Transactivation of proto‑oncogene c‑Myc by hepatitis B virus transactivator MHBst167
- Authors:
- Published online on: May 28, 2014 https://doi.org/10.3892/ol.2014.2190
- Pages: 803-808
Abstract
Introduction
Worldwide, hepatitis B virus (HBV) is an important pathogen causing both acute and chronic liver diseases. Chronic HBV carriers have an increased risk of developing hepatocellular carcinoma (HCC). The mechanism of HBV-related carcinogenesis is poorly understood. Almost all HBV-associated HCCs studied thus far harbor chromosomally integrated HBV DNA (1–3). The integrated HBV DNA can encode two types of transcriptional transactivators: The well studied HBxAg and the preS2 transactivators, large hepatitis B virus surface proteins (LHBs) and C-terminally truncated middle size surface proteins (MHBst) (4–6). The wild-type middle hepatitis B virus surface protein (MHBs) consists of a 55-amino acid (aa) preS2-domain and a 226 aa S-domain. To generate the transactivating forms of MHBs, deletion of at least 87 C-terminal aa is required, and the transcriptional transactivator function is based on the cytoplasmic orientation of the preS2-domain (7). Considerable advances have been made in the fields of transcriptional transactivation of MHBst; however, the molecular basis of MHBst-dependent transcriptional transactivation remains enigmatic. Studies in this area will provide a better understanding of the association between HBV and host hepatocytes, and pave the way for elucidating the pathogenesis of HBV-related HCC.
In the present study, the transactivating potential of MHBst C-terminally truncated at aa position 167 (MHBst167) on Simian virus (SV40) early promoter was analyzed and, subsequently, genes transactivated by MHBst167 were screened using suppression subtractive hybridization (SSH). SSH was designed to generate a cDNA library that is enriched in differentially expressed sequences and, more importantly, equalized for the number of individual cDNA species, thus allowing the detection of rare transcripts. The full-length genes from the library were searched for homologs in GenBank. Finally, the association between the human proto-oncogene c-Myc and MHBst167 was discussed.
Materials and methods
Construction of vectors
For construction of eukaryotic expression vector pcDNA3.1(−)-MHBst167, the MHBst167 fragment was PCR-amplified from pCP10 containing two copies of HBV DNA subtype ayw (GenBank accession: U95551), with the forward primer (5′-GCCGGGCCCATGCAGTGGAATTCCACAAC) containing an ApaI site and reverse primer (5′-GGAAAGCTTCTATCCTGGAATTAGAGGACAAAC) containing a HindIII site. The fragment was inserted into the cloning vector pGEM-T (Promega, Madison, WI, USA), resulting in pGEM-T-MHBst167. An ApaI-HindIII fragment was isolated from the vector and inserted into ApaI-HindIII-digested pcDNA3.1(−) (Invitrogen Life Technologies, Carlsbad, CA, USA), resulting in pcDNA3.1(−)-MHBst167. The pcDNA3.1(−)-MHBs coding for intact HBV middle surface protein was constructed previously in the laboratory (8). To construct the reporter vector pCAT3-c-Myc, the promoter of human c-Myc was amplified from the genomic DNA of the HepG2 human HCC cell line (HBsAg-negative) by PCR with a pair of forward (5′-GGTACCATCCTCTCTCGCTAATCTCC) and reverse (5′-AGATCTATGGG CAGAATAGCCTCCCC) primers containing a KpnI and a BglII site, respectively. The promoter fragment was inserted into pGEM-T, yielding pGEM-T-c-Myc. A KpnI-BglII fragment was isolated from the plasmid and inserted at the KpnI-BglII sites of pCAT3-basic (promoterless; Promega), resulting in the pCAT3-c-Myc reporter vector. DL2000 DNA marker (Takara Biotechnology (Dalian) Co., Ltd, Dalian, China) was used as a DNA molecular weight marker. All the vectors were sequenced and digested with corresponding restriction enzymes to confirm the sequence accuracy.
Cell culture and transient transfection
HepG2 cells were purchased from the Cell Resource Center, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences (Shanghai, China) and were cultivated in Dulbecco’s modified Eagle’s medium (Invitrogen Life Technologies) containing 100 IU penicillin and 100 μg streptomycin per milliliter, supplemented with 10% (v/v) heat-inactivated fetal bovine serum (Hyclone Laboratories, Inc., Logan, UT, USA), at 37°C in 5% CO2 and 90% relative humidity. The cells were seeded on the day before transfection at a density of 8×105 cells per 35-mm dish and reached 50% confluence at the time of transfection. All transfections were performed with FuGene® 6 Transfection Reagent (Roche Applied Science, Indianapolis, IN, USA) according to the manufacturer’s instructions. The medium was changed 5 h after transfection and cells were harvested 40–48 h following transfection. All transfections and assays were repeated independently three times in triplicate.
Detection of MHBst167 expression
mRNA from HepG2 cells transfected with pcDNA3.1(−)-MHBst167 and pcDNA3.1(−) was isolated using a QuickPrep Micro mRNA purification kit (Amersham Biosciences, Little Chalfont, UK), and cDNA was reverse-transcribed from the mRNA. MHBst167 expression was detected by reverse transcription-polymerase chain reaction (RT-PCR) with MHBst167-specific primers by using 35 amplification cycles, and by western blotting using lysates of the HepG2 cells. The extracts were boiled for 5 min and separated by SDS-polyacrylamide gel electrophoresis (SDS-PAGE), and then transferred to nitrocellulose membranes (Pierce Biotechnology, Inc., Rockford, IL, USA). The membranes were reacted with anti-pre-S2 mouse anti-human monoclonal antibody and HRP-labeled goat anti-mouse polyclonal IgG as the primary and secondary antibodies, respectively and then with a SuperSignal West Pico Chemiluminescent Substrate working solution (Pierce Protein Biology Products, Thermo Fisher Scientific, Inc., Rockford, IL, USA) according to the manufacturer’s instructions. The immunoreactive bands were visualized after exposure to X-ray film.
Detecting the effect of MHBst167 on SV40 early promoter and c-Myc promoter
To detect the effect of MHBst167 on the SV40 promoter, various quantities of reporter vector pCAT3-promoter (Promega) containing CAT reporter gene controlled by the SV40 immediate early promoter element were transiently transfected into HepG2 cells. Co-transfections were made with pcDNA3.1(−)-MHBst167 (2.0 μg) + pCAT3-promoter (0.4 μg) as the test group, and pcDNA3.1(−) (2.0 μg) + pCAT3-promoter (0.4 μg) and pcDNA3.1(−)-MHBs (2.0 μg) + pCAT3-promoter (0.4 μg) as the control groups, respectively. To detect the effect of MHBst167 on the c-Myc promoter, various quantities of pCAT3-c-Myc were transiently transfected into HepG2 cells. The co-transfections were made with 1.0 μg reporter vector pCAT3-c-Myc and 0.5, 1.0, 1.5 and 2.0 μg effector vector pcDNA3.1(−)-MHBst167. The relative CAT activity was measured using enzyme-linked immunosorbent assay according to the manufacturer’s instructions (CAT ELISA kit; Roche Applied Science).
Generation and analysis of a subtracted cDNA library
SSH was performed with the PCR-Select™ cDNA subtraction kit (Clontech Laboratories, Inc., Mountain View, CA, USA) according to the manufacturer’s instructions. In brief, 2.0 μg of poly A+ mRNA, each from the pcDNA3.1(−)-MHBst167 tester group and the pcDNA3.1(−) driver group was subjected to cDNA synthesis, respectively. Following restriction with RsaI, small sizes of cDNAs were obtained. The tester cDNAs were then subdivided into two parts, ligated with the specific adaptor 1 and adaptor 2, respectively. After two subtractive hybridization reactions and two suppression PCR amplifications, differentially expressed cDNAs were selectively amplified. Subsequently, the second PCR products were used as templates for PCR amplification of G3PDH (a housekeeping gene) at 18, 23, 28, 33 cycles, respectively, to analyze subtraction efficiency. The second PCR products were directly purified using the Wizard® PCR-Preps DNA Purification system (Promega), and inserted into pGEM-T Easy (Promega) to construct the subtracted library. Colony PCRs were conducted to confirm that the size of the cDNA inserts ranged between 200 and 1,000 bp by using T7/SP6 specific primers localized in pGEM-T Easy. Following DNA sequencing of the positive colonies, nucleotide homology searches were performed using the BLAST program at NCBI (http://blast.st-va.ncbi.nlm.nih.gov/Blast.cgi).
Detecting the effect of MHBst167 on c-Myc expression
To detect the effect of MHBst167 on c-Myc mRNA, total RNA was extracted from HepG2 cells transiently transfected by pcDNA3.1(−) and pcDNA3.1(−)-MHBst167 using TRIzol reagent (Invitrogen Life Technologies) according to the manufacturer’s instructions, and was used for RT-PCR. The following primers (sense, 5′-TTCGGGTAGTGGAAAACCAG and antisense, 5′-CAGCAGCTCGAATTTCTTC) were used to amplify the c-Myc cDNA. β-actin specific primers (sense, 5′-TGACGGGGTCACCCACACTGTGCCCATCTA and antisense, 5′-CTAGAAGCATTTGCGGTGGACGATGGAGGG) was used as internal reference. To detect the effect of MHBst167 on c-Myc protein, total soluble proteins were extracted in radioimmunoprecipitation assay buffer (Pierce Biotechnology, Inc.) from the transfected HepG2 cells and separated on 12.5% SDS-PAGE gels for immunoblotting assay (prepared in house, Institute of Infectious Diseases, Beijing Ditan Hospital, Capital Medical University, Beijing, China). The expression of c-Myc was probed by mouse monoclonal antibody against human c-Myc derived from a cell line from American Type Culture Collection, Manassas, VA, USA. Mouse anti-human monoclonal β-actin antibody (Santa Cruz Biotechnology, Inc., Santa Cruz, CA, USA) was used as internal reference.
Results
Transient expression of MHBst167 in HepG2 cells
Digestion of recombinant vector pcDNA3.1(−)-MHBst167 with ApaI/HindIII, EcoRI, XbaI and XhoI yielded the expected bands (data not shown). DNA sequencing results indicated that the recombinant vector contained HBV DNA fragment encoding the truncated middle surface protein in-frame and the sequence was completely correct. MHBst167 mRNA and protein expression in HepG2 cells was successfully detected by RT-PCR (Fig. 1A) and western blotting (Fig. 1B), respectively.
Transactivation of MHBst167 on SV40 immediate early promoter
To determine the sensitivity of the kit for CAT measurement, we first evaluated the CAT activities in total cell lysates of HepG2 cells transfected with different quantities of pCAT3-promoter. The results showed that CAT gene expression exhibited an approximately linear association with the quantity of reporter vector used in transfection (Fig. 2A). Subsequently, 0.4 μg of reporter vector was selected to be used in the transfection experiments, so that it was easy to detect the reporter activity with room for further increase if a greater quantity of reporter vector was used. In the transient co-transfection assays, CAT gene expression from the pCAT3-promoter was ~4.5-fold higher following co-transfection with pcDNA3.1(−)-MHBst167 compared with that after co-transfection with pcDNA3.1(−) or pcDNA3.1(−)-MHBs. The marked increase in CAT gene expression may be attributed to the transactivating effect of the truncated HBV MHBst167 on the SV40 early promoter element, leading to the observed increase in CAT expression, whereas the intact MHBs was not transactive (Fig. 2B).
Analysis of the cDNA subtracted library transactivated by MHBst167
To gain a general view of the genes which may be involved in the pathogenesis of HBV, genes that were upregulated in HepG2 cells expressing MHBst167 were identified by the generation of a subtracted cDNA library. Subtraction efficiency analysis showed that PCR products of the housekeeping gene G3PDH in the unsubtracted library were obviously visible after 18 cycles; however, 28 cycles were required in the subtracted library (Fig. 3), indicating that the abundance of non-differentially expressed genes was effectively reduced and the subtraction method had a high subtraction efficiency. Using SSH, a total of 94 positive clones were obtained. These clones were prescreened by using PCR amplification to ensure that they had different inserts before sequencing. Among these clones, 77 contained inserts of 200–1,000 bp. A total of 50 clones from the cDNA library were randomly chosen and sequenced, and their nucleotide sequence homology searches were performed using the BLAST program at NCBI. The analysis results showed that there were 22 coding sequences, of which 18 were known and 4 were unknown genes. Some of the proteins coded by these genes have been shown to be involved in cell cycle regulation, cell apoptosis, signal transduction pathways and tumor development. Notably, the cell proto-oncogene c-Myc was up-regulated by MHBst167. A summary of the data is presented in Table I.
 | Table ISequence analysis of 42 clones isolated from subtracted cDNA library transactivated by MHBst167. |
MHBst167 upregulates the c-Myc promoter activity
To examine the relationship between MHBst167 and c-Myc, the effect of MHBst167 on the promoter activity of c-Myc was investigated. The promoter activity was evaluated using a CAT assay in HepG2 cells transfected with pcDNA3.1(−)-MHBst167. As shown in Fig. 4, transiently expressed MHBst167 was found to markedly increase the promoter activity of c-Myc in HepG2 cells in a dose-dependent manner. The results suggested that MHBst167 protein could transactivate c-Myc expression by transcriptionally activating its promoter element.
MHBst167 upregulates the c-Myc expression
To further elucidate the mechanisms of MHBst167 on c-Myc expression at the transcription and translation levels, the effect of MHBst167 on expression of the gene was investigated. As shown in Fig. 5A, level of mRNA of c-Myc markedly increased following transient transfection with pcDNA3.1(−)-MHBst167. The western blot analysis indicated that the expression of the gene was low in the control groups, whereas in the experiment group, its expression was markedly enhanced (Fig. 5B). These results indicated that MHBst167 could transactivate the expression of c-Myc at both the transcription and translation levels.
Discussion
The molecular mechanism of HBV-related carcinogenesis is poorly understood. A possibility could be activation of the expression of cellular genes involved in cell growth regulation by viral proteins. For example, HBx has been shown to act as a transcriptional transactivator, stimulating various viral and cellular enhancer and promoter elements (9). Transactivating functions have also been attributed to viral proteins translated from 3′-truncated HBV preS/S sequences that are frequently found in human HCCs (10). Lauer et al found there are three hydrophobic regions in the S-domain, located at MHBs residues 62–78, 135–53 and 224–281, respectively, which are separated by two highly hydrophilic regions (at MHBs residues 79–134 and 154–223). The authors showed that if truncation occurred beyond the third hydrophobic region with the first hydrophobic region being complete, the truncated protein acquired transactivation functions (11). MHBst-encoding sequences are found in numerous integrates subcloned from HBV-associated HCC, and previous studies showed there was truncated-form S protein in the circulation of patients with chronic hepatitis B virus infection (12,13).
To evaluate the putative relevance of MHBst167 in the process in HBV-associated HCC development, a detailed analysis of MHBst167 activator function is of great biological significance. In the present study, the authors demonstrated that MHBst167 was successfully expressed in the transiently transfected HepG2 cells. In the co-transfection experiments, the relative CAT expression in the cells transfected with pcDNA3.1(−)-MHBst167 + pCAT3-promoter was approximately 4.5-fold higher than that with pcDNA3.1(−) + pCAT3-promoter or pcDNA3.1(−)-MHBs + pCAT3-promoter. This indicated that MHBst167 had a significant transactivating function on the SV40 early promoter, leading to the observed increase in the expression of the downstream gene CAT, while the intact MHBs did not show transactivation. This suggests that HBV MHBst167 transiently expressed in HepG2 cells retains its biological activity in transcriptional activation, which is consistent with previous reports (14).
To gain further insights into the genes transactivated by MHBst167, SSH was used to clone the genes transactivated by MHBst167. Sequencing of the genes obtained from the subtracted library revealed 22 different coding sequences, of which18 were known and 4 were unknown genes.
The genes with known functions can be divided into five groups, namely genes related to cell transcription and protein synthesis, cell energy and substance metabolism, the formation mechanism of hepatic fibrosis, cell signal transduction and apoptosis, and tumor development (15). Notably, upregulated expression of proto-oncogene c-Myc was observed. Yuen et al demonstrated that 74% of HCC tissues had a high level of c-Myc expression (16). Overexpression of c-Myc has been implicated in liver regeneration and hepatocarcinogenesis. It is also an indicator of malignant potential and poor prognosis (17). The biological significance of c-Myc gene upregulation by the truncated middle surface protein of HBV in human hepatocellular carcinoma, however, has not been confirmed.
To further elucidate the regulatory mechanisms of MHBst167 on c-Myc expression, a reporter vector pCAT3-c-Myc was generated where the CAT gene was placed under the control of the c-Myc promoter, which contains the partly 5′-flanking region and the majority of the exon 1 regions of the c-Myc gene (18). The upregulated expression of proto-oncogene c-Myc in HepG2 cells has been confirmed by cell transient transfection at the mRNA and protein levels. It is reasonable to believe that the transformation effect of MHBst167 is involved in the upregulation of the expression of proto-oncogene c-Myc.
In conclusion, the present study analyzed the transactivator function of MHBst167 and constructed a subtracted cDNA library of genes transactivated by MHBst167. Furthermore, it was confirmed that MHBst167 could transactivate the expression of c-Myc at the transcriptional and translational levels. These findings provide new insights into the biological functions of MHBst167 and new directions to elucidate the hepatocarcinogenesis mechanisms of HBV infection.
Acknowledgements
The authors thank the technical staff of the Viral Hepatitis Research Center, Institute of Infectious Diseases, Beijing PLA 302 Hospital (Beijing, China), for excellent technical assistance.
