Moon C, King L S, Agre P
Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205-2185, USA.
Am J Physiol. 1997 Nov;273(5):C1562-70. doi: 10.1152/ajpcell.1997.273.5.C1562.
The aquaporin-1 (AQP1) water channel protein is expressed in multiple mammalian tissues by several different developmental programs; however, the genetic regulation is undefined. The proximal promoter of mouse Aqp1 contains multiple putative cis-acting regulatory elements, and mouse erythroleukemia (MEL) cells are a well-characterized model for erythroid differentiation. Corticosteroid or dimethyl sulfoxide (DMSO) exposure induces AQP1 protein expression in MEL cells, and transcriptional regulation was investigated by transient transfections with Aqp1 promoter-reporter constructs. Dexamethasone induction is abrogated by deletion of two glucocorticoid response elements -0.5 kilobases (kb) from the transcription initiation site. Mutation of the GATA element at -0.62 kb has no effect, whereas mutation of the CACCC site at -37 bp significantly reduces DMSO-induced promoter activity. Hydroxyurea induces expression of AQP1 protein without acting through the proximal promoter. The MEL cell line is a reproducible erythroid model system for studying transcriptional regulation of the Aqp1 gene while determining the consequences on AQP1 protein biosynthesis.
水通道蛋白-1(AQP1)水通道蛋白通过几种不同的发育程序在多种哺乳动物组织中表达;然而,其基因调控尚不清楚。小鼠Aqp1的近端启动子包含多个假定的顺式作用调控元件,小鼠红白血病(MEL)细胞是红细胞分化的一个特征明确的模型。皮质类固醇或二甲基亚砜(DMSO)处理可诱导MEL细胞中AQP1蛋白表达,并通过用Aqp1启动子-报告基因构建体进行瞬时转染来研究转录调控。从转录起始位点缺失两个糖皮质激素反应元件-0.5千碱基(kb)可消除地塞米松诱导作用。-0.62 kb处GATA元件的突变没有影响,而-37 bp处CACCC位点的突变显著降低了DMSO诱导的启动子活性。羟基脲可诱导AQP1蛋白表达,且不通过近端启动子起作用。MEL细胞系是一个可重复的红细胞模型系统,用于研究Aqp1基因的转录调控,同时确定对AQP1蛋白生物合成的影响。