Sato T, Larner J, Larner A C
Department of Pharmacology, University of Virginia Medical School, Charlottesville 22908.
Biochem Biophys Res Commun. 1988 May 31;153(1):116-27. doi: 10.1016/s0006-291x(88)81197-5.
We have previously shown that when H4 hepatoma cells are pretreated with insulin, plant lectins, phorbol esters, or insulin mediator, the steady state concentration of gene 33 mRNA is markedly increased. The increase in gene 33 mRNA concentration with insulin is due to an increase in the transcription rate of this gene. In the present report we demonstrate that nuclear extracts prepared from H4 hepatoma cells pretreated with insulin exhibit enhanced transcription of gene 33 RNA from a DNA template containing the cap site and 1500 bp upstream of the 33 gene. This is a stable effect of insulin on the nuclear RNA polymerase II system since it is observed in frozen and thawed nuclear extracts as well as fresh nuclear extracts.
我们之前已经表明,当H4肝癌细胞用胰岛素、植物凝集素、佛波酯或胰岛素介质进行预处理时,基因33 mRNA的稳态浓度会显著增加。胰岛素导致基因33 mRNA浓度增加是由于该基因转录速率的提高。在本报告中,我们证明,从用胰岛素预处理的H4肝癌细胞制备的核提取物,能够增强来自含有33基因帽位点和其上游1500 bp的DNA模板的基因33 RNA的转录。这是胰岛素对核RNA聚合酶II系统的稳定作用,因为在冻融的核提取物以及新鲜核提取物中均能观察到。