人5-羟色胺(5-HT)转运基因的功能启动子和聚腺苷酸化位点定位。

A Heils, A Teufel, S Petri, M Seemann, D Bengel, U Balling, P Riederer, K P Lesch
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引用次数: 230

摘要

我们已经分离并鉴定了人类5- ht转运体基因的5'-侧翼区域和近端聚腺苷化位点。主基因转录物全长2793 bp,包含5'-未翻译区(5'-UTR) 208 bp和3'-UTR 694个碱基。虽然在大鼠和小鼠中只有一个单一的mRNA物种,但与大鼠和小鼠的基序相比,人类基因中聚腺苷酸化的最近端信号似乎高度退化。这种聚腺苷化信号样基序可能导致额外的聚腺苷化位点的交替使用,从而在人类中产生多个mRNA物种。在5'侧区存在一个tata样基序和几个转录因子的潜在结合位点,包括AP1、AP2、SP1和一个cAMP响应元件(CRE)样基序。从转录起始位点下游217 bp处开始的约1.7 kb片段被连接到荧光素酶报告载体中,并在JAR人胎盘绒膜癌细胞中短暂表达,显示出构成型和福斯克林/霍乱毒素诱导的启动子活性。功能启动子图谱显示,转录起始位点bp - 1428和- 1185之间存在负衰减元件,bp - 1184和-78之间存在正衰减元件。对缺失突变体的研究也表明,核心启动子序列包含在转录起始位点的78 bp内,camp诱导启动子活性的调节依赖于多个顺式作用元件,包括两个AP1结合位点和位于bp -99的单个crea样元件。我们的研究结果表明:(1)5- ht转运体基因启动子在人JAR细胞中有活性,但在缺乏5- ht转运体的人SK-N-SH神经母细胞瘤和HeLa细胞中无活性;(2)5'侧序列1.4 kb内包含的信息足以赋予其细胞特异性表达;(3)启动子对cAMP诱导有反应。(4) 5-HT转运体基因的表达受正、负顺式作用元件的组合调控,这些元件通过一个由tata样基序定义的基础启动子单元运作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Functional promoter and polyadenylation site mapping of the human serotonin (5-HT) transporter gene.

We have isolated and characterized the 5'-flanking region and the proximal polyadenylation site of the human 5-HT transporter gene. The major gene transcript is 2,793 bp in length and it contains 208 bp of 5'-untranslated region (5'-UTR) and 694 bases of 3'-UTR. While only a single mRNA species occurs in rats and mice, the most proximal signal for polyadenylation in the human gene appears to be highly degenerate in comparison to the rat and murine motif. This polyadenylation signal-like motif may lead to alternate usage of additional polyadenylation sites resulting in multiple mRNA species in humans. A TATA-like motif and several potential binding sites for transcription factors including AP1, AP2, SP1, and a cAMP response element (CRE)-like motif are present in the 5'-flanking region. A approximately 1.7 kb fragment beginning 217 bp downstream from the transcription start site, which had been ligated into a luciferase reporter vector and transiently expressed in JAR human placental choriocarcinoma cells, displayed both constitutive and forskolin/cholera toxin-induced promoter activity. Functional promoter mapping revealed that there are negative attenuating elements between bp -1,428 and -1,185 and positive elements between bp -1,184 and -78 from the transcription initiation site. Studies with deletional mutants also indicated that core promoter sequences are contained within 78 bp of the transcription start site and that regulation of cAMP-inducible promoter activity depends on multiple cis-acting elements including two AP1 binding sites and a single CRE-like element located at bp -99. Our findings suggest that (1) the 5-HT transporter gene promoter is active in human JAR cells, but inactive in 5-HT transporter-deficient human SK-N-SH neuroblastoma and HeLa cells, (2) the information contained within 1.4 kb of 5'-flanking sequence is sufficient to confer its cell-specific expression, (3) the promoter responds to cAMP induction, and (4) the expression of the 5-HT transporter gene is regulated by a combination of positive and negative cis-acting elements operating through a basal promoter unit defined by a TATA-like motif.

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