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甲状旁腺激素基因中维生素D反应元件的功能分析及其与骨钙素基因的比较。

Functional analysis of vitamin D response elements in the parathyroid hormone gene and a comparison with the osteocalcin gene.

作者信息

Hawa N S, O'Riordan J L, Farrow S M

机构信息

Department of Medicine, University College London Medical School, Middlesex Hospital, United Kingdom.

出版信息

Biochem Biophys Res Commun. 1996 Nov 12;228(2):352-7. doi: 10.1006/bbrc.1996.1665.

Abstract

We have previously localised two putative vitamin D response elements (VDRE) in the bovine parathyroid hormone (PTH) gene to within -485 to -452 and -451 to -348 base pairs (bp). To confirm the functional significance of these elements, a series of reporter gene constructs were generated and the ability of 1,25-dihydroxyvitamin D3 (1,25(OH)2D3) to suppress gene transcription was assessed. These data confirmed the presence of two regions within -485 to -348 bp which confer responsiveness to 1,25(OH)2D3 and mediate its down-regulatory effect on PTH gene transcription. Second, we investigated whether the putative bovine PTH VDRE and the osteocalcin VDRE require the same nuclear proteins in their interaction with VDR. In gel shift assays, three specific DNA-protein complexes were formed using CV-1 nuclear extract and PTH VDRE. However, unlabelled osteocalcin VDRE (50-fold) failed to inhibit the formation of these complexes. These results suggest that interactions of VDR with the PTH and osteocalcin genes require different accessory factors.

摘要

我们先前已将牛甲状旁腺激素(PTH)基因中的两个假定维生素D反应元件(VDRE)定位在-485至-452以及-451至-348碱基对(bp)范围内。为了证实这些元件的功能重要性,构建了一系列报告基因载体,并评估了1,25-二羟维生素D3(1,25(OH)2D3)抑制基因转录的能力。这些数据证实了在-485至-348 bp范围内存在两个区域,它们赋予对1,25(OH)2D3的反应性,并介导其对PTH基因转录的下调作用。其次,我们研究了假定的牛PTH VDRE和骨钙素VDRE在与维生素D受体(VDR)相互作用时是否需要相同的核蛋白。在凝胶迁移试验中,使用CV-1细胞核提取物和PTH VDRE形成了三种特异性DNA-蛋白质复合物。然而,未标记的骨钙素VDRE(50倍过量)未能抑制这些复合物的形成。这些结果表明,VDR与PTH和骨钙素基因的相互作用需要不同的辅助因子。

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