During transcription elongation, three flexibly connected parts of RNA
polymerase of Escherichia coli advance along the template so that the
front-end domain is followed by the catalytic site which in turn is f
ollowed by the RNA product binding site. The advancing enzyme was foun
d to maintain the same conformation throughout extended segments of th
e transcribed region. However, when the polymerase traveled across cer
tain DNA sites that seemed to briefly anchor the front-end domain, cyc
lic shifting of the three parts, accompanied by buildup and relief of
internal strain, was observed. Thus, elongation proceeded in alternati
ng laps of monotonous and inchworm-like movement with the flexible RNA
polymerase configuration being subject to direct sequence control.