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ULK1 磷酸化参与非经典自噬。

Involvement of phosphorylation of ULK1 in alternative autophagy.

机构信息

Department of Pathological Cell Biology, Medical Research Institute, Tokyo Medical and Dental University , Tokyo, Japan.

出版信息

Autophagy. 2020 Aug;16(8):1532-1533. doi: 10.1080/15548627.2020.1776476. Epub 2020 Jun 16.

Abstract

Alternative autophagy is an ATG5 (autophagy related 5)-independent, Golgi membrane-derived form of macroautophagy. ULK1 (unc-51 like kinase 1) is an essential initiator not only for canonical autophagy but also for alternative autophagy. However, the mechanism as to how ULK1 differentially regulates both types of autophagy has remained unclear. Recently, we identified a novel phosphorylation site of ULK1 at Ser746, which is required for alternative autophagy, but not canonical autophagy. We also identify RIPK3 (receptor-interacting serine-threonine kinase 3) as the kinase responsible for genotoxic stress-induced ULK1 S746 phosphorylation. These findings indicate that RIPK3-dependent ULK1 S746 phosphorylation plays a pivotal role in genotoxic stress-induced alternative autophagy.

摘要

选择性自噬是一种 ATG5(自噬相关蛋白 5)非依赖性、高尔基体膜来源的巨自噬形式。ULK1(UNC-51 样激酶 1)不仅是经典自噬的必需起始因子,也是选择性自噬的必需起始因子。然而,ULK1 如何差异调节这两种类型的自噬的机制仍不清楚。最近,我们在 ULK1 的丝氨酸 746 位上发现了一个新的磷酸化位点,该位点对于选择性自噬而非经典自噬是必需的。我们还发现 RIPK3(受体相互作用丝氨酸-苏氨酸激酶 3)是负责基因毒性应激诱导的 ULK1 S746 磷酸化的激酶。这些发现表明,RIPK3 依赖性 ULK1 S746 磷酸化在基因毒性应激诱导的选择性自噬中起着关键作用。

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