Cell and Developmental Biology


Tutorial on chick early development

1. Summary of early stages (stage X – 8)


click here to view animation

The following sections contain descriptions of the events of gastrulation and neural induction.

2. Avian gastrulation

(reprinted from Stern, C.D. (2004). Gastrulation in the chick. In: Gastrulation: from cells to embryo. (ed. C.D. Stern). Cold Spring Harbor Press. pp. 219-232. Copyright Claudio D Stern and Cold Spring Harbor Press) - please cite this reference if using any of this information. (if you want to reproduce figures you need to contact both the author and the publishers)


Early stages: blastoderm formation and early polarity

Avian eggs and early embryos differ in several respects from the majority of vertebrates, yet many of the principles governing the early steps of development are very similar. Unlike amphibians and some other embryos, the point of sperm entry is not a crucial determinant of polarity of the early embryo, because avian embryos are highly polyspermic – as many as 5-26 sperm may enter the egg in domestic fowl (chicken) while turkey eggs may be entered by several hundred sperm heads (Waddington et al., 1998; Stepinska and Olszanska, 2003). Cleavage, as in most species containing a large amount of yolk (Arendt and Nübler-Jung, 1999) (Figs. 1-2), is meroblastic – that is, cleavage occurs within a planar disc, and new cell membranes open into the yolk generating small cells in the center and large, yolk-laden, open cells at the periphery (Fig. 2 B, C) (Bellairs et al., 1978). Unfortunately these stages are difficult to study because cleavage occurs while the egg is still within the maternal oviduct and before the shell is deposited (Fig. 1) – in the chicken, laying occurs some 20 hours post-fertilization, when the embryo is a flat disc (blastodisc or blastoderm) containing at least 20,000 cells.


A rule of thumb (von Baer’s rule) can help to predict the orientation of the head-tail axis of the embryo from the outside of the egg: with the egg lying along its long axis, and its blunt end to the operator’s left, the axis of the embryo will run at right angles to the long egg axis with the head pointing away from the operator. However this rule only applies in about 60-70% of cases.

As in teleosts, which are also meroblastic, maternal determinants are likely to exist also in avian embryos. One such determinant is called δ-ooplasm (or subgerminal ooplasm) – this is contained in the thin, “white” yolk that makes up the latebra and the nucleus of Pander (Fig. 2 A, C). The former is a funnel-like structure extending from just under the blastoderm to the center of the yolk (Callebaut et al., 1998a; Callebaut et al., 1999a; Callebaut et al., 2000a). We do not know the molecular nature or the functions of this ooplasm or whether it plays any role in polarity, although it has been suggested that it determines the position from which the endoblast and Koller’s sickle (see below) will form (Callebaut, 1993; Callebaut et al., 1998a; Callebaut et al., 2001).

Avian embryos appear to generate bilateral symmetry under the influence of gravity (Kochav and Eyal-Giladi, 1971; Callebaut, 1978; Eyal-Giladi and Fabian, 1980; Callebaut, 1993; Eyal-Giladi et al., 1994; Callebaut et al., 2001). As the egg descends along the oviduct, it rotates with the blastoderm remaining at an angle of about 45o to the vertical – the lower edge of the blastoderm will become the future head end. However, we are still completely ignorant about the mechanism by which gravity breaks radial symmetry. It was suggested that opposite (upper and lower) poles of the disc are exposed to gravitational forces of different magnitude and that this causes differential amounts of cell shedding (Kochav and Eyal-Giladi, 1971; Eyal-Giladi and Kochav, 1976; Eyal-Giladi and Fabian, 1980; Eyal-Giladi et al., 1994). However, this has never been demonstrated and the alternative hypothesis that rotation exposes the poles of the blastoderm to subgerminal ooplasm to different extents (Callebaut, 1993) seems much more likely.

Importantly, neither gravity nor maternal determinants irreversibly fixes bilateral symmetry until gastrulation starts, because avian embryos are highly regulative – right up to the time of appearance of the primitive streak, blastoderms can be split into several pieces (pie slices) each of which can spontaneously generate a complete embryonic axis (Lutz, 1949; Spratt and Haas, 1960a; Callebaut and Van Nueten, 1995). Therefore, gravity and localized maternal components can, at best, only bias polarity but do not act as definitive determinants.

The blastoderm stage

By the time the egg is laid, the embryo is an almost flat disc in which an inner area pellucida can be distinguished from a more peripheral ring, the area opaca. Closest to the acellular vitelline membrane that envelops the yolk (“dorsal” side), a simple, one-cell-tick epithelium is continuous over both areas (Fig. 3) (Bancroft and Bellairs, 1974; Bellairs et al., 1975). This is the epiblast. At this stage the cells of the epiblast of the two concentric areas are almost indistinguishable morphologically except that at the very edge of the area opaca the cells are flattened and contact the vitelline membrane, against which they will later spread and help expand the blastoderm; the center of the disc is not attached to the membrane. At later stages however cells of the area opaca epiblast become less columnar than those of the area pellucida.

Deep (facing the yolk) to the epiblast the cellular composition is more complex. The area opaca contains several layers of large (up to 150-200μm) yolky cells; those closest to the epiblast are firmly attached to it. This is the germ wall. By contrast, the center of the disc (area pellucida) does not yet contain a continuous cell layer, but is peppered with small islands of about 5-10 cells each. These are also yolky but not as large as the deep part of the area opaca (about 100μm). The islands may arise by a process of polyingression (or shedding) that occurs throughout the area pellucida shortly before laying (Peter, 1938; Kochav et al., 1980; Fabian and Eyal-Giladi, 1981; Eyal-Giladi, 1984), but the fate of the shed cells has never been studied experimentally. The islands will later fuse with each other to generate the primitive endodermal layer, or hypoblast (“entophyll” or “primary hypoblast” in the earlier literature).

Between the area opaca and the area pellucida is a narrow region (known as the marginal zone). The epiblast of this region (to which the term refers) is not distinguishable from other regions of epiblast, except for the expression of Vg1 at its posterior end (posterior marginal zone; see below) (Seleiro et al., 1996; Shah et al., 1997) and a slight gradient of cWnt8C decreasing from posterior to anterior (Skromne and Stern, 2001). The only morphological landmark is that the deep part (germ wall) is not strongly attached to the epiblast, unlike the area opaca. This region is known as the germ wall margin. In carefully dissected blastoderms it forms a lip that protrudes under the area pellucida for a few cell diameters (Stern and Ireland, 1981; Stern, 1990).

The boundary between area pellucida and marginal zone is marked, at the future posterior edge, by a crescent-shaped ridge of small cells, tighly adherent to the epiblast – Koller’s sickle (also known as Rauber’s sickle) (Koller, 1882; Callebaut and Van Nueten, 1994), which expresses goosecoid (Izpisua-Belmonte et al., 1993). Together, these components define a blastoderm of stage X (Roman numerals from I-XIV are used to classify stages before formation of the primitive streak according to Eyal-Giladi and Kochav, 1976; Arabic numerals from 2 onwards are used for post-streak embryos following Hamburger and Hamilton, 1951).


In the following few hours of incubation the islands of hypoblast gradually fuse together, probably by a process of flattening of the cells, which proceeds from posterior to anterior to generate a continuous but relatively loose layer, the hypoblast proper (Vakaet, 1970; Stern, 1990) (see supplementary movie {movie1} and animation {movie2}). This layer covers half of the area pellucida at stage XII and almost all of it at stage XIII (Fig. 3). Shortly after, two changes take place: first, the posterior germ wall margin cells and their progeny start to move centripetally (Stern, 1990) and displace the hypoblast anteriorly; this new layer is the endoblast (or “sickle endoblast” or “secondary hypoblast” in the earlier literature). Hypoblast and endoblast can be distinguished by several markers including goosecoid (in White Leghorns and some other strains), Hex, Hesx1/Rpx, Cerberus/Caronte, Otx2 and Crescent, all of which are expressed in the hypoblast but not in the endoblast (Bachvarova et al., 1998; Foley et al., 2000; Bertocchini and Stern, 2002). The hypoblast is therefore similar to the anterior visceral endoderm (AVE) of the mouse embryo. At the same time, a posterior thickening (the posterior bridge), apparently derived from Koller’s sickle appears – this transient structure defines stage XIV, and the primitive streak starts to form immediately thereafter. None of the components of the deep layer (hypoblast, endoblast, germ wall or its margin) contribute to any embryonic tissues – they only generate extraembryonic membranes such as the yolk sac stalk, and later disappear.

Fate maps and cell movements at the blastoderm stage


Many authors have constructed fate and specification maps of the epiblast of the chick at the blastoderm stage (Rudnick, 1935, 1938; Hatada and Stern, 1994; Callebaut et al., 1996; Bachvarova et al., 1998). The most detailed ones (Hatada and Stern, 1994) reveal an orderly arrangement of prospective embryonic tissues which gradually changes with time (Fig. 4), due to extensive morphogenetic movements of the epiblast that begin well before primitive streak formation (Gräper, 1929; Vakaet, 1970; Izpisua-Belmonte et al., 1993; Callebaut et al., 1999b; Foley et al., 2000). At stage X, future “dorsal” tissues (prospective organizer and its derivatives: endoderm, prechordal mesoderm, notochord) are found just central to and adjacent to Koller’s sickle (Izpisua-Belmonte et al., 1993; Hatada and Stern, 1994; Bachvarova et al., 1998; Streit et al., 2000). These territories quickly move towards the center of the blastoderm, and gradually become replaced in their original position by more lateral regions of epiblast (progressively more “ventral” fates like somite, intermediate mesoderm, etc.) (see supplementary movies: {Weijer.avi} and {normal.avi}). Therefore at stage X the posterior margin of the area pellucida contains a bilateral gradation of dorsal-to-ventral fates, dorsal at the posterior mid-point – subsequent movements “fold” this arrangement into a posterior midline presaging the future primitive streak, so that the most dorsal fates become located most anteriorly along this line (see below). These movements comprise convergence of epiblast towards the posterior mid-point and extension along the midline, but do not seem to occur by the process normally called “convergent extension” in that it is not accompanied by significant cell shape changes. The combination of posterior midpoint convergence and midline extension resembles a Polish dance (“Polonaise”) (see supplementary movies: {movie1} and {movie3}), the name given by Gräper (Gräper, 1929) to these epiblast movements after his remarkable stereo-pair time-lapse films of labeled embryos, made as early as 1926.

It is truly remarkable that cells can move horizontally within a relatively tight epithelium, the epiblast. The mechanics of such migration, including the degree to which it is truly “active” (rather than a consequence of mechanical propagation of a remote event like cell loss through ingression), is not yet understood. However, recent observations of living, Bodipy-ceramide chick embryos using two-photon microscopy have started to reveal that individual cells within the epithelium and translocate by “bobbing” up and down, as if each individual cell is a foot in a giant millipede (O. Voiculescu, I.-J. Lau, F. Bertocchini and C.D. Stern, unpublished observations).

We have already described briefly above the movements in the lower layer (Waddington, 1932; Spratt and Haas, 1960b; Vakaet, 1970; Rosenquist, 1972; Stern and Ireland, 1981; Stern, 1990; Bakst et al., 1997; Callebaut et al., 1997a; Bachvarova et al., 1998; Foley et al., 2000; Bertocchini and Stern, 2002). Essentially the hypoblast expands as the islands fuse from posterior to anterior, and the newly-formed hypoblast sheet is then displaced further anteriorly by the incoming endoblast (see supplementary movie {movie1} and animation {movie2}),. The speed at which the hypoblast/endoblast layer spreads is similar to the midline extension in the epiblast (Hatada and Stern, 1994) and recent experiments have shown that there is a causal link: rotation of the deep layer generates a new set of Polonaise movements in the adjacent epiblast (Foley et al., 2000), although the mechanisms by which the two layers communicate are unknown.

These movements also deform Koller’s sickle, which appears to be subjected to a large amount of shear. Its anterior (centrally-facing) mid-point will later migrate anteriorly as the primitive streak forms, its lateral extremes converge to the midline, and the posterior aspect (facing the marginal zone) remains posterior and eventually becomes extraembryonic (Izpisua-Belmonte et al., 1993; Bachvarova et al., 1998; Streit et al., 2000).

Cell interactions leading to primitive streak formation

The fact that isolated fragments of blastodiscs can spontaneously initiate axis formation (Lutz, 1949; Spratt and Haas, 1960a) indicates that cell interactions, rather than definitive determinants, must be involved. What are the signals, and where do they come from? Three main sources have been proposed: the hypoblast and/or endoblast, Koller’s sickle and the posterior marginal zone (PMZ).

The idea that the hypoblast/endoblast layer regulates the site of primitive streak formation comes from important experiments by Waddington (Waddington, 1932, 1933) in which he demonstrated that rotation of the deep layer (which he called “endoderm”) influences the orientation of the primitive streak. When it was rotated by 90o the streak arose from its original site but developed a gradual bend. After 180o rotation of the hypoblast, a few embryos had formed an ectopic streak arising from the opposite (anterior) side. This led Waddington to suggest that the hypoblast layer induces the primitive streak (Waddington, 1933) but he was cautious to avoid ruling out a contribution from cell movements. Subsequent studies were more forceful in proposing induction by the hypoblast (Azar and Eyal-Giladi, 1979, 1981; Mitrani and Eyal-Giladi, 1981; Azar and Eyal-Giladi, 1983; Mitrani et al., 1983) but without providing direct evidence with molecular markers or markers for different cell populations. Later, two studies repeated Waddington’s original observations and highlighted the fact that since 90o hypoblast rotations do not induce primitive streak formation from a new site, this is unlikely to be a true inductive event (Khaner, 1995; Foley et al., 2000). Moreover, it was shown (Foley et al., 2000) that the hypoblast layer influences the movements of the overlying epiblast – when rotated, it initates a new set of Polonaise movements at 90o to the original. These compete with the original movements causing the streak to bend, but cells destined for different tissue types do not change their fates.

Recently, a new emphasis has been placed on the second component of the deep layer, the endoblast (Callebaut and Van Nueten, 1995; Callebaut et al., 1998b; Callebaut et al., 1999b; Callebaut et al., 2000b; Bertocchini and Stern, 2002). Specifically (Bertocchini and Stern, 2002), it was shown that complete removal of the hypoblast leads to the formation of multiple streaks at random positions, suggesting that the hypoblast emits an antagonist of axis formation. Analysis of expression patterns and misexpression experiments then suggested that Cerberus, a Nodal antagonist, is responsible. Cerberus is expressed in the hypoblast but not in the endoblast, which is consistent with the fact that the primitive streak starts to form precisely at the time when the hypoblast is displaced away from the posterior edge of the area pellucida by the incoming endoblatst (Bertocchini and Stern, 2002). Finally, it should be mentioned that the hypoblast does have some inducing activity, which can be revealed by assessing the expression of several epiblast genes after grafting a hypoblast ectopically: the homeobox gene Not1/GNOT (Knezevic and Mackem, 2001), and the early “pre-neural” markers ERNI, Sox3 and Otx2 are induced transiently by grafts of the hypoblast to ectopic sites (Foley et al., 1997; Streit et al., 2000) (see Neural induction). The induction of Not1/GNOT may be mediated by retinoids, while induction of ERNI and Sox3 is mediated by FGF. We do not yet know the factors responsible for inducing Otx2.

The second component suggested as playing a role in primitive streak initiation is Koller’s sickle (Izpisua-Belmonte et al., 1993; Callebaut and Van Nueten, 1994; Callebaut et al., 1997a; Callebaut et al., 1998b; Callebaut et al., 2003). This structure has been said to give rise to the endoblast (hence the alternative name of “sickle endoblast”) and has even been proposed to act as a passage for posterior marginal zone cells from the epiblast to the lower layer (Azar and Eyal-Giladi, 1979; Eyal-Giladi, 1997). However higher resolution fate mapping using different techniques has suggested instead that the sickle contributes cells to the primitive streak itself but not significantly to the endoblast (Izpisua-Belmonte et al., 1993; Bachvarova et al., 1998). Furthermore although grafts of the sickle can indeed generate a second primitive streak upon transplantation, the extensive cellular contribution to the ectopic streak and particularly to definitive (gut) endoderm cannot be dissociated from the inductive effect (Izpisua-Belmonte et al., 1993; Bachvarova et al., 1998).


The third and final tissue involved in induction of primitive streak formation is the posterior marginal zone (PMZ) (Spratt and Haas, 1960a; Azar and Eyal-Giladi, 1979; Eyal-Giladi and Khaner, 1989; Khaner and Eyal-Giladi, 1989; Callebaut et al., 1997b; Bachvarova et al., 1998; Bachvarova, 1999; Skromne and Stern, 2001, 2002). Even though its activity as a streak inducer has been challenged (Callebaut et al., 1997b; Callebaut et al., 1998b), there is no question that when grafted into an ectopic position the PMZ is able to induce the formation of a second axis without making a cellular contribution to it, as long as the host is younger than stage XI (Eyal-Giladi and Khaner, 1989; Khaner and Eyal-Giladi, 1989; Bachvarova et al., 1998). These properties of the PMZ have likened it to the amphibian Nieuwkoop center (see Chapters XXX – Keller amphibian; Lemaire Siamois). And like the Nieuwkoop center, whose activity appears to depend upon the overlap of TGFβ and Wnt pathways, the inducing ability of the PMZ can be mimicked by misexpression of cVg1 in regions where Wnt8C is expressed (Seleiro et al., 1996; Shah et al., 1997; Skromne and Stern, 2001, 2002) (Fig. 5). Surprisingly however, unlike PMZ grafts, misexpression of cVg1 in the anterior marginal zone will generate a full axis as late as stage XIII.

In conclusion, all three tissues (hypoblast/endoblast, Koller’s sickle and PMZ) proposed to have axis inducing activity do indeed have the ability to influence primitive streak formation. However, their mechanisms of action and relative importance differ. The sickle has inducing ability but this is probably only because it contains some of the cells fated to form Hensen’s node (the avian organizer – see below). The earliest influences appear to come from the PMZ, where Vg1 and Wnt activities overlap. Vg1+Wnt induce expression of Nodal in the neighboring area pellucida epiblast, but Nodal can only act (presumably to induce mesendoderm) when the hypoblast has been displaced by the incoming endoblast.

In addition to Vg1+Wnt and Nodal, it is likely that FGFs (emanating from the hypoblast and/or Koller’s sickle) (Chapman et al., 2002; Karabagli et al., 2002) also play a role in primitive streak initiation because inhibitors of FGF block this process (Mitrani et al., 1990; Streit et al., 2000) and because misexpression of FGF can generate an ectopic streak (F. Bertocchini, I. Skromne and C.D. Stern, unpublished observations). It is likely that FGF acts in concert with Nodal, as in amphibians (Kimelman and Kirschner, 1987; Cornell and Kimmelman, 1994; LaBonne and Whitman, 1994; Latinkic et al., 1997). Finally, BMP activity also regulates primitive streak formation since ectopic expression of the antagonist Chordin (but not Noggin) is sufficient to induce a streak, even as late as stage 3, and misexpression of BMP4 near the streak causes the streak to disappear (Streit and Stern, 1999). Chordin is normally expressed in Koller’s sickle at stages XI-XIV.

Several important questions still remain unanswered. They include: what positions Vg1 expression in the PMZ? What molecular mechanisms underlie regulation when the posterior half of the blastoderm is removed?

Primitive streak formation and elongation

We know surprisingly little about the cellular details of how the primitive streak forms and elongates. Time-lapse films (see movie1, movie3) show that the initial appearance of the streak is extremely rapid – the embryo goes from having no visible axial structures (stage XIV) to developing a triangular, dense streak (stage 2; Fig. 3) in about 30 min, suggesting that primitive streak initiation is accompanied by massive ingression. However, although the basement membrane under the epiblast does partially dissolve during streak formation, this early stage does not involve the loss of epithelial continuity of the epiblast in the region of the forming streak, which happens much later (stage 3+) (Vakaet, 1982; Andries et al., 1983; Sanders and Prasad, 1989; Harrisson et al., 1991). This suggests that the formation of the early, triangular-shape streak is the result of rapid poly-ingression of individual cells through the basal lamina of the epiblast. This process may therefore be analogous to the formation of primary mesenchyme in echinoderms.

Ingression of early, “pioneer” cells from the epiblast to the interior of the embryo can be seen starting as early as stage XII by staining either with the HNK-1 antibody (Canning and Stern, 1988; Stern and Canning, 1990; Canning et al., 2000; Mogi et al., 2000) or for activity of the enzyme Acetylcholinesterase (AChE) (Drews, 1975; Valinsky and Loomis, 1984; Laasberg et al., 1986; Parodi and Falugi, 1989). Indeed, the HNK-1 epitope is carried on a subunit of AChE (Bon et al., 1987), and AChE activity correlates very well with cell ingression and invasiveness in a variety of species (Drews, 1975). It is puzzling that HNK-1/AChE expression differs in different strains of fowl; the salt-and-pepper expression in the epiblast is seen in the Rhode Island Red/Light Sussex cross-breed but not in the more inbred strain, White Leghorn. It also seems clear that HNK-1/AChE expression does not correlate completely with cells destined to form the primitive streak (Cooke, 1993). A few of these cells do ingress but do not contribute to the streak (their fate remains unknown), other HNK-1-postive cells remain in the germ wall margin from where they contribute to the lower layer (Canning and Stern, 1988; Stern and Canning, 1990; Cooke, 1993), and yet others do ingress to the primitive streak but later seem to disappear. Careful fate maps examining the origin of cells that will form the primitive streak have revealed that the definitive primitive streak is largely derived from a relatively small population of epiblast cells local to the site of streak formation and from Koller’s sickle (Bachvarova et al., 1998; Wei and Mikawa, 2000).

The early triangular streak (stage 2) is made up of a dense accumulation of middle layer cells between epiblast and endoblast (Fig. 3); however it rapidly straightens, to become a mesenchymal rod of parallel sides (stage 3). At this stage there is still no groove in the overlying epiblast and the basement membrane is largely intact. Soon afterwards however two processes take place more or less simultaneously (Vakaet, 1970): the appearance of a longitudinal groove in the epiblast overlying the streak and the start of lateral migration of the mesenchyme of the streak, at right angles to the axis of the streak, to establish the lateral plate. These processes define stage 3+. Since grafts of early (stage 3) streak to a new area can generate an ectopic streak containing an epiblast groove (Vakaet, 1973), and by analogy to the interactions between primary and secondary mesenchyme in echinoderms, it seems likely that the early streak cells induce the formation of a groove (and subsequent invagination) in the overlying epiblast. The signals that mediate this interaction are unknown but FGF and/or Chordin are likely candidates since both can induce a streak at stage 3 (see above).

Stage 4 is marked by the appearance of a distinct bulge at the tip of the streak, encompassing all three layers – this is Hensen’s node (Hensen, 1876) (see below). We consider this to be the last phase of the “gastrula stage” in avian embryos – shortly afterwards (stage 4+) a small triangular mass of cells starts to protrude anteriorly from the node (the emerging tip of the head process, which contains precursors for the prechordal mesendoderm – see below). At this time the future neural plate starts to become morphologically and molecularly (Sox2-positive) distinct, and stage 4+ can therefore be considered the beginning of the “neurula stage”.

We also know virtually nothing about the mechanics of primitive streak elongation. Time-lapse films reveal that less than 2 hours elapse between the early short streak at stage 2 and the almost fully elongated (1.5mm long) stage 3 streak, making it very unlikely (L. Bodenstein, unpublished computer simulations) that cell division alone is the main force driving this elongation (Wei and Mikawa, 2000). Streak elongation most likely involves a process of cell reorganization and changes in cell shape similar to those seen in amphibian convergent-extension.

Hensen’s node

The function of Hensen’s node (the avian organizer) will be described elsewhere (see Neural induction). Here we will concentrate on the origin, maintenance and subdivision of the node into different cellular territories.

Various fate mapping techniques have established that Hensen’s node arises from two distinct populations of cells (Izpisua-Belmonte et al., 1993; Hatada and Stern, 1994; Bachvarova et al., 1998; Streit et al., 2000; Lawson and Schoenwolf, 2001). One cell population (called “posterior cells” by Streit et al., 2000) resides deep to the epiblast, at the midpoint of Koller’s sickle from stage X. It remains in this position until the primitive streak starts to form (stage 2), and then moves anteriorly with the tip of the advancing streak. The second population (called “central cells” by Streit et al., 2000) resides in the epiblast during these early stages – at stage X it is found immediately adjacent to the first population (in the Nodal-expressing territory; see Fig. 5 at stage X). However, the Polonaise movements almost immediately move these cells to the middle of the blastoderm, when these movements stop (stage XIII). As the primitive streak elongates, the posterior cells soon regain contact with the central cells (stages 3-3+). At this time, a morphological node forms (stage 4) and this is accompanied by the acquisition of expression of Sonic hedgehog (Shh) (Levin et al., 1995).

Neither the posterior nor the central cells possess full neural inducing ability by themselves (although posterior cells can induce transient expression of the pre-neural genes Sox3 and ERNI), but acquire this ability when combined (Streit et al., 2000). When transplanted ectopically into the area pellucida of a host embryo, posterior cells can induce neighboring epiblast cells to acquire expression of goosecoid, a marker of the organizer (Izpisua-Belmonte et al., 1993). These findings suggest that during their migration anteriorly from stages 2-3, the posterior cells recruit adjacent epiblast cells to form part of the organizer.

The cellular composition of Hensen’s node remains dynamic throughout the early stages of development: even after stage 3+, neighboring epiblast cells migrate to the node, acquire the expression of organizer markers and later migrate out again to emerge in the underlying layers as endoderm, notochord, prechordal mesendoderm or medial somites (Joubin and Stern, 1999). Inducing signals from within the streak (again, Vg1+Wnt, perhaps Nodal) and inhibitory signals from the node itself (ADMP) and from surrounding regions of the blastoderm (BMPs) form a complex network regulating the spatial and temporal expression of node markers including Chordin, Goosecoid, Shh, Not1, HNF3β and others (Joubin and Stern, 1999). These results account for the fact that primitive streak stage embryos from which the node has been extirpated can generate a new node (Grabowski, 1956; Psychoyos and Stern, 1996b; Joubin and Stern, 1999; Yuan and Schoenwolf, 1999).

Despite the dynamic composition of the node at these stages, single cell lineage analysis has suggested that the node also contains a small population of resident cells with stem-cell characteristics (Selleck and Stern, 1991; Selleck and Stern, 1992b). It was proposed that when these cells divide, one daughter remains in the node while the other leaves to contribute to notochord and/or medial somite (Selleck and Stern, 1992b; Stern et al., 1992).

The node is not a uniform structure, either molecularly or by tissue fate. At a molecular level, it displays left-right asymmetry of expression of a number of genes. The earliest of these are Activin receptor IIA (more likely to be a receptor for Nodal) which is expressed on the right and the transcription factor HNF3β which is expressed on the left (Levin et al., 1995; Stern et al., 1995), from stage 3+. By stage 4-4+, while the node starts to develop slight morphological asymmetry, Shh appears on the left, FGF8 on the right and Nodal just to the left of the node (Levin et al., 1995; Dathe et al., 2002). Different regions of the node also give rise preferentially to different structures (Fig. 6), although the boundaries between these fates are not sharp. Specifically, the tip of the node contains mainly prospective notochord, prechordal mesendoderm and floor plate cells, the sides and posterior aspect have mainly prospective medial somite and endodermal precursors (Selleck and Stern, 1991). Transplantation experiments have revealed that the prospective notochord region contains cells that are already committed to this fate while the lateral regions are more plastic (Selleck and Stern, 1992a), but that all regions of the node are indistinguishable in their ability to induce and pattern neural tissue (Storey et al., 1995).

Establishment and subdivision of embryonic endoderm and mesoderm

The study of endoderm formation in avian embryos, as in many other species, has been hindered considerably by the lack of any exclusive, permanent markers for the endoderm lineage. This is even more inconvenient because the endoblast (see above) also lacks specific molecular markers, which makes it very difficult to distinguish these two neighboring tissues except that the endoblast contains typical intracellular inclusions which can be seen under phase contrast in explanted tissues (Stern and Ireland, 1981). It was not until 1953 that Bellairs first recognized that the definitive endoderm is derived from the epiblast via the primitive streak (Bellairs, 1953a, b, 1955, 1957) rather than from the hypoblast layer as was previously thought. The endoderm probably starts to insinuate itself into the lower layer at the early primitive streak stage (stage 2), and this insertion process ends by stage 4 (Vakaet, 1962; Nicolet, 1965; Modak, 1966; Gallera and Nicolet, 1969; Nicolet, 1970; Selleck and Stern, 1991). We are still ignorant about the signals that induce and pattern the endoderm, from where they arise and at what stage, but based on studies in other species it seems likely that Nodal will turn out to play a major role.

By the time the endoderm inserts into the deep layer (stage 3+-4), the original hypoblast cells have become confined to the most anterior part of the blastoderm, a region called the “germinal crescent” because it also contains the primordial germ cells (Ginsburg and Eyal-Giladi, 1986, 1987, 1989; Ginsburg et al., 1989; Tsunekawa et al., 2000). Since the surface of the hypoblast is greater than that of the germinal crescent, the tissue often develops blister-like projections extending ventrally from the surface of the epiblast. The fate of the hypoblast cells after this stage has not been examined thoroughly but it is generally assumed that they contribute to the stalk of the yolk sac. It is equally likely however that a large proportion of hypoblast cells undergo apoptosis, since TUNEL staining at this stage shows heavy labeling in the hypoblast of the germinal crescent (A. Gibson and C.D. Stern, unpublished observations).


The bulk of the middle layer of the stage 3+ primitive streak will give rise to mesoderm: the notochord in the midline with prechordal mesoderm at its tip, the somites, intermediate mesoderm (prospective mesonephric kidney and its duct), heart, lateral plate mesoderm (which includes both embryonic and extraembryonic components). It is important to recognize that the long axis of the primitive streak does not correspond to the future head-tail axis of the embryo but rather to the future dorsoventral axis of the mesoderm: anterior streak (node) gives rise to the most dorsal/axial structures, with more ventral (lateral) structures arising from progressively more posterior streak positions (Schoenwolf et al., 1992; Psychoyos and Stern, 1996a; Sawada and Aoyama, 1999; Freitas et al., 2001; Lopez-Sanchez et al., 2001). This can be understood most easily by looking at the patterns of cell migration from the streak (Figs. 4, 6), and the same relationship is seen in the mouse primitive streak.

It is likely that the major player in imparting specific dorsoventral identity to prospective mesoderm is BMP signaling. The node, which emits BMP antagonists, can transform lateral plate mesoderm into somitic mesoderm (Nicolet, 1968) and this has been shown to be mimicked by Noggin (but not Chordin) (Streit and Stern, 1999). Since Noggin is not expressed in the chick until about stage 4+, it is likely that somite identity is not fixed until after this stage. Indeed, competence for lateral-to-medial transformation and vice-versa remain until at least the early somite stage (Tonegawa et al., 1997; Streit and Stern, 1999; James and Schultheiss, 2003).

Ingression from the epiblast to the deeper layers to form endoderm and the most medial (axial) mesoderm ends around the end of stage 4 (Vakaet, 1962; Nicolet, 1965; Modak, 1966; Gallera and Nicolet, 1969; Nicolet, 1970; Selleck and Stern, 1991; Joubin and Stern, 1999). A recent study has identified a zinc finger transcriptional activator, Churchill, which regulates the cessation of ingression at the primitive streak by activating Sip1, an antagonist of Brachyury (Sheng et al., 2003). This is described in more detail under Neural induction; here we will only point out that expression and activites of Churchill and Sip1 regulate the transition from the end of gastrular ingression to the start of neurulation opposite the anterior levels of the primitive streak.

Time-lapse films show that formation of the head process (the name given to the cranial portion of the notochord, rostral to the future level of the otic vesicle) begins at stage 4+ by forward migration of cells from the node (Spratt, 1947; Bellairs, 1953b). After a short delay (to the end of stage 5) these movements stop and the primitive streak starts to regress (see below), which continues to extend the notochord caudally. Elongation of the notochord appears to include both a process of convergent-extension (as in amphibians and fish) and the gradual deposition of progeny from resident stem cells (see above), but the major ingression movements from the epiblast opposite the anterior primitive streak have ceased by this stage. At more posterior levels, however, ingression to form lateral mesoderm continues for some time.

The emigration of prospective somite and lateral plate mesoderm from the primitive streak is controlled by chemorepulsion by FGF (perhaps FGF8) expressed in the streak (Yang et al., 2002). Yang et al. also proposed that after emerging from the streak, prospective somite tissue is then attracted back to the midline, specifically to FGF4 expressed in the notochord. However, since the entire embryo elongates and narrows at this stage it is difficult to determine whether the migration of somitic mesoderm towards the midline is as active a process as was proposed (Easton et al., 1990). Furthermore, embryos lacking a notochord make a midline row of somites underlying the neural tube, raising the question of what would attract cells to the midline if this model is indeed correct (Stern and Bellairs, 1984).

Ending gastrulation and regression of the primitive streak

The main period of gastrulation is characterized by massive movement of epiblast into the primitive streak to generate mesoderm and endoderm. These movements gradually stop from stages 4-4+ at the most anterior levels of the streak (prospective notochord and medial somite), and progressively more caudally. As mentioned above, the end of ingression through the anterior streak is regulated by Churchill and Sip1 (Sheng et al., 2003). Soon after this (between stages 5-6), the primitive streak starts to regress (see supplementary animation {ChickGastula_animation.avi}),.

Several studies have attempted to establish the main cellular forces driving regression of the primitive streak. The earliest (Spratt, 1947) made the important discovery that shortening of the streak is predominantly a morphological change, rather than a migration of node cells. However, convergent-extension also plays a major role in the process as mentioned earlier (Spratt, 1947; Bellairs, 1963; Lepori, 1966; Stern and Bellairs, 1984; Schoenwolf et al., 1992; Catala et al., 1996; Colas and Schoenwolf, 2001). We still know nothing, however, about the signals that regulate the timing, the speed or the specific changes in cell behavior that control regression.

The tail bud – a continuation of gastrulation?

While regression continues, the deposition of axial and paraxial mesoderm continue as the whole embryo narrows and elongates caudally to generate the tail bud (Sanders et al., 1986; Catala et al., 1996; Knezevic et al., 1998; Charrier et al., 2002). It was therefore proposed that the tail bud is a continuation of the process of gastrulation (Knezevic et al., 1998). While it is true that several processes characteristic of gastrulation do continue in the regressing streak and later in the forming tail bud, other critical processes do not. Specifically, massive ingression of epiblast to form axial tissues (notochord and somites) has ceased (except perhaps at the most caudal end), the formation of new endoderm from the streak has also ended, and regression of the streak is accompanied by cell depletion from this structure. Furthermore the node starts to lose its neural inducing ability just after stage 4 (Dias and Schoenwolf, 1990; Storey et al., 1995) (Neural Induction). Together with the fact that the neural plate starts to elevate at about stage 4+ (Bancroft and Bellairs, 1975), we consider that the end of gastrulation (as a stage) occurs between stages 4 and 4+.


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Fig. 1. Formation of the hens’ egg and its descent along the maternal oviduct. From (Duval, 1889).

Fig. 2. Cleavage in the chick embryo. A. A section through the yolk reveals concentric rings (3) of dense (darker) and white (lighter) yolk. Under the blastoderm (1), a sub-blastodermic space filled with white yolk forms a funnel (the latebra) that extends deep into the center of the yolk mass, where it forms a small cavity, the Nucleus of Pander (2). B. Cleavage in the chick embryo is meroblastic: the cleavage planes open into the surrounding yolk mass. C. A section through the blastoderm and the surrounding yolk reveals the subgerminal cavity and latebra. All three figures dapted from (Duval, 1889).

Fig. 3. Stages of gastrulation in the chick embryo. Stages are indicated on the left: Roman numerals denote pre-primitive streak stages (X-XIV) (Eyal-Giladi and Kochav, 1976) and Arabic numbers the stages from the appearance of the primitive streak (stage 2 onwards) (Hamburger and Hamilton, 1951). The left column shows diagrammatic mid-sagittal sections through part of the blastoderm, posterior to the right. The middle column depicts whole embryos viewed from the ventral (endodermal) side, and the rightmost column embryos viewed from the dorsal (epiblast) aspect. Grey: vitelline membrane; Yellow: epiblast; Dark green: hypoblast; Light brown: area opaca endoderm (germ wall and its margin); Dark brown: endoblast; Red: primitive streak mesendoderm; Purple: Koller’s sickle; Bright green: definitive (gut) endoderm.

Fig. 4. Summary fate maps of the epiblast and cell movement patterns at different stages. The two diagrams on the left hand column show the major movements in the epiblast: Polonaise movements before primitive streak formation, and convergence of the epiblast to the streak (which is strongest posteriorly) during gastrulation. The middle column of diagrams summarize the locations of territories of cells that give rise to different mesodermal tissues and the gut endoderm. The rightmost column summarizes the locations of subdivisions of the neural plate. The dashed line at stage XI indicates the most anterior extent of spread of the hypoblast layer at this stage, and the dashed outline at stage 3 is the profile of the primitive streak.

Fig. 5. Molecular interactions implicated in the initiation of primitive streak formation, shown at three successive stages (indicated on the left), in sections (left column) and in whole mounts (right). At stage X, Vg1 (red; expressed in the posterior marginal zone) cooperates with Wnt8C (blue; expressed throughout the marginal zone) to induce Nodal (bright green) in the neighboring epiblast of the area pellucida. However, Nodal cannot act further because it is inhibited by Cerberus (black) produced by the underlying hypoblast (stage XII). Shortly before primitive streak formation (stages XIV-2), the displacement of the hypoblast by the non-Cerberus-expressing endoblast allows Nodal signaling to act. Nodal, in cooperation with FGF (light brown; emanating from the hypoblast and from Koller’s sickle) and Chordin (dark green; produced by Koller’s sickle) then induce ingression of cells from the epiblast to form the primitive streak. (Based on data from several sources, mainly (Skromne and Stern, 2001; Bertocchini and Stern, 2002).

Fig. 6. Fate maps of the primitive streak and Hensen’s node. A. Morphology of the anterior tip of the primitive streak at different stages: stage 3 (no groove, parallel sides), 3+ (groove, parallel sides), 4 (distinct node), 4+ (incipient head process, elongated pit). B. Fates and movement patterns of mesoderm emerging from different portions of the streak at stage 4. Note that the anterior-posterior axis of the streak corresponds not to the head-tail axis of the embryo but rather to the mediolateral (axial-lateral, or dorsoventral) axis of the mesodermal organs. Based on data from several sources, mainly (Selleck and Stern, 1991; Psychoyos and Stern, 1996a).

3. Neural induction

(reprinted from Stern, C.D. (2004). Neural induction. In:  Gastrulation: from cells to embryo. (ed. C.D. Stern). Cold Spring Harbor Press. pp. 419-432. Copyright Claudio D Stern and Cold Spring Harbor Press) - please cite this reference if using this information. (if you want to reproduce figures you need to contact both the author and the publishers)

What is neural induction?

Embryonic induction has been defined by Gurdon as “... an interaction between one (inducing) tissue and another (responding) tissue, as a result of which the responding tissue undergoes a change in its direction of differentiation” (Gurdon, 1987). Neural induction is therefore the process by which cells acquire a neural fate in response to appropriate signals during development or after embryonic manipulations that bring two dissimilar cell types together. During normal vertebrate development, neural induction is generally believed to occur around the time of gastrulation, directed at least in part by signals emanating from a special region of the embryo: “the organizer”. The organizer resides in the embryonic shield of teleosts, the dorsal lip of the blastopore in amphibians and the tip of the primitive streak (Hensen’s node) in amniotes. This Chapter takes an historical approach to trace the development of our understanding of this process at the cellular and molecular levels.

Early history


The concept of induction originates in von Baer’s work (von Baer, 1828) and was further developed at the turn of the 20th Century notably by Curt Herbst (Oppenheimer, 1991). But the concept of neural induction really

evolved from the pioneering experiments of Warren Lewis (Lewis, 1907) and the better known work of Hans Spemann and Hilde Mangold (Spemann and Mangold, 1924; Hamburger, 1988; De Robertis and Aréchaga, 2001) (Figs. 1, 2). As part of an effort to resolve an on-going controversy about whether embryos are “regulative” or “mosaic”, Lewis found that transplantation of the dorsal lip of the blastopore of Rana to an ectopic position caused a second axis to form. However, he interpreted this as self-differentiation of the graft and it was not until Spemann’s use of interspecies grafts between three differently pigmented species of newts (Triturus taeniatus, T. cristatus and T. alpestris) (Spemann, 1921; Spemann and Mangold, 1924), allowing the cells of the donor and host to be distinguished, that it could be clearly concluded that this was an example of an inductive interaction. Spemann and Mangold termed the dorsal lip of the blastopore “the organizer”, because it could direct the formation of a coherently organized, ectopic axis from cells whose fate was other than to form axial structures.

It took only a few years for these findings to be extended to other vertebrates, including amniotes: first to avian species (chick and duck) (Hunt, 1929; Waddington, 1930, 1932; Waddington, 1933b) and shortly afterwards to mammalian embryos (rabbit), by interspecies grafts in all combinations (Waddington, 1932, 1934; Waddington, 1936, 1937). In all these cases the primitive streak, and specifically Hensen’s node at its anterior end, were found to contain the “organizer activity”.

The ability of the organizer to induce a nervous system is coupled with its ability to pattern the induced structures, the property that led to its name. Anteroposterior patterning is discussed elsewhere in this book (Fraser and Stern, 2004); suffice it to say here that several models have been proposed to account for this activity of the organizer, the main ones being the “head/trunk/tail” model most clearly formulated by Otto Mangold (Mangold, 1933), which proposes the existence of separate inducing activities for the head, trunk and tail portions of the axis, and the “activation/transformation” model of Nieukwoop (Nieuwkoop et al., 1952; Nieuwkoop and Nigtevecht, 1954), which proposes that the nervous system that is initially induced is of “anterior” (forebrain) character and that later signals “transform” parts of it to more caudal fates. Currently there is evidence both for and against both opposing models and the issue has not yet been fully resolved (see Stern, 2001). The rest of this essay will concentrate on neural induction proper – the cellular and molecular mechanisms leading to the specification of neural fate regardless of its rostrocaudal character.

Seven fruitless decades

Following the identification of the organizer and of neural induction, the hunt began for the “organizing principles”. Spemann himself favored a vitalistic explanation, while several laboratories (most notably those of Holtfreter and O. Mangold and later Tiedemann and Grunz in Germany, Toivonen and Saxén in Finland, Dorothy and Joseph Needham and Waddington in England, Nakamura and Yamada in Japan and Brachet in Belgium) embarked on trying to identify a chemical inducer (Holtfreter, 1933; Waddington, 1933a; Holtfreter, 1934; Needham et al., 1934; Spemann, 1938; Toivonen, 1938; Chuang, 1939, 1940; Toivonen, 1940; Waddington, 1940; Holtfreter, 1945; Saxén and Toivonen, 1962; Toivonen et al., 1975; Rollhauser-ter Horst, 1977b, a; Saxen, 1980; Chen and Solursh, 1992; reviewed in Nakamura and Toivonen, 1978). Early indications for a steroid, then for various protein or RNA extracts, led to transient flurries of excitement, which quickly waned as a result of the discovery that numerous “heterologous”, or non-specific inducers (including killed organizers, high or low pH, alcohol, histological dyes, …) were just as effective as an organizer graft in inducing a second axis in amphibians. Essentially no progress was made until well into the 1990s.

A turning point: BMP antagonism and the “default model”


Several seemingly unrelated observations gradually led to a new concept, commonly known as “the default model” for neural induction (Hemmati-Brivanlou and Melton, 1997) (Fig. 3). First, several groups had observed that in amphibians, dissociation of gastrula-stage animal caps into single cells for a short time before reaggregating them again leads to the formation of neural tissue (Born et al., 1989; Godsave and Slack, 1989; Grunz and Tacke, 1989; Sato and Sargent, 1989; Saint-Jeannet et al., 1990). A few years later, it was found that misexpression of a dominant-negative “activin”-receptor (it was later discovered that this construct inhibits several TGFβ-related factors) into Xenopus embryos not only blocks mesoderm formation but also generates ectopic neural tissue (Hemmati-Brivanlou and Melton, 1992, 1994). At about the same time, it was discovered that BMP4 is a ventralizing factor in Xenopus (Dale et al., 1992; Jones et al., 1992). Several of these authors speculated that neural induction might be induced by removal of some inhibitory substance (Hemmati-Brivanlou and Melton, 1994), but direct evidence was still lacking.

Soon, three genes encoding proteins with neuralizing activity were isolated and found to be expressed in the organizer: Noggin (Smith and Harland, 1992; Lamb et al., 1993; Smith et al., 1993), Follistatin (Hemmati-Brivanlou et al., 1994) and Chordin (Sasai et al., 1994; Sasai et al., 1995). But it took several other findings before the connections were established firmly: the turning points were the finding that BMP4 is an effective inhibitor of neural fate while promoting epidermal differentiation (even in dissociated cells) (Hawley et al., 1995; Wilson and Hemmati-Brivanlou, 1995) and the observations that all three neuralizing/dorsalizing proteins, Noggin, Chordin and Follistatin, are binding partners and antagonists of BMP signaling (De Robertis and Sasai, 1996; Piccolo et al., 1996; Zimmerman et al., 1996; Fainsod et al., 1997). The Drosophila homolog of Chordin (Short gastrulation, or Sog) also binds and inactivates the BMP4 homolog Decapentaplegic (Dpp) and vertebrate Chordin can even rescue sog mutants (Francois and Bier, 1995; Holley et al., 1995; Schmidt et al., 1995; Biehs et al., 1996; De Robertis and Sasai, 1996; Ferguson, 1996).

Together, these findings led to the “default model” (Hemmati-Brivanlou and Melton, 1997), which proposes that cells within the ectoderm layer of the frog gastrula have an autonomous tendency to differentiate into neural tissue. This tendency is inhibited by bone morphogenetic proteins - in particular, BMP4, which acts as an epidermal inducer (Fig. 3).


Consistent with this model (Fig. 4), neuralization does not occur after dissociation of animal caps obtained from embryos previously injected with RNA encoding effectors of BMP4 (Msx1, Smad1 or Smad5; Suzuki et al., 1997a; Suzuki et al., 1997b; Wilson et al., 1997), consistent with the view that the neural pathway is inhibited by an endogenous BMP-like activity. Moreover, the expression pattern of BMP4 in Xenopus conforms to its proposed anti-neural function: in the early gastrula, BMP4 transcripts are widely expressed in the entire ectoderm and then clear from the future neural plate at the time when the organizer appears (Fainsod et al., 1994). Transcription of BMP RNA is maintained by the activity of BMP protein (Biehs et al., 1996), which accou

nts for the disappearance of BMP4 and -7 expression from the vicinity of the organizer (which secretes BMP inhibitors) at the gastrula stage (Fainsod et al., 1994; Hawley et al., 1995).

The model is further supported by the effects of treatments that inhibit the BMP signaling pathway. Animal caps cut from embryos injected with either RNA encoding dominant-negative receptors that bind BMPs (Hemmati-Brivanlou and Melton, 1994; Xu et al., 1995), or non-cleavable forms of BMP4 or -7 (Hawley et al., 1995), or antisense BMP4 RNA (Sasai et al., 1995) adopt a neural fate instead of epidermis (Fig. 4). Finally, Chordin and Noggin protein can neuralize isolated animal caps (provided that these have been exposed briefly to low Ca++/Mg++-medium – effectively a partial dissociation, although the rationale given for this is that it helps the protein penetrate between the cells).

In addition to its role in neural induction, the organizer can also pattern the mesoderm at the gastrula stage (“dorsalization”). This activity can also be attributed to BMP inhibition. BMPs can modify dorsal mesoderm to give ventral cell types (Dale et al., 1992; Fainsod et al., 1994; Jones et al., 1996), while their inhibitors can generate notochord and muscle from ventral mesoderm (Smith et al., 1993; Sasai et al., 1994; Tonegawa et al., 1997; Tonegawa and Takahashi, 1998; Streit and Stern, 1999b). BMP inhibitors can also regulate the dorsoventral polarity of the whole embryo before gastrulation. For example, UV irradiated embryos lack dorsoventral polarity and fail to gastrulate, but can be rescued fully by injection of RNA encoding any of the BMP inhibitors: the blastopore (dorsal) will form close to the site of injection (Smith and Harland, 1992; Sasai et al., 1994).

In addition to Chordin, Noggin and Follistatin, other secreted molecules that antagonize BMP signaling have been found and several of these are expressed in, or close to, the organizer. These include Cerberus (Bouwmeester et al., 1996; Belo et al., 1997), Gremlin, Dan and Drm (Hsu et al., 1998; Pearce et al., 1999; Dionne et al., 2001; Eimon and Harland, 2001; Khokha et al., 2003), Ogon/Sizzled (Wagner and Mullins, 2002; Yabe et al., 2003b) and Twisted gastrulation (Chang et al., 2001).

Finally, a recent study by the De Robertis lab demonstrated that organizer activity, or at least dorsalization, requires functional Chordin (Oelgeschlager et al., 2003). Together, these findings provide compelling evidence that BMPs and their modulation by endogenous inhibitors are involved in the activities of the organizer, including the establishment of neural and non-neural domains in Xenopus. This model is very attractive both because of its simplicity and also because it provides the first truly coherent model to explain neural induction since the discovery of the organizer by Spemann and Mangold.

More complexity?

What followed was perhaps a little reminiscent of the events in the 1940s that eventually led to a temporary loss of interest in identifying neural inducers (see above) – a flurry of papers reporting neural inducing activity of a variety of other molecules (Otte et al., 1988; Otte et al., 1990; Otte et al., 1991; Bolce et al., 1992; Kengaku and Okamoto, 1995; Lamb and Harland, 1995; Sokol et al., 1995; Witta et al., 1995; Hansen et al., 1997; Rodriguez-Gallardo et al., 1997; Xu et al., 1997; Alvarez et al., 1998; Barnett et al., 1998; Mariani and Harland, 1998; Storey et al., 1998; Baker et al., 1999; Hongo et al., 1999; Kato et al., 1999; Leclerc et al., 1999; Matsuo-Takasaki et al., 1999; Beanan et al., 2000; Fekany-Lee et al., 2000; Hardcastle et al., 2000; Ishimura et al., 2000; Strong et al., 2000; Kim and Nishida, 2001; Pera et al., 2001; Sullivan et al., 2001; Wessely et al., 2001; Borchers et al., 2002; Peng et al., 2002; Tsuda et al., 2002; Osada et al., 2003; Pera et al., 2003; Yabe et al., 2003a). Some of these clearly act by inhibition of the BMP pathway at some level, while others do not obviously act that way. Many of those that do not, however, seem to act by regulating the pattern of the whole embryo at earlier stages of development. Misexpression experiments conducted by injection of RNA at early cleavage stages gives results that are difficult to interpret in terms of whether the encoded protein acts directly (as a true neural inducer) or through prior induction of a cell fate that can emit an inducer.

To some extent this explains some contradictory findings. For example, the Wnt pathway has been reported to act as a neural inducer by some (Sokol et al., 1995; Baker et al., 1999; Wessely et al., 2001) but to inhibit neural induction by others (Wilson et al., 2001). The difference could be accounted for if at early stages Wnt dorsalizes the embryo (inducing tissues with organizer properties), while at later stages Wnt activity somehow antagonizes other signals from the organizer (Bainter et al., 2001; Wilson and Edlund, 2001). It becomes important to use reagents that work in a cell-autonomous manner and to express them in a stage- and position-controlled way (as appropriate to the specific inductive event being studied).

A more complex literature surrounds the role of FGF signaling in neural induction. A first study implicated this pathway indirectly when Suramin (which inhibits FGF among other related proteins) was found to block neural induction in Xenopus (Grunz, 1992). Later, several labs found that FGF can induce neural tissue under certain circumstances (Lamb and Harland, 1995; Rodriguez-Gallardo et al., 1997; Alvarez et al., 1998; Barnett et al., 1998; Storey et al., 1998; Hongo et al., 1999; Hardcastle et al., 2000; Ishimura et al., 2000; Wilson et al., 2000; Kim and Nishida, 2001; Hudson et al., 2003), while other studies suggested that FGF is not a sufficient signal for neural induction (Amaya et al., 1991; Cox and Hemmati-Brivanlou, 1995; Kroll and Amaya, 1996; Holowacz and Sokol, 1999; Ribisi et al., 2000; Pownall et al., 2003). One explanation for this discrepancy is the observation that different FGF receptors are required to mediate different activities of FGF: FGFR1 is required for the mesoderm-inducing function of FGF, while FGFR4 appears to mediate its role in neuralization (Hardcastle et al., 2000; Umbhauer et al., 2000). The involvement of FGF signals in neural induction will be discussed further below.

FGF, Wnt and BMPs in neural induction

Despite the obvious attraction of the default model, several observations in different organisms do not fit its proposals so neatly. In Xenopus, inhibition of FGF signaling by a dominant-negative version of the FGF-receptor-1 (XFD) blocks the neuralizing activity of both Noggin and Chordin (Launay et al., 1996; Sasai et al., 1996). Furthermore, mere cutting of the animal cap activates MAP kinase by phosphorylation, at least transiently (LaBonne and Whitman, 1997), which could explain the finding made by several labs that “control” animal caps express markers for the cement gland (Fig. 4). These observations suggest that FGF signaling is required for neural induction in addition to BMP inhibition.


In chick (Figs. 5-6), the patterns of expression of components of the BMP pathway do not agree with the model: Chordin continues to be expressed in organizer at stages when this has lost its neural inducing activity, and Noggin and Follistatin are not expressed in the organizer at the appropriate stages at all, while BMP4 and BMP7 are expressed only weakly (if at all) in the ectoderm before neural induction begins, and their expression increases at the border of the neural plate starting from the end of gastrulation (stage 4) (Streit et al., 1998). Moreover, misexpression of Chordin or Noggin in competent epiblast does not neuralize the epiblast (Streit et al., 1998; Streit and Stern, 1999b; Linker et al., 2004) (Fig. 6) and dissociation of the epiblast leads to differentiation of muscle rather than neurons (George-Weinstein et al., 1996). In zebrafish, neither Noggin nor Follistatin are expressed in the organizer (Bauer et al., 1998) and Chordin (chordino) mutants, although ventralized, still have a neural plate (Hammerschmidt et al., 1996a; Hammerschmidt et al., 1996b; Kishimoto et al., 1997; Schulte-Merker et al., 1997; Bauer et al., 1998). In mouse, BMP4 mutants are uninformative (the embryos die too early with mesoderm and other generalized defects (Winnier et al., 1995), but BMP2 and BMP7 mutants lack an early neural phenotype (Dudley et al., 1995; Zhang and Bradley, 1996) and Chordin-, Noggin- and even Chordin-Noggin double mutants have a respectable neural plate (Brunet et al., 1998; McMahon et al., 1998; Bachiller et al., 2000). In the urochordate Ciona, FGF signaling through the MEK pathway but not BMP inhibition appears to be responsible for neural induction (Darras and Nishida, 2001; Hudson and Lemaire, 2001; Kim and Nishida, 2001; Bertrand et al., 2003; Hudson et al., 2003).


FGF signaling now appears to be a prerequisite for neural induction but this step occurs (or at least begins) very ear

ly, before gastrulation (Streit et al., 2000; Wilson et al., 2000). However, FGF does not appear to be a sufficient or direct neural inducer in vertebrates (Streit et al., 2000). Wilson and colleagues (Wilson et al., 2001) suggested that FGF only shows neural inducing activity when Wnt signaling is also blocked, and proposed that there are two divergent pathways both involving FGF: for “medial epiblast cells” (prospective neural plate), FGF signaling alone is sufficient to repress the BMP pathway and thus cause neuralization. For “lateral epiblast cells” (prospective epidermis), both FGF signaling and Wnt inhibition are required to block the BMP pathway and neuralize (Wilson and Edlund, 2001; Wilson et al., 2001). It has been proposed (Bainter et al., 2001; Wilson and Edlund, 2001) that the critical event involves regulation of BMP4 transcription. Most of these experiments have been conducted using explants, and in our own experiments in intact embryos we are unable to neuralize competent epiblast by any combination of FGF, Wnt antagonists and/or BMP antagonists at any stage of development (Streit et al., 2000; Linker et al., 2004). Furthermore, we find that misexpression of the intracellular BMP antagonist Smad6 in chick embryos is not sufficient to cause neuralization of competent epiblast even when combined with secreted BMP antagonists (Chordin and Noggin), FGF, secreted Wnt antagonists (NFz8, Dkk1 and crescent) and a multifunctional antagonist (Cerberus) (Linker et al., 2004). We therefore believe that not all the required signals have been identified, and that although down-regulation of BMP is almost certainly involved in the specification of the neural plate, this is not a sufficient signal, even in combination with FGF and Wnt inhibition.

Looking upstream from a critical promoter

To date, therefore, we have not yet arrived at a full understanding of the molecular signals that trigger the acquisition of neural fate by the ectoderm. One reason for this may be the diversity of approaches used in different “model” systems, and that many of the approaches used have not taken full account of the issue of developmental timing, which is particularly important when studying molecules with multiple, and sometimes opposing functions at different times. One might however gain further insight by changing the viewpoint to the promoter of a target gene. This has recently been attempted for the first time by analysis of the Sox2 promoter, which is a good marker for committed, developing neural plate in the chick (unlike the mouse where the early functions of Sox3 and Sox2 appear to have been exchanged). Kondoh and colleagues have identified many enhancers both upstream and downstream of the cSox2 gene, which are conserved in mouse and human (Uchikawa et al., 2003). Two of these enhancers, N1 and N2, appear to be responsible for the onset of expression of Sox2 in the early neural plate – they contain binding sites for several identified transcription factors, including a Sox-related protein (perhaps Sox3, which in the chick is expressed earlier in a similar domain to Sox2), TCF/LEF (Wnt pathway), homeodomain-containing proteins and an E-box sequence shown to be a target of Sip1/δEF1 (Verschueren et al., 1999). Sip1 was recently identified as a target of the zinc finger protein Churchill, and morpholino-mediated down-regulation of Churchill function leads to loss of the neural plate, while misexpression of Churchill can confer or maintain the competence of epiblast to neural inducing signals from the node (Sheng et al., 2003) (see Avian gastrulation).

A view from the streak/blastopore


Churchill was first isolated from a molecular screen designed to identify genes that a

re regulated by 5 hours of signaling from a graft of the organizer, Hensen’s node, in the chick embryo (Sheng et al., 2003). This was done because previous studies had revealed that 5 hours’ exposure to a node are required for epiblast cells to become sensitive to Chordin misexpression (by maintaining Sox3 expression, which is otherwise only transiently induced by a node graft) (Streit et al., 1998). Churchill is expressed in the prospective neural plate from the late gastrula stage and thereafter persists in the forming neural plate in a pattern similar to that of Sox2. Both a node graft and misexpression of FGF induce Churchill expression in about 4 hours, as expected from the screen (Sheng et al., 2003) (Fig. 7). Churchill misexpression close to the streak of the chick embryo or the blastopore of frog embryos causes down-regulation of the mesodermal marker Brachyury; however, Churchill is a transcriptional activator, which suggested that one of its targets may be a repressor of Brachyury. A selection strategy and gel mobility shift assays identified the sequence CGGGRR as a binding target of Churchill, and analysis of the putative regulatory regions of Sip1 identified numerous occurrences of this sequence. Indeed Sip1 is expressed identically to Churchill and morpholino-knockdown of the latter causes loss of Sip1 expression (Sheng et al., 2003). Sip1 is a good candidate to mediate the down-regulation of Brachyury by Churchill, since it this is one of its known functions (Verschueren et al., 1999; Lerchner et al., 2000; Papin et al., 2002).

Misexpression of Churchill near the primitive streak causes not only loss of Brachyury but also a failure of cells to continue to ingress through the streak to form mesendoderm. Since Churchill begins to be expressed at about the time this ingression stops through the anterior primitive streak (see Avian gastrulation), this raised the possibility that one of its functions may be to end the process of gastrulation to keep some epiblast cells on the surface. This hypothesis is supported by the finding that morpholino down-regulation of Churchill at the late gastrula/early neurula stage causes cells to continue to ingress through the streak, and ectopic contribution to the mesoderm rather than neural plate. This effect can be rescued by co-electroporation of either Churchill or of its target Sip1 (Sheng et al., 2003). Thus, Churchill regulates the end of ingression through the streak as well as the competence of the cells that express it to respond to neural inducing signals from the node, raising the possibility that this is a critical protein in the neural induction process, and particularly in regulating the transition from gastrulation to neurulation. This finding drew attention to the rather overlooked fact that at the gastrula stage, the prospective mesoderm territory lies adjacent to the prospective neural plate in all vertebrate classes, and to the possibility that during normal development the decisions leading to the acquisition of neural fate involves a switch between these two identities in addition to the choice between epidermis and neural plate, as suggested by the Spemann/Mangold transplantation experiment and its equivalent in other species. One possibility, therefore, is that two separate decisions lead to the establishment of the neural plate: one (a decision between mesendoderm and neural fates) at the medial edge of the neural plate, involving Churchill and Sip1 medially, which prevent further gastrular ingression, and the other (neural versus epidermis) at its lateral/anterior edges, which could involve inhibition of BMP signaling.

A view from the border

The same screen that led to the identification of Churchill also identified another early response to an organizer graft: ERNI (Early Response to Neural Induction) (Streit et al., 2000). Like Churchill, this is expressed in the prospective neural plate but its expression begins much earlier, before gastrulation. At the end of gastrulation ERNI is down-regulated starting from the center of the neural domain until it is expressed only at the neural-epidermis border, and then it disappears from this domain after stage 7. Also like Churchill, ERNI is induced by a graft of the node and by FGF, but this induction is much more rapid (just 1 hour). Analysis of the expression of different FGFs and comparison with these early “pre-neural” markers suggested that ERNI and Sox3 are first induced before gastrulation, by FGF emanating from either the hypoblast or from prospective organizer cells at the posterior end of the blastodisc or both (Streit et al., 2000). Indeed, transplantation of either of these tissues can induce ERNI and Sox3 just like a node or FGF, and blocking the FGF pathway abolishes their induction by any of these tissues. These and other findings (Streit and Stern, 1999a) led to the view that an early response to neural induction (and FGF signaling) is the specification of a region with “border-like” character, which is responsive to BMP and its antagonists (Streit et al., 1998; Streit and Stern, 1999a, b). Subsequent events confine these properties exclusively to the future neural/epidermal border, as the neural plate proper becomes insensitive to BMP during gastrulation. By stage 3+-4, the only region sensitive to BMP signaling is the border itself: up-regulation of BMP here moves the border towards the midline (but only by a modest amount), narrowing the neural plate, while down-regulation of BMP at the border widens the neural plate (but again only slightly). Sip1 was first identified by its interaction with phosphorylated Smad1, a target of BMP (Verschueren et al., 1999), raising the possiiblity that Churchill, through Sip1, contributes to sensitizing cells to BMP antagonists after 5 hours’ exposure to FGF.

The situation in amphibians may not be different from that in birds. Based on at least some fate maps from early (32-64-cell) stages in both Xenopus (Jacobson and Hirose, 1981; Moody, 1987; Moody and Kline, 1990) and in other amphibians (Moury and Jacobson, 1989, 1990; Saint-Jeannet and Dawid, 1994; Delarue et al., 1997), the most animal blastomeres (A2 and A3) will contribute progeny to the neural crest (i.e. the border of the neural plate). Since most injections designed to test the ability of BMP antagonists and other factors to induce a neural plate are placed in the animal pole, it is likely that they target, at least in part, what may be the most sensitive region: the neural/epidermal border. It is also possible that the observations that cutting an animal cap activates MAPK as well as inducing expression of cement gland markers (the cement gland is part of the anteriormost border of the neural plate; see above) are causally connected. In agreement with this view, injection of the dowstream inhibitory component of the BMP pathway, Smad6 in Xenopus at the 32-cell stage causes axis duplications and/or expansion of the neural plate when placed into the A1-A3 animal blastomeres, but no ectopic neural plate when placed into the most ventral, A4 animal blastomere (Delaune et al., 2004; Linker et al., 2004). Together these observations raise the possibility that inhibition of the BMP pathway may only be effective in generating ectopic neural plate (expansion of the endogenous neural plate) within or close to the border between neural and epidermal territories, but not within a region wholly destined to give rise to epidermis. The results also point to the border of the neural plate as a special region, distinct from both neural plate and epidermis.

The timing of neural induction

Organizer grafts are technically easiest after the start of gastrulation, when the blastopore, primitive streak or shield can be identified morphologically. Experiments in which the stage of the host and donor embryos were varied in different vertebrate classes established that neural induction is likely to end by the end of the gastrula stage. For example, in the chick, a Hensen’s node taken from an embryo up to stage 4 can induce a complete nervous system but older donors gradually lose their inducing ability, while hosts rapidly lose their competence between stages 4 and 4+ (Damas, 1947; Gallera and Ivanov, 1964; Gallera, 1971; Dias and Schoenwolf, 1990; Storey et al., 1992; Streit et al., 1997). Experiments such as these have suggested that neural induction by the organizer is likely to end by the end of gastrulation, but do not give insight into when the process starts. As mentioned above, at least some of the early signals may be present and active before the start of gastrulation (Streit et al., 2000; Wilson et al., 2000). At this time, a number of “pre-neural” genes are expressed in the epiblast (including ERNI, Sox3 and Otx2), in a fairly broad domain which includes but is not restricted to the future neural plate. Some cells expressing all three markers are destined to contribute to mesendoderm as well as neural/epidermis border and some epidermis. Further signals and other refining mechanisms are required downstream of this initial “pre-neural” specification to commit cells to a neural fate.

In the chick, grafts of the hypoblast (which expresses both FGF8 and the Wnt antagonists Dkk-1, crescent and Cerberus) can induce all three “pre-neural” genes, but only transiently (Foley et al., 2000; Streit et al., 2000). It has been suggested (Stern, 2001) that signals from the node or from its derivatives like the head process/notochord and/or the prechordal mesendoderm may be required to stabilize this early expression and to drive cells to Sox2 expression and commitment to a neural plate fate. The hypoblast is equivalent (in terms of fate as well as expression of various markers) to the Anterior Visceral Endoderm (AVE) of the mouse (see Avian gastrulation), which has been shown to be required for normal development of the mouse forebrain (Thomas and Beddington, 1996; Beddington and Robertson, 1998, 1999). However, it is important to point out that neither the chick hypoblast nor the mouse AVE are equivalent to Spemann’s organizer in that neither can induce the formation of a neural plate/axis when grafted to an ectopic site. In the mouse, it was shown that forebrain induction requires a combination of the AVE, the “early gastrula organizer” (EGO – which may contain some of the precursors of the later node) as well as the appropriate responding part of the epiblast (prospective forebrain) (Tam and Steiner, 1999).

The findings that grafts of a mouse node to a lateral site induce a nervous system lacking the most rostral structures (Beddington, 1994) and that homozygous HNF3β mutants, which lack a node (Klingensmith et al., 1999), still have a fairly acceptable neural tube, have been used by some to argue that the node is not essential for neural induction. Indeed, it is clear that the most rostral portions of the neural plate (prospective forebrain) are never adjacent to the mature node in either mouse or chick embryos. However, the former finding can be explained because mouse embryos are very small and it is virtually impossible to find a site to graft the node allowing a complete axis to form without fusing with the host, and the latter can be explained by the possibility that although no morphological node or its derivatives form, some of its properties are also expressed by other tissues. Furthermore, by the time a “node” can be defined morphologically in the mouse, the embryos are starting to produce a head process; chick nodes at the equivalent stage (4+/5) have already lost their ability to induce the most rostral parts of the CNS (Dias and Schoenwolf, 1990; Storey et al., 1992). Taking this evidence together, the most parsimonious view is therefore that during normal development, signals from the AVE and/or other areas initiate some of the earliest events of neural induction, but are not sufficient. As development proceeds to gastrulation, “maintenance” signals as well as regional identity are imparted by the node and/or its derivatives (prechordal and chordal tissues) (Stern, 2001). However, the node itself (provided that it is taken from an embryo at the full primitive streak stage but before any prechordal/head process cells emerge) contains sufficient signals to induce a complete axis when grafted far enough from the host neural plate. In the chick this can be done in the inner third of the area opaca, which only has extraembryonic fate (Gallera, 1971; Dias and Schoenwolf, 1990; Storey et al., 1992; Streit et al., 1998); in the mouse (and perhaps also in Xenopus), it is impossible to find a site far enough from the host neural plate to avoid recruitment of host neural plate cells.


Although very substantial progress has been made in understanding neural induction since the pioneering experiments of the 1920s, there are still substantial gaps in our knowledge of both the cellular and molecular aspects of this important process. It is now becoming more likely than rather than a single inducing factor, a whole cascade of molecular events and converging pathways are required to specify the neural plate, and that different mechanisms may contribute to define this territory in different embryonic locations at different times. Our view is that a full understanding will only come when the embryological/cellular processes can be fully correlated with their molecular basis – much the same as what Wolpert may have had in mind when criticizing excessive emphasis on signaling events (“inductions”) at the expense of understanding the resulting patterns: “… induction and its related concepts, which have so dominated embryological thinking, have completely obscured the problems of pattern formation by emphasizing the information coming from some other tissue rather than the response in the tissue which gives rise to the pattern … {a} failure of inductive theory to consider the problem of spatial organization” (Wolpert, 1970; quoted from Horder, 2001).


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Figure legends

Fig. 1: Diagram of the “organizer graft” experiment of Spemann & Mangold (1924). The dorsal lip (red) of the blastopore (thick black line) of a donor newt at mid-gastrula stage is transplanted to the opposite (ventral) side of a host.

Fig. 2: Diagrams bu Hilde Mangold, illustrating the results of her organizer graft experiments (Fig. 1). The upper four figures are Indian ink drawings prepared as for publication, showing her embryos (Um25b, Um27a and two views of Um16) in whole mount. The lower part of the figure shows sketches from the sections of her most famous grafted embryo (Um132) where the donor tissue is colored red. Note that the mesoderm including somite and notochord is derived from the donor, while the adjacent nervous system is not. Access to the notebook and permission to reproduce them by courtesy of Jenny Narraway and the Embryological Collection of the Hubrecht Laboratory, Utrecht.

Fig. 3: The “default model” in Xenopus. On the left is a rough fate map of a blastula-stage embryo (organizer in red, ventral mesoderm in pink, neural in blue, epidermis yellow, yolky endoderm green). The inhibitory arrows represent BMP antagonist activity emanating from the organizer. On the right is a “genetic” diagram of the inductive interactions proposed by the model: ectoderm cells (represented by the grey boxes) have an autonomous tendency to differentiate into neural tissue, but are prevented from doing this and directed instead to epidermis by BMP4, which is expressed ubiquitously. Near the organizer, BMP antagonists block BMP4 signaling allowing neighboring ectoderm cells to develop according to their “default” neural fate.

Fig. 4: Summary of the main experiments supporting the “default model” (Fig. 3) as done in Xenopus. The leftmost two columns illustrate the results of cell dissociation experiments, the next two show the effects of incubating animal caps with BMP antagonists, and the last two columns summarize the most common type of “animal cap” experiment. The lower box shows the usual results of these experiments where + implies expression of markers for the tissue shown, - means no expression, and up- or down-arrows represent up- or down-regulation respectively.

Fig. 5: Organizer graft experiment in the chick, also demonstrating the changes in inducing ability of the organizer with increasing age of the donor. The middle diagram shows a host chick embryo, at stage 4. This embryo simultaneously receives a graft of a quail stage 4 node on its left and a quail stage 6 node on its right. The lower panel shows the result of this experiment, after in situ hybridization (purple) for the hindbrain marker Krox-20 (expressed in rhombomeres 3 and 5, arrows) and staining with an anti-quail antibody (brown). The young graft has induced a complete axis including the entire head, while the older graft on the right has generated a short axis, mostly derived from the graft itself and lacking rostral structures including the Krox-20-expressing region. Experiment performed by Kate Storey (Storey et al. 1992).

Fig. 6: Results of chick misexpression experiments. The upper diagram shows the two main types of misexpression experiments usually done in whole chick embryos: a graft of cultured COS cells that had been transfected with an expression plasmid encoding a secreted factor (left), and in vivo electroporation of an expression plasmid encoding the desired protein (which may be a transcription factor, secreted protein or any other construct) directly into a test region of the epiblast. The lower table summarizes the results of the main experiments done in whole chick embryos. + indicates induction, - no induction, n.e. no effect. In the first three examples (node, hypoblast, FGF8) the time (hours) of exposure required to obtain induction of the marker is shown.

Brachyury (Bra) is a marker for mesoderm. Sox2 is the “definitive” neural plate marker and the remaining markers (ERNI, Otx2, Sox3, ChCh) are expressed in the early epiblast including the prospective neural territory but do not indicate commitment of the cells to a neural fate. “αWnt” is a mixture of three different Wnt antagonists (crescent, NFz8 and Dkk1) and a multifunctional antagonist of Wnt, BMP and Nodal (Cerberus). Note that no combination of factors can mimic the induction of Sox2 by the node.

† Chordin induces an ectopic primitive streak when misexpressed inside the embryo (Streit et al., 1999b) but does not induce neural markers in competent epiblast.

* BMP4 misexpressed by electroporation within the neural plate inhibits Sox2 but not Sox3. When using COS cells there is no effect.

Based on experiments by Streit et al. (1999a, b, 2000) and C. Linker, I. de Almeida and C. D. Stern (unpublished).

Fig. 7: Model summarizing the regulation and functions of ChCh during early development. A-D: the embryologist’s view; E: the geneticist’s view. In A-D, embryos are shown at four stages, with their germ layers exploded. A. At stages XI-XII, the hypoblast (brown) emits FGF8 which induces the early pre-neural genes ERNI and Sox3 (orange) in the overlying epiblast (yellow), but the cells in this domain are still uncommitted. At this stage Nodal is expressed in the posterior (right) epiblast but is inhibited by Cerberus secreted by the hypoblast. B. At stages XIII-2, the hypoblast is displaced from the posterior part of the embryo by the endoblast (white) which allows Nodal signaling, in synergy with FGF, to induce Brachyury and Tbx6L and ingression (red arrows) to form the primitive streak (red). C. At stages 3+-4, continued FGF signaling now induces Churchill in a domain of the epiblast (turquoise). The border of the epiblast territory destined to ingress to form mesoderm is shown with a dashed black line. D. At the end of stage 4, Churchill induces Sip1, which blocks Brachyury, Tbx6L and further ingression of epiblast into the streak. The epiblast remaining outside the streak (blue) is now sensitized to neural inducing signals emanating from the node (blue arrows). E. The same model shown as a genetic cascade. Interactions described in this paper are shown as black lines, those from the literature are faint. The time axis runs vertically, wherein the color gradients indicate progressive commitment to epidermis (yellow), neural (blue) and mesoderm (red). BMP/Smad/Sip1 interactions regulate the epidermis-neural plate border, while ChCh/Sip1/FGF/Bra/Tbx6 regulate the mesoderm-neural decision. Reproduced from Sheng et al. (2003) with permission of Cell Press.