Byrne P, Huang W, Wallace V M, Shean M K, Zhang Z, Zhong Q, Theodossiou C, Blakesley H, Kolls J K, Schwarzenberger P
Louisiana State University Health Sciences Center, New Orleans 70112, USA.
Biotechniques. 2002 Feb;32(2):279-80, 282-4, 286.
Marine experimental stem cell transplantations require the accurate discrimination and quantification of donor cells from host cells. A Y-chromosome-specific, quantitative real-time PCR (kinetic PCR) protocol for blood-derived DNA was developed. The assay sensitivity was extremely high with accurate detection of only 10 pg (six copies of Y target DNA) in a variable background of female DNA background ranging from 2.5 to 50 ng. The dynamic range of the assay provided accurate results ranging from 2.2 x 10(-2)% to 100% of male DNA in female background. The kinetic PCR assay can be used in all mouse strains, and a sample size as low as 2.5 ng total DNA is sufficient for analysis. Therefore, kinetic PCR allows engraftment kinetic studies on repeated blood draws of individual animals with no need for sacrifice. Compared to conventional PCR, the assay is much simplified, as neither the accurate adjustment of sample DNA concentration nor a post-reaction analysis procedure is required. The procedure is simple, free of radioactivity, and permits a throughput of 500-600 reactions per day.
海洋实验性干细胞移植需要准确区分和定量供体细胞与宿主细胞。我们开发了一种针对血液来源DNA的Y染色体特异性定量实时PCR(动力学PCR)方法。该检测方法灵敏度极高,在2.5至50 ng的女性DNA背景可变背景下,仅需准确检测10 pg(Y靶DNA的六个拷贝)。该检测方法的动态范围在女性背景中提供了从2.2×10(-2)%到100%男性DNA的准确结果。动力学PCR检测可用于所有小鼠品系,低至2.5 ng的总DNA样本量就足以进行分析。因此,动力学PCR允许对单个动物的重复采血进行植入动力学研究,而无需处死动物。与传统PCR相比,该检测方法大大简化,因为既不需要准确调整样品DNA浓度,也不需要反应后分析程序。该程序简单,无放射性,每天可进行500-600次反应。