Interleukin 2 (IL-2) plays an important part in the specific and non-specif
ic cellular immune response and therefore is a candidate gene for resistanc
e to infectious diseases. PCR-primers were designed to amplify genomic DNA
fragments for sequence and structure analysis which should contain exons, i
ntrons and parts of 5' and 3'UTR of the ovine IL-2 gene. A SSCP-polymorphis
m has been found in a 501 base pair fragment of the gene and could be demon
strated in Merinolandschaf, Rhonschaf, Romanov and Graue Gehomte Heidschnuc
ke. The causative mutation was identified as silent A/G substitution st pos
ition 117 of exon 1.