Adaptive evolution of the tumour suppressor BRCA1 in humans and chimpanzees. Australian Breast Cancer Family Study. Huttley, G., A., Easteal, S., Southey, M., C., Tesoriero, A., Giles, G., G., McCredie, M., R., Hopper, J., L., & Venter, D., J. Nat Genet, 25(4):410-3., 2000.
Adaptive evolution of the tumour suppressor BRCA1 in humans and chimpanzees. Australian Breast Cancer Family Study [link]Website  abstract   bibtex   
Mutations in BRCA1 (ref. 1) confer an increased risk of female breast cancer. In a genome-wide scan of linkage disequilibrium (LD), a high level of LD was detected among microsatellite markers flanking BRCA1 (ref. 3), raising the prospect that positive natural selection may have acted on this gene. We have used the predictions of evolutionary genetic theory to investigate this further. Using phylogeny-based maximum likelihood analysis of the BRCA1 sequences from primates and other mammals, we found that the ratios of replacement to silent nucleotide substitutions on the human and chimpanzee lineages were not different from one another (P=0.8), were different from those of other primate lineages (P=0.004) and were greater than 1 (P=0.04). This is consistent with the historic occurrence of positive darwinian selection pressure on the BRCA1 protein in the human and chimpanzee lineages. Analysis of genetic variation in a sample of female Australians of Northern European origin showed evidence for Hardy-Weinberg (HW) disequilibrium at polymorphic sites in BRCA1, consistent with the possibility that natural selection is affecting genotype frequencies in modern Europeans. The clustering of between-species variation in the region of the gene encoding the RAD51-interaction domain of BRCA1 suggests the maintenance of genomic integrity as a possible target of selection.
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 title = {Adaptive evolution of the tumour suppressor BRCA1 in humans and chimpanzees. Australian Breast Cancer Family Study},
 type = {article},
 year = {2000},
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 keywords = {*Evolution, Molecular,Adaptation, Biological,Animal,Breast Neoplasms/genetics,Female,Genes, BRCA1/*genetics,Genotype,Human,Likelihood Functions,Mutation,Pan troglodytes,Phylogeny,Polymorphism (Genetics),Support, Non-U.S. Gov't,Variation (Genetics)},
 pages = {410-3.},
 volume = {25},
 websites = {http://www.nature.com/cgi-taf/DynaPage.taf?file=/ng/journal/v25/n4/full/ng0800_410.html,http://www.nature.com/cgi-taf/DynaPage.taf?file=/ng/journal/v25/n4/abs/ng0800_410.html},
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 abstract = {Mutations in BRCA1 (ref. 1) confer an increased risk of female breast cancer. In a genome-wide scan of linkage disequilibrium (LD), a high level of LD was detected among microsatellite markers flanking BRCA1 (ref. 3), raising the prospect that positive natural selection may have acted on this gene. We have used the predictions of evolutionary genetic theory to investigate this further. Using phylogeny-based maximum likelihood analysis of the BRCA1 sequences from primates and other mammals, we found that the ratios of replacement to silent nucleotide substitutions on the human and chimpanzee lineages were not different from one another (P=0.8), were different from those of other primate lineages (P=0.004) and were greater than 1 (P=0.04). This is consistent with the historic occurrence of positive darwinian selection pressure on the BRCA1 protein in the human and chimpanzee lineages. Analysis of genetic variation in a sample of female Australians of Northern European origin showed evidence for Hardy-Weinberg (HW) disequilibrium at polymorphic sites in BRCA1, consistent with the possibility that natural selection is affecting genotype frequencies in modern Europeans. The clustering of between-species variation in the region of the gene encoding the RAD51-interaction domain of BRCA1 suggests the maintenance of genomic integrity as a possible target of selection.},
 bibtype = {article},
 author = {Huttley, G A and Easteal, S and Southey, M C and Tesoriero, A and Giles, G G and McCredie, M R and Hopper, J L and Venter, D J},
 journal = {Nat Genet},
 number = {4}
}

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