Galvani Alison P, Slatkin Montgomery
Department of Integrative Biology, University of California, Berkeley, CA 94720, USA.
Proc Natl Acad Sci U S A. 2003 Dec 9;100(25):15276-9. doi: 10.1073/pnas.2435085100. Epub 2003 Nov 25.
The high frequency, recent origin, and geographic distribution of the CCR5-Delta 32 deletion allele together indicate that it has been intensely selected in Europe. Although the allele confers resistance against HIV-1, HIV has not existed in the human population long enough to account for this selective pressure. The prevailing hypothesis is that the selective rise of CCR5-Delta 32 to its current frequency can be attributed to bubonic plague. By using a population genetic framework that takes into account the temporal pattern and age-dependent nature of specific diseases, we find that smallpox is more consistent with this historical role.
CCR5-Δ32缺失等位基因的高频性、近期起源和地理分布共同表明,它在欧洲受到了强烈的选择。尽管该等位基因赋予了对HIV-1的抗性,但HIV在人类群体中存在的时间还不够长,不足以解释这种选择压力。普遍的假说是,CCR5-Δ32选择性地上升到其当前频率可归因于腺鼠疫。通过使用一个考虑到特定疾病的时间模式和年龄依赖性的群体遗传框架,我们发现天花更符合这一历史角色。