Apolipoprotein E Variation at the Sequence Haplotype Level: Implications for the Origin and Maintenance of a Major Human Polymorphism

• Main Authors: Fullerton, Stephanie M., Clark, Andrew G., Weiss, Kenneth M., Nickerson, Deborah A., Taylor, Scott L., Stengård, Jari H., Salomaa, Veikko, Vartiainen, Erkki, Perola, Markus, Boerwinkle, Eric, Sing, Charles F.
• Format: Text
• Language: English
• Published: The American Society of Human Genetics 2000
• Subjects: Articles; Indel’; karelia*
• Online Access: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1287893; http://www.ncbi.nlm.nih.gov/pubmed/10986041

Three common protein isoforms of apolipoprotein E (apoE), encoded by the ε2, ε3, and ε4 alleles of the APOE gene, differ in their association with cardiovascular and Alzheimer's disease risk. To gain a better understanding of the genetic variation underlying this important polymorphism, we identified sequence haplotype variation in 5.5 kb of genomic DNA encompassing the whole of the APOE locus and adjoining flanking regions in 96 individuals from four populations: blacks from Jackson, MS (n=48 chromosomes), Mayans from Campeche, Mexico (n=48), Finns from North Karelia, Finland (n=48), and non-Hispanic whites from Rochester, MN (n=48). In the region sequenced, 23 sites varied (21 single nucleotide polymorphisms, or SNPs, 1 diallelic indel, and 1 multiallelic indel). The 22 diallelic sites defined 31 distinct haplotypes in the sample. The estimate of nucleotide diversity (site-specific heterozygosity) for the locus was 0.0005±0.0003. Sequence analysis of the chimpanzee APOE gene showed that it was most closely related to human ε4-type haplotypes, differing from the human consensus sequence at 67 synonymous (54 substitutions and 13 indels) and 9 nonsynonymous fixed positions. The evolutionary history of allelic divergence within humans was inferred from the pattern of haplotype relationships. This analysis suggests that haplotypes defining the ε3 and ε2 alleles are derived from the ancestral ε4s and that the ε3 group of haplotypes have increased in frequency, relative to ε4s, in the past 200,000 years. Substantial heterogeneity exists within all three classes of sequence haplotypes, and there are important interpopulation differences in the sequence variation underlying the protein isoforms that may be relevant to interpreting conflicting reports of phenotypic associations with variation in the common protein isoforms.