LaPak Kyle M, Saeidi Soma, Bok Ilah, Wamsley Nathan T, Plutzer Isaac B, Bhatt Dhaval P, Luo Jingqin, Ashrafi Ghazaleh, Ben Major M
Department of Cell Biology and Physiology, Washington University, St. Louis, MO 63110, USA.
Division of Public Health Sciences, Department of Surgery, WUSM and Siteman Cancer Center Biostatistics and Qualitative Research Shared Resource, Washington University, St. Louis, MO 63110, USA.
Sci Signal. 2023 Dec 12;16(815):eadi9018. doi: 10.1126/scisignal.adi9018.
The nuclear factor erythroid 2-related factor 2 (NRF2) transcription factor activates cytoprotective and metabolic gene expression in response to various electrophilic stressors. Constitutive NRF2 activity promotes cancer progression, whereas decreased NRF2 function contributes to neurodegenerative diseases. We used proximity proteomic analysis to define protein networks for NRF2 and its family members NRF1, NRF3, and the NRF2 heterodimer MAFG. A functional screen of co-complexed proteins revealed previously uncharacterized regulators of NRF2 transcriptional activity. We found that ZNF746 (also known as PARIS), a zinc finger transcription factor implicated in Parkinson's disease, physically associated with NRF2 and MAFG, resulting in suppression of NRF2-driven transcription. ZNF746 overexpression increased oxidative stress and apoptosis in a neuronal cell model of Parkinson's disease, phenotypes that were reversed by chemical and genetic hyperactivation of NRF2. This study presents a functionally annotated proximity network for NRF2 and suggests a link between ZNF746 overexpression in Parkinson's disease and inhibition of NRF2-driven neuroprotection.
核因子红细胞2相关因子2(NRF2)转录因子可响应各种亲电应激源激活细胞保护和代谢基因表达。NRF2的组成型活性促进癌症进展,而NRF2功能降低则导致神经退行性疾病。我们使用邻近蛋白质组学分析来定义NRF2及其家族成员NRF1、NRF3和NRF2异二聚体MAFG的蛋白质网络。对共复合蛋白的功能筛选揭示了以前未表征的NRF2转录活性调节因子。我们发现,与帕金森病有关的锌指转录因子ZNF746(也称为PARIS)与NRF2和MAFG发生物理相互作用,从而抑制NRF2驱动的转录。在帕金森病的神经元细胞模型中,ZNF746的过表达增加了氧化应激和细胞凋亡,而NRF2的化学和基因超激活可逆转这些表型。本研究展示了一个功能注释的NRF2邻近网络,并提示帕金森病中ZNF746过表达与抑制NRF2驱动的神经保护之间存在联系。