| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10927184 | Cellular Immunology | 2005 | 4 Pages |
Abstract
The promoters of genes of the major histocompatibility complex vary not only because of linkage disequilibrium with their coding sequences but also, we argue, because of natural selection that acts particularly strongly on MHC II gene promoters. Thus, the promoter of H2Eb varies more than that of H2K, to an extent that cannot be accounted for by coding variation, and the same applies to HLA.DRB1 in comparison with H2D. We discuss how transduction by lentivirus vectors followed by adoptive transfer of monoclonal T cells could be used to test the functional activity of variant mouse promoters in vivo, and how homologous recombination in suitable cell lines might provide a short cut to obtaining promoter knock-ins.
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Authors
N.A. Mitchison, S.J. Ono, H.A. Stephens,
