Wun Cheuk-Ling, Quan Yingfei, Zhuang Xiaohong
School of Life Sciences, Centre for Cell & Developmental Biology and State Key Laboratory of Agrobiotechnology, The Chinese University of Hong Kong, Hong Kong, China.
Front Plant Sci. 2020 May 28;11:565. doi: 10.3389/fpls.2020.00565. eCollection 2020.
Autophagy is an intracellular degradation process, which is highly conserved in eukaryotes. During this process, unwanted cytosolic constituents are sequestered and delivered into the vacuole/lysosome by a double-membrane organelle known as an autophagosome. The autophagosome initiates from a membrane sac named the phagophore, and after phagophore expansion and closure, the outer membrane fuses with the vacuole/lysosome to release the autophagic body into the vacuole. Membrane sources derived from the endomembrane system (e.g., Endoplasmic Reticulum, Golgi and endosome) have been implicated to contribute to autophagosome in different steps (initiation, expansion or maturation). Therefore, coordination between the autophagy-related (ATG) proteins and membrane tethers from the endomembrane system is required during autophagosome biogenesis. In this review, we will update recent findings with a focus on comparing the selected core ATG complexes and the endomembrane tethering machineries for shaping the autophagosome membrane in yeast, mammal, and plant systems.
自噬是一种细胞内降解过程,在真核生物中高度保守。在此过程中,不需要的胞质成分被隔离,并通过一种称为自噬体的双膜细胞器运输到液泡/溶酶体中。自噬体起源于一个名为吞噬泡的膜囊,在吞噬泡扩张和闭合后,外膜与液泡/溶酶体融合,将自噬体释放到液泡中。来自内膜系统(如内质网、高尔基体和内体)的膜来源被认为在自噬体形成的不同步骤(起始、扩张或成熟)中发挥作用。因此,在自噬体生物发生过程中,自噬相关(ATG)蛋白与内膜系统的膜连接蛋白之间需要协调。在这篇综述中,我们将更新最近的研究结果,重点比较酵母、哺乳动物和植物系统中用于塑造自噬体膜的选定核心ATG复合物和内膜连接机制。