Skip to main content
Genetics logoLink to Genetics
. 1984 Mar;106(3):517–528. doi: 10.1093/genetics/106.3.517

Some Models of Gene Conversion for Treating the Evolution of Multigene Families

Tomoko Ohta 1
PMCID: PMC1224254  PMID: 6706111

Abstract

A simple model of gene conversion presented earlier has been compared with a more general model under the assumption of no bias. The former is based on a simple concept that, by conversion, a gene (or a segment of a gene) is transferred from one locus to another in a multigene family. Intrachromatid symmetric conversion may result in reciprocal exchange of genes within a multigene family, and the previous theory of identity coefficients needs modification when it occurs. The relationship of various parameters of the two models was made clear in formulating the transition equations of identity coefficients. As an example of extending the analyses, a model of preferential conversion that is relevant to the observed uneven polymorphisms of class I genes in the major histocompatibility complex has been investigated. It differs from the biased conversion, in that directional process is through location of genes on the chromosome. It is shown that the model satisfactorily explains the observed data, even though the effect of preferential conversion is difficult to distinguish from that of natural selection.

Full Text

The Full Text of this article is available as a PDF (660.4 KB).

Selected References

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

  1. Baltimore D. Gene conversion: some implications for immunoglobulin genes. Cell. 1981 Jun;24(3):592–594. doi: 10.1016/0092-8674(81)90082-9. [DOI] [PubMed] [Google Scholar]
  2. Hedrick P. W., Thomson G. Evidence for balancing selection at HLA. Genetics. 1983 Jul;104(3):449–456. doi: 10.1093/genetics/104.3.449. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Hood L., Steinmetz M., Goodenow R. Genes of the major histocompatibility complex. Cell. 1982 Apr;28(4):685–687. doi: 10.1016/0092-8674(82)90046-0. [DOI] [PubMed] [Google Scholar]
  4. López de Castro J. A., Strominger J. L., Strong D. M., Orr H. T. Structure of crossreactive human histocompatibility antigens HLA-A28 and HLA-A2: possible implications for the generation of HLA polymorphism. Proc Natl Acad Sci U S A. 1982 Jun;79(12):3813–3817. doi: 10.1073/pnas.79.12.3813. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Meselson M. S., Radding C. M. A general model for genetic recombination. Proc Natl Acad Sci U S A. 1975 Jan;72(1):358–361. doi: 10.1073/pnas.72.1.358. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Nagylaki T. Evolution of a large population under gene conversion. Proc Natl Acad Sci U S A. 1983 Oct;80(19):5941–5945. doi: 10.1073/pnas.80.19.5941. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Ohta T. Allelic and nonallelic homology of a supergene family. Proc Natl Acad Sci U S A. 1982 May;79(10):3251–3254. doi: 10.1073/pnas.79.10.3251. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Ohta T., Dover G. A. Population genetics of multigene families that are dispersed into two or more chromosomes. Proc Natl Acad Sci U S A. 1983 Jul;80(13):4079–4083. doi: 10.1073/pnas.80.13.4079. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Ohta T. On the evolution of multigene families. Theor Popul Biol. 1983 Apr;23(2):216–240. doi: 10.1016/0040-5809(83)90015-1. [DOI] [PubMed] [Google Scholar]
  10. Ohta T. On the evolution of multigene families. Theor Popul Biol. 1983 Apr;23(2):216–240. doi: 10.1016/0040-5809(83)90015-1. [DOI] [PubMed] [Google Scholar]
  11. Pays E., Van Meirvenne N., Le Ray D., Steinert M. Gene duplication and transposition linked to antigenic variation in Trypanosoma brucei. Proc Natl Acad Sci U S A. 1981 May;78(5):2673–2677. doi: 10.1073/pnas.78.5.2673. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Petes T., Fink G. R. Gene conversion between repeated genes. Nature. 1982 Nov 18;300(5889):216–217. doi: 10.1038/300216a0. [DOI] [PubMed] [Google Scholar]
  13. Ploegh H. L., Orr H. T., Strominger J. L. Major histocompatibility antigens: the human (HLA-A, -B, -C) and murine (H-2K, H-2D) class I molecules. Cell. 1981 May;24(2):287–299. doi: 10.1016/0092-8674(81)90318-4. [DOI] [PubMed] [Google Scholar]
  14. Robertson M. The evolutionary past of the major histocompatibility complex and the future of cellular immunology. Nature. 1982 Jun 24;297(5868):629–632. doi: 10.1038/297629a0. [DOI] [PubMed] [Google Scholar]
  15. Schulze D. H., Pease L. R., Geier S. S., Reyes A. A., Sarmiento L. A., Wallace R. B., Nathenson S. G. Comparison of the cloned H-2Kbm1 variant gene with the H-2Kb gene shows a cluster of seven nucleotide differences. Proc Natl Acad Sci U S A. 1983 Apr;80(7):2007–2011. doi: 10.1073/pnas.80.7.2007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Steinmetz M., Winoto A., Minard K., Hood L. Clusters of genes encoding mouse transplantation antigens. Cell. 1982 Mar;28(3):489–498. doi: 10.1016/0092-8674(82)90203-3. [DOI] [PubMed] [Google Scholar]
  17. Weiss E. H., Mellor A., Golden L., Fahrner K., Simpson E., Hurst J., Flavell R. A. The structure of a mutant H-2 gene suggests that the generation of polymorphism in H-2 genes may occur by gene conversion-like events. Nature. 1983 Feb 24;301(5902):671–674. doi: 10.1038/301671a0. [DOI] [PubMed] [Google Scholar]
  18. Winoto A., Steinmetz M., Hood L. Genetic mapping in the major histocompatibility complex by restriction enzyme site polymorphisms: most mouse class I genes map to the Tla complex. Proc Natl Acad Sci U S A. 1983 Jun;80(11):3425–3429. doi: 10.1073/pnas.80.11.3425. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Zimmer E. A., Martin S. L., Beverley S. M., Kan Y. W., Wilson A. C. Rapid duplication and loss of genes coding for the alpha chains of hemoglobin. Proc Natl Acad Sci U S A. 1980 Apr;77(4):2158–2162. doi: 10.1073/pnas.77.4.2158. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Genetics are provided here courtesy of Oxford University Press

RESOURCES