Abstract
oriP is the origin of plasmid replication of Epstein-Barr virus. Replication from oriP requires both the cis-acting elements (the family of repeats and the dyad symmetry element) and the viral origin-binding protein, EBNA-1. The ability of plasmids containing oriP to be maintained stably in EBNA-1-positive cells reflects the efficiency both of their replication and of their segregation each cell cycle. The efficiency of plasmid maintenance was determined for plasmids containing derivatives of oriP with one copy of the dyad symmetry element and two copies of the family of repeats by measuring the rate at which they were lost from cells in the absence of selection. These measurements demonstrated that plasmids with derivatives of oriP with two copies of the family of repeats in one orientation are maintained only slightly less efficiently than is wild-type oriP. To determine whether plasmid maintenance could be affected by reinitiation at the dyad symmetry element (T. A. Gahn and C. L. Schildkraut, Cell 58:527-535, 1989), plasmids containing derivatives of oriP with two copies of the dyad symmetry element and one copy of the family of repeats were compared with plasmids containing wild-type oriP in EBNA-1-positive cells. These measurements showed that plasmids containing a derivative of oriP with two copies of the dyad symmetry element are maintained as efficiently as is wild-type oriP and are not amplified relative to wild-type oriP. These observations indicate that the trans-acting factors that regulate DNA to replicate once per S phase are insensitive to multiple cis-acting regulatory sites within a replicon.
MeSH Terms
DNA Replication
DNA-Binding Proteins/physiology
Genes, Regulator
Genes, Viral
Herpesvirus 4, Human/genetics
Plasmids
Viral Proteins/physiology
Virus Replication
Chemicals
DNA-Binding Proteins
Viral Proteins
origin-binding proteins, viral
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Kirchmaier A L
McArdle Laboratory for Cancer Research, University of Wisconsin Medical School, Madison 53706.
Sugden B
References (25)
25 references, click to expand
-
Definition of the sequence requirements for binding of the EBNA-1 protein to its palindromic target sites in Epstein-Barr virus DNA.
J Virol. 1990 May;64(5):2369-79
PMID: 2157891
-
Interaction of the lymphocyte-derived Epstein-Barr virus nuclear antigen EBNA-1 with its DNA-binding sites.
J Virol. 1989 Jan;63(1):101-10
PMID: 2535719
-
Multiple EBNA1-binding sites are required to form an EBNA1-dependent enhancer and to activate a minimal replicative origin within oriP of Epstein-Barr virus.
J Virol. 1989 Jun;63(6):2657-66
PMID: 2542579
-
The Epstein-Barr virus origin of plasmid replication, oriP, contains both the initiation and termination sites of DNA replication.
Cell. 1989 Aug 11;58(3):527-35
PMID: 2547525
-
High-resolution footprints of the DNA-binding domain of Epstein-Barr virus nuclear antigen 1.
Mol Cell Biol. 1989 Jun;9(6):2738-42
PMID: 2548088
-
A chimera of EBNA1 and the estrogen receptor activates transcription but not replication.
J Virol. 1992 Mar;66(3):1795-8
PMID: 1738208
-
A nuclear matrix attachment region organizes the Epstein-Barr viral plasmid in Raji cells into a single DNA domain.
EMBO J. 1992 Mar;11(3):1165-76
PMID: 1312463
-
Arrest of bacterial DNA replication.
Annu Rev Microbiol. 1992;46:603-33
PMID: 1444268
-
Host cell regulation of induction of Epstein-Barr virus.
J Virol. 1974 Jul;14(1):174-6
PMID: 4365330
-
Selective extraction of polyoma DNA from infected mouse cell cultures.
J Mol Biol. 1967 Jun 14;26(2):365-9
PMID: 4291934
-
Effect of number and position of EBNA-1 binding sites in Epstein-Barr virus oriP on the sites of initiation, barrier formation, and termination of replication.
J Virol. 1993 Mar;67(3):1739-45
PMID: 8382320
-
Detection of specific sequences among DNA fragments separated by gel electrophoresis.
J Mol Biol. 1975 Nov 5;98(3):503-17
PMID: 1195397
-
A simple, rapid, and sensitive DNA assay procedure.
Anal Biochem. 1980 Mar 1;102(2):344-52
PMID: 6158890
-
A new dominant hybrid selective marker for higher eukaryotic cells.
J Mol Biol. 1981 Jul 25;150(1):1-14
PMID: 6271971
-
Plasmid-encoded hygromycin B resistance: the sequence of hygromycin B phosphotransferase gene and its expression in Escherichia coli and Saccharomyces cerevisiae.
Gene. 1983 Nov;25(2-3):179-88
PMID: 6319235
-
A cis-acting element from the Epstein-Barr viral genome that permits stable replication of recombinant plasmids in latently infected cells.
Proc Natl Acad Sci U S A. 1984 Jun;81(12):3806-10
PMID: 6328526
-
A vector that replicates as a plasmid and can be efficiently selected in B-lymphoblasts transformed by Epstein-Barr virus.
Mol Cell Biol. 1985 Feb;5(2):410-3
PMID: 2983194
-
A putative origin of replication of plasmids derived from Epstein-Barr virus is composed of two cis-acting components.
Mol Cell Biol. 1985 Aug;5(8):1822-32
PMID: 3018528
-
The terminus region of the Escherichia coli chromosome contains two separate loci that exhibit polar inhibition of replication.
Proc Natl Acad Sci U S A. 1987 Apr;84(7):1754-8
PMID: 3550796
-
Inhibition of replication forks exiting the terminus region of the Escherichia coli chromosome occurs at two loci separated by 5 min.
Proc Natl Acad Sci U S A. 1987 Apr;84(7):1759-63
PMID: 3550797
-
Plasmid origin of replication of Epstein-Barr virus, oriP, does not limit replication in cis.
Mol Biol Med. 1988 Apr;5(2):85-94
PMID: 2840551
-
Core sequence of two separable terminus sites of the R6K plasmid that exhibit polar inhibition of replication is a 20 bp inverted repeat.
Cell. 1988 Aug 12;54(4):515-23
PMID: 3042153
-
Identification of the DNA sequence from the E. coli terminus region that halts replication forks.
Cell. 1988 Nov 4;55(3):459-66
PMID: 2846183
-
A consensus sequence of three DNA replication terminus sites on the E. coli chromosome is highly homologous to the terR sites of the R6K plasmid.
Cell. 1988 Nov 4;55(3):467-75
PMID: 3052852
-
Role of EBNA-1 in arresting replication forks at the Epstein-Barr virus oriP family of tandem repeats.
Mol Cell Biol. 1991 Dec;11(12):6268-78
PMID: 1658629