ATG9A控制自噬体生物发生的所有阶段。

Ruheena Javed, Muriel Mari, Einar Trosdal, Thabata Lopes Alberto Duque, Masroor Paddar, Lee Allers, Prithvi Akepati, Michal H Mudd, Fulvio Reggiori, Vojo Deretic
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引用次数: 0

摘要

典型自噬是细胞内降解和循环细胞成分的途径。该途径的一个关键步骤是双膜细胞器的形成,称为自噬体,这是巨噬的一个标志性特征。为方便起见,自噬体的形成可分为起始(X)、扩展(Y)和关闭(Z)三个顺序步骤。ATG9A是一种完整的膜蛋白,以其在X和Y步骤中的作用而闻名。从而组织吞噬体膜的组装和生长。在这里,我们报道了哺乳动物ATG9A在指导最后一步z中的一个以前未被认识到的功能。特别是,ATG9A通过IQGAP1与关键的esrt - iii组分CHMP2A合作,促进自噬体关闭。因此,ATG9A协调自噬体膜生物发生的所有阶段,从吞噬体起始到其关闭。这使得ATG9A成为一种独特的ATG因子,在自噬体生物发生中起着中心枢纽的作用。简称:ATG9A自噬相关9A;羰基氰化间氯苯腙;Co-IP co-immunoprecipitation;ESCRT转运所需的内体分选复合物;EBSS厄尔平衡盐溶液;内质网;HCM高含量显微镜;HT HaloTag;LC-MS/MS液相色谱串联质谱;KO击倒;MPL膜渗透配体;MIL膜非配体;结核分枝杆菌;体外溶剂封闭细胞器限制膜的研究咯tetramethylrhodamine;野生型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ATG9A controls all stages of autophagosome biogenesis.

Canonical autophagy is an intracellular pathway that degrades and recycles cellular components. A key step of this pathway is the formation of double-membraned organelles, known as autophagosomes, an emblematic feature of macroautophagy. For convenience, the formation of autophagosomes can be categorized into sequential steps, initiation (X), expansion (Y) and closure (Z). ATG9A is an integral membrane protein known for its role in the X and Y steps. whereby it organizes phagophore membrane assembly and its growth. Here, we report a previously unappreciated function of mammalian ATG9A in directing the last step Z. In particular, ATG9A partners with the key ESCRT-III component CHMP2A through IQGAP1 to facilitate autophagosome closure. Thus, ATG9A orchestrates all stages of autophagosome membrane biogenesis, from phagophore initiation to its closure. This makes ATG9A a unique ATG factor that works as a central hub in autophagosome biogenesis.Abbreviation: ATG9A autophagy related 9A; CCCP carbonyl cyanide m-chlorophenylhydrazone; Co-IP co-immunoprecipitation; ESCRT endosomal sorting complexes required for transport; EBSS Earle's balanced salt solution; ER endoplasmic reticulum; HCM high-content microscopy; HT HaloTag; LC-MS/MS liquid chromatography-tandem mass spectrometry; KO knockout; MPL membrane permeant ligand; MIL membrane impermeant ligand; Mtb Mycobacterium tuberculosis; SolVit sealing of organellar limiting membranes in vitro; TMR tetramethylrhodamine; WT wild type.

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