Polyps of the cnidarian Hydra maintain their adult anatomy through two developmental organizers, the head organizer located apically and the foot organizer basally. The head organizer is made of two antagonistic cross-reacting components, an activator, driving apical differentiation and an inhibitor, preventing ectopic head formation. Here we characterize the head inhibitor by comparing planarian genes down-regulated when β-catenin is silenced to Hydra genes displaying a graded apical-to-basal expression and an up-regulation during head regeneration. We identify Sp5 as a transcription factor that fulfills the head inhibitor properties: leading to a robust multiheaded phenotype when knocked-down in Hydra, acting as a transcriptional repressor of Wnt3 and positively regulated by Wnt/β-catenin signaling. Hydra and zebrafish Sp5 repress Wnt3 promoter activity while Hydra Sp5 also activates its own expression, likely via β-catenin/TCF interaction. This work identifies Sp5 as a potent feedback loop inhibitor of Wnt/β-catenin signaling, a function conserved across eumetazoan evolution.
The freshwater Hydra polyp, which belongs to Cnidaria, a sister group to Bilateria, has the remarkable talent to regenerate any lost body parts, including a fully functional head. Hydra, which is made of two cell layers, external named epidermis and internal named gastrodermis, shows a polarized tubular anatomy with a head at the apical/oral pole and a foot at the basal/aboral one, both extremities being enriched in nerve cells (Fig. 1a). Remarkably, the cnidarian oral pole has been proposed to correspond to the posterior end of bilaterians1. Head regeneration relies on the rapid transformation of a piece of somatic adult tissue, the amputated gastric tube, into a tissue with developmental properties named head organizer, which directs the patterning of the regenerating tissue (reviewed in2,3,4) (Fig. 1b). This process is highly robust in Hydra, occurring after bisection at any level along the body column. The concept of organizer was first discovered by Ethel Browne who performed lateral transplantation experiments between pigmented and depigmented Hydra5. By grafting a non-pigmented piece of head onto the body column of a pigmented host, she observed the development of an ectopic axis predominantly made of pigmented cells, demonstrating the recruitment of host cells by the graft. This discovery was later confirmed in hydrozoans6,7,8,9,10 but also in vertebrates where organizers play an essential role during embryonic development11. In Hydra regenerating its head, the organizer gets established within 10 to 12 h after mid-gastric bisection, restricted to the head-regenerating tip within the first 24 h, remaining stable until the new head is formed and subsequently persisting as a homeostatic head organizer9.
The Hydra model also helped understand the dual structure of organizers. By comparing the efficiency of apical grafts to induce ectopic axis on intact or decapitated hosts, Rand et al. showed that the Hydra head organizer exerts two opposite activities, one activator that promotes apical differentiation, and another inhibitory that prevents the formation of supernumerary or ectopic heads12. In Hydra the inhibitory activity is graded along the body axis, maximal at the apical pole8, and tightly modulated during head regeneration, rapidly decaying after amputation and slowly recovering13. Gierer and Meinhardt used the results obtained from a series of transplantation experiments to propose a general mathematical model of morphogenesis14. Their model revisits the Turing model based on the reaction-diffusion model, where two substances that exhibit distinct diffusion properties and interact with each other, form a minimal regulatory loop that suffices for de novo pattern formation15. Gierer and Meinhardt posed that the activation component acts over short-range distance and the inhibition one over long-range distance. They distinguished between “the effective concentrations of activator and inhibitor, on one hand, and the density of their sources on the other”14. These models proved to efficiently simulate basic properties of pattern formation and to fit molecular data in a variety of developmental contexts16.
In Hydra, the Holstein lab identified Wnt3 as a growth factor fulfilling the criteria of the head activator, expressed locally at the tip of the head in intact Hydra, rapidly re-expressed in head-regenerating tips after amputation, and able to trigger an autocatalytic feedback loop17,18,19. Concerning the head inhibitor necessary to maintain a single head in homeostatic polyps and to develop a single head in budding and regenerating contexts, several attempts were made to characterize it, either biochemically or genetically. A protease-resistant small hydrophilic molecule was identified, exhibiting an apical to basal graded activity although with some activity also detected in the basal disc20,21. This last property discouraged from any further characterization. A genetic screen identified a Hydra ortholog of the vertebrate Wnt dickkopf inhibitors, named hyDkk1/2/4, which efficiently antagonizes Wnt activity in Xenopus22. However, Dkk1/2/4 is not expressed apically, being negatively regulated by Wnt/β-catenin signaling and its downregulation does not induce a multiheaded phenotype22,23. A recent study suggests that Hydra Thrombospondin might be involved in head inhibition, however its downregulation does not lead to a multiheaded phenotype24. Therefore, the molecular nature of the negative regulator(s) of the Hydra head organizer remains unknown. Here we used a strategy based on the evolutionarily conservation of Wnt/β-catenin signaling to trace the Hydra head inhibitor. We identify the transcription factor Sp5 as a transcriptional repressor of Wnt3, leading to a robust multiheaded phenotype when knocked-down in Hydra, while Wnt/β-catenin signaling positively modulates Sp5 expression. Sp5 fulfills the requirements of a head inhibitor in Hydra, and we show that this feedback loop between Sp5 and Wnt/β-catenin signaling appears conserved across eumetazoan evolution.
Identification of putative Hydra head inhibitors
To identify inhibitors of apical patterning that regulate the activity of the head organizer in both homeostatic and regenerative conditions, we established five criteria to be fulfilled by head inhibitor (HI) gene(s): (1) be controlled by Wnt/β-catenin signaling, (2) display an apical-to-basal graded activity, (3) be upregulated within the first day of head regeneration, (4) inhibit Wnt/β-catenin signaling, (5) prevent head formation (Fig. 1b). To select β-catenin target genes, we used a dataset of 440 genes downregulated in planarians silenced for β-catenin25 to retrieve 124 Hydra cognate genes (Supplementary Data 1). We analyzed their spatial and temporal RNA-seq expression profiles and found 5/124 genes predominantly expressed in the head and 3/5 upregulated in head-regenerating tips at least 1.5 fold after 24 h of regeneration (Fig. 1c, d). Among these candidates, we found Wnt3 and Wnt5, known as positive regulators of morphogenetic processes17,18,26 and Sp5, previously identified as a Wnt/β-catenin target gene in vertebrates27,28,29,30,31, thus a putative HI candidate (Fig. 1e). Hydra Sp5 (HySp5) encodes a Sp/Klf-class transcription factor whose sequence clusters with the bilaterian Sp5 ones in phylogenetic analyses (Supplementary Figs. 1–3).
Whole mount in situ hybridization confirmed the RNA-seq Sp5 pattern in intact Hydra, predominantly expressed in the head although absent from the apical tip where Wnt3 expression is maximal (Fig. 1f, g). After mid-gastric bisection, Sp5 is rapidly upregulated in both head- and foot-regenerating tips but its expression is only sustained in head-regenerating ones (Fig. 1g, Supplementary Fig. 4) supporting the idea that Sp5 is involved in head but not foot regeneration. We also performed a RNA-seq analysis of the cell-type expression32 and found that both Sp5 and Wnt3 are predominantly expressed in the gastrodermal epithelial stem cells (gESCs), a cell type associated with morphogenetic processes (Supplementary Fig. 5).
Hydra Sp5 a robust head inhibitory component
Next, we silenced Sp5 by electroporating siRNAs in intact animals and observed that within two days following the third electroporation (RNAi3), Sp5(RNAi) animals develop ectopic axes, initially from the budding zone, few days later from the upper body column (Fig. 2a, Supplementary Fig. 6). These ectopic axes differentiate multiple heads when located in the basal half but not from the upper half. Both ectopic axes and ectopic heads express the apical markers Wnt3, Bra1 and Tsp1, and the gland cell marker Kazal1 in the gastric tissue (Fig. 2b). When single-headed animals silenced for Sp5 are bisected after RNAi2, they all regenerate multiple heads that express Wnt3 at the tip (Fig. 2c, Supplementary Fig. 7). This multiheaded phenotype is robust, emerging quite synchronously in 50% uncut animals one day after RNAi2, in 100% two days after RNAi3 (Fig. 2d, Supplementary Fig. 6a–c). Furthermore, these ectopic heads express the neuropeptide RF-amide and are able to catch and ingest live Artemia, indicating that each ectopic head is functional (Fig. 2e, Supplementary Fig. 6d, Supplementary Movies 1–4). These results indicate that Sp5 acts as a strong inhibitor of head formation in Hydra.
Sp5 antagonizes Wnt/β-catenin signaling in Hydra
Next, we tested whether the multiheaded phenotype corresponds to a de-repression of Wnt3. To do this, we first tested whether the phenotype occurs when the Wnt/β-catenin pathway is inactive and thus knocked-down Sp5 together with β-catenin (Fig. 3a). Silencing β-catenin on its own delays head regeneration (Supplementary Fig. 8) and causes the formation of ectopic bumps in intact animals (Fig. 3a, Supplementary Fig. 9). While knocking down Sp5 causes the formation of multiple heads, the simultaneous knockdown of Sp5 and β-catenin prevents the occurrence of the multiheaded phenotype (Fig. 3a, Supplementary Fig. 9), suggesting that an increase in Wnt/β-catenin signaling activity is necessary to trigger multiple head formation when Sp5 is knocked down.
To further demonstrate that Sp5 represses Wnt/β-catenin signaling via Wnt3 repression, we knocked-down Sp5 in combination with Alsterpaullone (ALP), a drug that activates the Wnt/β-catenin pathway by antagonizing GSK3β33,34. As anticipated this combination led to a significant increase in ectopic tentacle formation, while knocking down β-catenin provides the opposite effect (Fig. 3b, Supplementary Fig. 10a). In these Sp5(RNAi) animals, we could also detect an increase in Wnt3 expression along the body column, indicating that Sp5 does repress Wnt3 expression (Fig. 3c, Supplementary Fig. 10b).
We also performed reaggregation experiments with cells coming from ALP-treated animals knocked-down either for Sp5 or for β-catenin. In standard conditions of reaggregation, several head spots form, each of them containing 5–15 Wnt3 expressing cells at 24 hours35. When Sp5 is knocked-down, we noted that the reaggregates tend to form multiple axes with a number of Wnt3 expressing spots increased by two-fold (Fig. 3d, e, Supplementary Fig. 11). In contrast, when β-catenin is knocked-down, the reaggregation process proceeds slower with aggregates exhibiting only few tentacles at day-4, with a number of Wnt3-expressing clusters similar to that observed in scramble(RNAi) control animals (Fig. 3d). These results confirm that Sp5 directly or indirectly represses Wnt3 expression.
To test whether Sp5 can directly repress the Wnt3 promoter, we produced a transgenic strain expressing the HyWnt3–2149:GFP-HyAct:dsRed construct where 2’149 bp of the Hydra Wnt3 promoter drives GFP expression and the Hydra Actin promoter drives dsRed expression19. We noted distinct levels of Wnt3-driven GFP fluorescence in control transgenic animals, maximal at the apex, intermediate in the adjacent region above the tentacle ring, and null at the level of the tentacle ring and along the body column (Supplementary Fig. 12a). In such transgenic animals knocked-down for Sp5, we did not record any body-wide GFP fluorescence but rather the appearance of patches of GFP + cells at the tip of the ectopic axes (Supplementary Fig. 12b). We could confirm this patchy Wnt3 activation along the body column of Sp5(RNAi) animals by performing a detailed kinetic analysis of Wnt3 expression (Supplementary Fig. 12c–d). This Wnt3 ectopic expression pattern suggests that Sp5 is silenced in restricted regions along the body column where Wnt3 is de-repressed and enhances its own expression via β-catenin signaling as previously recorded.
Sp5 represses the Hydra and zebrafish Wnt3 promoter
To further investigate the repressing activity of HySp5 on the HyWnt3 promoter, we performed luciferase reporter assays in human HEK293T cells (Fig. 4a–c). As the HyWnt3–2149:Luc construct shows a very low basal activity, we co-expressed a constitutively active form of β-Catenin (CMV:huΔβ-Cat)36 that enhances by ~10-fold the luciferase activity (Fig. 4b). In such conditions, the co-expression of HySp5 significantly reduces the activity of the HyWnt3 promoter (Fig. 4b). This effect was not observed when a partial version of HySp5 lacking the DNA-binding domain was used, indicating that the repressive effect of HySp5 is DNA-binding dependent (Fig. 4b). Two adjacent cis-regulatory modules were previously identified in the HyWnt3 promoter, a 599 bp-long activator that contains three clustered TCF binding sites and a 386 bp-long repressor sequence19, located immediately downstream (Fig. 4a, Supplementary Fig. 13a). This repressor module, highly conserved across Hydra species (Fig. 4a), is necessary for the Sp5-mediated Wnt3 repression, as the repression is no longer observed when this element is removed (Fig. 4b). Among the four constructs that harbor limited deletions within the Wnt3 repressor element, the construct containing both the -386/-286 and the -95/-1 sequences is the only one repressed by Sp5 (Fig. 4c), suggesting that the Sp5-dependent Wnt3 repression requires the cooperative activity of these two elements.
To test whether Sp5 also represses Wnt3 transcription in vertebrates we tested the 4 kb promoter region of the zebrafish Wnt3 locus in reporter assays where the zebrafish paralogs ZfSp5a and ZfSp5l1 are expressed (Fig. 4d, e). As for the HyWnt3–2149 construct, the transcriptional activity of the ZfWnt3–3997 construct was strongly enhanced by huΔβ-Cat, but repressed upon co-expression of ZfSp5a or ZfSp5l1 (Fig. 4e). The repressor activity of ZfSp5a was abolished when the DNA-binding domain was deleted. Although the zebrafish Wnt3 promoter does not share obvious sequence homologies with that of the HyWnt3 promoter, we could identify regions evolutionarily-conserved across different teleost lineages as well as TCF binding sites (TCF-BS) (Fig. 4d, Supplementary Fig. 13b). ChIP-qPCR experiments performed in transfected HEK293T identified two evolutionarily-conserved elements within the ZfWnt3 promoter directly bound by ZfSp5a (Fig. 4f).
Wnt/β-catenin signaling regulates HySp5 expression
In planarians as in zebrafish and mammals, the canonical Wnt/β-catenin pathway positively regulates the expression of Sp525,27,31,37. In mammals, Sp5 has also been reported to auto-regulate its expression, although studies in human and mouse embryonic stem cells (ESCs) differ on whether Sp5 acts positively or negatively on its own promoter31,37. In Hydra, a two days exposure to ALP suffices to upregulate Sp5 expression along the body column (Fig. 5a, Supplementary Fig. 14), suggesting that Sp5 regulation by the Wnt/β-catenin pathway predates the divergence of cnidarians. To test this hypothesis, we cloned 2’992 bp of the HySp5 promoter, a region that is evolutionarily-conserved across Hydra species and contains five putative TCF binding sites (Fig. 5b, Supplementary Fig. 13c). We evidenced its responsiveness to Wnt/β-catenin signaling, as we recorded a significant upregulation of the activity of the HySp5–2992:Luc reporter construct when the human WNT3, LRP6 or huΔβ-Cat proteins were co-expressed (Fig. 5c). In addition, we found that HySp5 can bind its own promoter as in ChIP-qPCR experiments Sp5 binding is significantly enriched in two neighboring regions located immediately upstream of the Sp5 Transcriptional Start Site (TSS) (Fig. 5d). Furthermore, co-expression of HySp5–2992:Luc and HySp5, alone or in combination with huΔβ-Cat resulted in a strong increase in luciferase activity (Fig. 5e). In mouse ESCs, Sp5 interacts with β-catenin and Tcf-Lef1 to regulate gene expression31. As anticipated, we found in a ChIP-seq analysis the mouse Sp5 and β-catenin proteins enriched in the same region of the Sp5 promoter (Supplementary Fig. 15a), suggesting a possible cooperation to regulate Sp5 transcription. We performed co-immunoprecipitation experiments with HEK293T cells co-transfected with HySp5 and huΔβ-Cat or huTCF1 and observed an interaction between HySp5 and these factors (Fig. 5f, Supplementary Fig. 15b–c). These results indicate that HySp5, similarly to its mammalian cognates, can act as an activator or a repressor of transcription and that Hydra and vertebrate Sp5 can interact with β-catenin or TCF1.
Sp5 DNA-binding properties are evolutionarily-conserved
To further compare the transcriptional activities of HySp5 and ZfSp5a, we expressed HySp5 or ZfSp5a in HEK293T cells and analyzed the genomic occupancies and the transcriptional changes induced by their overexpression (Fig. 6a). ChIP-seq analysis revealed that HySp5 binds a much smaller fraction of sequences than ZfSp5a (Fig. 6b), while the number of genes bound by HySp5 and ZfSp5a is not so different, 13’251 vs. 18’619, 99% of the HySp5 bound genes are also ZfSp5a targets (Fig. 6c). Interestingly, HySp5 and ZfSp5a differ in the spatial distribution of their target sequences: the majority of HySp5 bound elements localize within the 5 kb proximal region of the assigned genes, while ZfSp5a proportionally binds more frequently elements located in upstream sequences, above 10 kb from the TSS (Fig. 6d, e). This suggests that vertebrate Sp5 more readily recognizes sequences enriched in long-range regulatory elements, which are not recognized by the HySp5 protein.
Motif enrichment analysis of the HySp5 and ZfSp5a bound elements revealed that the two orthologs recognize both similar and divergent consensus binding sites (Fig. 6f). In both cases, the most enriched motif resembled the general SP/KLF consensus sequence (GGGxGGG/A). We then used the enriched motifs to identify putative HySp5/ZfSp5a binding sites in the regulatory regions of HyWnt3, ZfWnt3 and HySp5. We could identify putative HySp5 binding sites in the two regions of the HyWnt3 repressor required to inhibit transcription (Supplementary Figs. 13). Similarly, we also found evolutionarily-conserved Sp5 binding sites in the regions of ZfWnt3 and HySp5 enriched in the ChIP-qPCR analysis, supporting the idea that Hydra and zebrafish Sp5 directly regulate the transcriptional activity of these promoters. Despite the similarity in the main consensus sites bound by HySp5 and ZfSp5a, we also identified motifs differentially enriched among the elements bound by these two orthologs (Fig. 6f). Interestingly, ZfSp5a binds elements that display an over-representation of Tbx1 and Sox13 motifs, which were not identified in the pool of HySp5 bound sequences (Fig. 6f). Members of the Tbx and Sox families are known to interact with Sp138 and β-catenin39 respectively, suggesting that they could also form transcriptional complexes with Sp5. Thus, the enrichment in Tbx/Sox consensus sequences suggests that vertebrate Sp5 but not Hydra Sp5 may regulate gene expression in complexes involving these transcription factors.
To further validate that HySp5 has similar DNA-binding properties than its vertebrate orthologs, we inspected the HySp5 genomic coverages in the proximities of genes identified as Wnt/β-catenin targets in mouse and human ESCs31,37. Comparable binding profiles of HySp5 and mSp5 were observed for the Axin2, Bra and Lrg5 loci in human and mouse cells, while quite different at the Nanog and Plk4 loci, the latter likely due to cell-type or species specific differences (Supplementary Fig. 16a). We also found a strong enrichment of HySp5 and ZfSp5a binding in the WNT3 intronic sequences, in the promoter and intronic sequences of the neighboring WNT9B locus and in the upstream and intronic sequences of SP5 (Supplementary Fig. 16b). The GO term enrichment analysis actually identified the Wnt pathway as the most enriched category (Supplementary Fig. 16c, Supplementary Data 2).
All together, these results point to similar DNA-binding capacities between HySp5 and ZfSp5a even though the latter recognizes a larger set of sequences, often located at mid-long distances upstream from the TSS, possibly acting in combination with Sox and/or Tbx proteins.
Conserved and divergent transcriptional functions of Sp5
To assess the transcriptional activity of HySp5 and ZfSp5a, we measured by qRNA-seq the transcriptional changes induced by the overexpression of HySp5 and ZfSp5a in HEK293T cells co-expressing or not the huΔβ-Cat construct (Fig. 6a). As controls we used HEK293T cells transfected with a mock plasmid, the huΔβ-Cat construct alone or the mutated HySp5-ΔDBD and ZfSp5a-ΔDBD constructs. Principal component analysis (PCA) showed that HySp5 and ZfSp5a transfected samples, either alone or in combination with huΔβ-Cat, segregated together, widely separated from the control or HySp5-ΔDBD/ZfSp5a-ΔDBD values (Fig. 6g). This suggests that HySp5 and ZfSp5a elicit overall similar transcriptional responses. Instead, the values obtained from huΔβ-Cat transfected cells grouped together with the values from mock-transfected samples, while the values corresponding to cells co-expressing huΔβ-Cat with HySp5 or ZfSp5a do not substantially differ from those overexpressing HySp5 or ZfSp5a alone (Fig. 6g, Supplementary Data 2). These results imply that HEK293T cells do not respond to huΔβ-Cat overexpression, in agreeement with previous reports showing that although HEK293T cells respond to Wnt signalling stimulation by translocating β-catenin to the nucleus40,41, they display limited transcriptional responses of their endogenous Wnt target genes37,42.
Next, we analyzed the genes whose expression is modulated upon HySp5 or ZfSp5a overexpression but remains unaffected when their respective DNA-binding domain is deleted (Fig. 6h, Supplementary Data 2). We focused our analysis on the modulated genes that were associated to HySp5- or ZfSp5a-bound elements in ChIP-seq analysis, suggesting that these genes are directly activated or directly repressed targets. We identified downregulated genes, 153 upon HySp5 expression, 113 by ZfSp5a, and 83 by both (Fig. 6i, Supplementary Fig. 17, Supplementary Data 3). This demonstrates that the cnidarian and vertebrate Sp5 proteins have a similar repressive capacity. We also identified 137 and 23 genes upregulated upon ZfSp5a and HySp5 overexpression, respectively. Of these, only 5 are activated by both Sp5 orthologs (Fig. 6i, Supplementary Fig. 17, Supplementary Data 3), indicating that the activator function of the cnidarian and vertebrate Sp5 transcription factors diverged during evolution. This is surprising, since both HySp5 and mammalian orthologs can interact with β-catenin (Fig. 5f) to promote target gene activation. As the HEK293T cells are largely insensitive to huΔβ-Cat overexpression (Fig. 6g), the observed upregulation of HySp5 and ZfSp5a direct targets relies on mechanisms largely independent of β-catenin signaling. By contrast, the overexpression of HySp5 and ZfSp5a in zebrafish embryos leads to similar developmental alterations, which resemble those produced by the over-activation of Wnt/β-catenin signaling (Supplementary Fig. 18, Supplementary Data 4).
Studies performed in developing vertebrates show that Sp5 is a target of Wnt/β-catenin signaling as recorded in zebrafish27,28, mice29, Xenopus30, as well as in self-renewing mouse and human ESCs31,37. In line with these results, we show that in Hydra, Sp5 is positively regulated by Wnt/β-catenin signaling as evidenced by its upregulation when Wnt/β-catenin signaling is pharmacologically enhanced. These results illustrate the deep conservation of the Wnt/β-catenin-dependent regulation of Sp5 across eumetazoans. Wnt5, another candidate identified in the screen might also play a role in head inhibition, as a putative inhibitor of the canonical Wnt pathway43,44 and a possible HySp5 target gene. By contrast, secreted Wnt antagonists such as Dickkopf (Dkk)45 or Notum46, both expressed in Hydra, were not identified in this screen.
Wnt3 and Sp5 upregulations in head-regenerating tips are consistent with a rapid head organizer formation after bisection. Sp5 is re-expressed early during head regeneration, although as expected, later than Wnt3. This temporal parameter is indeed essential for the establishment of a de novo head organizer as demonstrated by transplantation experiments that accurately measured the successive re-activation of the two head organizer components, with head activation restored within 12 hpa and head inhibition coming back later, detectable at 24 hpa9,13. Here we used the qRNA-seq data to compare the respective regulations of Wnt3 and Sp5 in regenerating tips after decapitation or mid-gastric bisection. While Wnt3 is rapidly upregulated to reach a plateau value at 4 hpa, Sp5 shows an initial drop in expression within the first two hours following bisection, then an upregulation and a peak of expression detected at 8 hpa, four hours after that measured for Wnt3. If one assumes that the reestablishment of active Wnt3 and Sp5 proteins follows similar kinetics, then this four hour time window corresponds to a period when Wnt3/β-catenin signaling is active but Sp5 still inactive as Wnt3 repressor, leaving sufficient time to instruct tissues to form a head.
A recent observation suggested that human SP5 can directly repress the WNT3 promoter in human ESCs37. Here we demonstrate that indeed Sp5 from Hydra and zebrafish inhibit Wnt/β-catenin signaling by repressing the activity of the Wnt3 promoter. Both the RNA-seq and the ChIP-seq data presented here confirm this view, by showing firstly that HySp5 and ZfSp5a when overexpressed in HEK293T cells repress largely overlapping sets of genes and secondly that both Hydra and zebrafish Sp5 preferentially bind genes of the Wnt/β-catenin signaling pathway, as observed in the promoter and intronic regions of the human WNT3 and WNT9B genes. The studies performed in HEK293T cells also highlighted the fact that HySp5 and ZfSp5a, as transcriptional repressors, likely bind to regulatory elements located in the proximity of the TSS of their target genes. All together, these results highlight the similarity between the repressor effect of cnidarian and vertebrate Sp5 transcription factors, which predominantly affects genes of the Wnt/β-catenin signaling pathway but is not restricted to it. It is thus tempting to speculate that the Sp5-dependent inhibition of Wnt/β-catenin signaling originated early in metazoan evolution and was maintained across eumetazoans. By contrast, the properties of HySp5 and ZfSp5a as transcriptional activators appear quite different: both can promote gene activation through β-catenin interaction, but they largely differ in their capacity to activate target genes in a β-catenin-independent mode. Therefore, we speculate that Sp5 possibly evolved the capacity to interact with partners not previously identified such as Tbx or Sox, and/or acquired the capacity to bind consensus motifs such as those enriched in the vertebrate long-range enhancers, after Cnidaria divergence.
Consistent with its Wnt3 repressor function, HySp5 silencing triggers in a highly robust way the ectopic formation of clusters of Wnt3-expressing cells, followed by the formation of multiple heads along the body column of intact animals, in head-regenerating regions and in reaggregates (Fig. 7). This phenotype is different from the ones obtained with pharmacological treatments, either with the GSK3-β inhibitor ALP22,23,33 or recombinant Wnt3 that directly enhances β-catenin signaling18,47, where ectopic tentacles form first, and heads appear several days later. In intact animals, the knockdown of HySp5 leads to the direct and rapid formation of fully functional ectopic heads, preferentially in the budding zone, a region that is developmentally competent in adult animals where the expression of both Wnt3 and β-catenin is quite dynamically regulated17,18. By increasing the number of dsRNA electroporations, we noted the formation of ectopic heads in the apical half of the body column, even though the development of these heads remained incomplete. Nevertheless, we never observed supernumerary heads at the apex of homeostatic HySp5(RNAi) animals, likely reflecting the difficulty to obtain a significant silencing in the apical region where Sp5 expression is high. In the peduncle and basal part of the animal, ectopic head formation upon HySp5(RNAi) does not occur either, most likely as the physiological activity of Wnt3/β-catenin signaling is too low in this region to elicit ectopic head formation when Sp5 is silenced. In head-regenerating animals or reaggregates, the Sp5(RNAi) phenotype is readily observed as, similarly to the budding zone, the expression of Wnt3, β-catenin and Sp5 is quite dynamically regulated.
To further investigate these dynamic modulations, we designed strategies to modulate the Sp5(RNAi) phenotype. We first noticed that when β-catenin is silenced, the Sp5(RNAi) phenotype is greatly reduced, indicating that an active Wnt3/β-catenin signaling is necessarily required for ectopic head formation. We also measured the spatial spreading of the ALP-induced phenotype when Sp5 is knocked-down, with ectopic Wnt3 expression and ectopic tentacle formation all along the body column. This last result indicates that the constitutive activation of Wnt3/β-catenin signaling by ALP is significantly enhanced upon Sp5 silencing. These modulations of the Sp5(RNAi) phenotype in response to β-catenin(RNAi) or the ALP-induced phenotype in response to Sp5(RNAi) again confirm the intimate dynamic cross-talk that takes place between Sp5 regulation, Sp5 activity and the Wnt3/β-catenin signaling activity.
The observed Sp5(RNAi) phenotypic modulations indicate that Sp5 silencing cannot be easily maintained stable along the mid-gastric region, namely because its regulation is quite dynamic in response to the level of Wnt3/β-catenin signaling. Therefore, we interpret the homeostatic HySp5(RNAi) phenotype in the budding region as the consequence of the transient downregulation of HySp5 activity in tissues that have the highest potential for setting up an organizer as evidenced by the transient upregulation of β-catenin in the budding zone17. As an evidence of this dynamic cross-talk, we noticed that a transient drop in HySp5 expression suffices to rapidly induce a de-repression of Wnt3 expression, which leads to an upregulation of β-catenin activity, and in turn to Wnt3 upregulation followed by that of Sp5 (Fig. 7). The oscillatory nature of HySp5 and β-catenin expression in regions competent for head organizer formation suggests a bistability state relying on an auto-regulatory loop involving two transcription factors48. This bistability as a prerequisite to head organizer induction and/or head organizer maintenance remains to be explored.
This study identifies the transcription factor Sp5 as a key inhibitory component of the Hydra head organizer. Indeed Sp5 fulfills the five criteria we initially fixed, derived from the predicted properties of the head inhibitor and from the previous identification of Wnt/β-catenin signaling as the head activator19. Sp5 globally fits the Turing/Gierer-Meinhardt model as HySp5 expression is controlled by Wnt3/β-catenin signaling, predominantly expressed in the head, reactivated during head regeneration, while HySp5, as a Wnt3 repressor, represses ectopic head formation (Fig. 7). However, several features diverge from the expected properties of the head inhibitor predicted by the Gierer-Meinhardt model.
Firstly, we noted the lack of Sp5 expression at the very apical tip of the hypostome in intact animals, the region where Wnt3 expression, and most likely Wnt3 activity, is maximal. Two distinct cis-regulatory elements in the Wnt3 promoter were previously identified, an activator and a repressor element, the latter restricting Wnt3 expression to the distal tip of the head19. The Sp5 pattern is thus consistent with the prediction that the inhibitor should be absent or unable to repress Wnt3 in this area. As Sp5 appears as a direct target of Wnt3/β-catenin signaling (see below), an additional negative regulation has to take place in this most apical area, to prevent Sp5 expression. This local regulation remains to be identified.
Secondly, this study supports a scenario where Wnt3 acts as a short-range activator to sustain its own activity in the head organizer, while Sp5 prevents the expression of Wnt3 and possibly other Wnt genes in non-apical tissues. The Gierer-Meinhardt model, proposed at a time when the concept of transcription factor was still unknown, predicts that the head inhibitor is a diffusible substance, acting non-cell autonomously across the tissue layers. As a transcription factor, HySp5 is suspected to act cell-autonomously and thus not diffusible. However, some transcription factors can be secreted, as reported for the helix-turn-helix transcription factor EspR in bacteria49 or for some homeoproteins that exert non-cell autonomous functions in the mammalian brain50. Also, Sp5 might upregulate target genes that encode secreted peptides or proteins that diffuse in the extra-cellular space and exert head inhibitory functions. Such target genes, possibly taxon-specific, remain to be identified.
Thirdly, we cannot exclude that Wnt signals, which are numerous to be emitted from the apical region18 are not short-range signals but rather act over long-range distances to activate HySp5 expression with lipid-binding proteins or cytonemes modulating the spread of Wnt proteins as observed in Drosophila, Xenopus and zebrafish51,52,53. The inhibition of Wnt3/β-catenin signaling along the Hydra body axis might thus solely be mediated by transcriptional repression, with Sp5 regulating its own expression and tightly tuning the level of Wnt signals.
As a fourth divergence with the Gierer-Meinhardt model, we found that HySp5 activates its own promoter. Both the reporter assays and the ChIP-qPCR data demonstrate that HySp5 directly binds its own promoter, while the ChIP-seq data also suggest that HySp5 is able to bind the human SP5 promoter. These observations are consistent with a study showing that the mouse Sp5 protein directly binds and activates its own promoter31. In addition, β-catenin slightly enhances the activating effect of HySp5 on its promoter, likely through direct interaction between HySp5, TCF1 and/or β-catenin as observed in vitro. A recent study demonstrates a direct interaction between the zinc finger domain of mouse Sp5 and the HMG domain of Tcf/Lef1, while no direct interaction was observed for β-catenin31. Also the formation of active Tcf/Lef1-β-catenin complexes appears necessary for Sp5 DNA-binding in mouse ESCs31. In contrary, in human ESCs, SP5 could directly repress the human SP5 promoter37. Thus, currently we cannot exclude that besides its auto-activating effect, HySp5 might also have an auto-repressing effect when it reaches high intracellular levels for example. Further studies should evidence this putative auto-repressing effect as well as the interactions between HySp5 and TCF/β-catenin that favor the switch from Sp5 auto-activation to Sp5 auto-repression.
Animal culture and drug treatment
All experiments were carried out with Hydra vulgaris (Hv) from the Basel, AEP or Hm-105 strains. Cultures were maintained in Hydra Medium (HM: 1 mM NaCl, 1 mM CaCl2, 0.1 mM KCl, 0.1 mM MgSO4, 1 mM Tris pH 7.6) or in Volvic water, supplemented with 0.5 mM CaCl2. Animals were fed two to three times per week with freshly hatched Artemia nauplii and starved for four days before any experiment. For drug treatments Hv_Basel were treated for two days with 5 μM Alsterpaullone (ALP, Sigma) diluted in HM, 0.015% DMSO then rinsed 3x in fresh HM. All animals were selected randomly for experiments.
Generation of the HyWnt3:GFP-HyAct:dsRED transgenic strain
To induce gametogenesis, H. vulgaris of the strain AEP were fed with freshly hatched Artemia nauplii 7× per week for three weeks and then 1× per week for 1 week. Thereafter, male and female animals were cultured together, resulting in fertilized embryos. The hoTG-HyWnt3FL-EGFP-HyAct:dsRED plasmid (kind gift from T. Holstein, Heidelberg)19 was injected into one-cell stage embryos. Out of 504 injected eggs, 104 embryos hatched and 7/104 embryos exhibited GFP fluorescence in the hypostome.
In short, intact Hydra were briefly washed and incubated for 45 min in Milli-Q water54. 20 animals per condition were placed in 200 µl 10 mM sterilized HEPES solution (pH 7.0) and then transferred into a 0.4 cm gap electroporation cuvette (Cell Projects Ltd). Animals were electroporated with 4 μM of Sp5 (siRNA-1+siRNA-2+siRNA-3) or scramble siRNAs (Supplementary Table 1b) using the Biorad GenePulser Xcell electroporation system. For double knockdown experiments 2 μM of Sp5 siRNAs were mixed with 2 μM of scramble of β-catenin siRNAs. The conditions of electroporation were: Voltage: 150 Volts; Pulse length: 50 milliseconds; Number of pulses: 2; Pulse intervals: 0.1 s. For subsequent ALP treatment, RNAi animals that did not show any phenotypic signs were kept for 18 h in HM containing 5 μM ALP. The animals were then relaxed in 2% urethane/HM for one minute, fixed in 4% PFA prepared in HM (pH 7.5) for 2 h at RT and either processed for WISH, or directly mounted with Mowiol for picturing.
Animals were electroporated twice (RNAi1, RNAi2) with siRNAs and treated with ALP as described above. Next, 50–60 animals of the same size that did not show any phenotypic signs, were dissociated in 10 mL of dissociation medium (DM) (3.6 mM KCl, 6 mM CaCl2, 1.2 mM MgSO4, 6 mM Na-Citrate, 6 mM Pyruvate, 4 mM Glucose and 12.5 mM TES; pH 6.9)55 and the cell suspension was centrifuged at 1’400 rpm for 30 min at 4 °C. The pellet was resuspended in 1 mL DM and 450 µl of the cell suspension equally distributed into 1.5 mL tubes, followed by centrifugation at 1’400 r.p.m. for 30 min. After detachment, the aggregates were kept for one hour at 18 °C in 75% DM/HM and overnight in 50% DM/HM. On the next day, the aggregates were transferred into HM.
Total RNA was extracted using the E.Z.N.A.® Total RNA kit (Omega) and cDNA synthesized using the qScriptTM cDNA SuperMix (Quanta Biosciences). qPCR was performed in a 96-well format using the SYBRTM Select Master Mix for CFX (Thermo Fisher Scientific) and a Biorad CFX96TM Real-Time System. The TBP gene was used as an internal reference gene. HySp5 and TBP primer sequences are listed in Supplementary Table 1c. For ChIP-qPCR, DNA was prepared as below (ChIP-seq section) and qPCR performed as above with primer sequences listed in Supplementary Table 1d.
Whole mount In Situ Hybridization and immunodetection
Hydra were relaxed in 2% urethane/HM for one minute, fixed in 4% PFA prepared in HM (pH 7.5) for 4 h at RT and stored in MeOH at −20 °C for at least one day. Samples were rehydrated through a series of EtOH, PBSTw (PBS, Tween 0.1%) washes (75%, 50%, 25%) for 5 min each, washed 3× with PBSTw for 5 min, digested with 10 μg/mL Proteinase K (PK, Roche) in 0.1% SDS, PBSTw for 10 min, stopped by adding Glycine (4 mg/mL) and incubated for 10 min. Samples were washed 2x in PBSTw for 5 min, treated with 0.1 M TEA for 2 × 5 min, incubated 5 min after adding acetic anhydride 0.25% (v/v), 5 min after adding again acetic anhydride 0.25% (final concentration 0.5% v/v). Samples were then washed in PBSTw 2 × 5 min, post-fixed in 4% formaldehyde, PBSTw for 20 min, washed in PBSTw 4 × 5 min before adding the pre-warmed pre-hybridization buffer (PreHyb: 50% Formamide, 0.1 % CHAPS, 1× Denhardt’s, 0.1 mg/mL Heparin, 0.1% Tween, 5x SSC) and incubated for 2 h at 58 °C. Next, 350 μL hybridization buffer (PreHyb containing 0.2 mg/mL t-RNA, 5% Dextran) containing 200 ng DIG-labeled riboprobe was heated 5 min at 80 °C, then placed on ice for 2 min. This mix was added onto the samples, then incubated for 19 h at 58 °C. Next, the samples were rinsed 3x in pre-warmed PostHyb-1 (50% formamide, 5x SSC) and successively incubated for 10 min at 58 °C in PostHyb-1, PostHyb-2 (75% PostHyb-1, 25% 2x SSC, 0.1% Tween), PostHyb-3 (50% PostHyb-1, 50% 2x SSC, 0.1% Tween) and PostHyb-4 (25% PostHyb-1, 75% 2× SSC, 0.1% Tween). Samples were then washed 2 × 30 min in 2× SSC, 0.1% Tween, 2 × 30 min in 0.2x SSC, 0.1% Tween, 2 × 10 min in MAB-Buffer1 (1× MAB, 0.1% Tween), blocked in MAB-Buffer2 (20% sheep serum, MAB-Buffer1) for 1 h and incubated with anti-DIG-AP antibody (1:4000, Roche) in MAB-Buffer2 overnight at 4 °C. Next, the samples were washed in MAB-Buffer1 for 4 × 15 min, then in NTMT (NaCl 0.1 M, Tris-HCl pH 9.5 0.1 M, Tween 0.1%) for 5 min and finally in NTMT, levamisole 1 mM for 2 × 5 min. The colorimetric reaction was started by adding staining solution (Tris-HCl pH 9.5 0.1 mM, NaCl 0.1 mM, PVA 7.8%, levamisole 1 mM) containing NBT/BCIP (Roche). The background color was removed by a series of washes in EtOH/PBSTw (30%/70%, 50%/50%, 70%/30%, 100% EtOH, 70%/30%, 50%/50%, 30%/70%), PBSTw 2 × 10 min. Samples were post-fixed for 20 min in FA 3.7% diluted in PBSTw, washed in PBSTw 3 × 10 min and mounted with Mowiol. All steps were performed at RT unless indicated otherwise. Whole mount immunofluorescence with the anti-RFamide antibody (kind gift of C. Grimmelikhuijzen, 1:1000) was performed as in ref. 32.
Hydra were relaxed in 2% urethane/HM for one minute and fixed in 4% PFA prepared in HM (pH = 7.5) for 2 h at RT. Samples were washed 3 × 10 min with PBS, followed by adding 500 μL DAB (SIGMAFASTTM 3,3′-Diamino-benzide) solution. The DAB solution was prepared as follows: 1 tablet of DAB was dissolved in 10 mL of PBS and filtered with a 0.22 μm filter. 5 mL of the filtered solution was added to 5 mL of PBS together with 20 μL of Triton X-100 (0.2%) and 1 μL of a 30% H2O2 solution. The animals were incubated for 10 min in DAB solution and the reaction stopped by washing the samples 3 × 10 min with PBS.
To generate the HyWnt3:Luc construct 2149 bp of the Hydra Wnt3 promoter were transferred from the hoTG-HyWnt3FL-EGFP construct (kind gift from T. Holstein, Heidelberg)19 into the pGL3 reporter construct (kind gift from Z. Kozmik, Prague)29. For the HyWnt3-ΔRep:Luc construct, the whole HyWnt3:Luc plasmid sequence was PCR-amplified except the 386 bp corresponding to the repressor element. For the ZfWnt3:Luc construct 3997 bp of the zebrafish Wnt3 promoter were transferred from pEGFP-Wnt3 (kind gift of Cathleen Teh, Singapore) into pGL3. For the HySp5:Luc construct, 2’992 bp of the Hydra Sp5 promoter were PCR-amplified from Hm-105 genomic DNA and subcloned into pGL3. To express HA-tagged HySp5, ZfSp5a, ZfSp5l1 proteins, a C-terminal HA-tag was introduced into the pCS2 + constructs encoding the Hydra Sp5 (human codon-optimized), zebrafish Sp5a and Sp5l1 full-length coding sequences. The HySp5-ΔSP construct was produced by inserting a human codon-optimized HySp5 sequence lacking 110 amino acids of the N-terminal end together with a C-terminal HA-tag into pCS2+. The HySp5-ΔDBD and HySp5-ΔSP-ΔDBD constructs were generated using the QuikChange Lightning Multi Site-Directed Mutagenesis Kit (Agilent Technologies), following the manufacturer’s instructions. To generate the ZfSp5a-ΔDBD construct, the ZfSp5a-FL plasmid sequence was PCR-amplified except the DNA-binding domain. For preparing riboprobes, the HyWnt3, HyBra1, HyTsp1, HyKazal1 and HySp5 PCR products were cloned into pGEM-T-Easy (Promega). All constructs were verified by sequencing. All plasmids are listed in Supplementary Table 2 and primer sequences in Supplementary Table 1a.
Reporter assays in human HEK293T cells
HEK293T cells were maintained in DMEM High Glucose, 1 mM Na pyruvate, 6 mM L-glutamine, 10% fetal bovine serum. For the luciferase assays HEK293T cells were seeded into 96-well plates (5000 cells/well) and transfected 18 h later with X-tremeGENETM HP DNA transfection reagent (Roche). The plasmids listed in Supplementary Table 2 were transfected as follows: pGL4.74(hRluc/TK) (Promega): 1 ng, luciferase reporter constructs: 40 ng, CMV:huΔβ-Cat: 10 ng, Sp5 expression constructs: 20 ng, huWnt3 and huLRP6: 40 ng. Total DNA amount was adjusted with pTZ18R to 100 ng per well. To measure Firefly and Renilla luciferase activities, the samples were prepared using the Dual-Luciferase Reporter Assay System (Promega), transferred to a white OptiPlateTM-96 (PerkinElmer) and measured with a multilabel detection platform (CHAMELEONTM).
ChIP-seq sample preparation
920’000 HEK293T (92 cells/μL) cells were seeded into a 10 cm dish containing 10 mL of cell culture medium and transfected as described above with HySp5 or ZfSp5a, both containing a C-teminal HA tag (3’666 ng). Twenty-four hours later, cells were collected, washed twice in pre-warmed culture medium, fixed in 1% formaldehyde (FA) solution (Sigma) for 15 min until Glycine was added (final 125 mM) for 3 more minutes. In subsequent steps numerous reagents were from Active MotifTM (AM). The cells were washed once in ice-cold PBS and re-suspended in 5 mL chromatin prep buffer (AM), containing 0.1 mM PMSF and 0.1% protease inhibitor cocktail (PIC). The sample was transferred into a pre-cooled 15 mL glas Douncer, dounced with 30 strokes and incubated on ice for 10 min. Nuclei were centrifuged at 1250 g for 5 min at 4 °C, resuspended in 500 μL sonication buffer (1% SDS, 50 mM Tris-HCl pH 8.0, 10 mM EDTA pH 8.0, 1 mM PMSF, 1% PIC), incubated on ice for 10 min. Next, the chromatin was sonicated with a Bioblock Scientific VibraCell 75042 sonicator (Amplitude: 25%, Time: 12 min, 30 s on, 30 s off, 24 cycles), in conditions optimized to have a fragmentation size of ~250 bp. Then 100 μL of the sonicated chromatin was added to 900 μL ChIP dilution buffer (0.1% NP-40, 0.02 M HEPES pH 7.3, 1 mM EDTA pH 8.0, 0.15 M NaCl, 1 mM PMSF, 1% PIC) and incubated with 4 μg anti-HA antibody overnight at 4 °C on a rotator. Next, the sample was loaded on a ChIP-IT ProteinG Agarose Column (AM), incubated for 3 h at 4 °C on a rotator, washed 6x with 1 mL AM1 buffer and the DNA eluted with 180 μL pre-warmed AM4 buffer. The sample was decrosslinked by adding 100 μL high salt buffer (1 M NaCl, 3× TE buffer) and incubated for 5 h at 65 °C. RNAse A (10 μg/μL) was added and the sample incubated at 37 °C for 30 min before adding PK (10 μg/μL) and further incubated for 2 h at 55 °C. The DNA was purified with the MiniElute PCR purification kit (Qiagen). For preparing the Input DNA, 5 μL sonicated chromatin was diluted in 45 μL 0.5 M NaCl, incubated for 15 min at 95 °C, then transferred to 37 °C, incubated for 5 min with RNAse A (10 μg/μL), adding PK (10 μg/μL) and incubated at 55 °C for 30 min. 10 μL were taken for purification (MiniElute PCR purification kit from Qiagen).
RNA-seq sample preparation
156’500 HEK293T (78.25 cells/μL) cells were seeded into a 6-well plate containing 2 mL of cell culture medium and transfected as described above with 626 ng of HySp5, ZfSp5a, HySp5-ΔDBD, ZfSp5a-ΔDBD and 313 ng of human Δβ-Catenin. RNA was extracted with the E.Z.N.A. total RNA kit I from OMEGA following the manufacturer’s instructions.
Co-immunoprecipitation assay and Western blotting
920’000 HEK293T cells (92 cells/μL) were seeded into a 10 cm dish containing 10 mL of cell culture medium and transfected with huΔβ-Cat (1830 ng), huTCF1 (1830 ng) and HySp5 (3660 ng). 24 h later, Co-IP samples were prepared using the nuclear complex Co-IP kit from Active Motif, following the manufacturer’s instructions (all steps at 4 °C with ice-cold buffers). 100 μg nuclear extracts were then diluted in 500 μL Co-IP incubation buffer containing 4 μg anti-HA antibody or 4 μg rabbit IgG (12–370, Merck Millipore) and incubated overnight on a rotator. The Co-IP reaction was then loaded on a Protein G Agarose column (AM) and incubated one hour on a rotating wheel. The column was washed 3x in 500 μL Co-IP wash buffer supplemented with 1 mg/mL BSA, 3x in 500 μL of Co-IP wash buffer supplemented with 300 mM NaCl. The column was centrifuged at 1250 × g for 3 min and 25 μL 2x reducing buffer directly added onto the column. After 60 s incubation and 3 min centrifugation at 1250 × g, 5 μL glycerol (Sigma) was added and the sample boiled for 5 min at 95 °C before loading on a 8% SDS-PAGE gel, electrophoresed and transferred onto PVDF membrane (Bio-Rad). Then all steps were performed at RT unless specified. The membrane was blocked with M-TBS-Tw (TBS containing 0.1% Tween, 0.5% dry milk) for one hour until primary antibodies diluted 1:2000 in M-TBS-Tw were added for overnight incubation at 4 °C. The membrane was then washed 4 × 10 min in TBS-Tw, incubated in anti-rabbit (ab99697, Abcam) or anti-mouse (W402B, Promega) IgG horseraddish peroxidase antibody (1:5000) for one hour, visualized with Western Lightning® Plus-ECL reagent (PerkinElmer). 10 μg extract were used as Input sample. Antibodies: anti-HA antibody (NB600–363, Novus Biologicals), anti-β-catenin antibody (610153, BD Biosciences), anti-TCF1 (sc-271453, Santa Cruz Biotechnology). All uncropped western blots can be found in Supplementary Fig. 15.
ChIP-seq data analysis
Demultiplexed ChIP-seq reads from our sequenced samples were mapped onto the Human GRCh37 (hg19) genome assembly using bowtie2, version 18.104.22.1686, implemented in galaxy57. Significantly enriched regions were identified using MACS258 (version 22.214.171.12451222.0). Coverage files were normalized by the millions of mapped reads in each sample using a manually created R script. Normalized bedgraph files were converted to bigwig using the Wig/BedGraph-to-bigWig converter tool (version 1.1.1) implemented in the pubblic Galaxy server (https://usegalaxy.org/) and visualized with UCSC genome browser. The fastq files from the two biological replicates of each condition were merged and remapped in order to obtain the average coverage profile. Only autosomal chromosomes were analysed in this study. MACpeaks regions were either extended or cropped from their respective center to match a final size of 500 bp using a personalized R script based on the GenomicRanges package (version 1.32.6). Fasta files containing the DNA sequences corresponding to the coordinates of the MACpeaks regions were obtained using the UCSC table browser tool. These files were used to identify enriched motifs for transcription factor binding sites using the MEME-ChIP Suite59 (http://meme-suite.org/tools/meme-chip) in classic mode. Significantly enriched motifs were identified and compared to previously described TF weight matrixes from the JASPAR CORE 2014 database59 using the TOMTOM tool of the MEME-ChIP suite. Significantly enriched motifs were used to scan the HySp5, HyWnt3 and ZfWnt3 promoters, using the FIMO tool (http://meme-suite.org/tools/fimo)60 to identify putative Sp5 binding sites. Gene assignment of the identified MACpeak region was performed using the ChipEnrich Package in R (version 2.4.0; locus definition: nearest TSS; gene set: gene ontology biological process; method: polyenrich). Calculations of the total HySp5 and ZfSp5a coverages (in Mb) and of the frequency distribution of the number of Sp5-enriched regions per gene were performed in R using personalized scripts. ChIP-seq data sets for the Sp5 and β-catenin occupancies in mouse ES cells31,61 were, respectively, downloaded from the GEO subseries GSE72989 and GSM1065517 and re-mapped on the mouse mm10 genome assembly using the same workflow describe above.
RNA-seq data analysis
Demultiplexed RNA-seq reads from our sequenced samples were mapped onto the Human GRCh37 (hg19) genome assembly using the STAR RNA-seq aligner62 workflow implemented in Galaxy. The fastq files from the three biological replicates of each condition were merged and remapped in order to obtain the average coverage profile. Coverage files were normalized by the millions of mapped reads in each sample using a manually created R script. Normalized bedgraph files were converted to bigwig using the Wig/BedGraph-to-bigWig converter tool implemented in the public Galaxy server (https://usegalaxy.org/) and visualized with UCSC genome browser. We used Htseq63 implemented in the Galaxy server to count the number of uniquely mapped reads attributable to each gene (based on human genomic annotations from Ensembl release 8264). We used DESeq265 to perform differential expression analyses. Specifically, we contrasted a generalized linear model that explains the variation in read counts for each gene, as a function of the different transfection conditions, to a null model that assumes no effect of the HySp5/HySp5-ΔDBD, ZfSP5a or ZfSp5a-ΔDBD. We ran the Wald test and the P values were corrected for multiple testing with the Benjamini–Hochberg approach. We computed reads per kilobase of exon per million mapped reads gene expression levels using Cufflinks66.
FPKM levels were Log2-transformed, after adding an offset of 1 to each value. The Log2-transformed values were centered across samples before Principal Component Analysis (PCA); no variance scaling was performed. Heatmap plots were produced using the gplot package (version 3.0.1 in R). For this we computed the Z score ((X − μ)/σ, where for each gene μ and σ are respectively the average and standard deviation of all the replicates of the two conditions being compared and X is the FPKM value of each sample) based on the FPKM value of each gene differentially expressed between HySp5 vs HySp5-ΔDBD or between ZfSp5a vs ZfSp5a-ΔDBD. Up- and downregulated genes from this analysis were considered as HySp5 and/or ZfSp5a putative targets if they were associated with a MACpeak enriched region for these proteins (based on the chipenrich analysis described above).
GO term enrichment analysis
We used the GOrilla tool67 to search for enriched GO term categories associated with HySp5/ZfSp5a bound genes and with upregulated or downregulated HySp5/ZfSp5a putative targets using a treshold of p < 10–3 (FDR < 0,05). In the latter case, when more than 10 significantly enriched GO term categories were identified, we used the REVIGO tool68 using 0,7 as treshold for allowed similarity between related GO term classes.
Hydra genome assembly
Five clonal animals of the species Hydra viridissima and Hydra oligactis were sampled independently to extract DNA material using the DNeasy Blood & Tissue kit (Qiagen). Sequencing libraries were prepared using the TruSeq Nano DNA kit (Illumina), with 350 bp insert sizes, and sequenced paired-end using 150 cycles on an Illumina HiSeq X Ten sequencer by Macrogen Inc. Average and standard deviations of insert sizes of the sequenced reads were measured using 10 mio reads mapped to a preliminary assembly of each genome, then the two genomes were assembled using MaSuRCA v3.2.169. All scaffolds (>300 bp) and unplaced contigs (>500 bp) were retained in the final set of sequences. The redundancy of each assembly was reduced by using CD-HIT-est v4.770 with a 100% identity threshold. Sequencing depth was evaluated from the number of reads and expected genome length: Hydra viridissima: 120×; Hydra oligactis: 50×. Scaffolds assembly statistics in bp: number of scaffolds: 85677 for viridissima and 447337 for oligactis; N50: 11871 for viridissima and 5391 for oligactis.
Hydra RNA-seq transcriptomics
Multiple sequence alignment and phylogenetic analysis
For Supplementary Figure 2, the multiple sequence alignment was generated using T-Coffee71. The conserved zinc finger domains, SP and Btd boxes were visualized by IBS72. For the phylogenetic analysis of the Sp5, Sp-related and Klf-related gene families (Supplementary Figure 3), sequences from Hydra as well as from other cnidarian, ecdysozoans, lophotrochozoans and deuterostomes representative species were retrieved from Uniprot or NCBI, aligned with Muscle align (www.ebi.ac.uk/Tools/msa/muscle/)73 or MAFFT (https://mafft.cbrc.jp/alignment/server/) and tested in iterative PhyML 3.0 analyses using the LG substitution model, 8 substitution rate categories and 100 bootstraps74.
Sp5 expression in zebrafish embryos
For all zebrafish experiments, colonies of the strain AB-Tu or Nacre were used, with animals maintained at 28 °C with a maximal density of five fish per liter in a 14 h light–10 h dark cycle. The fish were fed twice a day with 2-day-old Artemia and fish embryos incubated at 28 °C. For overexpression experiments, capped sense mRNAs were synthesized using the mMESSAGE mMACHINE® Transcription Kit from Ambion (Ambion, Austin, TX USA) and 400 pg of HySp5, HySp5-ΔDBD, HySp5-ΔSP or HySp5-ΔSP-ΔDBD mRNAs injected into one cell stage embryos. For mRNA co-injection experiments, injected amounts were as follows: 400 pg of HySp5 and 4 pg of ZfWnt8 mRNA. All embryos were scored for phenotypes 48 h post fertilization.
All statistical analyses were performed with the software GraphPad Prism7. The statistical tests were two-tailed unpaired.
Further information on experimental design is available in the Nature Research Reporting Summary linked to this article.
The Hydra Sp5 sequence has been deposited in GenBank under: MG437301. The genome assemblies and reads have been deposited in the BioProject under: PRJNA419866. RNA-seq and ChIP-seq data have been deposited in the GEO database under accession code GSE121321 [https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc = GSE121321]. The authors declare that all data supporting the findings of this study are available within the article and its supplementary information files or from the corresponding author upon reasonable request. The Source Data underlying Figs. 4f, 5d and Supplementary Figs. 6b, 12d are provided as a Source Data file.
Petersen, C. P. & Reddien, P. W. Wnt signaling and the polarity of the primary body axis. Cell 139, 1056–1068 (2009).
Bode, H. R. The head organizer in Hydra. Int. J. Dev. Biol. 56, 473–478 (2012).
Shimizu, H. Transplantation analysis of developmental mechanisms in Hydra. Int. J. Dev. Biol. 56, 463–472 (2012).
Vogg, M. C., Wenger, Y. & Galliot, B. How somatic adult tissues develop organizer activity. Curr. Top. Dev. Biol. 116, 391–414 (2016).
Browne, E. N. The production of new hydranths in hydra by the insertion of small grafts. J. Exp. Zool. 7, 1–37 (1909).
Mutz, E. Transplantationsversuche an Hydra mit besonderer Beriicksichtigung der Induktion, Regionalität, Polarität. Arch. EntwMech Org. 121, 210–271 (1930).
Yao, T. Studies on the organizer problem in Pelmatohydra oligactis. I. The induction potency of the implants and the nature of the induced hydranth. J. Exp. Biol. 21, 145–150 (1945).
Webster, G. Studies on pattern regulation in hydra. II. Factors controlling hypostome formation. J. Embryol. Exp. Morphol. 16, 105–122 (1966).
MacWilliams, H. K. Hydra transplantation phenomena and the mechanism of Hydra head regeneration. II. Properties of the head activation. Dev. Biol. 96, 239–257 (1983).
Broun, M. & Bode, H. R. Characterization of the head organizer in hydra. Development 129, 875–884 (2002).
Spemann, H. & Mangold, H. Über die induktion von embryonalanlagen durch implantation artfremder organisatoren. Wilhelm. Roux’s Arch. Entw Mech. 100, 599–638 (1924).
Rand, H. W., Bovard, J. F. & Minnich, D. E. Localization of formative agencies in Hydra. Proc. Natl Acad. Sci. USA 12, 565–570 (1926).
MacWilliams, H. K. Hydra transplantation phenomena and the mechanism of hydra head regeneration. I. Properties of the head inhibition. Dev. Biol. 96, 217–238 (1983).
Gierer, A. & Meinhardt, H. A theory of biological pattern formation. Kybernetik 12, 30–39 (1972).
Turing, A. M. The Chemical Basis of Morphogenesis. Philos. T Roy. Soc. B 237, 37–72 (1952).
Kondo, S. & Miura, T. Reaction-diffusion model as a framework for understanding biological pattern formation. Science 329, 1616–1620 (2010).
Hobmayer, B. et al. WNT signalling molecules act in axis formation in the diploblastic metazoan Hydra. Nature 407, 186–189 (2000).
Lengfeld, T. et al. Multiple Wnts are involved in Hydra organizer formation and regeneration. Dev. Biol. 330, 186–199 (2009).
Nakamura, Y., Tsiairis, C. D., Ozbek, S. & Holstein, T. W. Autoregulatory and repressive inputs localize Hydra Wnt3 to the head organizer. Proc. Natl Acad. Sci. USA 108, 9137–9142 (2011).
Berking, S. Bud formation in Hydra: Inhibition by an endogenous morphogen. Wilhem Roux’s Arch. Entw Mech. 181, 215–225 (1977).
Schaller, H. C., Schmidt, T. & Grimmelikhuijzen, C. J. P. Separation and specificity of action of four morphogens from hydra. Roux Arch. Dev. Biol. 186, 139–149 (1979).
Guder, C. et al. An ancient Wnt-Dickkopf antagonism in Hydra. Development 133, 901–911 (2006).
Augustin, R. et al. Dickkopf related genes are components of the positional value gradient in Hydra. Dev. Biol. 296, 62–70 (2006).
Lommel, M. et al. Hydra mesoglea proteome identifies thrombospondin as a conserved component active in head organizer restriction. Sci. Rep. 8, 11753 (2018).
Reuter, H. et al. Beta-catenin-dependent control of positional information along the AP body axis in planarians involves a teashirt family member. Cell Rep. 10, 253–265 (2015).
Philipp, I. et al. Wnt/beta-catenin and noncanonical Wnt signaling interact in tissue evagination in the simple eumetazoan Hydra. Proc. Natl Acad. Sci. USA 106, 4290–4295 (2009).
Weidinger, G., Thorpe, C. J., Wuennenberg-Stapleton, K., Ngai, J. & Moon, R. T. The Sp1-related transcription factors sp5 and sp5-like act downstream of Wnt/beta-catenin signaling in mesoderm and neuroectoderm patterning. Curr. Biol. 15, 489–500 (2005).
Thorpe, C. J., Weidinger, G. & Moon, R. T. Wnt/beta-catenin regulation of the Sp1-related transcription factor sp5l promotes tail development in zebrafish. Development 132, 1763–1772 (2005).
Fujimura, N. et al. Wnt-mediated down-regulation of Sp1 target genes by a transcriptional repressor Sp5. J. Biol. Chem. 282, 1225–1237 (2007).
Park, D. S. et al. Role of Sp5 as an essential early regulator of neural crest specification in xenopus. Dev. Dyn. 242, 1382–1394 (2013).
Kennedy, M. W. et al. Sp5 and Sp8 recruit beta-catenin and Tcf1-Lef1 to select enhancers to activate Wnt target gene transcription. Proc. Natl Acad. Sci. USA 113, 3545–3550 (2016).
Wenger, Y. & Buzgariu, W. & Galliot, B. Loss of neurogenesis in Hydra leads to compensatory regulation of neurogenic and neurotransmission genes in epithelial cells. Philos. Trans. R. Soc. Lond. B. Biol. Sci. 371, 20150040 (2016).
Broun, M., Gee, L., Reinhardt, B. & Bode, H. R. Formation of the head organizer in hydra involves the canonical Wnt pathway. Development 132, 2907–2916 (2005).
Leost, M. et al. Paullones are potent inhibitors of glycogen synthase kinase-3beta and cyclin-dependent kinase 5/p25. Eur. J. Biochem. 267, 5983–5994 (2000).
Technau, U. et al. Parameters of self-organization in Hydra aggregates. Proc. Natl Acad. Sci. USA 97, 12127–12131 (2000).
Melotti, A. et al. The river blindness drug Ivermectin and related macrocyclic lactones inhibit WNT-TCF pathway responses in human cancer. EMBO Mol. Med. 6, 1263–1278 (2014).
Huggins, I. J. et al. The WNT target SP5 negatively regulates WNT transcriptional programs in human pluripotent stem cells. Nat. Commun. 8, 1034 (2017).
Chen, G. Y., Osada, H., Santamaria-Babi, L. F. & Kannagi, R. Interaction of GATA-3/T-bet transcription factors regulates expression of sialyl Lewis X homing receptors on Th1/Th2 lymphocytes. Proc. Natl Acad. Sci. USA 103, 16894–16899 (2006).
Zorn, A. M. et al. Regulation of Wnt signaling by Sox proteins: XSox17 alpha/beta and XSox3 physically interact with beta-catenin. Mol. Cell 4, 487–498 (1999).
Tan, C. W., Gardiner, B. S., Hirokawa, Y., Smith, D. W. & Burgess, A. W. Analysis of Wnt signaling beta-catenin spatial dynamics in HEK293T cells. BMC Syst. Biol. 8, 44 (2014).
Tan, C. W. et al. Wnt signalling pathway parameters for mammalian cells. PLoS ONE 7, e31882 (2012).
Li, Z., Nie, F., Wang, S. & Li, L. Histone H4 Lys 20 monomethylation by histone methylase SET8 mediates Wnt target gene activation. Proc. Natl Acad. Sci. USA 108, 3116–3123 (2011).
Nemeth, M. J., Topol, L., Anderson, S. M., Yang, Y. & Bodine, D. M. Wnt5a inhibits canonical Wnt signaling in hematopoietic stem cells and enhances repopulation. Proc. Natl Acad. Sci. USA 104, 15436–15441 (2007).
Mikels, A. J. & Nusse, R. Purified Wnt5a protein activates or inhibits beta-catenin-TCF signaling depending on receptor context. PLoS Biol. 4, e115 (2006).
Glinka, A. et al. Dickkopf-1 is a member of a new family of secreted proteins and functions in head induction. Nature 391, 357–362 (1998).
Kakugawa, S. et al. Notum deacylates Wnt proteins to suppress signalling activity. Nature 519, 187–192 (2015).
Chera, S. et al. Apoptotic cells provide an unexpected source of Wnt3 signaling to drive hydra head regeneration. Dev. Cell. 17, 279–289 (2009).
Widder, S., Macia, J. & Sole, R. Monomeric bistability and the role of autoloops in gene regulation. PLoS ONE 4, e5399 (2009).
Raghavan, S., Manzanillo, P., Chan, K., Dovey, C. & Cox, J. S. Secreted transcription factor controls Mycobacterium tuberculosis virulence. Nature 454, 717–721 (2008).
Bernard, C. et al. A Mouse model for conditional secretion of specific single-chain antibodies provides genetic evidence for regulation of cortical plasticity by a non-cell autonomous homeoprotein transcription factor. PLoS Genet. 12, e1006035 (2016).
Stanganello, E. et al. Filopodia-based Wnt transport during vertebrate tissue patterning. Nat. Commun. 6, 5846 (2015).
Mulligan, K. A. et al. Secreted Wingless-interacting molecule (Swim) promotes long-range signaling by maintaining Wingless solubility. Proc. Natl Acad. Sci. USA 109, 370–377 (2012).
Mii, Y. & Taira, M. Secreted Frizzled-related proteins enhance the diffusion of Wnt ligands and expand their signalling range. Development 136, 4083–4088 (2009).
Watanabe, H. et al. Nodal signalling determines biradial asymmetry in Hydra. Nature 515, 112–115 (2014).
Gierer, A. et al. Regeneration of hydra from reaggregated cells. Nat. New Biol. 239, 98–101 (1972).
Langmead, B. & Salzberg, S. L. Fast gapped-read alignment with Bowtie 2. Nat. Methods 9, 357–359 (2012).
Blankenberg, D. et al. Galaxy: a web-based genome analysis tool for experimentalists. Curr. Protoc. Mol. Biol. Chapter 19(Unit 19 10), 11–21 (2010).
Feng, J., Liu, T., Qin, B., Zhang, Y. & Liu, X. S. Identifying ChIP-seq enrichment using MACS. Nat. Protoc. 7, 1728–1740 (2012).
Bailey, T. L. et al. MEME SUITE: tools for motif discovery and searching. Nucleic Acids Res. 37, W202–W208 (2009).
Grant, C. E., Bailey, T. L. & Noble, W. S. FIMO: scanning for occurrences of a given motif. Bioinformatics 27, 1017–1018 (2011).
Zhang, X., Peterson, K. A., Liu, X. S., McMahon, A. P. & Ohba, S. Gene regulatory networks mediating canonical Wnt signal-directed control of pluripotency and differentiation in embryo stem cells. Stem Cells 31, 2667–2679 (2013).
Dobin, A. et al. STAR: ultrafast universal RNA-seq aligner. Bioinformatics 29, (15–21 (2013).
Anders, S. & Huber, W. Differential expression analysis for sequence count data. Genome Biol. 11, R106 (2010).
Yates, A. et al. Ensembl 2016. Nucleic Acids Res. 44, D710–D716 (2016).
Love, M. I., Huber, W. & Anders, S. Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biol. 15, 550 (2014).
Roberts, A., Trapnell, C., Donaghey, J., Rinn, J. L. & Pachter, L. Improving RNA-Seq expression estimates by correcting for fragment bias. Genome Biol. 12, R22 (2011).
Eden, E., Navon, R., Steinfeld, I., Lipson, D. & Yakhini, Z. GOrilla: a tool for discovery and visualization of enriched GO terms in ranked gene lists. BMC Bioinforma. 10, 48 (2009).
Supek, F., Bosnjak, M., Skunca, N. & Smuc, T. REVIGO summarizes and visualizes long lists of gene ontology terms. PLoS ONE 6, e21800 (2011).
Zimin, A. V. et al. The MaSuRCA genome assembler. Bioinformatics 29, 2669–2677 (2013).
Li, W. & Godzik, A. Cd-hit: a fast program for clustering and comparing large sets of protein or nucleotide sequences. Bioinformatics 22, 1658–1659 (2006).
Notredame, C., Higgins, D. G. & Heringa, J. T-Coffee: a novel method for fast and accurate multiple sequence alignment. J. Mol. Biol. 302, 205–217 (2000).
Liu, W. et al. IBS: an illustrator for the presentation and visualization of biological sequences. Bioinformatics 31, 3359–3361 (2015).
Edgar, R. C. MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res. 32, 1792–1797 (2004).
Guindon, S. et al. New algorithms and methods to estimate maximum-likelihood phylogenies: assessing the performance of PhyML 3.0. Syst. Biol. 59, 307–321 (2010).
This work was supported by the Swiss National Foundation (SNF 31003A_149630; 31003_169930), the Canton of Geneva, the Human Frontier Science Program (grant no. RGP0016/2010), the NCCR ‘Frontiers in Genetics’, the Claraz donation and the de Staël foundation. The authors warmly thank Denis Duboule and Claude Desplan for valuable inputs on the manuscript, Ariel Ruiz I Altaba and Charisios Tsiairis for discussions and reagents, Carol Gauron for excellent technical assistance, Nenad Suknovic and Szymon Tomczyk for help with image acquisition and the IGe3 Genomic Platform for ChIP-seq and RNA-seq library preparation and sequencing.
The authors declare no competing interests.
Journal peer review information: Nature Communications thanks the anonymous reviewers for their contribution to the peer review of this work. Peer reviewer reports are available.
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Vogg, M.C., Beccari, L., Iglesias Ollé, L. et al. An evolutionarily-conserved Wnt3/β-catenin/Sp5 feedback loop restricts head organizer activity in Hydra. Nat Commun 10, 312 (2019). https://doi.org/10.1038/s41467-018-08242-2
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