Wordsworth P, Ogilvie D, Priestley L, Smith R, Wynne-Davies R, Sykes B
Nuffield Department of Pathology, John Radcliffe Hospital, Oxford.
J Med Genet. 1988 Aug;25(8):521-7. doi: 10.1136/jmg.25.8.521.
Seventy-seven persons with a variety of heritable chondrodysplasias were screened for gross rearrangements of the structural gene encoding the major cartilage collagen, collagen II. None was found. Segregation of the locus (COL2A1) was studied in 19 pedigrees using three restriction site dimorphisms (shown by PvuII, HindIII, and BamHI) and a length polymorphism as linkage markers. Discordant segregation between COL2A1 and the mutant locus was seen in pedigrees with multiple epiphyseal dysplasia, autosomal recessive spondyloepiphyseal dysplasia tarda, hypochondroplasia, pseudoachondroplasia, diaphyseal aclasis, and trichorhinophalangeal syndrome. One pedigree with diastrophic dysplasia was weakly concordant. Autosomal dominant spondyloepiphyseal dysplasia tarda and metaphyseal chondrodysplasia (type Schmid) were not informative. We conclude that mutations of the collagen II gene are not a common feature of the heritable chondrodysplasias. Since the chondrocyte binding protein, chondrocalcin, is also encoded at COL2A1 our conclusions apply equally to this gene.
对77名患有各种遗传性软骨发育不全的患者进行了筛查,以检测编码主要软骨胶原蛋白(胶原蛋白II)的结构基因的大片段重排。未发现此类重排。利用三种限制性酶切位点多态性(由PvuII、HindIII和BamHI显示)和一种长度多态性作为连锁标记,在19个家系中研究了该基因座(COL2A1)的分离情况。在患有多发性骨骺发育不良、常染色体隐性迟发性脊椎骨骺发育不良、软骨发育不全、假性软骨发育不全、骨干续连症和毛发鼻指综合征的家系中,观察到COL2A1与突变基因座之间的不一致分离。一个患有弯曲性发育不良的家系表现出弱一致性。常染色体显性迟发性脊椎骨骺发育不良和干骺端软骨发育不良(施密德型)未提供有效信息。我们得出结论,胶原蛋白II基因的突变不是遗传性软骨发育不全的常见特征。由于软骨细胞结合蛋白软骨钙素也由COL2A1编码,我们的结论同样适用于该基因。