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pubmed-article:7836405pubmed:abstractTextWe have isolated and characterized regions important for expression of the mouse Na+/H+ exchanger gene. A 1.1-kilobase fragment upstream of the 5'-untranslated region contains specific DNA motifs characteristic of promoter and enhancer elements including a TATA box, two CAAT boxes, an SP-1 site, a cyclic AMP response element-binding site, and an AP-2-like site. This 1.1-kilobase fragment directs transcription of a luciferase reporter gene in mouse fibroblasts (NIH 3T3) and human Hep G2 cells. Deletion or mutation of an AP-2-like site 100 base pairs from the start site of transcription resulted in loss of most of the reporter plasmid activity. In addition, cotransfection of an AP-2 expression plasmid and the mouse promoter/luciferase plasmid increased the amount of Na+/H+ exchanger-directed transcription in AP-2-deficient Hep G2 cells. Moreover, mobility shift analysis indicated that a putative AP-2-binding site is capable of binding purified AP-2 protein and a specific protein from nuclear extracts of NIH 3T3 cells. The results show that the transcription factor AP-2 may play an important role in regulation of transcription of the mouse Na+/H+ exchanger gene.lld:pubmed
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pubmed-article:7836405pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:7836405pubmed:articleTitleActivation of the Na+/H+ exchanger gene by the transcription factor AP-2.lld:pubmed
pubmed-article:7836405pubmed:affiliationDepartment of Pediatrics, Faculty of Medicine, University of Alberta, Edmonton, Canada.lld:pubmed
pubmed-article:7836405pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:7836405pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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