Liu Y, Nelson A N, Lipsky J J
Clinical Pharmacology Unit, Mayo Clinic and Foundation, Rochester, Minnesota 55905, USA.
Biochem Biophys Res Commun. 1996 Jul 16;224(2):549-54. doi: 10.1006/bbrc.1996.1063.
A cDNA encoding vitamin K-dependent gamma-glutamyl carboxylase was cloned from a human Hep G2 cDNA library. The RNA transcript of the enzyme was found to be widely distributed in various human and rat tissues with liver showing the highest level. The carboxylase transcription in liver was not affected in rats treated with a single dose of warfarin (10 mg/kg) when measured up to 48 hours after the dose, though, at 12 hours, carboxylase activity measured in liver microsomes was elevated 5.4 fold over controls (p < 0.001). In rats fasted for 72 hours there was no affect on transcription in the liver while hepatic carboxylase activity increased 4.1 fold (p < 0.001). These data suggest that the increase in activity of the liver carboxylase in warfarin treated or fasted rats was not regulated by transcription but more likely was due to a posttranscriptional mechanism.
从人肝癌细胞系Hep G2 cDNA文库中克隆出编码维生素K依赖性γ-谷氨酰羧化酶的cDNA。发现该酶的RNA转录本广泛分布于各种人和大鼠组织中,其中肝脏中的水平最高。在给予单剂量华法林(10 mg/kg)的大鼠中,直至给药后48小时测量,肝脏中的羧化酶转录未受影响,不过,在12小时时,肝微粒体中测得的羧化酶活性比对照升高了5.4倍(p < 0.001)。在禁食72小时的大鼠中,肝脏中的转录未受影响,而肝脏羧化酶活性增加了4.1倍(p < 0.001)。这些数据表明,华法林处理或禁食大鼠肝脏中羧化酶活性的增加不是由转录调节的,而更可能是由于转录后机制。