Yamamoto Kaori, Tsubota Toshio, Komatsu Takeshi, Katayama Atsushi, Murase Tetsuma, Kita Isao, Kudo Tadaaki
United Graduate School of Veterinary Science, Faculty of Agriculture, Gifu University, Japan.
J Vet Med Sci. 2002 Jun;64(6):505-8. doi: 10.1292/jvms.64.505.
A method for sex identification of the Japanese black bear was examined using a polymerase chain reaction (PCR) and sequencing of a part of the amelogenin gene. This gene is located on the X and Y chromosomes, and there are 54 nucleotide deletions on the Y chromosome-specific gene. Forty-seven (26 male and 21 female) DNA samples and 23 (13 male and 10 female) DNA samples, respectively extracted from white blood cells and hairs of Japanese black bears were analyzed. The primers SE47 and SE48 from this X-Y homologous region were used in sex identification by PCR amplification. These primers amplified X- and Y-specific bands, which could be used to discriminate between sexes by a length polymorphism in all samples. We suggest that PCR amplification using the primers SE47 and SE48 is useful for sex determination of the Japanese black bear and could be applied to DNA analysis of small samples such as hairs.
采用聚合酶链反应(PCR)和牙釉蛋白基因部分序列测序的方法对日本黑熊进行性别鉴定。该基因位于X和Y染色体上,Y染色体特异性基因上有54个核苷酸缺失。分别从日本黑熊的白细胞和毛发中提取了47份(26份雄性和21份雌性)DNA样本以及23份(13份雄性和10份雌性)DNA样本进行分析。利用该X-Y同源区域的引物SE47和SE48通过PCR扩增进行性别鉴定。这些引物扩增出X和Y特异性条带,可通过长度多态性在所有样本中区分性别。我们认为,使用引物SE47和SE48进行PCR扩增对日本黑熊的性别鉴定很有用,并且可应用于毛发等小样本的DNA分析。