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非洲人内部的基因差异比非洲人和欧亚人之间的基因差异更大。

Larger genetic differences within africans than between Africans and Eurasians.

作者信息

Yu Ning, Chen Feng-Chi, Ota Satoshi, Jorde Lynn B, Pamilo Pekka, Patthy Laszlo, Ramsay Michele, Jenkins Trefor, Shyue Song-Kun, Li Wen-Hsiung

机构信息

Department of Ecology and Evolution, University of Chicago, Chicago, Illinois 60637, USA.

出版信息

Genetics. 2002 May;161(1):269-74. doi: 10.1093/genetics/161.1.269.

Abstract

The worldwide pattern of single nucleotide polymorphism (SNP) variation is of great interest to human geneticists, population geneticists, and evolutionists, but remains incompletely understood. We studied the pattern in noncoding regions, because they are less affected by natural selection than are coding regions. Thus, it can reflect better the history of human evolution and can serve as a baseline for understanding the maintenance of SNPs in human populations. We sequenced 50 noncoding DNA segments each approximately 500 bp long in 10 Africans, 10 Europeans, and 10 Asians. An analysis of the data suggests that the sampling scheme is adequate for our purpose. The average nucleotide diversity (pi) for the 50 segments is only 0.061% +/- 0.010% among Asians and 0.064% +/- 0.011% among Europeans but almost twice as high (0.115% +/- 0.016%) among Africans. The African diversity estimate is even higher than that between Africans and Eurasians (0.096% +/- 0.012%). From available data for noncoding autosomal regions (total length = 47,038 bp) and X-linked regions (47,421 bp), we estimated the pi-values for autosomal regions to be 0.105, 0.070, 0.069, and 0.097% for Africans, Asians, Europeans, and between Africans and Eurasians, and the corresponding values for X-linked regions to be 0.088, 0.042, 0.053, and 0.082%. Thus, Africans differ from one another slightly more than from Eurasians, and the genetic diversity in Eurasians is largely a subset of that in Africans, supporting the out of Africa model of human evolution. Clearly, one must specify the geographic origins of the individuals sampled when studying pi or SNP density.

摘要

单核苷酸多态性(SNP)变异的全球模式引起了人类遗传学家、群体遗传学家和进化生物学家的极大兴趣,但仍未被完全理解。我们研究了非编码区的模式,因为它们比编码区受自然选择的影响更小。因此,它能更好地反映人类进化史,并可作为理解人类群体中SNP维持情况的基线。我们对10名非洲人、10名欧洲人和10名亚洲人的50个非编码DNA片段进行了测序,每个片段长度约为500 bp。数据分析表明,该抽样方案足以满足我们的研究目的。这50个片段的平均核苷酸多样性(pi)在亚洲人中仅为0.061%±0.010%,在欧洲人中为0.064%±0.011%,而在非洲人中几乎是其两倍(0.115%±0.016%)。非洲人的多样性估计甚至高于非洲人和欧亚人之间的多样性(0.096%±0.012%)。根据非编码常染色体区域(总长度 = 47,038 bp)和X连锁区域(47,421 bp)的现有数据,我们估计非洲人、亚洲人、欧洲人以及非洲人和欧亚人之间常染色体区域的pi值分别为0.105%、0.070%、0.069%和0.097%,X连锁区域的相应值分别为0.088%、0.042%、0.053%和0.082%。因此,非洲人之间的差异略大于他们与欧亚人之间的差异,欧亚人的遗传多样性在很大程度上是非洲人遗传多样性的一个子集,这支持了人类进化的“走出非洲”模型。显然,在研究pi或SNP密度时,必须明确所采样个体的地理来源。

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