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首页> 外文期刊>Archives of Biochemistry and Biophysics >Identification of a transcription factor that binds to the promoter region of the human parathyroid hormone gene.
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Identification of a transcription factor that binds to the promoter region of the human parathyroid hormone gene.

机译:鉴定与人甲状旁腺激素基因启动子区结合的转录因子。

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A putative transcription factor binds a site adjacent to the negative vitamin D responsive element (VDRE) in the promoter region of the human parathyroid hormone gene. Deletion and mutation analysis reveal the binding site for this factor overlaps with the proximal repeat element of the VDRE. It includes additional nucleotides at the 3' end of the VDRE. This site has the sequence TTTGAACCTATAGTTGAGAT and a core sequence TGAACCTAT needed for binding of the factor. Experiments with specific anti-vitamin D receptor (VDR) antibodies demonstrate that VDR is not found in the factor/DNA complex. However, removing the VDR from the nuclear extract by immunoprecipitation eliminated the binding complex, and the addition of recombinant VDR to the depleted extract did not restore the factor's ability to bind to the DNA, suggesting that the factor and VDR are closely associated. Transfection experiments with various reporter constructs indicate that the factor is required for the high transcriptional activity of the human PTH gene. This high activity is significantly suppressed by 1,25-dihydroxyvitamin D3. This factor seems to be expressed in several cell types including rat osteoblasts and pituitary. Additionally, some human cancer cell lines express a high level of this factor. Copyright 1999 Academic Press.
机译:假定的转录因子结合人甲状旁腺激素基因启动子区域中与负维生素D反应元件(VDRE)相邻的位点。缺失和突变分析显示该因子的结合位点与VDRE的近端重复元件重叠。它在VDRE的3'末端包含其他核苷酸。该位点具有序列TTTGAACCTATAGTTGAGAT和结合因子所需的核心序列TGAACCTAT。使用特定的抗维生素D受体(VDR)抗体进行的实验表明,在因子/ DNA复合物中未发现VDR。但是,通过免疫沉淀从核提取物中去除VDR消除了结合复合物,并且在耗尽的提取物中添加重组VDR不能恢复该因子与DNA结合的能力,这表明该因子与VDR紧密相关。用各种报告基因构建体进行的转染实验表明,该因子是人PTH基因高转录活性所必需的。 1,25-二羟基维生素D3显着抑制了这种高活性。该因子似乎在包括大鼠成骨细胞和垂体在内的几种细胞类型中表达。另外,一些人类癌细胞系表达高水平的该因子。版权所有1999,学术出版社。

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