Diverse Mutations in the Gene for Cartilage Oligomeric Matrix Protein in the Pseudoachondroplasia–Multiple Epiphyseal Dysplasia Disease Spectrum

• Published in: American journal of human genetics 1998-02, Vol.62 (2), p.311-319
• Main Authors: Briggs, Michael D., Mortier, Geert R., Cole, William G., King, Lily M., Golik, Steven S., Bonaventure, Jacky, Nuytinck, Lieve, De Paepe, Anne, Leroy, Jules G., Biesecker, Leslie, Lipson, Mark, Wilcox, William R., Lachman, Ralph S., Rimoin, David L., Knowlton, Robert G., Cohn, Daniel H.
• Format: Article
• Language: English
• Subjects: Achondroplasia - classification; Achondroplasia - genetics; Adolescent; Adult; Amino Acid Sequence; Base Sequence; Biological and medical sciences; Cartilage; Cartilage Oligomeric Matrix Protein; Child; Codon; Diseases of the osteoarticular system; DNA Primers; Dwarf; Extracellular Matrix Proteins; Female; Genes, Dominant; Glycoproteins - genetics; Humans; Infant, Newborn; Male; Malformations and congenital and or hereditary diseases involving bones. Joint deformations; Matrilin Proteins; Medical sciences; Multiple epiphyseal dysplasia; Mutation; Osteochondrodysplasia; Osteochondrodysplasias - classification; Osteochondrodysplasias - genetics; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational; Pseudoachondroplasia
• ISSN: 0002-9297; 1537-6605
• DOI: 10.1086/301713

Pseudoachondroplasia (PSACH) and multiple epiphyseal dysplasia (MED) are autosomal dominant osteochondrodysplasias that result in mild to severe short-limb dwarfism and early-onset osteoarthrosis. PSACH and some forms of MED result from mutations in the gene for cartilage oligomeric matrix protein (COMP; OMIM 600310). We report the identification of COMP mutations in an additional 14 families with PSACH or MED phenotypes. Mutations predicted to result in single–amino acid deletions or substitutions, all in the region of the COMP gene encoding the calmodulin-like repeat elements, were identified in patients with moderate to severe PSACH. We also identified within this domain a missense mutation that produced MED Fairbank. In two families, one with mild PSACH and the second with a form of MED, we identified different substitutions for a residue in the carboxyl-terminal globular region of COMP. Both the clinical presentations of these two families and the identification of COMP-gene mutations provide evidence of phenotypic overlap between PSACH and MED. These data also reveal a role for the carboxyl-terminal domain in the structure and/or function of COMP.