Skip to main content
Download PDF

Onychophoran Hox genes and the evolution of arthropod Hox gene expression

Frontiers in Zoology volume 11, Article number: 22 (2014) Cite this article

Abstract

Introduction

Onychophora is a relatively small phylum within Ecdysozoa, and is considered to be the sister group to Arthropoda. Compared to the arthropods, that have radiated into countless divergent forms, the onychophoran body plan is overall comparably simple and does not display much in-phylum variation. An important component of arthropod morphological diversity consists of variation of tagmosis, i.e. the grouping of segments into functional units (tagmata), and this in turn is correlated with differences in expression patterns of the Hox genes. How these genes are expressed in the simpler onychophorans, the subject of this paper, would therefore be of interest in understanding their subsequent evolution in the arthropods, especially if an argument can be made for the onychophoran system broadly reflecting the ancestral state in the arthropods.

Results

The sequences and embryonic expression patterns of the complete set of ten Hox genes of an onychophoran (Euperipatoides kanangrensis) are described for the first time. We find that they are all expressed in characteristic patterns that suggest a function as classical Hox genes. The onychophoran Hox genes obey spatial colinearity, and with the exception of Ultrabithorax (Ubx), they all have different and distinct anterior expression borders. Notably, Ubx transcripts form a posterior to anterior gradient in the onychophoran trunk. Expression of all onychophoran Hox genes extends continuously from their anterior border to the rear end of the embryo.

Conclusions

The spatial expression pattern of the onychophoran Hox genes may contribute to a combinatorial Hox code that is involved in giving each segment its identity. This patterning of segments in the uniform trunk, however, apparently predates the evolution of distinct segmental differences in external morphology seen in arthropods. The gradient-like expression of Ubx may give posterior segments their specific identity, even though they otherwise express the same set of Hox genes. We suggest that the confined domains of Hox gene expression seen in arthropods evolved from an ancestral onychophoran-like Hox gene pattern. Reconstruction of the ancestral arthropod Hox pattern and comparison with the patterns in the different arthropod classes reveals phylogenetic support for Mandibulata and Tetraconata, but not Myriochelata and Atelocerata.

Introduction

Arthropod segmentation – its origin and maintenance - is among the key topics of evolutionary developmental (Evo-Devo) research. Arthropods are of particular interest as they comprise the most speciose and disparate animal phylum. They form a clade together with the onychophorans and tardigrades, referred to as Panarthropoda [1]. The arthropods themselves include four or five (depending on the status of pygnogonids) classes [2, 3]: the insects, the crustaceans, the myriapods and the chelicerates (with or without the pycnogonids), although there is significant molecular support for insects being an ingroup to a paraphyletic “Crustacea”, the group in total being referred to as the Pancrustacea or Tetraconata [3, 4]. While the body plans of many arthropod groups have diversified significantly since the Cambrian Period, the lobopodian body plan, represented today by the onychophorans, appears to have changed relatively little [5–8]. Many of the key characteristics of the arthropods - such as jointed limbs and full adult body segmentation with pronounced segmental indentations - are not present in onychophorans, and, based on reconstructions of the arthropod stem-group, these absences are best interpreted as being primitive [9]. However, traces of such features, such as the genetic toolkit required for podomere patterning are present in the limbs of onychophorans [10], and arthropod-like appendages are present in stem-group arthropods such as the anomalocaridids [11, 12].

In Drosophila and to some extent in other arthropods, segmentation is under control of a hierarchic segmentation gene cascade reviewed in [13–15]. This cascade controls the expression of the Hox genes, which in turn specify segmental identity. It is believed that the Hox genes are involved in providing positional information in a combinatorial mode to give each segment its identity along the anterior-posterior body axis [16–19]. Thus, disturbance of the Hox patterning, such as loss-of-function or ectopic expression of Hox genes often results in homeotic transformations, the change of one segment’s identity into that of another [20–23]. Beyond that, Hox genes are believed to be involved in tagmosis, i.e. the grouping of segments into functional units (tagmata) e.g. [24, 25]. The Drosophila Hox clusters contain eight Hox genes, but the ancestral arthropod Hox cluster most likely contained ten Hox genes [26, 27]. Two of the Drosophila genes, however, have changed their function. These are fushi-tarazu (ftz) and Hox3. The latter gene evolved into bicoid (bcd), zerknüllt (zen), (also referred to as z1) and z2[28, 29]. These genes have lost their homeotic function and now have new expression patterns. In Drosophila, ftz acts as a pair rule gene [30], and bcd/zen-genes are involved in axis determination and formation of extraembryonic membranes [31]. However, in more basally branching arthropods, the expression patterns of Hox3 and ftz are consistent with canonical Hox-like domains [32–36].

As Hox gene expression in arthropods is quite diverse (reviewed in e.g. [27]), it is difficult to reconstruct the ancestral pattern of expression within the clade without reference to an outgroup, such as the onychophorans [37–39].

Here we report on the sequences and embryonic gene expression profiles of the complete set of the ten Hox genes in the onychophoran Euperipatoides kanangrensis. The new data contribute to our understanding of how the highly derived arthropod body plans have evolved from a rather uniform onychophoran-like ancestor. Based on the onychophoran data we reconstruct the ancestral arthropod Hox gene profile as far as possible and use this in a comparative approach to detect phylogenetic signal. We find support for Mandibulata and Tetraconata, but not Myriochelata and Atelocerata.

Material and methods

Species husbandry, embryo treatment, in situ hybridization, nuclei staining and data documentation

The collection, laboratory maintenance and dissection of embryos of Euperipatoides kanangrensis specimens are described in [40]. Whole mount in situ hybridization was performed as described in [10]. The developmental stage of all embryos was determined by analyzing embryos stained with the nuclear dye DAPI (4-6-Diamidino-2-phenylindole) and comparing to the stage table published by [41]. Embryos were analyzed under a Leica dissection microscope equipped with either an Axiocam (Zeiss) or a Leica DC100 digital camera. Brightness, contrast, and color values were adjusted in all images using the image processing software Adobe Photoshop CS2 (Version 9.0.1 for Apple Macintosh).

RT-PCR and gene cloning

Total RNA was isolated from freshly-dissected embryos of E. kanangrensis via TRIZOL (Invitrogen). Poly-A RNA was isolated with the PolyATtract mRNA isolation system III (Promega) and used to produce cDNA using the Superscript first strand synthesis system for RT-PCR (Invitrogen). Short fragments of the Hox gene orthologs of E. kanangrensis Sex combs reduced (Ek-Scr), fushi-tarazu (Ek-ftz) and Abdominal-B (Ek-Abd-B) were isolated via RT-PCR with degenerate primers. For that purpose mRNA was isolated and cDNA was synthesized from complete embryos representing all stages from the 1-cell stage up to stage 21 [41]. A list of the primers used is available from the authors upon request. Initial PCR fragments were elongated via 3′-RACE (for Ek-Scr, Ek-ftz and Ek-Abd-B) or 5′-RACE (for Ek-Antp) with the GENE RACER KIT (Invitrogen) to obtain sufficiently long fragments for subsequent in situ hybridization experiments. These sequences are available in GenBank under the accession numbers FR865437 (Ek-Scr), FR865438 (Ek-ftz), FR865439 (Ek-Antp), and FR865440 (Ek-Abd-B). We also screened two independently prepared embryonic transcriptomes of E. kanangrensis for the presence of Hox genes and found a single copy of each of the expected Hox gene orthologs. The embryonic transcriptomes were made from comparable stages as used for the RT-PCR screen (1-cell stage to stage 21) [41]. We discovered the complete open reading frames of all onychophoran Hox genes. These sequences are available under accession numbers HE979835 (Ek-lab), HE979836 (Ek-pb), HE979837 (Ek-Hox3), HE979838 (Ek-Dfd), HE979839 (Ek-Scr), HE979840 (Ek-ftz), HE979841 (Ek-Antp), HE979842 (Ek-Ubx), HE979843 (Ek-abd-A_splice variant I), HE979844 (Ek-abd-A_splice variant II), and HE979845 (Abd-B).

All fragments were cloned into the PCRII vector (Invitrogen). Sequences of all isolated fragments were determined from both strands by means of Big Dye chemistry on an ABI3730XL analyser by a commercial sequencing service (Macrogen, Korea).

Phylogenetic analysis

The complete homeodomains were aligned in Clustal_X [42, 43] and accuracy of the resulting alignment was checked by hand. Maximum likelihood analysis was performed using the LG substitution model [44] as implemented in PhyLM [45].

Segmental nomenclature

In order to facilitate description and comparison of the data, we label segments that express Hox genes in arthropods with the prefix “H”; H1 is thus the most anterior segment (corresponding variously to the onychophoran slime papilla segment, chelicerate pedipalps, insect and myriapod “intercalary” and crustacean second antenna segments) that expresses Hox genes (i.e. lab, pb and Hox3), thus avoiding the potentially thorny problem of how many segments lie in front of this. Onychophoran segments in general are labelled fap (frontal appendage), j (jaw), sp (slime papilla) and then L1-15 for the walking limb-bearing segments. L1 is thus H2.

Results

Sequence analysis of the ten onychophoran Hox genes

Partial sequences of the E. kanangrensis Hox gene orthologs Ek-lab, Ek-pb, Ek-Hox3, Ek-Dfd, and Ek-Ubx have been described in [40, 46]. We have now recovered the complete protein coding sequences of the ten onychophoran Hox genes. Orthology of the complete protein sequences of the E. kanangrensis Hox genes was determined by comparison with published orthologs of the beetle Tribolium castaneum. The published sequence of ftz in the sea spider Endeis spinosa was added to the analysis to reveal orthology of ftz genes (Additional file 1: Figure S1). We provide the alignment of conserved regions of the Hox genes from various arthropod and onychophoran species (see supplementary data for further information). Within the highly conserved regions lie diagnostic amino acids that are characteristic for each Hox gene (Additional file 2: Figure S2). We did not detect any duplicated Hox genes, neither in our PCR screens nor in the sequenced transcriptomes although two Abd-B paralogs have been reported for another onychophoran species, Akanthokara kaputensis (accession numbers AF011273 (Abd-B-1) and AF011274 (Abd-B-2)). Interestingly, we found one splice variant of Ek-abd-A with a hexapeptide (HX) sequence (Ek-abd-A-variant I), and one without this highly-conserved motif (Ek-abd-A-variant II). For all other onychophoran Hox genes we only identified transcripts with the HX motif (except for Ek-Abd-B, which generally lacks a HX motif) (Additional file 2: Figure S2). This result differs from the earlier published fragment of Ek-Dfd[40], which lacks a HX motif and also differs considerably in its complete N-terminal region from the newly recovered fragment of Ek-Dfd. The newly recovered fragment has significant sequence similarity with Dfd genes of other arthropods (Additional file 2: Figure S2). The previously published short fragment of Akanthokara Dfd[47] most probably represents an insect sequence since it contains a number of insect-specific amino acids (Additional file 2: Figure S2). The earlier published sequence of Ek-Hox3[40] also differs from the newly-recovered fragment. The former sequence contains a short string of additional amino acids between the HX motif and the homeodomain (HD). This sequence was found neither in the sequenced transcriptomes nor in newly-cloned fragments recovered by means of RT-PCR with gene specific primers that flanked the sequence in question (not shown). It remains unclear, however, whether the former sequence represents an artefact or a rare splice variant.

Expression of the ten onychophoran Hox genes

The expression profiles of Ek-lab, Ek-pb, Ek-Hox3 and Ek-Dfd have been described in [40] (Figures 1A-D and 2A-D). The expressions of all ten Hox genes are continuous from their respective anterior borders of expression back to the rear of the developing embryos.

Figure 1
figure 1

Expression of onychophoran Hox genes (lateral/ventral views). (A-H) Lateral views. (I-J) Ventral views. In all cases anterior is to the left. Upper row: schematic drawing of Hox gene expression. Middle row: bright-field photography (A-J). Lower row: DAPI staining (A’-J’) of the same embryos as shown in exactly the same position as in the middle row (A-J). Darker shading in schematic drawings indicates stronger expression. Lighter shading indicates weaker expression. Note that the expression of Ek-Ubx mRNA forms a posterior to anterior gradient with unclear anterior expansion (marked with a question mark (?)). Arrows in I-J point to expression in the anal valves. Abbreviations: e, eye; j, jaw; L1-L15, first to fifteenth walking limb; saz, segment addition zone; sp, slime papilla.

Full size image
Figure 2
figure 2

Expression of onychophoran Hox genes (ventral views). In all cases anterior is to the left. Arrows in A and B point to up-regulated expression of lab and pb in the ventral nervous system. The asterisk (*) in A indicates damage of ventral tissue as a result of the hybridization procedure. See text for further information. Abbreviations; av, anal valves; fap, frontal appendage; hl, head lobe; j, jaw, L1-L15, first to fifteenth walking limb; sp, lime papilla, vee, ventral extraembryonic ectoderm.

Full size image

labial

In addition to the previously-described expression we find that Ek-lab is expressed considerably more strongly in the slime papillae-bearing (sp) segment (Figures 1A and 2A) as compared to other segments, and expression is up-regulated in certain regions of the developing neuroectoderm of the trunk (Figure 2A). A spot of Ek-lab expression is located anteriorly and proximally in the slime papillae (Figure 2A).

proboscipedia

The only difference between the published expression pattern and our new data is that Ek-pb is up-regulated in some regions of the neuroectoderm (Figure 2B).

Hox3

Ek-Hox3 remains expressed in the posterior half of the slime papillae, and does not later disappear from this tissue (Figure 2C) cf. [40].

Deformed

The anterior border of Ek-Dfd is at the border between the jaw-bearing segment and the first trunk segment (L1) (Figures 1D and 2D). In embryos younger than stage 11, expression only extends into L2 (Additional file 3: Figure S3).

Sex combs reduced

The anterior border of Ek-Scr expression lies approximately in the middle of the first walking limb-bearing segment (L1) (Figures 1E, 2E and 3). From there the expression extends throughout the complete posterior body including the anal valves.

Figure 3
figure 3

Anterior borders of Ek-Hox3 , Ek-Scr, Ek-Dfd and Ek-ftz expression. A) Ek-Hox3 expression in sp and L1. Asterisk marks anterior border of expression in the middle of the slime papilla (sp) segment (cf. Eriksson et al. 2010). B) Expression of Ek-Dfd extends to the anterior of the L1 segment (cf. Eriksson et al. 2010). C) Ek-Scr. Asterisk marks anterior border of expression in the middle of the L1 segment. D) Ek-ftz. Asterisk marks anterior border of expression in the middle of the L2 segment. Abbreviations as in Figure 1. Dashed lines indicate segmental borders.

Full size image

fushi-tarazu

The anterior border of Ek-ftz lies in the middle of the second trunk segment (L2) (Figures 1F, 2F and 3). In embryos younger than stage 12, expression only extends anteriorly into L3 (Additional file 3: Figure S3).

Antennapedia

Ek-Antp is expressed in all posterior segments including all of L4. Expression in L4, however, is considerably weaker than in more posterior segments. In segments L5-L7, Ek-Antp is expressed stronger than in L4, but still slightly weaker than in L8 to L15, which is the last segment (Figures 1G and 2G). Whether expression in L5 to L7 forms a gradient, or if it is at the same level in these segments, is not revealed by our in situ hybridization technique. As described for Scr and ftz, expression of Antp also shifts towards the anterior at around stage 13 (Additional file 3: Figure S3).

Ultrabithorax

The Ek-Ubx gene is clearly expressed in an anterior to posterior gradient. The most anterior segment expressing Ek-Ubx at a detectable level is L6 (Figures 1H and 2H). The gradient makes it difficult to determine unambiguously the anterior-most extent of Ek-Ubx expression. Low-level transcription (below detectable range) may be present in L5.

abdominal-A

Ek-abd-A is exclusively expressed in the last trunk segment (L15) and the anal valves (Figure 1I). Notably, expression in the mesoderm is stronger than in the ectoderm and at late developmental stages Ek-abd-A is strongly expressed in the interface between L15 and the anal valves (Additional file 4: Figure S4). Note the difference between this specific staining and frequently occurring unspecific signal in L15 (Additional file 5: Figure S5).

Abdominal-B

Ek-Abd-B is expressed in the mesoderm of the entire anal valves, but ectodermal expression is restricted to the very posterior of the anal valves (Figure 1J and Additional file 4: Figure S4).

Generally, none of the ten onychophoran Hox genes are expressed in tissue dorsal to the base of the appendages (Figure 1). This is unlike the situation in arthropods where expression of the Hox genes is generally not restricted to ventral tissue e.g. [27, 34, 48].

Discussion

Comparison of arthropod and onychophoran Hox gene expression data

Although the expression patterns of the Hox genes are relatively conserved across the arthropods, some clade-specific differences exist [27]. Comparison between arthropod and onychophoran Hox gene expression patterns may aid in reconstructing ancestral and derived arthropod expression: firstly, shared features of onychophorans and arthropods are likely to have been present in the last common ancestor of both; and secondly, the onychophoran data can in some instances be used to polarise the order of Hox gene change within the arthropod tree itself. We have therefore mapped Hox gene expression patterns onto an arthropod plus onychophoran tree (Figure 4). The Mandibulata grouping (myriapods plus insects plus crustaceans) seems favoured over Paradoxopoda (myriapods and chelicerates) in recent phylogenies [49–53] and thus we have chosen this topology to map our data onto, although as noted below, some aspects of the onychophoran data do support Mandibulata and none support Paradoxopoda.

Figure 4
figure 4

Summary of phylogenetic signals based on onychophoran and arthropod Hox gene expression. Conserved and diverged characters are plotted on the nowadays best-supported arthropod phylogeny. Onychophora, and onychophoran data, serve as outgroup. Dark red boxes denote events during arthropod Hox gene evolution. Light red boxes denote unresolved character-state; in these cases the character-state cannot be determined ancestral or derived because outgroup data for a clade Onychophora + Arthropoda are not available.

Full size image

Onychophorans and arthropods share several important aspects of their Hox gene expression patterns. Firstly, in both onychophorans and arthropods, Hox gene expression is absent from tissue anterior to the slime papillae-bearing (intercalary/premandibulary/pedipalpal) segment [25, 34, 40, 54]: i.e., Hox gene expression never extends to the anterior-most segments in either clade. Secondly, all Hox genes, except onychophoran Ubx, have a distinct anterior expression border, although at early developmental stages in members of both phyla this border may be located one segment more posteriorly.

A difference between onychophorans and arthropods is that in arthropods Scr is expressed in H3, but in onychophorans it is in H2. It would appear that either the onychophoran pattern is derived, or that a shift in the anterior extension of Scr evolved in the lineage leading to the arthropods (Figures 4 and 5 and Additional file 6: Table S1). Another apparent difference concerns the posterior extent of gene expression. In E. kanangrensis the expression of all Hox genes extends back to the rear of the embryo [40], this study; but in arthropods, the “anterior” Hox genes are typically not expressed in the posterior part of the body. However, data on Hox gene expression in species of the Chelicerata and Myriapoda provide evidence that the onychophoran Hox gene pattern may in this respect reflect the ancestral condition for Onychophora + Arthropoda. In the harvestman Phalangium opilio[36] (Figure 5A), the spider Achaearanea tepidariorum[55], the mite Archegozetes longisetosus[56], the centipede Lithobius atkinsoni[54] and the millipede Glomeris marginata[34] (Figure 5A), the expression of at least some anterior Hox genes extends from their anterior border of expression to the rear end of the embryo. In other cases anterior Hox genes are also expressed in the most posterior segment(s) and/or the segment addition zone (SAZ) (Figure 5A). We believe that weak (but clearly detectable) expression of some Hox genes in the posterior segments and expression in the last segment (or the SAZ) may represent evolutionary remnants of an ancestral state more clearly retained in onychophorans. Taken together, these data indicate a tendency in arthropod evolution to restrict anterior Hox gene expression to distinct anterior regions.

Figure 5
figure 5

Comparison of Hox gene expression profiles in the onychophoran E. kanangrensis , the myriapod Glomeris marginata and the harvestman Phalangium opilio, and reconstruction of the putative Hox gene pattern in the common ancestor. Orthologous genes are with identical colours. Conserved anterior and posterior borders of expression (compared to E. kanangrensis) are marked with asterisks (*). Borders of expression that are conserved in the myriapod and the harvestman (but not the onychophoran) are marked with filled circles (•). Smaller bars indicate weaker expression. ‘Delayed’ expression is marked with ‘d]’. Green bar to the left indicates good support for the predicted corresponding expression patterns in the ancestor; yellow bars indicate ambiguous support for the reconstructed expression patterns; red bar indicates that the ancestral expression pattern of abd-A is not predictable. This is also indicated by question marks (?). Dashed vertical lines indicate an either segmental or parasegmental (dashed line) anterior expression border. Hox gene-expressing segments are labelled with the prefix ‘H’. Abbreviations are as in Figure 1, and an, antennal segment; ch, cheliceral segment; L1-L4 (in chelicerates), walking limb-bearing segments one to four; md, mandibular segment; mx, maxillary segment; O1-O9, first to ninth opisthosomal segment; pa, pre-antennal region; ped, pedipalpal segment; pmd, premandibular segment; pmx, postmaxillary segment; SAZ, segment addition zone; T1-T8, first to eighth walking limb-bearing segment.

Full size image

Clade-specific comparisons between onychophorans and arthropods

As well as the general similarities (and differences) highlighted above, onychophorans share several similarities at the arthropod clade-specific level, in particular in conservation of anterior Hox gene expression borders (summarised in Figure 4). Although the anterior Hox gene pattern of pb and Hox3 is highly conserved, it deviates in some clades at least in insects, and these latter seem therefore to be derived. Secondly, deviation from the pattern of ftz expression found in onychophorans is only found in crustaceans and insects, supporting the Tetraconata (Pancrustacea) hypothesis. Thirdly, the anterior border of Antp seen in onychophorans has switched from H5 to H4 in myriapods, crustaceans and insects, in agreement with the Mandibulata concept. Fourthly, the posterior reduction of expression of the anterior Hox genes discussed above progresses from onychophorans, where expression of all the Hox genes extend to the rear end, to crustaceans and insects, where expression is more confined to distinct anterior regions (Figure 5A and Figure twelve in [27]). This again is in agreement with the Tetraconata concept. Conversely, the polarisation possible with the onychophoran data does not support either Myriochelata or Atelocerata.

Taken together, the differences and similarities in the expression data between onychophorans and arthropods allow a reasonable degree of reconstruction of the ancestral Hox expression for the entire clade (Figure 5B). We find good support for the reconstruction of the pattern of anterior Hox genes (lab, pb, Hox3, Dfd, Scr, Antp), but also that the reconstruction of posterior Hox genes is difficult (Ubx, abd-A, Abd-B) (Figure 5B). The varying anterior border of abd-A in the onychophoran and various arthropods makes it impossible to reconstruct its ancestral pattern. The lability of abd-A is highlighted by the loss of this gene from e.g. the mite Tetranychus urticae[57]. Among the reconstructable patterns some uncertainties remain, such as whether the Ubx gradient in onychophorans is ancestral or derived, and the anterior expression boundary of Scr. These uncertainties might in principle be resolved by reference to a suitable outgroup such as a tardigrade or a cycloneuralian worm. Unfortunately, Hox gene expression and action in the nematode Caenorhabditis elegans is highly derived [58], and no other cycloneuralian expression patterns are known. Development of a priapulid in situ hybridization protocol [59], however, opens the possibility of such data being obtained in the future.

Hox gene expression and tagmosis in arthropods

Hox gene expression has long been associated with the evolution and maintenance of tagmosis, i.e. the characteristic grouping or fusion of functionally similar segments e.g. [24, 25, 36, 60]. Ever since the earliest days of Hox gene research, the dominant hypothesis has been that the Hox genes primarily act to specify regions of the body, including above all the tagmata [16].

Although onychophorans have a relatively unspecialised body plan, with only the head and most posterior segment being differentiated, their Hox gene expression patterns show a surprising degree of sophistication, for example in the gradient of expression of Ubx. This pattern mirrors a similar one documented in limb specification, which in onychophorans is also surprisingly sophisticated [10].

In the onychophoran studied, the anterior segments (sp-L5) and the last segment (L15) express a unique set of Hox genes, which allows for the characterization of each of these segments sensu[17] (Figure 5A). The posterior segments (L6-L14), however, all express the same eight Hox genes. The same is true for many arthropods where the posterior segments are usually not characterised by a unique set of Hox genes [27]. It is possible that posterior segments in onychophorans do not require a specific set of Hox gene input as they appear to be morphologically identical, but that would then raise the question why the anterior (morphologically identical) trunk segments in onychophorans do express distinct sets of Hox genes (Figure 5A). It is of course possible that there are some cryptic morphological differences in these segments that are being regulated by differential Hox gene expression. However, if this is the case, then it is possible that such cryptic morphological differences are present in the posterior segments too, and this would raise the question of how these segments are specified within identical Hox gene expression domains. Generally, the mRNA expression pattern can differ from the protein pattern as a result of translational repression, and this could lead to different Hox-protein and Hox-mRNA landscapes. Further differences in segmental Hox gene patterning might also involve Hox cofactors [61–63], the presence of alternative splice variants e.g. [64] (possibly as represented by the different splice variants of Ek-abd-A), and temporal differences in Hox gene expression [65, 66]. Such temporal differences include the shifting anterior expression borders of Ek-Scr, Ek-ftz, and Ek-Antp (Additional file 3: Figure S3).

Ek-Ubx mRNA is expressed in an anterior to posterior gradient with detectable transcripts from the very posterior of the embryo to at least L6. It is thus possible that the different levels of Ek-Ubx mRNA (and resulting Ek-Ubx protein) are sufficient to give these segments a unique Hox signature. Studies in at least Drosophila do indeed show that Ubx function in segmentation and limb development is dependent on different levels of expression [67, 68]. Similarly, in the crustacean Parhyale, different levels of Ubx expression may be responsible for the development of different types of appendages, and knock down of Ubx results in homeotic transformation of these segments [69]. The Ek-Ubx gradient thus offers one possibility of how each posterior segment is uniquely patterned, even though they express the same set of Hox genes.

References

  1. Campbell LI, Rota-Stabelli O, Edgecombe GD, Marchioro T, Longhorn SJ, Telford MJ, Philippe H, Rebecchi L, Peterson KJ, Pisani D: MicroRNAs and phylogenomics resolve the relationships of Tardigrada and suggest that velvet worms are the sister group of Arthropoda. Proc Natl Acad Sci USA. 2011, 108: 15920-15924. 10.1073/pnas.1105499108.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  2. Dunlop JA, Arango CP: Pycnogonid affinities: a review. J Zool Syst Evol Res. 2005, 43: 8-21. 10.1111/j.1439-0469.2004.00284.x.

    Article  Google Scholar 

  3. Giribet G, Edgecombe GD: Reevaluating the arthropod tree of life. Annu Rev Entomol. 2012, 57: 167-186. 10.1146/annurev-ento-120710-100659.

    Article  PubMed  CAS  Google Scholar 

  4. Dohle W: Are the insects terrestrial crustaceans? A discussion of some new facts and arguments and the proposal of the proper name “Tetraconata” for the monophyletic unit Crustacea + Hexapoda. Ann Soc Entomol Fr. 2001, 37: 85-103.

    Google Scholar 

  5. Whittington HB: The lobopod animal Aysheaia pedunculata Walcott, Middle Cambrian, Burgess Shale, British Columbia. Philos Trans R Soc Lond B Biol Sci. 1978, 284: 165-197. 10.1098/rstb.1978.0061.

    Article  Google Scholar 

  6. Thompson I, Jones DS: A possible onychophoran from the Middle Pennsylvanian Mazon Creek Beds of northern Illinois. J Paleontol. 1980, 54: 588-596.

    Google Scholar 

  7. Dzik J, Krumbiegel G: The oldest ‘onychophoran’ Xenusion: a link connecting phyla?. Lethaia. 1989, 22: 169-181. 10.1111/j.1502-3931.1989.tb01679.x.

    Article  Google Scholar 

  8. Ou Q, Liu J, Shu D, Han J, Zhang Z, Wan X, Lei Q: A rare onychophoran-like lobopodian from the Lower Cambrian Chengjiang Lagerstätte, Southwest China, and its phylogenetic implications. J Paleontol. 2011, 85: 587-594. 10.1666/09-147R2.1.

    Article  Google Scholar 

  9. Budd GE: Tardigrades as ‘stem-group arthropods’: the evidence from the Cambrian fauna. Zool Anz. 2001, 240: 265-279. 10.1078/0044-5231-00034.

    Article  Google Scholar 

  10. 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: 363-372. 10.1111/j.1525-142X.2010.00423.x.

    Article  PubMed  CAS  Google Scholar 

  11. Daley AC, Budd GE, Caron JB, Edgecombe GD, Collins D: The Burgess Shale anomalocaridid Hurdia and its significance for early euarthropod evolution. Science. 2009, 323: 1597-1600. 10.1126/science.1169514.

    Article  PubMed  CAS  Google Scholar 

  12. Daley AC, Budd GE: New anomalocaridid appendages from the Burgess Shale, Canada. Palaeontology. 2010, 53: 721-738. 10.1111/j.1475-4983.2010.00955.x.

    Article  Google Scholar 

  13. Klingler M, Tautz D: Formation of embryonic axes and blastoderm pattern in Drosophila. Development, Genetics, Epigenetics and Environmental Regulation. Edited by: Russo VEA, Cove DJ, Edgar LG, Jaenisch R, Salamini F. 1999, Berlin: Springer, 311-330.

    Google Scholar 

  14. Pankratz MJ, Jäckle H: Blastoderm segmentation. The development of Drosophila melanogaster. Edited by: Bate M, Martinez Arias A. 1993, Cold Spring Harbor: Cold Spring Harbor Laboratory Press, 467-516.

    Google Scholar 

  15. Damen WGM: Evolutionary conservation and divergence of the segmentation process in arthropods. Dev Dyn. 2007, 236: 1379-1391. 10.1002/dvdy.21157.

    Article  PubMed  CAS  Google Scholar 

  16. Lewis EB: A gene complex controlling segmentation in Drosophila. Nature. 1978, 276: 565-570. 10.1038/276565a0.

    Article  PubMed  CAS  Google Scholar 

  17. Struhl G: Genes controlling segmental specification in the Drosophila thorax. Proc Natl Acad Sci USA. 1982, 79: 7380-7384. 10.1073/pnas.79.23.7380.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  18. Lawrence PA, Morata G: Homeobox genes: their function in Drosophila segmentation and pattern formation. Cell. 1994, 78: 181-189. 10.1016/0092-8674(94)90289-5.

    Article  PubMed  CAS  Google Scholar 

  19. Akam M: Hox genes, homeosis and the evolution of segment identity: no need for hopeless monsters. Int J Dev Biol. 1998, 42: 445-451.

    PubMed  CAS  Google Scholar 

  20. Pultz MA, Diederich RJ, Cribbs DL, Kaufman TC: The proboscipedia locus of the Antennapedia complex: a molecular and genetic analysis. Genes Dev. 1988, 2: 901-920. 10.1101/gad.2.7.901.

    Article  PubMed  CAS  Google Scholar 

  21. Hughes CL, Kaufman TC: RNAi analysis of Deformed, proboscipedia and Sex combs reduced in the milkweed bug Oncopeltus fasciatus: novel roles for Hox genes in the hemipteran head. Development. 2000, 127: 3683-3694.

    PubMed  CAS  Google Scholar 

  22. Pavlopoulos A, Kontarakis Z, Liubicich DM, Serano JM, Akam M, Patel NH, Averof M: Probing the evolution of appendage specialization by Hox gene misexpression in an emerging model crustacean. Proc Natl Acad Sci USA. 2009, 106: 13897-13902. 10.1073/pnas.0902804106.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  23. Khadjeh S, Turetzek N, Pechmann M, Schwager EE, Wimmer EA, Damen WG, Prpic NM: Divergent role of the Hox gene Antennapedia in spiders is responsible for the convergent evolution of abdominal limb repression. Proc Natl Acad Sci USA. 2012, 109: 4921-4926. 10.1073/pnas.1116421109.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  24. Akam M: Arthropods: developmental diversity within a (super) phylum. Proc Natl Acad Sci USA. 2000, 97: 4438-4441. 10.1073/pnas.97.9.4438.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  25. Damen WGM, Hausdorf M, Seyfarth E-A, Tautz D: A conserved mode of head segmentation in arthropods revealed by the expression pattern of Hox genes in a spider. Proc Natl Acad Sci USA. 1998, 95: 10665-10670. 10.1073/pnas.95.18.10665.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  26. Cook CE, Smith LM, Telford MJ, Bastianello A, Akam M: Hox genes and the phylogeny of the arthropods. Curr Biol. 2001, 11: 759-763. 10.1016/S0960-9822(01)00222-6.

    Article  PubMed  CAS  Google Scholar 

  27. Hughes CL, Kaufman TC: Hox genes and the evolution of the arthropod body plan. Evol Dev. 2002, 4: 459-499. 10.1046/j.1525-142X.2002.02034.x.

    Article  PubMed  CAS  Google Scholar 

  28. Rushlow C, Doyle H, Hoey T, Levine M: Molecular characterization of the zerknüllt region of the Antennapedia gene complex in Drosophila. Genes Dev. 1987, 1: 1268-1279. 10.1101/gad.1.10.1268.

    Article  PubMed  CAS  Google Scholar 

  29. Stauber M, Jackle H, Schmidt-Ott U: The anterior determinant bicoid of Drosophila is a derived Hox class 3 gene. Proc Natl Acad Sci USA. 1999, 96: 3786-3789. 10.1073/pnas.96.7.3786.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  30. Jürgens G, Wieschaus E, Nüsslein-Volhard C, Kluding H: Mutations affecting the pattern of the larval cuticle in Drosophila melanogaster. II. Zygotic loci on the third chromosome. Wilhelm Roux’s Arch Dev Biol. 1984, 193: 283-295. 10.1007/BF00848157.

    Article  Google Scholar 

  31. Stauber M, Prell A, Schmidt-Ott U: A single Hox3 gene with composite bicoid and zerknüllt expression characteristics in non-Cyclorrhaphan flies. Proc Natl Acad Sci USA. 2002, 99: 274-279. 10.1073/pnas.012292899.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  32. Hughes CL, Liu PZ, Kaufman TC: Expression patterns of the rogue Hox genes Hox3/zen and fushi tarazu in the apterygote insect Thermobia domestica. Evol Dev. 2004, 6: 393-401. 10.1111/j.1525-142X.2004.04048.x.

    Article  PubMed  CAS  Google Scholar 

  33. Damen WGM, Janssen R, Prpic N-P: Pair rule gene orthologs in spider segmentation. Evol Dev. 2005, 7: 618-628. 10.1111/j.1525-142X.2005.05065.x.

    Article  PubMed  Google Scholar 

  34. Janssen R, Damen WGM: The ten Hox genes of the millipede Glomeris marginata. Dev Genes Evol. 2006, 216: 451-465. 10.1007/s00427-006-0092-5.

    Article  PubMed  CAS  Google Scholar 

  35. Papillon D, Telford MJ: Evolution of Hox3 and ftz in arthropods: insights from the crustacean Daphnia pulex. Dev Genes Evol. 2007, 217: 315-322. 10.1007/s00427-007-0141-8.

    Article  PubMed  CAS  Google Scholar 

  36. Sharma PP, Schwager EE, Extavour CG, Giribet G: Hox gene expression in the harvestman Phalangium opilio reveals divergent patterning of the chelicerate opisthosoma. Evol Dev. 2012, 14: 450-463. 10.1111/j.1525-142X.2012.00565.x.

    Article  PubMed  CAS  Google Scholar 

  37. Whitington PM, Mayer G: The origins of the arthropod nervous system: insights from the Onychophora. Arthropod Struct Dev. 2011, 40: 193-209. 10.1016/j.asd.2011.01.006.

    Article  PubMed  Google Scholar 

  38. Hering L, Henze MJ, Kohler M, Kelber A, Bleidorn C, Leschke M, Nickel B, Meyer M, Kircher M, Sunnucks P, Mayer G: Opsins in Onychophora (velvet worms) suggest a single origin and subsequent diversification of visual pigments in arthropods. Mol Biol Evol. 2012, 29: 3451-3458. 10.1093/molbev/mss148.

    Article  PubMed  CAS  Google Scholar 

  39. Eriksson BJ, Fredman D, Steiner G, Schmid A: Characterisation and localization of the opsin protein repertoire in the brain and retinas of a spider and an onychophoran. BMC Evol Biol. 2013, 13: 186-10.1186/1471-2148-13-186.

    Article  PubMed  PubMed Central  Google Scholar 

  40. 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: 117-122. 10.1007/s00427-010-0329-1.

    Article  PubMed  Google Scholar 

  41. 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: 224-234. 10.1016/j.ydbio.2013.07.010.

    Article  PubMed  CAS  Google Scholar 

  42. Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG: The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res. 1997, 25: 4876-4882. 10.1093/nar/25.24.4876.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  43. Henikoff S, Henikoff JG: Amino acid substitution matrices from protein blocks. Proc Natl Acad Sci USA. 1992, 89: 10915-10919. 10.1073/pnas.89.22.10915.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  44. Le SQ, Gascuel O: An improved general amino acid replacement matrix. Mol Biol Evol. 2008, 25: 1307-1320. 10.1093/molbev/msn067.

    Article  PubMed  CAS  Google Scholar 

  45. Guindon S, Gascuel O: A simpel, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Syst Biol. 2001, 52: 696-704.

    Article  Google Scholar 

  46. Janssen R, Budd GE: Gene expression suggests conserved aspects of Hox gene regulation in arthropods and provides additional support for monophyletic Myriapoda. EvoDevo. 2010, 1: 4-10.1186/2041-9139-1-4.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  47. Grenier JK, Garber TL, Warren R, Whitington PM, Carroll S: Evolution of the entire arthropod Hox gene set predated the origin and radiation of the onychophoran/arthropod clade. Curr Biol. 1997, 7: 547-553. 10.1016/S0960-9822(06)00253-3.

    Article  PubMed  CAS  Google Scholar 

  48. Shippy TD, Rogers CD, Beeman RW, Brown SJ, Denell RE: The Tribolium castaneum ortholog of Sex combs reduced controls dorsal ridge development. Genetics. 2006, 74: 297-307.

    Article  Google Scholar 

  49. Shultz JW, Regier JC: Phylogenetic analysis of arthropods using two nuclear protein-encoding genes supports a crustacean + hexapod clade. Proc Biol Sci. 2000, 267: 1011-1019. 10.1098/rspb.2000.1104.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  50. Regier JC, Shultz JW, Kambic RE: Pancrustacean phylogeny: hexapods are terrestrial crustaceans and maxillopods are not monophyletic. Proc Biol Sci. 2005, 272: 395-401. 10.1098/rspb.2004.2917.

    Article  PubMed  PubMed Central  Google Scholar 

  51. von Reumont BM, Jenner RA, Wills MA, Dell’ampio E, Pass G, Ebersberger I, Meyer B, Koenemann S, Iliffe TM, Stamatakis A, Niehuis O, Meusemann K, Misof B: Pancrustacean phylogeny in the light of new phylogenomic data: support for Remipedia as the possible sister group of Hexapoda. Mol Biol Evol. 2012, 29: 1031-1045. 10.1093/molbev/msr270.

    Article  PubMed  CAS  Google Scholar 

  52. Rota-Stabelli O, Campbell L, Brinkmann H, Edgecombe GD, Longhorn SJ, Peterson KJ, Pisani D, Philippe H, Telford MJ: A congruent solution to arthropod phylogeny: phylogenomics, microRNAs and morphology support monophyletic Mandibulata. Proc Biol Sci. 2011, 278: 298-306. 10.1098/rspb.2010.0590.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  53. Sombke A, Lipke E, Kenning M, Müller CH, Hansson BS, Harzsch S: Comparative analysis of deutocerebral neuropils in Chilopoda (Myriapoda): implications for the evolution of the arthropod olfactory system and support for the Mandibulata concept. BMC Neurosci. 2012, 13: 1-17. 10.1186/1471-2202-13-1.

    Article  PubMed  PubMed Central  Google Scholar 

  54. Hughes CL, Kaufman TC: Exploring the myriapod body plan: expression patterns of the ten Hox genes in a centipede. Development. 2002, 19: 1225-1238.

    Google Scholar 

  55. Abzhanov A, Popadic A, Kaufman TC: Chelicerate Hox genes and the homology of arthropod segments. Evol Dev. 1999, 1: 77-89. 10.1046/j.1525-142x.1999.99014.x.

    Article  PubMed  CAS  Google Scholar 

  56. Telford MJ, Thomas RH: Of mites and zen: expression studies in a chelicerate arthropod confirm zen is a divergent Hox gene. Dev Genes Evol. 1998, 208: 591-594. 10.1007/s004270050219.

    Article  PubMed  CAS  Google Scholar 

  57. Grbic M, Van Leeuwen T, Clark RM, Rombauts S, Rouze P, Grbic V, Osborne EJ, Dermauw W, Ngoc PC, Ortego F, Hernandez-Crespo P, Diaz I, Martinez M, Navajas M, Sucena E, Magalhaes S, Nagy L, Pace RM, Djuranovic S, Smagghe G, Iga M, Christiaens O, Veenstra JA, Ewer J, Villalobos RM, Hutter JL, Hudson SD, Velez M, Yi SV, Zeng J, et al: The genome of Tetranychus urticae reveals herbivorous pest adaptations. Nature. 2011, 479: 487-492. 10.1038/nature10640.

    Article  PubMed  CAS  Google Scholar 

  58. Aboobaker A, Blaxter M: Hox gene evolution in nematodes: novelty conserved. Curr Opin Genet Dev. 2003, 13: 593-598. 10.1016/j.gde.2003.10.009.

    Article  PubMed  CAS  Google Scholar 

  59. Martin-Duran JM, Janssen R, Wennberg S, Budd GE, Hejnol A: Deuterostomic development in the protostome Priapulus caudatus. Curr Biol. 2012, 22: 2161-2166. 10.1016/j.cub.2012.09.037.

    Article  PubMed  CAS  Google Scholar 

  60. Schwager EE, Schoppmeier M, Pechmann M, Damen WG: Duplicated Hox genes in the spider Cupiennius salei. Front Zool. 2007, 4: 1-10.1186/1742-9994-4-1.

    Article  Google Scholar 

  61. Mann RS: The specificity of homeotic gene function. Bioessays. 1995, 17: 855-863. 10.1002/bies.950171007.

    Article  PubMed  CAS  Google Scholar 

  62. Mahaffey JW: Assisting Hox proteins in controlling body form: are there new lessons from flies (and mammals)?. Curr Opin Genet Dev. 2005, 15: 422-429. 10.1016/j.gde.2005.06.009.

    Article  PubMed  CAS  Google Scholar 

  63. Joshi R, Sun L, Mann R: Dissecting the functional specificities of two Hox proteins. Genes Dev. 2010, 24: 1533-1545. 10.1101/gad.1936910.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  64. Reed HC, Hoare T, Thomsen S, Weaver TA, White RA, Akam M, Alonso CR: Alternative splicing modulates Ubx protein function in Drosophila melanogaster. Genetics. 2010, 184: 745-775. 10.1534/genetics.109.112086.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  65. Castelli-Gair J, Akam M: How the Hox gene Ultrabithorax specifies two different segments: the significance of spatial and temporal regulation within metameres. Development. 1995, 121: 2973-2982.

    PubMed  CAS  Google Scholar 

  66. Castelli-Gair J: Implications of the spatial and temporal regulation of Hox genes on development and evolution. Int J Dev Biol. 1998, 42: 437-444.

    PubMed  CAS  Google Scholar 

  67. Smolik-Utlaut SM: Dosage requirements of Ultrabithorax and bithoraxoid in the determination of segment identity in Drosophila melanogaster. Genetics. 1990, 124: 357-366.

    PubMed  CAS  PubMed Central  Google Scholar 

  68. Tour E, Hittinger CT, McGinnis W: Evolutionarily conserved domains required for activation and repression functions of the Drosophila Hox protein Ultrabithorax. Development. 2005, 132: 5271-5281. 10.1242/dev.02138.

    Article  PubMed  CAS  Google Scholar 

  69. Liubicich DM, Serano JM, Pavlopoulos A, Kontarakis Z, Protas ME, Kwan E, Chatterjee S, Tran KD, Averof M, Patel NH: Knockdown of Parhyale Ultrabithorax recapitulates evolutionary changes in crustacean appendage morphology. Proc Natl Acad Sci USA. 2009, 106: 13892-13896. 10.1073/pnas.0903105106.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

Download references

Acknowledgements

Financial funding was provided to GEB by the Swedish Natural Science Council (VR) and the Swedish Royal Academy of Sciences (KVA), and to GEB and RJ by the European Union via the Marie Curie Training networks “ZOONET” (MRTN-CT-2004-005624). We wish to thank Jean Joss, Robyn Stutchbury and Rolf Ericsson for their most appreciated help during onychophoran collection. The onychophoran transcriptome was analyzed with the help of Nico Posnien and Alistair McGregor.

We gratefully acknowledge the support of the NSW Government Department of Environment and Climate Change by provision of a permit SL100159 to collect onychophorans at Kanangra Boyd National Park, and to the Australian Government Department of the Environment, Water, Heritage and the Arts for export permits WT2009-4598 and WT2012-4704.

Author information

Authors and Affiliations

  1. Department of Earth Sciences, Palaeobiology, Uppsala University, Villavägen 16, 75236, Uppsala, Sweden

    Ralf Janssen & Graham E Budd

  2. Department of Neurobiology, University of Vienna, Althanstrasse 14, 1090, Vienna, Austria

    Bo Joakim Eriksson

  3. Department of Biological Sciences, Macquarie University, Sydney, NSW, 2109, Australia

    Noel N Tait

Authors
  1. Ralf Janssen
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Bo Joakim Eriksson
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Noel N Tait
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Graham E Budd
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding author

Correspondence to Ralf Janssen.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

RJ designed the project, carried out the experiments and wrote the first draft of the manuscript. BJE isolated fragments of some Hox genes prior to the availability of sequenced transcriptomes, and provided additional transcriptome data. NNT provided interpretation and discussion and was involved in writing of the final version of the manuscript. He also identified the species. GB provided interpretation and discussion and was involved in writing of the final version of the manuscript. All authors read and accepted the final manuscript.

Electronic supplementary material

12983_2013_311_MOESM1_ESM.tiff

Additional file 1: Figure S1: Phylogenetic analysis of E. kanangrensis Hox genes. The homeodomain sequences have been used for the analyses. The phylogram represents the unrooted majority rule consensus computed from 100 replicas. Numbers indicate the reliability values of the branches. (TIFF 6 MB)

12983_2013_311_MOESM2_ESM.tiff

Additional file 2: Figure S2: Conserved protein motifs in arthropod and onychophoran Hox genes. Onychophoran Hox sequences (E. kanangrensis and Akanthokara kaputensis) are aligned with orthologous genes of at least one species representing the four main arthropod classes (i.e. Insecta, Crustacea, Myriapoda and Chelicerata). Identical amino acids (compared to E. kanangrensis) are shaded in grey; amino acids that are conserved in arthropods are shaded in yellow; diagnostic amino acids are shaded in red. Amino acids in red font indicate insect-specific positions (see text for further information). Question marks (?) stand for unknown sequence. Dashes (-) indicate the absence of any amino acid in this position of the alignment. Sequences of E. kanangrensis are underlined. Asterisks (*) mark G. marginata sequences that are partially recovered from an embryonic transcriptome. Abbreviations: Af, Artemia franciscana (Crustacea); Ak, Akanthokara kaputensis (Onychophora); At, Achaearanea tepidariorum (Chelicerata); Cs, Cupiennius salei (Chelicerata); Dm, Daphnia magna (Crustacea) Dp, Daphnia pulex (Crustacea); Ek, Euperipatoides kanangrensis (Onychophora); Glomeris marginata (Myriapoda); Mb, Mamestra brassicae (Insecta); Sm, Strigamia maritima (Myriapoda); Tc, Tribolium castaneum (Insecta). (TIFF 19 MB)

12983_2013_311_MOESM3_ESM.tiff

Additional file 3: Figure S3: Shifted anterior borders of Hox gene expression. All embryos are oriented with anterior to the left. A/B: Ventral view. C-H: lateral view. A-H) bright field photographs; A’-H’) DAPI staining of the same embryos shown in A-H. Double-headed arrows point to anterior border of expression. Faint arrows indicate weak expression. A) Expression of Ek-Dfd is anteriorly restricted to L2 (stage 9/10). B) At stage 11 Ek-Dfd expression extends to the anterior border of L1. C) Expression of Ek-Scr extends into the middle of L2 at stage 12. D) At stage 13 Ek-Scr shifts towards anterior into the L1-segment. E) Anterior border of expression of Ek-ftz is in the middle of L3 at stage 11. F) At the subsequent stage 12, Ek-ftz is weakly present also in L2. G) Expression of Ek-Antp is restricted to L5 (and more posterior segments) at stage 12. H) At stage 13, Ek-Antp reaches anteriorly into the L4 segment where it remains expressed weakly during further development. Shifting of the anterior border of expression was never observed for any of the other onychophoran Hox genes. Abbreviations: L1-L5, first to fifth walking limb-bearing segment. (TIFF 15 MB)

12983_2013_311_MOESM4_ESM.tiff

Additional file 4: Figure S4: Additional aspects of Ek-abd-A and Ek-Abd-B expression. In all panels anterior is to the left. A) Expression of Ek-abd-A. Ventral view. Expression in the mesoderm (mes) is stronger than in the ectoderm (ec). B) Expression of Ek-abd-A; dorsal view. C) Expression of Ek-Abd-B. Ventral view. The arrow points to expression in the ectoderm of the anal valves. Abbreviations: a, anus; av, anal valve; ec, ectoderm; mes, mesoderm; L14 and L15, fourteenth and fifteenth walking-limb bearing segment. (TIFF 5 MB)

12983_2013_311_MOESM5_ESM.tiff

Additional file 5: Figure S5: Frequently occurring staining artefacts. In all panels anterior is to the left. A) Stage 19 embryo. Ventral view. Typical staining artefacts are often observed in older stage embryos where the surface of the frontal appendages attracts unspecific signal. A similar false positive signal appears regularly in the opening of the slime papillae. The coelomic cavity of the L15-segment often stains unspecifically. Long staining time frequently results in unspecific staining of the yolk. B/C) A typical artefact: staining of one of the two coelomic cavities (arrowheads) of the head in a stage 13 and a stage 20 embryo. Abbreviations: fap, frontal appendage; L15, fifteenth walking limb; sp, lime papilla. (TIFF 7 MB)

12983_2013_311_MOESM6_ESM.doc

Additional file 6: Table S1: Summary of available literature on Hox gene expression in arthropods and onychophorans. Compared is the anterior-most extension of Hox gene mRNA (in some cases protein) expression. (DOC 113 KB)

Authors’ original submitted files for images

Rights and permissions

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Cite this article

Janssen, R., Eriksson, B.J., Tait, N.N. et al. Onychophoran Hox genes and the evolution of arthropod Hox gene expression. Front Zool 11, 22 (2014). https://0-doi-org.brum.beds.ac.uk/10.1186/1742-9994-11-22

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://0-doi-org.brum.beds.ac.uk/10.1186/1742-9994-11-22

Keywords

Frontiers in Zoology

ISSN: 1742-9994