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单个鉴定神经元中电压门控离子通道的可变剪接的细胞特异性模式。

Cell-specific patterns of alternative splicing of voltage-gated ion channels in single identified neurons.

机构信息

Department of Biological Sciences, University of Missouri, Columbia, MO, USA.

出版信息

Neuroscience. 2010 Jun 16;168(1):118-29. doi: 10.1016/j.neuroscience.2010.03.001. Epub 2010 Mar 6.

DOI:10.1016/j.neuroscience.2010.03.001
PMID:20211705
Abstract

CbNa(v) and CbIH encode channels that carry voltage-gated sodium and hyperpolarization activated cation currents respectively in the crab, Cancer borealis. We cloned and sequenced full length cDNAs for both CbNa(v) and CbIH and found nine different regions of alternative splicing for the CbNa(v) gene and four regions of alternative splicing for CbIH. We used RT-PCR to determine tissue-specific differences in splicing of both channel genes among cardiac muscle, skeletal muscle, brain, and stomatogastric ganglion (STG) tissue. We then examined the splice variant isoforms present in single, unambiguously identified neurons of the STG. We found cell-type specific patterns of alternative splicing for CbNa(v), indicating unique cell-specific pattern of post-transcriptional modification. Furthermore, we detected possible differences in cellular localization of alternatively spliced CbNa(v) transcripts; distinct mRNA isoforms are present between the cell somata and the axons of the neurons. In contrast, we found no qualitative differences among different cell types for CbIH variants present, although this analysis did not represent the full spectrum of all possible CbIH variants. CbIH mRNA was not detected in axon samples. Finally, although cell-type specific patterns of splicing were detected for CbNa(v), the same cell type within and between animals also displayed variability in which splice forms were detected. These results indicate that channel splicing is differentially regulated at the level of single neurons of the same neural network, providing yet another mechanism by which cell-specific neuronal output can be achieved.

摘要

CbNa(v) 和 CbIH 分别编码在北美的螃蟹 Cancer borealis 中携带电压门控钠电流和超极化激活阳离子电流的通道。我们克隆并测序了 CbNa(v) 和 CbIH 的全长 cDNA,并发现 CbNa(v) 基因有九个不同的选择性剪接区域,CbIH 有四个。我们使用 RT-PCR 来确定这两个通道基因在心肌、骨骼肌、脑和 stomatogastric ganglion (STG) 组织中的组织特异性剪接差异。然后,我们检查了 STG 中单个、明确鉴定的神经元中存在的剪接变体同工型。我们发现 CbNa(v) 的剪接具有细胞类型特异性,表明存在独特的细胞特异性转录后修饰模式。此外,我们检测到了剪接的 CbNa(v) 转录本可能存在的细胞内定位差异;神经元的细胞体和轴突之间存在不同的 mRNA 同工型。相比之下,我们没有发现不同细胞类型的 CbIH 变体存在定性差异,尽管这种分析没有代表所有可能的 CbIH 变体的全部范围。在轴突样本中未检测到 CbIH mRNA。最后,尽管在 CbNa(v) 中检测到了细胞类型特异性的剪接模式,但同一动物内和动物之间的相同细胞类型也显示出了所检测到的剪接形式的可变性。这些结果表明,通道剪接在同一神经网络的单个神经元水平上受到差异调节,为实现细胞特异性神经元输出提供了另一种机制。

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