SOD1 MISSENSE MUTATION IN AN ITALIAN FAMILY WITH ALS

被引:66
作者
RAINERO, I
PINESSI, L
TSUDA, T
VIGNOCCHI, MG
VAULA, G
CALVI, L
CERRATO, P
ROSSI, B
BERGAMINI, L
MCLACHLAN, DRC
STGEORGEHYSLOP, PH
机构
[1] UNIV TURIN, DEPT NEUROL, TURIN, ITALY
[2] UNIV PISA, PISA, ITALY
[3] UNIV TORONTO, DEPT MED, DIV NEUROL, CTR RES NEURODEGENERAT DIS, TORONTO, ON, CANADA
关键词
D O I
10.1212/WNL.44.2.347
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We have discovered a new Italian pedigree with autosomal-dominant ALS. The pedigree, at present, comprises 75 members distributed in five generations. ALS was diagnosed in eight patients. The mean +/- SD age of onset of the disease was 46.8 +/- 13.5 years, with a range of 29 to 63 years. The mean +/- SD duration of the disease was 11.6 +/- 1.7 months. Molecular genetic studies showed a missense mutation (Gly-->Ser, codon 41) in exon 2 of the Cu/Zn superoxide dismutase gene (SOD1) on chromosome 21 in the available affected member and in 45% of the at-risk subjects of the pedigree. This study confirms the presence of SOD1 point mutations in families with autosomal-dominant ALS and suggests that additional genetic or environmental factors may be involved in the full expression of the disease.
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页码:347 / 349
页数:3
相关论文
共 10 条
[1]  
Bruni A C, 1992, J Geriatr Psychiatry Neurol, V5, P126
[2]  
Foncin JF, 1989, FAMILIAL ALZHEIMERS, P45
[3]   GLUTAMATE, NITRIC-OXIDE AND CELL CELL SIGNALING IN THE NERVOUS-SYSTEM [J].
GARTHWAITE, J .
TRENDS IN NEUROSCIENCES, 1991, 14 (02) :60-67
[4]   EXPANSION OF AN UNSTABLE DNA REGION AND PHENOTYPIC VARIATION IN MYOTONIC-DYSTROPHY [J].
HARLEY, HG ;
BROOK, JD ;
RUNDLE, SA ;
CROW, S ;
REARDON, W ;
BUCKLER, AJ ;
HARPER, PS ;
HOUSMAN, DE ;
SHAW, DJ .
NATURE, 1992, 355 (6360) :545-546
[5]   FAMILIAL MOTOR NEURON DISEASE - EVIDENCE FOR AT LEAST 3 DIFFERENT TYPES [J].
HORTON, WA ;
ELDRIDGE, R ;
BRODY, JA .
NEUROLOGY, 1976, 26 (05) :460-465
[6]  
HUSDON AJ, 1981, BRAIN, V104, P217
[7]   MOLECULAR AND PROSPECTIVE PHENOTYPIC CHARACTERIZATION OF A PEDIGREE WITH FAMILIAL ALZHEIMERS-DISEASE AND A MISSENSE MUTATION IN CODON 717 OF THE BETA-AMYLOID PRECURSOR PROTEIN GENE [J].
KARLINSKY, H ;
VAULA, G ;
HAINES, JL ;
RIDGLEY, J ;
BERGERON, C ;
MORTILLA, M ;
TUPLER, RG ;
PERCY, ME ;
ROBITAILLE, Y ;
NOLDY, NE ;
YIP, TCK ;
TANZI, RE ;
GUSELLA, JF ;
BECKER, R ;
BERG, JM ;
MCLACHLAN, DRC ;
STGEORGEHYSLOP, PH .
NEUROLOGY, 1992, 42 (08) :1445-1453
[8]   MUTATIONS IN CU/ZN SUPEROXIDE-DISMUTASE GENE ARE ASSOCIATED WITH FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS [J].
ROSEN, DR ;
SIDDIQUE, T ;
PATTERSON, D ;
FIGLEWICZ, DA ;
SAPP, P ;
HENTATI, A ;
DONALDSON, D ;
GOTO, J ;
OREGAN, JP ;
DENG, HX ;
RAHMANI, Z ;
KRIZUS, A ;
MCKENNAYASEK, D ;
CAYABYAB, A ;
GASTON, SM ;
BERGER, R ;
TANZI, RE ;
HALPERIN, JJ ;
HERZFELDT, B ;
VANDENBERGH, R ;
HUNG, WY ;
BIRD, T ;
DENG, G ;
MULDER, DW ;
SMYTH, C ;
LAING, NG ;
SORIANO, E ;
PERICAKVANCE, MA ;
HAINES, J ;
ROULEAU, GA ;
GUSELLA, JS ;
HORVITZ, HR ;
BROWN, RH .
NATURE, 1993, 362 (6415) :59-62
[9]   LINKAGE OF A GENE CAUSING FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS TO CHROMOSOME-21 AND EVIDENCE OF GENETIC-LOCUS HETEROGENEITY [J].
SIDDIQUE, T ;
FIGLEWICZ, DA ;
PERICAKVANCE, MA ;
HAINES, JL ;
ROULEAU, G ;
JEFFERS, AJ ;
SAPP, P ;
HUNG, WY ;
BEBOUT, J ;
MCKENNAYASEK, D ;
DENG, G ;
HORVITZ, HR ;
GUSELLA, JF ;
BROWN, RH ;
ROSES, AD .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (20) :1381-1384
[10]   A NOVEL BUT NONPATHOGENIC MUTATION IN EXON-4 OF THE HUMAN AMYLOID PRECURSOR PROTEIN (APP) GENE [J].
VAULA, G ;
MORTILLA, M ;
TUPLER, R ;
LUKIW, W ;
TANZI, R ;
NEE, L ;
POLINSKY, R ;
FONCIN, JF ;
BRUNI, AC ;
MONTESI, MP ;
SORBI, S ;
STGEORGEHYSLOP, P .
NEUROSCIENCE LETTERS, 1992, 144 (1-2) :46-48