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人类进化过程中不存在严重瓶颈:来自两个载脂蛋白C-II缺乏等位基因的证据。

No severe bottleneck during human evolution: evidence from two apolipoprotein C-II deficiency alleles.

作者信息

Xiong W J, Li W H, Posner I, Yamamura T, Yamamoto A, Gotto A M, Chan L

机构信息

Department of Medicine, Baylor College of Medicine, Houston, TX.

出版信息

Am J Hum Genet. 1991 Feb;48(2):383-9.

Abstract

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.

摘要

通过聚合酶链反应(PCR)扩增了一名日本人和一名委内瑞拉人载脂蛋白(apo)C-II缺乏等位基因、正常日本apo C-II基因以及黑猩猩apo C-II基因的DNA序列,并在PCR产物的多个克隆上测定了它们的核苷酸序列。正常的日本序列与先前发表的正常高加索人序列相同,而黑猩猩序列与该序列仅相差三个核苷酸。相比之下,两个人类突变序列与正常apo C-II基因序列相比,各自都有几个核苷酸的差异,包括缺失。数据表明,这两个突变等位基因都出现在50多万年前。研究表明,如果出现瓶颈效应,缺陷等位基因在种群中只能持续很短的时间。因此,这两个等位基因的古老性表明人类进化过程中没有严重的瓶颈效应。此外,一个等位基因来自日本,另一个来自委内瑞拉高加索家庭,这一事实与现代人类起源的多地区进化模型比与完全替代或“走出非洲”模型更为一致。

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