Wang Yuhao, Ruan Linhao, Zhu Jin, Zhang Xi, Chih-Chieh Chang Alexander, Tomaszewski Alexis, Li Rong
Center for Cell Dynamics and Department of Cell Biology, Johns Hopkins University School of Medicine; Baltimore, MD 21205, USA.
Biochemistry, Cellular and Molecular Biology (BCMB) Graduate Program, Johns Hopkins University School of Medicine; Baltimore, MD 21287, USA.
bioRxiv. 2023 Aug 31:2023.03.29.534670. doi: 10.1101/2023.03.29.534670.
Mitochondria are the cellular energy hub and central target of metabolic regulation. Mitochondria also facilitate proteostasis through pathways such as the 'mitochondria as guardian in cytosol' (MAGIC) whereby cytosolic misfolded proteins (MPs) are imported into and degraded inside mitochondria. In this study, a genome-wide screen in yeast uncovered that Snf1, the yeast AMP-activated protein kinase (AMPK), inhibits the import of MPs into mitochondria while promoting mitochondrial biogenesis under glucose starvation. We show that this inhibition requires a downstream transcription factor regulating mitochondrial gene expression and is likely to be conferred through substrate competition and mitochondrial import channel selectivity. We further show that Snf1/AMPK activation protects mitochondrial fitness in yeast and human cells under stress induced by MPs such as those associated with neurodegenerative diseases.
线粒体是细胞的能量枢纽和代谢调节的核心靶点。线粒体还通过诸如“线粒体作为胞质溶胶守护者”(MAGIC)等途径促进蛋白质稳态,即胞质中错误折叠的蛋白质(MPs)被导入线粒体并在线粒体内降解。在本研究中,对酵母进行的全基因组筛选发现,酵母中的AMP激活蛋白激酶(AMPK)Snf1在葡萄糖饥饿条件下抑制MPs导入线粒体,同时促进线粒体生物发生。我们发现这种抑制作用需要一个调节线粒体基因表达的下游转录因子,并且可能是通过底物竞争和线粒体导入通道选择性来实现的。我们进一步表明,Snf1/AMPK激活在由与神经退行性疾病相关的MPs等引起的应激条件下保护酵母和人类细胞中的线粒体健康。