Mitchell Sabrina L, Goodloe Robert, Brown-Gentry Kristin, Pendergrass Sarah A, Murdock Deborah G, Crawford Dana C
Department of Molecular Physiology and Biophysics, Center for Human Genetics Research, Vanderbilt University, 2215 Garland Avenue, 519 Light Hall, Nashville, Tennessee, USA,
Hum Genet. 2014 Jul;133(7):861-8. doi: 10.1007/s00439-014-1421-9. Epub 2014 Feb 1.
Mitochondrial DNA (mtDNA) haplogroups are valuable for investigations in forensic science, molecular anthropology, and human genetics. In this study, we developed a custom panel of 61 mtDNA markers for high-throughput classification of European, African, and Native American/Asian mitochondrial haplogroup lineages. Using these mtDNA markers, we constructed a mitochondrial haplogroup classification tree and classified 18,832 participants from the National Health and Nutrition Examination Surveys (NHANES). To our knowledge, this is the largest study to date characterizing mitochondrial haplogroups in a population-based sample from the United States, and the first study characterizing mitochondrial haplogroup distributions in self-identified Mexican Americans separately from Hispanic Americans of other descent. We observed clear differences in the distribution of maternal genetic ancestry consistent with proposed admixture models for these subpopulations, underscoring the genetic heterogeneity of the United States Hispanic population. The mitochondrial haplogroup distributions in the other self-identified racial/ethnic groups within NHANES were largely comparable to previous studies. Mitochondrial haplogroup classification was highly concordant with self-identified race/ethnicity (SIRE) in non-Hispanic whites (94.8 %), but was considerably lower in admixed populations including non-Hispanic blacks (88.3 %), Mexican Americans (81.8 %), and other Hispanics (61.6 %), suggesting SIRE does not accurately reflect maternal genetic ancestry, particularly in populations with greater proportions of admixture. Thus, it is important to consider inconsistencies between SIRE and genetic ancestry when performing genetic association studies. The mitochondrial haplogroup data that we have generated, coupled with the epidemiologic variables in NHANES, is a valuable resource for future studies investigating the contribution of mtDNA variation to human health and disease.
线粒体DNA(mtDNA)单倍群对于法医学、分子人类学和人类遗传学研究具有重要价值。在本研究中,我们开发了一个包含61个mtDNA标记的定制面板,用于对欧洲、非洲以及美洲原住民/亚洲线粒体单倍群谱系进行高通量分类。利用这些mtDNA标记,我们构建了一个线粒体单倍群分类树,并对来自国家健康与营养检查调查(NHANES)的18,832名参与者进行了分类。据我们所知,这是迄今为止在美国基于人群的样本中对线粒体单倍群进行特征描述的最大规模研究,也是首次将自我认定的墨西哥裔美国人与其他血统的西班牙裔美国人分开来描述线粒体单倍群分布的研究。我们观察到母系遗传血统分布存在明显差异,这与针对这些亚人群提出的混合模型一致,凸显了美国西班牙裔人群的遗传异质性。NHANES中其他自我认定的种族/族裔群体的线粒体单倍群分布在很大程度上与先前的研究相当。线粒体单倍群分类在非西班牙裔白人中与自我认定的种族/族裔(SIRE)高度一致(94.8%),但在包括非西班牙裔黑人(88.3%)、墨西哥裔美国人(81.8%)和其他西班牙裔(61.6%)在内的混合人群中则低得多,这表明SIRE并不能准确反映母系遗传血统,尤其是在混合比例较高的人群中。因此,在进行基因关联研究时,考虑SIRE与遗传血统之间的不一致性很重要。我们生成的线粒体单倍群数据,再加上NHANES中的流行病学变量,是未来研究mtDNA变异对人类健康和疾病贡献的宝贵资源。