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The epitranscriptomic mark N6 -methyladenosine (m6 A) is the most abundant RNA modification in eukaryotic mRNA, but various limitations in currently available m6 A detection methods have precluded routine identification of m6 A marks at the single-site level in mRNA transcripts. Herein, we report a single-base elongation- and ligation-based qPCR amplification method (termed "SELECT") that exploits the ability of m6 A to hinder 1) the single-base elongation activity of DNA polymerases and 2) the nick ligation efficiency of ligases; SELECT employs qPCR for quantitation. Following optimization and validation, SELECT was applied on three highly relevant proof-of-concept cases: determining 1) if a putative m6 A site is m6 A-modified in mRNAs and lncRNAs from biological samples, 2) the m6 A fraction at biological sites, and 3) if a particular m6 A modification enzyme functions on a specific target site. In summary, the rapid and flexible SELECT method facilitates the identification and verification of m6 A marks with unprecedented ease.
Xiao et al. (2018) studied this question.