The E3 ubiquitin ligase skp2 regulates neural differentiation independent from the cell cycle
© Boix-Perales et al.; licensee BioMed Central Ltd. 2007
Received: 3 May 2007
Accepted: 14 December 2007
Published: 14 December 2007
The SCFskp2 complex is an E3 ubiquitin ligase that is known to target a number of cell cycle regulators, including cyclin-dependent kinase inhibitors, for proteolysis. While its role in regulation of cell division has been well documented, additional functions in differentiation, including in the nervous system, have not been investigated.
Using Xenopus as a model system, here we demonstrate that skp2 has an additional role in regulation of differentiation of primary neurons, the first neurons to differentiate in the neural plate. Xenopus skp2 shows a dynamic expression pattern in early embryonic neural tissue and depletion of skp2 results in generation of extra primary neurons. In contrast, over-expression of skp2 inhibits neurogenesis in a manner dependent on its ability to act as part of the SCFskp2 complex. Moreover, inhibition of neurogenesis by skp2 occurs upstream of the proneural gene encoding NeuroD and prior to cell cycle exit. We have previously demonstrated that the Xenopus cyclin dependent kinase inhibitor Xic1 is essential for primary neurogenesis at an early stage, and before these cells exit the cell cycle. We show that SCFskp2 degrades Xic1 in embryos and this contributes to the ability of skp2 to regulate neurogenesis.
We conclude that the SCFskp2 complex has functions in the control of neuronal differentiation additional to its role in cell cycle regulation. Thus, it is well placed to be a co-ordinating factor regulating both cell proliferation and cell differentiation directly.
Ubiquitin-mediated proteolysis has recently emerged as a central player in regulating destruction of proteins controlling cell fate determination, cell proliferation and cell differentiation [1, 2]. Indeed, coordinating stability of proteins involved in these three processes is an efficient way for cells to decide to divide or to undergo differentiation.
Polyubiquitination, which targets proteins for destruction, is brought about by a multi-enzyme cascade, typically involving E1 ubiquitin-activating enzymes, E2 ubiquitin-conjugating enzymes and E3 ubiquitin ligases . Specificity for particular substrates resides in the E3 subunit, which is itself often a multi-subunit complex. The largest group of E3 ligases is the ring-finger domain family and within this family several so called SCF E3 ligases are known to target proteins important for maintenance of the balance between proliferation and differentiation [4–6]. One of the best studied ligases in this family is SCFskp2, which is composed of a cullin-1 scaffold, bound directly to the Ring finger protein Rbx1 and to Skp1 [4–9]. Specificity for ubiquitination resides in the skp2 subunit, which associates with Skp1 via its F box.
SCFskp2 has been shown to target a growing number of proteins important in cell cycle progression for ubiquitin-mediated proteolysis. These include the transcription factors E2F1  and c-myc [11, 12], and the cdk inhibitors (cdkis) p21 Cip1 [13, 14] and p27Kip1 , although the physiological relevance of some of these potential substrates has been questioned.
Importantly, targets of SCFskp2, of which p27Kip1 is the most studied, must generally be phosphorylated in a cell cycle dependent manner to be targeted by skp2 for polyubiquitination and destruction [16–18]. Xenopus skp2 has recently been cloned and has been shown to target the Xenopus cdki Xic1 [19, 20] for degradation in vitro and in egg extracts . However, in this case Xic1 appears not to require phosphorylation for targeting.
We have previously showed that Xic1 has an essential role in differentiation of primary neurons, the first neurons to differentiate in the neural plate in Xenopus . Neural differentiation in this system is driven by the neurogenic transcription factor, Neurogenin (XNgnr1), which is expressed in scattered neural precursors in the neural plate arranged in three stripes lateral to the midline . XNgnr1 transcriptionally upregulates another basic helix-loop-helix (bHLH) transcription factor NeuroD, whose expression coincides with cell cycle exit and terminal neural differentiation . Interestingly, we have shown that Xic1 is not required at these late stages downstream of NeuroD for cell cycle exit or differentiation. Instead, Xic1 acts at an early stage of neurogenesis, in parallel with XNgnr1, where it appears to stabilise the XNgnr1 protein . Moreover, this function is separable from the ability of Xic1 to inhibit overall cdk kinase activity . Thus, Xic1 has distinct roles in cell cycle regulation and differentiation, making it an appealing candidate for a protein that coordinates these two functions.
Skp2, by regulating the stability of cdkis as well as additional targets such as c-myc and E2F1, is also well placed to play a role in coordinating proliferation and differentiation. A skp2 null mouse has been generated, which although smaller than wild type, is phenotypically grossly normal despite an increase in polyploidy, multiple centrosomes and apoptosis . A skp2-/- p27Kip1-/- mouse has also been generated , which appears similar but not identical to the p27Kip1-/- mice, indicating that, while p27Kip1 may be its main target, SCFskp2 may ubiquitinate other important substrates. In mice, however, the presence of three cdkis and other redundancies makes analysis of the role of skp2 in proliferation and differentiation during development problematic.
Importantly, targets of SCFskp2, of which p27Kip1 is the most studied, must generally be phosphorylated in a cell cycle dependent manner to be targeted by skp2 for polyubiquitination and destruction [16–18]. Xenopus skp2 has recently been cloned and has been shown to target the Xenopus cdki Xic1 [19, 20] for ubiquitination in vitro and for degradation in egg extracts . However, in this case Xic1 appears not to require phosphorylation for targeting.
We find that Xenopus skp2 (skp2) shows dynamic expression in the neural plate and neural tube, indicating that it is well placed to regulate neural differentiation in a stage-specific manner. Loss of skp2 protein after morpholino injection has no effect on the cell cycle but results in differentiation of extra primary neurons, while over-expression of skp2 inhibits neurogenesis and this depends on the presence of an F box. Skp2 can degrade Xic1 in vivo and this can account for some, but not all, of skp2's ability to regulate primary neurogenesis. Therefore, skp2 is well placed to directly regulate the balance between proliferation and differentiation, in addition to a potential role in cell cycle control.
We also investigated the expression of skp2 relative to Xic1 in the late neural plate in embryos that had undergone in situ hybridisation to detect expression of the individual genes, which were subsequently sectioned (Figure 1h,i). As expected, Xic1 is expressed in deep layer cells, in addition to staining in the underlying myotome and notochord (which can be distinguished by light blue staining due to poor penetration by the BM purple substrate; see Materials and methods). Skp2 staining, by contrast, is weaker but is present in both the superficial and deep layers of the neural plate in a region overlapping Xic1 expression.
By stage 17, when the neural tube begins to close, skp2 message is found posteriorly in the neural folds, as well as remaining in the placodes, eye field and brain regions (Figure 1d). Primary neurons only form from the deep layer of the neural plate while superficial layer cells remain undifferentiated at this stage . By tailbud stage 25, skp2 message is expressed in the neural tube, eye and branchial arches (Figure 1e). At a similar stage (stage 26; Figure 1f), Xic1 is also expressed in the neural tube, eye and branchial arches but additional staining is seen in the myotome where skp2 is undetectable. By stage 33, skp2 expression remains strongest in the head (Figure 1g).
Thus, skp2 is expressed at the right time and in the right place to be playing a role in primary neurogenesis. Interestingly, at early neural plate stages skp2 RNA is excluded from the medial areas expressing the potential target Xic1 (compare Figure 1b and 1c), although overlap is seen in the lateral neural folds (Figure 1h,i). However, as neurulation proceeds, skp2 expression expands to the mid-line (Figure 1d). Therefore, skp2 expression is dynamic and is consistent with a stage dependent role in regulation of Xic1 protein, an in vitro target in primary neurons . As Xic1 is essential for primary neurogenesis, skp2 is also well placed for regulating this process. We have investigated this further.
We then investigated the effect of loss of skp2 on differentiation of primary neurons, by injecting skp2 Mo or Con Mo into one cell of a two-cell embryo along with β-galactosidase (ßgal) RNA as a lineage tracer. As the first plane of cleavage should bisect the embryo along the left/right axis, the injected and uninjected sides of the embryo can be compared. Embryos were allowed to develop to stage 15, fixed and then in situ hybridisation was performed to determine neural β-tubulin (nßt) expression, which is expressed in differentiated primary neurons (Figure 2c–g). Embryos were scored according to the number of neurons on the injected versus the uninjected side. Examples of representative embryos displaying the phenotypes described (Figure 2c) are given (Additional file 1). Skp2 Mo injection resulted in a subtle but reproducible increase in the number of primary neurons on the injected side versus the uninjected side of the embryo, generally proximal to or within the usual stripe of primary neurogenesis (Figure 2c, d, f; 20 ng, n = 120 embryos; 30 ng, n = 123 embryos; 40 ng, n = 100 embryos). This effect was dependent on the dose of skp2 Mo injected; the higher the dose of skp2 Mo, the greater the percentage of embryos showing an increase in neuron number (Figure 2c). A very small proportion of embryos injected with skp2 Mo at the highest doses showed a reduction of neurons. However, this was not strictly dose dependent and a similar, albeit slightly smaller, effect was also seen with the highest dose of Con Mo (30 ng, n = 73; 40 ng, n = 108), so it is unlikely to be a specific effect of loss of skp2 protein.
The increase in the number of primary neurons on the injected side was subtle and somewhat variable in wholemount embryos. To look more closely, stage 15 embryos were sectioned and analyzed by in situ hybridisation for nßt expression. Extra primary neurons were clearly seen after skp2Mo injection on the injected side only, and these were confined, as usual, to the deep layer of cells of the neuroectoderm (Figure 2f, arrow). Interestingly, we usually saw an increase in primary neurons lateral to or within the lateral stripe rather than at the mid-line. Cells in the lateral stripe will go on to form the sensory neurons and this is the region of neural plate-stage embryos where in situ hybridisation staining for both Xic1 and skp2 overlap (Figure 1b, c, h, i).
Thus, loss of skp2 protein leads to a moderate but dose-dependent and significant increase in the number of primary neurons. Notably extra neurons form generally dorso-laterally and near to or within the established stripes in the deep layer of the neural plate but not ectopically significantly ventrally (Figure 2d, f). A similar effect is seen on over-expression of the skp2 target, Xic1 .
SCFskp2 degrades cdkis [10, 13, 14, 29–32]. Therefore, loss of skp2 might be expected to result in a slowing of the cell cycle, and indeed skp2 knockout mice are small and their cells display a reduced growth rate . As proliferation is thought to be incompatible with differentiation in neurons, it is therefore possible that skp2 Mo is promoting neurogenesis by inducing cell cycle exit in the neural plate. To investigate this possibility, we injected skp2 Mo or Con Mo into one cell of a two cell embryo and allowed these embryos to develop to neural plate stage before staining for the mitotic marker phosphohistone H3 (pH3)  (Figure 2h, i). Numbers of pH3-expressing cells were counted in a fixed area of the neural plate on injected and uninjected sides and compared (Figure 2h', i'). There was no significant difference in the number of mitotic cells after injection of either skp2 Mo or Con Mo (n = 31 embryos and n = 38 embryos, respectively). Therefore, loss of skp2 does not promote neural differentiation by forcing cell cycle exit. A thickening of the epidermis was sometimes seen in sections (Figure 2f), indicating some alteration in neuroectodermal architecture. However, our pH3 analysis indicates this is not a result of increased proliferation of neuroectodermal cells.
To investigate the effect of over-expression of skp2, RNAs were injected into one cell of two cell embryos along with ßgal RNA, and then embryos were allowed to develop until stage 15. In situ hybridisation was subsequently performed to detect nßt expression; 84% of embryos (n = 359) injected with wild-type skp2 showed reduced nßt expression on the injected side (Figure 3a). In contrast, neither F box skp2 (Figure 3b) nor MAFbx (Figure 3c) affected nßt staining (100% n = 65 and 92% n = 49 unaffected, respectively). Thus, over-expression of skp2 inhibits neuronal differentiation and this is dependent on the ability of skp2 to interact with the SCF complex and, hence, target substrates for ubiquitin-mediated proteolysis. The effect of skp2 over-expression is dose-dependent; embryos injected with 250 pg skp2 mRNA showed only a modest decrease in neurons but this effect was progressively more pronounced on increasing skp2 mRNA, up to 1 ng, where more than 80% of embryos were affected (Figure 3f).
Elevated levels of skp2 correlate with cancer where cells proliferate inappropriately [38, 56]. Moreover, skp2 over-expression alone induces quiescent fibroblasts to replicate their DNA in low serum . Such an increase in cell proliferation might be expected to inhibit neural differentiation and, indeed, over-expression of cyclin A2/cdk2 alone in Xenopus embryos inhibits primary neurogenesis . Thus, we investigated whether skp2 over-expression alone could promote proliferation in early Xenopus embryos by injection of skp2 mRNA into one cell of a two cell embryo followed by analysis of pH3 staining in the neural plate. Unexpectedly, skp2 over-expression led to a 24% decrease in pH3-expressing cells on the injected side (p < 0.001, n = 27 embryos; Figure 3d). Moreover, the F box mutant of skp2 also produced an 18% decrease in pH3 cells (p < 0.001, n = 17 embryos; Figure 3e). This indicates that effects on proliferation are modest and are not due to the specific targeting of skp2-dependent substrates for ubiquitin-mediated proteolysis, and additionally cannot explain the ability of wild-type skp2 to inhibit neurogenesis.
Depletion of skp2 promotes primary neurogenesis (Figure 2) while over-expression of skp2 inhibits neuron formation (Figure 3). To demonstrate the specificity of these effects, we co-injected skp2 Mo or Con Mo along with RNA encoding skp2 missing the first six base-pairs after the ATG start site, which is not targeted by the skp2 Mo. Western blotting of protein lysates from stage 15 embryos revealed that skp2 Mo knocks down exogenous skp2 protein effectively, but is unable to reduce levels of this non-targeted skp2 protein (Figure 2a).
Skp2 has been demonstrated in the mammalian systems to degrade several substrates known for their roles in regulating proliferation and/or differentiation, including p27Kip1, p21Cip1, c-myc, E2F-1 and p107 [10, 13, 14, 29–31, 59]. Xic1, the Xenopus homologue of p27Kip1 and p21Cip1, is also targeted by skp2 for ubiquitin-mediated proteolysis . We have previously shown that Xic1 plays an essential role in primary neurogenesis in parallel with XNgnr1 and prior to cell cycle exit . As over-expression of skp2 inhibits neurogenesis at this stage, skp2 may regulate primary neurogenesis by controlling the levels of Xic1 protein. We have investigated this possibility further.
Skp2 message is most strongly expressed in the neural plate, underlying myotome and the notochord at stage 15. Xic1 is also transiently expressed in scattered cells in the epidermis at around stages 12–13  so protein may still be present in the skin of the embryo as well as these other tissues. To determine whether skp2 can target endogenous Xic1 for degradation in the neural plate, embryos were injected with wild-type or F Box skp2 dorsally along with green fluorescent protein as a lineage tracer. The dorsal region encompassing the neural plate and anterior neural folds of stage 16 embryos expressing green fluorescent protein in this area were dissected out, and the levels of Xic1 protein compared by western blotting. Over-expression of wild-type skp2 significantly decreased the level of endogenous Xic1 protein compared to neural plates from uninjected embryos (Figure 6d). In comparison to wildtype skp2, Fbox skp2 had no effect on the level of endogenous Xic1 protein (Figure 6d), consistent with its impaired ability to target Xic1 to the SCF complex.
Interestingly, over-expression of skp2 did not result in complete degradation of either endogenous Xic1 (Figure 6d) or Xic1 translated from co-injected cDNA (Figure 6b, c). As well as expression in the epidermis, primary neurons and neuronal placodes, Xic1 becomes increasingly strongly expressed in the myotome as neural plate stages progress (Figure 1). Xic1 is absolutely required for myotomal muscle differentiation in Xenopus , so if it can be degraded by skp2 in this tissue we would expect skp2 over-expression to inhibit myogenesis. Hence, we looked to see whether wild-type skp2, but not Fbox skp2, could inhibit muscle differentiation. Interestingly, and unlike differentiation of primary neurons, over-expression of skp2 did not inhibit early or late muscle differentiation (Figure 6e–h), indicating that Xic1 protein cannot be targeted for destruction in this tissue. This would account for our observation that only a proportion of Xic1 can be degraded by skp2 over-expression; Xic1 protein in the myotome would remain stable.
Thus, over-expression of Xic1 can partially rescue the effect of skp2 over-expression. However, it is of note that, after mRNA injection, Xic1 protein accumulates to levels considerably above endogenous (for example, compare lanes 1, 4 and 5 in Figure 6b), yet this is not enough to fully reverse the effects of skp2 over-expression on inhibition of neurogenesis. Thus, we consider it likely that skp2 is regulating levels of both Xic1 and other factors required for primary neurogenesis. These potentially novel substrates remain to be identified.
Ubiquitin-mediated proteolysis has recently emerged as a central regulator of numerous cellular pathways, although the role of E3 ubiquitin ligases in developmental processes has been poorly studied. We have investigated the role in early Xenopus development of skp2, a component of the E3 ligase SCFskp2 previously shown to be important for cell cycle regulation.
In situ hybridisation demonstrates that the developmental expression of skp2 is dynamic and is consistent with skp2 playing a role in neurogenesis (Figure 1). At early neural plate stages, skp2 is expressed in anterior regions corresponding to the neuronal placodes, eye field and brain, and the lateral neural folds where neuronal precursors are abundant, but is excluded from medial regions of the posterior neural plate. Expression in the neural plate at this time overlaps at least partially with that of its potential target, Xic1, although while Xic1 expression is confined to the deep layer of cells in the neural plate, skp2 mRNA is found in both the deep and superficial layers (Figure 1h). As neurulation progresses, skp2 becomes upregulated throughout the neural tube, although remaining most prominent in the anterior regions, including in the eye and in the migrating neural crest of the branchial arches. At later stages skp2 staining is lost in the posterior of the embryo, although it remains high in the head. Thus, the timing and localisation of skp2 message are consistent with it playing a role in regulation of Xic1 stability and primary neurogenesis. It is of note that Xic1 is also strongly expressed in the myotome (Figure 1c, i), where it is required for muscle differentiation, but skp2 is not expressed in this tissue (Figure 1h), indicating that any role of skp2 in regulating Xic1 levels may be confined to neural tissue.
SCFskp2 has a known role in cell cycle progression, which it effects by controlling the levels of a number of key cell cycle regulators, including cdkis, E2F and c-myc [10–14, 29–32]. We investigated the effect of up- or down-regulation of skp2 levels on cell cycling by measuring pH3 staining, a specific marker for mitotic cells . Surprisingly and in contrast to the mouse, loss of skp2 protein had no effect on cell proliferation in early Xenopus embryos (Figure 2f, h). One of the major points of regulation for progression through the cell cycle is called the restriction point, found in G1. Passage through the restriction point and, thus, commitment to cell cycling is controlled by phosphorylation of the retinoblastoma (pRb) protein. This results in release of the transcription factor E2F, which in turn drives transcription of genes required for S phase progression (for a review, see ). pRb phosphorylation is brought about by cdks, which are in turn inhibited by cdkis. Both cdkis and E2F are targets for skp2-mediated ubiquitination and destruction. Loss of skp2 in mammalian cells results in cdki accumulation , which will cause pRb to be maintained in a hypophosphorylated and, therefore, active state, thus inhibiting passage through G1 into S phase. Interestingly, at the early stages of Xenopus development studied here, E2F is found largely unbound to pRb  and, moreover, the Xenopus Rb protein is not required for cell cycle regulation or early embryonic development . Additionally, another potential skp2 target, c-myc, is predominantly expressed in the neural crest during early development in Xenopus and loss of protein after morpholino injection has little effect on cell proliferation . These observations may explain why loss of skp2 protein does not affect cell cycling at these stages, and indicates that c-myc and E2F are not likely targets for skp2 regulation at this stage.
Absolute levels of skp2 protein are regulated through the cell cycle, being higher in S and G2 phases , indicating that the absolute level of skp2 protein is important for its cell cycle function. One characteristic of cancer cells is inappropriate division, and indeed a variety of tumour cells have elevated skp2 levels [38, 56]. Moreover, over-expression of skp2 drives entry into S phase, inducing quiescent fibroblasts to replicate their DNA in low serum . Surprisingly, over-expression of skp2 in Xenopus embryos results in a small but significant decrease in pH3-staining cells (Figure 3d). However, this decrease is also seen after over-expression of skp2 in which the F box has been deleted and which is severely impaired in its ability to bind to the SCF complex (Figure 3e). Thus, this effect cannot be due to ubiquitin-mediated proteolysis of SCFskp2 targets. However, it is possible that skp2 binding disrupts the function of one of its targets, a positive cell cycle regulator, resulting in slowing of the cell cycle, although in this developmental context it is not clear what such a substrate would be. It has been suggested that in some cases, cdkis at low levels may be required for assembly of cdk complexes, so can act to stimulate the cell cycle, only becoming inhibitory above a certain stoichiometry . Binding by skp2 or F Box skp2 could disrupt this function. However, disruption of such a function of Xic1 in cdk complex assembly could not account for the F Box-dependent requirement for skp2 in primary neurogenesis.
Skp2 levels regulate primary neurogenesis in Xenopus; loss of skp2 results in formation of extra neurons (Figure 2) while skp2 over-expression inhibits neurogenesis (Figure 3). In vitro studies have shown that Xic1 is a potential target for skp2-mediated ubiquitination and destruction; skp2 can target Xic1 for degradation both in vitro and in vivo  (Figure 6). Supporting this hypothesis, Xic1 is required for primary neurogenesis; in its absence primary neurons do not form, mimicking the effect of skp2 over-expression, while over expression of Xic1 results in supernumery neurons within the usual stripes , similar to the pattern seen on injection of skp2 Mo. Interestingly, although Xic1 is a cdk inhibitor, it is not required for neurogenesis at the time of cell cycle exit, downstream of NeuroD. Instead, Xic1 acts at an early stage of neurogenesis in parallel with XNgnr1, the same point at which skp2 acts. Therefore, skp2 may regulate primary neurogenesis by targeting Xic1 for ubiquitin-mediated proteolysis. Most identified substrates of skp2 require cell cycle regulated phosphorylation, generally by cdks, to facilitate skp2 binding. Unusually, ubiquitination by SCFskp2 does not require the phosphorylation of Xic1 , indicating that Xic1 levels will be particularly sensitive to absolute levels of skp2 protein.
XNgnr1 over-expression induces extra neurons in neuroectoderm but this is blocked by skp2 over-expression. Can extra Xic1 rescue this loss of ectopic neurons? At the levels injected here, the co-injection of Xic1, skp2 and XNgnr1 frequently results in apoptosis, precluding further investigation. This may be a result of the combined mild pro-apoptotic effects of both XNgnr1 and Xic1 [22, 65] when they are co-injected. We would note, however, that Xngnr1 is the endogenous driver of formation of primary neurons in the normal stripes, these are suppressed by over-expression of skp2, and a partial rescue occurs when skp2 and Xic1 are co-injected. We show that Xic1 is required for normal primary neurogenesis, it is degraded by skp2, and a drop in its levels is crucial for over-expressed skp2 to inhibit neurogenesis in the neural plate. Thus, skp2 is perfectly placed to regulate Xic1 levels resulting in control of differentiation of primary neurons in vivo.
Over-expression of skp2 results in degradation of a significant proportion of co-expressed Xic1 protein (Figure 6b, c). However, increasing the amount of skp2 further does not result in full degradation of Xic1. In these assays, Xic1 is continually synthesised from micro-injected message and the level of remaining protein may represent an equilibrium between synthesised and degraded Xic1 protein. In addition, at high levels of skp2, it is likely that other components of the Scf E3 ligase complex become limiting. Skp2 mRNA injection has a small but somewhat inconsistent effect on levels of endogenous Xic1 protein in whole embryos that is made up of expression in epidermal, neural and mesodermal tissues. However, by dissecting out the neural plate and neural folds at mid-neurula stage, we can enrich for the population of endogenous Xic1 protein in differentiating primary neurons compared to mesodermal and epidermal Xic1, and when we do this we see that skp2 can target endogenous Xic1 for destruction more efficiently (Figure 6d). Xic1 plays an essential role in muscle differentiation . Interestingly, while skp2 over-expression inhibits neurogenesis, we see that it does not inhibit myotomal muscle differentiation (Figure 6e–h), indicating that it is unable to degrade Xic1 protein in the myotome. This could be due to either lack of other SCF complex members, modification or degradation of skp2 protein, modification of Xic1 or another unknown mechanism. Indeed, endogenously, skp2 is not expressed in muscle so the absence of any required co-factors might not be unexpected.
The mammalian homologue of Xic1, p27Kip1, is also targeted for ubiquitin-mediated proteolysis by the ubiquitin ligase KPC, where its destruction occurs after export from the nucleus . Homologues of its components KPC1 and 2 are found in Xenopus and are well conserved (76% and 73% identity with human KPC1 and 2, respectively; C Fiore-Heriche and AP, data not shown). Xic1 destruction in Xenopus eggs requires Xic1 to be in the nucleus , although it is not known whether later in development there may be an additional cytoplasmic Xic1 destruction pathway. As skp2 is not expressed in the myotome, such a pathway may control Xic1 levels in the developing muscle.
To determine further whether skp2 is acting on neurogenesis via its ability to regulate Xic1 levels, we investigated the effect of co-expression of skp2 and Xic1 on formation of primary neurons (Figure 7). Overexpression of skp2 inhibits neurogenesis while increasing Xic1 levels produces extra neurons: co-injection of the two results in an intermediate phenotype, demonstrating that a balance between levels of skp2 and Xic1 proteins regulates the number of differentiating primary neurons, again indicating that Xic1 is a bone fide in vivo substrate of SCFskp2. However, it should be noted that Xic1 protein expressed from injected mRNA accumulates to levels far higher than those usually found in embryos (Figure 6), yet rescue is not complete. We favour the possibility that there are unknown protein targets of SCFskp2, in addition to Xic1, that are involved in primary neuron differentiation, and that their stability is regulated in parallel with Xic1; levels of Xic1 and this additional target(s) must be restored to fully rescue primary neurogenesis in the presence of elevated skp2 protein. XNgnr1, the proneural protein that drives primary neurogenesis, is unstable but our preliminary data indicate it is unlikely to be a direct target of ubiquitin-mediated proteolysis by SCFskp2 (J Vosper, HB-P and AP, unpublished data). However, other cell cycle regulators known to be targets of SCFskp2, such as E2F1  and c-myc [11, 12], could play additional roles in regulating neuronal differentiation.
In conclusion, here we demonstrate a role for skp2 in regulating differentiation of primary neurons over and above any role it may have in regulating the cell cycle. Indeed, in Xenopus, at these early developmental stages, skp2's role in cell cycle progression appears to be minimal. Skp2 is widely expressed in the developing mouse so it is well placed to play a role in differentiation in mammalian embryos in addition to a role in cell cycle regulation.
Cancer cells divide inappropriately, but equally important is their failure to adopt a fully differentiated character and it is this that results in malignancy. Indeed, cancer may result from a failure to differentiate rather than from cell cycle defects per se  with cells reverting to a more embryonic phenotype. Skp2 is elevated in a range of tumours [38, 56], where our data indicate it may play a separable but complementary role in regulating cell cycle progression and differentiation. We would argue that any direct role in differentiation must be explained to understand the full impact of skp2 upregulation in cancer. In general, molecules that regulate cell cycle exit and differentiation may be crucial targets for cancer therapy, and if we are to make the best use of them we must have a greater understanding of how cell division and differentiation are co-ordinated during development. Identifying molecules with dual functions in these two processes is a good place to start.
Materials and methods
Plasmid construction and mutagenesis
To create skp2 without the F-box domain (F Box skp2), two separate fragments flanking the region to be deleted were amplified from skp2 plasmid DNA, using Taq and Vent DNA polymerases. The first fragment (amino acids 1–92 of wild-type skp2) was amplified using primers 5'-CGC AGG GAA TTC GCC ACC ATG CAC AGG AAA CAT CTT CAG GAG ATC TCG-3' and 5'-CGC AGT ACC GGT GAC TGA CTG AGC AAG-3'. The second fragment (amino acids 138–420) was amplified using primers 5'-GTC AGG ACC GGT GAT CTT ACT GGC AAA CAC GTG-3' and 5'-GCA CGC TAG GCC TTC ACA AGT AGT CCT TAT AGT TCA-3'. The PCR products were digested with Eco RI/Age I (fragment 1) or Age I/Stu I (fragment 2) and subcloned into the Eco RI/Stu I sites of pCS2+.
RNA/morpholino oligonucleotide injections
For generating capped mRNAs, vectors encoding XNgnr1 , XNeuroD , skp2, F-Box skp2, MAFbx, and ßgal were transcribed in vitro (mMessage mMachine Kit, Ambion (Applied Biosystems, Warrington UK). RNAs for XNgnr1 (50 pg), NeuroD (500 pg), skp2 (1 ng), F-Box skp2 (1 ng) or MAFbx (1 ng) were co-injected in a volume of 10 nl along with 100 pg of ßgal mRNA to act as a lineage tracer. Antisense morpholino oligonucleotide skp2 Mo (20–40 ng; 5'-ATG TTT ACC TGT GCA TGT TCA TCA G-3') or a five base-pair mismatch control morpholino (30–40 ng; 5'-ATC TTT AGC TCT GCA TCT TCT TCA G-3') (GeneTools LLC Philomath, Oregon, USA.), were also coinjected with 100 pg of ßgal mRNA.
Xenopus whole-mount in situ hybridisation, antibody staining, and in situ hybridisation on sections
Embryos were raised until indicated stages, fixed in MEMFA for 1.5 hours, X-gal (5-bromo-4-chloro-3-indolyl β-galactopyranoside) stained and analyzed by whole mount in situ hybridisation . Double in situ hybridisations were performed according to . Linearised plasmids from Sox3 (Not1/T7), Bluescript N-tubulin (BamH1/T3) , pCS2+ (T7 promoter repaired; Eco RI/T7) skp2 were used to generate antisense RNA probes by in vitro transcription with digoxigenin-11-UTP (Roche, Welwyn Garden City, UK.) and detected using alkaline-phosphatase-conjugated anti-digoxigenin antibodies (Roche). BM purple was used as a substrate (Roche). pH3 immunostaining was carried out as previously described  using a 1:1,000 dilution of primary antibody anti-pH3 (TCS Biologicals, Buckingham, UK.) pH3-positive cells were counted within regions of equal surface area on injected and uninjected bilateral halves of each embryo; percent changes were then determined for each embryo as the ratio of injected/uninjected values. Percent values shown represent averaged results. In situ hybridisation on tissue sections was carried out as previously described . Alternatively, embryos were post-fixed in MEMFA, embedded in gelatin/albumin and sectioned by Leica VT1000M vibratome, and mounted in 100% glycerol, (60 micron sections; Figure 1h, i). In Figure 1i, staining of deep mesodermal tissues appears light blue due to poor penetrance of the BM purple staining component.
Protein extracts were prepared as previously described . Skp2 was detected using an affinity purified polyclonal antibody , p27Xic1 was detected using an affinity purified polyclonal antibody . Blots were probed with monoclonal anti-tubulin antibody (1: 2,000; Sigma, Gillingham, UK) where appropriate as a loading control. Usually, protein from approximately one embryo equivalent or five dissected neural plates was loaded per lane.
We are grateful to Laura Itzhaki, Shinichi Ohnuma, Christelle Fiore-Heriche, Bill Harris and Christine Holt for helpful discussions, Paul Ko Ferrigno for technical advice, Sonia Tarazona-Campos for statistical advice, and Jonathan Vosper for providing reagents. HB-P was supported by the Harrison Watson Jr Studentship, Clare College, Cambridge. HW was supported by a studentship from the Wellcome Trust. PRY was supported by grants from the National Institute of Health (1RO1-GM066226) and the US Army Department of Defence (DAMD17-02-1-0589). AP and IH were supported by BBSRC grant BB/C004108/1.
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