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ATF-1-CREB异二聚体参与管家型钠钾ATP酶α1亚基基因的组成性表达。

ATF-1CREB heterodimer is involved in constitutive expression of the housekeeping Na,K-ATPase alpha 1 subunit gene.

作者信息

Kobayashi M, Kawakami K

机构信息

Department of Biology, Jichi Medical School, Tochigi, Japan.

出版信息

Nucleic Acids Res. 1995 Aug 11;23(15):2848-55. doi: 10.1093/nar/23.15.2848.

Abstract

Na,K-ATPase alpha 1 subunit is an essential protein for cell growth and homeostasis. The gene coding for the protein is expressed in various types of tissues. We previously demonstrated that the transcription regulatory element of the gene (ARE) is located in the position -102 to -61 from the transcription initiation site. To identify the minimal regions that are essential for the constitutive expression, the sequences of the ARE were analyzed in detail by in vitro transcription assays using nuclear extracts from rat kidney, brain and liver. The analyses of various mutations in the promoter demonstrated that the proximal region of the ARE is required for the efficient transcription in every nuclear extract. The factors binding to this region in these nuclear extracts exhibited identical mobility in gel retardation assays. The ATF/CRE core motif is indicated to be important for the factor binding and for the promoter function in all nuclear extracts. The common binding factor in the nuclear extracts was revealed to be an ATF-1/CREB heterodimer by gel retardation assays using specific antibodies. We conclude that the ATF-1/CREB heterodimer is involved in the constitutive expression of the Na,K-ATPase alpha 1 subunit gene.

摘要

钠钾-ATP酶α1亚基是细胞生长和体内平衡所必需的蛋白质。编码该蛋白质的基因在多种组织中表达。我们之前证明该基因的转录调控元件(ARE)位于转录起始位点上游-102至-61的位置。为了确定组成型表达所必需的最小区域,使用来自大鼠肾脏、大脑和肝脏的核提取物,通过体外转录分析详细分析了ARE的序列。对启动子中各种突变的分析表明,ARE的近端区域是每种核提取物中高效转录所必需的。在凝胶阻滞分析中,这些核提取物中与该区域结合的因子表现出相同的迁移率。ATF/CRE核心基序对所有核提取物中的因子结合和启动子功能都很重要。通过使用特异性抗体的凝胶阻滞分析,发现核提取物中的共同结合因子是ATF-1/CREB异二聚体。我们得出结论,ATF-1/CREB异二聚体参与钠钾-ATP酶α1亚基基因的组成型表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b0c/307121/faad7a0ba518/nar00015-0057-a.jpg

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