ArticleAmerican journal of human genetics2002
DNA sequence variation in a 3.7-kb noncoding sequence 5' of the CYP1A2 gene: implications for human population history and natural selection.
Article in American journal of human genetics, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.
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Who cites it
22 citing papers in PubMed, 91 citations in OpenAlex.
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- A Computational Approach for Modeling the Allele Frequency Spectrum of Populations with Arbitrarily Varying Size.Genomics, proteomics & bioinformatics · 2019Article
- Is there adaptation in the human genome for taste perception and phase I biotransformation?BMC evolutionary biology · 2019Article
- Complex evolution of the GSTM gene family involves sharing of GSTM1 deletion polymorphism in humans and chimpanzees.BMC genomics · 2018Article
- Population Structure of UK Biobank and Ancient Eurasians Reveals Adaptation at Genes Influencing Blood Pressure.American journal of human genetics · 2016Article
- Natural Selection and Functional Potentials of Human Noncoding Elements Revealed by Analysis of Next Generation Sequencing Data.PloS one · 2015Article
- Human loci involved in drug biotransformation: worldwide genetic variation, population structure, and pharmacogenetic implications.Human genetics · 2013Article
- Caffeine, selected metabolic gene variants, and risk for neural tube defects.Birth defects research. Part A, Clinical and molecular teratology · 2010Article
- How culture shaped the human genome: bringing genetics and the human sciences together.Nature reviews. Genetics · 2010Review
- Molecular population genetics of human CYP3A locus: signatures of positive selection and implications for evolutionary environmental medicine.Environmental health perspectives · 2009Article
- Constructing genomic maps of positive selection in humans: where do we go from here?Genome research · 2009Article
- CYP1A1/2 haplotypes and lung cancer and assessment of confounding by population stratification.Cancer research · 2009Article
- Pharmacogenomics and therapeutic prospects in dementia.European archives of psychiatry and clinical neuroscience · 2008Review
- Pharmacogenetic basis for therapeutic optimization in Alzheimer's disease.Molecular diagnosis & therapy · 2007Review
- Nucleotide variation and haplotype diversity in a 10-kb noncoding region in three continental human populations.Genetics · 2006Article
- Deciphering the ancient and complex evolutionary history of human arylamine N-acetyltransferase genes.American journal of human genetics · 2006Article
- Local adaptation and population differentiation at the interleukin 13 and interleukin 4 loci.Genes and immunity · 2004Article
- Nucleotide variation at Msn and Alas2, two genes flanking the centromere of the X chromosome in humans.Genetics · 2004Article
- Natural selection and population history in the human angiotensinogen gene (AGT): 736 complete AGT sequences in chromosomes from around the world.American journal of human genetics · 2004Article
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Authors and funding
6 authors at 1 institution in 1 country.
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Abstract
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.
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