Kim Na Young, Lee Hwan Young, Park Sun Joo, Yang Woo Ick, Shin Kyoung-Jin
Department of Forensic Medicine, Yonsei University College of Medicine, 50 Yonsei-ro, Seodaemun-gu, Seoul, 120-752, Korea.
J Forensic Sci. 2013 May;58(3):738-43. doi: 10.1111/1556-4029.12062. Epub 2013 Feb 13.
Two multiplex polymerase chain reaction (PCR) systems (Midiplex and Miniplex) were developed for the amplification of the mitochondrial DNA (mtDNA) control region, and the efficiencies of the multiplexes for amplifying degraded DNA were validated using old skeletal remains. The Midiplex system consisted of two multiplex PCRs to amplify six overlapping amplicons ranging in length from 227 to 267 bp. The Miniplex system consisted of three multiplex PCRs to amplify 10 overlapping short amplicons ranging in length from 142 to 185 bp. Most mtDNA control region sequences of several 60-year-old and 400-500-year-old skeletal remains were successfully obtained using both PCR systems and consistent with those previously obtained by monoplex amplification. The multiplex system consisting of smaller amplicons is effective for mtDNA sequence analyses of ancient and forensic degraded samples, saving time, cost, and the amount of DNA sample consumed during analysis.
开发了两种多重聚合酶链反应(PCR)系统(Midiplex和Miniplex)用于扩增线粒体DNA(mtDNA)控制区,并使用陈旧骨骼遗骸验证了多重系统扩增降解DNA的效率。Midiplex系统由两个多重PCR组成,用于扩增六个重叠的扩增子,长度在227至267bp之间。Miniplex系统由三个多重PCR组成,用于扩增10个重叠的短扩增子,长度在142至185bp之间。使用这两种PCR系统成功获得了多具60岁和400 - 500岁骨骼遗骸的大多数mtDNA控制区序列,且与之前通过单重扩增获得的序列一致。由较小扩增子组成的多重系统对于古代和法医降解样本的mtDNA序列分析有效,可节省时间、成本以及分析过程中消耗的DNA样本量。