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      The hairpin-type tail-anchored SNARE syntaxin 17 targets to autophagosomes for fusion with endosomes/lysosomes.

      Cell
      Amino Acid Motifs, Amino Acid Sequence, Animals, Autophagy, Cell Line, Cytosol, metabolism, Endosomes, Fibroblasts, HEK293 Cells, HeLa Cells, Humans, Lysosomes, Mice, Molecular Sequence Data, Phagosomes, Protein Structure, Tertiary, Qa-SNARE Proteins, chemistry, Sequence Alignment

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          Abstract

          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. Copyright © 2012 Elsevier Inc. All rights reserved.

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