Tseng-Crank J, Foster C D, Krause J D, Mertz R, Godinot N, DiChiara T J, Reinhart P H
Glaxo Research Institute, Research Triangle Park, North Carolina 27709.
Neuron. 1994 Dec;13(6):1315-30. doi: 10.1016/0896-6273(94)90418-9.
We have cloned and expressed nine Ca(2+)-activated K+ channel isoforms from human brain. The open reading frames encode proteins ranging from 1154 to 1195 amino acids, and all possess significant identity with the slowpoke gene products in Drosophila and mouse. All isoforms are generated by alternative RNA splicing of a single gene on chromosome 10 at band q22.3 (hslo). RNA splicing occurs at four sites located in the carboxy-terminal portion of the protein and gives rise to at least nine ion channel constructs (hbr1-hbr9). hslo mRNA is expressed abundantly in human brain, and individual isoforms show unique expression patterns. Expression of hslo mRNA in Xenopus oocytes produces robust voltage and Ca(2+)-activated K+ currents. Splice variants differ significantly in their Ca2+ sensitivity, suggesting a broad functional role for these channels in the regulation of neuronal excitability.
我们已经从人类大脑中克隆并表达了九种钙激活钾通道亚型。开放阅读框编码的蛋白质长度在1154至1195个氨基酸之间,并且所有亚型都与果蝇和小鼠中的慢poke基因产物具有显著的同源性。所有亚型都是由位于10号染色体q22.3带(hslo)上的单个基因通过可变RNA剪接产生的。RNA剪接发生在蛋白质羧基末端部分的四个位点,产生了至少九种离子通道构建体(hbr1 - hbr9)。hslo mRNA在人类大脑中大量表达,并且各个亚型表现出独特的表达模式。在非洲爪蟾卵母细胞中表达hslo mRNA会产生强大的电压和钙激活钾电流。剪接变体在其钙敏感性方面存在显著差异,这表明这些通道在调节神经元兴奋性方面具有广泛的功能作用。