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Temporal resolution of NAIL-MS of tRNA, rRNA and Poly-A RNA is overcome by actinomycin D

RNA is dynamically modified and has the potential to respond to environmental changes and tune translation. The objective of this work is to uncover the temporal limitation of our recently developed cell culture NAIL-MS (nucleic acid isotope labelling coupled mass spectrometry) technology and overco...

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Autores principales: Hagelskamp, Felix, Borland, Kayla, Ammann, Gregor, Kaiser, Stefanie M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10170653/
https://www.ncbi.nlm.nih.gov/pubmed/37181633
http://dx.doi.org/10.1039/d2cb00243d
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author Hagelskamp, Felix
Borland, Kayla
Ammann, Gregor
Kaiser, Stefanie M.
author_facet Hagelskamp, Felix
Borland, Kayla
Ammann, Gregor
Kaiser, Stefanie M.
author_sort Hagelskamp, Felix
collection PubMed
description RNA is dynamically modified and has the potential to respond to environmental changes and tune translation. The objective of this work is to uncover the temporal limitation of our recently developed cell culture NAIL-MS (nucleic acid isotope labelling coupled mass spectrometry) technology and overcome it. Actinomycin D (AcmD), an inhibitor of transcription, was used in the NAIL-MS context to reveal the origin of hybrid nucleoside signals composed of unlabelled nucleosides and labelled methylation marks. We find that the formation of these hybrid species depends exclusively on transcription for Poly-A RNA and rRNA but is partly transcription-independent for tRNA. This finding suggests that tRNA modifications adapt and are dynamically regulated by cells to overcome e.g. stress. Future studies on the tRNA modification mediated stress response are now accessible and the temporal resolution of NAIL-MS is improved by the use of AcmD.
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spelling pubmed-101706532023-05-11 Temporal resolution of NAIL-MS of tRNA, rRNA and Poly-A RNA is overcome by actinomycin D Hagelskamp, Felix Borland, Kayla Ammann, Gregor Kaiser, Stefanie M. RSC Chem Biol Chemistry RNA is dynamically modified and has the potential to respond to environmental changes and tune translation. The objective of this work is to uncover the temporal limitation of our recently developed cell culture NAIL-MS (nucleic acid isotope labelling coupled mass spectrometry) technology and overcome it. Actinomycin D (AcmD), an inhibitor of transcription, was used in the NAIL-MS context to reveal the origin of hybrid nucleoside signals composed of unlabelled nucleosides and labelled methylation marks. We find that the formation of these hybrid species depends exclusively on transcription for Poly-A RNA and rRNA but is partly transcription-independent for tRNA. This finding suggests that tRNA modifications adapt and are dynamically regulated by cells to overcome e.g. stress. Future studies on the tRNA modification mediated stress response are now accessible and the temporal resolution of NAIL-MS is improved by the use of AcmD. RSC 2023-02-24 /pmc/articles/PMC10170653/ /pubmed/37181633 http://dx.doi.org/10.1039/d2cb00243d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Hagelskamp, Felix
Borland, Kayla
Ammann, Gregor
Kaiser, Stefanie M.
Temporal resolution of NAIL-MS of tRNA, rRNA and Poly-A RNA is overcome by actinomycin D
title Temporal resolution of NAIL-MS of tRNA, rRNA and Poly-A RNA is overcome by actinomycin D
title_full Temporal resolution of NAIL-MS of tRNA, rRNA and Poly-A RNA is overcome by actinomycin D
title_fullStr Temporal resolution of NAIL-MS of tRNA, rRNA and Poly-A RNA is overcome by actinomycin D
title_full_unstemmed Temporal resolution of NAIL-MS of tRNA, rRNA and Poly-A RNA is overcome by actinomycin D
title_short Temporal resolution of NAIL-MS of tRNA, rRNA and Poly-A RNA is overcome by actinomycin D
title_sort temporal resolution of nail-ms of trna, rrna and poly-a rna is overcome by actinomycin d
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10170653/
https://www.ncbi.nlm.nih.gov/pubmed/37181633
http://dx.doi.org/10.1039/d2cb00243d
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