首页> 美国卫生研究院文献>American Journal of Human Genetics >No severe bottleneck during human evolution: evidence from two apolipoprotein C-II deficiency alleles.
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No severe bottleneck during human evolution: evidence from two apolipoprotein C-II deficiency alleles.

机译:在人类进化过程中没有严重的瓶颈:来自两个载脂蛋白C-II缺陷等位基因的证据。

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摘要

The DNA sequences of a Japanese and a Venezuelan apolipoprotein (apo) C-II deficiency allele, of a normal Japanese apo C-II gene, and of a chimpanzee apo C-II gene were amplified by PCR, and their nucleotide sequences were determined on multiple clones of the PCR products. The normal Japanese sequence is identical to--and the chimpanzee sequence differs by only three nucleotides from--a previously published normal Caucasian sequence. In contrast, the two human mutant sequences each differ from the normal apo C-II gene sequence by several nucleotides, including deletions. The data suggest that both mutant alleles arose greater than 500,000 years ago. It is shown that a defective allele can persist in a population for only a short time if a bottleneck occurs. Therefore, the antiquity of the two alleles suggests no severe bottleneck during human evolution. Moreover, the fact that one allele is from Japan and the other is from a Venezuelan Caucasian family is more consistent with the multiregional evolution model of modern human origins than with the complete replacement or "out of Africa" model.
机译:通过PCR扩增了日本和委内瑞拉载脂蛋白(apo)C-II缺乏等位基因,正常日本apo C-II基因和黑猩猩apo C-II基因的DNA序列,并在PCR产物的多个克隆。正常的日本人序列与以前发布的正常高加索人序列相同-黑猩猩序列仅相差三个核苷酸。相反,两个人类突变体序列各自与正常载脂蛋白C-II基因序列的区别在于几个核苷酸,包括缺失。数据表明,这两个突变等位基因都出现于500,000年前。结果表明,如果出现瓶颈,有缺陷的等位基因只能在短时间内持续存在。因此,两个等位基因的古代表明在人类进化过程中没有严重的瓶颈。此外,一个等位基因来自日本,另一个等位基因来自委内瑞拉的白种人家庭,这一事实与现代人类起源的多区域进化模型相比,与完全替代或“非非洲”模型更为一致。

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