Chen Jin-Wen, Uboh Cornelius E, Soma Lawrence R, Li Xiaoqing, Guan Fuyu, You Youwen, Liu Ying
University of Pennsylvania School of Veterinary Medicine, New Bolton Center Campus, 382 West Street Road, Kennett Square, PA 19348, USA.
J Forensic Sci. 2010 Nov;55(6):1610-4. doi: 10.1111/j.1556-4029.2010.01466.x.
A novel multiplex of independent dinucleotide tandem repeat (DTR) loci was previously described that is capable of not only discriminating human and equine DNA, but of identifying a single equine source. We report a case in which a bloodstained syringe and two needles were found during inspection of a barn by inspectors of the Pennsylvania Racing Commissions. Using the multiplex and single-locus detection, all 21 equine DTR markers were detected in a suspect horse and two evidence samples, indicating the evidence samples came from the suspect animal. Only six markers were detected in the third evidence sample because the volume of blood was limited. Following whole-genome amplification and single-locus PCR, the third evidence sample detected a total of 17 markers and the likelihood of identity (probability from suspect horse/probability from a random pacer) was 7.0 × 10⁶. The DTR multiplex has some technical limitations, but it is already practical for casework.
先前已描述了一种新型的独立二核苷酸串联重复(DTR)位点多重检测方法,该方法不仅能够区分人类和马的DNA,还能识别单一马源。我们报告了一个案例,宾夕法尼亚赛马委员会的检查员在检查一个马厩时发现了一个带血的注射器和两根针头。使用多重检测和单一位点检测,在一匹嫌疑马和两个证据样本中检测到了所有21个马DTR标记,表明证据样本来自嫌疑动物。由于第三个证据样本中的血量有限,仅检测到六个标记。经过全基因组扩增和单一位点PCR后,第三个证据样本共检测到17个标记,同一性可能性(来自嫌疑马的概率/来自随机一匹马的概率)为7.0×10⁶。DTR多重检测方法存在一些技术限制,但已适用于实际案件工作。