Structure and chromosomal localization of the beta 2 subunit of the human brain sodium channel

被引:18
作者
Eubanks, J
Srinivasan, J
Dinulos, MB
Disteche, CM
Catterall, WA
机构
[1] UNIV WASHINGTON,DEPT PHARMACOL,SEATTLE,WA 98195
[2] UNIV WASHINGTON,GRAD PROGRAM NEUROBIOL & BEHAV,SEATTLE,WA 98195
[3] UNIV WASHINGTON,DEPT NEUROL SURG,SEATTLE,WA 98195
[4] UNIV WASHINGTON,DEPT PATHOL,SEATTLE,WA 98195
关键词
beta; 2; subunit; Charcot-Marie-Tooth disease; chromosome; 11; demyelination; human brain sodium channel;
D O I
10.1097/00001756-199708180-00025
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
THE beta 2 subunit of rat brain voltage-gated sodium channels modulates their cell-surface expression and gating. It is a 33 kDa glycoprotein with a single transmembrane segment and an immunoglobulin-like fold resembling those of cell adhesion molecules in the extracellular domain. Here we report the cDNA sequence and genomic localization of the gene encoding the human beta 2 subunit. The mature human beta 2 protein has 89% amino acid sequence identity to rat beta 2 and has four conserved consensus sites for N-linked glycosylation. The extracellular cysteine residues which are predicted to form the disulfide linkage in the immunoglobulin-like fold are also conserved, indicating that the overall structure is preserved between these two species. Using fluorescent in situ hybridization (FISH), we localized the beta 2 gene to human chromosome 11q3. Mutations in this region of chromosome 11 in Charcot-Marie-Tooth syndrome type 4B and in other neurological diseases cause abnormal myelination and neurological deficits. The similarity of beta 2 to cell adhesion molecules, including myelin protein p0, and its chromosomal location at 11q23 suggest a potential role in these demyelinating diseases.
引用
收藏
页码:2775 / 2779
页数:5
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