Romero J A, Zatz M, Axelrod J
Proc Natl Acad Sci U S A. 1975 Jun;72(6):2107-11. doi: 10.1073/pnas.72.6.2107.
The lag period in the induction of rat pineal N-acetyltransferase (arylamine acetyltransferase or acetyl-CoA:arylamine N-acetyltransferase EC 2.3.1.5) by catecholamines via the beta-adrenergic receptor varies with the length of exposure of the rat to light or darkness. If rats have been exposed to light and reduced sympathetic nerve activity for more than 12 hr, this lag period is 1-2 hr long. Under these conditions, actinomycin D completely blocks the induction of N-acetyltransferase by isoproterenol and by dibutyryl adenosine 3':5'-cyclic monophosphate (cyclic AMP). In contrast, if enzyme activity is caused to fall by brief exposure to light at night when N-acetyltransferase activity is high, reinduction by catecholamines occurs almost immediately. In this case, actinomycin D does not block the reinduction of N-acetyltransferase by isoproterenol or by dibutyryl cyclic AMP. Cycloheximide blocks N-acetyltransferase induction under all conditions tested. Thus, new protein synthesis is always required for N-acetyltransferase induction; however, the requirement for RNA synthesis is variable, and contributes to the length of the lag period for induction. It is postulated that both beta-adrenergic stimulation and dibutyryl cyclic AMP act intracellularly at two separate sites in the induction of pineal N-acetyltransferase. One site is in the stimulation of transcription, and the other is in the stimulation of post-transcriptional events.
儿茶酚胺通过β-肾上腺素能受体诱导大鼠松果体N-乙酰转移酶(芳胺乙酰转移酶或乙酰辅酶A:芳胺N-乙酰转移酶,EC 2.3.1.5)的延迟期随大鼠暴露于光照或黑暗的时长而变化。如果大鼠暴露于光照且交感神经活动减弱超过12小时,此延迟期为1 - 2小时。在这些条件下,放线菌素D完全阻断异丙肾上腺素和二丁酰腺苷3':5'-环磷酸腺苷(环磷腺苷)对N-乙酰转移酶的诱导。相反,当N-乙酰转移酶活性较高时,若在夜间通过短暂光照使酶活性下降,儿茶酚胺几乎可立即重新诱导其活性。在这种情况下,放线菌素D并不阻断异丙肾上腺素或二丁酰环磷腺苷对N-乙酰转移酶的重新诱导。环己酰亚胺在所有测试条件下均阻断N-乙酰转移酶的诱导。因此,N-乙酰转移酶的诱导始终需要新的蛋白质合成;然而,对RNA合成的需求是可变的,且影响诱导延迟期的时长。据推测,β-肾上腺素能刺激和二丁酰环磷腺苷在诱导松果体N-乙酰转移酶的过程中在细胞内的两个不同位点起作用。一个位点是在转录刺激方面,另一个是在转录后事件刺激方面。