Department of Environmental Toxicology, University of California Davis, Davis, CA 95616, USA.
Forensic Sci Int Genet. 2012 Mar;6(2):290-5. doi: 10.1016/j.fsigen.2011.06.005. Epub 2011 Jul 20.
In the United States, human forensic evidence collected from crime scenes is usually comingled with biomaterial of canine and feline origins. Knowledge of the concentration of nuclear DNA extracted from a crime scene biological sample and the species from which the sample originated is essential for DNA profiling. The ability to accurately detect and quantify target DNA in mixed-species samples is crucial when target DNA may be overwhelmed by non-target DNA. We have designed and evaluated a species-specific (human, dog and cat) nuclear DNA identification assay based on the TaqMan(®) quantitative real-time PCR (qPCR) technology that can simultaneously detect and measure minute quantities of DNA specific to either humans, dogs and/or cats. The fluorogenic triplex assay employs primers and hydrolysis probes that target the human TH01 locus as well as the dog and cat Melanocortin 1 Receptor (MC1R) sequences in a species-specific manner. We also demonstrate that the assay is a highly sensitive, reliable and robust method for identifying and quantifying mixed-species templates of human-dog-cat origin with as little as 0.4 pg of human and cat nuclear DNA, respectively, and 4.0 pg of dog nuclear DNA.
在美国,从犯罪现场收集的人类法医证据通常与犬科和猫科动物的生物材料混合在一起。了解从犯罪现场生物样本中提取的核 DNA 的浓度以及样本来源的物种对于 DNA 分析至关重要。当目标 DNA 可能被非目标 DNA 淹没时,准确检测和定量混合物种样本中的目标 DNA 至关重要。我们设计并评估了一种基于 TaqMan(®)定量实时 PCR (qPCR)技术的种特异性(人类、狗和猫)核 DNA 鉴定检测方法,该方法可以同时检测和测量微量的特定于人类、狗和/或猫的 DNA。荧光三链检测方法采用了以种特异性方式靶向人类 TH01 基因座以及犬科和猫科黑素皮质素 1 受体 (MC1R) 序列的引物和水解探针。我们还证明,该检测方法是一种高度敏感、可靠和强大的方法,可用于鉴定和定量混合物种模板,其人类-犬-猫起源的模板最小检测量分别为 0.4pg 人类和猫核 DNA,以及 4.0pg 犬核 DNA。