Murakami M, Fujise H, Lee Y S, Matsuba C, Fujitani H
Laboratories of Molecular Biology, Azabu University School of Veterinary Medicine, Sagamihara, Kanagawa, Japan.
J Vet Med Sci. 2001 Jun;63(6):679-81. doi: 10.1292/jvms.63.679.
To find definitive RFLP sites for canine sex determination, DNA segments corresponding to parts of the canine ZFX and ZFY genes were amplified by PCR and were directly sequenced. According to the newly defined sequence data, the combination of Haelll and Cfr13I sites was found to be useful for not only identifying the sex of the canine DNA samples but also distinguishing them from the human DNA. Conveniently, these two enzymes worked simultaneously in the same single buffer. The double-digestion of the ZFX/ZFY PCR products with HaeIII and Cfr13I showed banding patterns unique to males and females in Canis familialis. This PCR/RFLP method was confirmed to be applicable to various breeds of dog.
为了找到用于犬类性别鉴定的确切限制性片段长度多态性(RFLP)位点,通过聚合酶链反应(PCR)扩增了与犬类ZFX和ZFY基因部分相对应的DNA片段,并进行了直接测序。根据新定义的序列数据,发现HaeIII和Cfr13I位点的组合不仅可用于鉴定犬类DNA样本的性别,还可将它们与人类DNA区分开来。方便的是,这两种酶可在同一单一缓冲液中同时起作用。用HaeIII和Cfr13I对ZFX/ZFY PCR产物进行双酶切,显示出犬科动物中雄性和雌性特有的条带模式。这种PCR/RFLP方法被证实适用于各种犬种。