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首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Alternative splicing as a molecular switch for Ca2+/calmodulin-dependent facilitation of P/Q-type Ca2+ channels.
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Alternative splicing as a molecular switch for Ca2+/calmodulin-dependent facilitation of P/Q-type Ca2+ channels.

机译:选择性剪接,作为P / Q型Ca2 +通道的Ca2 + /钙调蛋白依赖性促进的分子开关。

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摘要

Alternative splicing of the P/Q-type channel (Ca(V)2.1) promises customization of the computational repertoire of neurons. Here we report that concerted splicing of its main alpha1A subunit, at both an EF-hand-like domain and the channel C terminus, controls the form of Ca2+-dependent facilitation (CDF), an activity-dependent enhancement of channel opening that is triggered by calmodulin. In recombinant channels, such alternative splicing switches CDF among three modes: (1) completely ON completely "OFF," and (3) partially OFF but inducible by elevated global Ca2+ influx. Conversion from modes 1 to 3 represents an unprecedented dimension of control. The physiological function of these variants is likely important, because we find that the distribution of EF-hand splice variants is strikingly heterogeneous in the human brain, varying both across regions and during development.
机译:P / Q型通道(Ca(V)2.1)的替代拼接有望自定义神经元的计算库。在这里,我们报道其主要的alpha1A亚基在EF手状结构域和通道C末端的一致剪接,控制着Ca2 +依赖的促进作用(CDF)的形式,该活性依赖于通道开放的增强而被触发通过钙调蛋白。在重组通道中,此类替代剪接在三种模式之间切换CDF:(1)完全打开,完全“关闭”,以及(3)部分关闭,但可通过增加的整体Ca2 +流入量诱导。从模式1到3的转换代表了前所未有的控制范围。这些变体的生理功能可能很重要,因为我们发现EF手剪接变体在人脑中的分布非常异质,在整个区域和整个发育过程中都不同。

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