- Research article
- Open Access
The vertebrate ancestral repertoire of visual opsins, transducin alpha subunits and oxytocin/vasopressin receptors was established by duplication of their shared genomic region in the two rounds of early vertebrate genome duplications
- David Lagman†1,
- Daniel Ocampo Daza†1,
- Jenny Widmark1,
- Xesús M Abalo1,
- Görel Sundström1, 2 and
- Dan Larhammar1Email author
© Lagman et al.; licensee BioMed Central Ltd. 2013
Received: 27 June 2013
Accepted: 29 October 2013
Published: 2 November 2013
Vertebrate color vision is dependent on four major color opsin subtypes: RH2 (green opsin), SWS1 (ultraviolet opsin), SWS2 (blue opsin), and LWS (red opsin). Together with the dim-light receptor rhodopsin (RH1), these form the family of vertebrate visual opsins. Vertebrate genomes contain many multi-membered gene families that can largely be explained by the two rounds of whole genome duplication (WGD) in the vertebrate ancestor (2R) followed by a third round in the teleost ancestor (3R). Related chromosome regions resulting from WGD or block duplications are said to form a paralogon. We describe here a paralogon containing the genes for visual opsins, the G-protein alpha subunit families for transducin (GNAT) and adenylyl cyclase inhibition (GNAI), the oxytocin and vasopressin receptors (OT/VP-R), and the L-type voltage-gated calcium channels (CACNA1-L).
Sequence-based phylogenies and analyses of conserved synteny show that the above-mentioned gene families, and many neighboring gene families, expanded in the early vertebrate WGDs. This allows us to deduce the following evolutionary scenario: The vertebrate ancestor had a chromosome containing the genes for two visual opsins, one GNAT, one GNAI, two OT/VP-Rs and one CACNA1-L gene. This chromosome was quadrupled in 2R. Subsequent gene losses resulted in a set of five visual opsin genes, three GNAT and GNAI genes, six OT/VP-R genes and four CACNA1-L genes. These regions were duplicated again in 3R resulting in additional teleost genes for some of the families. Major chromosomal rearrangements have taken place in the teleost genomes. By comparison with the corresponding chromosomal regions in the spotted gar, which diverged prior to 3R, we could time these rearrangements to post-3R.
We present an extensive analysis of the paralogon housing the visual opsin, GNAT and GNAI, OT/VP-R, and CACNA1-L gene families. The combined data imply that the early vertebrate WGD events contributed to the evolution of vision and the other neuronal and neuroendocrine functions exerted by the proteins encoded by these gene families. In pouched lamprey all five visual opsin genes have previously been identified, suggesting that lampreys diverged from the jawed vertebrates after 2R.
Color vision is the ability to distinguish light of different wavelengths. This property has arisen independently in vertebrates and invertebrates through duplications of the genes encoding ciliary opsins and rhabdomeric opsins, respectively . In the vertebrates, three types of cones displaying distinct wavelength properties were initially described by Ragnar Granit who received the Nobel Prize for these achievements in 1967. Later studies, including molecular cloning of the visual opsins in various vertebrates, have shown that four major color opsin subtypes existed in early vertebrates [2–4]. Thus, together with the dim-light (scotopic) receptor rhodopsin expressed in rods, the family of visual opsins encompassed five members in early vertebrates: RH1 (rhodopsin), RH2 (green opsin), SWS1 (ultraviolet opsin), SWS2 (blue opsin), and LWS (red opsin).
Subsequently, the gene repertoire has changed by gains and losses of opsin genes in the different vertebrate lineages. For instance, the ancestor of placental mammals lost RH2 and SWS2 and extant mammals use SWS1 for vision in the blue part of the spectrum. Primates have a duplicate of LWS that has mutated to have its absorption maximum in green, namely OPN1MW. The platypus has retained SWS2 but lost SWS1. Other losses have occurred in frogs (RH2), in the coelacanth Latimeria chalumnae, and in cartilaginous fishes. In teleost fishes, on the other hand, many additional duplicates have arisen .
Phylogenetic analyses of the five visual opsin sequences in chicken showed that the rhodopsin sequence RH1 was most closely related to the green opsin RH2, suggesting that this gene duplication was the most recent and that the four color opsins existed before rhodopsin . Thus, it appeared that color vision was ancestral to the dim-light vision and the appearance of rhodopsin and rod photoreceptors facilitated the adaptation to nocturnal environments. As a rhodopsin sequence had already been described in a lamprey, this implied that all five opsins existed before the divergence of lampreys and gnathostomes, i.e., jawed vertebrates. Subsequently, also the four color opsins have been described in pouched lamprey (Geotria australis) .
Although the visual opsin gene duplications must have taken place before the lamprey-gnathostome divergence, it has remained unclear how they happened. We and others have previously reported that numerous gene families expanded in the two genome doublings, i.e. tetraploidizations, that took place before the radiation of gnathostomes [8–11] usually called 2R for two rounds of genome doubling. The two tetraploidizations resulted in a large number of quartets of related chromosome regions, and each such quartet is called a paralogon. Subsequently, a third tetraploidization, 3R, took place in the lineage leading to teleost fishes . By investigating gene families sharing chromosome regions, we have been able to deduce the evolution of multiple neuronal and endocrine gene families as well as their neighbors, namely the opioid peptides  and receptors , neuropeptide Y-family peptides  and receptors [16, 17], voltage-gated sodium channels and their neighboring TGF-β receptors , the IGFBP family , the paralemmin family  and, more recently, the three transducin subunit gene families activated by visual opsins . All of these families received additional members in 2R and all but one expanded further in 3R. Chromosomal positions thereby constitute a useful additional type of information for analyses of gene families, especially families that display different evolutionary rates among members or over time, both of which seem to afflict the visual opsins.
We have previously performed sequence-based phylogenetic analyses of several gene families in the phototransduction cascade, and also investigated their chromosomal positions in the human genome [21–23]. These analyses suggested that most of the phototransduction gene families expanded in the basal vertebrate tetraploidizations, including the visual opsin family. In our first study, we proposed that RH1, SWS1 and LWS arose as a result of duplications of a large chromosome block . Because teleost fishes and birds have the LWS and SWS2 genes in close proximity on the same chromosome [24–26], we suggested a scenario where two adjacent visual opsin genes were quadrupled by chromosome duplications . However, the paralogon harboring the opsin genes seemed to have undergone major rearrangements and only a few adjacent gene families were identified, thereby making our conclusions uncertain. Interestingly, one of the neighboring gene families was the transducin alpha subunit family (GNAT), involved in the phototransduction cascade, as well as its adjacent relative G protein alpha inhibiting subunit (GNAI) gene [21–23]. The GNAT family includes three genes located on three of the visual opsin chromosomes in several vertebrates, each flanked by a more distantly related GNAI gene [21, 27, 28].
In parallel, independent analyses in our laboratory of the oxytocin/vasopressin receptor (OT/VP-R) genes and the L-type voltage-gated calcium channel alpha subunit (CACNA1-L) genes converged to reveal large chromosomal regions that share evolutionary history with the visual opsin, GNAT and GNAI genes. The pituitary peptide hormones oxytocin and vasopressin have previously been reported to have five to six ancestral vertebrate receptors (OT/VP-R) based on phylogenetic analyses [29, 30]: one oxytocin receptor, OTR, encoded by OXTR genes, and four to five vasopressin receptors, including V1A (AVPR1A), V1B (AVPR1B) as well as several types of V2 receptors. We report here that the OT/VP-R family genes are located in the proposed visual opsin paralogon, thus resolving the issue of the evolutionary relationships between the ancestral members. Finally, the L-type voltage-gated calcium channel alpha subunits (CACNA1-L) form a family with four members whose genes are located on the visual opsin chromosomes.
We have used these gene families as starting points for extensive analyses of conserved synteny in species representing several vertebrate classes. We report here that these five main gene families and 34 neighboring gene families comprise large paralogous chromosomal regions with extensive similarities to one another that can most parsimoniously be explained by quadruplication of a large ancestral chromosome region. These results define the time points for expansion of the visual opsin family as well as the transducin alpha family, the oxytocin/vasopressin receptors, and the L-type voltage-gated calcium channels. Furthermore, our results have implications for the divergence time point of lampreys and jawed vertebrates relative to the two basal vertebrate tetraploidizations.
We used amino acid sequences identified in genome databases to produce alignments and phylogenetic trees for the visual opsins, the oxytocin and vasopressin receptors (OT/VP-R), the G-protein alpha transducing (GNAT) and inhibiting (GNAI) subunits, as well as the L-type voltage-gated calcium channel alpha subunits (CACNA1-L). Detailed information on these gene families, including database identifiers, location data, genome assembly information and annotation notes for all identified sequences, is provided in Additional file 1. Topologies of the visual opsin and OT/VP-R gene family trees are presented in this section and we have recently published our phylogenetic analyses of the GNAT and GNAI gene families . The phylogenetic analyses of the CACNA1-L family, which have not been published previously, are included in Additional file 2: Figures S7 and S8. These gene families have members located in overlapping regions of the human genome putatively considered as one paralogon and are henceforth referred to as the “main” gene families of this study.
We have also made phylogenetic trees for 34 neighboring gene families identified in the chromosomal regions of the main gene families. The positional data from the main gene families and the neighboring gene families have been compared between the genomes of human, chicken, zebrafish, three-spined stickleback and spotted gar. This combination of phylogenetic and synteny data is the basis for the description of our results below.
Phylogenetic analyses of vertebrate visual opsin genes
Summary of visual opsin sequences analyzed in this study
Species (genome assembly version)
Sequence names in phylogenetic analyses a
Chromosome, linkage group, or genomic scaffold
Hsa X OPN1LW
Hsa X OPN1MW2
Hsa X OPN1MW
Hsa 3 RHO
Hsa 7 OPN1SW
Mmu X Opn1mw
Mmu 6 Rho
Mmu 6 Opn1sw
Grey short-tailed opossum
Mdo X LWS
Mdo 6 RH1
Mdo 8 SWS1
Gga 12 RH1
Gga 26 RH2
Carolina anole lizard
Aca 2 LWS
Aca 4 RH2
Aca 2 SWS2
Western clawed frog
Loc LG1 LWS
Loc LG5 RH1-1d
Loc LG5 RH1-2
Loc LG3 RH2
Loc LG8 SWS1-1e
Loc LG8 SWS1-2d
Loc LG1 SWS2
Dre 11 opn1lw1
Dre 11 opn1lw2
Dre 8 rho
Dre 11 rhol
Dre 6 opn1mw1
Dre 6 opn1mw2
Dre 6 opn1mw3
Dre 6 opn1mw4
Dre 4 opn1sw1
Dre 11 opn1sw2
Gac XVII LWS
Gac XII RH1-1d,e
Gac XII RH1-2
Gac XVII SWS2
Ola 5 LWS-1
Ola 5 LWS-2
Ola 7 RH1-1
Ola 7 RH1-2
Ola 5 SWS2-1
Ola 5 SWS2-2
Spotted green pufferfish
Tni 11 LWS
Tni 9 RH1-1
Tni 9 RH1-2
Tni 11 RH2
Tni 11 SWS2
Visual opsin gene repertoires
The repertoires of visual opsins in mammals and birds have been described in detail in numerous previous studies, and the anole lizard (Anolis carolinensis) opsin genes have been described more recently . These data are consistent with our analyses (Figure 1), which confirm that the ancestral repertoire in jawed vertebrates consisted of five visual opsin genes with losses of SWS2 and RH2 in mammals. The Western clawed frog (Xenopus tropicalis) also seems to have lost the RH2 gene, although this could be due to gaps in the genome assembly. Three full-length and one fragmented visual opsin gene sequences were identified in the coelacanth (Latimeria chalumnae) genome assembly. The full-length sequences cluster within the RH1, RH2 and SWS2 branches (Figure 1). The RH1 and RH2 sequences have previously been reported . The presence of only three visual opsin sequences indicates that there seem to have been losses of visual opsin genes in this lineage. The fragmented gene sequence appears to be a pseudogene sharing sequence similarity to known SWS1 sequences, but with a premature stop-codon and a frame-shift mutation within the first exon. A sequence fragment bearing the same mutations at the same locations has been identified previously  as one of two non-overlapping clones postulated to be parts of an SWS1 pseudogene. However, the second clone reported by these authors, instead corresponds to a fragment of the full-length SWS2 sequence that we identified. All five ancestral types of vertebrate visual opsin genes are present in all the investigated actinopterygian genomes (including spotted gar and teleosts), except the spotted green pufferfish, where an SWS1 sequence could not be identified (Figure 1). Additionally, LWS, SWS2, RH1 and RH2 sequences often occur as multiple local duplicates in teleosts (Table 1). In the spotted gar genome assembly we could identify seven visual opsin genes: one gene each of the LWS, SWS2 and RH2 types and two genes each of the SWS1 and RH1 types (Figure 1). The two SWS1 genes are located adjacent to each other on the same linkage group (LG8) approximately 8 Kb apart (see Table 1), and are thus most likely the result of a local duplication. The two RH1 genes are located on the same linkage group (LG5) approximately 16.6 Mb apart, one with introns (RH1-1 in Table 1 and Figure 1) and one without (RH1-2). These duplicate RH1 genes on the same chromosome have previously been identified in teleost fish species: the one with introns, called exo-rhodopsin, is expressed outside of the retina; and the one without introns, called rhodopsin, is expressed in rods . The intron-less rhodopsin gene is the result of a retrotranscription event . We could identify these duplicate RH1 sequences in all investigated teleost genomes (RH1-1 and RH1-2 in Table 1 and Figure 1). Additionally, the zebrafish has two copies of the intron-less rhodopsin gene, located on two different chromosomes. These zebrafish genes have previously been called rh1 and rh1-2 or rho and rhol (for rhodopsin-like) (Table 1). The teleost exo-rhodopsins form a well-supported cluster in the phylogenetic analyses (marked exorh in Figure 1) while the putative spotted gar exo-rhodopsin (RH1-1) has an uncertain position within the RH1 cluster. On the other hand, the rhodopsin gene of the spotted gar clusters together with the teleost rhodopsin genes with high support, forming a well-defined actinopterygian cluster (marked rho in Figure 1).
Five visual opsins have previously been cloned and characterized from the pouched lamprey (Geotria australis)  and were therefore included in our phylogenetic analyses to provide relative dating. In line with previous analyses [2, 7, 36] the pouched lamprey LWS, SWS1 and SWS2 sequences cluster with high support within their respective branches (Figure 1). We also find that the sequences called RhA and RhB represent the RH1 and RH2 genes, with high support in all our phylogenetic analyses (Figure 1, Additional file 2). Thus it is likely that all five visual opsin genes were present before the divergence of cyclostomes, such as the lampreys, and jawed vertebrates.
Phylogenetic analysis of the oxytocin and vasopressin receptor genes
The clusters for oxytocin receptors (OTR) and V1-type vasopressin receptors (V1A, V1B) are well-supported, and the tree shows that the spotted gar, like teleosts, lacks the V1B subtype while the coelacanth has all three (Figure 2). With regard to V2-type vasopressin receptors, Yamaguchi et al (2012) were able to define three types by using synteny data . Our phylogenetic analyses and the analysis of conserved synteny described below are consistent with three ancestral V2-types, and we propose the nomenclature V2A, V2B and V2C for these receptors. As in the previously cited analyses, the V2C receptors form two paraphyletic branches, with teleost V2C sequences clustering basal to the other V2-type branches (Figure 2), likely due to a faster rate of sequence evolution. However, their chromosomal locations support their orthology with tetrapod and spotted gar V2C sequences (see below). The coelacanth lacks a V2C sequence but has both V2A and V2B, making it the only analyzed species in the sarcopterygian lineage (which also includes tetrapods) with a V2B gene. Since V2C sequences were found in the Western clawed frog, anole lizard and chicken genomes (Figure 2), the loss in the coelacanth is likely lineage-specific. Taken together with the spotted gar, which has all three V2-type sequences (Figure 2), this indicates that the V2A, V2B and V2C subtypes arose early in vertebrate evolution, although there have been several differential losses in different vertebrate classes. Sequences from the Southern platyfish were included since this species was found to have the V2C sequence that previously had only been found in zebrafish and three-spined stickleback . These three species do not form a monophyletic group within teleosts, which indicates that V2C genes could have been lost several times in teleost evolution. The Southern platyfish is also the only teleost where duplicate V2B sequences were found (V2B-1 and V2B-2 in Figure 2).
Database identifiers, location data, genome assembly information, and annotation notes for all identified OT/VP-R sequences are included in Additional file 1. The OT/VP-R phylogenetic tree files and the alignment they were made from are provided as a citable file set with a stable identifier – see reference .
Phylogenetic analysis of the L-type voltage-gated calcium channel alpha subunits
Four genes of the CACNA1-L family were identified in the tetrapod genomes investigated: CACNA1D, CACNA1F, CACNA1C and CACNA1S. However CACNA1F could not be identified in the chicken genome assembly or in any other avian genome available. The Western clawed frog was excluded from the analysis because the short scaffolds of the genome assembly (JGI4_1) did not allow complete gene sequences to be identified. In the teleost genomes investigated all four genes are present, with additional putative 3R duplicates of the CACNA1D, -1F and -1S genes in all four teleost genomes. These results are detailed in Additional file 1, with database identifiers, location data, genome assembly information, and annotation notes for all identified sequences.
The CACNA1F, -1C and -1S genes form three distinct clusters in the bootstrapped NJ (Additional file 2: Figure S7) and PhyML (Figure S8) analyses, while the putative teleost CACNA1D subtype cluster is only resolved in the NJ tree (Additional file 2: Figure S7). These results are presented in Additional file 2. All CACNA1-L phylogenetic tree files and the alignment they were made from are provided as a citable file set with a stable identifier – see reference .
Conserved synteny analysis
Neighboring gene families analyzed for conserved synteny
ATPase, Ca++ transporting, plama membrane
Calcium channel, voltage-dependent, alpha 2/delta subunit
Calcium/calmodulin dependent protein kinase
Cyclin-dependent kinase, members 16, 17 and 18
Cadherin, EGF LAG seven-pass G-type receptor (flamingo homolog, Drosophila)
Coatomer protein complex, subunit gamma
Kinase epsilon and TANK-binding kinase
IQ motif and Sec7 domain containing
Lysine specific demethylase 5
Kelch domain containing 8
L1 cell adhesion molecule
Leucine rich repeat neuronal
Membrane associated guanylate kinase, WW and PDZ domain containing
Putative homeodomain transcription factor
Protein phosphatase, Mg2+/Mn2+ dependent
Protein tyrosine phosphatase, non-receptor type
RNA binding motif protein
Round spermatid basic protein
Sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin)
SLIT-ROBO Rho GTPase activating protein
Translocase of inner mitochondrial membrane 17
Ubiquitin-like modifier activating enzyme, members 1 and 7
Ubiquitin specific peptidase, members 4, 11, 15 and 19
WNK lysine deficient protein kinase
For the majority of the identified neighboring gene families, 23 out of 34, both the NJ trees and the PhyML trees support duplications in the same time-window as the 2R events, i.e. after the divergence of invertebrate chordates and vertebrates, but before the divergence of sarcopterygians and actinopterygians. Several of the 34 identified families also have duplicate teleost branches supporting duplications in the same time-window as the teleost-specific 3R event. Four additional gene families are consistent with duplications in 2R, but lack invertebrate family members to date the duplications. The remaining seven gene families have some subtype clusters that are unresolved, or an unresolved branching of the identified tunicate or lancelet sequences, which makes them inconclusive with regard to the duplications in 2R. Detailed notes on the tree topologies for the neighboring gene families are provided in Additional file 4.
In order to date the translocations seen in the teleost genomes better, orthology predictions between the human neighboring family members and the spotted gar genome were made (see Methods). The locations of the predicted spotted gar orthologs were then recorded and compared with the human, chicken, zebrafish and three-spined stickleback chromosome regions (Additional file 5). While only around 75% of putative spotted gar orthologs could be found for the human neighboring gene family members, this analysis of conserved synteny between the human and spotted gar shows no translocations in the spotted gar genome. With a few exceptions, the identified putative spotted gar orthologs are located on linkage groups 1, 3 and 5, which correspond to the regions on human chromosomes X, 1 and 3 respectively, and linkage group 8 which corresponds to the regions on human chromosomes 7 and 12 (Figure 3).
In order to investigate the evolution of the visual opsin genes related to the two rounds of early vertebrate whole genome duplications, 2R, we have analyzed several neighboring gene families identified in the same chromosomal regions as the human visual opsin genes. Specifically, we investigated whether there were other gene families showing conserved synteny with these and whether they underwent gene duplications in the same time-window as the 2R events. During the process of these analyses we realized that the chromosomal regions of the visual opsin genes overlapped with similar ongoing analyses in our laboratory of the oxytocin and vasopressin receptor gene family (OT/VP-R), the G-protein alpha transducing subunit (GNAT) and G-Protein alpha inhibiting subunit (GNAI) gene families, as well as the gene family of L-type voltage-gated calcium channel alpha subunits (CACNA1-L). These gene families are referred to as the “main” gene families in our analyses. Their evolution will be discussed below in conjunction with the evolution of the visual opsins.
The chromosomal regions harboring the visual opsin genes were duplicated in the vertebrate whole genome duplications
Chromosomal rearrangements in teleost genomes, but not in the spotted gar genome
In the teleost genomes the investigated orthologous genes of the human genes located on chromosomes 1, 3 and X seem to have been rearranged so that the genes are intermingled. In zebrafish this involves chromosomes 8, 23, 11 and 6 (Figure 4) and in the three-spined stickleback linkage groups XII, XVII and scaffold 27 (Additional file 5). These major rearrangements are in line with previous whole genome analyses [10, 45]. Recently Amores et al. published an analysis of the genome of the spotted gar (Lepisosteus oculatus), which belongs to a actinopterygian lineage that diverged before 3R and thus should not have the same rearrangements . They found that the spotted gar seemed to have fewer rearrangements in general compared to the teleosts and that the synteny was more conserved between human and spotted gar than between spotted gar and zebrafish due to post-3R rearrangements in the teleost lineage. To see if this was the case for the regions housing the visual opsin genes, we performed an orthology prediction between human and spotted gar protein predictions and recorded the chromosomal locations of the putative spotted gar orthologs (Additional file 5). This is summarized in Figure 3. By comparing the chromosomal regions of human, chicken, spotted gar, zebrafish and three-spined stickleback we found that the synteny is indeed more conserved between human, chicken and spotted gar than between spotted gar and the teleosts, in agreement with the global genome analyses . This further supports the notion that 3R contributed to the major rearrangements seen in teleost genomes [10, 45].
Evolution of the visual opsin gene family
Five of the seven identified spotted gar genes represent the LWS, SWS1, SWS2 and RH2 types of visual opsin genes, while the other two represent the RH1 type (Figure 1): one intron-containing (RH1-1) and one intron-less (RH1-2). The intron-containing RH1 gene is likely the ortholog of the teleost exo-rhodopsin gene (exorh), named for its expression mainly in the pineal complex of the teleost brain instead of the retina . The intron-less RH1 gene is likely the ortholog of the teleost rhodopsin (rho) gene, a retrotranscript of the exo-rhodopsin gene . Our analyses indicate that the retrotransposition event occurred before the divergence of holostean fishes (including gars) and teleosts (Figure 6). The intron-less spotted gar RH1 is presumably the ortholog of a gene that has previously been identified in the longnose gar (Lepisosteus osseus) as rhodopsin . In the zebrafish there is an additional intron-less RH1 gene called rhol for rhodopsin-like (Figure 2), located on a different chromosome than the rho gene (Table 1). Morrow et al., who identified the two intronless RH1 genes in the zebrafish genome, also identified similar duplicated genes in a few other cyprinid species . Analyses performed by other researchers have shown that duplicated intron-less RH1 genes seem to be present in some non-cyprinid teleost species as well, including the deep-sea dwelling short-fin pearl-eye  and the Japanese and European eels [50, 51]. This suggests that the two intron-less RH1 genes might have originated in 3R, following the retrotransposition event. However, to confirm that rho and rhol are 3R duplicates, information about chromosomal locations is needed from several species. The presence of two intronless RH1 genes in the above-mentioned species, but not in the medaka, spotted green pufferfish and three-spined stickleback, suggests loss in the latter species or in their common ancestor. In the zebrafish, the regions harbouring the duplicated RH1 genes rho and rhol on chromosome 8 and 11 have undergone major rearrangements. Our analyses show that these chromosomes contain paralogous members of the CACNA1-L, ERC, CACNA2D, PRICKLE and MAGI families (see Additional file 5). The CACNA2D and MAGI tree topologies support a 3R duplication of these paralogous gene copies. However, the paralogous copies in the trees of the CACNA1-L, ERC and PRICKLE families are inconsistent. While it is a likely scenario, we cannot say for certain that the duplicate intron-less RH1 genes originated in 3R.
Evolution of the GNAT and GNAI gene families
In our previous analyses of the GNAT gene family we concluded that the GNAT-GNAI gene pairs seen today in many vertebrates had an origin in a local duplication preceding 2R. The 2R events subsequently gave rise to the GNAT1-GNAI2, GNAT2-GNAI3 and GNAT3-GNAI1 gene pairs . This is in line with previous studies from other research groups, see for instance . Consequently, independent losses of the GNAT3 gene have occurred in the teleost and amphibian lineages and possibly the sea lamprey (Petromyzon marinus) lineage after 2R [27, 28]. We identified putative 3R duplicates in the GNAI gene family for the GNAI1 and GNAI2 genes in our previous analysis , although we had no synteny data to support the hypothesis. In the present analyses 10 gene families have putative 3R duplicates located on the GNAI1-bearing chromosomes in zebrafish (chromosomes 4 and 25). Six of these families show a clear 3R topology in both phylogenetic analyses. In the three-spined stickleback 12 neighboring gene families have members on the GNAI1-bearing chromosomes (IV and XIX), seven of which show a clear 3R topology in both phylogenetic analyses. In addition, three of the 10 families in zebrafish as well as three out of 12 families in three-spined stickleback show a topology supporting 3R in either the NJ or PhyML tree. For the GNAI2 genes, four neighboring gene families have putative 3R duplicates on the GNAI2 bearing chromosomes in zebrafish (chromosomes 6 and 11). Three of these show a clear 3R duplication pattern. In three-spined stickleback only one family has members on the GNAI2 bearing chromosome and scaffold (XVII and scaffold 27), although its topology is unclear with regard to 3R. These results are summarized in Additional file 5. Our orthology predictions between human and spotted gar identified a single putative GNAT1 ortholog as well as a single putative GNAI1-3 ortholog (Figure 3). Taken together this analysis supports a possible 3R expansion of the GNAI1 and GNAI2 genes and their chromosomal regions. This also corroborates the loss of the GNAT3 gene in the teleost and amphibian lineages independently.
Evolution of the oxytocin and vasopressin receptor gene family
Our phylogenetic analysis of the OT/VP-R family (Figure 2) shows that the vertebrate gene family consists of six ancestral members, OTR, V1A, V1B, V2A, V2B and V2C. We propose a simplified nomenclature for the V2-type receptors based on the evolutionary scenario below. The V2A receptors form the largest branch and include the well-characterized mammalian V2 receptor encoded by the AVPR2 gene. The V2B receptor subtype was identified independently by us  and other researchers , and includes mostly actinopterygian sequences as well as coelacanth and elephant shark. The V2C receptor subtype was first reported by us as V2-like in zebrafish and three-spined stickleback , and it was later characterized as V2bR2 by Yamaguchi et al.. Unlike V2B, the V2C branch includes frog and lizard sequences, as well as the known chicken V2 receptor first characterized as VT1 . Like the receptors OTR, V1A and V1B, both V2B and V2C seem to signal via the DAG/IP3/Ca2+ pathway, while the adenylyl cyclase/PKA/cAMP signaling typical for V2A receptors seems to constitute an evolutionary switch in the OT/VP-R family .
Our current phylogenetic analysis and the analyses of the visual opsin gene-bearing chromosome regions allowed us to deduce the following evolutionary scenario for the OT/VP-R gene family: Two ancestral genes were present on the same ancestral vertebrate chromosome before 2R, one giving rise to V1A, V1B and OTR through 2R and one giving rise to V2A, V2B and V2C (Figure 5). The ancestral linkage is still conserved with V2B and OTR genes located together, and V1A and V2C genes located together on the same chromosomes. In the teleost lineage, the 3R event gave rise to two copies of V1A, called V1Aa and V1Ab, as part of the same chromosome regions as the teleost GNAI1 genes (Figure 4). The phylogenetic analysis (Figure 2) is consistent with this, although the V1Aa and V1Ab sequences do not form two well-supported clusters. In the teleosts we also identified local duplicates of OTR, called OTR1 and OTR2, and of V2A, called V2A1 and V2A2.
Evolution of the voltage-gated calcium channel, L-type gene family
The CACNA1-L gene family is one of three subfamilies of voltage-gated calcium channel alpha subunits. The CACNA1-L subfamily, which belongs to the paralogon described herein, has four members in mammals and up to seven members in teleost fish. A more comprehensive analysis of this gene region and the remaining two voltage-gated calcium channel families, located in other paralogons, is in progress (Widmark et al.).
The phylogenetic analyses (Additional file 2: Figures S7 and S8) as well as the analyses of conserved synteny performed in this study show that the CACNA1-L gene family expanded in 2R, before the radiation of vertebrates, with one ancestral gene giving rise to the CACNA1S, CACNA1D, CACNA1C and CACNA1F subtype genes. Subsequently the CACNA1S, -1D and -1F genes duplicated in 3R as part of the visual opsin gene-housing chromosome regions (Figure 5). As for several other gene families in this paralogon, these teleost duplicates have been translocated between the paralogous chromosome regions. For instance, teleost CACNA1S, CACNA1D and CACNA1F genes have all been translocated to zebrafish chromosome 8 (Figure 4) and stickleback linkage group XII (Additional file 5). As mentioned previously, we have observed similar rearrangements for other regions in teleost genomes during analyses of the somatostatin receptor gene regions . The CACNA1D teleost cluster is not well resolved in the phylogenetic maximum likelihood analysis (Additional file 2: Figure S8), and no putative spotted gar sequence could be identified in the orthology predictions. However, our conserved synteny analyses as well as previous whole-genome analyses [10, 45] are consistent with our conclusions.
Implications for early vertebrate radiation
Our analyses show that the gnathostome opsin repertoire with the four subtypes RH1, RH2, SWS1, SWS2 clearly resulted from a quadruplication of an ancestral chromosome block (that also included the adjacent but more distantly related LWS genes without surviving duplicates). The presence of orthologs of all these genes in the pouched lamprey (Geotria australis)  imply that these chromosome-based gene duplications took place before the lamprey-gnathostome divergence, as previously proposed . Our present extensive characterization of these paralogous gene regions in a broad range of vertebrates demonstrates that they resulted from the quadruplication of a very large chromosomal block in the time window of 2R. Thus, it would follow that the lamprey lineage diverged after the two basal vertebrate tetraploidizations. If hagfishes and lampreys together form a monophyletic clade in the superclass Cyclostomata, as seems to be the case , this would mean that all vertebrates, including hagfish [56, 57], share a common ancestor that had gone through 2R. To our knowledge, the opsin gene family is presently the only one that has been found to have retained a complete 2R quartet in a lamprey. Several previously investigated gene families in the literature display fewer family members in lampreys than in gnathostomes – see for instance [20, 58], suggesting more extensive gene loss in the lamprey lineage after 2R. Nevertheless, some incomplete gene families are consistent with post-2R divergence of cyclostomes and jawed vertebrates, including the retinoic acid receptors RAR . The genome-wide duplication pattern in the recently published sea lamprey (Petromyzon marinus) whole-genome sequence was found to be indicative of 2R .
We present an extensive analysis of the paralogous chromosome regions housing the gene families for visual opsins, the G-protein alpha subunit families for transducin (GNAT) and adenylyl cyclase inhibition (GNAI), the oxytocin and vasopressin receptors (OT/VP-R), and the L-type voltage-gated calcium channel alpha subunits (CACNA1-L), using both phylogenetic analyses and positional data for these as well as 34 chromosomal neighboring gene families. This combined dataset makes it possible to make a robust inference how this region evolved. We conclude that these related chromosome regions originated from an ancestral chromosome that was duplicated in the two basal vertebrate tetraploidizations (2R) resulting in four paralogous chromosome regions. The paralogon was duplicated again in the teleost-specific tetraploidization (3R) giving teleost fish additional gene family members. We could detect extensive post-3R chromosomal rearrangements between the paralogous chromosome regions in teleost genomes that obscure the view of these whole genome duplications, as noted previously [45, 46, 53]. However, the analyses of extant teleost genomes combined with the data presented here from the spotted gar, an out-group to teleost evolution, allowed us to resolve the rearrangements.
Referring also to our previous analyses of several gene families, we conclude that the basal vertebrate tetraploidizations contributed with new genetic material in several gene families involved in the phototransduction cascade, but also in other functions related to the vertebrate nervous system.
Sequence identification and genome database searches
Amino acid sequence predictions of the visual opsin genes were retrieved from the Ensembl genome browser (http://www.ensembl.org)  from a representative selection of vertebrate clades: human (Homo sapiens), mouse (Mus musculus), grey short-tailed opossum (Monodelphis domestica), anole lizard (Anolis carolinensis), chicken (Gallus gallus), Western clawed frog (Xenopus (Silurana) tropicalis), coelacanth (Latimeria chalumnae), zebrafish (Danio rerio), three-spined stickleback (Gasterosteus aculeatus), medaka (Oryzias latipes) and spotted green pufferfish (Tetraodon nigroviridis). Amino acid sequence predictions from the spotted gar (Lepisosteus oculatus) genome were identified through BLAST searches against the LepOcu1 assembly available at the Pre! Ensembl genome browser (http://pre.ensembl.org/Lepisosteus_oculatus/Info/Index) and included in the analyses. Chicken data was complemented with cloned sequences (GenBank accession numbers: NP_990769.1, P22329.1 and P28682.1) [6, 61]. Additionally, published visual opsin amino acid sequences from the pouched lamprey (Geotria australis) were used (GenBank accession numbers AAR14682.1, AAR14683.1, AAR14681.1, AAR14684.1 and AAR14680.1) .
For the oxytocin and vasopressin receptor gene family the same species repertoire as the visual opsins was used with a few exceptions: the Japanese pufferfish (Takifugu rubripes) was used instead of the related spotted green pufferfish and Southern platyfish (Xiphophorus maculatus) sequences (retrieved from Ensembl version 68) were added to increase resolution of the teleost branches. In addition, published oxytocin and vasopressin receptor sequences from the elephant shark (Callorhinchus milii) (GenBank accession numbers AB665985.1, AB665982.1, AB665983.1, AB665984.1, and AB671271.1) were added . A sequence from the tunicate transparent sea squirt (Ciona intestinalis) was also added. Known OT/VP-R gene family members in the common octopus (Octopus vulgaris) were used as out-group, as described in .
For the CACNA1-L gene family the same repertoire as the visual opsins were used excluding Western clawed frog, coelacanth and spotted gar. Invertebrate sequences from transparent sea squirt and fruit fly (Drosophila melanogaster) were included for relative dating and as a root, respectively.
Sequences were identified in several Ensembl versions for the different gene families, using Ensembl’s automatic protein family predictions, spanning between Ensembl 60 (November 2010) to Ensembl 68 (July 2012). For the visual opsin gene family, gene predictions were identified through Ensembl’s gene tree function  searches since the OPN genes are spread among several Ensembl protein family predictions. All sequences and database identifiers have been verified against the genome assembly versions in Ensemble database version 71 (April 2013). This information can be found in Additional files 1 and 3. To identify additional family members that may have been excluded from the automatic Ensembl protein family predictions, Basic Local Alignment Searches (BLAST)  were performed using identified amino acid sequences (tblastn) as search terms with standard settings on the Ensembl database and the National Center for Biotechnology Information (NCBI) databases.
Conserved synteny analysis
The locations of the identified visual opsin, OT/VP-R, GNAT, GNAI and CACNA1-L sequences were recorded for the genome assemblies detailed above. All locations were verified against the genome assembly versions in Ensemble database version 71 (April 2013). Using the BioMart function, lists of gene predictions corresponding to the chromosome blocks bearing these genes in the human genome assembly GRCh37 were downloaded from the Ensembl genome browser (versions specified below). This dataset was complemented with lists from the zebrafish genome (assembly Zv9) in some cases (see below). Chromosome blocks were defined as approximately 5 Mb in each direction of each of the genes in the above-mentioned gene families.
From these lists of syntenic gene predictions we identified Ensembl protein family predictions that had members on at least two of the included chromosome blocks: these protein family predictions represent the syntenic or neighboring gene families. Amino acid sequence predictions corresponding to each of the identified neighboring gene families were downloaded from the Ensembl genome browser in order to do amino acid sequence alignments and phylogenetic analyses, and the locations of all identified sequences were recorded. The species included in these analyses were: human, mouse, grey short-tailed opossum, chicken, three-spined stickleback, spotted green pufferfish, medaka, zebrafish, transparent sea squirt (Ciona intestinalis or Ciona savignyi) and fruit fly (Drosophila melanogaster). Sequence predictions from the following additional species were used in some families in order to ensure phylogenetic signal and/or taxonomic representation: Tasmanian devil (Sarcophilus harrisii), zebra finch (Taeniopygia guttata), anole lizard, Western clawed frog, Japanese pufferfish (Takifugu rubripes), Florida lancelet (Branchiostoma floridae) and the nematode Caenorhabditis elegans. Additional members that were not included in the automatic protein family predictions were identified by tblastn searches as described above. All sequences, database identifiers and locations have been verified against the genome assembly versions in Ensemble database version 71 (April 2013). For some of the neighboring gene families invertebrate sequences had to be identified by Hidden Markov Model searches (HMMER) using the HMMER web server (http://hmmer.janelia.org/)  and its pHMMER implementation against the UniProtKB database and the NCBI non-redundant (NR) protein database.
The identification of neighboring gene families was done independently for the regions corresponding to each of the visual opsin, OT/VP-R, GNAT/GNAI and CACNA1-L gene families. The neighboring gene families were subsequently pooled together into one dataset and used for the analyses of conserved synteny. Since several of the chromosome blocks used in the analyses overlapped, some of the gene families were identified twice.
Selection of neighboring gene families in the visual opsin chromosome regions
The chromosome regions bearing the visual opsin genes OPN1SW, RHO, OPN1LW and OPN1MW in the human genome were used to select neighboring gene families. The chromosome blocks range between map positions 124 Mb and 134 Mb on chromosome 3, between map positions 123 Mb and 133 Mb on chromosome 7, and between map positions 148 Mb and 158 Mb on the X chromosome in Ensembl 60 (November 2010). Ensembl protein families with members present in at least two of the above-mentioned chromosomal regions were included in the subsequent phylogenetic analyses.
Selection of neighboring gene families in the OT/VP-R chromosome regions
Since not all identified OT/VP-R genes could be identified in the human genome (Ocampo Daza et al 2012), both the zebrafish and the human genomes were used to identify neighboring gene families for the analysis of conserved synteny. Both sets of chromosome blocks were downloaded from Ensembl 60 (November 2010).
The chromosome blocks in the zebrafish genome range between map positions 3 Mb and 12.5 Mb as well as between map positions 12.5 Mb and 22 Mb on chromosome 4, between map positions 37 Mb and 52 Mb on chromosome 6, between map positions 13 Mb and 30 Mb on chromosome 23 and between map positions 1 bp and 7 Mb on chromosome 25. Since there are several OT/VP-R genes located on the same chromosomes, these blocks do not necessarily represent 5 Mb. For example, the V1aR1-type and V2bR2-type genes are both located on chromosome 4, but to investigate the paralogy relationship between these two genes the chromosome blocks were treated separately. Ensembl protein families with members on at least three of the chromosome blocks were selected for the analysis of conserved synteny.
In the human genome the chromosome blocks range between map positions 199 Mb and 209 Mb on chromosome 1, between map positions 3 Mb and 13 Mb on chromosome 3, between Map positions 56 Mb and 66 Mb on chromosome 12, and between map positions 147 Mb and 157 Mb on the X chromosome. Protein families with members on at least two of the chromosome blocks were selected.
Selection of neighboring gene families in the CACNA1-L chromosome regions
A list of all gene predictions located in the chromosome blocks between map positions 196 Mb and 206 Mb on chromosome 1, 48.5 Mb and 58.5 Mb on chromosome 3, 1 bp and 7 Mb on chromosome 12 and between map positions 44 Mb and 54 Mb on chromosome X in the human genome were downloaded from Ensembl 61 (February 2011). These blocks represent the chromosomal regions of the CACNA1S, CACNA1D, CACNA1C and CACNA1F genes respectively. Ensembl protein families with members located on at least two of the chromosome blocks were considered for the analysis of conserved synteny.
Selection of neighboring gene families in the GNAT and GNAI chromosome regions
Lists of genes in the GNAT-GNAI bearing chromosome regions were downloaded from Ensembl 59 (Aug 2010). The chromosome blocks range between map positions 74.8 Mb and 84.7 Mb on chromosome 7, between map positions 45.3 Mb and 55.2 Mb on chromosome 3, and between map positions 106 Mb and 115.1 Mb on chromosome 1 in the human genome. Ensembl protein families represented on at least two of the three human chromosome blocks were included in the analysis of conserved synteny.
Sequence annotation and curation
For short, incomplete or highly diverging sequences among the identified gene predictions, the genomic sequences, including intronic and flanking sequences, were collected and the GenScan gene prediction server (http://genes.mit.edu/GENSCAN.html)  was used to ratify faulty exon predictions or to predict exons or entire genes de novo. Whenever possible, short Ensembl predictions were replaced with NCBI RefSeq sequences identified by BLAST searches, or with overlapping GenScan-predictions included in the Ensembl browser. Sequences that were still divergent with regard to exon-intron boundaries were curated manually by following consensus for splice donor and acceptor sites as well as sequence homology to other family members. Remaining highly divergent and unalignable sequence stretches in some of these predictions were removed. Short amino acid sequences that could not be ratified and did not provide enough sequence information in the alignments were removed entirely in order to prevent artifacts in the phylogenetic analyses. However the chromosomal locations of the gene predictions were registered.
Sequence alignment and phylogenetic analyses
Amino acid sequences were aligned using the ClustalW algorithm (Gonnet weight matrix, gap opening penalty 10.0 and gap extension penalty 0.20)  or the MUSCLE algorithm (with 16 iterations)  and the resulting alignments were inspected manually in order to ratify faulty or divergent predictions and curate misaligned sequence stretches. The manually curated alignments were used to calculate phylogenetic trees, using both the Neighbor Joining (NJ) and Phylogenetic Maximum Likelihood (PhyML) methods.
NJ trees with non-parametric bootstrap support were made using standard settings (NJ clustering algorithm with 1000 bootstrap iterations) in ClustalX 2.0.12 . PhyML trees were made using the PhyML3.0 algorithm  with the following settings: amino acid frequencies (equilibrium frequencies), proportion of invariable sites (with optimized p-invar) and gamma shape parameters were estimated from the alignments, the number of substitution rate categories was set to 8, BIONJ was chosen to create the starting tree, both NNI and SPR tree optimization methods were considered and both tree topology and branch length optimization were chosen. The amino acid substitution model was selected for each alignment using ProtTest3.2  with the following settings: Likelihood scores were computed selecting between the JTT, LG, DCMut, Dayhoff, WAG, Blosum62 and VT substitution model matrices with no add-ons and a Fixed BioNJ JTT-based starting tree. Based on these analyses the LG model was chosen for the visual opsin gene family and the JTT model for the OT/VP-R and CACNA1-L gene families. The JTT model was also chosen for the majority of the neighboring gene families, except for the B4GALNT, CACNA2D, COL, L1CAM, PLG, PPP, QSOX and UBA gene families where the WAG model was chosen, and the RPL and TWF gene families where the LG model was chosen. The visual opsin, OT/VP-R and CACNA1-L PhyML topologies are supported by non-parametric bootstrap tests with 100 iterations. The PhyML tree topologies for the neighboring families are supported by non-parametric SH-like approximate likelihood ratio (aLRT) tests [68, 70] since this method is faster.
Relative dating and outgroup choice
For the majority of the phylogenetic analyses the identified fruit fly sequences were used as out-group to root the trees. In some cases where no fruit fly sequence could be identified, C. elegans or tunicate sequences were used instead. The inclusion of lancelet or tunicate sequences in the phylogenetic analyses provides the relative dating for the time-window of 2R. For a few families where no invertebrate sequences could be identified, midpoint-rooting  was used. The rooting of the phylogenetic trees for the neighboring gene families is summarized in Table 2. The OT/VP-R gene family was rooted with identified Octopus vulgaris family members, as described in . The visual opsin gene family was rooted with the human OPN3 gene.
Analysis of conserved synteny between the human and spotted gar genomes
A FASTA file containing all preliminary protein sequence predictions from the spotted gar genome assembly (LepOcu1) available in the Pre! Ensembl database was downloaded using the FTP server ( http://pre.ensembl.org/downloads.html, retrieved July 25, 2012). This file was used for orthology searches using InParanoid 4.1 [72, 73] (with standard settings) against a FASTA file containing translations of all human canonical transcripts (available from the InParanoid website: http://inparanoid.sbc.su.se/download/7.0_current/sequences/processed/H.sapiens.fa. From the resulting global dataset of orthology matches between the spotted gar and human genomes, the best spotted gar matches (highest bootstrap support) for each human gene prediction used in this study were mined. The locations of each of these spotted gar protein prediction matches in the spotted gar genome assembly were recorded and charted.
Description of additional files
The data sets supporting the results of this article, including all sequence alignments and phylogenetic tree files, are available in figshare and have been cited in the article where appropriate – see references [35, 42–44]. The following additional files are included with this article. Additional file 1 includes detailed information on the main gene families, such as database identifiers, location data and annotation notes for all analyzed sequences. Additional file 2 includes the phylogenetic trees of the main gene families (Figures S1-S8). Additional file 3 includes detailed information on the neighboring gene families. Additional file 4 includes supplementary notes on the phylogenies of neighboring gene families. Additional file 5 includes conserved synteny tables with the synteny data underlying our evolutionary scenario.
This work was supported by grants from the Swedish Research Council and the Carl Trygger Foundation. We are grateful to Ola Gustafsson and Susanne Dreborg who participated in the initial stages of the opsin analyses, to Venkatesh Chandra Reddy who carried out initial phylogenetic analyses on some of the neighboring gene families, and to Christina A. Bergqvist and Lars G. Lundin for fruitful discussions throughout this project.
- Hering L, Henze MJ, Kohler M, Kelber A, Bleidorn C, Leschke M, Nickel B, Meyer M, Kircher M, Sunnucks P, Mayer G: Opsins in onychophora (velvet worms) suggest a single origin and subsequent diversification of visual pigments in arthropods. Mol Biol Evol. 2012, 29: 3451-3458. 10.1093/molbev/mss148.PubMedView ArticleGoogle Scholar
- Davies WIL, Collin SP, Hunt DM: Molecular ecology and adaptation of visual photopigments in craniates. Mol Ecol. 2012, 21: 3121-3158. 10.1111/j.1365-294X.2012.05617.x.PubMedView ArticleGoogle Scholar
- Davies WL, Carvalho LS, Tay B-H, Brenner S, Hunt DM, Venkatesh B: Into the blue: gene duplication and loss underlie color vision adaptations in a deep-sea chimaera, the elephant shark Callorhinchus milii. Genome Res. 2009, 19: 415-426.PubMed CentralPubMedView ArticleGoogle Scholar
- Collin SP: Evolution and ecology of retinal photoreception in early vertebrates. Brain Behav Evol. 2010, 75: 174-185. 10.1159/000314904.PubMedView ArticleGoogle Scholar
- Rennison DJ, Owens GL, Taylor JS: Opsin gene duplication and divergence in ray-finned fish. Mol Phylogenet Evol. 2012, 62: 986-1008. 10.1016/j.ympev.2011.11.030.PubMedView ArticleGoogle Scholar
- Okano T, Kojima D, Fukada Y, Shichida Y, Yoshizawa T: Primary structures of chicken cone visual pigments: vertebrate rhodopsins have evolved out of cone visual pigments. Proc Natl Acad Sci USA. 1992, 89: 5932-5936. 10.1073/pnas.89.13.5932.PubMed CentralPubMedView ArticleGoogle Scholar
- Davies WL, Cowing JA, Carvalho LS, Potter IC, Trezise AEO, Hunt DM, Collin SP: Functional characterization, tuning, and regulation of visual pigment gene expression in an anadromous lamprey. FASEB J. 2007, 21: 2713-2724. 10.1096/fj.06-8057com.PubMedView ArticleGoogle Scholar
- Larhammar D, Lundin L-G, Hallböök F: The human Hox-bearing chromosome regions did arise by block or chromosome (or even genome) duplications. Genome Res. 2002, 12: 1910-1920. 10.1101/gr.445702.PubMed CentralPubMedView ArticleGoogle Scholar
- Dehal P, Boore JL: Two rounds of whole genome duplication in the ancestral vertebrate. PLoS Biol. 2005, 3: e314-10.1371/journal.pbio.0030314.PubMed CentralPubMedView ArticleGoogle Scholar
- Nakatani Y, Takeda H, Kohara Y, Morishita S: Reconstruction of the vertebrate ancestral genome reveals dynamic genome reorganization in early vertebrates. Genome Res. 2007, 17: 1254-1265. 10.1101/gr.6316407.PubMed CentralPubMedView ArticleGoogle Scholar
- Putnam NH, Butts T, Ferrier DEK, Furlong RF, Hellsten U, Kawashima T, Robinson-Rechavi M, Shoguchi E, Terry A, Yu J-K, Benito-Gutiérrez E, Dubchak I, Garcia-Fernàndez J, Gibson-Brown JJ, Grigoriev IV, Horton AC, de Jong PJ, Jurka J, Kapitonov VV, Kohara Y, Kuroki Y, Lindquist E, Lucas S, Osoegawa K, Pennacchio LA, Salamov AA, Satou Y, Sauka-Spengler T, Schmutz J, Shin-I T, et al: The amphioxus genome and the evolution of the chordate karyotype. Nature. 2008, 453: 1064-1071. 10.1038/nature06967.PubMedView ArticleGoogle Scholar
- Jaillon O, Aury J-M, Brunet F, Petit J-L, Stange-Thomann N, Mauceli E, Bouneau L, Fischer C, Ozouf-Costaz C, Bernot A, Nicaud S, Jaffe D, Fisher S, Lutfalla G, Dossat C, Segurens B, Dasilva C, Salanoubat M, Levy M, Boudet N, Castellano S, Anthouard V, Jubin C, Castelli V, Katinka M, Vacherie B, Biémont C, Skalli Z, Cattolico L, Poulain J, et al: Genome duplication in the teleost fish Tetraodon nigroviridis reveals the early vertebrate proto-karyotype. Nature. 2004, 431: 946-957. 10.1038/nature03025.PubMedView ArticleGoogle Scholar
- Sundström G, Dreborg S, Larhammar D: Concomitant duplications of opioid peptide and receptor genes before the origin of jawed vertebrates. PLoS One. 2010, 5: e10512-10.1371/journal.pone.0010512.PubMed CentralPubMedView ArticleGoogle Scholar
- Dreborg S, Sundström G, Larsson TA, Larhammar D: Evolution of vertebrate opioid receptors. Proc Natl Acad Sci USA. 2008, 105: 15487-15492. 10.1073/pnas.0805590105.PubMed CentralPubMedView ArticleGoogle Scholar
- Sundström G, Larsson TA, Brenner S, Venkatesh B, Larhammar D: Evolution of the neuropeptide Y family: new genes by chromosome duplications in early vertebrates and in teleost fishes. Gen Comp Endocrinol. 2008, 155: 705-716. 10.1016/j.ygcen.2007.08.016.PubMedView ArticleGoogle Scholar
- Larsson TA, Tay B-H, Sundström G, Fredriksson R, Brenner S, Larhammar D, Venkatesh B: Neuropeptide Y-family peptides and receptors in the elephant shark, Callorhinchus milii confirm gene duplications before the gnathostome radiation. Genomics. 2009, 93: 254-260. 10.1016/j.ygeno.2008.10.001.PubMedView ArticleGoogle Scholar
- Larsson TA, Olsson F, Sundström G, Lundin L-G, Brenner S, Venkatesh B, Larhammar D: Early vertebrate chromosome duplications and the evolution of the neuropeptide Y receptor gene regions. BMC Evol Biol. 2008, 8: 184-10.1186/1471-2148-8-184.PubMed CentralPubMedView ArticleGoogle Scholar
- Widmark J, Sundström G: Ocampo Daza D, Larhammar D: Differential evolution of voltage-gated sodium channels in tetrapods and teleost fishes. Mol Biol Evol. 2011, 28: 859-871. 10.1093/molbev/msq257.PubMedView ArticleGoogle Scholar
- Ocampo Daza D, Sundström G, Bergqvist CA, Duan C, Larhammar D: Evolution of the insulin-like growth factor binding protein (IGFBP) family. Endocrinology. 2011, 152: 2278-2289. 10.1210/en.2011-0047.View ArticleGoogle Scholar
- Hultqvist G, Ocampo Daza D, Larhammar D, Kilimann MW: Evolution of the vertebrate paralemmin gene family: ancient origin of gene duplicates suggests distinct functions. PLoS One. 2012, 7: e41850-10.1371/journal.pone.0041850.PubMed CentralPubMedView ArticleGoogle Scholar
- Lagman D, Sundström G, Ocampo Daza D, Abalo XM, Larhammar D: Expansion of Transducin Subunit Gene Families in Early Vertebrate Tetraploidizations. Genomics. 2012, 1-9.Google Scholar
- Larhammar D, Nordström K, Larsson TA: Evolution of vertebrate rod and cone phototransduction genes. Phil Trans Roy Soc Lond B Biol Sci. 2009, 364: 2867-2880. 10.1098/rstb.2009.0077.View ArticleGoogle Scholar
- Nordström K, Larsson TA, Larhammar D: Extensive duplications of phototransduction genes in early vertebrate evolution correlate with block (chromosome) duplications. Genomics. 2004, 83: 852-872. 10.1016/j.ygeno.2003.11.008.PubMedView ArticleGoogle Scholar
- Kawamura S, Blow NS, Yokoyama S: Genetic analyses of visual pigments of the pigeon (Columba livia). Genetics. 1999, 153: 1839-1850.PubMed CentralPubMedGoogle Scholar
- Chinen A, Hamaoka T, Yamada Y, Kawamura S: Gene duplication and spectral diversification of cone visual pigments of zebrafish. Genetics. 2003, 163: 663-675.PubMed CentralPubMedGoogle Scholar
- Yokoyama R, Yokoyama S: Molecular characterization of a blue visual pigment gene in the fish Astyanax fasciatus. FEBS Lett. 1993, 334: 27-31. 10.1016/0014-5793(93)81673-N.PubMedView ArticleGoogle Scholar
- Oka Y, Korsching SI: Shared and unique G alpha proteins in the zebrafish versus mammalian senses of taste and smell. Chem Senses. 2011, 36: 357-365. 10.1093/chemse/bjq138.PubMedView ArticleGoogle Scholar
- Ohmoto M, Okada S, Nakamura S, Abe K, Matsumoto I: Mutually exclusive expression of Gαia and Gα14 reveals diversification of taste receptor cells in zebrafish. J Comp Neurol. 2011, 519: 1616-1629. 10.1002/cne.22589.PubMed CentralPubMedView ArticleGoogle Scholar
- Yamaguchi Y, Kaiya H, Konno N, Iwata E, Miyazato M, Uchiyama M, Bell JD, Toop T, Donald JA, Brenner S, Venkatesh B, Hyodo S: The fifth neurohypophysial hormone receptor is structurally related to the V2-type receptor but functionally similar to V1-type receptors. Gen Comp Endocrinol. 2012, 178: 519-528. 10.1016/j.ygcen.2012.07.008.PubMedView ArticleGoogle Scholar
- Ocampo Daza D, Lewicka M, Larhammar D: The oxytocin/vasopressin receptor family has at least five members in the gnathostome lineage, including two distinct V2 subtypes. Gen Comp Endocrinol. 2012, 175: 135-143. 10.1016/j.ygcen.2011.10.011.PubMedView ArticleGoogle Scholar
- Peirson SN, Halford S, Foster RG: The evolution of irradiance detection: melanopsin and the non-visual opsins. Phil Trans Roy Soc Lond B Biol Sci. 2009, 364: 2849-2865. 10.1098/rstb.2009.0050.View ArticleGoogle Scholar
- Davies WL, Hankins MW, Foster RG: Vertebrate ancient opsin and melanopsin: divergent irradiance detectors. Photochem Photobiol Sci. 2010, 9: 1444-1457. 10.1039/c0pp00203h.PubMedView ArticleGoogle Scholar
- Sato K, Yamashita T, Ohuchi H, Shichida Y: Vertebrate ancient-long opsin has molecular properties intermediate between those of vertebrate and invertebrate visual pigments. Biochemistry. 2011, 50: 10484-10490. 10.1021/bi201212z.PubMedView ArticleGoogle Scholar
- Kusakabe T, Tsuda M: Photoreceptive systems in ascidians. Photochem Photobiol. 2007, 83: 248-252. 10.1562/2006-07-11-IR-965.PubMedView ArticleGoogle Scholar
- Phylogenetic analyses of the visual opsin genes of the LWS, SWS1, SWS2, RH1 and RH2 clades. http://0-dx.doi.org.brum.beds.ac.uk/10.6084/m9.figshare.705157Google Scholar
- Collin SP, Knight MA, Davies WL, Potter IC, Hunt DM, Trezise AEO: Ancient colour vision: multiple opsin genes in the ancestral vertebrates. Curr Biol. 2003, 13: R864-R865. 10.1016/j.cub.2003.10.044.PubMedView ArticleGoogle Scholar
- Alföldi J, Di Palma F, Grabherr M, Williams C, Kong L, Mauceli E, Russell P, Lowe CB, Glor RE, Jaffe JD, Ray DA, Boissinot S, Shedlock AM, Botka C, Castoe TA, Colbourne JK, Fujita MK, Moreno RG, ten Hallers BF, Haussler D, Heger A, Heiman D, Janes DE, Johnson J, de Jong PJ, Koriabine MY, Lara M, Novick PA, Organ CL, Peach SE, et al: The genome of the green anole lizard and a comparative analysis with birds and mammals. Nature. 2011, 477: 587-591. 10.1038/nature10390.PubMed CentralPubMedView ArticleGoogle Scholar
- Yokoyama S, Zhang H, Radlwimmer FB, Blow NS: Adaptive evolution of color vision of the Comoran coelacanth (Latimeria chalumnae). Proc Natl Acad Sci USA. 1999, 96: 6279-6284. 10.1073/pnas.96.11.6279.PubMed CentralPubMedView ArticleGoogle Scholar
- Mano H, Kojima D, Fukada Y: Exo-rhodopsin: a novel rhodopsin expressed in the zebrafish pineal gland. Brain research Molecular brain research. 1999, 73: 110-118. 10.1016/S0169-328X(99)00242-9.PubMedView ArticleGoogle Scholar
- Fitzgibbon J, Hope A, Slobodyanyuk SJ, Bellingham J, Bowmaker JK, Hunt DM: The rhodopsin-encoding gene of bony fish lacks introns. Gene. 1995, 164: 273-277. 10.1016/0378-1119(95)00458-I.PubMedView ArticleGoogle Scholar
- Morrow JM, Lazic S, Chang BSW: A novel rhodopsin-like gene expressed in zebrafish retina. Vis Neurosci. 2011, 28: 325-335. 10.1017/S0952523811000010.PubMedView ArticleGoogle Scholar
- Phylogenetic analyses of the vertebrate oxytocin and vasopressin receptor gene family. http://0-dx.doi.org.brum.beds.ac.uk/10.6084/m9.figshare.707336Google Scholar
- Phylogenetic analyses of the vertebrate voltage-gated calcium channel L-type alpha 1 subunit gene family. http://0-dx.doi.org.brum.beds.ac.uk/10.6084/m9.figshare.710637Google Scholar
- Phylogenetic analyses of syntenic gene families in visual opsin gene-bearing chromosome regions. http://0-dx.doi.org.brum.beds.ac.uk/10.6084/m9.figshare.705852Google Scholar
- Kasahara M, Naruse K, Sasaki S, Nakatani Y, Qu W, Ahsan B, Yamada T, Nagayasu Y, Doi K, Kasai Y, Jindo T, Kobayashi D, Shimada A, Toyoda A, Kuroki Y, Fujiyama A, Sasaki T, Shimizu A, Asakawa S, Shimizu N, Hashimoto S-I, Yang J, Lee Y, Matsushima K, Sugano S, Sakaizumi M, Narita T, Ohishi K, Haga S, Ohta F, et al: The medaka draft genome and insights into vertebrate genome evolution. Nature. 2007, 447: 714-719. 10.1038/nature05846.PubMedView ArticleGoogle Scholar
- Amores A, Catchen J, Ferrara A, Fontenot Q, Postlethwait JH: Genome evolution and meiotic maps by massively parallel DNA sequencing: spotted gar, an outgroup for the teleost genome duplication. Genetics. 2011, 188: 799-808. 10.1534/genetics.111.127324.PubMed CentralPubMedView ArticleGoogle Scholar
- Bellingham J, Tarttelin EE, Foster RG, Wells DJ: Structure and evolution of the teleost extraretinal rod-like opsin (errlo) and ocular rod opsin (rho) genes is teleost rho a retrogene. J Exp Zool B Mol Dev Evol. 2003, 297: 1-10.PubMedView ArticleGoogle Scholar
- Venkatesh B, Ning Y, Brenner S: Late changes in spliceosomal introns define clades in vertebrate evolution. Proc Natl Acad Sci USA. 1999, 96: 10267-10271. 10.1073/pnas.96.18.10267.PubMed CentralPubMedView ArticleGoogle Scholar
- Pointer MA, Carvalho LS, Cowing JA, Bowmaker JK, Hunt DM: The visual pigments of a deep-sea teleost, the pearl eye Scopelarchus analis. J Exp Biol. 2007, 210 (16): 2829-2835. 10.1242/jeb.006064.PubMedView ArticleGoogle Scholar
- Zhang H, Futami K, Horie N, Okamura A, Utoh T, Mikawa N, Yamada Y, Tanaka S, Okamoto N: Molecular cloning of fresh water and deep-sea rod opsin genes from Japanese eel Anguilla japonica and expressional analyses during sexual maturation. FEBS Lett. 2000, 469: 39-43. 10.1016/S0014-5793(00)01233-3.PubMedView ArticleGoogle Scholar
- Archer S, Hope A, Partridge JC: The molecular basis for the green-blue sensitivity shift in the rod visual pigments of the European eel. Proceedings Biological sciences/The Royal Society. 1995, 262: 289-295. 10.1098/rspb.1995.0208.PubMedView ArticleGoogle Scholar
- Tan F, Lolait SJ, Brownstein MJ, Saito N, MacLeod V, Baeyens DA, Mayeux PR, Jones SM, Cornett LE: Molecular cloning and functional characterization of a vasotocin receptor subtype that is expressed in the shell gland and brain of the domestic chicken. Biol Reprod. 2000, 62: 8-15. 10.1095/biolreprod62.1.8.PubMedView ArticleGoogle Scholar
- Ocampo Daza D, Sundström G, Bergqvist CA, Larhammar D: The evolution of vertebrate somatostatin receptors and their gene regions involves extensive chromosomal rearrangements. BMC Evol Biol. 2012, 12: 231-10.1186/1471-2148-12-231.PubMed CentralPubMedView ArticleGoogle Scholar
- Kuraku S, Meyer A, Kuratani S: Timing of genome duplications relative to the origin of the vertebrates: did cyclostomes diverge before or after?. Mol Biol Evol. 2009, 26: 47-59.PubMedView ArticleGoogle Scholar
- Heimberg AM, Cowper-Sal-lari R, Sémon M, Donoghue PCJ, Peterson KJ: microRNAs reveal the interrelationships of hagfish, lampreys, and gnathostomes and the nature of the ancestral vertebrate. Proc Natl Acad Sci U S A. 2010, 107: 19379-19383. 10.1073/pnas.1010350107.PubMed CentralPubMedView ArticleGoogle Scholar
- Ota KG, Fujimoto S, Oisi Y, Kuratani S: Identification of vertebra-like elements and their possible differentiation from sclerotomes in the hagfish. Nat Commun. 2011, 2: http://0-dx.doi.org.brum.beds.ac.uk/10.1038/ncomms1355Google Scholar
- Shimeld SM, Donoghue PCJ: Evolutionary crossroads in developmental biology: cyclostomes (lamprey and hagfish). Development. 2012, 139: 2091-2099. 10.1242/dev.074716.PubMedView ArticleGoogle Scholar
- Jakobsson J, Ackermann F, Andersson F, Larhammar D, Löw P, Brodin L: Regulation of synaptic vesicle budding and dynamin function by an EHD ATPase. J Neurosci. 2011, 31: 13972-13980. 10.1523/JNEUROSCI.1289-11.2011.PubMedView ArticleGoogle Scholar
- Smith JJ, Kuraku S, Holt C, Sauka-Spengler T, Jiang N, Campbell MS, Yandell MD, Manousaki T, Meyer A, Bloom OE, Morgan JR, Buxbaum JD, Sachidanandam R, Sims C, Garruss AS, Cook M, Krumlauf R, Wiedemann LM, Sower SA, Decatur WA, Hall JA, Amemiya CT, Saha NR, Buckley KM, Rast JP, Das S, Hirano M, McCurley N, Guo P, Rohner N, et al: Sequencing of the sea lamprey (Petromyzon marinus) genome provides insights into vertebrate evolution. Nat Genet. 2013, 45: 415-421. 10.1038/ng.2568.PubMed CentralPubMedView ArticleGoogle Scholar
- Flicek P, Amode MR, Barrell D, Beal K, Brent S, Carvalho-Silva D, Clapham P, Coates G, Fairley S, Fitzgerald S, Gil L, Gordon L, Hendrix M, Hourlier T, Johnson N, Kähäri AK, Keefe D, Keenan S, Kinsella R, Komorowska M, Koscielny G, Kulesha E, Larsson P, Longden I, McLaren W, Muffato M, Overduin B, Pignatelli M, Pritchard B, Riat HS, et al: Ensembl 2012. Nucleic Acids Res. 2012, 40: D84-D90. 10.1093/nar/gkr991.PubMed CentralPubMedView ArticleGoogle Scholar
- Tokunaga F, Iwasa T, Miyagishi M, Kayada S: Cloning of cDNA and amino acid sequence of one of chicken cone visual pigments. Biochem Biophys Res Commun. 1990, 173: 1212-1217. 10.1016/S0006-291X(05)80915-5.PubMedView ArticleGoogle Scholar
- Vilella AJ, Severin J, Ureta-Vidal A, Heng L, Durbin R, Birney E: EnsemblCompara GeneTrees: Complete, duplication-aware phylogenetic trees in vertebrates. Genome Res. 2009, 19: 327-335.PubMed CentralPubMedView ArticleGoogle Scholar
- Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ: Basic local alignment search tool. J Mol Biol. 1990, 215: 403-410.PubMedView ArticleGoogle Scholar
- Finn RD, Clements J, Eddy SR: HMMER web server: interactive sequence similarity searching. Nucleic Acids Res. 2011, 39 (2): W29-W37.PubMed CentralPubMedView ArticleGoogle Scholar
- Burge C, Karlin S: Prediction of complete gene structures in human genomic DNA. J Mol Biol. 1997, 268: 78-94. 10.1006/jmbi.1997.0951.PubMedView ArticleGoogle Scholar
- Larkin MA, Blackshields G, Brown NP, Chenna R, McGettigan PA, McWilliam H, Valentin F, Wallace IM, Wilm A, Lopez R, Thompson JD, Gibson TJ, Higgins DG: Clustal W and Clustal X version 2.0. Bioinformatics. 2007, 23: 2947-2948. 10.1093/bioinformatics/btm404.PubMedView ArticleGoogle Scholar
- Edgar RC: MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res. 2004, 32: 1792-1797. 10.1093/nar/gkh340.PubMed CentralPubMedView ArticleGoogle Scholar
- Guindon S, Dufayard J-F, Lefort V, Anisimova M, Hordijk W, Gascuel O: New algorithms and methods to estimate maximum-likelihood phylogenies: assessing the performance of PhyML 3.0. Syst Biol. 2010, 59: 307-321. 10.1093/sysbio/syq010.PubMedView ArticleGoogle Scholar
- Abascal F, Zardoya R, Posada D: ProtTest: selection of best-fit models of protein evolution. Bioinformatics. 2005, 21: 2104-2105. 10.1093/bioinformatics/bti263.PubMedView ArticleGoogle Scholar
- Anisimova M, Gascuel O: Approximate likelihood-ratio test for branches: A fast, accurate, and powerful alternative. Syst Biol. 2006, 55: 539-552. 10.1080/10635150600755453.PubMedView ArticleGoogle Scholar
- Hess PN, De Moraes Russo CA: An empirical test of the midpoint rooting method. Biol J Linn Soc. 2007, 92: 669-674. 10.1111/j.1095-8312.2007.00864.x.View ArticleGoogle Scholar
- Berglund A-C, Sjölund E, Ostlund G, Sonnhammer ELL: InParanoid 6: eukaryotic ortholog clusters with inparalogs. Nucleic Acids Res. 2008, 36: D263-D266.PubMed CentralPubMedView ArticleGoogle Scholar
- Remm M, Storm CE, Sonnhammer EL: Automatic clustering of orthologs and in-paralogs from pairwise species comparisons. J Mol Biol. 2001, 314: 1041-1052. 10.1006/jmbi.2000.5197.PubMedView ArticleGoogle Scholar
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