Department of Biology, University of Maryland, College Park, MD, USA.
Pharmacogenomics. 2011 Nov;12(11):1545-58. doi: 10.2217/pgs.11.88. Epub 2011 Oct 13.
Functional variability at the arylamine N-acetyltransferase genes is associated with drug response in humans and may have been adaptive in the past owing to selection pressure from diet and exposure to toxins during human evolution.
We have characterized nucleotide variation at the NAT1 and NAT2 genes, and at the NATP1 pseudogene in global human populations, including many previously under-represented African populations, in order to identify potential functional variants and to understand the role that natural selection has played in shaping variation at these loci in globally diverse populations.
MATERIALS & METHODS: We have resequenced approximately 2800 bp for each of the NAT1 and NAT2 gene regions, as well as the pseudogene NATP1, in 197 African and 132 nonAfrican individuals.
RESULTS & CONCLUSION: We observe a signature of balancing selection maintaining variation in the 3'-UTR of NAT1, suggesting that these variants may play a functional role that is currently undefined. In addition, we observed high levels of nonsynonymous functional variation at the NAT2 locus that differs amongst ethnically diverse populations.
芳基胺 N-乙酰基转移酶基因的功能变异性与人类对药物的反应有关,过去可能由于人类进化过程中饮食和接触毒素的选择压力而具有适应性。
我们已经对全球人类群体中的 NAT1 和 NAT2 基因以及 NATP1 假基因中的核苷酸变异进行了特征描述,包括许多以前代表性不足的非洲人群,以确定潜在的功能变异,并了解自然选择在塑造这些基因座在全球不同人群中的变异方面所起的作用。
我们对 197 名非洲人和 132 名非非洲人个体的 NAT1 和 NAT2 基因区域以及假基因 NATP1 进行了约 2800 个碱基的重测序。
我们观察到 NAT1 3'UTR 中维持变异的平衡选择特征,表明这些变异可能具有目前尚未定义的功能作用。此外,我们观察到 NAT2 基因座存在高水平的非同义功能变异,这些变异在不同种族的人群中存在差异。