INTRODUCTION

Top Abstract Introduction Materials and Methods Results Discussion References

Human cytomegalovirus (HCMV), a member of the betaherpesvirus family, exerts many different effects on the host cell during infection (15). The virus optimizes the conditions of the cell for its replication by activating the expression of genes that will assist in its DNA synthesis. At the same time, the virus inhibits host cell DNA synthesis by an undefined mechanism that coincides with viral gene expression (5, 11, 25, 35). Since the virus is not competing with the host cell for resources, it is able to maximize its replication. Our interest lies in how HCMV alters the cell cycle at the transcriptional level in order to achieve this effect.

The cell cycle is a dynamic process requiring that all components adhere to strict temporal and spatial requirements. The cyclins are key regulatory factors that are controlled by a variety of mechanisms including phosphorylation, association with their respective cyclin-dependent kinases (cdk's), gene expression, protein stability, subcellular localization, and degradation (2, 14, 21, 51, 54, 55). One of these cyclins, cyclin E, is expressed in the G₁ phase of the cell cycle and associates with cyclin-dependent kinase 2 (cdk2). This association along with phosphorylation of the kinase by cyclin-activating kinase activates cdk2. The activated kinase complex is then responsible for several phosphorylation events that are required for progression into the S phase of the cell cycle.

The E2F family of transcription factors also plays a central role in cell cycle control. These transcription factors regulate expression of genes involved in cell cycle progression (cyclin E, cyclin A, cdc2, and cdc25), transcription (E2F-1, b-myb, p107, and c-myc), and DNA synthesis (DNA polymerase , cdc6, dihydrofolate reductase [DHFR], thymidine kinase, HsOrc1, and H2A) (10, 18, 20, 22-24, 26, 29, 34, 43-45, 47, 48, 52, 56, 58, 63). In the classic model of E2F site regulation, an E2F family member, E2F-1 to -6, forms a heterodimer with a DP family member, DP-1 to -3, and this complex binds to an E2F site on the DNA (consensus TTTCGCGC). The presence of a pocket protein (Rb, p130, or p107) is thought to be repressive, and the sequential phosphorylation of the pocket protein by cyclin D-cdk4/6 and cyclin E-cdk2 results in its release from the complex and activation of transcription by the remaining heterodimeric complex. Subsequent phosphorylation of the heterodimeric complex by cyclin A-cdk2 is believed to lead to the release of the complex from the DNA.

Rb, p107, and even p130, which is most often associated with a repressive G₀ complex, have all been detected in E2F-containing complexes in S-phase cells, suggesting that the presence of a pocket protein is not always an indicator of inhibition (2, 33, 40). In addition to their role in transcription, the pocket proteins p107 and p130 can bind to cyclin E or A-cdk2 complexes and inhibit their kinase activity (7, 62). The role of p107 and p130 in the cell cycle is further complicated by the fact that they can simultaneously interact with E2F transcription factors and cyclin-cdk complexes. It is not clear what role the E2F-cyclin-cdk-pocket protein complexes may play in a cycling cell. These types of complexes are commonly detected in electrophoretic mobility shift assays (EMSAs) using extracts from S-phase cells, suggesting that these complexes are not inhibitors of transcription (33).

Our lab and others have shown that HCMV infection affects many factors involved in the regulation of the cell cycle, leading to arrest of the cell prior to mitosis (3-6, 11, 16, 25, 35, 42, 50). These effects include upregulation of cyclin E and its associated kinase activity, downregulation of cyclin A and its associated kinase activity, sustained levels of cyclin B, hyperphosphorylation of Rb, stabilization of p53, altered subcellular localization of cdk2, and sequestration of p53 and replication protein A into viral replication centers.

Recently, we demonstrated that cyclin E upregulation in HCMV-infected cells occurs at the transcriptional level (50). In uninfected cells, E2F factors appear to regulate the transcription of cyclin E in a cell cycle-dependent manner through specific binding sites in the promoter, which are located approximately 100, 600 (two sites), 1,000 (two sites), and 1,100 bp from the translation start site (18, 45). However, it is still not certain which of these sites are most important for regulation of cyclin E transcription, as two independent groups have arrived at different conclusions based on the results of mutagenesis experiments and transient-transfection studies (18, 45). In addition, these two groups detected transcription start sites different from those of one another. Different transformed cell lines were used by the two groups, and this may explain the discrepancies. In a separate study, Bresnahan et al. (3) used cyclin E promoter constructs and transient-transfection assays to examine the regulation of this promoter by HCMV. The results of their transfection studies suggested that the viral immediate-early (IE) protein IE2-86 was the major transactivator of the cyclin E promoter and that the E2F sites were not required.

The goal of the work presented here was to determine the molecular basis of the upregulation of cyclin E transcription by HCMV when the endogenous promoter is in its normal chromatin context. We show that the primary HCMV-induced cyclin E transcripts initiate further downstream than the cyclin E transcripts in mock-infected cells. In accord with these observations, we demonstrate, by in vivo footprinting of the cyclin E promoter, protection as well as hypersensitivity of downstream sites in infected cells. Some of these sites overlap the region that contains the two E2F sites that were shown by Ohtani et al. (45) to be important for cell cycle-mediated regulation of cyclin E transcription. At the same time, we observed that the steady-state levels and patterns of phosphorylation of E2F and Rb family members are specifically altered by infection. We further find that virus-induced complexes, one of which consists of E2F-4, DP-1, and p130, bind to this region of the promoter with kinetics that parallel the induction of the cyclin E transcript. We also show that the induction of cyclin E transcription requires viral gene expression. However, in contrast to what was suggested by the results of Bresnahan et al. (3), we find that IE2-86 alone cannot induce the endogenous cyclin E promoter. Another major viral IE protein, IE1-72, also cannot activate the endogenous cyclin E promoter when expressed alone or in combination with IE2-86. Rather, the results of kinetic experiments suggest that a viral gene product(s) in the early class, expressed after the IE phase, is necessary for the induction of cyclin E expression. Moreover, based on the results of infection with an HCMV mutant virus containing a deletion of the IE1-72 gene, it appears that this gene product is not required for the virus-mediated upregulation of cyclin E.

	MATERIALS AND METHODS

Top Abstract Introduction Materials and Methods Results Discussion References

Cell culture and virus. Human foreskin fibroblasts were obtained from the University of California, San Diego, Medical Center and cultured in minimum essential medium with Earle's salts (MEM) (Gibco-BRL) supplemented with 10% heat-inactivated fetal bovine serum (FBS) (Summit Biotechnology), 50 µg of gentamicin sulfate (Omega Scientific) per ml, 1.5 µg of amphotericin B (Omega Scientific) per ml, 2 mM L-glutamine (Bio-Whittaker), 200 U of penicillin (Omega Scientific) per ml, and 200 µg of streptomycin (Omega Scientific) per ml. Cells were kept in incubators maintained at 37°C and 7% CO₂. The Towne strain of HCMV was obtained from the American Type Culture Collection (VR 977) and propagated as previously described (57). The RC303Acc strain of HCMV contains a deletion in exon 4 of UL122-123 and was a generous gift from Edward Mocarski (41).

Synchronization and infections. Cells were synchronized in G₀ phase by allowing them to grow to confluence as previously described (16). Three days after confluence, the cells were trypsinized, replated at a lower density to allow progression into the cell cycle, and infected at a multiplicity of infection of 5 or mock infected with tissue culture supernatants. At appropriate times postinfection (p.i.), cells were washed with phosphate-buffered saline (PBS), scraped, and processed as described for each type of experiment. Alternatively, cells were synchronized by serum starvation for 48 h in medium with no serum and kept in medium with no serum during the course of the infection. The method of synchronization used for each experiment is given in the text.

Western blot analysis. Cells were lysed in Laemmli reducing sample buffer (2% sodium dodecyl sulfate [SDS], 10% glycerol, 100 mM dithiothreitol, 60 mM Tris [pH 6.8], 2 µg of aprotinin and leupeptin per ml, 1 mM phenylmethylsulfonyl fluoride [PMSF], 50 mM NaF, 0.5 mM Na₃VO₄, 4 mM EDTA, 10 mM Na₄P₂O₇, 1 mM benzamidine, and 1 mM NaS₂O₅). The lysates were then sonicated, boiled for 5 min, and centrifuged for 10 min at 16,000 × g. Samples (100 µg/lane) were run on 10% polyacrylamide gels unless otherwise stated. Proteins were transferred to Immobilon P (Millipore) or Protran (Schleicher & Schuell), and Western blot analysis was performed using the appropriate mouse or rabbit antibody followed by the appropriate horseradish peroxidase-linked secondary antibody (Amersham Life Science Products). Proteins were visualized using Pierce Supersignal or Blaze chemiluminescent detection methods (per manufacturer's instructions).

Cycloheximide block and release experiments. Confluence-synchronized cells were replated at a lower density in MEM plus 10% FBS and allowed to settle for 1 h prior to the addition of 100 µg of cycloheximide (Sigma) per ml. At 1 h after the addition of cycloheximide, cells were mock or HCMV infected in the presence of 100 µg of cycloheximide per ml. At 3 h p.i., cells were washed three times in MEM plus 10% FBS to release them from the cycloheximide block. At appropriate times post-release from cycloheximide, 20 µg of actinomycin D (Sigma) per ml was added to the culture medium or cells were maintained in 100 µg of cycloheximide per ml for the duration of the experiment. Cells were harvested at 18 h p.i. and processed as described for Western blot analysis.

Immunofluorescence. Glass coverslips were placed in tissue culture dishes at the time of plating prior to mock, HCMV, or baculovirus infection. At 24 h p.i., coverslips were removed from tissue culture dishes and washed twice in PBS, and cells were simultaneously fixed and permeabilized by placing them in 100% methanol at 20°C for 10 min. Coverslips were washed three times in PBS at this point and before and after all incubations. Coverslips were incubated for 20 min in blocking solution (10% normal goat serum [Jackson Laboratories] in PBS-0.5% bovine serum albumin [BSA]) and then incubated for 10 min in antibody against the IE1-72 and IE2-86 proteins (CH16.0; Goodwin Institute) diluted 1:3,000 in PBS-0.5% BSA. This was followed by a 10-min incubation in fluorescein isothiocyanate-conjugated goat anti-mouse secondary antibody (Jackson Laboratories) diluted 1:500 in PBS-0.5% BSA. Coverslips were then incubated for 10 min with 2 mg of Hoechst (Calbiochem) per ml diluted 1:500 in PBS-0.5% BSA and mounted onto slides using glycerol-paraphenylenediamine (an antiphotobleaching agent) (Sigma). Images were visualized using a Leitz DMRB fluorescent microscope and were photographed using a Leica DMLD slide camera. Images were arranged and labeled using Adobe Photoshop 3.0 and Adobe Illustrator 6.0.2.

Immunoprecipitation. p130 antibodies (Santa Cruz) or rabbit preimmune serum (collected from a naive New Zealand White female rabbit) was coupled to protein A-Sepharose beads (Pharmacia Biotech) as previously described (30). Cells were lysed in NETN (20 mM Tris [pH 8.0], 100 mM NaCl, 1 mM EDTA, 0.5% NP-40, 2 µg of aprotinin and leupeptin per ml, 1 mM PMSF, 50 mM NaF, 0.5 mM Na₃VO₄, 4 mM EDTA, 10 mM Na₄P₂O₇, 1 mM benzamidine, and 1 mM NaS₂O₅) and subjected to three cycles of freezing and thawing (5 min at 80°C and then 5 min at 37°C). Lysates were centrifuged to pellet debris, and 5 µg of coupled antibody was added to the supernatant and incubated overnight at 4°C during rocking. Coupled antibody was pelleted by centrifugation and washed three times in NETN. The pellet was resuspended in Laemmli reducing sample buffer, boiled, and loaded on a 10% polyacrylamide gel. Gels were transferred and Western blotted as described above, with the exception that protein A- or protein G-horseradish peroxidase was used as the secondary antibody.

Nuclear-cytoplasmic fractionation. For EMSA, nuclear and cytoplasmic fractionation was performed as follows. Cells were pelleted and resuspended in 1 ml of buffer A (20 mM HEPES [pH 7.9], 10 mM KCl, 1 mM MgCl₂, 10% glycerol, 0.1% NP-40, 2 µg of aprotinin and leupeptin per ml, 1 mM PMSF, 50 mM NaF, 0.5 mM Na₃VO₄, 4 mM EDTA, 10 mM Na₄P₂O₇, 1 mM benzamidine, and 1 mM NaS₂O₅). This cell lysate was immediately layered onto 1 ml of 37% sucrose and centrifuged for 10 min at 1,320 × g. The top layer (cytoplasmic fraction) was removed and centrifuged for an additional 10 min at 16,000 × g to clear it of membranes. The pellet below the sucrose was lysed in buffer A-300 mM NaCl and subjected to three cycles of freezing and thawing (5 min at 80°C and then 5 min at 37°C). This nuclear fraction was vortexed for 1 min and centrifuged for an additional 10 min at 16,000 × g to clear it of membranes. Protein concentrations were determined using the Bio-Rad protein assay, and lysates were stored at 80°C.

EMSA. Reaction mixtures contained the following: 1× buffer (9), 10% glycerol, 200 ng of sonicated salmon sperm DNA, 5 µg of nuclear extract, 20 fmol of appropriate radiolabeled probe, and in some cases a 30 to 300 molar excess of cold competitor probe or 1 to 2 µg of specific antiserum. Reaction mixtures were incubated for 20 min at room temperature and loaded on a 4% polyacrylamide gel with 5% glycerol in 0.5× Tris-borate-EDTA. Gels were run in 0.5× Tris-borate-EDTA for 2 h at 35 mA per gel, dried down for 1 h at 80°C, and exposed to film.

In vivo DMS footprinting and LMPCR. For in vivo dimethyl sulfate (DMS) treatment, cells were pelleted and resuspended in 1 ml of medium. Cells were warmed to 37°C, 10 µl of 10% DMS was added, and cells were incubated for 1 min at 37°C. Cells were immediately transferred to 50 ml of ice-cold PBS and pelleted. Cell pellets were washed in PBS and then resuspended in 2 ml of PBS. Genomic DNA was isolated according to the Qiagen Blood and Cell Culture DNA Midi Kit protocol. Isolated DNA was precipitated, resuspended in 10% piperidine, heated to 90°C for 30 min, and then dried in a SpeedVac concentrator overnight. Treated DNA was used in a ligation-mediated PCR (LMPCR) as previously described (1). Primers for cyclin E promoter footprinting were as follows: PE1, 5' GCG CTC CAG TCC CGG CAG GCG GCG G 3'; PE2, 5' CGG CGA CGG CAG TGG CGG CGG CGG C 3'; PE3, 5' CGG CGG CGG CGC CGG GAG TCG GCG G 3'; LMPCR.1, 5' GCG GCG GCC CCG GCG CTT CGC AGG C3'; and LMPCR.2, 5' GCC TGC GAA GC 3'. PCR was performed as follows. First, the samples were subjected to 5 min of denaturation at 95°C, 30 min of annealing at 72°C, and 12 min of extension at 76°C. During first-strand synthesis, the reaction mixtures contained 2 µg of the appropriate DNA, 0.2 mM deoxynucleoside triphosphates (dNTPs), 1 U of GC-rich enzyme mix (Roche Biochemicals), 0.5 M GC resolution solution (Roche Biochemicals), 1× reaction buffer (Roche Biochemicals), and 3 pmol of PE1. LMPCR.1 and LMPCR.2 were annealed to make the unidirectional linker that was then ligated to the first-strand synthesis products as previously described (1). For the amplification step, the samples contained 1 M G-C resolution solution (Roche Biochemicals), 1× reaction buffer (Roche Biochemicals), 0.2 mM dNTPs, 2 U of GC-rich enzyme mix (Roche Biochemicals), 10 pmol of PE2, and 10 pmol of LMPCR.1. The samples were denatured for 5 min at 95°C and subjected to 35 cycles of 30 s of denaturation at 95°C, 30 s of annealing at 75°C, and 30 s of extension at 78°C. Finally, the reactions were subjected to a 10-min extension at 72°C. For the end-labeling step, the samples contained 1 M GC resolution solution (Roche Biochemicals), 1× reaction buffer (Roche Biochemicals), 0.2 mM dNTPs, 0.5 U of AmpliTaq DNA polymerase (Perkin-Elmer), and 2 pmol of radiolabeled PE3. The reactions were then denatured at 95°C for 5 min and subjected to nine cycles of 30 s of denaturation at 95°C, 30 s of annealing at 76°C, and 1 min of extension at 79°C. A final 7-min extension was performed at 79°C. For in vitro samples and Maxam-Gilbert reactions, genomic DNA was isolated according to the Qiagen protocol and then treated with the appropriate chemical as previously described (1). The treated samples were subjected to the same LMPCRs as were the in vivo-treated samples. After LMPCR, samples were extracted once with phenol-chloroform-isoamyl alcohol (1) and then precipitated, resuspended in 3 µl of loading buffer, and run on a 6% denaturing polyacrylamide gel.

Antisera. Antibodies used in Western analysis were E2F-1 (sc-251), E2F-2 (sc-633), E2F-3 (sc-878), E2F-4 (sc-1082), E2F-5 (sc-1083), DP-1 (sc-610), DP-2 (sc-830), p130 (sc-317), p107 (sc-318), cyclin E (sc-198), and CREB binding protein (CBP) (sc-583), all obtained from Santa Cruz Biotechnologies. The Sp-1 antibody was a generous gift from James T. Kadanoga (University of California, San Diego). The G6PD antibody was a generous gift from Rod Nakayama (University of California, Irvine). The UL44 antibody was a generous gift from Lenore Periera (University of California, San Francisco). CH16.0 was obtained from the Goodwin Institute. Antibodies used for supershift analysis were the same as those used for Western analysis with the addition of Rb (14031A [Pharmingen]), E2F-4 (sc-866 [Santa Cruz]), cyclin E (14761C [Pharmingen]), cyclin A (14531C [Pharmingen]), and Sp-1 (sc-420 [Santa Cruz]).

Primer extension analysis. mRNA was isolated from cells using the Invitrogen FastTrack 2.0 mRNA isolation kit. Primer extension reactions were carried out as described previously (49) using 5 µg of mRNA per reaction and the cyclin E-specific primer E3 (5' CGG CAG GCG GCG GCG GCG ACG GCA GTG GCG GCG GC 3'). Reaction mixtures were precipitated, resuspended in loading buffer, and run on a 6% denaturing polyacrylamide gel. Sanger sequencing reactions were also performed with E3 using T7 Sequenase version 2.0 (U.S. Biochemical).

	RESULTS

Top Abstract Introduction Materials and Methods Results Discussion References

HCMV uses a new start site to upregulate cyclin E mRNA. Previously, our lab showed that the effect of HCMV infection on cyclin E expression was at the level of transcription (50). We found that, when G₀ synchronized cells were infected with HCMV as they were released from confluence into the G₁ phase of the cell cycle, there was a significant induction of cyclin E mRNA by 12 h p.i. that was sustained through 96 h p.i. To map the start sites of transcription from the cyclin E promoter in HCMV-infected cells, synchronized foreskin fibroblasts were again infected upon release into G₁. The mRNA was then isolated at 10 and 48 h p.i. and subjected to primer extension analysis. Figure 1 shows that new start sites were present in the infected cells at +21, +49, +51, +53, +64, +65, and +67 relative to the sequence published by Ohtani et al. (45). Mock-infected cells showed only one start site, at +32. Interestingly, most infected cell cyclin E mRNA start sites occurred downstream of the previously identified start site (+1 in Fig. 1) and of the start site that we detected in mock-infected cells (+32 in Fig. 1). As is noted in Fig. 1, we did not detect use of the previously identified start site at +1. Since there are limits to the primer extension assay, we also performed analysis using a primer that was closer to the previously identified start site and again did not detect use of this site in foreskin fibroblasts (data not shown). These results were confirmed by RNase protection analysis (data not shown).

View larger version (53K): [in this window] [in a new window]   FIG. 1.   Primer extension analysis of cyclin E mRNA at 10 and 48 h p.i. mRNA was isolated using Invitrogen FastTrack 2.0, and primer extension was performed as previously described (49). Arrows indicate locations of transcription start sites relative to the published sequence (45). The site at +1 is marked to indicate the start site that was previously identified by Ohtani et al. (45). We do not detect use of this site in fibroblasts. Sanger sequencing reactions using the same primer as was used in the primer extension were performed in parallel. M, mock-infected cells; V, virus-infected cells.

In vivo footprinting of the cyclin E promoter. Based on the results from the primer extension analysis, we proceeded to examine the downstream region of the cyclin E promoter at 10 and 24 h p.i. To determine if there was a change in the in vivo site occupancy of the cyclin E promoter during the infection, we used the technique of in vivo footprinting. Cells were confluence synchronized and released into G₁ at the time of infection. At 10 and 24 h p.i., cells were harvested, genomic DNA was isolated, and in vivo footprinting was performed as described in Materials and Methods. A large number of changes were observed, and the most notable ones are discussed below. By comparison with the in vitro-treated samples, all in vivo-treated samples showed protection at +20, +44, and +64 and hypersensitivity at +23, +31, +42, +57, and +59 (Fig. 2, part 1). Some level of hypersensitivity was detected in all in vivo samples at +75. However, this hypersensitivity was stronger in G₀ and infected cells at 10 h p.i. than in the other in vivo samples. We also found that there was protection at +33 in mock-infected cells, most notably at 24 h p.i., and that this residue was not altered in confluent cells in G₀. Changes in this region are consistent with use of the +32 start site that we detected in mock-infected cells.

View larger version (8426K): [in this window] [in a new window]   FIG. 2.   (Part 1) In vivo DMS footprinting analysis of the cyclin E promoter at 10 and 24 h p.i. Cells were treated with 0.1% DMS as described in Materials and Methods. After LMPCR, samples were run out on a 6% denaturing polyacrylamide gel. Hypersensitive sites are indicated by asterisks, and protected sites are identified by open circles. Lines denote changes that were seen in all in vivo samples compared to the in vitro sample. Arrows mark differences between mock (M)- and HCMV (V)-infected samples. In all cases, the corresponding location within the sequence is noted. The lane labeled G0 represents in vivo DMS treatment of confluent uninfected cells. The lane labeled VITRO represents in vitro treatment of DNA from uninfected cells. (Part 2) A summary of the events that occur on the cyclin E promoter. Solid arrows represent virus-induced transcription start sites. The open arrow designates the cellular start site for transcription. Solid asterisks denote hypersensitive sites that were detected in the in vivo footprint of infected cells. Solid circles mark protected sites from the in vivo footprint of infected cells. Open asterisks represent hypersensitivity that was seen in mock-infected cells, and open circles represent protection that was seen in mock-infected cells. The E2F site that is underlined in this panel is a component of the probe that was used in EMSAs.

Steady-state levels of the factors that regulate cyclin E transcription. Since we were able to detect in vivo site occupancy of a previously defined E2F site in infected cells, we examined the steady-state levels of the transcription factors that are thought to be responsible for regulation of cyclin E transcription (18, 45). Western blot analysis of members of the E2F family showed no changes in E2F-1, -2, or -3 during a 24-h time course (Fig. 3A to C). As has been observed by others, we detected several differently migrating forms of E2F-5 (59). Figure 3E shows that several of them were preferentially lost in infected cells at 16 h p.i. In contrast, the levels of the different forms of E2F-5 did not vary significantly in mock-infected cells throughout the time course.

View larger version (34K): [in this window] [in a new window]   FIG. 3.   Western blot analysis of the E2F family of proteins at various times p.i. One hundred micrograms of total cell lysate was run on a 20-cm 10% polyacrylamide gel (0.07% bisacrylamide final concentration) (31). Proteins were transferred to nitrocellulose and analyzed by Western blotting. (A) E2F-1. (B) E2F-2. (C) E2F-3. (D) E2F-4. (E) E2F-5. (F) Nuclear and cytoplasmic lysates were prepared at 0 and 8 h p.i., and 100 µg of nuclear (N), cytoplasmic (C), or nuclear lysates treated with CIAP were run on 10% polyacrylamide gels. Proteins were transferred to nitrocellulose and analyzed by Western blotting for E2F-4. Two different exposures of the same blot are shown. (G) One hundred micrograms of nuclear (N) or cytoplasmic (C) lysates from three independent experiments was run on 10% polyacrylamide gels. Proteins were transferred to nitrocellulose and analyzed by Western blotting for G6PD and CBP. M, mock infected; V, virus infected.

View larger version (35K): [in this window] [in a new window]   FIG. 4.   Western blot analysis of other proteins that might be involved in transcriptional regulation of cyclin E. Lysates were prepared at various times p.i., and 100 µg of total cell lysate was used for each lane. Samples for DP-1 (A) and DP-2 (B) detection were run on a 20-cm 10% polyacrylamide gel (0.07% bisacrylamide final concentration) (31), transferred to nitrocellulose, and analyzed by Western blotting. (C) Samples for Sp-1 detection were run on a 10% minigel (29:1 bis/acrylamide ratio), transferred to Immobilon, and analyzed by Western blotting. Samples for p130 (D) and p107 (E) detection were run on a 7.5% polyacrylamide gel (0.07% bisacrylamide final concentration) (31), transferred to nitrocellulose, and analyzed by Western blotting.

A virus-induced complex accumulates on the cyclin E promoter. In order to identify which of the above factors might form a complex with the cyclin E promoter, we performed EMSAs with mock- and HCMV-infected nuclear lysates that were prepared at various times after infection of confluence-synchronized fibroblasts. A region of the cyclin E promoter from nucleotide 21 to +20 was radiolabeled and used as the probe in these experiments. This region of the cyclin E promoter contains the two E2F binding sites located approximately 600 bp upstream from the translation start site that were previously identified by Ohtani and coworkers (45) as being important for cell cycle-dependent regulation of cyclin E transcription. Cells were harvested and fractionated as described in Materials and Methods. Both nuclear and cytoplasmic fractions were subjected to Western blot analysis using anti-CBP (nuclear) and anti-G6PD (cytoplasmic) specific antibodies to verify the purity of the fractions prior to their use in EMSAs (Fig. 3G).

View larger version (50K): [in this window] [in a new window]   FIG. 5.   EMSAs using sequences from the cyclin E promoter. (A) Nuclear extracts were prepared at various times p.i. Five micrograms of nuclear extract was combined with the radiolabeled probe CYCE E2F DS (5' CT AGC GCC GGT TCC GCG CGC AGG GAT TTT AAA TGT CCC GCT CTG AG 3') as described in Materials and Methods. The letter E designates the early virus- induced complex. The letter L designates the late virus-induced complex. The letter R designates the Rb-containing band shift. The letters NS designate nonspecific complexes. M, mock infected; V, virus infected. (B) Five micrograms of nuclear extract from infected cells at 18 h p.i. was combined with the same radiolabeled probe as in panel A. The indicated amount of competitor probe in molar excess was added to the reaction. The sequences of the competitor probes were as follows: FLAG, 5' GAT CTA TGG ACT ACA AGG ACG ACG ACG ACA AGG G 3'; CYCE DS MUT, 5' GCC GGT TCC GAT CGC AGG GAT TTT AAA TGT CAT GCT CTG AG 3'; DHFR E2F, 5' GGG CGG GGC GGC CAC AAT TTC GCG CCA AAC TTG ACC GCG CG 3'; CYCA CDE/CHR, 5' CCA TTT CAA TAG TCG CGG GAT ACT TGA ACT GCA AGA ACA GC 3'; and E2F CONS, 5' GAT CTA TGG ATT TAA GTT TCG CGC CCT TTC TCA TAC TA 3'.

View larger version (57K): [in this window] [in a new window]   FIG. 6.   Comparison of the E2F complexes that are present in mock- and HCMV-infected cells. (A) The DHFR probe was radiolabeled and combined with 5 µg of nuclear lysate obtained from mock-infected cells at 24 h p.i. The indicated antiserum was added to the reaction to determine if the band shifts could be supershifted or abrogated by the specific antiserum. (B) The CYCE E2F DS probe was radiolabeled and combined with 5 µg of nuclear lysate obtained from HCMV-infected cells at 18 h p.i. The indicated antiserum was added to the reaction to determine if complex E could be supershifted or abrogated by the specific antiserum. The supershift that was produced by the addition of p130 antibody is marked by an arrow. A portion of the gel was cropped and the contrast was adjusted in order to better visualize the effects of the antiserum.

p130 and E2F-4 remain associated in vivo in their specific states of phosphorylation in infected cells. The above experiments demonstrated that E2F-4 and p130 were maintained in specific phosphorylation states in infected cells. Moreover, these two proteins were present in nuclear lysates from infected cells and were shown to associate with the cyclin E promoter in EMSAs. To determine if these proteins were associating in vivo, a coimmunoprecipitation assay was performed. Rabbit preimmune serum or p130 antibody was incubated with total-cell lysates from mock-infected cells from 12 h p.i.; immunoprecipitates were subjected to SDS gel electrophoresis and Western blotted for p130 and E2F-4. Figure 7A shows that the p130-specific antibody, but not rabbit preimmune serum, was able to immunoprecipitate these proteins, demonstrating both their in vivo association and the specificity of the interaction with the p130 antibody. To determine which forms of these proteins were associating in vivo, total-cell lysates were prepared from mock- and HCMV-infected cells at 8 and 24 h p.i. The p130 was immunoprecipitated from the lysates using a p130 antibody, and the immunoprecipitates were subjected to SDS gel electrophoresis. The proteins were then analyzed by Western blotting with antibodies to p130 and E2F-4. Figure 7B demonstrates that there is an in vivo association between E2F-4 and p130 in mock-infected and infected cells at 8 and 24 h p.i. This association was clearly seen in both mock-infected and infected cells at 8 h p.i., with the infected cells showing association with only the highly phosphorylated form of E2F-4. However, at 24 h p.i. in mock-infected cells the association of the two proteins was greatly diminished as the cells were entering into S phase. In contrast, the association was maintained in infected cells, and the majority of the p130-associated E2F-4 was in the highly phosphorylated form.

View larger version (39K): [in this window] [in a new window]   FIG. 7.   In vivo association between p130 and E2F-4. (A) Mock-infected cell lysates (M) from 12 h p.i. were immunoprecipitated (IP) with p130 antibody or rabbit preimmune serum coupled to protein A-Sepharose. IgG, immunoglobulin G. (B) Mock-infected (M) or infected (V) cell lysates from 8 and 24 h p.i. were immunoprecipitated (IP) with p130 antibody coupled to protein A-Sepharose. Immunoprecipitates were run on a 7.5% polyacrylamide gel. Proteins were transferred to nitrocellulose and Western blotted for p130 and E2F-4.

HCMV IE proteins IE1-72 and/or IE2-86 is not sufficient to induce expression of endogenous cyclin E. Previously published data implicated the viral IE protein IE2-86 as playing a role in the HCMV-mediated upregulation of cyclin E (3). In that study, it was demonstrated that the viral IE protein IE2-86 but not IE1-72 could upregulate the cyclin E promoter in a transient-transfection assay in an E2F-independent manner (3). Using an in vitro footprinting assay, this group also showed that recombinant IE2-86 could bind to a region of the cyclin E promoter from +35 to +66. Interestingly, that region not only coincided with the region where we detected alterations in our in vivo footprint but flanked the initiation sites of the major HCMV-induced cyclin E transcripts. Because these prior experiments were performed as transient expression assays in which the cyclin E promoter linked to a reporter gene was transfected into U373 cells, an astrocytoma cell line, we felt that it was important to determine if IE2-86 could be playing a role in the upregulation of cyclin E in an in vivo context. We chose to do so by examining the effects of the viral IE proteins IE1-72 and IE2-86 on the endogenous cyclin E promoter in permissive human fibroblasts.

View larger version (44K): [in this window] [in a new window]   FIG. 8.   Recombinant baculoviruses express IE1-72 and IE2-86 in human fibroblasts. Cells were confluence synchronized and mock infected (M), infected with HCMV (V), or infected with recombinant baculovirus(es) (72, 86, or 72+86). Coverslips were taken at 24 h p.i., fixed and permeabilized in methanol, and stained with Hoechst stain to identify the total number of cells and CH16.0 to detect cells that expressed IE1-72 or IE2-86.

View larger version (19K): [in this window] [in a new window]   FIG. 9.   Expression of HCMV IE1-72 and that of IE2-86 are not sufficient to induce endogenous cyclin E. (A) Lysates were prepared at 24 h p.i. from the same experiment that was described in the legend to Fig. 8, and 50 µg of total cell lysate was run on a 10% polyacrylamide gel, transferred to nitrocellulose, and Western blotted for cyclin E. M, mock infected; V, virus infected. (B) Cells were serum starved and were mock infected (M), infected with HCMV (V), infected with UV-irradiated virus (UV), mock infected and infected with recombinant baculovirus (M and 72 or 86), or infected with both UV-irradiated virus and recombinant baculovirus (UV and 72 or 86). Cell lysates were prepared at 24 h p.i., and 50 µg of total cell lysate was run on a 10% polyacrylamide gel, transferred to nitrocellulose, and Western blotted for cyclin E.

IE1-72 is not required for the HCMV-mediated upregulation of cyclin E. While the above experiments demonstrated that expression of IE1-72 or IE2-86 does not lead to an increase in the levels of cyclin E, they did not address whether either of these proteins was required for the HCMV-mediated upregulation of cyclin E. To address this question, the use of a mutant virus was employed. RC303Acc is missing exon 4 of the UL122-123 coding region, which results in a virus that does not express the IE protein IE1-72 (41). Cells were serum starved and mock, HCMV, or RC303Acc infected. They were then harvested for Western blot analysis at 24 h p.i. Figure 10 shows that infection with RC303Acc led to an increase in the levels of cyclin E that was comparable to that seen in cells infected with the wild-type Towne strain. Hence, IE1-72 was not required for the HCMV-mediated upregulation of cyclin E. 

View larger version (34K): [in this window] [in a new window]   FIG. 10.   IE1-72 is not required for the HCMV-mediated upregulation of cyclin E. Cells were serum starved and were mock infected (M), infected with RC303Acc (72), or infected with the Towne strain (V). Cell lysates were prepared at 24 h p.i., and 100 µg of total cell lysate was run on a 10% polyacrylamide gel, transferred to nitrocellulose, and Western blotted for HCMV IE1-72-IE2-86 and cyclin E.

Early gene expression is required for the HCMV-mediated upregulation of cyclin E. Since our observations suggested that IE1-72 and IE2-86 were not directly responsible for the HCMV-mediated upregulation of cyclin E, we sought to determine which phase of viral gene expression was temporally associated with the upregulation of cyclin E. Cells were confluence synchronized and replated in MEM plus 10% FBS in the presence of cycloheximide in order to halt protein synthesis. They were then mock or HCMV infected in the presence of cycloheximide to allow for accumulation of viral IE transcripts and released from cycloheximide for various times prior to the addition of the transcription inhibitor, actinomycin D. Lysates were prepared from cells at 18 h p.i.; the proteins were subjected to SDS electrophoresis and analyzed by Western blotting for the presence of the HCMV IE1-72 and IE2-86 proteins (Fig. 11A and D), the HCMV 50-kDa UL44 early gene product (Fig. 11B and E), and cyclin E (Fig. 11C and F). Viral IE proteins were detected after release from the cycloheximide block (Fig. 11A, lanes 8, 10, 12, 14, and 16, and 11D, lanes 2, 4, 6, 8, 10, 12, and 14) but not in cells that were maintained in cycloheximide (Fig. 11A, lane 4), demonstrating that protein synthesis was completely inhibited. The activation of early genes by the IE factors was detected by the expression of UL44 at various times post-release from cycloheximide block. The level of this protein increased as the time interval between cycloheximide release and the addition of actinomycin D was lengthened (Fig. 11B, lanes 12, 14, and 16, and 11E, lanes 4, 6, 8, 10, 12, and 14). However, despite the appearance of the IE gene products and the demonstration of their ability to activate UL44 early gene expression, levels of cyclin E were not increased under these conditions (Fig. 11C). Only when cycloheximide was released at 3 h p.i. and actinomycin D addition was delayed until 7 h p.i. or later was there HCMV-induced cyclin E expression (Fig. 11C, lane 16, and 11F, lanes 8, 10, 12, and 14). As expected, HCMV-infected cells that were not treated with either drug showed a marked increase in the levels of cyclin E (Fig. 11C, lane 2). Taken together, these data suggest that viral early gene expression is required for the induction of cyclin E expression.

View larger version (45K): [in this window] [in a new window]   FIG. 11.   Viral early gene expression is required for the HCMV-mediated upregulation of cyclin E. Cells were confluence synchronized and mock (M)- or HCMV (V)-infected in the presence of cycloheximide (CHX). Cells were released from the cycloheximide block at 3 h p.i., and actinomycin D (ActD) was added at various times postrelease (0 to 15 h p.i.). Lysates were prepared at 18 h p.i., and 50 µg of total cell lysate was run on a 10% polyacrylamide gel, transferred to nitrocellulose, and Western blotted for IE1-72 and IE2-86 (CH16.0) (A and D), UL44 (B and E), or cyclin E (C and F). It should be noted that the apparent small increase in cyclin E in the mock-infected cells in panel F, lane 5, is due to the presence of BSA (due to inefficient washing of the cells prior to lysis) that comigrated at this position and nonspecifically bound some of the cyclin E antibody.

	DISCUSSION

Top Abstract Introduction Materials and Methods Results Discussion References

Downstream regions of the cyclin E promoter are important for HCMV-mediated upregulation. We have shown that the HCMV-induced cyclin E transcripts initiate further downstream than the cyclin E mRNA present in mock-infected cells. This change in start site is coincident with the appearance of protection and hypersensitivity in the in vivo footprint of infected cells. In G₀ cells, we detected protection at several sites, +20, +44, and +64, and hypersensitivity at +23, +31, +42, +57, +59, and +75. However, with the exception of the +75 hypersensitive site, the same changes were seen in all in vivo samples compared to the in vitro sample. Differences that were detected in the +33 to +36 region correlate with the use of the +32 start site in mock-infected cells. In accord with these results, mock-infected cells showed protection at +33, which was very near the transcription start site that was utilized in these cells. At 24 h p.i. in infected cells, we did not observe protection of the +33 site, but we did observe hypersensitivity of both the +34 and the +36 sites. This result was consistent with this region of the promoter not being utilized in the same manner in infected cells as it was in mock-infected cells.

E2F phosphorylation and complex formation during HCMV infection. HCMV infection altered the steady-state levels of several factors that are thought to regulate cyclin E gene expression. In HCMV-infected cells, DP-1 levels were maintained in a slower-migrating form. E2F-4 was maintained in a slower-migrating form in infected cells throughout the time course, while in mock-infected cells it shifted to a faster-migrating form at 8 h p.i. It remains to be determined whether the various forms of E2F-4, which arise from differential phosphorylation, differ in their transcriptional activity.

Expression of HCMV IE proteins IE1-72 and/or IE2-86 does not result in increased levels of endogenous cyclin Erequirement for early gene expression. Recently, transient-transfection experiments using a plasmid consisting of the cyclin E promoter and a luciferase reporter suggested that HCMV-mediated upregulation of cyclin E was E2F site independent (3). In that same study, it was reported that cotransfection with a plasmid expressing the HCMV IE protein IE2-86 could transactivate this reporter construct. Because there are many examples where transient-expression assays do not reflect the in vivo situation (19, 28), it is difficult to directly compare the prior work with our studies, where the endogenous cyclin E promoter was analyzed in an in vivo chromatin context. In order to determine if IE2-86 was indeed playing a role in upregulation of cyclin E in vivo, we asked if expression of IE1-72 or IE2-86 could lead to an increase in endogenous cyclin E levels. As our data clearly show, expression of either protein alone, of the two proteins together, or of the protein or proteins combined with infection with UV-inactivated virus does not lead to an increase in endogenous cyclin E levels. It is interesting to note that the region of the promoter that was identified in our in vivo footprinting studies contains the domain that appeared to form a complex with IE2-86 in an in vitro assay using the purified protein (3). However, the binding of IE2-86 to the cyclin E promoter has not yet been demonstrated in vivo. Moreover, since our studies demonstrate that IE2-86 cannot induce expression of endogenous cyclin E, the relevance of the reported in vitro binding is uncertain. The cycloheximide block and release experiment that was depicted in Fig. 11 demonstrated that, although IE gene products were present in amounts that equaled or exceeded those which are seen during HCMV infection, there was no induction of cyclin E. Only after early gene expression was observed were we able to detect an HCMV-induced increase in levels of cyclin E (Fig. 11E and F). These data indicate that IE gene expression is not sufficient for the HCMV-mediated upregulation of cyclin E but rather that some early gene product(s) or downstream effector of that product(s) is required for the increased cyclin E expression in infected cells. It should be noted that the possibility of a cooperative effect of an early gene product with an IE gene product cannot be excluded by the results of this experiment. However, it is unlikely that the viral IE protein IE1-72 plays a role in the HCMV-mediated upregulation of cyclin E, since infection with a mutant virus that was missing the IE1-72 gene product was able to efficiently induce cyclin E.