Fig. 5From: The histone and non-histone methyllysine reader activities of the UHRF1 tandem Tudor domain are dispensable for the propagation of aberrant DNA methylation patterning in cancer cellsDNA methylation maintenance is stable despite global disruptions to LIG1K126- and H3K9-associated lysine methylation signaling. a In vitro methylation of recombinant full-length LIG1 by the catalytic domain of G9a (EHMT2). 3H-SAM incorporation was monitored by autoradiography and Coomassie staining is used as a loading control. b Western blots of HCT116 cells treated with either DMSO control or the G9a inhibitor UNC0638 (1 µM) for 48 h. cbb, Coomassie brilliant blue stain of membrane. c Infinium MethylationEPIC BeadChip analysis of HCT116 cells from b. Data are presented as in Fig. 4b, c. d Western blots of HCT116 cells 12 days after incorporation of lentivirus expressing wild-type H3.3 (WT) or H3.3 K9M. e Infinium MethylationEPIC BeadChip analysis of HCT116 cells from d. Data are presented as in Fig. 4b, cBack to article page