Cargando…

tRNA is a new target for cleavage by a MazF toxin

Toxin-antitoxin (TA) systems play key roles in bacterial persistence, biofilm formation and stress responses. The MazF toxin from the Escherichia coli mazEF TA system is a sequence- and single-strand-specific endoribonuclease, and many studies have led to the proposal that MazF family members exclus...

Descripción completa

Detalles Bibliográficos
Autores principales: Schifano, Jason M., Cruz, Jonathan W., Vvedenskaya, Irina O., Edifor, Regina, Ouyang, Ming, Husson, Robert N., Nickels, Bryce E., Woychik, Nancy A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756823/
https://www.ncbi.nlm.nih.gov/pubmed/26740583
http://dx.doi.org/10.1093/nar/gkv1370
_version_ 1782416402142986240
author Schifano, Jason M.
Cruz, Jonathan W.
Vvedenskaya, Irina O.
Edifor, Regina
Ouyang, Ming
Husson, Robert N.
Nickels, Bryce E.
Woychik, Nancy A.
author_facet Schifano, Jason M.
Cruz, Jonathan W.
Vvedenskaya, Irina O.
Edifor, Regina
Ouyang, Ming
Husson, Robert N.
Nickels, Bryce E.
Woychik, Nancy A.
author_sort Schifano, Jason M.
collection PubMed
description Toxin-antitoxin (TA) systems play key roles in bacterial persistence, biofilm formation and stress responses. The MazF toxin from the Escherichia coli mazEF TA system is a sequence- and single-strand-specific endoribonuclease, and many studies have led to the proposal that MazF family members exclusively target mRNA. However, recent data indicate some MazF toxins can cleave specific sites within rRNA in concert with mRNA. In this report, we identified the repertoire of RNAs cleaved by Mycobacterium tuberculosis toxin MazF-mt9 using an RNA-seq-based approach. This analysis revealed that two tRNAs were the principal targets of MazF-mt9, and each was cleaved at a single site in either the tRNA(Pro14) D-loop or within the tRNA(Lys43) anticodon. This highly selective target discrimination occurs through recognition of not only sequence but also structural determinants. Thus, MazF-mt9 represents the only MazF family member known to target tRNA and to require RNA structure for recognition and cleavage. Interestingly, the tRNase activity of MazF-mt9 mirrors basic features of eukaryotic tRNases that also generate stable tRNA-derived fragments that can inhibit translation in response to stress. Our data also suggest a role for tRNA distinct from its canonical adapter function in translation, as cleavage of tRNAs by MazF-mt9 downregulates bacterial growth.
format Online
Article
Text
id pubmed-4756823
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-47568232016-02-18 tRNA is a new target for cleavage by a MazF toxin Schifano, Jason M. Cruz, Jonathan W. Vvedenskaya, Irina O. Edifor, Regina Ouyang, Ming Husson, Robert N. Nickels, Bryce E. Woychik, Nancy A. Nucleic Acids Res Nucleic Acid Enzymes Toxin-antitoxin (TA) systems play key roles in bacterial persistence, biofilm formation and stress responses. The MazF toxin from the Escherichia coli mazEF TA system is a sequence- and single-strand-specific endoribonuclease, and many studies have led to the proposal that MazF family members exclusively target mRNA. However, recent data indicate some MazF toxins can cleave specific sites within rRNA in concert with mRNA. In this report, we identified the repertoire of RNAs cleaved by Mycobacterium tuberculosis toxin MazF-mt9 using an RNA-seq-based approach. This analysis revealed that two tRNAs were the principal targets of MazF-mt9, and each was cleaved at a single site in either the tRNA(Pro14) D-loop or within the tRNA(Lys43) anticodon. This highly selective target discrimination occurs through recognition of not only sequence but also structural determinants. Thus, MazF-mt9 represents the only MazF family member known to target tRNA and to require RNA structure for recognition and cleavage. Interestingly, the tRNase activity of MazF-mt9 mirrors basic features of eukaryotic tRNases that also generate stable tRNA-derived fragments that can inhibit translation in response to stress. Our data also suggest a role for tRNA distinct from its canonical adapter function in translation, as cleavage of tRNAs by MazF-mt9 downregulates bacterial growth. Oxford University Press 2016-02-18 2016-01-05 /pmc/articles/PMC4756823/ /pubmed/26740583 http://dx.doi.org/10.1093/nar/gkv1370 Text en © The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Nucleic Acid Enzymes
Schifano, Jason M.
Cruz, Jonathan W.
Vvedenskaya, Irina O.
Edifor, Regina
Ouyang, Ming
Husson, Robert N.
Nickels, Bryce E.
Woychik, Nancy A.
tRNA is a new target for cleavage by a MazF toxin
title tRNA is a new target for cleavage by a MazF toxin
title_full tRNA is a new target for cleavage by a MazF toxin
title_fullStr tRNA is a new target for cleavage by a MazF toxin
title_full_unstemmed tRNA is a new target for cleavage by a MazF toxin
title_short tRNA is a new target for cleavage by a MazF toxin
title_sort trna is a new target for cleavage by a mazf toxin
topic Nucleic Acid Enzymes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756823/
https://www.ncbi.nlm.nih.gov/pubmed/26740583
http://dx.doi.org/10.1093/nar/gkv1370
work_keys_str_mv AT schifanojasonm trnaisanewtargetforcleavagebyamazftoxin
AT cruzjonathanw trnaisanewtargetforcleavagebyamazftoxin
AT vvedenskayairinao trnaisanewtargetforcleavagebyamazftoxin
AT ediforregina trnaisanewtargetforcleavagebyamazftoxin
AT ouyangming trnaisanewtargetforcleavagebyamazftoxin
AT hussonrobertn trnaisanewtargetforcleavagebyamazftoxin
AT nickelsbrycee trnaisanewtargetforcleavagebyamazftoxin
AT woychiknancya trnaisanewtargetforcleavagebyamazftoxin