Sabeti Pardis C, Reich David E, Higgins John M, Levine Haninah Z P, Richter Daniel J, Schaffner Stephen F, Gabriel Stacey B, Platko Jill V, Patterson Nick J, McDonald Gavin J, Ackerman Hans C, Campbell Sarah J, Altshuler David, Cooper Richard, Kwiatkowski Dominic, Ward Ryk, Lander Eric S
Whitehead Institute/MIT Center for Genome Research, Nine Cambridge Center, Cambridge, Massachusetts 02142, USA.
Nature. 2002 Oct 24;419(6909):832-7. doi: 10.1038/nature01140. Epub 2002 Oct 9.
The ability to detect recent natural selection in the human population would have profound implications for the study of human history and for medicine. Here, we introduce a framework for detecting the genetic imprint of recent positive selection by analysing long-range haplotypes in human populations. We first identify haplotypes at a locus of interest (core haplotypes). We then assess the age of each core haplotype by the decay of its association to alleles at various distances from the locus, as measured by extended haplotype homozygosity (EHH). Core haplotypes that have unusually high EHH and a high population frequency indicate the presence of a mutation that rose to prominence in the human gene pool faster than expected under neutral evolution. We applied this approach to investigate selection at two genes carrying common variants implicated in resistance to malaria: G6PD and CD40 ligand. At both loci, the core haplotypes carrying the proposed protective mutation stand out and show significant evidence of selection. More generally, the method could be used to scan the entire genome for evidence of recent positive selection.
在人类群体中检测近期自然选择的能力,将对人类历史研究和医学产生深远影响。在此,我们介绍一种通过分析人类群体中的长程单倍型来检测近期正选择遗传印记的框架。我们首先在感兴趣的位点识别单倍型(核心单倍型)。然后,我们通过核心单倍型与距该位点不同距离处等位基因关联的衰减情况来评估每个核心单倍型的年龄,这种衰减情况通过扩展单倍型纯合性(EHH)来衡量。具有异常高EHH和高群体频率的核心单倍型表明存在一种突变,该突变在人类基因库中崛起的速度比中性进化预期的要快。我们应用这种方法来研究两个携带与疟疾抗性相关常见变异的基因的选择情况:葡萄糖-6-磷酸脱氢酶(G6PD)和CD40配体。在这两个位点,携带推测的保护性突变的核心单倍型都很突出,并显示出显著的选择证据。更广泛地说,该方法可用于扫描整个基因组以寻找近期正选择的证据。