Distinct roles of two binding sites for the bovine papillomavirus (BPV) E2 transactivator on BPV DNA replication

The modulation of DNA replication by transcription factors was examined by using bovine papillomavirus type 1 (BPV), BPV replication in vivo requires two viral proteins: El, an origin-binding protein, and E2, a transcriptional transactivator, In the origin, El interacts with a central region flanked by two binding sites for E2 (BS11 acid BS12), of which only BS12 has been reported to be essential for replication in vivo. Using chemical interference and electrophoretic mobility shift assays, we found that the binding of E2 to each site stimulates the formation of distinct El-origin complexes, A high-mobility C1 complex is formed by using critical E2 contacts to BS12 and El contacts to the dyad symmetry element, In contrast, interaction of E2 with the BS11 element on the other origin flank promotes the formation of the lower-mobility C3 complex. C3 is a novel species that resembles C2, a previously identified complex that is replication active and formed by El alone. The binding of El greatly differs in the C1 and C3 complexes,,vith El in the C1 complex limited to the origin dyad symmetry region and El in the C3 complex encompassing the region from the proximal edge of BS11 through the distal edge of BS12. We found that the presence of both M-binding sites is necessary for wild-type replication activity in vivo, as well as for maximal production of the C3 complex. These results show that in the normal viral context, BS11 and BS12 play separate but synergetic roles in the initiation of viral DNA replication that are dependent on their location within the origin. Our data suggest a model in which the binding of E2 to each site sequentially stimulates the formation of distinct El-origin complexes, leading to the replication competent complex.