Thousands of cellular mRNAs contain the methyl modification m6A, which plays critical roles in mRNA processing and gene expression. We developed GEMS, a genetically encoded m6A sensor that provides a simple readout for m6A methylation in living cells and offers a platform for achieving m6A-coupled effector protein expression.
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References
Flamand, M. F. et al. The proteins of mRNA modification: writers, readers, and erasers. Annu. Rev. Biochem. 92, 145–173 (2023). This review discusses the function and regulation of m6A and its links to physiology and disease.
Owens, M. C. et al. Recent technical advances in the study of nucleic acid modifications. Mol. Cell 81, 4116–4136 (2021). This review describes methods for detecting m6A and other RNA modifications.
Meyer, K. D. DART-seq: an antibody-free method for global m6A detection. Nat. Methods 16, 1275–1280 (2019). This paper describes the DART-seq method for transcriptome-wide m6A mapping.
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This is a summary of: Marayati, B. F., Thompson, M. G., Holley, C. L., Horner, S. M. & Meyer, K. D. Programmable protein expression using a genetically encoded m6A sensor. Nat. Biotechnol. https://doi.org/10.1038/s41587-023-01978-3 (2024).
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GEMS enables mRNA m6A methylation sensing in living cells and m6A-coupled protein delivery. Nat Biotechnol (2024). https://doi.org/10.1038/s41587-023-01997-0
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DOI: https://doi.org/10.1038/s41587-023-01997-0