Cattle DRA and DRB genes, cloned by reverse-transcription polymerase c
hain reaction, were transfected into mouse L cells. The cattle DR-expr
essing L-cell transfectant generated was analyzed serologically, bioch
emically, and functionally. Sequence analysis of the transfected DRB g
ene clearly showed showed that it was DRB3 allele DRB30101, which cor
responds to the 1D-IEF-determined allele DRBF3. 1D-IEF analysis of the
transfectant confirmed that the expressed DR product was DRBF3. Funct
ional integrity of the transfected gene products was demonstrated by t
he ability of the transfectant cell line to present two antigens (the
foot-and-mouth disease virus-derived peptide FMDV15, and ovalbumin) to
antigen-specific CD4+ T cells from both the original animal used to o
btain the genes, and also from an unrelated DRBF3+ heterozygous animal
. Such transfectants will be invaluable tools, allowing us to dissect
the precise contributions each locus product makes to the overall immu
ne response in heterozygous animals, information essential for rationa
l vaccine design.