Brandon Chen, Drew Stark, Pankaj Jadhav, Theophilus Nguyen, Benjamin Halligan, Nicholas J. Rossiter, Nicole Sindoni, Myungsun Shin, Joao A. Paulo, Matthew Chang, Imhoi Koo, С. В. Кошкин, Sanjana Eyunni, Paolo Ronchi, Michelle T. Paulsen, Harrison S. Greenbaum, Mariana T. Ruckert, Pietro Morlacchi, David A. Hanna, Jason Lin, Rachel M. Guerra, Tao Liu, David J. Pagliarini, Ruma Banerjee, Abhijit Parolia, Mats Ljungman, Andrew D. Patterson, Joseph D. Mancias, Shyamal Mosalaganti, Jonathan Z. Sexton, Tito Calí, Costas A. Lyssiotis, Yatrik M. Shah
Inter-organellar communication is critical for cellular metabolism. One of the most abundant inter-organellar interactions occurs at the endoplasmic reticulum and mitochondria contact sites (ERMCSs). However, an understanding of the mechanisms governing ERMCS regulation and their roles in cellular metabolism is limited by a lack of tools that permit temporal induction and reversal. Through screening approaches, we identified fedratinib, an FDA-approved drug that dramatically increases ERMCS abundance by inhibiting the epigenetic modifier BRD4. Fedratinib rapidly and reversibly modulates mitochondrial and ER morphology, induces a distinct ER-mitochondria envelopment structure, and alters metabolic homeostasis. Moreover, ERMCS modulation depends on mitochondrial electron transport chain complex III function. Comparison of fedratinib activity to other reported inducers of ERMCSs revealed common mechanisms of induction and function, providing clarity to a growing body of experimental observations. In total, our results uncovered a novel epigenetic signaling pathway and an endogenous metabolic regulator that connects ERMCSs and cellular metabolism.