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GC盒和E盒基序作为神经元烟碱型受体α7亚基基因近端启动子区域中的调控元件。

GC- and E-box motifs as regulatory elements in the proximal promoter region of the neuronal nicotinic receptor alpha7 subunit gene.

作者信息

Carrasco-Serrano C, Campos-Caro A, Viniegra S, Ballesta J J, Criado M

机构信息

Department of Neurochemistry, Universidad Miguel Hernández, 03550 San Juan, Alicante, Spain.

出版信息

J Biol Chem. 1998 Aug 7;273(32):20021-8. doi: 10.1074/jbc.273.32.20021.

DOI:10.1074/jbc.273.32.20021
PMID:9685340
Abstract

The alpha7 subunit is a component of alpha-bungarotoxin-sensitive nicotinic acetylcholine receptors expressed in bovine adrenomedullary chromaffin cells. The proximal promoter of the gene coding for this subunit contains several GC-boxes and one E-box. Deletion analysis and transient transfections showed that a 120-base pair region (-77 to +43) including all of these elements gave rise to approximately 70 and 95% of the maximal transcriptional activity observed in chromaffin and SHSY-5Y neuroblastoma cells, respectively. Site-directed mutagenesis of the different elements indicated that both GC and E motifs contribute to the activity of the alpha7 gene in a very prominent way. Using electrophoretic mobility shift assays, the upstream stimulatory factor (USF) was shown to be a component of the complexes that interacted with the E-box when nuclear extracts from chromaffin and SHSY-5Y cells were used. Binding of the early growth response gene transcription factor (Egr-1) to three different GC-boxes was also demonstrated by shift assays and DNase I footprint analysis. Likewise, alpha7 promoter activity increased by up to 5-fold when alpha7 constructs and an Egr-1 expression vector were cotransfected into chromaffin cell cultures. Mutagenesis of individual GC-boxes had little effect on Egr-1 activation. By contrast, pairwise suppression of GC-boxes abolished activation, especially when the most promoter-proximal of the Egr-1 sites was removed. Taken together, these studies indicate that the alpha7 gene is likely to be a target for multiple signaling pathways, in which various regulatory elements are involved.

摘要

α7亚基是在牛肾上腺髓质嗜铬细胞中表达的α-银环蛇毒素敏感型烟碱型乙酰胆碱受体的一个组成部分。编码该亚基的基因的近端启动子包含几个GC盒和一个E盒。缺失分析和瞬时转染表明,一个包含所有这些元件的120个碱基对的区域(-77至+43)分别在嗜铬细胞和SHSY-5Y神经母细胞瘤细胞中产生了约70%和95%的最大转录活性。对不同元件的定点诱变表明,GC和E基序都以非常显著的方式促进α7基因的活性。使用电泳迁移率变动分析,当使用嗜铬细胞和SHSY-5Y细胞的核提取物时,上游刺激因子(USF)被证明是与E盒相互作用的复合物的一个组成部分。早期生长反应基因转录因子(Egr-1)与三个不同GC盒的结合也通过迁移率变动分析和DNase I足迹分析得到了证实。同样,当将α7构建体和Egr-1表达载体共转染到嗜铬细胞培养物中时,α7启动子活性增加了多达5倍。单个GC盒的诱变对Egr-1激活影响很小。相比之下,成对抑制GC盒则消除了激活作用,尤其是当去除Egr-1位点中最靠近启动子的位点时。综上所述,这些研究表明α7基因可能是多种信号通路的靶点,其中涉及各种调控元件。

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