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Examining the Roles of m6A Sites in mRNA Using the Luciferase Gene Fused With Mutated RRACH Motifs
Nobuko Katoku-Kikyo1,2, Nobuaki Kikyo1,2
1Stem Cell Institute, University of Minnesota, Minneapolis, MN, USA.
Abstract:
N 6-methyladenosine (m6A) is the most abundant internal modification in mRNA and is regulated primarily by the balance between the METTL3 methylase complex and two demethylases, FTO (fat mass and obesity-associated protein) and ALKBH5 (α-ketoglutarate-dependent dioxygenase alkB homolog). Reflecting this prevalence, m6A participates in virtually every step of RNA metabolism, influencing a wide range of physiological and pathological processes. The first step in studying m6A is genome-wide mapping, typically performed by m6A-seq, which sequences RNA fragments immunoprecipitated with an m6A-specific antibody. This is followed by identification of RRACH motifs (R = A or G; H = A, C, or U) within these sequences, with m6A being located at the third nucleotide. The second step involves mutating the putative m6A sites to establish a causal link between the modification and downstream biological effects. Since the mapping step has been covered in several detailed protocols, this article focuses on the second step-mutagenesis of RRACH motifs and subsequent functional analysis of the mutations by ectopic expression. The 3' untranslated region (UTR) of the mouse Runx2 gene is used as an example. The mutant and wild-type sequences are inserted into a luciferase reporter vector and transfected into 293FT cells to evaluate how loss of m6A affects luciferase protein levels. The same reporter plasmids are also used in an RNA stability assay with a transcription inhibitor. Although site-specific demethylation of endogenous mRNA would be preferable, it remains technically challenging despite many attempts. Thus, ectopic expression of the mutated target gene remains a widely used and practical alternative. Key features • This protocol assumes that the m6A-seq data and a list of putative target genes modified by m6A are already available. • Highly specialized techniques or equipment are not required. • The luciferase-based assessment in this protocol is widely used in the m6A field as a standard approach.
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