Suzuki Y, Matsushima A, Ohtake A, Mori M, Tatibana M, Orii T
Eur J Pediatr. 1986 Oct;145(5):406-8. doi: 10.1007/BF00439249.
In the autopsied liver of a neonate with carbamyl phosphate synthetase (CPS)-I deficiency, the activity of CPS-I was about 9% of the normal neonatal control. The enzyme protein of CPS-I was hardly detectable by sodium dodecyl sulphate/polyacrylamide gel electrophoresis (SDS/PAGE) and an immunoblotting method using anti-rat liver CPS-I. The level of translatable mRNA for CPS-I was markedly decreased in a cell-free protein synthesis system consisting of rabbit reticulocyte lysate and total RNA extracted from the autopsied liver of the patient. These observations indicate that the enzyme deficiency in this case is probably mainly due to a diminished level of translatable mRNA, which would lead to a decrease in the synthesis of the CPS-I precursor.
在一名患有氨甲酰磷酸合成酶(CPS)-I缺乏症的新生儿的尸检肝脏中,CPS-I的活性约为正常新生儿对照的9%。通过十二烷基硫酸钠/聚丙烯酰胺凝胶电泳(SDS/PAGE)以及使用抗大鼠肝脏CPS-I的免疫印迹法,几乎检测不到CPS-I的酶蛋白。在由兔网织红细胞裂解物和从该患者尸检肝脏中提取的总RNA组成的无细胞蛋白质合成系统中,CPS-I的可翻译mRNA水平显著降低。这些观察结果表明,该病例中的酶缺乏可能主要是由于可翻译mRNA水平降低,这将导致CPS-I前体合成减少。