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5HT3血清素受体基因的神经元表达需要核因子1复合物。

Neuronal expression of the 5HT3 serotonin receptor gene requires nuclear factor 1 complexes.

作者信息

Bedford F K, Julius D, Ingraham H A

机构信息

Department of Physiology, University of California at San Francisco, San Francisco, California 94143-0444, USA.

出版信息

J Neurosci. 1998 Aug 15;18(16):6186-94. doi: 10.1523/JNEUROSCI.18-16-06186.1998.

Abstract

The 5HT3 receptor (5HT3R) is a serotonin-gated ion channel whose expression is restricted to a subset of cells within the central and peripheral nervous systems. In vitro analysis shows that a small proximal region of the TATA-less 5HT3R promoter is sufficient to direct neuronal-specific reporter gene expression. Three potential regulatory elements conserved between the mouse and human genes were identified within this proximal promoter, two of which are known sites for the ubiquitously expressed factors Sp1 and nuclear factor 1 (NF1). Surprisingly, mutation of the NF1 binding site abolished all reporter activity in cell transfection studies, suggesting that this element is essential for neuronal-specific transcriptional activity of the 5HT3R. Furthermore, a complex of neuronal proteins that includes a member(s) of the NF1 family binds to this site, as shown by gel mobility super shift and DNaseI footprinting analyses. Although NF1 has been proposed to mediate basal transcription of many ubiquitously expressed genes, our data suggest that a member of the NF1 transcription factor family participates in neuronal-specific gene expression by promoting interactions with other regulatory factors found in sensory ganglia.

摘要

5-羟色胺3型受体(5HT3R)是一种5-羟色胺门控离子通道,其表达局限于中枢和外周神经系统内的一部分细胞。体外分析表明,无TATA盒的5HT3R启动子的一个小的近端区域足以指导神经元特异性报告基因的表达。在该近端启动子中鉴定出小鼠和人类基因之间保守的三个潜在调控元件,其中两个是普遍表达因子Sp1和核因子1(NF1)的已知结合位点。令人惊讶的是,在细胞转染研究中,NF1结合位点的突变消除了所有报告基因活性,这表明该元件对于5HT3R的神经元特异性转录活性至关重要。此外,凝胶迁移超迁移和DNaseI足迹分析表明,包括NF1家族成员在内的一种神经元蛋白复合物与该位点结合。虽然有人提出NF1介导许多普遍表达基因的基础转录,但我们的数据表明,NF1转录因子家族的一个成员通过促进与感觉神经节中发现的其他调控因子的相互作用来参与神经元特异性基因表达。

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