Schaller K L, Krzemien D M, McKenna N M, Caldwell J H
Department of Cellular and Structural Biology, University of Colorado Health Sciences Center, Denver 80262.
J Neurosci. 1992 Apr;12(4):1370-81. doi: 10.1523/JNEUROSCI.12-04-01370.1992.
Sodium (Na) channel cDNAs were synthesized from RNA isolated from rat brain, cardiac muscle, and skeletal muscle. Partial cDNAs coding for the largest cytoplasmic loop of the Na channel were amplified with PCR. Sequence analysis of these cDNAs revealed that Na channel cDNAs originally described as brain genes were also expressed in both cardiac and skeletal muscle. Some of these cDNAs were isoforms that differed by insertions or deletions and can be explained by alternative choices of a 5' splice site. Southern blot analysis of genomic DNA confirmed the presence of introns in this region of the gene. Transcripts of multiple isoforms were detected with RNase protection in brain, heart, and skeletal muscle. Several conclusions can be drawn from the data. (1) Some rat sodium channel genes are transcribed in all excitable tissues studied here: brain, cardiac muscle, and skeletal muscle. (2) Each of these three tissues expresses multiple sodium channel genes. (3) Alternative splicing of sodium channel transcripts occurs in these tissues. (4) Expression of multiple genes and alternative splicing of the transcripts is responsible for at least seven different sodium channel mRNAs in skeletal muscle.
从大鼠脑、心肌和骨骼肌中分离出的RNA合成了钠(Na)通道cDNA。用聚合酶链反应(PCR)扩增编码钠通道最大细胞质环的部分cDNA。这些cDNA的序列分析表明,最初被描述为脑基因的钠通道cDNA也在心肌和骨骼肌中表达。其中一些cDNA是通过插入或缺失而不同的异构体,这可以通过5'剪接位点的不同选择来解释。基因组DNA的Southern印迹分析证实了该基因区域存在内含子。在脑、心脏和骨骼肌中用核糖核酸酶保护法检测到多种异构体的转录本。从这些数据可以得出几个结论。(1)一些大鼠钠通道基因在本文研究的所有可兴奋组织中都有转录:脑、心肌和骨骼肌。(2)这三种组织中的每一种都表达多种钠通道基因。(3)钠通道转录本在这些组织中发生可变剪接。(4)多个基因的表达和转录本的可变剪接导致骨骼肌中至少有七种不同的钠通道mRNA。