Visualization and measurement of DNA methyltransferase activity in living cells

Journal article

In this unit, a live-cell assay to measure DNA (cytosine-5) methyltransferase (MTase) activity at the single-cell level is described. This method takes advantage of the irreversible binding of enzymatically active MTases to genomic DNA substituted with the mechanism-based inhibitor 5-aza-2′-deoxycytidine (5-aza-dC). The procedure comprises incorporation of this nucleoside analog into DNA during replication and quantification of the time-dependentMTase immobilization by fluorescence recovery after photobleaching (FRAP). This trapping assay monitors kinetic properties and activity-dependent immobilization ofMTases in their native environment and enables direct comparison of mutations and inhibitors that affect MTase regulation and catalytic activity in single living cells. In addition, a simplified protocol to obtain qualitative information on the activity of either endogenously or exogenously expressed MTases is provided. © 2008 by John Wiley and Sons, Inc.

Authors: Schermelleh, L; Spada, F; Leonhardt, H

• Journal: Current Protocols in Cell Biology
• Issue: SUPPL. 39
• Publication date: 2008-01-01
• DOI: 10.1002/0471143030.cb2212s39
• EISSN: 1934-2616
• ISSN: 1934-2500
• Language: English
• Keywords: DNA (cytosine-5) methyltransferase; Dnmt1; 5-aza-2′-deoxycytidine; Mechanism-based inhibitor; DNA methylation; Trapping assay; Fluorescence recovery after photobleaching