Skip to main content
Genetics logoLink to Genetics
. 1991 Nov;129(3):931–948. doi: 10.1093/genetics/129.3.931

Selection, Hitchhiking and Disequilibrium Analysis at Three Linked Loci with Application to Hla Data

W P Robinson 1, A Cambon-Thomsen 1, N Borot 1, W Klitz 1, G Thomson 1
PMCID: PMC1204759  PMID: 1752429

Abstract

The HLA system has been extensively studied from an evolutionary perspective. Although it is clear that selection has acted on the genes in the HLA complex, the nature of this selection has yet to be fully clarified. A study of constrained disequilibrium values is presented that is applicable to HLA and other less polymorphic systems with three or more linked loci, with the purpose of identifying selection events. The method uses the fact that three locus systems impose additional constraints on the range of possible disequilibrium values for any pair of loci. We have thus examined the behavior of the normalized pairwise disequilibrium measures using two locus (D'), and also three locus (D''), constraints on pairwise disequilibria in a three locus system when one of the three loci is under positive selection. The difference between these measures, δ = |D'| - |D''|, has a distribution for the two unselected loci differing from that for the selected locus with either of the unselected loci (the hallmark is a high positive value of δ for the two unselected loci). An examination of genetic drift indicates that positive δ values are unlikely to be found in human populations in the absence of selection when recombination is greater than about 0.1%. This measure can thus provide insight into which allele of several linked loci might have been subject to selection. Application of this method to HLA haplotypes from a large French population study (Provinces Francaise) identifies selected alleles on particular haplotypes. Application of a complementary method, disequilibrium pattern analysis also confirms the action of selection on these haplotypes.

Full Text

The Full Text of this article is available as a PDF (1.5 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Figueroa F., Günther E., Klein J. MHC polymorphism pre-dating speciation. Nature. 1988 Sep 15;335(6187):265–267. doi: 10.1038/335265a0. [DOI] [PubMed] [Google Scholar]
  2. Gyllensten U. B., Erlich H. A. Ancient roots for polymorphism at the HLA-DQ alpha locus in primates. Proc Natl Acad Sci U S A. 1989 Dec;86(24):9986–9990. doi: 10.1073/pnas.86.24.9986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Gyllensten U. B., Lashkari D., Erlich H. A. Allelic diversification at the class II DQB locus of the mammalian major histocompatibility complex. Proc Natl Acad Sci U S A. 1990 Mar;87(5):1835–1839. doi: 10.1073/pnas.87.5.1835. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Hedrick P. W., Thomson G. A two-locus neutrality test: applications to humans, E. coli and lodgepole pine. Genetics. 1986 Jan;112(1):135–156. doi: 10.1093/genetics/112.1.135. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Hedrick P. W., Whittam T. S., Parham P. Heterozygosity at individual amino acid sites: extremely high levels for HLA-A and -B genes. Proc Natl Acad Sci U S A. 1991 Jul 1;88(13):5897–5901. doi: 10.1073/pnas.88.13.5897. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hudson R. R. The sampling distribution of linkage disequilibrium under an infinite allele model without selection. Genetics. 1985 Mar;109(3):611–631. doi: 10.1093/genetics/109.3.611. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Hughes A. L., Nei M. Nucleotide substitution at major histocompatibility complex class II loci: evidence for overdominant selection. Proc Natl Acad Sci U S A. 1989 Feb;86(3):958–962. doi: 10.1073/pnas.86.3.958. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hughes A. L., Nei M. Pattern of nucleotide substitution at major histocompatibility complex class I loci reveals overdominant selection. Nature. 1988 Sep 8;335(6186):167–170. doi: 10.1038/335167a0. [DOI] [PubMed] [Google Scholar]
  9. Klein J. Origin of major histocompatibility complex polymorphism: the trans-species hypothesis. Hum Immunol. 1987 Jul;19(3):155–162. doi: 10.1016/0198-8859(87)90066-8. [DOI] [PubMed] [Google Scholar]
  10. Kuhner M., Watts S., Klitz W., Thomson G., Goodenow R. S. Gene conversion in the evolution of both the H-2 and Qa class I genes of the murine major histocompatibility complex. Genetics. 1990 Dec;126(4):1115–1126. doi: 10.1093/genetics/126.4.1115. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Lewontin R C. The Interaction of Selection and Linkage. I. General Considerations; Heterotic Models. Genetics. 1964 Jan;49(1):49–67. doi: 10.1093/genetics/49.1.49. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Robinson W. P., Asmussen M. A., Thomson G. Three-locus systems impose additional constraints on pairwise disequilibria. Genetics. 1991 Nov;129(3):925–930. doi: 10.1093/genetics/129.3.925. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Takahata N., Nei M. Allelic genealogy under overdominant and frequency-dependent selection and polymorphism of major histocompatibility complex loci. Genetics. 1990 Apr;124(4):967–978. doi: 10.1093/genetics/124.4.967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Thomson G., Baur M. P. Third order linkage disequilibrium. Tissue Antigens. 1984 Oct;24(4):250–255. doi: 10.1111/j.1399-0039.1984.tb02134.x. [DOI] [PubMed] [Google Scholar]

Articles from Genetics are provided here courtesy of Oxford University Press

RESOURCES