species. Using Escherichia coli as a model system, we explored stress-induced modulation of 2'-O-methylations in tRNAs by RiboMethSeq. This analysis and orthogonal analytical measurements by LC-MS show substantial, but not uniform, increase of the Gm18 level in selected tRNAs under mild bacteriostatic antibiotic stress, while other Nm modifications remain relatively constant. The absence of Gm18 modification in tRNAs leads to moderate alterations in E. coli mRNA transcriptome, but does not affect polysomal association of mRNAs. Interestingly, the subset of motility/chemiotaxis genes is significantly overexpressed in ΔTrmH mutant, this corroborates with increased swarming motility of the mutant strain. The stress-induced increase of tRNA Gm18 level, in turn, reduced immunostimulation properties of bacterial tRNAs, which is concordant with the previous observation that Gm18 is a suppressor of Toll-like receptor 7 (TLR7)-mediated interferon release. This documents an effect of stress induced modulation of tRNA modification that acts outside protein translation.

Indexed as

Escherichia coliGene Expression RegulationGuanosineHumansImmunity, InnateInterferonsMethylationRNA Processing, Post-TranscriptionalRNA, TransferToll-Like Receptor 7GuanosineInterferonsRNA, TransferTLR7 protein, humanToll-Like Receptor 7

Identifiers

PMID33275131
PMCPMC7736821
OpenAlexW3108918157

What OpenQuestion holds

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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.