Department of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Department of Biochemistry, School of Medicine, Zhejiang University, Hangzhou, China.
Trends Cell Biol. 2021 Jun;31(6):432-444. doi: 10.1016/j.tcb.2021.01.005. Epub 2021 Feb 8.
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.
自噬和泛素-蛋白酶体系统(UPS)是两种主要的蛋白质降解途径。Cullin-RING E3 连接酶(CRLs)是最大的 E3 连接酶家族,在维持蛋白质内稳态方面具有关键的生物学功能。我们提供了一个关于 CRLs 与自噬之间相互作用的最新综述,重点介绍了 CRLs 对由几个自噬相关蛋白(ATG)复合物及其关键上游信号通路组成的核心自噬机制的调节作用。还讨论了这种功能相互作用在健康和疾病中的参与。了解 CRLs 在自噬中的作用有助于开发针对 CRLs 和自噬失调的疾病(如癌症和神经退行性疾病)的治疗策略。