Bourgeois P, Harlin J C, Renouf S, Goutal I, Fairand A, Husson A
Groupe de Biochimie Physiopathologie Digestive et Nutritionelle, Institut Fédératif de Recherches Multidisciplinaires sur les Peptides no. 23, St-Etienne-du-Rouvray, France.
Eur J Biochem. 1997 Nov 1;249(3):669-74. doi: 10.1111/j.1432-1033.1997.t01-1-00669.x.
Expression of the hepatic gene for argininosuccinate synthase (ASS), one of the key enzymes of the urea cycle, was analysed during the perinatal period in the rat. To this end, the amount of specific mRNA was measured in the liver at various stages of development and in cultured foetal hepatocytes maintained in different hormonal conditions. The ASS mRNA was first detected in 15.5-day foetuses and its level increased concomitantly with a rise in the enzyme activity, suggesting that the appearance of the ASS activity reflects the turning on of specific gene transcription. This was demonstrated by run-on assay which showed an enhanced rate of transcription of the ASS gene during the perinatal period. When foetal hepatocytes were cultured with dexamethasone, a dose-dependent increase in ASS mRNA was measured, which was completely abolished by actinomycin D addition. The transcription rate of the gene was increased about twofold in the presence of the steroid, as measured by nuclear run-on assay. This transcriptional action could additionally require a protein factor since it could be inhibited by the simultaneous addition of puromycin. Insulin or glucagon respectively repressed or enhanced the dexamethasone-induced accumulation of ASS mRNA when added simultaneously with the steroid for 24 h. This developmental regulation of the ASS mRNA by glucocorticoids, insulin and glucagon could account for the modulation of the enzyme activity previously observed in vivo and in vitro in the foetal liver.
对大鼠围产期精氨酸琥珀酸合成酶(ASS,尿素循环的关键酶之一)的肝脏基因表达进行了分析。为此,在发育的各个阶段以及在不同激素条件下培养的胎儿肝细胞中,测量了肝脏中特异性mRNA的量。ASS mRNA首次在15.5天的胎儿中被检测到,其水平随着酶活性的升高而同步增加,这表明ASS活性的出现反映了特定基因转录的开启。这通过连续转录分析得到证实,该分析表明围产期ASS基因的转录速率增强。当胎儿肝细胞用地塞米松培养时,测量到ASS mRNA呈剂量依赖性增加,加入放线菌素D后这种增加完全被消除。通过细胞核连续转录分析测量,在类固醇存在下基因的转录速率增加了约两倍。这种转录作用可能还需要一种蛋白质因子,因为同时加入嘌呤霉素可抑制它。当与类固醇同时添加24小时时,胰岛素或胰高血糖素分别抑制或增强了地塞米松诱导的ASS mRNA积累。糖皮质激素、胰岛素和胰高血糖素对ASS mRNA的这种发育调控可以解释先前在胎儿肝脏体内和体外观察到的酶活性调节。