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5-羟色胺2A受体基因中的-1438A/G多态性影响启动子活性。

The -1438A/G polymorphism in the 5-hydroxytryptamine type 2A receptor gene affects promoter activity.

作者信息

Parsons Michael J, D'Souza Ursula M, Arranz Maria-Jesus, Kerwin Robert W, Makoff Andrew J

机构信息

Department of Clinical Neuropharmacology, Institute of Psychiatry, King's College London, London, United Kingdom.

出版信息

Biol Psychiatry. 2004 Sep 15;56(6):406-10. doi: 10.1016/j.biopsych.2004.06.020.

Abstract

BACKGROUND

The -1438A/G single nucleotide polymorphism (SNP) lies just upstream of two alternative promoters for the 5-hydroxytryptamine type 2A (5-HT2A) receptor gene (HTR2A) and is in strong linkage disequilibrium with the 102T/C SNP. Both SNPs are associated with numerous psychiatric disorders and related phenotypes. A possible functional affect of the -1438A/G SNP might underlie associations of both linked SNPs with these neuropsychiatric disorders. A prior investigation into affects of this SNP on promoter function, lacking the more downstream promoter, found no significant difference with a reporter gene assay.

METHODS

To investigate possible functional effects of -1438A/G on either promoter, two different reporter gene assays were used in three cell lines.

RESULTS

Promoter activity was consistently detected that, in the presence of the SV40 enhancer, was significantly greater in the presence of the A allele relative to the G allele but only in cell lines that express endogenous HTR2A, suggesting that transcriptional factor(s) and the presence of both promoters might be necessary to elicit this effect.

CONCLUSIONS

These findings show that the -1438A/G SNP has the potential to modulate HTR2A promoter activity and might be the functional variant responsible for the associations of both SNPs with many neuropsychiatric phenotypes.

摘要

背景

-1438A/G单核苷酸多态性(SNP)位于5-羟色胺2A型(5-HT2A)受体基因(HTR2A)两个可变启动子的上游,并且与102T/C SNP处于强连锁不平衡状态。这两个SNP均与多种精神疾病及相关表型有关。-1438A/G SNP可能的功能影响可能是这两个连锁SNP与这些神经精神疾病关联的基础。先前一项关于该SNP对启动子功能影响的研究,由于缺少更下游的启动子,通过报告基因检测未发现显著差异。

方法

为研究-1438A/G对任一启动子可能的功能影响,在三种细胞系中使用了两种不同的报告基因检测方法。

结果

持续检测到启动子活性,在SV40增强子存在的情况下,相对于G等位基因,A等位基因存在时的启动子活性显著更高,但仅在表达内源性HTR2A的细胞系中如此,这表明转录因子以及两个启动子的存在可能是引发这种效应所必需的。

结论

这些发现表明,-1438A/G SNP具有调节HTR2A启动子活性的潜力,可能是导致这两个SNP与许多神经精神表型相关联的功能变异体。

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