Two Orangutan Species Have Evolved Different KIR Alleles and Haplotypes.

Bibliographic Collection: 
CARTA-Inspired Publication
Publication Type: Journal Article
Authors: Guethlein, LA; Norman, PJ; Heijmans, CM; de Groot, NG; Hilton, HG; Babrzadeh, F; Abi-Rached, L; Bontrop, RE; Parham, P
Year of Publication: 2017
Journal: Journal of Immunology
Volume: 198
Number: 8
Pagination: 3157-3169
Date Published: Apr 15
Publication Language: eng
ISBN Number: 0022-1767
Accession Number: 28264973
Abstract:

The immune and reproductive functions of human NK cells are regulated by interactions of the C1 and C2 epitopes of HLA-C with C1-specific and C2-specific lineage III killer cell Ig-like receptors (KIR). This rapidly evolving and diverse system of ligands and receptors is restricted to humans and great apes. In this context, the orangutan has particular relevance because it represents an evolutionary intermediate, one having the C1 epitope and corresponding KIR but lacking the C2 epitope. Through a combination of direct sequencing, KIR genotyping, and data mining from the Great Ape Genome Project, we characterized the KIR alleles and haplotypes for panels of 10 Bornean orangutans and 19 Sumatran orangutans. The orangutan KIR haplotypes have between 5 and 10 KIR genes. The seven orangutan lineage III KIR genes all locate to the centromeric region of the KIR locus, whereas their human counterparts also populate the telomeric region. One lineage III KIR gene is Bornean specific, one is Sumatran specific, and five are shared. Of 12 KIR gene-content haplotypes, 5 are Bornean specific, 5 are Sumatran specific, and 2 are shared. The haplotypes have different combinations of genes encoding activating and inhibitory C1 receptors that can be of higher or lower affinity. All haplotypes encode an inhibitory C1 receptor, but only some haplotypes encode an activating C1 receptor. Of 130 KIR alleles, 55 are Bornean specific, 65 are Sumatran specific, and 10 are shared.

Author Address:

Department of Structural Biology, Stanford University, Stanford, CA 94305. Department of Microbiology and Immunology, Stanford University, Stanford, CA 94305. Department of Structural Biology, Stanford University, Stanford, CA 94305. Department of Microbiology and Immunology, Stanford University, Stanford, CA 94305. Comparative Genetics and Refinement, Biomedical Primate Research Centre, 2288 GJ Rijswijk, the Netherlands. Comparative Genetics and Refinement, Biomedical Primate Research Centre, 2288 GJ Rijswijk, the Netherlands. Department of Structural Biology, Stanford University, Stanford, CA 94305. Department of Microbiology and Immunology, Stanford University, Stanford, CA 94305. Stanford Genome Technology Center, Palo Alto, CA 94304; and. Department of Structural Biology, Stanford University, Stanford, CA 94305. Department of Microbiology and Immunology, Stanford University, Stanford, CA 94305. Comparative Genetics and Refinement, Biomedical Primate Research Centre, 2288 GJ Rijswijk, the Netherlands. Theoretical Biology and Bioinformatics, Utrecht University, 3584 CH Utrecht, the Netherlands. Department of Structural Biology, Stanford University, Stanford, CA 94305; peropa@stanford.edu. Department of Microbiology and Immunology, Stanford University, Stanford, CA 94305.

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