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New recombinant HLA-B alleles in a tribe of South American Amerindians
indicate rapid evolution of MHC class I loci David I. Watkins, Stephen N. McAdam, Xiaomin Liu, Clarice R. Strang*, Edgar L. Milford†, Cindy G. Levine, Theodore L. Garber‡, Alex L. Dogon, Carol I. Lord, Steven H. Ghim, Gary M. Troup§, Austin L. Hughes & Norman L. Letvin
Harvard Medical School, New England Regional Primate Research Center, One Pine Hill Drive,
Southborough, Massachusetts 01772, USA
*PO Box 9282,
Guayaquil, Ecuador, South America
†Brigham and Women's
Hospital, 75 Francis Street, Boston, Massachusetts 02115, USA
‡Texas A&M University, College of Veterinary Medicine,
College Station, Texas 77843, USA
§ Department of Pathology, School of
Medicine, University of New Mexico, New Mexico 87131, USA
Department of Biology, 208 Mueller Laboratory, Pennsylvania
State University, University Park, Pennsylvania 16802, USA
EVIDENCE suggests that the New World was colonized only 11,000–40,000 years
ago by Palaeo-Indians1. The descendants of these Palaeo-Indians therefore
provide a unique opportunity to study the effects of selection on major
histocompatibility complex class I genes over a short period. Here we analyse
the class I alleles of the Waorani of South America and the Zuni of North
America. Four of the Waorani HLA-B alleles were new functional variants which
could be accounted for by intralocus recombination. In contrast, all of the
Zuni HLA-A and -B molecules were present in Caucasians and orientals. This
suggests that the new Waorani HLA-B variants arose in South America. The
description of four new HLA-B alleles in the Waorani and another five new HLA-B
alleles from two other tribes of South American Amerindians2 indicates that the
HLA-B locus can evolve rapidly in isolated populations. These studies underline
the importance of gathering genetic data on endangered native human
populations3.
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