Sineo L, Martini R, Borghi G, Failli M
Istituto ricerche cliniche, Firenze, Italy.
Boll Chim Farm. 1993 Jun;132(6):201-2.
RAPD-PCR is a new technique that, starting from genomic DNA allows, with the use of a single primer of "random" base composition to amplify a variable number of sequences that can give important informations if analyzed for linkage studies, gene mapping or phylogenetic purposes. In order to detect the possible application of this simple way of DNA-fingerprinting in individual identification and in cell lineages characterization we analyzed human and non-human Primates DNA. Six different single primers of variable length were used and resulted in individual or specific electrophoretic patterns. As already reported we found a better resolution using "short" primers. The individual electrophoretic patterns obtained by RAPD-PCR can be a simple and reliable approach to DNA analysis.
随机扩增多态性DNA聚合酶链反应(RAPD-PCR)是一项新技术,它从基因组DNA开始,利用单个碱基组成“随机”的引物,扩增出数量可变的序列。如果对这些序列进行连锁研究、基因图谱绘制或系统发育分析,它们能够提供重要信息。为了检测这种简单的DNA指纹识别方法在个体识别和细胞谱系特征分析中的潜在应用,我们分析了人类和非人类灵长类动物的DNA。我们使用了六种不同长度的单引物,结果产生了个体特异性或特定的电泳图谱。正如之前所报道的,我们发现使用“短”引物能获得更好的分辨率。通过RAPD-PCR获得的个体电泳图谱可以成为一种简单而可靠的DNA分析方法。