Wooding S P, Watkins W S, Bamshad M J, Dunn D M, Weiss R B, Jorde L B
Department of Human Genetics, University of Utah, Salt Lake City, UT, 84112, USA.
Am J Hum Genet. 2002 Sep;71(3):528-42. doi: 10.1086/342260. Epub 2002 Aug 9.
CYP1A2 is a cytochrome P450 gene that is involved in human physiological responses to a variety of drugs and toxins. To investigate the role of population history and natural selection in shaping genetic diversity in CYP1A2, we sequenced a 3.7-kb region 5' from CYP1A2 in a diverse collection of 113 individuals from three major continental regions of the Old World (Africa, Asia, and Europe). We also examined sequences in the 90-member National Institutes of Health DNA Polymorphism Discovery Resource (PDR). Eighteen single-nucleotide polymorphisms (SNPs) were found. Most of the high-frequency SNPs found in the Old World sample were also found in the PDR sample. However, six SNPs were detected in the Old World sample but not in the PDR sample, and two SNPs found in the PDR sample were not found in the Old World sample. Most pairs of SNPs were in complete linkage disequilibrium with one another, and there was no indication of a decline of disequilibrium with physical distance in this region. The average +/- SD nucleotide diversity in the Old World sample was 0.00043+/-0.00026. The African population had the highest level of nucleotide diversity and the lowest level of linkage disequilibrium. Two distinct haplotype clusters with broadly overlapping geographical distributions were present. Of the 17 haplotypes found in the Old World sample, 12 were found in the African sample, 8 were found in Indians, 5 were found in non-Indian Asians, and 5 were found in Europeans. Haplotypes found outside Africa were mostly a subset of those found within Africa. These patterns are all consistent with an African origin of modern humans. Seven SNPs were singletons, and the site-frequency spectrum showed a significant departure from neutral expectations, suggesting population expansion and/or natural selection. Comparison with outgroup species showed that four derived SNPs have achieved high (>0.90) frequencies in human populations, a trend consistent with the action of positive natural selection. These patterns have a number of implications for disease-association studies in CYP1A2 and other genes.
细胞色素P450 1A2(CYP1A2)是一种参与人体对多种药物和毒素生理反应的细胞色素P450基因。为了研究群体历史和自然选择在塑造CYP1A2基因多样性中的作用,我们对来自旧世界三个主要大陆区域(非洲、亚洲和欧洲)的113个个体的多样化样本中CYP1A2基因5'端上游3.7 kb区域进行了测序。我们还研究了美国国立卫生研究院90个成员的DNA多态性发现资源库(PDR)中的序列。共发现了18个单核苷酸多态性(SNP)。在旧世界样本中发现的大多数高频SNP在PDR样本中也有发现。然而,在旧世界样本中检测到了6个SNP,而在PDR样本中未发现;在PDR样本中发现的2个SNP在旧世界样本中未发现。大多数SNP对彼此处于完全连锁不平衡状态,并且没有迹象表明该区域的连锁不平衡会随着物理距离而下降。旧世界样本中的平均核苷酸多样性为0.00043±0.00026(标准差)。非洲人群的核苷酸多样性水平最高,连锁不平衡水平最低。存在两个地理分布广泛重叠的不同单倍型簇。在旧世界样本中发现的17个单倍型中,12个在非洲样本中发现,8个在印度人样本中发现,5个在非印度亚洲人样本中发现,5个在欧洲人样本中发现。在非洲以外发现的单倍型大多是在非洲发现的单倍型的子集。这些模式都与现代人类起源于非洲一致。7个SNP是单例,位点频率谱显示明显偏离中性预期,表明群体扩张和/或自然选择。与外群物种的比较表明,4个衍生SNP在人类群体中达到了高频率(>0.90),这一趋势与正自然选择的作用一致。这些模式对CYP1A2及其他基因的疾病关联研究有许多启示。