A novel in vitro assay reveals SNARE topology and the role of Ykt6 in autophagosome fusion with vacuoles

被引:72
作者
Gao, Jieqiong [1 ]
Reggiori, Fulvio [2 ]
Ungermann, Christian [1 ,3 ]
机构
[1] Univ Osnabruck, Dept Biol Chem, Biochem Sect, Osnabruck, Germany
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Cell Biol, Groningen, Netherlands
[3] Univ Osnabruck, Ctr Cellular Nanoanalyt Osnabruck CellNanOs, Osnabruck, Germany
基金
瑞士国家科学基金会;
关键词
MEMBRANE-TRANSPORT PATHWAYS; TETHERING COMPLEX; SYNTAXIN; 17; RAB GTPASE; SACCHAROMYCES-CEREVISIAE; PROTEIN PALMITOYLATION; MONITORING AUTOPHAGY; NUCLEOTIDE EXCHANGE; EFFECTOR COMPLEX; HOPS CATALYZES;
D O I
10.1083/jcb.201804039
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Autophagy is a catabolic pathway that delivers intracellular material to the mammalian lysosomes or the yeast and plant vacuoles. The final step in this process is the fusion of autophagosomes with vacuoles, which requires SNARE proteins, the homotypic vacuole fusion and protein sorting tethering complex, the RAB7-like Ypt7 GTPase, and its guanine nucleotide exchange factor, Mon1-Ccz1. Where these different components are located and function during fusion, however, remains to be fully understood. Here, we present a novel in vitro assay to monitor fusion of intact and functional autophagosomes with vacuoles. This process requires ATP, physiological temperature, and the entire fusion machinery to tether and fuse autophagosomes with vacuoles. Importantly, we uncover Ykt6 as the autophagosomal SNARE. Our assay and findings thus provide the tools to dissect autophagosome completion and fusion in a test tube.
引用
收藏
页码:3670 / 3682
页数:13
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