Codon bias and base composition in major histocompatibility complex (MHC) s
equences have been studied for both class I and II loci in Homo sapiens and
Part troglodytes. There is low to moderate codon bias for the MHC of human
s and chimpanzees. In the class I loci, the same level of moderate codon bi
as is seen for HLA-B, HLA-C, Patr-A, Patr-B, and Patr-C, while at HLA-A the
level of codon bias is lower. There is a correlation between codon usage b
ias and G+C content in the A and B loci in humans and chimps, but not at th
e C locus. To examine the effect of diversifying selection on codon bias, w
e subdivided class I alleles into antigen recognition site (ARS) and non-AR
S codons. ARS codons had lower bias than non-ARS codons. This may indicate
that the constraint of codon bias on nucleotide substitution may be selecte
d against in ARS codons. At the class II loci, there are distinct differenc
es between alpha and beta chain genes with respect to codon usage, with the
beta chain genes being much more biased. Species-specific differences in b
ase composition were seen in exon 2 at the DRB1 locus, with lower GC conten
t in chimpanzees. Considering the complex evolutionary history of MHC genes
, the study of codon usage patterns provides us with a better understanding
of both the evolutionary history of these genes and the evolution of synon
ymous codon usage in genes under natural selection.