Xibing Xu
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
Authors
Roland Barriot
Bertille Voisin
Thomas Arrowsmith tom.arrowsmith@durham.ac.uk
PGR Student Doctor of Philosophy
Ben Usher
Claude Gutierrez
Xue Han
Carine Pagès
Peter Redder
Professor Tim Blower timothy.blower@durham.ac.uk
Professor
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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Publisher Licence URL
http://creativecommons.org/licenses/by/4.0/
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