The major factor influencing incidence of disease following challenge with
transmissible spongiform encephalopathies (TSEs) in sheep is the allotype a
t amino acid numbers 136, 154 and 171 of the PrP protein. There are at leas
t two groups of TSEs, one which targets the amino acid encoded at position
136 and the other which is more influenced by the amino acid at codon 171.
Within these groups of TSE types, there may additionally be sub-types, as r
esistance to some, but not all, "136-type" TSEs can also be affected by the
amino acid at codon 154. In goats, there are also PrP polymorphisms which
apparently influence incubation period of TSE disease, however, this has no
t found to be true for cattle and BSE incidence. Sheep PrP amino acid codon
s 136, 154 and 171 do not explain everything about, for example, natural sc
rapie occurrence in sheep flocks, and attention is now turning to the flank
ing regions of the PrP gene looking for sequence differences in gene expres
sion control motifs which may also have an influence on disease development
. The sheep PrP gene produces two mRNAs in peripheral tissues [17], the res
ult of alternative polyadenylation in the 3' untranslated region of the gen
e. Results from transfection assays of murine neuroblastoma cells with cons
tructs expressing different regions of ovine PrP mRNA have revealed the pre
sence of sequences in the 3' untranslated region that modulate protein synt
hesis and have therefore the potential to affect disease progression.