Literature DB >> 26685209

Complex MHC Class I Gene Transcription Profiles and Their Functional Impact in Orangutans.

Natasja G de Groot1, Corrine M C Heijmans2, Marit K H van der Wiel2, Jeroen H Blokhuis3, Arend Mulder4, Lisbeth A Guethlein5, Gaby G M Doxiadis2, Frans H J Claas4, Peter Parham5, Ronald E Bontrop6.   

Abstract

MHC haplotypes of humans and the African great ape species have one copy of the MHC-A, -B, and -C genes. In contrast, MHC haplotypes of orangutans, the Asian great ape species, exhibit variation in the number of gene copies. An in-depth analysis of the MHC class I gene repertoire in the two orangutan species, Pongo abelii and Pongo pygmaeus, is presented in this article. This analysis involved Sanger and next-generation sequencing methodologies, revealing diverse and complicated transcription profiles for orangutan MHC-A, -B, and -C. Thirty-five previously unreported MHC class I alleles are described. The data demonstrate that each orangutan MHC haplotype has one copy of the MHC-A gene, and that the MHC-B region has been subject to duplication, giving rise to at least three MHC-B genes. The MHC-B*03 and -B*08 lineages of alleles each account for a separate MHC-B gene. All MHC-B*08 allotypes have the C1-epitope motif recognized by killer cell Ig-like receptor. At least one other MHC-B gene is present, pointing to MHC-B alleles that are not B*03 or B*08. The MHC-C gene is present only on some haplotypes, and each MHC-C allotype has the C1-epitope. The transcription profiles demonstrate that MHC-A alleles are highly transcribed, whereas MHC-C alleles, when present, are transcribed at very low levels. The MHC-B alleles are transcribed to a variable extent and over a wide range. For those orangutan MHC class I allotypes that are detected by human monoclonal anti-HLA class I Abs, the level of cell-surface expression of proteins correlates with the level of transcription of the allele.
Copyright © 2016 by The American Association of Immunologists, Inc.

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Year:  2015        PMID: 26685209      PMCID: PMC4707110          DOI: 10.4049/jimmunol.1500820

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  32 in total

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Journal:  Mol Immunol       Date:  2009-11-22       Impact factor: 4.407

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  9 in total

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