Elias P, Gustafsson C M, Hammarsten O
Department of Medical Biochemistry, University of Göteborg, Sweden.
J Biol Chem. 1990 Oct 5;265(28):17167-73.
The origin binding protein (OBP) or herpes simplex virus 1 has been expressed in Escherichia coli and used to study the role of multiple OBP binding sites in the herpes simplex virus #1 origin of replication, oris. Our results showed that the sequence CGTTCGCACTT was required for the binding of OBP to duplex DNA with high affinity. The minimal oris contains three repeats of this sequence or close derivatives thereof. Filter binding experiments have demonstrated that specific binding occurs to two of these repeats, box I and box II. An investigation using the DNase I footprinting technique revealed that the binding of OBP to box I and box II was cooperative and led to the formation of a highly organized complex in which the entire oris sequence was induced. We observed furthermore that the AT-rich sequence of the oris dyad was readily accessible to macromolecules even in the OBP.oris complex. The DNase I cleavage pattern of this sequence was, however, altered radically, indicating that a significant conformational change had occurred. A tentative structural model for the OBP-oris interaction is discussed on the basis of these observations.
单纯疱疹病毒1型的起始结合蛋白(OBP)已在大肠杆菌中表达,并用于研究多个OBP结合位点在单纯疱疹病毒1型复制起点(oriS)中的作用。我们的结果表明,序列CGTTCGCACTT是OBP与双链DNA高亲和力结合所必需的。最小的oriS包含该序列或其紧密衍生物的三个重复。滤膜结合实验表明,特异性结合发生在其中两个重复序列,即盒I和盒II上。使用DNase I足迹技术的研究表明,OBP与盒I和盒II的结合是协同的,并导致形成一种高度有序的复合物,其中整个oriS序列被诱导。我们还观察到,即使在OBP-oriS复合物中,oriS二分体的富含AT的序列也很容易被大分子接近。然而,该序列的DNase I切割模式发生了根本改变,表明发生了显著的构象变化。基于这些观察结果,讨论了OBP与oriS相互作用的初步结构模型。