BAP1 inhibits the ER stress gene regulatory network and modulates metabolic stress response

F Dai, H Lee, Y Zhang, L Zhuang… - Proceedings of the …, 2017 - National Acad Sciences
F Dai, H Lee, Y Zhang, L Zhuang, H Yao, Y Xi, ZD Xiao, MJ You, W Li, X Su, B Gan
Proceedings of the National Academy of Sciences, 2017National Acad Sciences
The endoplasmic reticulum (ER) is classically linked to metabolic homeostasis via the
activation of unfolded protein response (UPR), which is instructed by multiple transcriptional
regulatory cascades. BRCA1 associated protein 1 (BAP1) is a tumor suppressor with de-
ubiquitinating enzyme activity and has been implicated in chromatin regulation of gene
expression. Here we show that BAP1 inhibits cell death induced by unresolved metabolic
stress. This prosurvival role of BAP1 depends on its de-ubiquitinating activity and correlates …
The endoplasmic reticulum (ER) is classically linked to metabolic homeostasis via the activation of unfolded protein response (UPR), which is instructed by multiple transcriptional regulatory cascades. BRCA1 associated protein 1 (BAP1) is a tumor suppressor with de-ubiquitinating enzyme activity and has been implicated in chromatin regulation of gene expression. Here we show that BAP1 inhibits cell death induced by unresolved metabolic stress. This prosurvival role of BAP1 depends on its de-ubiquitinating activity and correlates with its ability to dampen the metabolic stress-induced UPR transcriptional network. BAP1 inhibits glucose deprivation-induced reactive oxygen species and ATP depletion, two cellular events contributing to the ER stress-induced cell death. In line with this, Bap1 KO mice are more sensitive to tunicamycin-induced renal damage. Mechanically, we show that BAP1 represses metabolic stress-induced UPR and cell death through activating transcription factor 3 (ATF3) and C/EBP homologous protein (CHOP), and reveal that BAP1 binds to ATF3 and CHOP promoters and inhibits their transcription. Taken together, our results establish a previously unappreciated role of BAP1 in modulating the cellular adaptability to metabolic stress and uncover a pivotal function of BAP1 in the regulation of the ER stress gene-regulatory network. Our study may also provide new conceptual framework for further understanding BAP1 function in cancer.
National Acad Sciences