Divergent roles of BECN1 in LC3 lipidation and autophagosomal function

被引:113
作者
He, Ruina [1 ]
Peng, Jingyu [1 ]
Yuan, Pengfei [1 ]
Xu, Fang [2 ]
Wei, Wensheng [1 ]
机构
[1] Peking Univ, State Key Lab Prot & Plant Gene Res, Peking Tsinghua Ctr Life Sci, Biodynam Opt Imaging Ctr BIOPIC,Sch Life Sci, Beijing 100871, Peoples R China
[2] Tsinghua Univ, Peking Univ, Ctr Life Sci,Sch Life Sci, State Key Lab Biomembrane & Membrane Biotechnol, Beijing 100084, Peoples R China
基金
美国国家科学基金会;
关键词
autophagy; autophagosome; BECN1; LC3; PtdIns3K; BECLIN 1-INDEPENDENT AUTOPHAGY; 3-KINASE COMPLEX; ATG PROTEINS; PATHWAY; RUBICON; PHOSPHORYLATION; TUMORIGENESIS; ASSOCIATION; INHIBITION; SNON/SKIL;
D O I
10.1080/15548627.2015.1034404
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
BECN1/Beclin 1 is regarded as a critical component in the class III phosphatidylinositol 3-kinase (PtdIns3K) complex to trigger autophagy in mammalian cells. Despite its significant role in a number of cellular and physiological processes, the exact function of BECN1 in autophagy remains controversial. Here we created a BECN1 knockout human cell line using the TALEN technique. Surprisingly, the complete loss of BECN1 had little effect on LC3 (MAP1LC3B/LC3B) lipidation, and LC3B puncta resembling autophagosomes by fluorescence microscopy were still evident albeit significantly smaller than those in the wild-type cells. Electron microscopy (EM) analysis revealed that BECN1 deficiency led to malformed autophagosome-like structures containing multiple layers of membranes under amino acid starvation. We further confirmed that the PtdIns3K complex activity and autophagy flux were disrupted in BECN1(-/-) cells. Our results demonstrate the essential role of BECN1 in the functional formation of autophagosomes, but not in LC3B lipidation.
引用
收藏
页码:740 / 747
页数:8
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