Defects in the control of Wnt signaling have emerged as a recurrent mechanism involved in cancer pathogenesis and acute myeloid leukaemia (AML), including the hematopoietic regeneration-associated WNT10B in AC133bright leukaemia cells, although the existence of a specific mechanism remains unproven. We have obtained evidences for a recurrent rearrangement, which involved the WNT10B locus (WNT10BR) within intron 1 (IVS1) and flanked at the 5′ by non-human sequences whose origin remains to be elucidated; it also expressed a transcript variant (WNT10BIVS1) which was mainly detected in a cohort of patients with intermediate/unfavorable risk AML. We also identified in two separate cases, affected by AML and breast cancer respectively, a genomic transposable short form of human WNT10B (ht-WNT10B). The intronless ht-WNT10B resembles a long non-coding RNA (lncRNA), which suggests its involvement in a non-random microhomology-mediated recombination generating the rearranged WNT10BR. Furthermore, our studies supports an autocrine activation primed by the formation of WNT10B-FZD4/5 complexes in the breast cancer MCF7 cells that express the WNT10BIVS1. Chemical interference of WNT-ligands production by the porcupine inhibitor IWP-2 achieved a dose-dependent suppression of the WNT10B-FZD4/5 interactions. These results present the first evidence for a recurrent rearrangement promoted by a mobile ht-WNT10B oncogene, as a relevant mechanism for Wnt involvement in human cancer.
A longstanding question in cancer biology has been the nature of mechanisms that control initiation and growth of a hierarchically organized population of cells sustained by cancer stem cells (CSCs) at their apex1. It is well established that canonical Wnt signalling plays a major role in fuelling stem cell activity and sustaining tissue regeneration2,3 in a dose dependent manner in several adult stem cell niches including bone marrow4,5,6 and mammary gland7. Wnt proteins have also been extensively studied in connection with malignancy8,9 and they are causatively involved in the development of several types of leukaemias10,11,12,13,14,15. Nontheless, it remains unclear both what molecular features govern the specific functional properties of leukaemia initiating cells (LIC) and which genome-destabilizing processes promote leukaemia stemness16.
Recent insights into regenerative processes point to WNT10B as a candidate potentially linking tissue regeneration and cancer2,17,18,19. We recently reported evidence supporting the influence of the haematopoietic regeneration-associated WNT10B on AC133bright cells in human AML via an autocrine/paracrine loop20.
Results and Discussion
Transient wnt10b overexpression in zebrafish embryos promotes the accumulation of haematopoietic precursors
To asses if the reported WNT10B-overexpression in the hematopoietic microenvironment could be an important perturbing factor of myeloid cells and a possible adjuvant in AML development, synthetic mRNA was microinjected in the zebrafish zygote in order to determine the effects of transient wnt10b overexpression on early haematopoiesis. This was performed to mimic, in vivo, the Wnt pathway aberrant deregulation observed in the leukaemia bone marrow micro-environment. The injected embryos displayed developmental defects, such as expansion of the ventral tissues, dorsalization, and lack of the anterior-most cephalic regions, which was to be expected from the excessive activation of the Wnt pathway21. Remarkably, we also observed the expansion of the posterior blood island (PBI), and the caudal-most haematopoetic tissue hosting erythromyeloid progenitors, which suggest some effect on haematopoiesis (data not shown). We therefore focused on the consequences of wnt10b upregulation by analyzing the expression of scl (Fig. 1a), pu.1 (Fig. 1b), and gata1 (Fig. 1c), which are, respectively, distinctive markers of erythromyeloid, myeloid, and erythroid progenitors22. Our results show that elevated wnt10b expression caused the expansion of these cell populations (Fig. 1a–c and Supplementary Fig. 1a–d). While the number of progenitors increased, that of circulating neutrophils (Fig. 1d) reduced markedly (Fig. 1e) in the transgenic line expressing GFP under the neutrophil-specific myeloperoxidase (mpx) promoter. These findings indicate that wnt10b overexpression promotes the accumulation of haematopoietic precursors at the expense of more differentiated cell types, resembling conditions, such as pre-leukemic expansion of haematopoietic stem cell (HSC), which are characterized by an imbalance between immature and differentiated blood cells23. Taken together, these results support a critical role for wnt10b in haematopoietic progenitors homeostasis.
Identification of recurrent rearrangement generating the WNT10BR allele
To assess a possible involvement of a key genetic event behind the deregulated WNT10B expression observed in AML, we first performed on leukemic bone marrow mononuclear cells (BMNCs), a single-primer extension/amplification of the 5′ flanking sequences upstream of exon 2 which contains the starting codon of WNT10B (Fig. 2a), in a representative cohort of Italian AML patients and healthy donors (Supplementary Table 1).
A single amplification product of 400 bp was observed in genomic DNA (Fig. 2a) in all intermediate-adverse risk AML patients; subsequent sequence analysis revealed the insertion of a non-human DNA segment located 77 nucleotides upstream the end of IVS1 after a short G-rich stretch (Fig. 2b). The origin of the non-human DNA extending to the 5′ of WNT10BR locus (Fig. 2b) could not be identified, but it resembles transposable DNA.
A 5′ RACE and WNT10B-alleles specific expression analysis were performed on the same cohort of patients in order to test for the presence of an expressed form derived from the rearranged allele observed in genomic DNA within IVS1. As previously observed, the normal WNT10B allele was expressed in all AML patients but not in BMNCs of healthy donors20. Conversely, the rearranged form, hereafter named WNT10BIVS1, was expressed exclusively in patients harboring the corresponding rearrangement in the genomic DNA (Fig. 2a). Analysis performed on the AC133-positive leukemic cell fraction reported the same results observed on the whole MNCs.
WNT10B/WNT10BIVS1 expression ratio match with WHO risk stratification
In order to determine the prevalence of the genomic WNT10BR allele, we retrospectively investigated the WNT10B pattern of rearrangement acquisition on mononuclear cells from an Italian cohort of 125 AML patients (Supplementary Table 1 and Supplementary Fig. 2a–f). We analyzed the relative expression of the two transcript variants WNT10B and WNT10BIVS1 by Droplet Digital™ PCR (ddPCR) in the leukaemic patient population classified according to the scoring system of the Medical Research Council (MRC), the European LeukemiaNet (ELN), and the National Comprehensive Cancer Network (NCCN) scoring systems (Supplementary Figs 3a–f, and 5a–f). WNT10B was highly expressed in all groups, while WNT10BIVS1 expression was associated only with the intermediate/unfavourable-risk groups (Fig. 3a–d, and Supplementary Fig. 4a–d). Samples from individuals who developed a therapy-related AML (t-AML) were negative for both WNT10B (p < 0.002, Fig. 3e and Supplementary Fig. 4d,e) and WNT10BIVS1 alleles (p < 0.0005, Fig. 3d,f and Supplementary Fig. 4,f). These results therefore, evidenced a WNT10BR frequency of 56% in the present AML cohort, and link the WNT10B/WNT10BIVS1 expression pattern to the WHO risk stratification greatly strengthening the idea that this new genetic abnormality against WNT10B locus may have a role supporting the leukemic clone in clinical context without recurrent cytogenetic abnormalities (Fig. 3g,h). Furthermore, statistical analysis showed no significative difference for both WNT10B and WNT10BIVS1 levels according to FLT3-ITD (p 0.8818 and p 0.1271 respectively; Kruskal-Wallis test) and to KIT mutational status (p 0.4561 and p 0.4871 respectively; Kruskal-Wallis test).
We demonstrated transcripts in situ with specific padlock probes and target-primed rolling-circle amplification (RCA) in order to assess the distribution and localization of the WNT10B/WNT10BIVS1 mRNAs in AML bone marrow sections using an independent, non-PCR-based technique. Reassuringly, we obtained abundant signals from both transcripts in bone marrow sections from two independent AML patients, visualizing both transcriptional variants with similar detection efficiency (Fig. 4a,b and Supplementary Fig. 5).
Two prototypic cases (t-AML#6, AML#280, Supplementary Table 2) were found within the leukemia patients in this study who were diagnosed with t-AML after a personal history of breast cancer treated with chemotherapy (CMT) or radiation therapy (XRT) respectively. We investigated both the presence of the rearranged WNT10BR allele and the expression of WNT10BIVS1 in breast cancer tissues (T) and surrounding normal tissues (N) as well as in leukemia blasts (MNC) sampled at diagnosis (Fig. 4c,d).
In the case treated with XRT alone (AML#280), we could detect the presence of both the genomic WNT10BR allele and the expression of the related WNT10BIVS1 transcript in non-familial breast cancer (NFBC) tissue, but not in normal surrounding tissues, which was present also in the secondary AML sample at diagnosis three years later (Fig. 4c).
In contrast, the case affected by familial breast cancer (FBC) resulted negative for the presence of the WNT10BR genomic allele both in the breast cancer specimen and in the t-AML, which developed five years later following CMT (Fig. 4d).
These results were of particular interest considering recent observations that suggest AML diagnosed in patients after receiving XRT alone differ from t-AML occurring after CMT, and share genetic features and clinical behaviours with de novo AML24.
Identification of the intronless short form ht-WNT10B
Recent results in breast cancer research support the rationale that the WNT10B/β-catenin/HMGA2 axis has a functional role in highly aggressive triple-negative breast cancers (TNBC) in humans19. This led us to assume an integration event consistent with MMTV-viral activation of the Wnt-10b locus in mice, and to link its overexpression to a high transforming potential in the mammary gland25. We therefore analyzed the coding region of WNT10BR allele to assess the origin of the observed site-specific integration mechanism.
Amplification of the entire coding region using a primer pair specifically designed to detect the WNT10BR allele shows the expected 4,6-kb fragment in the samples we had previously shown to harbor the presence of the abnormal rearrangement (intermediate-unfavorable risk patients) (Fig. 4e).
In addition to this fragment, that represents the rearranged allele, an extra amplicon was observed in the lane for the patient sample AML#9 (Fig. 4e). Sequence analysis of this extra band revealed the existence on the genomic level of an intronless WNT10B oncogene short form, hereafter named human transposable-WNT10B (ht-WNT10B). Specific RT-PCR analysis showed that ht-WNT10B is currently being expressed (Fig. 4e lower panel). Additionally, in the course of screening an Italian cohort of 35 de novo breast cancer patients (manuscript in preparation) we detected the same ht-WNT10B genetic element in one independent non-familial breast cancer patient (NFBC#29, Fig. 4f, and Supplementary Table 3).
Furthermore, in both cases in which ht-WNT10B was isolated, the sequence analysis revealed the absence of exons 1 and 4, and the presence of a G/A single nucleotide variation at the junction of exons 2 and 3 flanked at 5′ by the same 77 IVS1 nucleotides followed by non-human DNA as observed in WNT10BR (Fig. 4g). This genetic element, resembling a long noncoding RNA (lncRNAs)26,27, is expressed as a single transcript containing the short form of WNT10B oncogene described here; a non-functional protein is predicted in silico however. For the first time these observations revealed the existence of a short version of the WNT10B oncogene, rarely integrated at the DNA level, which points to its potential involvement in the WNT10BR generation by non-random microhomology-mediated recombination as recently suggested in virus-mediated integration28.
Identification of the WNT10B-FZDs interacting complexes by in situ PLA in the MCF-7 cell line carrying the WNT10BR
WNT molecules can signal via binding to members of the seven-transmembrane-spanning Frizzled (FZD) receptors. Despite the involvement of aberrant Wnt signaling in a variety of human cancers, relatively little is known about the role of such receptors in cancer pathogenesis. Although we recently confirmed higher expression for FZD4 in AML20,29, it is still not known which FZD receptor(s) bind WNT10B. The MCF7 breast cancer cell line was selected for functional studies since it expresses the WNT10BIVS1 allele. By culturing them in conditions that form spheres they exhibit more cancer stem cell like features, e.g. expressing AC133+ that we in AML correlates to a cell population that responds to WNT10B via an autocrine/paracrine loop8.
In order to visualize interactions between WNT10B and FZD4/5/6 we used proximity ligation assay (PLA) (Fig. 5a) in both adherent cultures and in tumorspheres which are significantly enriched for AC133 on MCF7. Compaction of the RCA products, resulted in high intensity signals, were detected for WNT10B-FZD4/5 complexes, both in tumorsphere (Fig. 5b,d,h) and in adherent (Fig. 5c,e,h) MCF7 cells (Extended data Fig. 6a,b,d,e). In contrast, in situ PLA analysis of WNT10B-FZD6 interaction, did not generate specific detection signals (Fig. 5f,g) in the MCF7 cell system (Supplementary Fig. 6c,f). Co-immunoprecipitation was performed to confirm the PLA results (Fig. 5i).
Finally, we used the IWP2 compound acting on the acyltransferase Porcupine30 (Fig. 5l) to selectively inhibit the Wnt autocrine loop since small molecule inhibitors of regulatory events underlying production of WNT proteins facilitate a chemical-based interrogation of pathway function. The level of in situ PLA signals for WNT10B-FZD4/5 was reduced in IWP2-treated cells in a dose-dependent manner (Fig. 5m).
These results not only point to FZD4/5 as WNT receptors specifically synergizing with WNT10B, but they also confirm an autocrine mechanism for Wnt signaling activation in a cellular model characterized by the presence of the rearranged WNT10BR allele.
Overall, our data demonstrate the existence of a mobile element containing a ht-WNT10B short form, whose precise origin is unknown as are mechanisms involved in the transmission of this genetic element. These findings are consistent with recent evidence showing that exogenous DNA integrates in human somatic genomes more frequently in tumors than normal samples31. It is possible that viral and/or bacterial integrations by lateral gene transfer may lead to altered gene expression mainly in AML and breast cancers, as supported by recent data32. This would provide an additional avenue for viral/bacteria-associated oncogenesis, beyond inflammation-induced damage33.
Fish and embryos maintenance
Embryos were handled according to relevant guidelines. Fish were maintained at 28 °C on a 14-hour light/10-hour dark cycle and collected by natural spawning.
We used embryos from the AB strain and mpx:GFP34 and gata1:DsRed35 transgenic lines. Our facility strictly complies with the relevant Italian laws, rules and regulations (Legislative Decree No. 116/92), as confirmed by the authorization issued by the municipality Milan (Art. 10 of Legislative Decree No. 116, dated 27.1.1992). All of the procedures were carried out in accordance with the relevant guidelines and regulations.
wnt10b cDNA cloning and transcription
Two specific primers (Zf_P1 and Zf_P2, See Extended Table 4) were used to amplify the wnt10b ORF using reverse transcribed total RNA extracted from zebrafish embryos and larvae at 24–96 hours post fertilization (hpf). The obtained cDNA fragment was gel purified and cloned into pCMV–SC (Stratagene, Agilent Technologies, Santa Clara, CA, USA). Capped mRNA was transcribed using the mMessage mMachine Kit (Ambion, Austin, TX-Thermo Fisher Scientific) according to the manufacturer’s instructions. All control embryos were obtained injecting the zygote with GFP or DsRed synthetic mRNA, depending on the fluorescence of the transgenic lines under analysis.
Microinjection and analyses
wnt10b transcript microinjections were carried out on 1- to 2-cell stage embryos using 400 pg of capped mRNA per embryo.
Whole mount in situ hybridization (WISH) was performed as previously described36 on embryos collected at the desired developmental stages and fixed in 4% paraformaldehyde/phosphate buffered saline, using scl37 and pu.138 DIG-labeled riboprobes.
Live imaging of transgenic embryos was carried out using the Zeiss Axiovert 200 M. To determine the number of neutrophils in the mpx:GFP transgenics each embryo was photographed on 4–5 different focal planes, then the pictures were assembled in a single image on which the cell count was performed using the ImageJ 1.47 software.
Patients and Sample Collection
We collected BM MNCs from n = 125 AML patients at diagnosis and according to the 2015 National Comprehensive Cancer Network (NCCN) classification, samples included n = 48 favorable risk, n = 70 intermediate-adverse risk and n = 7 Therapy-related (t-AML) AML patients. We collected also one prototypic case resulted affected by t-AML after a personal history of breast cancer followed and radiation therapy (XRT). Patients’ characteristics are shown in Extended Table 1 and Extended Table 2. Human BM cells obtained from n = 6 healthy donors were also collected. Each patient gave his/her informed consent for collection of clinical data, the cryopreservation of bone marrow samples and the performance of DNA-analysis for scientific purposes, in accordance with institutional guidelines. For each patient, data regarding history, haematologic parameters, bone marrow morphology, immunophenotype, cytogenetic, molecular analysis, and diagnosis of extra-medullary leukemia were recorded. Treatment schedule and outcome data were available for 116 out of 125 patients.
Besides, in this study, n = 2 non-familial breast cancer patients (NFBC) were recruited from Niguarda Hospital, Milan (Italy). Tumor and adjacent normal tissues of the same patient were obtained during resection and immediately snap-frozen in liquid nitrogen. Patients’ clinical and histopathological informations are summarized in Extended Table 3. The study design adhered to the Declaration of Helsinki and approval for this study was obtained from the Niguarda Hospital Review Board (116_04/2010).
Definitions and criteria for treatment response
Complete remission (CR) was defined as less than 5% of bone marrow blasts, regression of extramedullary disease, transfusion independency with peripheral neutrophil count greater than 1000/μL and platelet count greater than 100000/μL and disappearance of the cytogenetic and molecular markers. Recurrent disease is defined as the reappearance of ≥5% blasts in the bone marrow or in the peripheral blood or as the appearance of a new extramedullary site of disease in patients with a previously documented CR. Extramedullary disease was defined as any leukemic collection outside the bone marrow and its presence was documented either by histological, cytological or radiological criteria.
Overall survival (OS) was calculated from the date of diagnosis until death, where all living patients were censored at the time of last contact. The duration of CR was calculated from the date of the first CR until the date of the first relapse. Relapse-free survival (RFS) was calculated from the date of the first CR until the date of the first relapse, where patients were censored at the time of last contact or death not due to recurrent disease.
5′ WNT10B Flanking Region analysis
Single Primer PCR
Genomic DNA was recovered using Dnazol (Invitrogen, Thermo Fisher), following manufacturer’s instructions. The reaction mixture of the Single Primer-PCR39 contained, in a total volume of 30 μl, 3 ng of DNA, 3 μl of 10X M-Buffer (500 mM Tris, 2.5 mg/ml BSA, 20 mM MgCl2, 5% Ficoll and 5 mM Cresol Red), 3 μl of 5 μM 1 P Primer and 3 μl of T/TS [10.5 ul of 2.5 mg/ml of BSA diluted in 100 mM Tris, 1 μl Taq Pol and 1 μl Hotstart Taq Pol, (NEB New England Biolabs, Mississauga, ON, Canada)]. The amplification was carried out in a Veriti thermal cycler (Applied Biosystems) as follows: 94 °C for 30 s, 20 cycles at 94° for 0 s, 55 °C for 0 s and 72 °C for 60 s; 30 cycles at 94° for 0 s, 55 °C for 0 s and 72 °C for 60 s; 30 cycles at 94° for 0 s, 55 °C for 0 s and 72 °C for 60 s. The PCR product was then analyzed by electrophoresis through a 1% agarose gel.
The purified templates were dissolved in sterile water and the Applied Biosystems Big-Dye ver. 1.1 chemistry kit was used to perform the sequencing reactions. Sequences were analysed on ABI3130XL automatic sequencers (Applied Biosystems, Foster City, CA, USA).
WNT10B/WNT10BIVS1 Gene expression analysis
Total RNA was extracted using the RNAqueous-4PCR kit following the manufacturer’s instructions (Ambion, Austin, TX-Thermo Fisher Scientific), and then were reverse transcribed with RT mixtures containing 500 ng of RNA, 100 U Improm II (Promega, Madison, WI, USA), 1x buffer, 1 mM dNTPs, 5 mM MgCl2, and 0.5 μg of P5 reverse primer in a total volume of 20 μl for 5 min at 25 °C and then 60 min at 42 °C. The reaction was terminated by heating at 75 °C for 5 min. All PCRs were performed containing 5 μl of DNA as template, 5X Green GoTaq Buffer (Promega Corporation, Madison, WI, USA), 4 mM of MgCl2, 0.2 μM of each primer, 0.2 mM dNTPs (Promega), 0.5 U of Taq DNA polymerase (Promega), and water to a final volume of 50 μl. The GAPDH retrotranscription was performed using random primers. The WNT10B (P4-P2 primers) amplification was performed with following thermal conditions: 94 °C for 1 min, 33 cycles at 94° for 30 s, 58 °C for 30 s, 72 °C for 30 s and 72 °C for 5 min. The amplification of WNT10BIVS1 (P3-P2 primers) was performed as follows: 94 °C for 1 min, 33 cycles at 94° for 30 s, 61 °C for 30 s, 72 °C for 30 s and 72 °C for 5 min. The GAPDH (P6-P7 primers) housekeeping gene amplification was carried out in a thermal cycler as follows: 94 °C for 1 min, 30 cycles at 94° for 20 s, 60 °C for 15 s, 72 °C for 15 s and 72 °C for 5 min. Primers are listed in Extended Table 4. At the end the PCR products were analysed by electrophoresis through a 2% agarose gel.
WNT10B/WNT10BIVS1 Absolute quantification
In our study, ddPCR40 experiments were performed in blind way at the BIORAD laboratories (Milan, Italy) using primers and probes listed in Extended Table 4. The 0.1 mM RNA, extracted using the RNAqueous-4PCR kit following the manufacturer’s instructions (Ambion, Austin, TX-Thermo Fisher Scientific), was denatured at 95 °C for 5 min and kept on ice prior addition to the reaction. We performed the experiment on Bio-Rad’s QX100 ddPCR system and the reaction mixtures in a final 20 μl volume consisted of 10 μl of 2× One-Step RT-ddPCR Supermix (Bio-Rad, CA, USA), 1 mM Manganese Acetate solution (Bio-Rad, CA, USA), 0.5 μM of primers (WNT10B: P4-P2, WNT10BIVS1 P3-P2), 0.25 μM WNT10B_dd1 and WNT10BIVS1_dd2 probes. The 20 μL ddPCR reaction mixture was then loaded into the Bio-Rad DG8 droplet generator cartridge (Bio-Rad, CA, USA). Then, each oil well was filled with 70 μl of droplet generation oil (Bio-Rad, CA, USA) and the prepared cartridge was then loaded into the QX100 droplet generator (Bio-Rad, CA, USA). The generated droplets were transferred to a 96-well PCR plate, and then samples were amplified on the T100 BioRad thermal cycler. The thermal cycling conditions consisted of 30 min reverse transcription at 60 °C, 5 min initial denaturation at 95 °C, followed by 40 cycles of a two-step thermal profile of 30 s denaturation at 94 °C and 60 s annealing-elongation at 60 °C and a final 10 min denaturation step at 98 °C. Then plates were transferred to the QX 100 droplet reader (Bio-Rad, CA, USA) and ddPCR data were analyzed with QuantaSoft analysis software (version 1.7.4).
All collected variables were submitted to usual descriptive methods. In particular, for continuous variables the distribution was firstly evaluated by the Shapiro-Wilk test, so that normally distributed variables were summarized with mean and standard deviation, while non-normal variables were summarized with median and range. The Pearson’s chi-square test with Yates’ correction for continuity and the Fisher’s exact test were used to check the association between categorical data, after cross-tabulation. Comparisons of normally distributed continuous variables were carried out by Student’s t-test or by Welch test (in the case of non-homogeneous variances between groups, previously verified by Levene’s test). The Kruskal-Wallis test and the Mann-Whitney U-test were used for comparison of continuous non-normally distributed variables.
The survival analysis was carried out using the Kaplan-Meier product limit method, followed by the logrank test, to evaluate the possible differences in survival between groups. Cox univariate and multivariate regression models were also used to analyse the effects of continuous variables on survivorship. The optimal multivariate model was chosen using a backward stepwise elimination after inserting all variables showing p < 0.20 at univariate analysis.
The receiver operating characteristics curve (ROC) was traced to analyse the role of WNT transcript levels on survivorship and to search for an optimal cut-off value for WNT transcript itself. For all possible cut-off points, the total accuracy was considered together with sensitivity, specificity, positive predictive value and negative predictive value; however, the choice was made according to Youden.
Statistical analysis was done using MedCal 188.8.131.52 and statistical significance was assumed for all tests with p < 0.05.
Patients subgroups were identified in gene expression data using consensus clustering, named “clustercons”, by R-package. Corresponding scatterplots were produced using the scatterplot3d (https://cran.r-project.org/web/packages/scatterplot3d/index.html).
mRNA in situ detection
All mRNA in situ experiments were performed according to Larsson et al.41 with modifications, in ordinance with guidelines established in the related patent (US 8551708 B2). Informed consents for in situ expression analysis on bone marrow biopsies were obtained, this study was approved by the Niguarda Hospital Review Board (116_04/2010).
Bone marrow biopsies of AML patients, previously embedded in paraffin blocks, were cut in 5 μm thick sections and mounted on slides. Slides were dewaxed as follows: twice in 100% xylene for 15 minutes and 10 minutes, twice in 100% EtOH for 2 minutes, twice in 95% EtOH for 2 minutes, twice in 70% EtOH for 2 minutes, and washed in DEPC-H2O for 5 minutes and in DEPC-PBS for 2 minutes. Tissue fixation was performed in 3.7% (w/v) paraformaldehyde in PBS for 10 minutes at room temperature. After a wash in DEPC‐PBS for 2 minutes, the tissue sections were then permeabilized with 2 mg/ml pepsin (Sigma Aldrich, St. Louis, US) in 0.1 M HCl at 37 °C for 2 minutes. Slides were washed in DEPC-H2O for 5 minutes, in DEPC-PBS for 2 minutes and then fixed in 3.7% (w/v) paraformaldehyde in PBS for 10 minutes at room temperature. Tissue sections were then dehydrated through a series of 70%, 85% and 100% ethanol for 1 min each. The in situ reactions were carried out with a reaction volume of 100 μl in secure-seals (13 mm in diameter and 0.8 mm deep; Grace Bio-Labs) mounted over the tissue. One μM of locked nucleic acid (LNA)-modified cDNA primer (Exiqon, Vedbaek, Denmark; P8 and P9, see Extended Table 4) was added to the slide with 10 U/μl of M‐MULV reverse transcriptase (Fermentas), 500 nM dNTPs (Invitrogen), 0.2 μg/μl BSA (New England Biolabs, NEB) and 1 U/μl RiboLock RNase Inhibitor (Fermentas) in the 1X M-MULV reaction buffer. Slides were incubated for 3 hours at 37 °C. After incubation, slides were washed in PBS-T (DEPC‐PBS with 0.05% Tween20), followed by a post-fixation step in 3.7% (w/v) paraformaldehyde in DEPC‐PBS for 30 min at room temperature. Then the samples were washed twice in DEPC PBS-T. Ligation was then carried out with 0.1 μM of the β‐actin, WNT10B and WNT10BIVS1 padlock probes (Sigma-Aldrich, St Louis, MO; PP1, PP2 and PP3, see Extended Table 4) and in a mix of 0.5 U/μl Ampligase (Epicentre), 0.4 U/μl RNase H (Fermentas), 1 U/μl RiboLock RNase Inhibitor (Fermentas), Ampligase buffer, 50 mM KCl and 20% formamide. Incubation was performed first at 37 °C for 30 minutes, followed by 45 minutes at 45 °C. After ligation reaction, the slides were washed twice in DEPC-PBS with 0.05% Tween20 and then the Rolling Circle Amplification (RCA) was performed with 1 U/μl DNA Polymerase (Fermentas) in the supplied reaction buffer, 1 U/μl RNase Inhibitor (Fermentas), 250 μM dNTPS (Invitrogen), 0.2 μg/μl BSA (NEB) and 5% glycerol. Incubation was carried out for 7 hours at 37 °C, and it was followed by a twice wash in PBS-T. Rolling Circle Particles (RCPs) were visualized using 100 nM of detection probe (Sigma-Aldrich; DP1 and DP2, see Extended Table 4) in 2X SSC and 20% formamide at 37 °C for 20 minutes. Slides were then washed in DEPC-PBS. Nuclei were counterstained with 100 ng/ml Hoechst 33258 (Sigma‐Aldrich). The Secure-seals were removed and the slides were dehydrated using a series of 70%, 85% and 100% ethanol for 3 minutes each. The dry slides were mounted with Invitrogen Slowfade. Images of bone marrow tissue slides were acquired using an Axioplan II epifluorescence microscope (Zeiss) equipped with a 100 W mercury lamp, a CCD camera (HRM, Zeiss), and a computer-controlled filter wheel with excitation and emission filters for visualization of DAPI, Cy3, and Cy5 at room temperature of 25 °C. A x20 (Plan Apocromat, Zeiss) and x40 (Plan Neofluar, Zeiss) objective were used for capturing the images. Images were collected using the Axiovision software (release 4.3, Zeiss). Exposure times for slides images were 520–680 ms (at 20X magnification), 320–480 ms for DAPI; 300–650 ms for Cy3; 580 ms for Cy5. Images were collected as z-stacks to ensure that all RCPs were acquired, with a maximum intensity project (MIP) created in Axiovision. For quantification, the numbers of RCPs and cell nuclei in three different images were counted digitally using CellProfiler (www.cellprofiler.org) on three x20 microscope images. The average for each sample was then calculated from the result of the three images and is reported as RCPs per cell. The threshold for different color channels was set with ImageJ 1.41.
Molecular characterization of WNT10BR and htWNT10B
All WNT10BR and ht-WNT10B genomic amplifications were performed using the reaction mixture of 50 μl consisted in 500 ng of DNA, 1× GoTaq Buffer, 1.5 mM MgCl2, 0.2 μM of P2, P1 and P5 primers listed in Extedended Table 4, 0.5 mM of dNTPs and 1U of TaqDNA Polymerase (Promega, Madison, WI, USA). Total RNA was extracted and reverse transcribed using the protocol previous described and PCRs were performed in a final volume of 50 μl containing 5 μl of DNA as template, 5X Green GoTaq Buffer (Promega Corporation, Madison, WI, USA), 4 mM of MgCl2, 0.2 μM of each primer, 0.2 mM dNTPs (Promega), 0.5 U of Taq DNA polymerase (5 U/μl; Promega). The amplifications were performed with following thermal conditions: P2-P1, 94 °C for 3 min, 30 cycles at 94° for 30 s, 58 °C for 30 s, 72 °C for 30 s and 72 °C for 5 min; P2-P10, 94 °C for 5 min, 33 cycles at 94° for 30 s, 59 °C for 45 s, 72 °C for 5 min and 72 °C for 10 min. Then the PCR products were visualized by 0.8% and 1.5% electrophoresis agarose gels and sequenced using the chemistry described above. The obtained P2-P10 fragment was gel purified and cloned into TOPO® TA Cloning® Kit (Invitrogen, Carlsbad, CA). We amplified GAPDH as housekeeping gene, following the protocol described above.
MCF-7 Adherent and Tumorspheres cell culture
The human breast adenocarcinoma cells (MCF-7) were purchased from ATCC (Manassas, VA) and was authenticated by STR profiling, using the AmpFlSTR® Identifiler kit and tested for mycoplasma (MycoProbe from RnD # number CUL001B). We grew MCF-7 cells in T-25 flasks (Corning) in DMEM (Gibco), supplemented with 10% (v/v) fetal bovine serum (FBS), 10 μg/ml insulin, 2 mM L-Glutamine and 0.02 μg/ml epidermal growth factor (EGF) (Sigma-Aldrich, USA). For slide preparation we trypsinized cells and seeded them into eight-well chamber slides (Lab-Tek, Nunc), allowing theme to adhere for 48 h. At the second day, medium was then aspirated and cells were fixed in 3.7% formaldehyde solution for 30 min on ice. Then, after a step to was away residual of fixative solution, we dried slides in absolute ethanol and stored them at −20 °C until further use. In order to generate tumorspheres, adherent cells were trypsinized with 0.05% Trypsin-EDTA (Gibco), washed three times with calcium-magnesium-free PBS and after adding 2 mL of DMEM/F12, tumorspheres were dissociated by gentle pipetting42. Cells are then seeded at concentration of 5 × 104 cells/ml in low adherent T-25 flasks (Corning, Manassas, VA), in NSA media [DMEM/F12, (Gibco), 20 ng/mL EGF (Sigma), 10 ng/mL recombinant human basic fibroblast growth factor bFGF (R&D Systems), 4 μg/ml heparin (Sigma), 10% human NeuroCult® (Stem Cell Technologies)], 0.15% bovine serum albumin BSA (Sigma) and 1% penicillin G-streptomycin solution (Gibco). Cells were grown at 37 °C in a humidified atmosphere with 5% CO2, for 6 days.
Inhibition of WNT palmitoyltransferase
MCF-7 cells were plated at a concentration of 1 × 103 cells/well on Lab-Tek II (Nunc) chamber slides. Cells were serum starved for 48 h and then the Wnt palmitoyltransferase inhibitor (IWP-2), (Sigma Aldrich, St. Louis, MO, USA) was used at 0 μM, 3 μM, 5 μM, 7 μM concentrations to treat cells, in a dose dependent manner.
In situ Proximity Ligation Assay
In situ PLA was performed according to the manufacturer’s instructions (Olink Bioscience), briefly the cells were permeabilized with 0.5% Triton X-100 for 10 min at room temperature (RT) and washed two times for 5 min in PBS. Slides were incubated with blocking solutions for 1 h at 37 °C and then were incubated with the primary antibodies (mouse monoclonal α-WNT10B [5 A7], Abcam; rabbit polyclonal α-FZD4, Abcam; rabbit polyclonal α-FZD5, Abcam; rabbit polyclonal α-FZD6 ThermoFisher Scientific) diluted in Duolink Blocking Solution (Olink Bioscience) for 2 h at room temperature. After overnight incubation at 4 °C with the antibodies, the samples were washed three times for 5 min in TBS plus 0.05% Tween 20 and therefore Duolink secondary probes Anti-Rabbit (Minus) and Anti-Mouse (Plus) probes (Olink Bioscience) were diluted (1:5) in Duolink Antibody Diluent (Olink Bioscience) and incubated over slides for 1 h at 37 °C. Then the slides were washed three times in TBS plus 0.05% Tween 20 for 10 min. Duolink ligase was added in Duolink Ligation Mix diluted to 1× in high purity water and then incubated for 30 min at 37 °C. Then samples were washed gently two times for 2 min in TBS plus 0.05% Tween 20 before the following amplification step. We performed the RCA with 25 nM of the compaction oligonucleotide43 (oligonucleotides C1 and D1, See Extended Table 4). The RCA took place in the presence of 25 nM of detection oligonucleotides in a RCA buffer containing 0.25 mg/ml BSA, 7.5 ng/ml poly-adenosine, 1× phi29 DNA polymerase buffer (Fermentas), 0.25 mM dNTPs (Thermo Scientific) and 0.25 U/μl phi29 DNA polymerase, followed by incubation at 37 °C for 1 h. In order to stain nuclei, we used 100 ng/ml of Hoechst (Sigma-Aldrich) and samples were incubated for 10 min at RT and then washed two times for 5 min each with TBS plus 0.05% Tween 20 and finally 5 min with TBS. After washing we dehydrated the slide by washing with an EtOH solution (70% EtOH and 30% TBS) for 2 min and secondly with a 99% solution of EtOH for 2 min. Slides were mounted with SlowFade Gold mounting medium (Invitrogen). Technical controls of isPLA, based on the omission of first antibodies in order to exclude possible cross-reactivity of secondary antibodies or non-specific PLA-signal generation, were performed (data not shown). The images were acquired as z-stacks with Zeiss AxioPlan2 microscope with a 20×/0.8 Plan-Apo objective and an Axiocam MRm camera and processed with Zeiss AxioVision 4.8 software at room temperature of 25 °C. In order to quantify RCPs/cells we used the CellProfiler software (www.cellprofiler.org) on five different x20 microscope images acquired.
Cells cultured in T-25 flasks, were washed with 0.5 ml ice-cold Cell Lysis Buffer adding 1 mM PMSF (Cell Signaling, Danvers, MA, USA)] with PhosSTOP (Roche), for 5 minutes. Then cells were gently scraped and collected in Eppendorf tubes and finally centrifuged for 10 min at 14,000 g, 4 °C. In order to measure the protein concentration in supernatant cell lysate, the Pierce™ BCA Protein Assay Kit (Pierce Biotechnology, Rockford, IL, USA) was used. Then, 100 μg of protein were incubated under rotation for 2 h at 4 °C with an antibody dilution of 1:100 (mouse monoclonal α-WNT10B [5 A7], Abcam; rabbit polyclonal α-FZD4, Abcam; rabbit polyclonal α-FZD5, Abcam; rabbit polyclonal α-FZD6 ThermoFisher Scientific). A total volume of 20 μl of 50% bead slurry Protein G Sepharose 4 Fast Flow beads (VWR, Wayne, NJ, USA) were added and incubated under rotation for 2 h at 4 °C. After three washing times with 500 μL cell lysis buffer the pellet was resuspended in 20 μl of SDS sample buffer (Cell Signaling), vortexed and centrifuged for 30 s, and finally incubated for 5 min at 95 °C. Samples were loaded on a NuPAGE 10% Bis-Tris Gel (Life Technologies) and gels were run at 130 V. In order to transfer proteins from the NuPAGE Gel to nitrocellulose membrane, an iBlot dry blotting system (Life Technologies) and iBlot Gel Transfer Stacks Nitrocellulose (Life Technologies) were used following the manufacturer’s instructions. Then the nitrocellulose membranes were blocked in LI-COR blocking buffer (LI-COR, Lincoln, NE, USA) for 1 h in RT, and primary antibodies were diluted 1:1000 in LI-COR blocking buffer and finally incubated with the membrane under gentle rotation overnight at 4 °C. After that the membrane was washed three times in 1× TBS supplemented with 0.05% Tween 20, secondary antibodies IRDye 680LT Donkey (polyclonal) Anti-Mouse IgG (H + L) Highly Cross Adsorbed (LI-COR) and IRDye 800CW Conjugated Goat (polyclonal) Anti-Rabbit (H + L) Highly Cross Adsorbed (LI-COR) were diluted 1:20,000 in LI-COR blocking buffer and incubated with the membrane under gentle rotation for 10 min at RT, followed by three washes in 1 × TBS supplemented with 0.05% Tween. Therefore we scanned membranes in the Odyssey infrared imaging system (LI-COR).
Frizzled receptors gene expression analysis
Total RNA was extracted and reverse transcribed using the protocol previous described and random primers. All PCRs were performed in a final volume of 50 μl containing 5 μL of DNA as template, 5X Green GoTaq Buffer (Promega Corporation, Madison, WI, USA), 4 mM of MgCl2, 0.2 μM of each primer (See Extended Table 4), 0.2 mM dNTPs (Promega), 0.5 U of Taq DNA polymerase (5 U/μl; Promega Corporation). The frizzled receptors gene expression analysis was performed using the following thermal cycle conditions: P12-P13, 94 °C for 3 min, 33 cycles at 94° for 30 s, 52 °C for 30 s, 72 °C for 30 s and 72 °C for 2 min; P14-P15, 94 °C for 3 min, 33 cycles at 94° for 30 s, 52 °C for 30 s, 72 °C for 30 s and 72 °C for 2 min; P16-P17, 94 °C for 3 min, 33 cycles at 94° for 30 s, 51 °C for 30 s, 72 °C for 30 s and 72 °C for 2 min; P18-P19, 94 °C for 3 min, 33 cycles at 94° for 30 s, 53 °C for 30 s, 72 °C for 30 s and 72 °C for 2 min. The GAPDH amplification was performed as standard control. The PCR products were visualized by electrophoresis through a 2% agarose gel.
How to cite this article: Lazzaroni, F. et al. Intronless WNT10B-short variant underlies new recurrent allele-specific rearrangement in acute myeloid leukaemia. Sci. Rep. 6, 37201; doi: 10.1038/srep37201 (2016).
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We are grateful to U. Landegren, O. Söderberg and K. Grannas for their valuable comments and support with the experiments developed at the SciLifeLab in Uppsala and A. Ghilardi for zebrafish care, maintenance, and her expert technical support. We would like to thank M. Bianchi and E. Cardillo (BIORAD-Italia) for experimental contributions and technical assistance with droplet digital PCR, and M. Nilsson for helpful discussion. A.B. was supported by the Association Como Hematology and Oncology (CHO), and by the Associazione Malattie del Sangue Onlus (AMS). F.L. was supported by a postdoctoral fellowship from C.M. Lerici Foundation.