Murray-McIntosh R P, Scrimshaw B J, Hatfield P J, Penny D
Institute for Molecular BioSciences, Massey University, P.O. Box 11222, Palmerston North, New Zealand.
Proc Natl Acad Sci U S A. 1998 Jul 21;95(15):9047-52. doi: 10.1073/pnas.95.15.9047.
The hypervariable 1 region of human mtDNA shows markedly reduced variability in Polynesians, and this variability decreases from western to eastern Polynesia. Fifty-four sequences from New Zealand Maori show that the mitochondrial variability with just four haplotypes is the lowest of any sizeable human group studied and that the frequency of haplotypes is markedly skewed. The Maori sequences, combined with 268 published sequences from the Pacific, are consistent with a series of founder effects from small populations settling new island groups. The distributions of haplotypes were used to estimate the number of females in founding population of New Zealand Maori. The three-step simulation used a randomly selected founding population from eastern Polynesia, an expansionary phase in New Zealand, and finally the random selection of 54 haplotypes. The results are consistent with a founding population that includes approximately 70 women (between 50 and 100), and sensitivity analysis shows that this conclusion is robust to small changes in haplotype frequencies. This size is too large for models postulating a very small founding population of "castaways," but it is consistent with a general understanding of Maori oral history as well as the results of recent canoe voyages recreating early trans-oceanic voyages.
人类线粒体DNA的高变区1在波利尼西亚人身上显示出明显降低的变异性,并且这种变异性从西波利尼西亚到东波利尼西亚逐渐减小。来自新西兰毛利人的54个序列表明,仅四种单倍型的线粒体变异性是所研究的任何相当规模人类群体中最低的,并且单倍型的频率明显偏向。毛利人的序列与来自太平洋地区已发表的268个序列相结合,与一系列由小群体定居新岛屿群所产生的奠基者效应相一致。单倍型的分布被用于估计新西兰毛利人奠基群体中的女性数量。三步模拟使用了从东波利尼西亚随机选择的奠基群体、在新西兰的扩张阶段,最后随机选择54个单倍型。结果与一个包含约70名女性(50至100名之间)的奠基群体相一致,敏感性分析表明这一结论对于单倍型频率的微小变化具有稳健性。这个规模对于假设一个非常小的“遇难者”奠基群体的模型来说太大了,但它与毛利人的口述历史的一般理解以及最近重现早期跨洋航行的独木舟航行结果相一致。