Toll signals regulate dorsal–ventral patterning and anterior–posterior placement of the embryo in the hemipteran Rhodnius prolixus
© Berni et al.; licensee BioMed Central Ltd. 2014
Received: 6 June 2014
Accepted: 11 September 2014
Published: 27 October 2014
Insect embryonic dorso-ventral patterning depends greatly on two pathways: the Toll pathway and the Bone Morphogenetic Protein pathway. While the relative contribution of each pathway has been investigated in holometabolous insects, their role has not been explored in insects with a hemimetabolous type of development. The hemimetabolous insect Rhodnius prolixus, an important vector of Chagas disease in the Americas, develops from an intermediate germ band and displays complex movements during katatrepsis that are not observed in other orders. However, little is known about the molecular events that regulate its embryogenesis. Here we investigate the expression and function of genes potentially involved in the initial patterning events that establish the embryonic dorso-ventral axis in this hemipteran.
We establish a staging system for early embryogenesis that allows us to correlate embryo morphology with gene expression profiles. Using this system, we investigate the role of Toll pathway genes during embryogenesis. Detailed analyses of gene expression throughout development, coupled with functional analyses using parental RNA interference, revealed that maternal Toll is required to establish germ layers along the dorso-ventral axis and for embryo placement along the anterior-posterior axis. Interestingly, knockdown of the Toll pathway effector Rp-dorsal appears to regulate the expression of the Bone Morphogenetic Protein antagonist Rp-short-gastrulation.
Our results indicate that Toll signals are the initiating event in dorso-ventral patterning during Rhodnius embryogenesis, and this is the first report of a conserved role for Toll in a hemipteran. Furthermore, as Rp-dorsal RNA interference generates anteriorly misplaced embryos, our results indicate a novel role for Toll signals in establishment of the anterior-posterior axis in Rhodnius.
KeywordsToll Dorso-ventral axis Embryogenesis NFκB Hemipteran
Morphological diversity in the class Insecta is reflected in its different developmental modes. In addition to attaining the adult form directly (ametabolous) through complete (holometabola) or incomplete (hemimetabola) metamorphosis, the size of the embryonic rudiment relative to the egg determines many of the morphogenetic events that ensue. Insect eggs are divided into long, intermediate, and short germ types according to the size of the embryonic rudiment and the number of segments that are specified before gastrulation (reviewed in). This diversity of developmental modes poses challenges for understanding the molecular basis of insect development.
As a first step in embryonic development, the dorso-ventral (DV) and anterior-posterior (AP) axes are specified, leading to patterned embryonic gene expression. In insects, patterning along the DV axis is required to subdivide mesodermal and ectodermal embryonic tissues and to drive formation of extraembryonic membranes. Two major pathways have been described that pattern the DV axis in arthropods: the Toll receptor pathway and the Bone Morphogenetic Protein (BMP) pathway. Their respective contribution to DV patterning, as well as their maternal versus zygotic functions, varies among species (see references in). For instance, in the long-germ diptera Drosophila melanogaster, the maternal Toll pathway establishes domains of zygotic gene expression along the DV axis. Drosophila Toll regulates the activity of the NFκB family downstream effector protein Dorsal (Dl). Upon activation of the Toll pathway, Dl is no longer targeted for degradation by the Cactus/IκB inhibitor and can translocate to the cell nuclei to regulate the expression of target genes, including localized expression of the BMP pathway genes decapentaplegic (dpp) and short gastrulation (sog) (see references in). In contrast, in the beetle Tribolium castaneum, which presents a more ancestral short-germ mode of embryogenesis, elements of the Toll pathway are maternally provided but most DV patterning occurs at the zygotic level[4–6]. Furthermore, BMPs play a key role in setting up the DV axis in Tribolium, and Tc-Toll does not regulate Tc-dpp expression[5, 7].
Based on the conserved role of BMPs in patterning the bilaterian DV axis, it has been hypothesized that Toll was co-opted from a more ancestral immune function for DV patterning in insects. Arthropod DV patterning has been studied in chelicerates such as the spider model Parasteatoda tepidariorium and holometabolous insects such as Nasonia vitripennis, T. castaneum, and D. melanogaster (reviewed in[2, 9]). Recently, the role of Toll and BMP pathways has been analyzed in two long germ hymenopteran species, the bee Apis mellifera and the wasp N. vitripennis[10, 11]. In N. vitripennis the BMP gradient and its dorsally expressed target genes are not regulated by Toll signaling. In A. mellifera Toll and BMP are involved not only in DV but also in AP axis establishment. However, embryonic DV patterning has not been investigated in hemimetabolous insects. Considering the lack of knowledge about DV patterning in insects with a more direct (hemimetabolous) type of development, we set out to investigate the relative contributions of the Toll and BMP pathways to DV patterning in the hemimetabolous insect Rhodnius prolixus, which develops with an intermediate germ type of embryogenesis.
The hemiptera Rhodnius prolixus is an important vector of Chagas disease, which affects over 8 million people in Latin America. As an established model for insect physiology, recent genomic analyses are contributing to a global understanding of R. prolixus genome size and organization, and tissue-specific sequences are being identified[13–15]. This community effort also provides the molecular basis for investigating the function and network of interactions between developmental genes.
Rhodnius egg production depends on blood feeding. After each blood meal, a female lays up to 40 eggs[16, 17]. Three extracellular membranes plus a hard chorion protect the resulting embryos from desiccation. While several morphological features of Rhodnius embryonic development have been described[18–21], the molecular aspects that regulate Rhodnius development remain unexplored. This is especially true for the initial embryonic stages where axial patterning events must take place, and before overall embryo morphology is set. The long-lasting effects of parental double-stranded RNA interference (pRNAi) assays recently described for this species now provide a tool for addressing these questions[22–27].
In this study, we established a staging system for early Rhodnius embryogenesis, which enabled us to correlate embryo morphology with gene expression, and provided a framework for functional studies. Next, we investigated whether the genes associated with the Toll and BMP pathways are expressed in the Rhodnius embryo, which revealed that Rp-Toll and Rp-dl are maternally and zygotically expressed. With this information, we performed functional analyses for Toll pathway elements. Our results suggest that the Toll pathway acts to specify germ layers along the DV axis and to localize the embryo along the long axis of the Rhodnius egg. Thus, our results implicate Toll signaling as a central pathway in Rhodnius embryonic development.
Insect rearing, tissue fixation, and histological sections
Rhodnius rearing was performed as previously described[26, 27]. Ovary collection and dissection were performed using standard protocols available for D. melanogaster. Briefly, ovary fixation was performed at room temperature with 4% paraformaldehyde (PFA) for 1 hour shortly before Toll immunostaining (see below). For embryonic fixation we have established a new protocol involving trypsin digestion, sonication, and increased fixation time (detailed protocol available upon request). Briefly, the embryos were fixed at 4% PFA in phosphate buffer pH 7.4 with Tween-20 0.1% at room temperature for 24 hours, sonicated for 2 minutes, and then treated with trypsin for chorion permeabilization for 5 minutes. The next step was post-fixation for 12 hours with 4% PFA. After manual dechorionation with fine forceps, embryos were stained with DAPI (1 μg/μL). For frozen histological sections, embryos were fixed overnight in 4% PFA, washed in PBS and included in OCT (Tissue-Tek, Sakura Finetek, Torrance, CA, USA) in 2-hour steps, from 25% to 100% OCT. Sections (20 μm) were obtained in a CM 1510S Leica cryostat (Leica, Wtzler, Germany).
For ovary immunostaining, egg chambers were fixed for 20 minutes in 4% PFA, washed in phosphate buffer pH 7.4 with Tween-20 0.1%, blocked with 0.1% normal goat serum and incubated overnight at 4°C with primary antibody Toll d-300 (Santa Cruz Biotechnology, Santa Cruz, CA, USA, 1:50 dilution). Detection was performed with secondary anti-rabbit 488 (1:1000, 1 hour/room temperature; Alexa Fluor, Invitrogen, Life Technologies) and counterstained with Alexa 546 conjugated phalloidin (1:100, 1 hour/room temperature; Invitrogen) and DAPI. Images were obtained with a Leica SP5 confocal microscope.
Identification of Bone Morphogenetic Protein- and Toll-related genes in R. prolixus genome and phylogenetic analysis
D. melanogaster or T. castaneum protein sequences were used as BLAST queries in the Rhodnius prolixus unpublished genome (http://genome.wustl.edu/genomes/detail/rhodnius-prolixus/). BLASTs were also performed in the recently published R. prolixus gut transcriptome. After manual curation, protein sequences were aligned using the CLUSTALW algorithm available in the MEGA6 package. The best substitution model for this set of Toll protein sequences (LG + G) was calculated also in MEGA6. Phylogenetic analysis of Toll-related genes was performed using a maximum likelihood method with 100 replicates for bootstrap, complete deletion of gaps and using the nearest-neighbor-interchange method.
Accession numbers for the genes analyzed were: EF1: RPRC015041; 18S, GenBank ID: AJ421962.1; Rp-dpp, GenBank ID: GU906792.1; Rp-dl, GenBank ID: ABU96698.1; Rp-sog: RPRC015365-RA Rp-cact: Asb-31044 (VectorBase). Accession numbers for Toll genes are in main text, RPRC accession numbers are from Vectorbase (https://www.vectorbase.org/).
Total RNA was isolated using TRIzol reagent (Invitrogen) from previtellogenic, vitellogenic, or choriogenic ovaries, and embryos collected for 6-hour time windows and aged to the periods described in the text. RNA was treated with RNAse free TURBO™ DNAse (Ambion, Life Technologies), and cDNA was synthesized from 1 μg total RNA using the Multiscribe kit (Applied Biosystems.Real-time quantitative PCR was performed on a StepOnePlus real-time PCR system using power SYBR-green PCR master mix (Applied Biosystems, Foster City, USA). The comparative Ct method[29, 30] was used to compare changes in gene expression levels. The ribosomal 18S (18S) and Elongation factor 1 (Ef1) genes were used as endogenous reference genes ( and Additional file1). Primer pairs are listed in Additional file1. All primers were designed with Primer 3 (http://frodo.wi.mit.edu/primer3/) and checked for dimer formation with Oligoanalyzer software (http://www.idtdna.com/analyzer/applications/oligoanalyzer/). All quantitative real-time PCR experiments were performed in triplicate, with four technical replicates. Bars in graphs correspond to standard error.
Parental RNA interference
Double-stranded RNA was synthesized from PCR products containing T7 promoter sequences at both ends as previously described. Briefly, two successive PCRs were performed; the first to amplify Rp-dl and Rp-cact from the cDNA and the second PCR added T7 promoter sequences at both ends. Primer pairs are listed in Additional file1. BLASTn against the Rhodnius prolixus genome did not detect unrelated sequences similar to the selected regions. The unrelated MalE gene (Gene ID: 948538), present in Escherichia coli, but absent from the R. prolixus genome, was used as a dsRNA control (dsMalE) for the off-target effects of dsRNA. The MalE 800 bp fragment was amplified from the Litmus 281-plasmid (New England Biolabs, Iswich, MA, USA) with a single primer (T7, 5-TAATACGACTCACTATAGGG-3) specific for the T7 promoter sequence that is on both sides of the MalE sequence. The different dsRNA concentrations used during the studies are described in Results. dsRNA injections into R. prolixus female virgins followed recently published protocols. Two days after dsRNA injection the females were fed with rabbit blood. Oviposition and egg collection were initiated 1 week after blood feeding. Eggs were collected, counted, and the hatch rate defined after 20 days at 28°C, to make sure all surviving embryos had hatched.
Proteins were separated under SDS-PAGE and analyzed by Western blots using standard protocols. PVDF membranes were blocked with 5% bovine serum albumin and incubated overnight at 4°C with primary antibody Toll d-300 (Santa Cruz Biotechnology, 1:50 dilution). Proteins were detected with peroxidase conjugated secondary antibody (Vector; 1:4000) and Pierce ECL Western Blot Substrate (Life Technologies).
Establishing a staging system to study Rhodnius prolixus early embryonic development
DV polarity of the Rhodnius egg is easily identified immediately after oviposition ([19, 20], this report) due to the oblique position of the anterior cap (Figure 1C). During Cleavage, the Rhodnius embryo develops as a syncytium (from 0 to 12 hours), with nuclear cleavages initially taking place at the center of the egg (0 to 6 hours, stage 1A). After migrating to the periphery (6 to 12 hours, stage 1B), two cell populations begin to segregate: the small syncytial blastoderm nuclei and the putative serosal cells[33, 34]. The syncytial nuclei concentrate at the posterior pole, forming the germ rudiment (GR), which corresponds to the embryonic rudiment plus amniotic rudiment[33, 35] (stage 2).
During the Blastoderm period (12 to 24 hours) membranes form around the blastoderm nuclei (by 18 hours, stage 2B; Figure 1B,C) and, shortly after, the not yet invaginated ventral GR is visible as a U-shaped cubical epithelium curved around the posterior pole, likely corresponding to the prospective head lobes. Germ cells appear at this stage, projecting into the yolk[20, 32].
At 24 hours (stage 3A; Figure 1D-F) gastrulation takes place, which is characterized by the invagination and inward proliferation of GR cells on the dorsal side and by the movement of the ventral part of the GR towards the posterior pole (characterizing immersion anatrepsis). As a result of this movement, the amnion is formed and the embryo proper extends with the anterior cephalic end at the posterior region of the egg (stage 3B; Figure 1G-I). Thus, by the end of gastrulation the embryo and egg AP axes are inverted relative to each other[20, 32]. In addition, the germ band is inverted relative to the egg DV axis and placed on the dorsal side of the egg, which differs from the pattern displayed by another hemiptera species, Oncopeltus fasciatus[36, 37].Following germ band extension, morphological Segmentation begins in the anterior region of the embryo (36 hours, stage 4; Figure 1J-L). At 48 hours (stage 5; Figure 1M-O), cephalic and thoracic appendages are visible. Segmentation of abdominal regions is visible at 60 hours (stage 6; Figure 1P-R).
Subsequent stages characterize the Growth phase, where the different appendages develop and most of the embryo, especially posterior regions, is immersed in yolk (stages 7 to 9, 72 to 108 hours; Figure 1S-V). During stage 10 the embryo undergoes the relatively rapid process of Katatrepsis (Figure 1W,X), where the embryo emerges from the yolk by rotating backwards 180°. As a result, the cephalic region of the embryo now aligns itself with the anterior of the egg. Similar movements are observed in most hemimetabolous insects and require the presence of the serosal membrane, which in Rhodnius contracts at the anterior side of the egg[19, 32]. After stage 7, secretion of the cuticle[26, 32] disturbs tissue visualization with fluorescent nuclear staining.
Major features of Rhodnius embryonic development until katatrepsis
Developmental time at 28°C
Characteristic features in whole mounts
Nuclei divide internally
Nuclei reach the periphery
Formation of germ rudiment
Nuclei progressively concentrate at egg posterior
Germ rudiment invagination begins
Germ band extension
Anterior segmentation (in head and thorax) begins
Appendage buds appear; non-segmented abdomen
segmented abdomen; neural groove evident
Thoracic appendages elongate, bigger than head appendages
Antennal appendages grow over first maxillary appendages
First maxillary appendages hidden by antennal appendages; embryo shortens and widens (germ band retraction)
Katatrepsis and Dorsal Closure
At the end of katatrepsis, embryo and egg anterior-posterior axes coincide; embryo closes dorsally
Several Toll and Bone Morphogenetic Protein pathway components are conserved in Rhodnius
In order to address which genes are required to pattern the Rhodnius DV axis, we first sought to identify Toll and BMP pathway genes that may be expressed during embryogenesis. We recently identified complete or partial sequences for genes in both pathways, including six different Toll sequences in the R. prolixus genome. Expression was confirmed for most of these in the recently published R. prolixus transcriptome raw data. Phylogenetic analysis suggests that Rp-Toll-like- 2 (RPRC009262), herein referred to as Rp-Toll, is a Drosophila Toll ortholog (Figure 2A). The Rp-Toll sequence was aligned to Drosophila and Tribolium Toll proteins, which revealed that this sequence comprises a transmembrane region, part of the extracellular segment and most of the intracellular domain that interacts with downstream elements (Figure 2B and Additional file2). The predicted Rp-Toll protein sequence presents 44% sequence identity with Drosophila Toll, and most of this identity covers the region identified by the anti-Dm-Toll antiserum used in this study (Figure 2B and Additional file2).
Sequences coding for a Dorsal transcription factor (an NFκB/c-Rel protein activated by Toll) have been previously identified in R. prolixus. These authors detected Rp-dl transcripts in the embryo (dl, 1A) as well as adult salivary glands, midgut, and fat body (dl, 1B and 1C). Accordingly, we identified an inhibitory cactus/IkB ortholog that is expressed in R. prolixus ovaries, embryos, fat body, and in the digestive tract.
BMP family proteins signal through heterodimeric transmembrane receptors to induce phosphorylation of R-Smads, leading to activation of Co-Smads and regulation of gene transcription. Classically, BMPs are regulated in the extracellular space by binding to Chordin (Chd)/Short gastrulation (Sog) antagonists. We have identified in the R. prolixus genome two sequences coding for BMP ligands (Rp-dpp and Rp-gbb) and one sequence for the antagonist Sog (Rp-sog). Furthermore, one type I (Rp-tkv) and one type II (Rp-punt) BMP receptor, two R-Smads (Rp-mad and Rp-mad-like), and one Co-Smad (Rp-medea) are represented as expressed sequences, implying that all elements necessary for BMP signaling are present (Mesquita and colleagues, manuscript in preparation). Given that Dpp/BMP and Sog/Chd sequences have been previously associated to embryonic DV patterning in arthropods and vertebrates, we chose to investigate these homologs in greater detail.
Expression of Toll and Dpp pathway genes varies throughout embryonic development
As part of the BMP pathway, Rp-dpp expression, on the other hand, was only observed at the onset of gastrulation (Figure 3D, Additional file4). This pattern is different from Rp-sog (Figure 3E), which is expressed at low levels during early stages and coincides with peak Rp-Toll and Rp-dl zygotic expression. High Rp-dpp and Rp-sog mRNA levels in stages 2B and 3 result from zygotic expression, given that these peaks are not observed in unfertilized eggs (data not shown). Therefore, it is unlikely that maternal Rp-dpp mRNA provides information for early patterning in Rhodnius.
Rp-dl knockdown alters embryonic patterning
Egg lay resulting from parental RNA interference
Egg lay (per female per feeding)†
Number of females
31.88 ± 5.35
3.5 ± 1.25
0.96 ± 0.26
26.0 ± 1.38
Embryo viability resulting from parental RNA interference
Embryo viability (%)†
Number of eggs
5.5 ± 2.03
1.55 ± 0.184
3.37 ± 1.71
89.54 ± 5.03
Embryonic phenotypes resulting from Rp-dl pRNAi
Embryonic phenotypes (%)
No germ rudiment*
Embryo anteriorly localized**
Embryo randomly localized
Embryo posteriorly localized
Rp-dl (0.5) stages 2-4
Rp-dl (1.0) stages 2-4
Rp-dl (0.5) stages 5-10
Rp-Toll (0.5) stages 2-10
control (1.0) stages 2-10
On the other hand, parental RNAi for Rp-cact results in oogenesis phenotypes that preclude embryonic formation: (Figure5). In order to unveil the role of cactus during Rhodnius embryogenesis, we performed pRNAi on adult females. Intriguingly, Rp-cact dsRNA-injected females showed underdeveloped ovaries and large undigested gut contents 1 week after blood feeding (Figure 5F, data not shown). In contrast, control dsRNA-injected females display ovaries at the choriogenic stage and largely absent gut content (Figure 5E, data not shown). After Rp-cact dsRNA, female adult mortality increased with time and reached 100% after 10 days, even when a low dsRNA concentration was adopted for the pRNAi assay (<100 ng/μL). The low number of eggs laid by surviving females (Table 3) precluded the analysis of possible Rp-cact during DV formation. Similar adult lethality has been observed in experiments investigating Tc-cact in the beetle Tribolium. Only the injection of embryonic RNAi, as done in Tribolium, would be able to unveil the role of Rp-cact during DV axis formation, a technique not yet applied in Rhodnius due to its hard chorionic structure. This suggests that Rp-cact has additional functions that may not involve Rp-dl or that excess Toll signals are more deleterious to oogenesis than lack of Toll.
Rp-dl regulates expression of the Bone Morphogenetic Protein pathway gene Rp-sog
In order to investigate hierarchical relationships between Toll and BMP pathway genes during embryogenesis, we analyzed the expression of Rp-Toll, Rp-cact, Rp-sog, and Rp-dpp under Rp-dl pRNAi. Functional assays for Rp-dl showed that a 60 to 80% decrease in Rp-dl mRNA levels (Figure 7) results in an approximately 60% decrease in stage 2B Rp-sog and Rp-cact mRNAs, while stage 1 mRNA levels are unchanged (Figure 7). In contrast, no significant changes in stage 1 mRNA levels were seen for Rp-dpp, Rp-cact, and Rp-Toll under the same condition (Figure 7). No differences are observed for Rp-dpp and Rp-Toll at later stage 2B either. Stage 2B mRNAs are likely composed of zygotic messages, since levels are greatly reduced in unfertilized embryos, while stage 1 mRNAs are in great part provided by the mother. Our results strongly suggest that zygotic Rp-sog and Rp-cact expression during gastrulation (stage 2B) may depend on the activity of the Toll pathway.
Rp-Toll is a conserved insect Toll ortholog
In this study, we sought to identify and perform functional analyses of genes required for DV patterning in the hemipteran Rhodnius, with the goal of better understanding the evolution of DV patterning in metazoans.
We identified six coding sequences for Toll-related receptors in the R. prolixus genome and gut transcriptome (Mesquita and colleagues, manuscript in preparation and), and phylogenetic analysis showed that Rp-Toll- 2 is the Toll ortholog associated with DV patterning during embryogenesis (Figure 1).
In addition to Toll, Drosophila expresses eight other Toll-related receptor genes that perform redundant or partially redundant functions[40–42]. Phylogenetic analysis of Toll receptors in the mosquito Anopheles gambiae, the beetle Tribolium castaneum, the bee Apis mellifera, the fruit fly Drosophila melanogaster, and the bug Oncopeltus fasciatus showed major variation among these species[43–45]. In addition, it has been established that Toll loci involved in embryonic DV patterning are part of an orthologous group in all insect species studied so far. Therefore, the presence of several Toll loci, but only one true Toll ortholog, indicates that the R. prolixus genome displays a repertoire of Toll receptors that is characteristic of insects.
In contrast to the receptor diversity, intracellular Toll pathway components appear less diversified in insect evolution. Toll adaptors such as MyD88, Tube, and Pelle display one-to-one orthologs in R. prolixus and other insects (; data not shown). Furthermore, a single IκB Cactus ortholog was identified in the R. prolixus genome (this report,). A dorsal immune factor (dif) ortholog, which codes for a second Rel-like protein in Drosophila, is absent in other insects as well as in the R. prolixus s genome (M. Sorgine, unpublished results). Thus, Rp-dl and Rp-cact should be effector and inhibitor, respectively, of all Toll functions in R. prolixus.
Toll signals pattern the Rhodnius embryonic dorso-ventral axis
Next, we analyzed the effects of parental knockdown on downstream elements of the Toll pathway. Because of the challenges associated with performing embryonic in situ hybridization in Rhodnius, we conducted an alternative staging protocol, which allowed us to correlate changes in pRNAi gene expression with temporally specific morphological phenotypes. This protocol can be used in future functional analyses conducted during early Rhodnius embryogenesis.
Rp-dl pRNAi embryos that reach gastrulation stages lack an internal mesodermal layer, which is consistent with a role for Toll signals in DV patterning, as shown for several insect species. Loss of extraembryonic tissues, as shown in our Rp-dl knockdowns, has also been associated with defective DV patterning[34, 36, 46–48]. Furthermore, the perpendicular placement of the GR in blastoderm stage Rp-dl pRNAi embryos is reminiscent of Tc-Toll and Tc-sog pRNAi embryos, where it has been suggested that the Toll pathway harbors an AP as well as DV component. Our molecular analysis showed that Rp-Toll and Rp-dl are expressed during oogenesis and embryonic cleavage stages, and that the mother delivers a great part of the Rp-Toll and Rp-dl mRNAs for use during embryogenesis. A second peak of Rp-Toll (24 to 36 hours) and Rp-dl (18 to 30 hours) mRNAs resulting from zygotic expression is observed at gastrulation. Thus, the fundamental question is whether the DV patterning phenotypes observed under Rp-dl pRNAi are due to blockage of maternally or zygotically provided Rp-dl and Rp-Toll.
Maternal messages are fundamental for the development of insect embryos. For example, maternal messages via the Epidermal Growth Factor Receptor pathway break the symmetry in Drosophila, Nasonia, and Tribolium and Gryllus bimaculatus ovarian follicles, setting up the embryonic DV axis. In Drosophila, this symmetry-breaking event leads to the differential activation of maternally provided Toll receptors along the DV axis, which is translated into the nuclear Dorsal gradient during embryogenesis. Indeed, in this diptera, Toll, dorsal, and cact functions in DV axis formation are exclusively maternal.
However, positional information derived from the mother is not a strict requirement. For instance, exposure of Atrachya beetle embryos to cold temperatures leads to the production of germ bands that are randomly condensed relative to the AP and DV axes, implying that axial patterning is regulated zygotically in this species. Moreover, careful investigation of DV axis establishment in T. castaneum showed that Toll and Dl are involved in a zygotic self-regulatory circuit. Evidence for this circuit was provided by the comparison of spatial expression patterns of DV target genes in embryonic versus parental RNAi of Tc-Toll, Tc-dorsal, and Tc-cactus. Embryonic and parental knockdown phenotypes are identical in T. castaneum, strongly suggesting that most DV patterning events take place at the zygotic level.
Unfortunately, we were unable to reproduce this level of spatial resolution in the expression of DV genes in Rhodnius since we were not able to reproduce the previously published in situ protocols[23, 24] and embryonic injections are remarkably difficult to administer due to the hard chorion of Rhodnius. However, at the morphological level, early misplacement of GR cells in the anterior of the egg under Rp-dl pRNAi suggests that the maternal Toll pathway performs an early axial patterning function that affects later developmental stages. Furthermore, perpendicular placement of the GR relative to the long axis of the egg under Rp-dl pRNAi resembles the loss of DV polarity phenotype reported for Tc-Toll and Tc-dpp, suggesting an early effect of Rp-dl in DV patterning. During the early stages, the decrease in Rp-dl mRNA levels under RNAi is greatest (>90%), with most resulting embryos (84%) being anteriorly misplaced and short. Therefore, it is reasonable to suggest that DV patterning is controlled by maternal Rp-dl.
Rhodnius Toll signals play a novel role in defining the embryo’s position along the anterior-posterior axis
Interestingly, our functional assays reveal that Rp-dl pRNAi leads to a severe defect in the positioning of the developing embryo, which is found at the anterior of the egg instead of being placed at the posterior. This observation strongly suggests that the Toll pathway exerts a role not only in the establishment of the DV axis, but also in the AP axis. The embryo’s anterior placement could result from incorrect specification of extraembryonic membranes, since we observed a small number of amniotic cells in Rp-dl RNAi embryos. However, we observed misplaced embryos as early as the syncytial blastoderm stages, before extracellular membranes are able to exert a tracking effect on the developing embryo. Therefore, an alternative hypothesis is that specification of the AP and DV axes are interdependent and that Rp-dl RNAi interferes with the expression of AP patterning genes. A recent study reported that patterning of the two major body axes is co-dependent in Apis mellifera. Considering that we found Rp-dl pRNAi embryos mislocalized along the AP axis, a similar mechanism may play a role during axis specification in Rhodnius.
Anteriorly placed Rhodnius embryos are short and do not emerge into the yolk, suggesting that anatrepsis has been disturbed. Such an effect has not been previously described for the Toll pathway in any of the arthropod species analyzed to date. However, it has been recently reported that interfering with the terminal system in the hemipteran Oncopeltus disturbs invagination of the blastoderm although, in this case, germ band extension and segmentation proceeds almost normally. This is consistent with the interpretation that part of the phenotypes displayed by interfering with the Toll pathway in Rhodnius may result from AP patterning defects.
Respective contribution of the Toll and Bone Morphogenetic Protein pathways to Rhodnius dorso-ventral patterning
A long-standing question in embryonic patterning concerns identifying the point in evolution at which the two main pathways (Toll and BMP) were deployed to pattern the DV axis, as well as elucidating their respective contributions along different clades. Studies in ancestral arthropod classes (for example, the crustacean Parhyale hawaiensis and the spider Parasteatoda tepidariorum) indicate no role of Toll in DV patterning, although Toll is detected during embryogenesis of the tick Riphicephalus (Boophilus) microplus. In fact, in these arthropods, BMPs seem to perform a more central role in setting the DV axis.
The role of Toll in immunity has been functionally assayed in several insects (see references in), unlike its role in DV patterning, which has only been studied in a few holometabolous insects[2, 10, 56] and more recently in Oncopeltus (J.A. Lynch and S. Roth, personal communication). The functional analyses of Rp-dl conducted in this study show that the Toll pathway plays a role in Rhodnius embryogenesis. However, Rp-dl and Rp-cact are also expressed in the salivary gland, intestine, and fat body, where they play a role in the response to infection (, this report). Therefore, considering the hypothesis that the ancestral function of the Toll pathway is in immunity, our results support the notion that acquisition of an embryonic role for Toll predates the common ancestor of hemiptera and hymenoptera.
The relative contribution of the Toll and BMP pathways to DV patterning varies across species. In vertebrates, BMPs perform a central role in setting the DV axis, and no functional role for an NFκB pathway in this context has been reported. In insects, sequences that respond to Dorsal/NFκB have been identified, which drive DV restricted expression patterns in Anopheles, Drosophila, and Tribolium[46, 58–61]. In Drosophila, maternal Toll signals play the greatest role in defining territories along the DV axis, spatially restricting the zygotic expression of target genes such as dpp and sog. Sog and Dpp proteins subsequently subdivide the dorsal domain and drive the formation of the extraembryonic amnioserosa[48, 62]. At the beginning of gastrulation in the scuttle fly Megascelia, BMP subdivides the extraembryonic amnion and serosa as well. In contrast, in Tribolium, both the Toll and BMP pathways set the entire DV axis: loss of Tc-Dpp signals causes loss of extraembryonic (dorsal-anterior) tissue and embryo expansion, while a decrease in Tc-Toll or Tc-sog results in expansion of dorsal-anterior structures at the expense of embryonic tissue[5, 63, 64].
In Rhodnius, the presence of maternal Rp-Toll and Rp-dl mRNAs in cleavage stage embryos, the absence of Rp-dpp expression at this stage, and the decrease in zygotic Rp-sog in Rp-dl pRNAi, suggest that maternal Toll sets the initial events in embryonic DV patterning, as shown for Drosophila (Figure 8). On the other hand, the presence of maternal Rp-sog messages during cleavage stages suggests an early function for Rp-sog that may differ from Sog function in either Drosophila or Tribolium. While no Rp-dpp expression is observed at these early stages, Rp-Sog may exert an effect on other BMPs such as Rp-Gbb, which is yet to be explored.
The lack of a central role for Rp-dpp in setting the DV axis in Rhodnius could argue against the hypothesis that the ancestral pathway responsible for DV pattering relied on BMPs. However, we have previously shown that in Drosophila, where maternal Toll signals initiate patterned gene expression along the DV axis, maternal expression of dpp[65, 66] and sog in follicle cells impacts DV axis formation, thus modifying the Dl gradient in the Drosophila early embryo[65, 67]. Therefore, despite the fact that Drosophila embryos rely on Toll and Dl activation as the main DV patterning event, there might still be a hidden component of maternal dpp in DV patterning that corresponds to an ancestral BMP function. Interestingly, we observed that Rp-sog and Rp-dpp are highly expressed during oogenesis (not shown). Thus, they may perform a patterning function in the follicular epithelium during oogenesis, or provide maternal messages and/or protein that may reflect on embryonic patterning as well. Future functional assays for BMP pathway genes should help clarify the role of the BMP pathway during Rhodnius embryogenesis, and provide insights as to the relative contribution of the BMP and Toll pathways in this hemiptera.
In this study, we investigated the role of the Toll pathway in Rhodnius prolixus embryonic development. We show that the Toll pathway presents maternal and zygotic components. Functional assays revealed that Rp-dl determines early placement of the germ rudiment at the egg’s posterior. In addition, embryos resulting from Rp-dl pRNAi lack a mesodermal layer and display decreased amnion. Thus Rp-dl is necessary for DV patterning. While Rp-dpp mRNAs are absent in early embryonic stages, we observe that the Toll pathway regulates zygotic expression of Rp-sog preceding gastrulation. In conclusion, the Toll pathway is a central component in Rhodnius embryonic DV patterning.
Bone Morphogenetic Protein
- chd :
- dl :
- dpp :
polymerase chain reaction
parental RNA interference
RNdaF is a Young Scientist of Rio de Janeiro Foundation for Research (FAPERJ, Brazil), supported by grants from Conselho Nacional de Desenvolvimento Científico e Tecnologico (CNPq). HA is supported by grants from FAPERJ and CNPq. The authors would like to thank Prof. Siegfried Roth and his group for sharing unpublished results, and acknowledge Prof. Roth and Dr. Attilio Pane for helpful comments on the manuscript. We are also indebted to José de S Lima and Gustavo Ali for insect care and to Dr. Pedro Oliveira for use of quantitative PCR equipment, to Carolina Batista and Nilson Santos for help with cryostat sections and Dr. Roberto Lent for use of the cryostat.
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