29 Dec 2015: Lowe CJ, Terasaki M, Wu M, Freeman RM Jr, Runft L, et al. (2015) Correction: Dorsoventral Patterning in Hemichordates: Insights into Early Chordate Evolution. PLOS Biology 13(12): e1002354. doi: 10.1371/journal.pbio.1002354 View correction
We have compared the dorsoventral development of hemichordates and chordates to deduce the organization of their common ancestor, and hence to identify the evolutionary modifications of the chordate body axis after the lineages split. In the hemichordate embryo, genes encoding bone morphogenetic proteins (Bmp) 2/4 and 5/8, as well as several genes for modulators of Bmp activity, are expressed in a thin stripe of ectoderm on one midline, historically called “dorsal.” On the opposite midline, the genes encoding Chordin and Anti-dorsalizing morphogenetic protein (Admp) are expressed. Thus, we find a Bmp-Chordin developmental axis preceding and underlying the anatomical dorsoventral axis of hemichordates, adding to the evidence from Drosophila and chordates that this axis may be at least as ancient as the first bilateral animals. Numerous genes encoding transcription factors and signaling ligands are expressed in the three germ layers of hemichordate embryos in distinct dorsoventral domains, such as pox neuro, pituitary homeobox, distalless, and tbx2/3 on the Bmp side and netrin, mnx, mox, and single-minded on the Chordin-Admp side. When we expose the embryo to excess Bmp protein, or when we deplete endogenous Bmp by small interfering RNA injections, these expression domains expand or contract, reflecting their activation or repression by Bmp, and the embryos develop as dorsalized or ventralized limit forms. Dorsoventral patterning is independent of anterior/posterior patterning, as in Drosophila but not chordates. Unlike both chordates and Drosophila, neural gene expression in hemichordates is not repressed by high Bmp levels, consistent with their development of a diffuse rather than centralized nervous system. We suggest that the common ancestor of hemichordates and chordates did not use its Bmp-Chordin axis to segregate epidermal and neural ectoderm but to pattern many other dorsoventral aspects of the germ layers, including neural cell fates within a diffuse nervous system. Accordingly, centralization was added in the chordate line by neural-epidermal segregation, mediated by the pre-existing Bmp-Chordin axis. Finally, since hemichordates develop the mouth on the non-Bmp side, like arthropods but opposite to chordates, the mouth and Bmp-Chordin axis may have rearranged in the chordate line, one relative to the other.
Citation: Lowe CJ, Terasaki M, Wu M, Freeman RM Jr, Runft L, Kwan K, et al. (2006) Dorsoventral Patterning in Hemichordates: Insights into Early Chordate Evolution. PLoS Biol 4(9): e291. doi:10.1371/journal.pbio.0040291
Academic Editor: Edward De Robertis, Howard Hughes Medical Institute, United States of America
Received: March 7, 2006; Accepted: June 28, 2006; Published: August 22, 2006
Copyright: © 2006 Lowe et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This research was supported by USPHS grants HD37277 to MK and HD42724 to JG and by NASA grant FDNAG2–1605 to JG and MK. CJL was supported in part by a Miller Institute Fellowship (University of California Berkeley) and a Colwin Fellowship (Woods Hole).
Competing interests: The authors have declared that no competing interests exist.
Abbreviations: Admp, anti-dorsalizing morphogenetic protein; Bmp, bone morphogenetic protein; Cv, crossveinless; dlx , distalless ; Hh, hedgehog; pitx , pituitary homeobox ; PoxN, pox neuro; RNAi, RNA interference; Shh, sonic hedgehog; Sim, single-minded; siRNA, small interfering RNA; Tsg, twisted gastrulation
Arthropods (especially Drosophila) and chordates (especially mouse, fish, frogs, and birds) and presumably all bilaterians are fundamentally similar in the development of their body plans [1,2]. Suites of genes are arranged in conserved domain maps in both the anteroposterior and dorsoventral dimensions of developing embryos. Paradoxically, this conservation of axial patterning provides the developmental platform for astonishing anatomical and physiological diversification both within and between phyla. Clearly a major step in the evolution of bilateral animals was the origination of these domain maps and the usage of transcription factors and signaling proteins by which diverse target genes could be expressed at specific times and places in development at subsequent stages.
The evolution of the dorsoventral axis (transverse to the anteroposterior axis) is not well understood. It may have originated during the transition from radial to bilateral animals , although recent evidence raises the possibility it was already cryptically present in radial animals [4,5]. Bilateral animals, at least back to the Cambrian, have numerous anatomical and physiological specializations located along this axis, in all three germ layers. The mesodermal tissues such as the heart, blood forming elements (and the direction of blood flow), gonads, visceral muscle, and striated muscle are arranged in dorsoventral patterns. The gill slits (in chordates and hemichordates) and other endodermal organs have similarly conserved patterns in the dorsoventral domain. Ectodermal examples include the central nervous system and epidermal territory. The dorsal and ventral poles of the axis are usually assigned based on the orientation of the animal related to gravity (dorsal up; ventral down) or on the location of the mouth (defining the ventral side). Some of these specializations were presumably added before others in the evolution of bilateral animals. The more widespread the specialization among bilateral animals, the older it is assumed to be. For example, since arthropods and chordates have central nervous systems, and since new molecular data reveal commonalities of their development and organization, the central nervous system has been considered a dorsoventral differentiation already present in the bilateral ancestor . We will address this point in our study of hemichordates.
Preceding the dorsoventral axis of anatomical and physiological specializations in the course of development is a molecular axis. In arthropods and chordates genes for bone morphogenetic protein (Bmp 2,4,7, or Dpp) are expressed in the embryo at one pole and the genes for Bmp antagonists, such as Chordin and Noggin, at the other. All subsequent tissues, organs, and cell types develop in accordance with this Bmp-Chordin axis [1,6]. It may be part of the fundamental body plan of all bilateral animals and may be a key innovation of the bilaterian ancestor (urbilaterian), to which all later dorsoventral differences of anatomy and physiology were attached .
Once established in the embryo, two phases of dorsoventral patterning can be distinguished in chordates and Drosophila . During the first stage, at pre-gastrula and gastrula stages, ectoderm segregates into two distinct domains, neural and non-neural (i.e., epidermis). Embryonic ectodermal cells that are exposed to high Bmp levels develop as epidermis, whereas cells exposed to low Bmp levels, due to the action of antagonists, develop as neural ectoderm. In both cases, the nervous system develops on the Chordin (low-Bmp) side (called dorsal in the former and ventral in the latter). In vertebrates, a neural default circuitry underlies the decisions, in which Bmp signals repress neural development and promote epidermal development of the ectoderm, whereas elimination of Bmp by antagonists de-represses neural development and represses epidermal . Bmp absence, though necessary, may not suffice for neural development in chordates; fibroblast growth factor may have a licensing role . Likewise, different antagonists of Bmp may operate in different organisms, such as noggin and follistatin in addition to Chordin; the extracellular modulators of Bmp distribution may also vary. This segregation of ectodermal territories along the Bmp-Chordin axis in the first phase accomplishes the centralization of the nervous system in chordates and Drosophila.
In the second phase, at post-gastrula stages, Bmp serves to pattern the germ layers in Drosophila and chordates . In the vertebrate neural tube there is a new round of bmp expression in the roof plate. Hedgehog (Hh) protein and Bmp antagonists emanate from the floorplate and notochord. More than 20 gene expression domains distribute along the dorsoventral axis of the tube in relation to these signals and specify neural cell types . Sensory cells and sensory interneurons (in the dorsal part of the neural tube) arise where there is high Bmp, whereas motor neurons arise in regions of low Bmp and high Hh protein [12,13]. Similar patterning occurs in the Drosophila neurogenic ectoderm, where Bmp is opposed by antagonists and by epidermal growth factor [14,15]. In the mesoderm of chordates and Drosophila, high Bmp specifies the heart, and visceral muscle, whereas low Bmp (high antagonists) specifies striated body wall muscle . In vertebrates, Bmp levels also specify gut regions and organs of the endoderm [17,18]. The similar anatomical and physiological specializations along the Bmp-Chordin axis in both Drosophila and chordates may imply that some of them date back to the bilateral ancestor and were conserved in later divergent lineages of bilaterians. However, it is also possible that some of them evolved independently in different bilaterian lineages within the context of the pre-existing Bmp-Chordin axis. A central question would be whether the segregation of epidermis and neurogenic ectoderm, as a means of centralizing the nervous system, dates back to the bilaterian ancestor or arose independently in several lines of descendents including chordates and arthropods .
We report here the study of the origins of the dorsoventral developmental axis in Saccoglossus kowalevskii, a member of the hemichordata, a phylum of bilateral adult animals, the sister taxon to echinoderms, and closely related to chordates. These three phyla along with the recently reclassified Xenoturbella constitute the deuterostome supertaxon . We expected hemichordate embryos to utilize a Bmp-Chordin axis to pattern their dorsoventral anatomical axis, in light of the conserved use of Bmp-Chordin in dorsoventral patterning of arthropods and chordates. However, hemichordates differ from those phyla in lacking a central nervous system: theirs is diffuse throughout the ectoderm. Nerve cells and epidermal cells are finely intermixed . The epidermis is not broadly segregated from neural ectoderm, and thus seems to lack phase 1 of neural development that is characteristic of arthropods and chordates.
Yet, despite its diffuse nervous system, hemichordates have a well-developed dorsoventral polarity in all three germ layers, as if phase 2 patterning occurs. On one side (sometimes called dorsal) are localized the gill slits, stomochord, heart/kidney complex, and gonads, as shown in Figure 1. On the other (called ventral) are localized the mouth and post-anal tail . Even for the diffuse nervous system, there are dorsoventral differences in neuronal cell types. The two axon tracts on the opposite midlines differ functionally (the ventral one more associated with motor function). The dorsal tract is internalized in the collar region by a neurulation-like developmental process . Giant neurons develop near the dorsal midline, and a specialized patch of sensory neurons develops near the mouth on the ventral side at the base of the proboscis . Despite these differences, the categorical assignment of dorsal and ventral poles to the hemichordate axis is ambiguous, because the animal lives mostly in a vertical orientation and its mouth is very wide . The mouth side is nonetheless often called ventral, by convention.
The ventral side, assigned because of the mouth location, is down in this schematic figure. Anterior is to the left. Note the three parts of the body: the prosome (proboscis) at the anterior end, the narrow mesosome (collar) in the middle, and the elongated metasome to the posterior (only half the length is shown). Ectodermal derivatives are colored blue, mesodermal red, and endodermal yellow. Prominent structures of the dorsoventral axis include the dorsal and ventral axon tracts, the dorsal and ventral blood vessels, the dorsal stomochord with the heart/kidney complex, the dorsal gill slits, the ventral mouth, and the ventral tail (only in the juvenile, not shown).
Redrawn with modification from Benito and Pardos .
Overall, this organization led Nübler-Jung and Arendt  to propose that hemichordates have a dorsoventral anatomical axis the inverse of chordates and the same as protostomes such as Drosophila. Said in other words, they predicted that the hemichordate mouth falls on the Chordin side of the animal, whereas in chordates it is on the Bmp side. If true, chordates would be unique among bilateral animals in having moved the mouth to the opposite side of the body. A venerable explanation for the chordate anomaly is the inversion hypothesis: an ancestor of the chordate lineage inverted the body dorsoventrally and then moved the mouth to the other side . Although the hypothesis, as usually presented, holds that the ancestor already had a centralized nervous system on one side (ventral in the ancestor, dorsal in chordates after inversion), this is not a necessary provision of the hypothesis. Other germ layers and organs might have had dorsoventral organization at the time of body inversion, and the nervous system might have centralized later.
We have examined the topology of expression of a range of orthologs of genes in S. kowalevskii embryos that are known in vertebrates to depend on the Bmp-Chordin axis for their domain location and to have roles in dorsoventral development. We also investigated the functional importance of Bmp signaling for dorsoventral patterning by RNA interference (RNAi) knockdown and by treatment with ectopic ligand. The comparison of hemichordates to chordates affords insights about which elements of dorsoventral patterning are likely ancestral to deuterostomes and which are unique to chordates or hemichordates. S. kowalevskii indeed expresses many orthologs in a topology that would support the hypothesis of conserved roles in patterning along a Bmp-Chordin axis. Other orthologs, we find, are expressed differently, most notably those that are targets of Hh signaling in the phase 2 patterning of the chordate nervous system. Our functional studies confirm that the Bmp-Chordin axis underpins the dorsoventral anatomical axis of members of this phylum. However, the segregation of neural and epidermal territories does not seem to be a part of this patterning, and this initial phase is not required for other aspects of dorsoventral patterning. Furthermore, dorsoventral patterning seems independent of anteroposterior patterning in S. kowalevskii, an independence well known in Drosophila but not found in chordates. We discuss the evolutionary implications of our data for the evolution of bilaterians and suggest that the developmental steps involved in centralization of the nervous system (that is, the epidermal-neural segregation) were added independently in different lineages, but always utilizing an existing Bmp/Chordin axis already involved in dorsoventral patterning in the ectoderm.
Despite the difficulties of assigning definitive dorsal and ventral poles in hemichordates, we will, for descriptive purposes in this section, use the classical definition with ventral represented by the position of the mouth (Figure 1).
Bmp Signaling and the bmp Synexpression Group
The site of Bmp signaling in the embryos of chordates and arthropods defines one pole of the Bmp-Chordin developmental axis. Genes whose encoded proteins participate in Bmp signaling, such as bmps 2, 4, and 7; tolloid; twisted gastrulation (tsg), crossveinless (cv-2), and bambi [1,27,28], have been grouped in the bmp4 synexpression group, because they are expressed in the same domain . We have isolated orthologous sequences from S. kowalevskii cDNA libraries. Bmp2/4 of S. kowalevskii is the ortholog of Drosophila dpp; a related ancestral sequence was duplicated in the chordate lineage and diverged to both bmp2 and bmp4. Bmp5/8 is the S. kowalevskii ortholog of an ancestral gene that duplicated and diverged in the chordate lineage to bmps 5,6, 7, and 8 and in the Drosophila lineage to screw and glass bottom boat . Expression results are shown in Figure 2.
All embryos are cleared (see Materials and Methods) otherwise specified. All embryos have a similar orientation: anterior in the top left and dorsal in the top right of each panel, unless otherwise specified.
(A) Expression of bmp2/4 at late gastrula stage and (B) at day 3 of development.
(C) Hatched juvenile oriented with dorsal toward the viewer. White arrowhead indicates the position of the collar where the bmp2/4 expression domain follows the submerged ectodermal track of the dorsal cord.
(D) Section of a juvenile of a similar stage to (C). Dorsal is at the top of the panel. Note the submerged bmp domain, stained purple.
(E) Dorsal view of bmp5/8 expression at day 3 of development with dorsal toward the viewer, and (F) in a hatching juvenile at day 5 of development. White arrowhead indicates the submerged domain in the collar (mesosome) similar to that of bmp2/4 in panel D.
(G) Expression of bmp5/8 in the far posterior of a late juvenile at day 13 of development. White arrow indicates the position of the anus, before which the bmp5/8 domain stops. Posterior to the anus is the post anal tail.
(H) Expression of tolloid/xolloid at day 3 of development.
(I) Expression of bambi at the late gastrula stage. (J) Expression of crossveinless at the late gastrula stage and (K) at day 3 of development, with the dorsal midline oriented toward the viewer.
(L) Tsg expression at day two of development.
(M–P) Chordin expression from early to late developmental stages.
(M) Expression at mid gastrula.
(N) Sagittal section an embryo at day 2 of development just anterior to the telotroch; ventral is at the bottom of the panel.
(O) Day 3 of development, a surface view of the lateral ectoderm, (P) and day 4 of development, in sagittal section.
(Q) Admp and bmp2/4 double in situ hybridization at day 2 of development; brown is admp and blue is bmp2/4, and (R) a cross section of the same stage just anterior to the telotroch.
(S) Admp expression at day 5 of development, and (T) surface view of an uncleared embryo, ventral midline toward the viewer.
In S. kowalevskii, bmp2/4 expression begins at gastrulation in the ectoderm on one side (Figure 2A). As development proceeds, it continues in a sector and eventually narrows by day 3 to a thin stripe on the dorsal midline of the ectoderm, from the apical organ to the anus (Figure 2B and 2C). As dorsal ectoderm of the collar rolls inward on day 3 (“neurulation”), bmp expression comes to lie in the submerged ectoderm of the collar axon tract (Figure 2D). In juveniles with 2–3 gill slits (14 d post fertilization), expression continues in a tight midline reaching to the anus, but not extending into the post-anal tail (unpublished data). The expression of bmp5/8 closely resembles that of bmp2/4 (Figure 2E–2G); it eventually narrows to a stripe on the dorsal midline and is excluded from the post-anal tail (Figure 2F and 2G). Xolloid is a metalloprotease that in chordates cleaves the complex of Bmp with Chordin, releasing Bmp to bind to its receptors [31,32]. In Drosophila, the orthologous protease, Tolloid, accomplishes cleavage of the Dpp/Sog complex, to similar ends. The proteins are essential for active Bmp/Dpp signaling. In S. kowalevskii the expression of tolloid begins after gastrulation in the posterior dorsal region of the ectoderm (unpublished data). By day 2 of development, it continues on the posterior dorsal midline in the ectoderm, but anteriorly only to the boundary of the metasome and mesosome. Expression is also detected at this stage in the prospective pharyngeal endoderm, and in a small patch of posterior dorsal endoderm (Figure 2H). Bambi, which encodes an inhibitory pseudoreceptor of Bmp that is co-expressed with bmp4 in Xenopus and mouse [33,34], is similarly co-expressed in S. kowalevskii, on the dorsal midline shortly after gastrulation (Figure 2I). Low levels of expression are also detected throughout the ectoderm. In later stages, its dorsal expression declines to undetectable levels (unpublished data). Tsg, a modifier of Bmp signaling, binds to Chordin and Tolloid to agonize or antagonize Bmp signaling, depending on the presence of yet other modifiers [35–37]. In S. kowalevskii, tsg is expressed on the dorsal midline (Figure 2L) at late gastrulation, and at low levels throughout the ectoderm. Like bambi, its dorsal expression declines after day 2 of development to undetectable levels. The final member of the bmp4 synexpression group in this study is cv-2, a crossveinless ortholog. Originally cloned from Drosophila melanogaster, it is expressed in regions of high Bmp signaling in the metamorphosing wing, but not during embryonic development . In chordates it is expressed in regions of high Bmp signaling, such as the roofplate of the neural tube, and its encoded protein modulates Bmp signaling [39–41]. In S. kowalevskii, cv-2 is expressed on the dorsal midline (Figure 2J) of the embryo. Like bambi and tsg, its expression diminishes in later stages. To conclude, five members of the bmp4 synexpression group, originally identified in D. melanogaster and vertebrates, show dorsal midline domains of expression in S. kowalevskii. We thus find significant correlative evidence of Bmp signaling from this midline in hemichordates. In a later section of results, we will experimentally investigate the role of Bmp signaling in hemichordate dorsoventral patterning.
We also cloned an ortholog encoding Chordin, a Bmp antagonist, from S. kowalevskii and examined its expression in relation to the bmp domain. Expression begins in a sector of ectoderm of the early gastrula, the presumed prospective ventral side, since it is opposite the bmp2/4 domain as shown by double in situ hybridization (see thumbnail photo). At early stages, its breadth of expression extends almost to the dorsal side in the mid-level ectoderm (Figure 2M–2P), though less extensively in the anterior and posterior ectoderm. At later stages, chordin expression remains broad, strongest in the mesosome and anterior metasome, and tapering off at the telotroch (a dense ciliated band) in the posterior metasome. Anteriorly, chordin is expressed in the ectoderm of the posterior prosome, tapering off toward the tip (Figure 2O). By day 4, its expression shrinks to a small ventral patch in the anterior metasome, mesosome, and posterior prosome ectoderm (Figure 2P). This pattern of expression of chordin, centered on the ventral midline, strongly suggests that its encoded protein and Bmp on the dorsal side are involved in an antagonistic interaction, as found in other bilateral animals. In S. kowalevskii as well as Drosophila, chordin is only expressed in the ectoderm, whereas in Xenopus, it is expressed in both the ectoderm and mesoderm . In the course of development of S. kowalevskii to the hatched juvenile stages, the only domains of expression of chordin and bmp are the midline stripes described above; there are no secondary domains.
Another gene from the Bmp sub-family of transforming growth factor-beta signaling molecules, which encodes a protein with a key role in vertebrate organizer function, is anti-dorsalizing morphogenetic protein (admp). No admp ortholog has been found in Drosophila. Like Bmp2, 4, and 7, the Admp protein may bind to Chordin and be rendered inactive in signaling until the Tolloid protease releases it . Unlike the genes of other Bmps, admp appears to be co-expressed with chordin, not opposite it, and to be repressed by Bmps. According to current views, Admp acts like a Bmp signal in concert with the other Bmps, when released on their side of the embryo . We cloned the S. kowalevskii ortholog of admp from an expressed sequence tag collection. The ortholog is expressed on the ventral midline of embryonic ectoderm and also in some regions of ventral midline endoderm (Figure 2Q–2T). Expression begins in the ventral ectoderm and endoderm of the late gastrula (unpublished data). Thereafter, as the embryo elongates, ectodermal admp expression extends in a thin line from the anterior tip to the anus, interrupted only by the telotroch (Figure 2Q). It is expressed directly opposite bmp2/4 as shown in Figure 2R. At day 4, admp is still expressed along the ventral midline of the embryo; however, its level is much lower in the mesosome and anterior prosome (Figure 2S). Ventral endoderm expression of admp is most prominent in two domains; the more anterior of these in the metasome becomes more intense than the other by day 4 of development (Figure 2S). Thus, as in chordates, chordin and admp are co-expressed in hemichordates on the side opposite Bmps. Unlike chordates, the hemichordate expression is in the ectoderm and endoderm, rather than in the mesoderm. Thus like chordin expression, admp does not identify organizer-like mesoderm in hemichordates.
Dorsally Restricted Domains of Target Gene Expression
Orthologs encoding seven transcription factors exhibit dorsal domains of expression in the different germ layers, providing evidence of a dorsoventral pattern of transcriptional regulation in hemichordates, previously unreported. These genes, which include distalless (dlx), tbx2/3, olig1/2, pox neuro (poxN), pituitary homeobox (pitx), hex, and nk2.3/2.5, are candidate targets of Bmp activation. Expression results are shown in Figure 3. In a later section of Results, we provide evidence that their domains indeed expand and contract when Bmp signaling is manipulated, but first we must describe their domains in normal development.
These genes were chosen as candidate targets of Bmp activation or repression. All embryos are oriented as in Figure 2 with anterior to the top and left of each panel and dorsal in the top right of each panel, unless otherwise specified. The telotroch or ciliated band is marked by white arrowheads. Expression of dlx at (A) day 2 of development, just after gastrulation and (B) at day 3 of development.
(C) Tbx 2/3 expression just after gastrulation, and (D) at day 3 of development.
(E) Expression of hex at day 3 of development (F) Expression of nk2.3/2.5 at day 4.
(G) Expression of olig on day 2, just after gastrulation, and (H) at day 3.
(I) poxN expression at day 4 of development.
(J) Pitx expression at day 2 of development, dorsal midline toward the viewer, a glancing optical section through the dorsal-most ectoderm.
(K) Pitx expression at day 4 of development. Note the two domains of expression.
(L) Netrin expression, a transverse section of a post-gastrula embryo at the level of the ciliated band. Note the broad ventral expression of netrin, and (M) the more narrow domain at day 3 of development.
(N) Expression of lim3 at day 3 of development.
(O) Expression of mnx at day 2 of development, and (P) at day 4. Note the ventral endodermal expression.
(Q) Expression of mox (also called gax) at day 3 of development, and (R) a close up of the ventral domain at day 3, ventral midline toward the viewer, displaying the metasome and part of the mesosome.
(S) Expression of sim at day 2 of development, and (T) at day 5.
In the ectoderm, dlx is expressed in a stripe on the dorsal midline, like bmp2/4 (Figure 3A). Also, it is expressed in a uniform speckled pattern in the prosome ectoderm, as reported earlier . Its expression begins after gastrulation in a sector of ectoderm, the prospective dorsal midline (Figure 3A), and continues throughout all stages examined, closely resembling bmp2/4 expression. Like bmp2/4 and bmp5/8, its domain is submerged in the anterior mesosome, where the dorsal axon tract is internalized (unpublished data). In vertebrates, dlx paralogs have multiple developmental roles, but all share a role in patterning neural crest cells on the dorsal midline where the neural folds meet, a site of high Bmp levels [46,47].
Similar expression is found for the S. kowalevskii T-box gene, tbx2/3. In vertebrates, tbx2 and tbx3 are distinct from other T-box genes by being transcriptional repressors rather than activators . Although tbx2 is expressed in several domains during chordate development, it is expressed in neural crest cells forming the sensory dorsal root ganglia, common to all vertebrate species investigated [49,50]. Interestingly, bmp2 regulates tbx2 and tbx3 in early cardiac development in vertebrates , and in sea urchins tbx2/3 responds to Bmp signaling in the establishment of the oral/aboral axis . In Drosophila, the ortholog of tbx2/3, optomotor blind, is also regulated by Dpp during wing disk development . In S. kowalevskii, expression of tbx2/3 begins during gastrulation in a sector of the ectoderm and rapidly restricts down to a dorsal stripe, with its strongest expression posterior to the telotroch ciliated band. Its midline domain is broader than found for bmp2/4 and dlx (Figure 3C and 3D). In the anterior metasome near the first gill slit, ectodermal expression extends ventrally and encircles the embryo as a band.
Three further genes, olig, pox neuro, and pitx exhibit dorsal midline expression in sub-regions of the embryo's length. In vertebrates, olig1 and 2 are expressed in the ventral spinal cord in the region that gives rise to oligodendrocytes and motor neurons, whereas olig 3 is expressed in the dorsal cord . Bmp and sonic hedgehog (Shh) have been implicated in their activation in these regions . We see the initial expression of the olig ortholog of S. kowalevskii in a dorsal spot at the base of the prosome, in a cluster of cells (Figure 3G). Later, the expression expands to the entire proboscis ectoderm and to a dorsal midline of spots of cells along the body length (Figure 3H).
Pox neuro is a pax gene of Drosophila and other arthropods, closely related to the pax 2/5/8 group of genes and the cnidarian paxA group , but there is no clear ortholog in vertebrates. The PoxN protein plays a role in both the peripheral and central nervous systems of Drosophila and may be involved in determining neuroblast identity . We have cloned five pax genes from S. kowalevskii, two previously published in Lowe et al. . In cladograms, poxN clusters with Pax A and C of cnidarians and poxN of Drosophila; it is distinct from the pax 2/5/8 group of genes (Figure S-2H). In S. kowalevskii its expression begins on day 3, quite late in development, after the three major body divisions have been established. It is detected in isolated cells of a tight line of expression on the dorsal midline of the metasome (Figure 3I).
Pitx plays multiple roles in chordate development. Though named for its role in pituitary development , it also participates with nodal in establishing deuterostome left/right asymmetries  and in ventral posterior patterning . In S. kowalevskii, pitx is expressed in two widely separated domains. One appears at gastrulation in the posterior ventral ectoderm in a broad band of scattered cells, just anterior to the telotroch (unpublished data). In later stages, expression narrows to a stripe along the ventral midline (Figure 3K). A second domain of strong expression appears at day two of development, as the three body regions begin to resolve, at the base of the proboscis on the dorsal midline (Figure 3J). This distinct spot is approximately at the site where the proboscis pore later forms, connecting the anterior coelom to the exterior, just left of the dorsal midline. During those later stages, as the stomochord projects into the prosome directly underneath this spot, pitx expression extends into the mesoderm of the heart/kidney complex, just dorsal to the stomochord. It remains unknown whether this prosome domain has any relation to an ancestral pituitary rudiment predicted by Goodrich  to occupy this location.
Three transcription factors show dorsal domains in the endoderm. The first is an nk homeobox gene, we have named nk-2.3/2.5 that is related to Drosophila tinman, amphink-tin, and a range of nk2 class vertebrate genes that all play roles in cardiac development (see gene tree in S-4P). We have succeeded in cloning only one member of this related group of vertebrate genes, as was also reported in amphioxus , suggesting that the vertebrate nk2 class cardiac genes represent a diversification of an ancestral copy of a tinman-related gene in basal chordates. We do not detect expression of nk-2.3/2.5 until relatively late in development (day 4) in the most dorsal part of the pharyngeal endoderm, between the first pair of gill pouches as they begin to develop (Figure 3F). A similar domain of expression is detected ventrally in the floor of the developing pharyngeal endoderm of amphioxus . Tinman and related genes are best known for their conserved roles in the development of cardiac mesoderm . However at no point in development do we detect expression of nk 2.3/2.5 of S. kowalevskii in the structure classically described as the heart in the axial complex, at the tip of the stomochord . Moreover, it is not expressed in mesoderm, only dorsal midline endoderm, at the stages we have examined.
The second gene detected in the dorsal endoderm is the transcriptional repressor hex. In vertebrates it is expressed in the anterior visceral endoderm and plays an early role in blocking mesoderm induction and favoring anterior neural development; later it plays a role in the development of the liver and the thyroid [65,66]. Expression of hex in S. kowalevskii begins very early in the gastrula and shows a tight restriction to the prospective dorsal endoderm in a region of expression directly beneath the bmp2/4 stripe (unpublished data). Expression continues in the dorsal endoderm in the post-gastrula from the very posterior endoderm to the most anterior endoderm except for the mouth (Figure 3E). In later developmental stages, the expression becomes thinner and more tightly associated with the dorsal midline. The expression in the anterior is stronger than more posteriorly (unpublished data). The final gene expressed in the dorsal endoderm is pax1/9. As we reported earlier , it is expressed during the formation of the gill slits.
To conclude, we report seven new genes with dorsal domains of expression in hemichordates. These seven were not difficult to find, and we expect that many more genes exhibit such dorsoventral expression, perhaps all dependent on the Bmp-Chordin axis.
Ventrally Restricted Domains of Target Gene Expression
Orthologs encoding a signaling ligand (Netrin) and four transcription factors (Mnx, Lim3, Mox, and single-minded [Sim]) are expressed in distinct ventral domains in the three germ layers of S. kowalevskii embryos, and hence they are candidate targets of Bmp repression. To these should be added the ventral domain of pitx expression, described above. In a later section of Results, we will provide evidence that these genes are indeed Bmp targets, since their domains are expanded and contracted when Bmp signaling is manipulated, but first we must describe the normal domains.
Comparative studies of netrin show that the encoded protein plays a conserved role in axonal guidance [67,68]. In Drosophila the two netrin genes, A and B, are expressed along the ventral midline, and the proteins are signals for axon repulsion and attraction by commissural neurons in short and long range signaling . In vertebrates, an ancestral netrin gene underwent a series of duplications and diversifications to at least four netrin genes. In the central nervous system, netrin 1 is expressed in the floorplate and netrin 2 in the ventral third of the developing spinal cord and floorplate [68,70]. As in Drosophila the proteins elicit either commissural axon attraction or repulsion depending on the receptor expressed by the responding growth cone. Gene tree analysis shows that our netrin from S. kowalevskii groups with the netrin 1 and 2 classes of genes (Figure S3-K). Lower deuterostomes probably have only one gene of the netrin1/2 class . Expression of netrin 1/2 begins at late gastrulation in a small spot in the posterior ventral ectoderm (unpublished data). After gastrulation, the domain extends from just behind the telotroch forward to the anterior proboscis, though not to the apical tip region (Figure 3M). When viewed in section, the early expression is strongest at the ventral midline, diminishing laterally (Figure 3L). In mid-stage embryos (day 4), its expression is uneven along the ventral midline, forming patches with large gaps at the telotroch and in the mesosome (unpublished data). In later stages the expression narrows to a ventral midline stripe extending from the telotroch to a point midway into the proboscis (Figure 3M and unpublished data). After hatching, it becomes restricted to a very thin line on the ventral midline under the ventral axon tract, extending into the tail. This expression is consistent with Netrin's possible involvement in S. kowalevskii in attracting some axons from the general ectoderm into the ventral axon tract and perhaps repelling others into the dorsal axon tract.
The homeobox gene mnx has been implicated in the development of motor neurons in Caenorhabditis elegans, Drosophila, and chordates . It is expressed in neurogenic regions, such as the ventral-lateral neural tube of chordates, and its encoded transcription factor may play a conserved role in motor neuron development . The mnx ortholog of S. kowalevskii has an initial expression profile similar to that found in amphioxus; that is, in the endoderm of post-gastrula embryos  rather than in neurogenic ectoderm. In amphioxus, this endoderm expression is restricted dorsally, whereas in hemichordates it is restricted ventrally in posterior endoderm (Figure 3O). Two small patches of expression appear in ventral ectoderm of the metasome, just anterior to the telotroch, and in dorsal ectoderm at the prosome-mesosome boundary. In later developmental stages (day 3), the expression in the endoderm splits into two domains, an anterior one in the ventral pharynx and a posterior one in the ventral endoderm (prospective gut). Ectodermal expression is eventually detected in a ventral patch of the metasome anterior to the telotroch, and in a thin ring of expression at the prosome-mesosome boundary (Figure 3P). Although the endoderm expression of mnx in hemichordates is not understood, it should be noted that hemichordates (like echinoderms) are reported to have an endodermal nervous system .
Some overlap of mnx expression is detected with another homeobox gene implicated in motor neuron patterning, lim3 . Lim3 is expressed in the same ventral population of ectodermal cells as mnx and pitx, and no expression of it is found in endoderm (Figure 3N). It is also expressed in the developing prosome ectoderm. Whether these domains in the ectoderm are really associated with the specification of motorneurons is unknown; currently no information is available on neuronal cell type specification in this animal. However, the ventral axon tract is more associated with motor function, and the body wall musculature of the trunk is primarily ventral .
Sim is another candidate Bmp target from S. kowalevskii. Its expression is known in D. melanogaster and chordates. In Drosophila, sim is considered a “master control gene” in the development of ventral midline mesectodermal cells , with significance for dorsoventral patterning of the nervous system. In chordates it has somewhat variable expression, including in the notochord of amphioxus , the axial mesoderm, and the ventral sector of the neural tube in vertebrates [78,79]. The evidence for a conserved role of the encoded protein in Drosophila and chordates remains weak. In hemichordates, it is expressed in the ventral endoderm of the mesosome and anterior metasome back to the first gill slit and in ventral ectoderm of the same region (Figure 3S and 3T). Although it is expressed on the ventral midline, further analysis of sim in S. kowalevskii is needed before it can be ascribed a role in the establishment of this midline.
Finally, the only restricted marker of mesoderm that we have detected in this study is mox (also called gax). This gene is a member of the extended hox complex and may play a conserved role in mesoderm development throughout chordates and lophotrochozoans, though absent in ecdysozoans such as in C. elegans and Drosophila [80,81]. In vertebrates, mox is expressed only in trunk mesoderm, not head mesoderm. In S. kowalevskii, mox expression begins post gastrulation after the coeloms have pouched out of the archenteron by enterocoely. Expression is initially detected exclusively in the paired coeloms of the metasome, with no obvious dorsoventral asymmetry (unpublished data). As development continues, expression in the dorsal-most region of the metacoels is down-regulated. Ventral expression continues until only a thin line of mox expression remains in the developing metasomal mesoderm and extends forward into the mesocoels at later stages (Figure 3Q and 3R).
In summary, we have obtained seven genes with distinctive dorsal expression domains (to which the previously reported pax1/9 should be added) and five with ventral domains, all of which are candidates for activation or repression by Bmp of the Bmp-Chordin axis of hemichordates.
Mechanisms of Neural Tube Dorsoventral Patterning: Are They Conserved in Hemichordates?
Three genes were chosen for study in S. kowalevskii because of their well-known roles in dorsoventral patterning of the chordate neural tube: shh, nk2.2, and msx. Shh is released from the floorplate of the neural tube, opposite Bmp from the roofplate, and it activates a suite of genes in the ventral sectors of the neural tube , whose encoded transcription factors specify different kinds of ventral neurons. Nk2.2 is one such gene; it is activated at high Shh levels found near the floorplate . Msx on the other hand is expressed in dorsal regions of the neural tube in response to Bmp signals from the roof plate and nearby epidermis, and its encoded transcription factor specifies sensory interneurons . The relative placement of netrin, nk2.2, gsx, and msx domains in the chordate neural tube is similar to the placement of the expression domains of orthologous genes in the Drosophila nerve cord. This similarity has been taken as evidence for the homology of the centralized nerve cords of the two groups . Countering the hypothesis of homology is the evidence that many other genes are expressed differently in the two cords and that, while Shh is the counter-posed signal to Bmp in the chordate case, epidermal growth factor may have that role in arthropods.
In S. kowalevskii, we find that the expression profiles of the hh, nk2.2, and msx orthologs do not at all resemble the expression domains of vertebrates or Drosophila, as shown in Figure 4. We could isolate only one kind of hedgehog ortholog from S. kowalevskii, but this may exhaust the hemichordate repertoire since basal deuterostomes such as amphioxus and sea urchins have but one gene [86,87], whereas vertebrates have up to four paralogs of hh . The expression of hh in S. kowalevskii begins at day 2, in a small patch at the apical tip of the prosome ectoderm (Figure 4A), and it continues in the same domain throughout all stages examined (Figure 4B). Low level expression also occurs in the anterior gut (unpublished data). At no time is hh expressed in a dorsal or ventral midline domain, for example, close to the netrin ventral domain. The nk2. 2 of S. kowalevskii was cloned by low stringency hybridization. Its expression begins at gastrulation in the endoderm (Figure 4C) rather than ectoderm, as has been also found in amphioxus but not other chordates . Its domain in S. kowalevskii clearly delineates endoderm from the anterior mesendoderm that becomes the prosome mesoderm. It is continuously expressed throughout the endoderm until hatching; however, it is down-regulated in the dorsal endoderm at the site where gill slits form on day 3, and thereafter (Figure 4D). As the stomodeum (mouth) opens at day 2–3 of development, the expression of nk2.2 extends into the ectoderm in two narrow wings near the mouth, leading toward but not reaching the dorsal midline (Figure 4D). No other ectodermal domain was found during development. Just as hh is not expressed in a chordate-like dorsoventral domain, the nk2.2 gene, which in chordates depends on Hh signaling for expression, also reveals no chordate-like domain.
All embryos are shown as optical sections, and oriented in a similar manner as in Figure 2 with anterior to the top and left of each panel and dorsal in the top right of each panel, unless otherwise specified.
(A) Hh expression in the apical tip of a day 3 embryo, and (B) at day 5 at the same location.
(C) Endodermal expression of nk2–2 (also called nkx2.2) in the late gastrula, with a sharp delineation between presumptive proboscis mesoderm and definitive endoderm, and (D) at day 4, with expression continuing in the endoderm but down-regulated in the pouches of the forming gill slits (black arrowhead).
(E) Expression of msx in the late gastrula, and (F) at day 3. Expression occurs exclusively in the ectoderm of the metasome and is down-regulated in the telotroch, the cilated band, as marked (white arrowhead).
Msx was cloned from S. kowalevskii cDNA libraries by low stringency hybridization using a probe based on the msx homeodomain of Strongylocentrotus purpuratus. Expression begins during gastrulation as a circumferential ectodermal stripe in the prospective anterior metasome (Figure 4E). Its early ring-like domain resembles that of engrailed  except that the ring of the latter is interrupted on the dorsal midline. At later developmental stages, as dorsal flexure occurs, the msx domain expands posteriorly into the dorsal metasome (Figure 4F). The highest expression occurs just anterior to the telotroch ciliated band.
Of these three genes, all of which have conserved roles in dorsoventral neural patterning in chordates, none shows evidence of such a role in the hemichordate S. kowalevskii. The similar domains and specification roles of msx and nk2.2 along with gsx (which we have not yet obtained) in the central nervous systems of vertebrates and Drosophila have served as evidence of the homology, ancestry, and conservation of central nervous systems across all bilaterians. Since we find no such correspondence in S. kowalevskii; either the domains and roles were lost in the lineage leading to hemichordates (and perhaps echinoderms), or they were independently co-opted in arthropods and chordates.
Functional Effects of Bmp Signaling
To test the importance of the Bmp-Chordin axis for the development of the definitive dorsoventral axis of S. kowalevskii, we exposed embryos globally to Bmp protein, or we depleted the embryo of Bmp using RNAi. To score the effects, we used most of the 13 genes we now know to be expressed in dorsal or ventral domains in S. kowalevskii, as well as features of the overall anatomy of the treated embryos. Of particular interest is the development of the nervous system in treated embryos, which is normally diffuse throughout the ectoderm even though the embryo possesses a Bmp-Chordin axis. Embryos and expression results are shown in Figures 5 and 6, and Table 1 summarizes the results of the following two sections.
Exogenous Bmp4 protein was applied to the late blastula embryo (14 h post fertilization), and development was allowed to continue. All embryos are shown at a similar developmental stage, day 3 of development.
(A) Side view of a control embryo cultured without Bmp4. The mouth is indicated by a black arrowhead on the ventral side. The normally developing endoderm shows a dorsal, anterior projection of the gut called the stomochord, indicated with a white arrowhead. One of the mesocoels is clearly visible on the dorsal midline, indicated by a yellow arrowhead. The endoderm is divided into two sections, the pharyngeal region in the anterior, divided from the posterior gut region by a posterior constriction shown by blue arrows. The first gills slit is indicated by a green arrowhead, just anterior to the gut division.
(B) Embryos treated with 250ng/ml of Bmp 4, fixed at the same time as the control in panel A. The dorsoventral orientation is not possible to determine since they are cylindrically symmetric. Black arrowheads indicate thick condensations of mesenchyme around the anterior gut.
(C) Embryos fixed at a similar development stage following a treatment with 500 ng/ml Bmp4 displaying a consistent phenotype between samples. Note the flattened anterior end and the thick connection of prosome and mesosome.
(D) Expression of bmp2/4 following treatment with Bmp4 protein showing activation of endogenous expression throughout the ectoderm.
(E) Stereomicrographs of uncleared embryos showing the expression of chordin in control embryos, with broad ventral expression, and (F) embryos following treatment with Bmp4 protein at 100 ng/ml.
(G) Stereomicrographs of uncleared embryos showing the expression of elv in control embryos, with broad expression, but stronger at the midlines, and (H) embryos following treatment with Bmp4 protein at 100 ng/ml. Note the persistence of elv expression; it is not repressed by Bmp4.
(I) Ubiquitous ectodermal expression of dlx following treatment with 100 ng/ml of Bmp4.
(J) Expression of tbx2/3 expands throughout the ectoderm following treatment of the embryo with Bmp4 protein (250 ng/ml). White arrowheads indicate the position of the telotroch/ciliated band.
(K) Expression of pitx expands from a spot to a ring around the base of the prosome in both the ectoderm and underlying mesenchyme, after Bmp4 protein treatment.
(L) Control expression of hex at day 4 of development, and (M) following treatment with Bmp4 at 100ng/ml.
(N) Pax1/9 expression expands from a dorsolateral spot to a circumferential ring in the endoderm following Bmp4 treatment at 100 ng/ml.
(O) Like pax1/9, the nk2–3/2–5 domain expands from a short dorsal stripe to a ring in the endoderm, after Bmp4 treatment.
(P) Expression of admp in the most anterior endoderm following treatment with 500 ng/ml of Bmp4. This is a residual spot (thus showing that the staining procedure has worked), whereas the entire ventral domains of ectoderm and endoderm have disappeared.
Eggs were injected immediately following fertilization with bmp siRNA and development was allowed to continue.
(A) Low magnification micrograph of a group of embryos at the beginning of day 3 of development from injected eggs, showing the consistency of the phenotype. The dorsoventral orientation cannot be determined since the embryos are cylindrically symmetric. Note the deep indentation between the prosome and mesosome, and the short posterior end beyond the telotroch (ciliated band).
(B) Optical section of an embryo at the same stage of development from an injected egg.
(C) In the siRNA treated embryo, the expression of dlx continues in scattered cells in the anterior ectoderm of the prosome but disappears from the dorsal midline.
(D) Expression of pitx at day 4 of development in a siRNA treated embryo, showing expanded expression throughout the majority of the metasome anterior to the telotroch, whereas the prosome dorsal spot is absent. The prosome has detached from the mesosome at this stage, as the mouth indentation encircles the embryo. The same developmental stage is shown in panel E and F.
(E) Expression of admp expands strongly throughout the ectoderm of the detached prosome.
(F) Low magnification micrograph of day 4 embryos showing expansion of expression of netrin from a ventral midline stripe to the entire ectoderm including that of the detached prosome. White arrowhead shows the position of the telotroch.
Over-Expression by Exposure to Exogenous Bmp Protein
When Bmp from vertebrates was applied directly to ascidian embryos, it had the same over expression effects as injection of mRNA for Bmp . We therefore added zebrafish recombinant Bmp 4 protein to seawater at a range of concentrations to assess its effects on the development of S. kowalevskii embryos. All treatments significantly altered development (Figure 5B and 5C). From a morphological and molecular perspective, the embryos are “dorsalized,” in a dose dependent manner (unpublished data). Treated embryos are cylindrical in shape, more elongated than normal, flattened at the proboscis tip, and lacking the dorsal flexure that normally results from asymmetric tissue extension. The mouth is absent, and instead of a thin neck, the mesosome is thickly connected to the prosome. Also the first gill slits are entirely lacking, although at very low levels of Bmp exposure (10 ng/ml) a deep circumferential groove forms in the ectoderm at the position along the anteroposterior axis at which the gill slits would first perforate. The organization of the anteroposterior axis is generally unaffected.
To supplement the morphological observations, we investigated the Bmp dependence of the expression of various genes in the three germ layers. First we assayed the expression of bmp2/4 itself and found that this mRNA is elevated to detectable levels throughout the ectoderm (Figure 5D), rather than remaining localized to the dorsal midline as in control embryos (Figure 2A–2D). This expanded expression may imply an auto-activating circuitry of the Bmp synexpression group, as is known for Drosophila and vertebrates . Then we assayed five genes that, in normal embryos, are expressed on or near the dorsal midline in either the ectoderm or endoderm, as candidates for activation by Bmp. Dlx, as described earlier (Figure 3A and 3B), is expressed in the ectoderm of the entire prosome  and on the dorsal midline of the meso- and metasome. In Bmp-treated embryos, dlx expression expands into all meso- and metasomal ectoderm (Figure 5I). A similar Bmp dependence is found for tbx2/3, a gene also normally expressed on the dorsal midline (Figure 3C and 3D). In Bmp-treated embryos, tbx2/3 is expressed around the entire circumference of the embryo (Figure 5J). In the case of pitx, which has two ectodermal domains normally, the dorsal spot at the base of the proboscis expands in the presence of excess Bmp to encircle the base of the proboscis, along with underlying mesenchyme expression, as if repressed by Bmp. As further evidence of repression, chordin expression could not be detected in Bmp-treated embryos (Figures 5E and F).
Then we examined three genes normally expressed asymmetrically in the endoderm. Hex is normally expressed along the dorsal midline, with stronger expression anteriorly (Figures 3E and 5). After Bmp ligand treatment, this domain is expanded circumferentially most prominently in the anterior endoderm, but also at lower levels in posterior endoderm. Expression seems entirely down-regulated in the mid endoderm region, possibly at the level where gill slits would normally begin to develop (Figure 5M). Pax 1/9 is normally expressed as a bilateral pair of spots in the dorsolateral endoderm as the first gill slit pair forms [45,91]. In treated embryos, these spots expand to a ring of expression around the body (Figure 5N). Similar results were also found with nk2.3/2.5, normally expressed on the dorsal midline of the endoderm, including the dorsal and medial region of the first gill slit pair. Like pax1/9, nk2.3/2.5 expression expands to a ring encircling the entire endoderm (Figure 5O). As a final case, we chose admp as a candidate for Bmp repression since this gene is normally expressed only on the ventral midline of the ectoderm and endoderm. In Bmp-treated embryos, admp expression is indeed repressed, except for a residual small spot in the anterior endoderm (Figure 5P). Thus, uniform exposure of the embryo to excess Bmp protein activates the widespread expression of those genes normally expressed dorsally, and represses those normally expressed ventrally. These findings implicate dorsal midline Bmp in normal dorsoventral patterning in at least the ectoderm and endoderm.
We might expect very different effects of Bmp in specifying the nervous system of hemichordates. In Drosophila and vertebrates, Bmp represses neurogenesis, but in hemichordates there is no apparent segregation of ectoderm into neurogenic and epidermal territories. To test this, we examined the expression of elv, a pan neural gene . In control embryos, elv is expressed throughout the ectoderm with its highest levels on the dorsal and ventral midlines and in the developing proboscis ectoderm (Figure 5G). In Bmp protein-exposed embryos, the expression of elv is not down-regulated; it is similar to controls along the anteroposterior axis and is expressed at uniform high levels around the embryo's circumference (Figure 5G and 5H). Therefore, unlike insects and vertebrates, hemichordates do not have a gene regulatory circuit by which Bmp represses neural fates during early development.
Knockdown of Bmp by Small Interfering RNA
To further test the role of Bmp in dorsoventral patterning, we knocked down endogenous Bmp levels by injecting into the newly fertilized egg either a pool of small interfering RNA (siRNA) generated by the cleavage of the full-length transcript by the dicer enzyme or individual synthetic siRNAs directed against two different regions of the open reading frame of the bmp2/4 mRNA. The phenotypes of the resulting embryos are identical and highly reproducible from all three kinds of materials and between injection runs. The embryos look normal throughout early stages; however, after gastrulation they fail to extend dorsally and remain cylindrical in organization, as we might expect from ventralized embryos. Anteroposterior organization is normal, as reflected by the fact that the prosome, mesosome, and metasome are set off by anterior and posterior grooves. On day 3, when the anterior groove would normally deepen on the ventral side to form the mouth (Figure 6A and 6B), the groove indents circumferentially and severs the mesosome from the prosome, which falls off (see Figure 6D–6F). Gill slits fail to form in the metasome. The telotroch remains close to the anus, and the posterior endoderm is wider than normal (Figure 6A and 6B). Overall, the effects of the siRNA injections to produce ventralized embryos complement those of Bmp ligand treatments to produce dorsalized embryos.
Indicative of the specificity of the anti-bmp siRNAs, control eggs injected with a scrambled siRNA sequence developed normally with a dorsoventral axis (unpublished data). Furthermore, when siRNA injected embryos were then treated with Bmp protein, they undertook Bmp-dependent gene expression, indicating that the siRNAs did not cause systemic damage unrelated to Bmp.
We examined the expression of four genes that normally have ventral domains and are therefore candidates for repression by endogenous Bmp from the dorsal side. As described earlier (Figure 3L and 3M), netrin is expressed in a broad band on the ventral side at early stages and then restricts down to a thin stripe on the ventral midline. In anti-bmp siRNA injected embryos, netrin expression expands uniformly throughout the ectoderm (Figure 6F), indeed suggesting that Bmp normally represses netrin dorsally. As a second example, pitx expression is altered in the embryos from eggs injected with anti-bmp siRNAs; the posterior ventral domain of pitx expands uniformly throughout the ectoderm (Figure 6D) whereas the anterior dorsal spot of expression is absent from the detached prosome. These data on pitx from Bmp knockdown embryos complement the results from the Bmp over-expression assays and suggest strongly that Bmp normally represses the expression of pitx to a posterior ventral stripe in the metasome but activates its expression in the anterior dorsal spot on the proboscis. Third, we examined admp, which is normally expressed in a ventral stripe. In anti-bmp siRNA embryos, admp expression expands uniformly, especially in the proboscis where it becomes very intense (Figure 6E). And fourth, in anti-bmp siRNA embryos, dlx expression in the prosome ectoderm remains patchy; however, the dorsal midline expression is absent (Figure 6C). Thus, Bmp is likely required for activation of dlx on the dorsal midline but not for prosome ectoderm expression.
In summary, Bmp2/4 activates and represses specific genes in the ectoderm, mesoderm, and endoderm germ layers to give unique dorsoventral patterns of expression in the embryonic body. Differences of Bmp availability along this axis are presumably related not only to the location of a Bmp source at the dorsal midline of the embryo and a Chordin (and perhaps Admp) source at the opposite midline, but also to the interactions of Bmp with a variety of modifiers encoded by genes of the Bmp synexpression group.
The anatomical components of the dorsoventral axis of hemichordates have been recognized for decades, such as the opposed midline axon tracts, giant neurons , the heart/kidney complex , gill slits, gonads, body wall muscle, and tail [93,94]. However, the homology of these to candidate counterparts in chordates has been ambiguous, making problematic the comparisons along the dorsoventral axes of the two groups. Molecular and developmental comparisons have been impossible given the paucity of data from hemichordates. We have improved the basis for comparison by supplementing anatomical observations with molecular data. In particular, our finding of the polarized expression of bmp and chordin on the two midlines of the early embryo establishes the existence of a Bmp-Chordin axis to which we can relate the locations of various gene expression domains and anatomical specializations of the definitive dorsoventral axis of the animal. These midlines seem to be the only sites of bmp and chordin expression in the embryo and juvenile. Furthermore, we have tested the developmental importance of the Bmp-Chordin axis and have found that at least 13 candidate target genes, which normally have dorsal or ventral expression, predictably expand or contract their domains in line with Bmp availability, as do all the observable anatomical specializations. At uniform high levels of exogenous Bmp we obtain cylindrical dorsalized embryos, and in the absence of endogenous Bmp we obtain ventralized embryos. All aspects of dorsoventral organization of ectoderm and endoderm, and likely also mesoderm (for which we lack good marker genes), depend on the Bmp-Chordin axis in the S. kowalevski embryo. As concluded previously for chordates and arthropods, and now supported by the hemichordate findings, this Bmp-Chordin axis is truly a developmental axis underlying the definitive anatomical dorsoventral axis, and it may date back to the earliest bilateral animals [1,27].
Furthermore, for comparisons with chordates, the Bmp-Chordin developmental axis of hemichordates can be defined intrinsically, without reference to unreliable features such as the orientation of the animal in the gravitational field or by the location of the mouth, features which have proven hard to compare across taxa. The expression of bmp mRNA at one pole of the Bmp-Chordin axis and chordin at the other suggests that a gradient of active Bmp protein across the embryo, high at the bmp pole and low at chordin, sets the quantitative conditions for selecting and organizing target gene expression. However, many modulators are known to affect the local level of active Bmp, such as the complexes it forms with Chordin, Tsg, and perhaps Cv-2, and its release from those complexes by the Tolloid protease . The Bmp midline is also the site of expression of bambi, encoding a pseudoreceptor of Bmp which is thought to inhibit Bmp auto-activation  Furthermore, admp, which is expressed on the ventral midline, encodes a protein with Bmp-like action when released by Tolloid from its complex with Chordin, and then Admp acts through a receptor not used by Bmps . Also, Bmp antagonists exist besides Chordin, such as Noggin and DAN. Preliminary tests indicate that these are widespread in the ectoderm of S. kowalevskii, not concentrated at a midline (unpublished data). Thus, the concentration profile of active Bmp protein across the embryo may not be a monotonic gradient. Still, whatever its shape, we propose that the Bmp profile constitutes the fundamental developmental axis for the selection and placement of components of the eventual anatomical dorsoventral axis.
While the Bmp-Chordin axis is shared by chordates and hemichordates, it remains to compare what target genes and anatomical specializations are indeed selected and placed on the axis in the two groups. On the Bmp side, both groups place gill slits, coelomic mesoderm, a contractile heart-like dorsal vessel, and nk2.3/2.5 expression; on the Chordin side, both groups place the post-anal tail, the majority of striated body wall muscle and motor neurons, and netrin1 expression. These shared features, including their similar placements along the Bmp-Chordin axis, can be ascribed to the deuterostome ancestor, and some perhaps even to the bilateral ancestor. These features were just brought forward in the chordate lineage (hemichordate, too), not evolved anew within the lineage.
There are two prominent exceptions to the list of targets of the Bmp-Chordin axis shared by hemichordates and chordates, namely, the nervous system and the mouth. The hemichordate diffuse nervous system does not reveal a dorsoventral asymmetry of neurogenesis or neuron abundance; it develops throughout the ectoderm, even at the midline of bmp expression. In chordates (and Drosophila, too) the central nervous system develops near the source of Chordin, and the large epidermal territory develops near the Bmp source. In hemichordates, neurogenic and epidermal cells are finely intermixed throughout the ectoderm . In chordates and Drosophila, increased Bmp contracts the developing territory of neurogenic ectoderm, and expands the epidermal territory, whereas decreased Bmp results in the reverse effect . However, as shown here, the exposure of the hemichordate embryo to a uniform excess of exogenous Bmp protein, which up-regulates endogenous bmp gene expression around the body, does not cause the territory of neurogenesis to contract, as shown by the persistence of widespread pan-neural gene expression (Figure 5H). This insensitivity of neurogenesis to Bmp in hemichordates, despite the presence of a Bmp-Chordin axis in the embryo, implies that the “anti-neurogenic phase” of Bmp signaling is absent in hemichordates.
Nonetheless hemichordates use the Bmp-Chordin axis for a second phase, the “morphogenetic phase” for patterning the three germ layers. The patterning of neuronal cell types within the diffuse nervous system is included in the patterning, for example, the giant neurons near the dorsal midline (the Bmp pole); a nerve tract rich in motor neuron axons at the ventral midline, a specialized patch of sensory neurons near the mouth, and a line of poxN expressing cells, perhaps specialized neurons, on the posterior dorsal midline. However, chordates appear to achieve much more patterning of neuronal cell types than do hemichordates. Indeed, the entire Bmp-Hh double gradient used by chordates to select and place ten gene expression domains in the dorsoventral axis of the neural tube , is absent from hemichordates. Hh is localized to the apical ectoderm and anterior gut in hemichordates; it has no dorsoventral expression. Whereas the neural tube domains of chordates include those of pax6, dbx, en, irx, nk2.2, and msx, none of these genes shows a dorsoventral domain in S. kowalevskii (see Results here and in ). Yet all of these are expressed in the hemichordate embryo in anteroposterior domains, as they are in chordates in domains additional to the dorsoventral domains. Particularly noteworthy are the nk2.2 and msx domains since these are thought to have similar expression in Drosophila neurectoderm and the chordate neural tube . Yet they have no dorsoventral domains in S. kowalevskii. These differences suggest that much of the regulatory architecture involved in dorsoventral patterning of chordate nervous system evolved subsequent to the divergence of hemichordates and chordates. If true, the dorsoventral axis would have been a locus of much more evolution in chordates than was the anteroposterior axis since, as we showed previously , the gene expression domains of this axis are extensively similar in both groups, hence in the deuterostome ancestor.
Further analysis will be needed to determine if the neural default circuitry of the kind operating in vertebrates  is entirely absent from hemichordates. If so, the circuitry and its role in segregating neural and epidermal territories must have arisen independently in the chordate and arthropod lines, and perhaps in other lines as well . Such segregation was presumably a key evolutionary step in the centralization of the nervous system, which is a major dorsoventral innovation. Presumably, intrinsic to the evolution of a restriction of neural and epidermal fates in the different lineages was the use in all lineages of the pre-existing Bmp-Chordin axis. Alternatively, hemichordates (and perhaps echinoderms) may have lost the central nervous system of a deuterostome ancestor, rendering it diffuse and presumably simplified. However, we think this unlikely because the domain map of anteroposterior neural patterning genes of hemichordates does not seem to be reduced in complexity relative to chordates  and because the germ layers of hemichordates seem otherwise rich in dorsoventral differentiations, except for neural-epidermal segregation.
In the context of the Bmp-Chordin axis, we must last discuss the location of the mouth in hemichordates. It is on the Chordin side, as in Drosophila, but in chordates it is on the Bmp side. Chordates then, among protostomes and deuterostomes, would be the only group to have this mouth location, a conclusion reached by Nubler-Jung and Arendt  from anatomical comparisons, now reinforced by our elucidation of the Bmp-Chordin axis in hemichordates. The recent finding of left-sided expression of pitx and nodal in sea urchin larvae has been presented as evidence that echinoderms are also uninverted , although direct comparisons of larval and adult body plans are problematic. Wherever the mouth is, that side is called ventral, by convention, thereby fixing the orientation of the anatomical dorsoventral axis. The inverse relation of the axes of chordates and arthropods was furthermore recognized by the positions of heart, coelomic mesoderm, body wall muscle, and nerve cords. Thus, the dorsoventral axis of chordates is the inverse of all other bilateral animals.
A venerable explanation of the inverse relationship is the inversion hypothesis (dating back to E. Geoffroy Saint-Hilaire ) in which a chordate ancestor inverted its entire body dorsoventrally and then moved the mouth to the opposite side (or the reverse order of events). Our current studies of altering Bmp levels in development indicate that mouth development is repressed by Bmp and hence it arises at the point farthest from Bmp, in the mesosome-metasome groove. Bmp-overexposed embryos lack a mouth, and Bmp-deficient embryos form a mouth circumferentially which causes the proboscis to fall off (Figures 5 and 6). The new mouth of chordates would seem to hold a new relationship to the Bmp-Chordin axis. The classical inversion hypothesis, despite its attractions, does not require the nervous system to have been already centralized before inversion occurred, even though such centralization is usually assumed. Our data raise the possibility that centralization and inversion are separate issues (outlined in Figure 7). The ancestor, even with a diffuse system, could have inverted its body, which already had dorsoventral differences in the other germ layers, and then moved its mouth. Subsequently it could have centralized its nervous system to the Chordin side. Such a scenario works just as well, indicating that inversion can't be used to argue the existence of a central nervous system in the uninverted deuterostome or bilateral ancestor.
Mesoderm is shown in red, endoderm in yellow and ectoderm in blue (neural) and grey (epidermis). An ancestral secreted Bmp axis was involved in dorsoventral patterning of the three germ layers in the bilaterian ancestor. This ancestor we propose was characterized by a diffuse organization of its nervous system, shown by blue dots. A Bmp gradient was involved in dorsoventral patterning of all three germ layers. In the basal deuterostome and hemichordates the role of the Bmp gradient is conserved in general dorsoventral patterning. During chordate (and protostome) evolution, the existing Bmp/Chordin axis was co-opted for an additional developmental role in nervous system centralization.
However, there are other ways to achieve inversion in chordates, other than assuming a major shift in the life history mode of an ancestor. One of the ways might be termed the “ectopic chordin hypothesis.” In chordates, Chordin is produced by both endomesoderm of Spemann's organizer, and the neurogenic region of the ectodermal blastula stage, at least in Xenopus laevis  whereas in all other phyla, including hemichordates, the source of Chordin is exclusively the ectoderm. As shown here for hemichordates and elsewhere for other bilateral animals, all organs, tissues, and expression domains of the definitive dorsoventral axis depend on the Bmp-Chordin axis for their selection and placement. If this developmental axis were inverted during very early development, without moving the mouth-forming agency, all aspects of definitive dorsoventral organization would necessarily invert. In chordates, Bmp is produced “at large” in the ectoderm whereas the Chordin-Admp source is primarily localized in the chordamesoderm which arises from the archenteron/gut midline. Wherever the Chordin-Admp source is placed, this defines the Bmp-Chordin axis in chordates. Perhaps this new germ layer source, so different from ectoderm, evolved on the side opposite the mouth in a chordate ancestor, thus inverting the axis. To further these inquiries, we plan to examine the means by which the Bmp and Chordin stripes are placed opposite one another in the ectoderm of the hemichordate embryo, and the means of placement of the mouth.
Whatever the means by which the mouth and the central nervous system are produced in chordates, these studies reinforce the prominence of the Bmp-Chordin axis as a patterning mechanism in perhaps all bilaterian animals. The hemichordate S. kowalevskii seems to be an exceptional object for the study of the origin of the chordate body plan. This is in part because of the functional independence of the dorsal-ventral and anterior-posterior axes and the fact that patterning genes often appear dedicated to a single use and not used successively in new patterns. From our studies we can conclude that in the deuterostome lineage, the anteroposterior pattern, delineated by hox and other genes, may have been established very early, as a modest but significant modification of the bilaterian ancestor. In the dorsoventral dimension, the basic Bmp-Chordin axis would have been just as fundamental in the common lineage of bilaterians, but considerable modification of the subdivisions of this axis has certainly occurred in deuterostomes. The centralized nervous system of arthropods and vertebrates, so important in the previous theories of anatomical evolution of the bilateral organisms, may itself have arisen independently in both groups but built on the pre-existing Bmp-Chordin gradient. The studies in hemichordates suggest strongly that the chordate body plan emerged from the deuterostome ancestor's body plan by maintaining the anteroposterior patterning and the Bmp-Chordin gradient, but re-specifying features such as the mouth, the nervous system, and numerous details of dorsoventral patterning.
Materials and Methods
Eggs, embryos, and juveniles.
Adult S. kowalevskii were collected intertidally in September near Woods Hole, Massachusetts. Ovulation and fertilization were achieved in the laboratory by the methods of Colwin and Colwin [98,99] with several modifications . Embryos were staged by the normal tables of Bateson [100–102] and Colwin and Colwin .
Two cDNA libraries were used in this study, one from mixed blastula and gastrula stages and another from mixed gastrula and neurula stages. These were constructed as described in Lowe et al. .
Cloning of orthologs.
Three strategies were used: 1) We surveyed 60,000 arrayed expressed sequence tag clones from the two libraries. 2) We screened cDNA libraries at low stringency using short probes complementary to highly conserved regions of orthologs from other deuterostomes using standard protocols. 3) We designed degenerate primers (Codehop http://blocks.fhcrc.org/codehop.html) for PCR assay of ortholog sequences in arrayed aliquots of the cDNA libraries.
Over-expression of Bmp2/4 was achieved by addition of recombinant Zebrafish Bmp4 protein (R&D Systems, Minneapolis, Minnesota, United States) at four concentrations (10, 100, 250, and 500 ng/ml) from the blastula stage until day 4 of development. Ligand protein was replaced every 24 h of the treatment. Samples were fixed in MEMFA and stored in ethanol . For the depletion of Bmp2/4, we injected siRNA. Two different strategies were carried out: 1) Double stranded transcripts of 800 bp in length were produced which were then digested with dicer enzyme (Gene Therapy Systems, San Diego, California, United States) according to the manufacturers protocols. The stock solution for injection was 50 ng/ul in water. 2) We designed synthetic siRNAs to two regions of the bmp2/4 open reading frame. In one case, the sequences were: sense 5′-CUACGGACUCGAAGUGGAAUU-3′ and antisense 3′-UUGAUGCCUGAGCUUCACCUU-5′ which were directed to region 1057–1077 of the bmp2/4 clone. In the other case, the sequences were: sense: 5′-CUCGACCAAUCAUGCGAUAUU-3′ and antisense: 3′-UUGAGCUGGUUAGUACGCUAU-5′ which were directed to positions 1396–1416. The stock solutions for injection were 50 ng/ul in water. For injection of the siRNAs, several eggs were added to a small dish containing freshly diluted sperm for 15 s and then transferred to a silicon rubber injection chamber. A quantitative injection method with front loaded needles was used . The injections were done under an upright microscope with a 10× 0.3 NA objective lens. The 360 μm diameter egg has a volume of approximately 25 nl, and each egg was injected with 0.23 nl of siRNA solution (50 pg/nl stock or a dilution thereof), that is, less than 1% volume. The optimal period for injection was from approximately 3 min to 6 min after fertilization. At other times, the eggs usually lysed while using this injection method. Successfully injected embryos were cultured in sterile seawater in 35 mm culture dishes (coated with agarose to reduce sticking).
In situ hybridization.
This was done as described in Lowe et al. . After staining, samples were fixed overnight in Bouins fixative and then rinsed multiple times in 80% EtOH/ 0.1M TrisHCl [pH 8] until the picric acid color was gone. Samples were then further dehydrated into 100% methanol and cleared in Murray clear (benzyl benzoate: benzaldehyde, 2:1) and mounted onto slides in Permount (Fisher Scientific, Pittsburgh, Pennsylvania, United States).
Gene orthology and phylogenetic analysis.
All genes of this study were assigned orthology by phylogenetic analysis. The results are presented in Figures S1–S4. Top amino acid blast hits were aligned with additional sequences in ClustalX (http://www.embl.de/~chenna/clustal/darwin/index.html). Neighbor-joining phylogenetic analyses were carried out in PAUP* (http://paup.csit.fsu.edu) restricting the analysis to conserved domains from the alignments. 1,000 bootstrap replicates were carried out, and nodes with less than 50% support were collapsed. Bayesian analysis was carried out using Mr Bayes (v3.0B4) (http://mrbayes.csit.fsu.edu). The parameters of the analysis are as follows: 10,000,000 generations, burn in 7,500, sampling frequency 100, and four chains, under a mixed model of evolution.
Figure S1. Gene Trees for Study Genes
(A) Transforming growth factor class genes admp, bmp2/4, and bmp5/8, (B) tsg, (C) cv2, (D) tbx2/3.
(8.2 MB TIF)
Figure S2. Gene Trees for Study Genes
(E) pitx, (F) hex, (G) olig, (H) pox neuro.
(8.2 MB TIF)
Figure S3. Gene Trees for Study Genes
(I) lim3, (J) sim, (K) netrin1/2, (L) mox.
(8.2 MB TIF)
Figure S4. Gene Trees for Study Genes
(M) mnx, (N) hh, (O) msx, (P) nk2.3/2.5.
(8.2 MB TIF)
The GenBank (http://www.ncbi.nlm.nih.gov/Genbank/index.html) accession numbers for the genes and gene products discussed in this paper are admp (DQ431039), bambi (DQ431032), bmp2/4 (DQ431030), bmp5/8 (DQ431031), chordin (DQ431034), cv (DQ431033), dlx(AY318740.1), hh(DQ431035), hex (DQ431047), lim3/4 (DQ431040), mnx (DQ431042), mox (DQ431050), msx (DQ431048), netrin1/2 (DQ431045), nk2–2 (DQ431049), nk2–3/2–5 (DQ431046), olig (DQ431044), pax1/9 (DQ869011), pitx (DQ431041), pox-neuro (DQ431038), sim (DQ431043), tbx2/3 (DQ431037), tolloid (DQ431036), and tsg (DQ810291).
We thank Dr. Rindy Jaffe for valuable help and advice with microinjection, Dr. Sharon Amacher for the use of her Axiophot 2 and Axiocam for collecting in situ images, Pam Angevine (Nikon), and Rudy Rottenfusser (Carl Zeiss) for the use of microscopes and for excellent advice, and the Waquoit Bay National Estuarine Research Reserve and the staff of the Marine Biology Laboratory, Woods Hole, Massachusetts, for support during our annual September collection of embryos.
CJL, MK, and JG conceived and designed the experiments. CJL, MT, MW, LR, KK, SH, JA, MK, and JG performed the experiments. CJL, MK, and JG analyzed the data. CJL, RMF, EL, CG, and MS contributed reagents/materials/analysis tools. CJL, MK, and JG wrote the paper.
- 1. De Robertis EM, Sasai Y (1996) A common plan for dorsoventral patterning in Bilateria. Nature 380: 37–40.
- 2. Lichtneckert R, Reichert H (2005) Insights into the urbilaterian brain: Conserved genetic patterning mechanisms in insect and vertebrate brain development. Heredity 94: 465–477.
- 3. Gerhart J, Lowe C, Kirschner M (2005) Hemichordates and the origin of chordates. Curr Opin Genet Dev 15: 461–467.
- 4. Finnerty JR, Pang K, Burton P, Paulson D, Martindale MQ (2004) Origins of bilateral symmetry: Hox and dpp expression in a sea anemone. Science 304: 1335–1337.
- 5. Martindale MQ, Finnerty JR, Henry JQ (2002) The Radiata and the evolutionary origins of the bilaterian body plan. Mol Phylogenet Evol 24: 358–365.
- 6. Ferguson EL (1996) Conservation of dorsal-ventral patterning in arthropods and chordates. Curr Opin Genet Dev 6: 424–431.
- 7. Dorfman R, Shilo BZ (2001) Biphasic activation of the BMP pathway patterns the Drosophila embryonic dorsal region. Development 128: 965–972.
- 8. De Robertis EM, Kuroda H (2004) Dorsal-ventral patterning and neural induction in Xenopus embryos. Annu Rev Cell Dev Biol 20: 285–308.
- 9. Delaune E, Lemaire P, Kodjabachian L (2005) Neural induction in Xenopus requires early FGF signalling in addition to BMP inhibition. Development 132: 299–310.
- 10. Rusten TE, Cantera R, Kafatos FC, Barrio R (2002) The role of TGF beta signaling in the formation of the dorsal nervous system is conserved between Drosophila and chordates. Development 129: 3575–3584.
- 11. Jessell TM (2000) Neuronal specification in the spinal cord: Inductive signals and transcriptional codes. Nat Rev Genet 1: 20–29.
- 12. Timmer JR, Wang C, Niswander L (2002) BMP signaling patterns the dorsal and intermediate neural tube via regulation of homeobox and helix-loop-helix transcription factors. Development 129: 2459–2472.
- 13. Liem KF Jr., Tremml G, Roelink H, Jessell TM (1995) Dorsal differentiation of neural plate cells induced by BMP-mediated signals from epidermal ectoderm. Cell 82: 969–979.
- 14. Skeath JB (1998) The Drosophila EGF receptor controls the formation and specification of neuroblasts along the dorsal-ventral axis of the Drosophila embryo. Development 125: 3301–3312.
- 15. von Ohlen T, Doe CQ (2000) Convergence of dorsal, DPP, and EGFR signaling pathways subdivides the Drosophila neuroectoderm into three dorsal-ventral columns. Dev Biol 224: 362–372.
- 16. Kishimoto Y, Lee KH, Zon L, Hammerschmidt M, Schulte-Merker S (1997) The molecular nature of zebrafish swirl: BMP2 function is essential during early dorsoventral patterning. Development 124: 4457–4466.
- 17. Bachiller D, Klingensmith J, Shneyder N, Tran U, Anderson R, et al. (2003) The role of chordin/Bmp signals in mammalian pharyngeal development and DiGeorge syndrome. Development 130: 3567–3578.
- 18. Rossi JM, Dunn NR, Hogan BL, Zaret KS (2001) Distinct mesodermal signals, including BMPs from the septum transversum mesenchyme, are required in combination for hepatogenesis from the endoderm. Genes Dev 15: 1998–2009.
- 19. Holland ND (2003) Early central nervous system evolution: An era of skin brains? Nat Rev Neurosci 4: 617–627.
- 20. Bourlat SJ, Nielsen C, Lockyer AE, Littlewood DT, Telford MJ (2003) Xenoturbella is a deuterostome that eats molluscs. Nature 424: 925–928.
- 21. Bullock TH, Horridge GA (1965) Structure and function in the nervous systems of invertebrates. San Francisco: W. H. Freeman. 919 p.
- 22. Hyman LH (1940) The invertebrates. New York: McGraw-Hill. 572 p.
- 23. Morgan T (1894) Development of Balanoglossus. J Morphol 9: 1–86.
- 24. Brusca RC, Brusca GJ (1990) Invertebrates. Sunderland (Massachusetts): Sinauer Associates. 922 p.
- 25. Nubler-Jung K, Arendt D (1996) Enteropneusts and chordate evolution. Curr Biol 6: 352–353.
- 26. Geoffroy St.-Hilaire E (1822) Considérations générales sur les vertebrés. Mem HIst Nat 9: 89–119.
- 27. Arendt D, Nubler-Jung K (1994) Inversion of dorsoventral axis? Nature 371: 26.
- 28. Karaulanov E, Knochel W, Niehrs C (2004) Transcriptional regulation of BMP4 synexpression in transgenic Xenopus. Embo J 23: 844–856.
- 29. Niehrs C, Pollet N (1999) Synexpression groups in eukaryotes. Nature 402: 483–487.
- 30. Martin AP (2000) Choosing among alternative trees of multigene families. Mol Phylogenet Evol 16: 430–439.
- 31. Marques G, Musacchio M, Shimell MJ, Wunnenberg-Stapleton K, Cho KW, et al. (1997) Production of a DPP activity gradient in the early Drosophila embryo through the opposing actions of the SOG and TLD proteins. Cell 91: 417–426.
- 32. Blader P, Rastegar S, Fischer N, Strahle U (1997) Cleavage of the BMP-4 antagonist chordin by zebrafish tolloid. Science 278: 1937–1940.
- 33. Onichtchouk D, Chen YG, Dosch R, Gawantka V, Delius H, et al. (1999) Silencing of TGF-beta signalling by the pseudoreceptor BAMBI. Nature 401: 480–485.
- 34. Grotewold L, Plum M, Dildrop R, Peters T, Ruther U (2001) Bambi is co-expressed with Bmp-4 during mouse embryogenesis. Mech Dev 100: 327–330.
- 35. Chang C, Holtzman DA, Chau S, Chickering T, Woolf EA, et al. (2001) Twisted gastrulation can function as a BMP antagonist. Nature 410: 483–487.
- 36. Oelgeschlager M, Larrain J, Geissert D, De Robertis EM (2000) The evolutionarily conserved BMP-binding protein Twisted gastrulation promotes BMP signalling. Nature 405: 757–763.
- 37. Ross JJ, Shimmi O, Vilmos P, Petryk A, Kim H, et al. (2001) Twisted gastrulation is a conserved extracellular BMP antagonist. Nature 410: 479–483.
- 38. Conley CA, Silburn R, Singer MA, Ralston A, Rohwer-Nutter D, et al. (2000) Crossveinless 2 contains cysteine-rich domains and is required for high levels of BMP-like activity during the formation of the cross veins in Drosophila. Development 127: 3947–3959.
- 39. Coffinier C, Ketpura N, Tran U, Geissert D, De Robertis EM (2002) Mouse Crossveinless-2 is the vertebrate homolog of a Drosophila extracellular regulator of BMP signaling. Mech Dev 119 Suppl 1: S179–S184.
- 40. Binnerts ME, Wen X, Cante-Barrett K, Bright J, Chen HT, et al. (2004) Human Crossveinless-2 is a novel inhibitor of bone morphogenetic proteins. Biochem Biophys Res Commun 315: 272–280.
- 41. Rentzsch F, Zhang J, Kramer C, Sebald W, Hammerschmidt M (2006) Crossveinless 2 is an essential positive feedback regulator of BMP signaling during zebrafish gastrulation. Development 133: 801–811.
- 42. Kuroda H, Wessely O, De Robertis EM (2004) Neural induction in Xenopus: requirement for ectodermal and endomesodermal signals via Chordin, Noggin, beta-Catenin, and Cerberus. PLoS Biol 2: e92.. DOI: 10.1371/journal.pbio.0020092.
- 43. Lele Z, Nowak M, Hammerschmidt M (2001) Zebrafish ADMP is required to restrict the size of the organizer and to promote posterior and ventral development. Dev Dyn 222: 681–687.
- 44. Reversade B, De Robertis EM (2005) Regulation of ADMP and BMP2/4/7 at opposite embryonic poles generates a self-regulating morphogenetic field. Cell 123: 1147–1160.
- 45. Lowe CJ, Wu M, Salic A, Evans L, Lander E, et al. (2003) Anteroposterior patterning in hemichordates and the origins of the chordate nervous system. Cell 113: 853–865.
- 46. Merlo GR, Zerega B, Paleari L, Trombino S, Mantero S, et al. (2000) Multiple functions of Dlx genes. Int J Dev Biol 44: 619–626.
- 47. Wada H (2001) Origin and evolution of the neural crest: A hypothetical reconstruction of its evolutionary history. Dev Growth Differ 43: 509–520.
- 48. Carreira S, Dexter TJ, Yavuzer U, Easty DJ, Goding CR (1998) Brachyury-related transcription factor Tbx2 and repression of the melanocyte-specific TRP-1 promoter. Mol Cell Biol 18: 5099–5108.
- 49. Hayata T, Kuroda H, Eisaki A, Asashima M (1999) Expression of Xenopus T-box transcription factor, tbx2 in Xenopus embryo. Dev Genes Evol 209: 625–628.
- 50. Takabatake Y, Takabatake T, Takeshima K (2000) Conserved and divergent expression of T-box genes Tbx2-Tbx5 in Xenopus. Mech Dev 91: 433–437.
- 51. Yamada M, Revelli JP, Eichele G, Barron M, Schwartz RJ (2000) Expression of chick Tbx-2, Tbx-3, and Tbx-5 genes during early heart development: Evidence for BMP2 induction of Tbx2. Dev Biol 228: 95–105.
- 52. Gross JM, Peterson RE, Wu SY, McClay DR (2003) LvTbx2/3: A T-box family transcription factor involved in formation of the oral/aboral axis of the sea urchin embryo. Development 130: 1989–1999.
- 53. Grimm S, Pflugfelder GO (1996) Control of the gene optomotor-blind in Drosophila wing development by decapentaplegic and wingless. Science 271: 1601–1604.
- 54. Filippi A, Tiso N, Deflorian G, Zecchin E, Bortolussi M, et al. (2005) The basic helix-loop-helix olig3 establishes the neural plate boundary of the trunk and is necessary for development of the dorsal spinal cord. Proc Natl Acad Sci U S A 102: 4377–4382.
- 55. Lu QR, Yuk D, Alberta JA, Zhu Z, Pawlitzky I, et al. (2000) Sonic hedgehog–regulated oligodendrocyte lineage genes encoding bHLH proteins in the mammalian central nervous system. Neuron 25: 317–329.
- 56. Sun H, Rodin A, Zhou Y, Dickinson DP, Harper DE, et al. (1997) Evolution of paired domains: Isolation and sequencing of jellyfish and hydra Pax genes related to Pax-5 and Pax-6. Proc Natl Acad Sci U S A 94: 5156–5161.
- 57. Dambly-Chaudiere C, Jamet E, Burri M, Bopp D, Basler K, et al. (1992) The paired box gene pox neuro: A determinant of poly-innervated sense organs in Drosophila. Cell 69: 159–172.
- 58. Christiaen L, Burighel P, Smith WC, Vernier P, Bourrat F, et al. (2002) Pitx genes in Tunicates provide new molecular insight into the evolutionary origin of pituitary. Gene 287: 107–113.
- 59. Duboc V, Rottinger E, Lapraz F, Besnardeau L, Lepage T (2005) Left-right asymmetry in the sea urchin embryo is regulated by nodal signaling on the right side. Dev Cell 9: 147–158.
- 60. Shapiro MD, Marks ME, Peichel CL, Blackman BK, Nereng KS, et al. (2004) Genetic and developmental basis of evolutionary pelvic reduction in threespine sticklebacks. Nature 428: 717–723.
- 61. Goodrich ES (1917) "Proboscis pores” in craniate vertebrates, a suggestion concerning the premandibular somites and hypophysis. Quart J Microscop Sci 62: 539–553.
- 62. Holland ND, Venkatesh TV, Holland LZ, Jacobs DK, Bodmer R (2003) AmphiNk2-tin, an amphioxus homeobox gene expressed in myocardial progenitors: Insights into evolution of the vertebrate heart. Dev Biol 255: 128–137.
- 63. Ranganayakulu G, Elliott DA, Harvey RP, Olson EN (1998) Divergent roles for NK-2 class homeobox genes in cardiogenesis in flies and mice. Development 125: 3037–3048.
- 64. Balser E, Ruppert E (1990) Structure, ultrastructure, and function of the preoral heart-kidney in Saccoglossus kowalevskii (Hemichchordata, Enteropneusta) including new data on the stomochord. Acta Zoologica 71: 235–249.
- 65. Brickman JM, Jones CM, Clements M, Smith JC, Beddington RS (2000) Hex is a transcriptional repressor that contributes to anterior identity and suppresses Spemann organiser function. Development 127: 2303–2315.
- 66. Martinez Barbera JP, Clements M, Thomas P, Rodriguez T, Meloy D, et al. (2000) The homeobox gene Hex is required in definitive endodermal tissues for normal forebrain, liver, and thyroid formation. Development 127: 2433–2445.
- 67. Harris R, Sabatelli LM, Seeger MA (1996) Guidance cues at the Drosophila CNS midline: Identification and characterization of two Drosophila Netrin/UNC-6 homologs. Neuron 17: 217–228.
- 68. Kennedy TE, Serafini T, de la Torre JR, Tessier-Lavigne M (1994) Netrins are diffusible chemotropic factors for commissural axons in the embryonic spinal cord. Cell 78: 425–435.
- 69. Keleman K, Dickson BJ (2001) Short- and long-range repulsion by the Drosophila Unc5 netrin receptor. Neuron 32: 605–617.
- 70. Serafini T, Colamarino SA, Leonardo ED, Wang H, Beddington R, et al. (1996) Netrin-1 is required for commissural axon guidance in the developing vertebrate nervous system. Cell 87: 1001–1014.
- 71. Shimeld S (2000) An amphioxus netrin gene is expressed in midline structures during embryonic and larval development. Dev Genes Evol 210: 337–344.
- 72. Arber S, Han B, Mendelsohn M, Smith M, Jessell TM, et al. (1999) Requirement for the homeobox gene Hb9 in the consolidation of motor neuron identity. Neuron 23: 659–674.
- 73. Ferrier DE, Brooke NM, Panopoulou G, Holland PW (2001) The Mnx homeobox gene class defined by HB9, MNR2 and amphioxus AmphiMnx. Dev Genes Evol 211: 103–107.
- 74. William CM, Tanabe Y, Jessell TM (2003) Regulation of motor neuron subtype identity by repressor activity of Mnx class homeodomain proteins. Development 130: 1523–1536.
- 75. Cameron CB, Mackie GO (1996) Conduction pathways in the nervous system of Saccoglossus sp. (Enteropneusta). Canadian J Zool 74: 15–19.
- 76. Nambu JR, Lewis JO, Wharton KA Jr., Crews ST (1991) The Drosophila single-minded gene encodes a helix-loop-helix protein that acts as a master regulator of CNS midline development. Cell 67: 1157–1167.
- 77. Mazet F, Shimeld SM (2002) The evolution of chordate neural segmentation. Dev Biol 251: 258–270.
- 78. Coumailleau P, Penrad-Mobayed M, Lecomte C, Bollerot K, Simon F, et al. (2000) Characterization and developmental expression of Sim, a Xenopus bHLH/PAS gene related to the Drosophila neurogenic master gene single-minded. Mech Dev 99: 163–166.
- 79. Moffett P, Dayo M, Reece M, McCormick MK, Pelletier J (1996) Characterization of msim, a murine homologue of the Drosophila sim transcription factor. Genomics 35: 144–155.
- 80. Hinman VF, Degnan BM (2002) Mox homeobox expression in muscle lineage of the gastropod Haliotis asinina: Evidence for a conserved role in bilaterian myogenesis. Dev Genes Evol 212: 141–144.
- 81. Minguillon C, Garcia-Fernandez J (2002) The single amphioxus Mox gene: Insights into the functional evolution of Mox genes, somites, and the asymmetry of amphioxus somitogenesis. Dev Biol 246: 455–465.
- 82. Roelink H, Augsburger A, Heemskerk J, Korzh V, Norlin S, et al. (1994) Floor plate and motor neuron induction by shh-1, a vertebrate homolog of hedgehog expressed by the notochord. Cell 76: 761–775.
- 83. Briscoe J, Ericson J (2001) Specification of neuronal fates in the ventral neural tube. Curr Opin Neurobiol 11: 43–49.
- 84. Liu Y, Helms AW, Johnson JE (2004) Distinct activities of Msx1 and Msx3 in dorsal neural tube development. Development 131: 1017–1028.
- 85. Cornell RA, Ohlen TV (2000) Vnd/nkx, ind/gsh, and msh/msx: Conserved regulators of dorsoventral neural patterning? Curr Opin Neurobiol 10: 63–71.
- 86. Shimeld SM (1999) The evolution of the hedgehog gene family in chordates: insights from amphioxus hedgehog. Dev Genes Evol 209: 40–47.
- 87. Hara Y, Katow H (2005) Exclusive expression of hedgehog in small micromere descendants during early embryogenesis in the sea urchin, Hemicentrotus pulcherrimus. Gene Expr Patterns 5: 503–510.
- 88. Holland LZ, Venkatesh TV, Gorlin A, Bodmer R, Holland ND (1998) Characterization and developmental expression of AmphiNk2–2, an NK2 class homeobox gene from Amphioxus. (Phylum Chordata; Subphylum Cephalochordata). Dev Genes Evol 208: 100–105.
- 89. Darras S, Nishida H (2001) The BMP/CHORDIN antagonism controls sensory pigment cell specification and differentiation in the ascidian embryo. Dev Biol 236: 271–288.
- 90. Biehs B, Francois V, Bier E (1996) The Drosophila short gastrulation gene prevents Dpp from autoactivating and suppressing neurogenesis in the neuroectoderm. Genes Dev 10: 2922–2934.
- 91. Lowe CJ, Tagawa K, Humphreys T, Kirschner M, Gerhart J (2004) Hemichordate embryos: Procurement, culture, and basic methods. Methods Cell Biol 74: 171–194.
- 92. Bullock TH (1945) The anatomical organization of the nervous system of enteropneusta. Quart J Microscrop Sci 86: 55–112.
- 93. Bateson W (1886) The ancestry of the chordata. Quart J Microscrop Sci 26: 535–571.
- 94. Hyman LH (1955) The invertebrates. New York: McGraw-Hill. 572 p.
- 95. Ashe HL, Levine M (1999) Local inhibition and long-range enhancement of DPP signal transduction by Sog. Nature 398: 427–431.
- 96. Echelard Y, Epstein DJ, St-Jacques B, Shen L, Mohler J, et al. (1993) Sonic hedgehog, a member of a family of putative signaling molecules, is implicated in the regulation of CNS polarity. Cell 75: 1417–1430.
- 97. Hemmati-Brivanlou A, Melton D (1997) Vertebrate embryonic cells will become nerve cells unless told otherwise. Cell 88: 13–17.
- 98. Colwin AL, Colwin LH (1950) The developmental capacities of separated early blastomeres of an enteropneust, Saccoglossus kowalevskii. J Experimental Zool 115: 263–296.
- 99. Colwin AL, Colwin LH (1962) Induction of spawning in Saccoglossus kowalevskii (Enteropneusta) at Woods Hole. Biological Bulletin 123: 493.
- 100. Bateson W (1884) Early stages in the development of Balanoglossus (sp. incert.). Quart J Microscrop Sci 24: 208–236.
- 101. Bateson W (1885) Later stages in the development of Balanoglossus kowalevskii with a suggestion as to the affinities of the Enteropneusta. Quart J Microscrop Sci 25: 81–128.
- 102. Bateson W (1886) Continued account of the later stages in the development of Balanoglossus kowalevskii, with a suggestion as to the affinities of the enteropneusta. Quart J Microscrop Sci 26: 511–534.
- 103. Colwin AL, Colwin LH (1953) The normal embryology of Saccoglossus kowalevskii. J Morphol 92: 401–453.
- 104. Jaffe LA, Terasaki M (2004) Quantitative microinjection of oocytes, eggs, and embryos. Methods Cell Biol 74: 219–242.
- 105. Benito J, Pardos F (1997) Hemichordata. In: Harrison FW, Ruppert EE, editors. Microscopic anatomy of invertebrates. New York: Wiley-Liss. pp. 15–101. pp.