| Literature DB >> 31971848 |
Weijing Yao1, Yixing Li1, Liming Wu2, Choufei Wu3, Yi Zhang4, Jing Liu5, Zhiyong He4, Xiaoyong Wu1, Chenjun Lu1, Liefeng Wang4, Huiming Zhong6, Zhi Hong7, Shiming Xu5, Wei Liu1, Cong Yi1.
Abstract
How energy deprivation induces macroautophagy/autophagy is not fully understood. Here, we show that Atg11, a receptor protein for cargo recognition in selective autophagy, is required for the initiation of glucose starvation-induced autophagy. Upon glucose starvation, Atg11 facilitates the interaction between Snf1 and Atg1, thus is required for Snf1-dependent Atg1 activation. Phagophore assembly site (PAS) formation requires Atg11 via its control of the association of Atg17 with Atg29-Atg31. The binding of Atg11 with Atg9 is crucial for recruiting Atg9 vesicles to the PAS and, thus, glucose starvation-induced autophagy. We propose Atg11 as a key initiation factor controlling multiple key steps in energy deprivation-induced autophagy. Abbreviations: AMPK: AMP-activated protein kinase; Ams1: α-mannosidase; Ape1: aminopeptidase I; Cvt: cytoplasm-to-vacuole targeting; GAPDH: glyceraldehyde 3-phosphate dehydrogenase; GFP: green fluorescent protein; MBP: myelin basic protein; MMS: methanesulfonate; PAS: phagophore assembly site; PNBM: p-nitrobenzyl mesylate; SD-G: glucose starvation medium; SD-N: nitrogen starvation medium; ULK1, unc-51 like autophagy activating kinase 1; WT: wild type.Entities:
Keywords: Atg11; Atg9; PAS; Snf1; glucose starvation-induced autophagy
Year: 2020 PMID: 31971848 PMCID: PMC7751503 DOI: 10.1080/15548627.2020.1719724
Source DB: PubMed Journal: Autophagy ISSN: 1554-8627 Impact factor: 16.016