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Journal of Virology, November 2001, p. 10603-10611, Vol. 75, No. 22
Department of Cancer Genetics, Roswell Park
Cancer Institute, Buffalo, New York 14263
Received 25 May 2001/Accepted 13 August 2001
oriP is a 1.7-kb region of the Epstein-Barr virus
(EBV) chromosome that supports replication and stable maintenance of
plasmids in human cells that contain EBV-encoded protein EBNA1.
Plasmids that depend on oriP are replicated once per
cell cycle by cellular factors. The replicator of oriP
is an ~120-bp region called DS which depends on either of two pairs
of closely spaced EBNA1 binding sites. Here we report that changing the
distance between the EBNA1 sites of a functional pair by inserting or
deleting 1 or 2 bp abolished replication activity. The results
indicated that, while the distance separating the binding sites is
critical, the specific nucleotide sequence between them is unlikely to
be important. The use of electrophoretic mobility shift assays to
investigate binding by EBNA1 to the sites with normal or altered
spacing revealed that EBNA1 induces DNA to bend significantly when it
binds, with the center of bending coinciding with the center of
binding. EBNA1 binding to a functional pair of sites which are spaced
21 bp apart center to center and which thus are in helical phase
induces a larger symmetrical bend, which based on electrophoretic
mobility approximates the sum of two separate EBNA1-induced DNA bends. The results imply that replication from oriP requires a
precise structure in which DNA forms a large bend around two EBNA1 dimers.
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.22.10603-10611.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Replication from oriP of
Epstein-Barr Virus Requires Exact Spacing of Two Bound Dimers of EBNA1
Which Bend DNA
*
Corresponding author. Mailing address: Department of
Cancer Genetics, Roswell Park Cancer Institute, Buffalo, NY 14263. Phone: (716) 845-8964. Fax: (716) 845-1698. E-mail:
john.yates{at}roswellpark.org.
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