粒体自噬
线粒体DNA
生物
遗传学
突变
线粒体
解旋酶
自噬
细胞生物学
突变
突变体
粒线体疾病
核DNA
DNAJA3公司
DNA
人类线粒体遗传学
线粒体融合
非孟德尔遗传
三磷酸腺苷
点突变
表型
线粒体肌病
DNA损伤
遗传(遗传算法)
线粒体脑肌病
核基因
分子生物学
作者
Michele Frison,Brandon S. Lockey,Yu Nie,Zoe Golder,Eleni Theiaspra,Cameron Ryall,Camilla Lyons,Stephen P. Burr,Malwina Prater,Lyuba V. Bozhilova,Angelos Glynos,James B. Stewart,Nick S. Jones,Marcos Roberto Chiaratti,Patrick F. Chinnery
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2025-10-09
卷期号:390 (6769): 156-163
被引量:5
标识
DOI:10.1126/science.adr5438
摘要
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.
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