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Visualization and Quantification of Single-Base mA Methylation. | LitMetric

Visualization and Quantification of Single-Base mA Methylation.

Angew Chem Int Ed Engl

Department of Chemistry, Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology, Tsinghua University, Beijing, 100084, China.

Published: November 2024

N-methyladenosine (mA) has emerged as the most prevalent form of RNA modification found across various RNA classes. The detection and quantification of mA RNA modifications under various physiological conditions are crucial for elucidating disease mechanisms and identifying potential therapeutic targets. However, visualizing intracellular mA modifications at single-base resolution remains a significant challenge. Existing methods based on high-throughput sequencing or in vitro assays are not suitable for in situ mA RNA imaging. In this work, we introduce the TadA8.20-assisted N-methyladenosine RNA imaging at single-base resolution (TARS) method for precise visualization and quantification of both A and mA forms at specific RNA sites within single cells. Validation studies using TARS on MALAT1 lncRNA in HeLa cells and CCND1 mRNA in breast cancer cell lines demonstrated its high specificity and efficiency in mapping and quantifying mA modifications at single-base resolution. TARS represents a novel tool that advances mA RNA modification research by offering accurate and detailed insights into mA modifications at the single-base level.

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Source
http://dx.doi.org/10.1002/anie.202420977DOI Listing

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