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Atg9 Vesicles Recruit Vesicle-tethering Proteins Trs85 and Ypt1 to the Autophagosome Formation Site

机译:Atg9囊泡招募囊泡束缚蛋白Trs85和Ypt1到自噬小体形成位点。

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摘要

Atg9 is a transmembrane protein that is essential for autophagy. In the budding yeast Saccharomyces cerevisiae, it has recently been revealed that Atg9 exists on cytoplasmic small vesicles termed Atg9 vesicles. To identify the components of Atg9 vesicles, we purified the Atg9 vesicles and subjected them to mass spectrometry. We found that their protein composition was distinct from other organellar membranes and that Atg9 and Atg27 in particular are major components of Atg9 vesicles. In addition to these two components, Trs85, a specific subunit of the transport protein particle III (TRAPPIII) complex, and the Rab GTPase Ypt1 were also identified. Trs85 directly interacts with Atg9, and the Trs85-containing TRAPPIII complex facilitates the association of Ypt1 onto Atg9 vesicles. We also showed that Trs85 and Ypt1 are localized to the preautophagosomal structure in an Atg9-dependent manner. Our data suggest that Atg9 vesicles recruit the TRAPPIII complex and Ypt1 to the preautophagosomal structure. The vesicle-tethering machinery consequently acts in the process of autophagosome formation.
机译:Atg9是自噬必不可少的跨膜蛋白。在发芽的酿酒酵母中,最近发现Atg9存在于被称为Atg9囊泡的细胞质小囊泡上。为了鉴定Atg9囊泡的成分,我们纯化了Atg9囊泡,并对其进行了质谱分析。我们发现,它们的蛋白质组成不同于其他细胞器质膜,特别是Atg9和Atg27是Atg9囊泡的主要成分。除了这两个组件外,还鉴定了Trs85(转运蛋白颗粒III(TRAPPIII)复合物的特定亚基)和Rab GTPase Ypt1。 Trs85直接与Atg9相互作用,并且包含Trs85的TRAPPIII复合物促进Ypt1与Atg9囊泡的缔合。我们还显示,Trs85和Ypt1以Atg9依赖的方式定位于前自噬体结构。我们的数据表明Atg9囊泡招募TRAPPIII复杂和Ypt1到前自噬体结构。囊泡束缚机制因此在自噬体形成过程中起作用。

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