Ago K, Ago M, Nakagawa S, Ogata M
Department of Legal Medicine, Graduate School of Medicine and Dental Sciences, Kagoshima University, Kagoshima, Japan.
Am J Primatol. 2006 Oct;68(10):1025-31. doi: 10.1002/ajp.20285.
Amplification products from male and female Japanese macaques were obtained by PCR with human Y-chromosomal DYS389 primers. These products were examined by electrophoresis and sequence analysis. The PCR products from the 12 Japanese macaques tested had different band patterns on an electrophoretogram. Sequence analysis of the products revealed that the high polymorphism originated from variable numbers of repeats of two separate CTAT sequences. The sequences of the Japanese macaque products were similar to those of the reference human DYS389 sequence. However, variable CTGT repeats and a difference in the second forward primer binding site yielded two products in human males, DYS389I and DYS389II, which do not exist in Japanese macaques. Our results suggest that the human DYS389 primers may be a potential tool not only for distinguishing between human and Japanese macaque DNA samples, but also for identifying individual macaques, because of the highly polymorphic alleles.
使用人类Y染色体DYS389引物通过聚合酶链反应(PCR)获得了雄性和雌性日本猕猴的扩增产物。通过电泳和序列分析对这些产物进行了检测。所检测的12只日本猕猴的PCR产物在电泳图上具有不同的条带模式。产物的序列分析表明,高度多态性源于两个独立的CTAT序列重复数目的变化。日本猕猴产物的序列与参考人类DYS389序列相似。然而,可变的CTGT重复序列以及第二个正向引物结合位点的差异在人类男性中产生了两种产物,即DYS389I和DYS389II,而在日本猕猴中不存在。我们的结果表明,由于等位基因的高度多态性,人类DYS389引物可能不仅是区分人类和日本猕猴DNA样本的潜在工具,也是识别个体猕猴的潜在工具。