Section of Molecular Biology, Division of Biological Sciences, University of California San Diego, La Jolla, CA 92093, USA.
Section of Molecular Biology, Division of Biological Sciences, University of California San Diego, La Jolla, CA 92093, USA.
J Mol Biol. 2020 Jan 3;432(1):104-122. doi: 10.1016/j.jmb.2019.06.017. Epub 2019 Jun 22.
Macroautophagy (referred to hereafter as autophagy) is an intracellular degradation pathway in which the formation of a double-membrane vesicle called the autophagosome is a key event in the transport of multiple cytoplasmic cargo (e.g., proteins, protein aggregates, lipid droplets or organelles) to the vacuole (lysosome in mammals) for degradation and recycling. During this process, autophagosomes are formed de novo by membrane fusion events leading to phagophore formation initiated at the phagophore assembly site. In yeast, Atg11 and Atg17 function as protein scaffolds, essential for selective and non-selective types of autophagy, respectively. While Atg17 functions in non-selective autophagy are well-defined in the literature, less attention is concentrated on recent findings regarding the roles of Atg11 in selective autophagy. Here, we summarize current knowledge about the Atg11 scaffold protein and review recent findings in the context of its role in selective autophagy initiation and autophagosome formation.
自噬(以下简称自噬)是一种细胞内降解途径,其中形成一种称为自噬体的双层膜囊泡是将多种细胞质货物(例如蛋白质、蛋白质聚集体、脂滴或细胞器)运输到液泡(哺乳动物中的溶酶体)进行降解和回收的关键事件。在这个过程中,自噬体通过膜融合事件从头形成,导致在噬泡组装位点起始噬泡的形成。在酵母中,Atg11 和 Atg17 作为蛋白质支架发挥作用,分别对选择性和非选择性自噬至关重要。虽然文献中对 Atg17 在非选择性自噬中的作用已有明确的定义,但对 Atg11 在选择性自噬中的作用的最新发现关注较少。在这里,我们总结了关于 Atg11 支架蛋白的现有知识,并回顾了其在选择性自噬起始和自噬体形成中的作用的最新发现。