A simple method for the determination of sex from the pulp of freshly extracted human teeth utilizing the polymerase chain reaction.

U Pillay, B Kramer
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Abstract

The polymerase chain reaction (PCR) has been used to amplify a region of the ZFX and ZFY genes from DNA in human blood and other tissues, for determination of the sex of an individual. In the present study DNA was extracted from the pulp of 21 male and 24 female fresh human third molar teeth. A region of the ZFX and ZFY genes was amplified by PCR and analysed by digestion of the amplified DNA with HaeIII restriction endonuclease. The digested PCR products were run on a 2 per cent agarose gel. Males were distinguished from females by having a fragment of 317 base pairs which was absent in females. Identification of the sex of the individual was 100 per cent accurate in each case. A blind study of random samples of the same teeth, used to assess the reproducibility of the technique evoked an identical result. This method provides an accurate alternative to skeletal measurements and histological staining techniques for the sexing of individuals from small amounts of DNA.

一种利用聚合酶链反应测定新拔牙牙髓性别的简单方法。
聚合酶链反应(PCR)已被用于从人类血液和其他组织的DNA中扩增ZFX和ZFY基因的一个区域,以确定个体的性别。本研究从21名男性和24名女性新鲜人第三磨牙的牙髓中提取DNA。用PCR扩增ZFX和ZFY基因的一个区域,用HaeIII限制性内切酶酶切扩增DNA进行分析。消化的PCR产物在2%琼脂糖凝胶上运行。雄性与雌性的区别在于,雄性具有317个碱基对的片段,而这在雌性中是缺失的。在每种情况下,对个体性别的识别都是100%准确的。对相同牙齿的随机样本进行盲法研究,用来评估该技术的可重复性,得出了相同的结果。这种方法提供了一种精确的替代骨骼测量和组织学染色技术,用于从少量DNA中确定个体的性别。
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