| Literature DB >> 28306502 |
Xiawei Cheng1, Xiuling Ma1, Xianming Ding1, Lin Li2, Xiao Jiang1, Zhirong Shen2, She Chen2, Wei Liu3, Weihua Gong4, Qiming Sun5.
Abstract
Class III PI3-kinase (PI3KC3) is essential for autophagy initiation, but whether PI3KC3 participates in other steps of autophagy remains unknown. The HOPS complex mediates the fusion of intracellular vesicles to lysosome, but how HOPS specifically tethers autophagosome to lysosome remains elusive. Here, we report Pacer (protein associated with UVRAG as autophagy enhancer) as a regulator of autophagy. Pacer localizes to autophagic structures and positively regulates autophagosome maturation. Mechanistically, Pacer antagonizes Rubicon to stimulate Vps34 kinase activity. Next, Pacer recruits PI3KC3 and HOPS complexes to the autophagosome for their site-specific activation by anchoring to the autophagosomal SNARE Stx17. Furthermore, Pacer is crucial for the degradation of hepatic lipid droplets, the suppression of Salmonella infection, and the clearance of protein aggregates. These results not only identify Pacer as a crucial multifunctional enhancer in autophagy but also uncover both the involvement of PI3KC3 and the mediators of HOPS's specific tethering activity in autophagosome maturation.Entities:
Keywords: Beclin1; HOPS; PI3KC3; Pacer; Rubicon; Stx-17; UVRAG; Vps34
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Year: 2017 PMID: 28306502 DOI: 10.1016/j.molcel.2017.02.010
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970