Please use this identifier to cite or link to this item: https://doi.org/10.1039/c8sc02163e
Title: A fluorescent methylation-switchable probe for highly sensitive analysis of FTO N6-methyladenosine demethylase activity in cells
Authors: Cheong, A. 
Low, J.J.A.
Lim, A. 
Yen, P.M.
Woon, E.C.Y. 
Issue Date: 2018
Publisher: Royal Society of Chemistry
Citation: Cheong, A., Low, J.J.A., Lim, A., Yen, P.M., Woon, E.C.Y. (2018). A fluorescent methylation-switchable probe for highly sensitive analysis of FTO N6-methyladenosine demethylase activity in cells. Chemical Science 9 (36) : 7174-7185. ScholarBank@NUS Repository. https://doi.org/10.1039/c8sc02163e
Rights: Attribution-NonCommercial 4.0 International
Abstract: N6-Methyladenosine (m6A) is one of the most abundant epigenetic modifications on mRNA. It is dynamically regulated by the m6A demethylases FTO and ALKBH5, which are currently attracting intense medical interest because of their strong association with several human diseases. Despite their clinical significance, the molecular mechanisms of m6A demethylases remain unclear, hence there is tremendous interest in developing analytical tools to facilitate their functional studies, with a longer term view of validating their therapeutic potentials. To date, no method exists which permits the analysis of m6A-demethylase activity in cells. To overcome this challenge, herein, we describe the first example of a fluorescent m6A-switchable oligonucleotide probe, which enables the direct detection of FTO demethylase activity both in vitro and in living cells. The m6A probe provides a simple, yet powerful visual tool for highly sensitive detection of demethylase activity. Through the use of m6A-probe, we were able to achieve real-time imaging and single-cell flow cytometry analyses of FTO activity in HepG2 cells. We also successfully applied the probe to monitor dynamic changes in FTO activity and m6A methylation levels during 3T3-L1 pre-adipocyte differentiation. The strategy outlined here is highly versatile and may, in principle, be adapted to the study of a range of RNA demethylases and, more widely, other RNA modifying enzymes. To the best of our knowledge, the present study represents not only the first assay for monitoring FTO activity in living cells, but also a new strategy for sensing m6A methylation dynamics. © The Royal Society of Chemistry.
Source Title: Chemical Science
URI: https://scholarbank.nus.edu.sg/handle/10635/213292
ISSN: 2041-6520
DOI: 10.1039/c8sc02163e
Rights: Attribution-NonCommercial 4.0 International
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