Bernard Amélie, Klionsky Daniel J
a Life Sciences Institute , and the Department of Molecular ; Cellular and Developmental Biology; University of Michigan ; Ann Arbor , MI USA.
Autophagy. 2015 Apr 3;11(4):718-9. doi: 10.1080/15548627.2015.1018503.
To maintain proper cellular homeostasis, the magnitude of autophagy activity has to be finely tuned in response to environmental changes. Many aspects of autophagy regulation have been extensively studied: pathways integrating signals through the master regulators TORC1 and PKA lead to multiple post-translational modifications affecting the functions, protein-protein interactions, and localization of Atg proteins. The expression of several ATG genes increases sharply upon autophagy induction conditions, and defects in ATG gene expression are associated with various diseases, pointing to the importance of transcriptional regulation of autophagy. Yet, how changes in ATG gene expression affect the rate of autophagy is not well characterized, and transcriptional regulators of the autophagy pathway remain largely unknown. To identify such regulators, we analyzed the expression of several ATG genes in a library of DNA-binding protein mutants. This led to the identification of Rph1 as a master transcriptional regulator of autophagy.
为维持适当的细胞内稳态,自噬活性的强度必须根据环境变化进行精确调节。自噬调控的许多方面已得到广泛研究:通过主要调节因子TORC1和PKA整合信号的途径会导致多种翻译后修饰,影响Atg蛋白的功能、蛋白质-蛋白质相互作用及定位。在自噬诱导条件下,几个ATG基因的表达会急剧增加,并且ATG基因表达缺陷与多种疾病相关,这表明自噬转录调控的重要性。然而,ATG基因表达的变化如何影响自噬速率尚未得到很好的表征,自噬途径的转录调节因子在很大程度上仍然未知。为了鉴定此类调节因子,我们在一个DNA结合蛋白突变体文库中分析了几个ATG基因的表达。这导致鉴定出Rph1是自噬的主要转录调节因子。