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Arc 泛素化在突触可塑性中的作用。

Arc ubiquitination in synaptic plasticity.

机构信息

Neuroscience Institute, Georgia State University, 100 Piedmont Ave., Atlanta, GA 30302, United States.

Biogen, Cambridge, MA 02142, United States.

出版信息

Semin Cell Dev Biol. 2018 May;77:10-16. doi: 10.1016/j.semcdb.2017.09.009. Epub 2017 Sep 7.

Abstract

The activity-regulated cytoskeleton-associated protein (Arc) is a neuron-expressed activity regulated immediate early gene (IEG) product that is essential for memory consolidation and serves as a direct readout for neural activation during learning. Arc contributes to diverse forms of synaptic plasticity mediated by the trafficking of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors. Notably, Arc protein expression abruptly increases and then rapidly decreases following augmented network activity. A large body of work has focused on Arc transcription and translation. Far fewer studies have explored the relevance of Arc protein stability and turnover. Here, we review recent findings on the mechanisms controlling Arc degradation and discuss its contributions to AMPA receptor trafficking and synaptic plasticity.

摘要

活性调节细胞骨架相关蛋白(Arc)是一种神经元表达的活性调节的早期基因(IEG)产物,对于记忆巩固是必不可少的,并且作为学习过程中神经激活的直接读出器。Arc 通过 α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体的运输,有助于多种形式的突触可塑性。值得注意的是,Arc 蛋白表达在增强的网络活动后突然增加,然后迅速减少。大量的工作集中在 Arc 的转录和翻译上。研究 Arc 蛋白稳定性和周转率的相关性的研究则少得多。在这里,我们回顾了控制 Arc 降解的机制的最新发现,并讨论了它对 AMPA 受体运输和突触可塑性的贡献。

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