自噬
卡林
生物
泛素连接酶
细胞生物学
泛素
泛素蛋白连接酶类
蛋白质降解
帕金
蛋白酶体
袋3
生物化学
疾病
细胞凋亡
医学
病理
基因
帕金森病
作者
Guang Lu,Liming Wang,Jing Zhou,Wei Liu,Han‐Ming Shen
标识
DOI:10.1016/j.tcb.2021.01.005
摘要
Autophagy and the ubiquitin-proteasome system (UPS) are two major pathways for protein degradation. The cullin-RING E3 ligases (CRLs) are the largest E3 ligase family and have key biological functions in maintaining protein homeostasis. We provide an updated review of the interactions between CRLs and autophagy, focusing on the regulatory effects of CRLs on the core autophagy machinery that consists of several autophagy-related protein (ATG) complexes and their key upstream signaling pathways. The involvement of such functional interactions in health and disease is also discussed. Understanding the role of CRLs in autophagy is helpful for the development of therapeutic strategies for diseases in which CRLs and autophagy are dysregulated, such as cancer and neurodegenerative conditions.
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