The first two cell-fate decisions of preimplantation mouse embryo development are not functionally independent

During mouse preimplantation embryo development, three distinct cell lineages are formed, represented by the differentiating trophectoderm (TE), primitive endoderm (PrE) and the pluripotent epiblast (EPI). Classically, lineage derivation has been presented as a two-step process whereby outer TE cells are first segregated from inner-cell mass (ICM), followed by ICM refinement into either the PrE or EPI. As ICM founders can be produced following the fourth or fifth cleavage divisions, their potential to equally contribute to EPI and PrE is contested. Thus, modelling the early sequestration of ICM founders from TE-differentiation after the fourth cleavage division, we examined ICM lineage contribution of varying sized cell clones unable to initiate TE-differentiation. Such TE-inhibited ICM cells do not equally contribute to EPI and PrE and are significantly biased to form EPI. This bias is not caused by enhanced expression of the EPI marker Nanog, nor correlated with reduced apical polarity but associated with reduced expression of PrE-related gene transcripts (Dab2 and Lrp2) and down-regulation of plasma membrane associated Fgfr2. Our results favour a unifying model were the three cell lineages are guided in an integrated, yet flexible, fate decision centred on relative exposure of founder cells to TE-differentiative cues.


Results
ICM founder cells are generated during or shortly after the fourth (the 8-to 16-cell transition) and fifth cleavage (the 16-to 32-cell transition) divisions 4,6 . The time between the completion of these divisions is approximately twelve hours 32 , during which outer-residing 16-cell stage blastomeres remain apical-basolaterally polarised and exposed to TE-differentiative cues, such as suppressed hippo-pathway signalling, whilst apolar inner-cells are protected from TE-differentiation by active hippo-pathway signalling [16][17][18][19]27,28 . As these outer-residing blastomeres can also generate further ICM founders after the fifth cleavage, it is questionable whether ICM progenitors produced by the fourth and fifth cleavage divisions have equal potential to contribute to EPI and PrE [24][25][26] . In order to test if ICM cells are generated with equal potential, irrespective of the extent of TE induction their parental cells received, we assayed ICM lineage contribution of TE-inhibited cell clones in the embryo. We hypothesised if the extent of TE induction was unimportant for PrE differentiation in the ICM, TE-inhibited clones would not be impaired in their potential to contribute to PrE. Conversely, if being able to initiate TE-differentiation facilitates PrE differentiation, such clones would be disadvantaged in populating the PrE, therefore supporting the integrated cell-fate model.
Tead4 down-regulation using long dsRNA phenocopies the zygotic Tead4 −/− knock-out. We employed an RNAi microinjection based strategy, targeting the Tead4 gene, to inhibit TE-differentiation within defined cell clones. We reasoned clonal Tead4 down-regulation would mimic the naturally occurring removal of cells from Tead4 regulation that occurs during their internalisation after the fourth cleavage division. We chose to target Tead4 as it is the earliest known transcription-factor to function in TE specification and its transcriptional activating properties are known to be regulated by hippo-signalling, thereby confining its regulatory output to polarised outer-cells 8,9,16 . Accordingly, we synthesised a Tead4 specific long double-stranded RNA (Tead4-dsRNA) for use in single cell microinjection experiments that could be used to elicit TE-inhibited cell clones in the preimplantation mouse embryo. We first confirmed the efficacy of the construct by microinjecting recovered 2-cell (E1.5) stage embryos, in both blastomeres, with RDBs (rhodamine dextran conjugated beads, lineage tracer) ± the Tead4-dsRNA. As shown in Fig. 1b, we observed > 95% reduced Tead4 mRNA expression, at the 16-(E3.1) and 32-cell (E3.6) stages, with accompanying undetectable levels of Tead4 protein, in Tead4-dsRNA injected embryos (Tead4-KD embryos) compared to microinjection controls (Fig. 1c); confirming the efficacy of the Tead4-dsRNA construct. We also observed robust reductions in the expression of two other TE-specific transcription factor genes known to function downstream of Tead4, namely Cdx2 10 (Fig. 1b,c) and Gata3 33,34 (Fig. 1b), demonstrating a successful block in TE-specification. Moreover, when we in vitro cultured such Tead4-KD embryos, they developed in-step with controls until the 32-cell (E3.6) stage but subsequently failed to initiate blastocoel formation and displayed considerable cell-death by the late blastocyst stage (E4.5); recapitulating the phenotype exhibited by genetically null Tead4 −/− zygotic knockout embryos 8,9 (Fig. 1d).

Clonal down-regulation of Tead4 expression inhibits PrE formation.
We next asked what would be the consequence for PrE derivation in a clone of Tead4-KD cells in the developing embryo? First, we microinjected 2-cell (E1.5) stage embryos in one blastomere with RDBs ± Tead4-dsRNA, to elicit a fluorescently marked and TE-inhibited clone comprising half the embryo. As shown in Fig. 2, we observed complete down-regulation of Tead4 and Cdx2 protein, only within the cells derived from the Tead4-dsRNA microinjected blastomere and throughout the preimplantation developmental period; confirming our clonal TE-inhibition approach. However, in contrast to the global down-regulation of Tead4 ( Fig. 1), clonal Tead4-KD embryos were able to initiate appropriate blastocoel formation, illustrating the regulative capacity of the preimplantation mouse embryo.
We next assayed the frequency that Tead4-KD cells contributed to each late blastocyst (E4.5) cell lineage, compared with the non-injected clone and the equivalent clone from control embryos in which RDBs alone had been microinjected (Fig. 3). It is important to note that blastocyst lineage contribution and the incidence of apoptosis in such control embryos were statistically identical to that observed in a second group of control embryos that had been similarly microinjected at the 2-cell stage with RDBs plus a GFP specific dsRNA (GFP-dsRNA; lacking an endogenous mouse mRNA target- Supplementary Fig. S1 and Supplementary  Tables ST1 & ST2). The lack of any statistically significant difference between these two groups, confirmed the appropriateness of using the RDB alone control in all the subsequently described assays.
Therefore, lineage contribution was assayed in RDB alone microinjected control and clonal Tead4-KD late blastocysts (E4.5) that had been double immuno-stained for either i) Gata4, a PrE marker 35 , and Cdx2, a marker of TE cells 10 , or ii) Sox17, an early PrE marker 15,22 , and Cdx2 (under each immuno-staining protocol, ICM cells devoid of either marker were classified as EPI, as ICM lineage segregation is reported to be completed by this time 36 ), or, iii) Gata4 and Nanog, an EPI marker 11 , (thus directly assaying both ICM cell lineages whilst designating outer cells negative for either marker as TE). Further comprehensive analyses relating to the relative spatial location of cell clones, ICM versus outer-TE location, and cells with fragmented nuclei typical of apoptosis were also undertaken. Note that each of the three respective immuno-staining regimes described above were associated with dedicated and matched control and Tead4-KD embryo groups that were microinjected during the same experimental sessions. Accordingly, n = 24, 13 and 25 for RDB alone control groups and n = 24, 9 and 23 for Tead4-KD embryo groups per respective immuno-staining regime. Figure 3 summarises these data and Supplementary Figs S2, S3, and S4 provide expanded summaries from each immuno-staining method used. Supplementary Tables ST3,  ST4 and ST5 provide individual embryo data for each of immuno-staining group and data relating to apoptosis can be found in Supplementary Fig. S5 and Supplementary Tables ST6, ST7 and ST8.
Our analyses showed that whilst clonal Tead4-KD embryos were able to develop into morphologically normal (E4.5) late blastocysts (Fig. 3b), the clonal origin of these cells, irrespective of how they were assayed in the differing immuno-staining regimes, were not equal. Specifically, Tead4-KD clones preferentially and significantly contributed to the ICM versus the outer TE with partial compensation coming from the non-microinjected clone (Fig. 3c); although Tead4-KD embryos presented with significantly less TE and more ICM than control embryos (Fig. 3c and Supplementary Figs S2-S4 and Supplementary  Tables ST3-ST5). Cells derived from the Tead4-dsRNA microinjected clone that remained in an outer TE position, did not express Cdx2 protein (with very few isolated exceptions detailing very weak anti-Cdx2 immuno-fluorescence) and were almost exclusively spatially restricted to the polar TE, overlying the ICM, rather than mural TE surrounding the expanding blastocoel. Albeit marked, this phenotype is entirely consistent with the well-characterised Tead4 role in TE-differentiation 16 . However, unlike the situation in control embryos, ICM cell lineage segregation was also unequal in Tead4-KD embryos, with the Tead4-dsRNA microinjected cell clones preferentially and significantly contributing to EPI rather than PrE (Fig. 3c). Whilst the ICMs of Tead4-KD embryos were significantly larger than control embryos, the number of PrE cells remained equal in both groups, with all the extra Tead4-KD ICM cells contributing to increased EPI cell number (Fig. 3c and Supplementary Figs S2-3 and Supplementary Tables ST3-ST5). Moreover, the smaller non-microinjected ICM clone in TE-inhibited embryos (for example comprising 7.0 ± 0.8 cells versus 22.6 ± 1.1 cells for the microinjected clone in embryos immuno-stained with Gata4/ Cdx2- Supplementary Fig. S2 and Supplementary Table ST3), contributed a statistically equal number of PrE cells than the microinjected clone (equating, in the Gata4/Cdx2 immuno-stained example, but  A schematic of experimental strategy to effect clonal Tead4 knockdown (KD) and TE-inhibition in one-half of the embryo using microinjected RDBs ± Tead4-dsRNA (see materials and methods) is given on the left. Representative single z-plane confocal micrographs of control and Tead4-KD embryos at either the mid-16-cell (E3.1), 32-cell (E3.6) or > 64-cell (E4.5) stages immuno-stained for Tead4 or Cdx2 (green) are given. Cells derived from the microinjected 2-cell stage clone are distinguishable by the co-injected RDB fluorescence (red). DNA counter-stain (blue) is also shown. In merged images the arrows denote cells exhibiting a lack of Tead4 or Cdx2 expression in the Tead4-KD microinjected cell clone, thus confirming the efficacy and the functional and clonal inhibition of TE-differentiation by Tead4-dsRNA until the late blastocyst stage (E4.5). ICM cells not from the microinjected clone, expressing Tead4 protein are marked with asterisks (in Tead4 alone micrographs). Note, in contrast to global Tead4-KD embryos (Fig. 1), such clonal Tead4-KD embryos initiate blastocoel formation in a manner indistinguishable from control microinjected embryos. Scale bars = 10 μ m.
Scientific RepoRts | 5:15034 | DOi: 10.1038/srep15034 a trend repeated in the other staining groups, to 50.3% of its overall size, versus 19.0% in the microinjected Tead4-KD ICM clone- Fig. 3d), emphasising the bias within the microinjected Tead4-KD clone against contributing to the PrE, despite forming the majority of the total cell number of the ICM. We also noted significant reductions in total cell number in Tead4-KD embryos (Supplementary Figs S2-S4  and Supplementary Tables ST3-ST5) accountable for by increased apoptosis within outer-residing cells of the microinjected clone, presumably unable to adapt to a spatial location requiring TE-differentiation (Supplementary Fig. S5 and Supplementary Tables ST6-ST8).
Overall, we found that individual ICM cells from either the non-microinjected and microinjected TE-inhibited clones of Tead4-KD embryos did not segregate between the EPI and PrE in a manner that would be consistent with them being generated with equal potential. Rather TE-inhibited ICM cells preferentially allocate to the EPI, with the non-microinjected cell clone contributing a greater proportion of its cells to the PrE. Importantly, this result was consistently observed irrespective of the combination of specific antibody markers used to assay the emerging late blastocyst (E4.5) cell lineages, thus validating the functional relevance of the ICM allocation phenotype observed. It has previously been reported that the ICMs of late blastocyst (E4.5) stage embryos can present with cells expressing neither an EPI or PrE marker 21,35 . Consistent with such reports we also observed incidences, using the anti-Gata4/Nanog antibody combination, of late blastocyst (E4.5) stage ICM cells that were either negative or positive for both ICM markers, albeit at very low frequencies and in both control and Tead4-KD embryo groups (on average less than one cell per embryo in both conditions- Fig. 3d, Supplementary Fig. S4 and Supplementary  Table ST5). Although there was a statistically significant increased frequency of cells exhibiting negative immuno-fluorescence for each marker in the microinjected clone of Tead4-KD embryos, when compared with both the non-microinjected clone or the equivalent clone of control embryos, it was in overall numbers extremely modest (0.9 ± 0.2 cells per embryo versus 0.0 and 0.3 ± 0.1, respectively). Moreover, it was insufficiently large to explain the increased contribution of cells classified as EPI in embryos that were assessed by immuno-fluorescent staining for either Gata4/Cdx2 or Sox17/Cdx2 ( Fig. 3 and Supplementary Figs S2 and S3 plus Supplementary Tables ST3 and ST4) as being derived from unspecified ICM cells.
We therefore interpret the collective sum of these experimental datasets as demonstrating that the clonal inhibition of TE cell-fate biases ICM progeny towards EPI rather than PrE formation, albeit with a very small number of ICM cells remaining uncommitted to either lineage. Moreover, this correlates with TE-differentiation potentiating later PrE differentiation, as suggested by the integrated cell-fate model. However, inhibition of TE-differentiation is not an impermeable block to future PrE formation, as cells derived from the TE-inhibited clone can populate the PrE but at much reduced frequency. TE-inhibition within smaller sized cell clones also inhibits PrE formation. We next created embryos containing smaller sized TE-inhibited clones to assay if the observed bias against PrE contribution, Figure 3. Clonal inhibition of TE-differentiation preferentially biases cells to EPI rather than PrE fates. (a) Experimental strategy to effect clonal Tead4-KD and TE-inhibition in one-half of the embryo and assess cell lineage allocation in late blastocysts (E4.5) via immuno-fluorescence detection of marker gene expression, using; i) Cdx2 (TE) & Gata4 (late PrE) -red, ii) Cdx2 & Sox17 (early PrE)-blue, and iii) Gata4 & Nanog (EPI)-green, (n.b. inner-cells devoid of either lineage marker in i) and ii) were classified as EPI and outer cells devoid of immuno-reactivity in iii) were designated as TE). (b) Representative single z-plane confocal micrographs of microinjection control and clonal Tead4-KD late blastocyst (E4.5) embryos immuno-stained for Cdx2 (pseudo-coloured yellow) and Gata4 (green) protein expression. Progeny of the microinjected cell are distinguishable by co-injected RDB fluorescence (red). DNA is counterstained with DAPI (blue). Merged image asterisks represent exemplar cells classified in our analyses as TE, arrows as PrE cells and arrow-heads as EPI. Note similar exemplar micrographs for the alternative immuno-staining regimes are given in Supplementary Figs S3 and S4. Scale bars = 10 μ m. (c) Average number of cells from either non-microinjected or microinjected cell clones contributing to late blastocyst (E4.5) lineages, in control and clonal Tead4-KD embryos, immuno-stained in each of the three regimes outlined in a). Error bars represent s.e.m; * / ** and ‡/ ‡ ‡ denote statistically significant differences between equivalent cell clones of control and clonal Tead4-KD embryos, or between cell clones within control and clonal Tead4-KD embryo groups, respectively (p < 0.05 and p < 0.005, 2-tailed student t-tests). The relative average percentage contribution of total cell number to each late blastocyst lineage in both control-and Tead4-KD embryos is also provided as a pie-chart.  (a) Experimental strategy to generate embryo chimeras containing marked TE-inhibited cells equivalent to one ninth of the embryo and to asses late blastocyst (E4.5) lineage formation, via immuno-fluorescent staining for Cdx2 and Gata4 (n.b. inner-cells devoid of either lineage marker were classified as EPI and immuno-staining using anti-Tead4 antibody was also used to confirm Tead4 KD in the marked chimeric clones). (b) Representative single z-plane confocal micrographs of control and Tead4-KD clone containing chimeras immuno-stained for Tead4 (green) expression. In the merged image, arrows denote cells not expressing detectable levels of Tead4 derived from original Tead4-KD donor blastomere (c) Further, representative single z-plane confocal micrographs of late blastocyst (E4.5) chimeras immuno-stained for Cdx2 (pseudo-coloured yellow) and Gata4 (green). Merged image asterisks represent exemplar cells classified in our analyses as belonging to the TE, arrows PrE and arrow-heads EPI. In (b,c) cells deriving from donor blastomeres, themselves originally derived from control or Tead4-dsRNA microinjected 2-cell (E1.5) stage embryos, within chimeras are distinguishable by co-injected RDB (red). DNA is counterstained (DAPI, blue). Scale bars = 10 μ m. (d) Average number of cells from either RDB-marked or non-marked cell clones in TE lineage (left) and ICM, EPI and PrE lineages (right), in control and Tead4-KD-chimeras; error bars represent s.e.m and * / ** denote statistically significant differences between equivalent cell clones of control-and Tead4-KD-chimeras (p < 0.05 and p < 0.005, respectively -2-tailed student t-tests). Inset pie-charts denote the relative average contribution of cells within each embryo group to each of the three late blastocyst (E4.5) lineages. (e) Averaged percentage contribution of unmarked and RDB-marked cell clones, of control and clonal Tead4-KD chimeric embryos, immuno-stained for Cdx2 and Gata4, between the TE (blue) & ICM (yellow) and the PrE (green) & EPI (orange) of analysed late blastocysts (E4.5). Overall, for control chimeras n = 30 and for clonal Tead4-KD chimeras n = 17. Note, further analysis and variant presentation of the above data is provided in Supplementary Fig. S7 and Supplementary Tables ST11 and ST12. at the late blastocyst (E4.5) stage, would persist. This was because, the above described experiments yielded embryos with relatively larger ICMs (e.g. Tead4-KD; 29.6 ± 1.5, versus controls; 21.8 ± 1.0 cells, in embryo groups immuno-stained for Gata4/Cdx2 - Supplementary Fig. S2 and Supplementary Table ST3) and we wanted to exclude the possibility that E4.5 stage late blastocysts could only support a finite number of PrE cells and that our results were not due to excessive developmental regulation (i.e. that once a finite number of PrE cells had been specified, any extra ICM cells would be defaulted to form EPI). Our first approach involved the direct microinjection of single individual blastomeres of mid-4-cell stage (E2.0) embryos, causing Tead4-KD in one quarter of the embryo (Supplementary Fig. S6 and Supplementary  Table ST9, for apoptosis data see Supplementary Fig. S5 and Supplementary Table ST10; n = 19 control embryos and n = 29 Tead4-KD embryos, immuno-stained for Gata4 and Cdx2). We observed the same bias, as for the above described 2-cell microinjections, in the Tead4-KD microinjected cell clone. However, the average size of such Tead4-KD embryo ICMs was still greater than that observed in control embryos. Therefore, we adopted another strategy to characterise late blastocyst (E4.5) cell lineage contribution of still smaller clones of TE-inhibited cells, involving the creation of chimeric embryos from non-compacted 8-cell stage (E2.5) embryos aggregated with single developmentally matched donor blastomeres in which Tead4 expression was down-regulated. Such chimeras contained marked TE-inhibited clones (Tead4-KD-chimeras) equivalent to one-ninth of their initial total cell number and when in vitro cultured to the last blastocyst stage were morphologically indistinguishable from control-clone containing chimeras (referred to as control-chimeras, see summarised data in Fig. 4, expanded in Supplementary  Fig. S7 with Supplementary Tables ST11 and ST12 documenting individual embryo allocation and apoptosis data, respectively; n = 30 control-chimeras and n = 17 Tead4-KD-chimeras, immuno-stained for Gata4/Cdx2). Importantly, such Tead4-KD-chimeras had a total number of ICM cells statistically equal to that observed in control-chimeras (20.9 ± 1.0 versus 19.0 ± 0.9 cells, respectively) and were  Table ST13). When we assayed late blastocyst (E4.5) cell lineage contribution, we found that the marked TE-inhibited clone of Tead4-KD-chimeras was not only biased to populate the ICM, it was also biased in a statistically significant manner to contribute to the EPI rather than the PrE. Therefore, we found that the inhibition of TE-differentiation within discreet small clones, within ICMs of more physiological appropriate size, also biases cell-fate against PrE formation. Thus, demonstrating that the observed anti-PrE biases observed in TE-inhibited ICM residing clones, derived from any of the three experimental strategies described, are not simply a function of generating unusually large ICMs. Moreover, the data reflect unequal cell-fate potential between such TE-inhibited clones when compared with non-manipulated, non-TE-inhibited, ICM cells of the same embryo. Expressed alternatively, clonal inhibition of TE-differentiation inhibits the progeny of that clone to differentiate towards a PrE cell-fate, when competing with otherwise unperturbed cells outwith the clone.

Molecular characterisation of attenuated PrE formation in TE-inhibited cell clones.
The extent of 8-cell stage blastomere, and subsequent outer-cell, apical-basolateral polarisation has previously been correlated with cell-division orientation and outer-cell engulfment, whereby reduced polarity is associated with inner-cell generation and active hippo-signalling 6,28 . We therefore assayed for apical polarisation and hippo-signalling deficits within TE-inhibited cell clones using previously described anti-phospho-ezrin/radixin/moesin (pERM) and Yap1 antibodies 6,19 , respectively. However, we observed no apical polarisation defects by the mid-16 cell (E3.1) stage (Fig. 5) although we sometimes documented outer mid-16-cell stage blastomeres with substantially reduced apical pERM (not correlating with any clone) at frequencies similar to recent reports 6 . Yap1 immuno-staining of clonal Tead4-KD embryos, detailed nuclear and unusually enriched cytoplasmic expression in outer-residing TE-inhibited cells of mid-16-cell stage embryos, contrasting with more typical nuclear enriched localisation in non-microinjected outer-cells (or control embryos); a similar pattern of Yap1 mis-localisation was also observed at the 32-cell (E3.6) stage, although outer cell staining was more prominently cytoplasmic by this stage. Using anti-sera previously reported 16 to only recognise phosphorylated Yap1 (pYap1- Supplementary Fig. S8), we determined that the mis-localised Yap1 was non-phosphorylated, confirming the atypical cytoplasmic localisation was not because of the induction of active hippo-signalling. We speculate it may be associated with a lack of mechanism to retain Yap1 in the nucleus given its binding partner's absence (i.e. Tead4), and thus reflects an equilibrium of the active nuclear import and passive export of non-phosphorylated Yap1. Curiously, we also observed nuclear localised pYap1 in outer mid-16-cell stage blastomeres both within and outside the Tead4-dsRNA microinjected clone ( Supplementary  Fig. S8a,b). pERM immuno-staining of 32-cell (E3.6) stage embryos revealed robust apical expression within outer-residing TE-inhibited clones, associated with rounded non-TE like morphology (Fig. 5) at frequencies consistent with subsequent apoptosis (see Supplementary Fig. S5 and Supplementary Tables  ST6-ST8). Overall, we did not observe any apical polarisation deficits/or intracellular mis-localisations within TE-inhibited clones that would be consistent with the generation of the extra ICM founder cells (Fig. 3), nor did we observe such deficits when assaying other apical polarity (Prkcz and Pard6b), basolateral polarity (Scrib) or cell adhesion molecular markers (Cdh1-see Supplementary Fig. S9).
We next ascertained if TE-inhibited clone segregation towards EPI cell-fate was associated with precocious and/or increased expression of the EPI marker gene Nanog 37 . We first assayed Nanog derived transcript levels in 16-(E3.1) and 32-cell (E3.6) stage embryos derived from embryos microinjected in both blastomeres at the 2-cell (E1.5) stage with RDBs ± Tead4-dsRNA, to effect global TE-inhibition in all cells of the embryo (Fig. 6a). We found that Nanog mRNA levels remained unchanged at both stages. We therefore assayed Nanog protein expression, but utilising the clonal down-regulation model by microinjecting one blastomere at the 2-cell (E1.5) stage to permit side-by-side comparison of Nanog protein levels in non-microinjected and TE-inhibited microinjected clones (Fig. 6b). Similarly, we did not detect any difference in Nanog protein expression levels between the microinjected and non-microinjected clones in both control and Tead4-KD embryos or between the embryo groups, confirming TE-inhibition by Tead4-KD is not associated with enhanced or precocious Nanog expression.
We next hypothesised that the EPI bias of TE-inhibited ICM residing clones may be associated with attenuated PrE-related gene expression, and thus indicative of a potential obstacle for such cells to initiate or maintain PrE differentiation. Accordingly, we investigated the expression levels of PrE-related gene mRNAs following TE-inhibition (Fig. 6a). We found that, in contrast to Nanog, the normalised transcript levels for the PrE marker genes Lrp2 38 , and Dab2 39 were down-regulated > 95%. Moreover, we also detected a ~40% reduction in Fgfr2 mRNA transcripts, a gene required to mediate PrE-promoting Fgf4-based signalling in the ICM 20,21 . We also observed the same trend of attenuated PrE-related gene mRNA expression in clonally TE-inhibited/Tead4-KD late blastocysts (E4.5), derived by microinjection of a single blastomere at the 2-cell (E1.5) stage ( Supplementary Fig. S10). Given the centrally important role of Fgf4 signalling within maturing ICMs 20,21 , we decided to assay Fgfr2 protein expression after clonal TE-inhibition (Fig. 6c-note microinjected clones were marked with Oregon-green-conjugated dextran beads/OGDBs rather than RDBs). In microinjection control embryos, we observed Fgfr2 in regions demarking approximate boundaries between TE and ICM cells, characteristic of plasma membrane association (the microscopic resolution used prevented exact cellular origin to be determined). Similarly, we also detected Fgfr2 expression at regions between some fellow ICM cells but notably not all Scientific RepoRts | 5:15034 | DOi: 10.1038/srep15034 potential ICM-to-ICM cell contact regions. We interpret these data to indicate heterogeneous inter-cell, membrane associated, Fgfr2 protein expression in the ICMs of control embryos; an expression pattern consistent with a concurrent and similar heterogeneous and reciprocal inter-cell 'salt and pepper' expression pattern for EPI (Nanog) and early PrE (Gata6) markers, already long described 37 . Importantly, in Tead4-KD embryos we did not detect Fgfr2 protein at any ICM-to-ICM cell contact region between cells of the microinjected clone. Moreover, such inner-cells also exhibited prominent nuclear localised Fgfr2. Interestingly, nuclear localised Fgfr2 was seen in some, but not all, inner-cells of control embryos, with the suggestion that nuclear-enriched cells also lack plasma membrane associated Fgfr2, akin to TE-inhibited clones (Fig. 6c). It is possible that nuclear sequestration, be it in some ICM cells of control embryos or within the TE-inhibited ICM clones of Tead4-KD embryos, blunts their capacity to respond to Fgf4-based signals at the plasma membrane and thus differentiate towards PrE fate.
In summary, the reported attenuated PrE formation of TE-inhibited ICM clones is not associated with increased expression of the EPI marker Nanog, nor with reduced apical-basolateral polarity. Inhibition of TE cell-fate, does however correlate with reduced transcript levels for PrE marker genes and down-regulation of Fgfr2 protein from the plasma membrane of ICM cells.

Discussion
We created variously sized cell clones within developing preimplantation mouse embryos that were unable to initiate TE-differentiation and assayed their ICM cell-fate potential to see if such clones would be predisposed towards EPI rather than PrE, in a similar manner to that described for ICM founders generated during the fourth cleavage 22 . In each of our experiments we found this to be true, as ICM cells derived from TE-inhibited clones preferentially contributed EPI versus PrE cells. These data indicate that level of TE-differentiation exposure ancestral cells of ICM progenitors are exposed to, is functionally relevant, although certainly not deterministic, in regard to guiding their ultimate fate. We conclude that our data are consistent with the integrated cell-fate model, whereby differing levels of exposure to TE-differentiative cues, provided by prolonged inhibition of hippo-signalling in outer-cells that yield ICM founders at the fifth cleavage division rather than those that do at the fourth, biases ICM cells to preferentially occupy either EPI or PrE.
A question arising from our clonal studies is: Are ICM progenitors generated as a result of the fourth or fifth cleavage, or more precisely from cells with differing exposures to TE-differentiation, molecularly equivalent? Others report, the first population of derived inner-cells are characterised by higher Fgf4 and lower Fgfr2 expression, whilst the second population exhibit relatively elevated Fgfr2 expression 26,31 , consistent with our observations of reduced Fgfr2 mRNA levels after Tead4-KD (Fig. 6a); these data support the hypothesis that prolonged exposure to TE-differentiation, primes cells to yield ICM progeny biased towards PrE, by becoming more responsive to Fgf4 21 . Moreover, still others report that the Fgfr2 gene itself, plus the Lrp2 and Dab2 genes, are occupied by promoter proximal Tead4 protein in TS cells 40 . We observed a lack of detectable Fgfr2 protein expression between adjacent ICM cells within the Tead4-KD clone (plus increased nuclear localisation), suggesting that TE inhibited clones are less able to differentiate to PrE because of reduced ability to receive Fgf4-based membrane signals. Interestingly, a similarly heterogeneous anti-Fgfr2 immuno-staining pattern has previously been reported in mouse Figure 6. Global and clonal TE-inhibition; no enhanced Nanog expression prior to 32-cell stage but attenuated PrE-specific marker expression. (a) The experimental strategy to down-regulate Tead4 and inhibit TE-differentiation throughout all cells of the embryo prior to Q-RTPCR analysis (upper). Normalised expression fold changes, resulting from Tead4-KD, of the stated transcripts at the mid-16-cell (E3.1) or 32cell (E3.6) stages (lower panels). Individual gene mRNA levels were normalised against Rpl23 and/or H2afz transcript levels within control and experimental knockdown conditions prior to fold change calculation. Errors = s.e.m, n = at least 2 for biological and 3 for technical replicates (n.b. Tead4 specific data is repeated from Fig. 1 as Q-RTPCR was performed from same cDNA preparations). (b) Confocal microscopy analysis of Nanog (green) expression after clonal Tead4-KD at the mid-16-cell (E3.1) and 32-cell (E3.6) stages. Arrows and arrow-heads denote exemplar Nanog expression in non-microinjected and microinjected clones, respectively. Asterisks highlight TE cells without Nanog expression reflecting previously characterised inter-cell heterogeneity. (c) Confocal microscopy analysis of Fgfr2 (red) expression after clonal Tead4-KD at the noncavitated 32-cell (E3.5) blastocyst stage. Representative single z-plane confocal micrographs are shown (middle panels) with the lower 4 panels detailing magnified anti-Fgfr2 immuno-stained images, according to numbered regions of interest. Arrow-heads highlight plasma membrane associated Fgfr2 between neighbouring ICM cells (control embryos) and arrows approximate equivalent regions of other neighbouring ICM cells without anti-Fgfr2 signal (illustrating heterogeneous Fgfr2 expression within control embryo ICMs). Similarly, arrows show ICM cell boundaries between cells of the microinjected clone devoid of Fgfr2 in Tead4-KD embryos. Asterisks and lollipop markers, in both control and Tead4-KD embryos, show nuclear Fgfr2 protein (especially in Tead4-KD embryos) or expression at the interface of TE and ICM cells, respectively. In both (b,c) progeny cells of microinjected clones are distinguishable by co-injected RDBs (red) or OGDBs (Oregongreen dextran beads-green). DNA was counterstained with DAPI (blue) and scale bars = 10 μ m.
blastocysts, although the significance of this observation was not discussed 41 . The reason for enhanced Fgfr2 nuclear localisation is unclear, although not unprecedented 42,43 and is observed heterogeneously in control embryo ICM cells populations (Fig. 6c).
A recent genetic study demonstrated that restricted inner-cell expression of the pluripotency-related transcription factor Sox2 is also regulated by hippo-signalling in a Tead4-dependant manner 44 . This report is consistent with the integrated cell-fate model as it highlights the importance of the relatively early and late removal of cells from TE-differentiative environments. The reported data also suggest that the EPI bias of TE-inhibited clones (Figs 3 and 4 and Supplementary Figs S2-S4, S6 and S7) maybe due to increased Sox2 expression. A previous study investigating ICM lineage contribution of varying ratios of marked inner-cells, in chimeric 16-cell stage embryos, demonstrates that the initial number of ICM founders has profound effects for cell-fate. Chimeras generated with fewer (e.g. 3) inner-cells exhibited EPI bias within these ICM founders, reminiscent of previous reports of non-manipulated in vitro cultured time-lapse observed embryos 22 , in addition to PrE bias of unmarked cells internalised following the fifth cleavage. However, generating chimeras with more initial inner-cells (e.g. 4 or 5) ablated the biases 26 . The authors speculated elevated extra-cellular Fgf4 levels in chimeras with more ICM founders, causes cells that may have otherwise contributed to EPI, to differentiate to PrE; a hypothesis also supported by mathematical modelling of ICM cell-fate 45 . In our data (Figs 3 and 4 and Supplementary Figs S2-S4, S6 and S7), we observed the greatest percentage PrE contribution of non-TE-inhibited ICM-resident clones when the TE-inhibited/Tead4-KD clone in the ICM was largest, and vice-versa. We interpret these results as indirect evidence that larger TE-inhibited clones may generate greater levels of extra-cellular Fgf4 within the ICM than smaller clones. As such, our data support the relevance of the number of generated ICM cells, and not just their developmental origin, as being important in biasing/directing lineage segregation 26,45 . In all our experimental strategies, we observed PrE contribution of cells derived from TE-inhibited clones, indicating that removal from TE-differentiation does not 'block' PrE differentiation. It is possible that elevated Fgf4 levels in ICMs containing TE-inhibited clones are sufficient to act upon cells within the clone itself. Alternatively, stochastic mechanisms could also be involved, whereby inherent self-reinforcing fluctuations in gene expression would predispose TE-inhibited ICM cells towards a profile favourable for PrE differentiation. Indeed, stochastic mechanisms are promoted as a means by which ICM lineage segregation normally occurs 46 . We would argue that our data indicate significant biases in ICM cell-fate derivation based on cell history but do not dismiss the existence, input nor importance of stochastic mechanisms. Indeed, early mammalian development is highly regulative, indicating, by definition, the existence of multiple complementary and overlapping pathways that must work together to guide, rather than restrict, the appropriate cell-fate decisions required 47 .
Theoretically our results are explainable by a direct and unprecedented PrE promoting role for Tead4 within the ICM, potentially acting via inactivation of the hippo-signalling pathway. However, existing ES cell evidence argue against this hypothesis. Firstly, as Tead4 −/− ES cell differentiation leads to the expression of multiple lineage marker genes, including the PrE markers Gata6 and Sox17, the evidence suggests that Tead4 is dispensable for PrE formation per se (agreeing with our clonal data) 9 . Moreover, when we performed double immuno-fluorescent staining of, control microinjected and Tead4-KD (microinjecting one blastomere at the 2-cell stage) or in vitro cultured control late blastocysts (E4.5) for Yap1 and Gata4 ( Supplementary Fig. S11), we did not observe any nuclear co-localisation of the two factors that would have been indicative of activated hippo-signalling in specified PrE cells. Nor, did we observe any indication of nuclear Yap1 in any inner/ICM cells at earlier developmental points prior to the late blastocyst (E4.5) stage ( Fig. 5 and Supplementary Fig. S8). We therefore consider it unlikely that Tead4 has a direct PrE promoting role within the ICM. Furthermore, given that it is even possible to derive Tead4 −/− ES cells, a direct requirement of Tead4 to maintain the pluripotent EPI lineage is also highly improbable 9 . However, it is important to note that ES cells may not share the same degree of functional similarity with cells of the early embryo 48 . Overall, the collective evidence points against any direct cell-fate role of Tead4 within the ICM. Consequently, our clonal Tead4-KD data are best explained by the inability of the ancestors of ICM progenitors to initiate/respond to TE-differentiative cues, rather than a lack of functionally relevant Tead4 protein within individual ICM cells.
Our observations of pERM and Yap1 immuno-staining ( Supplementary Fig. S8) are completely consistent with an earlier report detailing the existence of apolar outer-cells with cytoplasmically localised Yap1 protein, indicative of active hippo-signalling 6 . However, we did observe unexpected nuclear pYap1 in outer-residing, mid-16-cell stage blastomeres ( Supplementary Fig. S8a,b). This result is unintuitive, as phosphorylation of Yap1 is normally associated with its cytoplasmic sequestration in response to active hippo-signalling, and neither the reason nor its functional significance are clear. Possibly, the phospho-serine-127 epitope recognised by the antibody is not a sufficient/determining factor governing nuclear exclusion at this stage; for instance Yap1 has five known hippo-signalling directed (by Lats) phosphorylatable serine containing consensus motifs 49 .
We conclude our data are compatible with the integrated cell-fate model of early lineage segregation, whereby TE, EPI and PrE fates all begin their segregation at the fourth cleavage division and are guided by relative differences in the exposure of the founding cells to TE-differentiative cues and the timely activation (or liberation from suppression) of the hippo-signalling pathway. However, and in keeping with the remarkable regulative capacity of the early embryo, such mechanisms act to guide rather than dictate cell-fate and can be modulated by factors such as generated inner-cell number or the induction of self-reinforcing stochastic gene expression.

Methods
All described experimental procedures on mice and mouse embryos were approved, ratified and licensed by the local ethics committee of the Biology Centre (in České Budějovice) of the Czech Academy of Sciences and by the responsible committee of the Czech Academy of Sciences on the national level, in accordance with Czech and European Union law. Accordingly, the described experiments were implemented in full accordance with the approved guidelines provided by the two above stated committees.
Image analysis/cell counting. Individual E4.5 stage blastocyst cell contributions within and outwith the microinjected clone, or within inner or outer-cell populations, or within cell lineage marker protein positive or negative cells (after specific immuno-staining), plus the incidence of cells with fragmented/apoptotic nuclei, were determined in both experimental and control embryos by inspection of confocal z-sections using Fluoview ver.1.7.a (Olympus) and Imaris 6.2.1 (BitPlane) software. The above contribution criteria in in vitro culture control embryo groups (starting from 2-cell/E1.5 stage) was first established ( Supplementary  Fig. S12 and Supplementary Table ST13) to provide a baseline for the appropriate development of individual control and experimental embryos to be screened, removing those with generally poor development due to manipulation (particularly in chimeras). Accordingly, embryos with fewer than 64, or less than four Gata4 positive cells (minimum we observed in the reference data) were excluded from the analysis. Statistical analysis. The mean of cells within defined embryonic populations and the standard error of means (mean ± s.e.m.) were calculated and statistical significance determined using 2-tailed Student's t-tests.