Background: MHC class I antigens are encoded by a rapidly evolving gene family comprising classical and
non-classical genes that are found in all vertebrates and involved in diverse immune functions. However,
there is a fundamental difference between the organization of class I genes in mammals and non-mammals.
Non-mammals have a single classical gene responsible for antigen presentation, which is linked to the
antigen processing genes, including TAP. This organization allows co-evolution of advantageous class Ia/
TAP haplotypes. In contrast, mammals have multiple classical genes within the MHC, which are separated
from the antigen processing genes by class III genes. It has been hypothesized that separation of classical
class I genes from antigen processing genes in mammals allowed them to duplicate. We investigated this
hypothesis by characterizing the class I genes of the tammar wallaby, a model marsupial that has a novel
MHC organization, with class I genes located within the MHC and 10 other chromosomal locations.
Results: Sequence analysis of 14 BACs containing 15 class I genes revealed that nine class I genes, including
one to three classical class I, are not linked to the MHC but are scattered throughout the genome.
Kangaroo Endogenous Retroviruses (KERVs) were identified flanking the MHC un-linked class I. The
wallaby MHC contains four non-classical class I, interspersed with antigen processing genes. Clear
orthologs of non-classical class I are conserved in distant marsupial lineages.
Conclusion: We demonstrate that classical class I genes are not linked to antigen processing genes in the
wallaby and provide evidence that retroviral elements were involved in their movement. The presence of
retroviral elements most likely facilitated the formation of recombination hotspots and subsequent
diversification of class I genes. The classical class I have moved away from antigen processing genes in
eutherian mammals and the wallaby independently, but both lineages appear to have benefited from this
loss of linkage by increasing the number of classical genes, perhaps enabling response to a wider range of
pathogens. The discovery of non-classical orthologs between distantly related marsupial species is unusual
for the rapidly evolving class I genes and may indicate an important marsupial specific function