- Open Access
A glimpse into the past: phylogenesis and protein domain analysis of the group XIV of C-type lectins in vertebrates
BMC Genomics volume 23, Article number: 420 (2022)
The group XIV of C-type lectin domain-containing proteins (CTLDcps) is one of the seventeen groups of CTLDcps discovered in mammals and composed by four members: CD93, Clec14A, CD248 and Thrombomodulin, which have shown to be important players in cancer and vascular biology. Although these proteins belong to the same family, their phylogenetic relationship has never been dissected. To resolve their evolution and characterize their protein domain composition we investigated CTLDcp genes in gnathostomes and cyclostomes and, by means of phylogenetic approaches as well as synteny analyses, we inferred an evolutionary scheme that attempts to unravel their evolution in modern vertebrates.
Here, we evidenced the paralogy of the group XIV of CTLDcps in gnathostomes and discovered that a gene loss of CD248 and Clec14A occurred in different vertebrate groups, with CD248 being lost due to chromosome disruption in birds, while Clec14A loss in monotremes and marsupials did not involve chromosome rearrangements. Moreover, employing genome annotations of different lampreys as well as one hagfish species, we investigated the origin and evolution of modern group XIV of CTLDcps. Furthermore, we carefully retrieved and annotated gnathostome CTLDcp domains, pointed out important differences in domain composition between gnathostome classes, and assessed codon substitution rate of each domain by analyzing nonsynonymous (Ka) over synonymous (Ks) substitutions using one representative species per gnathostome order.
CTLDcps appeared with the advent of early vertebrates after a whole genome duplication followed by a sporadic tandem duplication. These duplication events gave rise to three CTLDcps in the ancestral vertebrate that underwent further duplications caused by the independent polyploidizations that characterized the evolution of cyclostomes and gnathostomes. Importantly, our analyses of CTLDcps in gnathostomes revealed critical inter-class differences in both extracellular and intracellular domains, which might help the interpretation of experimental results and the understanding of differences between animal models.
The evolution of vertebrate genes has been characterized by impressive chromosome rearrangements that include whole genome duplications (WGDs) as well as chromosomal reorganizations [1, 2]. As suggested by genomic data, showing an expansion of numerous gene families, the transition from cephalochordates to early vertebrates was characterized by multiple polyploidizations by which the ancestral vertebrate has expanded its gene repertoire . Among the gene families that expanded during the evolution of vertebrates, we found of particular interest the group XIV of C-type lectin domain-containing proteins (CTLDcps) and studied their evolution and protein domain composition by collecting publicly available genome annotations of numerous vertebrate species.
The group XIV of C-type lectins is part of the larger superfamily of CTLDcps which consists of seventeen groups in mammals . Four members compose the group XIV of CTLDcps: CD93, Clec14A, CD248, and Thrombomodulin, which have been studied extensively in human and mouse in the contexts of angiogenesis and cancer biology [5,6,7,8]. They are type I transmembrane proteins with an extended extracellular domain (ECD) which, from the N-terminus, consists of a CTLD, a sushi domain (except for Thrombomodulin) and a variable number of EGF-like repeats: CD93 has five, Clec14A one, CD248 three, and Thrombomodulin six. A Pro/Ser/Thr rich region (known as mucin-like region) extends from the last EGF-like repeat to the transmembrane domain and is responsible for a high degree of glycosylation. Lastly, a short cytotail extends into the cytoplasm .
Expression profile analyses have shown peculiar tissue distribution for each of the four proteins. CD93 has been predominantly studied in endothelial cells (EC) although it is also expressed by different cell types such as neurons, monocytes, platelets and hematopoietic stem cells . In ECs it has been shown to regulate adhesion and migration [10,11,12], and, by binding the extracellular matrix (ECM) protein Multimerin-2 (MMRN2), forms a complex with the β1 integrin inducing fibronectin fibrillogenesis important for EC migration [6, 13]. Moreover, CD93 can be cleaved from the membrane and released in a soluble form (sCD93) which acts as a potent inducer of angiogenesis through its EGF-like tandem repeats .
Clec14A expression is considered endothelial specific. Interestingly, the expression of Clec14A is barely detectable in healthy vessels but strongly upregulated in angiogenic tumor-associated blood vessels of non-small cell lung cancer and ovarian cancer tissues [15, 16]. It has been found to regulate EC tube formation and migration in vitro as well as tumor angiogenesis in vivo. Moreover, like CD93 and CD248, Clec14A binds to MMRN2, promoting tumor vascular growth in a Lewis lung carcinoma mouse model .
CD248 is the only member of the group XIV that is not expressed by ECs. Instead, it shows elevated expression in fibroblasts, perivascular, mesenchymal and some tumor cells . It was demonstrated that CD248 is able to bind different ECM proteins such as collagen I, fibronectin and MMRN2 [6, 8]. Despite its role in angiogenesis is still controversial, it has been shown that CD248 can act as a regulator of vessel normalization and vascular pruning [9, 17].
Thrombomodulin is expressed in endothelial and lymphatic blood vessels but can also be found in monocytes, neutrophils as well as dendritic cells [18, 19]. Thrombomodulin is the only protein of the group XIV that lacks some key amino acids necessary for the folding of a proper sushi-like domain and the region comprised between the CTLD and first EGF is instead indicated as hydrophobic stretch . Importantly, the absence of a proper sushi-like domain probably accounts for the incapability of Thrombomodulin to bind to MMRN2 . The soluble form of Thrombomodulin, generated after proteolytic cleavage, can modulate angiogenesis by binding the fibroblast growth factor 1 [20, 21]. Besides its role in angiogenesis, Thrombomodulin plays a key role in the coagulation cascade working as an anti-coagulative molecule. Indeed, in this framework, it binds to the serine protease thrombin thus inhibiting the pro-coagulant thrombin-mediated hydrolysis of fibrinogen to fibrin .
The human genome annotation shows a peculiar organization of the group XIV of CTLDcps coding genes with total absence of introns in CD248, Clec14A, and Thrombomodulin whereas CD93 bears a small intron that splits coding and regulatory sequences in two exons. Noteworthy, CD93 and Thrombomodulin lay on the same chromosome in humans, leading to the hypothesis that they may have arisen from a tandem duplication event .
Despite protein similarity of the members of the group XIV would suggest a common origin, phylogenetic analyses aimed to understand their phylogenetic relationship as well as their ancestry have never been attempted. Moreover, despite intensive studies on the human and mouse proteins, little is known about the evolution of their protein domains in other vertebrates.
The availability of a multitude of vertebrate genomic, transcriptomic and proteomic data allowed us to retrieve protein orthologs and paralogs used to study the gene synteny of each group XIV member in different vertebrate classes. Importantly, the current genome annotation of Petromyzon marinus allows the comparison of syntenic gene families between cyclostome and gnathostome CTLDcps-bearing chromosomes helping reconstruct their evolution across vertebrates. In the present work, gene and protein sequences were collected and used to perform comparative genomics and proteomics analyses. Based on the results of our study, we demonstrated that the group XIV of CTLDcps derived from a common ancestor and inferred an evolutionary scheme of their evolution in vertebrates, showing that modern CTLDcps established independently in cyclostomes and gnathostomes. In addition, we demonstrated the loss of CD248 in birds as well as the absence of Clec14A in monotremes and marsupials. By collecting public data from numerous vertebrate orders, we focused our attention on analyzing extracellular and intracellular domains. We revealed important similarities and differences of the group XIV of CTLDcps that may depend on environmental and species-specific adaptations and point out important differences between vertebrate classes.
Sequence mining and dataset creation
All the vertebrate protein and gene sequences belonging to the group XIV of C-type lectin superfamily and their syntenic genes were identified and retrieved from the Protein (NCBI) database. Doubtful protein annotations as well as taxon-missing sequences were manually checked and recovered via pairwise alignment through BLASTp. To retrieve cyclostomes and amphioxi protein sequences from available ill-annotated genomes, gnathostome protein sequences were employed to build HMMER profiles . Due to doubtful annotation, P. marinus CTLDcp genes and proteins were named as follows: CTLDcp-α (XM_032974273) and CTLDcp-β (XM_032974220) genes lying on chromosome 53, CTLDcp-γ gene lying on chromosome 17 (XM_032955932), CTLDcp-δ gene lying on chromosome 6 (XM_014554877). cDNA sequences of neighbor gene families (forkhead-box, ovo and fos) lying on the CTLDcp bearing-chromosomes were mined for at least one species per vertebrate class and lancelets as described above. A complete list of protein, CDS, cDNA and genome accession numbers used in this study is available in the Additional file 4: Supplementary Table 1.
Analysis of the group XIV CTLDcps sushi-like domain in Petromyzon marinus
In order to compare the sushi-like domain of the group XIV CTLDcps in P. marinus, protein domains were predicted using Batch-CD Search NCBI using the CDD database . Since Batch-CD Search failed to predict the sushi-like domain, we manually retrieved the protein region comprised between the CTLD and the first EGF-like (for CTLDcp-α, CTLDcp-β and CTLDcp-δ) or the transmembrane domain (for CTLDcp-γ). To understand if P. marinus CTLDcps showed typical amino acids required for the folding of the sushi-like domain , we aligned the retrieved sequences using PRALINE toolbox [26,27,28]. Structural insights of the sushi-like domain folding were obtained by means of the automated protein structure homology-modelling server SWISS-MODEL .
Synteny identification and analysis
Disposition of the syntenic genes was obtained by manually locating each syntenic gene position in the chromosome following the NCBI database annotation. Gene synteny was visualized using Simple Synteny web tool . The chromosome block interval analyzed for synteny was ~ 20Mbp in each direction of the CTLDcp gene of interest, although in many cases this definition encompassed the entire chromosome. One representative species per vertebrate class and a minimum of 15 syntenic genes per locus were used for the analysis.
Phylogenetic analyses and tree topology tests
For the phylogenetic reconstructions, we utilized well-annotated and largely reported species, including model organisms when possible and employing two representative species per vertebrate class. Species employed for the phylogenetic reconstructions: Homo sapiens (human), Mus musculus (house mouse), Monodelphis domestica (gray short-tailed opossum), Ornithorhynchus anatinus (platypus), Gallus gallus (chicken), Corvus moneduloides (new Caledonian crow), Lacerta agilis (lizard), Trachemys scripta elegans (red-eared slider), Xenopus tropicalis (western clawed frog), Microcaecilia unicolor (tiny Cayenne caecilian), Danio rerio (zebrafish), Latimeria chalumnae (coelacanth), Carcharodon carcharias (great white shark), Scyliorhinus canicula (small-spotted catshark) Petromyzon marinus (sea lamprey), Lethenteron camtschaticum (arctic lamprey), Entosphenus tridentatus (pacific lamprey), Eptatretus burgeri (inshore hagfish), Branchiostoma floridae (Florida lancelet) and Branchiostoma belcheri (Belcher’s lancelet). All phylogenetic analyses were performed using amino-acid or cDNA data matrices automatically aligned using the Aliview built in MUSCLE3.8 aligner [31, 32] and manually revised. Alignments were employed for a Maximum Likelihood (ML) analysis using 10,000 iterations of ultrafast bootstrap in IQ-TREE . Finally, the best evolutionary model was selected during the run with ModelFinder Plus . Rooting was performed on B. belcheri and B. floridae homologous sequences, which were employed as outgroups. All the final trees were visualized using iTOL . To assess orthology between cyclostome and gnathostome proteins, we constrained ten distinct tree topologies and tested them using five different statistical methods (bp-RELL, p-KH, p-SH, c-ELW, p-AU) through IQ-TREE. Topologies which showed a significant outcome in all the statistical tests were accepted and discussed in the Results section.
Protein domain identification and Ka/Ks ratio
Protein domains were identified for all the vertebrate taxon including one representative species per order through the Batch-CD Search NCBI using the CDD database . EGF-like domains were manually revised and categorized based on their typical signatures according to the current PROSITE annotation . EGF-like domains containing the CxCx(5)Gx(2)C (PS00022) or CxCx(2)[GP][FYW]x(4,8)C (PS01186) signature were considered EGF 1 or EGF 2, respectively .
EGF 2 containing the NxNNC-x(3,14)-C-x(3,7)-CxxBxxxxAxC-x(1,6)-C-x(8,13)-Cx (PS01187), (where ‘N’: negatively charged or polar residue [DEQN]; ‘B’: possibly β-hydroxylated residue [DN]; ‘A’: aromatic amino acid; ‘C’: cysteine involved in disulfide bond; ‘x’: any amino acid), were considered calcium-binding EGFs (cbEGFs) according to the PROSITE annotation . Predicted EGF-like domains falling in neither of the two categories were annotated as EGF-like. Thrombomodulin-like fifth EGF domains (cl07616) were successfully predicted by Batch-CD Search and named Tme5-EGF. For the sushi-like domain containing region identification, we considered the interval between the CTLD and the first EGF-like domain. Similarly, the mucin-like region was considered starting from the first amino acid after the last EGF-like domain and finishing before the transmembrane region. The CDS of each domain used for the analysis is shown in detail in the Additional files 8, 9, 10 and 11: Supplementary files 1–4. Transmembrane domain prediction was carried out by the TMHMM Server, v.2.0 [38, 39]. Phosphorylation of tyrosine residues laying in the cytoplasmic region was inferred by using the NetPhos3.1 server . Only consensus with a score > 0.5 were considered reliable and plotted with WebLogo2.8.2 [41, 42].
Protein domain regions were employed to retrieve the corresponding nucleotide sequences through an in-house python3 script to calculate the Ka/Ks ratio. The genetic dataset was aligned as translated amino-acids with MUSCLE3.8 available in the Aliview software [31, 32]. The Ka/Ks ratio was then calculated with the yn00 method available in PAML  as previously described , and plotted in the R environment v.4.1.1.
Data analyses were performed using the statistical function of R software and the values represent the mean ± SD obtained. Statistical differences among groups were evaluated using the One-way ANOVA followed by Tukey’s multiple-comparison test. All p-values reported were two-tailed and p < 0.05 was considered statistically significant.
Study of the group XIV CTLDcps paralogy in gnathostomes
Although CD93, Thrombomodulin, Clec14A, and CD248 are classified in the same protein group, no formal phylogenetic analysis has been conducted to clarify their phylogenetic relationships. Interestingly, it has been previously demonstrated that their bearing chromosomes derived from a series of duplication events as they show typical features of paralogons . To further corroborate these findings, we investigated the evolutionary relationships of three highly conserved transcription factor gene families (forkhead-box, fos and ovo), which we found being neighbors of the CTLDcps genes (Table 1 and Additional file 5: Supplementary Table 2). Our phylogenetic reconstruction showed that these gene families dispose in discrete clusters supporting an ancestral duplication scenario (Fig. 1). Therefore, to unravel the hypothesis that the members of the group XIV share a common ancestry, we retrieved amino acid sequences from the NCBI database and performed a phylogenetic reconstruction of numerous vertebrate species. Using amino acid sequences of CTLD-like proteins of two different lancelet species as outgroups, the resulting ML tree showed the CTLDcps disposition in discrete subtype clusters with a well-supported ancestral node, consistent with the assumption that the group XIV of CTLDcp genes arose from a gene duplication event (Fig. 2). To corroborate these findings, we analyzed the CTLDcp gene loci and studied gene synteny of a representative species per vertebrate class. A total of 15 gene families were analyzed showing that all the CTLDcps-bearing chromosomes share syntenic gene patterns (Table 1 and Additional file 5: Supplementary Table 2). Interestingly, all the analyzed gnathostome taxa presented CD93 and Thrombomodulin as linked genes since they lie in close proximity on the same chromosome. Moreover, we observed a gene loss of CD248 and its neighbor genes ascribable to chromosome disruption in birds (Additional file 5: Supplementary Table 2), and the loss of Clec14A in monotremes and marsupials, which probably represent a synapomorphy of these groups (Additional file 5: Supplementary Table 2).
Evolution of CTLDcps in cyclostomes and gnathostomes
To shed light on the evolutionary history of the CTLDcps, we retrieved CTLDcp genes in P. marinus, (namely CTLDcp-α, -β, -γ, or -δ), reconstructed their gene loci, and compared them to the human CTLDcps-bearing chromosomes (Fig. 3). Importantly, this reconstruction highlighted the presence of numerous shared gene families between the lamprey and the human chromosomes and showed that, on chromosome 53 of P. marinus, two CTLDcp genes were found in linkage as CD93 and Thrombomodulin in all gnathostomes (see Fig. 3 and Additional file 6: Supplementary Table 3).
To understand the evolutionary relationships between gnathostome and cyclostome CTLDcp genes, we retrieved additional cyclostome protein sequences from two different lamprey species and one hagfish by building appropriate HMMER profiles for each CTLDcp and performed phylogenetic analyses. In our first reconstruction, none of the cyclostome CTLDcps was unambiguously assigned as gnathostome ortholog and disposed in two distinct clusters (cyclostome clade A and clade B). Indeed, the phylogenetic tree showed sister relationships between cyclostome clade A and Clec14A as well as the cyclostome clade B with the (CD248,CD93) cluster (Fig. 4A). Since hidden paralogy and asymmetric gene retention, that follows gene duplication and loss, can confuse orthology assignment, we tested alternative tree topologies (see Additional file 7: Supplementary Table 4 for details and Additional file 1: Supplementary Fig. 1 for tested tree topologies). Our alternative hypotheses suggested two statistically accepted scenarios of the evolutionary relationships between gnathostome and cyclostome homologs (Fig. 4B). In the topology 1 scenario, CTLDcp-γ of P. marinus was found being Clec14A ortholog, while the other cyclostome proteins distributed across two different clades. Similarly, the topology 2 scenario inferred cyclostome proteins as monophyletic and sister to gnathostome Clec14A suggesting that the latter might resemble features of the last CTLDcp common ancestor before the divergence of proto-gnathostomes from proto-cyclostomes.
P. marinus CTLDcp-α lacks the sushi-like domain
To understand the nature of P. marinus CTLDcps, we wondered if P. marinus proteins might share important features with their gnathostome counterparts. The presence of a sushi-like domain is a hallmark of CTLDcps and important for CTLDcps protein–protein interaction. Importantly, this extracellular motif (composed by ∼60 amino acid residues) is characterized by conserved tryptophan, glycine, proline, and cysteine residues . Therefore, we retrieved the protein region bearing the sushi domain (see Analysis of the group XIV CTLDcps sushi-like domain in Petromyzon marinus and Protein domain identification and Ka/Ks ratio), and performed protein alignment and modeling prediction analyses of P. marinus proteins (Fig. 5). Protein alignment showed that one of the two CTLDcps found on chromosome 53 (CTLDcp-α) presented a short amino acid sequence as well as lacked key amino acid residues important for the sushi-like domain structure (red asterisks, Fig. 5A). This result was further substantiated by SWISS-MODEL, which failed to predict domain folding only for CTLDcp-α (Fig. 5B).
Protein domain analysis of gnathostome CTLDcps
Due to the importance of each CTLDcp domain in carrying out multiple and distinct functions, we sought to analyze in depth domain composition and study codon selection across gnathostome species. To do that, we collected amino acid sequences from one representative species per vertebrate order and identified protein domains using Batch-CD Search . Despite clearly identifying the CTLD, Batch-CD Search failed to predict the sushi-like domain, the Pro/Ser/Thr rich region and part of the EGF-like domains, whose proper identification required manual curation (see Protein domain identification and Ka/Ks ratio). Protein extracellular domains (except for the EGF-like domain subtype) of each CTLDcp showed conservation of number and order across the vertebrate taxa and were then schematically represented in Fig. 6A. Interestingly, the main difference in domain composition was ascribable to EGF-like domains. In detail, while EGF 2 and cbEGF are present in all the CTLDcps, the EGF 1 is specific of the only Clec14A bird clade, whereas EGF-like and Tme5 EGF are distinctive of Thrombomodulin (Fig. 6A). To gain insights into the evolutionary rate of each protein domain, the nonsynonymous (Ka) over synonymous (Ks) ratio was estimated by comparing CDS sequences. As expected, the CTLD and the EGF-like domains of all the proteins showed a Ka/Ks ratio < 1 indicating a tendency to undergo purifying selection (Fig. 6B). Similarly, the sushi-like domain-containing region revealed a Ka/Ks < 1, although higher in Clec14A compared to CD93 and CD248. Curiously, despite Thrombomodulin does not present a proper sushi-like domain, we found this region highly conserved (Fig. 6B). Similarly, a purifying selection was also discovered in all the examined EGF domains of all proteins. In contrast, the Pro/Ser/Thr rich region showed a Ka/Ks ratio > 1, indicating positive selection (Fig. 6B, violet plots).
CD93 and Thrombomodulin show tyrosine phosphorylation consensuses in their cytoplasmic domain
Tyrosine phosphorylation of transmembrane proteins is often a critical post-translational modification in regulating cell signaling and protein recycling. We therefore attempted to predict tyrosine phosphorylation of the entire group XIV using the NetPhos3.1 server. Analysis of the Clec14A sequence showed a lack of tyrosine residues in the cytoplasmic domain, while no significant predictions were found for CD248, despite the presence of a conserved tyrosine residue in the cytoplasmic domain. Consistent with previous findings on HUVECs , CD93 showed two tyrosine phosphorylation sites. Noteworthy, the first consensus was ubiquitous in all the vertebrate classes (Additional file 2: Supplementary Fig. 2) and showed a common amino acidic pattern (Fig. 7A, upper panel). Conversely, the second consensus differed between groups of gnathostomes and in fishes it was only found in the Neoteleostei clade (Fig. 7A, lower panel). Interestingly, a tyrosine consensus in the cytotail of Thrombomodulin was predicted as a possible phosphorylation site in six different vertebrate classes, resembling a common amino acid pattern, with the exception of fishes (Fig. 7B).
In this study, we investigated the evolution and the protein domain composition of the group XIV of CTLDcps in modern vertebrates. Here, we demonstrated that these proteins duplicated from a common ancestor and gained insights on their evolution in cyclostomes and gnathostomes. Moreover, we carefully analyzed CTLDcp domains by investigating their codon substitution rate and carefully identified and categorized EGF-like domains of several gnathostome species.
Combining both phylogenetic and synteny-based approaches, we demonstrated that gnathostome proteins belonging to the group XIV of CTLDcps are paralogs and descend from a common ancestor. Here, we also attempted to unravel the phylogenetic relationships between gnathostome and cyclostome CTLDcps. Based on our results, we inferred an evolutionary scheme where a proto-vertebrate evolved two CTLDcp genes after one WGD event occurred in the ancestral cephalochordate. Since, in both gnathostomes (CD93 and Thrombomodulin) and P. marinus (CTLDcp-α and -β), a pair of CTLDcps lies on the same chromosome only a few nucleotides apart, we assumed that their ancestral gene evolved by a tandem duplication event, likely due to asymmetric crossing-over as happened from other tandem duplicated genes . Interestingly, analysis of P. marinus proteins revealed that one of the two tandem paralog genes lacks the sushi-like domain, suggesting that, before the divergence of gnathostomes and cyclostomes, the common ancestor of Thrombomodulin and CTLDcp-α lost key amino acids necessary for the folding of the sushi-like domain. From three ancestral CTLDcps in the proto-vertebrate, independent polyploidization of the proto-gnathostome and proto-cyclostome has generated multiple copies of CTLDcp genes, of which four have been retained in the majority of modern species (Fig. 8). Although our phylogenetic reconstruction did not show unambiguous orthology relationships between cyclostome and gnathostome CTLDcps, one of the alternative topologies identified CTLDcp-γ of P. marinus as ortholog of the gnathostome Clec14A. Interestingly, analysis of numerous CTLDcp orthologs revealed that each CTLDcp presents a statistically significant typical length (Additional file 3: Supplementary Fig. 3) with Clec14A being the shortest and having retained one or none EGF-like domain. Importantly, P. marinus CTLDcp-γ, showed a loss of the EGF-like domains, which accounts for its short protein sequence. This data suggests that Clec14A might have speciated before the separation of proto-gnathostomes from proto-cyclostomes. Moreover, a scenario where Clec14A speciated in the proto-vertebrate would implicate that the gnathostome CD248 evolved from a proto-CD93 locus that underwent proto-Thrombomodulin loss. This assumption is substantiated by the fact that, according to our phylogenetic reconstructions, CD93 is sister to CD248 in gnathostomes (Figs. 2 and 4). In a similar fashion, the ortholog of CTLDcp-δ in cyclostomes might have arisen following a gene loss of one proto-CTLDcp-α copy (Fig. 8). Our findings are in line with the current view of evolution and divergence of modern cyclostomes and gnathostomes which suggests that, after a first WGD event, gnathostomes and cyclostomes underwent tetraploidization and hexaploidization respectively . Noteworthy, synteny analyses of gnathostome CTLDcp genes showed that, while CD93 and Thrombomodulin were found in all the representative vertebrate classes, a gene loss of CD248 in birds and Clec14A in monotremes and marsupials occurred via different mechanisms. Indeed, gene loci analyses showed that CD248 loss was due to a dismantling of its bearing chromosome since all the syntenic gene families were either lost or moved on other chromosomes. On the other hand, Clec14A loss was probably due to gene deletion or pseudogenization, and independently on chromosome rearrangements since its locus was maintained unaltered.
Since a preponderant role is attributed to the ECD in mediating group XIV protein function, we analyzed in depth ECD composition and investigated domain conservation by analyzing the mutation rate of each protein domain in gnathostomes. Consistent with the importance of the CTLD in maintaining protein folding and function , we found it to be deeply conserved in all the group XIV proteins and across the entire gnathostome clade. Interestingly, the region containing the sushi-like domain was also found to be highly conserved. Indeed, together with the CTLD, this relatively short region bears critical amino acid residues that mediate CD93, Clec14A and CD248 binding to the ECM protein MMRN2 [6, 48]. To our surprise, although Thrombomodulin lost key amino acids required for the folding of a proper sushi-like domain, we found the region comprised between the CTLD and the first EGF-like domain as highly conserved, indicating an important role in maintaining a functional protein structure. Our analysis pointed out some critical differences in the composition and organization of EGF-like domains between proteins. Although the EGF-like domains are annotated and have been previously described for the human and mouse proteins , some key differences in their composition have been overlooked. Except for the first Thrombomodulin EGF-like domain, all the other group members display the typical features of the complement C1r-like EGF domains (cEGF). Some EGF-like domains were found to bear a hydroxylation consensus of an asparagine residue as well as negatively charged residues at their N-termini, known to be critical in mediating calcium binding in accordance to the current PROSITE annotation  and previous studies . Importantly, Clec14A showed different types of EGF-like domains between classes. Indeed, although being both cEGF subtypes , we found that in birds the EGF-like domain displayed the typical EGF 1 subtype signature, while mammals, reptiles, sharks and fishes showed the EGF 2 signature instead. In addition, in fishes, the Clec14A EGF-like domain bears a calcium-binding motif, supporting the idea of a species-specific evolution of different EGF-like domains in Clec14A. Regarding the Pro/Ser/Thr rich region, we found that it is characterized by a high mutation rate and subjected to positive selection. However, we found that in all species this region was highly enriched in amino acid residues that can be O-linked glycosylated (see Additional files 8, 9, 10 and 11: Supplementary files 1–4), suggesting that the overall O-linked sugar moiety might not be impaired. Our characterization of the CTLDcp domains was not limited on the ECD, as we also extended our analysis to the cytoplasmic region in the attempt to predict tyrosine phosphorylation motifs. Although Clec14A and CD248 showed no prediction of phosphorylable tyrosines, CD93 and Thrombomodulin were predicted to be tyrosine phosphorylated. According to previous observations [10, 46], for CD93 two consensuses of tyrosine phosphorylation were found in its intracellular domain. It is important to underline that, while all species were found to share the first tyrosine phosphorylation motif with a common consensus, only a few groups showed a second. Interestingly, the second consensus was found to be different across species, and in fishes was predicted solely for the Neoteleostei clade. This result leads to the hypothesis that differently from the first tyrosine residue, which might have appeared in the early evolution of CD93, the second phosphorylation site evolved lately and independently for each vertebrate group. Finally, although a tyrosine phosphorylation of Thrombomodulin has never been demonstrated experimentally, our analysis predicted a conserved phosphorylation consensus across different gnathostome classes. Our observations concerning the protein domain composition showed important class-specific synapomorphies. If on one hand, our study on protein alignments shows that each CTLDcp is highly conserved within classes, on the other, it points out critical inter-class differences. These results gain increasing relevance when considering the employment of animal models. In fact, although of valuable importance, the translation of results from model organisms that diverged several million years ago from humans needs to take into account subtle species-specific differences that might be of critical importance in inferring protein function. As an example, Danio rerio (zebrafish) is largely used as model to study angiogenesis and vascular dynamics and, specifically, has been employed to study the role of CD93 and Clec14A in angiogenesis . As demonstrated by our analyses, the mammalian orthologs of CD93 and Clec14A in D. rerio showed differences in the protein domain composition. Indeed, CD93 in D. rerio only contains one phosphorylable tyrosine residue in its cytoplasmic domain compared to the two of mammals, suggesting relevant differences between fish and mammalian signaling pathways. Likewise, in fishes Clec14A showed a calcium-binding EGF-like domain which is not present in mammals and might entail important functional repercussions.
In conclusion, using a phylogenetic and synteny-based approach, our study provides insights on the evolution of the group XIV of CTLDcps in modern vertebrates. Moreover, our analysis on protein domains allowed a visualization of the evolutionary rate of each domain and proposed a protein-specific classification of EGF-like domains based on known sequence signatures. Taken together, our results might help to better interpret protein functions and underline differences of orthologous proteins between different animal classes.
Availability of data and materials
The datasets analyzed during the current study are available in the NCBI database repository, https://www.ncbi.nlm.nih.gov/. Protein domain CDS of each CTLDcp in the different gnathostome orders can be found as additional files.
Complement C1r-like EGF domain
C-type lectin domain-containing protein
Epidermal growth factor
Fibroblast growth factor receptor 1
Whole Genome Duplication
Dehal P, Boore JL. Two rounds of whole genome duplication in the ancestral vertebrate. PLoS Biol. 2005;3:e314.
Nakatani Y, Takeda H, Kohara Y, Morishita S. Reconstruction of the vertebrate ancestral genome reveals dynamic genome reorganization in early vertebrates. Genome Res. 2007;17:1254–65.
Nakatani Y, Shingate P, Ravi V, Pillai NE, Prasad A, McLysaght A, et al. Reconstruction of proto-vertebrate, proto-cyclostome and proto-gnathostome genomes provides new insights into early vertebrate evolution. Nat Commun. 2021;12:4489.
Zelensky AN, Gready JE. The C-type lectin-like domain superfamily. FEBS J. 2005;272:6179–217.
Hsu Y-Y, Shi G-Y, Wang K-C, Ma C-Y, Cheng T-L, Wu H-L. Thrombomodulin promotes focal adhesion kinase activation and contributes to angiogenesis by binding to fibronectin. Oncotarget. 2016;7:68122–39.
Khan KA, Naylor AJ, Khan A, Noy PJ, Mambretti M, Lodhia P, et al. Multimerin-2 is a ligand for group 14 family C-type lectins CLEC14A, CD93 and CD248 spanning the endothelial pericyte interface. Oncogene. 2017;36:6097–108.
Langenkamp E, Zhang L, Lugano R, Huang H, Elhassan TEA, Georganaki M, et al. Elevated expression of the C-type lectin CD93 in the glioblastoma vasculature regulates cytoskeletal rearrangements that enhance vessel function and reduce host survival. Cancer Res. 2015;75:4504–16.
Simonavicius N, Robertson D, Bax DA, Jones C, Huijbers IJ, Isacke CM. Endosialin (CD248) is a marker of tumor-associated pericytes in high-grade glioma. Mod Pathol. 2008;21:308–15.
Khan KA, McMurray JL, Mohammed F, Bicknell R. C-type lectin domain group 14 proteins in vascular biology, cancer and inflammation. FEBS J. 2019;286:3299–332.
Barbera S, Lugano R, Pedalina A, Mongiat M, Santucci A, Tosi GM, et al. The C-type lectin CD93 controls endothelial cell migration via activation of the Rho family of small GTPases. Matrix Biol. 2021;99:1–17.
Barbera S, Raucci L, Lugano R, Tosi GM, Dimberg A, Santucci A, et al. CD93 signaling via Rho proteins drives cytoskeletal remodeling in spreading endothelial cells. Int J Mol Sci. 2021;22:12417.
Orlandini M, Galvagni F, Bardelli M, Rocchigiani M, Lentucci C, Anselmi F, et al. The characterization of a novel monoclonal antibody against CD93 unveils a new antiangiogenic target. Oncotarget. 2014;5:2750–60.
Lugano R, Vemuri K, Yu D, Bergqvist M, Smits A, Essand M, et al. CD93 promotes β1 integrin activation and fibronectin fibrillogenesis during tumor angiogenesis. J Clin Invest. 2018;128:3280–97.
Kao Y-C, Jiang S-J, Pan W-A, Wang K-C, Chen P-K, Wei H-J, et al. The epidermal growth factor-like domain of CD93 is a potent angiogenic factor. PLoS One. 2012;7:e51647.
Krishna Priya S, Kumar K, Hiran KR, Bindhu MR, NagareRohit P, Vijaykumar DK, et al. Expression of a novel endothelial marker, C-type lectin 14A, in epithelial ovarian cancer and its prognostic significance. Int J Clin Oncol. 2017;22:107–17.
Mura M, Swain RK, Zhuang X, Vorschmitt H, Reynolds G, Durant S, et al. Identification and angiogenic role of the novel tumor endothelial marker CLEC14A. Oncogene. 2012;31:293–305.
Christian S, Winkler R, Helfrich I, Boos AM, Besemfelder E, Schadendorf D, et al. Endosialin (Tem1) is a marker of tumor-associated myofibroblasts and tumor vessel-associated mural cells. Am J Pathol. 2008;172:486–94.
Conway EM. Thrombomodulin and its role in inflammation. Semin Immunopathol. 2012;34:107–25.
Maruyama I, Salem HH, Ishii H, Majerus PW. Human thrombomodulin is not an efficient inhibitor of the procoagulant activity of thrombin. J Clin Invest. 1985;75:987–91.
Kuo C-H, Sung M-C, Chen P-K, Chang B-I, Lee F-T, Cho C-F, et al. FGFR1 mediates recombinant thrombomodulin domain-induced angiogenesis. Cardiovasc Res. 2015;105:107–17.
Shi C-S, Shi G-Y, Chang Y-S, Han H-S, Kuo C-H, Liu C, et al. Evidence of human thrombomodulin domain as a novel angiogenic factor. Circulation. 2005;111:1627–36.
Esmon CT, Esmon NL, Harris KW. Complex formation between thrombin and thrombomodulin inhibits both thrombin-catalyzed fibrin formation and factor V activation. J Biol Chem. 1982;257:7944–7.
Eddy SR. Accelerated profile HMM searches. PLoS Comput Biol. 2011;7:e1002195.
Lu S, Wang J, Chitsaz F, Derbyshire MK, Geer RC, Gonzales NR, et al. CDD/SPARCLE: the conserved domain database in 2020. Nucleic Acids Res. 2020;48:D265–8.
Tu Z, Cohen M, Bu H, Lin F. Tissue distribution and functional analysis of Sushi domain-containing protein 4. Am J Pathol. 2010;176:2378–84.
Simossis VA. Homology-extended sequence alignment. Nucleic Acids Res. 2005;33:816–24.
Simossis VA, Heringa J. PRALINE: a multiple sequence alignment toolbox that integrates homology-extended and secondary structure information. Nucleic Acids Res. 2005;33 Web Server:W289-94.
Simossis VA, Heringa J. The PRALINE online server: optimising progressive multiple alignment on the web. Comput Biol Chem. 2003;27:511–9.
Waterhouse A, Bertoni M, Bienert S, Studer G, Tauriello G, Gumienny R, et al. SWISS-MODEL: homology modelling of protein structures and complexes. Nucleic Acids Res. 2018;46:W296-303.
Veltri D, Wight MM, Crouch JA. SimpleSynteny: a web-based tool for visualization of microsynteny across multiple species. Nucleic Acids Res. 2016;44:W41–5.
Edgar RC. MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res. 2004;32:1792–7.
Larsson A. AliView: a fast and lightweight alignment viewer and editor for large datasets. Bioinformatics. 2014;30:3276–8.
Nguyen L-T, Schmidt HA, von Haeseler A, Minh BQ. IQ-TREE: a fast and effective stochastic algorithm for estimating maximum-likelihood phylogenies. Mol Biol Evol. 2015;32:268–74.
Kalyaanamoorthy S, Minh BQ, Wong TKF, von Haeseler A, Jermiin LS. ModelFinder: fast model selection for accurate phylogenetic estimates. Nat Methods. 2017;14:587–9.
Letunic I, Bork P. Interactive Tree Of Life (iTOL) v5: an online tool for phylogenetic tree display and annotation. Nucleic Acids Res. 2021;49:W293–6.
Sigrist CJA, de Castro E, Cerutti L, Cuche BA, Hulo N, Bridge A, et al. New and continuing developments at PROSITE. Nucleic Acids Res. 2012;41:D344–7.
Wouters MA, Rigoutsos I, Chu CK, Feng LL, Sparrow DB, Dunwoodie SL. Evolution of distinct EGF domains with specific functions. Protein Sci. 2005;14:1091–103.
Krogh A, Larsson B, von Heijne G, Sonnhammer ELL. Predicting transmembrane protein topology with a hidden markov model: application to complete genomes11Edited by F. Cohen. J Mol Biol. 2001;305:567–80.
Sonnhammer EL, von Heijne G, Krogh A. A hidden Markov model for predicting transmembrane helices in protein sequences. Proc Int Conf Intell Syst Mol Biol. 1998;6:175–82.
Blom N, Gammeltoft S, Brunak S. Sequence and structure-based prediction of eukaryotic protein phosphorylation sites. J Mol Biol. 1999;294:1351–62.
Crooks GE. WebLogo: a sequence logo generator. Genome Res. 2004;14:1188–90.
Schneider TD, Stephens RM. Sequence logos: a new way to display consensus sequences. Nucleic Acids Res. 1990;18:6097–100.
Yang Z. PAML 4: phylogenetic analysis by maximum likelihood. Mol Biol Evol. 2007;24:1586–91.
Yang X, Liu X, Zhou Y, Zhang F, Huang L, Wang J, et al. New insights on the function of plant acyl carrier proteins from comparative and evolutionary analysis. Genomics. 2021;113:1155–65.
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.
Galvagni F, Nardi F, Maida M, Bernardini G, Vannuccini S, Petraglia F, et al. CD93 and dystroglycan cooperation in human endothelial cell adhesion and migration. Oncotarget. 2016;7:10090–103.
Lallemand T, Leduc M, Landès C, Rizzon C, Lerat E. An overview of duplicated gene detection methods: why the duplication mechanism has to be accounted for in their choice. Genes. 2020;11:1046.
Galvagni F, Nardi F, Spiga O, Trezza A, Tarticchio G, Pellicani R, et al. Dissecting the CD93-Multimerin 2 interaction involved in cell adhesion and migration of the activated endothelium. Matrix Biol. 2017;64:112–27.
Du J, Yang Q, Luo L, Yang D. C1qr and C1qrl redundantly regulate angiogenesis in zebrafish through controlling endothelial Cdh5. Biochem Biophys Res Commun. 2017;483:482–7.
The authors would like to acknowledge Uppsala University for covering the cost of the Open Access publication. The authors would also like to thank Ms. Nayomi Illansinhage Don, Mr. Matteo Vitale, Mr. Nicola Iannotti and Dr. Chiara Leo for the valuable discussions and suggestions.
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Alternative tree topologies. Each tree represents the constrained topology tested with 10,000 RELL replicates for different statistical methods (bp-RELL, p-KH, p-SH, c-ELW, p-AU) through IQ-TREE. Outcomes of each analysis is detailed in Supplementary Table 4.
Identification of the first CD93 phospho-tyrosine consensus in each group of vertebrates. CD93 first phospho-tyrosine consensus was retrieved by NetPhos3.1 and plotted using WebLogo2.8.2. The predicted consensus for each group of vertebrates is shown as entropy rendering abundance to emphasize motif’s information content. Number of species used for the analysis: Chondrichthyes n = 3, Teleosts n = 27, Amphibians n = 2, Reptiles n = 2, Birds n = 11, Marsupials n = 3 and Mammals n = 17.
Average protein length of group XIV CTLDcps. Protein length was calculated and plotted in the R environment v.3.6.3. Number of species used for the analysis: CD93 n= 98, Clec14A n= 64, CD248 n= 61 and Thrombomodulin n= 88. Bars show SD. ****P < 0.0001 One-way ANOVA test.
List of protein (first sheet), CDS (second sheet), cDNA (third sheet) accession numbers used and genome accession number of Lethenteron camtschaticum, Entosphenus tridentatus, Eptatretus burgeri (fourth sheet).
Gnathostome CTLDcps loci synteny. List of the syntenic genes laying on the CD93/Thrombomodulin- (first sheet), CD248- (second sheet) and Clec14A- (third sheet) -bearing chromosomes in gnathostomes. Positions of genes that moved away from the chromosome are specified. § represents not found genes. # represents genes with an unplaced scaffold. * indicates chromosome disruption.
P. marinus gene synteny. Gene families laying on chromosome 6, 17 and 53 of P. marinus analyzed for conserved synteny with their gnathostome counterparts.
Alternative topology test results. Eleven topologies tested with five different statistical methods (bp-RELL, p-KH, p-SH, c-ELW, p-AU). Tested tree topologies follow unconstrained and constrained trees reported in Supplementary Fig. 1. Highlighted rows are significant topologies.
CDS of one representative species per vertebrate order of CD93 extracellular domain.
CDS of one representative species per vertebrate order of Clec14A extracellular domain.
CDS of one representative species per vertebrate order of CD248 extracellular domain.
CDS of one representative species per vertebrate order of Thrombomodulin extracellular domain.
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Barbera, S., Cucini, C. A glimpse into the past: phylogenesis and protein domain analysis of the group XIV of C-type lectins in vertebrates. BMC Genomics 23, 420 (2022). https://doi.org/10.1186/s12864-022-08659-6
- C-type lectin evolution
- Whole genome duplications