Department of Biology and Evolution, University of Ferrara, 44121 Ferrara, Italy.
Trends Genet. 2010 Jul;26(7):285-95. doi: 10.1016/j.tig.2010.04.002. Epub 2010 May 13.
Despite our relatively large population size, humans are genetically less variable than other primates. Many allele frequencies and statistical descriptors of genome diversity form broad gradients, tracing the main expansion from Africa, local migrations, and sometimes adaptation. However, this continuous variation is discordant across loci, and principally seems to reflect different blends of common and often cosmopolitan alleles rather than the presence of distinct gene pools in different regions of the world. The elusive structure of human populations could lead to spurious associations if the effects of shared ancestry are not properly dealt with; indeed, this is among the causes (although not the only one) of the difficulties encountered in discovering the loci responsible for quantitative traits and complex diseases. However, the rapidly growing body of data on our genomic diversity has already cast new light on human population history and is now revealing intricate biological relationships among individuals and populations of our species.
尽管我们的人口规模相对较大,但人类在基因上的变异性比其他灵长类动物要小。许多等位基因频率和基因组多样性的统计描述形成了广泛的梯度,这些梯度追踪了从非洲的主要扩张、局部迁移,有时还有适应的过程。然而,这种连续的变异在不同的基因座之间是不一致的,主要似乎反映了常见的和通常是世界性的等位基因的不同混合,而不是世界不同地区存在不同的基因库。如果不能正确处理共同祖先的影响,人类群体的难以捉摸的结构可能会导致虚假的关联;事实上,这是发现负责数量性状和复杂疾病的基因座所遇到的困难的原因之一(尽管不是唯一原因)。然而,关于我们基因组多样性的快速增长的数据已经为人类群体历史带来了新的启示,现在正在揭示我们物种个体和群体之间复杂的生物学关系。