RBBP5 is an epigenetic regulator of mammalian hepatic 12h oscillator [RNA-seq]

Proteostasis is vital for cellular health, with disruptions leading to pathologies including aging, neurodegeneration and metabolic disorders. Traditionally, proteotoxic stress responses were studied as acute reactions to various noxious factors; however, recent evidence reveals that many stress-response genes exhibit ~12-hour ultradian rhythms under physiological conditions in mammals. These rhythms, driven by an XBP1s-dependent 12h oscillator, are crucial for managing proteostasis. By exploring the chromatin landscape of the murine 12h hepatic oscillator, we identified RBBP5, a key subunit of the COMPASS complex, as an essential epigenetic regulator of proteostasis. RBBP5 is indispensable for regulating both the hepatic 12h oscillator and transcriptional response to acute proteotoxic stress, acting as a co-activator for master proteostasis transcription factor XBP1s. RBBP5 ablation leads to increased sensitivity to proteotoxic stress, chronic inflammation, and hepatic steatosis in mice, along with impaired autophagy and reduced cell survival in vitro. In humans, lower RBBP5 expression is associated with dampened adaptive stress-response gene expression and hepatic steatosis. Our findings establish RBBP5 as a critical regulator of proteostasis, essential for maintaining mammalian organismal health. Overall design: All mice used for biological rhythm study are in C57BL/6J background, male and between 3 and 4 months of age. Rbbp5 (flox/flox); Alb-CRE (-/-) (n=48) and Rbbp5 (flox/flox); Alb-CRE (+/-) mice (n=48) [Rbbp5 (flox/flox); Alb-CRE (-/-) and Rbbp5 (flox/flox); Alb-CRE (+/-) mice were littermates] were first entrained under LD12:12 conditions for 2 weeks before transferred to constant darkness for 24hrs. Mice were then sacrificed via cervical dislocation at a 2h interval for a total of 48 hours under constant darkness. Mice were fed ad libitum during the entire experiment. Liver were taken.