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. 2020 Dec 10;10:576362. doi: 10.3389/fonc.2020.576362

Figure 5.

Figure 5

Acetylation on K135 lysine residue does not alter sub-cellular localization of MeCP2 but influences its binding at gene promoters in MDA-MB-468 cells. (A) Immunofluorescence staining of empty vector (EV), HA-tagged MeCP2 (WT), K135R mutant (HA-K135R), and K135Q mutant (HA-K135Q) cells. Merge of HA-MeCP2 (green) and nuclear staining (blue) proteins is shown as HA/DAPI for each of the cells. Merge of DAPI (blue), HA-MeCP2 (green), and actin (red) is shown as MERGE for each of the cells. (B) Immunofluorescence staining of EV, WT, HA-K135R, and K135Q cells at higher magnification.