Vanecek T, Vorel F, Sip M
Sikl's Department of Pathology, Charles University Hospital, Pilsen, Czech Republic.
Int J Legal Med. 2004 Feb;118(1):14-8. doi: 10.1007/s00414-003-0407-2. Epub 2003 Oct 31.
In order to identify polymorphic sites and to find out their frequencies and the frequency of haplotypes, the complete D-loop of mitochondrial DNA (mtDNA) from 93 unrelated Czech Caucasians was sequenced. Sequence comparison showed that 85 haplotypes were found and of these 78 were unique, 6 were observed twice and 1 was observed three times. Genetic diversity (GD) was estimated at 0.999 and the probability of two randomly selected sequences matching (random match probability, RMP) at 1.2%. Additionally these calculations were carried out for hypervariable regions 1, 2 (HV1, HV2), for the area between HV1 and HV2 and for the area of the hypervariable region HV3. The average number of nucleotide differences (ANND) was established to be 10.2 for the complete D-loop. The majority of sequence variations were substitutions, particularly transitions. Deletions were found only in the region where HV3 is situated and insertions in the same place and in poly-C tracts between positions 303 and 315 in HV2. A high degree of length heteroplasmy was found especially in the regions of poly-C tracts between positions 16184 and 16193 in HV1 and between positions 303 and 315 in HV2. Position heteroplasmies were found in two cases.
为了鉴定多态性位点,找出它们的频率以及单倍型频率,对93名无亲缘关系的捷克高加索人的线粒体DNA(mtDNA)完整D环进行了测序。序列比较显示,共发现85种单倍型,其中78种是独特的,6种被观察到两次,1种被观察到三次。估计遗传多样性(GD)为0.999,两个随机选择的序列匹配的概率(随机匹配概率,RMP)为1.2%。此外,还针对高变区1、2(HV1、HV2)、HV1和HV2之间的区域以及高变区HV3的区域进行了这些计算。完整D环的平均核苷酸差异数(ANND)确定为10.2。大多数序列变异是替换,尤其是转换。仅在HV3所在区域发现了缺失,在HV2的303至315位之间的同一位置和多聚C序列中发现了插入。特别是在HV1的16184至16193位之间以及HV2的303至315位之间的多聚C序列区域发现了高度的长度异质性。在两例中发现了位置异质性。