Founder-haplotype analysis in Fukuyama-type congenital muscular dystrophy (FCMD)

被引:32
作者
Kobayashi, K
Nakahori, Y
Mizuno, K
Miyake, M
Kumagai, T
Honma, A
Nonaka, I
Nakamura, Y
Tokunaga, K
Toda, T
机构
[1] Univ Tokyo, Inst Med Sci, Ctr Human Genome, Lab Genome Med,Minato Ku, Tokyo 1088639, Japan
[2] Univ Tokyo, Grad Sch Int Hlth, Dept Human Genet, Tokyo 1130033, Japan
[3] Univ Tokushima, Sch Med, Dept Publ Hlth, Tokushima 7708503, Japan
[4] Aichi Welf Ctr Persons Dev Disabil, Dept Pediat Neurol, Kasugai, Aichi 4800392, Japan
[5] Yamagat Med Rehabil Ctr Disabled Persons, Dept Pediat, Kaminoyama 9993145, Japan
[6] NCNP, Natl Inst Neurosci, Dept Ultrastruct Res, Tokyo 1878502, Japan
[7] Univ Tokyo, Inst Med Sci, Ctr Human Genome, Lab Mol Med, Tokyo 1088639, Japan
关键词
D O I
10.1007/s004390050824
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Fukuyama-type congenital muscular dystrophy (FCMD) is an autosomal recessive, severe muscular dystrophy associated with brain anomalies. After our initial mapping of the FCMD locus to 9q31-33, we performed linkage disequilibrium analysis, which led us to suspect that the FCMD gene lay within a region of less than 100 kb containing D9S2107. In the present study, we developed two new microsatellites (D9S2170 and D9S2171) in close vicinity to D9S2107 and examined haplotypes of FCMD chromosomes by using four markers (cen-D9S2105-D9S2170-D9S2171-D9S2107-tel). As 82% of the FCMD chromosomes that we examined shared the founder haplotype (138-192-147-183) and 94% of the FCMD patients in our panel carried founder haplotypes on one or both chromosomes, the data supported the hypothesis of a single founder of this disease in the Japanese population. Eight haplotypes different from the founder's were observed in FCMD chromosomes, indicating that eight different FCMD mutations in addition to the founder's have occurred in Japan. Moreover, we have detected several historical recombinations that have disrupted the founder haplotype at D9S2105 or D9S2170 and conclude that the FCMD gene is probably located just centromeric to D9S2170.
引用
收藏
页码:323 / 327
页数:5
相关论文
共 13 条
[1]  
FUKUYAMA Y, 1981, BRAIN DEV-JPN, V3, P1
[2]   A GENETIC-STUDY OF THE FUKUYAMA TYPE CONGENITAL MUSCULAR-DYSTROPHY [J].
FUKUYAMA, Y ;
OHSAWA, M .
BRAIN & DEVELOPMENT, 1984, 6 (04) :373-390
[3]  
HAMMER MF, 1995, AM J HUM GENET, V56, P951
[4]  
JORDE LB, 1994, AM J HUM GENET, V54, P884
[5]  
JORDE LB, 1995, AM J HUM GENET, V56, P11
[6]   An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy [J].
Kobayashi, K ;
Nakahori, Y ;
Miyake, M ;
Matsumura, K ;
Kondo-Iida, E ;
Nomura, Y ;
Segawa, M ;
Yoshioka, M ;
Saito, K ;
Osawa, K ;
Hamano, K ;
Sakakihara, Y ;
Nonaka, I ;
Nakagome, Y ;
Kanazawa, I ;
Nakamura, Y ;
Tokunaga, K ;
Toda, T .
NATURE, 1998, 394 (6691) :388-392
[7]   LOCALIZATION OF THE EPM1 GENE FOR PROGRESSIVE MYOCLONUS EPILEPSY ON CHROMOSOME-21 - LINKAGE DISEQUILIBRIUM ALLOWS HIGH-RESOLUTION MAPPING [J].
LEHESJOKI, AE ;
KOSKINIEMI, M ;
NORIO, R ;
TIRRITO, S ;
SISTONEN, P ;
LANDER, E ;
DELACHAPELLE, A .
HUMAN MOLECULAR GENETICS, 1993, 2 (08) :1229-1234
[8]  
MCKUSICK VA, 1994, MENDELIAN INHERITANC, P2040
[9]   YAC and cosmid contigs encompassing the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region on 9q31 [J].
Miyake, M ;
Nakahori, Y ;
Matsushita, I ;
Kobayashi, K ;
Mizuno, K ;
Hirai, M ;
Kanazawa, I ;
Nakagome, Y ;
Tokunaga, K ;
Toda, T .
GENOMICS, 1997, 40 (02) :284-293
[10]   LOCALIZATION OF A GENE FOR FUKUYAMA TYPE CONGENITAL MUSCULAR-DYSTROPHY TO CHROMOSOME 9Q31-33 [J].
TODA, T ;
SEGAWA, M ;
NOMURA, Y ;
NONAKA, I ;
MASUDA, K ;
ISHIHARA, T ;
SUZUKI, M ;
TOMITA, I ;
ORIGUCHI, Y ;
OHNO, K ;
MISUGI, N ;
SASAKI, Y ;
TAKADA, K ;
KAWAI, M ;
OTANI, K ;
MURAKAMI, T ;
SAITO, K ;
FUKUYAMA, Y ;
SHIMIZU, T ;
KANAZAWA, I ;
NAKAMURA, Y .
NATURE GENETICS, 1993, 5 (03) :283-286