Brakenhoff R H, Henskens H A, van Rossum M W, Lubsen N H, Schoenmakers J G
Department of Molecular and Cellular Biology, University of Nijmegen, Toernooiveld, The Netherlands.
Hum Mol Genet. 1994 Feb;3(2):279-83. doi: 10.1093/hmg/3.2.279.
The locus for the hereditary human Coppock-like cataract (CCL) is closely linked to a particular combination of polymorphic TaqI sites within the human gamma-crystallin gene cluster. Mapping of these sites shows that they define a 15 kb region encompassing the gamma D and psi gamma E gene. The gamma D and the psi gamma E gene were cloned from the CCL chromosome and characterized. The gamma D gene was functionally equivalent to its allele cloned from a wild-type chromosome. The CCL psi gamma E gene contains a cluster of sequence changes within and around its TATA box. Together these cause a ten-fold increase in the activity of the psi gamma E promoter, raising the level of expression of this gene to 30% of that of the gamma D gene. The predicted protein product of the psi gamma E gene is a 6 kD N-terminal gamma-crystallin fragment. Reactivation of the psi gamma E gene and concomitant overexpression of the gamma-crystallin fragment could be the cause of the Coppock-like cataract.
人类遗传性科波克样白内障(CCL)的基因座与人类γ-晶状体蛋白基因簇内多态性TaqI位点的特定组合紧密连锁。对这些位点的定位显示,它们界定了一个包含γD和ψγE基因的15 kb区域。从CCL染色体克隆并鉴定了γD和ψγE基因。γD基因在功能上等同于从野生型染色体克隆的等位基因。CCL ψγE基因在其TATA盒及其周围包含一系列序列变化。这些变化共同导致ψγE启动子活性增加10倍,使该基因的表达水平提高到γD基因的30%。ψγE基因预测的蛋白质产物是一个6 kD的N端γ-晶状体蛋白片段。ψγE基因的重新激活以及γ-晶状体蛋白片段的伴随过表达可能是科波克样白内障的病因。