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转录因子AP-2调节多巴胺β-羟化酶基因的表达。

Transcription factor AP-2 regulates expression of the dopamine beta-hydroxylase gene.

作者信息

Greco D, Zellmer E, Zhang Z, Lewis E

机构信息

Department of Molecular and Medical Genetics, Oregon Health Sciences University, Portland 97201, USA.

出版信息

J Neurochem. 1995 Aug;65(2):510-6. doi: 10.1046/j.1471-4159.1995.65020510.x.

Abstract

Expression of the gene encoding the neurotransmitter biosynthetic enzyme dopamine beta-hydroxylase (DBH) is regulated in a tissue-specific pattern, and transcription is influenced by environmental stimuli. Using the promoter proximal region of the rat DBH gene and nuclear extracts from SHSY-5Y neuroblastoma cells, a DNA-protein complex was identified that is competitive with oligonucleotides containing the recognition site of transcription factor AP-2. DNase footprint analysis identified an AP-2 binding site between -136 and -115 of the DBH promoter. Mutation of that AP-2 site results in a sevenfold reduction of basal reporter gene expression, but second messenger-stimulated activity is retained. Cotransfection of an AP-2 expression vector and a DBH promoter-reporter construct into cultured cells results in a sixfold stimulation of reporter gene expression, demonstrating the ability of AP-2 to trans-activate the DBH promoter. These results identify a new regulatory element on the rat DBH gene and suggest that the AP-2 site plays a role in maintaining basal levels of DBH transcription.

摘要

编码神经递质生物合成酶多巴胺β-羟化酶(DBH)的基因表达以组织特异性模式受到调控,并且转录受环境刺激影响。利用大鼠DBH基因的启动子近端区域和SHSY-5Y神经母细胞瘤细胞的核提取物,鉴定出一种与含有转录因子AP-2识别位点的寡核苷酸具有竞争性的DNA-蛋白质复合物。DNase足迹分析确定了DBH启动子-136至-115之间的一个AP-2结合位点。该AP-2位点的突变导致基础报告基因表达降低7倍,但第二信使刺激的活性得以保留。将AP-2表达载体和DBH启动子-报告基因构建体共转染到培养细胞中,导致报告基因表达受到6倍的刺激,证明了AP-2反式激活DBH启动子的能力。这些结果确定了大鼠DBH基因上一个新的调控元件,并表明AP-2位点在维持DBH转录的基础水平中发挥作用。

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