Frech G C, VanDongen A M, Schuster G, Brown A M, Joho R H
Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, Texas 77030.
Nature. 1989 Aug 24;340(6235):642-5. doi: 10.1038/340642a0.
Voltage-activated potassium channels play an important part in the control of excitability in nerve and muscle. Different K+ channels are involved in establishing the resting potential, determining the duration of action potentials, modulation of transmitter release, and in rhythmic firing patterns and delayed excitation. Using in vitro transcripts made from a directional complementary DNA library we have isolated, by expression cloning in Xenopus oocytes, a novel K+-channel gene (drk1). Functionally, drk1 encodes channels that are K+ selective and belong to the delayed rectifier class of channels, rather than the A-type class encoded by the Shaker gene of Drosophila. The channels show sigmoidal voltage-dependent activation and do not inactivate within 500 ms. Structurally, drk1 encodes an amino-acid sequence which is more closely related to the Drosophila Shab gene than to the Shaker gene.
电压激活钾通道在神经和肌肉兴奋性的控制中起着重要作用。不同的钾离子通道参与建立静息电位、决定动作电位的持续时间、调节递质释放以及参与节律性放电模式和延迟兴奋。利用从定向互补DNA文库制备的体外转录本,我们通过在非洲爪蟾卵母细胞中进行表达克隆,分离出了一个新的钾通道基因(drk1)。在功能上,drk1编码的通道对钾离子具有选择性,属于延迟整流型通道,而不是由果蝇的Shaker基因编码的A型通道。这些通道表现出S形电压依赖性激活,并且在500毫秒内不会失活。在结构上,drk1编码的氨基酸序列与果蝇的Shab基因的关系比与Shaker基因的关系更为密切。