TFEB
自噬
细胞生物学
溶酶体
ATG16L1
生物发生
生物
碱性螺旋-环-螺旋-亮氨酸拉链转录因子
转录因子
激酶
袋3
磷酸化
自噬体
化学
生物化学
基因
DNA结合蛋白
细胞凋亡
酶
作者
Carmine Settembre,Chiara Di Malta,Vinicia Assunta Polito,Moisés Garcı́a-Arencibia,Francesco Vetrini,Serkan Erdin,Serpil Uckac Erdin,Tuong Huynh,Diego L. Medina,Pasqualina Colella,Marco Sardiello,David C. Rubinsztein,Andrea Ballabio
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2011-05-27
卷期号:332 (6036): 1429-1433
被引量:2776
标识
DOI:10.1126/science.1204592
摘要
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.
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