Zhang Lu, Ding Mei, Pang Hao, Xing Jiaxin, Xuan Jinfeng, Wang Chunhong, Lin Ziqing, Han Song, Liang Kewei, Li Chunmei, Yao Jun, Wang Baojie
China Medical University School of Forensic Medicine, Shenyang, P. R. China.
Department of Forensic Medicine, National Police University of China, Shenyang, P. R. China.
Electrophoresis. 2016 Aug;37(15-16):2273-7. doi: 10.1002/elps.201600009. Epub 2016 Jul 11.
The identification of individuals in a mixture of two semen samples usually involves an analysis of autosomal and Y chromosomal short tandem repeats (STR) which can exclude unrelated individuals but cannot achieve the purpose of individual identification. In sperm cells, there are multiple copies of mitochondrial DNAs (mtDNA) which exhibit genetic polymorphisms in different matrilineal-related individuals. Single-cell capture technology can be applied to obtain some single sperm cells in a mixed semen sample, then polymerase chain reaction can be employed to amplify the mtDNA hypervariable region I (HVR I) from each cell. By pooling the cells with the same HVR I sequence, we can obtain the sufficient nuclear DNA for STR typing.
在两份精液样本的混合物中识别个体通常涉及对常染色体和Y染色体短串联重复序列(STR)的分析,这可以排除无关个体,但无法实现个体识别的目的。在精子细胞中,存在多个线粒体DNA(mtDNA)拷贝,这些拷贝在不同的母系相关个体中表现出遗传多态性。单细胞捕获技术可用于从混合精液样本中获取一些单个精子细胞,然后可采用聚合酶链反应从每个细胞中扩增线粒体DNA高变区I(HVR I)。通过将具有相同HVR I序列的细胞汇集在一起,我们可以获得足够的核DNA用于STR分型。