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泛素系统突变与神经疾病。

Ubiquitin system mutations in neurological diseases.

机构信息

Cell Biology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA; Louis V. Gerstner, Jr. Graduate School of Biomedical Sciences, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

Cell Biology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

出版信息

Trends Biochem Sci. 2024 Oct;49(10):875-887. doi: 10.1016/j.tibs.2024.06.011. Epub 2024 Jul 6.

Abstract

Neuronal ubiquitin balance impacts the fate of countless cellular proteins, and its disruption is associated with various neurological disorders. The ubiquitin system is critical for proper neuronal cell state transitions and the clearance of misfolded or aggregated proteins that threaten cellular integrity. This article reviews the state of and recent advancements in our understanding of the disruptions to components of the ubiquitin system, in particular E3 ligases and deubiquitylases, in neurodevelopmental and neurodegenerative diseases. Specific focus is on enzymes with recent progress in their characterization, including identifying enzyme-substrate pairs, the use of stem cell and animal models, and the development of therapeutics for ubiquitin-related diseases.

摘要

神经元泛素平衡影响无数细胞蛋白的命运,其破坏与各种神经紊乱有关。泛素系统对于适当的神经元细胞状态转换和清除威胁细胞完整性的错误折叠或聚集的蛋白质至关重要。本文综述了泛素系统成分(特别是 E3 连接酶和去泛素化酶)在神经发育和神经退行性疾病中的破坏的现状和最新进展。特别关注的是在其特性鉴定方面有最新进展的酶,包括鉴定酶-底物对、使用干细胞和动物模型,以及开发针对泛素相关疾病的治疗方法。

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The CRL3 ubiquitin ligase-USP15 pathway governs the destruction of neurofilament proteins.CRL3 泛素连接酶-USP15 通路调控神经丝蛋白的降解。
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