Fig. 3
From: Live-cell single-molecule dynamics of PcG proteins imposed by the DIPG H3.3K27M mutation

Eed and Suz12 are required for the stability of Ezh2 on chromatin, but have different effects on its target search process. a Schematic representation of Ezh2. The N-terminus of Ezh2 interacts with Eed. The SANT2 domain (red rectangle) interacts with Suz12. The C-terminus of Ezh2 is the catalytic lobe, including cysteine-rich domain (CXC, yellow rectangle) and SET domain (green rectangle) that is the catalytic domain of Ezh2. b Cumulative distribution of displacements for HaloTag-Ezh2 replicated from Fig. 1, for HaloTag-Ezh2 (N = 64 cells, n = 11437 displacements) in Eed−/− mES cells, and for HaloTag-Ezh2ΔSANT2(N = 71 cells, n = 5981 displacements) in wild-type mES cells. The cumulative distributions were fitted with three populations. Fitted parameters are shown in Supplementary Table 3. c Fraction of the chromatin-bound population (F1) obtained from Fig. 3b. Results are means ± SD. d Survival probability distribution of the dwell times for HaloTag-Ezh2 replicated from Fig. 2, for HaloTag-Ezh2 (N = 93 cells, n = 2339 trajectories) in Eed−/− mES cells, and for HaloTag-Ezh2ΔSANT2 (N = 85 cells, n = 2728 trajectories) in wild-type mES cells. The distributions were fitted with a two-component exponential decay model. Fitted parameters are shown in Supplementary Table 4. e–g Fraction (e), residence time (f), and search time (g) of the long-lived population (F1sb) for HaloTag-Ezh2 replicated from Fig. 2, for HaloTag-Ezh2 in Eed−/− mES cells, and for HaloTag-Ezh2ΔSANT2 in wild-type mES cells. Results are means ± SD from three biological replicates