Hung, Y.C., Huang, K.L., Chen, P.L., Li, J.L., Lu, S.H., Chang, J.C., Lin, H.Y., Lo, W.C., Huang, S.Y., Lee, T.T., Lin, T.Y., Imai, Y., Hattori, N., Liu, C.S., Tsai, S.Y., Chen, C.H., Lin, C.H., Chan, C.C. (2021). UQCRC1 engages cytochrome c for neuronal apoptotic cell death.  Cell Rep. 36(12): 109729.

FBrf0251393

Research paper

Human ubiquinol-cytochrome c reductase core protein 1 (UQCRC1) is an evolutionarily conserved core subunit of mitochondrial respiratory chain complex III. We recently identified the disease-associated variants of UQCRC1 from patients with familial parkinsonism, but its function remains unclear. Here we investigate the endogenous function of UQCRC1 in the human neuronal cell line and the Drosophila nervous system. Flies with neuronal knockdown of uqcrc1 exhibit age-dependent parkinsonism-resembling defects, including dopaminergic neuron reduction and locomotor decline, and are ameliorated by UQCRC1 expression. Lethality of uqcrc1-KO is also rescued by neuronally expressing UQCRC1, but not the disease-causing variant, providing a platform to discern the pathogenicity of this mutation. Furthermore, UQCRC1 associates with the apoptosis trigger cytochrome c (cyt-c), and uqcrc1 deficiency increases cyt-c in the cytoplasmic fraction and activates the caspase cascade. Depleting cyt-c or expression of the anti-apoptotic p35 ameliorates uqcrc1-mediated neurodegeneration. Our findings identify a role for UQCRC1 in regulating cyt-c-induced apoptosis.