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Identification of animal skin of historical parchments by polymerase chain reaction (PCR)-based methods

机译:基于聚合酶链反应的历史羊皮膜动物皮肤的鉴定(PCR)的基础方法

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This study deals with establishing of a PCR-based strategy with the aim to recognize the animal origin of different historical parchments. This is one of relatively rare studies on the analysis of ancient DNA from parchments. Robustness of the PCR technology is demonstrated by successful identification of the animal species using only a small amount of DNA isolated from 12 parchment samples. Ten PCR-based assays specific for the detection of different animal species (Bos taurus, Ovis aries, Capra hircus, Sus scrofa, Oryctolagus domestica, Cervus elaphus, Capreolus capreolus, Dama dama) and two PCR assays utilizing universal primers were evaluated and optimized with the aim to find a rapid parchment identification method, which would be more reliable than the classical microscopic examination. The optimized PCR methods produced satisfactory results. Out of 12 investigated parchments, 9 items were unambiguously identified, DNA from 2 samples could not be amplified with any of the species-specific PCR assays, and only one parchment produced controversial results. The species-specific PCR results were confirmed by direct sequencing and PCR cloning with consequent sequencing. Our approach, including isolation of parchment DNA by chaotropic solid-phase extraction, optimization of the PCR programs and high-stringency annealing temperatures, demonstrated to be effective, easy and reliable for the analysis of historical parchment DNA. We consider this PCR-based strategy potentially useful also for investigation of other types of animal items conserved in museums, galleries or libraries.
机译:本研究涉及建立基于PCR的战略,其目的是识别不同历史植物的动物来源。这是关于羊皮纸古代DNA分析的相对罕见的研究之一。通过仅使用从12个羊皮纸样品中分离的少量DNA成功鉴定动物物种来证明PCR技术的鲁棒性。评估并优化利用通用引物的培养物种用于检测不同动物物种的基于PCR的基于PCR的测定,用于检测不同的动物物种(BOS Taurus,Ovis,Capra Hircus,SUS Scrophus,Caperolus Caperus,Dama Dama)和两个PCR测定。旨在找到一种快速羊皮纸鉴定方法,它比经典微观检查更可靠。优化的PCR方法产生了令人满意的结果。在12个调查的羊膜中,毫不含糊地识别出9项,其中2个样品中的DNA不能与任何物种特异性PCR测定扩增,只有一根羊皮纸产生有争议的结果。通过直接测序和PCR克隆来证实特异性PCR结果,随后的测序。我们的方法,包括通过旋流固相提取,优化PCR节目和高严格退火温度的母猪DNA的分离,证明是有效,容易可靠地分析历史羊皮膜DNA。我们认为这种基于PCR的战略可能还可用于调查在博物馆,画廊或图书馆保守的其他类型的动物物品。

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