Crosses of two independently derived transgenic mice demonstrate functional complementation of the genes encoding heavy (HLA-B27) and light (beta 2-microglobulin) chains of HLA class I antigens

EMBO J. 1987 Jun;6(6):1673-6. doi: 10.1002/j.1460-2075.1987.tb02416.x.

Abstract

In man a number of diseases are associated with certain alleles of MHC antigens. The most pronounced example is ankylosing spondylitis, which is strongly associated with HLA-B27. As a first step towards a model system to study the basis of this association, transgenic mice were generated that showed cell surface expression of the HLA-B27 antigen biochemically indistinguishable from HLA-B27 antigen expressed on human cells. This result was obtained by crossing two independently derived strains of mice, one of which is transgenic for the HLA-B27 heavy chain gene, and the other carrying and expressing the human beta 2m gene. Examination of HLA-B27 and human beta 2m mRNA in various tissues shows the two genes to be expressed in a coordinate fashion. The mRNA levels follow those of endogenous H-2 Class I genes.

MeSH terms

  • Animals
  • Cloning, Molecular
  • Crosses, Genetic
  • Female
  • Genes*
  • HLA Antigens / genetics*
  • HLA-B27 Antigen
  • Histocompatibility Antigens*
  • Humans
  • Lymphocytes / immunology
  • Macromolecular Substances
  • Male
  • Mice
  • beta 2-Microglobulin / genetics*

Substances

  • HLA Antigens
  • HLA-B27 Antigen
  • Histocompatibility Antigens
  • Macromolecular Substances
  • beta 2-Microglobulin