The T7 RNA polymerase-dependent transcription was studied as a functio
n of nucleotide sequence structures positioned upstream of the T7 prom
oter. Model double-stranded DNA templates were constructed for this pu
rpose. They contained a target sequence of 485 base pairs (cDNA fragme
nt of Venesuelian encephalomyelitis equine virus genome), T7 promoter
consensus and different extra base sequences upstream of the T7 promot
er. The level of the target sequence transcription was clearly determi
ned by the extra base sequence. The presence of one extra base pair G
. C ensured the most pronounced effect, transcription was increased on
e order of magnitude in comparison with template which has only a cano
nical T7 promoter sequence at the 5'-end.