Chan Vivian, Yip Ben, Yam Irene, Au Patrick, Lin Che-Kit, Wong Virginia, Chan Tai-Kwong
University Department of Medicine, Queen Mary Hospital, Pokfulam Road, Hong Kong.
J Neurol. 2004 Sep;251(9):1089-93. doi: 10.1007/s00415-004-0487-z.
A real time quantitative PCR (QPCR) method using TaqMan technology was used to assess the copy number of the two survival motor neuron genes (SMN1 and SMN2) on chromosome 5q13. This allows the accurate determination of carriers for spinal muscular atrophy (SMA), with one copy of SMN1. Analysis of 569 normal southern Chinese individuals revealed a carrier incidence of 1.6%, similar to that found in the western society. Study of 42 obligatory carriers showed a (2 + 0) genotype in two (4.8 %). In 27 SMA patients with homozygous deletion of the SMN1 gene, the number of SMN2 gene correlated with disease phenotype, with 68% of type II and III patients carrying three or more SMN2 genes, whilst the incidence of three or more SMN2 genes in the normal population was 1.57%.
采用TaqMan技术的实时定量聚合酶链反应(QPCR)方法,用于评估5号染色体q13区域两个生存运动神经元基因(SMN1和SMN2)的拷贝数。这使得能够准确确定脊髓性肌萎缩症(SMA)的携带者,即具有一个SMN1拷贝的个体。对569名正常中国南方个体的分析显示,携带者发生率为1.6%,与西方社会的发生率相似。对42名确定携带者的研究表明,其中两名(4.8%)呈现(2 + 0)基因型。在27名SMN1基因纯合缺失的SMA患者中,SMN2基因数量与疾病表型相关,II型和III型患者中有68%携带三个或更多SMN2基因,而正常人群中携带三个或更多SMN2基因的发生率为1.57%。