Augustin L, Mavinakere M, Morizono H, Tuchman M
Department of Medicine, University of Minnesota, Minneapolis, Minnesota 55455, USA.
Pediatr Res. 2000 Dec;48(6):842-6. doi: 10.1203/00006450-200012000-00023.
Chinese hamster ovary cultured cells were transformed to continuously express wild-type and two mutant ornithine transcarbamylase genes, R141Q and R40H. In addition, these cells were transfected to transiently express the same genes. The R141Q mutation abolishes the enzymatic activity, and the amount of "mature" protein present in transfected cells is equivalent to the wild type. The R40H mutation causes a reduction of enzymatic activity to approximately 26 to 35% of wild type concomitant with a significant reduction in the amount of protein present. Transfection with wild-type and mutant genes together in various proportions did not reveal dominant negative effects of the two mutations studied. This expression system can be used to examine the deleterious effect of private mutations or lack thereof in families with ornithine transcarbamylase deficiency as well as evaluate the potential dominant negative effects of gene delivery for treatment of ornithine transcarbamylase deficiency.
中国仓鼠卵巢培养细胞被转化以持续表达野生型和两个突变型鸟氨酸转氨甲酰酶基因,即R141Q和R40H。此外,这些细胞被转染以瞬时表达相同的基因。R141Q突变消除了酶活性,转染细胞中存在的“成熟”蛋白量与野生型相当。R40H突变导致酶活性降低至野生型的约26%至35%,同时存在的蛋白量显著减少。以各种比例共同转染野生型和突变型基因并未揭示所研究的两种突变的显性负效应。该表达系统可用于检查鸟氨酸转氨甲酰酶缺乏症家族中私人突变的有害作用或缺乏有害作用,以及评估基因递送治疗鸟氨酸转氨甲酰酶缺乏症的潜在显性负效应。