- Research article
- Open Access
The serendipitous origin of chordate secretin peptide family members
BMC Evolutionary Biology volume 10, Article number: 135 (2010)
The secretin family is a pleotropic group of brain-gut peptides with affinity for class 2 G-protein coupled receptors (secretin family GPCRs) proposed to have emerged early in the metazoan radiation via gene or genome duplications. In human, 10 members exist and sequence and functional homologues and ligand-receptor pairs have been characterised in representatives of most vertebrate classes. Secretin-like family GPCR homologues have also been isolated in non-vertebrate genomes however their corresponding ligands have not been convincingly identified and their evolution remains enigmatic.
In silico sequence comparisons failed to retrieve a non-vertebrate (porifera, cnidaria, protostome and early deuterostome) secretin family homologue. In contrast, secretin family members were identified in lamprey, several teleosts and tetrapods and comparative studies revealed that sequence and structure is in general maintained. Sequence comparisons and phylogenetic analysis revealed that PACAP, VIP and GCG are the most highly conserved members and two major peptide subfamilies exist; i) PACAP-like which includes PACAP, PRP, VIP, PH, GHRH, SCT and ii) GCG-like which includes GCG, GLP1, GLP2 and GIP. Conserved regions flanking secretin family members were established by comparative analysis of the Takifugu, Xenopus, chicken and human genomes and gene homologues were identified in nematode, Drosophila and Ciona genomes but no gene linkage occurred. However, in Drosophila and nematode genes which flank vertebrate secretin family members were identified in the same chromosome.
Receptors of the secretin-like family GPCRs are present in protostomes but no sequence homologues of the vertebrate cognate ligands have been identified. It has not been possible to determine when the ligands evolved but it seems likely that it was after the protostome-deuterostome divergence from an exon that was part of an existing gene or gene fragment by rounds of gene/genome duplication. The duplicate exon under different evolutionary pressures originated the chordate PACAP-like and GCG-like subfamily groups. This event occurred after the emergence of the metazoan secretin GPCRs and led to the establishment of novel peptide-receptor interactions that contributed to the generation of novel physiological functions in the chordate lineage.
The evolution of the secretin family of brain-gut peptides remains enigmatic despite being some of the first endocrine factors ever identified. For example, in 1902 the ground breaking experiments of Bayliss and Starling with dog intestinal extracts set off the search for the active principal and, by 1961, secretin (SCT) had been isolated and sequenced . Currently, 10 peptides belonging to the secretin family have been isolated in humans and include; SCT, vasoactive intestinal peptide (VIP), pituitary adenylate cyclase-activating polypeptide (PACAP), peptide histidine methionine (PHM), PACAP-related peptide (PRP), growth hormone-releasing hormone (GHRH), glucagon (GCG), glucagon-like peptide (GLP 1 and 2) and glucose-dependent insulinotropic peptide (GIP) [2–4]. Members of the secretin family share significant structural and conformational homology and their key metabolic and developmental functions in human make them of considerable pharmacological interest. Members of class 2 G-protein coupled receptors (a.k.a family B GPCRs), bind and are activated by the secretin family members (family B1 members or secretin family GPCRs) and specific peptide-receptor pairs have been identified in representatives of different vertebrate classes. Class 2 GPCRs is a larger family of receptors and also includes members of the metazoan adhesion (B2) and insect methuselah (B3) families and secretin family GPCRs (B1) are proposed to descend from the adhesion receptors prior to protostome-deuterostome divergence [5, 6].
In protostomes (nematodes, arthropods, annelids and platyhelminthes) and early deuterostomes such as Ciona and amphioxus, immunohistochemical (IHC) approaches using antisera raised against various mammalian secretin family members suggest they possess similar peptides to vertebrates (Table 1). PACAP-like genes (pacap1 and pacap2) have only been reported in the tunicate, Chelyosoma productum  and partial mRNAs (114bp) corresponding to the highly conserved PACAP coding exon  have been isolated in Hydra magnipapillata and several protostomes and deposited in public databases . The existing data has been taken to indicate that an ancestral secretin family gene was probably present prior to the deuterostome-protostome divergence and most likely resembled the vertebrate PACAP precursor [2, 8, 10–12]. Paradoxically, in protostomes with fully sequenced genomes and extensive molecular resources (Figure 1, Additional file 1), genes encoding ligands homologous to members of the vertebrate secretin family have not been reported. In contrast, secretin-like family GPCR encoding genes which share similar sequence, structure and conserved gene environment with the vertebrate members have been identified, making ligand-receptor evolution an interesting enigma [13–16].
The present study focuses on secretin family ligands and complements previous studies aimed at identifying and characterising the evolution of family 2 GPCRs [5, 6, 8, 14, 17]. A comparative approach which takes advantage of the wealth of information currently available (genome, ESTs, peptide) for porifera, cnidaria, protostomes, early deuterostomes and vertebrates (Figure 1), is undertaken to re-evaluate the origin of the secretin family in metazoa. The sequence, gene structure and gene environment of secretin family members in vertebrates with sequenced genomes was characterised and used to search for homologue peptides, genes or genome regions in non-vertebrates.
Vertebrate secretin family members
Sequence database searches using the nucleotide and mature peptide sequences of human and zebrafish secretin family members, readily identified homologues in lamprey, teleost and tetrapod (Xenopus, lizard, chicken) genomes. This is due to the high sequence conservation of the mature peptide region between the vertebrate members which facilitates their identification (Table 2) (see reviews [2, 4, 8, 18, 19]).
The tetrapod members
In humans, 10 peptides encoded by six genes have been isolated. In Aves, homologues of the mammalian members have been identified and peptides and corresponding transcripts were isolated in duck (Anas platyrhynchos), chicken (Gallus gallus) and turkey (Meleagris gallopavo) [20–27]. In silico analysis of the chicken genome identified six genes encoding secretin family members which share similar organisation to the human homologues and comparative analysis revealed they correspond to the peptides and nucleotide precursors previously described (Table 1 and Table 2). Searches in the reptile and amphibia genomes identified homologues for all human members with the exception of SCT and it remains to be established if the failure is due to the incomplete nature of their genome assemblies or to the absence of this gene. In reptiles, few members of this family have been reported to date. A VIP and GCG peptides were isolated from the Alligator mississippiensis, the nucleotide precursor of the latter peptide reported from the Heloderma suspectum [28–30] and a PRP/PACAP mRNA was recently characterised from the Italian wall lizard Podarcis sicula [31, 32]. Sequence database searches on the lizard Anolis carolinensis genome identified for the first time the genes encoding the reptile PHI/VIP (ENSACAG00000005619), PRP/PACAP (ENSACAG00000008729), GHRH (ENSACAG00000011836), GCG/GLP (ENSACAG00000014182) and GIP (ENSACAG00000006291) (Table 2). The predicted gene organisation suggests the coding exons for the mature peptides share identical structure with other metazoan genes and to date the exon encoding the lizard GLP2 remains to be identified.
Homologues of human secretin members have previously been reported in amphibians. VIP and PACAP and were isolated in Rana ridibunda [33, 34]; GCG from Rana catesbeiana  and in Xenopus laevis single transcripts for PRP/PACAP , PHI/VIP, GHRH , GCG/GLP  and GIP  have been described. The genome of Xenopus tropicalis contains secretin family homologues which share high sequence conservation with the tetrapod genes (Table 2), but one difference was the presence of three GLP1 exons (GLP1a, b and c) within the GCG/GLP gene structure as a result of a species-specific exon duplication.
The fish members
Peptides, transcripts and genes of the secretin family have also been isolated from the most diverse vertebrate clade, the teleosts. VIP was isolated from cod (Gadus morhua) [39, 40] and goldfish (Carassius auratus) , PACAP from the Japanese stargazer (Uranoscopus japonicus)  and GCG from the channel catfish (Ictalurus punctatus) [43, 44] (Table 1). The identification of two transcripts for PHI/VIP in goldfish Carassius auratus  and zebrafish (Danio rerio) (PHI/VIP a, EU031789 and PHI/VIP b, EU031790) and of two PRP/PACAP (PRP/PACAP a, NM_152885 and PRP/PACAP b, AF329633) [46, 47] and GCG/GLP precursors in zebrafish  suggests they are duplicates in fish and this has been confirmed by the identification of two PRP/PACAP and GCG/GLP genes in Takifugu (ENSTRUG00000003782 and ENSTRUG00000010059; ENSTRUG00000008721 and ENSTRUG00000004633, respectively) and Tetraodon (ENSTNIG00000017117 and ENSTNIG00000018649; ENSTNIG00000013278 and ENSTNIG00000000614, respectively) genomes (Table 2) . The greater number of secretin family genes identified in fish relative to tetrapods is most likely to be a result of the proposed teleost specific genome duplication and the absence of GIP and GHRH gene duplicates suggests they were probably deleted [49–51]. In common with Xenopus, no homologue of human SCT has been identified in fish genomes.
In the sea lamprey (Petromyzon marinus), a primitive vertebrate of the Agnatha clade, two homologues of human proglucagon (GCG/GLP) were characterised in the genome assembly Contig 31522 (GENSCAN00000079364) and Contig 32128 which correspond to the previously reported proglucagon I (AF159707) and proglucagon II (AF159708) transcripts, respectively . In the present study, searches of the partially sequenced lamprey genome retrieved putative PRP/PACAP (GENSCAN00000120210 on Contig3575.2) and PHI/VIP genes (shared between GENSCAN00000109335 and GENSCAN00000056150 localised on Contig20045.2 and Contig20045.3, respectively). However, GHRH, SCT and GIP were not identified possibly due to the present incomplete nature of its genome assembly.
Sequence and gene structure comparison
Sequence comparisons reveal that members of the secretin family are highly conserved and this also applies to their secondary structure which consists of a random N-terminal structure and a C-terminal alpha-helix [53, 54]. The lamprey, teleost, Xenopus, reptile and chicken members are in general 50% identical in amino acid sequence with the human homologues (Figure 2) and two main peptide subfamilies, which share in general a maximum of 60% sequence similarity between their members were identified; i) PACAP-like subfamily which includes 6 peptide groups (PACAP, PRP, VIP, PHI, GHRH and SCT) and ii) GCG-like subfamily which contains 4 peptide groups (GCG, GLP1, GLP2 and GIP). Highest sequence conservation from lamprey to human (>70% sequence identity) occurs within PACAP, VIP and GCG peptide groups which contrasts with PRP and GLP2 that are the most divergent and Takifugu PRP b and GLP2 predicted peptides are only 33% and 37% identical with the human homologues.
Consensus amino acids for peptide subfamilies were deduced and the overall conservation characterised. With few exceptions, 7 amino acid residues H1, D3, F6, T7, Y10, Q16 and L23 are the most abundant across the PACAP-like subfamily (Figure 2). The residues H1, D3 and L23 are present in all peptide groups with occasional exceptions in some taxa. However, the motif F6T7 is absent from the vertebrate PRP sequences and is only present in tunicate PRP and the residue Q16 is absent from the SCT mature peptide and Y10 is only present in the chicken SCT homologue. This suggests that specific modifications occurred within the conserved core domain of the PACAP-like subfamily members and their functional significance remains to be explored. A similar comparison of the vertebrate GCG-like subfamily indicates that 15 amino acid residues H1, A2, G4, T5, F6, S8, D9, S11, L14, A19, K20, F22, V23, W25, and L26 are generally maintained across the 4 peptide groups. Even if taxa variability is taken into consideration, the residues G4, F6 and F22 and the motifs S8 D9 and W25L26 are in general maintained (Figure 2). Peptide specific variations include for GIP, H1 which is replaced by Y, L14 which is replaced by M or V (with exception of lizard) and A19 which is replaced by K or Q. In the GCG mature peptide sequence A2 is replaced by S and in GLP2 with the exception of chicken and Takifugu T5 is replaced by S. Comparison of the metazoan PACAP-like and GCG-like subfamily consensus sequence revealed they overlap for the residues H1 and F6 which are key amino acids in secretin GPCR binding affinity [19, 53, 55, 56]. This suggests that, after exon/chromosome duplication of their common ancestor exon, distinct evolutionary pressures within each subfamily occurred.
The chordate PACAP shares in general 92% of amino acid sequence similarity with VIP and these two peptides are the most conserved members (Figure 3). In contrast, the vertebrate SCT demonstrates the lowest conservation (less than 62% within the PACAP-like subfamily) however this may be an artefact due to the restricted number of species in which it has been characterised. In addition, signature amino acid residues within or between peptide groups were also identified and they may reflect and support common evolutionary pathways and overlapping or specific functional roles. This includes, the PACAP Y13 and A24A25 motif, the V5, N9, F13 and N24 for VIP, the motif N7K8A9 and residue H24 within PRP, the L5, S8, E24 and I27 for PH, and the GHRH residues N8, I17, Q24 and I26 across the tetrapod and teleost members (Figure 2). Gene structure comparisons restricted to the mature peptide precursors revealed that PACAP and VIP exons are encoded in the same precursor as PRP and PH, respectively [2, 8] (Figure 3). Most common amino acids to the chordate PACAP and VIP members includes R14 and K15and the motifs M17A18V19 and V26L27 and they share a maximum of 37% amino acid sequence identity with PRP and PH indicating that after exon duplication considerable changes occurred. The latter peptides have a similar sequence (81% similar) which is closely related to vertebrate GHRH (88% similar) with which they partition the residues A2, K12, L14, G15 and the motif S18A19R20 and suggest a common evolutionary origin. The SCT gene has only been identified in tetrapods and the deduced peptide residues, E9 and Q20 are maintained in the mammalian and chicken homologues. The evolutionary origin of SCT is still enigmatic and it is proposed to have been lost in the fish lineage [14, 57].
Members of the GCG-like subfamily share at least 62% amino acid similarity and GLP1 and GLP2 have the highest identity (59%, Figure 3). In addition to the general sequence conservation of the GCG-like subfamily members, conserved amino acid positions within the vertebrate peptide groups were also identified (Figure 2). This includes S2, Q24, M27 and the motifs R17R18 and Q20D21 for GCG; V10, S12 and Q17 for GLP1; S5, N11 and L23 for GLP2; and Y1 and L27 in GIP. The GLP1 and GLP2 peptides are encoded in the same precursor (proglucagon precursor) as GCG with which they share 77% and 81% amino acid sequence similarity, respectively and the mature peptide coding exons are proposed to be a consequence of exon duplication events. Vertebrate GIP shares 37% and 40% sequence identity with GCG and GLPs, respectively and studies based upon gene structure comparisons suggest the latter emerged from the same exon as GCG, however the results of sequence analysis are inconclusive and more data is required [2, 27].
The secretin members in non-vertebrates
Database searches using the vertebrate nucleotide and peptide sequences of secretin family members and the duplicate urochordate Chelyosoma productum PRP/PACAP transcripts failed to identify conserved sequence and structure homologues in genome or EST databases from porifera, cnidaria, protostome and early deuterostomes (Ciona, amphioxus and sea urchin). Instead, short sequence matches were identified in unrelated genes or non-annotated genome segments. In depth analysis of the best matches, revealed homologies for the central region and C-terminal ends (outside the bioactive core) of the chordate mature peptides and, when the invertebrate fragments were used to interrogate vertebrate databases, they failed to retrieve a secretin family homologue suggesting that members of this family are absent from non-vertebrate genomes.
The exception is PACAP for which a highly conserved partial sequence corresponding to the exon encoding the mature peptide (>89% amino acid identity, ) has been isolated in Hydra magnipapillata (AB083650), in the tunicate, Halocynthia roretzi (AB121759) and in several protostomes such as planarian (Dugesia japonica, AB083649), crab (Eriocheir japonica, AB121765), squid (Sepioteuthis lessoniana, AB083651) and cockroach (Periplaneta americana, AB083652) . Database searches using the non-vertebrate PACAP nucleotide or deduced peptide sequences failed to retrieve homologues from protostomes with available genome data (Helobdella robusta, Capitella sp. I, Lottia gigantea, Daphnia pulex, Drosophila melanogaster, Aedes aegypti, Anopheles gambiae, Caenorhabditis elegans and Caenorhabditis briggsae). Moreover, searches performed in Hydra magnipapillata and related species Nematostella vectensis genome assemblies with the Hydra PACAP nucleotide or deduced peptide sequence also failed to confirm the existence of a gene encoding PACAP. In early deuterostomes, searches using the Chelyosoma productum PRP/PACAP nucleotide or deduced peptide sequences in Ciona intestinalis and Ciona savignyi genomes or available tunicate ESTs failed to identify possible sequence homologues in urochordate. Taken together these results raise questions about the authenticity of the previously reported sequences.
An alternative strategy utilized a secretin family prototype sequence model based on the assumption that the chordate members arose from a common precursor gene which duplicated to give PACAP-like and GCG-like subfamily exons (Figure 2 and 3). The prototype sequence deduced in silico was H1A2D3G4T5F6T7S8D9Y10S11xxL14xQ16xxA19K20xF22xxW25L26 (x represents variable position) and contains 18 conserved amino acid positions and high conservation was found for the N-terminal region. Structural characterisation using Pfam analysis classified the generated prototype sequence as a Hormone_2 member (PF00123, which includes the vertebrate secretin family members)  and sequence similarity searches performed retrieved secretin family members in vertebrates but failed to identify potential members in non-vertebrates. A second approach using HMM models and searching the general NCBI non-redundant (nr) peptide and an invertebrate subset of the NCBI nucleotide and EST (est_others) databases corroborated the preceding results.
The optimal maximum likelihood (ML) tree with bootstrap support values higher than 50% is presented in Figure 4. Despite the high level of sequence identity and short sequences utilized, phylogenetic analyses of the chordate mature peptides (1-27 aa) and their corresponding nucleotide sequences resulted in similar tree topologies and suggests that members of the secretin family share a common ancestry. In the optimal ML tree presented in Figure 4 two clades PACAP-like and GCG-like were obtained suggesting that after ancestral exon duplication two main peptide subgroups emerged and underwent distinct evolutionary trajectories. Similar tree topologies were obtained using Bayesian approaches (Supplementary table 2) and a PACAP-like derived clade includes the peptides PACAP, PRP, PH, VIP, GHRH and SCT and a GCG-like clade the peptides GCG, GLP1, GLP2 and GIP. The Chelyosoma PACAP deduced peptide sequences always grouped with the vertebrate peptide sequence homologues and the tunicate PRPs did not cluster with any particular peptide clade and in all the analysis performed tended to be more closely related to the tetrapod SCT.
Gene environment comparisons
The immediate gene environment of vertebrate secretin members was compared and indicates that PRP/PACAP, GCG/GLP, and GHRH genome regions are syntenic and gene order is in general maintained (Figure 5). The GCG/GLP gene environment shares at least 3 genes (KCNH7, IFIH1 and SLC4A10), PRP/PACAP, 2 genes (YES1 and METTL4) and GHRH, 1 gene (RPN2) when equivalent genome regions are compared between Takifugu, Xenopus, chicken and human. The VIP and GIP genomic regions are poorly conserved and no gene synteny or gene order was identified (data not shown). Moreover, searches also failed to identify conservation of gene linkage between the different vertebrate secretin family members.
In Takifugu, the neighbouring genes of the paralogue GCG/GLP (SLC4A10 and KCNH7, N000046 and N000036) and PACAP (YES1, N000223 and N000080) genes were also duplicates supporting the teleost gene or genome duplication event. Searches were extended to the lamprey and lizard genomes but contiguous sequences were too small to confirm the existence of gene environment conservation. Comparison of the SCT genome region between chicken (chromosome 5) and human (chromosome 11) revealed they are highly conserved and the order of 5 genes (MUCDHL, DRD4, DEAF1, EPS8L2 and PDDC1) is maintained. In Xenopus genome, the chicken and human SCT flanking genes are localised in the amphibian scaffold_296 and in Takifugu, where a gene homologue is proposed to be absent, they are distributed in two distinct genome regions: MUCDHL and DRD4 are localised in scaffold N000002 and the remaining genes in scaffold N000328 suggesting the existence of a conserved gene block prior to the emergence of the tetrapod gene (data not shown).
In order to identify a potential secretin family genome region in non-vertebrates, the conserved vertebrate gene environment was used to retrieve homologues in the C. elegans, Drosophila and Ciona genomes. Genes sharing similarity in sequence to those flanking the vertebrate GCG/GLP, PRP/PACAP and GHRH loci were identified although the genes encoding secretin family members were absent (Figure 6). In C. elegans the genes drh-3, abts-1, src-1 and M01A10.3 map to chromosome I and are respectively homologues of the human IFIH1 and SLC4A10 on chromosome 2, YES1 on chromosome 18 and RPN2 on chromosome 20. In Drosophila, sei and CG6370 are localised in chromosome 2R and are the homologues of human KCNH7 and RPN2 and the fruit-fly Dcr-2 and CG14906 genes in chromosome 3R the correspondent in sequence of the human IFIH1 and METTL4, respectively.
In the tunicate genome, homologues of the vertebrate secretin family flanking genes were identified scattered in the Ciona genome assembly. Homologues of human KCNH7 (ENSCING00000000802, scaffold_167), IFIH1 (ENSCING00000009744, scaffold_44) and SLC4A10 (ENSCING00000006669, chromosome 9p) genes which flank GCG/GLP in vertebrates were identified. The conserved gene environment of the vertebrate PRP/PACAP genes: YES1 (ENSCING00000008550 on scaffold_65) and METTL4 (ENSCING00000013236 on chromosome 8q) genes are also present as well the putative urochordate homologue of the RPN2 gene (ENSCING00000009122) conserved in the vertebrate GHRH genome region.
In the C. elegans genome chromosome 1 contained homologues of the genes which flank PRP/PACAP, GCG/GLP and GHRH in vertebrates. This suggests that this chromosome may be the protostome genome fragment that most resembles the potential metazoan ancestral secretin genome region from which the vertebrate members emerged. However, detailed analysis of chromosome positions (src-1, 1566932 to 1580204bp; M01A10.3, 5550508 to 5549145 bp; drh-3, 7820837 to 7826373 bp; and abst-1, 8307558 to 8296909 bp) revealed they are not mapped in close proximity and do not forms a gene cluster. Moreover, no conserved linkage between the putative Drosophila and the C. elegans gene homologues exists.
Comparative analysis of data from phylogenetically distant organisms is a major contributor for understanding gene and gene family evolution and the role of function and regulation in this process. The identification of gene homologues in vertebrates and early metazoan genomes provides a unique opportunity to perform comparative studies and to investigate gene family ancestries. The secretin family is a well-studied group of peptides which activate specific receptors of family 2 GPCRs to bring about their pleotropic actions in vertebrates. Secretin-like family GPCRs have been identified and cloned from non-vertebrate genomes [6, 14, 59, 60] and their putative peptide ligands identified by immunohistochemistry (IHC) using antisera raised against the mammalian peptide homologues (Table 1). Both peptides and their corresponding receptors are proposed to have arisen by gene duplication events prior to the vertebrate radiation [2, 6, 8, 10, 11, 18] and they represent an interesting model for studies of receptor-ligand evolution.
In the present study, despite extensive in silico database searches it was not possible to identify members of the secretin peptide family in non-vertebrates regardless of the report of a full-length PACAP cDNA in the tunicate, Chelyosoma productum  and cDNA of the PACAP coding exon in crab, cockroach, squid, planarian and Hydra magnipapillata [7, 9]. Moreover, using the partial PACAP cDNA previously identified in Hydra magnipapillata (a cnidaria) to interrogate its sequenced genome  failed to identify the gene homologue.
It seems unlikely that the failure to identify PACAP in non-vertebrates was related to the methodology used as a similar approach has been successfully utilized to identify the gene encoding the active nonapeptide hormone, vasotocin/vasopressin in the amphioxus genome assembly and also the gene loci in several chordates including teleosts . In fact, the existence of neurohypophysial hormones (eg. vasopressin and oxytocin) in deuterostomes and protostomes has been amply confirmed by the isolation of both genes and peptides from representatives of a number of different phyla (reviewed in ). Similarly, conserved sequence homologues of vertebrate neuropeptide Y family members have been isolated from molluscs and also from fruit-fly and mosquito and GPCR ligand-receptor pairs similar to the vertebrate NPY system have been characterised [63–65].
A comprehensive in silico analysis of the fully sequenced Drosophila genome identified and classified GPCRs and compared their number to putative neuropeptide ligands. Although 5 secretin family GPCR members were identified in the arthropod genome, only two potential ligands, corticotrophin releasing factor (CRF)-related peptides and amnesiac genes, unrelated to chordate secretin peptide family members were predicted . In contrast, recent studies performed in molluscs (Helix pomatia) using IHC and MALDI-TOF/TOF identified partial peptides with a similar mass to vertebrate PACAP in the snail whole hemolymph and CNS extracts . Should the identity of the peptide be confirmed by sequencing taking in consideration the results of the present study a new paradigm will be required to explain secretin family evolution.
There is evidence that genes for amnesiac in Drosophila and maxadilan in sand-fly might encode functional homologues of the vertebrate PACAP despite their lack of sequence similarity [2, 68–70] and the maxadilan peptide is able to activate mammalian PAC1 receptors in vitro [71, 72]. The activation of family 2 GPCRs members by the secretin family of ligands has been linked to their well conserved structure [53, 54] which comprises an alpha helix in the mid and C-terminal region and an N-terminal loop. The region of maxadilan implicated in PAC1 receptor activation has an identical structure to the N-terminal region of secretin family ligands and contains key amino acids involved in receptor activation (reviewed by ). In fact, mutation analysis with maxadilan demonstrated that despite its greater size compared to vertebrate secretin family peptides, the disruption of four conserved cysteine residues (1 - 5 and 14 - 51) responsible for the formation of two disulfide bonds led to loss of activity . Taking into consideration the degree of conservation of the N-terminal ligand binding domain of the secretin family GPCRs  and their relative promiscuity  it is unsurprising that protostome peptides activate vertebrate receptors. In nematode and Drosophila, PDF (Pigment Dispersing Factor) stimulated the homologues of vertebrate secretin GPCRs but they were not stimulated by secretin family members [14, 59, 60]. These observations suggest that specificity of the receptor members has changed during evolution and may explain the failure to identify conserved ligands.
A general model to explain peptide ligand binding and receptor activation has emerged recently for class B GPCRs (secretin family) . The proposed mechanism, known as the "two-domain model" suggests that initial ligand-receptor interactions are mediated by the central and C-terminal peptide segments with the extracellular N-terminal receptor region and that activation occurs subsequently when the bioactive N-terminus of the ligand binds the receptor juxtamembrane domain . In this context, the identification in the present study of putative "signature" amino acids conserved across taxa for each peptide groups may explain differences in selection and affinity for receptors. For example, mutation of conserved residues within the C-terminal region of VIP revealed that substitution of L23 (common to PACAP-like subfamily members) decreased peptide biological activity without altering the predicted structure . D3 is conserved across the PACAP-like peptides and this residue has a role in adenyl cyclase (AC) stimulation and interacts with basic residues (R188and K195) in the second transmembrane helix of VPAC . Similarly, D9 which is conserved across the GCG-like members is essential in the activation of mammalian GCGR . It will be of interest in the future to study the role of unique amino acid residues/motifs identified in the present study within the N-terminal and C-terminal regions of each peptide group.
Recently, a Darwinian evolutionary model was proposed to explain the origin of steroid hormones and their receptors and may also explain the emergence of metazoan secretin peptide-receptor pairs. The steroid hormones and receptors were proposed to have evolved through a molecular exploitation process in which structurally adapted receptors evolved prior to ligand emergence [79, 80]. By reconstructing the sequence of the ancestral steroid receptors (eg. corticoid receptor) the authors verified that they are activated by hormones (eg. aldosterone) that only emerged in the tetrapod lineage. At present, evolutionary comparisons of the metazoan receptor members and secretin peptide family suggests that, receptors emerged prior to the ligands which were subsequently acquired as a consequence of genome evolution in the chordate radiation. Generally, two major gene or genome duplication events are proposed to have occurred at the origin of vertebrates and have accompanied increased organismal complexity and emergence of gene novelties [81, 82]. Whilst the majority of gene duplicates were probably lost as a consequence of their functional redundancy, some were fixed in the genome by the gain of new biological functions or partitioning the function of the ancestral counterpart and this may be the case for the secretin family GPCRs and their ligands [8, 17, 83].
The origin of the chordate secretin peptide family has been previously associated with the insect adipokinetic hormone (AKH) and AKH-Precursor Related Peptides (APRP) precursor evolution . Despite their low sequence similarity, the arthropod AKH and APRP precursor was found to share a similar gene organisation and comparable functions with vertebrate GCG and GHRH and they were proposed to have shared common origin prior to protostome-deuterostome divergence (approximately 600 million years ago). However, against this hypothesis is the recent demonstration that insect ADK signals through a gonadotropin-releasing hormone (GnRH) like receptor (members of family 1 GPCRs) and also the isolation of putative nematode AKH-GnRH related precursors suggesting that the invertebrate ADK members may share common evolution with the metazoan GnRH system [85, 86].
The present study does not confirm the results of IHC studies in the early 70's and 80's which identified putative invertebrate secretin family members using antisera against mammalian peptides. It was not possible to identify sequence homologues of the Chelyosoma productum PRP/PACAP peptides in the sequenced Ciona genomes, although at least 8 putative secretin-like family GPCRs have been reported . The previous facts taken with i) the identification in snail of a putative PACAP peptide; and ii) the activation of a secretin-like family GPCRs in nematode and Drosophila by PDF but not by vertebrate secretin family members makes it difficult to establish when the peptide members emerged in the deuterostome lineage. It is hypothesised that the emergence of the full suite of receptors and their ligands accompanied the rapid genome changes during chordate evolution. The ancestral secretin family gene probably arose as part of an existing gene or gene fragment and via exon and gene duplication events generated the existing suite of family members (Figure 3). This occurred after the emergence of the secretin family GPCRs and led to the establishment of novel and specific receptor ligand interactions that contributed to the generation of novel physiological functions. In contrast, to other peptide families, such as NPY/PYY and Oxytocin/vasopressin which stimulate receptors of family 1 GPCRs and are highly conserved from protostomes to deuterostomes, members of the secretin family GPCRs appear to have adopted new ligands during evolution.
Using comparative sequence approaches the existence of putative non-vertebrate secretin family members were investigated in publicly available protostome and early deuterostome genome, EST and protein databases. The complete nucleotide and amino acid sequences of human secretin family members (PHM/VIP, P01282; PRP/PACAP, P18509; SCT, P09683; GHRH, P01286; GIP, P09681; and GCG/GLP, P01275) mature peptides and their homologues in zebrafish and tunicate Chelyosoma productum PRP/PACAP precursors were used to interrogate databases (Figure 1, Additional file 1). Searches were performed in the metazoan genomes of porifera (Amphimedon queenslandica), cnidarians (Nematostella vectensis and Hydra magnipapilata), planarian (Schmidtea mediterranea), annelids (Helobdella robusta and Capitella capitata), mollusc (Lottia gigantea), crustacean (Daphnia pulex), insects (Drosophila melanogaster, Aedes aegypti and Anopheles gambiae); nematodes (Caenorhabditis elegans and Caenorhabditis briggsae); and in the early deuterostomes, sea urchin (Strongylocentrotus purpuratus Build 2), cephalochordate (Branchiostoma floridae) and urochordates (Ciona savignyi and Ciona intestinalis); and also in the vertebrate sea lamprey (Petromyzon marinus), teleosts (zebrafish, Danio rerio; Takifugu rubripes; Tetraodon nigroviridis; medaka, Oryzias latipes; stickleback, Gasterosteus aculeatus) and tetrapods, frog (Xenopus tropicalis), lizard (Anolis carolinensis) and chicken (Gallus gallus). Searches of the Takifugu genome were also performed in http://fugu.nimr.mrc.ac.uk/blast. To substantiate the results, further searches for secretin family members were also carried out in the NCBI EST data sets for porifera (Porifera (taxid:6040), cnidaria (Cnidaria (taxid:6073), protostomes (Protostomia (taxid:33317)) and early deuterostome (Echinoderms (taxid:7586); Cephalochordata (taxid:7735); Urochordata (taxid:7712) and also in species specific EST databases for the planarian (Schmidtea mediterranea), crab (Celuca pugilator), pacific oyster (Crassostrea gigas) and mussel (Mytilus edulis) (Additional file 1). In addition, the complete nucleotide precursor or the sequence corresponding to the deduced mature peptide of secretin family members in deuterostome were used to interrogate the general nucleotide (nr/nt) and protein databases (nr) available at NCBI  and UniProt  using the BLAST programme.
For small mature peptide sequences the BLAST algorithm was adjusted (scoring matrix PAM30, word size 2, highest expected value parameters, low complexity filter off, no adjustment) to permit identification of short peptide hits with strong similarities. Searches using short nucleotide sequences were also performed with word size 7; expected value 1000 and low complexity filter off. Best matches with significant scores or low E values <0.01 were retrieved and analysed.
Searches using a hidden Markov model were performed with the HMMER3 (3.03b)  suite of software on the NCBI non-redundant (nr) peptide, and custom-made invertebrate nucleotide (nt) (1614126 records) and est_others (ests minus human and mouse) (11209486 records) databases using hmmsearch. Subset databases were constructed to reduce the computational burden of performing a HMMER3 search against the complete NCBI nucleotide and EST databases. The invertebrate subset databases were constructed by querying the NCBI databases using Entrez for all invertebrate GI numbers (Metazoa NOT Vertebrata) for both nt and est_others and filtered using fastacmd (part of the NCBI BLAST package). Peptide searches were performed with the Pfam model for the secretin peptide family members (Hormone_2 member, PF00123) and nucleotide queries with a model constructed in HMMER3 (3.03b) using the nucleotide aligned sequences of the 1-27 aa mature peptide regions of the secretin family members represented in Figure 2.
The potential secretin family members identified were compared with existing vertebrate members. The non-vertebrate sequences that shared similarity with previously annotated genes or gene intron regions were discarded and the remaining candidates used to interrogate the NCBI database to confirm identity and failed to retrieve a homologue of the vertebrate secretin family. In contrast, homologues in vertebrate datasets were identified and the deduced amino acid sequences of the retrieved transcripts or predicted exon coding regions were compared using ClustalX 2.0  with the conserved mature peptide region 1-27 aa of representatives of the secretin family with the exception of human GLP1 in which 5-32 aa were used that correspond to a unique coding exon. Peptide similarities/identities were determined using the GeneDoc programme  and amino acid consensus sequences within each peptide group were deduced and compared to demonstrate general levels of conservation for each subfamily. A prototype peptide representative of the chordate secretin family was constructed by fusing the most abundant amino acid residues within the PACAP-like and GCG-like peptides members. The in silico deduced sequence was submitted to Pfam  analysis to confirm identity as a secretin member and used to search the vertebrate and non-vertebrate NCBI databases with BLAST and adjusted parameters to identify homologues.
Phylogenetic analyses were performed using the ClustalX 2.0 alignment of the 1-27 aa mature peptide region of secretin members. The amino acid sequence alignment produced was analysed with PROTTEST to select the model of protein evolution that best fits dataset  and phylogenetic analyses were conducted using 95 taxa with the maximum likelihood and Bayesian estimation methods (MrBayes and PhyloBayes, Additional file 2). The maximum likelihood analysis was carried out using Phyml 3.0  with 100 bootstrap replicates with a JTT substitution model with a discrete gamma distribution of rates among sites with 4 categories (Г). A search for the optimal ML tree was also performed. Bayesian estimation using MrBayes  was performed with the Dayhoff model with Г and PhyloBayes  with the CAT model plus Г. The MrBayes analysis was conducted with two MCMC runs (each with 4 chains) for 200,000 generations with 20,000 samples. The PhyloBayes CAT analysis was performed using 2 independent run replicates (40727 and 40382 generations, respectively). Likelihoods were plotted against generation time and the MCMC chains were assumed to have reached stationarity when the curve plateaued. Phylogenetic sequence analysis was also performed using the nucleotide sequences of the 1-27 mature peptide domains with the ML method as previously described and the GTR model plus Г and the individual peptide clades present in both nucleotide and amino acid trees obtained were similar (data not shown).
Gene environment comparisons
The gene environment of vertebrate secretin family members was determined to identify potentially conserved gene blocks; these were then used to search for putative ancestral secretin genome-like regions in C. elegans, Drosophila and Ciona assemblies. The Takifugu NIX annotated scaffolds  were used as a guide to characterise the Xenopus (Xenopus tropicalis) , the chicken and human homologue regions . The NIX annotated scaffolds from Takifugu were used as they had greater information content than the homologue data deposited in ENSEMBL. The conserved vertebrate gene environment identified the genes YES1 and METTL4 for PRP/PACAP; the gene RPN2 for GHRH; and the KCNH7, IFIH1 and SLC4A10 genes within the vertebrate GCG/GLP genomic region. The, C. elegans, Drosophila and Ciona genomes were assessed using the ENSEMBL assembly annotation and homologues identified and compared with the vertebrate homologue region.
(Vasoactive Intestinal Peptide)
(Pituitary Adenylate Cyclase-Activating Polypeptide)
(Growth Hormone Releasing Hormone)
(PH-Methionine): GCG: (Glucagon)
(Glucose-dependent Insulinotropic Peptide)
(G-Protein Coupled Receptors).
Jorpes JE, Mutt V: The gastrointestinal hormones, secretin and cholecystokinin-pancreozymin. Ann Intern Med. 1961, 55: 395-405.
Sherwood NM, Krueckl SL, McRory JE: The Origin and Function of the Pituitary Adenylate Cyclase-Activating Polypeptide (PACAP)/Glucagon Superfamily. Endocr Rev. 2000, 21: 619-670. 10.1210/er.21.6.619.
Irwin DM: Molecular evolution of mammalian incretin hormone genes. Regulatory peptides. 2009, 155: 121-130. 10.1016/j.regpep.2009.04.009.
Vaudry D, Gonzalez BJ, Basille M, Yon L, Fournier A, Vaudry H: Pituitary adenylate cyclase-activating polypeptide and its receptors: from structure to functions. Pharmacol Rev. 2000, 52: 269-324.
Nordstrom KJ, Lagerstrom MC, Waller LM, Fredriksson R, Schioth HB: The Secretin GPCRs descended from the family of Adhesion GPCRs. Mol Biol Evol. 2009, 26: 71-84. 10.1093/molbev/msn228.
Harmar AJ: Family-B G-protein-coupled receptors. Genome Biology. 2001, 2: REVIEWS3013-10.1186/gb-2001-2-12-reviews3013.
McRory J, Sherwood NM: Two Protochordate Genes Encode Pituitary Adenylate Cyclase-Activating Polypeptide and Related Family Members. Endocrinology. 1997, 138: 2380-2390. 10.1210/en.138.6.2380.
Cardoso JC, Vieira FA, Gomes AS, Power DM: PACAP, VIP and their receptors in the metazoa: insights about the origin and evolution of the ligand-receptor pair. Peptides. 2007, 28: 1902-1919. 10.1016/j.peptides.2007.05.016.
National Center for Biotechnology Information: [http://www.ncbi.nlm.nih.gov/]
Campbell RM, Scanes CG: Evolution of the growth hormone-releasing factor (GRF) family of peptides. Growth Regul. 1992, 2: 175-191.
Montero M, Yon L, Kikuyama S, Dufour S, Vaudry H: Molecular evolution of the growth hormone-releasing hormone/pituitary adenylate cyclase-activating polypeptide gene family. Functional implication in the regulation of growth hormone secretion. J Mol Endocrinol. 2000, 25: 157-168. 10.1677/jme.0.0250157.
Hoyle CH: Neuropeptide families: evolutionary perspectives. Regul Peptides. 1998, 73: 1-33. 10.1016/S0167-0115(97)01073-2.
Hill CA, Fox AN, Pitts RJ, Kent LB, Tan PL, Chrystal MA, Cravchik A, Collins FH, Robertson HM, Zwiebel LJ: G protein-coupled receptors in Anopheles gambiae. Science. 2002, 298: 176-178. 10.1126/science.1076196.
Cardoso JC, Pinto VC, Vieira FA, Clark MS, Power DM: Evolution of secretin family GPCR members in the metazoa. BMC Evol Biol. 2006, 6: 108-10.1186/1471-2148-6-108.
Nordstrom KJ, Fredriksson R, Schioth HB: The amphioxus (Branchiostoma floridae) genome contains a highly diversified set of G protein-coupled receptors. BMC Evol Biol. 2008, 8: 9-10.1186/1471-2148-8-9.
Kamesh N, Aradhyam GK, Manoj N: The repertoire of G protein-coupled receptors in the sea squirt Ciona intestinalis. BMC Evol Biol. 2008, 8: 129-10.1186/1471-2148-8-129.
Cardoso JC, de Vet EC, Louro B, Elgar G, Clark MS, Power DM: Persistence of duplicated PAC1 receptors in the teleost, Sparus auratus. BMC Evol Biol. 2007, 7: 221-10.1186/1471-2148-7-221.
Tam JK, Lee LT, Chow BK: PACAP-related peptide (PRP)-molecular evolution and potential functions. Peptides. 2007, 28: 1920-1929. 10.1016/j.peptides.2007.07.011.
Irwin DM: Molecular evolution of proglucagon. Regul Peptides. 2001, 98: 1-12. 10.1016/S0167-0115(00)00232-9.
Yoo SJ, You S, Kim H, Kim SC, Choi YJ, El Halawani M, Farris J, Foster DN: Molecular cloning and characterization of alternatively spliced transcripts of the turkey pituitary adenylate cyclase-activating polypeptide. Gen Comp Endocrinol. 2000, 120: 326-335. 10.1006/gcen.2000.7567.
Mirabella N, Squillacioti C, Colitti M, Germano G, Pelagalli A, Paino G: Pituitary adenylate cyclase activating peptide (PACAP) immunoreactivity and mRNA expression in the duck gastrointestinal tract. Cell Tissue Res. 2002, 308: 347-359. 10.1007/s00441-002-0555-6.
Sundby F, Frandsen EK, Thomsen J, Kristiansen K, Brunfeldt K: Crystallization and amino acid sequence of duck glucagon. FEBS letters. 1972, 26: 289-293. 10.1016/0014-5793(72)80595-7.
Markussen J, Frandsen E, Heding LG, Sundby F: Turkey glucagon: crystallization, amino acid composition and immunology. Hormone Metab Res. 1972, 4: 360-363. 10.1055/s-0028-1094032.
Hasegawa S, Terazono K, Nata K, Takada T, Yamamoto H, Okamoto H: Nucleotide sequence determination of chicken glucagon precursor cDNA: Chicken preproglucagon does not contain glucagon-like peptide II. FEBS letters. 1990, 264: 117-120. 10.1016/0014-5793(90)80779-I.
McFarlin DR, Lehn DA, Moran SM, MacDonald MJ, Epstein ML: Sequence of a cDNA encoding chicken vasoactive intestinal peptide (VIP). Gene. 1995, 154: 211-213. 10.1016/0378-1119(94)00856-N.
McRory JE, Parker RL, Sherwood NM: Expression and alternative processing of a chicken gene encoding both growth hormone-releasing hormone and pituitary adenylate cyclase-activating polypeptide. DNA Cell Biol. 1997, 16: 95-102. 10.1089/dna.1997.16.95.
Irwin DM, Zhang T: Evolution of the vertebrate glucose-dependent insulinotropic polypeptide (GIP) gene. Comp Biochem Physiol D Genome Proteo. 2006, 1: 385-395. 10.1016/j.cbd.2006.09.001.
Wang Y, Conlon JM: Neuroendocrine peptides (NPY, GRP, VIP, somatostatin) from the brain and stomach of the alligator. Peptides. 1993, 14: 573-579. 10.1016/0196-9781(93)90147-9.
Lance V, Hamilton JW, Rouse JB, Kimmel JR, Pollock HG: Isolation and characterization of reptilian insulin, glucagon, and pancreatic polypeptide: complete amino acid sequence of alligator (Alligator mississippiensis) insulin and pancreatic polypeptide. Genl Comp Endocrinol. 1984, 55: 112-124. 10.1016/0016-6480(84)90135-7.
Chen YE, Drucker DJ: Tissue-specific Expression of Unique mRNAs That Encode Proglucagon-derived Peptides or Exendin 4in the Lizard. J Biol Chem. 1997, 272: 4108-4115. 10.1074/jbc.272.7.4108.
Valiante S, Prisco M, Capaldo A, Zambrano I, De Falco M, Andreuccetti P, Laforgia V, Varano L: Molecular characterization and gene expression of the pituitary adenylate cyclase-activating polypeptide (PACAP) in the lizard brain. Brain Res. 2007, 1127: 66-75. 10.1016/j.brainres.2006.09.103.
Valiante S, Prisco M, De Falco M, Sellitti A, Zambrano I, Sciarrillo R, Capaldo A, Gay F, Andreuccetti P, Laforgia V: Distribution and Molecular Evolution of the Neuropeptide Pituitary Adenylate Cyclase-Activating Polypeptide (PACAP) and its Receptors in the Lizard Podarcis sicula (Squamata, Lacertidae). J Mol Neurosci. 2009
Alexandre D, Vaudry H, Jegou S, Anouar Y: Structure and distribution of the mRNAs encoding pituitary adenylate cyclase-activating polypeptide and growth hormone-releasing hormone-like peptide in the frog, Rana ridibunda. J Comp Neurol. 2000, 421: 234-246. 10.1002/(SICI)1096-9861(20000529)421:2<234::AID-CNE8>3.0.CO;2-S.
Chartrel N, Wang Y, Fournier A, Vaudry H, Conlon JM: Frog vasoactive intestinal polypeptide and galanin: primary structures and effects on pituitary adenylate cyclase. Endocrinology. 1995, 136: 3079-3086. 10.1210/en.136.7.3079.
Pollock HG, Kimmel JR: Chicken glucagon. Isolation and amino acid sequence studies. J Biol Chem. 1975, 250: 9377-9380.
Hu Z, Lelievre V, Tam J, Cheng JW, Fuenzalida G, Zhou X, Waschek JA: Molecular cloning of growth hormone-releasing hormone/pituitary adenylyl cyclase-activating polypeptide in the frog Xenopus laevis: brain distribution and regulation after castration. Endocrinology. 2000, 141: 3366-3376. 10.1210/en.141.9.3366.
Lee LT, Siu FK, Tam JK, Lau IT, Wong AO, Lin MC, Vaudry H, Chow BK: Discovery of growth hormone-releasing hormones and receptors in nonmammalian vertebrates. Proc Natl Acad Sci USA. 2007, 104: 2133-2138. 10.1073/pnas.0611008104.
Irwin DM, Satkunarajah M, Wen Y, Brubaker PL, Pederson RA, Wheeler MB: The Xenopus proglucagon gene encodes novel GLP-1-like peptides with insulinotropic properties. Proc Natl Acad Sci USA. 1997, 94: 7915-7920. 10.1073/pnas.94.15.7915.
Thwaites DT, Young J, Thorndyke MC, Dimaline R: The isolation and chemical characterization of a novel vasoactive intestinal peptide-related peptide from a teleost fish, the cod, Gadus morhua. Biochim Biophys Acta. 1989, 999: 217-220.
Xu M, Volkoff H: Molecular characterization of ghrelin and gastrin-releasing peptide in Atlantic cod (Gadus morhua): cloning, localization, developmental profile and role in food intake regulation. Gen Comp Endocrinol. 2009, 160: 250-258. 10.1016/j.ygcen.2008.12.004.
Uesaka T, Yano K, Yamasaki M, Ando M: Somatostatin-, Vasoactive Intestinal Peptide-, and Granulin-like Peptides Isolated from Intestinal Extracts of Goldfish, Carassius auratus. Gen Comp Endocrinol. 1995, 99: 298-306. 10.1006/gcen.1995.1113.
Matsuda K, Takei Y, Katoh J, Shioda S, Arimura A, Uchiyama M: Isolation and structural characterization of pituitary adenylate cyclase activating polypeptide (PACAP)-like peptide from the brain of a teleost, stargazer, Uranoscopus japonicus. Peptides. 1997, 18: 723-727. 10.1016/S0196-9781(97)00122-8.
Andrews PC, Ronner P: Isolation and structures of glucagon and glucagon-like peptide from catfish pancreas. J Biol Chem. 1985, 260: 3910-3914.
Small BC, Nonneman D: Sequence and expression of a cDNA encoding both pituitary adenylate cyclase activating polypeptide and growth hormone-releasing hormone-like peptide in channel catfish (Ictalurus punctatus). Gen Comp Endocrinol. 2001, 122: 354-363. 10.1006/gcen.2001.7651.
Tse DL, Pang RT, Wong AO, Chan SM, Vaudry H, Chow BK: Identification of a potential receptor for both peptide histidine isoleucine and peptide histidine valine. Endocrinology. 2002, 143: 1327-1336. 10.1210/en.143.4.1327.
Krueckl SL, Fradinger EA, Sherwood NM: Developmental changes in the expression of growth hormone-releasing hormone and pituitary adenylate cyclase-activating polypeptide in zebrafish. J Comp Neuro. 2003, 455: 396-405. 10.1002/cne.10494.
Wang Y, Wong AO, Ge W: Cloning, regulation of messenger ribonucleic acid expression, and function of a new isoform of pituitary adenylate cyclase-activating polypeptide in the zebrafish ovary. Endocrinology. 2003, 144: 4799-4810. 10.1210/en.2003-0501.
Zhou L, Irwin DM: Fish proglucagon genes have differing coding potential. Comp Biochem Physiol B Biochem Mol Biol. 2004, 137: 255-264. 10.1016/j.cbpc.2003.11.009.
Taylor JS, Braasch I, Frickey T, Meyer A, Peer Van de Y: Genome duplication, a trait shared by 22000 species of ray finned fish. Genome Res. 2003, 13: 382-390. 10.1101/gr.640303.
Steinke D, Salzburger W, Braasch I, Meyer A: Many genes in fish have species-specific asymmetric rates of molecular evolution. BMC genomics. 2006, 7: 20-10.1186/1471-2164-7-20.
Meyer A, Peer Van de Y: From 2R to 3R: evidence for a fish-specific genome duplication (FSGD). Bioessays. 2005, 27: 937-945. 10.1002/bies.20293.
Irwin DM, Huner O, Youson JH: Lamprey proglucagon and the origin of glucagon-like peptides. Mol Biol Evol. 1999, 16: 1548-1557.
Bourgault S, Vaudry D, Segalas-Milazzo I, Guilhaudis L, Couvineau A, Laburthe M, Vaudry H, Fournier A: Molecular and conformational determinants of pituitary adenylate cyclase-activating polypeptide (PACAP) for activation of the PAC1 receptor. J Med Chem. 2009, 52: 3308-3316. 10.1021/jm900291j.
Wray V, Nokihara K, Naruse S: Solution structure comparison of the VIP/PACAP family of peptides by NMR spectroscopy. Ann N Y Acad Sci. 1998, 865: 37-44. 10.1111/j.1749-6632.1998.tb11160.x.
Gourlet P, Woussen-Colle MC, Robberecht P, de Neef P, Cauvin A, Vandermeers-Piret MC, Vandermeers A, Christophe J: Structural requirements for the binding of the pituitary adenylate-cyclase-activating peptide to receptors and adenylate-cyclase activation in pancreatic and neuronal membranes. FEBS. 1991, 195: 535-541.
Gallwitz B, Witt M, Paetzold G, Morys-Wortmann C, Zimmermann B, Eckart K, Folsch UR, Schmidt WE: Structure/activity characterization of glucagon-like peptide-1. FEBS. 1994, 225: 1151-1156.
Roch GJ, Wu S, Sherwood NM: Hormones and receptors in fish: do duplicates matter?. Gen Comp Endocrinol. 2009, 161: 3-12. 10.1016/j.ygcen.2008.10.017.
Pfam Database. [http://pfam.sanger.ac.uk/]
Janssen T, Husson SJ, Lindemans M, Mertens I, Rademakers S, Ver Donck K, Geysen J, Jansen G, Schoofs L: Functional characterization of three G protein-coupled receptors for pigment dispersing factors in Caenorhabditis elegans. J Biol Chem. 2008, 283: 15241-15249. 10.1074/jbc.M709060200.
Mertens I, Vandingenen A, Johnson EC, Shafer OT, Li W, Trigg JS, De Loof A, Schoofs L, Taghert PH: PDF receptor signaling in Drosophila contributes to both circadian and geotactic behaviors. Neuron. 2005, 48: 213-219. 10.1016/j.neuron.2005.09.009.
Gwee PC, Tay BH, Brenner S, Venkatesh B: Characterization of the neurohypophysial hormone gene loci in elephant shark and the Japanese lamprey: origin of the vertebrate neurohypophysial hormone genes. BMC Evol Biol. 2009, 9: 47-10.1186/1471-2148-9-47.
de Jong-Brink M, ter Maat A, Tensen CP: NPY in invertebrates: molecular answers to altered functions during evolution. Peptides. 2001, 22: 309-315. 10.1016/S0196-9781(01)00332-1.
Garczynski SF, Crim JW, Brown MR: Characterization of neuropeptide F and its receptor from the African malaria mosquito, Anopheles gambiae. Peptides. 2005, 26: 99-107. 10.1016/j.peptides.2004.07.014.
Larhammar D, Salaneck E: The NPY Family of Peptides in Immune Disorders, Inflammation, Angiogenesis and Cancer. 2005, Basel/Switzerland: Birkhäuser Verlag
Hewes RS, Taghert PH: Neuropeptides and neuropeptide receptors in the Drosophila melanogaster genome. Genome Res. 2001, 11: 1126-1142. 10.1101/gr.169901.
Hernadi L, Hiripi L, Gyori J, Szabo H, Vehovszky A: The terrestrial snail, Helix pomatia, adapts to environmental conditions by the modulation of central arousal. Acta Biol Hung. 2008, 59 (Suppl): 47-53. 10.1556/ABiol.59.2008.Suppl.7.
Hashimoto H, Shintani N, Baba A: Higher brain functions of PACAP and a homologous Drosophila memory gene amnesiac: insights from knockouts and mutants. Biochim Biophys Res Comm. 2002, 297: 427-431. 10.1016/S0006-291X(02)02144-7.
Lerner EA, Iuga AO, Reddy VB: Maxadilan, a PAC1 receptor agonist from sand flies. Peptides. 2007, 28: 1651-1654. 10.1016/j.peptides.2007.06.021.
Kandel E, Abel T: Neuropeptides, adenylyl cyclase, and memory storage. Science. 1995, 268: 825-826. 10.1126/science.7754367.
Tatsuno I, Uchida D, Tanaka T, Saeki N, Hirai A, Saito Y, Moro O, Tajima M: Maxadilan specifically interacts with PAC1 receptor, which is a dominant form of PACAP/VIP family receptors in cultured rat cortical neurons. Brain Res. 2001, 889: 138-148. 10.1016/S0006-8993(00)03126-7.
Pereira P, Reddy VB, Kounga K, Bello Y, Lerner E: Maxadilan activates PAC1 receptors expressed in Xenopus laevis xelanophores. Pigment Cell Res. 2002, 15: 461-466. 10.1034/j.1600-0749.2002.02077.x.
Shemesh R, Toporik A, Levine Z, Hecht I, Rotman G, Wool A, Dahary D, Gofer E, Kliger Y, Soffer MA, et al: Discovery and validation of novel peptide agonists for G-protein-coupled receptors. J Biol Chem. 2008, 283: 34643-34649. 10.1074/jbc.M805181200.
Hoare SR: Mechanisms of peptide and nonpeptide ligand binding to Class B G-protein-coupled receptors. Drug Discov Today. 2005, 10: 417-427. 10.1016/S1359-6446(05)03370-2.
Perry SJ, Junger S, Kohout TA, Hoare SR, Struthers RS, Grigoriadis DE, Maki RA: Distinct conformations of the corticotropin releasing factor type 1 receptor adopted following agonist and antagonist binding are differentially regulated. J Biol Chem. 2005, 280: 11560-11568. 10.1074/jbc.M412914200.
Nicole P, Lins L, Rouyer-Fessard C, Drouot C, Fulcrand P, Thomas A, Couvineau A, Martinez J, Brasseur R, Laburthe M: Identification of key residues for interaction of vasoactive intestinal peptide with human VPAC1 and VPAC2 receptors and development of a highly selective VPAC1 receptor agonist. Alanine scanning and molecular modeling of the peptide. J Biol Chem. 2000, 275: 24003-24012. 10.1074/jbc.M002325200.
Solano RM, Langer I, Perret J, Vertongen P, Juarranz MG, Robberecht P, Waelbroeck M: Two basic residues of the h-VPAC1 receptor second transmembrane helix are essential for ligand binding and signal transduction. J Biol Chem. 2001, 276: 1084-1088. 10.1074/jbc.M007686200.
Unson CG, Macdonald D, Ray K, Durrah TL, Merrifield RB: Position 9 replacement analogs of glucagon uncouple biological activity and receptor binding. J Biol Chem. 1991, 266: 2763-2766.
Thornton JW, Need E, Crews D: Resurrecting the ancestral steroid receptor: ancient origin of estrogen signaling. Science. 2003, 301: 1714-1717. 10.1126/science.1086185.
Bridgham JT, Carroll SM, Thornton JW: Evolution of hormone-receptor complexity by molecular exploitation. Science. 2006, 312: 97-101. 10.1126/science.1123348.
Ohno S: Evolution by gene duplication. 1970, Berlin, New York: Springer-Verlag
Holland PW, Garcia-Fernandez J, Williams NA, Sidow A: Gene duplications and the origins of vertebrate development. Dev Suppl. 1994, 125-133.
Wu S, Roch GJ, Cervini LA, Rivier JE, Sherwood NM: Newly-identified receptors for peptide histidine-isoleucine and GHRH-like peptide in zebrafish help to elucidate the mammalian secretin superfamily. J Mol Endocrinol. 2008, 41: 343-366. 10.1677/JME-08-0083.
Clynen E, De Loof A, Schoofs L: New insights into the evolution of the GRF superfamily based on sequence similarity between the locust APRPs and human GRF. Gen Comp Endocrinol. 2004, 139: 173-178. 10.1016/j.ygcen.2004.07.006.
Lindemans M, Liu F, Janssen T, Husson SJ, Mertens I, Gade G, Schoofs L: Adipokinetic hormone signaling through the gonadotropin-releasing hormone receptor modulates egg-laying in Caenorhabditis elegans. Proc Natl Acad Sci USA. 2009, 106: 1642-1647. 10.1073/pnas.0809881106.
Park Y, Kim YJ, Adams ME: Identification of G protein-coupled receptors for Drosophila PRXamide peptides, CCAP, corazonin, and AKH supports a theory of ligand-receptor coevolution. Proc Natl Acad Sci USA. 2002, 99: 11423-11428. 10.1073/pnas.162276199.
UniProt Database. [http://www.expasy.org/tools/blast/]
Eddy SR: A probabilistic model of local sequence alignment that simplifies statistical significance estimation. PLoS Comput Biol. 2008, 4: e1000069-10.1371/journal.pcbi.1000069.
Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG: The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res. 1997, 25: 4876-4882. 10.1093/nar/25.24.4876.
Ronquist F, Huelsenbeck JP: MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics. 2003, 19: 1572-1574. 10.1093/bioinformatics/btg180.
Lartillot N, Philippe H: A Bayesian mixture model for across-site heterogeneities in the amino-acid replacement process. Mol Biol Evol. 2004, 21: 1095-1109. 10.1093/molbev/msh112.
Fugu genome. [http://fugu.nimr.mrc.ac.uk/]
Ensembl Genome browser. [http://www.ensembl.org]
NCBI MapViewer. [http://www.ncbi.nlm.nih.gov/mapview/]
Giribet G: Relationships among metazoan phyla as inferred from 18S rRNA sequence data: a methodological approach. Exs. 2002, 85-101.
Gerhart J, Lowe C, Kirschner M: Hemichordates and the origin of chordates. Curr Opin Genet Dev. 2005, 15: 461-467. 10.1016/j.gde.2005.06.004.
Delsuc F, Brinkmann H, Chourrout D, Philippe H: Tunicates and not cephalochordates are the closest living relatives of vertebrates. Nature. 2006, 439: 965-968. 10.1038/nature04336.
Takeda J, Seino Y, Tanaka K, Fukumoto H, Kayano T, Takahashi H, Mitani T, Kurono M, Suzuki T, Tobe T, et al: Sequence of an intestinal cDNA encoding human gastric inhibitory polypeptide precursor. Proc Natl Acad Sci USA. 1987, 84: 7005-7008. 10.1073/pnas.84.20.7005.
Moody AJ, Thim L, Valverde I: The isolation and sequencing of human gastric inhibitory peptide (GIP). FEBS letters. 1984, 172: 142-148. 10.1016/0014-5793(84)81114-X.
Orskov C, Bersani M, Johnsen AH, Hojrup P, Holst JJ: Complete sequences of glucagon-like peptide-1 from human and pig small intestine. J Biol Chem. 1989, 264: 12826-12829.
Drucker DJ, Asa S: Glucagon gene expression in vertebrate brain. J Biol Chem. 1988, 263: 13475-13478.
Yiangou Y, Di Marzo V, Spokes RA, Panico M, Morris HR, Bloom SR: Isolation, characterization, and pharmacological actions of peptide histidine valine 42, a novel prepro-vasoactive intestinal peptide-derived peptide. J Biol Chem. 1987, 262: 14010-14013.
Linder S, Barkhem T, Norberg A, Persson H, Schalling M, Hokfelt T, Magnusson G: Structure and expression of the gene encoding the vasoactive intestinal peptide precursor. Proc Natl Acad Sci USA. 1987, 84: 605-609. 10.1073/pnas.84.2.605.
Guillemin R, Brazeau P, Bohlen P, Esch F, Ling N, Wehrenberg WB: Growth hormone-releasing factor from a human pancreatic tumor that caused acromegaly. Science. 1982, 218: 585-587. 10.1126/science.6812220.
Mayo KE, Vale W, Rivier J, Rosenfeld MG, Evans RM: Expression-cloning and sequence of a cDNA encoding human growth hormone-releasing factor. Nature. 1983, 306: 86-88. 10.1038/306086a0.
Kimura C, Ohkubo S, Ogi K, Hosoya M, Itoh Y, Onda H, Miyata A, Jiang L, Dahl RR, Stibbs HH, et al: A novel peptide which stimulates adenylate cyclase: molecular cloning and characterization of the ovine and human cDNAs. Biochem Biophys Res Comm. 1990, 166: 81-89. 10.1016/0006-291X(90)91914-E.
Whitmore TE, Holloway JL, Lofton-Day CE, Maurer MF, Chen L, Quinton TJ, Vincent JB, Scherer SW, Lok S: Human secretin (SCT): gene structure, chromosome location, and distribution of mRNA. Cytogenet Cell Genetics. 2000, 90: 47-52. 10.1159/000015658.
Wang Y, Li J, Wang CY, Kwok AH, Leung FC: Identification of the endogenous ligands for chicken growth hormone-releasing hormone (GHRH) receptor: evidence for a separate gene encoding GHRH in submammalian vertebrates. Endocrinology. 2007, 148: 2405-2416. 10.1210/en.2006-1013.
Nilsson A, Carlquist M, Jornvall H, Mutt V: Isolation and characterization of chicken secretin. FEBS. 1980, 112: 383-388.
Nilsson A: Structure of the vasoactive intestinal octacosapeptide from chicken intestine. The amino acid sequence. FEBS letters. 1975, 60: 322-326. 10.1016/0014-5793(75)80740-X.
You S, Silsby JL, Farris J, Foster DN, el Halawani ME: Tissue-specific alternative splicing of turkey preprovasoactive intestinal peptide messenger ribonucleic acid, its regulation, and correlation with prolactin secretion. Endocrinology. 1995, 136: 2602-2610. 10.1210/en.136.6.2602.
Pollock HG, Hamilton JW, Rouse JB, Ebner KE, Rawitch AB: Isolation of peptide hormones from the pancreas of the bullfrog (Rana catesbeiana). Amino acid sequences of pancreatic polypeptide, oxyntomodulin, and two glucagon-like peptides. J Biol Chem. 1988, 263: 9746-9751.
Yuen TTH, Mok PY, Chow BKC: Molecular cloning of a cDNA encoding proglucagon from goldfish, Carassius auratus. Fish Physiol Biochem. 1997, V17: 223-230. 10.1023/A:1007793705131.
McRory JE, Parker DB, Ngamvongchon S, Sherwood NM: Sequence and expression of cDNA for pituitary adenylate cyclase activating polypeptide (PACAP) and growth hormone-releasing hormone (GHRH)-like peptide in catfish. Mol Cell Endocrinol. 1995, 108: 169-177. 10.1016/0303-7207(94)03467-8.
Fradinger EA, Sherwood NM: Characterization of the gene encoding both growth hormone-releasing hormone (GRF) and pituitary adenylate cyclase-activating polypeptide (PACAP) in the zebrafish. Mol Cell Endocrinol. 2000, 165: 211-219. 10.1016/S0303-7207(00)00251-3.
Argenton F, Zecchin E, Bortolussi M: Early appearance of pancreatic hormone-expressing cells in the zebrafish embryo. Mech Dev. 1999, 87: 217-221. 10.1016/S0925-4773(99)00151-3.
Parker DB, Coe IR, Dixon GH, Sherwood NM: Two salmon neuropeptides encoded by one brain cDNA are structurally related to members of the glucagon superfamily. FEBS. 1993, 215: 439-448.
Valiante S, Prisco M, Ricchiari L, Laforgia V, Varano L, Andreuccetti P: Distribution of PACAP in the brain of the cartilaginous fish torpedo marmorata. Ann N Y Acad Sci. 2006, 1070: 591-596. 10.1196/annals.1317.087.
Matsuda K, Itoh Y, Yoshida T, Shioda S, Arimura A, Uchiyama M: The localization of pituitary adenylate cyclase-activating polypeptide (PACAP)-like immunoreactivity in the hypothalamo-pituitary region of an elasmobranch, stingray, Dasyatis akajei. Peptides. 1998, 19: 1263-1267. 10.1016/S0196-9781(98)00062-X.
Berks BC, Marshall CJ, Carne A, Galloway SM, Cutfield JF: Isolation and structural characterization of insulin and glucagon from the holocephalan species Callorhynchus milii (elephantfish). Biochem J. 1989, 263: 261-266.
Conlon JM, Bondareva V, Rusakov Y, Plisetskaya EM, Mynarcik DC, Whittaker J: Characterization of insulin, glucagon, and somatostatin from the river lamprey, Lampetra fluviatilis. Gen Comp Endocrinol. 1995, 100: 96-105. 10.1006/gcen.1995.1138.
Conlon JM, Nielsen PF, Youson JH: Primary structures of glucagon and glucagon-like peptide isolated from the intestine of the parasitic phase lamprey Petromyzon marinus. Gen Comp Endocrinol. 1993, 91: 96-104. 10.1006/gcen.1993.1109.
Pestarino M: Immunocytochemical Localization of Glucagon-Related Peptides in the Cerebral Ganglion of the Protochordate Ascidian, Styela-Plicata. J Neuroendocrinol. 1990, 2: 641-645. 10.1111/j.1365-2826.1990.tb00459.x.
Fritsch HA, Van Noorden S, Pearse AG: Gastro-intestinal and neurohormonal peptides in the alimentary tract and cerebral complex of Ciona intestinalis (Ascidiaceae). Cell Tiss Res. 1982, 223: 369-402. 10.1007/BF01258496.
Sherwood NM, Adams BA, Tello JA: Endocrinology of protochordates. Can J Zool. 2005, 83: 225-255. 10.1139/z04-178.
Pestarino M: Occurrence of different secretin-like cells in the digestive tract of the ascidian Styela plicata (Urochordata, Ascidiacea). Cell Tiss Res. 1982, 226: 231-235. 10.1007/BF00217097.
Pestarino M: Localization of peptide histidine isoleucine-like immunoreactivity in the gut of the ascidian, Styela plicata. Anim Biol. 1993, 2: 91-95.
Reinecke M: Immunohistochemical Localization of Polypeptide Hormones in Endocrine-Cells of the Digestive-Tract of Branchiostoma-Lanceolatum. Cell Tiss Res. 1981, 219: 445-456. 10.1007/BF00209985.
Dimaline R: Vasoactive Intestinal Peptide. Edited by: Susanne Holmgren. 1989, London, New York: Chapman and Hall
Foster N, Lee DL: Vasoactive intestinal polypeptide-like and peptide histidine isoleucine-like proteins excreted/secreted by Nippostrongylus brasiliensis, Nematodirus battus and Ascaridia galli. Parasitology. 1996, 113 (Pt 3): 287-292. 10.1017/S0031182000082056.
Andries JC, Belemtougri G, Tramu G: Immunohistochemical identification of growth hormone-releasing factor-like material in the nervous system of an insect, Aeshna cyanea (Odonata). Neuropeptides. 1984, 4: 519-528. 10.1016/0143-4179(84)90095-7.
Andries JCBG, Tramu G: Multiple peptide immunoreactivities in the nervous system of Aeschna cyanea (Insecta, Odonata). An immunohistochemical study using antisera to cholecystokinin octapeptide, somatoliberin, vasoactive intestinal peptide, motilin and proctolin. Histochemistry. 1991, 96: 139-148. 10.1007/BF00315984.
El-Salhy M, Abou-el-Ela R, Falkmer S, Grimelius L, Wilander E: Immunohistochemical evidence of gastro-entero-pancreatic neurohormonal peptides of vertebrate type in the nervous system of the larva of a dipteran insect, the hoverfly, Eristalis aeneus. Reg Pept. 1980, 1: 187-204. 10.1016/0167-0115(80)90271-2.
El-Salhy M, Falkmer S, Kramer KJ, Speirs RD: Immunohistochemical investigations of neuropeptides in the brain, corpora cardiaca, and corpora allata of an adult lepidopteran insect, Manduca sexta (L). Cell Tiss Res. 1983, 232: 295-317. 10.1007/BF00213788.
Fujita T, Yui R, Iwanaga T, Nishiitsutsujiuwo J, Endo Y, Yanaihara N: Evolutionary Aspects of Brain-Gut Peptides - an Immunohistochemical Study. Peptides. 1981, 2: 123-131. 10.1016/0196-9781(81)90023-1.
Kuramoto H, Yui R, Iwanaga T, Fujita T, Yanaihara N: PHI-like immunoreactivity in the nervous system of the cockroach (insect) and Aplysia (mollusc) with special reference to its relationship to VIP-like immunoreactivity. Arch Histol Jpn. 1985, 48: 427-433. 10.1679/aohc.48.427.
Osborne NN, Patel S, Dockray G: Immunohistochemical demonstration of peptides, serotonin and dopamine-beta-hydroxylase-like material in the nervous system of the leech Hirudo medicinalis. Histochemistry. 1982, 75: 573-583.
Sundler F, Hakanson R, Alumets J, Walles B: Neuronal localization of pancreatic polypeptide (PP) and vasoactive intestinal peptide (VIP) immunoreactivity in the earthworm (Lumbricus terrestris). Brain Res Bull. 1977, 2: 61-65. 10.1016/0361-9230(77)90027-2.
Reglodi D, Lengvari I, Szelier M, Vigh S, Arimura A: Distribution of PACAP-like immunoreactivity in the nervous system of oligochaeta. Peptides. 2000, 21: 183-188. 10.1016/S0196-9781(99)00201-6.
Dhainaut-Courtois N, Dubois MP, Tramu G, Masson M: Occurrence and coexistence in Nereis diversicolor O.F. Muller (Annelida Polychaeta) of substances immunologically related to vertebrate neuropeptides. Cell Tiss Res. 1985, 242: 97-108. 10.1007/BF00225567.
Kaufmann W, Kerschbaum HH, Hauser-Kronberger C, Hacker GW, Hermann A: Distribution and seasonal variation of vasoactive intestinal (VIP)-like peptides in the nervous system of Helix pomatia. Brain Res. 1995, 695: 125-136. 10.1016/0006-8993(95)00659-E.
Licata A, Ainis L, Martella S, Ricca MB, Licata P, Pergolizzi S, Calabro C, Zaccone G: Immunohistochemical localization of nNOS and VIP in the mantle integument of the mussel, Mytilus galloprovincialis. Acta Histochem. 2003, 105: 143-149. 10.1078/0065-1281-00700.
Ottaviani E, Cossarizza A: Immunocytochemical evidence of vertebrate bioactive peptide-like molecules in the immuno cell types of the freshwater snail Planorbarius corneus (L.) (Gastropoda, Pulmonata). FEBS letters. 1990, 267: 250-252. 10.1016/0014-5793(90)80937-E.
Ottaviani E, Franchini A, Fontanili P: The presence of immunoreactive vertebrate bioactive peptide substances in hemocytes of the freshwater snail Viviparus ater (Gastropoda, Prosobranchia). Cell Mol Neurobiol. 1992, 12: 455-462. 10.1007/BF00711546.
Gustafsson MKS: Immunocytochemical Demonstration of Neuropeptides and Serotonin in the Nervous-System of Adult Schistosoma-Mansoni. Parasitol Res. 1987, 74: 168-174. 10.1007/BF00536029.
The authors acknowledge the input of the reviewers which improved the manuscript and thank Cymon Cox for help with the phylogenetic analysis and HMM searches. This work was co-financed by POCI 2010 and the European social funds attributed by the Portuguese National Science Foundation (FCT) to project (POCI/CVT/61052/2004) and CCMAR Pluriannual project and PhD fellowship (BD/17630/04) to FV.
The majority of the practical work was carried out by JCRC in collaboration with FAV and ASG. JCRC and DMP planned the study, wrote, analysed the data and critically revised the manuscript for important intellectual content. All authors read and approved the final manuscript.
Electronic supplementary material
Additional file 1: Publicly available genome and EST databases searched using the nucleotide and mature peptide sequence of the tunicate (Chelyosoma productum)and human secretin family members.(PDF 39 KB)
Phylogenetic support values (bootstrap proportions, bp; and posterior probabilities, pp) of the secretin family peptide clusters constructed with maximum likelihood (ml) (Figure
Additional file 2: 4), MrBayes and PhyloBayes methods.(PDF 30 KB)
Authors’ original submitted files for images
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Cardoso, J.C., Vieira, F.A., Gomes, A.S. et al. The serendipitous origin of chordate secretin peptide family members. BMC Evol Biol 10, 135 (2010). https://doi.org/10.1186/1471-2148-10-135
- Vasoactive Intestinal Peptide
- Mature Peptide
- Peptide Group
- PAC1 Receptor