During chordate evolution, two genome-wide duplications facilitated acquisition of vertebrate traits, including emergence of neural crest cells (NCCs), in which neofunctionalization of the duplicated genes are thought to have facilitated development of craniofacial structures and the peripheral nervous system. How these duplicated genes evolve and acquire the ability to specify NC and their derivatives are largely unknown. Vertebrate SoxE paralogues, most notably Sox9/10, are essential for NC induction, delamination and lineage specification. In contrast, the basal chordate, amphioxus, has a single SoxE gene and lacks NC-like cells. Here, we test the hypothesis that duplication and divergence of an ancestral SoxE gene may have facilitated elaboration of NC lineages. By using an in vivo expression assay to compare effects of AmphiSoxE and vertebrate Sox9 on NC development, we demonstrate that all SOXE proteins possess similar DNA binding and homodimerization properties and can induce NCCs. However, AmphiSOXE is less efficient than SOX9 in transactivation activity and in the ability to preferentially promote glial over neuronal fate, a difference that lies within the combined properties of amino terminal and transactivation domains. We propose that acquisition of AmphiSoxE expression in the neural plate border led to NCC emergence while duplication and divergence produced advantageous mutations in vertebrate homologues, promoting elaboration of NC traits.
Urochordates (Tunicates), Cephalochordates (Lancelets) and Vertebrates constitute the three extant groups within the chordate lineage. Although they share the fundamental chordate body plan with a dorsal hollow nerve cord, notochord and paired gill arches, vertebrates uniquely possess neural crest cells (NCCs). The neural crest is a multipotent stem cell population that arises from the dorsal region of the neural tube, undergo an epithelial-mesenchymal transition and migrate to distant locations to differentiate into multiple, diverse derivatives, including melanocytes, peripheral ganglia and craniofacial cartilage. Acquisition of the NC is thought to have facilitated a shift in the chordate lineage from filter-feeders to active predators1. Deciphering the molecular underpinnings of how NC is evolved as a multipotent migratory population is essential for understanding the evolutionary origin of vertebrates.
The previous discoveries of migratory pigment cells2,3 and neuronal progenitors with a subset of neural crest-like properties4 within the neural plate border together with phylogenetic analysis place tunicates as the sister group of vertebrates5. In contrast, amphioxus completely lacks NC-like cells6. Tunicates have small genomes with loss of several developmental genes whereas the genome of amphioxus has retained synteny with vertebrate genome7,8. Thus amphioxus represents an excellent extant surrogate to the chordate ancestor for exploring conservation and divergence of evolutionary mechanism in NC development.
All vertebrates studied to date contain at least two to three paralogs of SoxE transcription factors family (Sox8, Sox9 and Sox10), which are crucial for NC development. The relative timing of their expression onset and function during NC development differ depending on the species9,10,11,12,13,14,15. In birds and mammals, Sox9 is the first SoxE gene to be expressed in the prospective NCCs and is rapidly downregulated as NC migrates further, whereas Sox10 expression is activated in the premigratory NC domain and maintained in migrating NCCs13. In developing chick embryos, SOX9 induces Sox10 expression and both are sufficient to transform neural tube progenitors into NC identity. In addition, SOX9 cooperates with SNAIL2 to induce ectopic NCCs with epithelial-mesenchymal transition (EMT) properties16,17. Prolonged Sox9 expression biased NC to form glial cells but not neurons13. However, NCCs are still specified in mouse embryos with germ-line specific deletion of Sox9 (genetically null) but undergo apoptosis resulting in defects in the formation of trunk NC-derivatives16. In contrast, Sox8 expression precedes that of Sox9 and Sox10 in NC progenitors of Xenopus embryos and is required for the proper onset of NC specification18. However, in mammals, SOX8 appears to be dispensable for NC development19, whereas SOX9 is essential for chondrogenic differentiation13,16,20, and SOX10 for specification of glial, melanocyte and enteric lineages21,22. These studies highlight species-specific differences in the relative importance of SOXE proteins during NC development. In addition, the chondrogenic expression and function of vertebrate Sox9 is conserved in three SoxE paralogs in lampreys (jawless vertebrates)9 and probably in the basal chordate amphioxus, which has a single SoxE gene (AmphiSoxE) with expression in oral skeleton23, suggesting an ancestral role of SoxE gene in chondrogenesis. Although previous studies demonstrated a large degree of functional similarity between a SoxE ortholog from Drosophila melanogaster, Sox100B and Sox10 in mouse NC development24, whether SoxE gene from amphioxus, the closest living relatives of vertebrates also retains function of and/or differs from vertebrate Sox9 to regulate NC ontogeny is not clear. Molecular analyses show that the neural-plate border region of amphioxus has many transcription factors common to vertebrates but lacks most “neural crest specifier” genes, most notably AmphiSoxE. The exception is AmphiSNAIL which is expressed in the dorsolateral portion of the amphioxus neural tube, though no neural crest cells arise from this domain25. This implies that the redeployment of AmphiSoxE gene and/or other ancestral NC-specifiers in the border region may have facilitated emergence of NCCs. Consistent with this, recent studies suggest that such co-option events could have helped to mediate acquisition of NC cis-regulatory sequences in the AmphiSoxE gene23. In addition, genome wide duplication results in increasing the number of SoxE paralogues and their functional diversity in vertebrates. However, it remains to be determined whether the changes in the coding sequence of SoxE genes contribute to their neofunctionalization in NC lineage diversification during the chordate evolution. To address whether duplication and divergence of an ancestral SoxE gene may have led to novel functions that facilitated emergence of the NC and its traits in vertebrates, we compared the activity of AmphiSOXE with its vertebrate homologue by analyzing their effects on chicken neural crest development as an assay system.
Phylogenetic analyses reveal the intermediate state of amphioxus SOXE during evolution
In contrast to vertebrate SoxE, AmphiSoxE is not expressed in the neural plate border region26. Phylogenetic analysis places AmphiSOXE between invertebrates and vertebrates, suggesting its intermediate state during evolution (Fig. 1). Comparative sequence analysis reveals AmphiSOXE shares only 39.1% amino acid identity with Human SOX9 (Supplemental Fig. 1), with highest conservation in the dimerization (71.4%) and HMG (96.2%) domains but only 22% identity in the transactivation domain.
Amphioxus SOXE and SOX9 show similar DNA binding and cooperative homodimerization
Next we asked whether there are detectable changes on the level of SOXE-DNA association that may have contributed to the evolution of new biochemical activities within the SOXE subgroup. AmphiSOXE shares a highly conserved amino acid sequence in both the high-mobility group (HMG) box and the DNA-dependent dimerization (DIM) domain with the mammalian SOXE proteins SOX8, SOX9 and SOX10 (Fig. 2a). The AmphiSOXE HMG box encodes two unique amino acids within the HMG box and a further four amino acids show variability within the SOXE subgroup (Fig. 2a). However, as these residues map to protein interfaces remote from the DNA they are unlikely to directly modulate DNA recognition (Fig. 2b). The N-terminal region upstream of the AmphiSOXE HMG box encodes the 40 amino acid DIM domain characteristic for the SOXE subgroup27. The DIM is evolutionarily less conserved than the HMG box and several amino acid variants within the AmphiSOXE-DIM map to positions that were previously reported to influence cooperative homodimerization on palindromic DNA elements28. Moreover, SOXE dimerization has recently been suggested to be mediated by DIM:HMG rather than by DIM:DIM interactions29 (Fig. 2b). The same study demonstrated that SOXE factors tolerate a flexible half-site spacing and dimeric complexes where observed on all tested elements with spacers ranging from 1 to 10 bp (ACAATG(n1–10)CATTGT). However, the cooperativity factor and thus the efficiency of the SOXE homodimerization was found to be highest when the half-spacing was 3, 4 or 5 bp29. We therefore compared DNA dependent dimerization of AmphiSOXE to mammalian SOX9 with quantitative electrophoretic mobility shift assays (EMSAs) using two palindromic SOXE binding sites with 4 or 5 bp spacers between the half-sites (Fig. 3a). In the absence of the DIM, the SOX9-HMG as well as the AmphiSOXE-HMG form additive dimers as indicated by a cooperativity factor ω of ~1 (Fig. 3b,d). In contrast, the SOX9-NHMG and AmphiSOXE-NHMG constructs possessing both DIM domain and HMG box dimerize substantially more effectively with strong positive cooperativity on CD-Rap and Zero DNA elements (Fig. 3c,d). However, both SOX9 and AmphiSOXE bound to and dimerized on DNA in an indistinguishable fashion indicating that they exhibit similar capacity for cooperative binding to the same DNA sequence, despite differences in amino acids within DIM and HMG regions.
Amphioxus SOXE is capable of inducing neural crest-like cells
To compare the activity of AmphiSOXE with its vertebrate homologue, we used an electroporation assay to introduce AmphiSoxE or chick Sox9 cDNA in the bicistronic pCIG nuclear-EGFP expression vector into the caudal neural tube of stage HH10–11 chick embryos prior to neural crest emigration and assessed subsequent effects on NC development (Fig. 4a). After one day (stage HH15), NCCs are actively migrating and by 2 days (HH19) have begun to differentiate into neurons within the ganglion core, whereas bipotential neural and glial precursors remain in the dorsal root ganglia (DRG) periphery16. Consistent with the possibility that recruitment of SOXE to the neural plate border may have facilitated emergence of NC, AmphiSOXE promoted NC specification and emigration from the dorsal neural tube similar to SOX9. By 24 hours post-transfection (hpt), like Sox9, AmphiSOXE also induced ectopic expression of markers characteristic of NC identity, including Sox10, FoxD3, Wnt3a, and HNK1, while repressing the neural marker SOX2 (Fig. 4b–i; Supplemental Fig. 2a–f). In contrast, neither ectopic expression of these markers nor alteration of their endogenous levels was observed in the untransfected side of the neural tube or embryos treated with pCIG control vector (Supplemental Figs 2 and 3). As with SOX913, transfected cells delaminated from lateral regions of the neural tube, accompanied by breakdown of LAMININ in the basal lamina (Fig. 5c,d,g,h) and reduction of N-CADHERIN expression in the apical region (Fig. 5a,b,e,f). Like co-expression of Sox9 and Snail216, combined electroporation of AmphiSoxE and Snail2 resulted in ectopic NC emigration due to loss of apical-basal polarity in the transfected cells (Fig. 5i–p).
Overexpression of Amphioxus SOXE drives both dorsally and ventrally migrating cells toward DRG lineages
Despite these similarities at early stages, marked differences were noted between AmphiSOXE, SOX9 and control electroporations at 48hpt. Whereas control electroporations result in GFP+ Schwann cell precursors expressing P0 along the ventral roots, cells overexpressing AmphiSOXE or SOX9 still colonized to the ventral root but failed to differentiate into Schwann cells, suggesting that prolonged expression of AmphiSoxE or Sox9 inhibited NC to differentiate into Schwann cell lineage (Supplemental Fig. 4a–c). In addition, we observed premature migration of GFP+ cells along the dorsolateral pigment pathway, which normally opens for melanoblast migration only one day later (HH21) in control embryos (Fig. 5q–t). These dorsolaterally located cells fail to express the melanocyte marker MelEM, instead expressing SOX2 (Fig. 5q–s; Fig. 6g,j, n = 10/10), characteristic of sensory neuron specification of NC30,31, suggesting a cell fate switch from melanocytic to DRG lineages.
Despite these functional similarities, we also noted marked differences in effects mediated by AmphiSOXE versus SOX9. Similar to GFP control, AmphiSOXE overexpressing embryos had GFP+ cells expressing early markers of neuronal differentiation HuC/D or ISLET1/232 and SOX2, within the core of the DRG that differentiated into neurons and glial (Fig. 6b–g; Supplemental Fig. 5 a–d’; n = 8/8). By contrast, GFP+ cells in SOX9-electroporated embryos did not express neuronal markers in the DRG core, instead localizing to the periphery where glial cells differentiate30 (Fig. 6h–j; Supplemental Fig. 5e,f’; n = 12/12). This difference in lineage specification was insensitive to dosage (Supplemental Fig. 6; n = 3/3). Thus, vertebrate SOX9 appears to be functionally divergent from AmphiSOXE in influencing glial versus neuronal differentiation.
Divergence of SOXE N- and C-terminal domains enabled glial versus neuronal differentiation bias
To examine which protein domains may be responsible for this differential activity, we generated chimeric proteins between the N-terminus, HMG-box and C-terminal transactivation domains of SOX9 and AmphiSOXE and compared their activities (Fig. 6a). N-, HMG or C-terminal domains were designated 9 when derived from SOX9 or E when derived from AmphiSOXE. All the chimeric proteins can induce HNK1 (Supplemental Fig. 7). Each combination (9-E-9; E-9-9; 9-9-E) behaved like SOX9, resulting in differentiation into glial cells but not neurons (Fig. 6k–m, q–s, t–v; Supplemental Fig. 5g,h’, k,l’; m–o’). However, NC expressing chimeric protein containing the SOX9 HMG box with both the N- and C- domains of AmphiSOXE (E-9-E), differentiated into both neurons and glial (Fig. 6n–p; Supplemental Fig. 5i,j’). These results suggest that N-and C-terminal domains of AmphiSOXE but not the HMG box are responsible for the different influence on neuronal and glial differentiation.
Transactivation activity of AmphiSOXE is weak compared with SOX9
Accordingly, we hypothesized that alterations in the ancestral SOXE N-terminus and transactivation domain may have resulted in differences in transactivation activity that could affect lineage decisions. To test this, we compared the transactivation activity of AmphiSOXE with SOX9 in vivo using Sox2- and Sox10-regulatory regions to drive luciferase (luc) reporters known to be active in the DRG33,34. Consistent with the fact that Sox2 expression is initiated in SOX9+ emigrating NCCs35 and levels of SOX2 expression are known to influence neuronal differentiation31, we found that SOX9 stimulated a marked increase of Sox2-luc reporter activity compared to AmphiSOXE, SOXE-9-E and vector control (Fig. 7a). These data suggest that AmphiSOXE is a weaker activator of Sox2 transcription, while SOX9 may inhibit neuronal differentiation by activating high levels of Sox2 expression (Sox2High). To test this, we inhibited SOX2 function by overexpressing a Sox2-EnR construct36 and Sox9 together and examined the effect on neuronal differentiation in the DRG. By 48hpt, the majority of GFP+ cells were localized in the periphery of the DRG rather than the core. Notably DRG size was unchanged and comparable numbers of HuC/D+ cells formed in both transfected and control sides (Fig. 7b). These results suggest that blocking SOX2 function in SOX9 overexpressing cells can overcome the differentiation bias in the DRG. In contrast to differences in activation of Sox2, we observed similarities in activation of the Sox10-luc reporter by AmphiSOXE, SOX9 and SOXE-9-E (Fig. 7a), consistent with their similar potency in directing GFP+ cells to differentiate into glial.
The basal jawless vertebrate, lamprey (Petromyzom marinus) (Fig. 1), has migrating NCCs and most of the NC derivatives. By ectopically expressing the lamprey Sox9 ortholog, SoxE3 (Supplemental Fig. 1), we found SoxE3 functions similarly to SOX9, inhibiting sensory neuronal formation without affecting glial differentiation (Fig. 7c). SOXE3 also transactivated Sox10-luc reporter activity to a similar degree to AmphiSOXE, SOX9 and SOXE-9-E, whereas SOXE3 activated the Sox2-luc reporter at levels less than for SOX9 but higher than for AmphiSOXE or SOXE-9-E (Fig. 7a). These data suggest that SOXE3 functions similar to SOX9 in directing NC cells to glial rather than neuron differentiation in the DRG.
Lastly, we examined the other two paralogs of vertebrate SOXE, SOX8 and SOX10, which also possessed NC-inducing activity when overexpressed in chick neural tube13,37. Similar to Sox9, overexpression of SOX8 or SOX10 inhibited neuronal fate without affecting glial cell formation (Supplemental Fig. 8a–l) and exhibited more efficient in transactivating Sox2-luc reporter activity than AmphiSOXE (Supplemental Fig. 8m), whereas the activity in transactivating Sox10-luc reporter is similar among all tested SOXE proteins (Supplemental Fig. 8n). These findings suggest that divergent function in lineage determination has been fixed and retained in the SoxE duplicate paralogs following the split of jawed vertebrates from their ancestors.
NC formation is a complex multi-step process38, regulated by a hierarchical NC gene regulatory network (NC-GRN) in vertebrates. Studies in lamprey reveal extensive functional conservation of the NC-GRN to the base of vertebrates39. In the basal chordate, amphioxus, homologues of vertebrate NC specifier genes are present in the genome but are not expressed at the neural plate border region, with the exception of AmphiSnail26. Recent data suggest that acquisition of SoxE expression in NCCs may have been driven by evolution of new cis-regulatory sequences23. In addition to regulatory changes, our data suggest that protein changes between AmphiSOXE and vertebrate SOXE may be critical. While AmphiSOXE, SOX9 and even the Drosophila ortholog SOX100B can induce NC traits at the expense of neural cell fate24, there are clear differences with respect to lineage specification. The domains largely responsible for this differential activity appear to be located in the N- and C-terminus, consistent with the finding that AmphiSOXE is a weaker transactivator of Sox2 when compared with SOX9 (Fig. 8). Previous studies showed that Sox2 expression is initiated in early migrating NCCs, maintained in the periphery of the DRG and later restricted to the satellite glial40. Overexpression of SOX2 in trunk NC culture inhibited both neuronal and glial differentiation40, whereas downregulation of Sox2 by shRNA in migrating NCCs or Wnt1-Cre mediated knockout of Sox2 in mouse NC lineage resulted in reduced sensory neurons formation in the DRG31. Since SOX2 expression and function was genetically manipulated in uncommitted NC progenitors, the findings from these studies indicate an essential requirement for optimal SOX2 dosage in maintaining bipotent state of NC progenitor in which either excessive or below the optimal level of SOX2 could lead to defects in lineage differentiation. Once NCCs reach the periphery of the DRG, SOX2 and SOX10 are co-expressed in bipotential neural progenitors, which subsequently segregate into SOX2low/SOX10− neurons and SOX2high/SOX10+ glial cells30,31. This suggests that downregulation of Sox2 is required for sensory neuron differentiation consistent with its role in the developing chick spinal cord36 while SOX2high may promote satellite glial differentiation similar to its function in the oligodendrocyte lineage41. In agreement with this, promotion of higher Sox2 expression by SOX9 compared to AmphiSOXE, correlated with a bias towards glial rather than neuronal differentiation, suggesting that proper levels of SOX2 are required for acquisition of neuronal fate within the DRG. This is further supported by the ability of SOX2-EnR protein to abolish the effect of SOX9 over-expression. Competition between the ectopic SOX2-EnR repressor and the induced endogenous SOX2 for transcriptional targets could lower effective SOX2 transactivation levels to permit neuronal differentiation. Therefore, overexpression of Sox9 exhibited two distinct effects on Sox2 expression at two different stages of NC development, induction (repression of Sox2) and differentiation into glial cells (activation of Sox2) likely through association with stage specific cofactors, which remain to be identified.
As lamprey SOXE3 behaved like SOX9 in promoting glial over neuronal fate, we speculate that the ability of all SOXE proteins to direct NC differentiation into glial may have been acquired in basal vertebrates. In contrast, although another NC specifier, vertebrate FoxD3, was able to induce ectopic NCCs when overexpressed in chick neural tube, neither Amphioxus FoxD (AmphiFoxD3) nor lamprey FoxD paralogs exhibited this activity. Domain mapping studies further revealed that N-terminal sequence is critical for the NCC differentiation-inducing activity of FoxD342. Altogether, these results suggest that co-option of SoxE into NC-GRN occurred before the genome duplication, whereas among the five known vertebrate FoxD paralogs, only FoxD3 is expressed in the NC and might have been recruited slightly later than other NC specifiers, after the genome duplication. In addition, duplicated paralogs of SoxE and FoxD family acquire neofunctionalization properties at the level of NC lineage determination and specification, respectively via changes of specific protein sequences. The reasons underlying the distinct onset of neofunctionalization in both NC specifiers are not clear. Since the C-terminal motif of FoxD3 essential for the differentiation of dorsal mesodermal in Xenopus embryos is conserved in AmphiFoxD42,43, it is tempting to speculate that ancestral FoxD might be important in mesoderm development, resulting in late onset of acquiring the novel ability to induce NCCs.
Our data also imply that acquisition of a stronger transactivation potential in vertebrate SOX9 may have been advantageous during evolution of transcriptional regulation to ensure activation of SOX9 target genes at appropriate levels for tissue development. Consistent with the important contribution of evolving a strongly transactivating SOXE factor for the neural crest in vertebrates, it is noted that heterozygous mutations in the transactivation domain of SOX9 may lead to differential severity of Campomelic Dysplasia because of hypomorphic effects44,45. It is also notable that some mutations in the transactivation domain of SOX10 can lead to milder Waardenberg syndrome phenotypes than those that cause loss of function46,47. Our findings indicate that a weaker transactivation activity leads to loss of differential differentiation fate. Thus, we speculate that the two genome-wide duplications in the vertebrate lineage allowed duplication and divergence of SoxE genes, conferring additional later functions that may be essential for controlling proper migration and cell lineage segregation. Altogether, our results suggest that acquisition of SOXE to the neural plate border (through a regulatory change) accompanied by duplication and divergence of its protein domains (via advantageous mutations) that strengthened its transactivation ability, allowed elaboration of NC derivatives into peripheral ganglia and perhaps also the craniofacial skeleton (Fig. 8).
Materials and Methods
All experimental protocols were approved by the Committee on the Use of Live Animals in Teaching and Research (CULATR) in the University of Hong Kong. All the methods were carried out in accordance with the guidelines approved by the Committee on the Use of Live Animals in Teaching and Research (CULATR) in the University of Hong Kong.
The SOX9-HMG and SOX9-NHMG proteins were prepared using a bacterial pET-vector based expression system as described29. AmphiSOXE-HMG and the AmphiSOXE-NHMG were PCR amplified using primers with overhangs for attB sites and an N-terminal tobacco etch virus (TEV) protease cleavage site and cloned into a pDEST-hisMBP expression plasmid48 using the Gateway BP and LR cloning system (Invitrogen). The expression plasmids were transferred into the BL21(DE3)pLySs E. coli strain and the proteins were expressed and purified using established methods29.
EMSAs were carried out as reported recently29. In brief, dsDNA probes were prepared by combining forward strands with 5′ cy5 label and unlabeled reverse strands (Life Technologies) in 1X annealing buffer (20 mM Tris–HCl, pH 8.0; 50 mM MgCl2; 50 mM KCl) followed by heating to 95 °C for 5 min and cooling to 4 °C at 1 °C/min. For each EMSA reaction, 50 nM dsDNA probes were mixed with varying concentrations of protein in 1X EMSA buffer (10 mM Tris–HCl pH 8.0, 0.1 mg/ml bovine serum albumin, 50 μM ZnCl2, 100 mM KCl, 10% (v/v) glycerol, 0.1% (v/v) Igepal CA630 and 2 mM beta-mercaptoethanol). Samples were loaded onto 12% 1X Tris-glycine (TG, 25 mM Tris-HCl pH 8.0, 192 mM glycine) native PAGE gels after incubating at 4 °C in the dark for 4 h. The gel were run at 200 V for 40 min in 1X TG buffer in the cold room and imaged with a Typhoon FLA-7000 PhosphorImager (FUJIFILM). The intensities were detected with the Image Quant software (GE Healthcare) and cooperativity factors were calculated using previously reported equations49.
In ovo electroporation and expression vectors
Fertilized white Leghorn eggs were obtained from Tin Hang Technology Co. Limited and incubated in a humidified incubator at 38 °C. Embryos were staged as described previously50. In ovo electroporation was carried out as described13. Expression constructs were generated in the pCAGGS vector for mouse Sox8, Sox9, Sox10, AmphiSoxE and LampreySoxE3. Chimeric SoxE-9-9, Sox9-E-9, Sox9-9-E and SoxE-9-E conrstructs were generated by DNA recombineering using DY380 bacteria51. For electroporation, each Sox construct was co-injected with an EGFP expression construct into the lumen of Hamburger Hamilton stage 10–12 neural tubes. Electroporation was carried out using a BTX electroporator delivering five 50-ms pulses of 30V across the neural tube. Transfected embryos were incubated for 24 and 48 h before processing. Sox2-Luc reporter was generated by cloning the Sox2-NC1 enhancer33 into the pGL3-promoter vector (Promega). Sox10-Luc reporter (pE1B-C-F/Sox10-MCS4) was purchased in Addgen (#20243)34.Sox2-EnR was a gift of Prof. Jonas Muhr36.
In situ hybridisation and immunohistochemistry
Transfected embryos were fixed for an hour at 4 °C in 4% paraformaldehyde in 0.1 M phosphate buffer (PB), cryoprotected with 30% sucrose in PB and cryosectioned. In situ hybridization on cryosections was performed as described13, using probes for chick, Sox1052, Wnt3a (a gift from N. Itasaki) and FoxD3 chick expressed sequence tag clone. Immunohistochemical staining was performed using the antibodies against: green fluorescent protein (GFP) (Molecular Probes), Laminin (Sigma), HNK-1 (Becton Dickinson), HuC/D (Invitrogen), SOX2 (Neuromics), Islet1/2 (DSHB), P0 (DSHB) and MelEM (DSHB). Immunofluorescence images were photographed using a Zeiss LSM700 confocal microscope in the Faculty Core Facility, Li Ka Shing Faculty of Medicine, the University of Hong Kong.
Sox2-NC1 or Sox10-MCS4 enhancer driven luciferase reporters were mixed with Renilla and the relevant Sox expression construct and electroporated into the lumen of the chick neural tube. The trunk parts of embryos were collected 1–2 days later, lysed and assayed following the Promega’s manual. Statistical analysis was performed using a Student’s t-test.
Accession codes: Accession numbers for the sequences used in this study are as follows: Rattus norvegicus (Sox8: NP_001100458; Sox10: NP_); Mus musculus (Sox8: NP_035577; Sox9: NM_035578; Sox10: NP_035567); Gallus gallus (Sox8: NP_990062; Sox9: NP_989612; Sox10: NP_990123); Homo sapiens (Sox8: NM_055402; Sox9: NP_000337; Sox10: NP_990123); Xenopus laevis (Sox8: NP_001083964; Sox9: NP_001084276; Sox10: NP_001082358); Danio rerio (Sox8: NP_001020636; Sox9a: NP_571718; Sox9b: AAH67133; Sox10: NP_571950); Petromyzon marinus (SoxE1: AAW34332; SoxE2: ABC58684; SoxE3: ABC58685); Eptatretus burgeri (Sox9: BAG11536); Ciona intestinalis (SoxE: CAD58841); Lytechinus variegatus (SoxE: ABY40629); Drosophila melanogaster (Sox100B: NP_651839); Apis mellifera (SoxE1: XP_001122993; SoxE2: XP_001122996) and Nasonia vitripennis (SoxE1: XP_001604913; SoxE2: XP_008213434).
How to cite this article: Tai, A. et al. SOXE neofunctionalization and elaboration of the neural crest during chordate evolution. Sci. Rep. 6, 34964; doi: 10.1038/srep34964 (2016).
Green, S. A., Simoes-Costa, M. & Bronner, M. E. Evolution of vertebrates as viewed from the crest. Nature 520, 474–482, doi: 10.1038/nature14436 (2015).
Jeffery, W. R., Strickler, A. G. & Yamamoto, Y. Migratory neural crest-like cells form body pigmentation in a urochordate embryo. Nature 431, 696–699, doi: 10.1038/nature02975 (2004).
Abitua, P. B., Wagner, E., Navarrete, I. A. & Levine, M. Identification of a rudimentary neural crest in a non-vertebrate chordate. Nature 492, 104–107, doi: 10.1038/nature11589 (2012).
Stolfi, A., Ryan, K., Meinertzhagen, I. A. & Christiaen, L. Migratory neuronal progenitors arise from the neural plate borders in tunicates. Nature 527, 371–374, doi: 10.1038/nature15758 (2015).
Delsuc, F., Brinkmann, H., Chourrout, D. & Philippe, H. Tunicates and not cephalochordates are the closest living relatives of vertebrates. Nature 439, 965–968, doi: 10.1038/nature04336 (2006).
Holland, L. Z., Laudet, V. & Schubert, M. The chordate amphioxus: an emerging model organism for developmental biology. Cell Mol Life Sci 61, 2290–2308, doi: 10.1007/s00018-004-4075-2 (2004).
Dehal, P. et al. The draft genome of Ciona intestinalis: insights into chordate and vertebrate origins. Science 298, 2157–2167, doi: 10.1126/science.1080049 (2002).
Putnam, N. H. et al. The amphioxus genome and the evolution of the chordate karyotype. Nature 453, 1064–1071, doi: 10.1038/nature06967 (2008).
McCauley, D. W. & Bronner-Fraser, M. Importance of SoxE in neural crest development and the evolution of the pharynx. Nature 441, 750–752, doi: 10.1038/nature04691 (2006).
McCauley, D. W. & Bronner-Fraser, M. Conservation and divergence of BMP2/4 genes in the lamprey: expression and phylogenetic analysis suggest a single ancestral vertebrate gene. Evolution & development 6, 411–422, doi: 10.1111/j.1525-142X.2004.04054.x (2004).
Yan, Y. L. et al. A pair of Sox: distinct and overlapping functions of zebrafish sox9 co-orthologs in craniofacial and pectoral fin development. Development 132, 1069–1083, doi: 10.1242/dev.01674 (2005).
Kluver, N., Kondo, M., Herpin, A., Mitani, H. & Schartl, M. Divergent expression patterns of Sox9 duplicates in teleosts indicate a lineage specific subfunctionalization. Development genes and evolution 215, 297–305, doi: 10.1007/s00427-005-0477-x (2005).
Cheung, M. & Briscoe, J. Neural crest development is regulated by the transcription factor Sox9. Development 130, 5681–5693, doi: 10.1242/dev.00808 (2003).
Sakai, D., Suzuki, T., Osumi, N. & Wakamatsu, Y. Cooperative action of Sox9, Snail2 and PKA signaling in early neural crest development. Development 133, 1323–1333, doi: 10.1242/dev.02297 (2006).
Kellerer, S. et al. Replacement of the Sox10 transcription factor by Sox8 reveals incomplete functional equivalence. Development 133, 2875–2886, doi: 10.1242/dev.02477 (2006).
Cheung, M. et al. The transcriptional control of trunk neural crest induction, survival, and delamination. Developmental cell 8, 179–192, doi: 10.1016/j.devcel.2004.12.010 (2005).
Liu, J. A. et al. Phosphorylation of Sox9 is required for neural crest delamination and is regulated downstream of BMP and canonical Wnt signaling. Proc Natl Acad Sci USA 110, 2882–2887, doi: 10.1073/pnas.1211747110 (2013).
O’Donnell, M., Hong, C. S., Huang, X., Delnicki, R. J. & Saint-Jeannet, J. P. Functional analysis of Sox8 during neural crest development in Xenopus. Development 133, 3817–3826, doi: 10.1242/dev.02558 (2006).
Sock, E., Schmidt, K., Hermanns-Borgmeyer, I., Bosl, M. R. & Wegner, M. Idiopathic weight reduction in mice deficient in the high-mobility-group transcription factor Sox8. Molecular and cellular biology 21, 6951–6959, doi: 10.1128/MCB.21.20.6951-6959.2001 (2001).
Mori-Akiyama, Y., Akiyama, H., Rowitch, D. H. & de Crombrugghe, B. Sox9 is required for determination of the chondrogenic cell lineage in the cranial neural crest. Proceedings of the National Academy of Sciences of the United States of America 100, 9360–9365, doi: 10.1073/pnas.1631288100 (2003).
Sonnenberg-Riethmacher, E. et al. Development and degeneration of dorsal root ganglia in the absence of the HMG-domain transcription factor Sox10. Mechanisms of development 109, 253–265 (2001).
Southard-Smith, E. M., Kos, L. & Pavan, W. J. Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model. Nature genetics 18, 60–64, doi: 10.1038/ng0198-60 (1998).
Jandzik, D. et al. Evolution of the new vertebrate head by co-option of an ancient chordate skeletal tissue. Nature 518, 534–537, doi: 10.1038/nature14000 (2015).
Cossais, F. et al. Replacement of mouse Sox10 by the Drosophila ortholog Sox100B provides evidence for co-option of SoxE proteins into vertebrate-specific gene-regulatory networks through altered expression. Developmental biology 341, 267–281, doi: 10.1016/j.ydbio.2010.01.038 (2010).
Yu, J. K. The evolutionary origin of the vertebrate neural crest and its developmental gene regulatory network–insights from amphioxus. Zoology 113, 1–9, doi: 10.1016/j.zool.2009.06.001 (2010).
Yu, J. K., Meulemans, D., McKeown, S. J. & Bronner-Fraser, M. Insights from the amphioxus genome on the origin of vertebrate neural crest. Genome research 18, 1127–1132, doi: 10.1101/gr.076208.108 (2008).
Peirano, R. I. & Wegner, M. The glial transcription factor Sox10 binds to DNA both as monomer and dimer with different functional consequences. Nucleic acids research 28, 3047–3055 (2000).
Schlierf, B., Ludwig, A., Klenovsek, K. & Wegner, M. Cooperative binding of Sox10 to DNA: requirements and consequences. Nucleic acids research 30, 5509–5516 (2002).
Huang, Y. H., Jankowski, A., Cheah, K. S., Prabhakar, S. & Jauch, R. SOXE transcription factors form selective dimers on non-compact DNA motifs through multifaceted interactions between dimerization and high-mobility group domains. Scientific reports 5, 10398, doi: 10.1038/srep10398 (2015).
Wakamatsu, Y., Maynard, T. M. & Weston, J. A. Fate determination of neural crest cells by NOTCH-mediated lateral inhibition and asymmetrical cell division during gangliogenesis. Development 127, 2811–2821 (2000).
Cimadamore, F. et al. Human ESC-derived neural crest model reveals a key role for SOX2 in sensory neurogenesis. Cell stem cell 8, 538–551, doi: 10.1016/j.stem.2011.03.011 (2011).
Cui, S. & Goldstein, R. S. Early markers of neuronal differentiation in DRG: islet-1 expression precedes that of Hu. Brain research. Developmental brain research 121, 209–212 (2000).
Uchikawa, M., Ishida, Y., Takemoto, T., Kamachi, Y. & Kondoh, H. Functional analysis of chicken Sox2 enhancers highlights an array of diverse regulatory elements that are conserved in mammals. Developmental cell 4, 509–519 (2003).
Antonellis, A. et al. Identification of neural crest and glial enhancers at the mouse Sox10 locus through transgenesis in zebrafish. PLoS genetics 4, e1000174, doi: 10.1371/journal.pgen.1000174 (2008).
Adameyko, I. et al. Sox2 and Mitf cross-regulatory interactions consolidate progenitor and melanocyte lineages in the cranial neural crest. Development 139, 397–410, doi: 10.1242/dev.065581 (2012).
Bylund, M., Andersson, E., Novitch, B. G. & Muhr, J. Vertebrate neurogenesis is counteracted by Sox1-3 activity. Nature neuroscience 6, 1162–1168, doi: 10.1038/nn1131 (2003).
McKeown, S. J., Lee, V. M., Bronner-Fraser, M., Newgreen, D. F. & Farlie, P. G. Sox10 overexpression induces neural crest-like cells from all dorsoventral levels of the neural tube but inhibits differentiation. Dev Dyn 233, 430–444, doi: 10.1002/dvdy.20341 (2005).
Bronner, M. E. & LeDouarin, N. M. Development and evolution of the neural crest: an overview. Developmental biology 366, 2–9, doi: 10.1016/j.ydbio.2011.12.042 (2012).
Sauka-Spengler, T., Meulemans, D., Jones, M. & Bronner-Fraser, M. Ancient evolutionary origin of the neural crest gene regulatory network. Developmental cell 13, 405–420, doi: 10.1016/j.devcel.2007.08.005 (2007).
Wakamatsu, Y., Endo, Y., Osumi, N. & Weston, J. A. Multiple roles of Sox2, an HMG-box transcription factor in avian neural crest development. Dev Dyn 229, 74–86, doi: 10.1002/dvdy.10498 (2004).
Hoffmann, S. A. et al. Stem cell factor Sox2 and its close relative Sox3 have differentiation functions in oligodendrocytes. Development 141, 39–50, doi: 10.1242/dev.098418 (2014).
Ono, H., Kozmik, Z., Yu, J. K. & Wada, H. A novel N-terminal motif is responsible for the evolution of neural crest-specific gene-regulatory activity in vertebrate FoxD3. Dev Biol 385, 396–404, doi: 10.1016/j.ydbio.2013.11.010 (2014).
Yaklichkin, S., Steiner, A. B., Lu, Q. & Kessler, D. S. FoxD3 and Grg4 physically interact to repress transcription and induce mesoderm in Xenopus. J Biol Chem 282, 2548–2557, doi: 10.1074/jbc.M607412200 (2007).
Bi, W., Deng, J. M., Zhang, Z., Behringer, R. R. & de Crombrugghe, B. Sox9 is required for cartilage formation. Nat Genet 22, 85–89, doi: 10.1038/8792 (1999).
Pop, R., Zaragoza, M. V., Gaudette, M., Dohrmann, U. & Scherer, G. A homozygous nonsense mutation in SOX9 in the dominant disorder campomelic dysplasia: a case of mitotic gene conversion. Human genetics 117, 43–53, doi: 10.1007/s00439-005-1295-y (2005).
Chaoui, A. et al. Identification and functional analysis of SOX10 missense mutations in different subtypes of Waardenburg syndrome. Human mutation 32, 1436–1449, doi: 10.1002/humu.21583 (2011).
Jung, H. J., Jin, S. A., Choi, S. J., Lee, S. C. & Yun, S. J. A de novo SOX10 mutation in a patient with Waardenburg syndrome type IV. Journal of the American Academy of Dermatology 68, e177–e178, doi: 10.1016/j.jaad.2012.10.021 (2013).
Nallamsetty, S. & Waugh, D. S. A generic protocol for the expression and purification of recombinant proteins in Escherichia coli using a combinatorial His6-maltose binding protein fusion tag. Nature protocols 2, 383–391, doi: 10.1038/nprot.2007.50 (2007).
BabuRajendran, N. et al. Structure of Smad1 MH1/DNA complex reveals distinctive rearrangements of BMP and TGF-beta effectors. Nucleic acids research 38, 3477–3488, doi: 10.1093/nar/gkq046 (2010).
Hamburger, V. & Hamilton, H. L. A series of normal stages in the development of the chick embryo. Journal of morphology 88, 49–92 (1951).
Zhang, Y., Buchholz, F., Muyrers, J. P. & Stewart, A. F. A new logic for DNA engineering using recombination in Escherichia coli. Nature genetics 20, 123–128, doi: 10.1038/2417 (1998).
Cheng, Y., Cheung, M., Abu-Elmagd, M. M., Orme, A. & Scotting, P. J. Chick sox10, a transcription factor expressed in both early neural crest cells and central nervous system. Brain research. Developmental brain research 121, 233–241 (2000).
Schwarz, R. & Dayhoff, M. Matrices for detecting distant relationships. (National Biomedical Research Foundation, 1979).
Kumar, S., Stecher, G. & Tamura, K. MEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for Bigger Datasets. Molecular biology and evolution 33, 1870–1874, doi: 10.1093/molbev/msw054 (2016).
M., N. & S., K. Molecular Evolution and Phylogenetics. (Oxford University Press, New York, 2000).
Palasingam, P. et al. The Structure of Sox17 Bound to DNA Reveals a Conserved Bending Topology but Selective Protein Interaction Platforms. J. Mol. Bio. 388, 619–630 (2003).
Sock, E. et al. Loss of DNA-dependent dimerization of the transcription factor SOX9 as a cause for campomelic dysplasia. Human molecular genetics 12, 1439–1447 (2003).
This work was supported by grants from the Research Grants Council and University Grants Council of Hong Kong (7337/01M), (AoE/M-04/04), (T12-708/12-N) and (T12C-714/14-R) to K.S.E.C., GRF_17110715 to M.C and NS086907 to M.E.B. We thank Robin Lovell-Badge and Patrick Tam for helpful discussion, and Hisato Kondoh and Masanori Uchikawa for providing the Sox2-NC1 construct. We thank Yogesh Srivastava (GIBH) for help with structural modeling and May Cheung for technical assistance. R.J. is supported by a 2013 MOST China-EU Science and Technology Cooperation Program (grant number 2013DFE33080), by the National Natural Science Foundation of China (grant number 31471238), a 100 talent award of the Chinese Academy of Sciences and a Science and Technology Planning Project of Guangdong Province, China (2014B030301058).
The authors declare no competing financial interests.
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Tai, A., Cheung, M., Huang, YH. et al. SOXE neofunctionalization and elaboration of the neural crest during chordate evolution. Sci Rep 6, 34964 (2016). https://doi.org/10.1038/srep34964