학술논문

The beginning of the end: how scaffolds nucleate autophagosome biogenesis
Document Type
article
Source
Trends in Cell Biology. 24(1)
Subject
Biochemistry and Cell Biology
Biological Sciences
Underpinning research
1.1 Normal biological development and functioning
Generic health relevance
Adaptor Proteins
Vesicular Transport
Animals
Autophagy
Biological Transport
Humans
Membrane Fusion
Phagosomes
Transport Vesicles
Vacuoles
SNAREs
Atg1
Atg9
Atg13
autophagy
ULK1
membrane bending
vesicle tethering
Medical and Health Sciences
Developmental Biology
Biochemistry and cell biology
Language
Abstract
Autophagy is a conserved mechanism that is essential for cell survival in starvation. Moreover, autophagy maintains cellular health by clearing unneeded or harmful materials from cells. Autophagy proceeds by the engulfment of bulk cytosol and organelles by a cup-shaped double-membrane sheet known as the phagophore. The phagophore closes on itself to form the autophagosome, which delivers its contents to the vacuole or lysosome for degradation. A multiprotein complex comprising the protein kinase autophagy-related protein 1 (Atg1) together with Atg13, Atg17, Atg29, and Atg31 (ULK1, ATG13, FIP200, and ATG101 in humans) has a pivotal role in the earliest steps of this process. This review summarizes recent structural and ultrastructural analysis of the earliest step in autophagosome biogenesis and discusses a model in which the Atg1 complex clusters high-curvature vesicles containing the integral membrane protein Atg9, thereby initiating the phagophore.