Danesch U, Hashimoto S, Renkawitz R, Schütz G
J Biol Chem. 1983 Apr 25;258(8):4750-3.
The enzyme tryptophan oxygenase (EC 1.13.11.11), which is synthesized in rat liver, is induced by glucocorticoids. We have used cloned tryptophan oxygenase genomic and cDNA sequences to study the mechanism of induction. Rat liver poly(A+) RNA was separated on a formaldehyde gel, blotted to nitrocellulose, and hybridized to a nick-translated tryptophan oxygenase cDNA clone to analyze the kinetics of tryptophan oxygenase mRNA accumulation. Transcription in isolated rat liver nuclei was investigated to determine the relative rate of transcription of the tryptophan oxygenase gene. Analysis of the accumulation of albumin mRNA, which is unaffected by glucocorticoids, served as an internal control. We show here that the synthetic glucocorticoid dexamethasone causes a 10-fold increase in the concentration of tryptophan oxygenase mRNA sequences in rat liver, and that this is a consequence of transcriptional activation of the tryptophan oxygenase gene.
色氨酸加氧酶(EC 1.13.11.11)在大鼠肝脏中合成,可被糖皮质激素诱导。我们利用克隆的色氨酸加氧酶基因组和cDNA序列来研究诱导机制。大鼠肝脏多聚腺苷酸(poly(A+))RNA在甲醛凝胶上分离,转移至硝酸纤维素膜上,然后与经缺口平移的色氨酸加氧酶cDNA克隆杂交,以分析色氨酸加氧酶mRNA积累的动力学。研究了分离的大鼠肝细胞核中的转录情况,以确定色氨酸加氧酶基因的相对转录速率。对不受糖皮质激素影响的白蛋白mRNA积累情况的分析作为内部对照。我们在此表明,合成糖皮质激素地塞米松可使大鼠肝脏中色氨酸加氧酶mRNA序列的浓度增加10倍,这是色氨酸加氧酶基因转录激活的结果。