Y. Cai
A nucleotidyltransferase toxin inhibits growth of Mycobacterium tuberculosis through inactivation of tRNA acceptor stems
Cai, Y.; Usher, B.; Gutierrez, C.; Tolcan, A.; Mansour, M.; Fineran, P.C.; Condon, C.; Neyrolles, O.; Genevaux, P.; Blower, T.R.
Authors
B. Usher
C. Gutierrez
A. Tolcan
M. Mansour
P.C. Fineran
C. Condon
O. Neyrolles
P. Genevaux
Professor Tim Blower timothy.blower@durham.ac.uk
Professor
Abstract
Toxin-antitoxin systems are widespread stress-responsive elements, many of whose functions remain largely unknown. Here, we characterize the four DUF1814-family nucleotidyltransferase-like toxins (MenT1–4) encoded by the human pathogen Mycobacterium tuberculosis. Toxin MenT3 inhibited growth of M. tuberculosis when not antagonized by its cognate antitoxin, MenA3. We solved the structures of toxins MenT3 and MenT4 to 1.6 and 1.2 Å resolution, respectively, and identified the biochemical activity and target of MenT3. MenT3 blocked in vitro protein expression and prevented tRNA charging in vivo. MenT3 added pyrimidines (C or U) to the 3′-CCA acceptor stems of uncharged tRNAs and exhibited strong substrate specificity in vitro, preferentially targeting tRNASer from among the 45 M. tuberculosis tRNAs. Our study identifies a previously unknown mechanism that expands the range of enzymatic activities used by bacterial toxins, uncovering a new way to block protein synthesis and potentially treat tuberculosis and other infections.
Citation
Cai, Y., Usher, B., Gutierrez, C., Tolcan, A., Mansour, M., Fineran, P., Condon, C., Neyrolles, O., Genevaux, P., & Blower, T. (2020). A nucleotidyltransferase toxin inhibits growth of Mycobacterium tuberculosis through inactivation of tRNA acceptor stems. Science Advances, 6(31), Article eabb6651. https://doi.org/10.1126/sciadv.abb6651
Journal Article Type | Article |
---|---|
Acceptance Date | Jun 12, 2020 |
Online Publication Date | Jul 29, 2020 |
Publication Date | Jul 29, 2020 |
Deposit Date | Jun 10, 2020 |
Publicly Available Date | Jul 30, 2020 |
Journal | Science Advances |
Publisher | American Association for the Advancement of Science |
Peer Reviewed | Peer Reviewed |
Volume | 6 |
Issue | 31 |
Article Number | eabb6651 |
DOI | https://doi.org/10.1126/sciadv.abb6651 |
Public URL | https://durham-repository.worktribe.com/output/1262981 |
Files
Published Journal Article
(2 Mb)
PDF
Publisher Licence URL
http://creativecommons.org/licenses/by-nc/4.0/
Copyright Statement
Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/
This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license, which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
You might also like
Phage anti-CRISPR control by an RNA- and DNA-binding helix–turn–helix protein
(2024)
Journal Article
Genomic and taxonomic evaluation of 38 Treponema prophage sequences
(2024)
Journal Article
Multi-layered genome defences in bacteria
(2024)
Journal Article
Downloadable Citations
About Durham Research Online (DRO)
Administrator e-mail: dro.admin@durham.ac.uk
This application uses the following open-source libraries:
SheetJS Community Edition
Apache License Version 2.0 (http://www.apache.org/licenses/)
PDF.js
Apache License Version 2.0 (http://www.apache.org/licenses/)
Font Awesome
SIL OFL 1.1 (http://scripts.sil.org/OFL)
MIT License (http://opensource.org/licenses/mit-license.html)
CC BY 3.0 ( http://creativecommons.org/licenses/by/3.0/)
Powered by Worktribe © 2024
Advanced Search