Expression of myriapod pair rule gene orthologs
© Janssen et al. 2011
Received: 18 October 2010
Accepted: 25 February 2011
Published: 25 February 2011
Segmentation is a hallmark of the arthropods; most knowledge about the molecular basis of arthropod segmentation comes from work on the fly Drosophila melanogaster. In this species a hierarchic cascade of segmentation genes subdivides the blastoderm stepwise into single segment wide regions. However, segmentation in the fly is a derived feature since all segments form virtually simultaneously. Conversely, in the vast majority of arthropods the posterior segments form one at a time from a posterior pre-segmental zone. The pair rule genes (PRGs) comprise an important level of the Drosophila segmentation gene cascade and are indeed the first genes that are expressed in typical transverse stripes in the early embryo. Information on expression and function of PRGs outside the insects, however, is scarce.
Here we present the expression of the pair rule gene orthologs in the pill millipede Glomeris marginata (Myriapoda: Diplopoda). We find evidence that these genes are involved in segmentation and that components of the hierarchic interaction of the gene network as found in insects may be conserved. We further provide evidence that segments are formed in a single-segment periodicity rather than in pairs of two like in another myriapod, the centipede Strigamia maritima. Finally we show that decoupling of dorsal and ventral segmentation in Glomeris appears already at the level of the PRGs.
Although the pair rule gene network is partially conserved among insects and myriapods, some aspects of PRG interaction are, as suggested by expression pattern analysis, convergent, even within the Myriapoda. Conserved expression patterns of PRGs in insects and myriapods, however, may represent ancestral features involved in segmenting the arthropod ancestor.
The expression of the pair rule genes (PRGs) in seven transversal stripes is the first sign of metamerization in Drosophila. Primary PRGs are regulated in a double segmental periodicity by upstream-acting maternal-effect genes and zygotically-expressed gap genes at the blastoderm stage. The primary PRGs then regulate the expression of the secondary PRGs in a similar double segmental pattern (reviewed in [1, 2]). This expression pattern in alternating segments is also reflected in the phenotypes of null mutants of these genes: the loss of alternating segmental structures (hence, the name "pair rule") . Later in the extended germ band stage secondary stripes of many PRGs intercalate between the primary stripes and the genes function as segment polarity genes at this time of development [4, 5].
However, this mode of segmentation where all segments are produced simultaneously (the so-called long-germ developmental mode) is derived within the insects and is apparently correlated with the high speed of Drosophila embryonic development [6, 7]. In the majority of arthropods (including many holometabolous insects) only the anterior segments form simultaneously, and all posterior segments are formed sequentially from a posterior segment addition zone (SAZ) . This mode of segment formation is called the short-germ developmental mode. Theoretically, this mode of sequential segment formation does not require the pair rule gene mechanisms operating during Drosophila segmentation. However, studies in the beetle Tribolium castaneum have shown that although the developmental mode is that of a typical short-germ arthropod, some of the PRG orthologs function as "true" pair rule genes [9, 10]. Functional studies in more basal hemimetabolous insects, such as Oncopeltus fasciatus or Gryllus bimaculatus, support the idea that PRGs are involved in segmentation, but question the existence of a pair rule mechanism [11, 12]. Studies on the expression of PRGs in chelicerates , crustaceans [14, 15] and myriapods  support this thesis. An exception is seen in the centipede Strigamia maritima, where posterior segments are initially determined in a two-segmental periodicity, revitalizing the question of whether an ancestral pair rule mechanism might exist in arthropods [17, 18].
Part of the hierarchic interactions of the PRGs as known from Drosophila is also conserved in the beetle Tribolium [9, 10] and may also be conserved in a spider . However, some levels of PRG interaction are obviously divergent and it is, thus, unclear to what extent the interactions of PRGs are generally conserved in arthropods.
In this paper we present the expression profiles of orthologs of most of the known Drosophila PRG orthologs in the pill millipede Glomeris marginata during trunk segmentation. The data support the idea that PRG orthologs are generally involved in segmentation, but do not function as classical pair rule genes like in Drosophila and Tribolium. Our data show that posterior segments are formed one at a time and not in a double segmental periodicity. The interaction of PRG orthologs in Glomeris, as inferred from gene expression data, displays more similarities to Tribolium than to Drosophila. Also some of the PRG orthologs appear to have either ventral or dorsal specific functions, suggesting that the earlier reported decoupling of ventral and dorsal segmentation [19, 20] is already obvious with the function of the PRGs. Finally, we discuss our data in the context of the assumed arthropod segmentation clock acting in the addition of posterior segments under the control of Delta-Notch signaling.
Materials and methods
RNA isolation and cDNA synthesis were carried out as described previously . Initial fragments of the Glomeris even-skipped, runt and hairy-1 gene orthologs were amplified using degenerate primer sets directed against the homeodomain (for even-skipped), the runt domain (for runt) and the helix-loop-helix domain (for hairy), respectively, as described by Damen et al. 2000 . The degenerate primers for the isolation of Glomeris sloppy-paired, odd-paired, odd-skipped and pairberry-1 orthologs have been described in Damen et al. 2005  and Schoppmeier and Damen 2005 . To obtain larger fragments of the genes we subsequently performed 3'-RACE PCR using the MARATHON RACE Kit (Clontech, Heidelberg, Germany).
Sequences of all fragments were determined from both strands of several clones on a 3100 automated sequencer, using Big Dye dye-terminators version 3.1 (Big Dye Terminator Cycle Sequencing Kit; Perkin-Elmer Applied Biosystems, Foster City, CA, USA). The sequences of Glomeris pair rule gene orthologs are available under the accession numbers AM279687 (Gm-eve), AM279688 (Gm-h1), FR715033 (Gm-h2), FR715033 (Gm-h3), AM279692 (Gm-run), FR715039 (Gm-slp), FR715035 (Gm-opa), FR715036 (Gm-odd), FR715037 (Gm-pby1) and FR715038 (Gm-pby2).
For the similarity analysis, we searched GenBank  using the pairwise alignment program Gapped BLAST . Sequences were aligned using the multiple alignment program Clustal X . The alignments were calculated from the blocks substitution matrix BLOSUM 62 using gap costs at 20 for existence and 0.2 for extension. Maximum likelihood analysis was performed using the Quartet Puzzling method  as implemented in PAUP 4.0b10 .
In situ hybridization and nuclei staining
Whole mount in situ hybridizations were performed as described in Prpic and Tautz (2003) . Double in situ staining with digoxigenin (DIG) and fluorescein (FL) labeled RNA probes in parallel is described in Janssen et al. (2008) . For reasons of enhanced signal clearness (yolk stains yellow when using INT/BCIP or FastRed) embryos were flat mounted prior to photography. A detailed in situ hybridization protocol is available from the authors upon request.
Cell nuclei distribution was visualized by using the fluorescent dye 4-6-Diamidin-2-phenylindol (DAPI). Incubation in 1 μg/ml DAPI in phosphate buffered saline with 0.1% Tween-20 (PBST) for 30 minutes was followed by extensive washes in PBST. Embryos were analyzed under a Leica dissection microscope (Leica, Heerbrugg, Switzerland) equipped with either an Axiocam (Zeiss, Jena, Germany) or a D70 digital camera (Nikon, Tokyo, Japan). 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 (Adobe Systems Inc. San Jose, CA, USA).
Transcripts and phylogenetic analysis
The Gm-slp fragment encodes the C-terminal part of the protein including part of the forkhead-domain and the complete 3'-UTR as indicated by the presence of a putative polyadenylation signal (AATAAA). Gm-odd and Gm-opa encode part of the zinc-finger domains. The 5'and 3'ends of these two genes have not been recovered.
We isolated three gene fragments that show significant similarities to Drosophila hairy (Figure 1B). Drosophila possesses several bHLH transcription factors related to hairy with deadpan and side showing most similarities to hairy (Figure 1B). Since the order of branches in our phylogenetic analysis is statistically unresolved (trees not shown; cf. ) we designated the Glomeris fragments simply as Gm-h1, Gm-h2, and Gm-h3. All fragments encode the bHLH-domain (except its basic N-terminal part), the orange-domain, and the complete C-terminal part of the ORF each ending in a WRPW motif which, like the orange-domain, is characteristic for the hairy-class of bHLH-domain genes. All Glomeris hairy fragments contain a 3'UTR ending in a poly-A tail with a putative polyadenylation signal (that is, AATAAA for Gm-h1 and ATTAAA for Gm-h2 and Gm-h3) just upstream.
We obtained partial fragments for two Glomeris PaxIII group genes, which we named pairberry-1 (Gm-pby1) and pairberry-2 (Gm-pby-2) because of their sequence similarity to the Drosophila PaxIII group genes (that is, paired, gooseberry-neuro and gooseberry). The conceptually translated protein fragment contains the paired-domain (except its very N-terminal part), the octapeptide domain and the homeodomain (except its very C-terminal part) (Figure 1B).
Expression of primary PRG orthologs during Glomeris trunk segmentation
Three of the known pair rule genes (PRGs) from Drosophila, that is, even-skipped, runt and hairy, are described as primary since they act upstream of the so-called secondary PRGs and control the expression of the latter . The following section focuses on the expression of the orthologs of the primary PRGs during trunk segmentation in Glomeris.
Expression of secondary PRG orthologs during Glomeris trunk segmentation
The Glomeris odd-paired ortholog (Gm-opa) is expressed in segmental stripes. Its expression, however, is strictly restricted to the ventral part of the embryo (Figures 3E, F and 4D-F). opa is expressed posterior adjacent to the expression of en (Figure 3E, F). opa is also expressed in the SAZ (Figures 3E, F and 4D-F), but in a way that is different from the dynamic expression of eve and run. Initially the anterior SAZ expresses opa in a broad domain, that later transforms into a single small stripe in the newly formed segment (Figure 4D-F). Gm-opa is expressed in rings around the outgrowing appendages, with the exception of the labrum. The pre-mandibular and postmaxillary segments do not form appendages and here opa is expressed in the tissue corresponding to where the appendages form in the other segments (Figure 3E, F).
Gm-odd is expressed dynamically in the SAZ (Figure 4G-I). This dynamic expression, however, never results in ventral segmental stripes, but only in dorsal stripes. Initially a faint propeller-shaped expression domain appears in the SAZ (Figure 4G, I) that later becomes more clearly visible (Figure 4G). This domain then disappears from its ventral part and continues to strengthen in its dorsal part, leaving a strong patch of expression in the dorsal tissue of the nascent segment (Figure 4H). This then transforms into dorsal stripes (Figure 4I). The dorsal segmental expression of odd lies posterior to that of the segmental marker engrailed (en) (Additional file 1: Figure S1I, J). As with h1 and h2, odd expression also extends dorsally into the dorsal extraembryonic tissue (Additional file 1: Figure S1M). Gm-odd is also strongly expressed in the region of the forming stomodaeum (Figure 4G), the ventral portion of the developing appendages (Figure 4G), a dot-like domain anterior to the proctodaeum (Figure 4G-I) and in the CNS (Figure 4G-I).
Gm-slp is expressed in segmental stripes anteriorly abutting the expression of en (Figures 3G, H and 4J-L). The segmental expression initially extends into dorsal tissue, but soon after this expression pattern disappears (Figures 3G, H and 4L). There is no dynamic expression in the SAZ. The most posterior segmental stripe appears anterior to en in the anterior part of the SAZ or the nascent segment (Figures 3G, H and 4J-L). At later stages the segmental expression ceases in the anterior segments and remains only in the ocular region, the antennae, the walking legs, a restricted ventral region in the CNS, and segmentally reiterated stripes along the ventral midline (Figure 4L). The posterior part of the SAZ remains free from slp transcripts at all stages (Figures 3G, H and 4J-L).
Gm-pby1 is neither expressed dynamically in the SAZ nor in stripes in the posterior part of the SAZ, but appears first in a segmental stripe in the anterior of the SAZ or the nascent segment (Figures 3I, J and 4M-O). However, its expression is restricted to the ventral tissue only. The segmental expression disappears soon after its appearance in the ventral midline and the legs (Figures 3I, J and 4M-O). Its intra-segmental position overlaps with the posterior part of wingless (wg) (not shown) and the anterior part of en (Figure 3I, J). Gm-pby2 expression is restricted to the tips of the legs at late embryonic stages (not shown).
Pair rule gene orthologs are involved in myriapod segmentation
The expression profiles of the PRGs examined here suggest a general role in segment formation, or at least the development of segmentally-iterated structures. Even if some of the reported PRGs in Glomeris - despite their expression patterns that are typical for segmentation genes - might not be involved in segmentation, the data from a wide range of arthropods including spiders and myriapods support the idea that PRGs are generally important factors in arthropod segmentation [13, 21].
Posterior segments form in a single segmental periodicity
In the hemimetabolous insect Schistocerca americana and the spider-mite Tetranychus urticae the prd/pby orthologs Sg-pby1 and Tu-Pax3/7 appear with delay in every other segment in the anterior embryo which may hint at an ancestral double segmental mechanism [36, 37]; discussed in . However, outside the higher insects such a pair rule mechanism may be restricted to the anterior part of the embryo, which is patterned similarly as the Drosophila embryo. Therefore, mechanisms found in anterior patterning are likely to be more conserved between short germ and long germ arthropods than it is the case for posterior patterning (discussed in [38–40]). Since expression data on PRGs in anterior patterning are scarce outside the insects, this theory remains open for further debate and study.
There is, however, one example that supports a posterior pair-rule like mechanism outside higher insects. In the centipede Strigamia maritima posterior segments are added with a double segmental periodicity [17, 18]. This pair-rule like mechanism appears, however, to be the result of parallel evolution rather than a conserved feature of arthropod posterior segmentation, because some of the genes involved, like, for example, caudal, appear to be co-opted for this special purpose , discussed in [41, 42]. The expression of another PRG, eve, in the centipede Lithobius atkinsoni, however, does not show any kind of a double segmental pattern  further supporting the thesis that the double segmental mechanism found in Strigamia may be a peculiarity of geophilomorphs rather than a general feature of myriapods or even short germ arthropods. This is also supported by data from the spider Cupiennius salei where PRGs show no double segmental expression [13, 21, 22].
We find that none of the investigated PRGs are expressed in alternating segments in the trunk. In fact, the dynamic expression patterns of Gm-eve and Gm-run demonstrate clearly that the posterior trunk segments appear with a single segmental period (Figure 2). The dynamic expression in the SAZ of either of these genes can be followed into each nascent segment demonstrating that every single stripe of eve or run is correlated with the formation of a single new posterior segment.
Conserved aspects of early PRG interaction
In Drosophila the PRGs are subdivided into two classes; the primary PRGs, which are under control of maternal factors and the gap genes; and the secondary PRGs, which receive their input from the primary PRGs . Recent studies in the beetle Tribolium have examined the possibility of this PRG hierarchy being conserved . Although a number of differences exist in the regulation of the PRGs, the principal hierarchy of PRGs between Drosophila and Tribolium is conserved. eve and run act high in the regulatory network in both species [9, 43–45] and prd and slp are under the control of these primary PRGs [9, 45, 46]. Data from the spider Cupiennius support the idea that a hierarchic order of PRGs may even be conserved in all arthropods, since Cs-eve and Cs-run are expressed more posterior (that is, earlier) in the SAZ than Cs-slp and Cs-pby-3 that are restricted to the anterior of the SAZ and the anterior rim of the SAZ, respectively [13, 21, 22].
In Glomeris eve and run both display the most prominent expression pattern in the SAZ passing through it from its very posterior to its anterior and finally into the nascent segments (Figure 2). Furthermore these two PRG orthologs are the only ones in Glomeris being additionally expressed in concentric circles around the proctodaeum, as is the case for odr-1 in Strigamia  or eve in Lithobius  (Figure 2M, N). The dominant expression profiles of eve and run in the SAZ thus make them good candidates for segmentation genes acting at high level in a possible network, as it is the case for their orthologs in Drosophila , Tribolium  and possibly also Cupiennius [13, 21].
The Glomeris orthologs of the secondary PRGs (that is, Gm-slp and Gm-pby1) are never expressed dynamically in the SAZ, but appear relatively late in the SAZ shortly before the inter-segmental borders form (Figure 4J-O). Notably these two genes also display highly conserved intra-segmental expression patterns (discussed below). In addition, both orthologs are never expressed in the posterior part of the SAZ in Cupiennius, but only in the anterior SAZ (that is, Cs-pby-3) or at the anterior rim of the SAZ (that is, Cs-slp) . This led Damen and colleagues  to suggest that these genes may be under the control of genes like eve and run, which are active earlier (that is, already in the posterior SAZ). Since the relative tempo-spatial expression of some of the putative primary and secondary PRGs in the SAZ is conserved between Tribolium, Cupiennius and Glomeris, we postulate that at least eve and run are acting at a high level in a possible regulatory network of PRG orthologs in all arthropods.
In Glomeris the odd gene, which is a primary PRG in Tribolium and a secondary PRG in Drosophila, is also expressed dynamically in the entire SAZ (Figure 4G-I), suggesting that odd may play an important role in segment formation in Glomeris. Moreover, expression of the odd ortholog odr-1 in the centipede Strigamia also suggests a crucial role of this gene in posterior segment formation . Taken together these data imply that odd may already have gained a dominant function in segmentation in lower arthropods. Later, it may then have been recruited as a primary PRG in Tribolium. Indeed, in a bioinformatics study on transcriptional regulation of segmentation gene interaction in Drosophila odd rather behaves like a primary PRG although functionally it is a secondary one . This result strengthens the idea that odd orthologs fulfill important tasks in arthropod segmentation, even in Drosophila, where its function in segmentation may be understated by the fact that it acts like a secondary PRG.
Conserved segmental expression of secondary PRGs
As already discussed above, there appears to be a hierarchy of PRGs in Glomeris where putative primary PRGs are expressed early and dynamically in the Glomeris SAZ; whereas the expression of putative target genes such as the secondary PRGs (and SPGs) is restricted to anterior regions of the SAZ and the nascent segment. However, in Drosophila some of the PRGs are also expressed at later stages, where they function to stabilize the parasegment boundary (PSB) . Several studies have shown that the parasegment boundary is a conserved entity among arthropods and characterized by the expression of SPGs, like engrailed and wingless, at either side of the parasegment boundary [8, 19, 29, 48–51].
We, therefore, also analyzed the intra-segmental expression of the Glomeris PRGs and discuss here to what extend this late function/interaction of the Glomeris PRGs may be conserved or have diverged. Expression and function of most PRGs is known only from Drosophila and Tribolium, which are both rather derived holometabolous insects. Apart from that, the only almost-complete set of PRG orthologs is known from the spider Cupiennius. But the focus of this study is on the early expression in the SAZ and does not include the examination of later segmental expression patterns . The data on "late" PRG expression are thus very limited except for data on Pax3/7 group genes (that is, the Gm-pby1 orthologs) that are very abundant due to the availability of cross-reacting antibodies detecting all genes of this family in various arthropods (that is, orthologs of Drosophila paired, gooseberry and gooseberry-neuro) [15, 36].
The segmental expression patterns of the primary PRGs in Glomeris are different from that in Tribolium and/or Drosophila. For example, Gm-eve and Gm-run are expressed posterior to Gm-en in the ventral segments with no or only very little overlap (Figure 3A-D), whereas, in Drosophila and Tribolium eve and run expression is overlapping with en .
The intra-segmental expression of Gm-slp and Gm-pby1 is conserved between Glomeris and various arthropods (for pby1) [15, 36] and Glomeris, Drosophila and Tribolium (for slp) [5, 10]. In all cases slp is expressed anteriorly adjacent to en, and the Pax3/7 ortholog pby-1 is expressed overlying the PSG boundary and, thus, partially overlapping the expression of wg and of en (Figure 6).
We, therefore, propose that the late function of slp and Pax3/7 orthologs is conserved in the formation of the PSB in that slp represses en, and in that pby1 might activate wg and en. Whether the segmental expression profiles of the other Glomeris PRG orthologs is conserved among basal arthropods and what their late function in segmentation may be has to be examined in the future. Data on expression and function of all PRG orthologs from various basal arthropods would possibly help in answering this question.
Decoupled dorsal and ventral segmentation
In Glomeris the germ band consists of ventral tissue from the beginning of germ band extension on, but dorsal tissue does not start developing before stage 3 (staging after ). We reported earlier that Glomeris dorso-ventral segmentation is decoupled at the level of the segment polarity (SPGs) and Hox genes suggesting that the process of decoupling must have its origin at earlier regulatory levels [19, 20]. Since in Drosophila, the SPGs are under control of the pair rule genes (PRGs) it appeared likely that the decoupling of segmentation in Glomeris is attributed to the level of the PRGs. Our screen on Glomeris PRGs now revealed that some genes display a profile that suggests restricted function in dorsal segmentation, while others are predominantly expressed in ventral tissue (Figure 5). By contrast, the genes opa and pby-1 are expressed in stripes only in the ventral segments. Thus, they are likely to be involved in ventral segmentation, but they are not required for the formation of the dorsal segments. The remaining genes are initially expressed in ventral and dorsal segmental tissue, but show dorso-ventral differences in their persistence of expression. The expression of eve, runt and h1 stripes persist longer in dorsal tissue, whereas the slp stripes persist longer on the ventral side (Figures 4 and 5). Our data thus suggest that decoupling of dorsal and ventral segmentation already starts with the action of the PRG orthologs. Especially those genes that are initially expressed on both sides, but then "decide" for either ventral or dorsal persistence, provide further insight into the possible mechanisms of dorso-ventral decoupling. These genes are likely members of a core segmentation network that is common to both ventral and dorsal segments, but then are regulated differently on both sides to achieve the specific metamerisms of the ventral and dorsal sides, respectively.
The finding that the ventral segmentation gene expressions in Glomeris show similarities to those in other arthropods not only on the level of the SPGs but also of the PRGs, while the dorsal patterns deviate on this level as well, strengthens the notion that the ventral metamerism in Glomeris is homologous to the segmentation in other arthropods, while the dorsal metamerism mechanisms have diversified independently in different arthropod lineages .
The idea of an arthropod "segmentation clock"
Segmentation in short-germ arthropods and vertebrates displays fundamental morphological similarities. Separate body units (that is, segments and somites, respectively) are added sequentially from a posterior region in the embryo: the SAZ in arthropods and the presomitic mesoderm (PSM) in vertebrates [53, 54]. The cyclic expression of genes that is involved in the formation of new somites in vertebrates very closely resembles the dynamic expression of the Glomeris PRGs eve, run and also odd. The cyclic gene expression in vertebrates is under control of a so-called "segmentation clock" or "oscillator", of which Notch/Delta signaling is a key component . Recent work on the spider Cupiennius salei and the cockroach Periplaneta americana [55, 56] has shown that Notch/Delta signaling is a main component of arthropod segmentation as well, and implies that the lack of Notch/Delta signaling in Drosophila segmentation is the derived state. The morphological similarities of segment formation in arthropods and vertebrates and the common usage of Notch/Delta expression suggest that segmentation in both phyla traces from a common ancestor . However, the functional similarities between segmentation in arthropods and vertebrates are more extensive than just using Notch/Delta signaling. Recent work in the spider Achaearanea tepidariorum has shown that a posterior expression of the Wnt8 gene is involved in the maintenance of SAZ activity [57–59] and the ortholog of this gene, Wnt8 is required for the proper function of the PSM in vertebrates [60, 61].
It is currently unclear how these newly discovered vertebrate-like mechanisms feed into the more canonical segmentation mechanisms in arthropods, that is, the level of the pair rule and segment polarity genes. It has been suggested that these levels are under control of a posterior segmentation clock involving Notch/Delta signaling . So far there is only circumstantial evidence that supports this idea. First, the vertebrate Her/Hes genes, that are orthologs of the arthropod PRG hairy, are controlled by the Notch/Delta oscillator [62, 63], thus providing a link between these two components in vertebrates. It is possible that this link has been conserved and extended during arthropod evolution. Indeed, in the spider Cupiennius hairy expression is changed upon Notch and Delta RNAi [55, 64]. Second, the PRG odd is regulated downstream of Notch signalling in Drosophila leg development . This fact caused Chipman et al.  to suggest that odd might be under the control of Notch/Delta signaling in other processes as well, including segment formation. In agreement with this idea, in Glomeris and two other myriapods, Strigamia and Lithobius, Notch and Delta are expressed dynamically in the SAZ [18, 66, 67], strikingly similar to the dynamic patterns that we find in the present work for the segmentation genes. In Glomeris this dynamic Notch pattern results in dorsal segmental Notch stripes  and we have shown here that the odd stripes in Glomeris also persist only in the dorsal segments, thus pointing to a possible link between Notch signaling and odd activation. Another argument for the involvement of Notch/Delta signalling in dorsal segment formation comes from the expression of Gm-h1 (Figure 4B, C). Like Gm-Notch and Gm-odd also Gm-h1 becomes restricted to dorsal segments soon after its expression in the SAZ (Figure 4B, C). The expression profiles of Notch, Delta, odd, and h1 would be in agreement with the suggested ancestral interaction of a posterior "segmentation clock" mechanism and PRG orthologs [39, 68].
Expression of PRGs in dorsal extraembryonic tissue
In most arthropods a thin layer of dorsal ectodermal tissue connects the separated dorsal edges of the developing embryo . The nature and function of this tissue is not very well understood and the lack of expression of the segmentation genes in this tissue in most species suggests that it is not metamerized or subdivided into separate developmental units. However, in Glomeris the primary PRGs, eve and run are expressed in circles around (or within) the SAZ, which is especially clear at early developmental stages (Figure 2); the segmental expression of these genes thus includes extraembryonic tissue. A similar expression profile has also been reported for pair rule genes, for example, odr1 (odd ortholog) and eve1/2, in Strigamia  and it was, thus, not unexpected to find similar patterns in Glomeris as well. In Glomeris, however, h1 and odd are not only expressed in the dorsal segments (discussed above), but their segmental expression in the extraembryonic tissue persists even in older stages (Additional file 1: Figure S1). Since neither the segment polarity genes nor the Hox genes are expressed in the extraembryonic tissue it appears unlikely that this tissue is patterned or metamerized in the classical sense. But what then is the function of h1, h2 and odd expression in the extraembryonic tissue?
We postulate that the expression of the hairy genes (h1 and h2) and odd may be involved in "guiding" the two dorsal sides of the embryo in order to assure that "matching" tissue meets during the process of dorsal closure. This would be especially important, because the matching cannot be guided via the connection across the ventral side, as the dorsal segments are functionally decoupled from the ventral side.
The activation of the pair rule genes (PRGs) appears to be a crucial step in arthropod segmentation as it marks the transition from a non-periodic pattern to a periodic pattern. It is, therefore, surprising to some degree that this step of the segmentation mechanisms appears to be the most variable and diverse level, especially when it is compared to the evolutionarily conserved steps of the SPGs or the Hox genes [40, 70, 71]. Expression of all investigated PRGs in the millipede Glomeris is consistent with a role in segmentation. The PRGs in Glomeris seem to act in a hierarchic manner, and can be subdivided into primary and secondary PRG, similar as has been described for insects and a spider [9, 13]. However, the exact interactions between the Glomeris PRGs remain unclear due to the lack of functional methods. The expression of the primary PRGs strongly supports the idea that the initial patterning of the segments is in a single segmental period. A similar single segmental period has also been observed in other arthropods implying that it represents the ancestral mode for segment patterning and formation .
Our work is the first analysis in a non-insect arthropod in which the late expression of the PRGs has been studied. The intrasegmental positions of the expression patterns show similarities but also differences among the species analysed (Figure 6A). The comparison of insect data (that is, Tribolium and Drosophila) with data from a myriapod may help to distinguish between conserved and derived features of segmentation and thus provide clues about the origin and evolution of segmentation mechanisms in the arthropods.
In both Tribolium and Glomeris the intra-segmental expression of opa, slp and prd/pby1 is conserved, and although its function is unclear, it may be part of the ancestral patterning system (Figure 6).
An interesting case of "partial" conservation is provided by the genes run and eve. These genes are co-expressed in Tribolium and Glomeris (but not in Drosophila) (Figure 6). However, the co-expression stripes of run and eve do not have the same intrasegmental position in the two species. Thus, co-expression of these two genes appears to be a conserved feature already present in the common ancestor of insects and myriapods, but the mechanisms that position the run/eve stripe within a segment must differ in the two species.
Our results also add to the previous finding that the segmentation mechanisms in the dorsal and ventral segments of Glomeris are decoupled . Previous results have shown that dorsal and ventral segmentation mechanisms differ mainly in their usage of the segmentation genes of the segment polarity group, but our present data show that strong dorso-ventral differences already exist in the expression of the orthologs of the PRGs.
The ancestral role of the PRGs in arthropod segmentation remains unclear until comparative data on expression and function are available for representatives of all groups of arthropods, as well as their assumed sister-groups, the onychophorans and the tardigrades . Shared conserved or diverged aspects of the segmentation process may then also contribute to the unraveling of arthropod phylogeny , which appears still not fully resolved [74, 75].
We would like to thank Hilary Pioro ( neé Dove) for Notch and Delta clones and two anonymous reviewers for their helpful comments and suggestions. This work has been supported by the Swedish Research Council (VR: grant to GEB), the European Union via the Marie Curie Training network "ZOONET" (MRTN-CT-2004-005624 (to GEB, RJ and WGMD)). The work of NMP is funded by the University of Göttingen, the Graduate School for Neurosciences and Molecular Biosciences (GGNB), and the Deutsche Forschungsgemeinschaft.
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