A New Bacterial Adenosine-Derived Nucleoside as an Example of RNA Modification Damage
- Publication type:
- Journal article
- Metadata:
-
- Autoren
- Larissa Bessler
- Lea-Marie Vogt
- Marc Lander
- Christina Dal Magro
- Patrick Keller
- Jonas Kuehlborn
- Christopher J Kampf
- Till Opatz
- Mark Helm
- Autoren-URL
- https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=fis-test-1&SrcAuth=WosAPI&KeyUT=WOS:000928874000001&DestLinkType=FullRecord&DestApp=WOS_CPL
- DOI
- 10.1002/anie.202217128
- eISSN
- 1521-3773
- Externe Identifier
- Clarivate Analytics Document Solution ID: P3BN7
- PubMed Identifier: 36629490
- ISSN
- 1433-7851
- Ausgabe der Veröffentlichung
- 11
- Zeitschrift
- ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Schlüsselwörter
- Epitranscriptome
- Isotopic Labeling
- Mass Spectrometry
- Nucleoside Analysis
- RNA Modification Damage
- Datum der Veröffentlichung
- 2023
- Status
- Published
- Titel
- A New Bacterial Adenosine-Derived Nucleoside as an Example of RNA Modification Damage
- Sub types
- Article
- Ausgabe der Zeitschrift
- 62
Data source: Web of Science (Lite)
- Other metadata sources:
-
- Abstract
- <jats:title>Abstract</jats:title><jats:p>The fields of RNA modification and RNA damage both exhibit a plethora of non‐canonical nucleoside structures. While RNA modifications have evolved to improve RNA function, the term RNA damage implies detrimental effects. Based on stable isotope labelling and mass spectrometry, we report the identification and characterisation of 2‐methylthio‐1,<jats:italic>N</jats:italic>6‐ethenoadenosine (ms<jats:sup>2</jats:sup>ϵA), which is related to 1,<jats:italic>N</jats:italic>6‐ethenoadenine, a lesion resulting from exposure of nucleic acids to alkylating chemicals in vivo. In contrast, a sophisticated isoprene labelling scheme revealed that ms<jats:sup>2</jats:sup>ϵA biogenesis involves cleavage of a prenyl moiety in the known transfer RNA (tRNA) modification 2‐methylthio‐<jats:italic>N</jats:italic>6‐isopentenyladenosine (ms<jats:sup>2</jats:sup>i<jats:sup>6</jats:sup>A). The relative abundance of ms<jats:sup>2</jats:sup>ϵA in tRNAs from translating ribosomes suggests reduced function in comparison to its parent RNA modification, establishing the nature of the new structure in a newly perceived overlap of the two previously separate fields, namely an RNA modification damage.</jats:p>
- Autoren
- Larissa Bessler
- Lea‐Marie Vogt
- Marc Lander
- Christina Dal Magro
- Patrick Keller
- Jonas Kühlborn
- Christopher J Kampf
- Till Opatz
- Mark Helm
- DOI
- 10.1002/anie.202217128
- eISSN
- 1521-3773
- ISSN
- 1433-7851
- Ausgabe der Veröffentlichung
- 11
- Zeitschrift
- Angewandte Chemie International Edition
- Sprache
- en
- Online publication date
- 2023
- Datum der Veröffentlichung
- 2023
- Status
- Published
- Herausgeber
- Wiley
- Herausgeber URL
- http://dx.doi.org/10.1002/anie.202217128
- Datum der Datenerfassung
- 2023
- Titel
- A New Bacterial Adenosine‐Derived Nucleoside as an Example of RNA Modification Damage
- Ausgabe der Zeitschrift
- 62
Data source: Crossref
- Abstract
- The fields of RNA modification and RNA damage both exhibit a plethora of non-canonical nucleoside structures. While RNA modifications have evolved to improve RNA function, the term RNA damage implies detrimental effects. Based on stable isotope labelling and mass spectrometry, we report the identification and characterisation of 2-methylthio-1,N6-ethenoadenosine (ms<sup>2</sup> ϵA), which is related to 1,N6-ethenoadenine, a lesion resulting from exposure of nucleic acids to alkylating chemicals in vivo. In contrast, a sophisticated isoprene labelling scheme revealed that ms<sup>2</sup> ϵA biogenesis involves cleavage of a prenyl moiety in the known transfer RNA (tRNA) modification 2-methylthio-N6-isopentenyladenosine (ms<sup>2</sup> i<sup>6</sup> A). The relative abundance of ms<sup>2</sup> ϵA in tRNAs from translating ribosomes suggests reduced function in comparison to its parent RNA modification, establishing the nature of the new structure in a newly perceived overlap of the two previously separate fields, namely an RNA modification damage.
- Addresses
- Institute of Pharmaceutical and Biomedical Sciences (IPBS), Johannes Gutenberg University Mainz, Staudingerweg 5, 55128, Mainz, Germany.
- Autoren
- Larissa Bessler
- Lea-Marie Vogt
- Marc Lander
- Christina Dal Magro
- Patrick Keller
- Jonas Kühlborn
- Christopher J Kampf
- Till Opatz
- Mark Helm
- DOI
- 10.1002/anie.202217128
- eISSN
- 1521-3773
- Externe Identifier
- PubMed Identifier: 36629490
- Funding acknowledgements
- Deutsche Forschungsgemeinschaft: HE 3397/14-2 in SPP1784
- Deutsche Forschungsgemeinschaft: TP C03 in TRR 319 Project-ID 439669440
- Open access
- false
- ISSN
- 1433-7851
- Ausgabe der Veröffentlichung
- 11
- Zeitschrift
- Angewandte Chemie (International ed. in English)
- Schlüsselwörter
- Nucleosides
- RNA
- RNA, Bacterial
- RNA, Transfer
- Adenosine
- Sprache
- eng
- Medium
- Print-Electronic
- Online publication date
- 2023
- Paginierung
- e202217128
- Datum der Veröffentlichung
- 2023
- Status
- Published
- Publisher licence
- CC BY
- Datum der Datenerfassung
- 2023
- Titel
- A New Bacterial Adenosine-Derived Nucleoside as an Example of RNA Modification Damage.
- Sub types
- Research Support, Non-U.S. Gov't
- Journal Article
- Ausgabe der Zeitschrift
- 62
Data source: Europe PubMed Central
- Abstract
- The fields of RNA modification and RNA damage both exhibit a plethora of non-canonical nucleoside structures. While RNA modifications have evolved to improve RNA function, the term RNA damage implies detrimental effects. Based on stable isotope labelling and mass spectrometry, we report the identification and characterisation of 2-methylthio-1,N6-ethenoadenosine (ms2 ϵA), which is related to 1,N6-ethenoadenine, a lesion resulting from exposure of nucleic acids to alkylating chemicals in vivo. In contrast, a sophisticated isoprene labelling scheme revealed that ms2 ϵA biogenesis involves cleavage of a prenyl moiety in the known transfer RNA (tRNA) modification 2-methylthio-N6-isopentenyladenosine (ms2 i6 A). The relative abundance of ms2 ϵA in tRNAs from translating ribosomes suggests reduced function in comparison to its parent RNA modification, establishing the nature of the new structure in a newly perceived overlap of the two previously separate fields, namely an RNA modification damage.
- Autoren
- Larissa Bessler
- Lea-Marie Vogt
- Marc Lander
- Christina Dal Magro
- Patrick Keller
- Jonas Kühlborn
- Christopher J Kampf
- Till Opatz
- Mark Helm
- Autoren-URL
- https://www.ncbi.nlm.nih.gov/pubmed/36629490
- DOI
- 10.1002/anie.202217128
- eISSN
- 1521-3773
- Ausgabe der Veröffentlichung
- 11
- Zeitschrift
- Angew Chem Int Ed Engl
- Schlüsselwörter
- Epitranscriptome
- Isotopic Labeling
- Mass Spectrometry
- Nucleoside Analysis
- RNA Modification Damage
- Nucleosides
- Adenosine
- RNA, Transfer
- RNA
- RNA, Bacterial
- Sprache
- eng
- Country
- Germany
- Paginierung
- e202217128
- Datum der Veröffentlichung
- 2023
- Status
- Published
- Datum, an dem der Datensatz öffentlich gemacht wurde
- 2023
- Titel
- A New Bacterial Adenosine-Derived Nucleoside as an Example of RNA Modification Damage.
- Sub types
- Journal Article
- Research Support, Non-U.S. Gov't
- Ausgabe der Zeitschrift
- 62
Data source: PubMed
- Author's licence
- CC-BY
- Autoren
- Larissa Bessler
- Lea-Marie Vogt
- Marc Lander
- Christina Dal Magro
- Patrick Keller
- Jonas Kühlborn
- Christopher J Kampf
- Till Opatz
- Mark Helm
- Hosting institution
- Universitätsbibliothek Mainz
- Sammlungen
- DFG-491381577-H
- Resource version
- Published version
- DOI
- 10.1002/anie.202217128
- Funding acknowledgements
- Deutsche Forschungsgemeinschaft (DFG)|491381577|Open-Access-Publikationskosten 2022–2024 Universität Mainz - Universitätsmedizin
- File(s) embargoed
- false
- Open access
- true
- ISSN
- 1521-3773
- Ausgabe der Veröffentlichung
- 11
- Zeitschrift
- Angewandte Chemie : International edition
- Schlüsselwörter
- 540 Chemie
- 540 Chemistry and allied sciences
- Sprache
- eng
- Open access status
- Open Access
- Paginierung
- e202217128
- Datum der Veröffentlichung
- 2023
- Public URL
- https://openscience.ub.uni-mainz.de/handle/20.500.12030/9069
- Herausgeber
- Wiley-VCH
- Datum der Datenerfassung
- 2023
- Datum, an dem der Datensatz öffentlich gemacht wurde
- 2023
- Zugang
- Public
- Titel
- A new bacterial adenosine-derived nucleoside as an example of RNA modification damage
- Ausgabe der Zeitschrift
- 62
Files
a_new_bacterial_adenosinederi-20230425113414785.pdf
Data source: OPENSCIENCE.UB
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