The f subunit of human ATP synthase is essential for normal mitochondrial morphology and permeability transition

The f subunit is localized at the base of the ATP synthase peripheral stalk. Its function in the human enzyme is poorly characterized. Because full disruption of its ATP5J2 gene with the CRISPR-Cas9 strategy in the HAP1 human model has been shown to cause alterations in the amounts of other ATP synthase subunits, here we investigated the role of the f subunit in HeLa cells by regulating its levels through RNA interference. We confirm the role of the f subunit in ATP synthase dimer stability and observe that its downregulation per se does not alter the amounts of the other enzyme subunits or ATP synthase synthetic/hydrolytic activity. We show that downregulation of the f subunit causes abnormal crista organization and decreases permeability transition pore (PTP) size, whereas its re-expression in f subunit knockdown cells rescues mitochondrial morphology and PTP-dependent swelling.

Automated summary

The f subunit plays a role in ATP synthase dimer stability, and its downregulation leads to abnormal cristae organization and decreased permeability transition pore size. Re-expression of the f subunit in knockdown cells rescues mitochondrial morphology and PTP-dependent swelling.