Suppressive role of OGT-mediated O-GlcNAcylation of BAP1 in retinoic acid signaling

Abstract BRCA1-associated protein 1 (BAP1) has been implicated in diverse biological functions, including tumor suppression. However, its regulation via glycosylation and its role in embryonic stem (ES) cells are poorly defined. BAP1 was recently reported to interact with O-linked N -acetylglucosamine ( O -GlcNAc) transferase (OGT). Here, we confirmed the physical interaction and investigated its functional significance. The O -GlcNAcylation of BAP1, which requires OGT, was examined in vivo and in vitro , and was proven using alloxan, an OGT inhibitor. OGT promoted the BAP1-induced repression of retinoic acid (RA)-induced RA receptor (RAR) activation. The repressive activity of BAP1 was relieved by alloxan but exacerbated by PUGNAc, an O -GlcNAcase (OGA) inhibitor. Finally, we addressed the role of O -GlcNAcylation in the RA-induced differentiation of murine ES cells. Alkaline phosphatase staining revealed the cooperation of RA and alloxan for impairing the pluripotency of ES cells. This cooperation was also observed by measuring the size of embryonic bodies and the expression of Sox2, a pluripotency marker. Overall, our data suggest that OGT-mediated O -GlcNAcylation of BAP1 prefers the maintenance of pluripotency, whereas its inhibition facilitates RA-induced differentiation in ES cells.