HPLC和uv -分光光度法检测古人类遗骸中古代DNA和PCR抑制剂

E. Arroyo-Pardo, M. A. Ocaña, J. J. Arroyo, A. Pérez‐Pérez, D. Turbón, G. Trancho, M. S. Rodríguez-Albarrán, J. Casas, B. Robledo, F. Bandrés
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引用次数: 2

摘要

古人类遗骸的研究可以通过聚合酶链反应(PCR)分析来进行,但主要的困难之一是克服强烈的PCR抑制。我们研究了六个考古遗址的遗骨。研究的遗骸共包括27个个体,时间跨度在2500年到400年之间。从35份样本中提取DNA,并扩增性别特异性的淀粉原蛋白序列以鉴定样本的性别。只考虑分子和人体测量数据一致的一致结果。尽管性别鉴定取得了成功,但为了建立一种快速预测古代DNA可能存在和状态的方案,研究人员使用紫外分光光度法和高效液相色谱法对样品进行了分析。紫外和高效液相色谱峰的组合似乎表明内源DNA的强烈降解。通过高效液相色谱法从6个样品中分离出一种PCR抑制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
HPLC and UV-Spectrophotometry Examination of Ancient DNA and PCR Inhibitors in Old Human Remains
The study of ancient human remains can be approached today through polymerase chain reaction (PCR) analysis, but one of the main difficulties involves overcoming strong PCR inhibitions. We studied skeletal remains from six archaeological sites. The remains studied include a total of 27 individuals and span between 2500 and 400 years before the present. DNA was extracted from 35 samples and sex-specific amelogenin sequences were amplified to identify the sex of the samples. Only consistent results for which molecular and anthropometrical data agreed were considered. Notwithstanding the success of the sex identification, the samples were analysed using ultraviolet (UV) spectrophotometry and high performance liquid chromatography (HPLC) in order to establish a rapid protocol to predict the possible presence and state of ancient DNA. A combination of UV and HPLC peaks seems to indicate a strong degradation of endogenous DNA. A PCR inhibitor was also isolated through HPLC in a set of six samples.
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