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The Xenopus laevis cyclin dependent kinase inhibitor p27Xic1 has been shown to be involved in exit from the cell cycle and differentiation of cells into a quiescent state in the nervous system, muscle tissue, heart and retina. We show that p27Xic1 is expressed in the developing kidney in the nephrostomal regions. Using overexpression and morpholino oligonucleotide (MO) knock-down approaches we show normal levels of p27Xic1 regulate pronephros organ size by regulating cell cycle exit. Knock-down of p27Xic1 expression using a MO prevented myogenesis, as previously reported; an effect that subsequently inhibits pronephrogenesis. Furthermore, we show that normal levels of p27Xic1 are required for somite segmentation also through its cell cycle control function. Finally, we provide evidence to suggest correct paraxial mesoderm segmentation is not necessary for pronephric induction in the intermediate mesoderm. These results indicate novel developmental roles for p27Xic1, and reveal its differentiation function is not universally utilised in all developing tissues.
In the amphibian Xenopus laevis, the first fully functional embryonic kidney to form is the pronephros. It is a paired organ, consisting of four distinct components; the glomus, coelomic cavity, nephrostomes and tubules (which are further characterized as proximal, intermediate, distal and connecting tubules), together these components form a non-integrated nephron.1–4 The pronephros develops from nephrogenic mesenchyme within the intermediate mesoderm lateral to the anterior somites.5–8 A signal from the somites establishes the intermediate mesoderm; therefore myogenesis is a necessary prerequisite to pronephrogenesis.9–11 The pronephros is a simple organ to study, showing both morphological and physiological similarities to more complex kidney forms, the meso- and metanephros, which make it an ideal model to study with reference to kidney development.3
p21Cip1, p27Kip1 and p57Kip2 are mammalian members of the Cip/Kip family of Cdk inhibitors (CKIs) that play important roles in development, particularly in cell fate determination, in addition to their function of blocking cell cycle progression.12 In Xenopus, three Cip/Kip family members have been described; p27Xic1, p16Xic2 and p17Xic3, the latter two are orthologues of p21Cip1 and p27Kip1 respectively.13–16 The expression of p16Xic2 and p17Xic3 is highly developmentally regulated, suggesting they might be involved in cell fate determination in a tissue-specific manner.15 However, expression was not detected within the pronephros. The other homologue is p27Xic1, which shows structural and functional similarities to p21Cip1, p27Kip1 and p57Kip2.16,17 The expression of p27Xic1 in early and tail bud embryos has been described and shown to play a role in neurogenesis, myogenesis, gliogenesis and cardiogenesis where it regulates cell fate and differentiation, in a similar manner to mammalian homologues.13,14,18–20 Analysis of the p27Xic1 domains has revealed the region responsible for this regulatory effect overlaps with but is distinct from the Cdk-cyclin binding domain located in the N-terminus.13,14,18 The phenotypic effect of p27Xic1 depletion in X. laevis, using morpholino oligonucleotides, on both muscle and neural development can be rescued by co-injecting the human homologue p21Cip1.13,14 If p27Xic1 functions in a similar manner to the mammalian p21Cip1, then it may be involved during development of the Xenopus kidney.
Here, we describe the characterization of p27Xic1 in X. laevis pronephric development. We report that p27Xic1 expression is detected within the developing pronephros at tadpole stages by in situ hybridization. We interfere with the normal expression of this gene by targeted overexpression, or knock-down of the endogenous protein with a specific antisense morpholino oligonucleotide (MO). Overexpression of p27Xic1 disrupted somitogenesis and reduced the size of the pronephric anlagen. MO knock-down also reduced the size of the pronephric anlagen and inhibited myogenesis. Pronephric phenotypes were lost upon injection of a mutant of p27Xic1 that had inactivated cyclin/cdk binding capabilities, suggesting p27Xic1 is not involved in regulating differentiation in the pronephros. These experiments identify previously unrecognized, functional roles for p27Xic1 in X. laevis pronephros development and somitogenesis and confirm the importance of this gene in diverse developmental processes.
p27Xic1 expression has been previously shown in the notochord, neural plate, differentiating muscle and in the eye and brain but its distribution has not been reported past stage 30 in whole embryos.13,14,19,21 To analyse p27Xic1 expression in pronephric development, we investigated expression in these stages and later using an improved whole mount in situ hybridization protocol.
p27Xic1 expression in early stage embryos followed similar domains to that previously reported (data not shown) but is also detected initially in the dorso-anterior part of the pronephric region and then in the region corresponding to the nephrostomes between stages 27 and 32 (Fig. 1). Prior to and past these stages no pronephric expression of p27Xic1 was detected by in situ hybridization. In conclusion, p27Xic1 expression is temporally and spatially appropriate for a role in pronephros development.
In order to examine the overexpression phenotype of p27Xic1 mRNA in vivo, we injected p27Xic1 mRNA and p21Cip1 mRNA into a single V2 blastomere of embryos at the 8-cell stage, βgal mRNA was co-injected to act as a lineage tracer. This targeted mRNA to the developing pronephric and somitic compartments. All microinjections described subsequently are carried out in this way unless otherwise stated. Little βgal staining was observed in pronephroi due to its immunostaining by antibody or in situ analysis. However, correct targeting could be determined by βgal staining in the somites. In each case the largest amount of mRNA (20–50 pg) that did not cause gross developmental defects was injected. Injected embryos were cultured to stage 41, correctly targeted embryos were sorted for βgal staining and then subjected to whole mount antibody staining with 3G8, which detects nephrostomes and proximal pronephric tubules, and 4A6, which detects intermediate and distal pronephric tubules.3 The effects on pronephric structure were scored by comparing the lineage labelled injected side against the control, uninjected side, of the same embryo and Chi squared analysis was carried out to assess the statistical significance. All experiments involving embryo microinjection were repeated multiple times and each time statistical analysis was carried out. Due to slight differences in embryo batches, results from individual repeat experiments were not pooled, a representative experiment is quoted in each case. Control embryos injected with βgal mRNA alone had a negligible effect on proximal tubule (2% reduced, n = 58) or intermediate and distal tubule (0% affected, n = 58) morphology (Fig. 2A). In embryos injected with p27Xic1 mRNA, the proximal tubules were reduced on the injected side in 91% of embryos (n = 23) (Fig. 2B). Inspection of the intermediate and distal tubules revealed that p27Xic1 mRNA also reduced their size to a similar degree (83%, n = 23) (Fig. 2B). Chi-squared analysis confirmed that the pronephros of p27Xic1 mRNA injected embryos was significantly reduced in size when compared to βgal mRNA injected embryos (p < 0.05).
p21Cip1 has functional and sequence homology with p27Xic1 and has been used to rescue the effect of the p27Xic1 MO.13 Injecting p21Cip1 mRNA produced a similar phenotype to that of p27Xic1 mRNA (Fig. 2C), the pronephric tubules were statistically significantly reduced in 82% of embryos (n = 52, p < 0.05).
p27Xic1 possesses three characteristic domains (Fig. S1A). The N-terminal half contains a Cyclin/Cdk binding domain, highly conserved between p21Cip1, p27Kip1 and p57Kip2. The C-terminal half possesses a PCNA-binding domain, also found in p21Cip1, and a QT-domain, a potential cdc2 phosphorylation site that occurs in p27Kip1.22,23 Similar to full length p27Xic1, p27Xic1 N (amino acids 1–96) inhibits Cyclin/Cdk kinase activity and stops cell division before MBT. p27Xic1 C (amino acids 97–210) can inhibit PCNA driven replication but cannot stop cell division before MBT.19 A third construct, p27Xic1 #2 (amino acids 35–96), possesses Cdk2 inhibitory activity but has been shown to lack the Müller cell inductive activity observed with p27Xic1 N in the Xenopus retina19 and lack the ability to promote primary neurogenesis.13 In order to investigate the effect these constructs had on pronephric development, we injected p27Xic1 N mRNA, p27Xic1 C mRNA and p27Xic1 #2 mRNA into a V2 blastomere as previously described. Inspection of p27Xic1 N mRNA injected embryos, revealed a significant reduction in proximal tubule (58% reduced, n = 33, p < 0.05) and intermediate and distal tubule (40% reduced, n = 33, p < 0.05) morphology similar to full length p27Xic1 mRNA when compared against the control, un-injected side (Fig. 2D). Therefore, p27Xic1 N, like the full length protein, perturbed pronephric development. In contrast, analysis of pronephric tubule morphology after p27Xic1 #2 mRNA (n = 34) and p27Xic1 C mRNA (n = 32) injections showed 0% effect on the pronephric development, similar to control embryos injected with βgal mRNA (Fig. 2E and F). In the absence of western analysis comparing the amounts of protein translated from the different constructs, it is formally possible that the differences in phenotype observed are due to differences in protein amounts as a consequence of different stability or translation efficiency.
In order to separate the effects of overexpressing p27Xic1 on cell cycle from potential later roles in differentiation, we injected a mutant of p27Xic1 that had inactivated cyclin and cdk binding domains, we term this mutant p27Xic1 CK− (Fig. S1B illustrates sites of mutagenesis, this mutant was a kind gift from Mehregan Movassagh, Cambridge University). Injection of p27Xic1 CK− mRNA failed to show a significant pronephric phenotype at stage 41, as observed by whole mount 3G8/ 4A6 immunostaining (8% reduced, n = 28, p > 0.05) (Fig. 2G).
To investigate whether depletion of p27Xic1 affects pronephric development, we utilized a previously characterized anti-sense morpholino oligonucleotide (MO) designed to be complementary to p27Xic1, and shown to specifically knock down p27Xic1 translation in vivo in our hands by western blot analysis13,20 (for MO sequence see Fig. S1C). Indeed, we have shown p27Xic1 MO knocked down p27Xic1 translation completely in vitro (Figs. S2 and S3). To determine if p27Xic1 depletion affected development of the pronephros, we targeted the p27Xic1 MO with βgal mRNA to the pronephric region as previously described. Embryos were allowed to develop to stage 32, when they were fixed and whole mount in situ hybridized for nephrin expression (a glomus marker), or were allowed to develop to stage 41 where whole mount antibody staining using 3G8 and 4A6 was performed. Injection of a Control MO had no effect on glomus development, reducing nephrin expression in a statistically insignificant 3% of embryos (n = 61, Fig. 3A), confirming that the process of injecting a random sequence MO does not adversely affect development. MO knock-down of p27Xic1 inhibited glomus development, 86% had reduced nephrin expression (n = 22, Fig. 3B). Overexpressing p27Xic1 reduced nephrin expression in 66% of embryos scored (n = 48, Fig. 3C). Additionally, injection of a Control MO had 0% effect on the morphology of the pronephric tubules (n = 24) as observed by 3G8 and 4A6 antibody staining (Fig. 3D). However, 3G8 immunostaining was reduced after p27Xic1 MO injection in 93% of embryos (n = 27) (Fig. 3E). Analysis of the intermediate and distal tubule morphologies revealed p27Xic1 MO reduced their size in 81% of embryos (n = 27).
Since p21Cip1 has functional homology with p27Xic1, but is not translationally inhibited by the p27Xic1 MO (Fig. S3),13 we attempted to rescue the p27Xic1 MO phenotype by coinjecting p21Cip1 mRNA with the p27Xic1 MO into a V2 blastomere of an 8-cell stage embryo. Embryos were co-injected with 20 ng p27Xic1 MO, 20 pg p21Cip1 mRNA, and βgal mRNA to act as a lineage tracer, and cultured to stage 41. Correctly targeted embryos were selected and whole mount antibody stained using 3G8 and 4A6. Alongside these co-injections, single injections of 20 ng p27Xic1 MO and 20 pg p21Cip1 mRNA were also performed to act as controls. Both p27Xic1 MO (78% reduced, n = 27) and p21Cip1 mRNA (91% reduced, n = 34) inhibited pronephros development. However when 20 ng p27Xic1 MO was coinjected together with 20 pg p21Cip1 mRNA pronephrogenesis is almost completely rescued, only a very small proportion of embryos had a reduced pronephros (9%, n = 23, p > 0.05, Fig. 3F). We have also attempted this rescue experiment with 10 pg p21Cip1 mRNA co-injected with 20 ng p27Xic1 MO. At these concentrations, we observed a reduction in pronephros size (58%, n = 26, data not shown).
Programmed cell death (PCD) is a key developmental process required by multi-cellular organisms to eliminate unwanted cells. Recently, molecular connections between cell cycle exit and PCD have been established.24 We have previously shown injection of p27Xic1 mRNA and the p27Xic1 MO, at the concentrations used here, did not increase levels of apoptosis during early development.13,14,19,20 To confirm this result, and ensure phenotypic pronephric reductions after p27Xic1 mis-expression were not a result of ectopic apoptosis, we inhibited apoptosis by co-injecting the apoptotic inhibitor BclXL with p27Xic1 mRNA or p27Xic1 MO. Injecting BclXL mRNA with βgal mRNA into one cell of a two cell stage embryo significantly reduced apoptosis in 36% of embryos assayed by TUNEL analysis at stage 22 (n = 55, p < 0.05, Fig. S4), indicating the correct biological activity of this mRNA. We injected p27Xic1 mRNA and p27Xic1 MO with or without BclXL mRNA into one cell of a two cell stage embryo and left the embryos to develop to stage 22. Expression of Lim-1, an early marker for the pronephros anlagen, was then detected by in situ hybridization (Fig. 4). The pronephros anlagen was reduced in 92% of embryos injected with the p27Xic1 MO (n = 24) (Fig. 4B) and 74% of embryos injected with p27Xic1 mRNA (n = 38) (Fig. 4D). The same phenotypes with similar degrees of severity were observed when BclXL was co-injected with the p27Xic1 MO (97% reduced, n = 41) (Fig. 4C) and p27Xic1 mRNA (84% reduced, n = 37) (Fig. 4E). In conclusion, PCD is not the mechanism by which pronephrogenesis is inhibited following injection of p27Xic1 mRNA and p27Xic1 MO.
To test whether an effect on cell cycle could explain the pronephric phenotype, we injected p27Xic1 mRNA and p27Xic1 MO into one cell of a two cell stage embryo and allowed development to proceed to stage 20, where Lim-1 in situ hybridizations and anti-phosphohistone H3 (pH3, a marker of dividing cells) immunostains were performed on the same embryos. Overexpressing p27Xic1 reduced Lim-1 expression in 75% of scored embryos (n = 24), similarly 84% of embryos injected with the p27Xic1 MO had reduced Lim-1 expression (n = 31) (Fig. 5B and C). Injection of p27Xic1 mRNA reduced the total number of pH3 immunostained cells on the injected side by 63% on average (n = 11) (Fig. 5E). However, MO depletion of p27Xic1 had no statistically significant effect on pH3 immunostaining. Injection of the Control MO had no significant effect on either Lim-1 expression (2% reduced, n = 55) or pH3 immunostaining (4% average reduction, n = 10) (Fig. 5A). Injection of the cyclin/cdk mutant p27Xic1 CK− mRNA showed that on average out of 10 embryos numerically scored for total pH3 immunostained cells, there was a statistically insignificant increase of 3.44% on the injected side over the un-injected side (p > 0.05) (Fig. 5D and E), confirming the lack of cell cycle inhibitory function in this mutant.
These results suggest that overexpressing p27Xic1 caused premature cell cycle exit, reducing the number of cells contributing to the anlagen, and therefore decreasing pronephros size. In contrast, reduction in size of the pronephros following p27Xic1 MO knock-down could not be attributed to a cell cycle effect.
To determine if p27Xic1 depletion induced gross developmental defects which could inhibit pronephrogenesis, we first injected the equatorial region of both cells of a 2-cell stage embryo with the p27Xic1 MO, along with βgal mRNA to act as a lineage tracer. Embryos were left to develop to stage 10/11, when they were fixed, stained for the lineage label and whole mount in situ hybridized for a marker of the early mesoderm, Xbrachyury (Xbra).25 Injection of the Control MO had 0% effect on Xbra expression (n = 73, Fig. 6A). Injection of the p27Xic1 MO also caused no effect (5% reduction n = 105, Fig. 6B). Although, V2 blastomere injections of the Control MO had no effect on MyoD or Lim-1 expression (n = 36) (Figs. 6C and S5Aa), injections of p27Xic1 MO caused severe reduction in expression of both the muscle marker MyoD, and an early pronephric anlagen marker, Lim-1 (79%, n = 33) (Figs. 6D and S5Ab). We suggest normal levels of p27Xic1 are required for myogenesis, the first phase of somite development, as loss of p27Xic1 expression inhibited MyoD expression. As early mesoderm development is not perturbed by p27Xic1 depletion, we suggest this effect on myogenesis is direct.
To test the effects overexpressing p27Xic1 had on myogenesis and somitogenesis, we injected p27Xic1 mRNA into a V2 blastomere of embryos at the 8-cell stage. The embryos were left to develop to stage 24, then fixed and subjected to double in situ hybridization for MyoD and Lim-1 expression. Overexpressing p27Xic1 caused the expected reduction in Lim-1 expression in 78% of embryos (n = 27) (Fig. 6E). 76% of these affected embryos also had fused, un-segmented somites, indicated by MyoD and MHC in situ analysis (MHC data not shown), without reducing MyoD and MHC expression. This effect could be attributed to cell cycle function since no significant effect on the pronephros anlagen formation or myogenesis, as seen by Lim-1/MyoD double in situ hybridizations, was observed (4.7% reduced Lim-1, 0% disrupted MyoD, n = 43) after p27Xic1 CK− overexpression (Fig. 6F). Thus we conclude that the reduced pronephros phenotype and the non-segmented somite phenotype we observed when we overexpressed p27Xic1 were due to premature cell cycle exit through inhibition of cyclinA2/cdk2 activity.
To confirm that the reduction in the size of the pronephros we observed when we overexpressed p27Xic1 mRNA could be achieved by premature cell cycle exit, we interfered with normal cell division by incubating embryos from stage 10.5 in the cell division inhibitors Hydroxyurea and Aphidicolin (HUA).27 HUA treatment inhibited cell division, as observed by an average 82% reduction in the number of positively stained pH3 cells on the left side of the embryos treated with HUA compared to the controls (Fig. S5, n = 10). At stage 41, 3G8/4A6 antibody staining was reduced in all embryos treated with HUA, with 4A6 staining completely absent (n = 14) (Fig. 7A). At these later stages embryos incubated in HUA had severely perturbed and delayed development. HUA treatment, like p27Xic1 mRNA overexpression, inhibited pronephros anlagen formation and disrupted somite segmentation in all the embryos treated (n = 17) (Figs. 7B and C; S7A and B). Incubation of embryos in HUA from stage 17 had no effect on muscle segmentation or pronephros anlagen formation (Fig. S7C and D).
p35.1 is a member of the p35 family, a group of proteins that bind to and activate cdk5. Philpott et al. showed p35.1 mRNA overexpression disrupted somite segmentation in a similar manner to our p27Xic1 mRNA overexpression phenotype.28 Reduced myogenesis is known to inhibit pronephrogenesis.9–11 To observe if disrupted somite segmentation affects pronephros development we injected p35.1 mRNA. Embryos injected into a V2 blastomere were then cultured to stage 24, where Lim-1/MyoD double in situ hybridizations were performed, and stage 41, where whole mount 3G8/4A6 immunostaining was carried out. At stage 24 we observed a similar muscle phenotype to that of overexpression of p27Xic1 mRNA, 69% of embryos had disrupted somite segmentation (n = 23). However, in 75% of embryos with disrupted somite segmentation Lim-1 expression covered a broader domain, but was not reduced (Fig. 8A and B). The remaining embryos showed no Lim-1 expression defects. At stage 41, p35.1 mRNA overexpression had no statistically significant effect on 3G8/4A6 staining (p > 0.05, n = 24, Fig. 8C). Thus the early broader domain of the pronephros anlagen induced by p35.1 mRNA injection was sufficient to form a mature pronephros in later stage embryos. In conclusion, we suggest correct somite segmentation is not essential for pronephros development.
The expression of p27Xic1 has been previously shown in the differentiating muscle and notochord at neurula stages and at lower levels in the neural plate and heart.13,19,20 We show by in situ hybridization and RT-PCR for the first time, p27Xic1 is expressed within the pronephros during development. Strong expression in the dorso-anterior region of the pronephros between stages 27 and 32, suggest p27Xic1 could have a role in pronephric development. To ascertain whether p27Xic1 is required for pronephros development, overexpression and depletion studies were performed.
Overexpressing p27Xic1 inhibited formation of all pronephric compartments. Injection of different domains of p27Xic1 mapped the N-terminus (amino acids 1–96) as the effector region inhibiting pronephrogenesis. Moreover, depleting endogenous p27Xic1 translation using a MO also inhibited development of distinct pronephric regions. We have demonstrated that overexpression and MO knock down of p27Xic1 indirectly inhibited formation of the pronephros, by different mechanisms. We have shown ectopic apoptosis was not a mechanism by which pronephros development was inhibited, and previous studies have shown that p27Xic1 mis-expression does not increase levels of apoptosis.13,14,19,20
Overexpressing p27Xic1 inhibited cell division and injection of the cyclin and cdk binding mutant, p27Xic1 CK−, had no effect on cell division or pronephros development. Thus injection of p27Xic1 mRNA impeded pronephrogenesis by inhibiting cdk2 kinase activity. Recent research has identified CKIs such as p27Xic1 and the mammalian Cip/Kip family as multifunctional proteins involved not only in cell cycle exit but also cell differentiation and migration.29 p27Xic1 has been shown to be involved in muscle, neural and heart differentiation, independent of its cell cycle exit function.13,14,20 p21-/- mutant mice have hypomyelinated cerebella due to failure of oligodendrocyte differentiation, importantly these mice had no aberrant cell cycle exit phenotypes.30 p27Kip1 has been shown to be involved in neuronal differentiation and migration.31 The N-terminus of p27Kip1 contains both the conserved cell cycle exit function and an uncharacterized differentiation function with the ability to stabilize Neurogenin-2. Nguyen et al. used a mouse homozygous for a cell cycle mutant allele of p27Kip1, p27CK−, to show the increase they observed in neuronal markers was independent of cell cycle exit. We overexpressed a similar cyclin/cdk mutant, p27Xic1 CK− which failed to show a pronephric phenotype. This suggests overexpression of p27Xic1, with concomitant cell cycle arrest, results in failure of the pronephric anlagen to proliferate. The function of p27Xic1 in myotome differentiation is separable from its ability to slow the cell cycle,14 so this differentiation function of p27Xic1 in the myotome will affect pronephric induction as myogenesis is a necessary prerequisite to pronephrogenesis.9–11 Since p27Xic1 CK− mRNA retains the differentiation function, but did not alter pronephrogenesis, we suggest that in contrast to other organs, pronephros development is only affected by cell cycle effects. Thus the effects of CKIs on differentiation may vary between tissues, for example p21Cip1 overexpression inhibits keratinocyte differentiation32 but promotes myelomonocytic leukemia cell differentiation.33
One of the earliest signals to the intermediate mesoderm to form pronephros originates from the anterior somites.9–11 Thus inhibition of myogenesis by the p27Xic1 MO may be sufficient to inhibit pronephros formation. Therefore, we suggest the p27Xic1 MO pronephric phenotype arises as an indirect effect, reduced myotome formation failing to induce the pronephric anlagen. Since MO knockdown of p27Xic1 expression did not inhibit expression of the early mesodermal marker Xbrachyury, our experiments suggest that the effect of p27Xic1 depletion on myogenesis was direct, and not a consequence of perturbed early mesoderm development.
MyoD has been shown to be stabilized by p57Kip2 in growing myoblasts through repression of Cyclin E/Cdk2 phosphorylation of MyoD, and by direct binding to and stabilization of MyoD.34,35 It is possible p27Xic1 interacts directly with MyoD, which would promote MyoD expression due to the positive feedback loop it has on its own expression.36 This would explain why MyoD expression is lost in p27Xic1 depleted embryos. Moreover, MyoD has been shown to stimulate expression of p21Cip1 in C2C12 cells and further control cell proliferation by acting as a negative intercessor of MRF4, which accelerates cell proliferation.37 Whether MyoD induces expression of cell cycle inhibitors to ensure cell cycle exit alone, or in addition to ensuring its stability in the cell, is not known.
The clock and wavelength model of segmentation38 requires synchronous cell division to aid allocation of somites within the presomitic mesoderm. In the myotome, p27Xic1 expression overlaps with MyoD expression from stage 15.14 Thus expression of p27Xic1 is temporally and spatially appropriate to have a role in directing cell cycle exit, and therefore somitogenesis. During gastrulation, mesodermal cells in the primitive streak divide synchronously in mice and chick embryos,39–41 this synchrony is maintained in somitogenic cells. Chick embryos incubated for 24 hours in S-phase inhibitors such as hydroxyurea display fused somites as a consequence of undirected cell cycle exit.42 p27Xic1 is a cell cycle inhibitor, thus the non-segmentation pattern observed when p27Xic1 is overexpressed is not surprising. Nevertheless, this result establishes a previously unrecognized role for p27Xic1 in somite segmentation in X. laevis.
The p27Xic1 MO reduced the somite size, as observed by reduced MyoD expression, consequently inhibiting pronephrogenesis. However, when p27Xic1 mRNA was overexpressed somite formed, but segmentation was disrupted. To see if disrupted muscle development inhibited pronephrogenesis we overexpressed p35.1, a gene known to disrupt somite segmentation but which is not expressed in the pronephros.28 These embryos displayed a slightly enlarged pronephros anlagen which subsequently recovered to form a normal mature pronephros at stage 41. Thus disrupted somite segmentation alone is insufficient to affect development of a mature pronephros. Overexpression of p27Xic1 did reduce mature pronephros development as well as disrupting somite segmentation, thus normal levels of p27Xic1 are essential for pronephrogenesis. We suggest this additional effect is due to premature cell cycle exit reducing the number of cells that can contribute to the pronephros anlagen. Thus in the pronephros, p27Xic1 does not promote differentiation like has been observed in primary neurogenesis and cardiogenesis.13,20
Whole-mount in situ hybridization was carried out as described elsewhere.43 The embryos were fixed in MEMFA (0.5 M MOPS, pH 7.4, 100 mM EGTA, 1 mM MgSO4, 4% formaldehyde) and linearized plasmid from p27Xic1 (XhoI/pBS), MyoD (HindIII/T7), MHC (NcoI/SP6) and Lim-1 (XhoI/T7) was used to generate digoxigenin-11-UTP-labelled (Boehringer Mannheim) antisense RNA probes from the polymerases indicated. Probes were visualized using anti-DIG-alkaline phosphatase secondary and NBT/BCIP for the color reaction according to the manufacturer's recommendations (Boehringer Mannheim).
Embryos were obtained by in vitro fertilization of hormonally stimulated Xenopus laevis and staged according to Nieuwkoop and Faber.1 Standard embryological procedures were used as described by Jones and Woodland.44 Embryos were dejellied in 2% cysteine hydrochloride pH 8 and cultured in 1/10th BarthX.
Capped RNAs were synthesized in vitro from p27Xic1,16 p27Xic1 N, p27Xic1 C, p27Xic1 #2,19 p21Cip1,45 p35.1,28 and p27Xic1 CK− using the SP6 Message Machine Kit (Ambion). Pod-1 mRNA46 was synthesized using T7 Message Machine Kit (Ambion). Typically 50 pg p27Xic1, p27Xic1 CK− and p27Xic1 N, 20 pg p21Cip1, 80 pg p27Xic1 #2 and p27Xic1 C, 2 ng p35.1 and 400 pg βgal mRNA was injected. The p27Xic1 antisense morpholino oligonucleotide used was: 5′-GCA GGG CGA TGT GGA AAG CAG CCA T-3′ and Pod-1 MO is: 5′-CGG TGG ACA TGA TCT GTT ATG CTG C-3′ (Gene Tools LLC). The control morpholino is a random sequence of the same length. Typically 20 ng of p27Xic1 MO and Control MO was injected. Embryos were dejellied and injected with mRNA alone or in combination with MO (as specified in the text) into one blastomere of a 2-cell stage embryo or a V2 blastomere of an 8-cell stage embryo to target the future pronephros,47,48 under 5% Ficoll in BarthX.
Whole mount immunohistochemistry was performed using standard methods on MEMFA fixed embryos. The primary antibodies used were monoclonal antibody 3G8, which detects the proximal tubules, and 4A6, which detects the intermediate and distal tubules.3 The secondary antibody was alkaline phosphatase-conjugated goat anti-mouse (Sigma). BCIP/NBT (Boehringer) or Fast Red TR/Napthol AS/MX (Sigma) was used for the color reaction, according to the manufacturer's recommendations. The primary antibody used to detect phosphohistone H3 was rabbit polyclonal IgG anti-phospho- Histone H3 (Ser10) (Upstate). For these experiments the secondary antibody was alkaline phosphatase-conjugated goat anti-rabbit (Sigma).
Total RNA from whole embryos and pronephroi were isolated and used for RT-PCR as described by Barnett et al.49 Primers used in this study are as follows. p27Xic1 primers: 5′-CAT CGA GCT CAG CAC TCA CA-3′ and 5′-GAC AGT CGG ACG CCT GGA TT-3′ (this work). ODC primers: 5′-GGA GCT GCA AGT TGG AGA-3′ and 5′-TCA GTT GCC AGT GTG TGG TC-3′.50
mRNA alone, or with MO, was translated in vitro in the Rabbit Reticulocyte Lysate System (Promega) with 35S-Met according to the manufacturer's protocol. Reactions (5 µl) were denatured at 95°C in 2xSDS loading buffer51 and run on a 12% (w/v) SDS-PAGE resolving gel using a vertical minigel apparatus for 2 hour at 100 V. The gel was exposed to Kodak X-ray film overnight at room temperature, before being developed.
We would like to thank Karine Massé for advice on molecular techniques and unpublished TUNEL assays, Mehregan Movassagh for making and supplying the p27Xic1 CK− mutant, Ian Horan for helpful comments and Paul Jarrett for maintenance of frogs. This work was supported by BBSRC grant, BB/C00406X/1 and The Wellcome Trust.
Previously published online: www.landesbioscience.com/journals/organogenesis/article/9973