Cs. Garland et al., Curvature of dinucleotide poised for formation of trinucleotide in transcription with Escherichia coli RNA polymerase, BIOCHEM, 38(11), 1999, pp. 3421-3425
A frequently used schematic model of transcriptional elongation shows an RN
A polymerase molecule moving along a linear DNA. This model is of course hi
ghly idealized and not compatible with promoter sequences [Gralla, J. D. (1
991) Cell 66, 415-418; Schleif, R. (1992) Annu. Rev. Biochem. 61, 199-223]
and regulatory proteins [Koleske, A. J., and Young, R. A. (1995) Trends Bio
chem. Sci. 20, 113-116; Dunaway, M., and Droge, P. (1989) Nature 341, 657-6
59; Muller, H. P., Sogo, J. M., and Schaffner, W. (1989) Cell 58, 767-777]
located some distance away from the point of transcription initiation [Kars
ten, R., von Hippel, P. H., and Langowski, J. (1995) Trends Biochem. Sci. 2
0, 500-506]. These circumstances lead to the expectation of curvature along
the DNA strand and require looping between sometimes distant points. We ha
ve now shown curvature in a dinucleotide formed at the very onset of transc
ription when it is poised for reaction with a mononucleotide to form a trin
ucleotide. The curvature became evident from the demonstration that a metal
ion bound with a mononucleotide in the i+1 (elongation) site is approximat
ely equidistant from bases at the 5' end (i-1 site) and 3' end (i site) of
the dinucleotide. Similar results were obtained with three different dinucl
eotides and four mononucleotides. Curvature of the RNA initiate may reflect
curvature of the DNA to which it is bound. These studies show curvature to
be a significant feature in the interaction between DNA template and RNA e
longate even at the very beginning of transcription.