Tumour cell plasticity is a major barrier to the efficacy of targeted cancer therapies but the mechanisms that mediate it are poorly understood. Here, we identify dysregulated RNA splicing as a key driver of tumour cell dedifferentiation in colorectal cancer (CRC). We find that Apc-deficient CRC cells have dysregulated RNA splicing machinery and exhibit global rewiring of RNA splicing. We show that the splicing factor SRSF1 controls the plasticity of tumour cells by controlling Kras splicing and is required for CRC invasion in a mouse model of carcinogenesis. SRSF1 expression maintains stemness in human CRC organoids and correlates with cancer stem cell marker expression in human tumours. Crucially, partial genetic downregulation of Srsf1 does not detrimentally affect normal tissue homeostasis, demonstrating that tumour cell plasticity can be differentially targeted. Thus, our findings link dysregulation of the RNA splicing machinery and control of tumour cell plasticity.
Colorectal cancer (CRC) is a leading cause of cancer related mortality responsible for around 900,000 deaths annually1. The emergence of novel targeted therapies for treatment has offered hope of improved outcome2, but these are generally beneficial to only small subsets of patients and emergence of resistance is common, even in initially responsive patients. For example, resistance to the highly specific EGFR inhibitor cetuximab, used for the treatment of some KRAS wild-type tumours, routinely emerges and survival benefit is limited3. In this case resistance emerges via multiple, distinct genetic and transcriptomic mechanisms that bypass the tumour’s requirement for signalling via EGFR, suggesting tumour heterogeneity may play a role in mediating therapy resistance3. Indeed, intra- and inter-tumoural mutational diversity within patients has been shown to result in CRC subpopulations having variable responses to therapeutic agents4, together suggesting that targeting single specific oncogenic driver genes may not deliver durable responses, even in highly stratified patient populations. Therefore, there is an urgent need to identify more general, clinically targetable biological mechanisms that exploit general cancer cell characteristics rather than the classically studied oncogenic driver genes that mediate them, such mutated APC, TP53 or RAS/MAPK5.
Another key therapeutic challenge is overcoming the plasticity of stem cell fate, where stem cells can not only differentiate into more specialised cell types, but these differentiated cells have the ability to revert back to the stem cell phenotype following tissue damage6,7,8. This is especially important when considering clinical treatment as this phenomenon has also been observed in tumours where differentiated tumour cells (non-Lgr5 + ) can be reactivated following cancer stem cell depletion and subsequently dedifferentiate and fuel tumour growth9,10.
Alternative RNA splicing increases proteome diversity and can induce radical effects on cellular phenotype including promoting carcinogenesis11,12,13. For example, the alternatively spliced Rac1 isoform, Rac1b, is constitutively active and is upregulated in Wnt-driven CRC driving efficient tumourigenesis14,15,16. Additionally, mRNA splicing is thought to be the rate-limiting step in generating functional transcripts and has been proposed as a potential therapeutic vulnerability in MYC driven breast cancer and lymphoma17,18,19. Therefore, activity levels of the RNA spliceosome may be an important facilitator of cancer cell growth and its targeting may present a viable therapeutic strategy.
Here, we aimed to identify universal therapeutic targets for CRC by determining the mechanisms important for cancer cell growth. We identified widespread dysregulation of RNA splicing factors and global reprogramming of RNA splice isoforms in a Wnt-driven animal model of CRC. Using 3D organoid cultures, we performed a synthetic lethal screen of splicing factors altered in CRC, identifying the splicing factor SRSF1 as a therapeutic vulnerability in CRC organoids. Moreover, we determined that SRSF1, by modulating the pro-proliferative Kras 4B isoform, alters cancer stem cell plasticity, the invasive potential of advanced tumours and the viability of primary CRC organoids derived from patients. Together, these data suggest that RNA splicing, and SRSF1 in particular, control the plasticity of tumour cells and is a viable therapeutic target in CRC.
RNA splicing is dysregulated following Wnt hyperactivation
To identify cellular processes activated at early stages of intestinal carcinogenesis, we deleted both copies of the CRC tumour suppressor gene Apc in mice using the intestinal specific villin-CreERT2 (villinCreERT2 Apcfl/fl). Five days after tamoxifen induced-gene recombination, small intestinal tissue was dissected and activation of the Wnt hyperproliferative phenotype confirmed by immunohistochemical staining of BrdU and Wnt/β-catenin target gene upregulation (Fig. S1a, S1b and S3a).
Wild-type and Apcfl/fl intestinal tissue was subjected to RNAseq (Supplementary Data 1) and biological pathway analysis (KEGG) used on differentially expressed transcripts to identify enriched biological processes. Compared to normal tissue, RNA processing events were the most significantly upregulated processes following Apc loss (Fig. 1a). Specifically, we found that 60 genes involved in RNA splicing were upregulated (Supplementary Data 2 and Fig. S1c). This suggests there may be an increased requirement for RNA splicing following CRC initiation.
To ascertain if splicing factor upregulation correlated with changes in RNA splicing events, we conducted differential splicing analysis using SUPPA220 and identified 1,661 alternative splicing events following Apc loss (p < 0.05) (Fig. 1b and Supplementary Data 3) indicating a global rewiring of alternative RNA splicing upon Wnt activation. The largest category of splicing event detected using this method was alternative first exon (46.4%) which could be an indication of alternative transcriptional regulation. To investigate this, we compared these events to differentially expressed genes identified in Supplementary Data 1. 140/631 alternative first exon events were also differentially expressed indicating the majority of these events are not linked to transcriptional changes and likely represent alternative use of first exons and/or differential promoter usage (Fig. S1d). SUPPA2 analysis detects annotated splicing events but is unable to detect unannotated events, limiting our analysis. To investigate whether loss of Apc also induces novel splicing events we carried out rMATS analysis, which can also detect novel splicing events21. Interestingly, this analysis identified a large number of splicing events utilising novel splice sites indicative of widespread splicing alterations (Supplementary Data 4 and Fig. S1e). Splicing changes were detected and validated in numerous cancer-related genes, including pro-tumourigenic Cd44 variant isoforms22, Fgfr2 and eIF4A2 (Fig. 1c and S1f–S1h). Notably, we found a significant change in the splicing ratio of the oncogene Kras (Fig. 1c and S1f) favouring the Kras4B isoform over the Kras4A isoform. These isoforms have been previously reported to have pro-proliferative and proapoptotic effects respectively (Figure S1g)23,24. We next analysed previously published RNA splicing analysis of The Cancer Genome Atlas (TCGA) data25 to determine whether the splicing events identified in our mouse model are found in human CRC samples. Of the top 100 identified skipped exon splicing events, 18 showed the same alteration in human CRC including KRAS, CD44 and EIF4A2 (Supplementary Data 5 and Fig. S1i). In summary, we identified widespread alterations of alternative splicing events following Apc loss, several of which are associated with cancer progression and a proportion of which are found in human CRC samples.
As RNA splicing activity is dysregulated in Apcfl/fl intestine, we investigated the effects of global splicing inhibition on oncogenic growth compared to wild-type. 3D intestinal organoids from normal or Apcfl/fl intestine were exposed to the highly potent splicing inhibitor pladienolide B26 (Fig. 1d). At low concentrations of the drug, Apcfl/fl organoids showed signs of cell death (Fig. 1d) and a drop in cell viability (Fig. 1e and S1j), whereas wild-type organoids were more resilient. We found a significant difference in the IC50 of pladienolide B for wild-type and Apcfl/fl intestinal organoids (Fig. 1e). We extended this analysis to organoids derived from human patient material. We found that CRC tumour organoids exhibited significant loss of viability upon pladienolide B treatment but organoids derived from normal tissue did not (Fig. 1f, g). These results support a proof-of-concept that the spliceosome may be a therapeutic vulnerability in Apc-deficient cells.
The splicing factor SRSF1 is critical for Apc-deficient growth
To identify which splicing factors are required for Apc-deficient cell growth, we conducted a splicing factor-targeted, synthetic lethal CRISPR screen comparing wild-type to Apcfl/fl intestinal organoids. We generated a guide RNA (gRNA) library targeting the 60 splicing factor genes upregulated following Apc deletion (Supplementary Data 2 and 6) and delivered them by lentiviral transduction into either wild-type-Cas9 or Apcfl/fl-Cas9 intestinal organoids (Fig. 1h) at low multiplicity of infection (MOI). Surviving organoids were harvested after 7 days of antibiotic selection and gRNA sequences in surviving clones analysed via deep sequencing. A comparison of the gRNAs present in surviving wild-type-Cas9 and Apcfl/fl-Cas9 organoids showed that guide RNAs targeting Ddx10 and Srsf1 were significantly underrepresented in Apcfl/fl-Cas9 population (Fig. 1i and Supplementary Data 7). This implies deletion of these genes is less well tolerated in the context of Apc loss compared to normal growth conditions. To confirm these findings, we CRISPR-targeted Ddx10 and Srsf1 individually in pooled gene-edited populations of both wild-type and Apcfl/fl organoids. Targeting Ddx10 or Srsf1 reduced Apcfl/fl organoid growth, but only Srsf1 showed a significant reduction in viability in Apcfl/fl organoids compared to wild-type organoids where Srsf1 is deleted (Fig. 2a, b and S2a, S2b). Therefore, we chose to investigate the function of Srsf1 in further detail.
Notably, despite showing significantly reduced viability in Apcfl/fl organoids, deletion of Srsf1 by CRISPR also reduced viability in wild-type organoids. However, previous reports have demonstrated that modest reductions in Srsf1 expression levels are well tolerated in mice suggesting a potential therapeutic window for targeting Srsf127. As therapeutic targeting does not lead to target inhibition equivalent to genetic knockout we aimed to phenocopy clinical intervention more accurately using doxycycline-inducible short hairpin RNA (shRNA) expression. This also allowed us to deplete Srsf1 levels in fully developed organoids of increasing genetic complexity and aggressiveness. Expression of the Srsf1 shRNA reduced SRSF1 levels in wild-type, Apc-deficient and AKP (Apc;∆/∆ Kras; G12D/+ Trp53∆/∆) organoids (Figures S2c, S2d). Validating the findings with CRISPR deletion, knockdown of Srsf1 significantly reduced the growth of fully mature Apc-deficient and AKP organoids (Fig. 2e–h). However, we observed no impact of Srsf1 depletion on wild-type organoid growth (Fig. 2c, d). Together, these data suggest a potential therapeutic vulnerability of CRC cells to depletion of Srsf1.
SRSF1 is required for epithelial cell hyperproliferation
To investigate the effects of targeting Srsf1 in vivo, we combined Apc deletion in our mouse model, where SRSF1 was upregulated (Fig. S3a), with a deletion of a single copy of Srsf1 (villinCreERT2 Apc;fl/fl Srsf1fl/+) (Figs. S3b–S3c and S3h). Homozygous deletion of Srsf1 led to gut toxicity with elevated levels of intestinal cell apoptosis (Fig. S3k) so heterozygous deletion of Srsf1 was selected to phenocopy a more clinically relevant scenario where impaired SRSF1 activity might be achieved rather than complete deletion.
A 30–50% reduction in Srsf1 levels (Figure S3h) had no proliferative or morphological effect in wild-type intestinal tissue (Fig. 3a, b and S3d–S3e). However, we observed a significant reduction in the number of BrdU-labeled (Fig. 3a, b) and Ki-67-positive cells (Figs. S3d, S3e) upon deletion of one copy of Srsf1 in the context of Apc loss. Interestingly we found that the proliferative reduction seen in villinCreERT2 Apc;fl/fl Srsf1fl/+ was observed predominantly in the intestinal villus zone (Fig. 3a–b and S3f) and this was independent of variations in crypt-villus size or levels of apoptosis (Figures S3g and S3i-S3j). We investigated this proliferative reduction further by harvesting villi from either Apcfl/fl or Apc;fl/fl Srsf1fl/+ tissue and generated villi-derived 3D organoids in vitro. The clonogenic capacity of these purified Apc;fl/fl Srsf1fl/+ epithelial cells was strongly impaired (Fig. 3c–e) demonstrating a persistence of this phenotype in a stromal-independent context. To determine in more detail whether Srsf1 depletion affected normal intestinal stem cell homeostasis we generated inducible vil-Cre-ERT2 WT and Srsf1fl/+ mice carrying the Lgr5GFP-CREERT2 transgene28. Following tamoxifen-induced gene deletion, we analysed the LGR5 + ISC population using GFP IHC to visualise LGR5-GFP expression and flow cytometry to determine the percentage of GFP positive cells. Both analyses showed that Srsf1 depletion had no impact on the LGR5 ISC population (Figure S3l–n). In addition, sorted single LGR5-GFP positive cells had the same capacity to form organoids when plated in vitro and showed no changes stem cell marker gene expression following Srsf1 depletion (Figure S3o–q). Together, these data indicate Srsf1 depletion does not affect normal LGR5 + intestinal stem cell homeostasis but significantly impairs the growth of Apc deficient cells.
Oncogenic SRSF1 levels affect cell-type plasticity
To investigate whether the reduced proliferative phenotype observed in the intestinal mucosa of Apc;fl/fl Srsf1fl/+ was due to changes in intestinal cell identity, we performed RNAseq analysis of Apcfl/fl and Apc;fl/fl Srsf1fl/+ intestines. We compared the Apc;fl/fl Srsf1fl/+ transcriptome (Supplementary Data 8) with previously defined signatures of intestinal cell types29,30 using gene set enrichment analysis (GSEA). Interestingly, we found a significant overlap between genes associated with late transit-amplifying and differentiated enterocytes and gene overexpressed in Apc;fl/fl Srsf1fl/+ intestinal cells (Figs. S3r–S3u) (Supplementary Data 9). Numerous differentiated cell marker genes were overexpressed in Apc;fl/fl Srsf1fl/+ compared to Apcfl/fl, including Slc13a2 and Apoc2 (Fig. 3f). We also found that expression of the Wnt target gene and cancer stem cell marker Prox1 was decreased in Apc;fl/fl Srsf1fl/+ (Fig. 3g). Interestingly, the increase in the splicing isoform ratio of Kras4B/Kras4A observed after Apc deletion (Fig. 1c and S1f) was reversed upon simultaneous deletion of Srsf1 (Fig. 3h). This was not due to alterations in nuclear localisation of β-catenin, a previously described function of Srsf1, as demonstrated by IHC analysis (Fig. S3v, w)31. These data suggest that Srsf1 promotes a less differentiated, stem cell-like phenotype following Apc deletion. To investigate the generality of these findings we depleted Srsf1 using shRNA in a number of tumourigenic organoid models (Fig. S3x–z)32,33 and determined stem cell function using clonogenicitiy assays. Validating our in vivo experiments, Srsf1 knockdown led to a significant reduction in clonogenicity, growth rate and viability of Apcfl/fl organoids suggesting reduced stem cell function (Fig. 3i–k and S3x–z). Notably, the same results were observed following Srsf1 knockdown in two mouse CRC organoid lines that model late-stage, metastatic disease (Fig. 3i–k and S3x–z). The expression of the stem cell marker Lgr5 was also reduced in Srsf1 depleted organoid lines (Fig. S2d). Together, these data demonstrate that Srsf1 depletion reduces stem cell properties and results in colorectal cancer cells adopting a more differentiated cell transcriptional phenotype.
SRSF1 facilitates intestinal cell dedifferentiation
Due to these findings we hypothesised that SRSF1 is required for differentiated enterocytes to dedifferentiate and acquire stem cell properties. Activation of KRAS or IκB kinase (IKK) combined with Apc loss has been shown to induce dedifferentiation of villus enterocytes34. Therefore, we generated mice carrying villinCreERT2 Apc;fl/fl KrasG12D or villinCreERT2 Apc;fl/fl Kras;G12D Srsf1fl/+ alleles and induced gene recombination with tamoxifen. As previously described34,35, a shorter 3-day post tamoxifen time point was employed so that dedifferentiating cells in the villus could be studied alone, without contamination from recombined cells migrating from the crypts. After 3-days, villi from the small intestines were dissected, digested to single cells and plated to determine dedifferentiation efficiency (Fig. S4a). We compared enterocyte dedifferentiation between villinCreERT2 Apc;fl/fl KrasG12D and villinCreERT2 Apc;fl/fl Kras;G12D Srsf1fl/+ mice and found that depletion of Srsf1 led to a significant reduction in the proportion of organoids formed (Fig. 4a, b). The clonogenic capacity of the organoid lines derived from these dedifferentiated cells was also reduced in the Srsf1fl/+ genotype (Fig. 4c) suggesting that the acquisition of stem cell properties was impaired. Intriguingly, Kras isoform splicing was still modulated by SRSF1 even in the context of constitutively active KRAS signalling (Figure S4b).
To confirm these observations, we employed a different dedifferentiation model driven by hyperactive NF-κB signalling34, (villinCreERT2 Apcfl/fl IKK2ca) and subjected these mice to the same experimental procedure. Again, we found a similar impairment in dedifferentiation capacity of villi cells and reduced clonogenicity in derived organoids following heterozygous Srsf1 deletion (Fig. 4d–f).
To rule out the possibility that these clonogenic cells derived from crypt cells migrating into the villi we sorted differentiated villus cells based on expression of EPHB2. EPHB2 marks a gradient of stem and progenitor crypt cells with expression absent in differentiated villus cells30. We sorted EPHB2 negative epithelial cells from wild-type crypts and confirmed that they did not have clonogenic capacity (Figure S4c–e). We next utilised this sorting strategy to obtain differentiated villus cells from induced villinCreERT2 Apc;fl/fl KrasG12D and villinCreERT2 Apc;fl/fl Kras;G12D Srsf1fl/+ mice (Fig. 4g). EPHB2 negative differentiated Apc;fl/fl KrasG12D cells were able to form colonies, indicative of cellular dedifferentiation. This ability was significantly impaired following Srsf1 depletion, demonstrating the requirement of Srsf1 for the acquisition of stem cell properties (Fig. 4h, i). To confirm these findings we utilised an analogous model where doxycycline-inducible shRNA depletion of Apc is used to activate Wnt signalling in KrasG12D mutant colonic organoids36. In the absence of doxycycline, organoid growth is dependent on media supplementation with Wnt3a and R-spondin. In addition, EPHB2 negative cells have poor clonogenic capacity indicative of a differentiated cell phenotype (Figure S4f). We used shRNA to deplete Srsf1 in these organoids and following doxycycline induction FACS sorted for EPHB2 negative, differentiated cells. Again, depletion of Srsf1 significantly impaired the ability of such cells to form colonies (Fig. 4j–l). In addition, organoids derived from Srsf1 depleted differentiated cells expressed significantly higher levels of the differentiated cell markers Muc2 and Krt20 (Figure S4g, S4h). Together, these data demonstrate a requirement for Srsf1 expression in mediating intestinal cell plasticity.
To determine whether Srsf1 also drives increased stem cell properties, we overexpressed wild-type Srsf1 (Srsf1WT) or Srsf1 with mutations in the second RNA recognition motif (RRM2) leading to impaired RNA binding37, (Srsf1D136A,K138A) in Apcfl/fl organoids (Figure S4i). Consistent with our deletion studies, Srsf1WT overexpression led to increased organoid growth, clonogenicity and increased expression of the stem cell marker Lgr5 (Figures S4i–l). By contrast the Srsf1 mutant did not affect organoid growth, demonstrating that the RNA-binding ability of SRSF1 is necessary for its dedifferentiation activity. Based on these findings, we conclude that SRFS1 mediates intestinal cell dedifferentiation and the acquisition of stem cell properties.
Wnt-induced SRSF1 levels enforce splicing dysregulation
To ascertain the extent to which Srsf1 contributes to Wnt-driven splicing dysregulation and identify potential splicing changes that mediate oncogenesis, we conducted differential splicing analysis on Apcfl/fl and Apc;fl/fl Srsf1fl/+ intestinal tissue, in which we observed reduced proliferation and stem cell activity, using SUPPA2. We identified 577 alternative splicing events (p < 0.05) (Fig. 5a and Supplementary Data 10). The majority of these were exon skipping alternative splicing events (30.5%), supporting previous work using in vitro models showing that SR proteins promote splice site selection through exonic splicing enhancer recognition38. We then determined the proportion of unique dysregulated alternative splicing events in Apcfl/fl that were SRSF1-dependent. We compared the alternative splicing events identified from our wild-type/Apcfl/fl analysis (Fig. 1b and Supplementary Data 3) with the alternative splicing events found in Apcfl/fl/Apc;fl/fl Srsf1fl/+ (Supplementary Data 10). There was a significant enrichment of alternative splicing events from Apcfl/fl/Apc;fl/fl Srsf1fl/+ that were also found in our wild-type/Apcfl/fl dataset (p < 1e−5) (Fig. 5b). In addition, a significant proportion of the alternative splicing events occurring after Apc deletion were reverted upon deletion of Srsf1fl/+ (127 alternative splicing events with discordant dPSIs, p = 0.049) (Supplementary Data 11). Again, rMATS analysis identified a large proportion of potentially novel splicing events suggesting widespread changes in alternative splicing mediated by SRSF1 (Figure S5a and Supplementary Data 12).
We validated several of the alternative splicing events discovered from our differential splicing analysis (Fig. 5c, d). Additionally, isoform level changes in Kras splicing were detected and validated confirming that the Wnt-induced increase in the pro-proliferative Kras4b isoform over the pro-apoptotic Kras4a isoform was reversed upon Srsf1 depletion. SRSF1-dependent changes in Kras isoform splicing levels were also present in multiple other models (Figs. 3h, S4b, S6j and S6m). To determine whether these transcripts were direct targets of SRSF1 we carried out RNA immunoprecipitation experiments. By pulling down SRSF1 from the CMT93 mouse colorectal cancer cells line and carrying out qRT-PCR we identified significant binding of Srsf1 to several of the alternatively spliced transcripts identified by RNAseq (Fig. S5b, c). In addition, alternative splicing events (events identified via SUPPA2 analysis, not including AF events) in our Apcfl/fl/Apc;fl/fl Srsf1fl/+ dataset, which were repressed following Srsf1 depletion, were enriched for SRSF1 binding motifs, together suggesting loss of direct, functional SRSF1 binding to these transcripts led to the splicing changes we observed (Fig. S5d). Besides the well-characterised role of SRSF1 in pre-mRNA splicing in the nucleus, this shuttling SR protein also has post-splicing functions, which include mRNA export, mRNA translation and nonsense-mediated decay12,39. We utilised a novel mouse model carrying a nucleo-cytoplasmic shuttling defective Srsf1 mutant to determine whether non-nuclear functions of SRSF1 could explain the phenotypes we observed40. Apc deficient organoids carrying a single allele of Srsf1-NRS (which is unable to shuttle to the cytoplasm) had no defect in clonogenic capacity (Fig. S5e–g). This is unlike organoids carrying heterozygous Srsf1 deletion (Fig. 3c, e) demonstrating that the cytoplasmic function of Srsf1 does not explain the phenotypes we observe in this model. Together, these data suggest the primary cause of the effects we observed are due to nuclear (presumably splicing) functions of SRSF1.
To functionally determine whether Kras4b plays a role in colorectal tumourigenesis we treated Apcfl/fl and metastatic KPN (Kras;G12D/+ Trp53;fl/fl Rosa26N1icd/+) organoids with the KRAS4B specific inhibitor deltarasin (Fig. S5h)41,42. Deltarasin is a small molecule inhibitor of the KRAS4B -PDEδ interaction, and PDEδ has been shown to chaperone and recruit KRAS4B to the plasma membrane, but is not required for KRAS4A recruitment. Treatment with deltarasin led to a rapid organoid dissociation and a highly significant reduction in viability of both Apcfl/fl and KPN organoid lines demonstrating an important role for KRAS4B in maintaining CRC organoid viability (Fig. 5e, f). Treatment of wild-type organoids led to a smaller reduction in viability (Fig. 5e, f). Treatment of human normal and CRC organoids showed a similar effect, with organoids derived from normal colon being resistant but those derived from tumours being highly sensitive to deltarasin treatment (Fig. S5i, S5j). To validate these findings we designed an antisense morpholino that inhibits the splicing of Kras4b. Treatment of organoids with this morpholino proved highly effective at reducing the Kras4b/Kras4a splice ratio (Fig. S5m, S5n) and significantly reduced the clonogenic capacity and viability of Apcfl/fl and KPN organoids (Fig. S5k–S5p).
To further this analysis, we next asked whether Kras4b expression is sufficient to rescue organoid viability in Srsf1 depleted organoids. We generated organoid lines overexpressing GFP alone, or Kras4b (also marked with GFP expression) both carrying a DOX inducible shSrsf1 RFP construct. In this model Kras4b expression (marked by GFP) can be maintained alongside Srsf1 depletion (marked by RFP expression) (Fig. S5q). We allowed organoids to form, induced with DOX and tracked GFP/RFP double-positive organoids over 3 days. Similar to our previous results, depletion of Srsf1 in GFP expressing controls led to a significant reduction in organoid growth (Fig. 5g, h). However, this growth reduction was significantly rescued to wild-type levels by ectopic expression of Kras4b indicative of a functional role for Kras4b in mediating the phenotypic effects of SRSF1 expression in this model (Fig. 5g, h).
To infer the biological function of the two Kras splicing isoforms in the context of CRC, we employed proximity-dependent biotin identification (BioID) to uncover interacting proteins of KRAS4A and KRAS4B (Fig. S5r–S5u). We found 83 proteins that significantly (p < 0.05) interacted with both KRAS4A and KRAS4B (Fig. S5t and Supplementary Data 13). We also identified 23 proteins that monogamously interacted with KRAS4A and 22 proteins that uniquely interacted with KRAS4B. Some of these uniquely interacting proteins were associated with contrasting cell signalling pathways and associated with unique cellular compartments (Supplementary Data 13). For example, IGF1R and RALA interacted only with KRAS4A whereas BRAF and RAP1A were exclusively associated with KRAS4B. These data show that KRAS4A and KRAS4B have specific subsets of protein interactors indicating SRSF1-controlled splicing changes can result in significant changes in the oncogenic protein interactome.
High Srsf1 expression mediates tumour cell plasticity and colorectal cancer invasiveness
To explore the role of SRSF1 in advanced stage colonic carcinogenesis we utilised a previously described model of carcinogen-induced tumourigenesis43. Cohorts of villinCreERT2 p53fl/fl and villinCreERT2 p53;fl/fl Srsf1fl/+ mice were treated with repeated rounds of azoxymethane (AOM) and aged until signs of colonic tumourigenesis became apparent (Fig. S6a). Mice treated with AOM presented predominantly with colonic tumours, with tumours of the small intestine rarely occurring (Fig. S6b). Although we did not find evidence that targeting Srsf1 provided a survival advantage or a change in tumour number or burden (Figs. S6c–S6e) we found that deletion of one copy of Srsf1 (Fig. S6f) significantly reduced the proportion of mice presenting with invasive tumours in this model (Fig. 6a, b). Additionally, overall number and percentage of invasive tumours per mouse and the presence of extensive collagen deposition was significantly reduced in Srsf1 depleted mice (Figs. 6c and S6g–S6i).
Upon examination of the invasive tumours, we found evidence of cell plasticity changes. Immunohistochemical analysis of the cancer stem cell marker PROX1 revealed a significant decrease in PROX1 expression in invasive p53;fl/fl Srsf1fl/+ tumour epithelial cells (Fig. 6d, e) corroborating our RNAseq results in short-term Cre-lox recombined Apc;fl/fl Srsf1fl/+ tissue (Fig. 3g). We also found a significant corresponding increase in expression in the differentiation marker, SLC13A2 (Figs. 6d, f), and altered Kras splicing in these tumours (Fig. S6j). These data suggest that impaired Srsf1 expression reduces the invasive and stem cell behaviour of colonic tumours in vivo.
To determine whether SRSF1 directly controls these phenotypes, we cultured 3D tumour organoids from invasive AOM p53fl/fl tumours and depleted Srsf1 expression using shRNA (Fig. S6k). We found that both PROX1 expression and Kras4b/Kras4a splicing ratio were impaired upon Srsf1 knockdown confirming a direct role for Srsf1 in mediating these effects (Figs. S6l, S6m). We then carried out an organoid invasion assay and observed a significant reduction in organoid cell invasion through matrigel upon Srsf1 depletion (Fig. 6g–i).
Together, these data suggest that SRSF1 directly controls tumour cell invasion and maintenance of stem cell properties in late-stage colon cancer.
SRSF1 depletion inhibits growth and stemness of human colorectal cancer-derived organoids
To ascertain how SRSF1 levels correlate with human CRC progression, we analysed colon cancer tissue microarrays (TMAs) containing varying severities of the disease. First, we investigated if the cancer stem cell marker PROX1, which has been show to promote metastatic outgrowth of cells44, correlated with SRSF1 expression. We found a positive correlation of SRSF1 and PROX1 expression (Fig. 7a, b and S7a) similar to that seen in our laboratory models (Figs. 3g and 6d, e). We next examined SRSF1 expression in different tumour stages and found that more invasive and metastatic tumours had significantly higher expression of SRSF1 (Fig. 7c) showing that SRSF1 levels correlate with advanced-stage colorectal cancer.
To phenocopy clinical intervention by way of attenuating SRSF1 levels in human CRC, we manipulated SRSF1 in patient-derived organoids (PDOs) using shRNA. Consistent with our animal experiments the clonogenicity, size and viability of the PDOs was impaired by depleting SRSF1 expression (Fig. 7d–g). Reduced SRSF1 expression was associated with a corresponding reduction in LGR5 suggesting that in human cancer, as in our mouse models, SRSF1 mediates stem cell function (Figs. 7h and S7b–S7d). We also observed an impairment in the ratio of KRAS4B/KRAS4A (Fig. 7h) which we had earlier found to be critical in facilitating oncogenic growth in mouse (Fig. 5e, f).
Taken together these data establish that, not only can SRSF1 attenuation mitigate the oncogenic potential of CRC in mouse models, but also in the human disease.
Tumour growth has been shown to increase the transcriptional output of cells leading to an elevated burden of pre-mRNAs requiring processing, including an increased requirement for RNA splicing45. The RNA addiction of hyperproliferative cells might therefore be exploited for clinical purposes. This idea was supported by earlier work showing that the spliceosome is a potential therapeutic vulnerability following MYC induction in 2D breast cancer cells and also during lymphomagenesis18,19. Here we have shown that genes associated with RNA metabolic processing are upregulated in a mouse model of colorectal cancer initiation. These include genes involved in RNA splicing. 60 splicing related genes are upregulated following Apc loss, accounting for approximately a quarter of all known splicing genes. Based on this, we surmised that splicing impairment might effectively target rapidly proliferating intestinal organoids with hyperactive Wnt signalling. Indeed, treating organoids with pladienolide B (which targets the SF3B complex) successfully targeted Apcfl/fl organoids without adversely affecting wild type organoids suggesting that RNA splicing generally may act as a therapeutic vulnerability in CRC. However, this drug has recently failed in clinical trials as it caused optic-nerve dysfunction and vision loss in patients46. On the other hand, a novel drug targeting the splicing factor SRSF1, ABX300, has been shown to impair SRSF1 splicing activity to treat diet-induced obesity in mice without any observed toxicity47. Furthermore, villinCreERT2 Srsf1fl/+ mice had normal intestinal morphology without any change in cell proliferation or normal stem cell function, and an inducible shRNA against Srsf1 had no observable phenotype in wild-type organoids. Thus, there is a clear therapeutic window for targeting SRSF1 in colorectal cancer.
In conjunction with an increased requirement for splicing factors, we identified dysregulation of splicing itself, as shown by the shift in RNA isoforms generated following Apc loss. We found that the Kras4a and 4b isoforms were alternatively spliced depending on the level of Wnt activation, and this was mediated by SRSF1. SRSF1 has previously been proposed to be oncogenic and is a direct transcriptional target of Myc48,49. In addition, SRSF1 expression has been shown to be dependent on Wnt signalling in colorectal cancer suggesting that Wnt driven dysregulation of RNA splicing is partially mediated by SRSF1 following Apc loss50. The Kras4a isoform has been shown to promote cell death24 and, when mutated, has significantly less oncogenic potential in mice than Kras4b51. Not only did we see a shift in splicing of these isoforms following Apc deletion, but we found that when we impaired the function of Apc-upregulated KRAS4B using deltarasin or an antisense morpholino, we could hamper oncogenic growth in our organoid models. Furthermore, the expression of Kras4b could rescue the growth of cells with impaired Srsf1 levels. As Srsf1 depletion leads to alterations in numerous splicing events it is unlikely that this single splicing event fully explains the role of SRSF1 in CRC. It is likely that numerous SRSF1 targets contribute to its phenotypic effect, making SRSF1 an attractive therapeutic target, depletion of which could impact on multiple different pathways.
Targeting Srsf1 resulted in reduced proliferation and stem cell function consistent with similarly described functions of SRSF1 in breast cancer50,52. Transcriptome analysis of Apc;fl/fl Srsf1fl/+ intestinal tissue revealed a role for SRSF1 in modulating cellular plasticity with the gene expression signature becoming distinctly enterocyte-like. Dedifferentiation of enterocytes has been shown to support a ‘top-down’ model of colorectal tumour morphogenesis where adenomas originate at the top of intestinal crypts34,53. Our data support a role for SRSF1-driven dedifferentiation in enterocytes. Following early activation of constitutive KRAS or NF-kB signalling with Apc loss, a reduction in dedifferentiation-driven clonal events arising from villi-derived differentiated cells was observed with impaired Srsf1 levels. Thus, SRSF1 can mediate cellular plasticity. As SRSF1 is a splicing factor, such plasticity changes might be brought about indirectly as a result of a general splicing repression response, or due to a change in the RNA isoform repertoire. As well as showing increased expression of differentiation marker genes, Srsf1 reduction resulted in a decrease in the stem cell marker Prox1. PROX1 is a Wnt-regulated transcription factor that has been shown to advance colon cancer progression by promoting dysplasia in colonic adenomas54, as well as enhancing metastasis in Wnt-driven progenitor cells44. Not only were Prox1 levels impaired in the intestines of Apc;fl/fl Srsf1fl/+ mice following acute Apc deletion, but this reduced level was observed in the advanced tumours of AOM treated p53;fl/fl Srsf1fl/+ mice. These tumours were also significantly less invasive and displayed evidence of the same cell differentiation phenotypes observed in our early-stage tumour model. Encouragingly, this demonstrates a potential to target SRSF1 mediated cellular plasticity even in the advanced stages of the disease.
In conclusion, our investigation using mouse models, ex-vivo organoid systems and patient-derived samples demonstrates that intestinal Wnt-driven cancers are addicted to the spliceosome. We have shown that targeting an individual oncogenic splicing factor, SRSF1, impairs cancer progression through a variety of mechanisms (Fig. 7i). Modulation of cell-type plasticity in favour of a gene expression signature with reduced stemness, an impaired ability of cells to dedifferentiate, as well as tumours having a lower invasive potential, all make targeting SRSF1 a highly attractive option, and may complement current standard-of-care therapies.
Contact for reagent and resources sharing
Requests for further information, reagents and resources should be directed to and will be fulfilled by the Lead Contact, Kevin B. Myant: (firstname.lastname@example.org).
Species used: Mus musculus. All animal experiments were performed in accordance with a UK Home Office licence (Project License 70/8885), and were subject to review by the animal welfare and ethics board of the University of Edinburgh. Both genders of mice were used for all experiments at an age of between 6 and 12 weeks once they had reached a minimum weight of 20 g. Mice were bred at the animal facilities of the University of Edinburgh and were kept in 12 h light–dark cycles and were given access to water and food ad libitum. Mice were maintained in a temperature- (20–26 °C) and humidity- (30–70%) controlled environment. Colonies had a mixed background (50% C57Bl6J, 50% S129). The genetic alleles used for this study were as follows: villinCreER55, Apc (floxed)56, ASF/SF2 (Srsf1 floxed)27, Kras (G12D)57, IKK2ca58, P53 (floxed)59. Mice were genotyped by Transnetyx (Cordoba, USA). At experiment endpoints, mice were humanely sacrificed by cervical dislocation (CD) in line with UK Home Office regulations.
Tumour models and treatments
For short-term Cre-Lox recombination where animals were taken at a specific time point of between 2 and 5 days postinduction of gene recombination (depending on the experimental model), mice were induced with a single dose of tamoxifen (Sigma-Aldrich, T5648) by intraperitoneal injection of 120 mg/kg on the first day and then optionally with a further treatment of 80 mg/kg on the second and third days.
For the long-term Cre-Lox recombination in tumour cohorts, mice were given a 300 µL, 10 mg/mL dose of tamoxifen on day 0 and a 200 µL, 10 mg/mL dose of tamoxifen dose on day 1. Mice were then treated via intraperitoneal injection with azoxymethane (AOM) (Sigma-Aldrich, A5486) at a dose of 10 mg/kg once a week, every week, starting on day 12, for 6 weeks.
Mice were aged until symptomatic of disease (rectal bleeding, weight loss, hunching and/or pale feet). Mice were randomly distributed by sex and age and a minimum of 20 or 3 mice were used for long and short-term experiments respectively. In long-term tumour cohort mice, tumour number and burden were macroscopically quantified in situ after mouse termination.
For animals which were used for BrdU analysis, 200 µL of cell proliferation labelling reagent (GE Healthcare, RPN201) was administered via intraperitoneal injection 2 h before culling.
Splicing factor-targeted synthetic lethal CRISPR screen & organoid transductions
A targeted guide RNA (gRNA) library for the 60 APC-induced splicing factors was generated using sequences from Mouse GeCKOv2 Library A (Zhang Lab/GeCKO website), using 3 guide RNAs per gene and 9 non-targeting control guides (Supplementary Data 6). In order to avoid ligation bias, oligonucleotides (Sigma) corresponding to each guide RNA were cloned individually into the lentiGuide-Puro vector (Addgene, 52963), Sanger sequenced, and then pooled at equimolar concentrations. LentiGuide-Puro was a gift from Feng Zhang60. Large-scale plasmid prep was achieved by electroporation of Endura electrocompetent cells (Lucigen) as previously described (Zhang Lab/GeCKO website). Equal guide RNA coverage within the library was confirmed via next-generation sequencing (NGS). The guide RNA library was used to generate infectious lentiviral vector particles.
The workflow of the synthetic lethal screen was as follows: Day 0 – Wild type-Cas9 and Apcfl/fl-Cas9 expressing organoids (derived from tamoxifen-inducible villinCreERT2 LSL-Cas9 mice) were plated and grown (full 24-well plate each, 20 µl Matrigel/well) in organoid growth media supplemented with 6 µM CHIR-99021 (GSK-3 inhibitor, Abcam, ab120890). Day 3 – Organoids were further expanded to two full 24-well plates each and grown in ‘Organoid+ media’: ADF (Advanced DMEM/F12 + B27 + N2) (500 µL/well), Noggin, EGF, R-spondin (only for Wild type organoids), 10 µM Y-27632 dihydrochloride (ROCK inhibitor, Tocris, 1254), 6 µM CHIR-99021, 1 µM Jagged-1 (188–204) (Notch Ligand, AnaSpec, AS-61298) and 1 mM valproic acid (Sigma, PHR1061). Day 5 – organoids were dissociated via mechanical disaggregation followed by treatment with StemPro Accutase Cell Dissociation Reagent (Gibco, A1110501) for 5 min at 37 °C and then neutralised in 1% BSA. Cells were counted using the Countess II Automated Cell Counter (Invitrogen) and 1×106 wild type-Cas9 or Apcfl/fl-Cas9 organoid cells were transduced at a multiplicity of infection (MOI) of 0.3 for each of the three biological replicates. (The precise working titre of the virus was calculated in advance by viral titration experiments on non-Cas9 expressing Apcfl/fl organoids and measuring survival following puromycin selection). Briefly, 250,000 cells were plated on an 80 µL bed of Matrigel in each of four wells of a 12-well plate (1×106 cells per genotype). Cells were incubated with 0.3 MOI lentivirus and 4 µg/mL of Hexadimethrine bromide/polybrene (Sigma, H9268) in a total volume of 500 µL of organoid+ media. Cells were allowed to transduce for 24 h. Day 6 – virus was removed and adhered organoid cells were overlaid and set with 100 µL Matrigel, followed by standard organoid growth media with Y-27632 only. Day 7 – Puromycin was added at a concentration of 2 µg/mL and Y-27632 was maintained in the media. Day 8 – fresh puromycin and Y-27632 containing media was added to organoids. Day 11 - puromycin and Y-27632 treatment was stopped and cells were grown in standard organoid growth media, and this was also refreshed on Day 13. Organoids were harvested on Day 14 and genomic DNA was purified using the DNeasy Blood & Tissue Kit (Qiagen, 69504). 4 independent replicate experiments were performed.
Intestinal organoids were passaged as usual via mechanical disaggregation and DMEM/PBS washes. After the last wash step, organoid cell pellets were treated with 1 mL StemPro Accutase cell dissociation Reagent (Gibco, A1110501) and incubated at 37 °C for 5–10 min in order to generate single cells. An equal volume of 1% BSA was added to stop the digestion reaction and then diluted in 10 mL DMEM/F-12 media. Cells were then passed through a 40 µm cell strainer and centrifuged at 300 g for 3 min. Cells were counted using the Countess II Automated Cell Counter (Invitrogen). Between 1–10 × 103 single cells were plated per 5 µL drop of Matrigel/BME and a minimum of 4 drops were plated for each genotype/condition. Organoid growth media was added and resultant spheres/clones were counted after 4 days. The clonogenic capacity was determined by calculating the average percentage of spheres formed in each drop per number of single cells plated.
Mice were administered 120 mg/kg tamoxifen on day 0 and 80 mg/kg tamoxifen on days 1 and 2. On day 3, mice were culled and the first 10 cm of the small intestine following the duodenum was dissected and washed twice with PBS. The intestine was opened longitudinally with small scissors and the opened intestine was rinsed in PBS. Villi were removed by scraping using a glass coverslip, and were collected in DMEM/F12 in a 50 mL centrifuge tube. The tube was gently inverted 5–6 times in order to dissolve the mucus and debris was allowed to settle for 30 s. After the larger aggregates settled down, the supernatant containing the villi was decanted into another centrifuge tube. This supernatant was then centrifuged at 100 g for 3 min and the collected villi pellet was resuspended gently in 10 mL DMEM/F12 so as not to fragment or disrupt the villi structure. Whole villi were observed under a light microscope and then counted. Equal numbers of villi were taken for each genotype/condition, centrifuged at 100 g for 3 min and then resuspended in 3–5 mL TryplE Express (Gibco, 12605010) and incubated at 37 °C for 30 min. During the incubation, the suspension was vigorous resuspended via pipetting every 10 min. After each resuspension, a droplet of the digestion medium was observed under the microscope to check digestion. After digestion to single cells, cells were resuspended in 10 mL DMEM/F12 and passed through a 40 µm cell strainer. Single cells were counted and then 12 droplets of Matrigel/BME of 10 µL containing 50,000 cells per droplet were plated in organoid growth media, with the addition of 10 µM Y-27632 dihydrochloride (ROCK inhibitor, Tocris, 1254). Colonies/spheres resulting from dedifferentiated villi-derived single cells were scored after 7 days.
For the wild type vs Apcfl/fl and Apcfl/fl vs Apc;fl/fl Srsf1fl/+ RNAseq experiments, 3 mice from each genotype were given intraperitoneal injections of tamoxifen of 120 mg/kg on day 0 and 80 mg/kg tamoxifen on day 1. The mice in the Apcfl/fl vs Apc;fl/fl Srsf1fl/+ experiment received an additional 80 mg/kg tamoxifen induction on day 2. Mice were culled on day 5, and the small intestine was dissected and flushed with PBS. A 1 cm piece of small intestine following the duodenum was placed in RNAlater solution (Sigma). RNA was later extracted as previously described and was sent to Edinburgh Genomics for sequencing. Truseq (Illumina) mRNA-seq libraries were prepared from total RNA and these were then sequenced using the Illumina HiSeq 4000 using 150 base paired-end sequencing.
Human organoid culture conditions
Human adenoma, carcinoma and liver met organoids were cultured in: 30% R-spondin conditioned media, 1% Noggin conditioned media, 1x B27, 50 ng/mL EGF, 10 nM Gastrin, 10 nM PGE2, 10 mM Nicotinamide, 10 µM SB202190, 600 nM A83-01, 12.5 mM N-Acetylcysteine in ADF (with 1X PenStrep, HEPES, Glutamine). Human organoid transduction conditions were the same as for mouse organoid transductions except that single-cell suspension were generated in TrypLE with 10 µM Y27632 for 10 min at 37 °C with mechanical dissociation every 3 min.
Human patient-derived organoids (PDOs)
C-002 is a cetuximab-resistant PDO generated from a biopsy of a liver metastasis from a gastrointestinal cancer patient and was generated elsewhere61. The following PDOs were generated by Dr Farhat Din and Prof Malcolm Dunlop, University of Edinburgh: MD175 is a 50 yr old female with familial adenomatous polyposis who previously underwent a colectomy and ileorectal anastomosis who then developed a stage 2 rectal cancer - individual polyp used in this study. MD20043 is an 81 yr old male with stage 4 rectal cancer, TNM (T3, 2, 1). MD19648 is a 45-year-old female with familial adenomatous polyposis complicated by a stage 3 rectal cancer - FAP rectum tumour, TNM (pT1, pN1a, 0). MD20853 is a 71 yr old male with a tubulovillous adenoma with low-grade dysplasia. MD20910 is a 60 yr old male with rectal cancer, TNM (pT2, N1b, 0). Ethical approval for human CRC organoid derivation was carried out under NHS Lothian Ethical Approval Scottish Colorectal Cancer Genetic Susceptibility Study 3 (SOCCS3) (REC reference: 11/SS/0109). All patients provided fully informed consent for the use of their tissues.
Biological pathway enrichment analysis
RNAseq data of the 2330 genes upregulated in Apcfl/fl relative to wild type were analysed using g:Profiler version e98_eg45_p14_ce5b097, accessed on 24/01/2020 using the following data sources: biological pathways-KEGG.
To generate organoids from wild type or genetically modified mice, the first 10 cm of small intestine following the duodenum was isolated, flushed with phosphate-buffered saline solution (PBS) and opened longitudinally using scissors. Villi were removed by scraping using a microscope coverslip. Remaining tissue was then washed several times with PBS and then incubated with 2 mM EDTA in PBS with gentle shaking at 4 °C for 30 min. Crypts were then removed from the tissue by vigorous pipetting and selecting through a 70 µm cell strainer. Crypts were scored and ~100 crypts were plated in 20 µL droplets of cold liquified Matrigel Growth Factor Reduced (GFR) Basement Membrane Matrix, Phenol Red-free, LDEV-free (Corning #356231/734-1101) or Cultrex Reduced Growth Factor Basement Membrane Extract Matrix, Type 2 (BME 2) (Trevigen #3533-010-02). A single 20 µl matrix droplet was grown in each well of a 24-well plate. Matrix droplets with suspended cells were allowed to solidify at 37 °C for 10 min prior to the addition of growth media. All organoids were grown in a humidified incubator at 37 °C supplemented with 5% CO2.
Organoids were grown in ‘organoid growth media’: Advanced DMEM/F-12 media (ADF, Gibco) supplemented with 100 units/mL penicillin, 100 µg/mL streptomycin, 2 mM L-Glutamine and 10 mM HEPES (Life technologies), N2 (Gibco, 17502048), B27 (Gibco, 17504044), 50 ng/mL EGF (Peprotech, 315-09-500) and 100 ng/mL Noggin (Peprotech, 250-38-500). Wild type organoids were grow with the addition of 500 ng/mL R-spondin-1 (Peprotech, 120-38-500). We later used Noggin and R-spondin via way of conditioned media made by transformed HEK 293 cell lines. The transformed Noggin producing cell line was a gift from Hans Clevers’ group (Hubrecht Institute) and the R-spondin producing cell line was purchased from Trevigen (#3710-001-01). Organoids were passaged via mechanical disaggregation using a serological pipette, where several rounds of ADF or PBS washing and centrifugation were used to remove the residual matrix, before resuspending organoid fragments in the fresh matrix.
Tumour cell isolation and organoid culture
Tumours were dissected from the intestine and then cut into pieces. Tumour tissue fragments were then incubated in 2 mL organoid growth media supplemented with 1 mg/mL collagenase II (Sigma, C1764), 0.5 mg/mL hyaluronidase (Sigma, H3506) and 10 µM Y-27632 dihydrochloride (ROCK inhibitor, Tocris, 1254). Incubation was at 37 °C for 60–90 min with vigorous shaking until the tumour was completely disaggregated. The digested reaction was then neutralised using 100 µL 1% BSA and then fragments were filtered through a 70 µm cell strainer. The filtered cells were then centrifuged at 600 g for 3 min and washed 2–3 times in DMEM/F12, before being resuspended and plated in an 20 µl droplets of BME in 24-well plates and overlaid with organoid growth media.
Pladienolide B treatment
Pladienolide B stock (Calbiochem, 5.30196.0001) was made up to 1 mM in DMSO. Wild type and Apcfl/fl organoids per broken into fragments via mechanical disaggregation and were plated at a density of ~40 fragments/5 µL drop of Matrigel in a 96-well plate, with at least 6 wells per Pladienolide B concentration for each of the three biological replicates. Organoids were allowed 48 h to develop prior to the addition of Pladienolide B, and were treated for 48 h with concentrations of Pladienolide B ranging from 0.5 nM–200 nM. For human organoid experiments the same protocol was used but a single dose of 1 nM Pladienolide B was used.
MTT/Resazurin cell viability analysis
For Thiazolyl Blue Tetrazolium Blue (MTT) cell viability assay, organoids were plated and treated in 96-well plates as already described. MTT (Sigma, M2128) solution was added to the organoid culture media at a final concentration of 500 µg/mL and incubated for 2–3 h at 37 °C, 5% CO2. The medium was then discarded and 20 µL of 2% SDS solution in H2O was added to solubilize the Matrigel (2 h, 37 °C). Then, 100 µL of DMSO were added for 1 h (37 °C) to solubilize the reduced MTT. The optical density was measured on a microplate absorbance reader (Wallac, 1420 Victor2 microplate reader) at 570 nm and a background read at 690 nm was subtracted from this value. Cell viability was normalised to either Wild type or Apcfl/fl DMSO control vehicle-treated organoids.
For Resazurin cell viability assay, Resazurin (R&D systems, AR002) was added at a volume equal to 10% of the cell culture media volume and incubated for 4 h at 37 °C. Fluorescence was read using 544 nm excitation and 590 nm emission wavelength. For CRISPR gene-targeting assays, cell viability was assessed by first removing the fluorescence of puromycin treated, non-transduced (and therefore dead) organoids, followed by normalisation relative to either wild type or Apcfl/fl non-targeting guide RNA control transduced organoids.
Overexpression of SRSF1 wild-type/DK mutant
Srsf1WT and Srsf1DK were generated as above and cloned into the pUltra-GFP vector (Addgene, 24129). The pUltra was a gift from Malcolm Moore62. PCR amplificaton used 5’-XbaI and 3’-BamHI restriction sites, with the addition of a C-terminal FLAG tag. Transduction was performed as already described and cells were expanded and subsequently subjected to cell sorting (FACS) for GFP + cells. For the clonogenicity assay – cells were subjected to FACS and seeded at 5000 cells/10 µl BME drop in Y27632, and cells were counted 5 days following FACS sorting.
Real-time quantitative polymerase chain reaction (qPCR)
Gene expression analysis was achieved via qPCR of mRNA. Total RNA was extracted using the RNeasy Mini Kit (Qiagen, 74106) followed by DNase treatment (Invitrogen, AM1906) and first-strand cDNA synthesis using 500 ng -1 µg RNA (Quantabio, 95048-100). qPCR was performed on 1/10 diluted cDNA using SYBR Select Master Mix (Applied Biosystems, 4472920) according to the manufacturer’s instructions on the CFX Connect Real-Time System (Bio Rad). Gene-specific oligonucleotides used are listed in (Supplementary Data 14). Ct-values were normalized to β-Actin, GAPDH or 18srRNA Ct-values, or the geometric mean of a combination of these loading controls. The delta-delta Ct method was used in order to calculate the relative fold change in gene expression of samples.
Reverse transcription polymerase chain reaction (RT-PCR) analysis of splicing isoforms
RNA extraction and first-strand cDNA synthesis using 500 ng RNA were performed as previously described. A PCR reaction was then performed with gene-specific oligonucleotides (Supplementary Data 14) using Phusion High-Fidelity DNA Polymerase (NEB, M0530S) following the manufacturer’s instructions using 5 µL of 1/10 diluted cDNA. PCR products were then separated by electrophoresis on a 1% agarose gel and fragment sizes were analysed using ImageJ63 using GAPDH RT-PCR for loading normalisation. Splicing isoform changes were calculated by generating a ratio of expression of each respective isoform in each condition.
CRISPR screen target validation experiments
For validation of individual genes arising from the CRISPR screen, the most effective guide RNA (based on Z-score) was selected for gene targeting. Guide RNAs used for the validation were: Non-targeting#2 (5’-GCTTTCACGGAGGTTCGACG-3’), Srsf1 (5’-CGGGTCCTCGAACTCAACGA-3’), Sf3b4 (5’-TTTAGATGCCACGGTGTACG-3’) and Ddx10 (5’-AATATCACCTACTCGAGAAC-3’). Guide RNAs were individually cloned into the lentiGuide-Puro vector (Addgene) and transformed into Stbl3 chemically competent E. coli (Invitrogen, C737303). Wild type-Cas9 and Apcfl/fl-Cas9 expressing organoids, as well as non-CAS9 expressing wild type and Apcfl/fl organoids, were transduced with lentivirus containing the specific guide RNA. This was done using 250,000 cells for each of the four cell genotypes. Two days after transduction, cells were selected with puromycin for 3 days. Surviving organoids were then digested to single cells using StemPro Accutase Cell Dissociation Reagent (Gibco, A1110501) and a clonogenicity assay was performed by plating 10,000 cells per 5 µl drop of Matrigel, with at least 4 Matrigel droplets per condition. Organoid growth media was added, with the addition of R-spondin-1 and 10 µM Y-27632 dihydrochloride (ROCK inhibitor, Tocris, 1254) to the Wild type-Cas9 and Wild type-Cas9-null organoids only. Four days after seeding, organoids resulting from single cells were scored and the clonogenic capacity was calculated as a percentage based on the number of cells seeded. Normalised clonogenicity values were then calculated by first normalising the Cas9-expressing cells with the Cas9-null cells for each genotype, followed by normalising these values to the nontargeting guide RNA expressing condition.
For the cell viability assay in Apcfl/fl organoids, 10,000 single cells of either Apcfl/fl-Cas9 or Apcfl/fl-Cas9-null single cells were plated onto a bed of 20 µl Matrigel in a well in a 96-well plate in triplicate and were transduced with lentivirus-containing media. The day after transduction (day 1), lentivirus was removed and cells were overlayed with 20 µl Matrigel and media. On day 2 puromycin selection was started. On day 8, resazurin (R&D systems, AR002) was added to the media for 4 h at 37 °C and fluorescence was read using 544 nm excitation and 590 nm emission wavelength. Cell normalisation was done as previously described, first using the Cas9-null organoids, and then using the non-targeting guide RNA condition as a reference.
Barcode PCRs and deep sequencing of integrated gRNAs
Genomically integrated guide RNAs were PCR amplified using staggered, barcoded PCR primers as previously described by Zhang lab64. Sequencing of amplified PCR products was achieved by Illumina deep sequencing (MiSeq v2).
Immunohistochemistry and histology
Intestinal tissue was dissected and washed with PBS, and fixed either as a Swiss-roll or a parcel in formaldehyde 4% for 24 h at 4 °C. For tumour scoring, intestinal tissue was fixed in Methacarn (60% Methanol, 30% Chloroform and 10% Glacial acetic acid) for 5 min at room temperature. Tissue processing was done using the Tissue-TeK VIP infiltration Processor (Sakura) followed by embedding in paraffin. Tissue sections were prepared at 5 µm using a microtome (Leica). Standard immunohistochemistry & histology techniques were used. Harris Hematoxylin and Eosin Y were used for nuclei and cytoplasmic staining respectively (Thermo Fisher Scientific).
The following antibodies were used: BrdU (BD Biosciences, 347580, pH6, 1/500), PROX1 (R&D systems, AF2727, pH6, 1/100 for human tissue array, 1/200 for mouse sections), SLC13A2 (Atlas antibodies, HPA014963, pH8, 1/100), SRSF1 (Invitrogen/Thermo Fisher Scientific, 32-4600, pH8, 1/10,000), Ki67 (Abcam, ab15580, pH6, 1/2000), Active Caspase-3 (R&D systems, AF835, pH6, 1/800). Secondary detection was achieved using Dako EnVision + /HRP rabbit/mouse System, neat (Agilent technologies, K400311-2), except for PROX1 where Rabbit anti-Goat IgG was used 1/200 (Thermo Fisher Scientific, 81–1620). Staining was achieved by Diaminobenzidine (DAB) Quanto Chromogen and Substrate (Thermo Fisher Scientific).
To stain collagen, Picro Sirius Red was used: de-waxed slides were submerged in Picro Sirius Red solution for 2 h. Picro Sirius Red Solution: 0.1% Direct red 80 (Sigma, 41496LH), 0.1% Fast green FCF (Abcam, ab146267) in Picric acid solution 1.3% in H2O (Sigma, P6744). Post staining, slides were washed twice in acidified water, dehydrated according to standard protocols and mounted.
Images were taken by using either the BX53 Upright Microscope (Olypmus) with the CellSens imaging software (Olympus) or the Nanozoomer Digital slide scanner (Hamamatsu) with the NDP.view2 software (Hamamatsu). Image analysis and quantification was done using QuPATH65.
The colon cancer human tissue arrays used were CO804b and CO2081b. (Biomax).
shApc;KrasG12D/+;shRNA de-differentiation assay
shApc;KrasG12D/+ organoids were previously described36, and cultured in ADF + + media with 1X B27, 1X N2, EGF (50 ng/mL), 1% Noggin CM, 10 mM Nicotinamide, 1.25mM N-acetylcysteine. Organoids were lentivirally transduced with either pTripZ-minP-shRenilla, or pTripZ-minP-shSrsf1. Organoids were given either a 12 hr or 24 hr treatment with or without doxycycline (1 µg/mL) before being collected and digested to single cells in TrypLE containing 10 µM Y-27632 for 30 min at 37 C. Cells were washed in ADF + + before being passed through a 40 µM cell strainer. Single cells were centrifuged at 500x g for 5 min at 4 C before being stained with 1:200 EphB2-APC conjugated antibody (BD Bioscience, Clone 2H9) for 30 min at room temperature in PBS with 0.1% BSA and 10 µM Y-27632. Cells were then washed twice in PBS at 500x g for 5 min at 4 C before being subjected to FACS (BD FACSARIA™ III) for EphB2low and EphB2high (no doxycycline) or GFP + /RFP + /EphB2low and EphB2high (doxycycline) populations. Single cells were then seeded into 20 µl BME in organoid media containing 10 µM Y-27632 for 48 h. Formed organoids were counted 7 days after FACS, and clonogenicity was calculated as (#GFP + /RFP + organoids/#single cells seeded x100).
EPHB2 negative in vivo dedifferentiation assay
Mice were administered 120 mg/kg tamoxifen on day 0. On day 2, mice were culled and the first 10 cm of the small intestine following the duodenum was dissected and washed twice with PBS. The intestine was opened longitudinally with small scissors and the opened intestine was rinsed in PBS. Villi were removed by scraping using a glass coverslip, and were collected in DMEM/F12 in a 50 mL centrifuge tube. The tube was gently inverted 5–6 times in order to dissolve the mucus and debris was allowed to settle for 30 s. After the larger aggregates settled down, the supernatant containing the villi was decanted into another centrifuge tube. This supernatant was then centrifuged at 100 g for 3 min and the collected villi pellet was resuspended gently in 10 mL DMEM/F12 so as not to fragment or disrupt the villi structure. Whole villi were observed under a light microscope and then counted. Equal numbers of villi were taken for each genotype/condition, centrifuged at 100 g for 3 min and then resuspended in 2 mL TryplE Express (Gibco, 12605010) and incubated at 37°C for 30 min. During the incubation, the suspension was vigorous resuspended via pipetting every 10 min. After each resuspension, a droplet of the digestion medium was observed under the microscope to check digestion. After digestion to single cells, cells were resuspended in 10 mL DMEM/F12 and passed through a 40 µm cell strainer. Single cells were washed once with 0.1% BSA in PBS and stained with 1:200 EphB2-APC conjugated antibody (BD Bioscience, Clone 2H9) and 1:200 Epcam-PE-conjugated antibody (BD Biosciences, 563477) for 30 min at room temperature in PBS with 0.1% BSA. Cells were then washed twice in 0.1% BSA in PBS at 500 g for 5 min at 4 C before being subjected to FACS (BD FACSARIA™ III) for Epcam positive, EphB2 negative populations. Single cells were then seeded into 10 µl BME in organoid media containing 10 µM Y-27632. Formed organoids were counted 7 days after FACS, and clonogenicity was calculated as (#organoids/#single cells seeded x100).
vil-Cre-ERT2 WT and Srsf1fl/+ mice carrying the Lgr5GFP-CREERT2transgene were administered 120 mg/kg tamoxifen on day 0 and 80 mg/kg tamoxifen on day 1. On day 7 mice were culled and the first 10 cm of the small intestine following the duodenum was dissected and washed twice with PBS. The intestine was opened longitudinally with small scissors and the opened intestine was rinsed in PBS. Villi were removed by scraping using a microscope coverslip. The remaining tissue was then washed several times with PBS and then incubated with 2 mM EDTA in PBS with gentle shaking at 4 °C for 30 min. Crypts were then removed from the tissue by vigorous pipetting and selecting through a 70 µm cell strainer. Equal numbers of crypts were taken for each genotype/condition, centrifuged at 100 g for 3 min and then resuspended in 2 mL TryplE Express (Gibco, 12605010) and incubated at 37 °C for 15 min. During the incubation, the suspension was vigorous resuspended via pipetting every 5 min. After each resuspension, a droplet of the digestion medium was observed under the microscope to check digestion. After digestion to single cells, cells were resuspended in 10 mL DMEM/F12 and passed through a 40 µm cell strainer. Cells were washed twice in 0.1% BSA in PBS at 500 g for 5 min at 4 C before being subjected to FACS (BD FACSARIA™ III) for the Lgr5-GFP positive population. Single cells were then seeded into 10 µl BME in organoid growth media containing 10 µM Y-27632. Formed organoids were counted 7 days after FACS, and clonogenicity was calculated as (#organoids/#single cells seeded x100).
Tumour stage classification
Staging of tumours was scored according to the TNM staging system; T0- no evidence of primary tumour, Tis- carcinoma in situ, T1- tumour invading submucosa, T2- tumour invading muscularis propria, T3- tumour invading through the muscularis propria into the pericolorectal tissue, T4a- tumour penetrating to the surface of the visceral peritoneum, T4b- tumour directly invading or adherent to other organs or structures.
BrdU cell counting
Images of stained small intestinal parcels were analysed in ImageJ where villi and crypts were first divided into villi and crypt compartments. BrdU positive cells in each compartment were scored from several images analysing an average of 24 villi/mouse and 82 corresponding crypts/mouse, using 3–5 mice per genotype.
cDNA constructs and SRSF1 mutagenesis
Srsf1 cDNA was purchased from GeneCopoeia (EX-Mm13449-Lv122) and Prox1 cDNA was from Origene (MR210370). Kras 4 A and Kras 4B were cloned from cDNA from Apcfl/fl mice.
The Srsf1 RNA recognition motif 2 (RRM2) mutant ‘DK’ was created by forcing amino acids 136D and 138 K both to mutate to alanine. This was achieved by conducting a mutagenesis PCR on Srsf1 within the Lv122 vector using the following overlapping oligonucleotides: 5’-CAAGTGGAAGTTGGCAGGCTTTAGCGGATCACATGCGTGAAG-3’ and 5’-CTTCACGCATGTGATCCGCTAAAGCCTGCCAACTTCCACTTG-3’.
SRSF1 RNA immunoprecipitation Protocol
10 million CMT93 cells were pelleted and washed twice with PBS. Cells were homogenised in 1 ml lysis buffer, pH 7.4 (100 mM NaCl, 10 mM MgCl2, 30 mM Tris-HCl, 1 mM DTT, Protease & phosphatase inhibitor, 40 U/ml RNase OUT, 0.5% Triton X-100). Homogenate was centrifuged at 10,000 g for 10 min and 100ul of supernatant removed for RNA and protein input samples. The remaining lysate was split in 2 with half used for IgG IP and half for SRSF1 IP. The lysate was precleared with 25ul washed Dynabeads, 0.05% BSA and 0.1ug/ml yeast tRNA for 1 h, 4 degC. Lysate was moved to a fresh tube and incubated with 2 ug SRSF1 antibody (sc-73026) or 2 ug mouse IgG (ab37335) for 1 h 4 degC pre-incubation with rotation, followed by a further 2 h incubation in the presence of 50ul dynabeads. The lysate was discarded and beads washed 3 x with lysis buffer. 1/3rd of the beads were taken for Western blots and the remaining resuspended in 100ul lysis buffer, followed by the addition of 50ug Proteinase K. Beads were incubated for 15 min 37 degC to elute RNA from beads. RNA was purified in Trizol and purified RNA reverse transcribed. cDNA was used for qRT-PCR reactions to determine relative binding of SRSF1 to various RNA transcripts.
BioID protein interaction screen
The pUltra vector (Addgene, 24129)62 was first modified, swapping out the EGFP for a gene encoding puromycin resistance. DNA sequence encoding the BirA enzyme with an N-terminal Myc tag (Myc-BioID2-MC, Addgene, 74223) was then subcloned into the pUltra vector (Addgene, 24129). Myc-BioID2-MCS was a gift from Kyle Roux66,67. Finally, primers containing the sequences of EcoRV and EcoRI restriction enzymes were used for Kras 4 A and Kras 4B amplification. Primer sequences were Kras 4 A/4B forward: 5’- CTCTCTGATATCGACTGAGTATAAACTTGTGGTGGTTGGAGCTGGTGGCGTAG -3’, Kras 4 A reverse: 5’-AGAGAGGAATTCTTACATTATAACGCATTTTTTAATTTTCACACAGCCAGGA-3’and Kras 4B reverse: 5’-AGAGAGGAATTCTCACATAACTGTACACCTTGTCCTTGACTTCTTCTTCTTC-3’. For the purpose of a BioID interaction control protein, the gene encoding GFP was cloned into the BirA-pUltra vector.
The BioID streptavidin affinity purification experiment was based on a previously published protocol66. In the first instance, 10 cm2 dishes were seeded each with 2 × 106 CMT-93 cells (mouse rectal carcinoma), 24 h prior to transfection. CMT-93 cells were grown in Dulbecco’s Modified Eagle’s Medium (DMEM, Sigma) supplemented with 10% foetal bovine serum, 2 mM glutamine and 1% of penicillin-streptomycin. Four plates were used for each of the three conditions: BirA-GFP, BirA-Kras4A and BirA-Kras4B. The following day, 8 µg of plasmid DNA was used for transfection in each plate using Lipofectamine 2000 (Invitrogen, 11668030) and Opti-MEM (Gibco, 51985026) according to the manufacturer’s instructions. 24 h later, growth media was replaced and supplemented with 50 µM biotin (Sigma, B4501). Cells were incubated for 24 h, washed in PBS, and then scraped into 500 µL RIPA buffer. Following protein clarification, 25 µL Streptavidin Sepharose slurry (GE Healthcare, 17-5113-01) was washed in RIPA buffer before being added to 1 mL of protein lysate, which was incubated for 6 h at 4 °C with rotation. Beads were purified by centrifugation at 1000 g for 5 min and washed four times with buffer (50 mM TrisCl and 8 M Urea, pH 7.4). On-bead digestion was done with trypsin as previously described68, followed by mass spectrometry using the Fusion Lumos mass spectrometer (Thermo Fisher Scientific). Proteins analysis was done using the MaxQuant-Perseus software69, and proteins were mapped to the mouse Uniprot database. Proteins enriched in BirA-Kras4A and BirA-Kras4B vs BirA-GFP were determined by first generating a Log2 of the LFQ values and then normalising by Z-score. A student’s t-test (p < 0.05) was performed versus the GFP control samples. Significant hits were also filtered by two additional parameters: >1.5 fold higher levels in Kras 4A/4B expressing cells and at least 2 peptides detected in each of the three biological replicates. Cluster analysis was done using STRING70.
Cells were lysed using RIPA buffer (Sigma, R0278) supplemented with 1% of phosphatase and protease inhibitors (Sigma, P0044 and P8340). Protein concentration was calculated using the BCA Protein Assay kit (Pierce). 10 µg of denatured protein lysate was separated by electrophoresis on NuPAGE 4–12% Bis-Tris precast protein polyacrylamide gels (Invitrogen) and blotted onto 4 µm nitrocellulose membrane (Amersham). Membranes were immersed in blocking solution (5% milk, 0.1% PBS-tween) for 1 h at room temperature, before being incubated in primary antibody at 4 °C overnight. Following 3 washes in 0.1% PBS-tween, the membrane was incubated in secondary antibody for 1 h at room temperature, followed by 3 more PBS-tween washes. Antibody signal was detected by using ECL Plus Western blotting substrate (Pierce, 32132) and visualised using the ImageQuant LAS 4000 (GE Healthcare). Primary antibodies used were: β-actin, 1/5000 (Cell Signalling Technology, 4970), SF2/SRSF1, 1/1000 (Abcam, ab133689), c-Myc, 1/1,000 (Cell Signalling Technology, 9402), Prox1, 1 µg/mL (R&D systems, AF2727), Ras (27H5), 1/1000 (Cell Signalling Technology, 3339), Myc-Tag (9B11), 1/10,000 (Cell Signalling Technology, 2276), and Streptavidin HRP, 1/10,000 (Abcam, ab7403). Secondary antibodies used were: Anti-Rabbit IgG HRP-linked, 1/1000 (Cell Signalling Technology, 7074), Anti-Mouse IgG HRP-linked, 1/1000 (Cell Signalling Technology, 7076) and Rabbit anti-Goat IgG, 1/1000 (Thermo Fisher Scientific, 81–1620). Western blot signal densitometry analysis was done using ImageJ63.
Lentiviral particles were made using cloned plasmid vectors, either at the Shared University Research Facility (University of Edinburgh), or in our own laboratory. Briefly, 10 µg gene-specific lentiviral vector was mixed with 7.5 µg lentiviral packaging vector psPAX2 (Addgene) and 2.5 µg envelope protein producing vector pCMV-VSV-G (Addgene) and transfected into HEK 293 T cells in a 10 cm2 dish using polyethylenimine transfection reagent (Polysciences, 23966). After 48 h virus was purified by first filtering the supernatant media with a 0.45 µm filter, followed by virus concentration using Lenti-X Concentrator (Takara Bio, 631232) and resuspension of viral particles in PBS.
Diagrams & illustrations
Organoids were mechanically dissociated by vigorous pipetting. 100 fragments were seeded in 10 µl BME in a 24-well plate. 24 h after seeding, media was removed and replaced with fresh media containing either Deltarasin (Tocris, 5424) (10 µM) or DMSO. Cell proliferation was assessed after 48 h adding 10% Resazurin (R&D systems, AR002). Fluorescence was measured using Victor2 Multilabel Plate Reader (PerkinElmer) as already described.
Kras 4b morpholino treatment
Organoids were mechanically dissociated by vigorous pipetting. 20–100 fragments were seeded in 10 µl BME in a 24-well plate. 24 h after seeding, media was removed and replaced with fresh media containing either 5 μM Kras4B vivo-morpholino (Genetools - GTATAGAAGGCATCGTCAACACCCT) or 5 μM control vivo-morpholino (Genetools - CCTCTTACCTCAGTTACAATTTATA). Cell proliferation was assessed after 6 days later by adding 10% Resazurin (R&D systems, AR002). Fluorescence was measured using Victor2 Multilabel Plate Reader (PerkinElmer) as already described.
Organoid invasion assay
The invasion assay was based on a previously described protocol71. FluoroBlok HTS 24 Multiwell Insert System with 8.0 µm Pore High Density PET Membrane (Scientific Laboratory Supplies Ltd., 351157) was used. Inserts were coated with 50 μg/mL Matrigel solution diluted in cooled DMEM/F12 media containing EGF and Noggin. The organoids were dissociated with TryplE (Gibco, 12605010), resuspended in DMEM/F12 media containing EGF, Noggin and 5 ng/ml TGF beta-1 (PeproTech EC Ltd, 100-21-10) and 3 × 104 cells were seeded in each apical chamber of the Fluoroblock insert, while DMEM/F12 media containing EGF and Noggin was added in the basal chambers. Following 72 h incubation at 37 °C, 5% CO2 atmosphere, cells were stained for 1 h with Calcein AM (Abcam, ab141420) and bottom and top fluorescence was read on a Victor2 Multilabel Plate Reader (PerkinElmer) at wavelengths of 485/535 nm (Ex/Em).
Differential Gene Expression of Wild type vs Apcfl/fl and Apcfl/fl vs Apc;fl/fl Srsf1:fl/+ Adaptor sequences were removed from paired reads using TrimGalore and cutadapt an8d reads mapped to mouse genome GRCm38 (mm10) using tophat 2.1.172. Differential expression was called using cuffdiff 2.2.173 making use of Ensembl gene annotation 84 for genes (for Wild type vs Apcfl/fl) and Ensembl gene annotation 87 for genes (for Apcfl/fl vs Apc;fl/fl Srsf1fl/+). Genes with an adjusted p value of less than 0.05 were considered significantly regulated.
Splicing analysis Wild type vs Apcfl/fl and Apcfl/fl vs Apc;fl/fl Srsf1:fl/+ Paired reads were pseudoaligned to the GRCm38 (mm10) Ensembl 87 transcriptome using salmon v0.9.174. Splicing changes were inferred from transcript TPMs using SUPPA220 from gene definitions in the Ensembl 87. A second splicing assessment was made with rMATS21 using the —novelSS setting to obtain splicing events involving unannotated splice sites.
Gene Set Enrichment analysis (GSEA): Enrichment analysis of differentially expressed genes in the Apcfl/fl vs Apc;fl/fl Srsf1fl/+comparison in gene sets defining enterocyte, paneth, goblet, tuft and enteroendocrine cell types was performed using the GSEA and enricher functions of Clusterprofiler75. The gene sets for these cell types was compiled previously29. Enrichment of differentially expressed genes in ISC, proliferating, late TA and Lgr5 gene sets, defined previously30, was performed similarly after mapping genes across species using homologs specified in biomart.
Splicing factor targeted CRISPR screen wild type vs Apc:fl/fl A library of 180 gRNAs targeting 60 genes (plus 9 non-targeting controls) was designed using Mouse GeCKOv2 Library A (Supplementary Data 6). Stagger sequences were removed from reads using cutadapt prior to read counting and statistical testing of counts in treatment vs control using MAGeCK v0.5.676. Statistics for gRNAs were used to select genes with gRNA having increased counts in treatment.
Enrichment of splicing events: An enrichment algorithm for the comparison of an ordered set (A) of splicing events with another (B) was implemented following the gene set enrichment method77. Splicing events in the reference set A were ordered by p value (for events with p < 0.1) and absolute dPSI used to associate a probability with each event. Events common to a test set B and A were considered hits and increased a cumulative enrichment score by the probability of each matching event, non-hit events decreased the score. The observed enrichment was the maximum of this score. The maximum enrichment possible was where the number of intersecting events occurred at the head of A, and a probability value for the actual enrichment was calculated from a null distribution of maximum scores found by randomly selecting 100,000 subsets of A with the size of the intersection of A and B.
Mouse shRNA constitutive & Tet-On system and organoid size experiments
For constitutive knockdown, the control (scramble) shRNA was a gift from David Sabatini (Addgene, 1864)78.
TRC lentiviral shRNAs (Mouse Srsf1 ENTREZGENE:110809) were purchased from Dharmacon. These were supplied in the pLKO.1 vector: shSrsf1-3 Clone Id: TRCN0000109142, sequence: AACATCAGCGTAACATACATC.
For inducible knockdown, shRenilla and shSrsf1–4 were cloned into Tet-ON inducible vector pTRIPZ, modified with a synthetic minimal promoter (minP) (synthesised by GenScript) to replace the minimum CMV promoter. shRNAs were cloned into pTripZ vector using 5’ XhoI and 3’EcoRI restriction sites. Organoids were seeded into BME and treated with 1 µg/ml doxycycline (Alfa Aesar by Thermo Scientific – J60579.22) dissolved in water.
shSrsf1–4 sequence (97mer): TGCTGTTGACAGTGAGCGATAGGCTTATGTTTGAACACTATAGTGAAGCCACAGATGTATAGTGTTCAAACATAAGCCTACTGCCTACTGCCTCGGA. shRenilla sequence: (97mer): TGCTGTTGACAGTGAGCGCAGGAATTATAATGCTTATCTATAGTGAAGCCACAGATGTATAGATAAGCATTATAATTCCTATGCCTACTGCCTCGGA.
Images were taken at the indicated time points and analysed using ImageJ 2.0. For organoid size (area) determination for the constitutive shRNA model, the minimum number of organoids used to calculate organoid area per biological replicate were: Apc:fl/fl 15, AKP: 20 and KPN: 40. For tracking and size determination in the Tet-On models, the number of organoids measured & tracked per biological repeat were: Wild-type organoids: 5–17, Apcfl/fl organoids: 8–20 and AKP organoids: 5. For the shRNA Srsf1/Kras 4B rescue experiments in Apcfl/fl organoids, 14–22 organoids were measured for size per biological replicate. For the human PDO organoids, the number of organoids measured were 33–250. All organoid size experiments had n = 3 biological replicates.
TRC lentiviral shRNAs (Human SRSF1 ENTREZGENE: 6426.) were purchased from Dharmacon. These were supplied in pLKO.1 vectors. shSRSF1–2 Clone ID: TRC0000001094, Sequence: TTAACCCGGATGTAGGCAGT.
Quantification and statistical analysis
Statistical analyses were performed using GraphPad Prism software (v8.3 GraphPad software, La Jolla, CA, USA) and Microsoft Excel (v2016, Redmond, WA, USA) performing the tests as indicated in the figure legends or main text. Significance levels were calculated according: p < 0.05 (*), p < 0.01(**) and p < 0.001 (***).
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
The RNAseq data generated in this study have been deposited in the GEO database under accession code GSE199623 (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE199623) and are freely available. All data are provided within the article, Supplementary Information and source data.
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This work was funded by Cancer Research UK (CRUK) under Career Development Fellowship, A19166 (K.B.M) and Small Molecule Drug Discovery Project Award, A25808 (K.B.M) and the European Research Council under Starting Grant, COLGENES – 715782 (K.B.M). Mass spectrometry was supported by the Wellcome Trust (Multiuser Equipment Grant 208402/Z/17/Z). We thank the University of Edinburgh’s Institute of Genetics and Cancer (IGC) technical staff for providing support for some of the experiments and we thank the animal technicians at the Biomedical Research Facility (BRF) facility for animal husbandry support. We thank Prof Owen Sansom for providing us with the VilCreERT2, Apcfl, P53fl, KrasG12D and Lgr5-CreERT2 mouse lines. We thank Dr Lukas Dow and Prof Scott Lowe for providing the shApc organoid line. We thank Prof Nicola Valeri for providing the C-002 PDO line.
The authors declare no competing interests.
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Hall, A.E., Pohl, S.ÖG., Cammareri, P. et al. RNA splicing is a key mediator of tumour cell plasticity and a therapeutic vulnerability in colorectal cancer. Nat Commun 13, 2791 (2022). https://doi.org/10.1038/s41467-022-30489-z