- Open Access
Phenotypic characterization with somatic genome editing and gene transfer reveals the diverse oncogenicity of ependymoma fusion genes
Acta Neuropathologica Communications volume 8, Article number: 203 (2020)
Recurrent RELA and YAP1 fusions are intimately associated with tumorigenesis in supratentorial ependymomas. Chromothripsis and focal copy number alterations involving 11q are hallmarks of these tumors. However, it is unknown whether the chromosomal alterations are a direct causal event resulting in fusion transcripts. In addition, the biological significance of the RELA fusion variants and YAP1 fusions is not yet fully characterized. In this study, we generated gene rearrangements on 11q with the CRISPR/Cas9 system and investigated the formation of oncogenic ependymoma fusion genes. Further, we examined the oncogenic potential of RELA fusion variants and YAP1 fusions in a lentiviral gene transfer model. We observed that endogenous RELA fusion events were successfully induced by CRISPR/Cas9-mediated genome rearrangement in cultured cells. In vivo genome editing in mouse brain resulted in the development of ependymoma-like brain tumors that harbored the Rela fusion gene. All RELA fusion variants tested, except a variant lacking the Rel homology domain, were able to induce tumor formation, albeit with different efficacy. Furthermore, expression of YAP1-FAM118B and YAP1-MAMLD1 fusions induced the formation of spindle-cell-like tumors at varying efficacy. Our results indicate that chromosomal rearrangements involving the Rela locus are the causal event for the formation of Rela fusion-driven ependymomas in mice. Furthermore, the type of RELA. fusion might affect the aggressiveness of tumors and that the Rel homology domain is essential for the oncogenic functions of RELA. fusions. The YAP1 fusion genes are also oncogenic when expressed in mice.
Ependymomas are primary tumors of the central nervous system which occur throughout the craniospinal axis. These tumors occur in all age groups, but intracranial tumors are more common in children [16, 20]. The current best available treatment for these patients is radical surgical removal, followed by local radiation therapy . Since there is currently no effective chemotherapy for ependymomas, recurrent tumors may be lethal in some cases if not fully surgically resected [2, 9, 14]. Therefore, survival of ependymoma patients has not been drastically improved over the past decades , indicating that the development of a new treatment regimen is necessary for these intractable tumors.
Recent large-scale genomic studies revealed that ependymomas segregate into distinct molecular subgroups, which are strongly associated with anatomical location [10, 20, 21]. Supratentorial ependymomas are classified into subependymoma (ST-SE) and ependymoma (ST-EPN) subgroups. The ST-EPN subgroup can be further stratified by mutually exclusive recurrent RELA and YAP1-related gene fusions. These ST-EPN gene fusions not only have diagnostic utility, but also provide potential therapeutic insights into these fusion-positive tumors.
The ST-EPN-RELA subgroup accounts for the majority of supratentorial ependymomas and is characterized by the presence of a gene fusion between C11orf95 and RELA gene [20, 21]. The C11orf95-RELA fusion (RELAFUS) genes are caused by chromothripsis, a single catastrophic genomic rearrangement involving 11q, consequently resulting in several RELAFUS variants . RELAFUS1 (Type 1) and RELAFUS2 (Type 2), the two most frequent variants, were able to induce human ependymoma-like tumors when expressed in murine neural stem cells, using either the RCAS/tv-a system for retroviral gene transfer or an allograft model [17, 21]. Although these findings strongly suggest that RELAFUS genes are responsible for human ependymoma formation, the oncogenic potential of other RELAFUS variants has not been determined yet. In addition, several other types of fusion transcripts involving genes on 11q were also identified concomitant with the RELAFUS transcripts in supratentorial ependymomas . This catastrophic genomic event might affect the status of other genes on 11q, and thereby contribute to the tumorigenesis of RELAFUS-positive tumors. However, the influence of these complex genomic rearrangements has not been captured in previous mouse models [17, 21].
The ST-EPN-YAP1 subgroup is a less common type of supratentorial ependymoma and harbors YAP1-related fusions, found as YAP1-MAMLD1 and YAP1-FAM118B gene fusions . In contrast to the ST-EPN-RELA subgroup, the genome of these tumors is relatively stable except for a focal copy number alteration involving the YAP1 gene locus on 11q , thus suggesting that a more limited number of gene alterations may be sufficient to drive the formation of ST-EPN-YAP1 tumors. The oncogenic potential of YAP1-MAMLD1 has recently been demonstrated by the forced expression via in utero gene transfer in the embryonic subventricular zone . However, the YAP1-FAM118B fusion failed to induce the formation of brain tumors in the same study. On the other hand, the tumor-forming potential of both fusions was observed when expressed in neonatal brains using the RCAS/tv-a system , thus suggesting a potentially different tumorigenic mechanism between these YAP1 fusion genes.
To clarify the biological significance of different chromosomal alterations in supratentorial ependymoma formation, we examined the oncogenic potential of ependymoma gene fusions in two independent mouse tumor models. First, we directly engineered chromosomal rearrangements in mice using the CRISPR/Cas9 system and reproduced the formation of oncogenic gene fusions found in human ependymoma. Second, we demonstrated the oncogenic potential of several variants of RELAFUS and YAP1-related fusion genes using in vivo lentiviral gene transfer into the brain of young adult and/or neonatal mice.
Materials and methods
293T cells (ATCC #CRL-3216) and NIH3T3 mouse fibroblasts (ATCC #CRL-1658) were obtained from ATCC and maintained with minor modifications according to the manufacture’s protocol. The primary mouse embryonic fibroblasts were established from Nestin-Cre+/−;Cag-Cas9+/+ mice and maintained in Dulbecco’s modified Eagle’s media (Gibco) supplemented with 10% fetal bovine serum (Gibco). Mouse neurospheres were generated and maintained as previously described .
Nestin-Cre and Cag-Cas9 mice were purchased from The Jackson Laboratories (Stock No. 003771 and 027650) and crossed to obtain Nestin-Cre+/−;Cag-Cas9+/+ mice. Genotyping protocol was described in the Additional file 1: Supplementary Methods .
Plasmids and lentivirus production
The pTomo lentiviral vector system was used as previously described . LV-EDIT-mRelafus vector was generated by Gibson Assembly of relevant U6-sgRNA fragments into the pTomo vector . The sgRNA sequences targeting Cdkn2a and control were previously described [1, 27]. Other sgRNAs were designed using the CRISPRDirect tool . The details of vector constructs and lentivirus production are described in the Additional file 1: Supplementary Methods. All vectors and sgRNA sequences used in this study are listed in Additional file 2 and 3: Table S1 and S2.
Generation of mouse brain tumors
Mice were injected with the relevant lentivirus and were monitored until they developed symptoms of disease or, if symptom-free, until 5 months after the lentivirus injection. Kaplan–Meier analysis demonstrating symptom-free survival of mouse brain tumors was performed using log-rank test in the GraphPad Prism 8 software. A value of p < 0.05 was considered significant in this study. See Additional file 1: Supplementary Methods for details.
Total RNA was extracted from cultured cells, flash-frozen brain tumor tissues, or formalin-fixed paraffin-embedded (FFPE) tissues using a miRNeasy Mini or RNeasy FFPE kit (Qiagen) according to the manufacturer’s protocol. cDNA libraries were synthesized with the Superscript IV VILO Master Mix (Invitrogen) according to the manufacturer’s protocol and used for subsequent PCR amplification. PCR reaction was performed in a 45-μl reaction volume under the following conditions: 0.3 μl of AmpliTaq Gold360 DNA polymerase (AppliedBiosystems), 4.5 μl of AmpliTaq Gold 360 buffer, 9 μl of GC enhancer, 1.8 μl of 25 mM Magnesium chloride, 1.2 μl of 10 mM dNTP mix, primer pairs (0.5 μM each), 50 ng of the cDNA template and autoclaved distilled water up to 45 μl. The protocol included pre-denaturation for 10 min at 95 °C, denaturation for 30 s at 95 °C, annealing for 30 s at 55 °C, extension for 30 s at 72 °C for 40 cycles and final extension for 10 min at 72 °C. The PCR products were resolved by electrophoresis on 2% agarose gel with GelRed Nucleic Acid Gel Stain (Biotium). Primer sequences are listed in Additional file 4: Table S3.
Western blot analysis
Cells were cultured, lysed, and processed for western blotting by standard methods as previously described . α-tubulin was used as an internal normalization control. Antibodies used in this study are listed in Additional file 5: Table S4.
H&E staining and immunohistochemistry
Mouse brains were paraffin-embedded, sectioned, and stained with hematoxylin and eosin (H&E) and immunohistochemistry (IHC) by standard methods (See Additional file 1: Supplementary Methods for details). In all H&E and IHC photomicrographs, dashed boxes in the top panels denote the enlarged regions as shown in the bottom panels. The length of all scale bars is 100 μm.
Lentiviral delivery of C11orf95-RELA type 1 fusion into mouse neural stem cells induces human ependymoma-like tumors
To examine the oncogenic potential of fusion genes found in human ependymomas, we initially established a model system for in vivo lentiviral gene transfer using the CRISPR/Cas9 system [7, 12]. Given previous studies where expression of the C11orf95-RELA type 1 fusion (RELAFUS1) was sufficient to induce formation of ependymoma-like brain tumors in mice [17, 21], we generated a pTomo-RELAFUS1-HA (containing a C-terminal human influenza hemagglutinin [HA] tag) lentiviral vector which can induce the exogenous gene expression in a cell-type-specific manner using the Cre-loxP system (Additional file 6: Fig. S1A and B) . Since loss of CDKN2A is a common event in the ST-EPN-RELA subgroup [20, 21], we also examined the impact of Cdkn2a inactivation on tumorigenesis by inserting sgRNAs against Cdkn2a or a non-targeting control sequence into the lentiviral vector (Additional file 6: Fig. S1A and B). These constructs were then tested in Nestin-Cre+/−;Cag-Cas9+/+ mice to target Nestin+ radial glia, the putative cell of origin for ependymomas (Additional file 6: Fig. S1C and D) .
Injection of the lentivirus encoding for RELAFUS1-sgCdkn2a into the brain of neonatal pups, brain tumor formation was observed around 2 months post-injection (Fig. 1a). Interestingly, the overall tumor latency was considerably shorter compared to our previous model (Fig. 1a, b) . We did not observe a significant difference in tumor incidence or latency between experimental groups with and without additional Cdkn2a loss (sgCdkn2a versus sgControl) (Fig. 1a, b and Additional file 6: Fig. S1E). This finding is consistent with our previous study in which Cdkn2a loss had no impact on the RELAFUS1-induced brain tumor formation . We did not observe tumor formation in control groups injected with an empty vector or lentiviruses containing sgCdkn2a or sgControl only (Fig. 1a, b).
In addition to pediatric cases, ST-EPN-RELA tumors also occur in adults [16, 20]. Thus, to examine whether expression of RELAFUS is able to induce tumor formation in the adult population, we injected our lentivirus encoding for RELAFUS1 into the subventricular zone of Nestin-Cre+/−;Cag-Cas9+/+ young adult mice. We found that brain tumors were reproducibly formed in the adult mice, albeit with a longer latency compared to our injections in neonatal mice (Fig. 1a–d). In contrast to neonatal pup injection, we observed a significant impact of additional Cdkn2a deletion in adult mice, suggesting different susceptibility to this gene inactivation between neonatal and adult brains (Fig. 1a–d).
Mouse brain tumors typically presented as well-circumscribed and uniform highly cellular masses adjacent to the ventricular system, or occasionally in the brain parenchyma (Fig. 1e and Additional file 6: Fig. S1F). The tumors were composed of relatively monomorphic cells with oval nuclei containing finely granular chromatin. Branching capillaries characteristic for human ST-EPN-RELA ependymomas were commonly seen throughout the mouse tumors [6, 17, 21]. Clear-cell change, another characteristic histological finding in human ST-EPN-RELA ependymomas, were occasionally observed. Ependymal rosettes, ependymal canals, and perivascular pseudorosettes were rarely seen in these tumors. Occasionally, the tumors demonstrated a fascicular architectural growth pattern, with spindled cells densely interwoven with epithelioid-type cells, reminiscent of high-grade glioma or sarcoma. Immunostaining for RELA and HA-tag antibodies displayed predominant nuclear immunopositivity, indicating successful vector expression in the tumors. Similar to human ependymomas, there was consistent extensive immunopositivity for the glial marker GFAP detected in the mouse tumor cells (Fig. 1e and Additional file 6: Fig. S1F). No pathological lesions were found in control mice (mock injection or injection of sgCdkn2a or sgControl alone) at the study endpoint.
Taken together, these RELAFUS1 tumors showed similar biological and histological features to previous RELAFUS1 models and recapitulated those of human ST-EPN-RELA ependymomas [17, 21]. Thus, the oncogenic function of RELAFUS1 was reproducible in the lentiviral gene transfer system.
CRISPR/Cas9-mediated gene rearrangement induces endogenous C11orf95-RELA fusion in human cultured cells
The C11orf95-RELA (RELAFUS) fusions are caused by a genomic rearrangement involving C11orf95 and RELA loci on 11q in human ependymomas. This rearrangement involves a multitude of other genes in this region with unknown effects on tumorigenesis. Although forced expression of RELAFUS1 was sufficient to induce brain tumor formation in mice, the status of neighboring genes involved in the genomic events was not considered in previous models [17, 21]. The generation of endogenous oncogenic gene fusion events, subsequently resulting in the formation of lung or brain tumors, has previously been achieved via CRISPR/Cas9-mediated chromosomal rearrangements in mice in vivo [4, 11]. Therefore, we examined whether the oncogenic gene rearrangement, consequently resulting in endogenous RELAFUS1, can be experimentally reproduced.
RELAFUS1 consists of the first two exons of C11orf95 and exons two to eleven of RELA . To reproduce the gene rearrangement giving rise to the RELAFUS1 transcript, we designed four sgRNAs (single guide RNAs) on the human C11orf95 and RELA gene loci around the breakpoints observed in human ependymomas harboring RELAFUS1 (Fig. 2a) . We then generated four expression vectors for these sgRNAs and transiently transfected them in two combinations into 293T cells (Fig. 2b). RT-PCR analysis across the fusion junction of RELAFUS1 detected the RELAFUS1 transcript in both sgRNA sets. The sequences were subsequently confirmed by Sanger sequencing of the PCR products (Fig. 2c). In addition, the presence of the RELAFUS1 protein in 293T cells carrying the rearranged gene loci could also be detected by Western Blot (Fig. 2d). Genomic PCR analyses revealed that the target sequences were cleaved through the CRISPR/Cas9 system as intended, thereby leading to the induction of the gene rearrangement (Additional file 7: Fig. S2A and B). These results suggested that the endogenous human RELAFUS1 gene can be experimentally generated by introducing the intended breakpoints in human cultured cells via CRISPR/Cas9 technology.
CRISPR/Cas9-mediated gene rearrangement induces oncogenic 2700081O15Rik-Rela fusion in mice
Successful detection of endogenous RELAFUS1 in human cultured cells encouraged us to examine whether this gene rearrangement can also be induced in mice, with subsequent formation of brain tumors. Rela is located upstream of the 2700081O15Rik (the mouse homolog of human C11orf95) on chr19, a similar pattern to the human RELA and C11orf95 genes on 11q (Figs. 2a and 3a). Therefore, to induce this gene rearrangement for the generation of the mouse 2700081O15Rik-Rela fusion (mRelafus), we designed sgRNAs in similar genomic positions compared to human RELAFUS1 (Figs. 2a and 3a). We then generated the vector constructs carrying sgRNAs with Cas9 and transiently transfected three (set-2) or four (set-1) sgRNAs into NIH3T3 cells (Fig. 3b). RT-PCR analysis detected mRelafus transcripts in both sgRNA sets and subsequent Sanger sequencing analyses of the PCR products confirmed the fusion junction sequence between exon 2 in 2700081O15Rik and exon 2 in Rela, resulting in an in-frame fusion structurally corresponding to human RELAFUS1 (Fig. 3c). The full-length cDNA of mRelafus was isolated and validated by Sanger sequencing. Further, the endogenous mRelafus protein was detected in cells transfected with the set-1 sgRNAs (Additional file 8: Fig. S3A).
Subsequently, we examined whether the endogenous mRelafus can induce brain tumors in mice. Given that the introduction of three breakpoints was sufficient to induce the fusion gene in vitro (Fig. 3c), we generated an all-in-one lentiviral vector including three sgRNAs (referred to as LV-EDIT-mRelafus) (Additional file 8: Fig. S3B) and co-injected the virus with or without the lentivirus for sgCdkn2a (#1 target sequence) into the brain of neonatal pups and young adult mice in Nestin-Cre+/−; Cag-Cas9+/+ mice (Fig. 3d, e). Brain tumor formation was observed in one out of ten mice that were injected as young adults (Fig. 3e, f). By contrast, injection of neonatal pups led to brain tumor formation in 5 out of 21 mice around 60 days post-injection (Fig. 3e, f). We observed a considerably lower tumor incidence compared to our other model that relies on the lentiviral overexpression of RELAFUS1 (Figs. 1b and 3f). Additional Cdkn2a loss had no significant impact on tumor formation upon injection in neonatal pups in this model (Fig. 3e).
Mouse brain tumors induced with the endogenous mRelafus gene presented with similar morphological and histologic features compared to tumors induced by the gene transfer of the RELAFUS1 (Figs. 1e and 3g). Immunohistochemical staining with a RELA antibody detected intense nuclear immunoreactivity, indicating mRelafus protein expression. Although the mRelafus gene rearrangement was not necessarily specific to Nestin-expressing cells of origin in this model, immunostaining for GFP suggested that tumors might have arisen from Nestin positive neural stem cells in some cases (Fig. 3h). These immunohistochemical findings strongly suggests that tumors were induced by endogenous mRelafus. We extracted RNA from mRelafus mouse brain tumors and were able to detect a fusion transcript corresponding to the human RELAFUS1 transcript by RT-PCR and subsequent sanger sequencing (Fig. 3i and Additional file 8: Fig. S3C). Another fusion transcript corresponding to human RELAFUS4 was also detected concomitantly in one mouse brain tumor sample (Fig. 3i) . In addition, the mRelafus1 protein was detected by western blot in a cell line derived from one of the mouse brain tumors (Fig. 3j). These results support the notion that gene rearrangements are the primary mechanism to create the oncogenic RELAFUS1 fusion gene, serving as the direct driver of tumorigenesis in human RELAFUS tumors.
C11orf95-RELA fusion variants present diverse oncogenic potential
Several RELAFUS variants have been identified in human ST-EPN-RELA tumors [5, 8, 21]. The oncogenic potential of RELAFUS1 and RELAFUS2, the most frequent RELAFUS variants, has previously been documented [17, 21]. However, the tumorigenic role of other less common RELAFUS variants has not been fully characterized. Therefore, we investigated which of these RELAFUS variants can induce brain tumor formation upon expression in neonatal pups using our lentiviral gene transfer system. RELAFUS variants 5, 6, and 7 have a similar structure to RELAFUS2, apart from small intronic intervening sequences, and share the same functional domains. Therefore, we focused our study on RELAFUS variants 2, 3 and 4 (Fig. 4a) . In addition, we tested a small fusion transcript (referred to as RELAFUS8) lacking the Rel homology domain which we have recently identified (Fig. 4a) .
We generated pTomo-lentiviral vectors encoding for RELAFUS variants 2, 3, and 4, along with a sgRNA targeting Cdkn2a (sgCdkn2a #1) (Additional file 9: Fig. S4A). Lentiviruses were injected into the brain of Nestin-cre+/−;Cag-Cas9+/+ neonatal pups. With the presence of C11orf95 and RELA preserved functional domains in the different RELAFUS variants, expression of RELAFUS2-4 induced brain tumor formation (Fig. 4b, c). Tumors generated by expression of RELAFUS1 and RELAFUS4 had the shortest tumor latencies. By contrast, tumors generated by expression of RELAFUS2 or RELAFUS3, which both possess two zinc finger domains of C11orf95, had significantly longer tumor latencies and lower tumor incidences, suggesting that an additional zinc finger domain might somehow negatively affect the tumorigenesis. There were no detectable lesions in the lentiviral injection of the RELAFUS8 and the control group (Fig. 4b, c). Thus, the Rel homology domain is likely essential for the oncogenic potential of the RELAFUS.
Histological features of these RELAFUS variants were almost indistinguishable from those of the RELAFUS1-driven tumors and partly recapitulated characteristic histologic features of human ependymomas (Fig. 1e and Additional file 9: Fig. S4B-D). These results show that all RELAFUS variants, except for the RELAFUS8 variant, are oncogenic with diverse tumor-forming potential.
YAP1 fusions induce brain tumors with different morphological and histologic features from RELAFUS-induced tumors in mice
ST-YAP1-EPN and ST-EPN-RELA tumors are recognized as clinically, genetically, and biologically distinct diseases [17, 19,20,21, 23]. To further understand the biology of ST-EPN-YAP1 tumors, we next examined the tumor-forming potential of recurrent YAP1-MAMLD1 and YAP1-FAM118B fusions in our system (Additional file 10: Fig. S5A). We generated pTomo-HA-YAP1-MAMLD1 and HA-YAP1-FAM118B lentiviral vectors and injected the lentiviruses into the brains of Nestin-Cre+/−;Cag-Cas9+/+ neonatal pups (Additional file 10: Fig. S5A and B). Injection of the YAP1-FAM118B fusion by itself caused the formation of mouse brain tumors with a similar latency to RELAFUS1 tumors, which is unlike the reported better clinical outcomes compared to RELAFUS tumors in human patients (Fig. 5a, b) . By contrast, no brain tumor formation was observed in the lentivirus injection with YAP1-MAMLD1 (without additional Cdkn2a loss) (Fig. 5b), whereas small tumor or neoplastic lesions were detected upon additional co-injection of sgCdkn2a (Fig. 5b and Additional file 10: Fig. S5C). Intracranial lentiviral injection of HA-YAP1 alone failed to induce brain tumor formation, reinforcing the necessity of the gene fusion partner for tumorigenesis (Fig. 5a, b) [19, 23].
YAP1-FAM118B fusion tumors mainly had a spindle-cell histomorphologic phenotype and tended to grow diffusely into the brain parenchyma, which is in contrast to the typical circumscribed growth pattern of RELAFUS-driven tumors (Fig. 5c). YAP1-FAM118B fusion tumors were rarely observed in the brain parenchyma and commonly localized to the adjacent intraventricular region, consistent with tumors arising from subventricular zone neural stem cells . Pseudopalisading necrosis was sometimes detected, whereas we did not observe ependymal rosettes, ependymal canals, or perivascular pseudorosettes in these tumors. Immunohistochemical analyses for YAP1 and HA-tag revealed nuclear expression of the YAP1-FAM118B fusion protein in the tumor cells (Fig. 5c). YAP1 regulates gene expression as a transcriptional co-activator in the nucleus, thus nuclear localization likely occurs in the setting of persistent YAP1 pathway activation in these tumors . Tumor cells were mostly negative for GFAP immunostaining. Excessive reactive astrocytes were commonly observed in the tumors as shown by extensive immunopositivity for GFAP adjacent to the HA-positive tumor cells (Fig. 5c). Overall, the YAP1-FAM118B-induced tumors appear to be high-grade spindle cell tumors rather than typical ependymoma. Similarly, small lesions induced with the YAP1-MAMLD1 fusion presented with an invasive phenotype that morphologically resembled the YAP1-FAM118B fusion tumors (Additional file 10: Fig. S5C). All together, these results provide evidence that the YAP1-FAM118B gene fusion is a potent oncogene capable of inducing brain tumors in mice.
In this study, we have successfully shown that the endogenous RELA fusion generated through targeted gene editing was sufficient to develop ependymoma-like brain tumors in mouse brains. Chromothripsis is one of the mechanisms to create a gene fusion event, but also simultaneously affects the status of neighboring genes on the involved chromosome . Thus, RELAFUS might have driven ependymoma formation in cooperation with numerous altered genes on 11q. However, it is not easy to determine which additional genes, if any, might be linked to RELAFUS-induced tumor formation. CRISPR/Cas9 system-mediated DNA double-strand breaks are repaired through Non-homologous end joining (NHEJ) more commonly and efficiently than the Homology Directed Repair (HDR) mechanism . NHEJ is a primary repair mechanism for DNA double-strand break in chromothripsis . Therefore, modeling gene rearrangements using the CRISPR/Cas9 technology seems to have reproduced at least one aspect of chromothripsis occurring in human ependymoma. Biological and histological similarities between mRelafus tumors and RELAFUS-induced tumors, as well as the successful detection of mRelafus transcript and protein, support the idea that mRelafus tumors are induced by endogenous mRelafus, which is generated as a direct result of CRISPR/Cas9-mediated gene rearrangement. Thus, our model highly suggests that the biological consequence of genomic rearrangement in ependymomas is likely driven by the creation of novel splice junctions leading to the formation of oncogenic RELA fusion transcripts, while the potential influence of any neighboring gene(s) on the chromothriptic chromosome might be minimum, if at all, for tumorigenesis.
Mouse RELA fusion tumors recapitulated the phenotypic and histologic features of the human counterparts at various degrees as exemplified by the consistent branching capillary formation and intense nuclear immunopositivity of RELA. However, abundant perivascular pseudorosettes and GFAP-highlighted radial perivascular processes, the cardinal histologic features of ependymoma were not reproducibly observed. Furthermore, the spindle cell tumor morphology observed is unusual for ependymoma, except in the case of the tanycytic histologic variant of ependymoma. Our mouse model demonstrates that the ependymoma gene fusion products drive tumor formation in a specific context, but they do not necessarily recapitulate all aspects of human tumors. Thus, while our animal models provide important insights into the oncogenic mechanism of gene fusions, it is essential to recognize the limitations of these models and have the ability to refine these models based on accurate genetics and biology.
All tested RELAFUS variants retaining the functional domain of RELA were oncogenic in our system. However, the tumor-forming potential of these variants were somewhat different, consistent with a previously published ex vivo model . RELAFUS1 and RELAFUS4 formed tumors with faster latency and higher incidence than RELAFUS2 and RELAFUS3. Multiple fusion variants can be seen within a single ependymoma [8, 20, 21]. Although the complete biological significance of these fusion variants in ependymoma are not fully understood, the presence of multiple fusion variants might give rise to intra- or inter-tumor molecular heterogeneity, possibly engendering different patient outcomes and treatment sensitivity.
The YAP1-MAMLD1 fusion was able to induce brain tumors in both prenatal and neonatal brains at varying efficacy [19, 23]. By contrast, the YAP1-FAM118B fusion was oncogenic by itself in neonatal, but not prenatal brains [19, 23]. ST-EPN-YAP1 tumors are commonly identified in children and approximately two-thirds are present in the infant population . Although the age distribution of these fusion-positive cases is not determined yet due to their relatively rare occurrence, the cell of origin for YAP1-FAM118B fusion might be possibly different from that of YAP1-MAMLD1 fusion tumors. Therefore, the oncogenic potential of YAP1-FAM118B fusion might rely on the temporal course of expression (e.g. during neonatal stage). Because inter-chromosomal rearrangement is indispensable for the creation of the YAP1-MAMLD1 fusion, additional genetic alterations might be acquired and contribute to the flexible oncogenic potential of the YAP1-MAMLD1 fusion. These findings indicate that the ST-EPN-YAP1 subgroup may be a heterogenous group of tumors which can be further subdivided according to their molecular features [8, 20]. Due to the unusual diffuse glioma or sarcoma like-histological findings in mouse YAP1 fusion tumors, a larger cohort of human ST-EPN-YAP1 tumors will need to be investigated histologically and molecularly to determine the relevance of mouse YAP1 fusion driven tumors as a model for human ependymoma.
Current molecular diagnosis of ST-EPN is focused on detection of the frequent splicing forms of RELAFUS. Given the oncogenic function of other RELAFUS variants and YAP1 fusions [19, 21, 23], detection of these less common fusion transcripts should be considered in routine surgical neuropathology practice. In addition to the diagnostic utility, detection of less common ependymoma gene fusions may have implications for potential therapeutic targeting strategies.
Genomic analyses of ependymomas have shed light onto some of the underlying tumor biology [8, 20, 21]. Nevertheless, the relative rarity of this tumor type still prevents the dynamic advance of ependymoma research and treatment because of the lack of currently available tumor derived-cell lines and patient-derived xenograft (PDX) models. Genetically accurate mouse models can provide a powerful platform for investigating such uncommon diseases. Genomic rearrangement models driven by an endogenous promoter that mirrors physiological gene expression have a great advantage as they are able to reproduce a more accurate biological situation compared to a gene transfer approach with an artificial promoter. Thus, we believe that our novel mouse ependymoma model has the potential to provide deeper insights into ependymoma biology, as well provide a platform to investigate therapeutic resistance and develop new treatment strategies for this aggressive disease [17, 19, 21].
The presence of RELA and YAP1 fusion transcripts is the hallmark of supratentorial ependymomas, and 11q chromosomal alterations are frequently associated with complex gene rearrangements. In order to gain a deeper understanding of ependymoma biology, it is essential to ascertain whether the presence of these fusion genes is sufficient for tumor formation or if additional abnormalities of neighboring genes involving in the genomic rearrangement are necessary. Our findings indicate that the biological function of chromosomal alterations in RELA fusion ependymomas is essentially to create a novel splice junction, consequently resulting in an oncogenic fusion gene. These findings are supported by the fact that simple overexpression of human variants of RELA fusions, without additional genetic alterations, induce tumor formation in mice. Thus, these observations not only support the need for precise neuropathological diagnosis of ependymoma molecular subgroups in the clinical setting, but also the exciting therapeutic potential for directly targeting specific fusion proteins found in supratentorial ependymoma.
- RELAFUS1 :
C11orf95-RELA type 1 fusion
Single guide RNA
- mRelafus :
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The research reported in this work was supported by the Grant-in-Aid for Scientific Research (C) (KAKENHI) (16K10775 to K. Ichimura and 19K09518 to T. Ozawa), Children’s Cancer Association of Japan (to T. Ozawa) and The Mother and Child Health Foundation (30-2 to T. Ozawa). We acknowledge the assistance of the Central Animal Division in the National Cancer Center Japan, Research Institute. We thank Sanae Matsuzaki and Mai Kitahara for technical assistance; Yuki Yomoda for secretarial assistance; all members of the Ichimura laboratory for helpful discussions. M. Takadera would also like to thank his family for their unparalleled love and support.
Availability of data and materials
All the data and materials generated in this study are available from the corresponding authors on reasonable request.
Ethics approval and consent to participate
All mouse experiments were approved and performed according to the guidelines of the Institutional Animal Care and Use Committee of the National Cancer Center Research Institute (protocol #T17-051).
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
. Supplementary materials and methods
. List of vector constructs
. List of sgRNA target sequence
. List of primers
. List of antibodies
. Lentiviral gene transfer of C11orf95-RELA type 1 fusion into mouse neural stem cells induces human ependymoma-like tumors (A) Schematic presentation of the pTomo-RELAFUS1-HA-sgRNA lentiviral vectors. Injection of the pTomo-lentivirus into the Nestin-Cre+/-;Cag-Cas9+/+ mouse brain induces RELAFUS1 expression specifically in the Nestin-expressing cells through the Cre-loxP system. The sgRNA targeting Cdkn2a or control sequence is expressed under the U6 promoter. LTR, long terminal repeat; CMV, human cytomegalovirus immediate early enhancer and promoter; RFP, red fluorescent protein; IRES, internal ribosome entry site; EGFP, enhanced green fluorescent protein; hU6, human U6 promoter; WPRE, woodchuck hepatitis virus posttranscriptional regulatory element (B) Western blot analysis for RELAFUS1-HA and p19ARF protein expression. NIH3T3 cells (left panel) or primary mouse embryonic fibroblasts (right panel) were infected with pTomo lentiviruses as indicated (left panel). Subsequently, pCAG-Cre vector was transiently transfected to induce Cre-meditated recombination in these cells. Cell lysates were then subjected to immunoblot analysis with the indicated antibodies. The upper (red) and lower (black asterisk) bands in the RELA antibody detection indicate RELAFUS1-HA and endogenous Rela protein, respectively. α-tubulin and β-actin were used as an internal control. (C) PCR genotyping of Nestin-Cre, Cag-Cas9 and Nestin-Cre+/-;CAG-Cas9+/+ mice (D) qRT-PCR analysis of Cdkn2a expression in primary mouse embryonic fibroblasts infected with the pTomo-RELAFUS1-HA-sgCdkn2a virus or sgControl virus. Expression was normalized using Rps18 as an internal control. Data represent Mean ± SEM with four samples per group. ***, P < 0.001. Data are representative of two independent experiments. (E) Sanger sequencing analyses of the colony-PCR products. Genomic DNAs were extracted from FFPE brain tumor tissues using a QIAamp DNA FFPE kit (Qiagen) according to the manufacturer’s protocol. The PCR products of the targeted loci were cloned into T-vector pMD20 (Takara). Each bacterial colony was PCR-amplified and sequenced (4 tumors, 5 clones each). The sgRNA sequence for Cdkn2a is shown in red and the 3’-PAM sequence is shown in green. Insertions or deletions are shown in blue. NBT-96, 100 and NBT-141, 164 denote DNA samples from the RELAFUS1-sgCdkn2a (#1) or sgControl (#1)-induced brain tumors, respectively. (F) Representative H&E and IHC analyses for HA tag, RELA and GFAP antibodies of the RELAFUS1-HA+sgCdkn2a (#1)-induced brain tumor in Nestin-Cre+/-;CAG-Cas9+/+ mice (n=3). Dashed boxes at the top panels denote the enlarged regions as shown at the bottom. Scale bars, 100 μm.
. CRISPR/Cas9-mediated gene rearrangement induces endogenous C11orf95-RELA fusion in human cultured cells. (A and B) Genomic PCR analyses in the gene-edited and parental 293T cells. DNAs were extracted from 293T cells transfected with set-1 (A) or 2 (B) sgRNAs and subjected to genomic PCR analysis. Blue and red boxes represent exons of the C11orf95 and RELA gene, respectively. Black arrowheads and Red arrows indicate cleavage sites by the sgRNAs and the position of PCR primers designed to detect gene rearrangement, respectively. Primer pairs as AB, CD, EF, GH, IJ, and KL detect an unedited intact gene. Positive bands with primer pair A/F and A/J indicate successful gene rearrangement between RELA exon 2 and C11orf95 exon 2 in the set-1 combination and between RELA exon 1 and C11orf95 exon 2 in the set-2 combination, respectively. The RT-PCR and sequencing analysis in the gene-editing with set-2 sgRNAs revealed that RELA exon 1 served as an intronic non-coding sequence (Fig. S2B, second top panel, grey box).
. CRISPR/Cas9-mediated gene rearrangement generated induces oncogenic 2700081O15Rik-Rela fusion in mice. (A) Western blot analysis in the NIH3T3 cells edited with the set-1 sgRNAs. The set-1 sgRNAs were transiently transfected into NIH3T3 cells, and GFP and RFP-positive cells were then selected using limiting dilution in puromycin containing media. Subsequently, cell lysates were subjected to immunoblot blot analysis with the indicated antibodies. Parental NIH3T3 cells were served as a control in this experiment. Upper (red) and lower (black arrow) bands in the RELA antibody detection indicate mRelafus and endogenous Rela protein, respectively. α-tubulin was used as an internal control. (B) RT-PCR detection of mRelafus transcript in the NIH3T3 cells. Cells were coinfected with the LV-EDIT-mRelafus and lentiCRISPRv2 virus for Cas9 expression and then subjected to RT-PCR analysis (left panel). RT and no RT denotes RT-PCR analysis with or without reverse transcriptase enzyme, respectively. The electropherogram of the PCR product in subsequent Sanger sequencing analysis was shown in the right panel. (C) RT-PCR detection of mRelafus transcript in the LV-EDIT-mRelafus-induced brain tumor (left panel) and electropherogram of the PCR product (right panel). Sanger sequencing analysis of the PCR product identified in-frame fusion transcript corresponding to human RELAFUS1 in this tumor (NBT-514).
. C11orf95-RELA fusion variants present diverse oncogenic potential (A) Western blot analysis for functional validation of pTomo-RELAFUS-HA-sgCdkn2a (#1) vector expression. NIH3T3 cells were infected with various pTomo lentiviruses as described. Subsequently, pCAG-Cre vector was transiently transfected to induce Cre-meditated recombination in the cells. Cell lysates were then subjected to immunoblot analysis with the indicated antibodies. Upper and lower bands in the RELA antibody detection indicate RELAFUS-HA protein and endogenous Rela protein, respectively. (B-D) Representative H&E and IHC analyses for HA tag, RELA and GFAP antibodies of the RELAFUS2-HA (B), RELAFUS3-HA (C) or RELAFUS4-HA (D) + sgCdkn2a (#1)-induced brain tumors in Nestin-Cre+/-;CAG-Cas9+/+ mice. Dashed boxes in the top panels denote the enlarged regions as shown in the bottom panels. Scale bars, 100 μm.
. YAP1 fusions induces brain tumors with different morphological and histologic features from RELAFUS-induced tumors in mice. (A) Schematic presentation of the predicted protein products of YAP1 fusions and wild-type YAP1 with HA tag in the N-terminus in the pTomo-lentiviral vectors. TID, TEA domain-containing factor-interaction domain for TEAD binding; WW, protein–protein interaction domain; MAML, mastermind-like domain; Ser, serine-rich region; Pro, proline-rich region; TAD, transcriptional activation domain for TEAD. (B) Western blot analysis for pTomo-HA-YAP1 fusion vector expression. NIH3T3 cells were infected with various pTomo lentiviruses as described. Subsequently, pCAG-Cre vector was transiently transfected to induce Cre-meditated recombination in the cells. Cell lysates were then subjected to immunoblot analysis with the indicated antibodies. (C) Representative H&E images of the HA-YAP1-MAMLD1 + sgCdkn2a (#1)-induced brain tumors in Nestin-Cre+/-;CAG-Cas9+/+ mice. Dashed boxes in the top panels denote the enlarged regions as shown in the bottom panels. Scale bars, 100 μm.
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Takadera, M., Satomi, K., Szulzewsky, F. et al. Phenotypic characterization with somatic genome editing and gene transfer reveals the diverse oncogenicity of ependymoma fusion genes. acta neuropathol commun 8, 203 (2020). https://doi.org/10.1186/s40478-020-01080-8
- Supratentorial ependymoma
- CRISPR/Cas9 system
- Brain tumor mouse model
- Gene rearrangement