a Department of Life Sciences , Korea University , Seongbuk-gu, Seoul , Republic of Korea.
b Department of Cancer Biomedical Science , National Cancer Center Graduate School of Cancer Science and Policy , Seongbuk-gu, Seoul , Republic of Korea.
Autophagy. 2018;14(12):2104-2116. doi: 10.1080/15548627.2018.1504716. Epub 2018 Aug 16.
The initiation of macroautophagy/autophagy is tightly regulated by the upstream ULK1 kinase complex, which affects many downstream factors including the PtdIns3K complex. The phosphorylation of the right position at the right time on downstream molecules is governed by proper complex formation. One component of the ULK1 complex, ATG101, known as an accessory protein, is a stabilizer of ATG13 in cells. The WF finger region of ATG101 plays an important role in the recruitment of WIPI1 (WD repeat domain, phosphoinositide interacting protein 1) and ZFYVE1 (zinc finger FYVE-type containing 1). Here, we report that the C-terminal region identified in the structure of the human ATG101-ATG13 complex is responsible for the binding of the PtdIns3K complex. This region adopts a β-strand conformation in free ATG101, but either an α-helix or random coil in our ATG101-ATG13 complex, which protrudes from the core and interacts with other molecules. The C-terminal deletion of ATG101 shows a significant defect in the interaction with PtdIns3K components and subsequently impairs autophagosome formation. This result clearly presents an additional role of ATG101 for bridging the ULK1 and PtdIns3K complexes in the mammalian autophagy process. Abbreviations: ATG: autophagy related; BECN1: beclin 1; GFP: green fluorescent protein; HORMA: Hop1p/Rev7p/MAD2; HsATG13: HORMA domain of ATG13 from Homo sapiens; KO: knockout; MAD2: mitotic arrest deficient 2 like 1; MAP1LC3/LC3: microtubule associated protein 1 light chain 3; PIK3C3/VPS34: phosphatidylinositol 3-kinase catalytic subunit type 3; PIK3R4/VPS15: phosphoinositide-3-kinase regulatory subunit 4; PtdIns3K: phosphatidylinositol 3-kinase; RB1CC1/FIP200: RB1 inducible coiled-coil 1; SAXS: small-angle X-ray scattering; ScAtg13: HORMA domain of Atg13 from Sccharomyces cerevisiae; SEC-SAXS: size-exclusion chromatography with small-angle X-ray scattering; SpAtg13: HORMA domain of Atg13 from Schizosaccharomyces pombe; SQSTM1/p62: sequestosome 1; ULK1: unc51-like autophagy activating kinase 1; UVRAG: UV radiation resistance associated; WIPI1: WD repeat domain: phosphoinositide interacting 1; ZFYVE1/DFCP1: zinc finger FYVE-type containing 1.
自噬的起始受到上游 ULK1 激酶复合物的严格调控,该复合物影响许多下游因子,包括 PtdIns3K 复合物。下游分子在适当的复合物形成条件下,在正确的位置和时间进行磷酸化。ULK1 复合物的一个组成部分 ATG101 作为一种辅助蛋白,是细胞中 ATG13 的稳定剂。ATG101 的 WF 指区域在招募 WIPI1(WD 重复域,磷酸肌醇相互作用蛋白 1)和 ZFYVE1(锌指 FYVE 型包含 1)中发挥重要作用。在这里,我们报告说,在人 ATG101-ATG13 复合物结构中鉴定的 C 末端区域负责与 PtdIns3K 复合物结合。在游离 ATG101 中,该区域采用β-链构象,但在我们的 ATG101-ATG13 复合物中采用α-螺旋或无规卷曲构象,从核心突出并与其他分子相互作用。ATG101 的 C 末端缺失显示与 PtdIns3K 成分的相互作用存在显著缺陷,随后会损害自噬体的形成。该结果清楚地呈现了 ATG101 在哺乳动物自噬过程中桥接 ULK1 和 PtdIns3K 复合物的另一个作用。缩写:ATG:自噬相关;BECN1:beclin 1;GFP:绿色荧光蛋白;HORMA:Hop1p/Rev7p/MAD2;HsATG13:来自人类的 ATG13 的 HORMA 结构域;KO:敲除;MAD2:有丝分裂阻滞缺陷 2 样 1;MAP1LC3/LC3:微管相关蛋白 1 轻链 3;PIK3C3/VPS34:磷脂酰肌醇 3-激酶催化亚基 3;PIK3R4/VPS15:磷酸肌醇-3-激酶调节亚基 4;PtdIns3K:磷脂酰肌醇 3-激酶;RB1CC1/FIP200:RB1 诱导卷曲螺旋 1;SAXS:小角 X 射线散射;ScAtg13:酿酒酵母的 Atg13 的 HORMA 结构域;SEC-SAXS:尺寸排阻与小角 X 射线散射;SpAtg13:裂殖酵母的 Atg13 的 HORMA 结构域;SQSTM1/p62:自噬相关蛋白 1;ULK1:UNC51 样自噬激活激酶 1;UVRAG:紫外线辐射抗性相关;WIPI1:WD 重复域:磷酸肌醇相互作用蛋白 1;ZFYVE1/DFCP1:锌指 FYVE 型包含 1。