DNA base sequence, once thought to be interesting only as a carrier of
the genetic blueprint, is now recognized as playing a structural role
in modulating the biological activity of genes. Primary sequences of
nucleic acid bases describe real three-dimensional structures with pro
perties reflecting those structures. Moreover, the structures are base
sequence dependent with individual residues adopting characteristic s
patial forms. As a consequence, the double helix can fold into tertiar
y arrangements, although the deformation is much more gradual and spre
ad over a larger molecular scale than in proteins. As part of an effor
t to understand how local structural irregularities are translated at
the macromolecular level in DNA and recognized by proteins, a series o
f calculations probing the structure and properties of the double heli
x have been performed. By combining several computational techniques,
complementary information as well as a series of built-in checks and b
alances for assessing the significance of the findings are obtained. T
he known sequence dependent bending, twisting, and translation of simp
le dimeric fragments have been incorporated into computer models of lo
ng open DNAs of varying length and chemical composition as well as in
closed double helical circles and loops. The extent to which the doubl
e helix can be forced to bend and twist is monitored with newly parame
terized base sequence dependent elastic energy potentials based on the
observed configurations of adjacent base pairs in the B-DNA crystallo
graphic literature.