Coding sequence, genomic organization, and conserved chromosomal localization of the mouse gene Scn11a encoding the sodium channel NaN

被引:53
作者
Dib-Hajj, SD
Tyrrell, L
Escayg, A
Wood, PM
Meisler, MH
Waxman, SG
机构
[1] Yale Univ, Sch Med, Dept Neurol, New Haven, CT 06510 USA
[2] Vet Affairs Med Ctr, Neurosci Res Ctr, West Haven, CT 06516 USA
[3] Univ Michigan, Sch Med, Dept Human Genet, Ann Arbor, MI 48109 USA
[4] Univ Miami, Sch Med, Miami Project Cure Paralysis, Miami, FL 33136 USA
[5] Univ Miami, Sch Med, Dept Neurol Surg, Miami, FL 33136 USA
关键词
D O I
10.1006/geno.1999.5890
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Previous studies have shown that sodium channel alpha-subunit NaN is preferentially expressed in small-diameter sensory neurons of dorsal root ganglia and trigeminal ganglia, These neurons include high-threshold nociceptors that are involved in transduction of pain associated with tissue and nerve injury. In this study, we show that mouse NaN is a 1765-amino-acid peptide that is predicted to produce a current that is resistant to tetrodotoxin (TTX-R), Mouse and rat NaN are 80 and 89% identical at the nucleotide and amino acid levels, respectively. The Scn11a gene encoding this cDNA is organized into 24 exons, Unlike some alpha-subunits, Scn11a does not have an alternative exon 5 in domain I. Introns of the U2 and U12 spliceosome types are present at conserved positions relative to other members of this family, Scn11a is located on mouse chromosome 9, close to the two other TTX-R sodium channel genes, Scn5a and Scn10a, The human gene, SCN11A, was mapped to the conserved linkage group on chromosome 3p21-p24, close to human SCN5A and SCN10A. The colocalization of the three sodium channel genes supports a common lineage of the TTX-R sodium channels. (C) 1999 Academic Press.
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页码:309 / 318
页数:10
相关论文
共 67 条
[41]   Alternative splicing of the sodium channel SCN8A predicts a truncated two-domain protein in fetal brain and non-neuronal cells [J].
Plummer, NW ;
McBurney, MW ;
Meisler, MH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (38) :24008-24015
[42]   Channelopathies: Ion channel disorders of muscle as a paradigm for paroxysmal disorders of the nervous system [J].
Ptacek, LJ .
NEUROMUSCULAR DISORDERS, 1997, 7 (04) :250-255
[43]   A tetrodotoxin-resistant voltage-gated sodium channel from human dorsal root ganglia, hPN3/SCN10A [J].
Rabert, DK ;
Koch, BD ;
Ilnicka, M ;
Obernolte, RA ;
Naylor, SL ;
Herman, RC ;
Eglen, RM ;
Hunter, JC ;
Sangameswaran, L .
PAIN, 1998, 78 (02) :107-114
[44]   SLOW SODIUM CONDUCTANCES OF DORSAL-ROOT GANGLION NEURONS - INTRANEURONAL HOMOGENEITY AND INTERNEURONAL HETEROGENEITY [J].
RIZZO, MA ;
KOCSIS, JD ;
WAXMAN, SG .
JOURNAL OF NEUROPHYSIOLOGY, 1994, 72 (06) :2796-2815
[45]   Mechanisms of paresthesiae, dysesthesiae, and hyperesthesiae: Role of Na+ channel heterogeneity [J].
Rizzo, MA ;
Kocsis, JD ;
Waxman, SG .
EUROPEAN NEUROLOGY, 1996, 36 (01) :3-12
[46]   SELECTIVE LOSS OF SLOW AND ENHANCEMENT OF FAST NA+ CURRENTS IN CUTANEOUS AFFERENT DORSAL-ROOT GANGLION NEURONS FOLLOWING AXOTOMY [J].
RIZZO, MA ;
KOCSIS, JD ;
WAXMAN, SG .
NEUROBIOLOGY OF DISEASE, 1995, 2 (02) :87-96
[47]   Structure and function of cardiac sodium and potassium channels [J].
Roden, DM ;
George, AL .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1997, 273 (02) :H511-H525
[48]  
ROWE LB, 1994, MAMM GENOME, V5, P463
[49]   MAPS FROM 2 INTERSPECIFIC BACKCROSS DNA PANELS AVAILABLE AS A COMMUNITY GENETIC-MAPPING RESOURCE [J].
ROWE, LB ;
NADEAU, JH ;
TURNER, R ;
FRANKEL, WN ;
LETTS, VA ;
EPPIG, JT ;
KO, MSH ;
THURSTON, SJ ;
BIRKENMEIER, EH .
MAMMALIAN GENOME, 1994, 5 (05) :253-274
[50]   Structure and function of a novel voltage-gated, tetrodotoxin-resistant sodium channel specific to sensory neurons [J].
Sangameswaran, L ;
Delgado, SG ;
Fish, LM ;
Koch, BD ;
Jakeman, LB ;
Stewart, GR ;
Sze, P ;
Hunter, JC ;
Eglen, RM ;
Herman, RC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (11) :5953-5956