The Beclin 1-VPS34 complex - at the crossroads of autophagy and beyond

被引:615
作者
Funderburk, Sarah F. [1 ,2 ]
Wang, Qing Jun [3 ]
Yue, Zhenyu [1 ,2 ]
机构
[1] Mt Sinai Sch Med, Dept Neurol, New York, NY 10029 USA
[2] Mt Sinai Sch Med, Dept Neurosci, New York, NY 10029 USA
[3] Univ Kentucky, Dept Mol & Cellular Biochem, Coll Med, Lexington, KY 40536 USA
关键词
PHOSPHATIDYLINOSITOL 3-KINASE COMPLEXES; BCL-X-L; SACCHAROMYCES-CEREVISIAE; REGULATES AUTOPHAGY; TUMOR-SUPPRESSOR; 1-DEPENDENT AUTOPHAGY; SIGNALING PATHWAYS; BH3-ONLY PROTEIN; MAMMALIAN-CELLS; UVRAG;
D O I
10.1016/j.tcb.2010.03.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
An increasing body of research on autophagy provides overwhelming evidence for its connection to diverse biological functions and human diseases. Beclin 1, the first mammalian autophagy protein to be described, appears to act as a nexus point between autophagy, endosomal, and perhaps also cell death pathways. Beclin 1 performs these roles as part of a core complex that contains vacuolar sorting protein 34 (VPS34), a class III phosphatidylinositol-3 kinase. The precise mechanism of Beclin 1-mediated regulation of these cellular functions is unclear, but substantial progress has recently been made in identifying new players and their functions in Beclin 1-VSP34 complexes. Here we review emerging studies that are beginning to unveil the physiological functions of Beclin 1-VPS34 in the central control of autophagic activity and other trafficking events through the formation of distinct Beclin 1-VPS34 protein complexes.
引用
收藏
页码:355 / 362
页数:8
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