Diastrophic dysplasia gene maps to the distal long arm of chromosome 5.
Open Access
- 1 October 1990
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 87 (20), 8056-8059
- https://doi.org/10.1073/pnas.87.20.8056
Abstract
We have used polymorphic DNA markers to map the gene for a clinically well-characterized form of osteochondrodysplasia, diastrophic dysplasia (DD), an autosomal recessive disorder of unknown pathogenesis. Linkage was analyzed in 13 families with two or three affected sibs comprising a total of 84 individuals. Positive two-point logarithm-of-odds (lod) scores were obtained between the DD locus and three polymorphic markers on chromosome 5. The highest pairwise lod score estimate of 7.37 with zero recombination to locus D5S72 suggests very tight linkage. There was no evidence of heterogeneity. Multipoint linkage analysis against the published order of the three loci gave the result centromere-D5S84-(DD, D5S72)-D5S61-terminus with a four-point lod score of 9.11. The present findings place the DD locus distal to the gene for adenomatous polyposis coli on the distal part of the long arm of chromosome 5. Our results provide a basis for refining the map position of the DD locus followed by physical localization, isolation, and characterization of the gene.Keywords
This publication has 25 references indexed in Scilit:
- Type II collagen screening in the human chondrodysplasiasAmerican Journal of Medical Genetics, 1989
- Inherited disorders of collagen gene structure and expressionAmerican Journal of Medical Genetics, 1989
- Exclusion of the COL2A1 gene as the mutation site in diastrophic dysplasia.Journal of Medical Genetics, 1989
- Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 622-643Cytogenetic and Genome Research, 1989
- Report of the committee on the genetic constitution of chromosome 5Cytogenetic and Genome Research, 1989
- Structural and segregation analysis of the type II collagen gene (COL2A1) in some heritable chondrodysplasias.Journal of Medical Genetics, 1988
- The Stickler syndrome: Evidence for close linkage to the structural gene for type II collagenGenomics, 1987
- A genetic linkage map of the human genomeCell, 1987
- The phenotypic variability of diastrophic dysplasiaThe Journal of Pediatrics, 1978
- DIASTROPHIC DWARFISMMedicine, 1972