MAPPING OF 2 NEW MARKERS WITHIN THE SMALLEST INTERVAL HARBORING THE SPINAL MUSCULAR-ATROPHY LOCUS BY FAMILY AND RADIATION HYBRID ANALYSIS

被引:30
作者
BRAHE, C
VELONA, I
VANDERSTEEGE, G
ZAPPATA, S
VANDEVEEN, AY
OSINGA, J
TOPS, CMJ
FODDE, R
KHAN, PM
BUYS, CHCM
NERI, G
机构
[1] UNIV GRONINGEN, DEPT MED GENET, GRONINGEN, NETHERLANDS
[2] LEIDEN UNIV, DEPT HUMAN GENET, SYLVIUS LAB, 2300 RA LEIDEN, NETHERLANDS
关键词
D O I
10.1007/BF00202811
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The locus responsible for the childhood-onset proximal spinal muscular atrophies (SMA) has recently been mapped to an area of 2-3 Mb in the region q12-q13.3 of chromosome 5. We have used a series of radiation hybrids (RHs) containing distinct parts of the SMA region as defined by reference markers. A cosmid library was constructed from one RH. Thirteen clones were isolated and five of these were mapped within the SMA region. Both RH mapping and fluorescence in situ hybridization analysis showed that two clones map in the region between loci D5S125 and D5S351. One of the cosmids contains expressed sequences. Polymorphic dinucleotide repeats were identified in both clones and used for segregation analysis of key recombinant SMA families. One recombination between the SMA locus and the new marker 9Ic (D5S685) indicates that 9Ic is probably the closest distal marker. The absence of recombination between the SMA locus and marker Fc (D5S684) suggests that Fe is located close to the disease gene. These new loci should refine linkage analysis in SMA family studies and may facilitate the isolation of the disease gene.
引用
收藏
页码:494 / 501
页数:8
相关论文
共 24 条
[1]   PRESYMPTOMATIC DIAGNOSIS OF SMA-III BY GENOTYPE ANALYSIS [J].
BRAHE, C ;
ZAPPATA, S ;
VELONA, I ;
BERTINI, E ;
SERVIDEI, S ;
TONALI, P ;
NERI, G .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 45 (03) :408-411
[2]   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
[3]  
CALLEN DF, 1993, AM J HUM GENET, V52, P922
[4]   COSMID VECTOR PCPG AND PLASMID VECTOR PKNUN1, AND THEIR USE FOR CLONING DNA-SEQUENCES ADJACENT TO SITES FOR RARE CUTTING RESTRICTION ENDONUCLEASES [J].
DAUWERSE, HG ;
VANOMMEN, GB ;
BREUNING, MH ;
PEARSON, PL .
NUCLEIC ACIDS RESEARCH, 1989, 17 (09) :3603-3603
[5]   AN ANONYMOUS HUMAN SINGLE COPY GENOMIC CLONE, D5S6 (M4) ON CHROMOSOME-5 IDENTIFIES A 3 ALLELE RFLP [J].
DIETZSCH, E ;
RETIEF, AE ;
LOTZE, MJ ;
WARNICH, L ;
NICHOLSON, DL ;
FOX, MF ;
FRICKE, J ;
DUPLESSIS, L ;
OOSTHUIZEN, CJJ .
NUCLEIC ACIDS RESEARCH, 1986, 14 (04) :1923-1923
[6]  
Dubowitz V., 1978, MUSCLE DISORDERS CHI, P146
[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]   ISOLATION AND CHROMOSOMAL ASSIGNMENT OF 100 HIGHLY INFORMATIVE HUMAN SIMPLE SEQUENCE REPEAT POLYMORPHISMS [J].
HUDSON, TJ ;
ENGELSTEIN, M ;
LEE, MK ;
HO, EC ;
RUBENFIELD, MJ ;
ADAMS, CP ;
HOUSMAN, DE ;
DRACOPOLI, NC .
GENOMICS, 1992, 13 (03) :622-629
[10]   DIRECT NONRADIOACTIVE INSITU HYBRIDIZATION OF SOMATIC-CELL HYBRID DNA TO HUMAN LYMPHOCYTE CHROMOSOMES [J].
KIEVITS, T ;
DEVILEE, P ;
WIEGANT, J ;
WAPENAAR, MC ;
CORNELISSE, CJ ;
VANOMMEN, GJB ;
PEARSON, PL .
CYTOMETRY, 1990, 11 (01) :105-109