Yao Jun, Ding Mei, Pang Hao, Xing Jia-Xin, Xuan Jin-Feng, Wang Bao-Jie
School of Forensic Medicine, China Medical University, Shenyang 110001, PR China.
School of Forensic Medicine, China Medical University, Shenyang 110001, PR China.
Neurosci Lett. 2015 Nov 16;609:120-3. doi: 10.1016/j.neulet.2015.10.034. Epub 2015 Oct 17.
The role of dopamine D1 receptor (DRD1) gene promoter polymorphisms in schizophrenia remains controversial. We aimed to characterize the polymorphisms in the promoter region because little is known about the extent of variance in this region and potential roles in gene transcription activity. In a previous case-control study, we amplified and genotyped the polymorphisms of DRD1 gene. According to its haplotype estimation, we identified eight SNPs and confirmed ten different haplotypes by cloning and sequencing the fragment spanning -1990 to +10. The promoter activity of these haplotypes was analyzed using dual luciferase assays in SH-SY5Y and HEK293 cells. Compared with the reference haplotype, the constructed haplotypes containing different variation sites could significantly alter the luciferase activity. Additionally, the prediction of the transcription factor binding sites was performed. Our examination could provide the informative reference for the role of DRD1 gene promoter in schizophrenia.
多巴胺D1受体(DRD1)基因启动子多态性在精神分裂症中的作用仍存在争议。我们旨在表征启动子区域的多态性,因为对此区域的变异程度以及在基因转录活性中的潜在作用了解甚少。在先前的病例对照研究中,我们对DRD1基因的多态性进行了扩增和基因分型。根据其单倍型估计,我们鉴定出8个单核苷酸多态性(SNP),并通过对跨度为-1990至+10的片段进行克隆和测序确认了10种不同的单倍型。使用双荧光素酶测定法在SH-SY5Y和HEK293细胞中分析了这些单倍型的启动子活性。与参考单倍型相比,包含不同变异位点的构建单倍型可显著改变荧光素酶活性。此外,还进行了转录因子结合位点的预测。我们的研究可为DRD1基因启动子在精神分裂症中的作用提供有益的参考。