Genetic variation in the equine leucocyte antigen-DRB (ELA-DRB) second exon
was investigated using polymerase chain reaction (PCR) amplification, rest
riction fragment length polymorphism (RFLP) of PCR products (PCR-RFLP) and
deoxyribonucleic acid (DNA) sequencing. Eight distinct PCR-RFLP patterns co
uld be identified in the studied Argentine Creole (AC) horses. The number o
f observed patterns per individual ranged from four to six, thus confirming
the presence of multiple DRB copies in AC horses. Three PCR-RFLP alleles a
nd three new sequences were identified. The estimated rates of synonymous a
nd non-synonymous substitutions among ELA-DRB exon 2 sequences were higher
within the antigen recognition site (ABS) than on the non-ABS. Phylogenetic
analysis showed that the nucleotide sequences clustered in two main groups
. while some sequences were not included in either group. Finally, the iden
tification of the number of alleles per animal. the phylogenetic and segreg
ation analyses allowed us to explain the number of ELA-DRB loci. However. i
t was not possible to identify specific alleles with specific loci.