Conforti F L, Sprovieri T, Mazzei R, Ungaro C, La Bella V, Tessitore A, Patitucci A, Magariello A, Gabriele A L, Tedeschi G, Simone I L, Majorana G, Valentino P, Condino F, Bono F, Monsurrò M R, Muglia M, Quattrone A
Institute of Neurological Sciences, National Research Council, Mangone, Cosenza, Italy.
Neuromuscul Disord. 2008 Jan;18(1):68-70. doi: 10.1016/j.nmd.2007.07.003. Epub 2007 Aug 20.
Mutations in the Angiogenin gene (ANG) linked to 14q11.2 have been recently discovered to be associated with Amyotrophic Lateral Sclerosis (ALS) in Irish and Scottish populations. In our study we investigated the role of ANG gene in ALS patients from southern Italy. We found a novel mutation in the signal peptide of the ANG gene in a sporadic patient with ALS (SALS). The molecular analysis of the ANG gene also demonstrated an allelic association with the rs11701 single nucleotide polymorphism (SNP) in familial ALS (FALS) but not in SALS patients. Our finding supports the evidence that the ANG gene is involved in ALS.
最近发现,与14q11.2相关的血管生成素基因(ANG)突变与爱尔兰和苏格兰人群的肌萎缩侧索硬化症(ALS)有关。在我们的研究中,我们调查了ANG基因在意大利南部ALS患者中的作用。我们在一名散发性ALS(SALS)患者的ANG基因信号肽中发现了一个新突变。ANG基因的分子分析还表明,在家族性ALS(FALS)中与rs11701单核苷酸多态性(SNP)存在等位基因关联,但在SALS患者中未发现。我们的发现支持了ANG基因参与ALS的证据。