A nonsense mutation of the mass1 gene in a family with febrile and aebrile seizures

被引:102
作者
Nakayama, J
Fu, YH
Clark, AM
Nakahara, S
Hamano, K
Iwasaki, N
Matsui, A
Arinami, T [1 ]
Ptácek, LJ
机构
[1] Univ Tsukuba, Inst Basic Med Sci, Dept Med Genet, Tsukuba, Ibaraki 3058575, Japan
[2] Univ Tsukuba, Inst Clin Med, Dept Pediat, Tsukuba, Ibaraki 3058575, Japan
[3] Univ Utah, Dept Neurobiol & Anat, Salt Lake City, UT USA
[4] Univ Utah, Howard Hughes Med Inst, Salt Lake City, UT USA
[5] Kensei Gen Hosp, Dept Pediat, Ibaraki, Japan
[6] Kitaibaraki Municipal Gen Hosp, Ibaraki, Japan
[7] Univ Utah, Dept Neurol & Human Genet, Salt Lake City, UT USA
关键词
D O I
10.1002/ana.10347
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A naturally occurring mutation of the mass1 (monogenic audiogenic seizure-susceptible) gene recently has been reported in the Frings mouse strain, which is prone to audiogenic seizures. The human orthologous gene, MASS1, was mapped to chromosome 5q14, for which we previously have reported significant evidence of linkage to febrile seizures (FEB4). We screened for MASS1 mutations in individuals from 48 families with familial febrile seizures and found 25 DNA alterations. None of nine missense polymorphic alleles was significantly associated with febrile seizures; however, a nonsense mutation (S2652X) causing a deletion of the C-terminal 126 amino acid residues was identified in one family with febrile and afebrile seizures. Our results suggest that a loss-of-function mutation in MASS1 might be responsible for the seizure phenotypes, though it is not likely that MASS1 contributed to the cause of febrile seizures in most of our families.
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页码:654 / 657
页数:4
相关论文
共 17 条
[1]   First genetic evidence of GABAA receptor dysfunction in epilepsy:: a mutation in the γ2-subunit gene [J].
Baulac, S ;
Huberfeld, G ;
Gourfinkel-An, I ;
Mitropoulou, G ;
Beranger, A ;
Prud'homme, JF ;
Baulac, M ;
Brice, A ;
Bruzzone, R ;
LeGuern, E .
NATURE GENETICS, 2001, 28 (01) :46-48
[2]   THE MEASUREMENT OF PAIN [J].
BIRD, HA ;
DIXON, JS .
BAILLIERES CLINICAL RHEUMATOLOGY, 1987, 1 (01) :71-89
[3]   Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2 [J].
Escayg, A ;
MacDonald, BT ;
Meisler, MH ;
Baulac, S ;
Huberfeld, G ;
An-Gourfinkel, I ;
Brice, A ;
LeGuern, E ;
Moulard, B ;
Chaigne, D ;
Buresi, C ;
Malafosse, A .
NATURE GENETICS, 2000, 24 (04) :343-345
[4]  
FREEMAN JM, 1980, PEDIATRICS, V66, P1009
[5]   Evidence for a novel gene for familial febrile convulsions, FEB2, linked to chromosome 19p in an extended family from the Midwest [J].
Johnson, EW ;
Dubovsky, J ;
Rich, SS ;
O'Donovan, CA ;
Orr, HT ;
Anderson, VE ;
Gil-Nagel, A ;
Ahmann, P ;
Dokken, CG ;
Schneider, DT ;
Weber, JL .
HUMAN MOLECULAR GENETICS, 1998, 7 (01) :63-67
[6]   Very large G protein-coupled receptor-1, the largest known cell surface protein, is highly expressed in the developing central nervous system [J].
McMillan, DR ;
Kayes-Wandover, KM ;
Richardson, JA ;
White, PC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (01) :785-792
[7]   Identification of epilepsy genes in human and mouse [J].
Meisler, MH ;
Kearney, J ;
Ottman, R ;
Escayg, A .
ANNUAL REVIEW OF GENETICS, 2001, 35 :567-588
[8]   Significant evidence for linkage of febrile seizures to chromosome 5q14-q15 [J].
Nakayama, J ;
Hamano, K ;
Iwasaki, N ;
Nakahara, S ;
Horigome, Y ;
Saitoh, H ;
Aoki, T ;
Maki, T ;
Kikuchi, M ;
Migita, T ;
Ohto, T ;
Yokouchi, Y ;
Tanaka, R ;
Hasegawa, M ;
Matsui, A ;
Hamaguchi, H ;
Arinami, T .
HUMAN MOLECULAR GENETICS, 2000, 9 (01) :87-91
[9]   Sequence similarities between a novel putative G protein-coupled receptor and Na+/Ca2+ exchangers define a cation binding domain [J].
Nikkila, H ;
McMillan, DR ;
Nunez, BS ;
Pascoe, L ;
Curnow, KM ;
White, PC .
MOLECULAR ENDOCRINOLOGY, 2000, 14 (09) :1351-1364
[10]  
Peiffer A, 1999, ANN NEUROL, V46, P671, DOI 10.1002/1531-8249(199910)46:4<671::AID-ANA20>3.0.CO