Opposing action of NCoR1 and PGC-1α in mitochondrial redox homeostasis

The ability to respond to fluctuations of reactive oxygen species (ROS) within the cell is a central aspect of mammalian physiology. This dynamic process depends on the coordinated action of transcriptional factors to promote the expression of genes encoding for antioxidant enzymes. Here, we demonstrate that the transcriptional coregulators, PGC-1α and NCoR1, are essential mediators of mitochondrial redox homeostasis in skeletal muscle cells. Our findings reveal an antagonistic role of these coregulators in modulating mitochondrial antioxidant induction through Sod2 transcriptional control. Importantly, the activation of this mechanism by either PGC-1α overexpression or NCoR1 knockdown attenuates mitochondrial ROS levels and prevents cell death caused by lipid overload in skeletal muscle cells. The opposing actions of coactivators and corepressors, therefore, exert a commanding role over cellular antioxidant capacity. [Display omitted] •The transcriptional coregulators PGC-1α and NCoR1 are essential mediators of mitochondrial redox homeostasis.•PGC-1α and NCoR1 act as activator and repressor of Sod2 expression, respectively.•This mechanism is essential for the cellular antioxidant capacity and viability during metabolic stress.