自噬
ULK1
亚科
生物
细胞内
ATG8型
计算生物学
细胞生物学
遗传学
基因
激酶
蛋白激酶A
细胞凋亡
安普克
作者
Jennifer C Y Chan,Sharon M. Gorski
出处
期刊:Biologia futura
[Springer Nature]
日期:2022-04-29
卷期号:73 (2): 157-169
被引量:3
标识
DOI:10.1007/s42977-022-00119-2
摘要
GABARAPL2 was initially characterized for its involvement in protein transport and membrane fusion events, but has since gained notoriety for its role in autophagy. GABARAPL2 is frequently studied alongside its GABARAP subfamily members, GABARAP and GABARAPL1. Although functional redundancy exists among the subfamily members, a complex network of molecular interactions, physiological processes and pathologies can be primarily related to GABARAPL2. GABARAPL2 has a multifaceted role, ranging from cellular differentiation to intracellular degradation. Much of what we know about GABARAPL2 is gained through identifying its interacting partners—a list that is constantly growing. In this article, we review both the autophagy-dependent and autophagy-independent roles of GABARAPL2, and emphasize their implications for both health and disease.
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