Merriwether D A, Ferrell R E
Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pennsylvania 15261, USA.
Mol Phylogenet Evol. 1996 Feb;5(1):241-6. doi: 10.1006/mpev.1996.0017.
It has been proposed that all native American mitochondrial DNA variation in the New World can be attributed to divergence from four "founding lineages" which entered the New World in three waves of migration from across the Bering Strait (T.G. Schurr et al., 1990, Am. J. Hum. Genet. 46: 613-623; A. Torroni and D. C. Wallace, 1995, Am. J. Hum. Genet. 56: 1234-1236; A. Torroni et al., 1994, Am. J. Hum. Genet. 54: 303-318; A. Torroni et al., 1994, Proc. Natl. Acad. Sci. USA 91: 1158-1162; A. Torroni et al., 1994, Am. J. Phys. Anthropol. 93: 189-199; A. Torroni et al., 1993a, Am. J. Hum. Genet. 53: 563-590; A. Torroni et al., 1993b, Am. J. Hum. Genet. 53: 591-608; Wallace and A. Torroni, 1992, Hum. Biol. 64(3): 403-416). Torroni et al. (1993a) believe that only one haplotype from each of these four founding lineages arrived in the New World via migration, and all the additional variation arose in the New World. Any other types were attributed to Caucasian admixture. G. Bailliet et al. (1994, Am. J. Hum. Genet. 55: 27-33), N. O. Bianchi and F. Rothhammer (1995, Am. J. Hum. Genet. 56: 1236-1238), and D. A. Merriwether (1994, Experientia 50: 592-601; 1995, Am. J. Phys. Anthropol. 98(4): 411-430) suggest that multiple variants of each lineage entered the New World, and that additional unrelated lineages also entered. We present the distribution of multiple variants of the four founding lineages, plus two additional lineages which we call X6 and X7, throughout the New World, Siberia, and Asia. These distributions are strong evidence that at least nine different founding lineage haplotypes entered the New World. Further, we find these distributions among Native Americans best fit a single wave of migration into the New World.
有人提出,新世界中所有美洲原住民的线粒体DNA变异都可归因于从四个“奠基谱系”分化而来,这四个谱系分三波从白令海峡对面迁徙进入新世界(T.G. 舒尔等人,1990年,《美国人类遗传学杂志》46卷:613 - 623页;A. 托罗尼和D.C. 华莱士,1995年,《美国人类遗传学杂志》56卷:1234 - 1236页;A. 托罗尼等人,1994年,《美国人类遗传学杂志》54卷:303 - 318页;A. 托罗尼等人,1994年,《美国国家科学院院刊》91卷:1158 - 1162页;A. 托罗尼等人,1994年,《美国体质人类学杂志》93卷:189 - 199页;A. 托罗尼等人,1993a,《美国人类遗传学杂志》53卷:563 - 590页;A. 托罗尼等人,1993b,《美国人类遗传学杂志》53卷:591 - 608页;华莱士和A. 托罗尼,1992年,《人类生物学》64(3)卷:403 - 416页)。托罗尼等人(1993a)认为,这四个奠基谱系中每个谱系只有一个单倍型通过迁徙抵达新世界,所有其他变异都在新世界产生。任何其他类型都归因于高加索人混血。G. 贝利耶等人(1994年,《美国人类遗传学杂志》55卷:27 - 33页)、N.O. 比安奇和F. 罗特哈默(1995年,《美国人类遗传学杂志》56卷:1236 - 1238页)以及D.A. 梅里韦瑟(1994年,《实验》50卷:592 - 601页;1995年,《美国体质人类学杂志》98(4)卷:411 - 430页)表明,每个谱系的多个变体进入了新世界,并且还有其他不相关的谱系也进入了。我们展示了这四个奠基谱系以及另外两个我们称为X6和X7的谱系在整个新世界、西伯利亚和亚洲的多个变体分布情况。这些分布有力地证明至少有九种不同的奠基谱系单倍型进入了新世界。此外,我们发现美洲原住民中的这些分布最符合一次进入新世界的单一迁徙浪潮。