Duzhyy Dmytro E, Sakai Yoshihisa, Sokolowski Bernd H A
Otology Laboratory, Department of Otolaryngology, University of South Florida, MDC83, 12901 Bruce B. Downs Blvd., Tampa, FL 33612, USA.
Brain Res Mol Brain Res. 2004 Feb 5;121(1-2):70-85. doi: 10.1016/j.molbrainres.2003.10.022.
Signal coding by the receptor and neuronal cells of the auditory system involves various ion channels that modulate a sound stimulus. The genes that encode a number of these ion channels and their accessory subunits are presently unknown for channels found in the sensory epithelium and cochlear nerve. Among these genes are those that encode delayed rectifier and transient type potassium channels found in both the sensory cells and the ganglion. Here, we report the cloning and developmental expression of Shaker family members that include cKv1.2, cKv1.3, cKv1.5, and the Shaker-related cGMP-gated potassium channel cKCNA10. Clones were obtained by screening a chicken embryonic cochlea cDNA library using, as a probe, a mixture of two DNA fragments of cKv1.2 and cKv1.3 obtained by the reverse transcription polymerase chain reaction (RT-PCR). Sequence analysis revealed chicken homologues of Kv1.2, Kv1.3, Kv1.5 and cGMP-gated potassium channels with a deduced amino acid homology of 96-98%, 82-84%, 67-71% and 67-79% to correspondent mammalian homologues. During development of chicken inner ear, RT-PCR studies show expression of cKv1.2, cKv1.3 and cKv1.5 as early as Embryonic Day (ED) 3, while cKCNA10 was detected at low levels beginning on ED6 and was highly expressed by ED9. Additionally, analysis of expression in different parts of the cochlea showed that these genes were co-expressed in different regions of the cochlea, including the cochlear ganglion, sensory epithelium, lagena, and tegmentum. This expression pattern suggests the potential for the formation of heteromeric channels from the corresponding alpha-subunits in these various tissues.
听觉系统的受体和神经元细胞进行的信号编码涉及多种调节声音刺激的离子通道。目前,对于感觉上皮和耳蜗神经中发现的这些离子通道,编码其中许多离子通道及其辅助亚基的基因尚不清楚。在这些基因中,包括那些在感觉细胞和神经节中都发现的编码延迟整流钾通道和瞬时型钾通道的基因。在这里,我们报告了Shaker家族成员的克隆和发育表达情况,这些成员包括cKv1.2、cKv1.3、cKv1.5以及与Shaker相关的cGMP门控钾通道cKCNA10。通过使用逆转录聚合酶链反应(RT-PCR)获得的cKv1.2和cKv1.3的两个DNA片段混合物作为探针,筛选鸡胚胎耳蜗cDNA文库来获得克隆。序列分析揭示了Kv1.2、Kv1.3、Kv1.5和cGMP门控钾通道的鸡同源物,其推导的氨基酸同源性与相应的哺乳动物同源物分别为96 - 98%、82 - 84%、67 - 71%和67 - 79%。在鸡内耳发育过程中,RT-PCR研究表明,早在胚胎第3天(ED3)就有cKv1.2、cKv1.3和cKv1.5的表达,而cKCNA10从胚胎第6天开始检测到低水平表达,并在胚胎第9天高度表达。此外,对耳蜗不同部位表达的分析表明,这些基因在耳蜗的不同区域共同表达,包括耳蜗神经节、感觉上皮、听壶和被盖。这种表达模式表明在这些不同组织中,相应的α亚基有可能形成异源通道。