Developmental Mechanism of Limb Field Specification along the Anterior–Posterior Axis during Vertebrate Evolution

Abstract

In gnathostomes, limb buds arise from the lateral plate mesoderm at discrete positions along the body axis. Specification of these limb-forming fields can be subdivided into several steps. The lateral plate mesoderm is regionalized into the anterior lateral plate mesoderm (ALPM; cardiac mesoderm) and the posterior lateral plate mesoderm (PLPM). Subsequently, Hox genes appear in a nested fashion in the PLPM and provide positional information along the body axis. The lateral plate mesoderm then splits into the somatic and splanchnic layers. In the somatic layer of the PLPM, the expression of limb initiation genes appears in the limb-forming region, leading to limb bud initiation. Furthermore, past and current work in limbless amphioxus and lampreys suggests that evolutionary changes in developmental programs occurred during the acquisition of paired fins during vertebrate evolution. This review presents these recent advances and discusses the mechanisms of limb field specification during development and evolution, with a focus on the role of Hox genes in this process.

1. Introduction

Paleontological evidence suggests that acquisition of the first pairs of fin-like structures occurred in the lineage of ancestral agnathans (jawless vertebrates; Figure 1a) [1,2]. The cephalochordate amphioxus and the agnathan lampreys are thought to have diverged prior to the acquisition of paired fins (Figure 1a) [3], and thus these animals could be good models for developmental comparisons to gain insights into the evolutionary sequence that lead to the acquisition of the limb-forming fields in the lateral plate mesoderm.

In gnathostomes (jawed vertebrates), limb buds appear as small bulges protruding from the body trunk at a specific position along the body axis during the development of gnathostome embryos. Specification of limb fields, which is tightly correlated with the initiation of limb bud formation, involves multiple steps [4]. The lateral plate mesoderm is regionalized into the anterior lateral plate mesoderm (ALPM; cardiac mesoderm) and the posterior lateral plate mesoderm (PLPM), which includes the presumptive limb-forming fields [5,6]. Retinoic acid signaling seems to play pivotal roles in this process [5,6]. In the PLPM, Hox genes are expressed in a nested fashion along the anterior–posterior axis and appear to be involved in the regionalization of the PLPM into forelimb, interlimb flank and hindlimb fields [7,8]. Then, the lateral plate mesoderm thickens and splits into the somatic and splanchnic layers sequentially from the anterior to posterior region of the embryos (Figure 1b) [9]. Subsequently, expression of limb initiation genes appears in the presumptive limb-forming fields [10]. Initiation of limb buds needs to occur at a precise position along the body axis, although little has been known until recently about the molecular mechanism linking limb positioning and initiation. Analyses of chick and mouse embryos, however, revealed that the Hox proteins that define the axial position of the limb-forming fields directly activate the transcription of the forelimb initiation gene, Tbx5 [11,12]. Furthermore, developmental analyses of limbless amphioxus and lampreys have provided evidence for the sequential events that occurred during the acquisition of limb-forming fields in the body of vertebrates during evolution [4]. This review highlights these recent advances and discusses the mechanisms of limb field specification during development and during vertebrate evolution, with a special focus on the function of Hox genes.

2. Regionalization of the Lateral Plate Mesoderm into the ALPM and the PLPM: Retinoic Acid and Hox Genes

During the development of gnathostome embryos, the lateral plate mesoderm is regionalized into the ALPM and the PLPM, including the presumptive limb-forming fields [5,6]. Recent developmental studies on zebrafish and mouse embryos suggested that such a regionalization of the lateral plate mesoderm is necessary to provide an environment permissive for forelimb-forming fields and that retinoic acid signaling has pivotal roles in this process [5,6]. In zebrafish, mutants for retinaldehyde dehydrogenase 2 (raldh2) lack pectoral fin buds (forelimb buds) [13,14], and embryos treated with retinoic acid inhibitor show the posterior expansion of the heart field and fail to initiate formation of pectoral fin buds [5]. During this process, retinoic acid signaling induces the expression of hoxb5b within the forelimb fields [5]. As hoxb5b restricts the number of atrial cells, it also restricts the posterior extension of the heart field to determine the anterior boundary of forelimb-forming fields, although its function is dispensable for forelimb formation [5]. Chick and mouse Hoxb5 orthologs have been implicated as direct targets of retinoic acid signaling [15,16,17]. Moreover, in mouse Hoxb5 mutants, the shoulder girdles shift their position, although morphological abnormalities of the heart have not been reported [18]. Thus, it is suggested that Hoxb5 mutants might have subtle cardiac defects, or be lethal, or other mouse Hox genes might have roles similar to those of zebrafish hoxb5b [5]. Multiple Hox genes are expressed in the heart fields of mouse and chick embryos [19,20]. However, heart phenotypes associated with the genetic inactivation of Hox genes have rarely been observed, which is probably due to the functional redundancy of paralogous Hox genes [21]. One notable exception is mouse Hoxa3 null mutants, which exhibit heart defects, including hypertrophy of the atria and the enlargement of the chief veins [22]. Heart phenotypes seen in Hoxa3 mutants, thus, have been implicated as a possible outcome of the expansion of the heart field [5].

Numerous studies on retinoic acid signaling in relation to the anterior-posterior patterning of the heart suggested roles for Hox genes in this process [21,23]. Treatment with retinoic acid enhances the expression of Hoxa4, Hoxd3 and Hoxb5 in chicken cardiogenic tissue [20]. In addition, Hoxb1, Hoxa1 and Hoxa3, downstream targets of retinoic acid signaling, define the distinct progenitor sub-domains of the secondary heart field in mouse embryos [24]. Furthermore, retinoic acid signaling is correlated with limb initiation and positioning in zebrafish, chick and mouse embryos [5,6,25,26]. Chick embryos treated with disulfiram, an inhibitor of retinoic acid synthesis, show hypoplasia, or a positional shift of the forelimb bud [25]. In mouse Raldh2 mutants, heart-forming fields expanded posteriorly, and forelimb initiation fails [6], as seen in zebrafish raldh2 mutants [5]. Thus, retinoic acid signaling seems to have a role in the regionalization of the lateral plate mesoderm into the ALPM and the PLPM [6,26,27]. In addition, in the pharyngeal endoderm and mesoderm of Raldh2 mouse mutants, Hoxa1 and Hoxb1 transcript levels are reduced [27], suggesting that the role of retinoic acid signaling in regionalizing the lateral plate mesoderm via regulation of Hox genes is conserved in mouse embryos.

An alternative model for the function of retinoic acid signaling in the regionalization process of the lateral plate mesoderm along the anterior–posterior axis has been proposed by Duester’s group. They suggested that retinoic acid signaling delimits the cardiac and epiblast Fgf8-positive domains, and provides a permissive environment for the induction of forelimb (but not hindlimb) development [6]. Chromatin immunoprecipitation analysis revealed that all three retinoic acid receptor (RAR) isoforms indeed bind to the retinoic acid responsive elements near the Fgf8 promoter, suggesting that retinoic acid signaling directly represses Fgf8 expression [28]. Interestingly, transgenic zebrafish embryos expressing ectopic Fibroblast growth factor (Fgf) signaling show expansion of the heart field and failure of initiation of pectoral fin development [29]. These results seem to support the view that FGF signaling is involved in the regionalization of the lateral plate mesoderm and provides a permissive environment for forelimb induction [6].

During embryonic development, regionalization of the lateral plate mesoderm into the ALPM and the PLPM provides a permissive environment for forelimb induction. Therefore, regionalization of the lateral plate mesoderm might have been a crucial step for acquisition of the limb-forming field during the evolution of vertebrates. In vertebrates, the heart is located at the anterior end of the body trunk, whereas the primitive heart of amphioxus—consisting of peristaltic blood vessels—is located at the posterior-ventral part of the body [30]. Recently, the distribution of the ALPM and the PLPM has been examined in amphioxus embryos by using molecular markers (Figure 2) [4]. In amphioxus, AmphiHand, an ortholog of Hand1 and Hand2, which are expressed throughout the lateral plate mesoderm of zebrafish, chick and mouse embryos [31,32,33], is expressed throughout the ventral mesoderm (Figure 2) [4]. Interestingly, in amphioxus, both AmphiNkx2-tin and AmphiTbx20—orthologues of Nkx2.5 and Tbx20, which are expressed in the cardiac mesoderm [32,34,35,36]—are also expressed throughout the ventral mesoderm. These results suggest that the amphioxus ventral mesoderm is not molecularly regionalized into cardiac versus posterior ventral mesoderm (Figure 2) [4]. In the limbless agnathan lamprey, Lethenteron japonicum Tbx20 (LjTbx20) is expressed in the anterior part of the lateral plate mesoderm [37], whereas LjMyb, an orthologue of c-myb that is expressed in the PLPM, is expressed in mesodermal cells posterior to the LjTbx20-positive area (Figure 2) [4]. These results suggest that the lateral plate mesoderm of lamprey, a limbless agnathan, is regionalized into the ALPM and the PLPM as seen in gnathostomes (Figure 2) [4].

In lampreys, expression of LjTbx1/10, an ortholog of Tbx1 and Tbx10 that is a marker of pharyngeal mesoderm [39], is restricted to the pharyngeal mesoderm [40]. Importantly, expression of AmphiTbx1/10 is also restricted to the pharyngeal ventral mesoderm [41], suggesting that the ventral mesoderm of amphioxus is indeed regionalized into the pharyngeal ventral mesoderm and ventral mesoderm caudal to the pharynx (Figure 2) [4]. Therefore, it seems that the system to regionalize the ventral mesoderm along the anterior–posterior axis was already established in the cephalochordate lineage, although the ventral mesoderm was not yet separated into the cardiac and posterior ventral mesoderm [4].

Previous studies suggest that retinoic acid signaling is involved in the patterning of various organs along the anterior–posterior axis both in amphioxus and lampreys [42,43,44,45,46,47]. RARs have been identified in amphioxus [42] and lampreys [43]. Furthermore, treatments with excess retinoic acid or retinoic acid inhibitors affect the anterior–posterior patterning of amphioxus and lampreys [42,43,44,45,46,47]. Interestingly, lamprey embryos treated with retinoic acid fail to form a heart [47], supporting the view that retinoic acid has retained its importance for the regionalization of the lateral plate mesoderm into the ALPM and the PLPM during evolution (Figure 3) [4]. Therefore, it is likely that retinoic acid signaling and its roles in the anterior–posterior patterning were present in the common ancestor of vertebrates and amphioxus. However, a recent study on amphioxus embryos revealed that the function of retinoic acid signaling in anterior–posterior patterning of somites in amphioxus might not be the same as in vertebrates [48]. Bertrand et al. showed that retinoic acid signaling has critical roles in somitogenesis in amphioxus; however, it does not antagonize Fgf signaling. Therefore, the anterior–posterior patterning system controlled by mutual inhibition between retinoic acid and Fgfs during somitogenesis might have been acquired after the divergence of amphioxus and ancestral vertebrates [48]. Zhao et al. proposed that, during mouse embryogenesis, antagonism between retinoic acid and Fgf8 provides the permissive environment for the forelimb-forming field in the PLPM [6]. Thus, we should consider the possibility that alteration of the distribution of retinoic acid in the lateral plate mesoderm and/or acquisition of a novel antagonistic function of retinoic acids and Fgfs might have been critical for subdividing the lateral plate mesoderm into the ALPM and the PLPM during vertebrate evolution (Figure 3).

In gnathostomes, several lines of evidence indicate that retinoic acid signaling regulates the transcription of Hox genes and leads to the regionalization of the lateral plate mesoderm along the anterior–posterior axis [5,21,23,27]. However, transcripts of Hox genes have not yet been observed in the segmented mesoderm (the progenitor of the ventral mesoderm) of amphioxus (Figure 3) [51,52]. In amphioxus, retinoic acid signaling regulates the expression of Hox genes in anterior–posterior patterning of the endoderm, central nervous system and ectoderm at the neurula stage [45,53,54]. In addition, retinoic acid signaling directly regulates expression of Hox genes to pattern the anterior–posterior axis during gastrulation [55], suggesting that the regulatory mechanism of Hox gene transcription by retinoic acid signaling has already been established in the common ancestors of amphioxus and ancestral vertebrates. As the nested expression of Hox genes has been observed in the PLPM of both lamprey and gnathostome embryos [4,7], the acquisition of the novel expression domain for Hox genes in the lateral plate mesoderm—possibly via alteration of distribution of retinoic acid and/or the acquisition of a novel function of retinoic acid signaling—seems to be required for the regionalization of the lateral plate mesoderm into the ALPM and the PLPM (Figure 3).

In lamprey embryos, Hox genes are indeed expressed in a nested fashion in the PLPM [4], although limb formation is not initiated in this region (Figure 3). In gnathostomes, subsequent to the regionalization of the lateral plate mesoderm into the ALPM and the PLPM, the lateral plate mesodermal cells proliferate and are subdivided into the somatic and splanchnic layers beginning from the anterior toward the posterior part of the body (Figure 1b) [9]. Limb buds then appear as protrusions of the somatic layers in the PLPM. In contrast, in lampreys, the lateral plate mesoderm is subdivided into the somatic and splanchnic layers in the ALPM, but not in the PLPM (Figure 2) [4]. Thus, it is possible that lampreys cannot form limb buds because the underdeveloped PLPM does not split into the somatic and splanchnic layers [4]. Until recently, subdivision of the PLPM had not been observed during embryogenesis of any teleost fishes. However, a recent histological analysis of pufferfish (Takifugu niphobles) embryos at a very early stage (eight-somite stage) revealed that the lateral plate mesoderm is indeed subdivided into somatic and splanchnic layers both in the ALPM and the PLPM [56]. Importantly, cells from the PLPM of lampreys contribute to the formation of peritoneal epithelium and blood cells, but not the body wall [4,57]. Therefore, it is likely that the proliferation and differentiation of the PLPM, as well as formation of the coelom cavity, might have been a crucial step in acquiring paired appendages during the evolution of vertebrates [4,57]. In gnathostomes, Forkhead box F (FoxF) is expressed throughout the PLPM prior to the separation; subsequent to the subdivision, FoxF transcripts are restricted to the splanchnic mesoderm and Iroquis homeobox 3 (Irx3) expression appears in the somatic mesoderm [9]. In lampreys, LjIrx1/3 is expressed in the somatic layers of the ALPM, but not in the PLPM, although LjFoxF is expressed throughout the PLPM [4] (Figure 2). Furthermore, in amphioxus, AmphiFoxF is expressed from the pharynx to the posterior end of the body trunk [4], and Branchiostoma floridae IrxC (BfIrxC) is expressed in the ventral mesoderm at the level of the pharynx, but not in the ventral mesoderm posterior to the pharynx (Figure 2) [58]. Therefore, it is likely that the common ancestor of amphioxus and ancestral vertebrates had the FoxF-positive lateral plate mesoderm, and Irx3-positive somatic mesoderm seems to have appeared at the cardiac level after the divergence of ancestral chordates and vertebrates. The FoxF-positive unseparated PLPM seems to have been acquired prior to the lamprey lineages. The Irx3-positive somatic layers seem to have appeared in the PLPM after the divergence of lampreys and vertebrates [4], and provided permissive environment needed for emergence of fin-forming fields during evolution.

3. Specification of Limb-Forming Fields: Tbx4, Tbx5 and Hox Genes

In gnathostomes, the lateral plate mesoderm is divided into the ALPM and the PLPM, and Hox genes seem to be involved in this process [5]. Although regionalization of the PLPM along the anterior–posterior axis by Hox genes has not been studied as extensively as in the nervous system or in somites, it has been proposed that expression patterns of Hox genes in the lateral plate mesoderm are somehow related to the specification of limb-forming fields [7]. Furthermore, the positioning of the forelimb buds at approximately the anterior border of the expression domains of Hox5 and Hox6 in the lateral plate mesoderm is conserved among zebrafish, chick and mouse [5,59,60,61]. Recently, it was shown that Hox proteins are involved in the regulation of the transcription of T-box transcription factor 5 (Tbx5) (Figure 3) [11,12,49]. Tbx5 is expressed in the anterior paired appendages of zebrafish, chick and mouse embryos [62,63,64] and initiates forelimb development [12,65,66,67,68,69]. In humans, mutations in TBX5 cause Holt–Oram syndrome (OMIM 142900), an autosomal-dominant disorder characterized by abnormalities of the upper limbs and cardiac defects [70,71]. Zebrafish with mutations in pbx4, which encodes a Hox protein co-factor, fail to induce tbx5 expression or initiate formation of pectoral fin buds [72]. In addition, developmental and molecular analyses of chick and mouse embryos revealed that rostral Hox genes expressed in the lateral plate mesoderm directly regulate the expression of Tbx5 and thereby control the axial position of forelimb-forming fields (Figure 3) [11].

Recent analyses of mouse mutants showed that Hox5 and Hox9 genes are involved in establishing the anterior and posterior domains of the forelimb, respectively [73,74]. Loss of function of all three Hox5 genes leads to anterior forelimb defects resulting from derepression of Shh expression [73]. In the anterior forelimbs, Hox5 proteins interact with promyelocytic leukemia zinc finger (Plzf) and cooperatively mediate repression of Shh expression [73]. In contrast, an analysis of a Hox9 quadruple knockout revealed that axial Hox9 paralogs establish the posterior field of forelimbs by triggering the posteriorly restricted expression of Hand2, which directly activates Shh at the posterior margin [74].

In chick and zebrafish, Wnt/β-catenin signaling has key roles in the initiation of limb formation [67,75]. In chick embryos, Wnt2b is expressed in the intermediate mesoderm and the lateral plate mesoderm in the presumptive forelimb-forming region, whereas Wnt8c is expressed in the presumptive hindlimb-forming region [75], and the implantation of Wnt2b- or Wnt8c-expressing cells into the interlimb flank region leads to the formation of an additional limb via induction of ectopic Fgf10 expression [75]. Consistent with this result, zebrafish embryos injected with wnt2b morpholinos show downregulation of tbx5 expression and fail to form pectoral fin buds [67]. In mouse embryos, however, Wnt ligands that act upstream of Fgf10 in the limb-forming field have not yet been found. Furthermore, double knockout mice for both Lef1 and Tcf1, which mediate Wnt signaling by forming a complex with β-catenin, form normal limb buds [76]. However, a recent study in mice showed that conditional removal of β-catenin from forelimb-forming regions leads to the reduction of Tbx5 expression and incomplete forelimbs, suggesting that the function of β-catenin to regulate Tbx5 transcription is conserved among zebrafish, chick and mouse [50]. The T-cell factor/lymphoid enhancer factor (TCF/LEF) binding sequence is required for the enhancer activity of the forelimb-specific Tbx5 regulatory element, suggesting that β-catenin directly regulates Tbx5 expression [50]. Furthermore, retinoic acid signaling directly activates transcription of Tbx5 in the forelimb-forming fields (Figure 3) [50]. Taken together, retinoic acid signaling, β-catenin/LEF/TCF and anteriorly nested Hox proteins seem to cooperatively activate Tbx5 transcription for inducing forelimb bud formation [50].

It has also been shown that caudally expressed Hox proteins, such as Hoxc8, Hoxc9 and Hoxc10, can form a repressive complex and bind to the forelimb-specific regulatory sequences of Tbx5 and repress its expression [49]. Interestingly, in chick embryos, transplantation of an Fgf-soaked bead into the interlimb flank region turns off Hoxc9 expression when an ectopic wing bud is induced, whereas it turns on Hoxc9 expression when an ectopic leg bud is induced [7]. Thus, these previous findings seem to support the view that Hoxc9 acts as a repressor of Tbx5 transcription [49]. In addition, rostrally expanded Hoxc8 distribution is present in the body trunk of a limbless vertebrate, the python [77], supporting the view that Hoxc8 represses Tbx5 expression [49].

Molecular mechanisms that specify the hindlimb-forming fields are not as well characterized as those of the forelimb-forming fields. Tbx4, which is closely related to Tbx5, is specifically expressed in the presumptive hindlimb forming fields of chick, mouse, teleosts and catshark (Scyliorhinus canicula) [62,63,64,78,79], and its expression is suggested to be regulated by Hox genes [12] and Pitx1 [12,80]. In addition, studies on transgenic mice, in which Tbx5 is replaced by Tbx4, revealed that Tbx4 is able to substitute for Tbx5 function in the initiation of the forelimb bud [12], suggesting that Tbx4 has a similar role in the initiation of hindlimb formation. However, unlike Tbx5 null mutants, mice deficient for Tbx4 are able to initiate Fgf10 expression in hindlimb fields and form truncated hindlimbs [81]. Additional studies in mice deficient for Tbx4 revealed that Tbx4 is crucial for initiating hindlimb outgrowth, but an additional factor(s) other than Tbx4 is likely to be involved in this process [82]. Islet1, a LIM-homeodomain transcription factor that is specifically expressed in the hindlimb progenitors, was recently shown to be required for hindlimb initiation [83,84]. Early inactivation of Islet1 as well as β-catenin in the lateral plate mesoderm leads to a failure to initiate hindlimb development [84]. Furthermore, Islet1 is required for the nuclear accumulation of β-catenin and thereby for activation of the β-catenin pathway, and that the β-catenin pathway is required for the maintenance of Islet1 expression [84]. Islet1 seems to be a missing piece in the regulation of hindlimb-specific initiation [84].

Pitx1, which encodes a member of the paired-like family of homeodomain transcription factors, is expressed in the presumptive hindlimb-forming fields in chick, mouse, stickleback (Gasterosteus aculeatus) and catshark embryos [79,85,86,87]. In mice, Pitx1 is required for normal initiation of hindlimb development by regulating transcription levels of Tbx4 [85,88,89]. It has recently been suggested that in Liebenberg syndrome (OMIM 186550) [90], an autosomal-dominant malformation of the upper limbs, the upper limbs have undergone a partial homeotic hindlimb transformation, and that this phenotype is associated with genomic rearrangements at the PITX1 locus [91].

In teleosts, the roles of tbx4 and pitx1 in pelvic fin formation seem to be more critical than their roles in the hindlimb formation of amniotes. In tbx4 mutant zebrafish, expression of fgf10 is not induced, and thus pelvic fin buds fail to initiate their formation at a very early stage of fin initiation [92]. In the spine-deficient morph of the three-spined sticklebacks, expressions of neither pitx1 nor tbx4 are detected in the lateral plate mesoderm at the level of the pelvic fin, and pelvic fin buds fail to initiate their formation [87]. Subsequently, the responsible regulatory sequence for pelvic spine deficiency was found within the pelvic fin-specific enhancer of pitx1 in three-spined stickleback [93,94]. In teleosts, pelvic fin formation is significantly delayed as it is triggered by thyroid hormone at the time of the larva-juvenile transition [95] (for instance, three weeks post–fertilization in zebrafish). Thus, the levels of molecules that affect the limb initiation process in the pelvic fin-forming region of teleosts at the time of pelvic fin initiation are not identical to those in the presumptive hindlimb-forming region of early chick and mouse embryos. Although we cannot exclude the possibility that the functions of Pitx1 and/or Tbx4 in the initiation of pelvic fin/hindlimb development in teleosts are different from those in mice, it is possible that the Pitx1-Tbx4 pathway is sufficient to activate the initiation of pelvic fin outgrowth in teleost fishes.

A shift in limb position is also observed in chick and mouse embryos in which expression of Gdf11 has been manipulated [96,97]. Mutant mice carrying a targeted deletion of Gdf11 exhibit posterior displacement of the hindlimbs, and patterns of expression of Hoxc6, Hoxc10 and Hoxc11 in spinal cord and paraxial mesoderm also shift posteriorly [96]. In chick embryos, overexpression of Gdf11 in the spinal cord leads to the rostral shift of both fore- and hindlimb [97]. In the spinal cord of chicks that overexpress Gdf11, expression of Hoxc6, Hoxc8, Hoxc9 and Hoxc10 shift rostrally and lead to the rostral shift of the lateral motor columns [97], which are defined by Hox6 and Hox10 [98,99,100]. Thus, the shift in limb buds in chick following the introduction of Gdf11-expressing constructs into the spinal cord was interpreted to be caused by a shift in the lateral motor columns [97]. Gdf11 expression in the caudal part of the body is conserved in chick, mouse, zebrafish and Nile tilapia embryos [101,102,103]. Furthermore, in zebrafish injected with gdf11 morpholinos, the pelvic fin shifts caudally, along with a posterior shift in Hoxc10 expression in the spinal cord [103], suggesting that the Gdf11-controlled mechanism that positions the hindlimb along the body axis is likely to be conserved in gnathostomes [103,104]. Gdf11 signaling is a central modulator of the trunk-to-tail transition during mouse development [105]. In Gdf11 mutants, the specification of the cloaca and the induction of the hindlimbs are significantly delayed, whereas precocious activation of Gdf11 signaling in the epiblast anteriorizes these structures with a concomitant reduction in trunk length [105]. In contrast, precocious activation of genes of the Hox9, Hox10 and Hox11 groups in the epiblast do not alter the phenotype, with one exception: transgenic mice expressing Hoxb9 show only a slight anterior displacement of the hindlimbs by one somite [105]. Thus, Jurberg and his colleagues proposed that Hox genes do not play a major role in specifying the hindlimb position along the anterior–posterior axis during the trunk-to-tail transition [105]. In early stages of hindlimb induction, Islet1 has a major role in establishing the posterior hindlimb field by regulating the Hand2-Shh pathway [84,106]. During the trunk-to-tail transition, Gdf11 directly activates Islet1 to promote formation of the most posterior progenitors of the lateral plate mesoderm, such as the hindlimbs and cloacal tissue [105].

It has been suggested that the nested Hox gene expression in the lateral plate mesoderm is necessary for acquiring the first pair of appendages during the evolution of vertebrates [107]. In limbless amphioxus species Branchiostoma floridae and Branchiostoma lanceolatum, Tbx4/5 is expressed throughout the ventral mesoderm (Figure 3) [108,109]. Interestingly, amphioxus Tbx4/5 has the ability to initiate forelimb formation in mouse transgenic lines [110]. This apparent contradiction can be explained by the regionalization of the ventral mesoderm and expression of Hox genes mentioned above. In amphioxus, the ventral mesoderm is not molecularly regionalized into the cardiac and posterior ventral mesoderm [4], and Hox genes are not expressed in the ventral mesoderm progenitors [51,52], suggesting that Tbx4/5 in the ventral mesoderm may contribute only to heart formation in amphioxus [4]. In lampreys, the lateral plate mesoderm is regionalized into the ALPM and the PLPM, and LjHox5i and LjHox6w are expressed in the PLPM in a nested fashion [4]. Nevertheless, lamprey LjTbx4/5 transcripts are not present in the PLPM but are in the ALPM [4,37]. Although we do not know whether lamprey Hox genes have the conserved function of inducing Tbx4/5 in the PLPM, one of the main reasons for limblessness seems to be the lack of separation of the PLPM into the somatic and splanchnic layers (Figure 3), which results in the contribution of cells from the PLPM to the peritoneal epithelium but not to the body wall [4,57].

4. Conclusions

In gnathostomes, the lateral plate mesoderm is regionalized into the ALPM and PLPM, and Hox genes are expressed in a nested fashion along the anterior–posterior axis in the PLPM. Then, the lateral plate mesoderm splits into the somatic and splanchnic layers, and the expression of limb initiation genes appears in the limb-forming fields. Figure 4 summarizes the genes implicated in the specification of limb-forming fields in the PLPM during mouse development. Tbx5 and Tbx4 are expressed in the forelimb- and hindlimb-forming fields, respectively [63,64], and play crucial roles in the initiation of limb outgrowth [12,65,66,67,68,69]. In the forelimb-forming field, retinoic acid signaling and β-catenin signaling act cooperatively with rostrally expressed Hox genes to directly regulate Tbx5 expression [11,50], whereas caudally expressed Hox genes repress Tbx5 to restrict its expression to this field [49]. In the hindlimb-forming field, Tbx4 expression, which is crucial for the induction of hindlimb development, is suggested to be activated by Hox genes [12] and Pitx1 [12,85]. Islet1-mediated activation of β-catenin signaling is also required for hindlimb induction [84]. In the early forelimb field, Hox9 paralogous genes are required for the expression of Hand2 to establish the posterior domain [74], whereas Hox5 genes and Plzf cooperatively mediate repression of Shh expression in the anterior domain [73]. In contrast, the hindlimb posterior domain is established by Islet1 to regulate Hand2 expression in this region [106].

Developmental analyses of limbless amphioxus and lampreys have provided clues to understand the evolutionary scenarios that led to the acquisition of limb-forming fields in the vertebrate body [4]. In amphioxus, the ventral mesoderm is not molecularly regionalized into cardiac versus posterior ventral mesoderm. In lamprey, the lateral plate mesoderm is regionalized into the ALPM and the PLPM, and Hox genes are expressed in a nested fashion in the PLPM [4], but the PLPM is not separated into the somatic and splanchnic layers [4]. These past and current findings suggest that, to acquire the limb-forming fields, novel expression domains of limb initiation genes in the lateral plate mesoderm, regionalization along its anterior–posterior axis, and its subdivision into somatic and splanchnic layers were likely to be required during vertebrate evolution.