Fujimoto B S, Schurr J M
Department of Chemistry, University of Washington, Seattle 98195.
Nature. 1990 Mar 8;344(6262):175-7. doi: 10.1038/344175a0.
The Escherichia coli phage 434 repressor binds as a dimer to the operator of the DNA helix. Although the centre of the operator is not in contact with protein, the repressor binding affinity can be reduced at least 50-fold by changing the sequence there: operators with A.T base pairs near their centre bind the repressor more strongly than do operators with G.C base pairs at the same positions. To explain these observations, it has been proposed that the base composition at the centre of the operator affects the affinity of the operator for repressor by altering the ease with which operator DNA can undergo the torsional deformation necessary for complex formation. In this model, the variation in binding affinity would require the torsion constant to have specific values and to change in a sequence-dependent manner. We have now measured torsion constants for DNAs with widely different base compositions. Our results indicate that the torsion constants depend only slightly on the overall composition, and firmly delimit the range of values for each. Even the upper-limit values are much too small to account for the observed changes in affinity of the 434 repressor. These results rule out simple models that rely on substantial generic differences in torsion constant between A.T-rich sequences and G.C-rich sequences, although they do not rule out the possibility of particular sequences having abnormal torsion constants.
大肠杆菌噬菌体434阻遏蛋白以二聚体形式结合到DNA螺旋的操纵基因上。尽管操纵基因的中心不与蛋白质接触,但通过改变该位置的序列,阻遏蛋白的结合亲和力可降低至少50倍:中心附近有A.T碱基对的操纵基因比相同位置有G.C碱基对的操纵基因更能紧密结合阻遏蛋白。为了解释这些观察结果,有人提出操纵基因中心的碱基组成通过改变操纵基因DNA进行复合物形成所需的扭转变形的难易程度来影响其对阻遏蛋白的亲和力。在这个模型中,结合亲和力的变化将要求扭转常数具有特定值并以序列依赖的方式变化。我们现在已经测量了具有广泛不同碱基组成的DNA的扭转常数。我们的结果表明,扭转常数仅略微依赖于整体组成,并严格限定了每个值的范围。即使是上限值也太小,无法解释观察到的434阻遏蛋白亲和力的变化。这些结果排除了依赖富含A.T序列和富含G.C序列之间扭转常数存在实质性一般差异的简单模型,尽管它们并不排除特定序列具有异常扭转常数的可能性。