The Ac element of maize has been modified by deletion of 537 bases (DE
LTANaeAc) from the untranslated leader of the transposase gene. In a s
econd modification the cauliflower mosaic virus 35S promoter has been
inserted into the truncated leader of DELTANaeAc, 21 bases upstream of
the natural translation start. The activity of these modified element
s has been compared with that of the unmodified element in transgenic
flax. Deletion of sequences in the untranslated leader only marginally
increased transposition in callus while insertion of the 35S promoter
enhanced transposition frequency 7-8-fold. Increased transposition co
rrelated with increased transcription of the transposase gene. The pre
sence of a 35S promoter upstream of the transposase gene, but outside
the Ac element, also enhanced both transcription and transposition.