An Expanded View of RNA Modification with Carbohydrate-Based Metabolic Probes

The discovery of glycosylated RNA (glycoRNA) revealed an unexpected association between glycans and RNA. This discovery, facilitated by the metabolic carbohydrate reporter per- O-acetylated N-azidoacetyl-mannosamine (Ac4ManNAz), underscores the potential for biological roles of previously unknown RNA modifications. Our study builds upon the detection of glycoRNA with other metabolic probes such as per-O-acetylated N-azidoacetyl-glucosamine (Ac4GlcNAz), N-azidoacetyl-galactosamine (Ac4GalNAz) and 6-azidofucose (Ac4FucAz). This broader analysis uncovered potential new glycosylated transcripts that warrant further study. However, our results also revealed unexpected resilience of the unidentified carbohydrate-RNA linkage to enzymatic cleavages by glycosidases. Therefore, we investigated non-enzymatic formation of carbohydrate-RNA linkages in vitro using per-acetylated probes. From these studies we draw two main conclusions. First, signals arising from metabolic incorporation using acetylated carbohydrate probes represent the main source of detectable glycoRNA species. Second, sequencing reveals that the most likely candidates for carbohydrate-modified RNAs are likely tRNAs. We demonstrated that an expanded repertoire of metabolic reporters can be incorporated into glycoRNA opening new perspectives on the nature of post-transcriptionally modified RNA.

Publication Details

Journal
Apollo (University of Cambridge)
Published
2025-04-28
DOI
https://doi.org/10.17863/cam.117704
Primary Topic
RNA modifications and cancer
Type
article
Field-Weighted Citation Impact
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article

An Expanded View of RNA Modification with Carbohydrate-Based Metabolic Probes

Apollo (University of Cambridge)
RNA modifications and cancer
article

An Expanded View of RNA Modification with Carbohydrate-Based Metabolic Probes

article en

Abstract

The discovery of glycosylated RNA (glycoRNA) revealed an unexpected association between glycans and RNA. This discovery, facilitated by the metabolic carbohydrate reporter per- O-acetylated N-azidoacetyl-mannosamine (Ac4ManNAz), underscores the potential for biological roles of previously unknown RNA modifications. Our study builds upon the detection of glycoRNA with other metabolic probes such as per-O-acetylated N-azidoacetyl-glucosamine (Ac4GlcNAz), N-azidoacetyl-galactosamine (Ac4GalNAz) and 6-azidofucose (Ac4FucAz). This broader analysis uncovered potential new glycosylated transcripts that warrant further study. However, our results also revealed unexpected resilience of the unidentified carbohydrate-RNA linkage to enzymatic cleavages by glycosidases. Therefore, we investigated non-enzymatic formation of carbohydrate-RNA linkages in vitro using per-acetylated probes. From these studies we draw two main conclusions. First, signals arising from metabolic incorporation using acetylated carbohydrate probes represent the main source of detectable glycoRNA species. Second, sequencing reveals that the most likely candidates for carbohydrate-modified RNAs are likely tRNAs. We demonstrated that an expanded repertoire of metabolic reporters can be incorporated into glycoRNA opening new perspectives on the nature of post-transcriptionally modified RNA.

Apollo (University of Cambridge)
Openalex Percentile: Top 62%
RNA modifications and cancer
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