van Holst Pellekaan S, Frommer M, Sved J, Boettcher B
School of Biological Sciences, University of Sydney, NSW, Australia.
Electrophoresis. 1997 Aug;18(9):1538-43. doi: 10.1002/elps.1150180909.
Population structure has been revealed in mitochondrial D-loop segment 1 (mt DLS1) sequences from Australian Aboriginal people in the Darling River region of NSW (Riverine) and from Yuendumu in central Australia (Desert). Comparison with five published global studies reveals that these Australians demonstrate greatest divergence from some Africans, least from Papua New Guinea (PNG) highlanders, and only slightly more divergence from some Pacific groups (Indonesian, Asian, Samoan, and coastal PNG). A median networks approach demonstrates that several hypervariable nucleotide sites within the DLS1 are likely to have undergone mutation independently. A comprehensive evaluation of specific nucleotide variants with the large amount of global sequence data now available has been achieved in three stages of analysis: (i) identification of key nucleotide variants (from the Cambridge reference sequence) in the Aboriginal Australian by pairwise comparison and construction of a 'local' median network, (ii) identification of key nucleotide variants in a selected global sample including Australian mtDLS1 types most different from each other, and (iii) calculation of the frequency with which these key nucleotide sites occur as variants in a greatly extended global sample. The third stage of the analysis revealed that nucleotides 16287 and 16356 are unique markers for representatives from the northern Riverine region. A 'thymine' at nucleotide 16223 is an informative signature of African and several identifiable non-African DLS1 types, whereas the 'cytosine' form is a marker for European, Pacific, and some Asian populations.
新南威尔士州达令河地区(河滨地区)和澳大利亚中部尤恩杜姆(沙漠地区)的澳大利亚原住民线粒体D环区域1(mt DLS1)序列中已揭示了群体结构。与五项已发表的全球研究进行比较发现,这些澳大利亚人与一些非洲人差异最大,与巴布亚新几内亚(PNG)高地人差异最小,与一些太平洋群体(印度尼西亚人、亚洲人、萨摩亚人和PNG沿海地区人群)的差异仅略大一些。一种中介网络方法表明,DLS1内的几个高变核苷酸位点可能独立发生了突变。利用现有的大量全球序列数据,通过三个分析阶段对特定核苷酸变体进行了全面评估:(i)通过成对比较和构建“局部”中介网络,确定澳大利亚原住民(相对于剑桥参考序列)的关键核苷酸变体;(ii)在一个选定的全球样本中确定关键核苷酸变体,该样本包括彼此差异最大的澳大利亚mtDLS1类型;(iii)计算这些关键核苷酸位点在大幅扩展的全球样本中作为变体出现的频率。分析的第三阶段表明,核苷酸16287和16356是河滨地区北部代表的独特标记。核苷酸16223处的“胸腺嘧啶”是非洲人和几种可识别的非非洲DLS1类型的信息性特征,而“胞嘧啶”形式是欧洲、太平洋和一些亚洲人群的标记。