Greengard O, Dewey H K
Proc Natl Acad Sci U S A. 1971 Aug;68(8):1698-701. doi: 10.1073/pnas.68.8.1698.
Livers of normal rats are devoid of catalytically or immunochemically reactive tryptophan oxygenase (EC 1.13.1.12) up to the 10th postnatal day; the enzyme reaches adult concentrations on about the twentieth day. Premature tryptophan oxygenase synthesis can be evoked in 4-day-old rats: if an injection of glucocorticoid is followed, a day later, by an injection of tryptophan, adult levels of tryptophan oxygenase activity and antigen content can be attained within 5 hr. The prematurely evoked tryptophan oxygenase is degraded in about 2 days, but the preparatory action of the glucocorticoid is longlasting. Even 4 days later, an injection of tryptophan can evoke significant enzyme formation. Actinomycin D, injected together with or 12 hr before the tryptophan, is not inhibitory, but if injected with the glucocorticoid it prevents enzyme formation upon later injection of tryptophan. The observations suggest that appearance of the new enzyme in developing tissue results from the sequential action of more than one stimulus and that the potentiality for its transcription may develop long before its actual synthesis.
正常大鼠的肝脏在出生后第10天之前没有催化活性或免疫化学活性的色氨酸加氧酶(EC 1.13.1.12);该酶在大约第20天达到成年浓度。4日龄大鼠可诱发色氨酸加氧酶的提前合成:如果先注射糖皮质激素,一天后再注射色氨酸,5小时内即可达到成年水平的色氨酸加氧酶活性和抗原含量。提前诱发的色氨酸加氧酶在约2天内降解,但糖皮质激素的预处理作用持久。即使4天后,注射色氨酸仍可诱发显著的酶形成。放线菌素D与色氨酸同时注射或在色氨酸注射前12小时注射,并无抑制作用,但如果与糖皮质激素一起注射,则会阻止随后注射色氨酸时酶的形成。这些观察结果表明,发育中的组织中新酶的出现是由多种刺激的顺序作用导致的,并且其转录的潜力可能在实际合成之前很久就已形成。