A ribosome-dependent small-ORF switch controls flagellar gene expression and virulence

RNA structures are active regulators of bacterial translation. Here, we identified a naturally occurring translation-enhancing small open reading frame (tesORF) that controls the expression of the flagellar operon fliFGHIJK in Salmonella enterica and other motile Enterobacterales. Nucleotide-resolution ribosome profiling revealed this previously unannotated 54-nucleotide ORF immediately upstream of fliF. Genetic, transcriptomic, and biochemical analyses support a model in which tesORF translation counteracts an inhibitory RNA structure, exposing the fliF ribosome-binding site and promoting translation initiation independently of the encoded peptide sequence. Disruption of tesORF translation reduced expression of the downstream operon and impaired motility and virulence-associated phenotypes in Escherichia coli, Salmonella, and Yersinia. Together, our findings reveal how translation of a conserved small ORF regulates an entire flagellar operon through RNA structural remodelling, with consequences expending to the wider flagellar regulon, linking RNA structural dynamics to bacterial motility and virulence.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-11-11
DOI
https://doi.org/10.64898/2026.11.10.765585
Primary Topic
RNA and protein synthesis mechanisms
Type
preprint
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preprint

A ribosome-dependent small-ORF switch controls flagellar gene expression and virulence

Owain J. Bryant, Betty Chung, Dominik Meggers, Filip Lastovka et al.
bioRxiv (Cold Spring Harbor Laboratory)
RNA and protein synthesis mechanisms
preprint

A ribosome-dependent small-ORF switch controls flagellar gene expression and virulence

Owain J. Bryant, Betty Chung, Dominik Meggers, Filip Lastovka, Franz Narberhaus, Elizaveta Alekseeva, Melina Knorr
preprint en

Abstract

RNA structures are active regulators of bacterial translation. Here, we identified a naturally occurring translation-enhancing small open reading frame (tesORF) that controls the expression of the flagellar operon fliFGHIJK in Salmonella enterica and other motile Enterobacterales. Nucleotide-resolution ribosome profiling revealed this previously unannotated 54-nucleotide ORF immediately upstream of fliF. Genetic, transcriptomic, and biochemical analyses support a model in which tesORF translation counteracts an inhibitory RNA structure, exposing the fliF ribosome-binding site and promoting translation initiation independently of the encoded peptide sequence. Disruption of tesORF translation reduced expression of the downstream operon and impaired motility and virulence-associated phenotypes in Escherichia coli, Salmonella, and Yersinia. Together, our findings reveal how translation of a conserved small ORF regulates an entire flagellar operon through RNA structural remodelling, with consequences expending to the wider flagellar regulon, linking RNA structural dynamics to bacterial motility and virulence.

bioRxiv (Cold Spring Harbor Laboratory)
University of Cambridge (GB), Ruhr University Bochum (DE)
RNA and protein synthesis mechanisms
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A ribosome-dependent small-ORF switch controls flagellar gene expression and virulence — Owain J. Bryant, Betty Chung, et al. · bioRxiv (Cold Spring Harbor Laboratory) (2026) | TGRS Research Map | TGRS