Santos Cristina, Alvarez Luis, Aluja Maria Pilar, Bruges-Armas Jacome, Lima Manuela
Centre of Research in Natural Resources and Department of Biology, University of the Azores, S. Miguel, Azores.
Coll Antropol. 2009 Dec;33(4):991-9.
The Azores archipelago (Portugal), located in the Atlantic Ocean, 1,500 km from the European mainland, is formed by nine islands of volcanic origin. The relative position of these islands allows the definition of three geographical groups: Eastern, Central and Western. Previous studies of the Azores using Short Tandem Repeats (STRs) have highlighted differences in the frequencies of several loci, when compared to Mainland Portugal or Madleira Island. Furthermore, linkage disequilibrium (LD), described for Azorean samples has been tentatively explained as reflecting the presence of genetic sub-structuring in the archipelago. To provide information concerning the genetic profile of the Azores Islands and to evaluate the presence of substructuring we have determined the allelic frequencies of 15 autosomal STR loci, using the AmpFlSTR Identifiler Kit, in representative samples from the Azorean Islands. Either considering the Azores as a whole, or analysing by island all the loci were in conformity with Hardy-Weinberg equilibrium. Average gene diversity ranged from 0.7669 in Corvo to 0.7972 in Terceira Island. Allelic independence between loci, tested for the global sample, detected significant LD (after correction for multiple tests) for pairs D21S11/D7S820 and D3S1358/D5S818. The exact test of population differentiation, combining the information of the 15 markers analysed, revealed significant differences between the three groups of islands, and between islands. Inter-island analysis reinforces the previous data that suggested the existence of sub-structuring in the Azores archipelago. Moreover, the data generated by this study can be used in a future forensic genetic database of the Azores after the appropriate enlacement of sample size by island, preventing, in that way, misinterpretations caused by population substructuring and small sample sizes.
亚速尔群岛(葡萄牙)位于大西洋,距离欧洲大陆1500公里,由九个火山岛组成。这些岛屿的相对位置可划分为三个地理区域:东部、中部和西部。此前利用短串联重复序列(STR)对亚速尔群岛进行的研究表明,与葡萄牙大陆或马德拉岛相比,该群岛若干基因座的频率存在差异。此外,对亚速尔群岛样本的连锁不平衡(LD)现象初步解释为反映了该群岛存在遗传亚结构。为了提供有关亚速尔群岛遗传特征的信息并评估亚结构的存在情况,我们使用AmpFlSTR Identifiler试剂盒,测定了亚速尔群岛代表性样本中15个常染色体STR基因座的等位基因频率。无论是将亚速尔群岛作为一个整体考虑,还是按岛屿进行分析,所有基因座均符合哈迪-温伯格平衡。平均基因多样性范围从科尔武岛的0.7669到特塞拉岛的0.7972。对总体样本进行的基因座间等位基因独立性测试发现,D21S11/D7S820和D3S1358/D5S818这几对基因座存在显著的连锁不平衡(经过多重检验校正)。结合15个分析标记的信息进行的群体分化精确检验显示,三组岛屿之间以及各岛屿之间存在显著差异。岛屿间分析强化了之前表明亚速尔群岛存在亚结构的数据。此外,本研究生成的数据在按岛屿适当调整样本量后,可用于未来亚速尔群岛的法医遗传数据库,从而避免因群体亚结构和小样本量导致的错误解读。