Kobayashi M, Kawakami K
Department of Biology, Jichi Medical School, Minamikawachi, Tochigi, Kawachi, 329-0498, Japan.
Biochem Biophys Res Commun. 1997 Dec 8;241(1):169-74. doi: 10.1006/bbrc.1997.7781.
Na,K-ATPase alpha1 subunit gene is constitutively expressed in a wide variety of tissues. Our previous studies revealed that the promoter region between -77 and +17 of the transcription initiation site of the rat Na,K-ATPase alpha1 subunit gene (Atp1a1) is sufficient for the promoter activity. In this region, an ATF/CRE site with an adjacent GC box exists. To elucidate how these sites are involved in the promoter activity, we analyzed effects of point mutations at these sites on transcription by in vitro transcription assays using nuclear extracts prepared from various rat tissues. Mutation at either site resulted in dramatic reduction of the promoter activity in all nuclear extracts, while mutation at both sites did not lead to further reduction. These results indicate that the ATF/CRE site and GC box are both essential for promoter activity and show synergistic activation. Electrophoretic mobility shift assay indicated that Sp1 and/or Sp3 bind to the GC box, and ATF1-CREB heterodimer binds to the ATF/CRE site. Since an element, ATF/CRE site-GC box, is conserved in mammalian Na,K-ATPase alpha1 subunit genes and in other constitutive promoters, we propose that this element is a critical unit for constitutive expression.
钠钾ATP酶α1亚基基因在多种组织中持续表达。我们之前的研究表明,大鼠钠钾ATP酶α1亚基基因(Atp1a1)转录起始位点-77至+17之间的启动子区域足以产生启动子活性。在该区域,存在一个带有相邻GC框的ATF/CRE位点。为了阐明这些位点如何参与启动子活性,我们通过使用从各种大鼠组织制备的核提取物进行体外转录分析,分析了这些位点的点突变对转录的影响。任何一个位点的突变都会导致所有核提取物中启动子活性显著降低,而两个位点的突变不会导致进一步降低。这些结果表明,ATF/CRE位点和GC框对于启动子活性都是必不可少的,并且显示出协同激活作用。电泳迁移率变动分析表明,Sp1和/或Sp3与GC框结合,而ATF1-CREB异二聚体与ATF/CRE位点结合。由于ATF/CRE位点-GC框元件在哺乳动物钠钾ATP酶α1亚基基因和其他组成型启动子中是保守的,我们提出该元件是组成型表达的关键单元。