Transporters associated with antigen processing molecules (TAP1 and TA
P2) mediate the transfer of cytosolic peptides into the lumen of the e
ndoplasmic reticulum for association with newly synthesized class I mo
lecules of the major histocompatibility complex. Previous molecular an
d functional analyses of rat and human TAP2 homologues indicated major
differences in gene diversification patterns and selectivity of pepti
des transported. Therefore, in this study, we analyzed the alleles of
the gorilla TAP2 locus to determine whether the pattern of diversifica
tion resembled that in either of those two species. Sequence analysis
of the TAP2 cDNAs from gorilla Epstein-Barr virus-transformed B-cell l
ines revealed four alleles with a genetic distance of less than 1%. Th
e nucleotide substitutions distinguishing the alleles are confined to
the 3' half of the coding region and occur individually or within two
small clusters of variability. Diversification of the locus appears to
have resulted from point substitutions and recombinational events. Ev
olutionary-rate estimates for the TAP2 gene in gorilla and human close
ly approximate those observed for other hominoid genes. The amino acid
polymorphisms within the gorilla molecules are distinct from those in
the human homologues. The absence of ancestral polymorphisms suggests
that gorilla and human TAP2 genes have not evolved in a trans-species
fashion but rather have diversified since the divergence of the linea
ges.