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An InCytes from MBC Selection: Atg8 Controls Phagophore Expansion during Autophagosome Formation

机译:从MBC选择中获得InCytes:Atg8在自噬小体形成过程中控制了荧光团的扩增。

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摘要

Autophagy is a potent intracellular degradation process with pivotal roles in health and disease. Atg8, a lipid-conjugated ubiquitin-like protein, is required for the formation of autophagosomes, double-membrane vesicles responsible for the delivery of cytoplasmic material to lysosomes. How and when Atg8 functions in this process, however, is not clear. Here we show that Atg8 controls the expansion of the autophagosome precursor, the phagophore, and give the first real-time, observation-based temporal dissection of the autophagosome formation process. We demonstrate that the amount of Atg8 determines the size of autophagosomes. During autophagosome biogenesis, Atg8 forms an expanding structure and later dissociates from the site of vesicle formation. On the basis of the dynamics of Atg8, we present a multistage model of autophagosome formation. This model provides a foundation for future analyses of the functions and dynamics of known autophagy-related proteins and for screening new genes.
机译:自噬是一种有效的细胞内降解过程,在健康和疾病中起关键作用。 Atg8是脂质缀合的泛素样蛋白,是自噬体(负责将细胞质物质传递至溶酶体的双膜囊泡)形成所必需的。但是,尚不清楚Atg8在此过程中如何以及何时起作用。在这里,我们显示Atg8控制自噬小体前体吞噬细胞的扩增,并给出自噬小体形成过程的第一个基于实时观察的瞬时解剖。我们证明Atg8的数量决定了自噬体的大小。在自噬体生物发生过程中,Atg8形成一个扩展结构,随后从囊泡形成部位解离。基于Atg8的动力学,我们提出了自噬小体形成的多阶段模型。该模型为未来分析已知自噬相关蛋白的功能和动力学以及筛选新基因提供了基础。

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