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The Journal of Immunology, 2000, 164: 1386-1398.
Copyright © 2000 by The American Association of Immunologists

Mamu-I: A Novel Primate MHC Class I B-Related Locus with Unusually Low Variability1

Julie A. Urvater2,*, Nel Otting§, Jamie H. Loehrke*, Richard Rudersdorf{dagger}, Igor I. Slukvin*, Marian S. Piekarczyk*, Thaddeus G. Golos*,{ddagger}, Austin L. Hughes, Ronald E. Bontrop§ and David I. Watkins3,*,||

* Wisconsin Regional Primate Research Center and Departments of {dagger} Genetics and {ddagger} Obstetrics and Gynecology, University of Wisconsin, Madison, WI 53715; § Department of Immunobiology, Biomedical Primate Research Centre, Rijswijk, The Netherlands; Department of Biology, Pennsylvania State University, University Park, PA 16802; and || Histocompatibility Laboratory, Division of Laboratory Medicine, Department of Pathology and Laboratory Medicine, University of Wisconsin, Madison, WI 53792

The rhesus macaque is an important animal model for several human diseases and organ transplantation. Therefore, definition of the MHC of this species is crucial to the development of these models. Unfortunately, unlike humans, lymphocytes from a single rhesus macaque express up to 12 different MHC class I cDNAs. From which locus these various alleles are derived is unclear. In our attempts to define the MHC class I loci of the rhesus macaque, we have identified an unusual MHC class I locus, Mamu-I. We isolated 26 I locus alleles from three different macaque species but not from three other Cercopithecine genera, suggesting that the I locus is the result of a recent duplication of the B locus occurring after the divergence of macaques from the ancestor of the other extant Cercopithecine genera. Mamu-I mRNA transcripts were detected in all tissues examined and Mamu-I protein was produced in rhesus B lymphoblastoid cell lines. Furthermore, Mamu-I protein was detected by flow cytometry on the surface of human 721.221 cells transfected with Mamu-I. In contrast to the polymorphism present at this locus, there is unusually low sequence variability, with the mean number of nucleotide differences between alleles being only 3.6 nt. Therefore, Mamu-I is less variable than any other polymorphic MHC class I locus described to date. Additionally, no evidence for positive selection on the peptide binding region was observed. Together, these results suggest that Mamu-I is an MHC class I locus in primates that has features of both classical and nonclassical loci.




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