The addition of various chemical modifications to RNA introduces an additional layer of complexity to the regulation of gene expression. Among all RNA modifications, N 6 ‐methyladenosine (m 6 A) has earned its status as the most abundant and well‐studied post‐transcriptional modification in mammalian mRNA. Nevertheless, understanding the role of m 6 A in shaping the fate of RNA molecules and its influence on gene expression heavily depends on the development and application of detection technologies. Among all m 6 A detection methods, chemical‐based sequencing methods show unique advantages. Our group recently developed an absolute quantification method named GLORI, which employs nitrite and glyoxal to convert adenosine to inosine efficiently. With its potential to emerge as the gold standard for m 6 A detection, GLORI showcases the promise of nitrite‐based approaches. This review provides a comprehensive overview of m 6 A detection techniques based on deamination or nitrosation, evaluating their strengths and limitations. Furthermore, we offer insights into the future directions of innovative approaches in m 6 A profiling.
No takes yet. Share an insight, caveat, or question.
Shen et al. (2024) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: