Autophagy initiation by ULK complex assembly on ER tubulovesicular regions marked by ATG9 vesicles

被引:234
作者
Karanasios, Eleftherios [1 ]
Walker, Simon A. [1 ]
Okkenhaug, Hanneke [1 ]
Manifava, Maria [1 ]
Hummel, Eric [2 ]
Zimmermann, Hans [2 ]
Ahmed, Qashif [1 ]
Domart, Marie-Charlotte [3 ]
Collinson, Lucy [3 ]
Ktistakis, Nicholas T. [1 ]
机构
[1] Babraham Inst, Signalling Programme, Cambridge CB22 3AT, England
[2] Carl Zeiss Microscopy GmbH, D-81379 Munich, Germany
[3] Francis Crick Inst, London NW1 1AT, England
基金
英国生物技术与生命科学研究理事会;
关键词
ENDOPLASMIC-RETICULUM; EARLY STEPS; PROTEINS; MITOCHONDRIA; BIOGENESIS; PHAGOPHORE; FIP200; GOLGI; YPT1; COMPARTMENT;
D O I
10.1038/ncomms12420
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Autophagosome formation requires sequential translocation of autophagy-specific proteins to membranes enriched in PI3P and connected to the ER. Preceding this, the earliest autophagy-specific structure forming de novo is a small punctum of the ULK1 complex. The provenance of this structure and its mode of formation are unknown. We show that the ULK1 structure emerges from regions, where ATG9 vesicles align with the ER and its formation requires ER exit and coatomer function. Super-resolution microscopy reveals that the ULK1 compartment consists of regularly assembled punctate elements that cluster in progressively larger spherical structures and associates uniquely with the early autophagy machinery. Correlative electron microscopy after live imaging shows tubulovesicular membranes present at the locus of this structure. We propose that the nucleation of autophagosomes occurs in regions, where the ULK1 complex coalesces with ER and the ATG9 compartment.
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页数:17
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