We derive the elastic theory suitable for describing the free energy r
equired to deform a stiff helical molecule with the symmetry of DNA. A
t quadratic levels in the strains we find, in addition to the independ
ent bending and torsional energies incorporated in previous theories,
a previously unknown coupling between twist and bend. If the backbone
is given constant curvature, minimization of the free energy with resp
ect to the twist degrees of freedom indicates that this coupling drive
s a decrease in the molecular twist, or an unwinding of the helix. New
experiments are proposed to bring out the symmetry-breaking effecTs o
f the twist-bend coupling: (i) ring closure experiments will indicate
a helix repeat that becomes progressively more underwound for smaller
rings, and (ii) gel mobilities of supercoiled rings of integral-helix-
repeat length, with equal and opposite added linking numbers, will dif
fer.