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STYK1 通过增强自噬特异性 III 类磷酸肌醇 3-激酶复合物 I 的组装来促进自噬。

STYK1 promotes autophagy through enhancing the assembly of autophagy-specific class III phosphatidylinositol 3-kinase complex I.

机构信息

National "111" Center for Cellular Regulation and Molecular Pharmaceutics, Hubei University of Technology , Wuhan, China.

The State Key Laboratory of Virology, College of Life Sciences, Wuhan University , Wuhan, Hubei, China.

出版信息

Autophagy. 2020 Oct;16(10):1786-1806. doi: 10.1080/15548627.2019.1687212. Epub 2019 Nov 7.

Abstract

Macroautophagy/autophagy plays key roles in development, oncogenesis, and cardiovascular and metabolic diseases. Autophagy-specific class III phosphatidylinositol 3-kinase complex I (PtdIns3K-C1) is essential for autophagosome formation. However, the regulation of this complex formation requires further investigation. Here, we discovered that STYK1 (serine/threonine/tyrosine kinase 1), a member of the receptor tyrosine kinases (RTKs) family, is a new upstream regulator of autophagy. We discovered that STYK1 facilitated autophagosome formation in human cells and zebrafish, which was characterized by elevated LC3-II and lowered SQSTM1/p62 levels and increased puncta formation by several marker proteins, such as ATG14, WIPI1, and ZFYVE1. Moreover, we observed that STYK1 directly binds to the PtdIns3K-C1 complex as a homodimer. The binding with this complex was promoted by Tyr191 phosphorylation, by means of which the kinase activity of STYK1 was elevated. We also demonstrated that STYK1 elevated the serine phosphorylation of BECN1, thereby decreasing the interaction between BECN1 and BCL2. Furthermore, we found that STYK1 preferentially facilitated the assembly of the PtdIns3K-C1 complex and was required for PtdIns3K-C1 complex kinase activity. Taken together, our findings provide new insights into autophagy induction and reveal evidence of novel crosstalk between the components of RTK signaling and autophagy. : AICAR: 5-aminoimidazole-4-carboxamide ribonucleotide; AMPK: adenosine 5'-monophosphate (AMP)-activated protein kinase; ATG: autophagy related; ATP: adenosine triphosphate; BCL2: BCL2 apoptosis regulator; BECN1: beclin 1; Bre A: brefeldin A; Co-IP: co-immunoprecipitation; CRISPR: clustered regularly interspaced short palindromic repeats; DAPI: 4',6-diamidino-2-phenylindole; EBSS: Earle's balanced salt solution; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; GFP: green fluorescent protein; GSEA: gene set enrichment analysis; MAP1LC3/LC3, microtubule associated protein 1 light chain 3; MAPK8/JNK1: mitogen-activated protein kinase 8; mRFP: monomeric red fluorescent protein; MTOR: mechanistic target of rapamycin kinase; MTT: 3-(4,5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide; PIK3C3: phosphatidylinositol 3-kinase catalytic subunit type 3; PIK3R4: phosphoinositide-3-kinase regulatory subunit 4; qRT-PCR: quantitative reverse transcription PCR; RACK1: receptor for activated C kinase 1; RUBCN: rubicon autophagy regulator; siRNA: small interfering RNA; SQSTM1: sequestosome 1; STYK1/NOK: serine/threonine/tyrosine kinase 1; TCGA: The Cancer Genome Atlas; Ub: ubiquitin; ULK1: unc-51 like autophagy activating kinase 1; UVRAG: UV radiation resistance associated; WIPI1: WD repeat domain, phosphoinositide interacting 1; ZFYVE1: zinc finger FYVE-type containing 1.

摘要

自噬在发育、肿瘤发生以及心血管和代谢疾病中发挥关键作用。自噬特异性的 III 类磷酸肌醇 3-激酶复合物 I(PtdIns3K-C1)对于自噬体的形成是必不可少的。然而,这种复合物形成的调节需要进一步研究。在这里,我们发现丝氨酸/苏氨酸/酪氨酸激酶 1(STYK1)是受体酪氨酸激酶(RTKs)家族的一个成员,是自噬的一个新的上游调节因子。我们发现 STYK1 在人类细胞和斑马鱼中促进自噬体的形成,其特征是 LC3-II 水平升高,SQSTM1/p62 水平降低,并且几个标记蛋白(如 ATG14、WIPI1 和 ZFYVE1)的斑点形成增加。此外,我们观察到 STYK1 作为同源二聚体直接与 PtdIns3K-C1 复合物结合。这种复合物的结合通过 Tyr191 磷酸化来促进,从而提高了 STYK1 的激酶活性。我们还证明 STYK1 升高了 BECN1 的丝氨酸磷酸化,从而降低了 BECN1 与 BCL2 的相互作用。此外,我们发现 STYK1 优先促进 PtdIns3K-C1 复合物的组装,并且是 PtdIns3K-C1 复合物激酶活性所必需的。总之,我们的研究结果为自噬诱导提供了新的见解,并揭示了 RTK 信号和自噬之间的成分之间存在新的串扰的证据。: AICAR:5-氨基咪唑-4-甲酰胺核糖核苷酸; AMPK:腺苷 5'-单磷酸(AMP)激活的蛋白激酶; ATG:自噬相关; ATP:三磷酸腺苷; BCL2:BCL2 凋亡调节剂; BECN1:beclin 1; Bre A:布雷菲德菌素 A; Co-IP:免疫共沉淀; CRISPR:成簇的规律间隔短回文重复序列; DAPI:4',6-二脒基-2-苯基吲哚; EBSS:Earle 的平衡盐溶液; GAPDH:甘油醛-3-磷酸脱氢酶; GFP:绿色荧光蛋白; GSEA:基因集富集分析; MAP1LC3/LC3,微管相关蛋白 1 轻链 3; MAPK8/JNK1:丝裂原活化蛋白激酶 8; mRFP:单体红色荧光蛋白; MTOR:雷帕霉素的机制靶标激酶; MTT:3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴盐; PIK3C3:磷脂酰肌醇 3-激酶催化亚基 3; PIK3R4:磷酸肌醇 3-激酶调节亚基 4; qRT-PCR:定量逆转录 PCR; RACK1:激活 C 激酶 1 的受体; RUBCN:rubicon 自噬调节剂; siRNA:小干扰 RNA; SQSTM1:自噬体 1; STYK1/NOK:丝氨酸/苏氨酸/酪氨酸激酶 1; TCGA:癌症基因组图谱; Ub:泛素; ULK1:unc-51 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 1; ZFYVE1:锌指 FYVE 型包含 1。

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