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American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 1994 Jul;55(1):160–167.

Analysis of HLA class II haplotypes in the Cayapa Indians of Ecuador: a novel DRB1 allele reveals evidence for convergent evolution and balancing selection at position 86.

E A Titus-Trachtenberg 1, O Rickards 1, G F De Stefano 1, H A Erlich 1
PMCID: PMC1918223  PMID: 8023844

Abstract

PCR amplification, oligonucleotide probe typing, and sequencing were used to analyze the HLA class II loci (DRB1, DQA1, DQB1, and DPB1) of an isolated South Amerindian tribe. Here we report HLA class II variation, including the identification of a new DRB1 allele, several novel DR/DQ haplotypes, and an unusual distribution of DPB1 alleles, among the Cayapa Indians (N = 100) of Ecuador. A general reduction of HLA class II allelic variation in the Cayapa is consistent with a population bottle-neck during the colonization of the Americas. The new Cayapa DRB1 allele, DRB1*08042, which arose by a G-->T point mutation in the parental DRB1*0802, contains a novel Val codon (GTT) at position 86. The generation of DRB1*08042 (Val-86) from DRB1*0802 (Gly-86) in the Cayapa, by a different mechanism than the (GT-->TG) change in the creation of DRB1*08041 (Val-86) from DRB1*0802 in Africa, implicates selection in the convergent evolution of position 86 DR beta variants. The DRB1*08042 allele has not been found in > 1,800 Amerindian haplotypes and thus presumably arose after the Cayapa separated from other South American Amerindians. Selection pressure for increased haplotype diversity can be inferred in the generation and maintenance of three new DRB1*08042 haplotypes and several novel DR/DQ haplotypes in this population. The DPB1 allelic distribution in the Cayapa is also extraordinary, with two alleles, DPB1*1401, a very rare allele in North American Amerindian populations, and DPB1*0402, the most common Amerindian DPB1 allele, constituting 89% of the Cayapa DPB1.(ABSTRACT TRUNCATED AT 250 WORDS)

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Selected References

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  1. Apple R. J., Erlich H. A. Two new HLA DRB1 alleles found in African Americans: implications for balancing selection at positions 57 and 86. Tissue Antigens. 1992 Aug;40(2):69–74. doi: 10.1111/j.1399-0039.1992.tb01962.x. [DOI] [PubMed] [Google Scholar]
  2. Begovich A. B., McClure G. R., Suraj V. C., Helmuth R. C., Fildes N., Bugawan T. L., Erlich H. A., Klitz W. Polymorphism, recombination, and linkage disequilibrium within the HLA class II region. J Immunol. 1992 Jan 1;148(1):249–258. [PubMed] [Google Scholar]
  3. Belich M. P., Madrigal J. A., Hildebrand W. H., Zemmour J., Williams R. C., Luz R., Petzl-Erler M. L., Parham P. Unusual HLA-B alleles in two tribes of Brazilian Indians. Nature. 1992 May 28;357(6376):326–329. doi: 10.1038/357326a0. [DOI] [PubMed] [Google Scholar]
  4. Brown J. H., Jardetzky T. S., Gorga J. C., Stern L. J., Urban R. G., Strominger J. L., Wiley D. C. Three-dimensional structure of the human class II histocompatibility antigen HLA-DR1. Nature. 1993 Jul 1;364(6432):33–39. doi: 10.1038/364033a0. [DOI] [PubMed] [Google Scholar]
  5. Bugawan T. L., Begovich A. B., Erlich H. A. Rapid HLA-DPB typing using enzymatically amplified DNA and nonradioactive sequence-specific oligonucleotide probes. Immunogenetics. 1990;32(4):231–241. doi: 10.1007/BF00187094. [DOI] [PubMed] [Google Scholar]
  6. Bugawan T. L., Erlich H. A. Rapid typing of HLA-DQB1 DNA polymorphism using nonradioactive oligonucleotide probes and amplified DNA. Immunogenetics. 1991;33(3):163–170. doi: 10.1007/BF01719235. [DOI] [PubMed] [Google Scholar]
  7. Cerna M., Falco M., Friedman H., Raimondi E., Maccagno A., Fernandez-Viña M., Stastny P. Differences in HLA class II alleles of isolated South American Indian populations from Brazil and Argentina. Hum Immunol. 1993 Aug;37(4):213–220. doi: 10.1016/0198-8859(93)90504-t. [DOI] [PubMed] [Google Scholar]
  8. Eberle M., Baxter-Lowe L. A. Molecular analysis of HLA-DRB1*08/12 alleles: identification of two additional alleles. Hum Immunol. 1992 May;34(1):24–30. doi: 10.1016/0198-8859(92)90081-w. [DOI] [PubMed] [Google Scholar]
  9. Erlich H. A., Gyllensten U. B. The evolution of allelic diversity at the primate major histocompatibility complex class II loci. Hum Immunol. 1991 Feb;30(2):110–118. doi: 10.1016/0198-8859(91)90079-o. [DOI] [PubMed] [Google Scholar]
  10. Miller S. A., Dykes D. D., Polesky H. F. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res. 1988 Feb 11;16(3):1215–1215. doi: 10.1093/nar/16.3.1215. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Moonsamy P. V., Suraj V. C., Bugawan T. L., Saiki R. K., Stoneking M., Roudier J., Magzoub M. M., Hill A. V., Begovich A. B. Genetic diversity within the HLA class II region: ten new DPB1 alleles and their population distribution. Tissue Antigens. 1992 Sep;40(3):153–157. doi: 10.1111/j.1399-0039.1992.tb02109.x. [DOI] [PubMed] [Google Scholar]
  12. Mullis K. B., Faloona F. A. Specific synthesis of DNA in vitro via a polymerase-catalyzed chain reaction. Methods Enzymol. 1987;155:335–350. doi: 10.1016/0076-6879(87)55023-6. [DOI] [PubMed] [Google Scholar]
  13. Rickards O., Tartaglia M., Martínez-Labarga C., De Stefano G. F. Genetic characterization of the Cayapa Indians of Ecuador and their genetic relationships to other Native American populations. Hum Biol. 1994 Apr;66(2):299–322. [PubMed] [Google Scholar]
  14. Saiki R. K., Gelfand D. H., Stoffel S., Scharf S. J., Higuchi R., Horn G. T., Mullis K. B., Erlich H. A. Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science. 1988 Jan 29;239(4839):487–491. doi: 10.1126/science.2448875. [DOI] [PubMed] [Google Scholar]
  15. Saiki R. K., Walsh P. S., Levenson C. H., Erlich H. A. Genetic analysis of amplified DNA with immobilized sequence-specific oligonucleotide probes. Proc Natl Acad Sci U S A. 1989 Aug;86(16):6230–6234. doi: 10.1073/pnas.86.16.6230. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Scacchi R., Corbo R. M., Rickards O., De Stefano G. F. The Cayapa Indians of Ecuador: a population study of seven protein genetic polymorphisms. Ann Hum Biol. 1994 Jan-Feb;21(1):67–77. doi: 10.1080/03014469400003082. [DOI] [PubMed] [Google Scholar]
  17. Scharf S. J., Griffith R. L., Erlich H. A. Rapid typing of DNA sequence polymorphism at the HLA-DRB1 locus using the polymerase chain reaction and nonradioactive oligonucleotide probes. Hum Immunol. 1991 Mar;30(3):190–201. doi: 10.1016/0198-8859(91)90034-7. [DOI] [PubMed] [Google Scholar]
  18. Scharf S. J., Horn G. T., Erlich H. A. Direct cloning and sequence analysis of enzymatically amplified genomic sequences. Science. 1986 Sep 5;233(4768):1076–1078. doi: 10.1126/science.3461561. [DOI] [PubMed] [Google Scholar]
  19. Verreck F. A., Termijtelen A., Koning F. HLA-DR beta chain residue 86 controls DR alpha beta dimer stability. Eur J Immunol. 1993 Jun;23(6):1346–1350. doi: 10.1002/eji.1830230624. [DOI] [PubMed] [Google Scholar]
  20. Watkins D. I., McAdam S. N., Liu X., Strang C. R., Milford E. L., Levine C. G., Garber T. L., Dogon A. L., Lord C. I., Ghim S. H. New recombinant HLA-B alleles in a tribe of South American Amerindians indicate rapid evolution of MHC class I loci. Nature. 1992 May 28;357(6376):329–333. doi: 10.1038/357329a0. [DOI] [PubMed] [Google Scholar]
  21. Williams R. C., Steinberg A. G., Gershowitz H., Bennett P. H., Knowler W. C., Pettitt D. J., Butler W., Baird R., Dowda-Rea L., Burch T. A. GM allotypes in Native Americans: evidence for three distinct migrations across the Bering land bridge. Am J Phys Anthropol. 1985 Jan;66(1):1–19. doi: 10.1002/ajpa.1330660102. [DOI] [PubMed] [Google Scholar]

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