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J. Biol. Chem., Vol. 276, Issue 26, 23689-23699, June 29, 2001
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From the Cold Spring Harbor Laboratory, Cold Spring Harbor,
New York 11724
DNA replication of papillomavirus requires the
viral initiator E1 and the transcription factor E2. Bovine
papillomavirus, type 1 (BPV-1), E1, and E2 bind cooperatively as dimers
to proximal sites in the viral replicator generating a
sequence-specific E1E2-ori complex. This complex is
critical for replication and can be converted to a multimeric
E1-ori initiator complex by displacement of E2 in the
presence of hydrolyzable ATP. However, E2 can function over extended
distances, and E2 at a distal position 33 base pairs upstream of the
E1-binding site also loads an E1 dimer onto ori. Under
these conditions, neither displacement of E2 nor ATP hydrolysis are
required for E1-ori formation, consistent with a need for ATP hydrolysis in E2 displacement from E1E2-ori. However,
ATP is required for stabilization of the resulting E1-ori
complex. These results indicate that BPV (with a proximal E2-binding
site) and human papillomaviruses (with distal E2-binding sites) utilize the same general mechanism for E1 loading but suggest that
E1E2-ori, which forms preferentially on ori,
may perform an additional role in BPV replication.
Mechanism and Requirements for Bovine Papillomavirus, Type 1, E1
Initiator Complex Assembly Promoted by the E2 Transcription Factor
Bound to Distal Sites*
*
This work was supported by National Institutes of Health
Grant CA 13106 (to A. S.) and in part by a Wellcome International Prize Traveling Fellowship (to C. M. S.).The costs of publication of this
article were defrayed in part by the
payment of page charges. The article
must therefore be hereby marked
"advertisement" in accordance with 18 U.S.C. Section
1734 solely to indicate this fact.
To whom correspondence should be addressed: Cold Spring Harbor
Laboratory, P. O. Box 100, Cold Spring Harbor, NY 11724. Tel.: 516-367-8407; Fax: 516-367-8454; E-mail: Stenlund@cshl.org.
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