- Research article
- Open Access
The neuropeptide complement of the marine annelid Platynereis dumerilii
BMC Genomics volume 14, Article number: 906 (2013)
The marine annelid Platynereis dumerilii is emerging as a powerful lophotrochozoan experimental model for evolutionary developmental biology (evo-devo) and neurobiology. Recent studies revealed the presence of conserved neuropeptidergic signaling in Platynereis, including vasotocin/neurophysin, myoinhibitory peptide and opioid peptidergic systems. Despite these advances, comprehensive peptidome resources have yet to be reported.
The present work describes the neuropeptidome of Platynereis. We established a large transcriptome resource, consisting of stage-specific next-generation sequencing datasets and 77,419 expressed sequence tags. Using this information and a combination of bioinformatic searches and mass spectrometry analyses, we increased the known proneuropeptide (pNP) complement of Platynereis to 98. Based on sequence homology to metazoan pNPs, Platynereis pNPs were grouped into ancient eumetazoan, bilaterian, protostome, lophotrochozoan, and annelid families, and pNPs only found in Platynereis. Compared to the planarian Schmidtea mediterranea, the only other lophotrochozoan with a large-scale pNP resource, Platynereis has a remarkably full complement of conserved pNPs, with 53 pNPs belonging to ancient eumetazoan or bilaterian families. Our comprehensive search strategy, combined with analyses of sequence conservation, also allowed us to define several novel lophotrochozoan and annelid pNP families. The stage-specific transcriptome datasets also allowed us to map changes in pNP expression throughout the Platynereis life cycle.
The large repertoire of conserved pNPs in Platynereis highlights the usefulness of annelids in comparative neuroendocrinology. This work establishes a reference dataset for comparative peptidomics in lophotrochozoans and provides the basis for future studies of Platynereis peptidergic signaling.
Neuropeptides, including peptide transmitters and hormones, are a diverse group of signaling molecules involved in chemical communication among neurons and neuroendocrine regulation. Neuropeptides represent by far the largest group of neurotransmitters and neuromodulators  and are considered the oldest neuronal signaling molecules in metazoans . Peptidergic signaling has deep evolutionary origins: essential enzymes for proneuropeptide (pNP) processing, maturation, and secretion have even been identified in organisms without a nervous system, such as the sponge Amphimedon queenslandica  and the placozoan Trichoplax adhaerens .
pNPs are translated as inactive precursors typically consisting of an N-terminal signal peptide (SP) that directs the pNP to the secretory apparatus, and one or several peptide elements flanked by basic cleavage sites . After pNP cleavage by neuronal prohormone convertases, the liberated peptides can be further modified. C-terminal alpha-amidation and N-terminal pyroglutamination are common forms of modification  and can affect peptide stability , peptide structure [8, 9], and bioactivity [10, 11].
Structurally and functionally important peptide elements often show sequence conservation among homologous pNPs or between the mature peptides within a single pNP . The strongest conservation is often restricted to a few key residues that confer bioactivity to the processed peptides [13, 14]. pNPs often contain spacer sequences between the conserved peptide stretches. These spacers are less conserved and therefore considered to be biologically inactive .
Most neuropeptides signal via G-protein coupled receptors (GPCR) . It has become clear in recent years that GPCRs and their peptide ligands are stably associated in evolution [16–18]. This co-evolutionary relationship of peptide-ligand pairs has been exploited to establish several conserved metazoan pNP families over large evolutionary distances [19, 20].
The classical approach to identifying novel bioactive neuropeptides was biochemical purification from the species of interest, followed by functional analysis [21–24]. With increasing genomic and transcriptomic sampling, pNP identification has been accelerated by in silico sequence analyses based on homology to previously described pNPs [25, 26], or on the presence of sequence features such as a SP, conserved C-terminal amidated motifs (e.g., RFa, “a” for amide) or cleavage sites [26–30].
Mass-spectrometry (MS) is also widely used as a powerful tool for the direct identification of bioactive peptides. This method relies on mapping the obtained peptide masses to a reference dataset (genome or transcriptome), and can be impeded by the presence of extensive post-translational modifications [31–33]. A combination of genomics and MS approaches has revealed the complete neuropeptide repertoire of several species in many metazoan phyla [34–38].
Annelids represent a diverse and species-rich phylum and have long been used in neuroendocrinological and behavioral studies . Comparative genomic approaches [19, 20, 40] and other studies identified multiple annelid pNPs and neuropeptides, including RFa [13, 41–47], FVRIa [48–50], excitatory peptide (EP) [51–53], egg-laying hormone (ELH) , myomodulin [55–57], RGWa , L11 or elevenin , vasopressin [39, 58, 59], gonadotropin releasing hormone (GnRH)[60, 61], insulin-related peptides , neuropeptide Y (NPY) [63, 64] and myoinhibitory peptide (MIP) . Despite these advances, a complete picture of annelid neuropeptide diversity is still missing.
Here we describe the neuropeptide complement of the marine polychaete annelid, Platynereis dumerilii, using a combination of transcriptomics, in silico pNP searches and MS-based peptide identification. Platynereis has recently been established as a powerful experimental organism for comparative and experimental neurobiology [50, 58, 65, 66]. Platynereis has a biphasic life cycle including free-swimming planktonic larval stages, followed by settlement and metamorphosis into the adult bottom-dwelling worm [67, 68]. The Platynereis larval nervous system is highly peptidergic and several neuropeptides were shown to be involved in the regulation of larval behaviors such as ciliary swimming and larval settlement [28, 65]. Previous studies described 15 Platynereis pNPs that are expressed in specific neuronal populations. Peptides generated from these pNPs include various RFa/RYa related peptides , vasotocin/neurophysin , FVRIa , RGWa , and MIP/allatostatin-B .
To complement this list, we used an integrative approach and identified 98 Platynereis pNPs, most of them verified by MS analysis. Our pNP catalog represents the most extensive list of annelid peptides to date. This catalog will provide a valuable resource for further studies of the peptidergic control of annelid behavior and physiology, and for the reconstruction of ancient metazoan peptide signaling systems and cell types .
Establishing the Platynereistranscriptome, predicted proteome and secretome datasets
To identify novel pNPs, we performed deep sequencing of the Platynereis transcriptome using a combination of Sanger, Roche/454 and Illumina technologies. We sequenced 77,419 expressed sequence tags (ESTs) from an arrayed, full-length normalized, mixed-stages cDNA library [GenBank JZ391525 - JZ468943]. This library was further sequenced using the Roche/454 technology. We also obtained Illumina paired-end sequencing reads from 13 Platynereis developmental stages including larvae, juveniles and adults. We assembled all acquired sequences into a reference transcriptome. The Platynereis transcriptome dataset contains 351,625 reads, with 87,686 of the contigs longer than 500 bp and 28,067 longer than 1000 bp. The transcriptome was annotated using the Basic Local Alignment Search Tool (BLAST) against SwissProt and well-annotated bilaterian proteomes (Additional files 1,2, 3 and 4). We also searched the transcriptome for open reading frames (ORFs) from which we derived a protein dataset. The predicted protein dataset contained 51,767 sequences longer than 120 amino acids (Additional file 5). To generate a Platynereis dataset of secreted proteins, the predicted protein dataset was analyzed for the presence of SPs . We identified 11,075 protein sequences with a SP. After the in silico removal of the SP, this secreted proteome database (Additional file 6), as well as the full predicted proteome database, were used for MS-based peptide identification.
Identification of PlatynereispNPs
In order to identify pNPs in the Platynereis transcriptome and predicted proteome datasets, we performed BLAST searches in these datasets using a large curated set of metazoan pNP query sequences . We also conducted pattern searches for repetitions of the motif x(3–10)-K[K/R]. The resulting sequences were examined for the presence of a SP, for cleavage sites, conserved peptide motifs, and other hallmarks of bioactive peptides and their processing (e.g. amidation signature C-terminal Gly, pyroglutamination signature N-terminal Gln, Cys-containing stretches, mono- or dibasic cleavage sites). These searches identified more than 80 Platynereis pNPs, including those previously described.
To complement the bioinformatics screen, and to find evidence for the presence of the predicted active peptides, we performed liquid chromatography - tandem mass spectrometry (LC-MS) on peptide extracts from various Platynereis larval and juvenile stages. We mapped the obtained MS hits to the Platynereis datasets. Using the MS analyses we discovered 15 further pNPs that were missed during our bioinformatic searches, extending the Platynereis repertoire to a total of 98 pNPs (Figure 1 and Additional files 7, 8, 9). We also analyzed the Platynereis neuropeptides for some of the most common peptide modifications and detected several modified peptides (Figure 1 and Additional files 8 and 9).
All full-length Platynereis pNPs have a SP and at least one potential basic cleavage site, and they lack non-neuropeptide protein domains as defined in the PFAM database. Besides, all 98 pNPs had to meet at least one of several criteria to be considered as bona fide prohormones. These include homology to known metazoan prohormones (e.g., NPY, AKH, 7B2 [70, 71]), a confirmed expression in Platynereis neurons (e.g., FVMa, SPY ), MS evidence (e.g., NGEW, GYa), conservation across lophotrochozoans or annelids (e.g., CCWa, QSGa) and other structural and functional hallmarks of a prohormone, such as a repetitive structure or peptide modifications (e.g., SPRa, QRIa).
Overview and classification of PlatynereispNP diversity
For most Platynereis pNPs we obtained the full-length open reading frame sequence (including a SP) and for 51 pNPs we have an available EST clone or a PCR-cloned cDNA. We annotated all pNP sequences with various sequence features, including the presence of a SP, cysteine-rich stretches (potentially also involved in processing ), prohormone-convertase cleavage-sites, modified (amidated or pyroglutaminated) or non-modified active peptides and the presence of a MS-hit. For all Platynereis pNPs containing repetitive peptides we also generated sequence logos (Figure 1 and Additional file 8). We classified the Platynereis pNP families according to their phylogenetic distribution, distinguishing ancient eumetazoan, ancient bilaterian, and ancient protostome families, as well as annelid/lophotrochozoa specific pNPs, and pNPs with no currently recognizable homologs outside Platynereis (Figure 1).
For the phylogenetic classification, we performed a sequence-similarity-based (BLAST p-values) clustering approach . We used a curated dataset of 6,225 pNPs from 10 phyla  combined with all Platynereis pNPs and their lophotrochozoan homologs collected from EST databases. We clustered this dataset using PSI-BLAST with 3 iterations. All Platynereis pNP sequences with no similarity to known metazoan pNPs were removed from the map. Metazoan pNPs that did not connect to any Platynereis pNP were also removed (e.g., parathyroid hormone, growth hormone) (Figure 2). Many of the repetitive pNPs formed a strongly connected cluster at the center of the map. These sequences were reanalyzed with clustering using non-iterative BLAST (Figure 3). The resulting maps were used to obtain an initial overview, which indicated a relationship of several Platynereis pNPs to known pNP families. The conservation of some Platynereis pNPs is limited to small stretches (the mature peptides) in the precursor and is difficult to identify using BLAST-based clustering (e.g., diuretic hormone 44 (DH44)). For this reason, we also performed motif searches and multiple-sequence alignments, which reinforced the family assignments, obtained by our clustering approach (Additional file 10).
Careful inspection of unassigned Platynereis pNPs for the presence of short conserved motifs using the motif discovery tool MEME  and known peptide profiles  led to the assignment of further Platynereis pNPs to known families (e.g., DH44, SIFa, pyrokinin/small cardio active peptide (sCAP); Additional file 10). We also discovered several Platynereis pNPs that belong to newly defined lophotrochozoan and annelid pNP families (Figure 1 and Additional file 10).
PlatynereispNPs belonging to ancient eumetazoan families
Platynereis also has three pNPs that belong to the eumetazoan R[F/Y]a family, FMRFa, RYa, and YFa (Figure 1 and Figure 3 and Additional file 10). The FMRFa pNP represents the ortholog of other protostome FMRFa pNPs. RYa has orthologs in other lophotrochozoans, sharing a Pro-rich C-terminal peptide (Additional file 10). The Platynereis YFa pNP is also part of the FMRFa cluster (Figure 3), however, direct orthologs of YFa pNPs could not be identified outside Platynereis.
A member of the eumetazoan Wamide/MIP/GWamide family, the Platynereis MIP/allatostatin-B pNP, gives rise to peptides involved in the regulation of larval settlement . Platynereis has another related pNP, yielding non-amidated W[I/L] peptides (Additional file 8 and Additional file 10). The two Trp residues that WI peptides share with MIPs (x-W-x6-7-W-[G/I/L]), and the position of the WI pNP in the Wamide/MIP/GWamide cluster (Figure 3) supports a close relationship between MIPs and WI pNPs. We only identified an orthologous WI pNP in the distantly related annelid Capitella teleta, suggesting that WI pNPs are annelid divergences of the MIP family.
Platynereis also has a pNP with a cysteine-rich prokineticin/colipase domain . Directly after the SP, the Platynereis prokineticin pNP contains amidated LFVa peptides. A similar peptide could also be identified in the C. teleta prokineticin pNP (Additional file 10).
PlatynereispNPs belonging to ancient bilaterian families
Recent comparative genomic analyses defined more than 25 pNP families that are ancestral to bilaterians [19, 20]. We found Platynereis representatives of most of these families that could readily be classified as one-to-one or many-to-one orthologs. These include glycoprotein hormone beta, vasotocin-neurophysin, NPY, RGWa, adipokinetic hormone (AKH), GnRH, 7B2, proenkephalin, DH44, achatin, luqin, tachykinin, calcitonin, diuretic hormone 31 (DH31), pedal peptide, allatotropin, sCAP, sulfakinin, crustacean cardio-active peptide (CCAP), allatostatin-A, allatostatin-C, SIFamide, L11, EP, pigment dispersing factor (pdf), and leucokinin (Figures 1, 2, 3 and Additional file 10). Two of these families, calcitonin/DH31 and DH44, show interesting gene or peptide repeat duplications in their evolutionary histories and will be discussed in detail below.
Platynereis has two pNPs belonging to the calcitonin/DH31 family, calcitonin and DH31. The calcitonin pNP shows high sequence similarity to the Cys-containing calcitonin peptides from vertebrates (Figure 4). In C. teleta, a second calcitonin-like pNP has recently been identified that is lacking the Cys residues . We also found an orthologous Platynereis sequence. These annelid pNPs are more similar to insect DH31 pNPs, also lacking the Cys residues, as shown by clustering (Figure 2) and sequence alignments (Figure 4). These results suggest that the ancestral bilaterian calcitonin peptide contained two Cys residues. The gene of this pNP duplicated in stem protostomes to give rise to DH31, followed by the loss of the Cys residues. Calcitonin has been retained in mollusks and annelids, but lost from the arthropod lineage. DH31 was lost from mollusks, and preserved in annelids and arthropods (Figure 4C).
We also identified two members of the corticotropin releasing factor/DH44 pNP family. DH44 has been shown to be related to mollusk egg-laying hormone (ELH) . We identified two pNPs in Platynereis that showed high sequence similarity on the level of mature peptides to mollusk ELH and also to insect DH44, with several highly conserved amino acid positions (Figure 5). The Platynereis DH44 pNPs are highly repetitive (13 and 16 copies) compared to their mollusk or insect counterparts that have only one peptide copy per pNP (Figure 5).
PlatynereispNPs belonging to ancient protostome families
Several members of ancient protostome pNP families are present in Platynereis, including myomodulin, prohormone-3, and whitnin (Figure 1).
The Platynereis myomodulin pNP has two alternative transcripts, both yielding several peptides with an LRMa C-terminus, characteristic of myomodulins (Additional file 8 and Additional file 10). Comparison of the Platynereis myomodulin pNP with the C. teleta sequence revealed other highly conserved peptide-stretches, flanked by monobasic cleavage sites, which may potentially yield non-amidated peptides (PRXGX, Additional file 8 and Additional file 10).
Lophotrochozoan-specific pNP families
We identified various pNPs belonging to lophotrochozoan pNP families including the fulicin related pNPs FLa and FVa/EFLGa, NKY, FVRIa, GNXQN, LXRX, CLCCY, CCWa, QSGa, CCRFa, and HFAa (Figure 1). Many of these could only be identified in annelids, mollusks, and sometimes also platyhelminths. We refer to these as lophotrochozoan families for simplicity. However, further sampling in other lophotrochozoan phyla will be needed to clarify their history.
Annelid FLa and FVa pNPs are related to mollusk fulicins, forming a lophotrochozoan pNP family. The Platynereis FVa mRNA has an unusual structure. Following the stop codon at the end of the coding region containing the FVa peptides, a second putative coding region is present, potentially yielding fulicin-like EFLGa peptides with an extra Gly residue (Figure 6A). A similar structure has been described for the FVa/EFLGa pNP in C. teleta . The region encoding the EFLGa peptides lacks a start Met and a SP, therefore it is not clear whether this region could be translated to yield mature peptides. The analysis of Illumina reads did not reveal any alternative transcripts with in-frame EFLGa peptides following a start site and a SP. The conservation of the EFLGa peptide-stretches across annelids (Additional file 10) suggests that these peptides are functional. Since MS evidence for EFLGa peptides was missing, we raised and affinity purified a specific antibody against EFLGa and performed immunostainings on Platynereis larvae. The EFLGa antibody labeled two neurons in the dorsal episphere of 48 h and two pairs of neurons in 72 h larva (Figure 6B and C), in the region where a subset of the precursor-expressing cells are found . When we pre-incubated the antibody with 5 mM EFLGa peptide, we no longer observed cellular staining (Figure 6C). In agreement with previous studies [13, 28], a cross-species reactive FVa antibody  labeled more neurons in the larval episphere at 48 h and 72 h (Figure 6B and C). EFLGa-positive neurons were a subset of these FVa expressing neurons as confirmed by their position, cell shape, and the presence of characteristic sensory dendrites abutting the cell bodies. (Figure 6D and E). These results suggest a translational stop-codon read-through mechanism  to yield bioactive EFLGa peptides, occurring in a subset of the precursor-expressing cells.
Annelid- and Platynereis-specific pNP families
For several pNPs we could not find orthologs outside Platynereis. Although we could not rely on pNP conservation as an indication of biological activity, we are confident that these pNPs produce bioactive peptides. In the case of WLD and SPY an effect on ciliary beating has previously been established . Other pNPs harbor two or more copies of similar peptides, often confirmed by MS evidence, including HIGA, NGEW, AYNPY, YTL, PPLPa, PY, Qpeptin, THDa, FGa and SPRa (Additional file 8 and Additional file 9). Many pNPs contain peptides with hallmarks of biological activity including amidation (SPY, HIGA, AYNPY, PPLPa, THDa, YYQa, FGa, LPWa, GYa, SPRa, QRIa, QDNa, PCNa and CCAa), pyroglutamination (YTL, PPLPa, SLL-1, QRIa, QDNa) or various Cys residues that potentially form disulfide bridges (WLD, AYNPY, FGa, SLL-1, SLL-2, SHM, RNT, QRIa, QDNa, PCNa and CCAa) (Figure 1 and Additional file 8). Further sampling in annelids could lead to the identification of orthologous pNPs in closely related species.
Stage-specific profile of PlatynereispNP expression
The Platynereis transcriptome dataset was acquired from various larval, juvenile and adult stages. To profile pNP expression, we mapped the obtained stage-specific Illumina paired-end reads to all pNP transcripts. The total number of pNP reads increases through larval development, peaks in 15-day-old juveniles, followed by a drop in adult stages. There are also large differences in pNP expression levels between sexually mature males and females (Figure 7).
We also performed a Pearson-clustering of pNPs based on their normalized stage-specific expression values. The Platynereis pNPs formed distinct clusters with expression peaking in different life cycle stages. We also found variable expression between 1-month pre- and 1-month post-cephalic-metamorphosis, and sexually mature male and female samples (Figure 8 and Additional file 11). For example, FMRFa, allatostatin-C and allatotropin were highly expressed in males, and lowly expressed in females.
An integrative approach to obtain the PlatynereispNP repertoire
To obtain a broad complement of Platynereis pNPs, we used an integrative approach combining transcriptomics, peptidomics, and bioinformatics. Such an integrative methodology was indispensable to extend the Platynereis pNP repertoire to 98 sequences.
In particular, MS analysis was often necessary to reveal pNPs with more restricted phyletic distribution, lower sequence conservation, or non-repetitive precursor structure. For example, in the GYa and SLL pNPs only one short potential bioactive peptide occurs in the precursor sequence. Moreover, MS evidences combined with the conservation of the peptide in orthologous annelid and mollusk pNPs allowed us to conclude that these sequences represent bona fide pNPs with likely biological activity (e.g. GNXQN, LEQ).
Expression profiling of PlatynereispNPs
The transcriptional profiling of pNP expression throughout the life cycle revealed that most of the pNPs are expressed at multiple stages. This indicates that the Platynereis nervous system is strongly peptidergic throughout the life cycle. The broad temporal expression of most pNPs also suggests that several of the Platynereis neuropeptides have pleiotropic functions. For example, we have recently shown that 12 different neuropeptides affect ciliary swimming and larval settlement in early larval stages [28, 65]. Since larvae settle after a brief planktonic stage (approximately 6 days) and locomotor cilia disappear after cephalic metamorphosis (approximately 1 month), the later expression of these peptides implies functions unrelated to ciliary swimming. The other specific differences we uncovered between different stages may be related to changing physiology (e.g., initiation of feeding). The differences between males and females indicate the presence of sex-specific neuroendocrine regulation potentially related to sex-specific physiology or behavior (e.g., in pheromone production or during the nuptial dance of Platynereis ).
Platynereis,a powerful marine invertebrate model for studying the function of ancient peptidergic signaling
Nervous systems evolved in a marine environment. Consequently, comparative studies of neuropeptide signaling in bilaterians would benefit from marine models with a rich set of conserved pNPs. Among the lophotrochozoans, a predominantly marine super-phylum, there are many emerging model species . However, few studies used a comprehensive approach to identify pNPs in lophotrochozoans [20, 25, 40]. A recent study in the freshwater planarian Schmidtea meditterranea established the first broad pNP resource in a lophotrochozoan . Compared to S. meditterranea, Platynereis has a richer repertoire of conserved pNPs. For example, S. meditterranea has no recognizable orthologs of achatin, luqin, AKH, allatotropin, CCAP, pdf, leucokinin, tachykinin, proenkephalin and whitnin [34, 78], all present in Platynereis. Previous studies also highlight the potential of Platynereis as a powerful lophotrochozoan model for studying neuropeptides. Peptide functions can be easily investigated in Platynereis larvae by bath application of synthetic neuropeptides [28, 65]. Recent technical advances now allow various genetic and other manipulations of peptidergic systems. For example, laser nanosurgery , transgenesis , morpholino-mediated gene knockdown , cellular resolution RNA in situ hybridization , complete neuronal reconstruction from TEM sections [65, 81], and whole-body gene expression pattern registration [66, 82] can be applied to explore the function of peptidergic systems in Platynereis.
Here we used an integrative approach, combining transcriptomics, peptidomics and sequence homology searches, to obtain a broad pNP complement for the model annelid Platynereis dumerilii. Using homology-based sequence clustering and a comprehensive set of multiple sequence alignments and peptide-motif screens, we classified many Platynereis pNPs into conserved families. This work will serve as the foundation for further research of neuropeptide functions in Platynereis and for the study of conserved bilaterian peptidergic cells. Our pNP catalog will also provide a useful resource for the identification of pNPs in other annelids and mollusks (comprising more than 100,000 extant species), as well as understudied non-model marine invertebrates (e.g. bryozoans or brachiopods).
Platynereis samples were obtained from an in-house culture at 18°C as previously described . Samples were collected for RNA extraction at the following stages: fertilized egg, 24 hpf, 36 hpf, 48 hpf, 72 hpf, 4 days post fertilization (dpf), 10 dpf, 15 dpf, 1 month post fertilization with pre-cephalic metamorphosis morphology, 1 month fertilization with post-cephalic metamorphosis morphology, 3 month adult asexual (atokous) worm, male and female sexually mature (epitokous) worm. Total larval RNA was extracted from pooled batches of larvae (minimum 3 batches), consisting of hundreds of individuals. Total RNA for the 3-month adult stage was extracted from the combined tissue of 10 worms. Male and female epitoke RNA was extracted from the combined tissue of 4 epitokes for each sex.
Total RNA was extracted from all samples using TRIreagent (Sigma) according to the manufacturer’s protocol, with two additional phenol:chloroform:isoamyl alcohol (25:24:1) phase separations, followed by one additional 1-Bromo-3-chloropropane (BCP) phase separation step prior to isopropanol precipitation.
Transcriptome sequencing, assembly and annotation
We used a combination of techniques to obtain a high-coverage Platynereis dumerilii transcriptome sequence. First, we generated a custom, normalized, full-length, mixed-stages cDNA library (with m7Gppp affinity purification to avoid bacterial RNA contamination; Invitrogen), cloned into the pCMV-Sport6 vector. After plating, we sequenced 83,152 randomly picked clones using the Sanger technology (ABI 3730) and the SP6 primer. 1,115 of the clones were also sequenced with the T7 primer. For base calling and vector trimming we used Phred [84, 85] and Cross-match. Mitochondrial and ribosomal RNA sequences were removed using Ribopicker 0.4.3  and a database of Platynereis mtDNA and rRNAs. The sequences were filtered with dustmasker, and every sequence with more than 20% low complexity regions was removed. The resulting 77,419 sequences were submitted to dbEST [GenBank: JZ391525 - JZ468943]. Second, we performed 454 sequencing (GS FLX, Roche/454) on the PCR-amplified cDNA library, following concatenation and fragmentation. We obtained 2,757,258 reads following adaptor trimming, quality (0.05), and length filtering (50 bp cutoff), using the software package CLC Genomics Workbench 4.5.1. Third, we performed Illumina sequencing on total RNA isolated from different developmental stages. Construction of sample-specific cDNA libraries from 5 μg total RNA, and paired-end transcriptome sequencing with an Illumina Hiseq 2000, was performed by GATC Biotech (Konstanz, Germany). Transcriptome Sequencing data was analysed using CLC Genomics Workbench 4.5.1 and 5.5.1 (CLC Bio). The raw read data for each stage-specific library was first filtered to remove Illumina adapter sequences, low quality sequences (Quality Limit 0.05) and short fragments (less than 30 base pairs).
All filtered 454 and Illumina reads were assembled using CLC Genomics Workbench 4.5.1. The resulting contigs and singletons were joined with all EST sequences, and passed to the CAP3 assembler with default parameters . Transcript sequences were searched for the longest ORF and translated.
The stage-specific filtered libraries were mapped to a subset of the assembled transcriptome of Platynereis (including only those sequences that had a BLASTX hit with an e-value < 1e-5 to the SwissProt database, and the 98 pNPs, a total of 52,631 transcripts) using the RNA-Seq Analysis function, with the following mapping parameters: paired distance 250 – 350 base pairs, minimum length fraction 0.8, minimum similarity fraction 0.9, maximum number of mismatches 2.
The total number of reads mapped to each gene in each stage-specific sample was normalized for total library size (reads per million (rpm)). For the subsequent analysis we focused only on the 98 pNP genes. To view the global pattern of neuropeptide expression throughout the Platynereis life cycle, we plotted the total sum of normalized expression values for all 98 pNPs in each stage-specific library.
The pNP genes were filtered based on their normalized expression values using the EdgeR RNA-Seq analysis package (Bioconductor)  in R version 3.0.1 to retain only those genes with at least 2 rpm in at least one developmental stage. The expression values were also further normalized for gene length (reads per kilobase million (RPKM)). The transcriptional profiles of the remaining 79 pNPs were clustered using hierarchical clustering with a Pearson correlation distance measure. The expression values were plotted using both the normalized expression values and the same values transformed to a fraction of 1.
Platynereis larval and juvenile stages from 2 days post fertilization until 15 days post fertilization were collected in a small net of 100 μm mesh size (approximately 500–1000 animals in total). To remove contamination, animals were washed several times in sterile-filtered natural seawater. Excessive salts were washed off by rinsing animals 1–2 seconds in distilled water. Specimens were immediately transferred to ice-cold extraction solution (methanol : glacial acetic acid : distilled water, 90:9:1). Samples were centrifuged for 1 h at 4°C. The supernatant that contained the dissolved peptides was evaporated completely. Peptides were dissolved in 100 μl double distilled H2O and used for mass-spectrometry.
Mass spectrometry: peptide sample preparation and LC-MS analysis
Neuropeptide mixtures were either directly desalted with C18 StageTips  or reduced and alkylated as described before . LC-MS analyses were performed on an EasyLC nano-HPLC (Proxeon Biosystems) coupled to an LTQ Orbitrap Elite mass spectrometer (Thermo Scientific). Separations of the peptide mixtures were done as described elsewhere  with slight modifications: Peptides were eluted with a 87-min segmented gradient of 5–33-90% HPLC solvent B (80% ACN in 0.5% acetic acid).
The mass spectrometer was operated in the positive ion mode. Precursor ions were recorded in the Orbitrap mass analyzer at a resolution of 120,000. The target value for the Orbitrap was 106 charges and the maximum allowed fill time was 100 ms. The 15 most intense precursor ions were sequentially fragmented in each scan cycle. High-resolution HCD MS/MS spectra were acquired with a resolution of 15,000 and a target value of 40,000. The normalized collision energy was set to 35, activation time to 0.1 ms and the first mass to 120 thomson. A minimum of 5000 counts were required to trigger MS/MS fragmentation and the maximum allowed fill time was 150 ms. The isolation window for MS/MS fragmentation was set to 2 thomson. Precursor ions were excluded from sequencing for 60 s after MS/MS. In one of the measurements MS/MS on singly charged precursor ions was enabled.
MS data processing, bioinformatic analysis and validation
In total three MS measurements were performed. The acquired MS raw files were processed separately using the MaxQuant software (v220.127.116.11) . Extracted peak lists were submitted to database search using the Andromeda search engine  to query a target-decoy  database consisting of the predicted Platynereis proteome (51,767 entries), the predicted secretome (11,075 entries), predicted neuropeptides (347 entries), commonly observed lab contaminants (248 entries), and the reversed complements of a those sequences (130,831 entries). We required full tryptic specificity allowing up to three missed cleavages and set the minimal peptide length to five amino acids. The initial precursor mass tolerance was set to 6 ppm, for fragment ions we used a mass tolerance of 20 ppm. For reduced and alkylated samples we defined carbamidomethylation of cysteins as fixed modification in the database search.
In order to screen for potential peptide modifications we performed a pre-run on one of the measurements by defining a fixed set of commonly observed (oxidation of methionine, acetylation of the protein N-terminus) and expected variable modifications (amidation of the peptide C-terminus) and iteratively included the following modifications in the database search: amidation of glycine; methylation of lysine and arginine; sulfation of tyrosine; acetylation of serine, threonine, alanine, glycine; pyroglutamic acid. Based on the results of this analysis we chose to include the following variable modifications in the actual database search: oxidation of methionine, sulfation of tyrosine, acetylation of the protein N-terminus, amidation of the peptide C-terminus, pyroglumatic acid.
Identified peptide spectrum matches (PSM) were statistically scored by MaxQuant software by calculation of posterior error probabilities (PEP) for each PSM. We considered all PSMs having a PEP below 0.01 for further analysis. The complete list of all identified peptide evidences including the respective spectra can be found in Additional file 9.
Antibody purification, immunohistology and imaging
A specific rabbit antibody against CEFLGa was raised and affinity-purified following a previously described protocol . The specificity of the obtained EFLGa antibody was also confirmed by pre-absorbing the antibody in 5 mM EFLGa for 2 h before applied in immunostainings, which completely blocked the antibody signal. The specificity of the cross-species reactive rabbit FVa antibody has been documented previously . All samples were counterstained with a mouse acetylated tubulin antibody (Sigma, Saint Louis, USA). Immunostaining on 48 hpf and 72 hpf Platynereis larvae as well as image acquisition was performed as described .
Basic Local Alignment Search Tool
Crustacean cardio active peptide
Cardio active peptide of the conus snail
Corticotropin releasing factor
Diuretic hormone 31
Diuretic hormone 44
Days post fertilization
Egg laying hormone
Annelid excitatory peptide
Expressed sequence tag
Gonadotropin releasing hormone
Hours post fertilization
Insulin related peptide
Liquid chromatography - tandem mass spectrometry
Abdominal ganglion neuropeptide L11 of A. californica
Mollusk neuropeptide KY
Open reading frame
Pheromone biosynthesis activating neuropeptide
Pigment dispersing factor
Posterior error probabilities
Peptide spectrum matches
Red pigment concentrating hormone
Small cardio active peptide
Liu F, Baggerman G, Schoofs L, Wets G: The construction of a bioactive peptide database in metazoa. J Proteome Res. 2008, 7: 4119-4131. 10.1021/pr800037n.
Watanabe H, Fujisawa T, Holstein TW: Cnidarians and the evolutionary origin of the nervous system. Dev Growth Differ. 2009, 51: 167-183. 10.1111/j.1440-169X.2009.01103.x.
Srivastava M, Simakov O, Chapman J, Fahey B, Gauthier ME, Mitros T, Richards GS, Conaco C, Dacre M, Hellsten U, Larroux C, Putnam NH, Stanke M, Adamska M, Darling A, Degnan SM, Oakley TH, Plachetzki DC, Zhai Y, Adamski M, Calcino A, Cummins SF, Goodstein DM, Harris C, Jackson DJ, Leys SP, Shu S, Woodcroft BJ, Vervoort M, Kosik KS, et al: The Amphimedon queenslandica genome and the evolution of animal complexity. Nature. 2010, 466: 720-726. 10.1038/nature09201.
Attenborough RM, Hayward DC, Kitahara MV, Miller DJ, Ball EE: A “neural” enzyme in nonbilaterian animals and algae: preneural origins for peptidylglycine alpha-amidating monooxygenase. Mol Biol Evol. 2012, 29: 3095-3109. 10.1093/molbev/mss114.
Hook V, Funkelstein L, Lu D, Bark S, Wegrzyn J, Hwang SR: Proteases for processing proneuropeptides into peptide neurotransmitters and hormones. Annu Rev Pharmacol Toxicol. 2008, 48: 393-423. 10.1146/annurev.pharmtox.48.113006.094812.
Eipper BA, Stoffers DA, Mains RE: The biosynthesis of neuropeptides: peptide alpha-amidation. Annu Rev Neurosci. 1992, 15: 57-85. 10.1146/annurev.ne.15.030192.000421.
Marks N, Stern F, Kastin AJ: Biodegradation of α-MSH and derived peptides by rat brain extracts, and by rat and human serum. Brain Res Bull. 1976, 1: 591-593. 10.1016/0361-9230(76)90086-1.
In Y, Ono H, Ishida T: Structural studies on C-amidated amino acids and peptides: function of amide group in molecular association in crystal structures of Val-Gly-NH2, Ser-Phe-NH2, Gly-Tyr-NH2 and Pro-Tyr-NH2 hydrochloride salts. Chem Pharm Bull. 2002, 50: 571-577. 10.1248/cpb.50.571.
Edison AS, Espinoza E, Zachariah C: Conformational ensembles: the role of neuropeptide structures in receptor binding. J Neurosci. 1999, 19: 6318-6326.
Merkler DJ: C-terminal amidated peptides: production by the in vitro enzymatic amidation of glycine-extended peptides and the importance of the amide to bioactivity. Enzyme Microb Technol. 1994, 16: 450-456. 10.1016/0141-0229(94)90014-0.
Prigge ST, Mains RE, Eipper BA, Amzel LM: New insights into copper monooxygenases and peptide amidation: structure, mechanism and function. Cell Mol Life Sci. 2000, 57: 1236-1259. 10.1007/PL00000763.
Wegener C, Gorbashov A: Molecular evolution of neuropeptides in the genus Drosophila. Genome Biol. 2008, 9: R131-10.1186/gb-2008-9-8-r131.
Conzelmann M, Jékely G: Antibodies against conserved amidated neuropeptide epitopes enrich the comparative neurobiology toolbox. Evodevo. 2012, 3: 23-10.1186/2041-9139-3-23.
Liu F, Baggerman G, Schoofs L, Wets G: Uncovering conserved patterns in bioactive peptides in Metazoa. Peptides. 2006, 27: 3137-3153. 10.1016/j.peptides.2006.08.021.
Hewes RS: Neuropeptides and Neuropeptide receptors in the Drosophila melanogaster genome. Genome Res. 2001, 11: 1126-1142. 10.1101/gr.169901.
Cho HJ, Acharjee S, Moon MJ, Oh DY, Vaudry H, Kwon HB, Seong JY: Molecular evolution of neuropeptide receptors with regard to maintaining high affinity to their authentic ligands. Gen Comp Endocrinol. 2007, 153: 98-107. 10.1016/j.ygcen.2006.12.013.
Kim D-K, Cho EB, Moon MJ, Park S, Hwang J-I, Do Rego J-L, Vaudry H, Seong JY: Molecular coevolution of neuropeptides gonadotropin-releasing hormone and kisspeptin with their cognate G protein-coupled receptors. Front Neurosci. 2012, 6: 3-
Jurenka R, Nusawardani T: The pyrokinin/pheromone biosynthesis-activating neuropeptide (PBAN) family of peptides and their receptors in Insecta: evolutionary trace indicates potential receptor ligand-binding domains. Insect Mol Biol. 2011, 20: 323-334. 10.1111/j.1365-2583.2010.01065.x.
Jékely G: Global view of the evolution and diversity of metazoan neuropeptide signaling. Proc Natl Acad Sci U S A. 2013, 110: 8702-8707. 10.1073/pnas.1221833110.
Mirabeau O, Joly J-S: Molecular evolution of peptidergic signaling systems in bilaterians. Proc Natl Acad Sci U S A. 2013, 110: E2028-E2037. 10.1073/pnas.1219956110.
Schoofs L, Holman GM, Hayes TK, Nachman RJ, De Loof A: Isolation, identification and synthesis of locusta myoinhibiting peptide (LOM-MIP), a novel biologically active neuropeptide from Locusta migratoria. Regul Pept. 1991, 36: 111-119. 10.1016/0167-0115(91)90199-Q.
Meunier JC, Mollereau C, Toll L, Suaudeau C, Moisand C, Alvinerie P, Butour JL, Guillemot JC, Ferrara P, Monsarrat B: Isolation and structure of the endogenous agonist of opioid receptor-like ORL1 receptor. Nature. 1995, 377: 532-535. 10.1038/377532a0.
Reinscheid RK, Nothacker HP, Bourson A, Ardati A, Henningsen RA, Bunzow JR, Grandy DK, Langen H, Monsma FJ, Civelli O: Orphanin FQ: a neuropeptide that activates an opioid like G protein-coupled receptor. Science. 1995, 270: 792-794. 10.1126/science.270.5237.792.
Katafuchi T, Kikumoto K, Hamano K, Kangawa K, Matsuo H, Minamino N: Calcitonin receptor-stimulating peptide, a new member of the calcitonin gene-related peptide family. Its isolation from porcine brain, structure, tissue distribution, and biological activity. J Biol Chem. 2003, 278: 12046-12054. 10.1074/jbc.M207970200.
Veenstra JA: Neurohormones and neuropeptides encoded by the genome of Lottia gigantea, with reference to other mollusks and insects. Gen Comp Endocrinol. 2010, 167: 86-103. 10.1016/j.ygcen.2010.02.010.
Nathoo AN, Moeller RA, Westlund BA, Hart AC: Identification of neuropeptide-like protein gene families in Caenorhabditis elegans and other species. Proc Natl Acad Sci. 2001, 98: 14000-14005. 10.1073/pnas.241231298.
Hinuma S, Shintani Y, Fukusumi S, Iijima N, Matsumoto Y, Hosoya M, Fujii R, Watanabe T, Kikuchi K, Terao Y, Yano T, Yamamoto T, Kawamata Y, Habata Y, Asada M, Kitada C, Kurokawa T, Onda H, Nishimura O, Tanaka M, Ibata Y, Fujino M: New neuropeptides containing carboxy-terminal RFamide and their receptor in mammals. Nat Cell Biol. 2000, 2: 703-708. 10.1038/35036326.
Conzelmann M, Offenburger S-L, Asadulina A, Keller T, Münch TA, Jékely G: Neuropeptides regulate swimming depth of Platynereis larvae. Proc Natl Acad Sci U S A. 2011, 108: E1174-E1183. 10.1073/pnas.1109085108.
McVeigh P, Mair GR, Atkinson L, Ladurner P, Zamanian M, Novozhilova E, Marks NJ, Day TA, Maule AG: Discovery of multiple neuropeptide families in the phylum Platyhelminthes. Int J Parasitol. 2009, 39: 1243-1252. 10.1016/j.ijpara.2009.03.005.
Rowe ML, Elphick MR: The neuropeptide transcriptome of a model echinoderm, the sea urchin Strongylocentrotus purpuratus. Gen Comp Endocrinol. 2012, 179: 331-344. 10.1016/j.ygcen.2012.09.009.
Hummon AB, Amare A, Sweedler JV: Discovering new invertebrate neuropeptides using mass spectrometry. Mass Spectrom Rev. 2006, 25: 77-98. 10.1002/mas.20055.
Boonen K, Landuyt B, Baggerman G, Husson SJ, Huybrechts J, Schoofs L: Peptidomics: the integrated approach of MS, hyphenated techniques and bioinformatics for neuropeptide analysis. J Sep Sci. 2008, 31: 427-445. 10.1002/jssc.200700450.
Menschaert G, Vandekerckhove TTM, Baggerman G, Schoofs L, Luyten W, Criekinge WV: Peptidomics coming of Age: a review of contributions from a bioinformatics angle. J Proteome Res. 2010, 9: 2051-2061. 10.1021/pr900929m.
Collins JJ, Hou X, Romanova EV, Lambrus BG, Miller CM, Saberi A, Sweedler JV, Newmark PA: Genome-wide analyses reveal a role for peptide hormones in planarian germline development. Plos Biol. 2010, 8: e1000509-10.1371/journal.pbio.1000509.
Li B, Predel R, Neupert S, Hauser F, Tanaka Y, Cazzamali G, Williamson M, Arakane Y, Verleyen P, Schoofs L, Schachtner J, Grimmelikhuijzen CJP, Park Y: Genomics, transcriptomics, and peptidomics of neuropeptides and protein hormones in the red flour beetle Tribolium castaneum. Genome Res. 2007, 18: 113-122. 10.1101/gr.6714008.
Hauser F, Neupert S, Williamson M, Predel R, Tanaka Y, Grimmelikhuijzen CJ: Genomics and peptidomics of neuropeptides and protein hormones present in the parasitic wasp Nasonia vitripennis. J Proteome Res. 2010, 9: 5296-5310. 10.1021/pr100570j.
Dircksen H, Neupert S, Predel R, Verleyen P, Huybrechts J, Strauss J, Hauser F, Stafflinger E, Schneider M, Pauwels K, Schoofs L, Grimmelikhuijzen CJP: Genomics, transcriptomics, and peptidomics of Daphnia pulex neuropeptides and protein hormones. J Proteome Res. 2011, 10: 4478-4504. 10.1021/pr200284e.
Xie F, London SE, Southey BR, Annangudi SP, Amare A, Rodriguez-Zas SL, Clayton DF, Sweedler JV: The zebra finch neuropeptidome: prediction, detection and expression. BMC Biol. 2010, 8: 28-10.1186/1741-7007-8-28.
Oumi T, Ukena K, Matsushima O, Ikeda T, Fujita T, Minakata H, Nomoto K: Annetocin - an oxytocin-related peptide isolated from the earthworm, Eisenia foetida. Biochem Biophys Res Commun. 1994, 198: 393-399. 10.1006/bbrc.1994.1055.
Veenstra JA: Neuropeptide evolution: neurohormones and neuropeptides predicted from the genomes of Capitella teleta and Helobdella robusta. Gen Comp Endocrinol. 2011, 171: 160-175. 10.1016/j.ygcen.2011.01.005.
Salzet M, Bulet P, Wattez C, Malecha J: FMRFamide-related peptides in the sex segmental ganglia of the Pharyngobdellid leech Erpobdella octoculata. Identification and involvement in the control of hydric balance. Eur J Biochem. 1994, 221: 269-275. 10.1111/j.1432-1033.1994.tb18738.x.
Evans BD, Pohl J, Kartsonis NA, Calabrese RL: Identification of RFamide neuropeptides in the medicinal leech. Peptides. 1991, 12: 897-908. 10.1016/0196-9781(91)90035-N.
Simon TW, Schmidt J, Calabrese RL: Modulation of high-threshold transmission between heart interneurons of the medicinal leech by FMRF-NH2. J Neurophysiol. 1994, 71: 454-466.
Díaz-Miranda L, de Motta GE, García-Arrarás JE: Monoamines and neuropeptides as transmitters in the sedentary polychaete Sabellastarte magnifica: Actions on the longitudinal muscle of the body wall. J Exp Zool. 1992, 263: 54-67. 10.1002/jez.1402630107.
Krajniak KG, Greenberg MJ: The localization of FMRFamide in the nervous and somatic tissues of Nereis virens and its effects upon the isolated esophagus. Comp Biochem Physiol. 1992, 101: 93-100.
Ukena K, Oumi T, Matsushima O, Takahashi T, Muneoka Y, Fujita T, Minakata H, Nomoto K: Inhibitory pentapeptides isolated from the gut of the earthworm, Eisenia foetida. Comp Biochem Physiol A Physiol. 1996, 114: 245-249. 10.1016/0300-9629(95)02134-5.
O'Gara BA, Brown PL, Dlugosch D, Kandiel A, Ku JW, Geier JK, Henggeler NC, Abbasi A, Kounalakis N: Regulation of pharyngeal motility by FMRFamide and related peptides in the medicinal leech, Hirudo medicinalis. Invert Neurosci. 1999, 4: 0041-0053. 10.1007/s101580050006.
Herbert Z, Pollák E, Zougman A, Boros A, Kapan N, Molnár L: Identification of novel neuropeptides in the ventral nerve cord ganglia and their targets in an annelid worm, Eisenia fetida. J Comp Neurol. 2009, 514: 415-432. 10.1002/cne.22043.
Matsushima O, Takahashi T, Morishita F, Fujimoto M, Ikeda T, Kubota I, Nose T, Miki W: Two S-Iamide Peptides, AKSGFVRIamide and VSSFVRIamide, Isolated from an Annelid, Perinereis vancaurica. Biol Bull. 2002, 184: 216-222.
Jékely G, Colombelli J, Hausen H, Guy K, Stelzer E, Nédélec F, Arendt D: Mechanism of phototaxis in marine zooplankton. Nature. 2008, 456: 395-399. 10.1038/nature07590.
Minakata H, Fujita T, Kawano T, Nagahama T, Oumi T, Ukena K, Matsushima O, Muneoka Y, Nomoto K: The leech excitatory peptide, a member of the GGNG peptide family: isolation and comparison with the earthworm GGNG peptides. FEBS Lett. 1997, 410: 437-442. 10.1016/S0014-5793(97)00567-X.
Matsushima O, Takahama H, Ono Y, Nagahama T, Morishita F, Furukawa Y, Iwakoshi-Ukena E, Hisada M, Takuwa-Kuroda K, Minakata H: A novel GGNG-related neuropeptide from the polychaete Perinereis vancaurica. Peptides. 2002, 23: 1379-1390. 10.1016/S0196-9781(02)00075-X.
Nagahama T, Ukena K, Oumi T, Morishita F, Furukawa Y, Matsushima O, Satake H, Takuwa K, Kawano T, Minakata H, Nomoto K: Localization of leech excitatory peptide, a member of the GGNG peptides, in the central nervous system of a leech (Whitmania pigra) by immunohistochemistry and in situ hybridization. Cell Tissue Res. 1999, 297: 155-162. 10.1007/s004410051343.
Salzet M, Verger-Bocquet M, Vandenbulcke F, Van Minnen J: Leech egg-laying-like hormone: structure, neuronal distribution and phylogeny. Brain Res Mol Brain Res. 1997, 49: 211-221. 10.1016/S0169-328X(97)00145-9.
Wang Y, Price DA, Sahley CL: Identification and characterization of a myomodulin-like peptide in the leech. Peptides. 1998, 19: 487-493. 10.1016/S0196-9781(97)00419-1.
Tobin A-E, Calabrese RL: Myomodulin increases Ih and inhibits the Na/K pump to modulate bursting in leech heart interneurons. J Neurophysiol. 2005, 94: 3938-3950. 10.1152/jn.00340.2005.
Takahashi T, Matsushima O, Morishita F: A myomodulin-CARP-related peptide isolated from a polychaete annelid, Perinereis vancaurica. Zoolog Sci. 1994, 11: 33-38.
Tessmar-Raible K, Raible F, Christodoulou F, Guy K, Rembold M, Hausen H, Arendt D: Conserved sensory-neurosecretory cell types in annelid and fish forebrain: insights into hypothalamus evolution. Cell. 2007, 129: 1389-1400. 10.1016/j.cell.2007.04.041.
Wagenaar DA, Hamilton MS, Huang T, Kristan WB, French KA: A hormone-activated central pattern generator for courtship. Curr Biol. 2010, 20: 487-495. 10.1016/j.cub.2010.02.027.
Tsai PS, Zhang L: The emergence and loss of gonadotropin-releasing hormone in protostomes: orthology, phylogeny, structure, and function. Biol Reprod. 2008, 79: 798-805. 10.1095/biolreprod.108.070185.
Luis Quintanar J, Gutiérrez-García K, Castillo-Hernández L: The neuropeptide Gonadotropin-releasing hormone modifies the spontaneous muscular contraction in the earthworm: Eisenia foetida. Invert Neurosci. 2011, 11: 113-116. 10.1007/s10158-011-0120-7.
LeRoith D, Lesniak MA, Roth J: Insulin in Insects and Annelids. Diabetes. 1981, 30: 70-76. 10.2337/diab.30.1.70.
Díaz-Miranda L, Escalona De Motta G, Garc A-A, JE S: Localization of neuropeptides in the nervous system of the marine annelid Sabellastarte magnifica. Cell Tissue Res. 1991, 266: 209-217. 10.1007/BF00678726.
Curry WJ, Fairweather I, Johnston CF, Halton DW, Buchanan KD: Immunocytochemical demonstration of vertebrate neuropeptides in the earthworm Lumbricus terrestris (Annelida, Oligochaeta). Cell Tissue Res. 1989, 257: 577-586. 10.1007/BF00221468.
Conzelmann M, Williams EA, Tunaru S, Randel N, Shahidi R, Asadulina A, Berger J, Offermanns S, Jékely G: Conserved MIP receptor-ligand pair regulates Platynereis larval settlement. Proc Natl Acad Sci U S A. 2013, 110: 8224-8229. 10.1073/pnas.1220285110.
Tomer R, Denes AS, Tessmar-Raible K, Arendt D: Profiling by image registration reveals common origin of annelid mushroom bodies and vertebrate pallium. Cell. 2010, 142: 800-809. 10.1016/j.cell.2010.07.043.
Fischer AH, Henrich T, Arendt D: The normal development of Platynereis dumerilii (Nereididae, Annelida). Front Zool. 2010, 7: 31-10.1186/1742-9994-7-31.
Fischer A, Dorresteijn A: The polychaete Platynereis dumerilii (Annelida): a laboratory animal with spiralian cleavage, lifelong segment proliferation and a mixed benthic/pelagic life cycle. Bioessays. 2004, 26: 314-325. 10.1002/bies.10409.
Petersen TN, Brunak S, Heijne Von G, Nielsen H: SignalP 4.0: discriminating signal peptides from transmembrane regions. Nat Methods. 2011, 8: 785-786. 10.1038/nmeth.1701.
Mbikay M, Seidah NG, Chretien M: Neuroendocrine secretory protein 7B2: structure, expression and functions. Biochem J. 2001, 357: 329-342. 10.1042/0264-6021:3570329.
Senatorov VV, Yang CR, Marcinkiewicz M, Chrétien M, Renaud LP: Depolarizing action of secretory granule protein 7B2 on Rat supraoptic neurosecretory neurons. J Neuroendocrinol. 1993, 5: 533-536. 10.1111/j.1365-2826.1993.tb00518.x.
Rayne RC, O'Shea M: Reconstitution of adipokinetic hormone biosynthesis in vitro indicates steps in prohormone processing. Eur J Biochem. 1994, 219: 781-789. 10.1111/j.1432-1033.1994.tb18558.x.
Frickey T, Lupas A: CLANS: a Java application for visualizing protein families based on pairwise similarity. Bioinformatics. 2004, 20: 3702-3704. 10.1093/bioinformatics/bth444.
Baggerman G, Liu F, Wets G, Schoofs L: Bioinformatic analysis of peptide precursor proteins. Ann N Y Acad Sci. 2005, 1040: 59-65. 10.1196/annals.1327.006.
Aravind L, Koonin EV: A colipase fold in the carboxy-terminal domain of the Wnt antagonists - the Dickkopfs. Curr Biol. 1998, 8: R477-R478. 10.1016/S0960-9822(98)70309-4.
Dunn JG, Foo CK, Belletier NG, Gavis ER, Weissman JS: Ribosome profiling reveals pervasive and regulated stop codon readthrough in Drosophila melanogaster. eLife. 2013, 2: e01179-10.7554/eLife.01179.
Tessmar-Raible K, Arendt D: Emerging systems: between vertebrates and arthropods, the Lophotrochozoa. Curr Opin Genet Dev. 2003, 13: 331-340. 10.1016/S0959-437X(03)00086-8.
Robb SMC, Ross E, Sánchez Alvarado A: SmedGD: the Schmidtea mediterranea genome database. Nucleic Acids Res. 2008, 36: D599-D606.
Backfisch B, Veedin Rajan VB, Fischer RM, Lohs C, Arboleda E, Tessmar-Raible K, Raible F: Stable transgenesis in the marine annelid Platynereis dumerilii sheds new light on photoreceptor evolution. Proc Natl Acad Sci U S A. 2013, 110: 193-198. 10.1073/pnas.1209657109.
Jékely G, Arendt D: Cellular resolution expression profiling using confocal detection of NBT/BCIP precipitate by reflection microscopy. Biotech. 2007, 42: 751-755. 10.2144/000112462.
Randel N, Bezares-Calderón LA, Gühmann M, Shahidi R, Jékely G: Expression dynamics and protein localization of rhabdomeric opsins in Platynereis larvae. Integr Comp Biol. 2013, 53: 7-16. 10.1093/icb/ict046.
Asadulina A, Panzera A, Verasztó C, Liebig C, Jékely G: Whole-body gene expression pattern registration in Platynereis larvae. Evodevo. 2012, 3: 27-10.1186/2041-9139-3-27.
Hauenschild CFA: Platynereis dumerilii. Mikroskopische Anatomie, Fortpflanzung, Entwicklung. 1969, Stuttgart: Gustav Fischer
Ewing B, Hillier L, Wendl MC, Green P: Base-calling of automated sequencer traces using phred. I. Accuracy assessment. Genome Res. 1998, 8: 175-185. 10.1101/gr.8.3.175.
Ewing B, Green P: Base-calling of automated sequencer traces using phred. II. Error probabilities. Genome Res. 1998, 8: 186-194.
Schmieder R, Lim YW, Edwards R: Identification and removal of ribosomal RNA sequences from metatranscriptomes. Bioinformatics. 2012, 28: 433-435. 10.1093/bioinformatics/btr669.
Huang X, Madan A: CAP3: A DNA sequence assembly program. Genome Res. 1999, 9: 868-877. 10.1101/gr.9.9.868.
Robinson MD, McCarthy DJ, Smyth GK: edgeR: a Bioconductor package for differential expression analysis of digital gene expression data. Bioinformatics. 2010, 26: 139-140. 10.1093/bioinformatics/btp616.
Rappsilber J, Mann M, Ishihama Y: Protocol for micro-purification, enrichment, pre-fractionation and storage of peptides for proteomics using StageTips. Nat Protoc. 2007, 2: 1896-1906. 10.1038/nprot.2007.261.
Borchert N, Dieterich C, Krug K, Schütz W, Jung S, Nordheim A, Sommer RJ, Macek B: Proteogenomics of Pristionchus pacificus reveals distinct proteome structure of nematode models. Genome Res. 2010, 20: 837-846. 10.1101/gr.103119.109.
Franz-Wachtel M, Eisler SA, Krug K, Wahl S, Carpy A, Nordheim A, Pfizenmaier K, Hausser A, Macek B: Global detection of protein kinase D-dependent phosphorylation events in nocodazole-treated human cells. Mol Cell Proteomics. 2012, 11: 160-170. 10.1074/mcp.M111.016014.
Cox J, Mann M: MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification. Nat Biotechnol. 2008, 26: 1367-1372. 10.1038/nbt.1511.
Cox J, Neuhauser N, Michalski A, Scheltema RA, Olsen JV, Mann M: Andromeda: a peptide search engine integrated into the MaxQuant environment. J Proteome Res. 2011, 10: 1794-1805. 10.1021/pr101065j.
Elias JE, Gygi SP: Target-decoy search strategy for increased confidence in large-scale protein identifications by mass spectrometry. Nat Methods. 2007, 4: 207-214. 10.1038/nmeth1019.
This work was supported by Max Planck Society Sequencing Grant
M.IF.A.ENTW8050 to GJ. The research leading to these results was supported by the European Research Council under European Union Seventh Framework Program FP7/2007–2013 and European Research Council Grant Agreement 260821.
The authors declare that they have no competing interests.
MC extracted peptide samples, analyzed the transcriptome and mass-spectrometry data, performed immunoassays, participated in the design of the study and drafted the manuscript. EAW generated the transcriptome resource, performed the stage-specific transcription profiling and helped to draft the manuscript. KK performed the processing, bioinformatic analysis and validation of the MS-data and helped to draft the manuscript. MFW processed and analyzed mass-spectrometry peptide samples. BM designed and coordinated the mass-spectrometry analysis and helped to draft the manuscript. GJ designed the study, generated the transcriptome resource, performed sequence analysis and sequence clustering and drafted the manuscript. All authors read and approved the final manuscript.
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- Diuretic hormone