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小鼠神经肽Y Y1受体基因转录的调控:核因子-κB/Rel蛋白的潜在作用。

Regulation of mouse neuropeptide Y Y1 receptor gene transcription: a potential role for nuclear factor-kappa B/Rel proteins.

作者信息

Musso R, Grilli M, Oberto A, Gamalero S R, Eva C

机构信息

Institute of Pharmacology and Experimental Therapeutics, Medical School, University of Torino, Italy.

出版信息

Mol Pharmacol. 1997 Jan;51(1):27-35. doi: 10.1124/mol.51.1.27.

Abstract

We previously isolated a 1.3-kb genomic fragment in the 5'-flanking region of the murine neuropeptide Y (NPY) Y1 receptor gene, which is able to drive the expression of LacZ reporter gene in neuronal cells. We determined the ability of deletion mutants of this region to modulate transcription of the heterologous luciferase gene in the Y1 receptor-expressing neuroblastoma/ glioma NG108-15 cells and the Y1 receptor-deficient 293 cells. Results suggest the presence of a cell type-specific core promoter (-399 to -218 from the initiator ATG) and, upstream, of two positive and two negative regulatory elements. Sequence analysis of the Y1 receptor promoter identified two decameric sequences corresponding to consensus binding sites for nuclear factor-kappa B/Rel proteins. Gel shift analysis indicated that a 29-bp oligonucleotide comprising the two putative kappa B sites, which we refer to as Y1-kappa B sequence, specifically binds kappa B-related complexes in nuclear extracts from rat brain areas, NG108-15 cells, and the murine T cell clone A.E7. In nuclear extracts from A.E7 and NG108-15 cells, the Y1-kappa B sequence specifically binds an additional complex whose molecular nature remains to be elucidated. Through transient transfection studies, we also demonstrated that the Y1-kappa B sequence acts as an enhancer element, inferring its potential role in regulation of the Y1 receptor gene expression.

摘要

我们先前在小鼠神经肽Y(NPY)Y1受体基因的5'侧翼区域分离出一个1.3kb的基因组片段,该片段能够驱动LacZ报告基因在神经元细胞中表达。我们测定了该区域缺失突变体调节异源荧光素酶基因在表达Y1受体的神经母细胞瘤/胶质瘤NG108-15细胞和缺乏Y1受体的293细胞中转录的能力。结果表明存在一种细胞类型特异性核心启动子(从起始ATG起-399至-218),并且在其上游存在两个正调控元件和两个负调控元件。对Y1受体启动子的序列分析鉴定出两个与核因子-κB/Rel蛋白共有结合位点相对应的十聚体序列。凝胶迁移分析表明,一个包含两个假定κB位点的29bp寡核苷酸(我们称之为Y1-κB序列)能特异性结合大鼠脑区、NG108-15细胞和小鼠T细胞克隆A.E7核提取物中的κB相关复合物。在A.E7和NG108-15细胞的核提取物中,Y1-κB序列能特异性结合另一种分子性质有待阐明的复合物。通过瞬时转染研究,我们还证明Y1-κB序列作为增强子元件起作用,推断其在调节Y1受体基因表达中的潜在作用。

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