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...
Autores principales: | , , , , , , , |
---|---|
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 |