Evidence map›Paper›PMID 41680142›Full record

ArticleNature communications2026

Extended Shine-Dalgarno motifs govern translation initiation in Staphylococcus aureus.

Maximilian P Kohl, Roberto Bahena-Ceron, Béatrice Chane-Woon-Ming, Maria Kompatscher, Matthias D Erlacher, Charles Barchet, Ottilie von Loeffelholz, Pascale Romby, Bruno P Klaholz, Stefano Marzi

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

10 authors.

Maximilian P KohlUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, Strasbourg, France.
Roberto Bahena-CeronUniversité de Strasbourg, CNRS, INSERM, Centre for Integrative Biology, Department of Integrated Structural Biology, IGBMC, Strasbourg, Illkirch, France.
Béatrice Chane-Woon-MingUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, Strasbourg, France.
Maria KompatscherInstitute of RNA Biology and Genomics, Biocenter, Medical University of Innsbruck, Innsbruck, Austria.
Matthias D ErlacherInstitute of RNA Biology and Genomics, Biocenter, Medical University of Innsbruck, Innsbruck, Austria.ORCID http://orcid.org/0000-0001-5570-9437
Charles BarchetUniversité de Strasbourg, CNRS, INSERM, Centre for Integrative Biology, Department of Integrated Structural Biology, IGBMC, Strasbourg, Illkirch, France.
Ottilie von LoeffelholzUniversité de Strasbourg, CNRS, INSERM, Centre for Integrative Biology, Department of Integrated Structural Biology, IGBMC, Strasbourg, Illkirch, France.
Pascale RombyUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, Strasbourg, France.
Bruno P KlaholzUniversité de Strasbourg, CNRS, INSERM, Centre for Integrative Biology, Department of Integrated Structural Biology, IGBMC, Strasbourg, Illkirch, France.ORCID http://orcid.org/0000-0001-8674-8674
Stefano MarziUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, Strasbourg, France. s.marzi@ibmc-cnrs.unistra.fr.ORCID http://orcid.org/0000-0003-0399-4613

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-10-IDEX-0002Agence Nationale de la Recherche (French National Research Agency) ANR-17-EURE-0023Agence Nationale de la Recherche (French National Research Agency) ANR 20-SFRI-0012Agence Nationale de la Recherche (French National Research Agency) ANR-21-CE12-0030-01Agence Nationale de la Recherche (French National Research Agency) ANR-23-CE12-0041-01Agence Nationale de la Recherche (French National Research Agency) ANR-24-CE11-7652
6 · The paper itself

Abstract

Regulation of translation initiation is central to bacterial adaptation, but species-specific mechanisms remain poorly understood. We present high-resolution mapping of translation start sites in Staphylococcus aureus, revealing distinct features of initiation alongside numerous unannotated small ORFs. Our analysis, combined with cryo-EM of a native mRNA-ribosome complex, shows that S. aureus relies on extended, start codon proximal Shine-Dalgarno (SD) interactions, creating specificity against phylogenetically distant bacteria. Several natural S. aureus initiation sites are not correctly decoded by E. coli ribosomes. We identify new and conserved non-canonical start codons, whose regulatory initiation sites contain these characteristic extended SD sequence motifs. Finally, we characterize a novel example of uORF-mediated translational control in S. aureus, demonstrating that translation of a small leader peptide modulates expression of a key biofilm regulator. The described mechanism involves codon rarity, ribosome pausing, and arginine availability, linking nutrient sensing to biofilm formation in this major human pathogen.

Indexed as

Nucleotide MotifsPeptide Chain Initiation, TranslationalStaphylococcus aureusBacterial ProteinsBiofilmsCodon, InitiatorCryoelectron MicroscopyEscherichia coliGene Expression Regulation, BacterialOpen Reading FramesProtein BiosynthesisRibosomesRNA, BacterialRNA, MessengerBacterial ProteinsCodon, InitiatorRNA, BacterialRNA, Messenger

Identifiers

PMID41680142
PMCPMC13009471

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Registered trials

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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.