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Conceived and designed the experiments: SJK. Performed the experiments: MK JR KAI. Analyzed the data: MK CP FE CMW SJK. Contributed reagents/materials/analysis tools: CP FE CMW. Wrote the paper: MK SJK.
In preimplantation mammalian development the transcription factor Sox2 (SRY-related HMG-box gene 2) forms a complex with Oct4 and functions in maintenance of self-renewal of the pluripotent inner cell mass (ICM). Previously it was shown that Sox2−/− embryos die soon after implantation. However, maternal Sox2 transcripts may mask an earlier phenotype. We investigated whether Sox2 is involved in controlling cell fate decisions at an earlier stage.
We addressed the question of an earlier role for Sox2 using RNAi, which removes both maternal and embryonic Sox2 mRNA present during the preimplantation period. By depleting both maternal and embryonic Sox2 mRNA at the 2-cell stage and monitoring embryo development in vitro we show that, in the absence of Sox2, embryos arrest at the morula stage and fail to form trophectoderm (TE) or cavitate. Following knock-down of Sox2 via three different short interfering RNA (siRNA) constructs in 2-cell stage mouse embryos, we have shown that the majority of embryos (76%) arrest at the morula stage or slightly earlier and only 18.7–21% form blastocysts compared to 76.2–83% in control groups. In Sox2 siRNA-treated embryos expression of pluripotency associated markers Oct4 and Nanog remained unaffected, whereas TE associated markers Tead4, Yap, Cdx2, Eomes, Fgfr2, as well as Fgf4, were downregulated in the absence of Sox2. Apoptosis was also increased in Sox2 knock-down embryos. Rescue experiments using cell-permeant Sox2 protein resulted in increased blastocyst formation from 18.7% to 62.6% and restoration of Sox2, Oct4, Cdx2 and Yap protein levels in the rescued Sox2-siRNA blastocysts.
We conclude that the first essential function of Sox2 in the preimplantation mouse embryo is to facilitate establishment of the trophectoderm lineage. Our findings provide a novel insight into the first differentiation event within the preimplantation embryo, namely the segregation of the ICM and TE lineages.
Sox genes are expressed throughout embryogenesis and encode a subclass of high mobility group (HMG) box proteins driving cell fate decisions by acting as transcription factors and architectural components of chromatin , . Sox2 is developmentally regulated  and is detected in the inner cell mass (ICM) of the murine blastocyst  and subsequently in primitive ectoderm, extraembryonic ectoderm  and the developing nervous system . Expression of Sox2 is observed in mouse and human eye lens ; in humans, heterozygous loss-of-SOX2 function causes several defects including bilateral anophthalmia , and defects in the hypothalamo-pituitary-gonadal axis . It is essential for inner ear sensory organ  and taste bud sensory cell  development. Sox2 acts cooperatively with the pluripotency factor Oct4 at promoters activating transcription of Fgf4, Utf1 and Fbx15 genes –, and interacts with Nanog in regulating transcription of Rex1 . It has been reported that the crucial role for Sox2 in mouse embryonic stem (ES) cells is to maintain them in a pluripotent state by preserving the required level of Oct4 expression . Furthermore, mouse embryonic and adult fibroblasts can be induced to a pluripotent state in vitro through ectopic expression of the transcription factors Sox2, Oct4, c-Myc and Klf4 , , .
Sox2 expression is essential during embryogenesis; Sox2 homozygous null embryos die soon after implantation  and Sox2 is the earliest marker of inner cells prior to ICM formation . Furthermore, Sox2 in association with the POU domain transcription factor Oct4 and homeobox transcription factor Nanog form a regulatory core, which maintains self-renewal of the pluripotent ICM in the embryo and ES cells , , –, and is unique to mammals . A contiguous pair of highly evolutionarily conserved Oct- and Sox-binding sites is essential for activating expression of genes specific to the pluripotent state in ES cells . Sox2 transcription is regulated by an enhancer containing this composite Sox-Oct cis-regulatory element that Sox2 and Oct4 bind synergistically . This element also occurs within the proximal promoter of Nanog , essential for retaining pluripotency , . The Sox2-Oct4-Nanog regulatory complex controls expression of pluripotency genes through feed-forward loops  including these three genes in an autoregulatory circuit . As well as activating target genes essential for self-renewal, the Sox2-Oct4-Nanog complex represses genes initiating differentiation .
Blastocyst formation coincides with demarcation of the first two lineages in the mammalian preimplantation embryo: the ICM that gives rise to the embryo proper, extraembryonic endoderm and mesoderm, and the trophectoderm (TE) that generates the placenta , . ES cells are derived from the ICM/epiblast population of the blastocyst –. Although this is a transitory cell-population in the embryo, cultured ES cells can undergo unlimited self-renewal and are pluripotent, giving rise to all embryonic cell types. At the late blastocyst-stage, three distinct cell lineages are observed: the epiblast, the primitive endoderm (PE) and the trophectoderm . Key binary switches in the mouse blastocyst are regulated by pairs of transcription factors ,  that govern cell fate decisions. Oct4, Sox2 and Nanog are fundamental regulators maintaining undifferentiated ES cell and epiblast fate , , , , while caudal-type homeobox transcription factor Cdx2 regulates TE gene expression and maintenance in the mouse blastocyst, repressing Oct4 and Nanog in the TE . Recently Gata3 has been demonstrated to regulate trophoblast development in parallel to Cdx2, and both genes are dependent on a third gene, Tead4 , . Gata6 regulates PE genes  antagonising Nanog within the mouse blastocyst . In addition, the Spalt transcription factor Sall4 has been reported to regulate transcription of Pou5f1 (encoding Oct4) and thereby formation of the ICM-derived lineages, namely the epiblast and the PE , .
Fgf4, regulated by the Sox2-Oct4 synergy , is expressed in the ICM  and has a role in ICM maintenance as well as trophoblast stem cell proliferation . It has been suggested that Fgf4 could have a paracrine effect in inducing polar TE, adjacent to the ICM . Fgf4 interacts with the receptor Fgfr2  which is expressed by the TE and extraembryonic ectoderm . Cdx2 and Eomesodermin (Eomes), a T-box transcription factor expressed in TE and responsible for its proliferation , , have been suggested as potential down-stream targets of Fgf4 signalling . Regulation of these gene families have also been associated with Fgf4 signalling in Danio rerio and Xenopus laevis , .
Homozygous Sox2 knock-out embryos die soon after implantation . Implantation sites lacked the epiblast and extraembryonic ectoderm components although trophoblast giant cells could be distinguished. In culture, Sox2 null embryos formed abnormal outgrowths lacking an ICM. Sox2 homozygous mutant embryos could be rescued by wild-type ES cells suggesting cell autonomous function. However by targeted deletion of the Sox2 gene, only mRNA from Sox2 zygotic transcription can be eliminated; any persisting maternal Sox2 mRNA or protein in the preimplantation embryo might fulfill earlier essential roles. We have addressed the question of an earlier role for Sox2 in controlling cell fate decisions using RNAi, which removes both maternal and embryonic Sox2 mRNA present during the preimplantation period. By depleting both sources of Sox2 mRNA at the 2-cell stage and monitoring embryo development in vitro, we showed that in the absence of Sox2, embryos arrest at the morula stage, and they fail to form TE or to cavitate. Furthermore, by performing rescue experiments using cell-permeant Sox2 protein, we observed reversal of the Sox2-siRNA phenotype, as demonstrated by blastocyst formation and expression of ICM, as well as TE markers.
Temporal and spatial expression of Sox2 protein was examined in preimplantation mouse embryos by immunofluorescence. Sox2 protein was found in oocytes and 2-cell stage embryos; fluorescence intensity increased from the 4-8-cell stage to the morula stage, peaking at the blastocyst, where it was present in both TE and ICM. Sox2 protein was located in nuclei in cleavage stage embryos, although nuclear staining at the 2-cell stage was weak and cytoplasmic staining was observed. However in some 4-cell embryos, Sox2 was localized in nuclei in all blastomeres, while in others, nuclear localization was observed in half of the blastomeres, while still in others Sox2 staining was detected only in the cytoplasm and not in nuclei (Figure 1A). In blastocysts it was observed in some nuclei and cytoplasm of TE as well as in all ICM nuclei (Figure 1A). Pluripotent mouse ES cells and ES cells induced to form neural lineages were used as positive controls for Sox2 immunostaining (Figure S1A). Western blotting with the Sox2 antibody on protein extracts from mES cells revealed a single band of 37 kDa, the expected size for Sox2 protein (Figure S1B). To confirm these results, Sox2 transcripts were also detected by RT-PCR at the oocyte, 2-cell, 4-cell, 8-cell, morula and blastocyst stages (Figure 1B).
Sox2 was transiently knocked down in 2-cell MF1xCD1 embryos with three different siRNA duplexes using electroporation. Duplexes for an irrelevant protein, Firefly Luciferase, and Galanin, a protein expressed throughout preimplantation mouse development (J. Razavi, D. Brison and S. Kimber, unpublished) were used as controls. Electroporation efficiency was 100%, as determined by rhodamine fluorescence detected immediately after electroporation and penetration of the siRNA duplexes into both cells of the 2-cell mouse embryos, which were compared to mock-electroporated embryos to exclude any autofluorescence effects. UV visualised embryos were not cultured further.
Sox2-siRNA duplexes were electroporated separately; embryos were cultured and scored daily until day 4 and 5 of development (plug = day 1), when control embryos were at the morula (16–32 cells) and blastocyst stage respectively. No difference in development between groups was detected until day 4. The effects of the three Sox2-siRNA duplexes are presented in Figure 2. On day 4, the majority of embryos of all groups formed morulae (Figure 2A, 2C, 2E) at percentages from 60% to 73.5%. All Sox2-siRNA duplexes were effective in perturbing development; by day 5, Sox2-duplex-1 had led to developmental arrest of 24% of embryos at the 4-8-cell stage and 51.7% at the morula stage. Sox2-duplex-2 resulted in arrest mainly at the morula stage (71.5%). Sox2-duplex-3 caused 69% arrest at the morula stage. Morulae were compact and showed similar organization to control groups. Only 18.7% of the Sox2-duplexes -1 and -2, and 21% of the Sox2-duplex-3-siRNA embryos formed blastocysts, compared to 76.2% to 83% for incubator, 61.8% to 62.5% for Galanin and 55.4% to 56.5% for FFL controls respectively (Figures 2B, 2D, 2F and and3A).3A). Thus absence of Sox2 prevented mouse preimplantation embryos developing beyond the morula stage. Sox2-duplex-1 appeared to have a more severe effect than duplexes -2 and -3, since a greater proportion of the embryos remained at the 4-8-cell stage rather than forming compacted morulae.
In order to rule out that the effects observed were not specific to the cross used (MF1xCD1), we also examined the effect of Sox2-duplex-1-siRNA on MF1xMF1 embryos. As observed in the MF1xCD1 embryos, after Sox2-siRNA knock-down >90% of the embryos underwent compaction but arrested at the morula stage (Figure S2).
To determine whether developmental arrest resulted from loss of Sox2 protein, we assessed protein expression by immunofluorescence with three different Sox2 antibodies (Figures 3B, 3D and S3) in Sox2-siRNA treated embryos at days 4 and 5 (MF1xCD1). Control groups (incubator-control, Galanin- and FFL-siRNA embryos) showed strong staining for Sox2 (Figure 3B). On both days, all embryos in the Sox2-siRNA group that remained at the morula stage were negative for Sox2 or showed extremely faint Sox2 staining. However, embryos in this group which reached the blastocyst stage on day 5, invariably showed Sox2 staining (Figure 3B), although generally decreased compared to control blastocysts. Therefore some of the Sox2-siRNA treated embryos may have escaped the RNAi effect and maintained Sox2 levels sufficient for blastocyst development. Compared to controls, there was a general delay in time of formation of the few blastocysts within the Sox2-siRNA embryos. Assessing levels of fluorescence after Sox2 staining, and dividing the number of embryos negative for Sox2 by the total number of embryos electroporated and examined per experiment, the knock-down efficiency after siRNA was found to be 71%, whereas 29% escaped the RNAi effect. Lethality of the Sox2-siRNA phenotype on day 5 was confirmed by Trypan-Blue uptake (Figure 3B). The majority (83%) of the knock-down embryos assessed for viability on day 5, contained a significant number of necrotic (blue-stained) cells. Therefore further follow-up of the Sox2-siRNA knock-down phenotype (e.g. embryo transfer) was not possible.
The Sox2 knock-down was also confirmed by RT-PCR in pools of 30 embryos. A loss of Sox2 transcript in day 4 Sox2-siRNA morulae (Figures 4A and S4) was observed compared to incubator-control (untreated) morulae, in which Sox2 transcripts were always detected. To determine whether the developmental arrest of Sox2 RNAi treated embryos was associated with loss of other genes (some of them Sox2 targets), we examined transcript expression of Fgf4, Fgfr2, Oct4, Nanog, Cdx2, Eomes and Tead4 (Figures 4A and S4). In embryos where Sox2 transcript was undetectable, Fgfr2 transcripts were barely visible, Fgf4, Cdx2, Eomes and Tead4 transcripts were untraceable after amplification of cDNA to 40 cycles, whereas Oct4 and Nanog transcripts remained unaffected (Figures 4A and S4). Comparable transcript levels for Atp1b1 (ATPase, Na+/K+ transporting, beta 1 polypeptide), Gata3, Gata4 and Gata6 were detected in Sox2 knock-down morulae compared to incubator-control morulae (Figure 4A). This implies that loss of Sox2 led to down-regulation of Fgf4, Fgfr2, Cdx2, Eomes and Tead4 transcripts, but did not affect Oct4, Nanog, Atp1b1, Gata3, Gata4 and Gata6 transcripts in the morula. Similar levels of βeta-actin transcripts (control) were detected in Sox2-siRNA and incubator-control embryos.
Due to the similarity of sequence in the HMG domain (which Sox2-duplex-1 targeted), between Sox2 and Sox1, Sox3, Sox14, Sox15 and Sox21, the presence of the latter transcripts was also investigated to verify the specificity of the Sox2 knock-down. Transcripts for none of these genes were detected at the morula stage in control or knock-down embryos after siRNA for each of the 3 duplexes (Figures 4A and S4). To confirm that the Sox2 knock-down phenotype was due to specific depletion of Sox2, we performed rescue experiments using recombinant cell-permeant Sox2 protein fused with a TAT protein transduction domain to allow intracellular delivery, which has been previously shown to be highly efficient in compensating for loss of RNAi-induced knock-down of Sox2 in ES cells .
The cell-permeant Sox2 protein was added 24 h after RNAi in the Sox2 siRNA group as well as incubator control embryos and it was renewed every 24 h as reported in Materials and Methods. Up-take of the Sox2-TAT protein was monitored by immunofluorescence 6 h, 12 h and 18 h after its first addition. Gradual increase in Sox2 protein expression and signs of possible protein uptake through an endocytic pathway were detected, as demonstrated by the patchy Sox2 expression (Figure S5). A significant rescue phenotype was observed among the Sox2 siRNA embryos by day 5 of development (Figures 2G, 3C and 3D). While 43–47.7% of the Sox2 siRNA (duplexes 2 and 3) embryos arrested at morula stages with only 18.7–21% forming blastocysts, their equivalent Sox2 siRNA R (rescue groups) formed blastocysts at percentages from 59.7% to 62.6% (Figures 2G, ,3C),3C), indicating substantial phenotype reversal upon addition of the Sox2 protein in the Sox2 siRNA groups. At the same time, 72.75% of the untreated incubator control embryos formed blastocysts, whereas 50.9% of the embryos treated with the cell-permeant Sox2 protein (Inc ctrl R) reached the blastocyst stage (Figures 2G, ,3C).3C). A significant proportion of the remaining incubator control Sox2-treated embryos appeared perturbed at earlier stages, indicating some detrimental effect of higher than normal levels of Sox2 in these embryos.
In order to investigate the Sox2-siRNA phenotype, we stained embryos for a number of ICM and TE markers, expressed at the morula and blastocyst stage (Figure 4B). Both day 4 and day 5 embryos were assessed after Sox2-siRNA for Sox2 protein expression, which was shown to be almost or completely absent. When Sox2-siRNA embryos were compared with incubator-control embryos, reduction in a number of TE proteins was observed. Yap, Cdx2, Eomes and Occludin were present in control embryos but could not be detected or were weakly detected in Sox2-siRNA embryos (Figures 3D and and4B).4B). Fgfr2 and Fgf4 proteins were also decreased (Figure 4B), coinciding with the absence of transcripts for these and other TE markers (Tead4, Cdx2, Eomes) in Sox2-siRNA embryos (Figures 4A and S4). However, the early trophoblast stem cell marker Gata3, as well as Oct4, Nanog, ZO1, Desmoplakin, E-cadherin, Gata4 and Gata6 protein expression remained unaffected (Figures 3D and and4B)4B) by Sox2 knock-down. Although Nanog protein was expressed in day 4 and day 5 in Sox2-siRNA embryos, it did not appear to be located in the nuclei. In the absence of Sox2 transcripts in Sox2-siRNA embryos, Oct4 and Nanog transcripts remained unaffected (Figures 4A and S4). The rabbit polyclonal Cdx2 antibody gave more prominent nuclear staining than the mouse monoclonal Cdx2, however both stained TE nuclei and cytoplasm. Immunological controls for all antibodies were negative (Figure S6).
After reversal of Sox2 knock-down phenotype, day 5 Sox2-siRNA R blastocysts expressed Sox2 in ICM and TE nuclei, Oct4 in ICM nuclei and Yap and Cdx2 in TE nuclei, resembling the day 5 incubator control and control R blastocysts (Figures 3B, 3D, ,4B).4B). The arrested day 5 Sox2-siRNA morulae did not demonstrate any Sox2, Yap or Cdx2 staining but did express Oct4 in inner cell nuclei (Figure 3D), resembling the originally observed Sox2 knock-down phenotype (Figures 3B, ,4B4B).
Sox2-siRNA, FFL-siRNA and incubator-control embryos were assessed for apoptosis at day 4 and 5 of development. While no apoptotic cells were identified at day 4 in either the control groups or the Sox2-siRNA groups, lack of Sox2 appeared to induce increased apoptosis in day 5 Sox2-siRNA embryos (Figure 5A), as indicated by an increased apoptotic index both in embryos with ≤32 cells (Figure 5B) and in arrested morulae (Figure 5C). The relative distribution of apoptosis between inner and outer cells (ICM and TE, respectively, where blastocysts had formed) in siRNA and control groups was the same (30% inner cells, 70% outer cells), thus most of the apoptosis appeared to be in the outer cells in all groups. Furthermore, Sox2 knock-down did not affect total cell numbers when considering both morulae and blastocysts at day 4 or 5 (Figure 6). Nevertheless, arrested morulae in the Sox2 knock-down group had lower cell numbers than control blastocysts. To conclude, more apoptotic cells were observed in Sox2 knock-down embryos compared to control embryos. However when compared by morphology, morulae and blastocysts (incubator-control versus Sox2-siRNA ‘escapee’ blastocysts) of both groups contained the same number of cells.
We found that Sox2 is expressed throughout preimplantation mouse development with cytoplasmic or nuclear Sox2 protein detected from the unfertilized oocyte to the blastocyst stage. This finding is partially in agreement with Avilion et al.  who showed that Sox2 protein was present in the cytoplasm of the fertilized oocyte, but its translocation into nuclei occurred at the 2-cell stage. Moreover, in our study, Sox2 transcripts of maternal origin were detected in oocytes and Sox2 protein was found in both nucleus and cytoplasm of the oocyte. Some 4-cell embryos had mainly cytoplasmic staining while others mainly nuclear; indeed some had blastomeres in both categories. This may relate to the increasing zygotic transcription at the 4-cell stage and suggests that Sox2 nuclear translocation may be initiated a bit later, at the 4-cell stage, in the strain of mice we examined compared to that used by Avilion et al. In later cleavage-stage embryos nuclear staining was invariably observed. The strong expression of Sox2 in TE and ICM at the blastocyst stage is generally in agreement with Avilion et al. . They showed that in early blastocysts Sox2 was uniquely cytoplasmic in TE cells, whereas we observed nuclear and cytoplasmic expression of Sox2 in some TE cells. They reported that Sox2 was mostly nuclear in ICM and our observations are in agreement.
The aim of our study was to define the effect of knocking down Sox2 in developing preimplantation mouse embryos, in order to uncover early functions in maintaining developmental potential of early mouse embryos and marking the pluripotent lineage . After knock-out, in the absence of zygotic Sox2, the epiblast was not maintained but rather differentiated into diverse cell types . The authors suggested that maternal Sox2 protein derived from the oocyte may carry the embryo through preimplantation development in the absence of oocyte Sox2 mRNA. However, in our study Sox2 transcripts were detected in oocytes and siRNA for Sox2 led to developmental arrest at the morula stage, suggesting a significant contribution of maternal Sox2, and that Sox2 protein and transcripts are crucial in the mouse preimplantation embryo for an additional earlier cell function than previously described. When Sox2-siRNA is applied early in preimplantation development, Sox2 protein levels are barely detectable or absent 3 days later, confirming the efficacy of siRNA as a technique for examining preimplantation protein function –. After knocking down Sox2 in 2-cell mouse embryos with three different siRNA duplexes, most morulae had very low levels of Sox2 and failed to develop to blastocysts, while this effect was not seen in control groups. The slightly smaller numbers of blastocysts forming after Galanin- and FFL-siRNA compared with incubator-control embryos suggests that the technique of siRNA causes some stress to embryos, but without statistically significant effect on development. This is further supported by the viability and normal post-implantation development following Galanin siRNA by electroporation in 2-cell stage mouse embryos and subsequent embryo-transfer at the blastocyst-stage to pseudopregnant mice (J. Razavi, D. Brison and S. Kimber, unpublished). The difference of severity of the Sox2 knock-down outcome when using the two different crosses (MF1xMF1, MF1xCD1) may be explained in the light of different genetic background and possibly dosage or polymorphisms of interacting genes of the mouse strains , .
Sox2-duplex-1 had a stronger impact on developing mouse embryos than duplexes -2 and -3, causing a proportion of them to arrest earlier, namely at the 4-8-cell stage. However, the Sox2-duplex-1 was designed to target within the conserved region of the HMG box, and might affect additional genes. We have controlled for this by using two siRNA sequences designed outside the HMG box and targeting Sox2 alone. In this case, for most of the Sox2 knock-down embryos developmental arrest occurred at the transition from the morula to the blastocyst stage, with Sox2-siRNA morulae failing to cavitate or undergo cell division beyond the 32-cell stage. However, a small number of Sox2-siRNA embryos ‘escaped’ the RNAi effect. These developed to blastocysts and showed moderate levels of Sox2 protein expression, though generally lower than control blastocysts. This indicates that in some embryos knock-down is incomplete, allowing sufficient Sox2 protein to accumulate by the late morula stage to permit development to the blastocyst stage. Thus a threshold level of Sox2 might be required for the developmental transition from a compacted morula to a fully differentiated blastocyst. Furthermore, Sox2-siRNA ‘escapee’ embryos were generally delayed in forming blastocysts compared to incubator-control embryos, whereas arrested Sox2-siRNA morulae did not form TE or a cavity when left in culture. This observation was further supported by confirming the lethality of the Sox2-siRNA phenotype on day 5, with the majority of the embryos becoming necrotic, as indicated by incorporation of Trypan-Blue.
After rescue experiments, using Sox2 protein fused with a TAT protein transduction domain , the Sox2-siRNA phenotype was reversed and blastocysts were formed. This confirms that Sox2 depletion was indeed the cause of the siRNA induced phenotype. The same cell-permeant Sox2 protein has been successfully used to rescue the stem cell phenotype observed in mES cells after Sox2-siRNA knock-down . Indeed, a series of recent publications demonstrate that TAT-mediated protein transduction is an efficient strategy to deliver biologically active proteins such as transcription factors into a variety of cells –, also reviewed in .
Loss of Tead4 (a molecule recently shown to be essential for TE formation in preimplantation mouse embryos ), Cdx2 and Eomesodermin, as well as the Tead4 coactivator protein Yap, (which localizes in nuclei of outer TE cells before Cdx2 does ), occurred after Sox2 knock-down in mouse embryos. Moreover, regular expression of all these genes after Sox2-mediated rescue of blastocysts, indicates that Sox2 may regulate genes that control differentiation of the outer cells of the morula to form TE. This is supported by the reduction in cell surface expression of Occludin, a component of tight junctions . However since ZO1, Desmoplakin and E-cadherin protein expression, as well as Na+/K+-ATPase β-subunit (Atp1b1) transcript expression were not affected, the initiation of epithelia formation appears to be intact in Sox2 knock-down embryos. The absence of Fgfr2 in Sox2-siRNA embryos also implies malfunction of the outer cells of the embryo, whereas the reduction of Fgf4, a direct target gene of the Sox2-Oct4 synergy, would reflect malfunction of the ICM . In this respect, the identification of Sox2 transcripts as the earliest marker of inner cells of the embryo should be noted . Tead4 −/− embryos  arrested at the morula stage, did not form blastocyst cavities and downregulated TE associated markers Cdx2, Eomes and Fgfr2. Similarly, in Tead4 −/− arrested morulae, E-cadherin was not affected . The striking similarity between the Sox2 RNAi embryo phenotype and that of the Tead4-null embryos, suggests a potential link. The early trophoblast marker Gata3 is expressed along with Cdx2 during preimplantation development and also maintained by Tead4 although expressed independently of Cdx2 . Gata3 also regulates trophectoderm, but it did not seem to be affected by the absence of Sox2 in our study, implying the existence of still poorly defined transcription factor circuitries affecting cell fate decisions .
Sox2 knock-down did not affect total cell numbers up to the morula stage (days 3–4). However, whilst control embryos cultured up to day 5 (approximately 72 h post 2-cell stage) reached roughly 64 cells and formed blastocysts, Sox2 knock-down embryos did not progress beyond 30 cells. In Tead4 −/− embryos cell division occurred on schedule up to 60 h post 2-cell stage, reaching 32 cells and a morula-like morphology, which was maintained, as embryos did not form clear blastocyst cavities. The authors stated that cell proliferation in the Tead4 −/− embryos was not arrested or significantly delayed  although they did not examine cell numbers later than 60 h post 2-cell. In our study, Sox2 RNAi embryos also failed to form blastocyst cavities and arrested at the morula stage. Sox2 may facilitate the maintenance of cell division in the embryo of Oct4 +ve cells, since embryos did not continue beyond the 30-cell stage when it was depleted. Sox2 could potentially regulate TE formation in the preimplantation embryo at some point upstream of Tead4, since Tead4 expression is affected in the absence of Sox2 (this study) but Sox2 is not affected in the absence of Tead4 . The lack of blastocyst cavity formation observed in our Sox2 RNAi embryos, as well as in the Tead4 −/− embryos , suggests a more severe phenotype than in Cdx2 −/− embryos, which gradually cavitate despite the absence of Cdx2 . Furthermore, whilst Sox2 RNAi and Tead4 −/− embryos downregulate Cdx2, Eomes and Fgfr2, Cdx2 −/− embryos express Eomes (though weakly) and Fgfr2 . In addition, the absence of the Tead4 co-activator and upstream Cdx2 regulator protein, Yap, in day 5 Sox2-siRNA embryos, but its presence in the rescued Sox2-siRNA blastocysts, make Sox2 a likely early regulator in the sequence of events leading to TE formation in the preimplantation mouse embryo. The observation that rescued Sox2-siRNA blastocysts express protein for Sox2 in ICM and some TE nuclei, Oct4 in ICM nuclei, as well as Cdx2 and Yap in TE nuclei, and now form blastocysts, is also consistent with Sox2 involvement in regulating the trophectoderm associated markers Yap and Cdx2, whether directly or indirectly.
In our study, the pluripotency marker proteins Oct4 and Nanog remained unchanged despite the lack of Sox2. This is surprising taking into account their interconnected regulation in ES cells. A similar maintenance of pluripotency markers was also observed in the absence of Tead4 . Enhancers of a number of pluripotency associated genes contain a Sox-Oct element, which both Sox2 and Oct4 bind in a combinatorial interaction . The complex formed regulates several genes (among them Oct4 and Sox2 themselves, as well as Nanog) that have been identified as essential for the formation of the ICM during mouse preimplantation development and for self-renewal of pluripotent ES cells , , , . The retention of Oct4 and Nanog expression, despite the depletion of Sox2 in this study, should be viewed in the light of their own auto-regulation which is likely to allow their transcription and translation even in the absence of Sox2. Alternatively, the well described trio-motif-network of Sox2-Oct4-Nanog might not function at the morula stage, so that Oct4 and Nanog can persist in the absence of Sox2. This network may only come into force at the blastocyst stage, when formation of the ICM leading to the epiblast occurs. However, Nanog expression appeared more cytoplasmic in Sox2-siRNA embryos compared to controls. Since Nanog is first expressed at the late morula stage , , it is likely that after Sox2 knock-down, embryos arrest at about the time Nanog is first transcribed/translated and hence staining may represent newly synthesised cytoplamic protein, not yet translocated into the nucleus , . Since the Sox2 knock-down embryos are delayed compared to controls, this might explain why control morulae already show a strong nuclear Nanog signal.
Fgf4 is expressed at the blastocyst stage ,  and regulates the 5th cell cycle in the mouse embryo . Thus loss of Fgf4 could account for the predominance of morulae with less than 32 cells after Sox2-siRNA. Later Fgf4, originating from the ICM and epiblast, acts upon TE cells in a paracrine manner . The Fgf4 gene has both core HMG and POU regulatory elements that are mutually dependent, and an additional independent Sox2-binding HMG regulatory element –. In Sox2-siRNA embryos both Fgf4 and Fgfr2 were downregulated, and there were almost undetectable levels of the TE markers Cdx2 and Eomes. FGF signalling is essential for the regulation of Cdx1, Cdx2 and Cdx4 during gastrulation in Xenopus laevis . Therefore it is possible that Fgf4/Fgfr2 signalling induces Cdx2 and Eomes, thereby facilitating TE formation. On the other hand Sox2 may be required in early cells expressing Cdx2 or for its maintenance. In its absence, Cdx2 is not expressed, with concurrent lack of Eomes and Fgfr2 expression. It has previously been shown that Eomes is downstream of Cdx2 in TE differentiation , . Furthermore, the parallel expression of Fgfr2 and Cdx2 in outer cells of the preimplantation embryo , and the established role of FGF signalling at the 5th cell cycle when overt TE is generated , could imply a concurrent requirement for FGF signalling with Cdx2 expression during TE development. The association of Sox2 and Cdx2 genes has also been shown in a different system, that of gastric cancer where Sox2 and Cdx1/Cdx2 are inversely related , . Interestingly, the extra-embryonic endoderm markers Gata4 and Gata6 were not affected by Sox2-siRNA, showing similar patterns of expression as previously reported , . Our finding therefore reinforces previous observation that Sox2 does not seem to exert an effect on extra-embryonic endoderm .
Recent findings in mES cells show an inverse relationship between Sox2 and TE associated markers, as ES cells can differentiate into trophectoderm in the absence of Sox2 , [76, Keramari, Ward and Kimber unpublished]. However ES cells are derived from the ICM, generally from blastocysts in implantation delay, and are a completely different cell population to the cleavage and morula stage embryo investigated in our study. Murine ES cells do not, unless experimentally forced, differentiate to TE , while the outer cells of the morula spontaneously differentiate to TE in utero or in simple media in vitro . Furthermore, the cross-talk between ICM and TE that takes place in the embryo is different from the signalling between ES cells in culture. It has also been shown that Sox proteins can act either as activators or repressors in different cellular contexts , and that critical thresholds of Sox2 are associated with different phenotypes in early cell lineage commitment events in neural and foregut endoderm differentiation , . This could explain the observation that Sox2 seems to positively regulate Cdx2 and Eomes in the morula, but to repress both genes in ES cells , [76, Keramari et al. unpublished]. For example, it has been reported that a single transcription factor, namely Sall4, regulates two distinctively different stem cell populations within the blastocyst, ES cells arising from the ICM, and XEN stem cells originating from the extra-embryonic endoderm . Sall4 is interconnected with the Sox2, Oct4 and Nanog auto-regulatory circuit to preserve pluripotency of ES cells, but at the same time induces genes critical for extra-embryonic endoderm formation like Gata4, Gata6, Sox7 and Sox17 . Furthermore, it was recently shown that the transcription coactivator Yap, previously thought to regulate only trophectoderm in the mouse embryo , also seems to exert a role in regulation of self-renewal and differentiation in mouse ES cells . This illustrates the common finding that transcriptional regulators of lineage segregation events can exert distinctly different functions within closely associated cell populations. In addition, it has been demonstrated that Nanog, previously thought to be a core transcription factor of the network that regulates pluripotency, though essential for ICM and germ cell formation, is dispensable for murine ES-cell self-renewal .
Our results lead us to conclude that Sox2 plays two distinctively different roles at two different early developmental stages, namely the morula and the ICM-derived ES cells and early epiblast , , [19, our data]. In addition, the association of Sox2 with Yap/Tead4/Cdx2/Eomes/Fgfr2 expression and TE formation in the early mouse embryo arising from our study suggests Sox2 may play a role in regulation of TE fate.
Sox2-siRNA embryos showed higher levels of apoptosis compared to incubator-control and FFL-siRNA embryos at day 5 of development. Electroporation did not appear to cause increased apoptosis, since FFL-siRNA embryos exhibited similarly low levels of apoptosis to the incubator-control embryos. Therefore knock-down of Sox2 seems to induce apoptosis, suggesting that Sox2 may regulate survival factors. Interestingly, in all groups, there were more apoptotic cells among outer (TE) cells than inner (ICM) cells. This may indicate a strain difference since most studies ,  revealed higher apoptosis in the ICM than trophectoderm of mouse embryos cultured from the zygote to the blastocyst stage. Although many studies have shown equal levels of apoptosis between ICM and TE in human embryos, Hardy et al.  reported increased apoptosis in TE. Strumpf et al.  demonstrated that Cdx2 disruption caused peri-implantation embryonic lethality due to lack of establishment of the TE. Cdx2 mutant morulae initiated cavitation and cellular polarisation for TE commitment, but ultimately cells underwent apoptosis. The potential link between Sox2 and Cdx2, revealed by our study, concurs with the similar induction of apoptosis when either Sox2 or Cdx2 are eliminated.
In summary, after knocking down Sox2 in 2-cell stage mouse embryos using siRNA, most embryos arrested at the morula stage and apoptosis was increased. While pluripotency markers Oct4 and Nanog remained unaffected, trophectoderm markers Tead4, Yap, Cdx2, Eomes and Fgfr2 were downregulated. The RNAi phenotype was rescued by introduction of Sox2 protein fused with a TAT protein transduction domain, leading to blastocyst formation and re-expression of Sox2, Yap and Cdx2. This indicates that Sox2 plays an important role in the preimplantation mouse embryo and its earliest essential function appears to involve establishment of the trophectoderm lineage either by directly or likely indirectly regulating Tead4 and Cdx2, or alternatively through Fgf4-Fgfr2 signalling. Future experiments would be essential in order to investigate further the mechanism by which Sox2 regulates these or other signalling pathways to promote trophectoderm induction in the preimplantation embryo. Furthermore, it has become apparent that Sox2 maternal transcripts and protein are likely to play an important role in the earliest function of Sox2.
This study was approved by the Ethics Review Committee of the University of Manchester and the UK Home Office (Licence Numbers 40/1939 and 40/2669).
Outbred female MF1 mice (Harlan Olac Ltd, Bicester, UK, as used in our previous work) were crossed with male CD1 mice with some preliminary data obtained from MF1xMF1 crosses. Mice were kept under standard conditions (20–22°C, 40–60% humidity, 12 h light/dark cycle). Female mice were superovulated with 5 IU of pregnant mare's serum gonadotrophin (PMSG, Calbiochem) by intraperitoneal injection (0.1 ml). Ovulation was synchronised by a 5 IU intraperitoneal injection (0.1 ml) of human chorionic gonadotrophin (hCG, Intervet) 46–48 hours later. Female mice were paired with males overnight and monitored the following morning for the presence of a vaginal plug, which was designated day 1 of pregnancy.
On day 2 female mice were killed by cervical dislocation, oviducts were dissected and transferred into M2 medium (Sigma) with 4 mg/ml bovine serum albumin (BSA, ICN Biomedical) before flushing. Embryos were flushed using sterile M2/BSA and a 34-Gauge blunt-ended stainless steel needle (Coopers Needleworks) attached to a 1 ml syringe.
Embryos were washed and cultured in a 30 µl drop of KSOM (EmbryoMax, Chemicon), under embryo-tested mineral oil (Sigma) at 37°C with 5% CO2 as described previously .
E14 mouse ES cells were cultured as described by Ying et al. , in order to be induced to differentiate towards neuroectodermal precursors. The medium was renewed every two days and the cells were cultured for 14 days. They were then fixed and immunostained as embryos, described below.
Specific oligonucleotide RNAi duplexes (Eurogentec) to Sox2 (NM_011443), Galanin (NM_010253) and Firefly Luciferase (FFL, D25416, Photuris pennsylvanica luciferase) were designed, using the Dharmacon short interference RNA (siRNA) oligo-designer-tool (http://design.dharmacon.com/default.aspx), taking into account 8 criteria for siRNA specificity and efficiency, as determined by Reynolds et al. . Sequences were copied into the NCBI BLAST database to confirm matching with the sequences of interest. Sox2-duplex-1 was designed to target Sox2 sequence within the HMG box, also found in other Sox genes; Sox2-duplexes -2 and -3 were designed to target Sox2 sequences outside the conserved region of the HMG box (both homologous to Sox2 only). Sense and antisense siRNA oligos used for electroporation are as follows:
Sox2-duplex-1 sense: 5′-GAUGCACAACUCGGAGAUCdTdT-3′
Sox2-duplex-1 antisense: 5′-GAUCUCCGAGUUGUGCAUCdTdT-3′
Sox2-duplex-2 sense: 5′-ACAGCUACGCGCACAUGAAdTdT-3′
Sox2-duplex-2 antisense: 5′-UUCAUGUGCGCGUAGCUGUdTdT-3′
Sox2-duplex-3 sense: 5′-GCACAUGAACGGCUGGAGCAAdTdT-3′
Sox2-duplex-3 antisense: 5′-UUGCUCCAGCCGUUCAUGUGCdTdT-3′
Galanin-duplex-1 sense: 5′-GCAACAUUGUCCGCACUAUdTdT-3′
Galanin-duplex-1 antisense: 5′-AUAGUGCGGACAAUGUUGCdTdT-3′
Galanin-duplex-2 sense: 5′-UAAUGGAGUUUCUCAGUUUdTdT-3′
Galanin-duplex-2 antisense: 5′-AAACUGAGAAACUCCAUUAdTdT-3′
Galanin-duplex-3 sense: 5′-AGAGGGAGUUACAACUGGAdTdT-3′
Galanin-duplex-3 antisense: 5′-UCCAGUUGUAACUCCCUCUdTdT-3′
FFL sense: 5′-CUCUUCAGGUUCUACGGGAdTdT-3′
FFL antisense: 5′-UCCCGUAGAACCUGAAGAGdTdT-3′
The 5′-end of each sense oligo was conjugated to rhodamine. 30 µl of each sense and antisense oligo from the stock solutions (100 µM) were mixed and 15 µl of annealing buffer (50 mM Tris/pH 7.5, 100 mM NaCl, Eurogentec) was added. Oligos were annealed by heating to 95°C for 2 minutes and then allowed to cool for 1 hour at 4°C. The annealed duplex was diluted 120 in 4-(2-hydroxyethyl)-1 piperazine ethanesulfonic acid (HEPES)-buffered saline (HBS) supplemented with 4 mg/ml BSA to give a final concentration of 2 µM (individual Sox2-siRNA duplexes and FFL-siRNA duplex). Combination of the three Galanin-siRNA duplexes created a final concentration of 6 µM.
Flushed 2-cell embryos were washed in HBS/BSA, transferred into the electroporation microchamber slides (VWR) in a minimal volume of medium and electroporated using an ECM®830 electroporator (VWR). Thirty embryos per group in 60 µl of each annealed siRNA (50 µM) were loaded onto the electroporation slides. The embryos were electroporated based on an assessment of several voltages and times, the optimum conditions being those used by Grabarek et al. : 10 V voltage, 750 microseconds pulse length, 6 pulses, 100 millisecond interval between pulses, unipolar pulse. After electroporation the embryos were washed through HBS/BSA and cultured up to day 5 (as above). Development was scored at 24-hour intervals after electroporation (daily between 3 and 4 pm). At days 4 and 5 of culture some embryos were harvested for RT-PCR, others stained by immunocytochemistry or assessed for cell number and apoptosis by TUNEL assay.
Glycerol stocks of purified recombinant Sox2-TAT fusion protein were generated as described previously . The stocks were freshly diluted 120 in KSOM media containing 0.5% Albumax II (Invitrogen) yielding final Sox2-TAT concentrations between 100 and 300 nM. Sox2-siRNA embryos were transferred and cultured in the above supplemented media 24 h after RNAi. Half the medium containing the Sox2-TAT protein was replenished every 24 h and embryos were cultured up to day 5. Rescue experiments were performed with Sox2-duplex-2 and Sox2-duplex-3 siRNA embryos.
Embryos were fixed in 4% paraformaldehyde (PFA, Sigma), washed through PBS-Tween with 4 mg/ml BSA (PBS/BSA), permeabilised with 1% Triton X-100 (Sigma) and washed through PBS/BSA. In order to decrease background staining, embryos were incubated for 10 min at room temperature in a solution of 2.6 mg/ml NH4Cl (Sigma) in PBS, and subsequently permeabilised and washed as above. They were then immersed in 120 normal goat serum (NGS, Sigma) or normal donkey serum (NDS, Sigma) before incubation in the appropriate dilution of the primary antibody in PBS/BSA at 4°C overnight. They were then washed and transferred into the appropriate secondary antibody (Alexa-Fluor, Molecular Probes) at 1200 dilution in PBS/BSA and incubated for 1 hour in the dark at room temperature. After washing, embryos were mounted in DAPI Vectashield mountant (Vector Laboratories) and aspirated by capillary action into 0.2 µM diameter microcapillaries (Camlab), which were sealed in both ends. Primary antibodies were as follows: Sox2 mouse monoclonal (150, R&D), Sox2 rabbit polyclonal (1500, Abcam), Sox2 rabbit polyclonal (1100, Chemicon), Oct4 mouse monoclonal (1250, BD Biosciences), Nanog goat IgG (110, R&D systems), Yap rabbit polyclonal (125, Cell Signaling), Cdx2 rabbit polyclonal (1500, raised in rabbits to an N-terminal KLH-linked peptide of mouse Cdx2 by Dr J. Collins, University of Southampton), Cdx2 mouse monoclonal IgG (1400, Biogenex, gift from Dr J. Draper, Toronto Hospital for Sick Children, Toronto), Eomesodermin rabbit polyclonal (1100, Orbigen), Fgfr2 mouse IgG (1100, Santa Cruz Biotechnology), Fgf4 goat polyclonal (150, Santa Cruz Biotechnology), Occludin rabbit polyclonal (1100, Zymed), ZO1 mouse monoclonal IgG (1100, Zymed), Desmoplakin mouse monoclonal IgG (110, gift from Prof. D. Garrod, University of Manchester), E-cadherin rat monoclonal IgG (1500, Sigma), Gata4 goat IgG (1200, Santa Cruz Biotechnology), Gata6 goat IgG (1200, R&D). Irrelevant antibodies of the same species/isotype as the primary antibodies replaced the primary antibodies, as negative controls: rabbit IgG (Vector laboratories); mouse IgG (Serotec); goat IgG (Santa Cruz Biotechnology); rat IgG (Santa Cruz Biotechnology).
Embryos were viewed under a multi-photon scanning laser confocal microscope (MRC 1024, BioRad) or a Leica (TCS Sp2 AOBS) inverted confocal microscope at the Bioimaging Facility, University of Manchester. A Z-series of 2.5 µM optical sections was collected and analysed using Confocal Assistant software (version 4.02) or LCS Lite software.
In order to assess the lethality of the Sox2 siRNA phenotype, day 5 Sox2 siRNA embryos were incubated in Trypan Blue (Sigma) solution, diluted 110 in KSOM embryo culture medium at room temperature for 10 min before assessment by bright-field microscopy. Blue-stained cells were considered non-viable.
Control and Sox2-siRNA embryos were assessed for apoptosis using the TUNEL assay (Fluorescein conjugated In Situ Cell Death Detection Kit, Roche) as in Kamjoo et al. . Day 4 and 5 embryos were fixed in 4% PFA, permeabilised in 0.5% Triton X-100, washed in PBS/PVP, and incubated for 1 hour at 37°C in the dark in TUNEL solution, a mixture of terminal deoxynucleotidyl transferase and fluorescein-conjugated dUTP in a ratio of 19. Positive control embryos were incubated in DNase (Roche) for 20 minutes at 37°C before TUNEL labelling. Negative control embryos were incubated in fluorescein-conjugated dUTP only. After TUNEL-labelling, embryos were washed in 0.5% Triton X-100 and PBS/PVP, mounted with DAPI Vectashield and aspirated into microcapillary tubes, which were then examined by confocal microscopy.
Apoptotic indices were calculated as number of apoptotic cells divided by total number of cells (DAPI stained nuclei) per embryo. Cell number per embryo was calculated by counting DAPI stained nuclei in confocal images produced by a compressed Z-series of 2.5 µM optical sections for each embryo by means of Confocal Assistant software (version 4.02).
SPSS software (version 11.5) was used to perform Independent Samples T-test for the apoptosis assessment. GraphPad Prism software (version 4) was used for the chi-square tests to monitor distribution of embryos among preimplantation developmental stages.
RNA was extracted from groups of 30 embryos by Dynabeads mRNA Direct Micro Kit (Dynal). cDNA was synthesized using Superscript II reverse transcriptase (Invitrogen) according to manufacturer's guidelines. The primers used (5′-3′) were:
Sox2 (NM_011443) CACAACTCGGAGATCAGCAA/CTCCGGGAAGCGTGTACTTA
β-actin (NM_007393) AGCCATGTACGTAGCCATCC/CTCTCAGCTGTGGTGGTGAA
Fgf4 (NM_010202) TCGGTGTGCCTTTCTTTACC/ACCTTCATGGTAGGCGACAC
Fgfr2 (NM_201601) CACCAACTGCACCAATGAAC/GAATCGTCCCCTGAAGAACA
Cdx2 (NM_007673) AGGCTGAGCCATGAGGAGTA/CGAGGTCCATAATTCCACTCA
Eomes (NM_010136) CCTGGTGGTGTTTTGTTGTG/TTTAATAGCACCGGGCACTC
Tead4 (NM_011567) AGCTAAGAACAAGGCCCTGC/TGCCAAAACCCTGAGATTGC
Oct4 (NM_013633) ATGGGGAAAGAAGCTCAGTG/CAAAATGATGAGTGACAGACAGG
Nanog (NM_028016) CACCCACCCATGCTAGTCTT/ACCCTCAAACTCCTGGTCCT
Sox1 (NM_009233) TACAGCCCCATCTCCAACTC/TCCGACTTGACCAGAGATCC
Sox14 (XM_907434) TGCGCAATTTAGTTCCAGTG/ATGCCTGGGAAGAGGATGTA
Sox21 (NM_177753) TCCAAGCCTGTGGACCACGT/GAGCCATGCACATGAAGGAG
Sox3 (NM_009237) TCCGTGGTGAAGTCGGAG/GCCCTGGTAGTGCTGGTG
Sox15 (NM_009235) GGCGTAAGAGCAAAAACTCG/TGGGATCACTCTGAGGGAAG
Atp1b1 (NM_009721) CAGATTCCCCAGATCCAGAA/CTGCACACCTTCCTCTCTCC
Gata3 (NM_008091) GTGGTCACACTCGGATTCCT/GCAAAAAGGAGGGTTTAGGG
Gata4 (NM_008092) TCTCACTATGGGCACAGCAG/CGAGCAGGAATTTGAAGAGG
Gata6 (NM_010258) GAGCTGGTGCTACCAAGAGG/TGCAAAAGCCCATCTCTTCT
Forty-cycle PCR amplification was performed using thermal cycler Mastercycler Gradient (Eppendorf). Amplicons, each amplified from 50 ng cDNA, were run by electrophoresis alongside a 100 bp DNA ladder (Invitrogen) or Hyperladder IV (Bioline) on 2% agarose gels, at 100 V and 150 mA for 1 hour. Mouse genomic DNA (Bioline) was used as positive control.
PCR product bands of the correct size were confirmed to contain the expected gene product by DNA sequencing. Bands were excised from the agarose gels and DNA extracted and purified using QIAquick Gel-Extraction-Kit (QIAGEN) which were then sequenced (in the Sequencing Unit) using an ABI Prism 377 sequencer (Applied Biosystems). Chromas software was used to read the base compositions, which were copied into the NCBI BLAST database (http://www.ncbi.nih.gov/BLAST/) to identify the sequences.
Validation of Sox2 antibody specificity was performed by Western blotting using 2×107 mouse ES cells (line R1)/ml of lysis buffer (50 mM Tris-Cl, 150 mM NaCl, 0.02% Na azide, 1% Triton X-100) with 1 protease inhibitor cocktail tablet (Complete Mini, Roche)/10 ml lysis buffer. A protein assay was performed using the bicinchoninic acid (BCA) Kit (Pierce), following the Microplate procedure, according to manufacturers' instructions. Twenty five µl lysates samples (50 µg of protein) were resolved by a 4–12% NuPAGE Bis-Tris gel according to manufacturer's recommendations (Invitrogen). 10 µl of BioRad kaleidoscope Multi-Coloured Standard markers were run in parallel at 200 V, 110 mA for 50 minutes. Samples were transferred to a PVDF membrane (Amersham Biosciences), which was blocked in 5% w/v dried milk powder (Marvel) in 0.1% PBS-Tween, incubated with Sox2 antibody (11000, Abcam) in 5% w/v dried milk powder (Marvel) at 4°C overnight and then with a peroxidase-labelled anti-rabbit IgG (13000, DAKO) in 5% w/v dried milk powder (Marvel) for 1 hour. The enhanced chemiluminescence (ECL) detection system (Amersham Biosciences) was used to visualize the protein bands.
(A) Sox2 antibody positive controls: pluripotent mES cells (Sox2-ES) stained for Sox2 (Abcam) in nuclei with some cytoplasmic staining, as well as neurally differentiated E14 cells (Sox2-N) with mainly nuclear Sox2 protein localisation and negative immunological controls (rabbit IgG isotype control and 2° Ab only control) for Sox2 embryo staining. Bars: 100 μm. (B) Western blot to validate specificity of the Sox2 (Abcam) antibody; 50μg mES protein loaded. Lane 1: 2o antibody only; 2: Sox2 (37kDa).
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Development of MF1xMF1 embryos after RNAi. Sox2-duplex-1-siRNA embryos (hatched, N=30) were compared with incubator-control (grey, N=20), FFL-siRNA (black, N=27) and bench-control embryos (white, N=22). On day 5, while control embryos formed blastocysts from 80% to 92.6%, only 3.3% of the Sox2-siRNA embryos formed blastocysts, with 96.7% arresting at the morula stage. On day 5, chi-square tests revealed significant differences (p<0.0001) between the % of Sox2-siRNA morulae and all control morulae, as well as between the % of Sox2-siRNA blastocysts and all control blastocysts.
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Immunostaining of day 4 and day 5 incubator ctrl (untreated) and Sox2-duplex-3-siRNA embryos, with different Sox2 (Chemicon) and Cdx2 (Biogenex) antibodies than the ones presented in Figure 4. This confirms the expression pattern described in Figures 3 and and44 for both markers, as well as absence of Sox2 and Cdx2 proteins after Sox2 RNAi. The images are single optical sections from confocal Z-series. At least 10 embryos were stained for each antigen and representative embryos (not Sox2 siRNA ‘escapees’) are shown. Bars: 50 μm.
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RT-PCR for Sox2, Fgfr2, Fgf4, Cdx2, Eomes, Tead4, Oct4, Nanog, Sox1, Sox3, Sox14, Sox15, Sox21 and Beta-actin (40 cycles) on day 4: incubator-control embryos (lanes 1 and 3); Sox2-duplex-1-siRNA embryos (lane 2); Sox2-duplex-3-siRNA embryos (lane 4). In the absence of Sox2 transcripts after siRNA, a clear reduction of Fgfr2, Ffg4, Cdx2, Eomes and Tead4 transcripts in Sox2-siRNA embryos was observed. Oct4 and Nanog transcripts were unaffected in Sox2 knock-down morulae compared to incubator-control morulae. Sox1, Sox3, Sox14, Sox15 and Sox21 transcripts were not expressed in any of the control or Sox2 knock-down morulae. Beta actin transcripts were detected in all embryos.
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Immunofluorescence confirmation of transferred Sox2 after initiation of the rescue experiment using the Sox2-TAT protein. Sox2 siRNA R embryos were immunostained with Sox2 6h, 12h and 18h after the first addition of Sox2-TAT protein, to assess Sox2 protein recovery efficiency. Gradual expression of Sox2 protein was confirmed, with signs of possible endocytic uptake of the protein, as indicated by patchy expression of Sox2.
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Immunological controls of embryo staining presented in Figures 3 and and4;4; the upper panel (A to K) shows controls for dual staining, the lower panel (L to S) illustrates controls for staining with single antibodies. The images are single optical sections from confocal Z-series. In all cases, the controls were negative. A: anti-Sox2 1o + goat anti-mouse IgG (2o to Oct4, Cdx2Biogenex, Fgfr2, ZO1, Desmoplakin); B: anti-Oct4 1o + goat anti-rabbit IgG (2o to Sox2); C: anti-Cdx2Biogenex 1o + goat anti-rabbit IgG (2o to Sox2); D: anti-Fgfr2 1o + goat anti-rabbit IgG (2o to Sox2); E: anti-ZO1 1o + goat anti-rabbit IgG (2o to Sox2); F: anti-Desmoplakin 1o + goat anti-rabbit IgG (2o to Sox2); G: anti-Sox2 1o + donkey anti-goat IgG (2o to Nanog and Fgf4); H: anti-Nanog 1o + donkey anti-rabbit IgG (2o to Sox2); I: anti-Fgf4 1o + donkey anti-rabbit IgG (2o to Sox2); J: anti-E-cadherin 1o + goat anti-rabbit IgG (2o to Sox2); K: anti-Sox2 1o + goat anti-rat IgG (2o to E-cadherin); L: Rabbit IgG isotype control to Sox2, Cdx2Jane Collins, Eomes, Occludin 1o antibodies; M: Mouse IgG isotype control to Oct4, Cdx2Biogenex, Fgfr2, ZO1, Desmoplakin 1o antibodies; N: Goat IgG isotype control to Nanog, Fgf4 1o antibodies; O: rat IgG isotype control to E-cadherin 1o antibody; P: Goat anti-rabbit IgG 2o antibody only control to Sox2, Cdx2Jane Collins, Eomes, Occludin; Q: Goat anti-mouse IgG 2o antibody only control to Oct4, Cdx2Biogenex, Fgfr2, ZO1, Desmoplakin; R: Donkey anti-goat IgG 2o antibody only control to Nanog, Fgf4; S: Goat anti-rat IgM 2o antibody only control to E-cadherin; T: Goat anti-rabbit IgG 2o antibody only control to Yap; U: Donkey anti-goat IgG 2o antibody only control to Gata4, Gata6; V: Goat IgG isotype control to Gata4, Gata6. Bars: 50 μm.
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We thank Robert Fernandez and Jane Kott at the University of Manchester Bioimaging Facility for help with confocal microscopy, and Dr Fozia Chaudry for help with optimization of the siRNA electroporation parameters. We also thank Professor Daniel Brison and Dr Nicoletta Bobola (University of Manchester, UK) for useful comments on the manuscript, Dr Jenny Nichols (University of Cambridge, UK) for the Gata4 and Gata6 antibodies, Dr Jane Collins (University of Southampton, UK), as well as Dr Jon Draper (Toronto Hospital for Sick Children, Canada), for the Cdx2 antibodies.
Competing Interests: The authors have declared that no competing interests exist.
Funding: Greek State's Scholarship Foundation (IKY-Greece), Infertility Research Trust (UK), Medical Research Council (MRC/UK, R107358) and Deutsche Forschungsgemeinschaft (DFG, ED79/1-1). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.