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人类线粒体DNA变异与巴斯克人的起源。

Human mitochondrial DNA variation and the origin of Basques.

作者信息

Bertranpetit J, Sala J, Calafell F, Underhill P A, Moral P, Comas D

机构信息

Laboratori d'Antropologia, Facultat de Biologia, Universitat de Barcelona, Spain.

出版信息

Ann Hum Genet. 1995 Jan;59(1):63-81. doi: 10.1111/j.1469-1809.1995.tb01606.x.

DOI:10.1111/j.1469-1809.1995.tb01606.x
PMID:7762985
Abstract

The hypervariable segment I of the control region of the mtDNA (positions 16024-16383) was PCR-amplified from mouth scrape and hairs and sequenced in 45 unrelated individuals of pure matrilineal Basque descent. Twenty-seven different sequences were found, of which 21 are unique to the Basques. The allelic partition observed, together with resampling experiments, suggested that much more variation remained to be discovered. The mean pairwise difference in number of nucleotides between individuals was 3-15, a very low value. Moreover, the number of steps for the most parsimonious tree is very low compared to the number of different sequences. Both findings suggest that the Basque population was founded by a few lineages that diverged in a short time span. The number of nucleotide differences between individuals was shown not to be influenced by the distance between their birthplaces, thus validating the sampling strategy used a posteriori. The pairwise difference distribution agreed well with the three-parameter model proposed by Rogers & Harpending (1992). The parameter estimates found for the Basques implied that a demographic expansion (or perhaps two, given the bimodal shape of the distribution) took place sometime between 14500 and 42000 BP which is in agreement with archaeological data. Our sample was compared to other populations for which D-loop sequences were available through the Nei & Miller (1990) distance. In a neighbour-joining tree, all the Caucasoid samples, including the Basques, appeared tightly clustered, whereas African samples were the most distant to the Caucasoids and also the most heterogeneous. Although classical markers, such as blood groups and protein polymorphisms, clearly separate the Basques (and the Sardinians) from other European populations, this distinctiveness was not found using D-loop sequences.

摘要

从45名纯母系巴斯克血统的无亲缘关系个体的口腔刮擦物和毛发中,对线粒体DNA控制区的高变区I(位置16024 - 16383)进行PCR扩增并测序。共发现27种不同序列,其中21种是巴斯克人特有的。观察到的等位基因划分以及重采样实验表明,仍有更多变异有待发现。个体间核苷酸数量的平均成对差异为3 - 15,这是一个非常低的值。此外,与不同序列的数量相比,最简约树的步骤数非常少。这两个发现都表明,巴斯克人群是由少数在短时间内分化的谱系建立的。个体间核苷酸差异的数量不受其出生地之间距离的影响,从而验证了事后使用的采样策略。成对差异分布与罗杰斯和哈彭丁(1992)提出的三参数模型吻合良好。为巴斯克人找到的参数估计表明,在公元前14500年至42000年之间的某个时候发生了人口扩张(鉴于分布的双峰形状,也许是两次),这与考古数据一致。通过内和米勒(1990)距离,将我们的样本与其他有D环序列的人群进行了比较。在邻接树中,所有高加索样本,包括巴斯克人,都紧密聚类,而非洲样本与高加索人距离最远,且也是最具异质性的。尽管经典标记,如血型和蛋白质多态性,清楚地将巴斯克人(和撒丁岛人)与其他欧洲人群区分开来,但使用D环序列未发现这种独特性。

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