Metabolic regulation of misfolded protein import into mitochondria

被引:0
|
作者
Wang, Yuhao [1 ,2 ,3 ]
Ruan, Linhao [1 ,2 ]
Zhu, Jin [4 ,5 ]
Zhang, Xi [1 ,2 ]
Chang, Alexander Chih-Chieh [1 ,2 ,6 ]
Tomaszewski, Alexis [1 ,2 ,3 ]
Li, Rong [1 ,2 ,4 ,5 ,6 ]
机构
[1] Johns Hopkins Univ, Ctr Cell Dynam, Sch Med, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Dept Cell Biol, Sch Med, Baltimore, MD 21218 USA
[3] Johns Hopkins Univ, Sch Med, Biochem Cellular & Mol Biol BCMB Grad Program, Baltimore, MD USA
[4] Natl Univ Singapore, Mechanobiol Inst, Singapore, Singapore
[5] Natl Univ Singapore, Dept Biol Sci, Singapore, Singapore
[6] Johns Hopkins Univ, Dept Chem & Biomol Engn, Whiting Sch Engn, Baltimore, MD 21218 USA
来源
ELIFE | 2024年 / 12卷
基金
美国国家卫生研究院;
关键词
mitochondria; proteostasis; metabolism; AMPK; misfolded protein; protein import; MAGIC; Human; S; cerevisiae; HSP70 HOMOLOG SSB; GLUCOSE REPRESSION; KINASE; AMPK; PHOSPHATASE; IDENTIFICATION; PREPROTEINS; REG1-GLC7; AUTOPHAGY; GENES;
D O I
10.7554/eLife.87518
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 Saccharomyces cerevisiae 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.
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页数:28
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