4.3 Article

High diversity of MIC genes in non-human primates

Journal

IMMUNOGENETICS
Volume 66, Issue 9-10, Pages 581-587

Publisher

SPRINGER
DOI: 10.1007/s00251-014-0791-4

Keywords

MHC class I chain-related genes; Gorilla gorilla; Pan troglodytes; Macaca fascicularis; Allelic diversity

Funding

  1. French government [ANR-11-LABX-0070_TRANSPLANTEX]
  2. Genomax
  3. Strasbourg School of Medicine Next Generation Sequencing center
  4. French Ministry of Research
  5. Institut Universitaire de France (IUF)

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The human MHC class I (MHC-I) chain-related genes A and B (MICA and MICB) encode stress-induced glycoproteins, ligands for the activating receptor NKG2D. They display an unusually high degree of polymorphism, next only to that of classical MHC-I. The functional relevance and selective pressure behind this peculiar polymorphism, which is quite distinct from that of classical MHC-I, remain largely unknown. This study increases the repertoire of allelic sequences determined for the MIC genes of non-human primates. Sequencing (mainly exons 2, 3, 4, 5) MIC genes of 72 Macaca fascicularis (Mafa), 63 Pan troglodytes (Patr), and 18 Gorilla gorilla (Gogo) individuals led to the identification of 35, 14, and 3 new alleles, respectively. Additionally, we confirm the existence of three independent MIC genes in M. fascicularis, i.e., Mafa-MICA, Mafa-MICB, and Mafa-MICB/A, the latter being a hybrid of Mafa-MICB and Mafa-MICA. By multiple sequence alignment and phylogenetic analysis, we further demonstrate that the present day MIC genes most likely derive from a single human MICB-like ancestral gene.

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