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

被引:203
|
作者
Parsons, MJ
D'Souza, UM
Arranz, MJ
Kerwin, RW
Makoff, AJ
机构
[1] Kings Coll London, Inst Psychiat, Div P Med, Dept Clin Neuropharmacol, London SE5 8AF, England
[2] Kings Coll London, Inst Psychiat, Social Genet & Dev Psychiat Ctr, London SE5 8AF, England
基金
英国医学研究理事会; 美国国家科学基金会;
关键词
-1438A/G polymorphism; 5-HT2A receptor; enhancer; promoter; psychiatric disorders; reporter gene assay;
D O I
10.1016/j.biopsych.2004.06.020
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Backgroun& The-1438A/G single nucleotide polymorphism (SAP) lies just upstream of two alternative promoters for the 5-bydroxytryptamine type 2A (5-HT2A) receptorgene (HTR2A) and is in strong linkage disequilibrium with the 102TICSNP. Both SNPs are associated with numerous psychiatric disorders and related phenotypes. A possible functional affect of tbe-1438A/G SNP might underlie associations of both linked SNPs with these neuropsycbiatric disorders. A prior investigation into affects of this SNP on promoterfunction, 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 neuropsycbiatric phenotypes.
引用
收藏
页码:406 / 410
页数:5
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