4.5 Review

Autophagosomes are formed at a distinct cellular structure

Journal

CURRENT OPINION IN CELL BIOLOGY
Volume 65, Issue -, Pages 50-57

Publisher

CURRENT BIOLOGY LTD
DOI: 10.1016/j.ceb.2020.02.012

Keywords

ATG1; ATG2; ATG5; ATG12; ATG13; ATG16; ATG17; ATG18; ATG29; ATG31; VAC8; Autophagosome; Phagophore; Isolation membrane; Autophagosome formation site; Phagophore assembly site; Pre-auto-phagosomal structure; PAS; ER; Vacuole; Autophagy; Lipid transfer; Organelle contact site; Tether; Phase separation; Liquid droplet

Categories

Funding

  1. Vienna Science and Technology Fund (WWTF) [VRG10-001]
  2. FWF Austrian Science Fund [P25522-B20, P28113-B28, W1261]
  3. European Research Council (ERC) under the European Union's Horizon 2020 research and innovation program [769065]
  4. European Union's Horizon 2020 research and innovation program [765912]
  5. Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) [403222702-SFB 1381, 259130777-SFB 1177]
  6. EMBO Young Investigator Program

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Autophagy is characterized by the formation of double-membrane vesicles called autophagosomes, which deliver bulk cytoplasmic material to the lytic compartment of the cell for degradation. Autophagosome formation is initiated by assembly and recruitment of the core autophagy machinery to distinct cellular sites, referred to as phagophore assembly sites (PAS) in yeast or autophagosome formation sites in other organisms. A large number of autophagy proteins involved in the formation of autophagosomes has been identified; however, how the individual components of the PAS are assembled and how they function to generate autophagosomes remains a fundamental question. Here, we highlight recent studies that provide molecular insights into PAS organization and the role of the endoplasmic reticulum and the vacuole in autophagosome formation.

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