Affiliation:
1. Institute of Pharmaceutical and Biomedical Sciences (IPBS) Johannes Gutenberg University Mainz Staudingerweg 5 55128 Mainz Germany
2. Department of Chemistry Johannes Gutenberg University Mainz Duesbergweg 10–14 55128 Mainz Germany
Abstract
AbstractThe 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 (ms2ϵA), 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 ms2ϵA biogenesis involves cleavage of a prenyl moiety in the known transfer RNA (tRNA) modification 2‐methylthio‐N6‐isopentenyladenosine (ms2i6A). The relative abundance of ms2ϵA 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.
Funder
Deutsche Forschungsgemeinschaft
Subject
General Chemistry,Catalysis
Cited by
8 articles.
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