Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China.
University of Chinese Academy of Sciences, Beijing, China.
Autophagy. 2020 Apr;16(4):724-734. doi: 10.1080/15548627.2019.1656957. Epub 2019 Aug 26.
PRKN/parkin activation through phosphorylation of its ubiquitin and ubiquitin-like domain by PINK1 is critical in mitophagy induction for eliminating the damaged mitochondria. Deubiquitinating enzymes (DUBs) functionally reversing PRKN ubiquitination are critical in controlling the magnitude of PRKN-mediated mitophagy process. However, potential DUBs that directly target PRKN and antagonize its pro-mitophagy effect remains to be identified and characterized. Here, we demonstrated that USP33/VDU1 is localized at the outer membrane of mitochondria and serves as a PRKN DUB through their interaction. Cellular and assays illustrated that USP33 deubiquitinates PRKN in a DUB activity-dependent manner. USP33 prefers to remove K6, K11, K48 and K63-linked ubiquitin conjugates from PRKN, and deubiquitinates PRKN mainly at Lys435. Mutation of this site leads to a significantly decreased level of K63-, but not K48-linked PRKN ubiquitination. deficiency enhanced both K48- and K63-linked PRKN ubiquitination, but only K63-linked PRKN ubiquitination was significantly increased under mitochondrial depolarization. Further, knockdown increased both PRKN protein stabilization and its translocation to depolarized mitochondria leading to the enhancement of mitophagy. Moreover, silencing protects SH-SY5Y human neuroblastoma cells from the neurotoxin MPTP-induced apoptotic cell death. Our findings convincingly demonstrate that USP33 is a novel PRKN deubiquitinase antagonizing its regulatory roles in mitophagy and SH-SY5Y neuron-like cell survival. Thus, inhibition may represents an attractive new therapeutic strategy for PD patients. CCCP: carbonyl cyanide 3-chlorophenylhydrazone; DUB: deubiquitinating enzymes; MPTP: 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine; OMM: outer mitochondrial membrane; PD: Parkinson disease; PINK1: PTEN induced kinase 1; PRKN/PARK2: parkin RBR E3 ubiquitin protein ligase; ROS: reactive oxygen species; TM: transmembrane; Ub: ubiquitin; UBA1: ubiquitin like modifier activating enzyme 1; UBE2L3/UbcH7: ubiquitin conjugating enzyme E2 L3; USP33: ubiquitin specific peptidase 33; WT: wild type.
PRKN/parkin 通过 PINK1 磷酸化其泛素和泛素样结构域的激活对于诱导消除受损线粒体的线粒体自噬至关重要。去泛素化酶 (DUB) 可通过功能逆转 PRKN 泛素化来控制 PRKN 介导的线粒体自噬过程的幅度。然而,直接针对 PRKN 并拮抗其促线粒体自噬作用的潜在 DUB 仍有待鉴定和表征。在这里,我们证明 USP33/VDU1 位于线粒体的外膜上,并通过相互作用作为 PRKN 的 DUB。细胞和测定表明,USP33 以 DUB 活性依赖性方式去泛素化 PRKN。USP33 更喜欢从 PRKN 上去除 K6、K11、K48 和 K63 连接的泛素缀合物,并且主要在 Lys435 上去泛素化 PRKN。该位点的突变导致 K63-,但不是 K48-连接的 PRKN 泛素化水平显著降低。缺失增强了 K48-和 K63-连接的 PRKN 泛素化,但仅在线粒体去极化下,K63-连接的 PRKN 泛素化显著增加。此外,沉默增加了 PRKN 蛋白的稳定性及其向去极化线粒体的易位,导致线粒体自噬增强。此外,沉默可保护 SH-SY5Y 人神经母细胞瘤细胞免受神经毒素 MPTP 诱导的细胞凋亡死亡。我们的发现令人信服地表明,USP33 是一种新型的 PRKN 去泛素酶,拮抗其在线粒体自噬和 SH-SY5Y 神经元样细胞存活中的调节作用。因此,抑制可能代表 PD 患者有吸引力的新治疗策略。CCCP:羰基氰化物 3-氯苯腙;DUB:去泛素化酶;MPTP:1-甲基-4-苯基-1,2,3,6-四氢吡啶;OMM:外线粒体膜;PD:帕金森病;PINK1:PTEN 诱导激酶 1;PRKN/PARK2:parkin RBR E3 泛素蛋白连接酶;ROS:活性氧;TM:跨膜;Ub:泛素;UBA1:泛素样修饰激活酶 1;UBE2L3/UbcH7:泛素缀合酶 E2 L3;USP33:泛素特异性肽酶 33;WT:野生型。