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FoxB, a new and highly conserved key factor in arthropod dorsal–ventral (DV) limb patterning


Forkhead box (Fox) transcription factors evolved early in animal evolution and represent important components of conserved gene regulatory networks (GRNs) during animal development. Most of the researches concerning Fox genes, however, are on vertebrates and only a relatively low number of studies investigate Fox gene function in invertebrates. In addition to this shortcoming, the focus of attention is often restricted to a few well-characterized Fox genes such as FoxA (forkhead), FoxC (crocodile) and FoxQ2. Although arthropods represent the largest and most diverse animal group, most other Fox genes have not been investigated in detail, not even in the arthropod model species Drosophila melanogaster. In a general gene expression pattern screen for panarthropod Fox genes including the red flour beetle Tribolium castaneum, the pill millipede Glomeris marginata, the common house spider Parasteatoda tepidariorum, and the velvet worm Euperipatoides kanangrensis, we identified a Fox gene with a highly conserved expression pattern along the ventral ectoderm of arthropod and onychophoran limbs. Functional investigation of FoxB in Parasteatoda reveals a hitherto unrecognized important function of FoxB upstream of wingless (wg) and decapentaplegic (dpp) in the GRN orchestrating dorsal–ventral limb patterning.


Arthropod limbs develop along three different axes, the proximal–distal (PD) axis, the anterior–posterior (AP) axis, and the dorsal–ventral (DV) axis. In the model system Drosophila melanogaster, leg allocation and AP axis determination is under control of segment polarity genes such as wingless (wg) and hedgehog (hh) (e.g. [1, 2]). This is likely conserved in arthropods and onychophorans as indicated by gene expression and functional data (e.g., [3,4,5,6,7,8,9,10]). The PD axis is established by the function of the so-called limb gap genes and the morphogens Wg and Decapentaplegic (Dpp) (e.g., [1, 11,12,13]), and gene expression data suggest that the function of limb gap genes is generally conserved among arthropods and onychophorans (e.g., [3, 10, 14,15,16,17,18,19]). In Drosophila, the morphogens Dpp and Wg are also involved in the determination of the DV axis [20,21,22]. The wg gene is expressed in the ventral region of the leg imaginal discs and loss of Wg protein causes dorsalisation of these limbs [22,23,24]. Downstream of Wg act two T-box genes, the paralogs H15 and midline (mid), both of which are like wg expressed in ventral ectodermal cells of the limbs [4, 20, 25,26,27]. dpp is expressed along the dorsal side of the Drosophila leg imaginal disc and loss of Dpp causes ventralization of these limbs [28, 29]. Downstream of Dpp functions another T-box gene, optomotor-blind (omb), which is expressed along the dorsal side of the legs [20, 29]. Expression of omb can induce dorsal fate in ventral cells of the developing legs [29]. Comparative gene expression data suggest that the role of ventral and dorsal leg patterning genes is conserved in arthropods, and partially also in onychophorans (e.g., [10, 26, 30,31,32]). However, functional evidence of a conserved DV patterning system in arthropods is sparse and exclusively based on data in insects [33, 7, 9, 25, 34]. While wg appears to be involved in DV limb development in holometabolous insects [7, 9], this does not appear to be the case for hemimetabolous insects [33].

Notably, many of the genes involved in DV limb patterning are duplicated in Drosophila, as well as in other studied arthropods and onychophorans. There are two H15-type genes in Drosophila and the millipede Glomeris marginata, and at least three H15 genes in spiders, and two copies of omb in onychophorans and spiders (summarized in [32]). Many of these genes have retained conserved expression patterns along the ventral and dorsal region of the developing limbs, respectively. Therefore, it is likely that their function(s) in DV patterning are at least partially conserved as well. This makes functional studies difficult because of likely redundant functions of such paralogs. Although wg is not duplicated in arthropods and onychophorans [6, 35, 36], it is a member of the Wnt class of genes (wg is Wnt1) of which arthropods ancestrally possess 12 classes (reviewed in [36, 37]). Many Wnt genes, although not paralogs of wg/Wnt1, are expressed in very similar patterns along the ventral side of the developing arthropod limbs (e.g., [38, 36]). It is therefore possible that other Wnt genes may substitute for wg function, and that functional data on the role of wg in arthropod limb development are inconclusive and potentially misleading (cf. [7, 9, 33]).

Here we report on the discovery of a hitherto unrecognized gene that is expressed along the ventral side of the investigated arthropods and an onychophoran, the forkhead transcription factor-encoding gene FoxB (Drosophila paralogs Dmfd4/Dmfd5 aka fd96Ca/fd96Cb [39, 40]. Although it exists in two copies (paralogs) in the model arthropods Drosophila and the flour beetle Tribolium castaneum, there is only one copy in the spider Parasteatoda tepidariorum. We therefore targeted the spider FoxB gene (Pt-FoxB) in our study and investigated its function in appendage development. Among other phenotypes, Pt-FoxB knockdown leads to altered leg morphologies, likely correlated with disturbed DV patterning during limb development. The expression of other known (or implied by conserved expression patterns) DV limb patterning genes such as omb, H15, and wg/Wnt1 is disturbed in Pt-FoxB knockdown appendages. This indicates a high-ranking function of FoxB in the gene regulatory network orchestrating DV limb patterning in spiders as well as Panarthropoda as a whole.


Research animals, embryo collection and developmental staging

Drosophila flies and embryos were obtained from the cultures in Göttingen (Oregon-R strain). Tribolium embryos were obtained from the cultures in Göttingen (San Bernardino strain). Glomeris embryos were collected and prepared as described in Janssen et al. [7]. Parasteatoda spiders were obtained from the established Göttingen strain for RNA-interference experiments. They were kept separately in plastic vials at approximately 21 °C. They were supplied with water and fed with either sub-adult crickets (Acheta domesticus) or Drosophila. Euperipatoides kanangrensis embryos were obtained as described in Hogvall et al. [41]. Developmental staging is after Janssen et al. [8] (Glomeris), Janssen and Budd [42] (Euperipatoides), Mittmann and Wolff [43] (Parasteatoda), and Strobl and Stelzer [44] (Tribolium).

Gene cloning, probe synthesis, whole mount in situ hybridization and nuclear staining

All gene fragments were isolated by means of RT-PCR with gene-specific primers based on sequence information from either sequenced genomes (Tribolium, Tribolium Genome Sequencing Consortium [45] and Parasteatoda, Schwager et al. [46]), or sequenced embryonic transcriptomes (Glomeris and Euperipatoides). Primer sequences are listed in Additional file 1: Table S1. Genes were cloned into either the PCRII vector (Invitrogen) or the PCR4-TOPO vector (Invitrogen). Sequences of the cloned fragments were verified by means of Big Dye chemistry on an ABI3730XL sequence analyser by a commercial sequencing service (Macrogen, Seoul, South Korea). Accession numbers of all gene fragments are listed in Additional file 2: Table S2.

Antisense RNA probes were in vitro transcribed with either Sp6, T7 or T3 RNA Polymerase (Roche) after amplification of the gene products from the plasmids using M13F and M13R oligonucleotides (Additional file 1: Table S1). Embryos of Tribolium were fixed as described in Schinko et al. [47]. Embryos of Parasteatoda were fixed as described in Pechmann et al. [48], or, after RNAi treatment, were fixed in a formaldehyde–heptane mix (1:15) for 4 h. Thereafter, the vitelline membranes were removed with Dumont-5 forceps. There is no significant difference in the result of in situ hybridization with either of the spider fixation protocols. Embryos of Glomeris were fixed in the same way as spider embryos after RNAi treatment. Embryos of Euperipatoides were fixed in a 1:15 formaldehyde-PBS mix for 4–6 h; membranes were removed with Dumont-5 forceps prior to fixation. For all single-colour stainings in all embryos, we applied the whole mount in situ hybridization protocol as described in Janssen et al. [49]. Double in situ hybridization was performed as described in Janssen et al. [50] with the exception that BM Purple (blue signal) (Roche) and SIGMAFAST Fast Red TR/Naphthol AS-MX (red signal) (SIGMA) were used for probe detection. Cell nuclei were visualized incubating embryos in 2 μg/ml of the fluorescent dye 4-6-diamidino-2-phenylindole (DAPI) in phosphate-buffered saline with 0.1% Tween-20 (PBST) for 20–30 min.

dsRNA synthesis and parental RNAi

After amplification from the plasmid using T7 and T7-Sp6 overhang primers (Additional file 1: Table S1), double-stranded RNA (dsRNA) for Pt-FoxB was synthesized using the MEGAscript T7 Kit (Life technologies). Sodium acetate was used for precipitation and RNA was dissolved in injection buffer (1.4 mM NaCl, 0.07 mM Na2HPO4, 0.03 mM KH2PO4, 4.0 mM KCL). Female spiders were injected laterally into the opisthosoma and either mated several hours prior to injection, or several hours after the first injection. We performed two independent rounds of injection that differed in the concentration of injected dsRNA. Each spider was injected three times (on 3 consecutive days) with each time 2.5 µl of 2.8 µg/µl dsRNA (first round of injections) or 4 µg/µl dsRNA (second round of injections) in injection buffer. Control spiders were injected with 2.5 μl of injection buffer. Altogether, 20 adult females were injected with Pt-FoxB dsRNA and 20 females with buffer only. Of all surviving spiders, cocoons of dsRNA-injected spiders were kept in glass vials separately. All dsRNA-injected and all control cocoons, respectively, were pooled and investigated each as one batch (see Additional file 3: Figure S1 for quantification). Embryos with morphologically distinguishable phenotypes were categorized into four distinct classes of which one, Class-I, is of particular interest for this study (see “Results”).

Phylogenetic analysis

Amino acid sequences of the FoxA, FoxB and FoxC forkhead domains of Parasteatoda, Glomeris, Tribolium, Euperipatoides and Drosophila were aligned using ClustalX with default parameters in MacVector v12.6.0 (MacVector, Inc., Cary, NC). In our analysis, the forkhead domain of Drosophila FoxQ2 serves as an outgroup sequence.

Bayesian phylogenetic analysis was performed with MrBayes [51] using a fixed WAG amino acid substitution model with gamma-distributed rate variation across sites (with four rate categories). Unconstrained exponential prior probability distribution on branch lengths and an exponential prior for the gamma shape parameter for among-site rate variation were applied. Topologies were estimated using 0.5 million generations for the Metropolis-coupled Markov chain Monte Carlo analysis with four chains. The chain-heating temperature was set to 0.2, and the chains were sampled every 200 cycles. 25% of samples were used as burnin. Clade support values were computed with posterior probabilities in MrBayes. See Additional file 4: Figure S2.

Imaging and image processing

All pictures were taken with a Leica DFC490 digital camera mounted on a Leica dissection microscope (MZ-FLIII). The image processing software Adobe PHOTOSHOP CC 2015 (v. 1.0 for Apple Macintosh) was used for the application of linear corrections of contrast and brightness.


Expression of panarthropod FoxB genes in developing appendages

The embryonic expression of Drosophila FoxB orthologs [i.e., Dmfd4/Dmfd5 (aka fd96Ca/fd96Cb)] has been described before [52]. However, in their paper, Häcker et al. [52] only describe embryonic expression patterns, and since appendages develop from imaginal discs in Drosophila, expression in the developing limbs remains unclear. We therefore investigated expression in the imaginal discs of third instar larvae. We found that both FoxB orthologs are expressed in identical, albeit weaker for FoxB2, patterns in the leg discs and in the antennal discs, but not in the haltere discs, the wing discs, or the eye discs (Fig. 1a–c and Additional file 5: Figure S3). Expression in the leg and antennal discs is restricted to ventral tissue. In both structures, this region of expression is interrupted by a small, most ventral zone of lower (or no) expression.

Fig. 1

Expression of FoxB genes in the developing limbs in Drosophila melanogaster (a–c dissected imaginal discs), Tribolium castaneum (d, e flat mounted embryos; anterior to the left; ventral view. e Inlay shows dissected legs), Glomeris marginata (fi dissected limbs; anterior view), and Euperipatoides kanangrensis (jl whole mount embryos; anterior to the left; j lateral view; k, l ventral view). Note that expression is always in the ventral sector of the ventral appendages, except for the arthropod labrum where expression is dorsal. Dorsal appendages, i.e., the wings and halteres in Drosophila do not express FoxB. Asterisks (*) mark dorsal tissue in ventral appendages. Arrows in b, c point to weaker (or no) expression in the very ventral region of the leg disc and the antennal disc. ad antennal disc, an antenna, ed eye disc, fap frontal appendage, hd haltere disc, hl head lobe, j jaw, L1/8 first and eighth walking limb, lb labium, ld leg disc, lr labrum, md mandible, mx maxilla, sp slime papilla, T1 first thorax segment, v/d ventral and dorsal side of leg, v ventral view on leg, wd wing disc

In all three sequentially segmenting arthropods investigated here, i.e., Tribolium, Glomeris and Parasteatoda, FoxB genes are expressed in the ventral sector of the developing appendages, except for the labrum where expression is dorsal (and thus in line with the rotation theory [53]) (Figs. 1d–i, 2, 3l and Additional file 6: Figure S4; Additional file 7: Figure S5; Additional file 8: Figure S6). At later developmental stages, expression in the walking limbs refines into a pattern of transverse ventral stripes of stronger expression that likely correspond to the beginning podomerisation (leg segmentation) (Figs. 1e, i and 3). This is most obvious in Parasteatoda with its relatively long legs and pedipalps (Fig. 3e–k).

Fig. 2

Expression of Parasteatoda tepidariorum FoxB. In all panels, anterior is to the left representing ventral views, except b, f, and u (lateral views). Dotted lines in ad mark borders of the embryo proper. The asterisk in c marks a first stripe of enhanced expression. Arrows in h, k and m point to expression in the ventral nervous system. Embryos of the same stage (er, t, u) represent different views on the same embryo. ch chelicera, cu cumulus, L1–L4 first to fourth walking leg, O2–O5 second to fifth opisthosomal segment, pp pedipalp, s stomodaeum, saz segment addition zone

Fig. 3

Expression of Parasteatoda tepidariorum FoxB and odd-skipped (odd) in dissected limbs. Note that expression of FoxB is exclusively in ventral tissue in all investigated stages and appendage types (aj) [except for the labrum, l where expression is in dorsal tissue. See text for further explanation]. In a and di, the left photograph represents a lateral view, the right photograph shows a posterior view on the same appendage. b, c, l Anterior view. j Posterior view. k Lateral view. Note the appearance of segmental transverse stripes of enhanced expression within the ventral region of FoxB expression in the pedipalps and legs (e.g., e, i, j) co-expressed with odd (k). Arrows in k point to co-expression of odd and FoxB. cw claw, cx coxa, e endite, fe femur, mt metatarsus, pt patella, ti tibia, ta tarsus, tr trochanter

Expression of FoxB in the onychophoran Euperipatoides (as a panarthropod outgroup species) is restricted to ventral expression early during limb development (Fig. 1j–l). While the slime papillae, the jaws and the walking limbs express FoxB in this way, the most anterior appendages, the protocerebral frontal appendages (= the onychophoran antennae) do not express FoxB (Fig. 1j). Additionally, FoxB genes are expressed in the developing ventral nervous system in Drosophila [51], Tribolium, Glomeris, Parasteatoda, and Euperipatoides (Figs. 1 and 2, Additional file 7: Figure S5 and Additional file 8: Figure S6), and in Glomeris, FoxB is strongly expressed in the anal valves (Additional file 7: Figure S5). At early developmental stages, Parasteatoda FoxB is expressed in the centre of the germ disc where the cumulus forms (Fig. 2a), and slightly later when the germ field forms, FoxB is expressed ubiquitously (Fig. 2b). When the segments form, FoxB is expressed in the form of transverse segmental stripes that later refine to the position of the forming limb buds (Fig. 2c–i).

FoxB function in the spider Parasteatoda

First, we studied the hatching rates of Pt-FoxB knockdown embryos after parental RNAi versus control embryos. We found that the hatching rate decreased significantly to < 1% in FoxB knockdown embryos, while the hatching rate of approximately 80–90% in control embryos is comparable to that for non-injected wild-type females, cf., e.g., hatching rates in McGregor et al. [54], Königsmann et al. [55]. These first results strongly implied that there is an RNAi-specific effect after injection of Pt-FoxB dsRNA. We analysed the few hatchlings (first instars) and found that many of these had mildly malformed appendages (Fig. 4). Some of the hatchlings were not able to moult successfully and remained stuck with the distal end of their limbs in the old cuticle.

Fig. 4

Malformations of the limbs in FoxB knockdown first instars. In all panels, anterior is to the left. ac Show dorsal views, a′c′ show the same embryos in ventral views. Arrows point to malformations. Asterisk (*) in b′ and c′ mark disturbed ventral bristle pattern (cf. a′). Abbreviations as in Fig. 2, and sp spinnerets

We then investigated the morphology of embryos of all recovered cocoons of both, RNA-injected females, and buffer-injected females. We discovered four different classes of embryonic phenotypes after Pt-FoxB knockdown. Quantification of the observed phenotypes is summarized in Additional file 3: Figure S1. Class-I is represented by abnormally developing limbs (Fig. 5). This represents the mildest observed phenotype, and it is most obvious in the relatively long pedipalps and legs, while it is less clearly visible (if at all) in the relatively short chelicerae, the labrum and the opisthosomal appendages. From approximately stage 8.2 onwards, it becomes obvious that the developing pedipalps and legs are broadened compared to wild-type appendages of embryos at comparable developmental stages; at stage 11 this is already very obvious (Fig. 5a, d). As these appendages proceed to develop, they start bending in a peculiar way resembling the shape of a “Bandyklubba” (Swedish, a term that describes the stick used to play the Nordic version of ice hockey) (Fig. 5b, e). Compared with the better known North American ice hockey stick, this stick is shorter and its distal end is more bent, hence the name Bandyklubba for this leg phenotype (Fig. 5c, f). At late embryonic stages, these limbs begin to disintegrate in a way that distal region(s) bud off from the proximal region of the legs and pedipalps (Fig. 5g–l). Legs and pedipalps of knockdown embryos are broader than comparable wild-type structures. In Class-I knockdown embryos, the overall morphology is not significantly altered by the appendage function of Pt-FoxB.

Fig. 5

Morphological disturbances in FoxB knockdown embryos. Class-I phenotype “Bandyklubba”. ac Show wild-type embryos. dl Show FoxB knockdown embryos. Note the crooked “Bandyklubba”-shaped legs and pedipalps and the budding off of distal limb segments in later stage embryos (arrows). In all panels, anterior is to the left, ventral views. Abbreviations as in Fig. 2 and hl head lobe, vs ventral sulcus

Class-II embryos show an unusually slim germ band. Class-III embryos develop a partially duplicated germ band. In Class-IV embryos, the germ disc does not form correctly. In many of these embryos, the disc is either fully malformed or disintegrated. The yolk is exposed as if the overlying so-called extraembryonic ectoderm did either not form, or disintegrate after formation.

Completely undeveloped eggs likely represent unfertilized eggs that never developed a protective vitelline membrane, and therefore appear as hardened yolk masses after fixation. Our analysis shows that the number of dead embryos is similar in knockdown embryos and wild-type (or control) embryos (Additional file 3: Figure S1).

We also recognized a small percentage of Class-II and Class-IV phenotypes in control embryos, indicating that delayed and small embryos as well as disintegrating (or not-forming) germ discs occasionally occur under natural conditions as well (Additional file 3: Figure S1). This shows that the transition from radial to bilateral symmetry and the onset of germ band formation are critical steps in spider development. However, we did not find a single Class-I or Class-III embryo in control embryos (Additional file 3: Figure S1).

In FoxB knockdown cocoons, the number of embryos identified as wild type after fixation at different embryonic stages is higher than the hatching rate suggesting that FoxB knockdown may lead to additional effects that are difficult to recognize (e.g., defects of the nervous system).

Expression of DV appendage patterning genes in FoxB knockdown embryos

In Class-I embryos, legs and pedipalps are abnormally crooked. Since we observed strong expression of FoxB along the ventral side of these appendages in the wild type, we tested if DV patterning of the appendages is disturbed after Pt-FoxB knockdown by analysing the expression patterns of ventral and dorsal marker genes in these embryos. We found that the expression of the conserved arthropod ventral appendage markers Pt-wg/Wnt1 (e.g., [8, 10, 38]) and Pt-H15.2 (e.g., [10, 26, 27, 31]) was significantly altered in Class-I appendages (Fig. 6a–l and Additional file 9: Figure S7 and Additional file 10: Figure S8). Pt-wg/Wnt1 is absent from the ventral tissue of the appendages except for the most proximal tissue (Fig. 6d–f, Additional file 9: Figure S7). This indicates that FoxB is differently required for wg expression in the distinct ventral regions along the proximal–distal (PD) axis of the limbs. Similarly, the expression of H15.2 is absent from ventral tissue in Class-I appendages (Fig. 6j–l, Additional file 10: Figure S8).

Fig. 6

Expression of wingless (wg) (af), H15.2 (gl) and optomotor-blind (omb) (mr) in wild type and FoxB knockdown appendages. Class-I phenotype “Bandyklubba”. All panels represent ventral views. Arrows point to areas of altered gene expression in knockdown appendages. Note that wg and H15.2 are expressed along the ventral side of all appendage types in wild-type embryos, and that this expression is lacking in FoxB knockdown appendages. The dorsally expressed gene omb is expressed in ventral regions in knockdown appendages. Abbreviations as in Fig. 2

The conserved arthropod dorsal limb marker optomotor-blind (omb) (e.g. [10, 27, 31] is still strongly expressed in the dorsal tissue of the limbs in Pt-FoxB knockdown embryos (Fig. 6p–r, Additional file 11: Figure S9). Interestingly, however, we observed an extension of the omb expression pattern into ventral tissue, that normally does not express Pt-omb (Fig. 6p–r), indicating a partial dorsalisation of the appendages after loss of Pt-FoxB function. This is predominantly (if not exclusively) observed for the distal region of the pedipalps and legs.

The gene Decapentaplegic (dpp) encodes a dorsal morphogen acting upstream of omb in Drosophila [20, 29]. In wild-type P. tepidariorum embryos, Pt-dpp is initially expressed in the tips of the prosomal appendages (Fig. 7a, b), and is later expressed in a striped fashion in the pedipalps and legs (Fig. 7c, Additional file 12: Figure S10). Intriguingly, this pattern is disrupted in FoxB knockdown embryos and is replaced by an entirely new expression pattern (Fig. 7d–f, Additional file 12: Figure S10). In the early stages of limb development, Pt-dpp is expressed along the ventral side of the appendages; initially this includes the ventral portion of the distal tip (Fig. 7d), but subsequently Pt-dpp is not at all expressed in the distal tip (Fig. 7e, f). The ringed Pt-dpp pattern that develops in the wild type at approximately stage 12 (Fig. 7c) does not emerge in Pt-FoxB knockdown embryos.

Fig. 7

Expression of Decapentaplegic (dpp) in wild type (WT) (ac) and FoxB knockdown appendages (df). Class-I phenotype “Bandyklubba”. Note the appearance of dpp expression along the ventral region of all appendages after FoxB dsRNA treatment. Abbreviations as in Fig. 2

Since the wild-type expression pattern of FoxB includes reiterated patterns in the spider limbs which is likely correlated with the position of the developing joints, we investigated the expression of the spider joint marker odd-skipped (odd) [56, 57] in Class-I embryos. In wild-type embryos, Pt-odd is expressed in nine rings in late developmental stages in the legs, in seven rings in the pedipalps, and two rings in the chelicerae (Fig. 8a). In Class-I limbs, the most distal rings do not form, or expression is very weak (Fig. 8b). Also, in all Class-I appendages, expression disappears from ventral tissue (or is strongly reduced ventrally) (Fig. 8b).

Fig. 8

Expression of odd-skipped (odd) in dissected limbs of WT embryos (a) and FoxB knockdown embryos (b). Class-I phenotype “Bandyklubba”. Lateral views. Numbers indicate domains of odd expression from proximal to distal. Numbers in brackets indicate weak expression after FoxB dsRNA treatment. Black asterisks indicate the most distal domain of odd. Note the much weaker or missing ventral expression of odd in FoxB knockdown embryos. The odd gene is likely involved in joint formation, and these results suggest a connection between FoxB function and appendage podomerization. Abbreviations as in Fig. 2; d distal; p proximal


FoxB genes represent evolutionary conserved markers of ventral limb tissue in ventral appendages

We could show that FoxB genes are expressed along the ventral side of all ventral appendages and that this expression is conserved in species of diverse panarthropod groups, namely the fly Drosophila, the beetle Tribolium, the millipede Glomeris, the spider Parasteatoda, and the onychophoran Euperipatoides. This suggests a conserved role for FoxB in DV appendage patterning in the entire clade Panarthropoda. Dorsal appendages, like the wings and halteres in Drosophila, in contrast, do not express FoxB, indicating that its function is restricted to ventral appendages. In all ventral appendage types including the highly modified spider opisthosomal appendages (i.e., the book lungs, the tracheal system, and the spinnerets), FoxB is expressed along the ventral ectoderm. This pattern is very similar to that of wg and H15, two other highly conserved ventral limb marker genes [5, 10, 27, 31].

Exceptions from this rule are the conserved FoxB expression domains in the dorsal tissue of the labrum in Tribolium, Glomeris and Parasteatoda (note that we did not investigate expression of FoxB in the labral discs of Drosophila). This apparent discrepancy, however, can be explained by the hypothesis that the labrum is the result of rotation and fusion of a pair of limbs. As a consequence, ventral and dorsal tissue is reversed in the labrum [52]. The second exception concerns the frontal appendages of the onychophoran which do not express FoxB. These appendages are innervated from the protocerebrum and likely are homologous with the arthropod labrum ([58, 59]; discussed in e.g., [60]), although expression of FoxB does not support this notion.

Knockdown of FoxB in the spider Parasteatoda reveals a specific role in DV appendage development

The highly conserved expression of FoxB in the limbs of arthropods and the onychophoran strongly suggests an important and evolutionarily conserved function in panarthropod DV limb development. The functional analysis of FoxB in the spider Parasteatoda tepidariorum indeed revealed that FoxB is required for proper DV patterning during limb axis formation. The Class-I phenotype shows an abnormally crooked distal region of pedipalps and legs, most probably explained by a reduction of ventral tissue. Class-I appendages are also broader and softer than wild-type appendages, indicating that the overall integrity of the limbs is disturbed. This becomes even more evident in later stage Class-I appendages which are characterized by the occurrence of abnormal constrictions that finally lead to the complete budding off of limb parts, especially in the distal region (Fig. 5).

A very similar phenotype has been reported for wg/Wnt1 and its receptor-encoding gene frizzled-1 (fz1) in the beetle Tribolium [7, 61]. Here the phenotypes are called “candy cane” and “nonpareille”/“pearls on a chain” referring to the bending of the limbs (“candy cane”) and the budding off and fusion of distal limb segments (“nonpareille” and “pearls on a chain”) [7]. Tribolium fz1 is expressed ubiquitously, but it fulfils a specific function in limb development as revealed by fz1 knockdown [61]. Although the function of fz1 is not yet studied in other arthropods, it is also ubiquitously expressed in Parasteatoda, allowing for a conserved interaction of Wg and Fz1 in spider limb development [62].

The effect of knockdown of Pt-FoxB and Tc-wg, both of which are expressed in conserved patterns along the ventral side of appendages in all hitherto investigated arthropods, is strikingly similar (“Bandyklubba” phenotype and “candy cane” phenotype, respectively) suggesting that they might work in the same conserved gene regulatory network (GRN) in DV limb patterning.

FoxB acts as a key factor in the gene regulatory network (GRN) controlling DV appendage patterning

In the model system Drosophila melanogaster, the DV limb axis is determined by the action of the dorsal and ventral morphogens Dpp and Wg, respectively. While dpp is specifically expressed in the dorsal sector of the limb imaginal discs, wg is specifically expressed in ventral tissue. The expression of the dorsal morphogen encoding gene dpp is different in the outgrowing appendages of arthropods with direct development, i.e., the vast majority of all arthropods. Instead of being expressed along the dorsal surface of the limbs, its expression is restricted to the tip (Fig. 9a). Despite these significant differences in gene expression, the so-called topology model has been proposed, that argues for a conserved function of Dpp as dorsal morphogen in a three-dimensional system as represented by directly developing limbs compared to the rather two-dimensional system as represented by the imaginal discs of Drosophila [10, 33]. The T-Box transcription factor optomotor-blind (omb) acts downstream of dpp in Drosophila and is expressed in the dorsal region of the leg imaginal discs (e.g., [63]) (Fig. 9a). This dorsal omb expression along the developing limbs was previously shown to be conserved in Panarthropoda [10, 26, 31, 32]. The ventral morphogen encoding gene wg is expressed in the ventral sector of the Drosophila leg imaginal disc, and its expression in other arthropods is highly conserved as well (e.g., [7, 10, 30]) (Fig. 9a). Downstream of wg functions another T-Box transcription factor-encoding gene, H15 (aka midline). Like wg, at least one of the H15 paralogs in each arthropod species is expressed along the ventral side of the outgrowing appendages (e.g., [10, 26, 31]) (Fig. 9a). In summary, the available data are compatible with the notion that the role of dpp and omb in specifying the dorsal side, as well as the role of wg and H15 in specifying the ventral side are evolutionarily conserved in panarthropods.

Fig. 9

Summary of gene expression in WT legs and FoxB-RNAi knockdown legs. Regulatory interactions of the investigated genes as known from Drosophila and as suggested by our results from the spider are indicated. Question marks indicate that it is unclear if the suggested activation of H15 and repression of omb are direct effects of FoxB, or whether they represent indirect effects

After FoxB knockdown in the spider, expression of both ventral marker genes, wg and H15.2, is missing (Fig. 9b, c). This indicates that FoxB acts upstream of wg in the GRN required for DV patterning. Since wg is acting upstream of H15 in Drosophila, the lack of H15.2 in FoxB knockdown appendages could be the result of the lack of wg, and thus a secondary effect of FoxB, or it could (as assumed for wg) be under direct control of FoxB. Our experimental setup cannot distinguish between these two possibilities, but it would be interesting to study in future experiments.

The expansion of dpp expression along the ventral region in limbs after FoxB knockdown indicates that FoxB normally acts as a repressor of dpp in ventral tissue, either directly, or via wg and/or H15.2 (Fig. 9d). We note, however, that no aspect of the topology model predicts our observation that the expression of Pt-dpp is progressively removed from the distal tip in Pt-FoxB knockdown embryos (Fig. 9d), and therefore this effect of Pt-FoxB RNAi cannot be explained by the model.

Also, the dorsal factor omb is intruding ventral and distal areas of appendages in FoxB knockdown embryos, which suggests that FoxB acts directly (or indirectly via Wg and H15.2) as a repressor of omb (Fig. 9e). The assumption that Dpp could act as a direct activator of omb [10] is not supported by our data, because the expansion of dpp along the ventral side of the limbs apparently does not cause ectopic expression of omb in this tissue (Fig. 9e). However, it is also possible that ventral tissue is not competent for omb expression, even in the presence of dpp.

In Drosophila, Hedgehog (Hh) activates dpp and wg in the leg disc due to an early asymmetry that allows ventral and dorsal cells to respond differently to Hh signalling (in dorsal tissue, dpp is activated, and in ventral tissue, wg is activated). Such asymmetry is provided by the relative earlier expression of Wg in ventral tissue [2, 20, 23]. Consequently, in the absence of Wg, Hh would activate dpp in ventral tissue, instead of wg [20].

This scenario is in line with our data. Since wg is absent from ventral tissue in FoxB knockdown embryos as a result of the missing function of FoxB, now dpp is dominantly expressed in this tissue. Once the asymmetry between wg and dpp expressing tissue is established, Dpp and Wg act as mutual antagonists in the Drosophila imaginal discs [20]. If this mutual antagonistic function is conserved, or at least the repressive function of Wg on Dpp, this might explain why dpp expands into the now wg-free ventral limb tissue after FoxB knockdown. Again, we cannot distinguish between a possible direct or indirect repression of dpp via FoxB or/and Wg. Either way, our data suggest that FoxB is acting at a high level in the GRN orchestrating DV limb patterning.

Evidence for different regulatory mechanisms acting along the AP axis of developing limbs

It has been shown that different regions along the AP axis of the Drosophila leg are under control of different GRNs, or that given GRNs act differently in different regions of the leg. For example, the most proximal region of the Drosophila leg, the coxa, never expresses Distal-less (Dll), a gene that is otherwise involved in the formation of all other podomeres (leg segments) (reviewed in [64]). It has also been shown that wg plays a specific role in the development of the coxa [65]. Similarly, it also appears that the proximal region (including the coxa) is patterned differently in the beetle Tribolium. Interestingly, here wg appears to have the opposite effect. While distal regions of the legs are affected in wg knockdown and Fz1 knockdown embryos, this is not the case for the coxal region [7, 61]. Therefore, it is possible that the proximal region and the distal region (defined as distal to the coxa) are generally regulated differently in arthropods [66, 67].

Our results on Parasteatoda FoxB function support this hypothesis and suggest that the differences between proximal and distal leg development may indeed date back to the last common ancestor of insects and spiders, i.e., the arthropod ancestor. Although Pt-FoxB is expressed all along the ventral side of pedipalps and legs, its knockdown affects only the distal and medial, but not the proximal Pt-wg expression (Fig. 9b). Similarly, Pt-FoxB knockdown leads to the misexpression of Pt-omb in the distal portions of pedipalps and legs, while medial and proximal portions are not affected (Fig. 9e). The most intriguing result, however, is the complete change of the Pt-dpp expression pattern after Pt-FoxB RNAi, especially in the distal tip. In this case, the loss of Pt-FoxB influences Pt-dpp expression even in portions of the limbs that never express Pt-FoxB. The reason for this is currently not clear.

Evidence for the coupling of DV patterning and joint formation

In Drosophila, the correct formation of joints depends on the PD patterning system and the so-called leg gap genes (e.g. [68, 69]; summarized in [70]). In a combinatorial mode, they activate Delta/Notch signalling (e.g., [71,72,73]) and downstream of Delta/Notch signalling act, e.g., the odd-skipped family genes, including odd-skipped (odd) itself [74, 75]. It has been shown that the involvement of Delta/Notch signalling and its downstream factors such as odd in arthropod joint formation is conserved in arthropods beyond Drosophila [76]. In the spider Cupiennius salei, the odd ortholog odd-related-1 (one of three identified odd-related genes in this spider) is expressed in concentric rings in the limbs downstream of Delta/Notch signalling and its function is clearly correlated with that of joint formation [76]. The same expression pattern is seen for odd in the limbs of Parasteatoda (Fig. 8).

Remarkably, we find that odd expression in concentric rings is disturbed after knocking down FoxB, but only in the ventral sector, while expression along the dorsal side of the limbs is not affected (except for the distal region where expression of odd is completely lost) (Fig. 8). Double in situ revealed that odd is indeed co-expressed with the patches of enhanced expression of FoxB (Fig. 3k). Together, this implies that odd expression in the limbs is likely under control of the DV patterning system downstream of FoxB function, at least ventrally. Since odd is one of the genes that is involved in joint formation in spiders, this finding is the first potential evidence that joint formation and DV patterning may be connected.


  1. 1.

    Campbell G, Weaver T, Tomlinson A. Axis specification in the developing Drosophila appendage: the role of wingless, decapentaplegic, and the homeobox gene aristaless. Cell. 1993;74:1113–23.

    CAS  PubMed  Article  Google Scholar 

  2. 2.

    Cohen B, Simcox AA, Cohen SM. Allocation of the thoracic imaginal primordia in the Drosophila embryo. Development. 1993;117:597–608.

    CAS  PubMed  Google Scholar 

  3. 3.

    Abzhanov A, Kaufman TC. Homologs of Drosophila appendage genes in the patterning of arthropod limbs. Dev Biol. 2000;227:683–9.

    Article  CAS  Google Scholar 

  4. 4.

    Prpic NM, Janssen R, Wigand B, Klingler M, Damen WG. Gene expression in spider appendages reveals reversal of exd/hth spatial specificity, altered leg gap gene dynamics, and suggests divergent distal morphogen signaling. Dev Biol. 2003;264:119–40.

    CAS  PubMed  Article  Google Scholar 

  5. 5.

    Brook WJ. T-box genes organize the dorsal ventral leg axis in Drosophila melanogaster. Fly (Austin). 2010;4:159–62.

    CAS  Article  Google Scholar 

  6. 6.

    Damen WGM (2002) Parasegmental organization of the spider embryo implies that the parasegment is an evolutionary conserved entity in arthropod embryogenesis. Development 129:1239-50

    CAS  PubMed  Google Scholar 

  7. 7.

    Janssen R, Prpic NM, Damen WG. Gene expression suggests decoupled dorsal and ventral segmentation in the millipede Glomeris marginata (Myriapoda: Diplopoda). Dev Biol. 2004;268:89–104.

    CAS  PubMed  Article  Google Scholar 

  8. 8.

    Ober KA, Jockusch EL. The roles of wingless and decapentaplegic in axis and appendage development in the red flour beetle, Tribolium castaneum. Dev Biol. 2006;294:391–405.

    CAS  PubMed  Article  Google Scholar 

  9. 9.

    Grossmann D, Scholten J, Prpic NM. Separable functions of wingless in distal and ventral patterning of the Tribolium leg. Dev Genes Evol. 2009;219:469–79.

    PubMed  PubMed Central  Article  Google Scholar 

  10. 10.

    Eriksson BJ, Tait NN, Budd GE, Akam M. The involvement of engrailed and wingless during segmentation in the onychophoran Euperipatoides kanangrensis (Peripatopsidae: Onychophora) (Reid 1996). Dev Genes Evol. 2009;219:249–64.

    PubMed  Article  Google Scholar 

  11. 11.

    Diaz-Benjumea FJ, Cohen B, Cohen SM. Cell interaction between compartments establishes the proximal-distal axis of Drosophila legs. Nature. 1994;372:175–9.

    CAS  PubMed  Article  Google Scholar 

  12. 12.

    Abu-Shaar M, Mann RS. Generation of multiple antagonistic domains along the proximodistal axis during Drosophila leg development. Development. 1998;125:3821–30.

    CAS  PubMed  Google Scholar 

  13. 13.

    Estella C, Mann RS. Logic of Wg and Dpp induction of distal and medial fates in the Drosophila leg. Development. 2008;135:627–36.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  14. 14.

    Prpic NM, Wigand B, Damen WG, Klingler M. Expression of dachshund in wild-type and Distal-less mutant Tribolium corroborates serial homologies in insect appendages. Dev Genes Evol. 2001;211:467–77.

    CAS  PubMed  Article  Google Scholar 

  15. 15.

    Inoue Y, Mito T, Miyawaki K, Matsushima K, Shinmyo Y, Heanue TA, Mardon G, Ohuchi H, Noji S. Correlation of expression patterns of homothorax, dachshund, and Distal-less with the proximodistal segmentation of the cricket leg bud. Mech Dev. 2002;113:141–8.

    CAS  PubMed  Article  Google Scholar 

  16. 16.

    Angelini DR, Kaufman TC. Functional analyses in the hemipteran Oncopeltus fasciatus reveal conserved and derived aspects of appendage patterning in insects. Dev Biol. 2004;271:306–21.

    CAS  PubMed  Article  Google Scholar 

  17. 17.

    Janssen R, Eriksson BJ, Budd GE, Akam M, Prpic NM. Gene expression patterns in an onychophoran reveal that regionalization predates limb segmentation in pan-arthropods. Evol Dev. 2010;12:363–72.

    CAS  PubMed  Article  Google Scholar 

  18. 18.

    Sharma PP, Schwager EE, Extavour CG, Giribet G. Evolution of the chelicera: a dachshund domain is retained in the deutocerebral appendage of Opiliones (Arthropoda, Chelicerata). Evol Dev. 2012;14:522–33.

    PubMed  Article  Google Scholar 

  19. 19.

    Schaeper ND, Wimmer EA, Prpic NM. Appendage patterning in the primitively wingless hexapods Thermobia domestica (Zygentoma: Lepismatidae) and Folsomia candida (Collembola: Isotomidae). Dev Genes Evol. 2013;223:341–50.

    PubMed  Article  Google Scholar 

  20. 20.

    Struhl G, Basler K. Organizing activity of wingless protein in Drosophila. Cell. 1993;72:527–40.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  21. 21.

    Brook WJ, Cohen SM. Antagonistic interactions between wingless and decapentaplegic responsible for dorsal–ventral pattern in the Drosophila leg. Science. 1996;273:1373–7.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  22. 22.

    Morimura S, Maves L, Chen Y, Hoffmann FM. Decapentaplegic overexpression affects Drosophila wing and leg imaginal disc development and wingless expression. Dev Biol. 1996;177:136–51.

    CAS  PubMed  Article  Google Scholar 

  23. 23.

    Couso JP, Bate M, Martinez-Arias A. A wingless-dependent polar coordinate system in Drosophila imaginal discs. Science. 1993;259:484–9.

    CAS  PubMed  Article  Google Scholar 

  24. 24.

    Wilder EL, Perrimon N. Dual functions of wingless in the Drosophila leg imaginal disc. Development. 1995;121:477–88.

    CAS  PubMed  Google Scholar 

  25. 25.

    Prpic NM, Janssen R, Damen WG, Tautz D. Evolution of dorsal-ventral axis formation in arthropod appendages: H15 and optomotor-blind/bifid-type T-box genes in the millipede Glomeris marginata (Myriapoda: Diplopoda). Evol Dev. 2005;7:51–7.

    CAS  PubMed  Article  Google Scholar 

  26. 26.

    Svendsen PC, Formaz-Preston A, Leal SM, Brook WJ. The Tbx20 homologs midline and H15 specify ventral fate in the Drosophila melanogaster leg. Development. 2009;136:2689–93.

    CAS  PubMed  Article  Google Scholar 

  27. 27.

    Pflugfelder GO, Eichinger F, Shen J. T-box genes in Drosophila limb development. Curr Top Dev Biol. 2017;122:313–54.

    CAS  PubMed  Article  Google Scholar 

  28. 28.

    Held LI, Heup MA, Sappington JM, Peters SD. Interactions of decapentaplegic, wingless, and Distal-less in the Drosophila leg. Roux Arch Dev Biol. 1994;203:310–9.

    PubMed  Article  Google Scholar 

  29. 29.

    Maves L, Schubiger G. A molecular basis for transdetermination in Drosophila imaginal discs: interactions between wingless and decapentaplegic signaling. Development. 1998;125:115–24.

    CAS  PubMed  Google Scholar 

  30. 30.

    Giorgianni MW, Patel NH. Patterning of the branched head appendages in Schistocerca americana and Tribolium castaneum. Evol Dev. 2004;6:402–10.

    PubMed  Article  Google Scholar 

  31. 31.

    Janssen R, Feitosa NM, Damen WG, Prpic NM. The T-box genes H15 and optomotor-blind in the spiders Cupiennius salei, Tegenaria atrica and Achaearanea tepidariorum and the dorsoventral axis of arthropod appendages. Evol Dev. 2008;10:143–54.

    CAS  PubMed  Article  Google Scholar 

  32. 32.

    Janssen R, Jörgensen M, Prpic NM, Budd GE. Aspects of dorso-ventral an proximo-distal limb patterning in onychophorans. Evol Dev. 2015;17:21–33.

    CAS  PubMed  Article  Google Scholar 

  33. 33.

    Angelini DR, Kaufman TC. Functional analyses in the milkweed bug Oncopeltus fasciatus (Hemiptera) support a role for Wnt signaling in body segmentation but not appendage development. Dev Biol. 2005;283:409–23.

    CAS  PubMed  Article  Google Scholar 

  34. 34.

    Nakamura T, Mito T, Tanaka Y, Bando T, Ohuchi H, Noji S. Involvement of canonical Wnt/Wingless signaling in the determination of the positional values within the leg segment of the cricket Gryllus bimaculatus. Dev Growth Differ. 2007;49:79–88.

    CAS  PubMed  Article  Google Scholar 

  35. 35.

    Janssen R, Le Gouar M, Pechmann M, Poulin F, Bolognesi R, Schwager EE, Hopfen C, Colbourne JK, Budd GE, Brown SJ, Prpic NM, Kosiol C, Vervoort M, Damen WG, Balavoine G, McGregor AP. Conservation, loss, and redeployment of Wnt ligands in protostomes: implications for understanding the evolution of segment formation. BMC Evol Biol. 2010;10:374.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  36. 36.

    Franke FA, Mayer G. Controversies surrounding segments and parasegments in Onychophora: insights from the expression patterns of four “segment polarity genes” in the peripatopsid Euperipatoides rowelli. PLoS ONE. 2014;9:e114383.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  37. 37.

    Murat S, Hopfen C, McGregor AP. The function and evolution of Wnt genes in arthropods. Arthropod Struct Dev. 2010;39:446–52.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  38. 38.

    Bolognesi R, Beermann A, Farzana L, Wittkopp N, Lutz R, Balavoine G, Brown SJ, Schröder R. Tribolium Wnts: evidence for a larger repertoire in insects with overlapping expression patterns that suggest multiple redundant functions in embryogenesis. Dev Genes Evol. 2008;218:193–202.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  39. 39.

    Mazet F, Yu JK, Liberles DA, Holland LZ, Shimeld SM. Phylogenetic relationships of the Fox (Forkhead) gene family in the Bilateria. Gene. 2003;316:79–89.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  40. 40.

    Lee HH, Frasch M (2004) Survey of forkhead domain encoding genes in the Drosophila genome: Classification and embryonic expression patterns. Dev Dyn 229:357–66.

    CAS  PubMed  Article  Google Scholar 

  41. 41.

    Hogvall M, Schönauer A, Budd GE, McGregor AP, Posnien N, Janssen R. Analysis of the Wnt gene repertoire in an onychophoran provides new insights into the evolution of segmentation. Evodevo. 2014;5:14.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  42. 42.

    Janssen R, Budd GE. Deciphering the onychophoran ‘segmentation gene cascade’: gene expression reveals limited involvement of pair rule gene orthologs in segmentation, but a highly conserved segment polarity gene network. Dev Biol. 2013;382:224–34.

    CAS  PubMed  Article  Google Scholar 

  43. 43.

    Mittmann B, Wolff C. Embryonic development and staging of the cobweb spider Parasteatoda tepidariorum C. L. Koch, 1841 (syn.: Achaearanea tepidariorum; Araneomorphae; Theridiidae). Dev Genes Evol. 2012;222:189–216.

    PubMed  Article  Google Scholar 

  44. 44.

    Strobl F, Stelzer EH. Non-invasive long-term fluorescence live imaging of Tribolium castaneum embryos. Development. 2014;141:2331–8.

    CAS  PubMed  Article  Google Scholar 

  45. 45.

    Tribolium Genome Sequencing Consortium, Richards S, Gibbs RA, Weinstock GM, et al. The genome of the model beetle and pest Tribolium castaneum. Nature. 2008;452:949–55.

    Article  CAS  Google Scholar 

  46. 46.

    Schwager EE, Sharma PP, Clarke T, et al. The house spider genome reveals an ancient whole-genome duplication during arachnid evolution. BMC Biol. 2017;15:62.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  47. 47.

    Schinko J, Posnien N, Kittelmann S, Koniszewski N, Bucher G. Single and double whole-mount in situ hybridization in red flour beetle (Tribolium) embryos. Cold Spring Harb Protoc. 2009;8:pdb.prot5258.

    Google Scholar 

  48. 48.

    Pechmann M, Benton MA, Kenny NJ, Posnien N, Roth S. A novel role for Ets4 in axis specification and cell migration in the spider Parasteatoda tepidariorum. Elife. 2017;6:e27590.

    PubMed  PubMed Central  Article  Google Scholar 

  49. 49.

    Janssen R, Andersson E, Betner E, Bijl S, Fowler W, Höök L, Lehr J, Mannelqvist A, Panara V, Smith K, Tieman S. Embryonic expression patterns and phylogenetic analysis of panarthropod Sox genes: insight into nervous system development, segmentation and gonadogenesis. BMC Evol Biol. 2018;18:88.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  50. 50.

    Janssen R, Budd GE, Damen WG, Prpic NM. Evidence for Wg-independent tergite boundary formation in the millipede Glomeris marginata. Dev Genes Evol. 2008;218:361–70.

    CAS  PubMed  Article  Google Scholar 

  51. 51.

    Huelsenbeck JP, Ronquist F. MRBAYES: bayesian inference of phylogenetic trees. Bioinformatics. 2001;17:754–5.

    CAS  Article  Google Scholar 

  52. 52.

    Häcker U, Grossniklaus U, Gehring WJ, Jäckle H. Developmentally regulated Drosophila gene family encoding the fork head domain. Proc Natl Acad Sci USA. 1992;89:8754–8.

    PubMed  Article  Google Scholar 

  53. 53.

    Kimm MA, Prpic NM. Formation of the arthropod labrum by fusion of paired and rotated limb-bud-like primordial. Zoomorphology. 2006;125:147–55.

    Article  Google Scholar 

  54. 54.

    McGregor AP, Pechmann M, Schwager EE, Feitosa NM, Kruck S, Aranda M, Damen WG. Wnt8 is required for growth-zone establishment and development of opisthosomal segments in a spider. Curr Biol. 2008;18:1619–23.

    CAS  PubMed  Article  Google Scholar 

  55. 55.

    Königsmann T, Turetzek N, Pechmann M, Prpic NM. Expression and function of the zinc finger transcription factor Sp6-9 in the spider Parasteatoda tepidariorum. Dev Genes Evol. 2017;227:389–400.

    PubMed  Article  CAS  Google Scholar 

  56. 56.

    Prpic NM, Damen WG. Notch-mediated segmentation of the appendages is a molecular phylotypic trait of the arthropods. Dev Biol. 2009;326:262–71.

    CAS  PubMed  Article  Google Scholar 

  57. 57.

    Zhang N. Developmental studies of appendage patterning and formation in spiders. Ph.D. Thesis. Georg-August-Universiät Göttingen, Göttingen, Germany. 2016.

  58. 58.

    Eriksson BJ, Budd GE. Onychophoran cephalic nerves and their bearing on our understanding of head segmentation and stem-group evolution of Arthropoda. Arthropod Struct Dev. 2000;29:197–209.

    CAS  PubMed  Article  Google Scholar 

  59. 59.

    Eriksson BJ, Tait NN, Budd GE, Janssen R, Akam M. Head patterning and Hox gene expression in an onychophoran and its implications for the arthropod head problem. Dev Genes Evol. 2010;220:117–22.

    PubMed  Article  Google Scholar 

  60. 60.

    Jockusch EL. Developmental and evolutionary perspectives on the origin and diversification of arthropod appendages. Integr Comp Biol. 2017;57:533–45.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  61. 61.

    Beermann A, Prühs R, Lutz R, Schröder R (2011) A context-dependent combination of Wnt receptors controls axis elongation and leg development in a short germ insect. Development 138:2793-2805.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  62. 62.

    Janssen R, Schönauer A, Weber M, Turetzek N, Hogvall M, Goss GE, Patel NH, McGregor AP, Hilbrant M. The evolution and expression of panarthropod frizzled genes. Front Ecol Evol. 2015;3:96.

    Article  Google Scholar 

  63. 63.

    Grimm S, Pflugfelder GO. Control of the gene optomotor-blind in Drosophila wing development by decapentaplegic and wingless. Science. 1996;271:1601–4.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  64. 64.

    Kojima T. The mechanism of Drosophila leg development along the proximodistal axis. Dev Growth Differ. 2004;46:115–29.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  65. 65.

    Kubota K, Goto S, Hayashi S. The role of Wg signaling in the patterning of embryonic leg primordium in Drosophila. Dev Biol. 2003;257:117–26.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  66. 66.

    González-Crespo S, Morata G. Genetic evidence for the subdivision of the arthropod limb into coxopodite and telopodite. Development. 1996;122:3921–8.

    PubMed  Google Scholar 

  67. 67.

    Casares F, Mann RS. The ground state of the ventral appendage in Drosophila. Science. 2001;293:1477–80.

    CAS  PubMed  Article  Google Scholar 

  68. 68.

    Mardon G, Solomon N, Rubin GM. dachshund encodes a nuclear protein required for normal eye and leg development in Drosophila. Development. 1994;120:3473–86.

    CAS  PubMed  Google Scholar 

  69. 69.

    Lecuit T, Cohen SM. Proximal-distal axis formation in the Drosophila leg. Nature. 1997;388:139–45.

    CAS  PubMed  Article  Google Scholar 

  70. 70.

    Rauskolb C. The establishment of segmentation in the Drosophila leg. Development. 2001;128:4511–21.

    CAS  PubMed  Google Scholar 

  71. 71.

    Parody TR, Muskavitch MAT. The pleiotropic function of Delta during postembryonic development of Drosophila melanogaster. Genetics. 1993;135:527–39.

    CAS  PubMed  PubMed Central  Google Scholar 

  72. 72.

    Speicher SA, Thomas U, Hinz U, Knust E. The Serrate locus of Drosophila and its role in morphogenesis of the wing imaginal discs: control of cell proliferation. Development. 1994;120:535–44.

    CAS  PubMed  Google Scholar 

  73. 73.

    de Celis JF, Tyler DM, de Celis J, Bray SJ. Notch signaling mediates segmentation of the Drosophila leg. Development. 1998;125:4617–26.

    PubMed  Google Scholar 

  74. 74.

    Rauskolb C, Irvine KD. Notch-mediated segmentation and growth control of the Drosophila leg. Dev Biol. 1999;210:339–50.

    CAS  PubMed  Article  Google Scholar 

  75. 75.

    Hao I, Green RB, Dunaevsky O, Lengyel JA, Rauskolb C. The odd-skipped family of zinc finger genes promotes Drosophila leg segmentation. Dev Biol. 2003;263:282–95.

    CAS  PubMed  Article  Google Scholar 

  76. 76.

    Angelini DR, Smith FW, Jockusch EL (2012) Extent With Modification: Leg Patterning in the Beetle Tribolium castaneum and the Evolution of Serial Homologs. G3 (Bethesda) 2:235–48

    Article  Google Scholar 

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We thank the following colleagues for providing clones, cDNAs and embryos: Matthias Pechmann (University of Cologne, Germany), Alistair McGregor (Oxford Brookes University, England) and Gregor Bucher (University of Göttingen, Germany). We gratefully acknowledge the support of the New South Wales Government Department of Environment and Climate Change by provision of a permit SL100159 to collect onychophorans at Kanangra-Boyd National Park. We thank Glenn Brock, David Mathieson, Robyn Stutchbury and especially Noel Tait, for their help during onychophoran collection. Financial funding was provided by the Swedish Natural Science Council (VR), Grant No. 621-2011-4703 (to R.J.), and the Deutsche Forschungsgemeinschaft (Grant Nos. PR 1109/4-1 and PR 1109/6-1 to N.M.P.). In situ hybridization experiments were partially executed under the supervision of RJ by Katerina Günter and Johanna Sundqvist during the “Evolution and Development” course at Uppsala University in the spring of 2016, course no. 1BG397.

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Correspondence to Ralf Janssen.

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Supplementary information

Additional file 1: Table S1. Primer sequences.

Additional file 2: Table S2. Accession numbers.

Additional file 3: Figure S1. Summary of phenotypes found in FoxB knockdown embryos compared to control embryos. The total numbers of investigated control and FoxB knockdown embryos is indicated on top of the bars in the diagram. The table gives a quantification of the observed phenotypes in relation to control embryos that show mostly wild-type phenotypes. Legend explanation: WT, wild type; Class-I, “Bandyklubba” phenotype (crooked limbs); Class-II, embryos with small germ bands; Class-III, partially duplicated germ band; Class-IV, germ band not forming (irregular germ disc); dead, unfertilized/not developing.

Additional file 4: Figure S2. Phylogenetic analysis. Bayesian phylogeny of forkhead domain amino acid sequences of FoxA, FoxB and FoxC genes of Drosophila melanogaster (Dm), Tribolium castaneum (Tc), Glomeris marginata (Gm), and Parasteatoda tepidariorum (Pt). Drosophila FoxQ2 serves as outgroup. Branch support (posterior probabilities) is given for each main branch. This simple analysis shows that FoxB orthologs can easily be distinguished from other closely related Fox genes such as FoxA and FoxC.

Additional file 5: Figure S3. Expression of Drosophila melanogaster FoxB2 in leg discs, the antennal disc, and the eye disc. Note that the expression is identical to that of FoxB1. Like FoxB1, FoxB2 is not expressed in the wing discs and the haltere discs (not shown).

Additional file 6: Figure S4. Expression of Tribolium FoxB1 in legs of embryos of different developmental stages. Note that the prepared appendages are still connected showing that expression is indeed along their ventral side. Abbreviations: d, dorsal side; v, ventral side.

Additional file 7: Figure S5. Expression of Glomeris marginata FoxB. In all panels, anterior is to the left, ventral views. Developmental stages are indicated. Except for expression in the appendages (see main text), Glomeris FoxB is also expressed in the ventral nervous system (arrows) and the anal valves. Abbreviations: an, antenna; av, anal valves; lr, labrum; mx, maxilla; T1, first trunk segment.

Additional file 8: Figure S6. Expression of Tribolium castaneum FoxB2. In all panels, expression in to the left, ventral views. Note that the expression of Tribolium FoxB1 (main text) and FoxB2 is identical. Arrows point to expression in the ventral nervous system. Abbreviations: an, antenna; T1, first thoracic segment.

Additional file 9: Figure S7. Expression of wingless (wg) in wild type (A–C) and FoxB knockdown embryos (D–F). In all panels, anterior is to the left, ventral views. Embryos shown in panels A–C and D–F represent different views on the same embryo. Note the reduced/lacking expression in the appendages. Abbreviations as in Fig. 2; hl, head lobe.

Additional file 10: Figure S8. Expression of H15.2 in wild type (A–D) and FoxB knockdown embryos (E–H). In all panels, anterior is to the left, ventral views (except panel D, lateral view). Arrows point to missing expression in ventral tissue of the legs and pedipalps. Embryos shown in panels A–D and E–H represent different views on the same embryo. Abbreviations as in Fig. 2; hl, head lobe; vs, ventral sulcus.

Additional file 11: Figure S9. Expression of optomotor-blind (omb) in wild type (A–D) and FoxB knockdown embryos (E–H). In all panels, anterior is to the left, ventral views (except panel D, lateral view). Arrows point to ectopic expression of omb in the pedipalps and legs, but not the chelicerae (arrowhead). Embryos shown in panels A–D and E–H represent different views on the same embryo. Abbreviations as in Fig. 2; hl, head lobe.

Additional file 12: Figure S10. Expression of Decapentaplegic (dpp) in wild type (A–C) and FoxB knockdown embryos (D–F). In all panels, anterior is to the left, ventral views. Abbreviations as in Fig. 2.

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Heingård, M., Turetzek, N., Prpic, N. et al. FoxB, a new and highly conserved key factor in arthropod dorsal–ventral (DV) limb patterning. EvoDevo 10, 28 (2019).

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  • Appendage patterning
  • Forkhead domain
  • Limb segmentation
  • Development