非裔美国人的线粒体DNA多样性。

Mitochondrial Dna Pub Date : 2015-06-01 Epub Date: 2013-10-09 DOI:10.3109/19401736.2013.840591
Derek C Johnson, Sadeep Shrestha, Howard W Wiener, Robert Makowsky, Ashish Kurundkar, Craig M Wilson, Brahim Aissani
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引用次数: 21

摘要

线粒体DNA (mtDNA)的遗传多态性定义了称为mtDNA单倍群的种群特异性特征。估计mtDNA单倍群分布可能容易出错,特别是如果研究样本不是来自多中心队列。在这里,我们报告了在一个多中心队列中登记的非裔美国人样本(n = 343)的mtDNA多样性。对D-loop控制区高变区I和II的测序显示,最常见的线粒体变异是73G、146C、150T、152C、189G、16278T和16311C。与已发表的数据一致,我们观察到17个常见的mtDNA单倍群:L0、L1、L1b、L1c、L2、L2a、L2b、L2c、L2e、L3、L3b、L3d、L3e、L3f、L3h、L3x和L4。最常见的单倍群是L2a(19.8%),其次是L1b(10.2%)。总的来说,我们研究中观察到的mtDNA单倍群分布与非裔美国人和非洲人口的分布相似。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mitochondrial DNA diversity in the African American population.

Mitochondrial DNA diversity in the African American population.

Genetic polymorphism along mitochondrial DNA (mtDNA) defines population-specific signatures called mtDNA haplogroups. Estimation of mtDNA haplogroup distribution may be prone to errors, notably if the study sample is not drawn from a multicenter cohort. Here, we report on mtDNA diversity in a sample of African American individuals (n = 343) enrolled in a multicenter cohort. Sequencing of the hypervariable regions I and II of the D-loop control region showed that the most common mitochondrial variants are 73G, 146C, 150T, 152C, 189G, 16278T, and 16311C. In agreement with the published data, we observed 17 common mtDNA haplogroups: L0, L1, L1b, L1c, L2, L2a, L2b, L2c, L2e, L3, L3b, L3d, L3e, L3f, L3h, L3x, and L4. The most commonly observed haplogroup is L2a (19.8%), followed by L1b (10.2%). Overall, the observed mtDNA haplogroup distribution in our study is similar to those published for the African American and the African populations.

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来源期刊
Mitochondrial Dna
Mitochondrial Dna 生物-遗传学
自引率
0.00%
发文量
0
审稿时长
2.4 months
期刊介绍: Previously published under the title DNA Sequence (Vols 1-19.3), Mitochondrial DNA accepts original high-quality reports based on mapping, sequencing and analysis of mitochondrial DNA and RNA. Descriptive papers on DNA sequences from mitochondrial genomes, and also analytical papers in the areas of population genetics, medical genetics, phylogenetics and human evolution that use mitochondrial DNA as a source of evidence for studies will be considered for publication. The editorial board will also consider manuscripts that examine population genetic and systematic theory that specifically address the use of mitochondrial DNA sequences.
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