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小鼠感觉神经元河豚毒素抗性电压门控钠通道基因Scn10a的克隆与特性分析

Cloning and characterization of a mouse sensory neuron tetrodotoxin-resistant voltage-gated sodium channel gene, Scn10a.

作者信息

Souslova V A, Fox M, Wood J N, Akopian A N

机构信息

Department of Anatomy and Developmental Biology, Galton Laboratory, University College, London, United Kingdom.

出版信息

Genomics. 1997 Apr 15;41(2):201-9. doi: 10.1006/geno.1997.4669.

Abstract

Small-diameter sensory neurons associated with unmyelinated axons express a tetrodotoxin-insensitive (TTXi) voltage-gated sodium channel (VGSC) that may play an important role in the transmission of nociceptive information to the spinal cord. A TTXi VGSC, named SNS, that accounts for the tetrodotoxin-resistant sodium current described in sensory neurons has been cloned from rat dorsal root ganglia. Using recombinant lambda phage clones encoding a mouse 129/SV genomic library, we have determined the detailed structure of the mouse SNS gene (Scn10a), including the location of exon-intron boundaries and the nucleotide sequence of the exons. The gene consists of 27 exons spanning approximately 90 kb on chromosome 9. Mouse SNS shows 95.3% overall amino acid identity to rat SNS and 98.5% identity throughout the putative transmembrane segments and the intracellular loop linking domains 3 and 4. The sizes of the exons and the exon-intron junction positions of the mouse SNS and the human skeletal muscle VGSC genes are remarkably conserved. These results provide the basis for an evolutionary comparison of sodium channels, the construction and analysis of a mouse SNS null mutant as a direct approach to understanding the biological function of SNS, and the identification of regulatory elements that are responsible for the tissue- and cell-specific expression of SNS.

摘要

与无髓鞘轴突相关的小直径感觉神经元表达一种对河豚毒素不敏感(TTXi)的电压门控钠通道(VGSC),该通道可能在伤害性信息向脊髓的传递中起重要作用。一种名为SNS的TTXi VGSC已从大鼠背根神经节中克隆出来,它解释了感觉神经元中描述的河豚毒素抗性钠电流。利用编码小鼠129/SV基因组文库的重组λ噬菌体克隆,我们确定了小鼠SNS基因(Scn10a)的详细结构,包括外显子-内含子边界的位置和外显子的核苷酸序列。该基因由27个外显子组成,跨越9号染色体上约90 kb的区域。小鼠SNS与大鼠SNS的总体氨基酸同一性为95.3%,在假定的跨膜区段以及连接结构域3和4的细胞内环中同一性为98.5%。小鼠SNS和人类骨骼肌VGSC基因的外显子大小和外显子-内含子连接位置非常保守。这些结果为钠通道的进化比较、构建和分析小鼠SNS无效突变体以直接了解SNS的生物学功能以及鉴定负责SNS组织和细胞特异性表达的调控元件提供了基础。

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