Chen Ming-Houng, Lee Horng-Mo, Tzen Chin-Yuan
St. Paul's Hospital, Taoyuan.
J Formos Med Assoc. 2002 Apr;101(4):268-76.
Although the displacement loop (D-loop) of mitochondrial DNA (mtDNA) is known to have a large number of sequence variations, data on this variation are lacking. This study investigated D-loop sequence polymorphism in Taiwanese subjects.
The D-loop mtDNA region was amplified from whole blood samples of 63 unrelated Taiwanese individuals using the polymerase chain reaction (PCR). PCR products were sequenced and analyzed. Sequence electropherograms of nucleotides 303 to 315 that showed particularly high background after C-stretch were subcloned to the PGEM-TE vector for sequencing analysis.
A total of 126 variable sites in 788 polymorphisms including 19 novel sites were found. The genetic diversity of the highly variable region (HVR)-I, HVR-II, HVR-III, and a region elsewhere were 0.999, 0.993, 0.850, and 0.707, respectively. The power of discrimination of these regions was 0.983, 0.977, 0.837, and 0.696, respectively. Both HVR-I and HVR-II contained segments of homopolymeric sequence. A high frequency (30%) of heteroplasmy made up of cytosine between nucleotides 303 and 315 appeared to be a unique feature of the Taiwanese population. Nucleotide substitutions at position 16,362 (T to C) in HVR-I have been found with high frequency in Taiwanese.
In this study, 19 polymorphisms in the D-loop of mtDNA in Taiwanese were newly identified, and an unusually high frequency of heteroplasmy was found in the region between nucleotides 303 and 315 in this population.
尽管已知线粒体DNA(mtDNA)的置换环(D环)存在大量序列变异,但关于这种变异的数据却很缺乏。本研究调查了台湾人群的D环序列多态性。
使用聚合酶链反应(PCR)从63名无亲缘关系的台湾个体的全血样本中扩增D环mtDNA区域。对PCR产物进行测序和分析。对C链延伸后背景特别高的303至315位核苷酸的序列电泳图进行亚克隆至PGEM - TE载体进行测序分析。
在788个多态性位点中总共发现了126个可变位点,其中包括19个新位点。高变区(HVR)-I、HVR-II、HVR-III和其他区域的遗传多样性分别为0.999、0.993、0.850和0.707。这些区域的鉴别力分别为0.983、0.977、0.837和0.696。HVR-I和HVR-II均包含同聚物序列片段。303至315位核苷酸之间由胞嘧啶组成的异质性高频(30%)似乎是台湾人群的一个独特特征。在台湾人群中,HVR-I的16,362位(T到C)核苷酸替换出现频率较高。
在本研究中,新鉴定出台湾人群mtDNA D环中的19个多态性,并且在该人群的303至315位核苷酸区域发现了异常高频率的异质性。