Briggs M D, Mortier G R, Cole W G, King L M, Golik S S, Bonaventure J, Nuytinck L, De Paepe A, Leroy J G, Biesecker L, Lipson M, Wilcox W R, Lachman R S, Rimoin D L, Knowlton R G, Cohn D H
Ahmanson Department of Pediatrics, Steven Spielberg Pediatric Research Center, Burns and Allen Cedars-Sinai Research Institute, Los Angeles, CA, USA.
Am J Hum Genet. 1998 Feb;62(2):311-9. 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 [http://www3.ncbi.nlm. nih.gov:80/htbin-post/Omim/dispmim?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.
假性软骨发育不全(PSACH)和多发性骨骺发育不良(MED)是常染色体显性遗传的骨软骨发育异常疾病,可导致轻至重度短肢侏儒症和早发性骨关节炎。PSACH和某些类型的MED是由软骨寡聚基质蛋白(COMP;OMIM 600310 [http://www3.ncbi.nlm.nih.gov:80/htbin-post/Omim/dispmim?600310])基因突变引起的。我们报告了另外14个具有PSACH或MED表型的家系中COMP基因突变的鉴定情况。在中度至重度PSACH患者中,发现了预计会导致单氨基酸缺失或替换的突变,所有这些突变都在COMP基因编码钙调蛋白样重复元件的区域内。我们还在该结构域内发现了一个导致MED Fairbank的错义突变。在两个家系中,一个患有轻度PSACH,另一个患有某种形式的MED,我们在COMP羧基末端球状区域的一个残基上发现了不同的替换。这两个家系的临床表现以及COMP基因突变的鉴定都为PSACH和MED之间的表型重叠提供了证据。这些数据还揭示了羧基末端结构域在COMP结构和/或功能中的作用。