Kornienko I V, Vodolazhskiĭ D I, Afanas'eva G V, Ivanov P L
Sud Med Ekspert. 2004 Nov-Dec;47(6):27-32.
Polymorphism of mDNA D-loop central region (CR), positions 16366-0072) was studied versus hypervariable sections (HVS1), positions 16024-16365, and HVS2, positions 00073-00340, for a sample of 71 residents of the Russian Federation. Ten polymorphic positions with 56 nucleotide substitutions, 55 of which are transitions, were detect in the CR section; no insertions or deletions were found there. It was proven as possible to use the mDNA CR locus as an additional identification marker in the forensic-expert of the mDNA control region. The probability of random coincidence (RC) of haplotypes in joint typing of HVS1, HVS2 and CR made 0.0208, which is 1.4-fold less versus the same parameter for haplotypes HVS1/HVS2 (RC = 0.0284).
针对71名俄罗斯联邦居民的样本,研究了线粒体DNA(mDNA)控制区(CR)中央区域(位置16366 - 0072)相对于高变区1(HVS1,位置16024 - 16365)和高变区2(HVS2,位置00073 - 00340)的多态性。在CR区域检测到10个具有56个核苷酸替换的多态性位点,其中55个为转换,未发现插入或缺失。已证明在法医鉴定线粒体DNA控制区时,可将mDNA CR位点用作额外的鉴定标记。HVS1、HVS2和CR联合分型时单倍型随机匹配概率(RC)为0.0208,相较于HVS1/HVS2单倍型的相同参数(RC = 0.0284)低1.4倍。