The Meq oncoprotein of Marek's disease virus interacts with p53 and inhibits its transcriptional and apoptotic activities
© Deng et al; licensee BioMed Central Ltd. 2010
Received: 26 September 2010
Accepted: 26 November 2010
Published: 26 November 2010
Marek's disease virus (MDV) is an oncogenic herpesvirus, which causes malignant lymphoma in chickens. The Meq protein of MDV, which is expressed abundantly in MDV-infected cells and in Marek's disease (MD) tumor cells, functions as a transcriptional activator and has been proposed to play an important role in oncogenic transformation. Preliminary studies demonstrated that Meq is able to bind p53 in vitro, as demonstrated using a protein-binding assay. This observation prompted us to examine whether the interaction between Meq and p53 occurs in cells, and to investigate the biological significance of this interaction.
We confirmed first that Meq interacted directly with p53 using a yeast two-hybrid assay and an immunoprecipitation assay, and we investigated the biological significance of this interaction subsequently. Exogenous expression of Meq resulted in the inhibition of p53-mediated transcriptional activity and apoptosis, as analyzed using a p53 luciferase reporter assay and a TUNEL assay. The inhibitory effect of Meq on transcriptional activity mediated by p53 was dependent on the physical interaction between these two proteins, because a Meq deletion mutant that lacked the p53-binding region lost the ability to inhibit p53-mediated transcriptional activity and apoptosis. The Meq variants L-Meq and S-Meq, but not VS-Meq and ∆Meq, which were expressed in MD tumor cells and MDV-infected cells, exerted an inhibitory effect on p53 transcriptional activity. In addition, ∆Meq was found to act as a negative regulator of Meq.
The Meq oncoprotein interacts directly with p53 and inhibits p53-mediated transcriptional activity and apoptosis. These findings provide valuable insight into the molecular basis for the function of Meq in MDV oncogenesis.
Marek's disease (MD), which is caused by Marek's disease virus (MDV), is a lymphoproliferative disease of chickens that causes significant economic losses in the poultry industry. MDV belongs to the genus Mardivirus of the Alphaherpesvirinae subfamily, but it shares biological characteristics with gammaherpesviruses, for example its ability to induce T-cell lymphoma and its slow growth in cell culture . MDV replicates in B and T lymphocytes during early cytolytic infection and subsequently establishes a latent infection of T lymphocytes that are finally transformed, which leads to the development of lymphomatous lesions in the visceral organs, peripheral nerves and skin . MD, therefore, serves as an elegant model for understanding the molecular mechanisms of herpesvirus-induced latency and oncogenesis .
The tumor suppressor protein p53 plays a major role in the protection of cells from malignant transformation via its ability to transactivate target gene expression and mediate downstream events, such as apoptosis and cell cycle arrest . Inhibition of p53-mediated transcriptional activity by viral oncoproteins contributes to virus-mediated oncogenesis. The main mechanism involved is the binding of viral proteins to p53, which reduces its transcriptional activity . For example, SV40 T antigen, adenovirus E1B55K, and HBx from hepatitis B virus bind directly to p53 and inhibit p53-mediated transcriptional activity [17–19]. In the Herpesviridae family, the immediate-early protein BZLF1 and the latency protein EBNA3C of Epstein-Barr virus, a gammaherpesvirus that shares biological characteristics with MDV, have been shown to form a complex with p53 and to disrupt p53-mediated transcriptional activity [20, 21]. Given the nature of p53 as a common target for several viral oncoproteins, it is reasonable to speculate that p53 may be a target of the Meq oncoprotein of MDV.
It has been shown previously that p53 has a similar distribution to Meq in MD tumor cells , and that Meq is able to bind p53 in vitro as demonstrated using a protein-binding assay . These observations prompted us to examine whether the interaction between Meq and p53 occurs in cells, and to investigate the biological significance of this interaction. We found that Meq binds directly to p53 and that this interaction resulted in inhibition of the transcriptional and apoptotic activities of p53.
Meq binds directly to p53
The Meq protein has been shown to interact with p53 in vitro in a protein-binding assay, and the p53 binding region resides between aa residues 54 and 127  (Figure 1A). To test whether this interaction occurs in cells, we employed a yeast two-hybrid assay. Recombinant plasmids pGBKT7-Meq (wild-type Meq) or pGBKT7-Meq-Δp53BD (a Meq deletion mutant that lacks the p53 binding region), expressing the bait fusion protein, were co-transformed with recombinant plasmid pGADT7-p53 (chicken p53), expressing the prey fusion protein, into yeast AH109 cells and selected on low-stringency and high-stringency media. The yeast cells co-transformed with the vectors pGBKT7-Meq and pGADT7 did not grow on high-stringency medium (Figure 1B, section 1), which suggests that Meq did not activate reporter genes autonomously. However, when pGBKT7-Meq was co-transformed with pGADT7-p53, the yeast cells grew on high-stringency medium (Figure 1B, section 2), which suggests that Meq interacted with p53. The yeast cells co-transformed with pGBKT7-Meq-Δp53BD and pGADT7-p53 did not grow on high-stringency medium (Figure 1B, section 4), confirming that the region of the Meq protein that spans aa residues 54 to 127 is required for the interaction with p53.
To determine whether the interaction between Meq and p53 occurs in host cells naturally permissive for MDV, primary chick embryo fibroblasts (CEFs) were co-transfected with Flag-tagged chicken p53 (Flag-p53) and GFP-tagged Meq (GFP-Meq) or GFP-tagged Meq-Δp53BD (GFP-Meq-Δp53BD) and analyzed by an immunoprecipitation assay. The Flag-tagged influenza virus M1 protein (Flag-M1) was used as a negative control. CEFs were used in this assay for the following reasons: (i) they are naturally permissive for MDV replication, and (ii) they can be transformed by MDV . Flag-p53 immunoprecipitated GFP-Meq, but not GFP-Meq-Δp53BD (Figure 1C), which confirms that the interaction between Meq and p53 occurs in host cells that are naturally permissive for MDV.
It has been reported previously that the subcellular localization of p53 is similar to that of Meq in MD tumor cells . Given that there is no commercial antibody suitable for the detection of chicken p53, we visualized the subcellular localization of Meq and p53 in CEFs that were co-transfected transiently with GFP-p53 and Flag-tagged Meq (Flag-Meq). The Flag-Meq protein was expressed in the nucleus (Figure 1D, panel a), as reported previously . The co-localization of Flag-Meq and GFP-p53 was observed in CEFs (Figure 1D, panel c), and also in other types of cells, such as H1299, DF-1 and Vero cells (data not shown).
Meq inhibits the transcriptional activity of p53
To assess the inhibitory effect of Meq on the transcriptional activity of p53 further, we analyzed the influence of Meq on the expression of the p53 targeting genes p21  and MDM2  in CEFs using a luciferase assay. A p21 promoter luciferase reporter plasmid (p21-Luc) and an MDM2 promoter luciferase reporter plasmid, both containing p53 response elements, were co-transfected separately with Flag-Meq into CEFs, and the luciferase activities were measured 24 h post-transfection. As shown in Figure 2D and 2E, Meq reduced the luciferase activity of both p21-Luc and MDM2-Luc significantly, when compared with the Flag-vector (Flag-Vec). Taken together, these observations suggested that Meq inhibits p53-mediated transcriptional activity.
p53-mediated apoptosis is suppressed by Meq expression
Meq inhibits p53 transcriptional activity, dependent on physical interaction
A number of tumor virus proteins, such as SV40 T antigen, E1B55K and HBx, disrupt the function of p53, and this inhibition is dependent on the physical interaction between these proteins [17–19]. We explored, therefore, whether the inhibitory effect of Meq on p53 transcription was dependent on their physical interaction. Flag-p53 was co-transfected with Flag-Meq or Flag-Meq-Δp53BD into H1299 cells in the presence of p53-Luc. The deletion mutant of Meq-Δp53BD was unable to bind p53, as shown in Figure 1. The inhibitory effects of Flag-Meq and Flag-Meq-Δp53BD on the luciferase activity of p53-Luc were compared subsequently. The expression of Flag-Meq reduced the luciferase activity significantly; however, in contrast, no inhibitory effect on luciferase activity was observed in the cells transfected with Flag-Meq-Δp53BD (Figure 2A and 2B). Similar results were observed in experiments that compared the inhibitory effects of Flag-Meq and Flag-Meq-Δp53BD on the luciferase activities of p21-luc and MDM2-Luc (Figure 2D and 2E). Next, we compared the inhibitory effects of Flag-Meq and Flag-Meq-Δp53BD on apoptosis mediated by p53. As expected, Flag-Meq-Δp53BD did not inhibit p53-mediated apoptosis (Figure 3). Taken together, these data suggested that Meq inhibits p53 transcription and that this inhibition is dependent on the physical interaction between Meq and p53.
Effects of Meq variants on p53 transcriptional activity
It has been reported previously that L-Meq and ∆Meq are negative regulators of Meq, and suppress the transactivational activities of Meq [28, 29]. It was therefore of interest to investigate the effects of the Meq variants on the p53-inhibitory activity of Meq. Flag-Meq was co-transfected with increasing amounts of each Meq variant into H1299 cells in the presence of Flag-p53 and p53-Luc, and the luciferase activities were measured 24 h post-transfection. L-Meq and S-Meq showed no enhanced or suppressive effect, while VS-Meq showed a slight, but not significant, inhibitory effect on the p53-inhibitory activity of Meq (data not shown). In contrast, the inhibitory effect of Meq on the transcriptional activity of p53 was attenuated significantly by co-expression of ∆Meq, in a dose-dependent manner (Figure 5B), which suggests that ∆Meq is a negative regulator of Meq. Taken together, these data suggested that the variants of Meq have different effects on the transcriptional activity of p53, and may play different roles during cytolytic infection and the establishment of latency or transformation.
Herpesviruses are important pathogens that are associated with a wide range of diseases in humans and other animals. MDV is one of the most contagious and highly oncogenic herpesviruses, and MD is the only neoplastic disease for which an effective vaccine has been employed widely . However, with increasing reports of vaccination breaks and the emergence of more virulent pathotypes, MD continues to pose a severe threat to the poultry industry, and the development of more effective control strategies remains a significant challenge . Therefore, a fundamental understanding of the molecular mechanisms of MD oncogenesis is important, not only for the development of more sustainable control strategies, but also to increase understanding of some of the principles of virus-induced lymphomagenesis.
The tumor suppressor protein p53 plays a major role in the protection of cells from malignant transformation and has been targeted by numerous viral oncoproteins . A preliminary study reported that Meq binds to p53 in vitro, as determined by a protein-binding assay . In this study, we used a yeast two-hybrid assay to show that Meq interacts directly with p53 (Figure 1B). We also demonstrated the interaction between Meq and p53 in host cells naturally permissive for MDV (Figure 1C), which confirmed further the interaction between these two proteins. Given that the tumor suppressor function of p53 is linked closely to its ability to transactivate target gene expression and mediate downstream events , we investigated the biological significance of the interaction between Meq and p53 on p53-mediated transcriptional activities. Exogenous expression of Meq resulted in inhibition of p53-mediated transcriptional activity and apoptosis (Figures 2 and 3), which suggests that p53 is targeted by the Meq oncoprotein of MDV.
Although the mechanisms of the abrogation of p53 transcriptional activity in virus-induced oncogenesis are not understood fully, the main mechanism employed by oncoviruses involves the direct binding of viral proteins to p53. This results in modulation of the functions of p53, mainly via acceleration of its degradation, sequestration of p53 in the cytoplasm, blockage of the DNA-binding capacity of p53, and/or blockage of the interaction of p53 with transcription coactivators . We found that Meq-Δp53BD, the Meq deletion mutant that lacks the p53 binding region and is unable to bind p53 (Figure 1), did not inhibit p53-mediated transcriptional activity and apoptosis (Figures 2 and 3). This suggests that the inhibitory effect of Meq on the transcription of p53 is dependent on the physical interaction of these two proteins. However, this interaction between Meq and p53 did not affect the stability of the protein or the subcellular localization of p53 (data not shown). The mechanism that underlies the p53-inhibitory effect of Meq is a current topic of investigation in our laboratory.
Several variants of Meq, including L-Meq, S-Meq, VS-Meq and ∆Meq (Figure 4A), have been characterized in MD tumor cells and MDV-infected cells [27–29], but their functions during cytolytic infection and the establishment of latency or transformation have not been elucidated fully. In the context of the inhibition of the function of p53, L-Meq and S-Meq were found to inhibit p53 transcriptional activity with a similar efficiency to Meq (Figure 5A). This implies that L-Meq and S-Meq may also play a role in cellular transformation, in a similar way to the Meq protein. Interestingly, VS-Meq, which contains the p53-binding region but lacks a 92-aa region located in the transactivation domain, showed no inhibitory effect on the transcriptional activity of p53 (Figure 5A), which suggests that Meq requires additional region(s) to exert this inhibitory function cooperatively. Although ∆Meq did not show a significant inhibitory effect on the transcriptional activity of p53, it suppressed the p53-inhibitory activity of Meq significantly (Figure 5B), which suggests that it acts as a negative regulator of Meq, as demonstrated in a previous study . These data also suggested that Meq proteins play complex roles during cytolytic infection and the establishment of latency or transformation.
In conclusion, we confirmed that Meq interacted directly with p53. Exogenous expression of Meq resulted in the inhibition of p53-mediated transcriptional activity and apoptosis. The inhibitory effect of Meq on p53-mediated transcriptional activity was dependent on the physical interaction between these two proteins. The Meq variants L-Meq and S-Meq, but not VS-Meq and ∆Meq, exerted inhibitory effects on the transcriptional activity of p53. In addition, ∆Meq was found to work as a negative regulator of Meq. Our findings provide valuable insight into the molecular basis of the function of Meq in the oncogenesis of MDV.
Cells, viruses and antibodies
The CEFs were prepared from nine-day-old embryonated specific-pathogen-free chicken eggs and cultured using standard techniques. The human non-small lung cancer cell line H1299 (p53-null) and the MD tumor cell line MSB-1 were maintained in Dulbecco's modified Eagle's medium and RPMI 1640 medium, respectively, supplemented with 10% fetal bovine serum, in an atmosphere containing 5% CO2. A very virulent strain of MDV, strain RB1B, was propagated on CEFs. The commercial antibodies used were an anti-Flag monoclonal antibody (M2, Sigma, St. Louis, MO, USA), a rabbit anti-Flag polyclonal antibody (Sigma), an anti-GFP monoclonal antibody (ab1218, Abcam, Cambridge, MA, USA), an anti-β-actin monoclonal antibody (AC-15, Sigma), a horseradish peroxidase (HRP)-conjugated goat anti-rabbit IgG antibody (sc-2004, Santa Cruz Biotechnology, Santa Cruz, CA, USA), a HRP-conjugated goat anti-mouse IgG antibody (sc-2005, Santa Cruz) and an Alexa Fluor 594-conjugated goat anti-mouse IgG (H+L)2 monoclonal antibody (Molecular Probes, Eugene, OR, USA).
Construction of expression plasmids and transient transfection
Primer sequence (5' to 3')
Cells were transfected with the indicated expression plasmids in the presence of the luciferase reporter plasmid and the control plasmid, Renilla luciferase pRL-TK (Promega, Madison, WI, USA). The chicken p53 luciferase reporter plasmid (p53-Luc) was provided generously by Dr. Byung-Whi Kong from the University of Arkansas, USA . The p21 luciferase reporter plasmid (p21-Luc) and MDM2 luciferase reporter plasmid (MDM2-Luc) were gifts from Dr. Kenji Fukasawa (H. Lee Moffitt Cancer Center & Research Institute, USA). Transfectants were harvested 24 h post-transfection and luciferase assays were carried out with the Dual-luciferase reporter assay system (Promega), according to the manufacturer's protocol. The firefly luciferase activity of individual cell lysates was normalized to Renilla luciferase activity. All assays were performed at least in triplicate.
CEFs grown on coverslips were co-transfected transiently with Flag-p53 and Flag-Meq or Flag-Meq-Δp53BD at a molar ratio of 1:10 and incubated for 24 h.
The transfectants were fixed with 4% paraformaldehyde, stained using the In Situ Cell Death Detection Kit, TMR red (Roche, Mannheim, Germany), and examined under a fluorescence microscope.
Yeast two-hybrid assay
The yeast two-hybrid assay was carried out using the MATCHMAKER GAL4 two-hybrid system 3 (Clontech, Palo Alto, CA, USA), and all procedures were performed according to the manufacturer's protocols. Meq and Meq-Δp53BD were subcloned in-frame with the GAL4 DNA binding domain into the pGBKT7 vector to generate the bait plasmids pGBKT7-Meq and pGBKT7-Meq-Δp53BD, respectively. Cells of the yeast host strain AH109 were transformed with pGBKT7-Meq or pGBKT7-Meq-Δp53BD to confirm that they did not activate reporter genes autonomously. Chicken p53 was subcloned in-frame with the GAL4 activation domain into the pGADT7 vector to generate the prey plasmid pGADT7-p53. To investigate the interaction between p53 and Meq, pGADT7-p53 was co-transformed with pGBKT7-Meq or pGBKT7-Meq-Δp53BD into yeast AH109 cells. The transformants were selected on low-stringency medium plates lacking tryptophan and leucine, and on high-stringency medium plates lacking tryptophan, leucine, histidine and adenine. The positive clones were confirmed by PCR analysis.
Western blot analysis, immunofluorescence and immunoprecipitation assays
Western blot analysis, immunofluorescence and immunoprecipitation assays were performed as described previously .
All measured values are expressed as the mean ± SE. The significance of the results was analyzed using Student's t-test, and p values less than 0.05 were considered significant.
We thank Dr. Thierry Soussi (Universite' Pierre et Marie Curie-Paris, France) for providing the chicken p53 cDNA, Dr. Byung-Whi Kong (University of Arkansas, USA) for providing the chicken p53 luciferase reporter plasmid, and Dr. Kenji Fukasawa (H. Lee Moffitt Cancer Center & Research Institute, USA) for providing the p21 luciferase reporter plasmid and MDM2 luciferase reporter plasmid. We also thank the Key Open Laboratory of Animal Parasitology, Ministry of Agriculture of China, for the provision of laboratory equipment. This research was supported by the Outstanding Overseas Chinese Scholar Research Fund from the Ministry of Personnel of China.
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