Accumulating evidence indicates that circular RNAs (circRNAs) are abundant in the human transcriptome. However, their involvement in biological processes, including pluripotency, remains mostly undescribed. We identified a subset of circRNAs that are enriched in undifferentiated human embryonic stem cells (hESCs) and demonstrated that two, circBIRC6 and circCORO1C, are functionally associated with the pluripotent state. Mechanistically, we found that circBIRC6 is enriched in the AGO2 complex and directly interacts with microRNAs, miR-34a, and miR-145, which are known to modulate target genes that maintain pluripotency. Correspondingly, circBIRC6 attenuates the downregulation of these target genes and suppresses hESC differentiation. We further identified hESC-enriched splicing factors (SFs) and demonstrated that circBIRC6 biogenesis in hESCs is promoted by the SF ESRP1, whose expression is controlled by the core pluripotency-associated factors, OCT4 and NANOG. Collectively, our data suggest that circRNA serves as a microRNA “sponge” to regulate the molecular circuitry, which modulates human pluripotency and differentiation.
Circular RNAs (circRNAs) are closed RNA transcripts, generated by back-splicing of a single pre-mRNA. In this process, the 5′ terminus is covalently linked to the 3′ terminus, resulting in a scrambled exon order. The first circRNA was identified in the early 1990s1, however, in the subsequent two decades, only a few additional circRNAs were reported1,2,3. These circular transcripts were originally considered errors or byproducts of splicing, but with the emergence of next-generation sequencing (NGS), circRNAs are now known to be abundant and conserved among various biological systems. Moreover, the expression of circRNAs has recently been shown to be tissue specific and regulated in different biological processes, such as epithelial–mesenchymal transition (EMT) and brain development4,5,6.
The biogenesis of individual circRNAs must be tightly controlled to produce these expression profiles, and studies on circRNA generation indicate that both cis-elements and trans-acting factors are involved in regulating biogenesis. Cis-elements, such as canonical splicing sites, GU-AG, are necessary for circRNA biogenesis7, and complementary base-pair sequences in the flanking introns (e.g., Alu elements) also contribute to promoting circRNA formation by bringing two distal introns together8, 9. Trans-factors, such as SFs (e.g., Muscleblind and Quaking), interact with the flanking introns of circRNAs to regulate circRNA synthesis5, 10. Thus, it has become clear that the biogenesis of circRNAs is tightly regulated in different biological processes to allow them to fulfill their regulatory roles. However, these regulatory roles are still largely unknown. The biological functioning of circRNAs was first described by Memczak et al.6 and Hansen et al.11, who demonstrated that circRNAs can act as microRNA “sponges” to regulate gene expression. Since then, various functional roles have been reported for circRNAs in controlling biological processes12,13,14, suggesting that circRNAs may have important roles in widespread cellular functions.
Human embryonic stem cells (hESCs), which are derived from the pluripotent inner cell mass of preimplantation blastocysts, have the capacity for unlimited self-renewal and pluripotency, giving rise to many cell types in the human body15. A functional analysis of the core pluripotency-associated transcription factors (PATFs), NANOG, OCT4, and SOX2, has revealed that they are indispensable for the maintenance of pluripotency in hESCs16. In addition to transcription factors, non-coding RNAs (ncRNAs), which have little or no protein-coding potential, have also been shown to have important roles in pluripotency maintenance. For example, small ncRNAs (less than 200 nucleotides), such as the microRNAs (miRNAs), miR-302/367, and miR-372 clusters, repress the expression of differentiation-related genes in hESCs17. Conversely, miR-34a and miR-145 are known to repress pluripotency-associated genes to promote in vitro differentiation of hESCs18, 19. In addition, long ncRNAs (lncRNAs; more than 200 nucleotides), such as lncRNA-ES1 and lncRNA-ROR, repress hESC differentiation by recruiting the polycomb repressive complex, PRC2, and inhibiting miRNA activity, respectively20, 21. Furthermore, the trans-spliced lncRNA, tsRMST, has recently been demonstrated to promote the undifferentiated status of hESCs by repressing early lineage-associated transcription factors22 and WNT signaling23 through the PRC2 complex. These studies clearly establish the importance of ncRNAs in pluripotency maintenance; however, a functional role for circRNAs in pluripotency status has not been previously reported.
To explore the functional roles of circRNAs in regulating human pluripotency, we identified and validated a subset of hESC-enriched circRNAs. Through gain-of-function and loss-of-function experiments, we further demonstrated that two circRNAs, circBIRC6 and circCORO1C, are functionally associated with pluripotency maintenance and reprogramming. Furthermore, we showed that circBIRC6 is enriched in the RNA-induced silencing complex (RISC), containing the catalytic subunit AGO2, and promotes the pluripotent state by inhibiting miR-34a-mediated and miR-145-mediated suppression of NANOG, OCT4, and SOX2 expression. Studies on circBIRC6 biogenesis showed that the pluripotency-associated genes NANOG and OCT4 regulate expression of the SF ESRP1 (epithelial-splicing regulatory protein 1), which is responsible for the generation of circBIRC6 in hESCs. Collectively, our results demonstrate that circRNAs participate in the molecular circuitry that controls human pluripotency.
Identification and validation of hESC-enriched circRNAs
To identify a pool of potential circRNAs that may be expressed in hESCs, we utilized a human circRNA database that comprises candidates identified from various cell types6, and selected 61 strong candidates for circRNAs that had more than 40 reads supporting a circular junction (step 1 in Fig. 1a and Supplementary Data 1). Combining RT-PCR analysis that uses divergent primers to specifically target the circular junction (Fig. 2a) and sequencing validation, we detected the presence of 20 circRNAs in hESCs (step 2 in Fig. 1a). As circRNAs may share the same junction sequence as their linear trans-spliced counterparts, and experimental artifacts may be generated by template switching during RT-PCR24, we treated total RNA from hESCs with RNaseR, which digests only linear RNAs containing a free 3′ terminus and not circRNAs25. This further analysis confirmed the circular nature of all 20 hESC-expressed circRNAs, by showing that these molecules were resistant to RNaseR digestion, whereas the linear isoforms were not (Fig. 1b). To determine whether these circRNAs are functionally associated with pluripotency, we first examined their temporal expression pattern during embryoid body (EB) differentiation. RT-qPCR analyses showed that 11 out of the 20 hESC-expressed circRNAs were enriched in hESCs (>0.1% of GAPDH levels; Fig. 1c). Among the 11 hESC-enriched circRNAs, nine were downregulated in EBs (Fig. 1d). In addition, all hESC-enriched circRNAs were upregulated in induced pluripotent stem cells (iPSCs) as compared with the parental fibroblasts (Fig. 1e). Notably, the RT-qPCR analyses also revealed that circRNA expression was often co-regulated with the corresponding linear isoform during differentiation. This was true for all circRNAs except for circBIRC6, circMAN1A2, and circILKAP (Fig. 1d), suggesting that these three circRNAs and their linear counterparts are differentially regulated with cell status. We further confirmed the presence of transcripts for circBIRC6, circCORO1C, and circMAN1A2, which exhibited the highest association with pluripotency status (fold change > 4 during differentiation and reprogramming), in hESCs by Northern blot analysis using probes that specifically target the circular junction of these circRNAs (Supplementary Fig. 1). This analysis conclusively excluded that these circRNAs were in vitro artifacts resulting from template switching. Collectively, we identify a set of circRNAs that are enriched in hESCs and iPSCs, and show that their expression is associated with the pluripotent state.
Disrupting circBIRC6 or circCORO1C impairs hESC pluripotency
To determine whether the hESC-enriched circRNAs function in pluripotency maintenance, we disrupted circBIRC6, circCORO1C, or circMAN1A2 expression in hESCs by overexpressing small hairpin RNAs (shRNAs) that specifically target the circular junction of each circRNA (shcircRNAs in Fig. 2a). Notably, expressing shcircRNAs in hESCs only disrupted the expression of circRNAs and not their linear counterparts, as demonstrated by RT-qPCR (Fig. 2b). After expressing shcircRNA in hESCs, we found that alkaline phosphatase (AP) activity was significantly reduced in circBIRC6-knockdown (H9-shcircB) and circCORO1C-knockdown (H9-shcircC), but not in circMAN1A2-knockdown (H9-shcircMa) hESCs, as compared with hESCs that express paired control shRNAs (Fig. 2e). RT-qPCR further revealed that expression levels of the PATFs, NANOG, OCT4, KLF4, and MYC, were downregulated in H9-shcircB and H9-shcircC (Fig. 2c), whereas expression of the lineage-related transcription factors (LRTFs) Brachyury, GSC, MIXL1, SOX17, and SOX1 was significantly upregulated (Fig. 2d). Immunocytochemistry (ICC) showed that the number of NANOG+ and OCT4+ cells was significantly reduced in H9-shcircB and H9-shcircC, whereas the number of Brachyury+ and SOX17+ cells was significantly increased (Fig. 2f). To exclude the possibility of off-target effects from the shcircRNA constructs, we re-expressed circBIRC6 and circCORO1C (Fig. 3a for vector construction) in H9-shcircB and H9-shcircC, respectively. After confirming, the expression levels of circBIRC6 and circCORO1C were rescued in H9-shcircB-res and H9-shcircC-res cells by RT-qPCR analysis (Fig. 2h), we performed RT-qPCR and ICC to show that the expression levels of PATFs and the number of NANOG+ or OCT4+ cells were similarly rescued (Fig. 2g, h). Consistent with our hESC results, various assays showed that disruption of circBIRC6 and circCORO1C expression downregulated PATFs expression in iPSCs (Supplementary Fig. 2).
To rule out the possibility that the above observations are caused by linear BIRC6, we transduced hESC with shRNAs that specifically targets linear BIRC6 (shLinB), or the common exon of both circBIRC6 and linear BIRC6 (shcircB-2). After confirming the specific disruption of shLinB and shcircB-2 on their target isoforms by RT-qPCR (Supplementary Fig. 3a), we found that the AP activity was decreased in shcircB-2, but not shLinB, transduced hESCs (Supplementary Fig 3e). RT-qPCR and ICC further showed the downregulation of PATFs (NANOG, OCT4, KLF4, and MYC), and miRNA-targeting gene expression (MDM4, SIRT1, ADAM17, and NEDD9), and upregulation of LRTFs expression (Brachyury, GSC, MIXL1, and SOX17) in shcircB-2-transduced hESCs, as compared to shLinB-transduced hESCs (Supplementary Fig. 3b–d). Further, ICC analyses revealed a decreased number of NANOG+ and OCT4+ cells, and an increased number of Brachyury+ and SOX17+ cells in shcircB-2-transduced hESCs (Supplementary Fig. 3f), suggesting that circBIRC6, but not linear BIRC6, is critical for pluripotency maintenance. Altogether, these results indicate that circBIRC6 and circCORO1C may be functionally involved in the maintenance of hESC pluripotency.
Expressing circBIRC6 or circCORO1C retains hESC pluripotency
To examine whether the aforementioned circRNAs maintain pluripotency, we performed gain-of-function experiments by overexpressing circRNAs with minigene constructs and examined the expression of circRNAs and their precursors by RT-qPCR and Northern analyses, using primer pairs that specifically target the circular junction site and the 5′ intron–exon junction (Fig. 3a, see details in “Methods”). The result showed that expression levels of circBIRC6, circCORO1C, and circMAN1A2 were all significantly increased in hESCs transfected with minigenes expressing circBIRC6 (H9-circB), circCORO1C (H9-circC), or circMAN1A2 (H9-circMa) compared with mock-transfected controls, whereas there was no increase in un-spliced precursors (Fig. 3b; Supplementary Fig. 4a). RT-qPCR and ICC staining revealed that ectopic expression of these circRNAs in hESCs, cultured under ESC culture conditions, did not reduce the number of cells expressing PATFs or increase the number of cells expressing LRTFs, suggesting that high expression levels of circRNAs in hESCs did not cause a loss of pluripotency (Supplementary Fig. 4b, c). However, ectopic expression of circBIRC6 or circCORO1C, but not circMAN1A2, in differentiating hESCs upregulated expression of the PATFs, OCT4, NANOG, and SOX2, and downregulated expression of the LRTFs Brachyury, GSC, MIXL1, SOX17, and PAX6 (Fig. 3c, d). Accordingly, ICC analysis revealed an increased number of NANOG+ and OCT4+ cells in differentiated H9-circB and H9-circC, and a decreased number of Brachyury+, SOX17+, and PAX6+ cells (Fig. 3e, f). These results show that circBIRC6 and circCORO1C, but not circMAN1A2, maintain pluripotency marker expression in differentiated hESCs.
Expressing circBIRC6 or circCORO1C promotes reprogramming
As our results demonstrated that circBIRC6 and circCORO1C contribute to human pluripotency maintenance, it was of interest to know whether their expression is sufficient to reprogram somatic cells into iPSCs. To this end, we first generated pluripotency reporter hESCs by knocking green fluorescent protein (GFP) into the endogenous OCT4 promoter using a CRISPR and Cre-loxP system (H9-OCT4pGFP; Supplementary Fig. 5a, b). Next, we differentiated H9-OCT4pGFP hESCs into a homogeneous population of fibroblast-like cells (H9-OCT4pGFPdFs) that do not express the OCT4pGFP transgene or PATFs (Fig. 4a; Supplementary Fig. 5b). To determine whether circRNAs are sufficient to promote reprogramming, we then expressed circBIRC6 or circCORO1C minigene constructs in H9-OCT4pGFPdFs. The RT-qPCR analyses showed that circBIRC6 and circCORO1C expression were significantly increased in H9-OCT4pGFPdFs transfected with the corresponding minigene construct (Fig. 4b). The expression of circBIRC6 or circCORO1C alone did not reactivate the PATFs OCT4, SOX2, and NANOG in H9-OCT4pGFPdFs (Fig. 4a), suggesting that expression of circBIRC6 or circCORO1C alone is insufficient to restore pluripotency status in fibroblasts. To determine whether circBIRC6 or circCORO1C may improve the efficiency of TF-mediated reprogramming, we infected H9-OCT4pGFPdF with Sendai virus encoding OCT4, SOX2, KLF4, and c-MYC (OSKM), with or without co-expression of circRNA. On day 14 after viral infection, RT-qPCR analysis showed that the expression levels of endogenous NANOG, OCT4, and SOX2 were increased in H9-OCT4pGFPdF populations co-expressing OSKM and circBIRC6 (OSKMB) or circCORO1C (OSKMC) compared with H9-OCT4pGFPdFs expressing only OSKM (Supplementary Fig. 5c). By day 21 after viral infection, small compact colonies started to appear among fibroblasts undergoing reprogramming. Further AP staining and quantitative analyses showed that the numbers of AP+ and OCT4-GFP+ colonies were significantly increased in OSKMB or OSKMC compared with OSKM cells (Fig. 4c, d). By day 28 post infection, fluorescence-activated cell sorting (FACS) showed that the number of reprogrammed OCT4-GFP+ iPSCs was also significantly increased in OSKMB or OSKMC compared OSKM cells (Fig. 4e). These results suggest that circBIRC6 and circCORO1C potentiate OSKM-mediated reprogramming.
C ircBIRC6 acts as a sponge for miR-34a and miR-145 in hESCs
It is known that circRNAs can act as miRNA sponges to regulate gene expression in different cell types6, 13, 26. To determine whether circ BIRC6 and circ CORO1C regulate pluripotency through the same mechanism, we first examined the relative expression levels of circRNAs in the cytoplasmic and nuclear compartments of hESCs. RT-qPCR results demonstrated that circ BIRC6 and circ CORO1C were enriched in the cytoplasm (Fig. 5a). RNA immunoprecipitation (RIP) assays further showed that circBIRC6, but not circCORO1C or either linear isoform, was enriched in AGO2 immunoprecipitates (Fig. 5b), suggesting that only circBIRC6 possesses miRNA-related functions. To determine which miRNAs potentially interact with circBIRC6, we analyzed putative miRNA-targeting sites on the circBIRC6 sequence using a probability of interaction by target accessibility (PITA) algorithm27. Selecting miRNA-targeting sites with strong binding energy (ΔG < −14 kcal mol−1) and allowing one G:U wobble pair or one mismatch in the miRNA seed regions, we found 431 sites that were targeted by 306 different miRNAs (Supplementary Data 2). Among the 95 miRNAs having multiple targeting sites on circBIRC6, miR-34a, and miR-145 have been reported to induce hESC differentiation by directly suppressing the expression of pluripotency-associated genes18, 19. Thus, we asked whether circBIRC6 was capable of regulating pluripotency in hESCs through interactions with miR-34a and/or miR-145. To this end, we transfected 3′ terminal-biotinylated miR-34a and miR-145 mimics into H9-circB, and precipitated RNA transcripts that interact with these mimics by streptavidin beads. RT-qPCR analyses revealed that circBIRC6 was enriched in the precipitates of miR-34a and miR-145 mimics compared with precipitates of scrambled oligonucleotide (Fig. 5c). Next, we carried out luciferase reporter assays and showed that miR-34a or miR-145 expression significantly reduced the luciferase activity of a reporter containing the complete circBIRC6 sequence appended to the 3′-untranslated region of luciferase (luc-circB), whereas the luciferase activity of luc-circB containing mutated miR-34a and miR-145 binding sites (luc-circBm1-m4) was not noticeably affected (Fig. 5d–f). For circRNAs to act as miRNA sponges and regulate miRNA activity, the relative expression level of circRNAs and their targeted miRNAs should be within an appropriate range. Accordingly, Northern blotting using probes specific for circBIRC6 showed the downregulation of circBIRC6 expression in differentiated hESCs (Supplementary Fig. 6) and RT-qPCR showed that miR-34a and miR-145 expression levels were lower than that of circBIRC6 in undifferentiated hESCs, but were higher than those of circBIRC6 in differentiated hESC derivatives (Fig. 5g). Taken together, these results suggest that circBIRC6 may exert its function through direct interactions with miR-34a and miR-145.
To ascertain whether circBIRC6 contributes to pluripotency maintenance by acting as a sponge for miR-34a and miR-145, we transfected hESCs with miR-34a or miR-145 mimics, and examined their impact on hESC status. RT-qPCR results showed that overexpression of miR-34a or miR-145 significantly reduced expression of miR-34a target genes (MDM4 and SIRT1) and miR-145 target genes (ADAM17 and NEDD9), thus confirming that miR-34a and miR-145 mimics were functional in hESCs (Supplementary Fig. 7a, b). RT-qPCR and immunoblot analyses further showed that overexpression of miR-34a or miR-145 significantly reduced expression of the PATFs (NANOG, OCT4, and SOX2) at both mRNA and protein levels (Fig. 5h, i). The reduction in PATFs caused by ectopic expression of miR-34a or miR-145 was accompanied by upregulated expression of the LRTFs Brachyury, GSC, MIXL1, SOX17, SOX1, and PAX6 (Fig. 6b, d), as well as PAX6, Brachyury, and SOX17 proteins (Fig. 6e). We then examined whether the expression of circBIRC6 was capable of rescuing the loss of pluripotency and/or in vitro differentiation caused by miR-34a or miR-145 mimics in hESCs. RT-qPCR demonstrated that expression of circBIRC6-promoted expression of the PATFs, miR-34a, and miR-145-targeted genes (MDM4, SIRT1, ADAM17, and NEDD9) in hESCs ectopically expressing miR-34a and miR-145. Furthermore, expression of the LRTFs was suppressed (Fig. 6a–d; Supplementary Fig. 7a, b). Notably, these rescue effects were further enhanced by increasing the relative level of circBIRC6 expression (circB (3 μg) in Fig. 6a–d. Furthermore, ICC staining showed that circBIRC6 expression results in an increased number of NANOG+ and OCT4+ cells in hESCs ectopically expressing miR-34a or miR-145, and a decreased number of Brachyury+, SOX17+, and PAX6+ cells (Fig. 6e), suggesting that circBIRC6 suppresses miR-34a-mediated and miR-145-mediated hESCs differentiation. Expression of circBIRC6, with mutations in miR-34a and miR-145 binding sites (circB4m), failed to rescue miR-34a-mediated and miR-145-mediated in vitro differentiation and the decrease of miR-34a-targeted and miR-145-targeted gene expression levels, further confirming that miRNA–circBIRC6 interactions are necessary for circBIRC6 function (Fig. 6a–d). Northern blotting using probes recognizing both circBIRC6 and its linear precursors confirmed that circBIRC6, but not its linear precursors, was the major isoform expressed in hESC H9 transfected with circB or circB4m minigenes, supporting the idea that the rescue effects were related to circBIRC6 expression (Supplementary Fig. 7c). In addition, RT-qPCR showed that expression levels of miR-34a-targeted and miR-145-targeted genes (MDM4, SIRT1, ADAM17, and NEDD9) were downregulated in H9-shcircB and rescued by re-expressing circBIRC6 in H9-circB-res, supporting the notion that circ BIRC6 acts as an miRNA sponge (Supplementary Fig. 7d). Collectively, our results support the conclusion that circBIRC6 promotes pluripotency maintenance in hESCs by reducing the activity of miR-34a and miR-145.
ESRP1 promotes the generation of circBIRC6 in hESCs
As splicing factors (SFs) have been shown to regulate cell-type-specific circRNA expression5, 10, and we hypothesized that hESC-associated SF may be involved in generating circBIRC6 in hESCs. Using microarray analyses, we identified three SFs, ESRP1, SNRPN, and HNRNPA1, that were enriched (fold change > 10) in hESC/iPSCs compared with human fibroblasts (Supplementary Data 3). RT-qPCR analyses further confirmed that these SFs were highly expressed in hESCs, with ESRP1 being the highest expressed, when compared to the differentiated derivatives (H9-dF) (Fig. 7a), suggesting their expression may be associated with hESC pluripotency. To examine whether ESRP1 is involved in circBIRC6 generation in hESCs, we disrupted ESRP1 expression using two different shRNA variants (Supplementary Fig. 8) and investigated the effects of ESRP1-knockdown on circBIRC6 expression. RT-qPCR analyses showed that ESRP1-knockdown resulted in a significant reduction of circBIRC6 expression in hESCs, but increased the expression of linear BIRC6 isoform (Fig. 7b). Notably, ESRP1 disruption also resulted in downregulation of the PATFs, NANOG and OCT4, in hESCs (Fig. 7b). It has been demonstrated that SFs promote circRNA generation by directly binding to recognition motifs in the introns flanking circRNA-forming exons5, 10. To examine whether ESRP1-binding sequences are critical for circBIRC6 formation, we searched for ESRP1-binding sequences (GGT-rich)28, 29 in circBIRC6 and its flanking introns, and identified three putative ESRP1-binding sites (Fig. 7c). Next, we generated two short circBIRC6 minigenes, circB-s and circB-s-Em. The circB-s minigene contains putative ESRP1-binging sites on both flanking introns that are preserved, but in contrast to the circBIRC6 minigene, the inversely inserted 5′ intron was removed to exclude the involvement of complementary sequences (Fig. 7c). The circB-s-Em minigene is similar to circB-s, but the putative ESRP1 sites have been deleted from the flanking introns. RIP analysis demonstrated the clear interaction between ESRP1 and circB-s, but not circB-s-Em (Fig. 7d), suggesting that ESRP1 indeed binds to the putative binding sites on the flanking introns. We then expressed circB-s in ESRP1 disrupted or control hESCs, and found that the circB-s minigene produced lower levels of circBIRC6 transcript in the absence of ESRP1, confirming that ESRP1 is critical for circBIRC6 formation in hESCs (Fig. 7e). Next, we expressed the circB-s-Em minigene in control hESCs, and found that circB-s-Em produced significantly less circBIRC6 compared with circB-s. This result suggested that the putative ESRP1-binding motifs on flanking introns are critical for circBIRC6 production (Fig. 7e). Notably, disruption of ESRP1 expression in circB-s-Em-transduced hESCs did not further decrease circBIRC6 transcript levels. To extend these observations, we investigated whether exons that do not normally form circRNAs (based on the circRNA collection in circBase30) could be made competent to generate circRNAs in hESCs by inserting ESRP1-binding sites into the flanking introns. We selected one exon with a length that was compatible to circBIRC6 (exon 11 of ZEB1) and another exon with shorter length (exon 25 of EGFR) to generate the minigene constructs. The minigenes were constructed to express regions containing the exons and the endogenous flanking introns (Fig. 7f) and were subsequently expressed in hESCs. Our RT-PCR results revealed that the expression of the aforementioned minigenes, harboring introduced ESRP1-binding motifs, produced circRNAs, whereas the minigenes without the inserted ESRP1-binding motif did not yield circRNAs (Fig. 7g). Then, we disrupted ESRP1 expression in hESCs that also expressed the ESRP1-binding motif inserted minigenes containing exon 11 of ZEB1 or exon 25 of EGFR and analyzed circRNA expression by RT-PCR. Our analysis showed that the circRNA formation was severely compromised by disrupting the expression of ESRP1 in hESCs (Fig. 7g), suggesting that the flanking intronic sequences, which contain ESRP1-binding motifs, can induce ESRP1-dependent circularization from transcripts that are normally linearly spliced. Taken together, these experiments demonstrate that ESRP1 plays an important role in regulating the formation of circBIRC6 in hESCs through binding to recognition sites in the introns flanking the circBIRC6-forming exons.
NANOG and OCT4 regulate ESRP1 expression in hESCs
As ESRP1 was highly expressed in human pluripotent stem cells (Fig. 7a; Supplementary Data 3), we hypothesized that the expression of ESRP1 may be directly regulated by PATFs. To explore this possibility, we first searched the ENCODE ChIP-seq database31 for PATFs that may occupy the ESRP1 promoter. Our analysis showed that NANOG and OCT4 occupancy, and H3K27Ac histone modifications were enriched on the ESRP1 promoter (Fig. 8a). ChIP-qPCR analyses further revealed that NANOG and OCT4 occupancy and H3K27Ac histone modifications were enriched in hESCs, but not in differentiated derivatives (Fig. 8b). Furthermore, a binding-motif analysis showed two putative binding sites for NANOG and one for OCT4 on the ESRP1 promoter (Fig. 8c). Finally, to determine whether NANOG and OCT4 directly regulate ESRP1 expression, we created an ESRP1 promoter-luciferase reporter (ESRP1-luc) construct and showed that its activity was increased by NANOG and OCT4 (Fig. 8d). This increase was attenuated by deletion of ESRP1 promoter NANOG binding sites (ESRP1-m1-Luc and ESRP1-m2-Luc) or the OCT4 binding site (ESRP1-m3-Luc) (Fig. 8d). Taken together, these results demonstrate that NANOG and OCT4 bind to the ESRP1 promoter to promote ESRP1 expression in hESCs.
It is evident that large numbers of circRNAs exist in the human transcriptome, and accumulating evidence suggests that they may have important roles in regulating cellular function6, 13, 14. However, the role of circRNA in hESCs and the mechanism by which circRNAs regulate pluripotency has not been previously described. In this study, we identified a subset of circRNAs that are enriched in hESCs and demonstrated that two circRNAs, circBIRC6 and circCORO1C, are functionally associated with the pluripotent state. Loss-of-function experiments demonstrated that compromised circBIRC6 or circCORO1C expression impeded pluripotency and induced differentiation of hESCs. In addition, ectopic expression of circBIRC6 or circCORO1C in hESCs-promoted pluripotency and enhanced the efficiency of iPSCs generation. Mechanistically, we found that circBIRC6 suppressed miR-34a-mediated and miR-145-mediated differentiation by directly interacting with these miRNAs. Our data thus suggest that circBIRC6 functions as a miRNA sponge to attenuate miRNA-mediated activity. Our study also demonstrates that ESRP1, a hESC-enriched SF, promotes circBIRC6 synthesis through interactions with its flanking introns. Furthermore, by using ChIP-qPCR and reporter analyses, we found that the ESRP1 expression is regulated by NANOG and OCT4 in hESCs. Our study suggests the existence of a regulatory network in hESCs, wherein coordinated interactions between PATFs and SFs modulate the expression of a distinct group of circRNAs, which can directly interact with miRNAs and influence the pluripotency state.
It was shown that circRNAs play roles in various biological processes, including neural development (ciRS-7/CDR1as), spermatogenesis (SRY), and cancer cell proliferation (circFOXO3, circHIPK3, and circITCH)6, 12,13,14. Here, we demonstrate that both circBIRC6 and circCORO1C are functionally associated with the human pluripotency. Our miRNA-targeting analysis showed that circBIRC6 harbors 431 targeting sites for 306 different miRNAs, suggesting that circBIRC6 may act as a miRNA sponge. Among these 306 miRNAs, there are 70 with two binding sites on circBIRC6, 21 with three binding sites, and four with four binding sites (Supplementary Data 2). These results are in agreement with a previous report, which showed that no particular miRNA exhibited highly enriched binding to circRNAs, with the exceptions of CDR1as, SRY, and ZNF91 32. Furthermore, our results confirmed that circBIRC6 can interact with and sequester at least two miRNAs, miR-34a and miR-145, to prevent in vitro differentiation. In addition, circBIRC6 has binding sites for several other miRNAs, including let-7, miR-92, and miR-103 (Supplementary Data 2), which have previously been reported to have functional roles in early-lineage differentiation. Therefore, in line with recent studies12,13,14, our results support the idea that circBIRC6 can serve as a miRNA sponge for multiple miRNAs to regulate gene expression.
Our results suggest that, unlike circBIRC6, circCORO1C likely contributes to controlling hESC pluripotency through a mechanism other than sequestration of miRNA(s). CircCORO1C does not associate with AGO2, which is a critical component for the miRNA-sponge role of circRNAs. Instead, we considered that circCORO1C may potentially function by regulating its linear isoform through competition with pre-mRNA synthesis, as recently demonstrated for circMbl 10. However, disrupting circCORO1C expression did not affect the expression of its linear counterpart (Fig. 2b), thus precluding this possibility. Alternatively, circCORO1C may regulate hESC pluripotency through interactions with proteins, for example, circFoxo3 can inhibit cell-cycle progression by trapping p21 and CDK2 in the cytoplasm33. Further experiments will be necessary to clarify whether this mechanism, or another, governs circCORO1C activity.
Although our data indicate that circBIRC6 and circCORO1C are functionally associated with pluripotency, we found that expression of either circBIRC6 or circCORO1C in human fibroblasts was not sufficient to reactivate the pluripotency program and effect iPSC formation. On the other hand, co-expression of either circBIRC6 or circCORO1C with OSKM in human fibroblasts potentiated iPSC formation. One likely explanation for these findings is that circBIRC6 and circCORO1C alone may not be sufficient to reactivate all the major pathways of early stage pluripotency reprogramming34, and thus cannot initiate the reprogramming process in somatic cells. Nevertheless, we found that these circRNAs enhance OSKM-initiated reprogramming. It is possible that circBIRC6 may contribute to improving reprogramming efficiency by blocking P53, a major roadblock of pluripotency reprogramming35, through upregulation of the P53 suppresser MDM2, which is a common target of miR-14536. Similar to miR-145, miR-34a has also been described as a suppressive factor for reprogramming, and inhibition of miR-34a expression has been shown to enhance reprogramming efficiency18. Although we did not find that pluripotency reprograming is possible using circBIRC6 or circCORO1C alone, it remains conceivable that in the future, iPSCs may be created using combinations of circRNAs that target and regulate miRNAs to control the major reprogramming pathways, thus allowing circRNAs to replace transcription factors for iPSC generation37.
The differential expression of circBIRC6 between human fibroblasts and hESCs suggests that biogenesis of circBIRC6 is regulated in a cell-type-specific manner, and that hESCs possess specific elements involved in circRNA biogenesis. Indeed, we found that ectopic expression of a circBIRC6 minigene in hESCs, or their differentiated derivatives, promoted the generation of circBIRC6 and its linear precursor (Figs. 3b and 4b). However, the linear precursor of circBIRC6 was less efficiently converted into circBIRC6 in hESC-derived fibroblasts than in hESCs, suggesting that circBIRC6 biogenesis may be regulated in a cell-type-dependent manner. Furthermore, we identified several splicing factors that are highly enriched in hESCs, and demonstrated that ESRP1 is involved in circBIRC6 biogenesis. These observations support the idea that splicing factors can contribute to cell-type-specific circRNA biogenesis5, 10. We also showed that the pluripotency-associated factors OCT4 and NANOG could directly regulate the expression of ESRP1, providing evidence to further support the interpretation that the ESRP1–circBIRC6 axis is a pluripotency-associated regulatory pathway. Although we showed that ESRP1 promoted circBIRC6 formation, ESRP1-knockdown only reduced circBIRC6 expression by ~50%. This incomplete suppression may be attributable to the redundant effects of ESRP2, a close family member of ESRP1 that recognizes a similar binding motif. We cannot rule out the possibility that circBIRC6 biogenesis is regulated by multiple hESC-enriched SFs, as was shown in other systems38. Future studies will be required to elucidate how other hESC-enriched SFs function to control human pluripotency.
We have shown that altered ESRP1 expression may have profound impact on circBIRC6 biogenesis. Moreover, our mechanistic studies revealed that deletion of the ESRP1-binding motifs in the introns flanking circBIRC6 resulted in a dramatic reduction of circBIRC6 generation. However, insertion of ESRP1-binding motifs into introns, which flank exons that normally do not form circRNA, induced circRNA formation from these exons. Altogether, these results suggest that ESRP1 may directly regulate back-splicing to promote circBIRC6 generation in hESCs through interaction with the putative binding motifs on both flanking introns of circBIRC6.
SFs are emerging regulators of pluripotency. For instance, MBNL promotes in vitro differentiation of hESCs through regulation of FOXP1 isoform-switching39. In contrast, the SR-related SFs SON and SFRS2 contribute to the maintenance of pluripotency by regulating the splicing of OCT440 and methyl-CpG binding domain protein (MBD2)41, respectively. In this study, we showed that disruption of ESRP1 reduced the expression of NANOG and OCT4, suggesting that ESRP1 indirectly regulates pluripotency by controlling circBIRC6 biogenesis. However, we cannot exclude that ESRP1, like SFRS2, directly regulates OCT4 and NANOG to promote pluripotency41. If this is the case, ESRP1 and OCT4 or NANOG could form a positive-feedback loop to reciprocally control the level and function of themselves and circRNAs, and thereby prevent loss of pluripotency in hESCs (see model in Supplementary Fig. 9). Nevertheless, these results suggest that, in addition to regulating the core transcription factor network in pluripotency, SFs could generate another layer of regulation by promoting circRNA synthesis or inducing pluripotency-associated genes.
Mouse (strain ICR) embryonic fibroblasts (MEFs) and human fibroblasts (HFs) were expanded in Dulbecco’s Modified Eagle Medium (DMEM) supplemented with 10% fetal bovine serum (FBS; Hyclone), 1% non-essential amino acids (Invitrogen), and 2 mM l-glutamine (Invitrogen). Mitomycin C (Sigma) was used to inactivate MEFs at P4 for generation of feeder cells. Human ESCs H9 and iPSCs were grown on MEF feeder layers (2 × 104 per cm2) in DMEM/F12 medium (Invitrogen) plus 20% Knockout Serum Replacement (Invitrogen), 1 mM l-glutamine, and 4 ng ml−1 basic fibroblast growth factor (bFGF; BD Biosciences). For in vitro differentiation, hESC colonies were detached by treating cells with 1 mg ml−1 dispase (Invitrogen) for 20 min at 37 °C and then transferring detached cells to ultra-low-attachment plates (Corning) to allow formation of embryoid bodies (EBs). The medium for EB culture was changed daily for 4 d using the same medium for culturing hESCs, and then replaced with MEF medium for further differentiation. The hESC H9 are obtained from WiCell Research institute and HFs are obtained from ATCC. Mycoplasma contamination was monthly examined by EZ-PCR mycoplasma test kit (Biological Industries). All animal experiments were performed under protocols approved by the Academia Sinica Institutional Animal Care and Utilization Committee.
RNA extraction and qRT-PCR
Total RNA was isolated from cells using the TRIzol reagent (Invitrogen) according to the manufacturer’s instructions. Purified RNA was treated with DNase I (Qiagen) to remove genome contamination and then was reverse transcribed using a Superscript II reverse transcriptase kit (Invitrogen) to generate a cDNA library. PCR products were amplified for 35 cycles using GoTag Mastermix (Promega), and RT-qPCR analyses were performed in triplicate using a KAPA SYBR Fast Kit (KAPA). All primers used are listed in Supplementary Table 1.
Total RNA (10 μg) from hESC H9 cells was incubated with 40 U RNaseR at 37 °C for 1 h in 1× buffer provided with the enzyme (Epicentre). RNA transcripts resistant to RNaseR treatment were precipitated with ethanol and resuspended in RNase-free H2O for the indicated analyses.
Identification and validation of circRNAs
Step 1: A total of 61 circRNAs with greater than 40 reads supporting a circular junction were selected from a database previously described by Memczak et al.6 Step 2: Circular junctions of the 61 circRNAs selected in step 1 were validated by sequential RNaseR treatment, RT-PCR, and sequencing assays; 20 circRNAs were validated. Step 3: hESC-enriched circRNAs were selected from the 20 circRNAs validated in step 2 using RT-qPCR assays (>0.1% GAPDH); 11 circRNAs were selected. Step 4: circRNAs highly associated with the pluripotent state were selected using RT-qPCR assays (fold change > 4 in reprogramming and differentiation); three circRNAs were selected. Step 5: Three circRNAs whose expression was highly associated with the pluripotent state (fold change > 4 in reprogramming and differentiation) were subjected to further functional tests (gain-of-function and loss-of-function assays). Full length of DNA electrophoresis of validated circRNAs and their linear counterpart shown in Fig. 1 are provided in Supplementary Fig. 10.
Expression vectors and miRNA mimics
For circRNA-expressing FUW vectors, full-length circRNAs without intervening introns were cloned from a cDNA library of H9 hESCs. The endogenous 5′-flanking and 3′-flanking 1 kb introns were cloned from the genome and fused to the corresponding ends of the circRNA. Notably, the exon–intron boundaries and canonical splicing sites (GT-AG) at the 5′ and 3′ termini of circRNAs were preserved for correct splicing. The most upstream 1 kb sequence of the 5′-flanking intron was copied and inversely inserted downstream of the 3′-flanking intron. To generate the circB-s minigene vector, the inversely inserted 5′-flanking intron at the 3′ terminus of the circBIRC6 minigene was removed by restriction enzyme digestion. For the circB-s-Em minigene vector (circB-s minigene with deleted ESRP1-binding sites), the region spanning between two ESRP1-binding sites at the 5′ and 3′ termini of the circB-s minigene vector was cloned by PCR and fused into the FUW vector. For minigenes expressing EGFR Exon 25 and ZEB1 Exon 11, the targeted exons with endogenous 5′-flanking and 3′-flanking 0.5 kb introns were cloned from the genome and fused into the FUW vector. The ESRP1-binding sequences were added to the 5′ and 3′ termini of EGFR Exon 25 and ZEB1 Exon 11 minigenes by PCR using primers that included ESRP1-binding sequences at the 5′ termini. For shRNA-expressing vectors, shRNA oligonucleotides specifically targeting the circular junction were synthesized (Genedragon), cloned into the pLKO vector according to the standard annealing protocol provided by the RNAi core (Academia Sinica, Taiwan), and verified by sequencing. Targeting sequences are listed in Supplementary Table 1. Lentiviral particles carrying circRNAs or shRNA or minigenes were generated in HEK293T cells using standard procedures. hESCs were infected with lentivirus and then cultured in standard hESC medium. The hESCs were then harvested for indicated analyses 3 days after infection. The miR-34a and miR-145 mimics or scrambled oligonucleotides (MDBio) were transfected into hESCs using Lipofetamine RNAiMAX (Thermo) at a final concentration of 20 nM. Transfected cells were harvested for indicated analyses 3 days after transfection.
Immunofluorescence staining and cell counting
Human ESCs and iPSCs were cultured on cover glass and fixed by incubating with 4% paraformaldehyde for 20 min at room temperature (RT). Fixed cells were then washed with PBS and permeabilized using a non-ionic detergent (0.1% Triton X-100 and 0.2% Tween-20) in PBS for 40 min at RT. Permeabilized cells were blocked by incubating with 2% goat serum (Invitrogen) for 1 h, washed with PBS containing 0.01% Tween-20 (PBST), and incubated with primary antibody. Primary antibodies used included anti-SOX17 (1:200; R&D Systems; AF1924), anti-PAX6 (1:500; Abcam; Ab5790), anti-NANOG (1:50; Abcam; Ab21624), anti-OCT4 (1:1000; Millipore; MAB4401), and anti-Brachyury (1:50; R&D Systems; AF2085). Cells were then washed with PBST and incubated with the appropriate fluorescein-conjugated secondary antibody. Stained samples were mounted using Vectashield H-1200 mounting media (Vector Laboratories), and images were captured using a fluorescence microscope (Leica). Positive signals in IF images were processed and counted using Image J with a consistent intensity threshold.
Cells on regular Petri dishes were fixed by incubating with 4% paraformaldehyde for 20 min at RT and then washed with PBS. Fixed cells were then incubated at RT with an AP substrate working solution, according to the instructions of the Blue Alkaline Phosphatase Substrate Kit (Vector Laboratories), to allow color development. The number of AP+ colonies was counted using Image J with a consistent intensity threshold.
Cells were detached with trypsin, washed with PBS, fixed with 1% paraformaldehyde and then permeabilized with 0.1% Triton X-100 in PBS. Fixed/permeabilized cells (1 × 106) were suspended in 100 μl PBS containing 1% bovine serum albumen (BSA) FACSCalibur (BD Biosciences) was used to count GFP+ cells, and collected data were analyzed with Cell Quest software (BD Biosciences).
Protein was extracted with RIPA buffer and quantified using a BCA protein assay kit (Pierce). For sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), 20 μg of protein from each sample was resolved on 10% gels and electro-transferred to a nitrocellulose membrane. After blocking non-specific binding by incubating in 3% non-fat milk in PBST for 1 h, at RT, membranes were incubated at 4 °C overnight with diluted primary antibody. The primary antibodies used were anti-OCT4 (1:1000; Millipore; MAB4401), anti-NANOG (1:1000; Abcam; Ab21624), anti-SOX2(1:2000; Millipore; AB5603), anti-AGO2 (1:1000; Abcam; ab57113), anti-ESRP1 (Novus; NBP1-82201), and mouse anti-β-actin (1:5000; Sigma; A5441). After washing with PBST, membranes were incubated with the appropriate horseradish peroxidase (HRP)-conjugated secondary antibody for 1 h, at RT. Signals were developed using Supersignal West Femto Substrate (Pierce) and recorded with an LAS-4000 luminescence image analyzer (Fujifilm). Full scans of the western blots shown in Fig. 5 are provided in Supplementary Fig. 11.
CRISPR-Cas9n-mediated genome editing
Homologous recombination between the first exon of OCT4 and donor vector through the homologous left arm (HL) and right arm (HR) was promoted by co-transfecting hESCs with donor vectors containing GFP, EF1α-RFP (RFP driven by an EF1α promoter), and puromycin (PURO) together with two guide RNAs (sequences in Supplementary Table 1). EF1α-RFP and PURO were subsequently removed using Cre protein after selection of transgenic hESC clones for expansion.
Biotinylated miRNA mimic capture
The biotinylated miRNA mimic pull-down assay was performed as described by Lal et al.42 In brief, 3′ end-biotinylated miR-34a and miR-145 mimics or scrambled oligonucleotides (MDBio) were transfected into hESCs using Lipofetamine RNAiMAX (Thermo) at a final concentration of 20 nM. After 1 day, the molecules interacting with biotinylated miRNA mimics were pulled-down by incubating the cell lysates with streptavidin-coated magnetic beads (Life Technologies). The abundance of circBIRC6 or circCORO1C in bound fractions was evaluated by RT-qPCR analysis.
RNA immunoprecipitation (RIP) assays were performed with using a Magna RIP Kit (Millipore) following the manufacturer’s instructions. In brief, 2 × 107 H9 hESCs were UV-crosslinked at 600 mj cm−2 and lysed in 100 μl RIP lysis buffer containing a proteinase inhibitor cocktail (Roche) and RNase inhibitor (Promega). Lysate was treated with DNase I (Roche) at 37 °C for 10 min and centrifuged at 12,000×g for 30 m. The lysate was then diluted with 900 μl RIP immunoprecipitation buffer and incubated for 3 h with 5 μg anti-ESRP1 (Novus, NBP1-82201) or 5 μg anti-AGO2 (Abcam, ab57113) antibodies that were pre-bound on magnetic beads. A 10-μl aliquot of the RIP mixture was saved as input. Beads were then washed six times with RIP wash buffer. A portion (20%) of the immunoprecipitate was saved for western blot analysis and the remainder (80%) was treated with proteinase K at 37 °C for 30 min. RNA was extracted using TRIzol regent (Invitrogen) according to the manufacturer’s instructions.
Chromatin immunoprecipitation assay
Chromatin immunoprecipitation (ChIP) assays were performed as follows22: briefly, hESCs H9 and their differentiated derivate (H9-EB) were treated with 1% (v/v) formaldehyde for 8 min at room temperature, and quenched with 125 mM glycine. The crosslinked chromatin was sonicated to an average size of 100–150 bp. Each ChIP reaction contained sonicated chromatin from 5 × 105 cells and 2 μg antibody (anti-OCT4 antibody, Millipore, MAB4401; anti-NANOG antibody, Abcam, Ab21624; anti-H3K27Ac, Abcam, Ab4729). The isolated DNA was purified using a QIAquick PCR purification kit (Qiagen). NANOG and OCT4 binding to the ESRP1 promoter was quantified by qPCR. Primers are listed in Supplementary Table 1. Enrichment (% of Input) was determined as (ChIP DNA/input DNA) × 100%. Each experiment was repeated at least three times, with each replicate producing a similar pattern. The results are expressed as mean ± SD of three qPCR replicates.
All quantitative data were obtained from three independent biologically replicated experiments and are presented as means ± SDs (error bars). P-values < 0.05, determined by two-tailed two-sample t-tests (unless otherwise indicated), were considered statistically significant.
The microarray data for the splicing factors expression reported in Supplementary Data 3 are available in Gene Expression Omnibus with accession numbers GSE28406 (HF and iCFB50) and GSE19964 (H9). All relevant data are available from the authors.
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This work was supported by grants from Academia Sinica (Thematic Project, AS-104-TP-B09 and AS-103-TP-B10) and the Ministry of Science and Technology (MOST103-2321-B-001-065, MOST104-0210-01-09-02/105-0210-01-13-01) and National Health Research Institutes (NHRI-EX104-10320SI).
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