INTRODUCTION

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The Epstein-Barr virus (EBV) lytic regulatory protein Zta (BZLF1, ZEBRA, Z) plays a key role in both regulation of EBV lytic gene expression and in lytic viral DNA replication. Zta is related to the Fos/CEBP family of cellular bZIP transcription factors but contains a unique coiled-coil dimerization domain that lacks the standard heptad leucine repeat (13, 19, 21). As a consequence, Zta forms homodimers and does not heterodimerize with the cellular Jun, Fos, and CREB bZIP proteins. Zta binds to both AP-1 sites and related sequences called Zta response elements (ZREs) (19, 38, 57). Both DNA binding and Zta activity are modulated by phosphorylation (7, 31). Zta activates transcription through stabilization of a TFIIA-TFIIID complex (17, 37, 40) and by recruiting the CREB-binding protein CBP (1, 14, 62). CBP and the related p300 possess intrinsic histone acetylase activity. They stimulate transcription through acetylation of histones, which leads to chromatin remodeling, through the acetylation of nonhistone transcription factors and by serving as a bridging factor between transcription factors and polymerase II (6, 33, 46, 48).

Two cis-acting regions have been defined as essential components of the EBV lytic origin of replication, oriLyt (25, 54). One of these comprises the promoter for the BHLF1 open reading frame which contains four ZREs and the second region, which is located 530 bp distally and does not contain ZREs, is required for oriLyt replication but not for transcriptional regulation of BHLF1 (8, 47). Mutation of all four of the ZREs in the promoter proximal region abolished oriLyt replication, indicating the necessity for Zta binding to this region for origin function (53). In a complementary approach, examination of the trans-acting EBV proteins needed for replication of an oriLyt containing plasmid in a Challberg cotransfection assay in EBV-negative cells also revealed an absolute requirement for Zta. In this assay, oriLyt replication was dependent on the presence of Zta plus six core replication proteins, the DNA polymerase (BALF5), polymerase processivity factor (BMRF1), single-stranded DNA-binding protein (BALF2), helicase (BBLF4), primase (BSLF1), and the primase-associated factor (BBLF2/3) (20, 52).

Zta is likely to contribute to oriLyt replication through a variety of mechanisms. Zta induces growth arrest, in part through posttranscriptional p53 stabilization and upregulation of the cyclin-dependent kinase inhibitors p21 and p27 (11, 49). Unlike the smaller DNA viruses, herpesviruses encode many of the enzymes necessary for DNA replication, and it may be advantageous for these viruses to replicate their genomes at a time when they are not competing with cellular DNA replication. The Zta activation domain is not required for Zta-induced growth arrest (12). Recent work has revealed that incoming viral genomes of adenovirus, simian virus 40 (SV40), herpes simplex virus (HSV), human cytomegalovirus (HCMV), and Kaposi's sarcoma-associated herpesvirus (KSHV) accumulate and replicate at promyelocytic leukemia protein (PML)-associated nuclear bodies called PODs (PML oncogenic domains) or ND10 (nuclear domain 10) (4, 10, 28, 42, 56, 59). In HSV- and HCMV-infected cells the POD structure is disrupted prior to lytic DNA replication (3, 32, 43), but replication compartments were detected in KSHV-infected cells that were decorated on the periphery with PODs (59). Induction of lytic replication in EBV-positive D98-HR1 cells revealed a complex process in which the POD protein Sp100 was dispersed prior to the onset of DNA replication, but PML dispersion and loss of POD structure was delayed until after the detection of replicating viral DNA (9). Zta appears to be the EBV protein that mediates late-stage dispersion of PODs, and the N terminus of the Zta activation domain is required for this function (2). The ability of Zta to disperse PML may be related to competition between Zta and PML for SUMO-1 modification (2).

Zta may also contribute to origin function through its transcriptional activity. Transcription factors frequently bind to auxiliary sequences flanking the minimal origin region where they stimulate replication efficiency (15, 24, 45) by contributing to the relief of nucleosomal repression (27, 35, 44). Initial deletion analyses of the Zta transcriptional activation domain found concurrent reductions in both the transcription and the replication functions of Zta (5, 53). However, there were indications that the Zta transactivation domain might have a role in oriLyt replication beyond that made by its contribution to transcriptional activation. An oriLyt plasmid in which the ZRE sites were converted to binding sites for either human papillomavirus E2 or yeast Gal4 could not be efficiently replicated by these proteins but was replicated by Zta fusion proteins targeted to the altered binding sites (53). Further, an activation domain deletion, Zta(11-25) that had no negative effects on transactivation function resulted in a Zta protein that was replication deficient in cotransfection replication assays (51).

In herpesvirus-infected cells, lytic viral DNA replication takes place in globular or kidney-shaped nuclear subdomains that stain for viral replication proteins (3, 41, 52, 58, 59, 66). Replication compartment formation has not been extensively examined in EBV-infected cells but Zta and BMRF1 were shown to colocalize in replication compartments formed after induction of the lytic cycle in EBV-infected Akata cells (55). In the present study we examined the interaction between the EBV helicase BBLF4 and Zta. The BBLF4 interaction site mapped to the amino acid (aa) 22 to 86 segment of the Zta transactivation domain adjacent to the interaction site for the BSLF1-BBLF2/3 primase subcomplex, further illustrating the complexity of contacts made by the core replication proteins. Zta mutants that were defective for helicase interaction failed to efficiently associate with replication compartments in Zta-transfected D98-HR1 cells, providing evidence for an additional role for the helicase in the intranuclear targeting of Zta.

	MATERIALS AND METHODS

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Plasmid constructions. A 750-bp BglII fragment containing the green fluorescent protein (GFP) coding sequences was obtained by introducing a 10-mer BglII linker into the NheI site of pEGFP-C1 (Clontech, Inc.) and cleaving with BglII. BBLF4-GFP was constructed by ligating the 750 bp fragment into BclI-cleaved pRTS28 (23). The Zta inserts from the plasmids pPL228 (39), pZQ239, and pZBS39-45 (obtained from P. Lieberman) were transferred as EcoRI or BamHI fragments, respectively, into the appropriate sites of the SG5 vector (Stratagene) to generate Zta 24-86, Zta 3-39, and Zta 39-45 eukaryotic expression plasmids. Zta 61-81 was constructed by PCR amplification of Zta aa 1 to 60 using the primers 5'-CAGTGGATCCTAATGATGGACCCAAACTCG and 5'-GCTAGCGGCCGCTGGCCTTGTGGCAGA, and Zta aa 82 to 245 was constructed using the primers 5'-GCTAGCGGCCGCCTCCTGAGAATGCTTAT and 5'-GCTAGGATCCTTACTTGTCATCGTCGTCC. The NotI-cleaved PCR products were ligated, and the Zta aa 1 to 60 plus 82-to-245 fragment was purified and ligated into the BamHI site of the SG5 vector. A pPL230 (51) EcoRI fragment was ligated into pGH416 to create the glutathione S-transferase (GST)-Zta 94-140 fusion protein expression plasmid. GST-Zta(wt)(pDH237), GST-Zta(26-133)(pDH279), and GST-Zta(1-133)(pDH245) have been described elsewhere (23), as have the oriLyt-chloramphenicol acetyltransferase (CAT) reporter, pDH123, and the expression plasmid for Zta(wt), pRTS21, and Zta(2-25). (51). The Zta(m22/24,74/75) and GST-Zta(22/24,74/75) plasmids were a gift from Paul M. Lieberman (40).

Immunofluorescence assays. Vero cells were seeded at 8 × 10⁴ cells per well in two-well slide chambers. Cells were transfected with a maximum of 3 µg of DNA by the calcium phosphate procedure. After transfection, cells were incubated in Dulbecco modified Eagle medium plus 10% fetal bovine serum for 16 h at 35°C in 3% CO₂, followed by a medium change and a further 24-h incubation. When appropriate, bromodeoxyuridine (BrdU) was added to the culture medium at a final concentration of 10 µM for 45 min before fixation. Cells were washed in phosphate-buffered saline (PBS; 0.144 g of KH₂PO₄, 9.0 g of NaCl, and 0.795 g of Na₂HPO₄ · 7H₂O per liter), fixed with 1% paraformaldehyde in PBS for 10 min at room temperature, and permeabilized for 20 min on ice in 0.2% Triton X-100 in PBS. For BrdU staining, pulse-labeled cells were incubated with 4 N HCl for 10 min at room temperature in order to expose incorporated BrdU residues and then washed in PBS three times for 5 min each time before permeabilization. Cells were incubated with primary antibody for 60 min at 37°C and with secondary antibody at 37°C for 30 min. The antibodies used were anti-BMRF1 monoclonal antibody (1:200; ABI Advanced Biotechnologies, Inc., Columbia, Md.), anti-BZLF1 polyclonal antibody (1:800; a gift of Marie Hardwick, Johns Hopkins School of Hygiene and Public Health), and sheep anti-BrdU antibody (1:200; Fitzerald Industries International, Inc., Concord, Mass.), fluorescein isothiocyanate (FITC)-conjugated goat anti-mouse immunoglobulin G (IgG; 1:200; Cappel Organon Teknika, Durham, N.C.), FITC-conjugated donkey anti-rabbit IgG (1:200), rhodamine-conjugated donkey anti-mouse immunoglobulin (1:200) and anti-rabbit immunoglobulin (1:200), and rabbit anti-sheep IgG (1:200; Chemicon, Temecula, Calif.).

CAT assay. Hela cells were plated in six-well cluster dishes at 2 × 10⁵ cells per well 16 h before transfection, with a medium change 4 h before transfection. Cells were transfected by calcium phosphate precipitation with the oriLyt-CAT reporter (pDH123, 1 µg) and Zta or Zta variants. Vector SG5 DNA was used to equalize the amount of DNA in each transfection to 5 µg. Each experiment was repeated at least two times. CAT assays were performed as previously described (26). Total protein was measured using the BCA Protein Assay Reagent (Pierce, Rockford, Ill.), and equal amounts of protein were analyzed for CAT activity.

GST-protein affinity assay. GST and GST-Zta fusion proteins were induced by growth in medium containing 100 µM isopropyl--D-thiogalactopyranoside (IPTG) for 3 h at 30°C. Pelleted bacteria were resuspended in binding buffer (50 mM Tris-HCl [pH 7.9], 100 mM NaCl, 5 mM MgCl₂, 0.5 mM EDTA, 2 mM dithiothreitol [DTT], 0.2% Nonidet P-40) and sonicated. Cell debris was removed by centrifugation at 10,000 × g for 10 min. The supernatant was incubated with glutathione agarose beads (Sigma, St. Louis, Mo.) at 4°C overnight, followed by three washes in binding buffer. The amount of protein bound to the beads was determined by Coomassie brilliant blue staining of protein separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). Equal amounts of each GST protein were used in the affinity assays.

DNA replication assays. The DNA transfection-replication assay was performed using a modification of the previously described protocol (51, 52). Briefly, 1.5 × 10⁶ Vero cells per 100-mm dish were transfected with 10 µg of pEF52(ori-Lyt) DNA, 1.6 µg of Zta expression plasmid, and 0.8 µg of expression plasmids for each of the six core replication proteins, as well as Mta and Rta. At 80 h after the posttransfection medium change, the cell monolayer was washed twice with PBS and scraped into 4 ml of 40 mM Tris-HCl (pH 7.5), 1 mM EDTA, and 150 mM NaCl. The cells were then pelleted and lysed in 2 ml of lysis buffer (10 mM Tris-HCl [pH 8.0], 10 mM EDTA, 2% SDS, 100 µg of proteinase K per ml). After overnight incubation at 37°C, the samples were diluted to 4 ml with Tris-EDTA (pH 8.0); extracted with phenol, phenol-chloroform, and chloroform; and ethanol precipitated after the addition of sodium acetate (pH 5.2) to a final concentration of 0.3 M. The DNA pellets were resuspended in 450 µl of distilled H₂O, treated with 100 µg of RNase A per ml, ethanol precipitated, and resuspended in 300 µl of H₂O. Then, 10 µg of extracted cellular DNA was digested overnight with 30 U of DpnI at 37°C. Replicated DNA was detected by PCR amplification using oligonucleotide primers specific for pBR322 DNA. The primers 5'-GAAGCCAGTTACCTTCGG and 5'-GCAGGACCACTTCTGCG amplified a 510-bp fragment containing seven DpnI restriction sites, while the primers 5'-CTGTGGAACACCTACATCTG and 5'-AGATGTCTGCCTGTTCATCC amplified a 330-bp control fragment that lacked DpnI sites. The products were visualized by electrophoresis on a 1.2% agarose gel containing 500 ng of ethidium bromide per ml.

	RESULTS

Top Abstract Introduction Materials and Methods Results Discussion References

Zta interaction with the EBV helicase, BBLF4. The EBV helicase, BBLF4, has previously been shown to localize to the cytoplasm of transfected cells (23). Cotransfection with Zta was found to result in nuclear translocation of BBLF4, suggesting an interaction between these two proteins (23). A BBLF4-GFP expression vector was generated to further characterize this interaction. BBLF4-GFP was transfected into Vero cells alone or with the series of Zta expression plasmids shown in Fig. 1A and the intracellular localization of BBLF4-GFP was determined by fluorescence microscopy (Fig. 1B). In transfected cells, BBLF4-GFP showed a cytoplasmic distribution. This localization was converted to nuclear when BBLF4-GFP was cotransfected with wild-type Zta. However, Zta(24-86) was ineffective at mediating nuclear localization of BBLF4-GFP. Deletions were created across the aa 24 to 86 region in an attempt to further define the sequences required for BBLF4 binding. Deletion of either the front portion of this domain [Zta(3-69)] or the back portion [Zta(61-81)] had a similar effect. In each case, cotransfection with BBLF4-GFP led to the detection of nuclear BBLF4-GFP, although the efficiency of nuclear translocation was reduced, and cytoplasmic BBLF4-GFP was also detected in a significant proportion of the cells (Fig. 1B; Table 1). Changing the spacing between the boundaries of the domain by introducing a small 6-aa deletion in the central region [Zta(39-45)] also had the effect of reducing the effectiveness of the interaction as measured by BBLF4-GFP nuclear localization (Fig. 1B; Table 1). These results suggested that BBLF4 might make contacts within each half of the aa 24 to 86 region of Zta. In support of this conclusion, a mutant [Zta(m22/26,74/75)] that carried a pair of mutations at each margin of the aa 24 to 86 region was severely impaired for nuclear translocation of BBLF4-GFP (Fig. 1B) (Table 1).

View larger version (42K): [in this window] [in a new window]   FIG. 1.   Effect of cotransfected Zta on the intracellular localization of BBLF4-GFP. (A) Diagrammatic representation of the Zta plasmids used in the cotransfection assays. (B) Representative photomicrographs of Vero cells transfected with BBLF4-GFP either alone or in the presence of the indicated wt or mutant Zta plasmids. The intracellular localization of BBLF4-GFP was determined by fluorescence microscopy.

Mapping the interaction domain for BBLF4-GFP using GST affinity assays. To provide additional evidence that Zta binds to BBLF4 and that the aa 22 to 86 region of Zta was required for the interaction. GST affinity assays were performed using the GST-Zta constructions illustrated in Fig. 2A. Extracts from 293T cells transfected with either BBLF4-GFP or a GFP control vector were incubated with glutathione beads containing equal amounts of the different GST-Zta proteins. The relative amounts of GST-Zta proteins used were determined by Coomassie brilliant blue staining of the SDS-PAGE-separated proteins (Fig. 2B, lower panel). Western blot analysis to detect protein binding to the GST-Zta proteins was performed using anti-GFP antibody and a chemiluminescence visualization procedure. Wild-type GST-Zta bound BBLF4-GFP, as did the GST-Zta activation domain construction, Zta(1-133) (Fig. 2B, upper panel). Zta carrying an internal deletion of the carboxy-terminal region of the activation domain, GST-Zta(94-140), also bound BBLF4-GFP, although with slightly reduced affinity (Fig. 2B, upper panel). Neither GST-Zta(26-133) nor Zta(m22/26,74/75) bound BBLF4-GFP (Fig. 2B, upper panel), again emphasizing the importance of sequences in the aa 22 to 26 and aa 74 to 86 regions of Zta for BBLF4 binding. There was no binding of BBLF4-GFP to GST alone (Fig. 2B, upper panel), nor did the control GFP protein bind to any of the GST constructions (Fig. 2B, middle panel).

View larger version (71K): [in this window] [in a new window]   FIG. 2.   Binding of BBLF4-GFP to GST-Zta constructions. (A) Diagrammatic representation of the GST-Zta constructions used. (B, upper panel) GST affinity assay in which a BBLF4-GFP transfected 293T cell extract was incubated with equal amounts of GST or the indicated GST-Zta proteins bound to glutathione beads. Bound protein was detected by Western blot analysis using anti-GFP antibody and a chemiluminescence visualization procedure. A total of 5 µl of extract was directly loaded in the extract lane. (Middle panel) GST affinity assay performed as described above using an extract of 293T cells transfected with control vector expressing GFP. (Lower panel) SDS-polyacrylamide gel stained with Coomassie brilliant blue showing the GST and GST-Zta proteins used in the binding assays presented in the upper and middle panels.

Zta(m22/26,74/75) is defective for DNA replication. To examine the functional consequences of loss of BBLF4 binding, Zta(m22/26,74/75) was tested for its ability to support lytic EBV DNA replication. We first used a PCR-based cotransfection-replication assay to compare the replication function of wild-type Zta with that of the Zta mutant Zta(m22/26,74/75). Vero cells were transfected with an oriLyt containing plasmid, along with expression plasmids for the six core EBV replication proteins, Rta and Mta plus either wild-type Zta, Zta(m22/26,74/75) or vector DNA. At 80 h posttransfection the cells were harvested, the DNA was extracted, and the concentration was determined by absorbance at 260 nm. Equal amounts of DNA from each transfection were either digested overnight with DpnI or were left untreated. Segments of the oriLyt plasmid DNA backbone were then amplified in a PCR reaction using two different sets of primers. The first set of primers amplified a 510-bp segment of the oriLyt plasmid backbone. This 510-bp region contains seven DpnI sites. The bacterially grown oriLyt plasmid DNA that is transfected into the cells is methylated and will be cleaved by DpnI, whereas DNA that has been replicated in the transfected mammalian cells will no longer carry the bacterially imposed methylation pattern and will not be cleaved. Thus, after DpnI digestion of the DNA, the 510-bp fragment should be readily amplifiable only from cells in which Zta has been able to support oriLyt DNA replication. On the other hand, in the absence of DpnI digestion the 510-bp fragment should be equally amplifiable from each of the DNA samples. A second set of PCR primers was used to control for any nonspecific effects of DpnI digestion. This primer pair amplified a 330-bp segment of the oriLyt plasmid backbone that does not contain any DpnI sites. In this case, the DpnI-digested DNA samples should be equally amplifiable regardless of whether or not the oriLyt plasmid had been replicated.

View larger version (17K): [in this window] [in a new window]   FIG. 3.   Zta(m22/26,74/75) is unable to replicate an oriLyt plasmid. Ethidium bromide-stained gel of electrophoretically separated PCR-amplified fragments of the non-EBV backbone sequences of the oriLyt plasmid pEF52. Vero cells were transfected with pEF52, expression plasmids for the six core replication genes, Mta and Rta plus either control vector DNA or expression plasmids for wild-type Zta or Zta(m22/26,74/75). DNA was isolated from the transfected cells, and segments of the oriLyt plasmid backbone were amplified by PCR either before or after digestion of the DNA with the methylation-sensitive restriction enzyme DpnI. The test primers amplify a 510-bp fragment that contains seven DpnI sites, while the control primers amplify a 330-bp fragment that does not contain any DpnI sites. After DpnI digestion of the transfected cell DNA, the 510-bp fragment should only be amplifiable if the input DNA has been replicated in the transfected cells. Lane 1, marker DNA ladder; lanes 2 to 8, DpnI-digested DNA amplified with the test primers; lanes 9 to 12, undigested DNA amplified with the test primers; lanes 13 to 17, DpnI-digested DNA amplified with the control primers. Plasmid DNA, the PCR reaction was performed directly on the input plasmid DNA; water, no DNA added.

View larger version (36K): [in this window] [in a new window]   FIG. 4.   Zta(m22/26,74/75) and Zta(24-86) are unable to replicate endogenous P3HR1 genomes. (A) Schematic representation of the righthand end of the EBV genome showing the relative locations of the terminal EcoRI and BamHI restriction fragments. TR, terminal repeats. (B) Southern blot of DNA isolated from P3HR1 cells electroporated with the indicated plasmids. After cleavage with BamHI, the electrophoretically separated DNA fragments were transferred to a nitrocellulose membrane and probed with a 32P-labeled EcoRI-Dhet probe. As indicated by the increase in the amount of the BamHI-Nhet fragment, linear EBV genomes were efficiently amplified only in wild-type Zta-transfected cells. Lanes 1 to 5, DNA isolated from electroporated P3HR1 cells; lane 6, cosmid 302-21 DNA digested with BamHI.

Zta(m22/26,74/75) and Zta(24-86) retain transactivation activity. Replication assays performed in P3HR1 or D98-HR1 cells are dependent on the expression of the core EBV replication proteins from the endogenous genomes. The Zta(m22/26,74/75) and Zta(24-86) mutations lie within the transcriptional activation domain of Zta. The activation domain has been shown to have a modular construction, and deletion of any one segment reduces, but does not eliminate, transcriptional activity (16, 37). The behavior of the Zta(m22/24,74/75) and Zta(24-86) mutants compared to wild-type Zta is illustrated in the reporter assay in Fig. 5. At low concentrations of transfected effector DNA, the Zta(m22/24,74/75) and Zta (24-86) mutants were severely impaired in their ability to activate expression from an oriLytp-CAT reporter relative to wild-type Zta. However, the deficiency could be partially compensated for by increasing the dose of input DNA. This was not the case for wild-type Zta, which gave maximal transactivation responses at low levels of input plasmid DNA. The wild-type and Zta(m22/24,74/75) and Zta(24-86) mutants express comparable levels of Zta protein in transfected cells as measured by Western blotting.

View larger version (19K): [in this window] [in a new window]   FIG. 5.   CAT reporter assay comparing transactivation activity of wild-type Zta and the Zta(m22/24,74/75) and Zta(24-86) mutants. HeLa cells were transfected with an oriLytp-CAT reporter (1 µg) and increasing amounts of expression vectors for wild-type or mutant Zta. Cells were harvested for determination of CAT activity 40 h after transfection.

View larger version (89K): [in this window] [in a new window]   FIG. 6.   Zta(m22/26,74/75) and Zta(24-86) activate expression of BMRF1 from endogenous EBV genomes. Immunofluorescence assay performed on D98-HR1 cells before and after transfection with the indicated Zta plasmids. Cells were stained with anti-BMRF1 (polymerase processivity factor) monoclonal antibody and FITC-conjugated secondary antibody.

Zta(m22/26,74/75) and Zta(24-86) fail to target efficiently to replication compartments. We wished to address the requirements for DNA replication compartment formation in transfected D98-HR1 cells. Replication compartments are visible in immunofluorescence assays as large intranuclear bodies. Replication compartments were detected in D98-HR1 cells transfected with wild-type Zta by staining for BMRF1 (polymerase processivity factor) (Fig. 7). These structures were shown to represent functional replication compartments by incubating the cells with BrdU and double staining for sites of BrdU incorporation with anti-BrdU antibody. The BrdU staining colocalized with BMRF1 in the intranuclear bodies (Fig. 7).

View larger version (21K): [in this window] [in a new window]   FIG. 7.   Demonstration of replication compartment formation in D98-HR1 cells. Immunofluorescence assay performed on D98-HR1 cells that were transfected with wild-type Zta and incubated with BrdU 45 min prior to fixation. Cells were double stained for the polymerase processivity factor BMRF1 (a and d) using anti-BMRF1 monoclonal antibody and FITC-conjugated anti-mouse immunoglobulin secondary antibody and for BrdU (b and e) using anti-BrdU sheep antibody and rhodamine-conjugated anti-sheep immunoglobulin as the secondary antibody. Merge, overlays of the FITC and rhodamine images (c and f). Replication bodies are visible that double stain for BrdU incorporation and the presence of viral replication proteins, as exemplified by BMRF1.

View larger version (37K): [in this window] [in a new window]   FIG. 8.   Zta(m22/26,74/75) and Zta(24-86) fail to associate with replication compartments. An immunofluorescence assay was performed on D98-HR1 cells transfected with expression vectors for wild-type or mutant Zta. Cells were stained for BMRF1 using anti-BMRF1 monoclonal antibody and for Zta using rabbit anti-Zta antiserum. Wild-type Zta colocalized with the replication compartments, whereas the two Zta mutants were excluded from these bodies. Merge, overlays of the FITC and rhodamine images.

	DISCUSSION

Top Abstract Introduction Materials and Methods Results Discussion References

A central role for Zta in lytic EBV DNA replication lies with the recruitment and assembly of a replication complex on oriLyt. The interactions that have been described between Zta and the core replication proteins and between individual viral replication proteins indicate that complex formation relies on multiple contact points among the participating proteins. The helicase (BBLF4), primase (BSLF1), and primase-associated factor (BBLF2/3) form a tripartite complex, as do the equivalent proteins in HSV (18). In DNA-transfected cells in which changes in intracellular localization of the proteins were used as a measure of interaction, BSLF1 was shown to interact with BBLF2/3, and evidence for a tripartite complex was also presented (23). These interactions were confirmed in immunoprecipitation assays using baculovirus-expressed proteins, with additional evidence provided for separate contacts by both BSLF1 and BBLF2/3 with BBLF4 (60). We had previously mapped the site of interaction of the primase subcomplex (BSLF1-BBLF2/3) with Zta to the N terminus of the Zta activation between Zta aa 11 and 25 (23). We now show that BBLF4 interacts with the adjacent region of Zta between aa 22 and 86. The helicase-primase complex has also been found to interact with polymerase (BALF5) (22). Polymerase interacts with the polymerase processivity factor (BMRF1) (29, 34), which in turn interacts with the bZIP domain of Zta (65). The single-stranded DNA-binding protein BALF2 has also been found to contact the BALF5-BMRF1 proteins (61). Thus, direct contacts on Zta are made by two of the proteins of the helicase-primase complex (BBLF2/3 and BBLF4) and by BMRF1, and the other core replication proteins appear to be tethered by interactions to one or more of these three proteins.

The possibility of additional tethering of the replication complex to oriLyt by cellular transcription factors was raised by the observation that cotransfected BMRF1 activated transcription from BHLF1 oriLyt promoter-reporter constructions and that the sequences required for this activation mapped to the essential promoter distal replication domain (63, 64). A yeast one-hybrid screen identified Sp1 and ZBP-89 as cellular transcription factors that bound to the essential promoter distal domain of oriLyt, and these proteins proved to also interact with BMRF1 and BALF5 (7). Thus, multiple protein-protein interactions between individual members of the virally encoded replication complex and between this complex and the DNA-bound Zta and cellular Spl and ZBP-89 transcription factors contribute to the origin tethering of the replication complex.

The mapping of the helicase interaction region to aa 22 to 86 within the Zta activation domain raises questions about the relationship between Zta's transcription and replication functions. The Zta(m22/26,74/75) mutant that lost interaction with BBLF4 also shows some impairment in transactivation function. Zta(m22/26,74/75) was significantly impaired for activation of the BHLF1(oriLyt) promoter in in vitro transcription assays but showed no deficit on an artificial promoter containing seven upstream ZREs (40). In transfection assays the Zta(m22/26,74/75) mutant was less effective in activating the BHLF1 promoter, with the deficit being partially compensated for by increasing the amount of transfected Zta(m22/26,74/75) (40) (Fig. 5). Analysis of the underlying nature of the deficit in Zta(m22/26,74/75) function revealed that this mutant had a reduced ability to stimulate the formation of a stable TFIID-TFILA complex (40) and also was impaired in its ability to recruit the coactivator CBP to Zta (14). The loss of interaction with CBP correlated with a reduced ability to detect Zta-mediated acetylation of histones. The Zta transactivation domain appears to have a modular structure, in that the loss of individual segments can be compensated for by increasing the number of Zta binding sites on the promoter or increasing the copy number of the other domains (16). It seems likely that the contacts made by the coactivators, basal transcription factors, and TAFs (37) are just as complex as those made by the replication proteins. However, the apparent overlap of the binding region for the helicase with that for CBP raises the possibility that individual DNA-bound Zta dimers may be capable of interacting with either a transcriptional complex or a replication complex but not both simultaneously. If such were the case, this might explain the requirement for multiple Zta binding sites within the origin. oriLyt of the EBV-related baboon virus herpesvirus papio is essentially identical in structure to EBV oriLyt and also contains multiple Zta binding sites (50).

Zta(m22/26,74/75) was defective for oriLyt DNA replication in a cotransfection replication assay and was similarly unable to induce replication of the endogenous genomes in P3HR1 cells. However, structures resembling replication compartments were detected in D98-HR1 cells transfected with this Zta mutant. We observed that Zta(m22/26,74/75) was excluded from the replication compartments and concluded that this inability to localize to the sites of DNA replication was a contributing factor in the DNA replication deficit displayed by Zta(m22/26, 74/75). This Zta mutant is also deficient for helicase interaction, and the implication is that the helicase targets Zta to the replication compartments. The formation of replication compartment-like structures in D98-HR1 cells transfected with Zta(m22/26,74/75) also implies that replication compartment formation in EBV does not require the presence of Zta or an active origin of replication. In cells transfected with the HSV replication machinery, replication compartment formation was found to be independent of the origin binding protein UL9 or an origin containing plasmid, and a similar observation was made for KSHV, where transfection of plasmids encoding the six core replication proteins was sufficient to allow the formation of replication compartments (41, 58, 59, 66). In contrast, the formation of CMV replication compartments in transfected cells required the presence of an oriLyt plasmid and both ancillary and core replication proteins (52).

Zta(24-86), which is also defective for helicase interaction, was unable to induce replication of the endogenous genomes in P3HR1 cells and was also not associated with replication compartments in D98-HR1 cells. Previously, Zta(25-86) had been found to replicate an oriLyt-containing plasmid in a cotransfection-replication assay (51). A differential ability to replicate a transfected oriLyt plasmid but not endogenous EBV genomes was also observed with a Zta aa 200 mutation in studies of Zta-BMRF1 interaction (65). The reason for the discrepancy between the two assays is not known but, given the functions mediated by the aa 24 to 86 region of Zta, it is possible to speculate. First, BBLF4 forms a tripartite complex with BSLF1 and BBLF2/3. These latter proteins bind to the aa 11 to 25 segment of Zta and can bind to Zta(24-86). In the presence of high concentrations of the proteins in transfected cells, it seems likely that BBLF4 could be tethered to Zta indirectly through the helicase subcomplex and hence permit Zta to be targeted to replication foci in the normal manner. A second difference between the assays is the presence of oriLyt on a transfected plasmid versus the endogenous and presumably more extensively nucleosome-associated oriLyt present within the episomal EBV genomes. This region of Zta is also involved in the recruitment of CBP, which has intrinsic histone acetylase activity. Ineffective histone acetylation and clearance from the DNA is likely to be a greater handicap for replication of the endogenous genomes than for transfected DNA. The complex nature of the interactions involved in Zta's transcriptional and replication functions has made it difficult to tease apart the contributions of individual domains of the Zta protein. This is exemplified by the aa 22 to 86 domain, where protein-protein interactions mediating replication complex formation, replication compartment targeting, and nucleosome clearance all contribute to oriLyt DNA replication.