...
首页> 外文期刊>The Royal Society Proceedings B: Biological Sciences >Identification of Ca2+ activated K+ channel splice variants and their distribution in the turtle cochlea
【24h】

Identification of Ca2+ activated K+ channel splice variants and their distribution in the turtle cochlea

机译:Ca2 +激活的K +通道剪接变体的鉴定及其在海龟耳蜗中的分布

获取原文
获取原文并翻译 | 示例

摘要

Turtle auditory-hair cells are frequency-tuned by the activity of calcium-activated potassium (K-Ca) channels, a cell's characteristic frequency being determined by the K-Ca channel density and kinetics which both vary systematically along the cochlea. As a first step towards identifying the source of K-Ca channel variation, we have isolated, by reverse-transcription polymerase chain reaction on dissociated hair cells, the main cDNAs homologous to the slo gene which encodes the channel's alpha-subunit. A total of six alternatively spliced variants were identified, the smallest of which is 94% identical to a mouse Slo sequence. Variation occurs by insertion of exons at only two splice sites, two of these exons encoding novel 31- and 61-amino acid sequences. As we were unable to detect splicing at other potential sites, we infer that the six variants correspond to naturally occurring combinations. The spatial distribution of the variants, defined by isolating hair cells from different regions of the cochlea, indicated that some isoforms were non-uniformly distributed. Those containing large inserts in the first splice site were notably absent from the highest-frequency region. We suggest that alternative splicing of the slo gene may contribute to variation in K-Ca channel properties. [References: 23]
机译:乌龟听觉毛发细胞通过钙激活的钾(K-Ca)通道的活动进行频率调谐,细胞的特征频率由K-Ca通道密度和动力学决定,二者沿耳蜗系统地变化。作为确定K-Ca通道变异来源的第一步,我们通过在解离的毛细胞上进行逆转录聚合酶链反应,分离了与slo基因同源的主要cDNA,该基因编码该通道的α-亚基。总共鉴定出六个剪接的变体,其中最小的与小鼠Slo序列具有94%的同一性。通过仅在两个剪接位点插入外显子而发生变异,这些外显子中的两个编码新的31和61氨基酸序列。由于我们无法检测到其他潜在位点的剪接,因此我们推断这六个变体对应于天然存在的组合。通过从耳蜗的不同区域分离毛细胞来定义变体的空间分布,这表明某些同工型是不均匀分布的。那些在第一个剪接位点包含大插入片段的片段在最高频率区域明显不存在。我们建议slo基因的可变剪接可能有助于K-Ca通道特性的变化。 [参考:23]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号