首页> 美国卫生研究院文献>BMC Genomics >Cloning and expression of a zebrafish SCN1B ortholog and identification of a species-specific splice variant
【2h】

Cloning and expression of a zebrafish SCN1B ortholog and identification of a species-specific splice variant

机译:斑马鱼SCN1B直系同源基因的克隆与表达及物种特异性剪接变体的鉴定

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

BackgroundVoltage-gated Na+ channel β1 (Scn1b) subunits are multi-functional proteins that play roles in current modulation, channel cell surface expression, cell adhesion, cell migration, and neurite outgrowth. We have shown previously that β1 modulates electrical excitability in vivo using a mouse model. Scn1b null mice exhibit spontaneous seizures and ataxia, slowed action potential conduction, decreased numbers of nodes of Ranvier in myelinated axons, alterations in nodal architecture, and differences in Na+ channel α subunit localization. The early death of these mice at postnatal day 19, however, make them a challenging model system to study. As a first step toward development of an alternative model to investigate the physiological roles of β1 subunits in vivo we cloned two β1-like subunit cDNAs from D. rerio.
机译:背景电压门控性Na + 通道β1(Scn1b)亚基是多功能蛋白,在电流调节,通道细胞表面表达,细胞粘附,细胞迁移和神经突生长中发挥作用。先前我们已经证明,使用小鼠模型,β1在体内调节电兴奋性。 Scn1b无效小鼠表现出自发性癫痫和共济失调,动作电位传导减慢,髓鞘轴突中Ranvier结节数量减少,淋巴结结构改变以及Na + 通道α亚基定位的差异。然而,这些小鼠在出生后第19天的早期死亡,使其成为具有挑战性的模型系统。作为开发替代模型以研究体内β1亚基的生理作用的第一步,我们克隆了来自D. rerio的两个β1样亚基cDNA。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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