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The B cell transcription program mediates hypomethylation and overexpression of key genes in Epstein-Barr virus-associated proliferative conversion
Genome Biologyvolume 14, Article number: R3 (2013)
Epstein-Barr virus (EBV) infection is a well characterized etiopathogenic factor for a variety of immune-related conditions, including lymphomas, lymphoproliferative disorders and autoimmune diseases. EBV-mediated transformation of resting B cells to proliferating lymphoblastoid cells occurs in early stages of infection and is an excellent model for investigating the mechanisms associated with acquisition of unlimited growth.
We investigated the effects of experimental EBV infection of B cells on DNA methylation profiles by using high-throughput analysis. Remarkably, we observed hypomethylation of around 250 genes, but no hypermethylation. Hypomethylation did not occur at repetitive sequences, consistent with the absence of genomic instability in lymphoproliferative cells. Changes in methylation only occurred after cell divisions started, without the participation of the active demethylation machinery, and were concomitant with acquisition by B cells of the ability to proliferate. Gene Ontology analysis, expression profiling, and high-throughput analysis of the presence of transcription factor binding motifs and occupancy revealed that most genes undergoing hypomethylation are active and display the presence of NF-κB p65 and other B cell-specific transcription factors. Promoter hypomethylation was associated with upregulation of genes relevant for the phenotype of proliferating lymphoblasts. Interestingly, pharmacologically induced demethylation increased the efficiency of transformation of resting B cells to lymphoblastoid cells, consistent with productive cooperation between hypomethylation and lymphocyte proliferation.
Our data provide novel clues on the role of the B cell transcription program leading to DNA methylation changes, which we find to be key to the EBV-associated conversion of resting B cells to proliferating lymphoblasts.
Infection of B cells with Epstein-Barr virus (EBV), which is highly prevalent in humans, is an excellent model to investigate the molecular mechanisms associated with the acquisition of unlimited growth during disease. EBV-associated changes in B cells are relevant to the development and progression of lymphomas  and lymphoproliferative disorders in immune-suppressed individuals, and various autoimmune disorders like rheumatoid arthritis, systemic lupus erythematosus and multiple sclerosis . In early primary human infection, EBV infects peripheral resting B cells and expresses six nuclear (EBNA1, 2, 3A, 3B, 3C and -LP) and two latent membrane proteins and small non-coding RNAs. This type of infection, in which these two groups of proteins transform resting B lymphocytes into continuously proliferating lymphoblastoid cell lines, is referred to as type III latency [1, 3]. This process mimics antigen-induced clonal expansion of resting B cells associated with MYC-mediated proliferation and upregulation of NF-κB, MAP kinases and antiapoptotic factors. Recent data have shown that EBNA2, which is essential to this process, enhances and exploits the B cell transcription program by binding to a variety of B cell transcription factor sites to achieve transformation . In vivo, the vigorous cellular immune response directed against EBV-immortalized cells limits the proliferation and expansion of such latently infected cells at early stages of infection of a naïve host or in immunocompromised individuals. Studying type III latency lymphoblastoid cells is relevant because it not only allows the investigation of early steps in infection and the effects that the viral activity exerts on B cell function, but also is an excellent strategy for investigating changes related to the triggering of unlimited proliferation of B cells, before any additional secondary transforming genetic and epigenetic events occur.
The mechanisms by which B cell identity is altered in this process towards unlimited proliferation, triggered by EBV infection, involve the acquisition of epigenetic changes. In this context, DNA methylation might play a key role, since this epigenetic mark participates in regulating transcriptional activity  and is known to be highly aberrant in several types of EBV-associated lymphomas [6, 7] and autoimmune diseases . Despite its role in gene control, DNA methylation is not only a mechanism of transcriptional control but also guarantees genomic stability. The relationship between methylation and transcriptional activity has been best studied in promoter regions, particularly CpG island-associated promoters, where methylation is generally associated with transcriptional repression. In the context of the hematopoietic system, DNA methylation profiling has revealed overall higher methylation levels in the lymphoid branch relative to the myeloid one, and with respect to less differentiated progenitors .
A number of studies have addressed the analysis of DNA methylation changes associated with EBV infection of B cells. Several of these have revealed that whereas the EBV genomic sequence is virtually unmethylated in free viral particles and lymphoblastoid cells, the genome is heavily methylated in both Burkitt and Hodgkin lymphomas . Also, the DNA methylation status of EBV promoters has been widely studied in association with the activity of latency promoters [11–14]. By contrast, fewer studies have addressed the acquisition of DNA methylation changes by the host cell during EBV-mediated transformation between resting B cells and proliferating lymphoblasts. EBV influences changes in the DNA methylation status at specific sequences [15–17] and these are likely to influence or modify the B cell phenotype and function. It is therefore of inherent interest to investigate the extent and mechanisms of acquisition of changes in DNA methylation by B cells following EBV infection as well as their potential contribution to phenotypic changes during this process.
In this study we investigated the acquisition of DNA methylation changes during EBV-mediated transformation of resting B cells to lymphoblastoid cell lines by using methylation bead arrays. We exclusively observed significant hypomethylation of around 250 genes. No hypermethylation was found. Time course analysis indicated that hypomethylation occurs only when cell proliferation has started, suggesting the exclusive participation of replication-dependent mechanisms. Gene Ontology (GO) analysis, comparison with the expression patterns of different cell types and between resting B cells and proliferating lymphoblasts, high-throughput analysis of the presence of transcription factor binding motifs and occupancy revealed that most genes undergoing hypomethylation are active and display the presence of NF-κB p65 and other B cell-specific transcription factors. In addition, hypomethylation associates with upregulation of several genes that are essential in the transformation of resting B cells to continuously proliferating lymphoblasts. Pharmacologically induced DNA demethylation increases B cell transformation efficiency. Our data provide novel clues to the contribution of epigenetic mechanisms associated with EBV-associated conversion of resting B cells to proliferating lymphoblasts, the relevance of the cell type context and why DNA hypomethylation could be key in the efficiency of this process.
DNA methylation profiling reveals that EBV-mediated B cell to lymphoblastoid transformation is associated with gene-specific hypomethylation
To investigate the acquisition of DNA methylation changes in association with EBV-associated transformation of resting B lymphocytes (RBLs), we first compared the DNA methylation profiles of six samples before and after EBV infection, once they had become lymphoblastoid cell lines (LCLs). To this end, we used methylation bead arrays that interrogate the DNA methylation status of over 27,000 informative CpG sites, including the region near the transcription start sites of more than 14,000 promoters. Statistical analysis of the combined data from the six pairs of samples revealed that 256 genes were hypomethylated (fold change (FC) > 2; false discovery rate (FDR) adjusted P < 0.05, Student's t-test) in B lymphoblastoid cells compared with resting B cells (Figure 1a; Additional file 1). By contrast, no hypermethylated genes were observed under these conditions. Scatterplots comparing the average DNA methylation patterns of the six RBLs and matching LCLs had highly reproducible DNA methylation profiles among different samples (Figure 1b). Changes corresponding to the average six pairs of B cells/lymphoblastoid cells were almost identical to the pattern obtained for only male or only female RBL/LCL comparisons, or those changes obtained for each individual pair of samples (Figure 1b), highlighting the specificity of the differences observed.
Since disease-related hypomethylation alterations generally affect repetitive elements, we also investigated changes in CpG sites in this type of sequence. In humans, most of the methylated cytosines are found in CpG-rich sequences within the tandem and interspersed repeats that constitute up to 45% of the human genome, of which Alu repeats are the most common family. We used genome-wide amplification of unmethylated DNA Alu repeats (AUMA)  to perform high-throughput screening of DNA methylation at these sequences. This experiment revealed no differences between RBLs and LCLs, suggesting that loss of methylation does not occur in repetitive sequences (Figure 1c).
Our analysis revealed a mean 21.5% methylation among the 256 genes undergoing demethylation in RBLs (Figure 1d). This average level of methylation at or near promoters is compatible with active gene expression in resting B cells. In fact, GO analysis showed significant enrichment (P < 0.05) for the following categories assigned to biological processes: immune response (GO:0006955; P-value = 8.8 × 10-5), humoral immune response (GO:0006959; P-value = 2.2 × 10-4), B cell receptor signaling pathway (GO:0050853; P-value = 8.8 × 10-4), inflammatory response (GO:0006954; P-value = 1.8 × 10-3) and chemotaxis (GO:0006935; P-value = 2.0 × 10-3) (Figure 1e). These categories include the presence of key markers of B cell function and identity, such as CD19, CD79a and BLNK. Among the list of hypomethylated genes, the presence of genes that are EBV-induced, such as CCR7 (EBI1), GPR183 (EBI2), EBI3 (IL27 subunit beta) and TRAF1 (EBI6), is also noteworthy.
To confirm that differences identified in DNA methylation between B cells and B lymphoblasts were robust, we carried out bisulfite genomic pyrosequencing of selected genes looking at CpG sites corresponding to the oligonucleotide probe represented in the methylation array, which is generally located around the transcription start site. We selected 20 genes on the basis of the magnitude of change in methylation, as revealed by the analysis of our methylation arrays, and their functional relevance in the context of B cell biology: CD19, CD79a, BLK, FCER2, LCK, BLNK, IL21, CCL3L1, SLAMF7, IL25, IRS2, TAP1, COLEC12, MAP3K7IP1, TCL1A, CD1C, CD80 and DOK3, including two of the genes originally described as EBV-induced (CCR7 and TRAF1). In all cases, bisulfite pyrosequencing of these genes confirmed an at least two-fold significant decrease for the aforementioned genes (Figure 2a; Additional file 2).
Hypomethylation associated with EBV-mediated transformation of RBLs to LCLs occurs in association with proliferation and does not involve active demethylation mechanisms
Our results indicated that the transformation of resting B cells to proliferating B lymphoblastoid cells is associated with gene promoter hypomethylation. Loss of methylation may occur as a result of the defective maintenance of DNA methylation as DNA replication and subsequent cell divisions start or, alternatively, as an active mechanism. To discriminate between these two possibilities, we first performed bisulfite genomic pyrosequencing of the genes previously analyzed in samples generated over time, including points at 1, 3 and 24 hours, before cell proliferation had been initiated , and LCLs after 1 and 2 weeks. To this end, we used a form of EBV that infects B cells very efficiently  and in which around 90% of B cells express EBNA2 (Figure 2b). The results showed that significant demethylation only occurred after cell divisions have started to take place (Figure 2c), although the coincidence in time with replication does not necessarily mean that hypomethylation takes place through a passive mechanism.
A variety of factors are known to be involved in active demethylation. Recent studies have drawn attention towards a family of enzymes, the Tet proteins, that convert 5-methylcytosine (5mC) to 5-hydroxymethylcytosine (5hmC) and other modified forms of cytosine. 5hmC may represent intermediates in the process leading to active DNA demethylation [21, 22]. In addition, activation-induced deaminase (AID) participates in active demethylation in a two-step process, whereby 5mC is first deaminated by AID to thymine, followed by G/T mismatch-specific thymine DNA glycosylase (TDG)-mediated excision repair [22, 23]. This process could potentially take place on 5mC, although some studies have shown that hydroxymethylation may target the methylcytosine residues that are going to be demethylated through this process . Analysis of the 5hmC levels at different times in several genes that become hypomethylated during RBL to LCL transformation showed neither a significant presence of 5hmC on the CpGs that undergo hypomethylation nor any changes during this process (Figure 2d). We did not see any significant change in the expression levels of Tet proteins (not shown) during this process. We also investigated the potential involvement of AID in hypomethylation. AID is overexpressed during EBV-mediated conversion of RBLs to LCLs. RT-PCR and western blot analysis of AID revealed an increased expression of AID during this process (Figure 2e). Recent ChIP-seq data have also served to identify direct AID targets in B cells . Comparison of these data with our own hypomethylation data showed that 71 out of 256 genes overlapped with AID binding sites (Figure 2f), although a chi-square test indicated that there is no significant enrichment. We also generated a retroviral inducible system for AID in a B cell line to test whether forced expression of this factor could lead to hypomethylation in the aforementioned genes. Bisulfite pyrosequencing of the same CpG sites of the previously validated genes before and after expression of AID showed no differences in methylation (not shown).
Given that EBV-mediated transformation and B cell activation share common pathways , we also performed bisulfite pyrosequencing of these genes in B cells activated/stimulated with IL4 and CD40L to test the EBV-associated specificity of the observed DNA demethylation changes. Under our conditions we achieved similar levels of both cell activation, measured by cytometry analysis of CD86 surface marker, and proliferation, measured by bromodeoxyuridine (BrdU) incorporation (Figure 2g, top) in both types of stimulation of B cells. However, no changes in the DNA methylation levels of these genes were observed during CD40L/IL4-stimulation of B cells (see examples in Figure 2g, bottom) even after 1 week, suggesting that methylation changes associated with EBV-mediated transformation to LCLs are independent of B cell activation.
Hypomethylated genes are enriched for binding of NF-κB and other lymphocyte-specific transcription factors
Our analysis of the dynamics of DNA demethylation suggests that this process occurs in a replication-associated manner, since changes only occurred once cell divisions had started and did not involve changes in 5hmC or the action of AID. In this context, hypomethylation could potentially associate with genomic sites that are less efficient in maintaining methylation during DNA replication, perhaps in regions that are associated with active transcription in the context of B cell function.
Previous studies have shown that EBV transcription factor EBNA2 enhances and exploits the RBL transcription program by binding to a variety of B cell transcription factor sites . We wondered whether hypomethylation is taking place at genomic sites bound by specific transcription factors, perhaps associated with active transcription in B cells. To address this, we investigated the possible enrichment of transcription factor motifs from the TRANSFAC database in a region of 500 bp around the CpG sites in which hypomethylation had been detected in our study. Significant enrichment of a small set of transcription factors was observed. Remarkably, significant enrichment of the binding motifs of two subunits of the NF-κB complex, specifically c-REL (9.3%, P-value = 2.0 × 10-5) and p65/RELA (6.3%, P-value = 3.1 × 10-3) (Figure 3a) was observed. NF-κB is known to be involved in the survival of LCLs and latency III-regulated cell gene expression . We also found enrichment of additional hematopoietic transcription factor binding motifs in this 500-bp window around hypomethylated CpG sites, such as GATA3, STAT1 and the MEF2 family (Figure 3a).
To evaluate the extent to which hypomethylated genes correlate with NF-κB occupancy, we used our methylation data and ChIP-seq data for NF-κB p65. Enriched NF-κB p65 peaks from a ChIP-seq study in lymphoblastoid cells  were annotated to the nearest Ensembl gene build (version 54)  using the Bioconductor package ChIPpeakAnno . All the targets from all four replicates were uniquely combined. Overlap of hypomethylated genes and NF-κB p65 targets were represented in a Venn diagram and the significance of overlap was determined by a standard chi-square test, written in the syntax of the R statistical program (Figure 3b).
We found that among the entire set of unique direct NF-κB p65 targets, 131 genes were shared with our list of 256 hypomethylated genes, that is, 51% of our hypomethylated genes were directly associated with the NF-κB p65 subunit (Figure 3b). Examples of the detailed binding of NF-κB p65 to these hypomethylated regions are shown in Figure 3c. Additional ChIP-seq data for other transcription factors were also used to investigate the overlap with hypomethylated genes. Specifically, we used ChIP-seq data from EBF1, IRF4, MEF2A, MEF2C, PAX5 and PU1 obtained from GM12878 cells (LCLs) from the ENCODE project (Figure 3D). Remarkably, significant enrichment was obtained for the binding of EBF1, IRF4 and MEF2C (P-value < 0.05). EBF1 is a transcription factor that is critical for both B lymphopoiesis and B cell function . IRF4 is as a crucial transcription factor in the generation of functionally competent plasma B cells . Finally, transcription factor Mef2c is required for B cell proliferation and survival after antigen receptor stimulation .
Our results suggested an association between genes that are regulated by B cell-specific transcription factors, particularly some associated with B cell activation and proliferation, and those that become hypomethylated. It is possible that during transformation of B cells to proliferative lymphoblasts, cells are less efficient in maintaining DNA methylation at actively transcribed sites, perhaps due to a lower presence of DNA methyltransferases (DNMTs), which are preferably bound to heterochromatic regions [33, 34]. One could argue that in quiescent B cells there is a tendency for inactive genes to become methylated, and when the cells are activated to grow and proliferate, genes that become active lose methylation. This possibility was partially discarded by analyzing the methylation levels in CD40L/IL4-activated B cells (Figure 2g). Also, the analysis of bone marrow CD19+ cells, where a high proportion of B cells are proliferating , showed no methylation differences with respect to peripheral blood CD19+ cells, which are quiescent (Additional file 3). It could also be possible that the finding of lower methylation levels in proliferating B cells was due to the specific infection by EBV of a B cell subpopulation with lower levels of methylation. To address that, we pyrosequenced several genes in different B cell subpopulations present in peripheral blood, including naïve B cells, as well as unswitched and switched memory B cells. No differences in methylation were observed with respect to total CD19+ cells from peripheral blood or RBLs and they all displayed higher methylation than LCLs (Additional file 3).
Several key genes are overexpressed is association with hypomethylation during EBV-mediated transformation to LCLs
Our findings suggest that many of the genes undergoing hypomethylation are actively transcribed in B cells, and therefore loss of methylation may not directly affect their expression levels. However, it is important to determine whether hypomethylation is also associated with overexpression of genes that may confer an advantage to proliferating B lymphoblasts.
To address this matter, we performed quantitative PCR of the selected genes in the set of six paired RBL and LCL samples (Figure 4a). Loss of methylation was in some cases associated with an increase in gene expression. This happens for instance for all bona fide EBV-induced genes (EBI), like EBI1, EBI2 and EBI3 (Figure 4a). Individual analysis also showed increase in mRNA levels for other genes, although in other cases this correlation with hypomethylation did not occur, and no changes or even a decrease in expression was observed, although the fold change was relatively low (see central and bottom panels in Figure 4a). This is not surprising, given that the DNA methylation levels of some of the genes undergoing hypomethylation in this process were already relatively low in resting B cells. As mentioned above, many of these hypomethylated genes are key factors in B cell function (CD19, CD79a, BLNK, and so on) and they are expected to be highly expressed in resting B cells. To test whether RNA polymerase II (Pol II) is associated with these genes we overlapped our data with the ChIP-seq data and found that at least 111 of them were Pol II-bound genes (Figure 3b). Examples of the detailed binding of Pol II to these hypomethylated regions are shown in Figure 3c.
We tested whether our 256 hypomethylated genes were generally highly expressed in B cells relative to other cell types. Thus, we compared normalized Affymetrix mRNA expression data of 73 normal human tissues . Comparison of expression of the 256 hypomethylated genes indicated that around 28% of them were more highly expressed in B cells than the average expression level of the 73 other tissue types (Figure 4b), reinforcing our findings on the relevance of the B cell context in the genes that undergo hypomethylation.
For a general comparison in the context of transformation of RBLs to LCLs, we compared the expression profiles of the 256 genes hypomethylated in B and LCLs (available at the Gene Expression Omnibus (GEO) database under series accession number GSE26212) . This revealed that around 41% of the genes displayed high levels of expression in RBLs (Figure 4c). However, around 59% of the remaining genes accomplished significant increase in gene expression (Figure 4b; Additional file 4), correlating with the over two-fold reduction in DNA methylation. Remarkably, the list of genes that become hypomethylated and are overexpressed includes several key genes in RBL to LCL conversion (Additional file 4). For instance, EBI3 undergoes an approximately five-fold change in methylation and becomes overexpressed. This gene is a subunit of the heterodimeric cytokine IL27, known to be regulated through NF-κB activation  and to induce B cell proliferation, which is stronger in naïve than in memory B cells . Another example is LTA, or lymphotoxin alpha, a member of the tumor necrosis factor family, and an autocrine growth factor induced upon binding of NF-κB . Other examples in our list include genes like SLAM1 and SLAMF7, two members of the 'signaling lymphocyte activation molecule' (SLAM) family, also implicated in B cell proliferation .
Pharmacologically induced DNA demethylation enhances proliferation during RBL to LCL transformation
Our analysis revealed that a high proportion of the genes that undergo hypomethylation during RBL to LCL transformation become overexpressed and that several of them are important for the transformation on continuous proliferating B lymphoblasts. To determine whether hypomethylation has any effect on the efficiency of transformation, we investigated whether pharmacologically induced hypomethylation influences RBL to LCL transformation. We tested the proliferation rate in RBLs infected with EBV and incubated in the presence of increasing concentrations with the demethylating agent 5-azadeoxycytidine (azadC) at concentrations between 50 pM and 50 μM. MTT assays showed that mock-treated cells started to proliferate around day 6 after infection with EBV (Figure 5a). Cell viability and proliferation rate decreased at very high doses of azadC, consistent with the toxicity properties of azadC at high doses, which we tested on cultured LCLs (Figure 5a). However, at low azadC concentrations (50 pM, 500 pM and 5 nM), where viability of cells is comparable to that of control cells (Figure 5a), a significant increase in cell proliferation was observed after day 8 (Figure 5b). This increase in proliferation in the presence of azadC was not observed when established LCLs were used as a control in proliferation experiments in the presence of azadC, suggesting that the effect of azadC is associated with the transformation of RBLs to proliferating B cells. Bisulfite genomic analysis of several of the target genes confirmed the loss of methylation at the studied CpG sites upon treatment with 5azadC at low concentrations (Figure 5c). In fact, we observed that azadC-treated cells had lower levels of methylation than control cells at day 10 (Figure 5c). Analysis of viral promoters showed that these were unmethylated in both free viral particles and in LCLs, ruling out the possibility that demethylation at EBV promoters and overexpression of EBV-encoded genes are responsible for more efficient transformation of RBLs to LCLs.
Our results provide evidence that EBV-mediated transformation of RBLs to LCLs results in the demethylation of a cluster of around 250 genes. Conversely, no significant hypermethylation is observed. Hypomethylation has been described in various immune disease-related contexts, including ICF (immunodeficiency, centromere instability and facial anomalies) syndrome  and autoimmune diseases . In most cases, disease-associated hypomethylation occurs at repetitive sequences, including Alu elements . However, in RBL to LCL transformation, hypomethylation takes place near the transcription start sites of around 250 genes, and no apparent hypomethylation occurs at the major type of repetitive elements. Lack of hypomethylation in repetitive sequences is consistent with the minimal changes in genomic stability associated with EBV-associated lymphoproliferation.
Given that hypomethylation occurs in association with the acquisition of proliferation, it is likely to be related to the decreased efficiency in DNA methylation maintenance as cells start to divide. The lack of evidence for active demethylation mechanisms during this process also supports the above possibility. The transition of a differentiated resting cell to a proliferative status would require the participation of DNMTs to maintain the DNA methylation profiles throughout replication/division cycles. Various lines of evidence indicate that DNMTs are associated with repetitive sequences [33, 34] and that heterochromatic regions act as a reservoir for DNMTs . This would explain why active regions, which are less rich in DNMTs, lose methylation in the transformation from resting to proliferative B cells, whereas in ICF syndrome, which is characterized by mutations in DNMT3B, hypomethylation takes place in heterochromatic regions, which act as reservoirs of DNMTs.
In fact, analysis of the regions associated with hypomethylation during RBL to LCL transformation shows enrichment of highly expressed genes and target sites of transcription factors that are expressed in B cells or are specifically activated during EBV infection, such as factors in the NF-κB pathway [26, 43]. The modulation of the NF-κB signaling by EBV is not only important for viral infection, but also contributes to the development of malignant neoplasia . In addition, our results indicate that hypomethylated genes are regulated by B cell-specific factors like EBF1, IRF4 and MEF2C, the last two of which are implicated in B cell activation and proliferation processes. We also observed that many of the genes that undergo hypomethylation, like CD19, CD79a, BLNK, BLK and LCK, are highly expressed in B cells. This suggests that active regions are either more accessible to putative demethylating machinery or are less efficient at maintaining methylation as proliferation starts. Given the lack of demethylation events before proliferation begins, and that we were unable to detect links between any of the proposed mechanisms associated with active demethylation, we favor the occurrence of a replication-coupled mechanism of demethylation, due to the inefficient maintenance of DNA methylation as replication is initiated. Similar to studies of the EBNA2 binding sites  in which EBV exploits intrinsic B cell transcription programs, hypomethylation takes place preferentially in genes that are expressed. Comparison of the lists of significantly hypomethylated genes and the presence of transcription factor binding motifs and occupancy reinforced this notion. Data from different sources suggest that transcriptionally active regions are devoid of DNMTs, making the maintenance of DNA methylation less efficient. On the other hand, since the main functional consequence of promoter hypomethylation would potentially be an increase in transcription, it is likely that demethylation contributes to overexpression of some of these genes. In this sense, we have identified several key genes that undergo both hypomethylation and overexpression during the conversion of RBLs to LCLs. These include genes like EBI3 [37, 38], a subunit of the cytokine IL27, LTA  and members of the SLAM family  among others that are known to contribute to lymphocyte proliferation (Additional file 4).
In addition, demethylation of genes that already have high expression levels in the first set of infected cells might also lock its transcriptional status, and therefore would reinforce the B cell phenotype, and might be key to enable infection of more B cells. EBV initially infects oropharynx epithelial cells, establishing a lytic replication that spreads to some B cells in nearby lymphoid tissues. Those expand as EBV establishes a type III latency growth-transforming infection of B cells that elicit a strong T-cell-specific response. Maintaining a B cell phenotype would favor recirculation and generalized expansion to B cell areas in secondary lymphoid organs where surviving B cells downregulate EBV antigen expression and establish long-term silent latency .
The functional relevance of demethylation in this process is highlighted by the observation that treatment of RBLs with azadC at low sub-toxic concentrations enhances RBL to LCL transformation. Since the EBV genome is virtually unmethylated in free viral particles, demethylation at EBV promoters and overexpression of EBV-encoded genes can be ruled out as responsible for more efficient transformation of RBLs to LCLs. Our findings on the enhanced cell proliferation concomitantly associated with the presence of low sub-toxic amounts of azadC suggests that initial DNA methylation changes may cooperate in the efficiency of this process.
Although type III latency lymphoblastoid cells do not necessarily correspond to initial steps of lymphomagenesis, they both share enhanced proliferation . It is likely that hypomethylation occurs in early steps towards to lymphomagenesis, when enhanced proliferation starts. In other hematological neoplasias, like in acute myeoloid leukemia, DNMT3A mutations are highly recurrent , and it has been proposed that these mutations in an enzyme responsible for the establishment of DNA methylation are an early event of clonal evolution . In B-cell chronic lymphocytic leukemia, increased levels of TCL1 result in inhibition of DNA methylation . Inhibition of methylation is proposed to be a common oncogenic mechanism in leukemogenesis . These findings highlight the relevance of our study as a potential early mechanism in this group of tumors.
Our study of DNA methylation changes in EBV-mediated transformation of RBLs to LCLs reveals that only promoter hypomethylation occurs during this process. Neither significant hypermethylation nor methylation changes at repetitive elements are observed. Hypomethylation takes place only when proliferation has started, and the analysis of putative elements of the active demethylation machinery does not indicate their implication during this process. Most genes undergoing hypomethylation are active and display the presence of NF-κB p65 and other B-cell-specific transcription factors. Since DNMTs tend to associate with heterochromatic regions, it is likely that maintenance of DNA methylation is less efficient in transcriptionally active regions as cells start to proliferate triggered by EBV; however, this process does not occur during CD40L/IL4-stimulation of B cells where no changes are observed. Our results show that hypomethylation is associated with further upregulation of gene expression of many of these genes. Also, pharmacologically induced demethylation increases B cell transformation efficiency and proliferation. Collectively, our data indicate that the B cell transcription machinery is associated with the subset of genes that undergo hypomethylation. The finding that relevant genes in EBV-mediated transformation of B cells are further upregulated indicates a key role of this mechanism. Hypomethylation has been proposed to play a role in early stages of hematological malignancies, including other B cell malignancies. Our data reinforce the notion of the role of hypomethylation in early lymphomagenesis and shed light on underlying mechanisms.
Materials and methods
Human samples (blood) used in this study come from anonymous blood donors and were obtained from the Catalan blood donation center (Banc de Sang i Teixits). Since the samples are anonymous, no informed consent is therefore required. The protocol used to transform with EBV B cells obtained from these anonymous donors was approved by the Committee of Biosecurity of IDIBELL (CBS) on 5 May 2011 and the Ethics Committee of the University Hospital of Bellvitge (CEIC) on 28 May 2011.
Subjects and sample preparation
Buffy-coats from anonymous blood donors were obtained from the Catalan blood donation center (Banc de Sang i Teixits). Viable peripheral blood mononuclear cells were isolated using LymphoprepTM density gradient centrifugation. Resting B cells were isolated by positive selection using CD19 MicroBeads (Miltenyi Biotec, Bergisch Gladbach, Germany), or by depletion using a B Cell Isolation Kit (Miltenyi Biotec). Isolated B cells were immortalized with the supernatant of the EBV producer cell line B95.8 for the methylation studies and with the 2089 EBV made from 293 cells carrying a recombinant B95.8 EBV genome  for expression analysis.
DNA methylation profiling using universal bead arrays
Infinium Methylation Assay (Illumina, Inc., San Diego, CA, USA) was used to analyze DNA methylation. The HumanMethylation27 panel allows researchers to interrogate 27,578 highly informative CpG sites per sample at single-nucleotide resolution. This panel targets CpG sites located within the proximal promoter regions of transcription start sites of 14,475 consensus coding sequencing (CCDS) in the NCBI Database (Genome Build 36). In addition, 254 assays cover 110 microRNA promoters. On average, two assays were selected per CCDS gene and from 3 to 20 CpG sites for > 200 cancer-related and imprinted genes. Bisulfite conversion of DNA samples was done using the EZ DNA methylation kit (Zymo Research, Orange, CA, USA). After bisulfite treatment, the remaining assay steps were identical to those of the Infimium Methylation Assay, using reagents and conditions supplied and recommended by Illumina. Two technical replicates of each bisulfite-converted sample were run. The results were all in close agreement and were averaged for subsequent analysis. The array hybridization was conducted under a temperature gradient program, and arrays were imaged using a BeadArray Reader (Illumina Inc.). The image processing and intensity data extraction software and procedures were those described by Bibikova and colleagues . Each methylation data point was represented as a combination of the Cy3 and Cy5 fluorescent intensities from the M (methylated) and U (unmethylated) alleles. Background intensity computed from a set of negative controls was subtracted from each data point.
Detection of differentially methylated genes from the methylation array and functional analysis
A t-test was carried out to identify probes differentially methylated between primary B cells relative to their counterparts obtained in the LCL. P-values were corrected for multiple testing using the method proposed by Benjamini and Hochberg  to control the FDR. Genes showing a FDR adjusted P-value < 0.05 and a minimum mean methylation FC of two were considered to be differentially methylated. Functional annotation of hypomethylated genes was based on GO (Consortium, 2000), as extracted from EnsEMBL  and the KEGG pathway database . Accordingly, all genes were classified into three ontologies, based on their involvement in biological processes, molecular functions and cellular components. We took only the GO/pathway categories that had at least ten annotated genes. We used GiTools for enrichment analysis and heatmap generation . Resulting P-values were adjusted for multiple testing using Benjamini and Hochberg's FDR method . An FDR cutoff of 0.25 was used for selection of enriched terms. The relationships between the DNA methylation data (from standard bisulfite sequencing and/or quantitative bisulfite pyrosequencing) and the age and sex of the individuals were evaluated by the Pearson chi-square test.
Analysis of gene promoter methylation: bisulfite sequencing and pyrosequencing
CpG island DNA methylation status was determined by sequencing bisulfite-modified genomic DNA. Bisulfite modification of genomic DNA was carried out as described by Herman et al. . To validate the DNA methylation data obtained by the Infinium methylation assay, bisulfite pyrosequencing was performed according to standard protocols and evaluated with the Pyro Q-CpG 1.0.9 program (Biotage, Uppsala, Sweden). Primer sequences, product lengths and annealing temperatures used in the bisulfite sequencing and bisulfite pyrosequencing PCR reactions are shown in Additional file 5. Raw data for bisulfite sequencing of all samples is presented in Additional file 6.
Amplification of unmethylated Alus (AUMA)
DNA digestion with SmaI enzyme and ligation to the linker were performed as described elsewhere . The product was purified using the GFX Kit (Amersham Biosciences, Uppsala Sweden) and eluted in 250 μl of sterile water. A chimeric primer comprising the complementary linker sequence (ATTCGCAAAGCTCTGA), the cut SmaI site (GGG) and three additional nucleotides homologous to the Alu consensus sequence were used to enrich for Alu sequences: AUMA-TTC (ATTCGCAAAGCTCTGAGGGTTC). Single primers were used for each PCR reaction. Products were resolved on denaturing sequencing gels. Bands were visualized by silver staining the gels. Faint bands with inconsistent display due to small variations in gel electrophoresis resolution were not considered. Band reproducibility was assessed with the analysis of PCR duplicates. AUMA fingerprints were visually checked for methylation differences between bands in different samples. Based on these premises, a given band was scored according to three possible behaviors: hypomethylation (increased intensity), hypermethylation (decreased intensity) and no change (no substantial difference between samples). Only those bands showing clear changes in their fingerprint intensities were considered to represent methylation changes.
Quantitative RT-PCR expression analyses
We reverse-transcribed total RNA extracted with TRIzol (Invitrogen), using a Transcriptor First Strand cDNA Synthesis Kit from Roche Diagnostics (Indianapolis, Indiana, USA). Quantitative real-time PCR analysis was performed in a PCR Real Time LightCycler 480 (Roche) with Sybr green. Primer sequences are shown in Additional file 5.
Analysis of transcription factor binding
Possible enrichment of transcription factor motif in the 500- to 1,000-bp region around the center of the hypomethylated probes and all other probes were predicted with the STORM algorithm , assuming P-value cutoffs of 0.00002 and 0.00001, respectively, using position frequency matrices (PFMs) from the TRANSFAC database (Professional version, release 2009.4) . Enrichment analysis of predicted transcription factors in the probes of significant hypomethylated probes (n = 421) were conducted using GiTools . We calculated a two-tailed P-value, and a finally adjusted FDR P-value (with 0.25 cutoff) was considered in establishing statistical significance.
We downloaded EBF1, IRF4, MEF2A, MEF2C, PAX5 and PU1 binding ChIPseq data for the GM12878 cell line from the ENCODE project . Original hg19 genomic co-ordinates were converted to hg18 using the USCS 'liftover' tool. RUNX ChIPseq target data were obtained from the study of Hollenhorst and colleagues  (Jurkat cell line, GEO Database ID: GSE17954). RBPJ and EBNA2 taken from a 2011 study of Zhao et al.  (GEO database ID: GSE29498). In this case, mapped data were analyzed using the MACS (version 220.127.116.11)  pipeline to call peaks. In all cases, peaks were annotated to the nearest EnsEMBL  gene (version 54) using the Bioconductor package ChIPpeakAnno .
Expression analysis of hypomethylated genes in various tissue types
Expression data on RBL and LCL from the study of Caliskan and colleagues  (GEO accession GSE26210) were used to determine the relative expression of hypomethylated genes in these two cell types. Probes were annotated to Refseq genes and when more than one probe was present for the same gene, they were averaged. Also, all replicates on same sample were averaged. Expression data were normalized by median-centering the expression value of each gene across all the samples and dividing the value by the standard deviation. These normalized values were delineated in a color-coded heatmap using GiTools .
Normalized mRNA expression of data of 73 normal human tissues was downloaded from the BioGPS database  and analyzed similarly.
Cell proliferation and viability assays
In cell proliferation analysis, different dilutions of cells were plated and cultured at 37°C in 5% CO2/95% O2 for 20 days. AzadC (Sigma, St. Louis, MO, USA) was used in serial dilutions between 50 pM and 50 μM and refreshed on day 4 of treatment. Every 2 days, cells were fixed and stained with MTT and incubated for 4 hours at 37°C. The reaction was stopped with 50% N,N-dimethylformamide, 30% SDS, 2.5% glacial acetic acid and 2.5% acid chloride 1 N, and incubated overnight at 37°C in 5% CO2/95% O2. Cell quantities were determined by measuring the optical density at 560 nm. All assays were performed in triplicate. Cell viability was determined by the incorporation of propidium iodide in dead cells measured by flow cytometry.
CD40L activation of B cells
B cells were cultured at 1.5 × 106 cells/ml and activated with 50 ng/ml of M.CD40L (Enzo Life Sciences, Lausen, Switzerland) and 50 ng/ml of IL4 (Gentaur, Kampenhout, Belgium). The percentage of activated RBLs was determined by CD86 expression measured by flow cytometry and proliferating B cells were detected by measuring BrdU incorporation.
Use of a B-cell-based inducible system to test AID activity
Jiyoye B cells with inducible expression of AID were generated using the Retro-X TM Tet-ON® Advanced Inducible Expression System (Clontech, Saint-Germain-en-Laye, France). This system works through the sequential infection of the RetroX-Tet-ON advanced vector and the pRetroX-Tight-Pur vector. Carboxy-terminal hemagglutinin (HA)-tagged human AID was cloned in the pRetroX-Tight-Pur vector. The stable doubly infected cell line was selected with Geneticin (1 mg/ml) and Puromycin (0.3 μg/ml). AID expression was induced by the addition of doxycycline (500 ng/ml) for 24 hours. Nuclear export was inhibited by the addition of leptomycin B (10 ng/ml) for 2 hours.
Methylation array data for this publication have been deposited in NCBI's GEO and is accessible through GEO series accession number GSE41957 .
amplification of unmethylated Alu repeats
false discovery rate
Gene Expression Omnibus
lymphoblastoid cell line
resting B lymphocyte
- Pol II:
RNA polymerase II.
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This work was supported by grants PI081346 (FIS) and SAF2011-29635 from the Spanish Ministry of Science and Innovation (MICINN) and grant 2009SGR184 from AGAUR (Catalan Government). AI was supported by fellowship from AGAUR, Government of Catalonia, Spain. MP is supported by Ramon y Cajal Programme.
The authors declare that they have no competing interests.
HH, CS-L, JR-U, VR-C, BJ, CM and MP performed experiments, AI, FA-S, AF, MF performed analysis, H-JD contributed with key tools, ME, EL-G, NL-B contributed with key analytic tools and interpreted data, and EB designed the project and wrote the paper. All authors read and approved the final manuscript.
Electronic supplementary material
Additional file 3: A comparison of the DNA methylation levels of selected genes in different B cell types. Bisulfite pyrosequencing was performed for the genes selected from experiments with methylation arrays. The analysis includes bone marrow (BM) CD19+ cells, naïve B cells, unswitched (US) memory B cells and switched (S) memory cells. Also peripheral blood resting B cells (RBLs) and corresponding lymphoblastoid B cells (LCLs) are included. (PDF 22 KB)
About this article
- Active Demethylation
- Transcription Factor Binding Motif
- Bisulfite Pyrosequencing
- Promoter Hypomethylation
- Hypomethylated Gene