Darlington G J, Tsai C C, Samuelson L C, Gumucio D L, Meisler M H
Mol Cell Biol. 1986 Apr;6(4):969-75. doi: 10.1128/mcb.6.4.969-975.1986.
The tissue-specific expression of two types of mouse amylase genes does not overlap in vivo; the Amy-1 locus is transcribed in the parotid gland and the liver, while expression of Amy-2 is limited to the pancreas. We identified a mouse hepatoma cell line, Hepa 1-6, in which both amylase genes can be simultaneously expressed. Amy-1 is constitutively active in these cells and is inducible by dexamethasone at the level of mRNA. We demonstrated that the liver-specific promoter of Amy-1 is utilized by the dexamethasone-treated hepatoma cells, and that glucocorticoid consensus sequences are present upstream of this promoter. Amy-2 is not detectable constitutively, but can be activated if the cells are cultured in serum-free medium containing dexamethasone. Expression of Amy-2 in a nonpancreatic cell type has not previously been observed. We speculate that induction of Amy-1 and activation of Amy-2 may involve different regulatory mechanisms. Hepa 1-6 cells provide an experimental system for molecular analysis of these events.
两种小鼠淀粉酶基因的组织特异性表达在体内并不重叠;Amy-1基因座在腮腺和肝脏中被转录,而Amy-2的表达仅限于胰腺。我们鉴定出一种小鼠肝癌细胞系Hepa 1-6,在该细胞系中两种淀粉酶基因可同时表达。Amy-1在这些细胞中组成性激活,并且在地塞米松作用下mRNA水平可被诱导。我们证明,地塞米松处理的肝癌细胞利用了Amy-1的肝脏特异性启动子,并且该启动子上游存在糖皮质激素共有序列。Amy-2组成性时不可检测,但如果细胞在含有地塞米松的无血清培养基中培养则可被激活。此前未观察到Amy-2在非胰腺细胞类型中的表达。我们推测,Amy-1的诱导和Amy-2的激活可能涉及不同的调控机制。Hepa 1-6细胞为这些事件的分子分析提供了一个实验系统。