Cali F, Le Roux M G, D'Anna R, Flugy A, De Leo G, Chiavetta V, Ayala G F, Romano V
OASI Istituto per la Ricerca sul Ritardo Mentale e l'Involuzione Cerebrale (IRCCS), Via Conte Ruggero 73, 94018 Troina, Enna, Italy.
Int J Legal Med. 2001;114(4-5):229-31. doi: 10.1007/s004140000169.
The forensic application of mtDNA typing requires large databases which are regionally well defined. To further this aim, we have typed mtDNA in a sample of 111 French and 106 Sicilians. The French were typed for both hypervariable segments (HVR1 and HVR2) of the mtDNA control region, whereas the Sicilians were only typed for HVR1, but in addition for the coding region RFLP markers for mtDNA groups H, I, J, K, L, M, T, U, V and X. In both samples, the predominant sequence type by far was the Cambridge reference sequence. Comparing HVR1 sequences, we found that the French sample was twice as diverse as the Sicilian sample as measured by sequence matches. A further set of sequence match comparisons including the French, Sicilian, and the published British mtDNA samples, demonstrate that sequence matching probabilities within samples differ by less than a factor of 2 from the matching probabilities between samples.
线粒体DNA分型的法医应用需要区域界定明确的大型数据库。为实现这一目标,我们对111名法国人和106名西西里人的样本进行了线粒体DNA分型。对法国人的线粒体DNA控制区的两个高变区(HVR1和HVR2)进行了分型,而对西西里人仅进行了HVR1分型,但此外还对线粒体DNA组H、I、J、K、L、M、T、U、V和X的编码区RFLP标记进行了分型。在两个样本中,到目前为止最主要的序列类型是剑桥参考序列。比较HVR1序列,我们发现通过序列匹配测量,法国样本的多样性是西西里样本的两倍。包括法国、西西里以及已发表的英国线粒体DNA样本在内的另一组序列匹配比较表明,样本内的序列匹配概率与样本间的匹配概率相差不到2倍。