ADGRL4/ELTD1 is a highly conserved angiogenesis-associated orphan adhesion GPCR that emerged with the first vertebrates and comprises 3 evolutionary variants
Our laboratory identified ADGRL4/ELTD1, an orphan GPCR belonging to the adhesion GPCR (aGPCR) family, as a novel regulator of angiogenesis and a potential anti-cancer therapeutic target. Little is known about how ADGRL4/ELTD1 (and aGPCRs in general) function, a problem compounded by a lack of known ligands or means of activation. With this in mind, we turned to computational evolutionary biology with the aim of better understanding ADGRL4/ELTD1.
We identified ADGRL4/ELTD1 as a highly conserved early angiogenic gene which emerged in the first true vertebrates (bony fish) approximately 435 million years ago (mya), evolving alongside key angiogenic genes VEGFR2 and DLL4. We identified 3 evolutionary ADGRL4/ELTD1 variants based on EGF domain deletions with variant 2 first emerging 101 mya (95% CI 96–105) in Afrotheria and 82 mya (95% CI 76–89) in Primates. Additionally, conservation mapping across all orthologues reveals highest level conservation in EGF Ca binding domain 1, suggesting that this motif plays an essential role, as well as specific regions of the GAIN domain, GPS motif and 7TM domain, suggesting possible activation mechanisms and ligand binding positions. Additionally, we found that ADGRL4/ELTD1 (a member aGPCR family 1) is possibly ancestral to members of aGPCR family 2.
This work establishes ADGRL4/ELTD1’s evolution, sheds light on its possible activation and ligand binding zones, and establishes the first temporal references for the emergence of ADGRL4/ELTD1 variants during vertebrate evolution. Our approach is applicable to the greater aGPCR family and opens up new avenues for future experimental work.
KeywordsADGRL4 ELTD1 Adhesion GPCR evolution
Delta-like ligand 4
Epidermal growth factor
GPCR autoproteolysis inducing domain
GPCR proteolysis site
Glutamate, Rhodopsin, Adhesion, Frizzled/Taste2, Secretin
Vascular endothelial growth factor
Discovered in 2001 , ELTD1/ADGRL4 is an orphan member of the G protein-coupled receptor (GPCR) superfamily, belonging to the 33 member ‘Adhesion GPCR’ family as per the Glutamate, Rhodopsin, Adhesion, Frizzled/Taste2, Secretin (GRAFS) classification . Adhesion GPCRs (aGPCRs) are so named because unlike other GPCRs, they all contain large extracellular domains with adhesion motifs . Human ELTD1/ADGRL4’s adhesion motifs comprise an epidermal growth factor (EGF) domain and an EGF Ca2+ binding domain. Recently, all aGPRCs underwent a nomenclature change  with ELTD1 being renamed ADGRL4. In this manuscript, all aGPCRS will be referred to by their new names followed by their old names (i.e. ADGRL4/ELTD1).
Our laboratories have previously identified ADGRL4/ELTD1 as a novel regulator of physiological and tumour angiogenesis . This work revealed ADGRL4/ELTD1 to be upregulated in tumour-associated endothelial cells and vascular smooth muscle cells (head and neck, renal, colorectal and ovarian cancers) and to be essential for sprouting angiogenesis in both zebrafish and humans as well as being regulated by two key angiogenic ligands, namely upregulation by vascular endothelial growth factor (VEGF), and downregulation by the Notch ligand delta-like ligand 4 (DLL4). Additionally, Adgrl4/Eltd1 silencing in ovarian and colorectal tumour xenografts in mice was found to substantially limit tumour growth by suppressing tumour-vessel angiogenesis. In human cancer patients, high tumour-vessel endothelial ADGRL4/ELTD1 expression was shown to correlate with improved overall survival (OS) in patients who subsequently received anti-cancer therapy (head and neck squamous carcinoma, renal, colorectal and ovarian cancers) implicating ADGRL4/ELTD1 as a putative prognostic marker of favourable outcome for these cancers types when treated with systemic therapy. This may be due to higher ADGRL4/ELTD1 expression correlating with higher microvessel density and vessel maturity, which thus allows for better systemic anti-cancer drug delivery to the tumour. ADGRL4/ELTD1 is not expressed by the majority of cancer cell lines , however it is highly upregulated in some glioblastoma tumour cells and has been shown to be important for glioblastoma cell survival, although the mechanism remains unclear [8, 9, 10].
Although ADGRL4/ELTD1 is now recognised as an important angiogenesis gene in both zebrafish and humans, very little is known about ADGRL4/ELTD1’s function. This is further compounded by the general lack of knowledge surrounding other members of the aGPCR family as historically, the Adhesion family is the most poorly studied of the five GPCR families. This stems from the difficulty in activating these receptors, the majority of them being orphans that lack a known ligand. Recently, a growing number of orphan aGPCRs have had their activation mechanism solved using the Stachel Hypothesis [11, 12, 13, 14, 15, 16, 17, 18]. This proposes that all expressed aGPCRs (except GPR123) contain a short 10–20 amino acid tethered agonist (the Stachel peptide) C-terminally to the GPS cleavage site which is essential for aGPCR activation through its action of striking the 7TM receptor loops and initiating signalling . Despite this, ADGRL4/ELTD1’s activation remains unsolved.
With this in mind, we turned to computational evolutionary biology to try and better understand ADGRL4/ELTD1’s evolutionary history and identify domains with the highest conservation that are likely to be those involved in important biological functions. Previous work on the subject of GPCR evolution has revealed that the aGPCR group is ancient and is ancestral to the Secretin GPCR family, with the first Adhesion member arising in the amoeba Dictyostelium discoideum before diversifying in the free-living, basal metazoan Trichoplax adhaerens [19, 20, 21]. However, to date, no work has specifically investigated ADGRL4/ELTD1’s evolution.
To investigate ADGRL4/ELTD1’s evolution and conservation across extant sequenced species and to compare this to established angiogenesis core genes.
To investigate whether ADGRL4/ELTD1 has lost or gained any domains during its evolution (and if so, when?) and whether this is informative in regard to ADGRL4/ELTD1’s function.
To investigate and compare ADGRL4/ELTD1 to other closely related aGPCRS to shed light on shared ligands or additional functions as well as the origin of closely related families
ADGRL4/ELTD1 is a highly conserved early core angiogenic gene which arose approximately 435 million years ago within bony fish
The first question investigated was which is the oldest extant species whose genome encodes an ADGRL4/ELTD1 orthologue? As ADGRL4/ELTD1 has been shown to be important in vessel sprouting, we hypothesised that the acquisition of ADGRL4/ELTD1 would correlate with the development of endothelial cells in a closed circulatory system. The very first endothelial cells in a closed circulatory system arose approximately 550 million years ago (mya) with the first vertebrates: the jawless fish . Today, members of this ancient group still exist: the hagfish and the lamprey. As the lamprey has been fully genome sequenced , it was chosen as the representative jawless fish and its annotated genome interrogated for the presence of an ADGRL4/ELTD1 orthologue as well as orthologues of two important angiogenesis associated genes: VEGFR1 (vascular endothelial growth factor receptor 1) and VEGFR2 (vascular endothelial growth factor receptor 2). These two genes were chosen because of their core importance to the field of angiogenesis  and because ADGRL4/ELTD1 is known to be regulated by VEGF .
This analysis revealed that the lamprey encodes a precursor to vegfr1 but not adgrl4/eltd1 nor vegfr2. Following this, the next evolutionary vertebrate group (bony fish; n = 11 annotated genomes) as well as all evolutionarily subsequent vertebrate groups (total n = 61 annotated genomes) were interrogated for the presence of orthologues to ADGRL4/ELTD1, VEGFR1 and VEGR2. Results revealed that eltd1 and vegfr2 are present in the genomes of all bony fish and all subsequent vertebrates (Fig. 1b). The genomic presence of VEGFR2 and ADGRL4/ELTD1 orthologues in bony fish and all subsequent vertebrates suggests that these genes were acquired during the during the evolution of jawless fish to bony fish. In terms of evolutionary time, as bony fish appeared approximately 435 mya ago [25, 26], these results suggest that ADGRL4/ELTD1 and VEGFR2 became established in vertebrates during the same time period.
Next, ADGRL4/ELTD1’s conservation across vertebrate genomes was investigated. This was performed by comparing ADGRL4/ELTD1’s amino acid sequence to the longest predicted amino acid sequences of ADGRL4/ELTD1 orthologues in extant members of all the major vertebrate groups retrieved from Ensembl (n = 61 annotated genomes). As a comparison, this was also done for VEGFR2 and for the evolutionarily ancient angiogenesis-associated Notch signalling pathway ligand DLL4.
ADGRL4/ELTD1’s amino acid sequence is highly conserved across all 61 sequenced vertebrate genomes with even the least similar orthologues (bony fish) having a similarity of > 50% to human ADGRL4/ELTD1 (Fig. 1c). Additionally, ADGRL4/ELTD1’s conservation across all 61 species is similar to that of the highly conserved angiogenesis genes VEGFR2 and DLL4 (unpaired Student’s t-test p = 0.1 and p = 0.05). (Additional file 1: Figure S1). As a control, an extended panel of unrelated genes were reviewed, comprising 9 DNA repair genes and 16 receptor tyrosine kinases (RTK) (Additional file 1: Figure S1). Whilst the majority are as conserved as ADGRL4/ELTD1, some are significantly less conserved than ADGRL4/ELTD1, whilst a smaller minority are more conserved (Additional file 1: Figure S1A). This shows that the high-level conservation found in ADGRL4/ELTD1 and core angiogenesis regulators VEGFR2 and DLL4 is a common feature of many genes but does not apply uniformly to all genes. For the majority of species, exome similarity to the human exome follows a trend similar to ADGRL4/ELTD1 and VEGFR2. Interestingly, in all bony fish reviewed (n = 11 annotated genomes), adgrl4/eltd1 is conserved to a far greater extent than the conservation of the fish exome (unpaired Student’s t-test p < 0.0001) with the same being true for the core angiogenic orthologues vegfr2 and dll4 and the majority of the extended panel of important control genes (Additional file 1: Figure S1B).
ADGRL4/ELTD1 has three evolutionary variants based on EGF domain deletions with 3 areas of major conservation indicating possible functional domains for future drug targeting
Next, the evolution of ADGRL4/ELTD1’s sequence during vertebrate evolution was investigated to shed light on conservation as a means to better understand ADGRL4/ELTD1’s domain function (e.g. which of ADGRL4/ELTD1’s domains are most critical for its function) in order to develop future cancer therapies targeting these domains. This was performed by aligning ADGRL4/ELTD1’s longest predicted amino acid sequences in 59 extant vertebrate species, representative of all major vertebrate groups from Bony Fish to Primates. An amino acid conservation score was then calculated for each aligned amino acid using a quantitative method which takes into account the physico-chemical properties of each aligned column . Additionally, each sequence was scanned for conserved domains using the results from three amino acid sequence conservation databases and then annotated with domain information. Exon-intron data was retrieved from each orthologue’s genomic sequence and annotated with the domain information. Finally, results from the amino acid alignment were used to create a phylogenetic tree showing evolutionary distance between ADGRL4/ELTD1 orthologues.
A snake-plot depicting human ADGRL4/ELTD1’s domains with the highest conservation across all orthologues is presented in Additional file 1: Figure S2. These comprise the EGF Ca2+ domain 1, the N-terminal half of the GAIN domain, the majority of the GPS motif, and the first five transmembrane loops of the 7TM. As canonical GPCR signalling occurs when a ligand binds to the extracellular loops of the 7TM, it can be hypothesised that ADGRL4/ELTD1’s 7TM extracellular loops with the highest evolutionary conservation (loops 2–3 and 4–5) could potentially the most important for ligand binding leading to signal transduction. As ADGRL4/ELTD1’s activation and signalling remains unsolved, the above external 7TM loops present prime opportunities for using mutagenesis or antibody targeting experiments to determine how ADGRL4/ELTD1 is activated. A phylogenetic tree showing the amino acid evolutionary distance between the above ADGRL4/ELTD1 orthologues reveals that each ADGRL4/ELTD1 orthologue localises to a grouping representing their respective evolutionary vertebrate group (Additional file 1: Figure S2). Furthermore, the phylogenetic tree shows how evolutionary similar mammalian ADGRL4/ELTD1 sequences are to each other, despite differences in EGF domain number in ADGRL4/ELTD1 variant 1 and 2 forms of the receptor. All predicted amino acid domain mapping details for each orthologue are listed in Additional file 1: Table S1.
ADGRL4/ELTD1 variant 2 first appeared approximately 101 million years ago within Afrotheria and then within Primates 82 million years ago
Next, we investigated when ADGRL4/ELTD1’s variants could have developed during vertebrate evolution. To answer this, an evolutionary phylogenetic timetree (a phylogenetic tree superimposed with robust estimates of evolutionary time) was created for the 59 extant vertebrate species analysed above. A minimum of two vertebrates from each major group were included. Evolutionary time estimates were derived from the curated “Timetree: timescales of life” database  with annotations added to this detailing which ADGRL4/ELTD1 variant is encoded in each species. The model for determining the approximate initial time period for the emergence of ADGRL4/ELTD1 variants 2 and 3 relied on the assumption that ADGRL4/ELTD1 variant 1 was the first form of ADGRL4/ELTD1. Evolutionary time was then measured from the earliest point of divergence from an ancestor common to an ADGRL4/ELTD1 variant 1 and variant 2 or 3 expressing vertebrate (in other words, from the point of emergence of an ancestor unique to an ADGRL4/ELTD1 variant 2 or 3 encoding vertebrate).
ADGRL4/ELTD1 is a hybrid comprising elements common to both aGPCR family 1 and 2 and is possibly ancestral to family 2 aGPCRs
We then compared the similarity of ADGRL4/ELTD1’s predicted domains to those expressed on the members of aGPCR family 1 and 2. Results reveal that ADGRL4/ELTD1’s EGF domains are most similar to those of aGPCR family 2’s ADGRE3/EMR3 receptor (Fig. 4b). As members of aGPCR family 4 also contain EGF domains (in addition to cadherin repeats and laminin G domains), a comparison of all aGPCR EGF domains (ADGRL4/ELTD1, family 2 members and family 4 members) was conducted with the same result (Additional file 1: Figure S3B). In addition, ADGRL4/ELTD1’s GAIN domain, GPS motif and 7TM domain are most similar to aGPCR family 1’s ADGRL3/LPHN3 receptor (Fig. 4b).
These results, combined with the knowledge that the majority of aGPCR families segregate into groups containing extracellular domains unique to that family, suggest that ADGRL4/ELTD1 is a hybrid comprising domain elements from both aGPCR family 1 and 2. As regards possible shared ligands, although ligands to ADGRE3/EMR3 remain unknown, the EGF motif ligands of other family 2 members are known, namely: dermatan sulfate  for both ADGRE2/EMR2 and ADGRE5/CD97; and CD55 , CD90 , and integrins α5β1, avβ3  for ADGRE5/CD97. Interestingly, none of these molecules has been shown to activate signalling in these receptors and, although none are known to associate with ADGRL4/ELTD1, they present a way forward for initiating ADGRL4/ELTD1’s ligand experiments.
The above ADGRL4/ELTD1 domain homology data beg the question: which developed first, the members of aGPCR family 1 or those of GPCR family 2 and could ADGRL4/ELTD1 possibly be ancestral to members of family 2? This question was approached by searching for orthologues of both aGPCR family 1 and family 2 members in early vertebrates. Results reveal that the lamprey genome contains a precursor to a single member of aGPCR family 1 (a precursor to ADGRL2/LPHN2 or ADGRL3/LPHN3) but none to any member of aGPCR family 2 (Fig. 4c). All bony fish genomes reviewed (n = 11) contained orthologues to all members of aGPCR family 1. In contrast, only 1 member of aGPCR family 2 was found as an orthologue in these genomes (ADGRE5/CD97). Looking forward in evolutionary time, the mouse similarly encodes all family 1 members with a larger repertoire of family 2 members, whilst the human genome contains all members of both families (Fig. 4c). These results suggest that Family 1 is likely to be the older of the two families, and that ADGRL4/ELTD1 was likely present before the first members of Family 2 evolved, suggesting the possibility of ADGRL4/ELTD1 being ancestral to members of aGPCR family 2 through having shared some of its EGF exons with the evolving members of family 2. The close similarity between ADGRL4/ELTD1’s EGF domains with ADGRE3/EMR3’s EGFs suggests that ADGRE3/EMR3 is the most recent descendant of ADGRL4/ELTD1.
Since the advent of the human genome project, several studies have been undertaken to determine the aGPCR repertoire in vertebrates using the following species as model organisms: human, rat, mouse, chicken, zebrafish and pufferfish [3, 32, 33, 34, 35, 36, 37]. These studies clearly showed that not all vertebrates contained homologs to all the human aGPCR repertoire and that ADGRL4/ELTD1 was present in all 6 reviewed organisms. Whilst contributing greatly to the understanding and classification of aGPCRs, these were limited by the number of available sequenced vertebrates at the time. ADGRL4/ELTD1 was first discovered in rat and human cardiomyocytes, with rat being noted to have 1 EGF domain and 2 EGF Ca binding domains whilst human contained 1 EGF domain and 1 EGF Ca binding domain . Since this initial discovery, no further systematic work has been undertaken to explore ADGRL4/ELTD1’s variants with the aim of understanding ADGRL4/ELTD1’s function. Studies performed in a range of ancient invertebrates have revealed that aGPCRs are of ancient origin. In ancient invertebrates however, many aGPCRS are species-specific, comprising a smaller limited range of human aGPCR homologs which do not include ADGRL4/ELTD1 [19, 20, 38, 39, 40, 41, 42, 43].
The current study builds on this previous evolutionary aGPCR work. Firstly, it systematically interrogates ADGRL4/ELTD1’s homologues within a far wider and more representative range of vertebrates as well as confirming that ADGRL4/ELTD1 first emerged with the evolution of the first true vertebrates. Secondly, this study systematically reviews ADGRL4/ELTD1’s sequence and domain evolution across a wide range of vertebrate homologs, establishing a temporal reference for the emergence of ADGRL4/ELTD1 variants during vertebrate evolution, and investigating whether ADGRL4/ELTD1 is ancestral to other aGPCRS. The study provides novel insights into ADGRL4/ELTD1’s evolution, its variants, potential functional elements as well as means of activation, and its relationship to other aGPCRs. These insights provide many useful ideas not only for future ADGRL4/ELTD1 studies but also for investigating the remainder of the aGPCR family, which remain poorly functionally understood due to the majority having orphan status with no known ligand. This work reveals that ADGRL4/ELTD1 arose within the first true vertebrates and has remained present in the genomes of all subsequent vertebrates. Additionally, ADGRL4/ELTD1 appears to be as highly conserved as members of the VEGF and Notch angiogenic pathways, key pathways which our laboratory has previously shown to affect ADGRL4/ELTD1 expression . Interestingly, it can be hypothesised that the minority of vital DNA repair and RTK genes which are significantly less conserved than ADGRL4/ELTD1 have evolved more complex interactions and are therefore less conserved, whilst those that are more conserved play a more fundamental early role in cellular biology. Similar to other core angiogenic genes, ADGRL4/ELTD1’s higher orthologue-human similarity compared to orthologue-human exome similarity in bony fish suggests that adgrl4/eltd1 has an important biological role in fish. This is supported by the finding that adgrl4/eltd1 silencing in zebrafish embryos is lethal, causing major disruption to the developing vasculature (although this data was obtained with morpholinos, we used two antisense morpholinos targeting the start codon and a splicing junction of the adgrl4/eltd1 pre-mRNA) . The finding that Adgrl4/Eltd1 knockout in murine embryos is not lethal or disruptive to the vasculature either as a single gene knockout  or as a double knockout in combination with the adhesion GPCR Adgrf5/Gpr116  suggests that higher vertebrate genomes have incorporated additional protective redundancy against such events (i.e. the incorporation of additional angiogenic genes). Taken together, this positions ADGRL4/ELTD1 as an evolutionarily early angiogenic gene in vertebrates. It remains an open question whether ADGRL4/ELTD1 and the above-mentioned angiogenesis genes reciprocally affected each other’s evolution. To investigate this, future experiments are needed to interrogate whether ADGRL4/ELTD1 EGF domain losses within individual species are linked to any structural changes in VEGF or Notch genes or any intermediaries – or vice versa. The hypothesis that ADGRL4/ELTD1 possibly arose in the first endothelial cells is based on ADGRL4/ELTD1 being expressed nearly exclusively by endothelial cells  and that both endothelial cells  and ADGRL4/ELTD1 emerged in the first vertebrates.
The finding that ADGRL4/ELTD1 across vertebrates comprises three evolutionary variants with a minority of vertebrates expressing more than 1 ADGRL4/ELTD1 variant is also novel and sheds light on ADGRL4/ELTD1’s important domains and possible means of activation. As more data becomes available, this opens the door to future RNASeq studies investigating the expression of these variants across a wide range of vertebrates. Interestingly, in all vertebrates, ADGRL4/ELTD1’s EGF Ca2+ binding domain 1 is never deleted. This high-level conservation suggests that this is possibly the most important ‘adhesion’ domain of ADGRL4/ELTD1’s multiple EGF adhesion domains and is most likely to be involved in receptor activation and function. Although ADGRL4/ELTD1’s ligand remains unknown, we hypothesise that it most likely interacts with an EGF domain. The finding that more recent vertebrates have lost an EGF domain suggests that this probable ligand is able to sufficiently activate the receptor through its interaction with only one or two EGF domains. It is also probable that the ligand(s) itself has evolved and changed conformation, prompting a change in the number of EGFs required for activation.
The recently proposed ‘Stachel’ Hypothesis states that each aGPCR contains a tethered agonist located C-terminal to the GPS point of cleavage (located at the N-terminal end of the CTF) (Fig. 1a) . Furthermore, the GAIN domain including its GPS motif are important for the function of the GPS cleavage site . Although ADGRL4/ELTD1’s activation and signalling mechanism(s) remain unknown, a growing number of aGPCRS have been shown to function through the Stachel mechanism [11, 12, 13, 14, 15, 18]. In these examples, aGPCR signalling is initiated when the tethered agonist (or a ligand analogous to that amino acid sequence) binds to a specific extracellular portion of the 7TM (the exact binding region remaining unsolved at present). ADGRL4/ELTD1’s high level GAIN domain and GPS motif conservation across all vertebrates suggests that ADGRL4/ELTD1‘s activation might follow a similar mechanism. With this in mind, one can use ADGRL4/ELTD1’s conservation mapping across orthologues to hypothesise that its highly conserved external 7TM regions (external loops 2–3, and 4–5) could potentially represent functionally important sites for ligand binding and the possible initiation of ADGRL4/ELTD1’s signal transduction (which remains unsolved). Once ADGRL4/ELTD1’s signalling is better understood, this finding presents ample opportunity for future experiments including 7TM mutation or antibody activating/blocking experiments targeting these specific 7TM regions in order to reveal exactly which residues are important for agonist/antagonist binding. Additionally, conservation mapping across vertebrate orthologues can also be used to guide receptor activation studies in other aGPCRs.
The evolutionary timetree findings are the first temporal approximations of ADGRL4/ELTD1’s evolution within vertebrates. These findings present an interesting view into the past and strengthens the suggestion that ADGRL4/ELTD1’s EGF domain and EGF Ca2+ binding domain 2 are evolutionarily expendable and that losing them has been evolutionarily beneficial for newer species as no ADGRL4/ELTD1 orthologue regains these domains once a common ancestor has lost them. As the EGF Ca binding domain 1 is present in every examined ADGRL4/ELTD1 orthologue, it can be hypothesised that this is most functionally important of ADGRL4/ELTD1’s EGF domains and should be targeted in future ADGRL4/ELTD1 functional experiments. It is also worth noting that there have been no other domain deletions or major additions apart from the EGF domain to ADGRL4/ELTD1’s sequence during vertebrate evolution. Exactly why the number of EGF domains has decreased as vertebrates have evolved remains open to speculation. A possible hypothesis includes the consideration that this has occurred in response to an evolutionary modification of ADGRL4/ELTD1’s yet unsolved ligand(s) or through evolutionary pruning of excess or redundant domains. A minority of vertebrates were predicted to express more than one ADGRL4/ELTD1 variant, suggesting that these receptors are in the midst of evolutionary change. Interestingly, only two vertebrate genomes in our dataset were predicted to express ADGRL4/ELTD1 variant 3 only: the platypus (which diverged from its common ancestor 177 mya and the zebrafinch, which diverged from its common ancestor most recently 38 mya. Why this has happened and whether these represent a true third ADGRL4/ELTD1 variant remains unclear because of their low frequency amongst our sampled vertebrates. Although it appears that ADGRL4/ELTD1 variants 2 and 3 have been selected across multiple vertebrate groups, it is possible that a different picture will appear when a larger repertoire of vertebrate genomes is available for assessment in the future.
This study also sheds light on the possible origins of aGPCR family 2, suggesting that ADGRL4/ELTD1’s exons containing EGF domains are possibly ancestral to this family. Although aGPCR family 2 members are mostly expressed by immune cells, there is a known functional overlap between ADGRL4/ELTD1 and at least one family 2 member: AGRE5/CD97, which stimulates angiogenesis in an integrin-dependant manner . The close EGF similarity between ADGRL4/ELTD1 and members of aGPCR family 2 suggests the possibility that the extracellular matrix (ECM) ligands known to bind to members of aGPCR family 2 may also bind to ADGRL4/ELTD1, opening the door to future functional experiments. This possibility is further strengthened by the ECM itself being known to play a key role in regulating angiogenesis . A limitation to this hypothesis is that EGF domains are found in many proteins not sharing homology to ADGRL4/ELTD1 and that family 2’s EGFs may have been acquired from a different ancestor. The close similarity between ADGRL4/ELTD1’s EGFs and those in family 2 make this less likely.
This work reveals that the orphan aGPCR receptor ADGRL4/ELTD1 is a highly conserved early angiogenic gene which emerged in the vertebrate genome during the evolution of bony fish approximately 435 mya with a similar high-level conservation to established core regulators of angiogenesis. This work further establishes the first temporal references for the emergence of three ADGRL4/ELTD1 variants during vertebrate evolution, based on EGF domain deletions. These ADGRL4/ELTD1 variant findings establish the importance of EGF Ca binding domain 1 as the adhesion domain most likely to be important for ADGRL4/ELTD1’s functional activity. Results from conservation mapping describe the most likely external 7TM sites important for ligand binding and subsequent receptor activation, which present useful target sites for future in vitro angiogenesis activation/blocking experiments. Results show that ADGRL4/ELTD1 contains structural elements common to both aGPCR family 1 and 2 and that ADGRL4/ELTD1 may possibly be ancestral to members of family 2. In summary, these findings open up new horizons and ideas for further experiments to better understand both ADGRL4/ELTD1, and other members of the historically poorly studied aGPCR family.
ADGRL4/ELTD1’s evolutionary bioinformatics work was performed using the Ensembl database of publically available annotated, sequenced genomes  as well as with BioMart . All nucleotide coding sequences and protein sequences as well as similarity comparisons between human ADGRL4/ELTD1, VEGFR2, DLL4 and BRCA1 and its orthologues were extracted from Ensembl. Amino acid sequences were extracted from NCBI RefSeq and Ensembl. Orthologues were extracted from Ensembl (which uses gene order conservation scoring as well as whole genome alignment scoring to assign orthologues). Exome comparisons were also extracted from Ensembl (which uses pairwise whole-genome comparisons to make comparisons between the human genome and other genomes). Furthermore, Ensembl was used to interrogate splice variants. Each sequence was scanned for conserved domains using three amino acid sequence conservation databases (Pfam using KEGG motif , SMART  and CDD ). For comparison of two groups, the Student’s t-test was used. For unpaired data, an unpaired Student’s t-test was performed. For comparison of two or more groups, a one-way ANOVA was computed. Significance is denoted as: * p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001, **** p ≤ 0.0001. All sequence alignment was performed using Clustal Omega  using either nucleotide or amino acid sequences as stated. Conservation scores were calculated using Jalview . Sequence conservation scanning was performed as mentioned above. Phylograms and cladograms were computed from the Clustal outputs and arranged using Dendroscope . Evolutionary timetree data was extracted from the public Timetree.org database . Orthologues and homologues of all interrogated genes in extant organisms were extracted from the Ensembl and KEGG databases .
DMF performed the analyses. DMF, AHB and ALH wrote the manuscript. All authors read and approved the final manuscript.
DMF was funded by the Rhodes Trust, the Clarendon Scholarship and the Oppenheimer Memorial Trust. AHB and ALH were funded by CRUK and Breast Cancer Research Foundation (ALH). Funding bodies had no role in the study design, analysis, interpretation of data or writing of the manuscript.
Ethics approval and consent to participate
Consent for publication
The authors declare that they have no competing interests.
- 7.Masiero M, Simoes FC, Han HD, Snell C, Peterkin T, Bridges E, Mangala LS, Wu SY, Pradeep S, Li D, et al. A core human primary tumor angiogenesis signature identifies the endothelial orphan receptor ELTD1 as a key regulator of angiogenesis. Cancer Cell. 2013;24(2):229–41.PubMedPubMedCentralGoogle Scholar
- 8.Ziegler J, Pody R, Coutinho de Souza P, Evans B, Saunders D, Smith N, Mallory S, Njoku C, Dong Y, Chen H, et al. ELTD1, an effective anti-angiogenic target for gliomas: preclinical assessment in mouse GL261 and human G55 xenograft glioma models. Neuro-oncology. 2017;19(2):175–85.PubMedGoogle Scholar
- 10.Serban F, Daianu O, Tataranu LG, Artene SA, Emami G, Georgescu AM, Alexandru O, Purcaru SO, Tache DE, Danciulescu MM, et al. Silencing of epidermal growth factor, latrophilin and seven transmembrane domain-containing protein 1 (ELTD1) via siRNA-induced cell death in glioblastoma. J Immunoassay Immunochem. 2017;38(1):21–33.PubMedGoogle Scholar
- 14.Muller A, Winkler J, Fiedler F, Sastradihardja T, Binder C, Schnabel R, Kungel J, Rothemund S, Hennig C, Schoneberg T, et al. Oriented cell division in the C. elegans embryo is coordinated by G-protein signaling dependent on the adhesion GPCR LAT-1. PLoS Genet. 2015;11(10):e1005624.PubMedPubMedCentralGoogle Scholar
- 18.Brown K, Filuta A, Ludwig MG, Seuwen K, Jaros J, Vidal S, Arora K, Naren AP, Kandasamy K, Parthasarathi K, et al. Epithelial Gpr116 regulates pulmonary alveolar homeostasis via Gq/11 signaling. JCI insight. 2017;2(11).Google Scholar
- 41.Nagarathnam B, Kalaimathy S, Balakrishnan V, Sowdhamini R. Cross-genome clustering of human and C. elegans G-protein coupled receptors. Evol Bioinformatics Online. 2012;8:229–59.Google Scholar
- 49.Guberman JM, Ai J, Arnaiz O, Baran J, Blake A, Baldock R, Chelala C, Croft D, Cros A, Cutts RJ, et al. BioMart central portal: an open database network for the biological community. Database (Oxford). 2011;2011:bar041.Google Scholar
- 54.Waterhouse AM, Procter JB, Martin DM, Clamp M, Barton GJ. Jalview version 2--a multiple sequence alignment editor and analysis workbench. Bioinformatics (Oxford, England). 2009;25(9):1189–91.Google Scholar
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.