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Nucleotidyltransferase toxin MenT extends aminoacyl acceptor ends of serine tRNAs to control Mycobacterium tuberculosis growth

Xu, Xibing; Barriot, Roland; Voisin, Bertille; Arrowsmith, Tom J.; Usher, Ben; Gutierrez, Claude; Han, Xue; Pagès, Carine; Redder, Peter; Blower, Tim R.; Neyrolles, Olivier; Genevaux, Pierre

Nucleotidyltransferase toxin MenT extends aminoacyl acceptor ends of serine tRNAs to control Mycobacterium tuberculosis growth Thumbnail


Authors

Xibing Xu

Roland Barriot

Bertille Voisin

Ben Usher

Claude Gutierrez

Xue Han

Carine Pagès

Peter Redder

Olivier Neyrolles

Pierre Genevaux



Abstract

Toxins of toxin-antitoxin systems use diverse mechanisms to inhibit bacterial growth. In this study, we characterize the translation inhibitor toxin MenT3 of Mycobacterium tuberculosis, the bacterium responsible for tuberculosis in humans. We show that MenT3 is a robust cytidine specific tRNA nucleotidyltransferase in vitro, capable of modifying the aminoacyl acceptor ends of most tRNA but with a marked preference for tRNASer, to which long stretches of cytidines are added. Furthermore, transcriptomic-wide analysis of MenT3 targets in M. tuberculosis identifies tRNASer as the sole target of MenT3 and reveals significant detoxification attempts by the essential CCA-adding enzyme PcnA in response to MenT3. Finally, under physiological conditions, only in the presence the native menAT3 operon, an active pool of endogenous MenT3 targeting tRNASer in M. tuberculosis is detected, likely reflecting the importance of MenT3 during infection.

Citation

Xu, X., Barriot, R., Voisin, B., Arrowsmith, T. J., Usher, B., Gutierrez, C., Han, X., Pagès, C., Redder, P., Blower, T. R., Neyrolles, O., & Genevaux, P. (2024). Nucleotidyltransferase toxin MenT extends aminoacyl acceptor ends of serine tRNAs to control Mycobacterium tuberculosis growth. Nature Communications, 15(1), Article 9596. https://doi.org/10.1038/s41467-024-53931-w

Journal Article Type Article
Acceptance Date Oct 28, 2024
Online Publication Date Nov 6, 2024
Publication Date Nov 6, 2024
Deposit Date Nov 12, 2024
Publicly Available Date Nov 12, 2024
Journal Nature Communications
Electronic ISSN 2041-1723
Publisher Nature Research
Peer Reviewed Peer Reviewed
Volume 15
Issue 1
Article Number 9596
DOI https://doi.org/10.1038/s41467-024-53931-w
Public URL https://durham-repository.worktribe.com/output/3088841

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