Energy homeostasis in mice is maintained through coordinated activity among hypothalamic nuclei that regulate food intake and thermogenesis. These processes must adapt to the sleep-wake cycle, yet the underlying pathways, cell types, and molecular mechanisms governing their diurnal regulation remain poorly understood. We show that mice lacking the E3 ubiquitin ligase are lean and resistant to diet-induced obesity, owing to reduced food intake and enhanced brown adipose tissue (BAT) thermogenesis. We identify GABAergic neurons in the suprachiasmatic nucleus (SCN)-components of the central circadian clock-as mediators of these effects. Specifically, in RIP-Cre neurons governs daily thermogenic rhythms, while in vasoactive intestinal peptide (VIP)-expressing neurons modulates diurnal feeding behavior. Thus, is a key regulator of diurnal rhythms controlling energy balance.