Wellcome Trust Centre for Human Genetics, Oxford University, Roosevelt Drive, Oxford OX3 7BN, UK.
Nature. 2011 Jul 20;476(7359):170-5. doi: 10.1038/nature10336.
Recombination, together with mutation, gives rise to genetic variation in populations. Here we leverage the recent mixture of people of African and European ancestry in the Americas to build a genetic map measuring the probability of crossing over at each position in the genome, based on about 2.1 million crossovers in 30,000 unrelated African Americans. At intervals of more than three megabases it is nearly identical to a map built in Europeans. At finer scales it differs significantly, and we identify about 2,500 recombination hotspots that are active in people of West African ancestry but nearly inactive in Europeans. The probability of a crossover at these hotspots is almost fully controlled by the alleles an individual carries at PRDM9 (P value < 10(-245)). We identify a 17-base-pair DNA sequence motif that is enriched in these hotspots, and is an excellent match to the predicted binding target of PRDM9 alleles common in West Africans and rare in Europeans. Sites of this motif are predicted to be risk loci for disease-causing genomic rearrangements in individuals carrying these alleles. More generally, this map provides a resource for research in human genetic variation and evolution.
重组与突变一起导致了种群中的遗传变异。在这里,我们利用非洲和欧洲裔人群最近在美洲的混合,根据 30000 名无关的非裔美国人中的大约 210 万个交叉点,构建了一个测量基因组中每个位置交叉概率的遗传图谱。在超过 300 万个碱基对的间隔处,它与在欧洲人中构建的图谱几乎相同。在更精细的尺度上,它有显著的差异,我们确定了大约 2500 个重组热点,这些热点在西非裔人群中活跃,但在欧洲人中几乎不活跃。这些热点处发生交叉的概率几乎完全由个体在 PRDM9 携带的等位基因控制(P 值 < 10(-245))。我们确定了一个 17 碱基对的 DNA 序列基序,它在这些热点中富集,与在西非裔人群中常见但在欧洲裔人群中罕见的 PRDM9 等位基因的预测结合靶标非常匹配。携带这些等位基因的个体中,这个基序的位点被预测为导致疾病的基因组重排的风险位点。更一般地说,这个图谱为人类遗传变异和进化的研究提供了资源。