Wang C K, Chen C M, Chang C Y, Chang K H, Chen I C, Li M L, Lee-Chen G-J, Wu Y R
Department of Life Science, National Taiwan Normal University, Taipei, Taiwan.
J Neural Transm (Vienna). 2006 Oct;113(10):1425-33. doi: 10.1007/s00702-006-0435-4. Epub 2006 Apr 11.
Increased alpha-synuclein expression may be involved in the pathogenesis of Parkinson's disease (PD). We investigated the association of Rep1 microsatellite and RsaI T-to-C substitution in the alpha-synuclein promoter region with the risk of PD by a case-control study. The RsaI C/C genotype and C allele were found less frequently in PD patients than in controls. A reduced risk of the Rep1-RsaI 0-C haplotype (OR = 0.57, 95% CI = 0.36-0.90) with PD was evident. The quantitative real-time PCR study showed that the alpha-synuclein mRNA expression was increased (although not significantly) in PD patients with RsaI T/T genotype or Rep1-RsaI 0-T haplotype as compared to T/C genotype or 0-C haplotype. Reporter constructs containing the RsaI C allele drove significantly lower transcriptional activity compared with the RsaI T allele in both IMR32 and 293 cells. The findings suggest that the RsaI T-to-C substitution may have a functional relevance to the susceptibility to PD.
α-突触核蛋白表达增加可能与帕金森病(PD)的发病机制有关。我们通过病例对照研究调查了α-突触核蛋白启动子区域的Rep1微卫星和RsaI T到C替换与PD风险的关联。在PD患者中发现RsaI C/C基因型和C等位基因的频率低于对照组。Rep1-RsaI 0-C单倍型与PD的风险降低明显(OR = 0.57,95% CI = 0.36 - 0.90)。定量实时PCR研究表明,与T/C基因型或0-C单倍型相比,RsaI T/T基因型或Rep1-RsaI 0-T单倍型的PD患者中α-突触核蛋白mRNA表达增加(尽管不显著)。在IMR32和293细胞中,含有RsaI C等位基因的报告基因构建体与RsaI T等位基因相比,驱动的转录活性显著降低。这些发现表明,RsaI T到C替换可能与PD易感性具有功能相关性。