Quantitative real-time PCR (qPCR) assay for human-dog-cat species identification and nuclear DNA quantification

被引:28
作者
Kanthaswamy, S. [1 ,2 ]
Premasuthan, A. [1 ]
Ng, J. [1 ]
Satkoski, J. [1 ]
Goyal, V. [1 ]
机构
[1] Univ Calif Davis, Mol Anthropol Lab, Dept Anthropol, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Environm Toxicol, Davis, CA 95616 USA
关键词
DNA quantification; Species identification; Human; dog and cat forensic DNA analysis; DEVELOPMENTAL VALIDATION; FORENSIC SAMPLES; DEGRADATION;
D O I
10.1016/j.fsigen.2011.06.005
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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 (R) 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. Published by Elsevier Ireland Ltd.
引用
收藏
页码:290 / 295
页数:6
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