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Allelic repertoire of the humanMHC class IMICA gene
Authors:Nassima Fodil  Laurent Laloux  Valérie Wanner  Philippe Pellet  Georges Hauptmann  Nobuhisa Mizuki  Hidetoshi Inoko  Thomas Spies  Ioannis Theodorou  Seiamak Bahram
Affiliation:1. Centre de Recherche d'Immunologie et d'Hématologie, 4 rue Kirschleger, 67085, Strasbourg Cedex, France
2. Laboratoire d'Immunologie Cellulaire et Tissulaire, H?pital Pitié-Salpêtrière, 83 Boulevard de l'H?pital, 75651, Paris Cedex 13, France
3. Tokai University School of Medicine, Bohseidai, 259-11, Isehara, Kanagawapref, Japan
4. Clinical Research Division, Fred Hutchinson Cancer Research Center, 1124 Columbia Street, 98104, Seattle, WA, USA
5. Basel Institute for Immunology, Grenzacherstrasse 487, Postfach, CH-4005, Basel, Switzerland
Abstract: The hallmark of the classical major histocompatibility complex (MHC) class I molecules is their astonishing level of polymorphism, a characteristic not shared by the nonclassical MHC class I genes. A distinct family of MHC class I genes has been recently identified within the human MHC class I region. The MICA (MHC class I chain-related A) gene in this family is a highly divergent member of the MHC class I family and has a unique pattern of tissue expression. We have sequenced exons encoding the extracellular α1, α2, and α3 domains of the MICA gene from twenty HLA homozygous typing cell lines and four unrelated individuals. We report the identification of eleven new alleles defined by a total of twenty-two amino acid substitutions. Thus, the total number of MICA alleles is sixteen. Interestingly, a tentative superimposition of MICA variable residues on the HLA-A2 structure reveals a unique pattern of distribution, concentrated primarily on the outer edge of the MICA putative antigen binding cleft, apparently bordering an invariant ligand binding site. Received: 13 May 1996 / Revised: 29 May 1996
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