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MiR-25 Regulates Wwp2 and Fbxw7 and Promotes Reprogramming of Mouse Fibroblast Cells to iPSCs

  • Dong Lu,

    Affiliation Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom

  • Matthew P. A. Davis,

    Affiliations Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom, European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom

  • Cei Abreu-Goodger,

    Affiliation European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom

  • Wei Wang,

    Affiliation Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom

  • Lia S. Campos,

    Affiliation Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom

  • Julia Siede,

    Affiliation Laboratory of Lymphocyte Signalling and Development, Babraham Institute, Cambridge, United Kingdom

  • Elena Vigorito,

    Affiliation Laboratory of Lymphocyte Signalling and Development, Babraham Institute, Cambridge, United Kingdom

  • William C. Skarnes,

    Affiliation Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom

  • Ian Dunham,

    Affiliation European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom

  • Anton J. Enright,

    Affiliation European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom

  • Pentao Liu

    Affiliation Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom

MiR-25 Regulates Wwp2 and Fbxw7 and Promotes Reprogramming of Mouse Fibroblast Cells to iPSCs

  • Dong Lu, 
  • Matthew P. A. Davis, 
  • Cei Abreu-Goodger, 
  • Wei Wang, 
  • Lia S. Campos, 
  • Julia Siede, 
  • Elena Vigorito, 
  • William C. Skarnes, 
  • Ian Dunham, 
  • Anton J. Enright



miRNAs are a class of small non-coding RNAs that regulate gene expression and have critical functions in various biological processes. Hundreds of miRNAs have been identified in mammalian genomes but only a small number of them have been functionally characterized. Recent studies also demonstrate that some miRNAs have important roles in reprogramming somatic cells to induced pluripotent stem cells (iPSCs).


We screened 52 miRNAs cloned in a piggybac (PB) vector for their roles in reprogramming of mouse embryonic fibroblast cells to iPSCs. To identify targets of miRNAs, we made Dgcr8-deficient embryonic stem (ES) cells and introduced miRNA mimics to these cells, which lack miRNA biogenesis. The direct target genes of miRNA were identified through global gene expression analysis and target validation.

Results and conclusion

We found that over-expressing miR-25 or introducing miR-25 mimics enhanced production of iPSCs. We identified a number of miR-25 candidate gene targets. Of particular interest were two ubiquitin ligases, Wwp2 and Fbxw7, which have been proposed to regulate Oct4, c-Myc and Klf5, respectively. Our findings thus highlight the complex interplay between miRNAs and transcription factors involved in reprogramming, stem cell self-renewal and maintenance of pluripotency.


Mouse and human fibroblast cells can be reprogrammed to iPSCs by expressing the four Yamanaka factors: Oct4, Sox2, Klf4 and c-Myc [1], [2], [3], [4], [5], [6], [7]. Other somatic cell types have also been reported to be reprogrammed to iPSCs [8], [9], [10], [11], [12]. Besides retroviral vectors, alternative routes are used to deliver the genetic factors such as lentivirus [2], adenovirus [13], plasmid-based vectors [14], episomal vectors [15], and the piggyBac (PB) DNA transposon [16], [17]. A growing number of genetic factors and chemical compounds are described to either improve reprogramming or even to replace one of the Yamanaka factors [18], [19], [20], [21], [22], [23], [24]. Moreover, perturbating several biological processes such as the cell cycle and DNA repair has profound effects on reprogarmming [25], [26], [27], [28].

MicroRNAs function to promote target mRNA degradation or as repressors of translation by binding the target sites usually located in the 3′ UTRs [29]. The long primary miRNAs (pri-miRNAs) are processed by the microprocessor complex, composed of the double-stranded RNA-binding protein DGCR8 and the RNase III enzyme DROSHA, into short hairpins called precursor miRNAs (pre-miRNAs) [30], [31], [32], [33]. These hairpins are exported to the cytoplasm and are processed by Dicer into mature miRNAs [34], [35]. Mouse ES cells express abundant miRNAs which play important roles in ES cell biology. As a consequence Dicer- or Dgcr8-deficient mouse ES cells are defective in cell cycle progression and differentiation [36], [37], [38]. These defects can be partially rescued by introduction of certain mature miRNAs. For instance, introduction of a subset of the miR-290 cluster is able to rescue the cell cycle defects in Dgcr8-deficient ES cells [39]. These miRNAs, which include miR-291-3p, miR-294 and miR-295, are thus named ES cell-specific cell cycle-regulating (ESCC) miRNAs based on their ability to regulate G1-S transition [39]. Moreover, proteins important in ES cell pluripotency are found to bind the promoter regions of miRNAs and regulate their transcription activities [40]. Therefore, miRNAs appear to have significant roles at the centre of the regulatory networks that control pluripotency. Indeed, overexpressing ESCC miRNAs can improve reprogramming by replacing c-Myc [41], and expressing the miR-302 cluster is sufficient to reprogram a cancer cell line to cells expressing pluripotency genes [42]. In a dramatic show of miRNA's function in reprogramming, Morrisey and colleagues recently demonstrated that expressing the miR-302/367 cluster alone is sufficient to reprogramme mouse and human fibroblast cells to iPSCs [43]. A combination of mir-200c plus mir- 302 and mir-369 family miRNAs is also shown to produce mouse and human iPSCs [44]. Conversely, inhibition of the let-7 family, which silences ES cell self-renewal by suppressing many of the same downstream targets that are indirectly activated by the ESCC miRNA family, promotes de-differentiation of somatic cells and reprogramming [45].

To identify additional miRNAs that affect reprogramming, we performed a genetic screen focusing on miRNAs that are expressed in mouse ES cells [46], [47], or over-expressed in cancer [48], [49]. From this screen, we found that overexpressing miR-25 substantially improved reprogramming, which was confirmed by introducing miR-25 mimics. The iPSCs produced were fully pluripotent as they contributed efficiently to both somatic cells and the germline in chimeras. Moreover, through bioinformatics analysis and experimental validation, we identified that miR-25 directly regulated Wwp2, an E3 ubiquitin ligase that targets Oct4 for ubiquitination, and Fbxw7, which is known to regulate c-Myc, Klf5 and other important factors. These results thus reveal a mechanism for miR-25 to regulate pluripotency genes and provide new information for efficient reprogramming.


MicroRNAs that promote reprogramming

The piggyBac (PB) transposition works efficiently in mammalian cells. We have previously comprehensively characterized PB transposition in mammalian cells and used it in reprogramming experiments [16], [50], [51]. To start exploring the roles of miRNAs in reprogramming, we selected 52 miRNAs or miRNA clusters, based on their expression in ES cells or in tumour cells (Table S1) [46], [47], [48], [49]. These miRNAs were cloned in the PB vector by PCR-amplifying 500–800 bp genomic DNA fragments that encompass the ‘precursor’ miRNA sequences (Table S2). In these PB vectors, miRNA expression was under the control of the CAG promoter (PB-CAG-mir) (Fig. 1a).

Figure 1. Reprogramming MEFs using PB transposons carrying the four Yamanaka factors and miRNAs.

a. Schematic diagrams of the PB transposon constructs. Mouse cDNAs for Oct4, c-Myc, Klf-4 and Sox2 (OCKS) were cloned under the control of either the CAG promoter or the TRE (Tet responsive element). Expression of rtTA (reverse tetracycline transactivator) and the miRNAs was controlled by the CAG promoter. cDNAs of OCKS were joined by a linker encoding the 2A peptide. b. The Oct4-reporter allele. The IRES-PuroGFP cassette was targeted to the 3′ UTR of Oct4 locus, immediately after the TGA stop codon in exon 5. c. Timeline of the reprogramming strategy. MEF cells were transfected with the transposon constructs and plated onto STO feeder cells. Puromycine (2.0 µg/ml) was added to select for Oct4 expression on day 10. If the Dox-inducible transposon (PB-TRE-OCKS) was used, Dox (1.0 µg/ml) was added one day after transfection.

ES cell pluripotency requires proper levels of Oct4 (Pou5f1) expression [52], and activation of Oct4 is a critical event in the reprogramming process [4]. We constructed and used an Oct4-reporter mouse line where an IRES-PuroGFP cassette was targeted to the 3′ UTR of the Oct4 locus (Fig. 1b) [51]. Fully pluripotent iPSCs reprogrammed from these Oct4-reporter MEFs are resistant to 2.0 µg/ml puromycin (Puro) selection and identifiable as GFP+ in flow cytometry [51]. Therefore we use resistance to 2.0 µg/ml Puro or GFP expression to assess primary reprogrammed colonies, followed by comprehensive characterization.

To reprogram mouse embryonic fibroblasts (MEFs) to iPSCs, we constructed the PB transposon carrying the four Yamanaka factor cDNAs controlled either by the CAG promoter (PB-CAG-OCKS, for Oct4, cMyc, Klf4 and Sox2) for constitutive expression, or by the Tet-response element (PB-TRE-OCKS) for inducible expression by Doxycycline (Dox) (Fig. 1a). As the baseline reprogramming control, we transfected the PB-CAG-OCKS transposon to Oct4-reporter MEFs, and plated the cells on STO feeder cells (Fig. 1c). To examine the effects of miRNAs in addition to the Yamanaka factors on reprogramming, we co-transfected the PB-CAG-OCKS plasmid with each of the 52 PB-CAG-miRNA plasmids and selected the reprogrammed colonies for puromycin resistance (2.0 µg/ml). We usually began Puro selection 10 days after transfection when ES cell-like colonies started to appear. Puror colonies were subsequently picked for expansion and further analysis.

Four out of the 52 tested miRNAs or miRNA clusters: the miR-302 cluster, miR-25, miR-290 and miR-298, gave substantially more Puror iPSC colonies (2–4 fold) than the control where only the four factors were used (PB-CAG-OCKS) (Fig. 2a). Identification of miR-302 and miR-290 in our screen confirmed the previous studies [41], [42]. However, we were unable to reproduce the result reported by Morrisey and colleagues [43] that expressing the miR-302/367 cluster alone is sufficent to reprogramme MEFs to iPSCs. This discrepancy is possibly caused by the miRNAs delivery approaches. We used the PB transposon where miR-302/367 cluster expression was controlled by the CAG promoter whereas in Morrisey's work, this cluster was delivered using a lentiviral vector. However, this possibility needs to be further investigated experimentally. Although miR-290 itself was not known to promote reprogramming, several members of the miR-290 family, miR-291-3p, miR-294 and miR-295, enhance reprogramming of MEFs in the absence of c-Myc [41]. The other two miRNAs identified in this screen, miR-25 and miR-298, were not previously reported for their role in ES cells or in reprogramming when the project started. We therefore chose initially to further characterize miR-25 since it was found to be expressed in ES cells (Fig. 2b), and its mature sequence is conserved across all vertebrate genomes examined (Table S3). On the other hand, miR-298 expression was not found in ES cells [47].

Figure 2. Co-expressing OCKS and microRNAs improved reprogramming.

a. Four microRNAs: miR302 (cluster), miR-25/93, miR-290 and miR-298 were able to improve reprogramming. Shown here is the fold change of iPSC colony number (2.0 µg/ml Puror). Fold changed was calculated based on the iPSC colony number using the four factors only (mean ± SEM. N = 4). b. qPCR analysis of the mature form of miR-25 expression. Expression was determined by qPCR and normalized using Sno202 miRNA. Data are mean ± SEM from three cell lines. * P<0.05. c. Reprogrammed colonies (2.0 µg/ml Puror) stained either by Methylene blue or for Alkaline Phophatase activity (AP). NC: negative control using a PB-Neo plasmid with no reprogramming factors; 4F-iPSC: iPSCs reprogramming by expressing OCKS (Dox inducible); 25-iPSC: iPSCs reprogramming by expressing OCKS (Dox inducible) and miR-25. Mimic: Transfection used a miR-25 mimic instead of the PB-CAG-mir25. d. A primary iPSC colony reprogrammed with the four Yamanaka factors and miR-25. e. GFP expression from the Oct4 locus in 4F-iPSCs and 25-iPSCs detected by flow cytometry.

To confirm the effects of miR-25 over-expression on reprogramming, we transfected 1×106 MEFs with PB-TRE-OCKS, PB-CAG-rtTA and PB-CAG-mir25 (Fig. 1a). Dox was added to the culture media to induce expression of the four Yamanaka factors. Again expression of miR-25 substantially increased the number of Puror iPSCs (Fig. 2c–d). The iPSC colonies were picked 16 days after transfection, and initially expanded in M15 plus LIF media. Dox was subsequently removed from the culture during colony expansion and the medium was changed from M15 plus LIF to the 2i medium. This medium is considered to be able to select and maintain ground state or naïve pluripotent ES cells by inhibiting the activities of ERK and GSK3β [53]. iPSCs produced from using either the 4 Yamanaka factors (4F-iPSC) or 4F plus miR-25 (25-iPSC) proliferated well in the 2i medium. Consistent with their resistance to 2.0 µg/ml Puro, the cells also expressed GFP in flow cytometry thus demonstrating robust expression of the endogenous Oct4 locus (Fig. 2e).

The miR-25 genomic DNA cloned in the PB also contains miR-93 (Table S2). However, we did not detect noticeable effect on reprogramming by expressing miR-93 from another genomic DNA containing only miR-93 (Table S2). To further examine the specific effect of miR-25 on reprogramming, we repeated the above reprogramming experiments using a miR-25 mimic instead of the genomic DNA containing miR-25. Adding miR-25 mimic increased AP+ colony number similar to using PB-CAG-mir-25/93 (Fig. 2C)

Characterization of iPSCs produced by over-expressing miR-25

Dox induced iPSCs of both 4F-iPSC and 25-iPSC were expanded for over 20 passages in the 2i medium without Dox. Both iPSCs expressed pluripotency markers as well as a panel of pluripotency-associated genes at levels comparable with that in ES cells (Fig. 3a and 3b). However, compared to MEFs and 4F-iPSCs, 25-iPSCs expressed higher levels of miR-25 (Fig. 2b). Bisulphite genomic DNA sequencing analysis of the promoter regions of Oct4 and Nanog loci revealed extensive demethylation in both 25-iPS and 4F-iPS cells as seen in ES cells, thus further confirming activation of these pluripotency gene loci (Fig. 3c). Importantly, even after extensive in vitro passage, these iPSCs retained a normal karyotype (Fig. 3d). To ensure that the exogenous factors were not expressed in the absence of Dox, we designed primers to amplify junction fragments between the Yamanaka factor cDNAs in PB-TRE-OCKS, and performed RT-PCR using RNA samples from iPSCs growing in the presence or the absence of Dox. As shown in Fig. 3e, Dox induced robust expression of the Yamanaka factors, while withdrawing Dox completely shut down their expression in the majority of examined iPSC lines (Fig. 3e).

Figure 3. Characterization of 25-iPSCs.

a. Immunofluorescence-staining of iPSCs to detect SSEA1 and Nanog expression. DNA was stained with DAPI (blue). b. RT-PCR analysis of pluripotency gene expression in 25-iPSCs and 4F-iPSCs. MEFs and ES cells serve as the negative and positive controls, respectively. Beta-actin was used as the PCR control. dH2O: no DNA template. c. Bisulfide genomic sequencing of the promoter regions of Oct4 and Nanog loci to detect CpG methylation. Open and filled circles represent unmethylated or methylated CpG dinucleotides, respectively. d. Normal karyotypes in a male 4F-iPS cell and a male 25-iPS cell. e. No exogenous Yamanaka factor expression in 25-iPSCs. RT-PCR was performed using primers to amply OCKS junctions (Primer sequences are in Table S2). Robust expression from PB-TRE-OCKS was detected in the presence of Dox. No expression was found if Dox was removed from the media. +RT: reverse transcriptase; -RT: no reverse transcriptase in reverse transcription. Beta-actin was used as the PCR control. f. Haematoxylin eosin stained sections of teratomas derived from 25-iPSCs. Cells representing all three germ layers were readily identifiable. g. Germline-transmission pups (agouti) from two chimeras derived from 25-iPSCs that were crossed to wild-type C57BL6 (albino) females.

To determine differentiation potentials of iPSCs, we injected 4F- and 25-iPSCs into F1 mice of C57BL/6 and 129S5 because Oct4-reporter MEFs had a C57BL/6/129S5 mixed genetic background. Both 4F- and 25-iPSCs efficiently formed teratomas containing tissues of all three germ layers (Fig. 3f). The 4F- and 25-iPSCs were also injected to C57BL/6 (albino) blastocysts for chimera production. Chimeras with extensive donor cell contribution were obtained from both iPSCs (Fig. 3g). Two male chimeras produced from injecting 25-iPSCs were crossed to wild type C57BL/6 (albino) females to test germline contribution of the iPSCs in the chimeras. In the first eight litters, 50 out of 52 pups were agouti coat colour indicative of very efficient contribution of 25-iPSCs in the germline of the chimeras (Fig. 3g). Similarly, two male chimeras produced from 4F iPSCs were also crossed to wild type C57B6 females (albino). Out of total 32 pups in the first four litters, 24 were agouti. Since the Dox induced iPSCs did not express detectable levels of exogenous factors in the absence of Dox (Fig. 3E), chimeras derived from either 4F- or 25-iPSCs did not develop any tumour or abnormalities in the aging period (14 months, n = 10).

To further characterize the 4F- and 25-iPSCs, we performed genome-wide gene expression microarray analysis. Expression profiles of 4F-iPSCs and 25-iPSCs were highly correlated, and clustered together with the profiles of ES cells and distinct from those of MEFs (Fig. 4a and b).

Figure 4. Genome-wide gene expression analysis in iPSCs and ES cells.

a. Heatmap showing the (log2) absolute expression intensities in MEFs, 25-iPS, 4F-iPS and ES cells of the top 100 differentially expressed genes between MEFs and ES cells. Expression profiles are clustered based on correlation, and the dendrogram represents the relationship between different cell types. b. Venn diagram showing the number of shared differentially expressed genes among 25-iPSCs, 4F-iPSCs and ES cells when compared to MEFs.

Identification of miR-25 targets

Dgcr8 is a critical component of the complex that processes primary miRNAs. Dgcr8-deficient ES cells have defects in miRNA biogenesis [38]. These cells thus provide an ideal platform to facilitate identifying potential miRNA targets once a mature miRNA is introduced into these ES cells. The obvious advantage of this system over transfecting miRNA mimics in another cell type (e.g. HeLa or normal ES cells) is that the target sites are not saturated by the endogenous miRNAs and there will be no functionally redundant miRNAs to confound the results.

We thus used a Dgcr8-deficient ES cell line where one allele was mutated by gene trapping and the other allele contained a targeted gene trap cassette (Davis et al. co-submission with this manuscript). To identify the direct target genes of miR-25, we introduced either a mimic version of miR-25 or a control miRNA (C. elegans miRNA, cel-miR-239b) (Fig. 5a) into the Dgcr8-deficient ES cells and generated gene expression profiles using Illumina BeadChip microarrays. Potential miR-25 target genes were expected to be down-regulated in cells with the miR-25 mimic but not in control cells. We used Sylamer to further characterise the effect of miR-25 expression [54]. Briefly, Sylamer tests for miRNA effects by searching sorted lists of genes for enrichment or depletion of words complementary to all possible miRNA “seed” regions, which are the most important determinants of target specificity. The 3′UTR sequences of all the transcripts profiled on the microarrays were sorted starting with the most down-regulated in the miR-25 transfection experiment. The only 7mers that were enriched within the 3′UTRs of these down-regulated genes correspond to words complementary to the miR-25 seed sequence, indicating that the experimental profile can be used to derive lists of genes enriched for direct targets of miR-25 (Fig. 5b). From this experiment we obtained a list of 72 transcripts, which were down-regulated after transfection of the miR-25 mimic, with a fold change of at least 1.2 and with an estimated false discovery rate less than 10%. Of these genes, 54 possessed at least one seed-matching site for miR-25 in their 3′UTR and constitute the initial set of experimentally derived miR-25 targets (Table S4). To test if these targets are being actively repressed by miR-25 in our iPSCs, we compared the 25-iPS microarray samples against the 4F-iPS samples. We observed that these miR-25 candidate targets were down-regulated in the 25-iPS cells (p value 9×10−4 by a Wilcoxon signed-rank test) (Fig. 5C). From these targets, we prioritized a list of 12 gene by selecting those that were also up-regulated in the Dgcr8-deficient cells, besides being down-regulated in 25-iPSCs relative to 4F-iPSCs (Table 1). Of particular interest on this gene list were Wwp2 and Fbxw7, which have been shown to modulate Oct4 and c-Myc respectively [55], [56], [57], [58], [59], [60].

Figure 5. Identification of miR-25 targets.

a. Timeline of miR-25 mimic transfection into the Dgcr8-deficient ES cells for discovering transcripts that were repressed by miR-25. The C. elegans miRNA, cel-miR-239b, was used as the negative control. b. Sylamer plots following the analysis of microarray data. The x-axis represents the 3′UTR sequences of all transcripts, sorted from the most down-regulated after miR-25 transfection compared to the cel-miR-239b transfection. Sylamer was used to analyze the enrichment or depletion of all possible heptamers matching mouse miRNA seeds, at every 500 sequences of the gene list. The horizontal dashed lines denote Bonferroni corrected p-value thresholds of 0.05. Words matching the mmu-miR-25 and cel-miR-293b seeds are highlighted. c. Cumulative fraction plot of the fold-changes obtained by comparing 25-iPS vs 4F-iPS microarrays. The fold-changes for all genes are indicated by the black curve; the green curve represents the 54 miR-25 targets from Table S4.

Validation of wwp2 and fbxw7 as miR-25 targets

We next proceeded to validate the experimentally predicted miR-25 targets. We first used quantitative (real-time) RT-PCR (qRT-PCR) to examine the expression of two selected miR-25 targets, Wwp2 and Fbxw7, as well as the pluripotency markers Oct4 and Nanog in MEF, 4F-iPSCs, 25-iPSCs and mouse ES cells. No significant difference in the expression of Oct4 or Nanog was detected, possibly due to the tightly regulated expression of pluripotency genes in ES cells and in iPSCs. Wwp2 is expressed at much higher levels in MEFs than in ES cells (Fig. 6a). The level of the Wwp2 transcript was significantly lower in 25-iPSCs compared to 4F-iPSCs, and was comparable to that in ES cells (Fig. 6a). Although we consistently detected lower Fbxw7 expression in 25-iPSCs and ES cells than in 4F-iPSCs, this decrease was not statistically significant (Fig. 6a). The expression results were thus consistent with the predictions of Wwp2, and to a certain degree Fbxw7, as the potential targets of miR-25.

Figure 6. Validation of miR-25 targets.

a. Realtime RT-PCR analysis of expression of Oct4, Nanog, Wwp2 and Fbxw7 in MEFs, iPSCs and ES cells. A significant decrease of Wwp2 was detected in 25-iPSCs, compared to 4F-iPSCs. Gene expression was normalized against Gadph. Error bar (mean ± SEM. N = 3 cell lines). * P<0.05 compared with 25-iPS cells for Wwp2 expression. b–c. Luciferase reporter assay to the validate miR25 binding sites in the 3′UTRs of Wwp2 and Fbxw7. Schematic diagrams of the reporters for Wwp2 (b) and Fbxw7 (c). The wild type and mutated miR-25 binding sites (highlighted in red) were indicated. The 3′ UTR of Wwp2 has one miR-25 binding site, whereas Fbxw7 has two. The 3′UTR genomic regions amplified for both Wwp2 and Fbxw7 are about 1.6 kb. d. Luciferase reporter assays for validating Wwp2 and Fbxw7 as direct targets of miR-25. Wild-type (Wt) or Mutant (Mut) reporter plasmids were co-transfected with miR-25 mimic or a control mimic into HeLa S3 cells to assay for the miR-25 dependent repression of Wwp2 and Fbxw7 reporter. Data are presented as mean ±SEM (N = 3). Comparison between groups were performed using one-way ANOVA followed by the Newman-Keuls post test to determine statistical significance. ** P<0.001.

To demonstrate that miR-25 directly regulates Wwp2 and Fbxw7, we performed the luciferase reporter assay based on pmirGLO Dual-Luciferase system where the full-length 3′ UTR of either Wwp2 or Fbxw7 was inserted into the 3′ side of the firefly luciferase gene (luc2) (Fig. 6b–c).

The wild type 3′ UTR of Wwp2 carries one miR-25 target site. We introduced a point mutation into this target site, which would abolish miR-25 binding based on computational prediction. The reporter plasmids carrying either the wild type or the mutant 3′ UTR of Wwp2 were co-transfected with the miR-25 mimics or the negative control mimics into HeLa S3 cells. The negative control mimics did not have any significant effect on reporter activity. However, the miR-25 mimic significantly repressed luciferase activity from the wild type reporter plasmid (Fig. 6d). Once the miR-25 binding target site was mutated, the repressing effect of the miR-25 mimic was lost (Fig. 6d). These results thus confirmed the critical role of the miR-25 binding site in regulating the luciferase activity in the reporter plasmid and thus Wwp2.

The 3′ UTR of Fbxw7 has two miR-25 binding sites. Point mutations were subsequently introduced into both sites in the mutant reporter plasmid. Again, we co-transfected the reporter plasmids with the miR-25 mimics and the negative control mimic into HeLa S3 cells. The negative control mimic did not show any effect on the reporter activity, whereas the miRNA-25 mimics caused significant repression on the luciferase activity from the wild type reporter but not the mutated reporter (Fig. 6d). These data thus confirmed Fbxw7 as another direct target of miR-25.


In an effort to identify new genetic factors in reprogramming, we screened 52 miRNAs/clusters that are expressed in ES cells or over-expressed in cancer. Two candidates, miR-25 and miR-298, were found to substantially improve reprogramming with the four Yamanaka factors. We focused on characterizing miR-25 in this study as miR-25 had a strong phenotype in promoting reprogramming, is highly conserved during evolution and is expressed in ES cells. The iPSCs produced by overexpressing miR-25 together with the four Yamanaka factors were pluripotent stem cells, based on their gene expression profiles, and on their ability to contribute to both the somatic lineages and the germline in chimeras. Further experiments designed to elucidate the contribution of miR-25 to this process combining computational prediction and experimental analysis using Dgcr8-deficient ES cells, demonstrated that miR-25 regulates a number of genes in mouse ES cells. We chose Wwp2 and Fbxw7 for further analysis and confirmed that miR-25 directly regulated Wwp2 and Fbxw7 in the luciferase reporter assay.

Wwp2, an E3 ubiquitin ligase, promotes Oct4 degradation by ubiquitination in both mouse and human ES cells [55], [56], thus suggesting a potential mechanism for improving reprogramming efficiency by miR-25. Importantly, Wwp2 expression levels in 25-iPSCs were slightly but consistently lower than that in iPSCs reprogrammed by the four Yamanaka factors alone (Fig. 6a). We did not however detect an obvious increase of Oct4 protein levels in 25-iPSCs (data not shown). The stable Oct4 expression level is likely caused by the pluripotent gene expression regulatory circuit in iPSCs where Oct4 is regulated by multiple factors. Fbxw7, on the other hand, is a component of SCF ubiquitin ligases that catalyzes the ubiquitination of cyclin E, Notch, c-Jun and c-Myc [57], [58], [59], [60]. Interestingly, Fbxw7 also directly targets Klf5 for ubiquitination and degradation [61]. Klf2, Klf4, and Klf5 are the core KLF protein circuitry with redundant function in regulating self-renewal of ES cells and Nanog expression [62], and Klf2 and Klf5 can replace Klf4 in reprogramming [63]. Thus, repression of Fbxw7 induced by over-expression of miR-25 might also contribute to improving reprogramming through upregulation of Klf5. While this manuscript was under preparation, miR-25 was shown to directly regulate p53 in tumour cells, and possibly p21 and Tgfβ signalling in MEFs [64], [65]. Both p53 and Tgfβαρε implicated in reprogramming [66], [67]. MiR-25 has also been recently suggested to function in IGF signalling, Wnt signalling and apoptosis in several cell types [68], [69], [70], [71]. In this study, we identified a different set of miR-25 targets in Dgcr8-deficient mouse ES cells. These targets include Wwp2 and Fbxw7, which may regulate three of the four reprogramming factors, Oct4, cMyc and Klf5. Other miR-25 targets identified in this study still remain to be characterised for their role in reprogramming. Our results, together with the other studies, show that, miR-25 promotes reprogramming by several mechanisms and possibly at distinct reprogramming stages. Given the conservation of miR-25 mature sequence during evolution and its role in regulating pluripotency genes, it will be interesting to determine whether its role is conserved in reprogramming human cells.

Materials and Methods

Ethics statement

All animal experiments were performed in accordance with the UK's 1986 Animals Scientific Procedure Act and local institute ethics committee regulations. Wellcome Trust Sanger Institute Ethical Review Committee approved this study.

Construction of transposon plasmids encoding microRNA and the 4 factors

Candidate miRNAs were selected from published papers based on their expression in mouse ES cells, in the mouse oocyte or in cancer [40], [42], [46], [47], [48], [49], [77], [78], [79], [80], [81], [82], [83], [84] (Table S1). Genomic DNA fragments harbouring miRNAs were cloned into a PB vector carrying a CAG promoter-driven expression cassette (PB-CAGG-miRNA). cDNAs of Oct4, Sox2, Klf4 and c-Myc were cloned into a PiggyBac vector under either the control of the CAG promoter or the Tetracycline operator (PB-CAG-OCKS and PB-TRE-OCKS). The cDNAs of the 4 factors were generated by PCR amplification to insert 2A peptide sequence in between the four cDNAs. A separate PB vector, with M2rtTA insert was also cloned under the tetracycline operator (PB-TRE-rtTA). All plasmids had the pBlueScript backbone.

Reprogramming of MEFs and iPS cell culture

MEFs with Oct4-GFP-Puro reporter allele were prepared from 13.5 d.p.c. embryos (C57BL/6 and 129S5 F1) cultured in M10 media: DMEM containing 10% FBS (HyClone), 1,000 units/ml Penicillin, 1,000 ug/ml Streptomycin, 2.92 mg/ml L-Glutamine and 1× non essential amino acids (Invitrogen). Individual PB-miRNAs were co-transfected with PB-OCKS into MEFs. Electroporation was performed using an Amaxa device to introduce 2 µg of PB-CAG-OCKS transposon and 2 µg of PB-CAG-miRNA transposon. The cells were then allowed to be reprogrammed to iPSCs in normal ES cell M15 media: DMEM containing 15% of FBS (Hyclone), 1,000 units/ml Penicillin, 1,000 ug/ml Streptomycin, 2.92 mg/ml L-Glutamine, 1× non essential amino acids, 0.1 mM 2-mercaptoethanol and 1,000 Uml−1 Leukemia inhibitory factor (LIF, Chemicon). For the Tet-inducible system, a PB-Tet-OCKS was co-electroporated with 1.0 µg of PB-CAG-rtTA plasmid. After 10 days of Doxycyclin induction, Puromycin selection (2.0 µg/ml) was applied. The plates were stained with methyl Blue or for Alkaline Phosphatase activities to score iPSC colonies. The iPSC colonies were cultured for 4 days in 2i media (iSTEM, Stem cell sciences). All ES cells and iPSCs were cultured on Mitomycin C–treated STO feeder cells.

Transfection of the miR-25 mimics in reprogramming

MEF cells were transfected with 2.0 µg of PB-CAG-OCKS plasmid, together with 16 nM of miRNA-25 mimic (Dharmacon) using the Amaxa transfection device. At 3, 6 and 9 days post initial transfection, these cells were transiently transfected with 16 nM of miRNA-25 mimic (Dharmacon) with Lipofectamin 2000 (Invitrogen) according to manufacture's instructions. Reprogrammed colonies were stained with Alkaline Phosphate.

Dgcr8-deficient ES cell lines were maintained in GMEM media supplemented with 100 µg/ml hygromycin B (Calbiochem). These cells were split every 2–3 days as they approached confluency.

Flow cytometry

Flow cytometric analysis was performed using iPSCs growing in 96-well plates to detect the GFP expression under the Oct4 promoter. We used a Cytomics FC500 series (Beckman Coulter) in this work.


Reverse transcription reactions were performed using SuperScript II (Invitrogen) and the Oligo dT20 primer. PCR was then carried out using the primers for ES cell marker genes listed in table 1 and an Extensor Hi-Fidelity PCR master mix 2 (ABgene). PCR was performed using the following settings: 94°C for 4 min, followed by 30 cycles of 94°C for 30 sec, 65°C for 30 sec and 68°C for 45 sec. Final incubation was at 68°C for 10 min.

Real time PCR

Quantitative real time PCR was performed using Taqman Gene Expression assays (Applied Biosystems) according to manufacture's instructions. The amount of target RNA was determined from the appropriate standard curve and normalized relative to GAPDH mRNA. The assay was custom designed using the Primer Express Software 3.0 (Applied Biosystems).


IPSCs were fixed with 4% paraformaldehyde in PBS for 20 min at room temperature (16–25°C) and permeabilized in 0.2% Triton in PBS for 10 min at room temperature. Cells were then blocked by incubation for 20 min with 5% donkey serum in PBS at room temperature. Cells were washed three times with PBS before the addition of PBS containing antibodies against Nanog (1∶500, Rabbit polyclonal; ab21603, Abcam) and SSEA1 (1∶100, mouse monoclonal, MC80; Cell Signaling Technology). After incubation for 1 hour at room temperature, cells were then washed 3 times with PBS and labelled with Alexa 488- or Alexa 546-conjugated secondary antibodies (Invitrogen). After a final wash with PBS, a drop of Vectashield (containing DAPI) mounting solution was applied to the slide and a coverslip fitted. The samples were then analyzed using a LSM700 confocal microscope (Zeiss) according to manufacture's instructions.

Bisulfide genomic sequencing

The promoters of Oct4 and Nanog were analyzed using bisulfide genomic sequencing for the DNA methylation status of MEF, 4F-iPS, 25 iPSCs and ES cells. The bisulfide treatment was performed using the CpGenome modification kit (Qiagen) according to manufacture's instructions. The PCR primers for Oct4 and Nanog were similar to those described previously by Takahashi and Yamanaka.





PCR products were cloned into pGEM T-vector (Promega) and sequenced using the M13 forward and reverse primers.


iPSCs were. F1 mice of C57BL/6 and 129S5 were anesthetized with diethyl ether. 1×106 iPSCs resuspended in PBS were administered subcutaneously into the dorsal flank. Tumours were visible 3 to 5 weeks after the injection, which were surgically dissected from the mice. Samples were weighed, fixed in PBS containing 4% formaldehyde, and embedded in paraffin. Sections were prepared and stained with hematoxylin and eosin.

Microarray analysis

Total RNA from MEFs, ES cells or iPSCs were hybridized onto MouseWG-6 expression BeadChip (Illumina) according to manufacture's instructions. Arrays were then scanned using the BeadXpress Reader (Illumina). Raw expression files were exported directly from BeadStudio and loaded into R/Bioconductor [72]. The lumi package was used to perform Vanriance-stabilizing Transformation and Robust Spline Normalization on the expression values [73]. For analysis of differential expression, limma was used to fit linear models to every probe, using an empirical Bayes approach to shrink the estimated variance [74], [75]. Probes that passed a detection threshold <0.01 in at least one sample (these values are included in Illumina's BeadStudio output) were called ‘present’. To establish False Discovery Rates (FDR), the p-values of all the ‘present’ probes were adjusted using the Benjamini and Hochberg method. To highlight the similarities and differences between different cell types, a FDR of 10% was chosen as a cut-off point.

Identification of potential miR-25 targets

The homozygous mutant cells were used for analysis as follows. Dgcr8gt1/tm1 mouse embryonic stem cells were maintained in 100 µg/ml hygromycin B (Calbiochem) selective ES cell culture medium (500 ml GMEM (Sigma), 50 ml Foetal Bovine Serum (Gibco), 5 ml 200 mM L-Glutamine (Gibco), 5 ml 100 mM Sodium Pyruvate (Gibco), 5 ml 100× Non-Essential Amino Acids (Gibco), 70 µl 0.05 M ß-mercaptoethanol (Sigma) and LIF) in gelatinized plates. Prior to transfection the cells were cultured for 4 days in non-selective media. On the fourth day the cells were plated to gelatinised 6 well plates, 96×104 cells per well in 7.2 ml of non-selective media. Wells were transfected after 3 hours. 240 pmoles of miRNA control mimic (miRIDIAN Negative Control #2 (Dharmacon CN-002000-01-05) or miRIDIAN mmu-miR-25 mimic (Dharmacon C-310564-01-0005)) were added to 240 µl OptiMEM I (Gibco). 7.2 µl of Lipofectamine 2000 (Invitrogen) was added to further 240 µl of OptiMEM and incubated for 5 minutes at room temperature. The two mixtures were subsequently combined. This mixture was incubated for 25 minutes at room temperature. Then the media in each well was replaced by 2.4 ml of fresh, non-selective media. The miRNA-lipid complexes were transferred to the wells and these were mixed gently. 5 hours later, the media was replaced with a further 7.2 ml of non-selective media. 10 hours after the initiation of transfection cells were washed twice with DPBS (-CaCl2 and MgCl2) (Gibco) and lysed with 1 ml of Trizol. Transfections were conducted in duplicate. Purified RNA was cleaned up with an RNeasy MiniElute Cleanup Kit (Qiagen) and labeled using the Total Prep RNA Amplification Kit (Illumina). 1500 ng of biotinylated RNA was hybridised to Illumina Mouse-6 v1.1 Expression Beadchips overnight at 58°C. The chips were washed, detected and scanned according to the manufacturers instructions and the scanner output was imported into Beadstudio v.3.1.8 (Illumina).

In addition Trizol was used to prepare RNA in triplicate from the 2 independently derived homozygous mutant mouse ES cell lines (Dgcr8gt1/tm1 and Dgcr8gt2/tm1) and 2 corresponding heterozygous cell lines (Dgcr8tm1,gt1/+ and Dgcr8tm1,gt2/+). The RNA was prepared for array analysis as described above.

Microarray analysis was conducted in R/Bioconductor [72] using the lumi [73] and limma [74] packages. All arrays relevant for this study were vst [75] transformed and quantile normalised alongside further array sets, the results of which will be discussed in a subsequent paper (Davis et al in preparation). The probes from the array were mapped to transcripts based upon the annotation of Ensembl v53. Where a probe maps to multiple transcripts, Vega [76] annotation was accepted in preference followed by Ensembl transcripts and EST transcripts respectively. In each category the transcript with the longest 3′UTR was chosen. If a probe was not associated with an Ensembl annotated transcript, where possible probes were annotated with a transcript according to the Illumina annotation file. Only probes with an annotated transcript were considered for the expression analysis. Where multiple probes mapped to the same transcript, the probe with the greatest inter-quartile range across the normalised arrays was selected for expression analysis. In order to determine a list of transcripts down-regulated by miR-25 a linear model was fitted across a large set of similar experiments prior to the comparison of the relevant samples (Davis et al in preparation); these include arrays considering a transfection time series and the transfection of alternative miRNAs. Arrays derived from Dgcr8gt1/tm1 cells transfected with a miR-25 mimic, lysed 10 hours after transfection were compared to those derived from cells transfected with a control mimic lysed after the same interval. Probes down-regulated in the presence of the miRNA mimic with a log fold change greater than log2(1.2) and a p-value less than 0.1 were considered for further analysis.

The transcripts associated with these probes were mapped to further annotation based upon Ensembl version 53, where possible, or to EntrezIDs based upon the Ilumina annotation file if Ensembl annotation was unavailable. Sylamer [54] was used to count the number of miRNA seed sequences associated with miR-25 in the 3′UTR of the annotated transcripts. The final miRNA target list comprises of those transcripts from this potential target list with one or more 7mer[1A] or 7mer[2] seed sequence within their annotated 3′UTRs. This list was further refined through a comparison to those genes whose expression changed between heterozygote Dgcr8 cells with two gene traps in the same allele of Dgcr8 and homozygous mutant cells with a gene trap cassette in each allele of Dgcr8. A linear model was fitted across all of the heterozygous and homozygous mutant arrays and a fifth set incorporating wild-type ES cells (E14). Using the same set of refined probes described and considering each of the heterozygous lines and homozygous mutant lines with equal weight the limma [74] package in bioconductor [72] was used to determine the relative expression change for each probe and corresponding gene between the cell lines of differing genotype.

Microarray data in this study can be accessed at:

E-MTAB-409 <>

E-MTAB-418 <>

Quantitation of miRNA

Quantitative real time PCR was performed using Taqman Gene Expression assays (Applied Biosystems) according to manufacture's instructions. The assay was custom designed using the Primer Express Software 3.0 (Applied Biosystems). The amount of target RNA was determined from the appropriate standard curve and normalized relative to Gapdh mRNA. Primer sequences are shown in Table S1. For mature miR-25 real time PCR analysis, we used a kit from the Taqman MicroRNA assays (Applied Biosystems). miR-25 expression was normalized against expression of Sno202 (Applied Biosystems).

Sylamer target enrichment analysis

Sylamer utilizes the over- and under-representation P-values in nested bins across a ranked sequence universe. It is optimized for four letter alphabets (i.e. DNA/RNA) and computes P-values for all words of a fixed length. The method has been tested on different miRNA expression databases. A convenient post-processing step is to plot the Sylamer output as lines of log-transformed P-values across all bins, giving a comprehensive view of word distribution behaviour across the sequence universe.

Luciferase plasmid construction

The Wwp2 3′UTR was amplified using primers Wwp2-F: 5′-TTTAACTCGAGCT-GAGGCTGCTGTCTCACAC-3′ and Wwp2-R: 5′-AAGCCGCGGCCGCGGCTGCTG-ATTCTTTATTGC-3′. The amplified fragment was digested using XhoI and NotI and ligated the psiCheck-2 renilla luciferase reporter plasmid (Promega). For the mutagenesis reactions, Quick Change Lightning Mutagenesis Kit (Strategne) was used. The mutagenic primers were Wwp2-mF: 5′-TCGGTATTGC-CAGTTTCTTGTAGACTAAAGAATCAGCAGC-3′ and Wwp2-mR: 5′-GCTGCT-GATTCTTTAGTCTACAAGAAACTGGCAATACCGA-3′.

Following the same cloning strategy, the Fbxw7 3′UTR was amplified using primers Fbxw7-F: 5′- TTTAACTCGAGAAAGCAGACATGATGAATTTTG-3′ and Fbxw7-R: 5′– AAGCCGCGGCCGCTAACATGAAAAAACACATTTTAT-3′. For the mutagenesis reactions, the following primers were used: Fbxw7-mF1: 5′ – GACGACTC-TCTAAATCCAACCAGGTGGAATTATTCTTTG-3′ and Fbxw7-mR1: 5′ – CAAAG-AATAATTCCACCTGGTTGGATTTAGAGAGTCGTC-3′ for site 1. Fbxw7-mF2: 5′- CTTATAACTTAAGTGGAATAAAATGTGTTTTTTCATGTTAGCGGC-3′ and Fbxw7-mR2: 5′-GCCGCTAACATGAAAAAACACATTTTATTCCACTTAAG-TTATAAG-3′ for site 2.

All plasmids were verified by sequencing.

Luciferase assays

Luciferase reactions were performed in 96 well plates. HeLaS3 cells were transfected using the Lipofectamin 2000 reagents (Invitrogen) with 5 ng of the Wwp2 or the Fbxw7 3′UTR plasmids. This value was derived after a concentration curve of the plamid was tested. A miR-25 mimic (Dharmacon) was added at a concentration of 20 nM. Different concentrations were tested and 20 nM was chosen as the lowest concentration to cause significant inhibition (data not shown). Reporter activity was analysed 24 hours after transfection with the Dual-Luciferase Reporter Assay System (Promega). Expression data are given as a ratio, with the Renilla reporter normalized against the luciferase reporter values.

Data analysis

Data are presented as mean ±SEM. Comparison between groups were performed using one-way ANOVA followed by the Newman-Keuls post test to determine statistical significance. A P value of <0.05 was taken as statistically significant.

Supporting Information

Table S2.

PCR primers for amplifying miRNA genomic DNA fragments and for other experiments in this work.


Table S3.

Conservation of miR-25 and miR-298 mature sequences. All mature sequences of miR-25 and miR-298 are obtained from miRBase database.


Table S4.

Candidate target genes of miR-25. The table lists 54 genes based on microarray expression and Sylamer analysis following transfection of miR-25 mimic to the Dgcr8-deficient ES cells.



We thank the Sanger RSF facility for assistance in animal work, microarray facility for gene expression analysis, Baiyun Fu and Fengtang Yang for karyotyping, and Yvette Hooks for histology sections.

Author Contributions

Conceived and designed the experiments: DL MPAD WW ID AJE PL. Performed the experiments: DL MPAD WW JS EV. Analyzed the data: DL MPAD CA LC. Contributed reagents/materials/analysis tools: WS. Wrote the paper: DL MPAD CA PL.


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