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人类血清素(5-羟色胺,5-HT)转运体基因的功能性启动子及聚腺苷酸化位点定位

Functional promoter and polyadenylation site mapping of the human serotonin (5-HT) transporter gene.

作者信息

Heils A, Teufel A, Petri S, Seemann M, Bengel D, Balling U, Riederer P, Lesch K P

机构信息

Department of Psychiatry, University of Würzburg, Germany.

出版信息

J Neural Transm Gen Sect. 1995;102(3):247-54. doi: 10.1007/BF01281159.

Abstract

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.

摘要

我们已经分离并鉴定了人类5-羟色胺转运体基因的5'-侧翼区和近端聚腺苷酸化位点。主要基因转录本长度为2793 bp,包含208 bp的5'-非翻译区(5'-UTR)和694个碱基的3'-UTR。虽然大鼠和小鼠中只出现一种mRNA,但与大鼠和小鼠的基序相比,人类基因中最近端的聚腺苷酸化信号似乎高度简并。这种类似聚腺苷酸化信号的基序可能导致额外聚腺苷酸化位点的交替使用,从而在人类中产生多种mRNA。5'-侧翼区存在一个类似TATA的基序以及几个转录因子的潜在结合位点,包括AP1、AP2、SP1和一个类似cAMP反应元件(CRE)的基序。一个从转录起始位点下游217 bp开始的约1.7 kb片段,已被连接到荧光素酶报告载体中,并在JAR人胎盘绒毛膜癌细胞中瞬时表达,显示出组成型和福斯可林/霍乱毒素诱导的启动子活性。功能性启动子图谱分析表明,在转录起始位点的-1428至-1185 bp之间存在负性衰减元件,在-1184至-78 bp之间存在正性元件。缺失突变体研究还表明,核心启动子序列包含在转录起始位点的78 bp内,并且cAMP诱导的启动子活性调节取决于多个顺式作用元件,包括位于-99 bp处的两个AP1结合位点和一个单一的类似CRE元件。我们的研究结果表明:(1)5-羟色胺转运体基因启动子在人JAR细胞中具有活性,但在缺乏5-羟色胺转运体的人SK-N-SH神经母细胞瘤细胞和HeLa细胞中无活性;(2)5'-侧翼序列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-羟色胺转运体基因的表达受通过类似TATA基序定义的基础启动子单元起作用的正负顺式作用元件组合的调节。

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