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Abstract Mitochondrial homeostasis is maintained through complex regulatory mechanisms, including the balance of mitochondrial dynamics involving fusion and fission processes. A central player in this regulation is the ubiquitin–proteasome system (UPS), which controls the degradation of pivotal mitochondrial proteins. In this study, we identified cullin–RING E3 ligase 2 (CRL2) and its substrate receptor, FEM1B, as critical regulators of mitochondrial dynamics.
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