VCP/p97 UFMylation 能稳定 BECN1 并促进自噬的启动。

Autophagy Pub Date : 2024-09-01 Epub Date: 2024-05-26 DOI:10.1080/15548627.2024.2356488
Zhifeng Wang, Shuhui Xiong, Zhaoyi Wu, Xingde Wang, Yamin Gong, Wei-Guo Zhu, Xingzhi Xu
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引用次数: 0

摘要

大自噬/自噬对细胞质物质的降解和再循环至关重要。这一过程的启动由磷脂酰肌醇-3-激酶(PtdIns3K)复合物决定,而磷脂酰肌醇-3-激酶复合物受因子 BECN1(beclin 1)调控。UFMylation 是一种新型泛素样修饰,已被证明可调节多种细胞活动。然而,UFMylation 在调节自噬中的作用尚未完全阐明。在这里,我们发现 VCP/p97 在 K109 上被 E3 UFL1(UFM1 特异性连接酶 1)UFMylated,这种修饰促进了 BECN1 的稳定和 PtdIns3K 复合物的组装,这表明 VCP/p97 UFMylation 在自噬启动过程中发挥作用。从机理上讲,VCP/p97 UFMylation 通过 ATXN3(ataxin 3)介导的去泛素化稳定了 BECN1。作为 PtdIns3K 复合物的关键成分,稳定的 BECN1 有助于该复合物的组装。重新表达 VCP/p97,而不是 UFMylation 缺陷突变体,可以挽救 VCP/p97 缺失引起的 MAP1LC3B/LC3B 蛋白表达的增加。我们还发现,在多种神经系统疾病和癌症中发现的几种致病性 VCP/p97 突变与 UFMylation 减少有关,因此 VCP/p97 UFMylation 是这些疾病的潜在治疗靶点。
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VCP/p97 UFMylation stabilizes BECN1 and facilitates the initiation of autophagy.

Macroautophagy/autophagy is essential for the degradation and recycling of cytoplasmic materials. The initiation of this process is determined by phosphatidylinositol-3-kinase (PtdIns3K) complex, which is regulated by factor BECN1 (beclin 1). UFMylation is a novel ubiquitin-like modification that has been demonstrated to modulate several cellular activities. However, the role of UFMylation in regulating autophagy has not been fully elucidated. Here, we found that VCP/p97 is UFMylated on K109 by the E3 UFL1 (UFM1 specific ligase 1) and this modification promotes BECN1 stabilization and assembly of the PtdIns3K complex, suggesting a role for VCP/p97 UFMylation in autophagy initiation. Mechanistically, VCP/p97 UFMylation stabilizes BECN1 through ATXN3 (ataxin 3)-mediated deubiquitination. As a key component of the PtdIns3K complex, stabilized BECN1 facilitates assembly of this complex. Re-expression of VCP/p97, but not the UFMylation-defective mutant, rescued the VCP/p97 depletion-induced increase in MAP1LC3B/LC3B protein expression. We also showed that several pathogenic VCP/p97 mutations identified in a variety of neurological disorders and cancers were associated with reduced UFMylation, thus implicating VCP/p97 UFMylation as a potential therapeutic target for these diseases. Abbreviation: ATG14:autophagy related 14; Baf A1:bafilomycin A1;CMT2Y: Charcot-Marie-Toothdisease, axonal, 2Y; CYB5R3: cytochromeb5 reductase 3; DDRGK1: DDRGK domain containing 1; DMEM:Dulbecco'smodified Eagle's medium;ER:endoplasmic reticulum; FBS:fetalbovine serum;FTDALS6:frontotemporaldementia and/or amyotrophic lateral sclerosis 6; IBMPFD1:inclusion bodymyopathy with early-onset Paget disease with or withoutfrontotemporal dementia 1; LC-MS/MS:liquid chromatography tandem mass spectrometry; MAP1LC3B/LC3B:microtubule associated protein 1 light chain 3 beta; MS: massspectrometry; NPLOC4: NPL4 homolog, ubiquitin recognition factor;PIK3C3: phosphatidylinositol 3-kinase catalytic subunit type 3;PIK3R4: phosphoinositide-3-kinase regulatory subunit 4; PtdIns3K:phosphatidylinositol 3-kinase; RPL26: ribosomal protein L26; RPN1:ribophorin I; SQSTM1/p62: sequestosome 1; UBA5: ubiquitin likemodifier activating enzyme 5; UFC1: ubiquitin-fold modifierconjugating enzyme 1; UFD1: ubiquitin recognition factor in ERassociated degradation 1; UFL1: UFM1 specific ligase 1; UFM1:ubiquitin fold modifier 1; UFSP2: UFM1 specific peptidase 2; UVRAG:UV radiation resistance associated; VCP/p97: valosin containingprotein; WT: wild-type.

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