Naito E, Dewa K, Yamanouchi H, Kominami R
Department of Forensic Science, Niigata University School of Medicine, Japan.
J Forensic Sci. 1994 Jul;39(4):1009-17.
Forensic DNA samples have been examined to ascertain the feasibility of a sex-typing procedure that we have recently developed. This uses two sets of primers complementary to the DXZ4 and SRY genes for polymerase chain reaction (PCR). PCR target in the DXZ4, an 80-bp sequence within the 130-bp fragment specific to females, is generated from inactive chromosome X by the DNA digestion with a methylation-sensitive restriction enzyme, HpaII. Therefore, the DXZ4 amplification and subsequent agarose gel electrophoresis detect the 80-bp fragment from female DNA. On the other hand, the SRY probe identifies a male-specific sequence on chromosome Y. Testing DNAs from fresh Turner's blood and from postmortem tissues exhibited band-signals confirming the sex identification. Degraded DNAs isolated from severely decomposed specimens were also identifiable when high-molecular-weight DNA was isolated before the assay. This demonstrates the usefulness of this method in forensic identification.
已对法医DNA样本进行检测,以确定我们最近开发的一种性别鉴定程序的可行性。该程序使用两组与DXZ4和SRY基因互补的引物进行聚合酶链反应(PCR)。DXZ4中的PCR靶点是一段80个碱基对的序列,位于女性特有的130个碱基对片段内,通过用甲基化敏感限制酶HpaII消化DNA,从失活的X染色体产生。因此,DXZ4扩增及随后的琼脂糖凝胶电泳可检测到来自女性DNA的80个碱基对片段。另一方面,SRY探针可识别Y染色体上的男性特异性序列。对来自新鲜特纳氏综合征患者血液和死后组织的DNA进行检测,显示出条带信号,证实了性别鉴定。当在检测前分离出高分子量DNA时,从严重腐败标本中分离出的降解DNA也可被识别。这证明了该方法在法医鉴定中的实用性。