Atg8 controls phagophore expansion during autophagosome formation
被引:563
作者:
Xie, Zhiping
论文数: 0引用数: 0
h-index: 0
机构:
Univ Michigan, Inst Life Sci, Ann Arbor, MI 48109 USA
Univ Michigan, Dept Mol Cellular & Dev Biol, Ann Arbor, MI 48109 USAUniv Michigan, Inst Life Sci, Ann Arbor, MI 48109 USA
Xie, Zhiping
[1
,2
]
Nair, Usha
论文数: 0引用数: 0
h-index: 0
机构:
Univ Michigan, Inst Life Sci, Ann Arbor, MI 48109 USA
Univ Michigan, Dept Mol Cellular & Dev Biol, Ann Arbor, MI 48109 USAUniv Michigan, Inst Life Sci, Ann Arbor, MI 48109 USA
Nair, Usha
[1
,2
]
Klionsky, Daniel J.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Michigan, Inst Life Sci, Ann Arbor, MI 48109 USA
Univ Michigan, Dept Mol Cellular & Dev Biol, Ann Arbor, MI 48109 USA
Univ Michigan, Dept Biol Chem, Ann Arbor, MI 48109 USAUniv Michigan, Inst Life Sci, Ann Arbor, MI 48109 USA
Klionsky, Daniel J.
[1
,2
,3
]
机构:
[1] Univ Michigan, Inst Life Sci, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Mol Cellular & Dev Biol, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Biol Chem, Ann Arbor, MI 48109 USA
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.