Alfonso-Sánchez M A, Cardoso S, Martínez-Bouzas C, Peña J A, Herrera R J, Castro A, Fernández-Fernández I, De Pancorbo M M
Departamento de Genética y Antropología Física, Facultad de Ciencia y Tecnología, Universidad del País Vasco, 48080 Bilbao, Bizkaia, Spain.
Am J Hum Biol. 2008 Mar-Apr;20(2):154-64. doi: 10.1002/ajhb.20706.
This study provides a more complete characterization of the mitochondrial genome variability of the Basques, including data on the hypervariable segment HVII of the D-loop region, which remains relatively unknown. To that end, genomic DNA from 55 healthy men living in the Arratia Valley (Biscay province) and the Goiherri region (Guipúzcoa province) was examined by direct sequencing. Three-generation pedigree charts were compiled to ensure the collection from autochthonous individuals. The most notable findings emerging from the analysis of haplogroup composition are: (i) lack of U8a mitochondrial lineage, a rare subhaplogroup recently identified in Basques and proposed as a Paleolithic marker, (ii) low frequency of haplogroup V, which conflicts with results of earlier analyses describing high frequencies in southwestern Europe, and (iii) high frequency of haplogroup J, especially subhaplogroups J1c1 and J2a. The frequency of haplogroup J does not coincide with previous mtDNA studies in present-day Basques, but is congruent with frequencies found in prehistoric and historic Basque populations. In explaining divergence in haplogroup composition between modern Basque samples, we hypothesized spatial heterogeneity promoted by population fragmentation due to extreme limitation of dispersal opportunities during the Pleistocene glaciations. Similarities between extinct and extant Basque populations as for the high frequency of lineage J, as well as the abundance of this haplogroup in northern Spain endorse a shift in the focus of attention of mtDNA analysts. A refined dissection of haplogroup J might provide more solid evidence about the process of postglacial recolonization of Europe, and thus about the shaping of the European gene pool.
本研究对巴斯克人的线粒体基因组变异性进行了更全面的描述,包括D环区域高变区HVII的数据,该区域仍相对鲜为人知。为此,通过直接测序检测了来自居住在阿拉蒂亚山谷(比斯开省)和戈伊埃里地区(吉普斯夸省)的55名健康男性的基因组DNA。编制了三代谱系图以确保采集到本地个体的样本。单倍群组成分析得出的最显著发现是:(i)缺乏U8a线粒体谱系,这是一种最近在巴斯克人中发现的罕见亚单倍群,并被提议作为旧石器时代的标记;(ii)单倍群V的频率较低,这与早期分析中描述的西南欧高频率结果相矛盾;(iii)单倍群J的频率较高,尤其是亚单倍群J1c1和J2a。单倍群J的频率与当今巴斯克人的先前线粒体DNA研究结果不一致,但与史前和历史时期巴斯克人群中的频率一致。在解释现代巴斯克样本中单倍群组成的差异时,我们假设由于更新世冰川期扩散机会极度有限导致的种群碎片化促进了空间异质性。已灭绝和现存的巴斯克人群在谱系J高频率方面的相似性,以及该单倍群在西班牙北部的丰富程度,都支持线粒体DNA分析人员转移关注重点。对单倍群J进行更精细的剖析可能会为欧洲冰后期重新定居过程,进而为欧洲基因库的形成提供更确凿的证据。