Morita K, Ebert S N, Wong D L
Nancy Pritzker Laboratory of Developmental and Molecular Neurobiology, Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, California 94305-5485, USA.
J Biol Chem. 1995 May 12;270(19):11161-7. doi: 10.1074/jbc.270.19.11161.
Transfection of PC12-variant RS1 cells with an Egr-1 expression construct has previously been shown to stimulate phenylethanolamine N-methyltransferase (PNMT) promoter activity, thus suggesting a putative role of Egr-1 as a factor regulating PNMT gene expression. To elucidate the physiological implication of this finding, the effects of phorbol 12-myristate 13-acetate (PMA) on PNMT promoter activity and Egr-1 expression were examined. PMA stimulated luciferase expression in RS1 cells transfected with a rat PNMT promoter-luciferase reporter gene construct, and also elevated both Egr-1 mRNA and Egr-1 protein levels in the untransfected cells. Further study on the concentration dependence of PMA action showed that the stimulation of luciferase expression correlated with the elevation of Egr-1 mRNA level. Finally, the stimulatory action of PMA on luciferase expression was dramatically diminished in the cells transfected with a mutant construct in which the Egr-1 binding site in PNMT promoter was mutated. These findings suggest that PMA-stimulated PNMT gene expression requires the enhancement of Egr-1 expression, thus providing further evidence for the physiological role of Egr-1 in the regulation of PNMT gene expression in the adrenergic cell.
先前已表明,用Egr-1表达构建体转染PC12变体RS1细胞可刺激苯乙醇胺N-甲基转移酶(PNMT)启动子活性,因此提示Egr-1作为调节PNMT基因表达的因子可能发挥作用。为阐明这一发现的生理学意义,研究了佛波醇12-肉豆蔻酸酯13-乙酸酯(PMA)对PNMT启动子活性和Egr-1表达的影响。PMA刺激了用大鼠PNMT启动子-荧光素酶报告基因构建体转染的RS1细胞中的荧光素酶表达,并且还提高了未转染细胞中Egr-1 mRNA和Egr-1蛋白水平。对PMA作用的浓度依赖性的进一步研究表明,荧光素酶表达的刺激与Egr-1 mRNA水平的升高相关。最后,在用PNMT启动子中的Egr-1结合位点发生突变的突变构建体转染的细胞中,PMA对荧光素酶表达的刺激作用显著减弱。这些发现表明,PMA刺激的PNMT基因表达需要增强Egr-1表达,从而为Egr-1在肾上腺素能细胞中调节PNMT基因表达的生理学作用提供了进一步的证据。