自噬
贝肯1
自噬体
细胞生物学
生物
生物发生
ATG16L1
磷脂酰肌醇
激酶
细胞器生物发生
粒体自噬
袋3
ULK1
泛素
蛋白质稳态
溶酶体
ATG5型
蛋白质降解
ATG8型
未折叠蛋白反应
蛋白激酶A
蛋白酶体
mTORC1型
泛素连接酶
自噬相关蛋白13
ATG12
液泡
生物化学
基因
细胞凋亡
安普克
作者
Lidia Wróbel,Sandra Malmgren Hill,Avraham Ashkenazi,David C. Rubinsztein
出处
期刊:Autophagy
[Informa]
日期:2021-03-09
卷期号:17 (4): 1052-1053
被引量:2
标识
DOI:10.1080/15548627.2021.1898742
摘要
VCP/p97 is an essential multifunctional protein implicated in a plethora of intracellular quality control systems, and abnormal function of VCP is the underlying cause of several neurodegenerative disorders. We reported that VCP regulates the levels of the macroautophagy/autophagy-inducing lipid phosphatidylinositol-3-phosphate (PtdIns3P) by modulating the activity of the BECN1 (beclin 1)-containing phosphatidylinositol 3-kinase (PtdIns3K) complex. VCP stimulates the deubiquitinase activity of ATXN3 (ataxin 3) to stabilize BECN1 protein levels and also interacts with and promotes the assembly and kinase activity of the PtdIns3K complex. Acute inhibition of VCP activity impairs autophagy induction, demonstrated by a diminished PtdIns3P production and decreased recruitment of early autophagy markers WIPI2 and ATG16L1. Thus, VCP promotes autophagosome biogenesis, in addition to its previously described role in autophagosome maturation.
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