干扰FUS的相位行为是肌缩性侧面硬化症中聚PR诱导的DNA损伤的基础
Yixin Wang1, Liu Liu2, Hui Chen1
1Department of Pharmacology, Laboratory of Molecular Neuropathology, Jiangsu Key Laboratory of Neuropsychiatric Diseases and College of Pharmaceutical Sciences, Soochow University, Suzhou, Jiangsu 215123, China.
Human molecular genetics
|September 27, 2023
概括
聚PR是C9ORF72基因扩展的有毒蛋白质,在ALS和FTD中引起严重的DNA损伤. FUS蛋白与聚PR的相互作用减轻了这种损伤,这表明了治疗点.
科学领域:
- 神经科学是一个神经科学.
- 遗传学 遗传学 是一个
- 分子生物学分子生物学
背景情况:
- C9ORF72基因扩展导致ALS和FTD.
- 聚PR蛋白具有高度毒性,与神经退行有关.
- 聚PR毒性的机制尚未完全理解.
研究的目的:
- 研究聚PR诱导的细胞毒性的分子机制.
- 确定DNA损伤在聚PR毒性的作用.
- 探索聚PR和FUS在DNA修复中的相互作用.
主要方法:
- 细胞培养和初级神经元模型.
- 聚PR表达的转基因小鼠模型.
- 在体外和体内相互作用研究 (co-IP,相分离试验).
- DNA损伤测定 (微辐射,彗星测定).
主要成果:
- 在各种模型中,聚PR过度表达会诱导显著的DNA损伤.
- 聚PR与FUS.的相分离相互作用并改变相分离.
- 聚PR 损害了FUS和XRCC1对DNA损伤部位的招募.
- 过度表达FUS可以减少DNA损伤和聚PR诱导的细胞死亡.
结论:
- 聚PR会导致严重的DNA损伤,导致ALS/FTD的发病.
- 通过参与DNA修复,FUS对聚PR毒性起着保护作用.
- 针对多-PR-FUS相互作用可能为C9ORF72相关疾病提供治疗策略.
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