Chordates undergo a characteristic morphogenetic process during neurulation to form a dorsal hollow neural tube. Neurulation begins with the formation of the neural plate and ends when the left epidermis and right epidermis overlying the neural tube fuse to close the neural fold. During these processes, mitosis and the various morphogenetic movements need to be coordinated. In this study, we investigated the epidermal cell cycle in Ciona intestinalis embryos in vivo using a fluorescent ubiquitination-based cell cycle indicator (Fucci). Epidermal cells of Ciona undergo 11 divisions as the embryos progress from fertilization to the tadpole larval stage. We detected a long G2 phase between the tenth and eleventh cell divisions, during which fusion of the left and right epidermis occurred. Characteristic cell shape change and actin filament regulation were observed during the G2 phase. CDC25 is probably a key regulator of the cell cycle progression of epidermal cells. Artificially shortening this G2 phase by overexpressing CDC25 caused precocious cell division before or during neural tube closure, thereby disrupting the characteristic morphogenetic movement. Delaying the precocious cell division by prolonging the S phase with aphidicolin ameliorated the effects of CDC25. These results suggest that the long interphase during the eleventh epidermal cell cycle is required for neurulation.
At the initial stages of animal embryogenesis, blastomeres undergo rapid and synchronous cell division called cleavage, which is characterized by very short gap (G1 and G2) phases. When embryogenesis proceeds, longer G1 and/or G2 phases are introduced, and from then on, blastomeres undergo the conventional cell cycle (Kipreos, 2005; Philpott and Yew, 2008). This transition in cell cycle composition is thought to be an adjustment that allows morphogenetic movement to occur (Duncan and Su, 2004). Studies in the protostome Drosophila melanogaster have shown that the G2 phase is added at the 14th cell cycle from fertilization (Grosshans and Wieschaus, 2000; Nabel-Rosen et al., 2005). The addition of the G2 phase is necessary for proper morphogenetic movement, as disruption of the G2 phase insertion in tribbles mutants leads to gastrulation defects (Mata et al., 2000). A similar phenomenon has been observed in the vertebrate Xenopus laevis, in which cell cycle arrest around the midblastula transition (MBT) is necessary for gastrulation (Murakami et al., 2004) and for the convergent extension of paraxial mesoderm (Leise and Mueller, 2004). These studies suggest the importance of changes in cell cycle composition for morphogenesis in both protostomes and deuterostomes. To understand the mechanisms of morphogenesis, we must determine how morphogenetic movement and the cell cycle are balanced.
Neurulation is a key morphogenetic movement of chordate embryos that involves the dorsal hollow neural tube (Gilbert, 2006). Neurulation occurs in two parts, primary neurulation and secondary neurulation. Primary neurulation consists of multiple steps: formation of the neural plate; invagination of the neural plate to form the neural groove; convergent extension of the neural plate cells; and closure of the neural tube by the fusion of the left and right neural folds, including the epidermal layer that overlays the neural tube (Colas and Schoenwolf, 2001). Cellular and molecular mechanisms of neurulation have been analyzed extensively; the invagination of the neural plate occurs by apical constriction mediated by Shroom (Hildebrand and Soriano, 1999) and p190RhoGAP (Brouns et al., 2000), and convergent extension of the neural plate is caused by the planar cell polarity (PCP) pathway (Wallingford, 2006). It has been shown that neurulation cannot be accomplished solely by means of the intrinsic movement of the neural plate: contribution from the surrounding epidermis is required for appropriate neural tube formation. The transcription factor AP-2, which is expressed in the epidermis but not in the neural plate, is necessary for proper neural tube closure (Zhang et al., 1996). It has been suggested that the expansion of the epidermal layer, which can be attributed to changes in cell shape, position and number, produces the pushing force that causes the neural plate to bend (Sausedo et al., 1997). Hence, epidermal cells engage in both cell division and morphogenetic movement during neurulation. However, coordination between the cell cycle and the morphogenetic movement of the epidermal layer has not been fully elucidated in vertebrate neurulation. One limitation is that vertebrate neurula-stage embryos consist of an enormous number of cells, and it is thus difficult to trace the cell cycle in a tissue-specific manner. Another experimental system is needed to overcome this problem.
The ascidian Ciona intestinalis is an excellent species in which to observe cell cycle progression during neurulation (Satoh, 2003). Like vertebrate embryos, Ciona embryos undergo neurulation to construct a dorsal hollow neural tube. The manner of Ciona neurulation is closely related to primary neurulation in vertebrates (Nicol and Meinertzhagen, 1988a; Nicol and Meinertzhagen, 1988b; Lowery and Sive, 2004). Ciona embryos and larvae are semi-transparent, and the number of constituent cells is extraordinarily small. The larva consists of ∼2,600 cells, with approximately 800 monolayer epidermal cells (Satoh, 1994). The small cell number is advantageous for observing the cell cycle during neurulation at cellular resolution (Nicol and Meinertzhagen, 1988a; Nicol and Meinertzhagen, 1988b). Cell lineage studies have allowed the observation of cell cycle progression in a specific lineage (Nishida, 1987; Pasini et al., 2006). The lineage tracing experiments have shown that epidermal cells undergo seven divisions before the initiation of gastrulation at the 110-cell stage, and divide four times during gastrulation, neurulation and tailbud formation. The epidermal cells then stop dividing until the hatching of larvae (Pasini et al., 2006).
A fluorescent ubiquitination-based cell cycle indicator (Fucci) was recently developed to trace the cell cycle during development in vivo (Sakaue-Sawano et al., 2008). The Fucci system utilizes fusions of fluorescent proteins and the ubiquitination boxes of two proteins, Geminin and Cdt1. Geminin is accumulated in the S, G2 and M phases and degraded in the late M phase, whereas Cdt1 is accumulated in the G1 phase and degraded during the S, G2 and M phases (Nishitani et al., 2004). Therefore, fluorescence of the Geminin-based indicator corresponds to the S/G2/M phases and the Cdt1-based indicator corresponds to the G1 phase. In this study, we introduced this system into Ciona embryos together with time-lapse imaging to observe cell cycle progression during neurulation. We found that a long G2 phase is inserted in the specific cell cycle between the tenth and eleventh divisions of epidermal cells. This cell cycle event coincides with the timing of neural tube closure by means of the fusion of the left and right epidermis. Through genetic and pharmacological analyses we show that the prolongation of the cell cycle is necessary for neural tube closure to occur.
MATERIALS AND METHODS
A Ci-EF1α promoter (Sasakura et al., 2010) was inserted into the multicloning site of pcDNA3-mAG-hGem(1/110), pcDNA3-mVenus-hGem(1/110), pcDNA3-mKO2-hCdt1(1/100), pcDNA3-mKO2-hCdt1(30/120) or pT2-mKO2-zCdt1(1/170). An RfC1 cassette was inserted into pcDNA3-CiEF1α–mKO2-hCdt1(1/100), pcDNA3-CiEF1α–mKO2-hCdt1(30/120) and pT2-CiEF1α–mKO2-zCdt1(1/170). Ci-EF1α–mAG-hGem(1/110) was inserted by the Gateway system (Invitrogen). gap43-egfp of pSP72-pFOG::B1-GAP43-GFP-B2 (Roure et al., 2007) was inserted into pSP-eGFP, then egfp was replaced by ecfp to create pSPGAP43C. A Ci-Epi1 promoter was inserted into pSPGAP43C to create pSPCiEpi1GAP43C. A CAAX box (Fukano et al., 2007) was subcloned into pSPKaede (Hozumi et al., 2010), pSP-Venus and pSP-mCherry to create pSP-KCAAX, pSPVCAAX and pSPmCheCAAX, respectively. A Ci-Epi1 promoter was inserted into pSPKCAAX to create pSPCiEpi1KCAAX. A BamHI fragment of Ci-ETR promoter was inserted into pSPmCheCAAX to create pSPCiETRmCheCAAX. The egfp cDNA of pSP-eGFP was replaced by a cDNA of Ci-cdc25, then a Ci-Epi1 promoter was inserted to create pSPCiEpi1Cicdc25. CiEpi1-gap43-ecfp, CiEpi1-KCAAX, CiEpi1-VCAAX, and CiEpi1-mCheCAAX were subcloned into pSPCiEpi1Cicdc25 to create pSPCiEpi1Cicdc25CiEpi1GAP43C, pSPCiEpi1Cicdc25CiEpi1KCAAX, pSPCiEpi1Cicdc25CiEpi1VCAAX and pSPCiEpi1Cicdc25CiEpi1mCheCAAX, respectively. The egfp cDNA of pSP-eGFP was replaced by a histone 2B ORF (Roure et al., 2007) fused with mCherry, and then a Ci-Epi1 promoter was inserted to create pSPCiEpi1H2BmCherry. Fucci constructs and H2BmCherry cassettes were inserted into pBS-HTB (Akanuma et al., 2002). mRNA was synthesized with the Megascript T3 (Ambion), cap structure analog (New England Biolabs), and poly(A) tailing kit (Ambion).
Time-lapse imaging using wide-field microscopy
The vectors shown in Fig. 1A were electroporated into one-cell-stage embryos (Corbo et al., 1997). The embryos were reared at 18°C until imaging. Time-lapse imaging was performed using the AxioImager Z1 wide-field fluorescent microscope system (Carl Zeiss). Imaging was performed in a room maintained at 20°C. We found no significant deviation from the developmental table (Hotta et al., 2007) defined at 18°C until 8.5 hours post fertilization (hpf). pSPCiEpi1GAP43C and pSPCiEpi1CiCdc25CiEpi1GAP43C (linearized with XhoI) were microinjected into unfertilized eggs together with mVenus-hGem(1/110) mRNA. At 6.0 hpf, the embryos were mounted on a glass-based dish, and time-lapse imaging was performed. The recording interval was 5 minutes. In the aphidicolin administration experiment, imaging was halted at 6 hours 55 minutes, aphidicolin was added at the concentration of 2 μg/ml, and imaging was restarted from 7.0 hpf.
Time-lapse imaging using confocal laser scanning microscopy
To observe the global cell cycle progression pattern, we microinjected mAG-hGem(1/110) and mKO2-hCdt1(1/100) mRNA into unfertilized eggs. For epidermal cell tracking experiments, mRNA of H2BmCherry was microinjected with mRNA of mAG-hGem(1/110). At 5-6 hpf, the embryos were mounted on a glass-based dish, and time-lapse 3D imaging was performed using an FV10i confocal microscope (Olympus) at 20°C. The recording interval was either 5 minutes or 10 minutes. At each time point, z-stack images were generated in the Fluoview viewer (Olympus). To observe cell shape change during the neural tube closure, pSPCiEpi1KCAAX or pSPCiEpi1Cicdc25CiEpi1KCAAX was electroporated into one-cell-stage embryos. At 5-6 hpf, the embryos were mounted on a glass-based dish and 10 μM FM4-64 (Molecular Probes) was added. Embryos were treated with 100 μM Y-27632 from 6.0 hpf.
Whole-mount in situ hybridization
Whole-mount in situ hybridization was performed essentially according to Yasuo and Satoh (Yasuo and Satoh, 1994). pSPCicdc25 was digested with SalI and EcoRI, and this partial cDNA fragment of Ci-cdc25 was inserted into the SalI and EcoRI sites of pBluescript SKII+. This vector was used as a template to synthesize digoxigenin-labeled probes for in situ hybridization. Probes were washed at 55°C and the final washing step was carried out using 30 mM NaCl, 3 mM sodium citrate, 0.1 % Tween 20.
Incorporation of EdU
The embryos were treated with 10 μM 5-ethynyl-2′-deoxyuridine (EdU) at 6.5 hpf, 7.0 hpf or 7.5 hpf for 30 minutes at 18°C. After fixation with 5% formaldehyde in sea-water, EdU incorporation was detected with a Click-iT EdU Alexa Fluor Imaging Kit (Invitrogen).
Immunostaining and phalloidin staining
mVenus-hGem(1/110) was immunostained with anti-GFP antibody (1:1000; Nacalai Tesque) and Alexa-488-conjugated anti-rabbit antibody (Invitrogen) for observation of EdU incorporation in Fucci-expressing embryos. To detect Phospho-histone H3 (PH3), pSPCiEpiIH2BmCherry was introduced into embryos, which were fixed at 7.75 hpf. PH3 was stained with anti-PH3 Ser10 antibody (1:100) (Tarallo and Sordino, 2004) and Alexa-488 conjugated anti-rabbit antibody. Embryos were stained with Alexa-488-conjugated phalloidin (Invitrogen) to detect F-actin.
Application of live-imaging probes to monitor cell cycle progression in Ciona intestinalis embryos
Several derivatives of Fucci probes have been created that are optimized for vertebrates (Sakaue-Sawano et al., 2008; Sugiyama et al., 2009). We tested whether these Fucci probes could monitor cell cycle progression in Ciona. For the Geminin-based Fucci, we tested mAG-hGem(1/110) and mVenus-hGem(1/110), which are fusions of a part of human Geminin (amino acids 1-110) with monomeric Azami Green (mAG) and monomeric Venus-YFP (mVenus), respectively. The Geminin-based Fucci probes emit green fluorescence. For Cdt1-based Fucci, there are two different human Cdt1 (hCdt1)-based Fucci probes: one includes amino acids 1-100 [hCdt1(1/100)] and the other includes amino acids 30-120 [hCdt1(30/120)]. We also tested a zebrafish Cdt1 (zCdt1)-based probe that includes amino acids 1-170. DNAs encoding these partial Cdt1 proteins were fused with cDNAs of monomeric Kusabira Orange 2 (mKO2), resulting in emission of orange fluorescence upon expression.
Expression of these Fucci probes was driven in the Ciona embryos and larvae with a ubiquitous promoter of Ci-EF1α (Fig. 1A) (Sasakura et al., 2010). At the larval stage, most cells in the tail stop cell cycle progression, and therefore cells in the S/G2/M phases are restricted to the trunk region (Nakayama et al., 2005). Accordingly, the fluorescence of mAG-hGem(1/110) and mVenus-hGem(1/110) was observed exclusively in the trunk (Fig. 1B, left), suggesting that these Fucci probes successfully monitor the S/G2/M phases in Ciona embryos. When mKO2-hCdt1(1/100) and mAG-hGem(1/110) were simultaneously expressed, the orange fluorescence rarely overlapped with the green fluorescence, suggesting that mKO2-hCdt1(1/100) is degraded at the S/G2/M phases. Almost all cells in the tail showed orange fluorescence exclusively, suggesting that their cell cycle is arrested at the G1/G0 phase. When mKO2-hCdt1(30/120) and mAG-hGem(1/110) were simultaneously expressed, the green fluorescence in the trunk always overlapped with the orange fluorescence (Fig. 1B, middle), suggesting that mKO2-hCdt1(30/120) is not degraded in the S/G2/M phases. Because cells at the tail region showed mKO2-hCdt1(30/120) fluorescence exclusively, cell cycle progression was not strongly affected by mKO2-hCdt1(30/120). When mKO2-zCdt1(1/170) was expressed together with mAG-hGem(1/110), the cells in the tail expressed both green and orange fluorescence (Fig. 1B, right), suggesting that mKO2-zCdt1(1/170) inhibits normal cell cycle progression. Our results indicate that mAG-hGem(1/110), mVenus-hGem(1/110) and mKO2-hCdt1(1/100) can be used to monitor cell cycle progression during Ciona embryogenesis.
To confirm this, we imaged mAG-hGem(1/110) and mKO2-hCdt1(1/100) fluorescence at single-cell resolution. After these two Fucci probes were simultaneously expressed in the epidermal cells of a tailbud embryo, epidermal cells with green nuclei were time-lapse imaged (Fig. 1C). The intense mAG-hGem(1/110) fluorescence in the nucleus was redistributed throughout the cells, probably upon nuclear envelope breakdown (Fig. 1C, 30 minutes). The dispersion of the Geminin-based Fucci signal can be used to determine the timing of the beginning of prometaphase. The cytokinesis of these cells that follows the prometaphase was observed in the form of dispersed mAG-hGem(1/110) fluorescence making an outline of the cell shape (Fig. 1C, 45 minutes). After cell division was completed, mAG-hGem(1/110) fluorescence was again accumulated in the nuclei (Fig. 1C, 60-75 minutes) and then disappeared after 30 minutes. mKO2-hCdt1(1/100) started to accumulate in the nuclei soon after cell division was finished (Fig. 1C, 60-90 minutes), and the timing was complementary to that of mAG-hGem(1/110). We concluded that mAG-hGem(1/110), mVenus-hGem(1/110) and mKO2-hCdt1(1/100) can be used to observe cell cycle progression in Ciona embryos and larvae.
Cell cycle progression of epidermal cells during neurulation
By using mAG-hGem(1/110) and mKO2-hCdt1(1/100), we monitored cell cycle progression in the epidermis at whole-embryo resolution (Figs 2 and 3). In vitro-synthesized mRNAs of the two Fucci probes were simultaneously introduced into unfertilized eggs by microinjection, and observation was begun after fertilization. This method reduces the mosaicism of the expression levels of probes among cells in comparison with DNA electroporation. The eighth mitosis of the epidermal cells was completed by 5.0 hpf and could not be followed by the accumulation of mAG-hGem(1/110) due to a lack of detectable fluorescence. The accumulation of mAG-hGem(1/110) was observed at ∼5.0 hpf (see Movie 1 in the supplementary material), after the eighth mitosis. The ninth mitosis occurred at 5.5-6.0 hpf (Fig. 2, Fig. 3A,E; see Movie 1 in the supplementary material). The b-line (posterior) epidermal cells divided ∼5 minutes faster than the a-line (anterior) cells, as was described previously (Nishida 2005). After this ninth division, the accumulation of mKO2-hCdt1(1/100) was not detected and mAG-hGem(1/110) accumulation was soon restarted (Fig. 2; see Movie 1 in the supplementary material), suggesting that there is only a short G1 phase and that cells enter the S/G2 phase soon after the ninth division. The tenth mitosis occurred at 6.5-7.0 hpf (Fig. 2, Fig. 3B,E; see Movie 1 in the supplementary material). We found that the timing of this division differed along the anterior-posterior (A-P) axis of the embryo. Posterior cells tended to start dividing earlier than anterior cells (Fig. 3B). After this tenth division, the accumulation of mKO2-hCdt1(1/100) was not detected, and mAG-hGem(1/110) accumulation was soon restarted (Fig. 2; see Movie 1 in the supplementary material). The fluorescence of mAG-hGem(1/110) showed that the eleventh division occurred at ∼8.0-9.0 hpf (Fig. 2, Fig. 3C,E; see Movie 1 in the supplementary material). At the time of the eleventh cell division, epidermal cells can be subdivided into four groups with different mitotic domains: cells around the ventral midline (MD1) and dorsal midline (MD2) and cells on the trunk lateral side (MD3a) and tail lateral side (MD3b) (Fig. 3C,D). In this study, the term `mitotic domain' (Foe and Odell, 1989) indicates a group of cells consisting of a single mitotic wave and sharing the timing of the entrance into the prometaphase. The eleventh mitosis started in the following order: MD1, MD2, MD3 (Fig. 3C). In MD1, MD2 and MD3a, posterior cells started mitosis earlier and the mitotic wave moved toward the anterior (Fig. 3D). Cells at MD3b showed a different pattern: mitosis started from both the anterior and posterior sides, and cells in the middle part underwent mitosis later (Fig. 3D). After the eleventh division, the epidermal cells started to accumulate mKO2-hCdt1(1/100) (Fig. 2; see Movie 1 in the supplementary material).
The intervals between the prometaphases of the tenth and eleventh cell divisions were an average of 36-47 minutes longer than those between the ninth and tenth divisions for cells of each mitotic domain, suggesting that the eleventh cell cycle is longer than the tenth cell cycle (Table 1). Because mAG-hGem(1/110) was accumulated in the nuclei at the early phase of the eleventh cell cycle (namely between the tenth and eleventh divisions) and no accumulation of mKO2-hCdt1(1/100) was detected, the longer interval in this period is thought to be due to the long S phase and/or G2 phase. EdU was incorporated around this cell cycle to determine the timing of the S phase at the eleventh cell cycle. When embryos were treated with EdU at 6.5-7.0 hpf, incorporation of EdU was not observed in the epidermal cells, whereas the neural plate cells showed strong EdU incorporation at this stage (Fig. 4A, left). Because epidermal cells enter the prometaphase of the tenth division at 6.5-7.0 hpf (Fig. 3E), these cells are in the M phase in most of this time window. We cannot exclude the possibility that there is a G1 phase that is too short to detect with Fucci. At 7.0-7.5 hpf, strong EdU incorporation was observed in the epidermal cells (Fig. 4A, middle), suggesting that they were in the S phase. At 7.5-8.0 hpf, incorporation of EdU was again lost in the epidermal cells (Fig. 4A, right). Therefore, the S phase at the eleventh cell cycle occurs within 30 minutes at 7.0-7.5 hpf. Because epidermal cells start to enter the M phase at 8.0 hpf, they are arrested for at least 30 minutes in the G2 phase of this cell cycle. To confirm that epidermal cells are in the G2 phase at 7.5-8.0 hpf, EdU incorporation was performed using embryos in which mVenus-hGem(1/110) was expressed in this time window. Epidermal cells showed accumulation of mVenus-hGem(1/110) in the nuclei, the hallmark of S/G2 phases, whereas no EdU incorporation was detected (Fig. 4B), suggesting that epidermal cells were in the G2 phase.
Time-lapse imaging revealed that closure of the neural tube by the fusing of the left and right epidermis occurred during this long G2 phase (Fig. 4C). Fusion of the epidermis started in the posterior-most region, and the fused plane moved in the anterior direction (see Movie 2 in the supplementary material). Membrane-bound fluorescent proteins were expressed in the epidermal cells to label their plasma membranes, allowing us to observe the cell shape changes of the epidermal cells during the fusion. Epidermal cells that had finished their tenth division were round, and no cell polarity was recognized. At the onset of neural tube closure, epidermal cells at the posterior midline become elongated towards a focus at the dorsal midline (Fig. 4C, arrowheads). These epidermal cells made contact at the focus, which then became the origin of zippering. The left and right lateral epidermal cells moved towards the midline, changed their shape to fill the gap and aligned tightly along the midline to close the furrow (Fig. 4C, 55 minutes). Short filopodia were formed during the cell movement (Fig. 4E), and F-action was accumulated strongly at the medial end of the midline epidermis (Fig. 4F). The movement and alignment of midline epidermal cells were transmitted towards the anterior and the midline was closed as if zipped (Fig. 4C, 80 minutes; see Movie 2 in the supplementary material). After this zippering, the epidermal cells underwent the eleventh division (Fig. 4C, 170 minutes). Epidermal cells of all mitotic domains tended to divide parallel to the A-P axis (Fig. 4C, 170 minutes; Fig. 4D). During neural tube closure, the tail started elongating toward the posterior end of the embryo.
Different timing of cdc25 expression in epidermal cells along the A-P axis
CDC25 is a conserved cell cycle regulator that promotes both G1/S and G2/M transitions (Boutros et al., 2006). Transcriptional regulation of cdc25 is crucial for tissue-specific timing of G2/M progression (Edgar et al., 1994; Lehman et al., 1999). If Ciona cdc25 is responsible for the regulation of epidermal cell G2/M progression, this gene might be expressed at different times along the A-P axis of the embryo. To examine this possibility, we investigated the expression profile of a cdc25 homolog of Ciona intestinalis (Ci-cdc25) by whole-mount in situ hybridization (Kawashima et al., 2003). Expression of Ci-cdc25 was observed in all of the epidermal cells in the early gastrula stage at 5.0-5.5 hpf (see Fig. S1A,B in the supplementary material). At 5.5 hpf, strong expression of Ci-cdc25 was also observed in cells of the neural lineage (see Fig. S1B in the supplementary material). At 6.0 hpf, ∼30 minutes before the start of the tenth mitosis, Ci-cdc25 expression was observed exclusively in the trunk epidermal cells, and the expression was reduced at 6.5 hpf, except for the anterior-most epidermis (see Fig. S1C,D in the supplementary material). At 7.0 hpf, when the epidermal cells had finished the tenth division and entered the S/G2 phase of the eleventh cell cycle, no expression of Ci-cdc25 was observed in the epidermal cells (see Fig. S1E in the supplementary material). At 7.5 hpf, when the epidermal cells were in the long G2 phase, expression of Ci-cdc25 at the posterior-most epidermis restarted (see Fig. S1F in the supplementary material). At 8.0 hpf, when the posterior-most epidermal cells started the eleventh mitosis, strong expression of Ci-cdc25 was observed in the epidermal cells near the posterior pole of the embryo (see Fig. S1G in the supplementary material). At 8.5-9.0 hpf, when the embryos had finished closing the tail neural tube, weak expression of Ci-cdc25 was detected in all of the tail epidermal cells (see Fig. S1H,I in the supplementary material). These results indicate that the timing of the expression of Ci-cdc25 was different in the anterior and posterior epidermal cells. This difference is in accordance with the above-mentioned observation that the timing of cell division in the epidermis differs along the A-P axis of the embryo, and that Ci-CDC25 is a candidate regulator of cell cycle progression of embryonic cells, or at least epidermal cells, during Ciona embryogenesis.
A long G2 phase at the eleventh cell cycle of epidermal cells is required for neural tube closure
The temporal correlation between the insertion of the long G2 phase at the eleventh cell cycle of epidermal cells and the closure of the neural tube suggests a causal relationship of these two developmental events. We attempted to reduce the period of this long G2 phase by overexpression of Ci-cdc25 in epidermal cells in order to observe its effects on neural tube closure (Fig. 5A). Ci-Epi1 is an epidermis-specific gene that starts to be expressed around the neurula stage (Chiba et al., 1998), and we utilized its cis element for overexpression of Ci-cdc25. The cell cycle progression of the epidermal cells of Ci-cdc25-overexpressing embryos was normal until the tenth division, as was revealed by the fluorescence of mVenus-hGem(1/110) (Fig. 5B). At the eleventh cell division, a clear difference was observed compared with the control embryos. The Ci-cdc25-overexpressing embryos started the eleventh division an average of 40 minutes earlier than the controls. Namely, the period of the eleventh cell cycle (between the tenth and eleventh divisions) was shortened to ∼50 minutes compared with 90 minutes in normal embryos. Precocious eleventh epidermal cell division in the Ci-cdc25-overexpressing embryos was confirmed by immunostaining of phospho-histone H3 (PH3), a marker of cells during mitosis, at 7.75 hpf (see Fig. S2 in the supplementary material). These Ci-cdc25-overexpressing embryos failed to close the neural tube (80%, n=25; Table 2). When viewed from the cross-section, the nerve cord of the normal embryos formed a clear tube consisting of four rows of neural cells (see Fig. S3 in the supplementary material). By contrast, neural plate cells of Ci-cdc25-overexpressing embryos were aligned laterally to maintain `sheet' morphology (see Fig. S3 in the supplementary material), suggesting that the sheet-to-tube transition of the neural tissue is arrested by shortening the G2 phase. Forty percent of Ci-cdc25-overexpressing embryos had a severe phenotype (Table 2); they did not demonstrate neural tube closure in either the tail or trunk regions (Fig. 5B; see Fig. S4A,B in the supplementary material). In these embryos, epidermal cells underwent the eleventh cell division before the initiation of closure. Formation of a clear zippering origin was not observed at the posterior end of the embryos, and movement of the epidermal cells towards the midline did not occur (Fig. 5C; see Movie 3 in the supplementary material). Forty percent of the embryos (Table 2) showed a milder phenotype; their epidermal cells completed neural tube closure at the tail region but not at the trunk region (see Fig. S4C in the supplementary material). The remaining 20% of the embryos completed neural tube closure (n=25; Table 2). In these embryos the eleventh division took place just after the closure, although the timing of the division was earlier than in the wild-type controls (see Fig. S4D in the supplementary material). These results suggest that the eleventh cell division of epidermal cells must take place after neural tube closure for this morphogenetic movement to occur. We examined the orientation of the eleventh epidermal cell division in Ci-cdc25-overexpressing embryos. The epidermal cells tended to divide parallel to the A-P axis as in the control embryos, suggesting that the induction of a precocious eleventh mitosis by Ci-cdc25 did not disrupt its orientation (see Fig. S5 in the supplementary material).
The above data suggest that a long G2 phase at the eleventh cell cycle might be necessary for the eleventh division to occur after the completion of neural tube closure. If this is the case, the long interval between the tenth and eleventh cell divisions is not necessarily the G2 phase. To examine this possibility, we treated embryos with aphidicolin, an inhibitor of DNA replication (Ikegami et al., 1978), between the tenth and eleventh divisions of the epidermal cells, and observed its effect on neural tube closure. When embryos were treated with aphidicolin just after the tenth division and before the eleventh division, neural tube closure at the tail region occurred as in the normal embryos (86%, n=21). The trunk neural plate did not completely close in the aphidicolin-treated embryos. This could have been because cell cycle progression of the trunk neural plate cells was also affected by aphidicolin. The aphidicolin-treated embryos showed either delayed or no eleventh mitosis of epidermal cells, suggesting that aphidicolin effectively suppressed progression through the S phase of the eleventh cell cycle.
By utilizing aphidicolin, we performed a rescue experiment of the overexpression phenotype of Ci-cdc25 by arresting cells at the S phase. We noted the occurrence of neural tube closure at the tail. As a result, the Ci-cdc25-overexpressing and aphidicolin-treated embryos showed neural tube closure at the tail much more frequently than did Ci-cdc25-overexpressing control embryos (Fig. 6 and Table 3), suggesting that induction of a longer interval after the tenth cell division rescued the effect of Ci-cdc25 overexpression. Fluorescent cross-section showed that a proper tail nerve cord was formed in the Ci-cdc25-overexpressing and aphidicolin-treated embryos (see Fig. S3 in the supplementary material). Taken together, these findings suggest that a long interval between the tenth and eleventh cell divisions of epidermal cells is crucial for neural tube closure. The interval is not necessarily the G2 phase, but in normal embryogenesis it occurs as a long G2 phase.
We performed a quantitative analysis to determine how much the shortening of the G2 phase affected the shape change of epidermal cells. As mentioned above, the dorsal midline epidermis was elongated towards the midline during neural tube closure. We measured the length of the cells along the mediolateral axis and the width along the A-P axis to calculate the length/width (L/W) ratio (Table 4); the scores were about 2.21 and 1.69 in the tail and trunk epidermal cells of control embryos, respectively. When Ci-cdc25 was overexpressed, the L/W ratios were reduced to 1.58 and 1.38, respectively, and aphidicolin administration restored the scores to 1.98 and 1.69, respectively. Therefore, the prolongation of the interphase is necessary for the dorsal midline epidermis to elongate towards the midline. The elongation was also interfered with by treating embryos with Y-27632, an inhibitor of Rho-kinase (ROCK) (Uehata et al., 1997), suggesting that this cell shape change is a result of Rho-mediated ROCK regulation. Y-27632 treatment did not affect the timing or pattern of cell cycle progression (data not shown).
We examined further the effect of the shortening of the G2 phase on F-actin accumulation at the medial end of the dorsal midline epidermis. As a result, F-actin accumulation was significantly decreased in the dorsal midline epidermal cells of Ci-cdc25-overexpressing embryos (see Fig. S6 in the supplementary material). F-actin accumulation was ameliorated by prolongation of the S phase with aphidicolin in Ci-cdc25-overexpressing embryos (see Fig. S6 in the supplementary material). Therefore, a prolonged interphase at the eleventh cell cycle is necessary for F-actin to accumulate at the medial end of the dorsal midline epidermis. Y-27632 treatment also abolished the accumulation of F-actin (see Fig. S6 in the supplementary material), suggesting that this phenomenon is also dependent on the Rho/ROCK pathway.
Cell division requires a large quantity of cytoskeletal elements for forming the mitotic spindle and contractile ring. Morphogenetic movement also requires a large amount of actin filament for forming filopodia/lamellipodia and microtubules for coordinated cellular movement (Rodriguez et al., 2003). It is thought that these two developmental events are incompatible, because they compete for the cytoskeletal components (Mata et al., 2000). Therefore, these two events cannot take place simultaneously and embryonic cells must regulate their timing for coordinated embryogenesis. In ascidian embryogenesis, we observed strong coordination between a single round of cell cycle progression in epidermal cells and neural tube closure. Epidermal cells prolong the G2 phase at the eleventh cell cycle to adjust the timing of the eleventh cell division so that it follows neural tube closure. This regulation is necessary because neural tube closure and the eleventh mitosis cannot take place simultaneously; epidermal cells achieve the coordination of mitosis and their morphogenetic movement by delaying the timing of mitosis. Disrupting the morphogenetic movement of the epidermis affected the sheet-to-tube morphogenesis of the neural plate, suggesting that the epidermis is necessary for the neural plate to form a tube. The contribution of the epidermis to neurulation seems to be a general feature among chordates.
During the G2 phase, dorsal midline epidermal cells elongate towards the midline to close the furrow. This cell shape change and movement, which is dependent on Rho/ROCK-mediated actin filament accumulation, could make the force that pushes the neural plate to form a tube. The morphogenetic movement and mitosis might compete against the actin filament in the epidermis during neurulation. Precocious eleventh mitosis inhibited both cell shape change and F-actin accumulation, whereas Y-27632 treatment could not alter the timing of the cell cycle/division. Therefore, mitosis and morphogenesis in this case are not equal for the competition of actin; mitosis can overwhelm the Rho/ROCK-mediated pathway. The significance of the prolongation of the G2 phase is to make time for the Rho/ROCK-mediated pathway to accumulate F-actin and conduct cell shape change.
Epidermal cells show different mitotic timings along the A-P axis. The posterior cells divide earlier than the anterior cells. This might be another adjustment for neural tube closure, because this morphogenetic movement proceeds from posterior to anterior regions. Previous observations with a scanning electron microscope suggested that a-line epidermal cells divide slightly later than b-line cells (Nishida, 1986). This is consistent with our findings. Our observations suggest that the divisions along the A-P axis are much finer and more detailed than the broad difference between the a-line and b-line. For example, tail midline epidermal cells, which are derivatives of b4.2, start the tenth and eleventh cell divisions from the posterior side. The regulator determining the timing of cell division might work gradually along the A-P axis of the embryo. We have also shown that the epidermis can be divided into four regions with different mitotic timings in the eleventh division. Curiously, the detection of four regions with different mitotic timings coincides with the classification of epidermal cells based on clonal analysis (Pasini et al., 2006), suggesting lineage-specific determination of cell division timing. Ci-cdc25 is probably a key regulator of the cell cycle progression of epidermal cells. The dynamic transcriptional change of this gene in the epidermis suggests that its transcriptional regulation is a crucial event for the regulation of the cell cycle. The importance of the transcriptional regulation of Ci-cdc25 has been reported in several organisms (Edgar et al., 1994; Bissen, 1995; Wickramasinghe et al., 1995; Nogare et al., 2007) and this regulation could be common among various animals.
The orientation of mitosis is also regulated in epidermal cells during neural tube closure. At their eleventh division, epidermal cells tend to divide along the A-P axis, which is perpendicular to the orientation of neural tube closure. A plausible role of this regulation is that it provides an adjustment for the rapid elongation of the body length at this stage, which is caused by elongation of the tail. In the neurulation of chick embryos, epidermal cells divide in both a rostrocaudal and a mediolateral orientation (Sausedo et al., 1997). The former division is suggested to play a role in longitudinal lengthening, which seems to be common with Ciona. By contrast, the latter division might play a role in the medial expansion of the epidermis. This is in contrast with Ciona, in which epidermal cells do not divide during the closing of the neural tube, and cell shape change and movement towards the midline are major driving forces behind the fusion of the epidermal layer at the midline.
For the closure of the neural tube to occur, many developmental events have to be carried out in coordination. To achieve this coordination, the cell cycle of Ciona epidermal cells has to be regulated at the single-cell-cycle level. Such strict regulation might have been adopted because of the small cell number of ascidian embryos, in which a single round of cell division has a strong effect on overall development. It is important to elucidate the detailed mechanisms by which such cell cycle regulation is achieved. These molecular mechanisms of cell cycle regulation should be linked with those regulating neural tube closure. In vertebrates, the PCP/Wnt pathway plays crucial roles in morphogenesis, including neural tube closure (Ueno and Greene, 2003; Gong et al., 2004; Ciruna et al., 2006; Wallingford, 2006), and it is possible that similar genetic cascades regulate cell cycle progression, the orientation of cell division and morphogenesis during neural tube closure in ascidian embryos. Additionally, the description of cell cycle regulation in other cell types and morphogenetic movements in Ciona development is important. Previous studies have shown that neural cells of Ciona exhibit elongation of the cell cycle during neurulation (Nicol and Meinertzhagen, 1988a; Nicol and Meinertzhagen, 1988b). Cell cycle regulation similar to that of epidermal cells might occur in neural-fated cells; this possibility will be investigated in a future study. Fucci probes are valuable tools for observing cell cycle progression and mitosis in detail. Finally, neural tube closure is a key event in neurulation among chordates (Colas and Schoenwolf, 2001). As mentioned above, the epidermal layer contributes to proper neural tube formation in vertebrates. Epidermal cells generate the force needed to bend the neural plate via both cell division and morphogenesis (Sausedo et al., 1997). There is likely to be a mechanism that coordinates the two cellular processes in the epidermis of vertebrates. The present study indicates that fusion of the epidermis during neural tube closure occurs at the G2 phase and that cell shape change via actin regulation during this phase is a key event in Ciona embryos. Whether mechanisms similar to these are conserved among chordates is an interesting question.
We thank the National Bio-resource Project, Shigeki Fujiwara and all members of the Maizuru Fishery Research Station of Kyoto University and the Education and Research Center of Marine Bioresources of Tohoku University for providing us with Ciona adults. We are grateful to Hiroki Nishida and Patrick Lemaire for providing pBS-HTB and gateway vector set, respectively. This study was supported by Grants-in-Aid for Scientific Research from JSPS to Y.S. and N.S.
The authors declare no competing financial interests.
Competing interests statement