Alonso Antonio, Martin Pablo, Albarrán Cristina, García Pilar, Primorac Dragan, García Oscar, Fernández de Simón Lourdes, García-Hirschfeld Julia, Sancho Manuel, Fernández-Piqueras Jose
Instituto Nacional de Toxicología, Servicio de Biología, Luis Cabrera 9, 28002 Madrid, Spain.
Croat Med J. 2003 Jun;44(3):273-80.
We reviewed the current methodologies used for human DNA quantitation in forensic and ancient DNA studies, including sensitive hybridization methods based on the detection of nuclear alpha-satellite repetitive DNA regions or more recently developed fluorogenic real-time polymerase chain reaction (PCR) designs for the detection of both nuclear and mitochondrial DNA regions. Special emphasis has been put on the applicability of recently described different real-time PCR designs targeting different fragments of the HV1 mtDNA control region, and a segment of the X-Y homologous amelogenin gene. The importance of these quantitative assays is to ensure the consistency of low copy number DNA typing (STR profiling and mtDNA sequencing).
我们回顾了法医和古DNA研究中用于人类DNA定量的当前方法,包括基于检测核α卫星重复DNA区域的灵敏杂交方法,以及最近开发的用于检测核DNA和线粒体DNA区域的荧光实时聚合酶链反应(PCR)设计。特别强调了最近描述的针对HV1线粒体DNA控制区域不同片段以及X-Y同源牙釉蛋白基因片段的不同实时PCR设计的适用性。这些定量分析的重要性在于确保低拷贝数DNA分型(STR分型和线粒体DNA测序)的一致性。