Molecular and population analysis of natural selection on the human haptoglobin duplication

Santi Rodriguez, Dylan M Williams, Philip A I Guthrie, Wendy L McArdle, George Davey Smith, David M Evans, Tom R Gaunt, Ian N M Day

Research output: Contribution to journalArticle (Academic Journal)peer-review

15 Citations (Scopus)

Abstract

Haptoglobin binds free haemoglobin that prevents oxidative damage produced by haemolysis. There is a copy number variant (CNV) in the haptoglobin gene (HP) consisting of two alleles, Hp1 (no duplication), and Hp2 (1.7kb duplication involving two exons). The spread of the Hp2 allele is believed to have taken place under selective pressures conferred by malaria resistance. However, molecular evidence is lacking and Hp did not emerge in genomewide SNPs surveys for evidence of selection. In Europe, there is geographical constancy of Hp2 frequency, indicative of absence of clinal pressures and that modern day European alleles represent a "snapshot" of their out-of-Africa migrations. In this work we test for signatures of natural selection acting on the Hp CNV in a sample from the UK population (Avon Longitudinal Study of Parents and Children, ALSPAC). We present here heterozygosity decay, pairwise F(ST) values observed between ALSPAC and 301 populations from all five populated continents, extended haplotype homozygosity analyses involving the CNV and 80 SNPs surrounding the CNV ∼500kb in each direction, and linkage disequilibrium and pairwise haplotypic analyses involving 160 SNPs on chromosome 16q22.1. Taken together, our results represent the first molecular analysis of natural selection in the Hp CNV genetic region.
Translated title of the contributionMolecular and Population Analysis of Natural Selection on the Human Haptoglobin Duplication
Original languageEnglish
Pages (from-to)352-362
Number of pages11
JournalAnnals of Human Genetics
Volume76
Issue number5
DOIs
Publication statusPublished - Sep 2012

Keywords

  • Haptoglobin
  • natural selection
  • copy number variant
  • ALSPAC
  • RECENT POSITIVE SELECTION
  • HUMAN GENOME
  • FALCIPARUM-MALARIA
  • ASSOCIATION
  • HEMOGLOBIN
  • GENOTYPE
  • CHILDREN
  • IDENTIFICATION
  • INDIVIDUALS
  • SIGNATURES

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