Sequence of the voltage-gated sodium channel beta(1)-subunit in wild-type and in quivering mice

被引:8
作者
Grosson, CLS
Cannon, SC
Corey, DP
Gusella, JF
机构
[1] MASSACHUSETTS GEN HOSP EAST,MOL NEUROGENET UNIT,CHARLESTOWN,MA 02129
[2] HARVARD UNIV,DEPT GENET,CHARLESTOWN,MA 02129
[3] MASSACHUSETTS GEN HOSP,DEPT NEUROL,BOSTON,MA 02114
[4] HOWARD HUGHES MED INST,BOSTON,MA 02114
[5] HARVARD UNIV,SCH MED,DEPT NEUROBIOL,BOSTON,MA 02114
来源
MOLECULAR BRAIN RESEARCH | 1996年 / 42卷 / 02期
关键词
voltage-gated sodium channel; beta(1)-subunit; mouse; quivering; neuromuscular disease; chromosome;
D O I
10.1016/S0169-328X(96)00123-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
SCN1B, the human gene encoding the beta(1)-subunit of the voltage-gated sodium channel has previously been cloned and mapped to Chr 19q13.1. The sequence of the homologous mouse gene, Scn1b, has now been determined from cDNA. The mouse gene is highly conserved, encoding a predicted protein with 99%, 98% and 96% amino acid identity to the rat, rabbit, and human homologs, respectively DNA sequence conservation is also striking in the 3' untranslated region which shows 67% and 98% to human and rat, respectively. Unlike the human and rat homologs, high expression of mRNA from the mouse gene is confined to adult skeletal muscle and brain, and is not observed in heart. As Scn1b maps to Chr 7, in close genetic proximity to the quivering gene (qv), the coding region of Scn1b was also cloned from a qv(J)/qv(J) homozygous mouse and assessed as a candidate for the site of this genetic defect. Comparison of qv and wild-type cDNAs showed no changes in the predicted amino acid sequence that could cause the go phenotype. However, three silent polymorphisms in the DNA coding region indicate that Scn1b is dose to qv, and is within a region of genetic identity with DBA/2J, the inbred background on which the qv(J) allele arose.
引用
收藏
页码:222 / 226
页数:5
相关论文
共 19 条
[1]  
BEIER D, 1995, R74624 GENB
[2]   SODIUM-CHANNEL INACTIVATION IS IMPAIRED IN EQUINE HYPERKALEMIC PERIODIC PARALYSIS [J].
CANNON, SC ;
HAYWARD, LJ ;
BEECH, J ;
BROWN, RH .
JOURNAL OF NEUROPHYSIOLOGY, 1995, 73 (05) :1892-1899
[3]   MODIFICATION OF THE NA+ CURRENT CONDUCTED BY THE RAT SKELETAL-MUSCLE ALPHA-SUBUNIT BY COEXPRESSION WITH A HUMAN BRAIN BETA-SUBUNIT [J].
CANNON, SC ;
MCCLATCHEY, AI ;
GUSELLA, JF .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1993, 423 (1-2) :155-157
[4]   FUNCTIONAL EXPRESSION OF SODIUM-CHANNEL MUTATIONS IDENTIFIED IN FAMILIES WITH PERIODIC PARALYSIS [J].
CANNON, SC ;
STRITTMATTER, SM .
NEURON, 1993, 10 (02) :317-326
[5]   CELLULAR AND MOLECULAR-BIOLOGY OF VOLTAGE-GATED SODIUM-CHANNELS [J].
CATTERALL, WA .
PHYSIOLOGICAL REVIEWS, 1992, 72 (04) :S15-S48
[6]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[7]   GENETIC DEAFNESS OF CENTRAL ORIGIN [J].
DEOL, MS ;
FRANK, MP ;
STEEL, KP ;
BOCK, GR .
BRAIN RESEARCH, 1983, 258 (01) :177-179
[8]  
DIBHAIJ SD, 1996, FEBS LETT, V377, P435
[9]  
FEINBERG AP, 1984, ANAL BIOCHEM, V137, P266
[10]   MOLECULAR-CLONING OF AN ATYPICAL VOLTAGE-GATED SODIUM-CHANNEL EXPRESSED IN HUMAN HEART AND UTERUS - EVIDENCE FOR A DISTINCT GENE FAMILY [J].
GEORGE, AL ;
KNITTLE, TJ ;
TAMKUN, MM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (11) :4893-4897