5-Formylcytidine (f C) is one of the epigenetic nucleotides in tRNA. Despite the evident importance of f C in gene expression regulation, little is known about its exact amount and position. To capture this information, we developed a modification-specific functionalization with a semi-stabilized ylide. The chemical labelling exhibited a high selectivity towards f C and allowed distinction from similar 5-formyluridine. We realized a detection strategy based on the fluorescence signal of the cyclization product 4,5-pyridin-2-amine-cytidine paC, which exhibited a high quantum yield. The results clearly identified f C with a limit of detection at 0.58 nM. This method altered the hydrogen bonding activities of f C and modulated its reverse transcription signature in its sequencing profile. We showed that f C can be detected from tRNA segments with a single-base resolution. Taken together, this approach is a sensitive, antibody-free, and applicable detection and sequencing method for f C-containing RNA.
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http://dx.doi.org/10.1002/anie.202210652 | DOI Listing |
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