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Identification of RNA helicases with unwinding activity on angiogenin-processed tRNAs
Stress-induced tRNA fragmentation upon environmental insult is a conserved cellular process catalysed by endonucleolytic activities targeting mature tRNAs. The resulting tRNA-derived small RNAs (tsRNAs) have been implicated in various biological processes that impact cell-to-cell signalling, cell su...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9943664/ https://www.ncbi.nlm.nih.gov/pubmed/36718960 http://dx.doi.org/10.1093/nar/gkad033 |
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author | Drino, Aleksej König, Lisa Capitanchik, Charlotte Sanadgol, Nasim Janisiw, Eva Rappol, Tom Vilardo, Elisa Schaefer, Matthias R |
author_facet | Drino, Aleksej König, Lisa Capitanchik, Charlotte Sanadgol, Nasim Janisiw, Eva Rappol, Tom Vilardo, Elisa Schaefer, Matthias R |
author_sort | Drino, Aleksej |
collection | PubMed |
description | Stress-induced tRNA fragmentation upon environmental insult is a conserved cellular process catalysed by endonucleolytic activities targeting mature tRNAs. The resulting tRNA-derived small RNAs (tsRNAs) have been implicated in various biological processes that impact cell-to-cell signalling, cell survival as well as gene expression regulation during embryonic development. However, how endonuclease-targeted tRNAs give rise to individual and potentially biologically active tsRNAs remains poorly understood. Here, we report on the in vivo identification of proteins associated with stress-induced tsRNAs-containing protein complexes, which, together with a ‘tracer tRNA’ assay, were used to uncover enzymatic activities that can bind and process specific endonuclease-targeted tRNAs in vitro. Among those, we identified conserved ATP-dependent RNA helicases which can robustly separate tRNAs with endonuclease-mediated ‘nicks’ in their anticodon loops. These findings shed light on the existence of cellular pathways dedicated to producing individual tsRNAs after stress-induced tRNA hydrolysis, which adds to our understanding as to how tRNA fragmentation and the resulting tsRNAs might exert physiological impact. |
format | Online Article Text |
id | pubmed-9943664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-99436642023-02-22 Identification of RNA helicases with unwinding activity on angiogenin-processed tRNAs Drino, Aleksej König, Lisa Capitanchik, Charlotte Sanadgol, Nasim Janisiw, Eva Rappol, Tom Vilardo, Elisa Schaefer, Matthias R Nucleic Acids Res Nucleic Acid Enzymes Stress-induced tRNA fragmentation upon environmental insult is a conserved cellular process catalysed by endonucleolytic activities targeting mature tRNAs. The resulting tRNA-derived small RNAs (tsRNAs) have been implicated in various biological processes that impact cell-to-cell signalling, cell survival as well as gene expression regulation during embryonic development. However, how endonuclease-targeted tRNAs give rise to individual and potentially biologically active tsRNAs remains poorly understood. Here, we report on the in vivo identification of proteins associated with stress-induced tsRNAs-containing protein complexes, which, together with a ‘tracer tRNA’ assay, were used to uncover enzymatic activities that can bind and process specific endonuclease-targeted tRNAs in vitro. Among those, we identified conserved ATP-dependent RNA helicases which can robustly separate tRNAs with endonuclease-mediated ‘nicks’ in their anticodon loops. These findings shed light on the existence of cellular pathways dedicated to producing individual tsRNAs after stress-induced tRNA hydrolysis, which adds to our understanding as to how tRNA fragmentation and the resulting tsRNAs might exert physiological impact. Oxford University Press 2023-01-31 /pmc/articles/PMC9943664/ /pubmed/36718960 http://dx.doi.org/10.1093/nar/gkad033 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. 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 (https://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 Drino, Aleksej König, Lisa Capitanchik, Charlotte Sanadgol, Nasim Janisiw, Eva Rappol, Tom Vilardo, Elisa Schaefer, Matthias R Identification of RNA helicases with unwinding activity on angiogenin-processed tRNAs |
title | Identification of RNA helicases with unwinding activity on angiogenin-processed tRNAs |
title_full | Identification of RNA helicases with unwinding activity on angiogenin-processed tRNAs |
title_fullStr | Identification of RNA helicases with unwinding activity on angiogenin-processed tRNAs |
title_full_unstemmed | Identification of RNA helicases with unwinding activity on angiogenin-processed tRNAs |
title_short | Identification of RNA helicases with unwinding activity on angiogenin-processed tRNAs |
title_sort | identification of rna helicases with unwinding activity on angiogenin-processed trnas |
topic | Nucleic Acid Enzymes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9943664/ https://www.ncbi.nlm.nih.gov/pubmed/36718960 http://dx.doi.org/10.1093/nar/gkad033 |
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