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核呼吸因子 1 正向调控人 PINK1 和 Parkin 基因的表达。

Positive regulation of human PINK1 and Parkin gene expression by nuclear respiratory factor 1.

机构信息

Institute of Special Environmental Medicine, Nantong University, Nantong 226019, China.

Institute of Special Environmental Medicine, Nantong University, Nantong 226019, China.

出版信息

Mitochondrion. 2020 Mar;51:22-29. doi: 10.1016/j.mito.2019.12.002. Epub 2019 Dec 18.


DOI:10.1016/j.mito.2019.12.002
PMID:31862413
Abstract

Previous studies have demonstrated that two Parkinson'sdisease-associatedgenes PINK1 and Parkin play a key role in mitochondrial quality control. But until now, the transcriptional regulation of these two genes under normal physiological conditions are not well understood. In this study, the transcriptional regulation of PINK1 and Parkin genes by nuclear respiratory factor 1 (NRF-1) and its effect on PINK1/Parkin-mediated mitophagy were studied. The NRF-1 binding sites in the promoter regions of human PINK1 and Parkin genes were analyzed by JASPER software and were confirmed by chromatin immunoprecipitation (ChIP) assay. The transcriptional activities and the expressions of PINK1 and Parkin genes were positively regulated by NRF-1 in HEK293T cells and in SH-SY5Y cells. Furthermore, NRF-1 over-expression (OE) up-regulated the protein level of full-length PINK1 in CCCP-treated cells, indicating the enhanced PINK1/Parkin-mediated mitophagy. When NRF-1 expression was transient orstableknockdown, the CCCP-induced mitophagy was alleviated as characterized by the reduced protein level of full-length PINK1, the declined ratio of LC3 II to LC3 I, and the decreasedratioof Mt-keimafluorescenceintensityexcited at 552 nm to that excited at 488 nm. In conclusion, NRF-1 has a positive regulatory effect on the transcription of PINK1 and Parkin genes, and involves in mitochondrial quality control through regulating PINK1/Parkin-mediated mitophagy.

摘要

先前的研究表明,两种帕金森病相关基因 PINK1 和 Parkin 在线粒体质量控制中发挥着关键作用。但直到现在,这两种基因在正常生理条件下的转录调控还不是很清楚。在这项研究中,研究了核呼吸因子 1(NRF-1)对 PINK1 和 Parkin 基因的转录调控及其对 PINK1/Parkin 介导的线粒体自噬的影响。通过 JASPER 软件分析了人 PINK1 和 Parkin 基因启动子区域的 NRF-1 结合位点,并通过染色质免疫沉淀(ChIP)实验进行了验证。NRF-1 在 HEK293T 细胞和 SH-SY5Y 细胞中正向调节 PINK1 和 Parkin 基因的转录活性和表达。此外,NRF-1 过表达(OE)上调了 CCCP 处理细胞中全长 PINK1 的蛋白水平,表明增强了 PINK1/Parkin 介导的线粒体自噬。当 NRF-1 表达瞬时或稳定敲低时,CCCP 诱导的线粒体自噬减轻,表现为全长 PINK1 的蛋白水平降低、LC3 II 与 LC3 I 的比值降低以及 Mt-keima 荧光强度在 552nm 处激发的比值降低到 488nm 处激发的比值降低。总之,NRF-1 对 PINK1 和 Parkin 基因的转录具有正向调节作用,并通过调节 PINK1/Parkin 介导的线粒体自噬参与线粒体质量控制。

相似文献

[1]
Positive regulation of human PINK1 and Parkin gene expression by nuclear respiratory factor 1.

Mitochondrion. 2020-3

[2]
Intermittent hypoxia preconditioning protects WRL68 cells against oxidative injury: Involvement of the PINK1/Parkin-mediated mitophagy regulated by nuclear respiratory factor 1.

Mitochondrion. 2021-7

[3]
PGAM5 regulates PINK1/Parkin-mediated mitophagy via DRP1 in CCCP-induced mitochondrial dysfunction.

Toxicol Lett. 2018-3-1

[4]
Alleviation of CCCP-induced mitochondrial injury by augmenter of liver regeneration via the PINK1/Parkin pathway-dependent mitophagy.

Exp Cell Res. 2021-12-1

[5]
Peroxiredoxin 6 Is a Crucial Factor in the Initial Step of Mitochondrial Clearance and Is Upstream of the PINK1-Parkin Pathway.

Antioxid Redox Signal. 2016-3-20

[6]
Mitochondrial and lysosomal biogenesis are activated following PINK1/parkin-mediated mitophagy.

J Neurochem. 2016-1

[7]
Nix restores mitophagy and mitochondrial function to protect against PINK1/Parkin-related Parkinson's disease.

Sci Rep. 2017-3-10

[8]
Role of glucose metabolism and ATP in maintaining PINK1 levels during Parkin-mediated mitochondrial damage responses.

J Biol Chem. 2015-1-9

[9]
Parkinson's disease-associated VPS35 mutant reduces mitochondrial membrane potential and impairs PINK1/Parkin-mediated mitophagy.

Transl Neurodegener. 2021-6-15

[10]
FBS/BSA media concentration determines CCCP's ability to depolarize mitochondria and activate PINK1-PRKN mitophagy.

Autophagy. 2019-5-7

引用本文的文献

[1]
Different Expression of Nuclear Respiratory Factor 1 (NRF-1) Gene in COVID-19: An Insight into Disease Severity.

Curr Microbiol. 2025-5-30

[2]
Novel reporter of the PINK1-Parkin mitophagy pathway identifies its damage sensor in the import gate.

bioRxiv. 2025-2-20

[3]
sdRNA-D43 derived from small nucleolar RNA snoRD43 improves chondrocyte senescence and osteoarthritis progression by negatively regulating PINK1/Parkin-mediated mitophagy pathway via dual-targeting NRF1 and WIPI2.

Cell Commun Signal. 2025-2-11

[4]
Glucose-6-phosphate dehydrogenase regulates mitophagy by maintaining PINK1 stability.

Life Metab. 2024-12-13

[5]
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Int J Mol Sci. 2023-12-24

[6]
Wild-type S100A3 and S100A13 restore calcium homeostasis and mitigate mitochondrial dysregulation in pulmonary fibrosis patient-derived cells.

Front Cell Dev Biol. 2023-11-30

[7]
Knockdown of KLF5 ameliorates renal fibrosis in MRL/lpr mice via inhibition of MX1 transcription.

Immun Inflamm Dis. 2023-7

[8]
NRF1-mediated mitochondrial biogenesis antagonizes innate antiviral immunity.

EMBO J. 2023-8-15

[9]
Mitochondrial quality control and its role in osteoporosis.

Front Endocrinol (Lausanne). 2023

[10]
Transcriptional regulation of NRF1 on metabotropic glutamate receptors in a neonatal hypoxic‑ischemic encephalopathy rat model.

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