The Role of the m6A RNA Methyltransferase METTL16 in Gene Expression and SAM Homeostasis

The RNA methylation of adenosine at the N6-position (m(6)A) has attracted significant attention because of its abundance and dynamic nature. It accounts for more than 80% of all RNA modifications present in bacteria and eukaryotes and regulates crucial aspects of RNA biology and gene expression in numerous biological processes. The majority of m(6)A found in mammals is deposited by a multicomponent complex formed between methyltransferase-like (METTL) proteins METTL3 and METTL14. In the last few years, the list of m(6)A writers has grown, resulting in an expansion of our understanding of the importance of m(6)A and the methylation machinery. The characterization of the less familiar family member METTL16 has uncovered a new function of the m(6)A methylation apparatus, namely the fine-tuning of the cellular levels of the major methyl donor S-adenosylmethionine (SAM). METTL16 achieves this by adjusting the levels of the enzyme that synthesizes SAM in direct response to fluctuations in the SAM availability. This review summarizes recent progress made in understanding how METTL16 can sense and relay metabolic information and considers the wider implications. A brief survey highlights similarities and differences between METTL16 and the better-known METTL3/14 complex, followed by a discussion of the target specificity, modes of action and potential roles of METTL16.

Automated summary

The RNA methylation of adenosine at the N6-position (m(6)A) plays a crucial role in RNA biology and gene expression. METTL3 and METTL14 are the main methyltransferases responsible for m(6)A deposition, while METTL16 regulates the cellular levels of the major methyl donor S-adenosylmethionine (SAM). This review summarizes recent progress in understanding the function of METTL16 in sensing and relaying metabolic information and discusses its similarities and differences with the better-known METTL3/14 complex, as well as its target specificity and potential roles.