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Mitochondrial synthesis of adenosine triphosphate is essential for eukaryotic life but is dependent on the cooperation of two genomes: nuclear and mitochondrial DNA (mtDNA). mtDNA mutates ~15 times as fast as the nuclear genome, challenging this symbiotic relationship. Mechanisms must have evolved to moderate the impact of mtDNA mutagenesis but are poorly understood. Here, we observed purifying selection of a mouse mtDNA mutation modulated by Ubiquitin-specific peptidase 30 (Usp30) during the maternal-zygotic transition. In vitro, Usp30 inhibition recapitulated these findings by increasing ubiquitin-mediated mitochondrial autophagy (mitophagy). We also found that high mutant burden, or heteroplasmy, impairs the ubiquitin-proteasome system, explaining how mutations can evade quality control to cause disease. Inhibiting USP30 unleashes latent mitophagy, reducing mutant mtDNA in high-heteroplasmy cells. These findings suggest a potential strategy to prevent mitochondrial disorders.

More information Original publication

DOI

10.1126/science.adr5438

Type

Journal article

Publication Date

2025-10-09T00:00:00+00:00

Volume

390

Pages

156 - 163

Total pages

7

Keywords

Animals, Female, Humans, Mice, DNA, Mitochondrial, Heteroplasmy, Mitochondria, Mitochondrial Diseases, Mitophagy, Mutation, Proteasome Endopeptidase Complex, Thiolester Hydrolases, Ubiquitin, Zygote, Mitochondrial Proteins