The Hairpin-type Tail-Anchored SNARE Syntaxin 17 Targets to Autophagosomes for Fusion with Endosomes/Lysosomes

被引:1012
作者
Itakura, Eisuke [1 ]
Kishi-Itakura, Chieko [1 ]
Mizushima, Noboru [1 ]
机构
[1] Tokyo Med & Dent Univ, Dept Physiol & Cell Biol, Tokyo 1138519, Japan
基金
日本学术振兴会;
关键词
ENDOPLASMIC-RETICULUM; MEMBRANE-PROTEINS; MAMMALIAN-CELLS; ATG PROTEINS; HOMOLOG; SYSTEM; TRAFFICKING; BIOGENESIS; STARVATION; TRANSPORT;
D O I
10.1016/j.cell.2012.11.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The lysosome is a degradative organelle, and its fusion with other organelles is strictly regulated. In contrast to fusion with the late endosome, the mechanisms underlying autophagosome-lysosome fusion remain unknown. Here, we identify syntaxin 17 (Stx17) as the autophagosomal SNARE required for fusion with the endosome/lysosome. Stx17 localizes to the outer membrane of completed autophagosomes but not to the isolation membrane (unclosed intermediate structures); for this reason, the lysosome does not fuse with the isolation membrane. Stx17 interacts with SNAP-29 and the endosomal/lysosomal SNARE VAMP8. Depletion of Stx17 causes accumulation of autophagosomes without degradation. Stx17 has a unique C-terminal hairpin structure mediated by two tandem transmembrane domains containing glycine zipper-like motifs, which is essential for its association with the autophagosomal membrane. These findings reveal a mechanism by which the SNARE protein is available to the completed autophagosome.
引用
收藏
页码:1256 / 1269
页数:14
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