deletion mitigates respiratory deficiency caused by mutations in the gene encoding the coenzyme Q chaperone protein Coq10.

Coenzyme Q (Q ) is a vital lipid component of the electron transport chain that functions in cellular energy metabolism and as a membrane antioxidant. In the yeast , deletion mutants are respiratory-incompetent, sensitive to lipid peroxidation stress, and unable to synthesize Q The yeast deletion mutant is also respiratory-deficient and sensitive to lipid peroxidation, yet it continues to produce Q at an impaired rate. Thus, Coq10 is required for the function of Q in respiration and as an antioxidant and is believed to chaperone Q from its site of synthesis to the respiratory complexes. In several fungi, Coq10 is encoded as a fusion polypeptide with Coq11, a recently identified protein of unknown function required for efficient Q biosynthesis. Because "fused" proteins are often involved in similar biochemical pathways, here we examined the putative functional relationship between Coq10 and Coq11 in yeast. We used plate growth and Seahorse assays and LC-MS/MS analysis to show that deletion rescues respiratory deficiency, sensitivity to lipid peroxidation, and decreased Q biosynthesis of the Δ mutant. Additionally, immunoblotting indicated that yeast Δ mutants accumulate increased amounts of certain Coq polypeptides and display a stabilized CoQ synthome. These effects suggest that Coq11 modulates Q biosynthesis and that its absence increases mitochondrial Q content in the ΔΔ double mutant. This augmented mitochondrial Q content counteracts the respiratory deficiency and lipid peroxidation sensitivity phenotypes of the Δ mutant. This study further clarifies the intricate connection between Q biosynthesis, trafficking, and function in mitochondrial metabolism.