Nagai Atsushi, Nakamura Isao, Shiraki Futoru, Bunai Yasuo, Ohya Isao
Department of Legal Medicine, Gifu University School of Medicine, 40 Tsukasa-machi, Gifu 500-8705, Japan.
Leg Med (Tokyo). 2003 Mar;5 Suppl 1:S210-3. doi: 10.1016/s1344-6223(02)00114-1.
Sequence polymorphisms of the hypervariable region HV1 in mitochondrial DNA (mtDNA) were analyzed in a sample of 137 unrelated Japanese individuals living in Gifu Prefecture (central region of Japan) using polymerase chain reaction amplification and direct sequencing. Eighty-two different haplotypes resulting from 81 variable sites were found in the mtDNA HV1 region between positions 16061 and 16450. The most frequent haplotype (16223T, 16362C) was shared by ten individuals. The genetic diversity and the genetic identity were 0.985 and 0.022, respectively. The C-stretch region located around position 16189 was observed in 23.4% of this population sample. Sequence heteroplasmy at the position 16103 (A/G) was found in one individual.
利用聚合酶链反应扩增和直接测序技术,对居住在日本岐阜县(日本中部地区)的137名无血缘关系的日本人的样本进行了线粒体DNA(mtDNA)高变区HV1的序列多态性分析。在mtDNA HV1区域位于16061至16450位置之间,发现了由81个可变位点产生的82种不同单倍型。最常见的单倍型(16223T,16362C)为10个人所共有。遗传多样性和遗传同一性分别为0.985和0.022。在该群体样本的23.4%中观察到位于16189位置附近的C-重复序列区域。在一名个体中发现了16103位置(A/G)的序列异质性。