A vector is described for the expression of genomic or cDNA copies of
bovine major histocompatibility complex (MHC) class I genes in transfe
cted mouse Ltk(-) cells. Class I gene fragments are amplified by the p
olymerase chain reaction, using primers in conserved parts of exon 2 a
nd the 3'-untranslated region of the gene. Amplified class I gene frag
ments can then be subcloned into the expression vector, pBoLA-21, whic
h contains the necessary 5'-and 3'-sequences for correct expression. T
he vector was tested by subcloning and expressing genomic and cDNA clo
nes.