Center for Cell Dynamics and Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, United States.
Biochemistry, Cellular and Molecular Biology (BCMB) Graduate Program, Johns Hopkins University School of Medicine, Baltimore, United States.
Elife. 2024 Jun 20;12:RP87518. doi: 10.7554/eLife.87518.
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 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中心和代谢调节的核心靶点。线粒体还通过“细胞质中线粒体作为守护者”(MAGIC)等途径促进蛋白质稳态,即细胞质中错误折叠的蛋白质(MPs)被导入并在线粒体内部降解。在这项研究中,通过全基因组筛选发现,酵母 AMP 激活蛋白激酶(AMPK)Snf1 抑制 MPs 向线粒体的导入,同时在葡萄糖饥饿时促进线粒体生物发生。我们表明,这种抑制需要一个下游转录因子来调节线粒体基因表达,并且可能通过底物竞争和线粒体导入通道选择性来实现。我们进一步表明,Snf1/AMPK 的激活可以保护酵母和人类细胞在 MPs (如与神经退行性疾病相关的 MPs)诱导的应激下的线粒体功能。