Center for Experimental Medicine, the Third Xiangya Hospital, Central South University, Changsha, China.
Neurobiol Aging. 2013 Aug;34(8):2078.e3-4. doi: 10.1016/j.neurobiolaging.2013.03.001. Epub 2013 Apr 9.
We conducted genetic analysis of the fused in sarcoma gene (FUS) in Chinese Han patients with essential tremor (ET) in a case-control association study. One hundred eighty unrelated patients with ET were screened for mutations in the coding region and exon-intron boundaries of FUS. Reverse transcriptase polymerase chain reaction analysis was performed to evaluate if the c.1176G>A variant results in change of splice site. Two hundred seventy-three normal control subjects were also analyzed when DNA variants were identified in ET cohort. A novel missense mutation, c.1176G>A (p.M392I), in FUS was identified in a 62-year-old patient. Four known variants (c.52C>A, p.P18T; c.147C>A, p.G49G; c.291T>C, p.Y97Y; c.684C>T, p.G228G) were observed in the case-control study without statistically significant differences in genotype and allele distributions. Mutation(s) in FUS might be associated with a small subset of ET cases in the Chinese population.
我们在一项病例对照关联研究中对融合肉瘤基因(FUS)进行了遗传分析,研究对象为汉族原发性震颤(ET)患者。我们筛选了 180 名无血缘关系的 ET 患者,以检测 FUS 编码区和外显子-内含子边界的突变。采用逆转录聚合酶链反应分析评估 c.1176G>A 变异是否导致剪接位点改变。当在 ET 队列中发现 DNA 变异时,我们还分析了 273 名正常对照。在一名 62 岁患者中发现了 FUS 的一种新错义突变 c.1176G>A(p.M392I)。在病例对照研究中观察到了四个已知的变异(c.52C>A,p.P18T;c.147C>A,p.G49G;c.291T>C,p.Y97Y;c.684C>T,p.G228G),但基因型和等位基因分布无统计学差异。FUS 的突变可能与中国人群中的一小部分 ET 病例有关。