Section on Statistical Genetics, Department of Biostatistics, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
BMC Evol Biol. 2011 Jun 20;11:173. doi: 10.1186/1471-2148-11-173.
HIV susceptibility and pathogenicity exhibit both interindividual and intergroup variability. The etiology of intergroup variability is still poorly understood, and could be partly linked to genetic differences among racial/ethnic groups. These genetic differences may be traceable to different regimes of natural selection in the 60,000 years since the human radiation out of Africa. Here, we examine population differentiation and haplotype patterns at several loci identified through genome-wide association studies on HIV-1 control, as determined by viral-load setpoint, in European and African-American populations. We use genome-wide data from the Human Genome Diversity Project, consisting of 53 world-wide populations, to compare measures of FST and relative extended haplotype homozygosity (REHH) at these candidate loci to the rest of the respective chromosome.
We find that the Europe-Middle East and Europe-South Asia pairwise FST in the most strongly associated region are elevated compared to most pairwise comparisons with the sub-Saharan African group, which exhibit very low FST. We also find genetic signatures of recent positive selection (higher REHH) at these associated regions among all groups except for sub-Saharan Africans and Native Americans. This pattern is consistent with one in which genetic differentiation, possibly due to diversifying/positive selection, occurred at these loci among Eurasians.
These findings are concordant with those from earlier studies suggesting recent evolutionary change at immunity-related genomic regions among Europeans, and shed light on the potential genetic and evolutionary origin of population differences in HIV-1 control.
HIV 的易感性和致病性均表现出个体间和群体间的变异性。群体间变异的病因仍知之甚少,部分原因可能与不同种族/民族群体之间的遗传差异有关。这些遗传差异可能源于自人类走出非洲的 6 万年来,不同种族群体间自然选择的不同模式。在这里,我们研究了通过对 HIV-1 控制的全基因组关联研究确定的几个位于病毒载量设定点的 HIV 易感性和致病性相关的基因座的群体分化和单倍型模式,这些基因座位于欧洲人和非裔美国人中。我们使用了人类基因组多样性计划的全基因组数据,该计划由来自全球 53 个群体的样本组成,以比较候选基因座与各自染色体其余部分的 FST 和相对扩展单体型同质性(REHH)的衡量标准。
我们发现,在与撒哈拉以南非洲群体的大多数成对比较中,最强烈关联区域的欧洲-中东和欧洲-南亚 FST 较高,而与撒哈拉以南非洲群体的 FST 非常低。我们还发现,除了撒哈拉以南非洲人和美洲原住民之外,所有群体在这些相关区域都存在近期正选择的遗传特征(更高的 REHH)。这种模式与以下模式一致,即在欧亚人群中,这些基因座的遗传分化(可能是由于多样化/正选择)发生了。
这些发现与早期研究结果一致,表明欧洲人免疫相关基因组区域近期发生了进化变化,并揭示了 HIV-1 控制人群差异的潜在遗传和进化起源。