Folding of the DNA and RNA strands in an arrested T7 RNA polymerase (RNAP)
transcription complex was studied by radioprobing, a novel method based on
an analysis of the strand breaks produced by decay of the iodine-125 incorp
orated at the C5 position of cytosine. I-125- labeled cytosines were incorp
orated into transcripts at different positions relative to the site of the
arrest. The intensities of the DNA breaks inversely correlate with the dist
ances from the I-125 decay site, so the radioprobing data provide informati
on about the spatial RNA/DNA folding during transcription.
We found that the yield of DNA strand breaks is significantly higher in the
template than the non-template strand. This is consistent with local openi
ng of the DNA duplex and formation of a hybrid between RNA and the template
DNA strand. Our data demonstrate that the RNA-DNA hybrid has a nonuniform
A-like structure. When the I-125 is incorporated seven nucleotides from the
active center of RNAP, the yield of strand breaks is substantially lower t
han if I-125 is positioned at the ends of the hybrid. Consequently, the DNA
and RNA strands are located closer to each other at the ends of the hybrid
and somehow separated in the middle. Surprisingly, the I-125-induced break
s were detected in both DNA strands upstream from the transcription "bubble
" indicating that DNA and RNA are closely associated outside the RNAP cleft
.
Thus, radioprobing data imply that the RNA/DNA fold in the complex with T7
RNAP is more complicated than had been anticipated by the existing models.
Based on the present data, we suggest a sterically feasible model explainin
g how formation of the long RNA-DNA hybrid can result in the initiation-to-
elongation switch in the T7 transcription complex. According to this model,
the topological linkage between the DNA and RNA strands provides the neces
sary stability for the elongation complex, while permitting movement of the
polymerase along the DNA duplex.