Kreike J, Lehner A
Institut für Gerichtliche Medizin, Universität Wien, Austria.
Int J Legal Med. 1995;107(5):235-8. doi: 10.1007/BF01245480.
Sex determination of pure and mixed blood samples and stains was performed by amplification of the X-specific and Y-specific alphoid sequences by PCR (XY-PCR). From mixed blood samples with female DNA present in large excess of male DNA, the Y-specific sequence still amplified efficiently. In the analysis of vaginal secretions in a case of sexual assault, XY-PCR was performed to test the efficiency of the selective lysis procedure in order to investigate whether alleles found with other PCR systems were of male or female origin. Our studies with mixed blood samples revealed pronounced DNA competition in the HLA-DQ alpha and D1S80 PCR systems: the alleles from a minor DNA component could not be detected in the presence of a large excess of DNA from a second person.
通过聚合酶链反应(XY-PCR)扩增X特异性和Y特异性α卫星序列,对纯血样和混合血样及污渍进行性别鉴定。在女性DNA大大超过男性DNA的混合血样中,Y特异性序列仍能高效扩增。在一例性侵犯案件的阴道分泌物分析中,进行XY-PCR以测试选择性裂解程序的效率,从而调查用其他PCR系统检测到的等位基因是男性还是女性来源。我们对混合血样的研究表明,在HLA-DQα和D1S80 PCR系统中存在明显的DNA竞争:在存在大量来自另一个人的DNA时,无法检测到微量DNA成分的等位基因。