Yao Yanhua, Tsuchiyama Scott, Yang Ciyu, Bulteau Anne Laure, He Chong, Robison Brett, Tsuchiya Mitsuhiro, Miller Delana, Briones Valeria, Tar Krisztina, Potrero Anahi, Friguet Bertrand, Kennedy Brian K, Schmidt Marion
Department of Biochemistry, Albert Einstein College of Medicine, Bronx, New York, New York, United States of America.
Buck Institute, Novato, California, United States of America.
PLoS Genet. 2015 Jan 28;11(1):e1004968. doi: 10.1371/journal.pgen.1004968. eCollection 2015 Jan.
Elevated proteasome activity extends lifespan in model organisms such as yeast, worms and flies. This pro-longevity effect might be mediated by improved protein homeostasis, as this protease is an integral module of the protein homeostasis network. Proteasomes also regulate cellular processes through temporal and spatial degradation of signaling pathway components. Here we demonstrate that the regulatory function of the proteasome plays an essential role in aging cells and that the beneficial impact of elevated proteasome capacity on lifespan partially originates from deregulation of the AMPK signaling pathway. Proteasome-mediated lifespan extension activity was carbon-source dependent and cells with enhancement proteasome function exhibited increased respiratory activity and oxidative stress response. These findings suggested that the pro-aging impact of proteasome upregulation might be related to changes in the metabolic state through a premature induction of respiration. Deletion of yeast AMPK, SNF1, or its activator SNF4 abrogated proteasome-mediated lifespan extension, supporting this hypothesis as the AMPK pathway regulates metabolism. We found that the premature induction of respiration in cells with increased proteasome activity originates from enhanced turnover of Mig1, an AMPK/Snf1 regulated transcriptional repressor that prevents the induction of genes required for respiration. Increasing proteasome activity also resulted in partial relocation of Mig1 from the nucleus to the mitochondria. Collectively, the results argue for a model in which elevated proteasome activity leads to the uncoupling of Snf1-mediated Mig1 regulation, resulting in a premature activation of respiration and thus the induction of a mitohormetic response, beneficial to lifespan. In addition, we observed incorrect Mig1 localization in two other long-lived yeast aging models: cells that overexpress SIR2 or deleted for the Mig1-regulator HXK2. Finally, compromised proteasome function blocks lifespan extension in both strains. Thus, our findings suggest that proteasomes, Sir2, Snf1 and Hxk2 form an interconnected aging network that controls metabolism through coordinated regulation of Mig1.
蛋白酶体活性升高可延长酵母、蠕虫和果蝇等模式生物的寿命。这种延长寿命的效应可能是由改善的蛋白质稳态介导的,因为这种蛋白酶是蛋白质稳态网络的一个不可或缺的模块。蛋白酶体还通过信号通路成分的时空降解来调节细胞过程。在这里,我们证明蛋白酶体的调节功能在衰老细胞中起着至关重要的作用,并且蛋白酶体能力升高对寿命的有益影响部分源于AMPK信号通路的失调。蛋白酶体介导的寿命延长活性依赖于碳源,蛋白酶体功能增强的细胞表现出呼吸活性和氧化应激反应增加。这些发现表明,蛋白酶体上调的促衰老影响可能与通过过早诱导呼吸导致的代谢状态变化有关。删除酵母AMPK、SNF1或其激活剂SNF4可消除蛋白酶体介导的寿命延长,支持了这一假设,因为AMPK途径调节代谢。我们发现,蛋白酶体活性增加的细胞中呼吸的过早诱导源于Mig1周转率的提高,Mig1是一种由AMPK/Snf1调节的转录抑制因子,可阻止呼吸所需基因的诱导。增加蛋白酶体活性还导致Mig1从细胞核部分重新定位于线粒体。总的来说,这些结果支持了一个模型,即蛋白酶体活性升高导致Snf1介导的Mig1调节解偶联,从而导致呼吸过早激活,进而诱导线粒体应激反应,对寿命有益。此外,我们在另外两个长寿酵母衰老模型中观察到Mig1定位错误:过表达SIR2或缺失Mig1调节因子HXK2的细胞。最后,蛋白酶体功能受损会阻止这两种菌株的寿命延长。因此,我们的研究结果表明,蛋白酶体、Sir2、Snf1和Hxk2形成了一个相互连接的衰老网络,通过对Mig1的协同调节来控制代谢。