首页> 美国卫生研究院文献>Nucleic Acids Research >Identification of a functional thyroid hormone response element in the upstream flanking region of the human NaK-ATPase beta 1 gene.
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Identification of a functional thyroid hormone response element in the upstream flanking region of the human NaK-ATPase beta 1 gene.

机译:鉴定人类NaK-ATPase beta 1基因上游侧翼区域中的功能性甲状腺激素反应元件。

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摘要

The human Na,K-ATPase beta 1 subunit gene promoter activity is stimulated by thyroid hormone (T3) in the human intestinal Caco-2 cells. To identify potential cis-acting transcriptional regulatory elements involved in this process, chimeric plasmids containing varying lengths of the 5' flanking region of the human beta 1 Na,K-ATPase gene linked to the firefly luciferase reporter gene were introduced into Caco-2 cells by transient transfection. Analysis of T3-regulated luciferase activity of cells carrying these plasmids, and subsequent use of site-directed mutagenesis revealed that a region from -459 to -438 (relative to the transcriptional start site) is required for the induction of the beta 1 Na,K-ATPase gene by T3. An oligonucleotide containing this sequence from -465 to -433 confers T3 responsiveness to a heterologous promoter. Gel mobility shift assays showed specific binding of nuclear proteins of Caco-2 cells to this region and immunoreactive T3 receptor was identified in one of these complexes. These data demonstrate that there is a cis-acting thyroid hormone responsive element in the 5' flanking region of the human beta 1 Na,K-ATPase gene and induction of transcription of this gene by T3 involves specific binding of the thyroid hormone receptor to the TRE located at position -459 to -438.
机译:人体肠道Caco-2细胞中的甲状腺激素(T3)刺激了人类Na,K-ATPaseβ1亚基基因启动子的活性。为了鉴定该过程中潜在的顺式作用转录调控元件,将包含与萤火虫荧光素酶报道基因连接的人β1 Na,K-ATPase基因5'侧翼区域长度不同的嵌合质粒引入Caco-2细胞通过瞬时转染。对带有这些质粒的细胞进行T3调节的荧光素酶活性分析,然后进行定点诱变,发现诱导β1Na所需的区域为-459至-438(相对于转录起始位点), T3的K-ATPase基因。含有从-465到-433的该序列的寡核苷酸赋予T3对异源启动子响应性。凝胶迁移率变动分析表明,Caco-2细胞核蛋白与该区域特异性结合,并且在这些复合物中的一种中鉴定出了免疫反应性T3受体。这些数据表明,在人beta 1 Na,K-ATPase基因5'侧翼区域有一个顺式作用的甲状腺激素响应元件,T3诱导该基因转录涉及甲状腺激素受体与T3的特异性结合。 TRE位于-459至-438的位置。

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