FINE-MAPPING OF THE SPINAL MUSCULAR-ATROPHY LOCUS TO A REGION FLANKED BY MAP1B AND D5S6

被引:38
作者
BRZUSTOWICZ, LM
KLEYN, PW
BOYCE, FM
LIEN, LL
MONACO, AP
PENCHASZADEH, GK
DAS, K
WANG, CH
MUNSAT, TL
OTT, J
KUNKEL, LM
GILLIAM, TC
机构
[1] COLUMBIA UNIV COLL PHYS & SURG,DEPT PSYCHIAT,722 W 168TH ST,BOX 23,NEW YORK,NY 10032
[2] JOHN RADCLIFFE HOSP,IMPERIAL CANC RES FUND,INST MOLEC MED,OXFORD OX3 9DU,ENGLAND
[3] COLUMBIA UNIV COLL PHYS & SURG,DEPT GENET & DEV,NEW YORK,NY 10032
[4] NEW YORK STATE PSYCHIAT INST & HOSP,NEW YORK,NY 10032
[5] HARVARD UNIV,SCH MED,DEPT GENET,BOSTON,MA 02115
[6] CHILDRENS HOSP MED CTR,DEPT PEDIAT,DIV GENET,BOSTON,MA 02115
[7] CHILDRENS HOSP MED CTR,HOWARD HUGHES MED INST,BOSTON,MA 02115
[8] TUFTS UNIV,NEW ENGLAND MED CTR,DEPT NEUROL,BOSTON,MA 02111
关键词
D O I
10.1016/0888-7543(92)90012-H
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
The microtubule-associated protein 1B (MAP1B) locus has been mapped in closed proximity to spinal muscular atrophy (SMA) on chromosome 5q13. We have identified a second microsatellite within a MAP1B intron, which increases the heterozygosity of this locus to 94%. Two unambiguous recombination events establish MAP1B as a closely linked, distal flanking marker for the disease locus, while a third recombinant establishes D5S6 as the proximal flanking marker. The combination of key recombinants and linkage analysis place the SMA gene in an approximately 2-cM interval between loci D5S6 and MAP1B. Physical mapping and cloning locate MAP1B within 250 kb of locus D5S112. The identification and characterization of a highly polymorphic gene locus tightly linked to SMA will facilitate isolation of the disease gene, evaluation of heterogeneity, and development of a prenatal test for SMA. © 1992.
引用
收藏
页码:991 / 998
页数:8
相关论文
共 29 条
[1]  
ANDERSON MA, 1984, IN VITRO CELL DEV B, V20, P856
[2]  
Brooke MH, 1985, CLIN VIEW NEUROMUSCU, P36
[3]   GENETIC-MAPPING OF CHRONIC CHILDHOOD-ONSET SPINAL MUSCULAR-ATROPHY TO CHROMOSOME-5Q11.2-13.3 [J].
BRZUSTOWICZ, LM ;
LEHNER, T ;
CASTILLA, LH ;
PENCHASZADEH, GK ;
WILHELMSEN, KC ;
DANIELS, R ;
DAVIES, KE ;
LEPPERT, M ;
ZITER, F ;
WOOD, D ;
DUBOWITZ, V ;
ZERRES, K ;
HAUSMANOWAPETRUSEWICZ, I ;
OTT, J ;
MUNSAT, TL ;
GILLIAM, TC .
NATURE, 1990, 344 (6266) :540-541
[4]  
Dubowitz V., 1978, MUSCLE DISORDERS CHI, P146
[5]  
DUBOWITZ V, 1991, NEUROMUSCULAR DISORD, V1, P47
[6]  
FEINBERG AP, 1984, ANAL BIOCHEM, V137, P266
[7]   GENETIC HOMOGENEITY BETWEEN ACUTE AND CHRONIC FORMS OF SPINAL MUSCULAR-ATROPHY [J].
GILLIAM, TC ;
BRZUSTOWICZ, LM ;
CASTILLA, LH ;
LEHNER, T ;
PENCHASZADEH, GK ;
DANIELS, RJ ;
BYTH, BC ;
KNOWLES, J ;
HISLOP, JE ;
SHAPIRA, Y ;
DUBOWITZ, V ;
MUNSAT, TL ;
OTT, J ;
DAVIES, KE .
NATURE, 1990, 345 (6278) :823-825
[8]   DELETION MAPPING OF DNA MARKERS TO A REGION OF CHROMOSOME-5 THAT COSEGREGATES WITH SCHIZOPHRENIA [J].
GILLIAM, TC ;
FREIMER, NB ;
KAUFMANN, CA ;
POWCHIK, PP ;
BASSETT, AS ;
BENGTSSON, U ;
WASMUTH, JJ .
GENOMICS, 1989, 5 (04) :940-944
[9]   LOCALIZATION OF THE HUNTINGTONS-DISEASE GENE TO A SMALL SEGMENT OF CHROMOSOME-4 FLANKED BY D4S10 AND THE TELOMERE [J].
GILLIAM, TC ;
TANZI, RE ;
HAINES, JL ;
BONNER, TI ;
FARYNIARZ, AG ;
HOBBS, WJ ;
MACDONALD, ME ;
CHENG, SV ;
FOLSTEIN, SE ;
CONNEALLY, PM ;
WEXLER, NS ;
GUSELLA, JF .
CELL, 1987, 50 (04) :565-571
[10]   REPORT OF THE COMMITTEE ON LINKAGE AND GENE ORDER [J].
KEATS, B ;
OTT, J ;
CONNEALLY, M .
CYTOGENETICS AND CELL GENETICS, 1989, 51 (1-4) :459-502