Thonberg Håkan, Fallström Marie, Björkström Jenny, Schoumans Jacqueline, Nennesmo Inger, Graff Caroline
Genetics Unit, Dept of Geriatric Medicine, Karolinska University Hospital, Huddinge, Sweden.
BMC Res Notes. 2011 Nov 1;4:476. doi: 10.1186/1756-0500-4-476.
Missense mutations in three different genes encoding amyloid-β precursor protein, presenilin 1 and presenilin 2 are recognized to cause familial early-onset Alzheimer disease. Also duplications of the amyloid precursor protein gene have been shown to cause the disease. At the Dept. of Geriatric Medicine, Karolinska University Hospital, Sweden, patients are referred for mutation screening for the identification of nucleotide variations and for determining copy-number of the APP locus.
We combined the method of microsatellite marker genotyping with a quantitative real-time PCR analysis to detect duplications in patients with Alzheimer disease.
In 22 DNA samples from individuals diagnosed with clinical Alzheimer disease, we identified one patient carrying a duplication on chromosome 21 which included the APP locus. Further mapping of the chromosomal region by array-comparative genome hybridization showed that the duplication spanned a maximal region of 1.09 Mb.
This is the first report of an APP duplication in a Swedish Alzheimer patient and describes the use of quantitative real-time PCR as a tool for determining copy-number of the APP locus.
编码淀粉样前体蛋白、早老素1和早老素2的三个不同基因中的错义突变被认为会导致家族性早发性阿尔茨海默病。淀粉样前体蛋白基因的重复也已被证明会导致该病。在瑞典卡罗林斯卡大学医院老年医学科,患者被转诊进行突变筛查,以鉴定核苷酸变异并确定APP基因座的拷贝数。
我们将微卫星标记基因分型方法与定量实时PCR分析相结合,以检测阿尔茨海默病患者中的重复情况。
在来自临床诊断为阿尔茨海默病的个体的22个DNA样本中,我们鉴定出一名患者在21号染色体上携带一个包含APP基因座的重复。通过阵列比较基因组杂交对染色体区域进行进一步定位显示,该重复跨度最大为1.09 Mb。
这是瑞典阿尔茨海默病患者中APP重复的首次报告,并描述了使用定量实时PCR作为确定APP基因座拷贝数的工具。