Telethon Institute of Genetics and Medicine (TIGEM), Via Pietro Castellino 111, 80131 Naples, Italy.
Science. 2011 Jun 17;332(6036):1429-33. doi: 10.1126/science.1204592. Epub 2011 May 26.
Autophagy is a cellular catabolic process that relies on the cooperation of autophagosomes and lysosomes. During starvation, the cell expands both compartments to enhance degradation processes. We found that starvation activates a transcriptional program that controls major steps of the autophagic pathway, including autophagosome formation, autophagosome-lysosome fusion, and substrate degradation. The transcription factor EB (TFEB), a master gene for lysosomal biogenesis, coordinated this program by driving expression of autophagy and lysosomal genes. Nuclear localization and activity of TFEB were regulated by serine phosphorylation mediated by the extracellular signal-regulated kinase 2, whose activity was tuned by the levels of extracellular nutrients. Thus, a mitogen-activated protein kinase-dependent mechanism regulates autophagy by controlling the biogenesis and partnership of two distinct cellular organelles.
自噬是一种依赖于自噬体和溶酶体合作的细胞分解代谢过程。在饥饿时,细胞会扩张这两个隔室以增强降解过程。我们发现,饥饿会激活一个转录程序,该程序控制着自噬途径的主要步骤,包括自噬体的形成、自噬体-溶酶体融合和底物降解。转录因子 EB(TFEB)是溶酶体生物发生的主基因,通过驱动自噬和溶酶体基因的表达来协调这个程序。TFEB 的核定位和活性受细胞外信号调节激酶 2 介导的丝氨酸磷酸化调节,其活性受细胞外营养物质水平的调节。因此,一个丝裂原激活蛋白激酶依赖的机制通过控制两个不同的细胞细胞器的生物发生和伙伴关系来调节自噬。