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Membrane curvature response in autophagy
被引：12
作者：
Wilz, Livia
[1
]
Fan, Weiliang
[1
]
Zhong, Qing
[1
]
机构：
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Div Biochem & Mol Biol, Berkeley, CA 94720 USA
来源：
关键词：
autophagy;
PtdIns3KC3;
Barkor;
Atg14(L);
BATS;
membrane curvature;
ALPS;
amphipathic alpha helix;
autophagosome;
PtdIns(3)P;
D O I：
10.4161/auto.7.10.16738
中图分类号：
Q2 [细胞生物学];
学科分类号：
071013 [干细胞生物学];
摘要：
Membrane trafficking is key for signal transduction, cargo transportation, and in the case of autophagy, delivering cytoplasmic substrates to the lysosome for degradation. Autophagy requires the formation of a unique double membrane vesicle, the autophagosome. However, the mechanism by which the autophagosome forms is unknown. Our recent study focused on the role of Barkor/Atg14(L) in targeting the autophagy-specific class III phosphatidylinositol-3-kinase (PtdIns3KC3) complex to the early autophagosome has implicated this complex in autophagosome formation. This study found that the BATS domain of Barkor targets the PtdIns3KC3 complex to early autophagic structures and senses highly curved membranes enriched in phosphatidylinositol- 3-phosphate (PtdIns(3) P). Consequently, this study uncovered an exciting new role for the PtdIns3KC3 complex as a potential inducer of autophagosome formation.
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页码：1249 / 1250
页数：2
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