Fuchs Julia, Tichopad Ales, Golub Yulia, Munz Marita, Schweitzer Katherine J, Wolf Björn, Berg Daniela, Mueller Jakob C, Gasser Thomas
University of Tübingen, Hertie-Institute for Clinical Brain Research, Department of Neurodegenerative Diseases, Hoppe-Seyler Str. 3, 72076 Tübingen, Germany.
FASEB J. 2008 May;22(5):1327-34. doi: 10.1096/fj.07-9348com. Epub 2007 Dec 27.
Genetic variability in the promoter and 3' region of the SNCA gene coding alpha-synuclein modulates the risk to develop sporadic Parkinson's disease (PD). Whether this is mediated by regulating alpha-synuclein expression levels remains unknown. Therefore, we analyzed levels of alpha-synuclein in blood and human post mortem brain tissue including the substantia nigra using quantitative real-time reverse transcriptase-polymerase chain reaction and enzyme linked immunosorbent assay in vivo. Single nucleotide polymorphism (SNP) rs356219, a tagging SNP for a disease-associated haplotype in the 3' region of the SNCA gene, has a significant effect on SNCA mRNA levels in the substantia nigra and the cerebellum. Further, the "protective" genotype 259/259 of the PD-associated promoter repeat NACP-Rep1 is associated with lower protein levels in blood than genotypes 261/261, 259/261, and 259/263. In conclusion, we provide evidence that alpha-synuclein levels are influenced by genetic variability in the promoter and 3' region of the SNCA gene in vivo.
编码α-突触核蛋白的SNCA基因启动子和3'区域的遗传变异性调节了散发性帕金森病(PD)的发病风险。这是否通过调节α-突触核蛋白的表达水平介导尚不清楚。因此,我们在体内使用定量实时逆转录聚合酶链反应和酶联免疫吸附测定法分析了血液和包括黑质在内的人类死后脑组织中α-突触核蛋白的水平。单核苷酸多态性(SNP)rs356219是SNCA基因3'区域中与疾病相关单倍型的标签SNP,对黑质和小脑中的SNCA mRNA水平有显著影响。此外,PD相关启动子重复序列NACP-Rep1的“保护性”基因型259/259与血液中比基因型261/261、259/261和259/263更低的蛋白质水平相关。总之,我们提供了证据表明α-突触核蛋白水平在体内受到SNCA基因启动子和3'区域遗传变异性的影响。