Abstract
WWOX (WW domain containing oxidoreductase) expression loss is common in various cancers and characteristic of poor prognosis. Deletions, translocations, and loss of expression affecting the WWOX gene are a common feature of various B cell neoplasms such as certain B cell lymphomas and multiple myeloma. However, the role of this common abnormality in B cell tumor initiation and/or progression has not been defined. In this study, we conditionally deleted Wwox early in B cell development by means of breeding Cd19-Cre transgenic mice crossed to Wwox floxed mice (Cd19 Wwox KO). We observed a significant reduced survival in Cd19 Wwox KO mice and the development of B cell neoplasms including B cell lymphomas, plasma cell neoplasias characterized by increased numbers of CD138+ populations as well as monoclonal gammopathies detected by serum protein electrophoresis. To investigate whether Wwox loss could play a role in genomic instability, we analyzed DNA repair functions during immunoglobulin class switch joining between DNA segments in antibody genes. While class switch recombination (CSR) was only slightly impaired, Wwox deficiency resulted in a dramatic shift of double strand break (DSB) repair from normal classical-NHEJ toward the microhomology-mediated alternative-NHEJ pathway, a pathway associated with chromosome translocations and genome instability. Consistent with this, Wwox deficiency resulted in a marked increase of spontaneous translocations during CSR. This work defines for the first time a role for Wwox for maintaining B cell genome stability during a process that can promote neoplastic transformation and monoclonal gammopathies.
Introduction
WWOX (WW domain containing oxidoreductase) is a ubiquitously expressed tumor suppressor gene mapping to chr16q23, which spans one of the most common chromosomal fragile sites in the human genome, FRA16D (–). Tumor copy number alterations analyses revealed WWOX to be one of the most frequently deleted genes in cancer (, ) and loss of WWOX expression is characteristic of poor prognosis [Reviewed in ()]. Although loss of WWOX is correlated with cancer development and progression, it does not behave as a highly penetrant classical tumor suppressor in most mouse models. Complete Wwox deletion results in post-natal death by 3–4 weeks of age (, ) and tissue specific deletion using a variety of Cre expression mouse models did not result in spontaneous tumor formation in mice from mixed genetic background [Reviewed in ()]. Recently however, increased mammary carcinogenesis has been reported in a cancer susceptible mouse genetic background, supporting the hypothesis of Wwox operating as a tumor suppressor (). We have previously observed that hypomorphic Wwox mice developed B cell lymphomas at old age () and this appears in agreement with observations indicating that heterozygous mice with only a functional Wwox allele (i.e., Wwox+/−) develop an increased B cell lymphoma incidence when exposed to the carcinogen ethyl-nitrosourea (). Thus, both of these studies (, ) suggest a propensity of B cells for neoplastic transformation upon Wwox deficiency.
In humans, alteration and loss of WWOX has been associated with certain B cell tumors (–), and most notably Multiple Myeloma (MM). In MM, the t(14;16) (q32;q23) involving IGH (Immunoglobulin heavy chain) and WWOX is a primary genetic event that results in upregulation of MAF and characteristic of a subgroup of high-risk MM (, , , ). Importantly, besides of WWOX participation in t(14;16), lower WWOX expression appears to be associated with poor MM prognosis (–). Loss of heterozygosity at the WWOX locus was shown to correlate with loss of WWOX expression in MM cases (). Homozygous WWOX deletions are indicative of poor prognosis () and alteration of 16q, which includes deletion of WWOX, were recognized by International Myeloma Working Groups as a recurrent secondary genetic event in high-risk MM (, ). Furthermore, in recent analyses of data from the Myeloma Genome Project, Walker et al. identified deletion 16q23.1 affecting WWOX, among the most common recurrent minimal copy number changes, detected in 252 out of 1,074 (23.5%) newly diagnosed MM cases characterized by whole-exome sequencing. Thus, WWOX deletion is one of the most common genomic abnormalities observed in MM overall (, ). In addition, WWOX gene promoter methylation was also reported to associate with disease progression (). Despite the overwhelming evidence suggesting a connection between WWOX loss of function and B cell neoplasia, the pathophysiological role of WWOX in B cells remains unclear.
In B cell lymphomas and MM, translocations between the IGH locus and oncogenes are recurrent events that drive transformation (, ). They are thought to be primarily generated by aberrant double strand break (DSB) formation during the antibody diversification processes of class-switch recombination (CSR) and V(D)J recombination (, ). Site-specific break formation at the IGH locus and off-target sites are determinants that impact the location, while break frequency and persistence impact the rate of translocations (). As such, efficient DNA damage response and repair of DSBs is important in suppressing translocations (). The major DSB pathway that operates during CSR and VDJ is the Ku70/80-dependent classical non-homologous end-joining (C-NHEJ) pathway. In the absence of C-NHEJ factors, DSBs are repaired by alternative end-joining pathways (Alt-NHEJ). These ill-defined pathways are thought to be less efficient, requiring more extensive end-processing and are biased toward microhomology based repair. In this context, studies suggest that Alt-NHEJ is prone to generating translocations while efficient repair by C-NHEJ suppresses translocations and genomic instability (, ). In this study, we examine the consequence of conditional B cell Wwox deletion in mice and find reduced survival, tumor formation, and evidence of plasma cell neoplastic transformation. Analysis of CSR from Wwox-deficient B cells reveals inappropriate utilization of the Alt-NHEJ pathway together with an increase in the generation of oncogenic translocations. Thus, this study demonstrates a direct role for Wwox in B cell genome stability during processes that lead to neoplastic transformation.
Materials and Methods
Animals
All animal research was conducted in facilities accredited by the Association for Assessment and Accreditation of Laboratory Animal Care International at the University of Texas MD Anderson Cancer Center, Science Park and all research was approved by the Institutional Animal Care and Use Committee. BK5-CreTG and Cd19Cre mice (, ) and the protocol to generate Wwoxflox/flox and Wwox knock-out (KO) mice have been previously described (, ). In brief, to generate Wwox KO mice we crossed Wwoxflox/wtmales with BK5-CreTG/TG, Wwoxflox/wtfemales (both in mixed 129SV/C57Bl/6 background). Cre expression and deletion occurs in the oocyte and embryo resulting in general recombination and deletion (). As controls (denoted Wwox WT) BK5-CreTG/0Wwox+/+were used. Two-week-old Wwox KO mice and age matched control Wwox WT were compared in experimental analyses. For the generation of Cd19 Wwox KO we crossed Wwoxflox/wt with Wwoxflox/wtCd19Cre/+ mice. For control mice (littermates denoted Cd19 Wwox WT) Wwoxwt/wt, Cd19Cre/+ mice were used. Mice of both genders were used in analysis. Genotypes were confirmed by PCR using primers previously described (, ) and see Supplementary Figure 1.
Antibodies
The following antibodies were used: Anti-CD3 (Biolegend 100237), anti-CD11b, (Biolegend 101237), anti-IgM (Biolegend 406525), anti-CD19 (BD Biosciences 561739), anti-CD95 (BD Biosciences 561856), anti-GL7 (BD Biosciences 553666), anti-CD21 APC (BD Biosciences 561770), anti-CD138 (BD Biosciences 553714), Horseradish peroxidase conjugated anti-mouse Light Chain Specific goat polyclonal antibody (Jackson Immunoresearch #115-035-174), anti-IgG1 (BD Biosciences 560089), and for histology anti-CD45R/B220 (Bio-Rad, MCA1258G) and anti-CD138 (Biolegend 142502).
Flow Cytometry and Wwox Expression Analysis in Primary Lymphocytes
The following cell populations were isolated from spleen or bone marrow by FACS sorting: Pro-B B220+/CD43hi/IgM−, Pre-B B220+/CD43lo/IgM−, Plasmablasts B220+/CD138+/CD19lo, Plasma cells B220−/CD138+/CD19−, Follicular B220+/CD19+/CD23hi/CD21lo, Marginal zone B220+/CD19+/Cd23lo/CD21hi, Germinal center CD19+/GL7+/CD95+. Viable cells were identified by forward and side scatter as well as propidium iodide dye exclusion. CD3+ and CD11b+ cells were used to exclude non-B cell populations. Samples were sorted using a BD FACSARIA Fusion. RNA from each B lymphocyte subpopulation was isolated using Trizol Reagent (Ambion) and cleaned up with RNeasy kit (Qiagen). Quantitative gene expression by reverse transcription real time PCR was determined using primer/probe Taqman set spanning exons 6–7 of Wwox (Thermo Fisher Scientific Assay ID Mm01247384, 4351372) and normalized to 18S RNA.
Histology and Immunohistochemistry
Full necropsy was performed on all mice and samples from major organs and tumors (whenever available) were collected. Tissues were processed by means of formalin fixation, paraffin embedding and hematoxylin and eosin (H&E) staining. Tumor samples were also analyzed by immunohistochemistry (IHC) following standard procedures and staining with anti-CD45R/B220 and anti-CD138. Histological analyses were performed by two pathologists without prior knowledge of genotypes. Based on IHC staining pattern and cell morphology, tumors were classified following guidelines of the Bethesda classification of lymphoid neoplasms in mice and a more recent classification of mouse plasmacytomas (, ).
Serum Protein Electrophoresis (SPEP)
Mice blood samples were collected at time of euthanasia. Samples were allowed to coagulate at room temperature and spun at 3000 × G for 10 min; 0.5 μl of sera were loaded in precast QuickGels (Helena Laboratories, 3505T) and run on a QuickGel Chamber (Helena Laboratories, 1284) according to the manufacturer's instructions. Samples were analyzed in triplicate with M-spike positive samples visible in all three analyses.
Statistical Analysis for Mouse Survival and Tumor Incidence
Analyses were performed using SPSS statistical software. Log-rank test was applied to compare survival curves. Fisher's exact test was used to compare tumor incidence rates. P-values of < 0.05 were considered significant.
B Cell Culture and Analysis
B cell isolation and culture have been previously described (). Naïve B cells were purified from spleens of wild-type and Wwox KO 16–17 day-old mice (, ) by anti-CD43 bead depletion (Miltenyi Biotec). Cells were cultured in LPS (25 μg/ml, Sigma-Aldrich) and IL-4 (5 ng/ml, RD) for 72 h. To determine CSR to IgG1, cultured B cells were stained with anti-IgG1 antibodies and flow cytometric analysis of surface Ig expression was performed on a LSRFortessa (BD) with scatter gating and propidium iodide staining to exclude dead cells (). Results were analyzed with FlowJo (Tree Star) and averages were obtained from triplicate cultures of six individual spleens in four independent experiments. Cell proliferation was analyzed with Cell Trace Violet (Invitrogen) according to manufacturer's protocol (). Fluorescent intensity was measured at culture initiation and at 72 h. Two independent experiments were performed. The chromosome translocation assay has been previously described (, ). Genomic DNA was isolated from naïve B cells cultured to undergo CSR with LPS and IL-4 for 72 h. PCR with genomic DNA of 105 cells per reaction was performed. 1st round PCR primers:(5′-ACTATGCTATGGACTACTGGGGTCAAG-3′ and 5′-GTGAAAACCGACTGTGGCCCTGGAA-3′) and 2nd round PCR primers (5′-CCTCAGTCACCGTCTCCTCAGGTA-3′ and 5′-GTGGAGGTGTATGGGGTGTAGAC-3′) were used to amplify Myc/Igh translocations. Amplicons were confirmed as translocations with reactivity to both southern blot probes Myc (5′-GGACTGCGCAGGGAGACCTACAGGGG-3′) and Igh (5′-GAGGGAGCCGGCTGAGAGAAGTTGGG-3′). The data shown is the summary of three independent experiments and the p-value was calculated by two-tailed Fisher's exact test.
Class Switch Recombination Junction Analysis
CSR junctions were amplified from genomic DNA by PCR with primers and conditions previously described (): 36 cycles of PCR (94°C 30 s, 62°C 30 s, 68°C 8 min) using first round primers (5′-CAGGCTAAGAAGGCAATCCTGG-3′) and (5′-TTGACCTGTAACCTACCCAGGAGAC-3′); and 36 cycles of PCR (94°C 30 s, 64°C 30 s, 68°C 8 min) using second round primers (5′-GATCCAAGGTGAGTGTGAGAGGACA-3′) (5′-CATCCTGTCACCTATACAGCTAAGCTG-3′). PCR products between 0.5 and 3 Kb were purified and cloned into pCR4-TOPO (Invitrogen), individual bacterial clones were picked up and sequenced. Sequences were analyzed from three independent experiments for microhomology and mutation. To identify junctions, donor and acceptor switch regions were aligned. MH was determined by identifying the longest overlap region at the junction. A single mismatch or gap was permitted if at least 5 bp from end of the overlapping sequence in the alignment (, ). For mutational analysis, 100 bp from junction were analyzed on both acceptor and donor regions.
Results
Wwox Ablation in Cd19+ B Cells Reduces Survival and Induces Neoplastic Transformation
In order to better understand the role of WWOX in B cell neoplasms we targeted deletion of this gene early in B-cell development by crossing Wwoxflox/flox mice () to Cd19Cre transgenic mice (). We confirmed Wwox protein ablation in Cd19+ B cells from Cd19Cre/+Wwoxflox/flox(Cd19 Wwox KO) mice by means of immunoblot (Supplementary Figure 1). Wwox protein was not detected in B cell samples from all analyzed Cd19 Wwox KO mice indicating efficient deletion in B cells (data not shown). Survival of Cd19 Wwox KO mice was compared with Cd19Cre/+Wwox+/+(Cd19 Wwox WT) control littermates. Overall survival was plotted using the Kaplan-Meier method and analyzed by the Log-rank test. Cd19 Wwox KO mice had a statistically significant lower survival rate than control (p = 0.007, Figure 1). Cd19 Wwox KO mice displayed a mean survival of 777 vs. 922 days for control mice. Animals were necropsied and histology samples obtained at either the end of the experiment or when moribund. Importantly, we observed that several Cd19 Wwox KO mice developed intra-abdominal tumors with the characteristics of B cell neoplasms (Figure 2). Tumors were broadly classified into lymphomas and plasmacytomas based on the IHC staining pattern (Table 1). Neoplastic lesions that were exclusively B220+ indicative of B cell lymphomas were further classified into mature and immature lymphomas based on published guidelines (). Several of the observed intra-abdominal tumors were positive for B220 and CD138, suggestive of plasmablastic plasmacytomas predominantly affecting mesenteric and retroperitoneal lymph nodes, and were histologically classified as previously described () (Figure 2 and Table 1). Tumors were also tested for Wwox immunoreactivity and were negative (not shown). Of 34 Cd19 Wwox KO mice, 8 (23.4%) developed (B220+) B cell lymphomas and 8 other mice developed plasmacytomas (B220+,CD138+) predominantly affecting mesenteric and retroperitoneal lymph nodes. Thus, a total of 16 of 34 (47%) Cd19 Wwox KO mice developed B cell neoplasms. In the Cd19 Wwox WT control group, only 2 of 14 (14.3%) mice developed B cell lymphomas and none developed plasmacytomas. In summary, the B-cell tumor incidence rates between the Cd19 Wwox KO group and the Cd19 Wwox WT group were significantly different (p < 0.05).
Figure 1
Figure 2
Table 1
| Mouse ID | Genotype [Cd19 Wwox] | Age (ds) | Histopathology | M SPIKE in SPEP |
|---|---|---|---|---|
| 15 | KO | 735 | Mature B cell lymphoma | + |
| 16 | KO | 735 | Mature B cell lymphoma | n/d |
| 68 | KO | 648 | Plasmablastic plasmacytoma (in MLN) | – |
| 70 | KO | 648 | Plasmablastic plasmacytoma (in MLN) | + |
| 93 | KO | 827 | Anaplastic plasmacytoma | + |
| 95 | KO | 820 | Anaplastic plasmacytoma | + |
| 97 | KO | 820 | Plasmacytoma (in MLN) | + |
| 103 | KO | 626 | Anaplastic plasmacytoma | – |
| 104 | KO | 625 | Precursor B cell lymphoma | n/d |
| 161 | KO | 602 | Precursor B cell lymphoma | n/d |
| 189 | KO | 769 | Precursor B cell lymphoma | + |
| 231 | KO | 737 | Mature B cell lymphoma | – |
| 254 | KO | 725 | Precursor B cell lymphoma | – |
| 261 | KO | 746 | Plasmablastic plasmacytoma (in MLN) | n/d |
| 269 | KO | 717 | No macroscopic tumor | + |
| 312 | KO | 921 | Mature B cell lymphoma | + |
| 332 | KO | 917 | No macroscopic tumor | + |
| 334 | KO | 891 | Anaplastic plasmacytoma | + |
| 180 | WT | 729 | No macroscopic tumor | + |
| 295 | WT | 926 | Mature B cell lymphoma | – |
| 325 | WT | 922 | Mature B cell lymphoma | n/d |
Histopathology of detected tumors and status of SPEP results.
MLN, Mesenteric Lymph Node; + indicates positive for M spikes; − indicates negative for M spikes as per SPEP analysis; n/d, not determined.
A characteristic of multiple myeloma, plasmacytomas and other plasma cell neoplasms is the secretion of immunoglobulin (Ig), detected in serum protein electrophoresis (SPEP) as Ig monoclonal bands (M-spikes) which is a routine method used in the clinic for the diagnosis of plasma cell dyscrasias. Serum samples were obtained from morbid mice prior to euthanasia whenever possible and those that survived to the end of the experimental period. SPEP analyses revealed M-spikes in multiple Cd19 Wwox KO mice (Figure 3A). In total 10 of 27 (37%) Cd19 Wwox KO mice but only 1 of 9 (11%) tested Cd19 Wwox WT control mice had detectable M-spikes. Full histopathologic analyses also indicated that some of the mice with M-spikes displayed evidence of myeloma cast nephropathy (myeloma kidney). This is characterized by the presence of obstructing casts in the lumen of kidney tubules. These eosinophilic (pink) deposits are formed by aggregates of monoclonal Ig light chains (Figures 3B–D).
Figure 3
Wwox Is Expressed in B Cells and Functions During Ig Class Switching
To address when during B cell development Wwox may be suppressing tumorigenesis, we first assessed normal Wwox expression in various B cell compartments. B cells from Pro-B, Pre-B, marginal zone, follicular B, germinal center (GC), plasmablast, and plasma cell compartments were purified from the spleen or bone marrow of wild-type mice. Wwox expression was analyzed by qPCR and compared to that of splenic CD8+ lymphocytes and CD11b+ leukocytes (Figure 4A). We find Wwox expression throughout B cell development including germinal center cells where Ig genes undergo mutagenic rearrangement. During Igh CSR, the enzyme AID (activation-induced cytidine deaminase) induces DSB in the switch regions, a process that is a significant source of genomic instability. To determine if Wwox functions during CSR we analyzed B cells for the ability to undergo proper CSR. Naïve (IgM+) B cells were isolated from the spleens of wild-type, Wwox KO and Wwox+/− 15 days old mice. Cells were cultured with LPS and IL-4 for 72 h to stimulate proliferation and CSR to IgG1. Cell proliferation was normal and flow cytometric analysis of cell surface antibody isotype expression revealed that Wwox KO cells supported IgG1 CSR at a rate of ~75% of wild-type controls (Figures 4B–D).
Figure 4
Wwox Deficiency Impairs C-NHEJ and Promotes Alt-NHEJ During Ig Class Switching
CSR requires end-joining between DSBs to exchange one isotype constant region for another. DSBs are induced and resolved during phase G1 of the cell cycle predominantly by the C-NHEJ pathway. In the absence of C-NHEJ, CSR is supported at a slightly reduced rate by alternative end-joining activity (Alt-NHEJ), with recombination junctions biased toward microhomology-mediated (MH) end-joining (MMEJ) (, –). To determine if Wwox deficiency altered C-NHEJ engagement we analyzed CSR junctions for MH usage following standard methods (–). To this end, the Sμ-Sγ1 junctions were amplified, PCR products were purified, cloned and sequenced from pools of B cells induced to undergo CSR to IgG. Sequence analysis of individual clones representative of both conditions (i.e., Wwox WT vs. Wwox KO B cells) revealed significant differences in the overall use of donor/acceptor homology at the CSR junctions (two-tailed Mann-Whitney test, p < 0.001). Wwox-deficient B cells displayed a significant shift toward microhomology (average MH Wwox WT 1.2 bp vs. Wwox KO 2.6 bp). Importantly, there was a significant decrease in blunt end joins (Wwox WT, 26 blunt of 77 total junctions [i.e., 33.8%] vs. Wwox KO, 5 blunt [8.2%] of 61 total junctions analyzed, p < 0.001 Fisher's exact test). Long MHs (>5 bp MH) were rare in WT B cells but significantly increased in Wwox KO B cells (Wwox WT, 1 of 77 [1.3%] vs. Wwox KO, 8 of 61 [13.1%], p < 0.01 Fisher's exact test) (Figure 5A and Supplementary Figure 2). The overall frequency of nucleotide insertions at CSR junctions was not significantly different, although Wwox KO B cells displayed a slight increase of insertions >1 bp (Figure 5A). Mutations occur in the vicinity of the junctions and are thought to be due to the AID induced mutational processes engaged during CSR (). Analysis of mutation frequency within 100 bp of the CSR junction revealed no difference between Wwox WT and Wwox KO (5.2 × 10−3 vs. 5.0 × 10−3 mutations/bp respectively, p = 0.8 t-test) (Figure 5B). We conclude that Wwox deficiency results in a significant shift toward MMEJ between switch regions, consistent with a shift toward the Alt-NHEJ pathway in the repair of AID induced DSBs.
Figure 5
Increased Translocations in Wwox KO B Cells Undergoing Class Switch Recombination
Although AID preferentially targets Ig genes, off-target AID activity can induce DSBs at other sites providing recombination substrates that result in characteristic chromosome translocations frequently found in B cell tumors (, ). One example is the oncogenic MYC/IGH translocation found in Burkitt's lymphoma and other B cell tumors. This translocation is mediated by AID induced DSBs at both MYC and IGH, with breaks in the MYC gene being rate-limiting (, ). Chromosome translocations display signatures of Alt-NHEJ repair in B cells while C-NHEJ suppresses translocation formation (). To determine if Wwox had a role in the incidence of spontaneous chromosome translocations during CSR, we used a previously described PCR/Southern blot assay to measure the frequency of AID induced Myc/Igh translocations (, ) (Figure 6A). It has been shown that naïve B cells do not harbor Myc/Igh translocations while cells induced to undergo CSR display translocations in an AID dependent fashion (, ). We observed that compared to Wwox WT, Wwox-deficient B cells had a significant 2.5-fold increase in spontaneous translocations (Figures 6B,C). Thus, we find that lack of Wwox expression is affecting the generation of spontaneous chromosome translocations, a process known to be promoted by the Alt-NHEJ pathway ().
Figure 6
Discussion
The incidence of plasma cell dyscrasias observed in our mouse model demonstrates that ablation of Wwox contributes to disease. Several mechanisms can mediate the loss of WWOX expression in human plasma cell dyscrasias including promoter methylation (), genomic deletions (, –) and translocations (, ). One translocation example, t(14;16), is known as a MM high-risk indicator (). The chromosome 16 breakpoints of t(14;16) are found within the WWOX gene and as a consequence structurally disruptive of the affected allele. The MAF locus, located 3' of WWOX, is brought within the influence of chromosome 14 IGH control elements and the resulting MAF overexpression has a causative role in MM. It is unclear however whether WWOX haploinsufficiency plays any role, or if silencing of the remaining allele via additional structural disruption (e.g., deletion) or epigenetic mechanisms is required in order to contribute to disease progression.
It has been shown that Wwox does not behave like a highly penetrant tumor suppressor gene [Reviewed in ()]. The limited tumor incidence, long latency and heterogeneity of neoplastic transformation in our mouse model suggests that additional secondary genetic events have to occur for full-blown malignancy to develop. Nevertheless, the lack of tumorigenesis when Wwox is conditionally deleted in various other tissues in mice with the same mixed genetic background as those here used () together with previous observations (, ), suggests that B cells are indeed a target tissue in which Wwox ablation contributes to neoplastic transformation.
Lymphocytes are unique in that they undergo programmed DNA damage during their receptor diversification processes. While T and B cells undergo V(D)J recombination only B cells undergo CSR and somatic hypermutation. The genomic instability induced by these B cell specific processes likely drives the imbalance of 95% of lymphomas being B cell derived with the majority being of post-germinal center origin (). During CSR, activation-induced cytidine deaminase (AID) induces DSB in the IGH switch regions to trigger recombination between isotype constant regions. The generation and resolution of these breaks occurs during the G1 phase of the cell cycle when NHEJ repair, but not homologous recombination, is readily available. Breaks randomly occur throughout each isotype switch region which are sequence diverse from each other. The result generates incompatible DSB end structures that require end-processing for ligation. The Ku70/80-mediated C-NHEJ pathway is the major pathway engaged during CSR. Recombination junctions normally lack microhomology consistent with the ability of C-NHEJ factors including XRCC4-DNA Ligase IV (Lig4) to process non-compatible ends (). If C-NHEJ is unavailable, CSR proceeds with reduced efficiency via Alt-NHEJ, which tends to utilize MMEJ (). We find that Wwox-deficient B cells support CSR at a slightly reduced rate and display MMEJ at recombination junctions consistent with Alt-NHEJ repair (). MMEJ is always mutagenic since extensive end resection occurs to find microhomologous regions with repair deleting some intervening sequence (). Alt-NHEJ has been implicated in chromosome translocations, as junction MH is a frequent feature of breakpoints and loss of C-NHEJ activity increases translocations (, ). For example, Ku70 or Lig4-deficient B cells generate frequent Myc/Igh translocations via an Alt-NHEJ joining mechanism (). Therefore, inappropriate usage of the Alt-NHEJ pathway has the potential to destabilize the genome. In this study, we find that Wwox deficiency increased generation of spontaneous B cell Myc/Igh translocations. This translocation is generated by AID induced DSBs at both Myc and Igh in primary B cells undergoing CSR (, ). Such translocation is a primary event in lymphomas such as Burkitt's and a common MM secondary event. Translocation capture assays show Myc/Igh to be indicative of genome wide Igh translocation and so determination of the spontaneous occurrence of such translocation event serves as a surrogate marker for overall genome instability (, ). In Wwox deficient B cells AID levels are not higher than WT (Supplementary Figure 3) and mutation frequency in the vicinity of recombination junctions is not increased. This further supports that Wwox deficiency influences DSB repair and not the mutation-generating machinery. Although AID is not expressed in MM cell lines, interaction of MM with dendritic cells in the in vivo microenvironment provides conditions that could induce AID expression and genomic instability (). Furthermore, mutational signatures from APOBEC deaminase family members are found in MM and are associated with poor prognosis (). Therefore, a primary event involving loss of WWOX could influence genome stability during periodic AID or APOBEC expression in MM.
The mechanism by which Wwox influences C-NHEJ and Alt-NHEJ during B cell CSR is not clear. Previous studies have indicated that WWOX deficiency in human cell lines results in genome instability and abnormalities in DNA damage repair pathways (, ). Abu-Odeh et al. have reported that WWOX depletion can lead to reduced ATM checkpoint kinase activation and impaired DNA repair (). In support of the observations here described, we have previously reported that WWOX depletion decreased C-NHEJ efficiency in human cell lines and is associated to the generation of phenotypes displaying increased resistance to the effects of DNA damaging agents (, ). However, WWOX function in B cells had not been previously examined. Since the DNA damage response is often dysregulated in cell lines, we here analyzed Wwox deficiency in primary B cells both in culture and in vivo. These results not only provide a clear and novel role for Wwox in B cell transformation and plasma cell dyscrasias but also further strengthen the notion of WWOX as an important player in maintaining genome integrity.
Statements
Data availability statement
All datasets generated for this study are included in the manuscript and/or the Supplementary Files.
Ethics statement
All animal research was conducted in facilities accredited by the Association for Assessment and Accreditation of Laboratory Animal Care International at the University of Texas MD Anderson Cancer Center, Science Park and all research was approved by the Institutional Animal Care and Use Committee.
Author contributions
CA and KM designed research. HK, YM, JP, JL, and MZ performed research. MS and CA performed pathology analyses. CA, MA, and KM analyzed the data. CA and KM wrote the paper.
Funding
. This work was partially supported by the grants from the Leukemia and Lymphoma Society Specialized Center of Research award #7016-18 (Project 2 to CA), Developmental Research Project from NIH/NCI P50 CA142509 to CA and The Three Strohm Sisters Family Foundation to KM.
Acknowledgments
We also acknowledge the University of Texas MD Anderson Cancer Center (UTMDACC) Research Animal Support Facility (P30 NIH CA16672), flow cytometry and cell imaging core (CPRIT RP170628), and molecular biology core.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fonc.2019.00517/full#supplementary-material
Supplementary Figure 1Mouse genotyping and Wwox expression ablation in B cells from Cd19 Cre+, Wwoxflox/flox mice. (A) PCR genotype analysis of DNA from two Cd19Cre/+;Wwoxwt/flox, two Cd19Cre/+;Wwoxwt/wt, and two Cd19Cre/+;Wwoxflox/flox mice as indicated. Genotyping was performed using Cre primers F; 5′ GCC TGC ATT ACC GGT CGA TGC AAC G 3′ and R; 5′ GTG GCA GAT GGC GCG GCA ACA CCA T 3′ generating a PCR product of 700 bp in size. For amplifying the Wwox wt and Wwox floxed loci we used primers Wwox-N1; 5′ ATG GGA CGA AAC TGG AGC TCA GAA 3′, Wwox-N2; 5′ TCA GCA ACT CAC TCT GGC TTC AAC 3′ and Wwox-L; 5′ GCA TAC ATT ATA CGA AGT TAT TCG AG 3′, as previously described (). The Wwox wt amplicon generates a 463 bp PCR product while the Wwox floxed allele generates a 344 bp product as indicated. (B) Representative immunoblot using Wwox antibody on protein extracts from FACS isolated Cd19+ B cells (first and fifth lanes) and from various other tissues (cerebellum, lung and kidney) from a Cd19Cre/+;Wwoxflox/flox(Cd19 Wwox KO) mouse and a Cd19Cre/+;Wwoxwt/wt(Cd19 Wwox WT) counterpart. As can be observed Wwox protein ablation is exclusive of B cells in the Cd19 Wwox KO mouse with other tissues expressing normal Wwox protein levels. Loading control using Actin antibody, lower panel.
Supplementary Figure 2Summary and alignments of CSR junctions. Summary table of number of clones with each type of junction. Representative alignments of a blunt, a 1 bp, a 2 bp, and all CSR junctions with more than 4 bp microhomology (MH). Sequence of a CSR junction (Blue, Middle) is aligned with germline switch donor (Top) and acceptor (Bottom) regions. Vertical lines denote identity between germline switch region and the sequenced CSR junction, bold lines mark continuous identity used to identify the breakpoint. Red denotes overlap between switch donor and acceptor region.
Supplementary Figure 3AID levels are not altered in Wwox KO B cells. Mouse splenocytes from wild-type (WT), AID KO (Aicda), or Wwox KO mice were cultured in LPS and IL-4 for 3 days. Anti-AID (Cell Signaling Technology L7E7) and anti-tubulin (Sigma) Western blot was performed on cell lysates and the relative signal ratio of AID to tubulin is displayed. Experiment representative of 3 independent experiments.
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Summary
Keywords
Wwox, B cells, monoclonal gammopathies, plasmacytomas, multiple myeloma, genomic instability
Citation
McBride KM, Kil H, Mu Y, Plummer JB, Lee J, Zelazowski MJ, Sebastian M, Abba MC and Aldaz CM (2019) Wwox Deletion in Mouse B Cells Leads to Genomic Instability, Neoplastic Transformation, and Monoclonal Gammopathies. Front. Oncol. 9:517. doi: 10.3389/fonc.2019.00517
Received
11 February 2019
Accepted
29 May 2019
Published
19 June 2019
Volume
9 - 2019
Edited by
Rongtuan Lin, McGill University, Canada
Reviewed by
Rami I. Aqeilan, Hadassah Medical Center, Israel; Jing Hong Wang, University of Colorado Anschutz Medical Campus, United States; Muhannad Mohammed Ali Abu-Remaileh, Dana–Farber Cancer Institute, United States; Omer Keinan, University of California, San Diego, United States
Updates
Copyright
© 2019 McBride, Kil, Mu, Plummer, Lee, Zelazowski, Sebastian, Abba and Aldaz.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Kevin M. McBride kmcbride@mdanderson.orgC. Marcelo Aldaz maaldaz@mdanderson.org
This article was submitted to Molecular and Cellular Oncology, a section of the journal Frontiers in Oncology
Disclaimer
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