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一种灵敏的变性梯度凝胶电泳分析方法显示,人类线粒体DNA控制区高变区1中异质性频率很高。

A sensitive denaturing gradient-Gel electrophoresis assay reveals a high frequency of heteroplasmy in hypervariable region 1 of the human mtDNA control region.

作者信息

Tully L A, Parsons T J, Steighner R J, Holland M M, Marino M A, Prenger V L

机构信息

University of Maryland, School of Medicine, Division of Human Genetics, Baltimore, MD, USA.

出版信息

Am J Hum Genet. 2000 Aug;67(2):432-43. doi: 10.1086/302996. Epub 2000 Jun 28.

Abstract

A population study of heteroplasmy in the hypervariable region 1 (HV1) portion of the human mtDNA control region was performed. Blood samples from 253 randomly chosen individuals were examined using a sensitive denaturing gradient-gel electrophoresis (DGGE) system. This method is capable of detecting heteroplasmic proportions as low as 1% and virtually all heteroplasmy where the minor component is > or = 5%. Heteroplasmy was observed in 35 individuals (13.8%; 95% confidence interval [CI] 9.6-18.0). Of these individuals, 33 were heteroplasmic at one nucleotide position, whereas 2 were heteroplasmic at two different positions (a condition known as "triplasmy"). Although heteroplasmy occurred at a total of 16 different positions throughout HV1, it was most frequently observed at positions 16093 (n=13) and 16129 (n=6). In addition, the majority of heteroplasmic variants occurred at low proportions and could not be detected by direct sequencing of PCR products. This study indicates that low-level heteroplasmy in HV1 is relatively common and that it occurs at a broad spectrum of sites. Our results corroborate those of other recent reports indicating that heteroplasmy in the control region is more common than was previously believed-a finding that is of potential importance to evolutionary studies and forensic applications that are based on mtDNA variation.

摘要

对人类线粒体DNA控制区高变区1(HV1)部分的异质性进行了一项群体研究。使用灵敏的变性梯度凝胶电泳(DGGE)系统检测了253名随机选取个体的血样。该方法能够检测低至1%的异质比例,并且实际上能检测到所有次要成分≥5%的异质性。在35名个体中观察到了异质性(13.8%;95%置信区间[CI] 9.6 - 18.0)。在这些个体中,33人在一个核苷酸位置存在异质性,而2人在两个不同位置存在异质性(一种称为“三质性”的情况)。尽管在整个HV1中总共16个不同位置出现了异质性,但最常出现在位置16093(n = 13)和16129(n = 6)。此外,大多数异质变体以低比例出现,通过PCR产物直接测序无法检测到。这项研究表明,HV1中的低水平异质性相对常见,且发生在广泛的位点。我们的结果证实了其他近期报告的结果,表明控制区的异质性比之前认为的更为常见——这一发现对基于线粒体DNA变异的进化研究和法医应用具有潜在重要性。

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