Messer W, Hartmann-Kühlein H, Langer U, Mahlow E, Roth A, Schaper S, Urmoneit B, Woelker B
Max-Planck-Institut für molekulare Genetik, Berlin, Federal Republic of Germany.
Chromosoma. 1992;102(1 Suppl):S1-6. doi: 10.1007/BF02451779.
We probed the complex between oriC and DnaA protein using two types of mutants in oriC. Base changes in the DnaA binding sites, DnaA boxes, had little effect on origin function. Mutations which change the distance between DnaA boxes R3 and R4, on the other hand, inactivated oriC unless the mutation deleted or inserted one complete helical turn. Origins with other 10 base pair insertions in the interval between DnaA boxes R2 and R3 were functional, but not insertions in the R1-R2 interval. FIS protein binds to a bipartite site in oriC between DnaA boxes R2 and R3. A model for the oriC/DnaA complex based on these results suggests an array of DnaA monomers with a 34 A spacing upon which oriC is arranged.
我们使用oriC中的两种突变体探究了oriC与DnaA蛋白之间的复合物。DnaA结合位点(即DnaA框)中的碱基变化对起始功能影响很小。另一方面,改变DnaA框R3和R4之间距离的突变会使oriC失活,除非该突变缺失或插入一整圈螺旋。在DnaA框R2和R3之间的间隔中有其他10个碱基对插入的起始点是有功能的,但在R1 - R2间隔中插入则无功能。FIS蛋白结合在oriC中DnaA框R2和R3之间的一个双位点上。基于这些结果的oriC/DnaA复合物模型表明,存在一系列间距为34 Å的DnaA单体阵列,oriC排列在其上。