通过C端域的替代拼接来调节NMDA受体酸化
W G Tingley1, K W Roche, A K Thompson
1Department of Neuroscience, Howard Hughes Medical Institute, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Nature
|July 1, 1993
概括
替代性剪接NMDA受体亚单元NR1调节蛋白激酶C (PKC) 酸化. 这种mRNA拼接机制影响着谷氨酸受体的敏感性,并暗示NR1.
科学领域:
- 神经科学是一个神经科学.
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
背景情况:
- NMDA受体对于像突触可塑性这样的大脑功能至关重要.
- 建议对NMDA受体的蛋白质酸化来调节它们的活性.
- NMDA受体子单元NR1由同源子单元组成.
研究的目的:
- 通过蛋白激酶C (PKC) 对NMDA受体亚单元NR1的酸化进行研究.
- 确定替代拼接在NR1酸化中的作用.
- 为了探索NR1C终端域的细胞内定位.
主要方法:
- 在表达重组NR1的细胞中通过PKC检查NR1酸化.
- 在初级皮层神经元培养物中研究了NR1酸化.
- 分析了替代拼接对NR1酸化位点的影响.
主要成果:
- PKC在多个不同的部位化NR1.
- 许多酸化位点位于NR1 C终端域中的替代拼接外子内.
- NR1 mRNA的替代拼接调节了其PKC酸化.
结论:
- mRNA拼接是一种控制谷氨酸受体对酸化敏感性的新机制.
- NR1的C端域位于细胞内.
- 建议的谷氨酸受体的跨膜拓模型可能需要修订.
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