Aqp1 expression in erythroleukemia cells: genetic regulation of glucocorticoid and chemical induction

被引:19
作者
Moon, C
King, LS
Agre, P
机构
[1] JOHNS HOPKINS UNIV, SCH MED, DEPT BIOL CHEM, BALTIMORE, MD 21205 USA
[2] JOHNS HOPKINS UNIV, SCH MED, DEPT MED, BALTIMORE, MD 21205 USA
[3] JOHNS HOPKINS UNIV, SCH MED, DIV PULM & CRIT CARE MED, BALTIMORE, MD 21205 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 1997年 / 273卷 / 05期
关键词
transcriptional regulation; water channels; erythroid tissue; promoter; protein biosynthesis; aquaporin-1;
D O I
10.1152/ajpcell.1997.273.5.C1562
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:C1562 / C1570
页数:9
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