A general strategy exploiting m(5)C duplex-remodelling effect for selective detection of RNA and DNA m(5)C methyltransferase activity in cells

RNA:5-methylcytosine (m(5)C) methyltransferases are currently the focus of intense research following a series of high-profile reports documenting their physiological links to several diseases. However, no methods exist which permit the specific analysis of RNA:m(5)C methyltransferases in cells. Herein, we described how a combination of biophysical studies led us to identify distinct duplex-remodelling effects of m(5)C on RNA and DNA duplexes. Specifically, m(5)C induces a C3′-endo to C2′-endo sugar-pucker switch in CpG RNA duplex but triggers a B-to-Z transformation in CpG DNA duplex. Inspired by these different ‘structural signatures’, we developed a m(5)C-sensitive probe which fluoresces spontaneously in response to m(5)C-induced sugar-pucker switch, hence useful for sensing RNA:m(5)C methyltransferase activity. Through the use of this probe, we achieved real-time imaging and flow cytometry analysis of NOP2/Sun RNA methyltransferase 2 (NSUN2) activity in HeLa cells. We further applied the probe to the cell-based screening of NSUN2 inhibitors. The developed strategy could also be adapted for the detection of DNA:m(5)C methyltransferases. This was demonstrated by the development of DNA m(5)C-probe which permits the screening of DNA methyltransferase 3A inhibitors. To our knowledge, this study represents not only the first examples of m(5)C-responsive probes, but also a new strategy for discriminating RNA and DNA m(5)C methyltransferase activity in cells.