We have identified bent DNA sites in the distal and proximal DNA puff BhC4-
1 amplified gene promoter region of Bradysia hygida. The 2D modeling of the
3D DNA path and the ENDS ratio values calculated in this promoter region r
esulted in the identification of ten pronounced bent sites named BhC4B - 9
to + 1. The 1847 bp fragment (- 3697 to - 1850) in relation to the transcri
ption start site shows multiple bending sites, BhC4B - 9 to BhC413 - 4, wit
h periodicity similar to 300 bp. The analysis of the other identified bent
region, starting at position - 957, reveals that the BhC413 + 1 bent site c
olocalizes with the putative BhC4-1 minimal promoter. The sequence analysis
of bent site BhC4B -4 shows a distribution of dA.dT at similar to 10 bp in
tervals between the middle of each tract, but intervals with more than one
turn, similar to 20 bp, two helix turns, were detected in the other bent si
tes described here. The bent sites BhC4B - 6 and BhC4B - 4, contain two con
sensus sequences, with 60 bp each. The apparent molecular weight of fragmen
ts in the BhC4-1 promoter region were estimated in agarose gels and compare
d with the data obtained in polyacrylamide gels without and with ethidium b
romide. The mobility reduction ratios (R-values) were determined, and a hig
h R-value, 1.80, for a 1215 bp fragment in the distal promoter region and a
1.23 significant R-value for a 662 bp fragment in the proximal segment wer
e found. To further analyze the predicted bent DNA sites in these fragments
, the 2D trajectories of the 3D DNA path and other parameters, AT percentag
e, roll angle, ENDS ratio and AG, were determined. The role of these bent s
ites in the BhC4-1 transcription regulation is discussed. J. Cell. Biochem.
83: 1-13, 2001. (C) 2001 Wiley-Liss, Inc.