Department of Neurology, Mount Sinai School of Medicine, New York, NY 10029, USA.
Trends Cell Biol. 2010 Jun;20(6):355-62. doi: 10.1016/j.tcb.2010.03.002. Epub 2010 Mar 29.
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.
越来越多的自噬研究提供了大量证据,证明其与多种生物功能和人类疾病有关。Beclin 1 是第一个被描述的哺乳动物自噬蛋白,它似乎作为自噬、内体和可能的细胞死亡途径之间的连接点。Beclin 1 作为包含液泡分选蛋白 34(VPS34)的核心复合物的一部分发挥这些作用,VPS34 是一种 III 类磷酸肌醇 3 激酶。Beclin 1 介导的这些细胞功能的调节的确切机制尚不清楚,但最近在鉴定新的参与者及其在 Beclin 1-VSP34 复合物中的功能方面取得了实质性进展。在这里,我们回顾了一些新兴的研究,这些研究开始揭示 Beclin 1-VPS34 在通过形成不同的 Beclin 1-VPS34 蛋白复合物来中央控制自噬活性和其他运输事件中的生理功能。