Regulation of DNMT1 Stability through Set7-Mediated Lysine Methylation in Mammalian Cells

Inheritance of epigenetic information encoded by cytosine DNA methylation patterns is crucial for mammalian cell survival, in large part through the activity of the maintenance DNA methyltransferase (DNMT1). Here, we show that SET7, a known histone methyltransferase, is involved in the regulation of protein stability of DNMTL SET7 co loca lizes and directly interacts with DNMT1 and specifically monomethylates Lys-142 of DNMTL Methylated DNMT1 peaks during the S and G 2 phases of the cell cycle and is prone to proteasome-mediated degradation. Overexpression of SET7 leads to decreased DNMT1 levels, and siRNA-mediated knockdown of SET7 stabilizes DNMTL These results demonstrate that signaling through SET7 represents a means of DNMT1 enzyme turnover.