Fine mapping and narrowing of the genetic interval of the spinal muscular atrophy region by linkage studies
- PMID: 8432521
- DOI: 10.1006/geno.1993.1018
Fine mapping and narrowing of the genetic interval of the spinal muscular atrophy region by linkage studies
Abstract
The gene for autosomal recessive proximal spinal muscular atrophy (SMA) has recently been mapped to chromosome 5q12.2-q13, within a genetic distance of about 6 cM, and is proximally flanked by the locus D5S6 and distally by D5S112. Here, we report linkage analyses in 64 SMA families with nine polymorphic markers closely linked to the SMA gene, which allowed us to narrow the SMA region to about 4 cM and to define a new proximal genetic border by the locus D5S125 (EF(TG/AG)n. Based on haplotype analysis and specific recombination events, the following order of the loci was determined: 5cen-D5S76-D5S6-D5S125-SMA-(5'MAP-1B-3'MAP- 1B)/D5S112-JK53CA1/2-(D5S39-D5S127)-5qter. The location of the SMA gene between D5S125 and MAP-1B is further supported by multipoint linkage analysis.
Similar articles
-
Large linkage analysis in 100 families with autosomal recessive spinal muscular atrophy (SMA) and 11 CEPH families using 15 polymorphic loci in the region 5q11.2-q13.3.Genomics. 1994 Mar 1;20(1):84-93. doi: 10.1006/geno.1994.1130. Genomics. 1994. PMID: 7912691
-
High-resolution genetic map around the spinal muscular atrophy (SMA) locus on chromosome 5.Am J Hum Genet. 1992 Mar;50(3):520-7. Am J Hum Genet. 1992. PMID: 1539593 Free PMC article.
-
Isolation of microsatellites from the spinal muscular atrophy (SMA) candidate region on chromosome 5q and linkage analysis in Spanish SMA families.Eur J Hum Genet. 1995;3(2):96-101. doi: 10.1159/000472282. Eur J Hum Genet. 1995. PMID: 7552147
-
[Molecular genetic diagnosis and deletion analysis in Type I-III spinal muscular atrophy].Schweiz Med Wochenschr. 1996 May 25;126(21):907-14. Schweiz Med Wochenschr. 1996. PMID: 8693311 Review. German.
-
Molecular studies of spinal muscular atrophy.Neuromuscul Disord. 1991;1(2):83-5. doi: 10.1016/0960-8966(91)90053-u. Neuromuscul Disord. 1991. PMID: 1822785 Review.
Cited by
-
Lethal congenital contracture syndrome: further delineation and genetic aspects.J Med Genet. 1994 Jul;31(7):521-7. doi: 10.1136/jmg.31.7.521. J Med Genet. 1994. PMID: 7966188 Free PMC article.
-
Linkage disequilibrium and haplotype analysis among Polish families with spinal muscular atrophy.Am J Hum Genet. 1995 Jan;56(1):210-5. Am J Hum Genet. 1995. PMID: 7825580 Free PMC article.
-
Lethal congenital contracture syndrome (LCCS), a fetal anterior horn cell disease, is not linked to the SMA 5q locus.J Med Genet. 1995 Jan;32(1):36-8. doi: 10.1136/jmg.32.1.36. J Med Genet. 1995. PMID: 7897624 Free PMC article.
-
Evidence of autosomal dominant mutations in childhood-onset proximal spinal muscular atrophy.Am J Hum Genet. 1994 Jul;55(1):112-9. Am J Hum Genet. 1994. PMID: 8023839 Free PMC article.
-
Mapping of a human rRNA gene in the YAC contig surrounding the SMA candidate gene.Hum Genet. 1995 Sep;96(3):335-8. doi: 10.1007/BF00210418. Hum Genet. 1995. PMID: 7649552
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous