Protein variation in Adh and Adh-related in Drosophila pseudoobscura. Linkage disequilibrium between single nucleotide polymorphisms and protein alleles.
Journal
  Genetics.
Citation
  Genetics. 159(2):673-87
Publication date
  2001 Oct
Authors
  Schaeffer SW
Walthour CS
Toleno DM
Olek AT
Miller EL
Investigators
  Stephen Schaeffer
Grant agencies
  National Institute of General Medical Sciences
Grants
  NIGMS GM-42472
MeSH headings
  Alcohol Dehydrogenase
Alleles
Drosophila
Linkage Disequilibrium
Polymorphism, Single Nucleotide
MeSH qualifiers
  genetics
Abstract
  A 3.5-kb segment of the alcohol dehydrogenase (Adh) region that includes the Adh and Adh-related genes was sequenced in 139 Drosophila pseudoobscura strains collected from 13 populations. The Adh gene encodes four protein alleles and rejects a neutral model of protein evolution with the McDonald-Kreitman test, although the number of segregating synonymous sites is too high to conclude that adaptive selection has operated. The Adh-related gene encodes 18 protein haplotypes and fails to reject an equilibrium neutral model. The populations fail to show significant geographic differentiation of the Adh-related haplotypes. Eight of 404 single nucleotide polymorphisms (SNPs) in the Adh region were in significant linkage disequilibrium with three ADHR protein alleles. Coalescent simulations with and without recombination were used to derive the expected levels of significant linkage disequilibrium between SNPs and 18 protein haplotypes. Maximum levels of linkage disequilibrium are expected for protein alleles at moderate frequencies. In coalescent models without recombination, linkage disequilibrium decays between SNPs and high frequency haplotypes because common alleles mutate to haplotypes that are rare or that reach moderate frequency. The implication of this study is that linkage disequilibrium mapping has the highest probability of success with disease-causing alleles at frequencies of 10%.
Medline ID
  21518598