Research Center of Neurology, Moscow, Russia.
Bull Exp Biol Med. 2020 Sep;169(5):673-676. doi: 10.1007/s10517-020-04952-0. Epub 2020 Sep 29.
We studied the expression of C9orf72 gene in pathologies associated with hexanucleotide repeats expansion in this gene: frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). The study included 7 patients with hexanucleotide repeats expansion in the C9orf72 gene and 9 patients of the control group. The expression of C9orf72 mRNA was evaluated in blood leukocytes by real-time PCR. Methylation of CpG-sites in C9orf72 promotor region was evaluated by DNA sequencing after bisulfite conversion. A 2-fold decrease in the C9orf72 gene expression was found in patients with hexanucleotide repeats expansion in comparison with controls, though the difference did not reach statistical significance due to small sample size. The highest expression was shown for ALS in comparison with FTD and FTD-ALS phenotype. A trend to inverse correlation between C9orf72 mRNA level and promoter methylation of this gene as well as between mRNA level and age of disease onset was demonstrated.
我们研究了与 C9orf72 基因六核苷酸重复扩展相关的病理学中 C9orf72 基因的表达:额颞叶痴呆(FTD)和肌萎缩侧索硬化症(ALS)。该研究包括 7 名 C9orf72 基因六核苷酸重复扩展的患者和 9 名对照组患者。通过实时 PCR 评估血液白细胞中 C9orf72 mRNA 的表达。通过亚硫酸氢盐转化后的 DNA 测序评估 C9orf72 启动子区域 CpG 位点的甲基化。与对照组相比,六核苷酸重复扩展患者的 C9orf72 基因表达降低了 2 倍,但由于样本量小,差异未达到统计学意义。与 FTD 和 FTD-ALS 表型相比,ALS 的表达最高。表明 C9orf72 mRNA 水平与该基因启动子甲基化之间以及 mRNA 水平与疾病发病年龄之间呈负相关趋势。