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Natural Polymorphisms in Tap2 Influence Negative Selection and CD4 : CD8 Lineage Commitment in the Rat

Research output: Contribution to journalArticle

  • Jonatan Tuncel
  • Sabrina Haag
  • Anthony C Y Yau
  • Ulrika Norin
  • Amelie Baud
  • Erik Lönnblom
  • Klio Maratou
  • A Jimmy Ytterberg
  • Diana Ekman
  • Soley Thordardottir
  • Martina Johannesson
  • Alan Gillett
  • Pernilla Stridh
  • Maja Jagodic
  • Tomas Olsson
  • Alberto Fernández-Teruel
  • Roman A Zubarev
  • Richard Mott
  • Timothy J Aitman
  • Jonathan Flint
  • Rikard Holmdahl
  • EURATRANS Consortium

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    Rights statement: Copyright: © 2014 Tuncel et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Original languageEnglish
Article numbere1004151
JournalPLoS Genetics
Issue number2
Publication statusPublished - Feb 2014


Genetic variation in the major histocompatibility complex (MHC) affects CD4∶CD8 lineage commitment and MHC expression. However, the contribution of specific genes in this gene-dense region has not yet been resolved. Nor has it been established whether the same genes regulate MHC expression and T cell selection. Here, we assessed the impact of natural genetic variation on MHC expression and CD4∶CD8 lineage commitment using two genetic models in the rat. First, we mapped Quantitative Trait Loci (QTLs) associated with variation in MHC class I and II protein expression and the CD4∶CD8 T cell ratio in outbred Heterogeneous Stock rats. We identified 10 QTLs across the genome and found that QTLs for the individual traits colocalized within a region spanning the MHC. To identify the genes underlying these overlapping QTLs, we generated a large panel of MHC-recombinant congenic strains, and refined the QTLs to two adjacent intervals of ∼0.25 Mb in the MHC-I and II regions, respectively. An interaction between these intervals affected MHC class I expression as well as negative selection and lineage commitment of CD8 single-positive (SP) thymocytes. We mapped this effect to the transporter associated with antigen processing 2 (Tap2) in the MHC-II region and the classical MHC class I gene(s) (RT1-A) in the MHC-I region. This interaction was revealed by a recombination between RT1-A and Tap2, which occurred in 0.2% of the rats. Variants of Tap2 have previously been shown to influence the antigenicity of MHC class I molecules by altering the MHC class I ligandome. Our results show that a restricted peptide repertoire on MHC class I molecules leads to reduced negative selection of CD8SP cells. To our knowledge, this is the first study showing how a recombination between natural alleles of genes in the MHC influences lineage commitment of T cells.

    Research areas

  • ATP-Binding Cassette Transporters, Alleles, Animals, Antigen Presentation, CD4-Positive T-Lymphocytes, CD8-Positive T-Lymphocytes, Cell Differentiation, Cell Lineage, Gene Expression Regulation, Histocompatibility Antigens, Major Histocompatibility Complex, Rats, Recombination, Genetic, Selection, Genetic

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