Messina J L
Department of Physiology, State University of New York Health Science Center, Syracuse 13210.
Endocrinology. 1989 Feb;124(2):754-61. doi: 10.1210/endo-124-2-754.
Experiments were conducted to investigate the actions of glucocorticoids and insulin on the induction of a specific mRNA (p33-mRNA) expressed in rat H4 hepatoma cells. Previous studies have found a 10-fold increase in this mRNA following 60 min of insulin addition. In the present study, dexamethasone (Dex) induced the cellular concentration of p33-mRNA 10- to 15-fold. This effect was time and dose dependent. The effect of Dex could be accounted for by a 10- to 15-fold increase in p33-mRNA transcription. However, insulin administration resulted in only a 3-fold increase in the transcription of p33-mRNA. The insulin induction of transcription was time and dose dependent and was blocked by the addition of alpha-amanitin. There was no increase in the transcription of a control gene, beta-tubulin, by either insulin or Dex. Neither insulin nor Dex altered the stability of p33-mRNA. Since the cellular concentration of p33-mRNA was induced to a greater extent than was transcription, insulin must be regulating at least one other step in the sequence between RNA synthesis and RNA stability.
进行实验以研究糖皮质激素和胰岛素对大鼠H4肝癌细胞中表达的一种特异性mRNA(p33 - mRNA)诱导作用。先前的研究发现,添加胰岛素60分钟后,这种mRNA增加了10倍。在本研究中,地塞米松(Dex)使p33 - mRNA的细胞浓度增加了10至15倍。这种效应具有时间和剂量依赖性。Dex的作用可归因于p33 - mRNA转录增加了10至15倍。然而,给予胰岛素仅使p33 - mRNA转录增加了3倍。胰岛素对转录的诱导具有时间和剂量依赖性,并被添加α-鹅膏蕈碱所阻断。胰岛素或Dex均未使对照基因β-微管蛋白的转录增加。胰岛素和Dex均未改变p33 - mRNA的稳定性。由于p33 - mRNA的细胞浓度比转录诱导的程度更大,胰岛素必定在RNA合成与RNA稳定性之间的序列中至少调控了另一个步骤。