Cryo-EM structures of two insect Ors have been obtained: the fig wasp (Apocrypta bakeri) Or co-receptor (Orco) (Butterwick et al., 2018; Figure 1A–B), which is a highly conserved member of the repertoire across most insect species (Benton et al., 2006; Jones et al., 2005; Larsson et al., 2004) and MhOr5 from the jumping bristletail (Machilis hrabei), a broadly tuned volatile sensor (Del Mármol et al., 2021). Despite sharing only 18% amino acid identity, these proteins adopt a highly similar fold (Del Mármol et al., 2021). As Orco shows higher sequence similarity to Grs – the ancestral family of insect chemosensory receptors from which Ors derived (Brand et al., 2018; Dunipace et al., 2001; Robertson et al., 2003) – we used A. bakeri Orco as the query structure in our analysis.

In our previous work (Benton et al., 2020), we generated ab initio protein models of Orco and candidate homologs in various unicellular eukaryotes using trRosetta (Yang et al., 2020) and RaptorX (Källberg et al., 2012). We therefore first examined the AlphaFold2 structural model of A. bakeri Orco (Figure 1C; Jumper et al., 2021; Varadi et al., 2022). This model displays striking qualitative similarity to the experimental structure (PDB 6C70 chain A) (Figure 1C). We assessed structural similarity quantitatively using two algorithms: first, using pairwise structural alignment in Dali (Holm, 2022), we extracted the resultant Z-score (the sum of equivalent residue-wise C_α-C_α distances between two proteins); second, we determined the template modeling (TM)-score from TM-align (Zhang and Skolnick, 2004; Zhang and Skolnick, 2005) (a measure of the global similarity of full-length proteins) (Table 1). These measures confirmed the visual impression that the modeled and experimental structures are almost identical (e.g., TM-score=0.96, where 1 would be a perfect match). We extended our assessment of available (or newly generated) AlphaFold2 models to other well-established members of the 7TMIC family from animals as well as much more divergent unicellular 7TMIC homologs previously identified (Benton et al., 2020; Source data 1). Using the same quantitative assessments, these all displayed substantial tertiary structural similarity to A. bakeri Orco (Table 1), reinforcing our previous conclusions that these proteins form part of the same superfamily. Moreover, the observation that multiple distinct algorithms (AlphaFold2, trRosetta, and RaptorX) predict the same global fold of these proteins strengthens confidence in the validity of ab initio structural models.

We proceeded to screen the AlphaFold Protein Structure Database for other proteins that are structurally similar to A. bakeri Orco using the hierarchical search function in Dali (Holm, 2022). This algorithm currently permits pairwise alignment of Orco to the complete predicted structural proteomes of 47 species – encompassing several vertebrates, invertebrates, plants, unicellular eukaryotes and prokaryotes – returning hits ordered by Z-score (Source data 2). We focused on those hits with a Z-score of >10 (Figure 1D). This threshold successfully captured known 7TMICs, while removing a large number of proteins (generally with a much lower Z-score) that did not fulfill other criteria for structural similarity, as described below. Of the expected hits, within the D. melanogaster structural proteome we recovered all models of the members of the Or and Gr repertoires. From Caenorhabditis elegans, we found all members of the gustatory receptor (GUR) family (Robertson et al., 2003) – including the photoreceptor LITE-1 (formerly GUR-2) (Edwards et al., 2008; Gong et al., 2016; Liu et al., 2010) – and the serpentine receptor R (SRR) family (which are of unknown function, but display diverse neuronal and non-neuronal expression patterns Vidal et al., 2018; Figure 1D and Source data 2). From the four plant species screened, all members of the DUF3537 family were successfully identified (Figure 1 and Source data 2). Inspection of several models below our Z-score threshold indicated that the proteins (typically multipass membrane proteins) have likely spurious resemblance to subregions of Orco rather than displaying similarity in their overall fold.

As will be illustrated below for individual novel candidate 7TMIC homologs, other hits were subsequently analyzed for their fulfillment of several criteria: (i) the presence of seven predicted TM domains, (ii) a predicted intracellular location of the N-terminus, and (iii) longer intracellular than extracellular loops (like insect Ors [Otaki and Yamamoto, 2003], while also recognizing that intracellular loops can vary enormously in length in homologs [Benton et al., 2020]). For hits that fulfilled these criteria, ‘reverse’ searching of the D. melanogaster structural proteome with Dali was performed to verify that Ors and Grs were structurally the most similar proteins in this species (Source data 3). We next qualitatively assessed the predicted tertiary structural similarity to A. bakeri Orco (Figure 1A–C; Butterwick et al., 2018), verifying: (i) the characteristic packing of the TMs, (ii) the projection of the long TM4, TM5, and TM6 below the main bundle of helices (forming the ‘anchor’ domain where most inter-subunit contacts occur in complexes; Butterwick et al., 2018; Del Mármol et al., 2021), and (iii) the exceptional splitting of TM7 into two subregions (TM7a, part of the anchor domain, and TM7b, which lines the ion conduction pathway; Butterwick et al., 2018; Del Mármol et al., 2021). Structures were also quantitatively compared to A. bakeri Orco, as described above (Table 1). As negative controls, we also performed comparisons with a variety of other multipass membrane proteins belonging to other superfamilies, including several with seven TMs (e.g., Rhodopsin, Frizzled, and the Adiponectin receptor) (Table 1). The new candidate homologs all displayed quantitative measures of similarity that were within the range of previously identified 7TMIC homologs, and clearly superior to the scores of negative control proteins (Table 1). We now present these candidate homologs from different species and the potential evolutionary and biological implications for the 7TMIC family, bearing in mind the caveat that some of these may represent cases of structural convergence (discussed below).

Extending our previous discovery of 7TMICs in various single-celled eukaryotes (informally grouped here under the term Protozoa) (Benton et al., 2020), we identified single proteins in two species belonging to the Trypanosomatida order: L. infantum and T. brucei, the causal agents in humans of trypanosomiasis (sleeping sickness) and visceral leishmaniasis (black fever), respectively (Figure 1D–F and Table 1). Beyond the 7TMIC-like protein fold (Figure 1E–F and Table 1), these proteins are characterized in their N-terminal regions by a Membrane Occupation and Recognition Nexus (MORN)-repeat domain, which is implicated in protein-protein interaction and possibly lipid binding (Sajko et al., 2020). BLAST searches identified homologous proteins only within trypanosomes (Figure 1G), consistent with our failure to recover these sequences in earlier primary structure-based screens for 7TMICs. We did not detect any structurally related proteins to Orco in Prokaryota or Fungi (previously, fungal GRLs were only identified in chytrids [Benton et al., 2020], which are not currently surveyed via Dali). Together, these results reinforce our previous conclusion (Benton et al., 2020) that 7TMICs evolved in or prior to the last eukaryotic common ancestor, and provide a first example of fusion of this TM protein fold with a distinct, cytoplasmic protein domain.

Given previous lack of success in identifying homologs of 7TMICs within any chordate genome, we were intrigued that our screen recovered two hits from H. sapiens (and orthologous proteins of the three other vertebrate species screened) (Figure 1D and Source data 1–3). The human proteins, PHTF1 and PHTF2, are very similar to each other (54.1% amino acid identity) and have the characteristic topology of 7TMICs (Figure 2A). The next most similar vertebrate proteins to Orco had substantially lower Dali Z-scores than PHTFs and represented a variety of likely spurious matches (Source data 2). The single D. melanogaster ortholog (Phtf) (Manuel et al., 2000) displays a similar topology to the vertebrate proteins (Figure 2A), and is the next most similar protein model to A. bakeri Orco after the D. melanogaster Grs, Ors, and Grls (see next section) (Source data 2). PHTF is an acronym of ‘Putative Homeodomain Transcription Factor’, a name originally proposed because of presumably artifactual sequence similarity of a short region around TM4 to homeodomain DNA-binding sequences (Raich et al., 1999); subsequent histological and biochemical studies (discussed below) established that PHTF1 is an integral membrane protein (Oyhenart et al., 2003).

To visually compare AlphaFold2 models of PHTF orthologs with A. bakeri Orco, we masked the long (>300 amino acid) first intracellular loop (Figure 2A), whose structure is mostly unpredicted but contains a few α-helical regions, as well as the ~100-residue N-terminus (Figure 2B). This visualization revealed the clear similarity in the organization of the seven TM helical core of the protein, including the split TM7 (Figure 2B–C), which was verified by quantitative structural comparisons (Table 1).

In contrast to other, taxon-restricted members of the 7TMIC superfamily, highly conserved PHTF homologs were found across Eukaryota, including in Bilateria, Cnidaria, and several unicellular species (Figure 2D). Phylogenetic analyses of a representative PHTF protein sequence dataset revealed that there is a single eukaryotic PHTF clade (Figure 2E and Figure 2—figure supplements 1–3). Bayesian and maximum likelihood phylogenetics largely agree on the topology of this tree and suggest that the PHTF1-PHTF2 duplication occurred specifically in the jawed vertebrate lineage (Gnathostomata) (Figure 2E).

Previous tissue-specific RNA expression analysis by northern blotting of H. sapiens PHTF1 and PHTF2 revealed enrichment in testis and muscle, respectively (Manuel et al., 2000). We confirmed and extended these conclusions by analyzing publicly available bulk RNA-sequencing (RNA-seq) datasets: PHFT1 is most abundantly detected in cerebellum and testis, and PHTF2 in skeletal muscle and arteries (Figure 2F and Figure 2—figure supplement 4). D. melanogaster Phtf displays highly enriched expression in the testis, and much lower expression in neural tissues in the FlyAtlas 2.0 bulk RNA-seq datasets (Figure 2F and Figure 2—figure supplement 5; Krause et al., 2022), potentially indicating a closer functional relationship to PHTF1 than PHTF2. Higher resolution expression analysis of Phtf in male reproductive tissue, using the Fly Cell Atlas (Li et al., 2022), revealed the most prominent expression in developing spermatocytes and spermatids (Figure 2G). The transcript expression of D. melanogaster Phtf is concordant with detection of rat (Rattus norvegicus) PHTF1 protein from primary spermatocytes to the end of spermatogenesis, predominantly localized to the endoplasmic reticulum (Oyhenart et al., 2005b; Oyhenart et al., 2003). The N-terminal region of mouse (M. musculus) PHTF1 associates with the testis-enriched FEM1B E3 ubiquitin ligase and is suggested to recruit it to the endoplasmic reticulum (Oyhenart et al., 2005a). Overexpression and/or knock-down studies of PHTF1 and PHTF2 in cell lines hint at roles in regulating cell proliferation and survival, and possible links to various cancers (Chi et al., 2020; Huang et al., 2015). However, the biological function of any PHTF protein in any organism is unclear. Nevertheless, PHTFs represent the first candidate homologs of insect Ors/Grs in chordates, indicating that they might not have been completely lost from this lineage, as previously thought (Benton, 2015; Robertson, 2015); we suggest they also act as ion channels.

Within the hits of our screen of D. melanogaster protein structures, we noticed 10 proteins that do not belong to the canonical Gr or Or families (Source data 1–3). These proteins have a similar length and TM topology as Grs and Ors (Figure 3A). Visual inspection and quantitative analyses confirmed that their predicted fold is very similar to that of A. bakeri Orco (Figure 3A and Table 1). As they almost completely lack other defining sequence features of these families (see below), we named these Grl proteins, using the same cytogenetic-based gene nomenclature conventions of other chemosensory gene families (e.g., Drosophila Odorant Receptor Nomenclature Committee, 2000), with one exception (GrlHolozoa [GrlHz], see below).

For seven D. melanogaster Grls, BLAST searches identified homologs only in drosophilids; for two others (Grl40a and Grl65a) we recovered drosophilid and other fly homologs. By contrast, the Grl originally designated CG3831 has homologs across a wide range of Holozoa (i.e., animals and their closest single-celled, non-fungal relatives), including chordates (e.g., the lancelet Branchiostoma floridae) and single-cell eukaryotes (e.g., Capsaspora owczarzaki) (Figure 3—figure supplements 1–4), leading us to name it GrlHolozoa (GrlHz). A subset of GrlHz homologs bear a long N-terminal domain containing WD40 repeats, which form a structurally predicted beta-propeller domain that is typically involved in protein-protein interactions (Figure 3—figure supplement 1D; Kim and Kim, 2020).

Given that nine of these Grls are restricted to flies, a reasonable hypothesis is that they evolved from fly Grs. To infer their evolutionary origins, we therefore examined sequence similarity of Grls with a representative set of Grs, as well as Ors and other animal (i.e., non-insect) GRLs. We found that fly Grls share little or no obvious sequence similarity with any of these other 7TMICs, precluding confident standard phylogenetic analysis and leading us to use an all-to-all graph-based methodology, which does not require a multiple sequence alignment. This approach infers relationships between sequences based on pairwise sequence similarity. This analysis first generates an all-to-all sequence similarity network via MMseqs2, in which sequence families can be identified as clusters in a 2D projection (Figure 3B), and then a tree by recursive spectral clustering (Figure 3—figure supplement 5; see Methods; Matsui and Iwasaki, 2020; Steinegger and Söding, 2017). In the network, we observed that several of the Grls were intermingled in clusters (e.g., Grl62b/Grl62c and Grl36a/Grl43a), suggesting relatively recent common ancestry (Figure 3B). These two clusters were recapitulated as clades in the graph splitting phylogeny (Figure 3—figure supplement 5). For Grl62a/b/c, the possibility of recent ancestry is consistent with the tandem genomic organization of the corresponding genes, which implies their evolution by gene duplication through non-allelic homologous recombination, similar to other families of chemosensory genes (Nei et al., 2008). None of the Grl clusters grouped with those of Ors, Grs, or other animal GRLs, rather connecting broadly, but weakly, with all other clusters (Figure 3B). Consistent with this clustering pattern, all Grls were placed near the presumed root of the graph splitting tree (Figure 3—figure supplement 5). This basal placement of Grls was inconsistent with their conservation only in flies, and is likely a phylogenetic artifact (see legend to Figure 3—figure supplement 5).

Although analysis of amino acid sequences did not provide evidence of ancestry between Grs and Grls, we noted that Grl36a was adjacent (separated by 306 bp) to the Gr36a/b/c cluster in the D. melanogaster genome. This proximity suggested that Grl36a might have arisen by gene duplication of a Gr36-like ancestor. Indeed, Grl36a homologs across drosophilid species were always found in tandem with Gr36-related genes in various arrangements (Figure 3C, Figure 3—figure supplement 6). To further investigate the hypothetical ancestry of Grl36a and Gr36, we first examined their gene structure. We incorporated into this analysis Gr59c and Gr59d homologs, which are closely related to Gr36a/b/c even though they are distantly located in the genome (Robertson et al., 2003), as well as Grl43a, the most closely related paralog to Grl36a (Figure 3B). The Gr family is characterized by the general, but not universal, conservation of three phase 0 introns near the 3’ end of these genes (Robertson et al., 2003). Gr36, Gr59c/d, and homologous non-drosophilid genes possess only one of these introns, which corresponds to the second ancestral Gr intron located just before the exon encoding TM7. Both D. melanogaster Grl36a and Grl43a also have a phase 0 intron immediately before the TM7-encoding exon, which aligns with the Gr intron position on a multiple protein sequence alignment (Figure 3D), suggesting that these Gr and Grl introns are homologous. We next examined the TM7 motifs in these Grs and Grls. The canonical TM7 motif of Grs is TYhhhhhQF, where h is a hydrophobic residue (Figure 3D; Robertson, 2019; Scott et al., 2001). However, Gr36 and Gr59c/d share a variant motif, T(H/N)(S/A)hhhhQ(Y/F/W), and we observed a very similar motif in Grl36a and Grl43a (Figure 3D).

The genomic proximity of Gr36 and Grl36a, and similarity in introns and TM7 motifs of these genes (as well as Gr59c/d and Grl43a) provide evidence that these genes have a relatively recent common ancestry within drosophilids. Phylogenetic analyses of this proposed clade support that a Grl36a/Grl43a clade is the sister clade to Gr36, and that this split occurred after the emergence of the Gr59c/d clade (Figure 3E, Figure 3—figure supplements 6–9). None of the other Grl genes are located adjacent to Gr genes, nor do the proteins possess a recognizable TM7 motif. Some other Grls might possess conserved introns of Grs (e.g., Grl40a with the first ancestral intron, and Grl36b and Grl65a with the second ancestral intron [data not shown]), but we cannot conclude with confidence that these are homologous. Thus, the ancestry of most Grls remains unresolved. Nevertheless, the highly restricted taxonomic representation of nine of these Grls and their structural similarity to Grs support a model in which Grls have rapidly evolved and diverged from ancestral Grs.

To gain insight into the potential role(s) of Grls, we first examined their expression in tissue-specific bulk RNA-seq datasets from the FlyAtlas 2.0 (Krause et al., 2022). Most Grls were expressed at very low (<1 fragment per kilobase of exon per million mapped fragments [FPKM]) or undetectable levels in essentially all tissues in these datasets, although Grl36b was detected in neuronal tissues (eye, brain, thoracicoabdominal ganglion) (Figure 2—figure supplement 5). The one exception was GrlHz, which was expressed (>8 FPKM) in various tissues (e.g., heart, ovary, testis, and larval fat body and garland cells [nephrocytes]). The unique expression and conservation properties of GrlHz suggest it has a different function from other Grls.

The lack of detection of transcripts for most Grls in the FlyAtlas 2.0 suggested that these genes might have highly restricted cellular expression patterns. Given the structural similarity of Grls to Grs, we examined their expression in an RNA-seq dataset of the major taste organ (labellum; a tissue not specifically represented in the FlyAtlas 2.0) (Dweck et al., 2021). D. melanogaster Gr genes display a wide range of expression levels in the labellar transcriptome, in part reflecting the breadth of expression in different classes of taste neurons. For example, Gr66a and Gr64f – broadly expressed markers for ‘bitter/aversive’ and ‘sweet/appetitive’ neuronal populations, respectively (Freeman and Dahanukar, 2015) – are detected at comparatively high levels (>5 FPKM) (Figure 3F). By contrast, many receptors expressed in subsets of these major neuron types (e.g., Gr22e for bitter and Gr61a for sweet; Freeman and Dahanukar, 2015) are expressed at much lower levels (~1 FPKM). Similar to this latter type of Gr, transcripts for four Grls were detected at >0.5 FPKM: GrlHz, Grl62c, Grl62a, and Grl36a (Figure 3F). Importantly, within the Fly Cell Atlas dataset of the proboscis and maxillary palp (Li et al., 2022), three of these were specifically expressed in the cluster of cells corresponding to Gr66a-expressing bitter/aversive neurons (Figure 3G). The fourth, GrlHz, was very sparsely expressed in non-neuronal cell types in this tissue, including hemocytes (data not shown; Li et al., 2022). None of the other six Grls were detectable in this dataset, consistent with their lower expression in the labellar bulk RNA-seq transcriptome (Figure 3F). Moreover, no Grl (except the broadly expressed GrlHz) was detectably expressed in other chemosensory tissue transcriptomes (leg, wing, or antenna) (data not shown; Li et al., 2022; Menuz et al., 2014). These observations raise the possibility that at least three Grls (Grl36a, Grl62a, and Grl62c) are chemosensory receptors for aversive stimuli.

Two hypotheses could explain the similarities between well-established 7TMICs and the candidate homologs described in this work: homology (i.e., shared ancestry), and thus the existence of a unified 7TMIC superfamily, or convergent evolution of the 7TMIC structure. We discuss the latter possibility in the following section. Here, we consider a detailed hypothesis of a 7TMIC superfamily of single evolutionary origin. Because confident multiprotein alignment of all members was impossible, we used the same all-to-all graph-based approach as for insect Grls to generate a sequence similarity network, and families were identified as clusters in a 2D projection (Figure 4A). We used the gross connectivity of clusters, and the presence or (putative) absence of these proteins across taxa (Figure 4B), to make inferences about the ancestry of these proteins.

In the sequence similarity network, clusters of Ors, Grs, and non-insect animal GRLs (excluding GrlHz) were closely located or intermingled, while insect Grl clusters were more distantly located from this grouping (Figure 4A). GrlHz formed a distinct cluster, but this connects only with the Or/Gr/Grl clusters (and not plant DUF3537 or PHTF clusters) (Figure 4A), suggesting that it descended from a Gr-like ancestor. Given that GrlHz was not detected outside of Holozoa (Figure 4B), the simplest hypothesis is that an ancestral holozoan had a 7TMIC gene that duplicated to produce an ancestral GrlHz and an ancestral Gr (Figure 4C). The diversity of Ors, Grs, and Grls would then have resulted from taxon-specific diversification of a single, holozoan branch of a hypothetical 7TMIC superfamily (Figure 4C).

The plant DUF3537 protein cluster was relatively well connected to the Or/Gr/Grl clusters (Figure 4A), consistent with the previously recognized sequence similarity between DUF3537 and Grs, which supported their proposed shared ancestry (Benton, 2015; Benton et al., 2020). If this is correct, a DUF3537/Or/Gr/Grl ancestor must have been present in a common ancestor of plants (part of Diaphoretickes) and animals (part of Amorphea) (Figure 4B–C). Unicellular eukaryotic 7TMICs were dispersed between Or/Gr/Grl and DUF3537 proteins (Figure 4A); the simplest hypothesis is that these are related to other 7TMICs in accordance with their species’ taxonomy (e.g., SAR [stremenopiles, alveolates, and Rhizaria] 7TMICs are more closely related to plant DUF3537 proteins than to animal Grs). Alternatively, the generally sparse conservation of unicellular eukaryotic 7TMICs might indicate horizontal gene transfer(s).

Finally, PHTF also forms a separate cluster (Figure 4A), and its broad taxonomic representation argues that the PHTF ancestral gene must also have been present in a common Amorphea-Diaphoretickes ancestor (Figure 4B–C). If there was a single ancestral 7TMIC, we hypothesize that this gene must have duplicated in a common eukaryotic ancestor to produce the distinct PHTF and Or/Gr/Grl/DUF3537 lineages (Figure 4C).

Exploiting recent advances in protein structure predictions, we have used a tertiary structure-based screening approach to identify new candidate members of the 7TMIC superfamily. While the founder members of this superfamily, insect Ors and Grs, were thought for many years to define an invertebrate-specific protein family (Benton, 2006; Robertson et al., 2003), there is now substantial evidence that these proteins originated in a eukaryotic common ancestor. We also counter previous assumptions that 7TMICs were completely lost in Chordata, through discovery of two lineages within this superfamily: PHTF and GrlHz. Finally, we have identified many previously overlooked putative chemosensory receptors in D. melanogaster (and related flies).

Two important issues remain open. First, are all of the candidate 7TMICs homologous, or does shared tertiary structure reflect convergent evolution in protein folding in at least some cases? Doubts about homology stem, reasonably, from the extreme sequence divergence between 7TMICs to beyond the twilight zone of sequence similarity (Rost, 1999). However, sequence divergence over many millions of years of accumulated amino acid substitutions is well appreciated in this superfamily (e.g., pairs of D. melanogaster Grs can display as little as 8% amino acid identity; Robertson et al., 2003). Thus, sequence dissimilarity alone is not compelling evidence for structural convergence. Examples of convergent evolution of tertiary protein structures have been described (Alva et al., 2010; Alva et al., 2015; Tomii et al., 2012) but the vast majority of these are small protein domains or motifs, some of which might represent relics of the evolution of proteins from short peptide ancestors (Alva et al., 2015; Lupas et al., 2001). The core of the 7TMIC fold is >300 amino acids, and the question of homology or convergence is most akin to the unresolved, long-standing debate regarding the evolution of the 7TM G protein-coupled receptor fold of type I and type II rhodopsins (Mackin et al., 2014; Rozenberg et al., 2021). In the case of 7TMICs, if PHTFs and other family members are not homologous, their taxonomic representation indicates that structural convergence must have occurred in a eukaryotic common ancestor. While it might be impossible to definitively distinguish homology from convergence, both hypotheses have interesting implications for this protein fold: convergent evolution of at least some 7TMICs from several distinct origins would argue that the fold is an energetically favorable packing of seven TMs; if the superfamily had a single origin, this would further highlight the remarkable potential for sequence diversification while maintaining a common tertiary structure (Schaeffer and Daggett, 2011).

Second, what are the biological roles of different 7TMICs? One aspect of this question pertains to their mechanism of action, that is, whether they assemble in multimeric complexes to form ligand-gated ion channels, similar to insect Ors and Grs. The apparent presence of an anchor domain in all 7TMICs, where most inter-subunit contacts occur in Ors (Butterwick et al., 2018; Del Mármol et al., 2021), raises the possibility that complex formation is a common biochemical property. Whether they function as ligand-gated ion channels is not necessarily trivial to answer. Even for insect Grs – for which abundant evidence exists for their in vivo requirement in tastant-evoked neuronal activity (Chen and Dahanukar, 2020) – definitive demonstration of their chemical ligand-gated ion conduction properties has (with rare exceptions, e.g., Morinaga et al., 2022) been elusive. For PHTF or GrlHz proteins, for example, it is currently difficult to anticipate what might be relevant ligands and we cannot exclude that they have a completely different type of biological activity. Nevertheless, available expression data points to roles of different proteins in specific, but diverse cell types, including chemosensory neurons, (developing) spermatocytes, and muscle. The discoveries in this work should stimulate interest in an even broader community of researchers to understand the evolution and biology of 7TMICs.

Structural screens for candidate 7TMIC homologs were performed with the AF-DB search tool on the Dali server (http://ekhidna2.biocenter.helsinki.fi/dali/; Holm, 2022) using as query the A. bakeri Orco structure (PDB 6C70-A) (Butterwick et al., 2018). As of December 2022, this server permitted screening of the structural proteome of 47 phylogenetically diverse species. Proteins whose structural models had a Z-score >10 were retained for further analysis. Candidate homologs from these screens were assessed first by using these as queries in Dali AF-DB searches of the D. melanogaster proteome to ensure Ors and Grs were the best ‘reverse’ hits, and subsequently for secondary structural features using DeepTMHMM (https://dtu.biolib.com/DeepTMHMM/) (Hallgren et al., 2022) and Phobius (https://phobius.sbc.su.se/) (Käll et al., 2007). Of the newly identified D. melanogaster Grls, we note that three were initially classified as being members of the Gr repertoire (Grl36a (Gr36d), Grl43a (Gr43b), and Grl65a (Gr65a), but later excluded (Flybase [flybase.org/] and [Robertson et al., 2003])). We also contrast the term ‘Grl’, referring to the proteins in insects (following nomenclature conventions of D. melanogaster [Flybase]) with ‘GRL’, referring to proteins in other animals and more distant eukaryotes; the same acronym does not reflect a monophyletic origin. To identify sequences of candidate homologs from other species that were not screened with Dali AF-DB, PSI-BLAST searches against the NCBI refseq_protein database were performed, using the query sequences indicated in each figure and dataset. PSI-BLAST was run with an expected threshold of 1E-10 until convergence. BLASTP searches for Gr36/59 homologs were performed more permissively, using an expected threshold of 0.05. All sequences analyzed in this work are provided in Source data 4.

AlphaFold2 protein models (Jumper et al., 2021; Varadi et al., 2022) were downloaded from the AlphaFold Protein Structure Database (alphafold.ebi.ac.uk; release July 2022). For proteins for which structural predictions were not already available, we generated AlphaFold2 models using ColabFold (Mirdita et al., 2022). Positive and negative control protein structures were downloaded from the RCSB Protein Data Bank (PDB codes are indicated in Table 1). Pairwise structural similarities of protein models were quantitatively assessed with Dali (Holm, 2022) and TM-align (https://zhanggroup.org/TM-align/) (Zhang and Skolnick, 2005). Proteins were aligned to the same coordinate space with Coot (https://www2.mrc-lmb.cam.ac.uk/personal/pemsley/coot/) (Emsley et al., 2010) and visualized in PyMol v2.5.4. All models analyzed in this work are provided in Source data 1.

Sequence databases assembled using PSI-BLAST (see above) were first curated in a semi-automated pipeline. First, sequences annotated as ‘partial’ or ‘low quality’, or that contained ambiguous sequence characters (e.g., X), were removed. CD-HIT (http://cd-hit.org) (Fu et al., 2012; Li and Godzik, 2006) was used to cluster redundant sequences (100% amino acid identity). Using Phobius TM domain predictions, we removed sequences with fewer than four TMs (this number was chosen to allow for the different sensitivity of Phobius compared to DeepTMHMM). In the final PHTF database, we manually excluded a single sequence as a spurious hit (B. floridae XP_035670545.1, zinc transporter ZIP10-like); this sequence sorted independently in first-pass phylogenetic analyses (via FastTree2; Price et al., 2010), and a search via InterPro (ebi.ac.uk/interpro/) revealed that it had no obvious similarity to the other proposed homologs. The database of Gr39/Gr59 homologs was manually curated due to its relatively small size and accurate automatic annotation by RefSeq; here, we excluded BLAST hits not annotated as Grs, and visually inspected a sequence alignment for good alignment.

To reduce the large curated sequence databases to a size that could be locally analyzed by both maximum likelihood and Bayesian phylogenetic methods, CD-Hit was used to cluster sequences by 70–90% sequence identity, using the longest sequence as the representative for phylogenetic analyses. The clustering used to generate each phylogeny is indicated in the corresponding figure legend.

We took two separate approaches to infer ancestry. In initial analyses, when comparing insect Grls to Ors/Grs/non-insect GRLs (Figure 3B) or for the entire 7TMIC superfamily (Figure 4A), we observed that extremely low sequence similarity severely constrained our ability to generate meaningful multiple sequence alignments (data not shown). We therefore generated all-to-all sequence similarity networks using MMSeqs2 and inferred phylogenies from these networks by the graph splitting method (both implemented in gs2) (Matsui and Iwasaki, 2020). MMSeqs2, as implemented in gs2, employs high sensitivity to sequence similarity and is thus capable of networking non-homologous sequences via spurious sequence identity, should it be present. This method does not distinguish between homology and convergence. Rather, the purpose of this analysis was to make inferences about relatedness under the assumption that all sequences are homologous. In the networks, edge weights are E-values from MMSeqs2. In the graph splitting trees, branch support values were generated by the edge perturbation method (1000 replicates) with a transfer bootstrap expectation (Lemoine et al., 2018). For visualization of sequence similarity networks, recursive, same-to-same sequence comparisons (resulting in an E-value of 0) were removed using an R script.

For all other trees, multiple sequence alignments were generated by MAFFT. We made no a priori assumptions about the alignment, so used default settings. Phylogenetic trees were inferred by maximum likelihood and Bayesian methods. Maximum likelihood trees were generated by IQ-TREE (Minh et al., 2020), using the best model selected for each analysis by ModelFinder (Kalyaanamoorthy et al., 2017) according to the Bayesian information criterion, and with bootstrapping by UFBoot2 (1000 replicates) (Hoang et al., 2018). Bayesian trees were generated by MrBayes (Ronquist and Huelsenbeck, 2003) using a mixed amino acid substitution model (Markov chain Monte Carlo analyses run until standard deviation of split frequencies <0.05, with 25% burn in). To generate the most parsimonious hypotheses of protein evolution, we used NOTUNG (Chen et al., 2000) to rearrange poorly supported branches and resolve polytomies in a species tree-aware fashion (i.e., favoring speciation to gene duplication/horizontal gene transfer in poorly supported branches and polytomies), using default weights/costs (gene duplication 1.5, transfers 3.0, gene loss 1.0). Branches were eligible for rearrangement at branch support values less than UFboot 95 or posterior probability 0.95. Species trees used for rearrangement were based on the NCBI Taxonomy Common Tree, with polytomies randomly resolved for each analysis using the ape (Paradis and Schliep, 2019) and phytools (Revell, 2012) packages. Strict consensus trees were generated by comparing the species tree-aware maximum likelihood and Bayesian trees via the consensus function in ape.

The 7TMIC sequence similarity network was visualized and annotated in Cytoscape (Shannon et al., 2003). Trees were visualized and annotated in NOTUNG, iTOL (itol.embl.de/) (Letunic and Bork, 2007), and Adobe Illustrator. Consensus sequence illustrations were adapted from figures generated by WebLogo (weblogo.berkeley.edu/) (Crooks et al., 2004).

The locations of Grl36a, Grl43a, Gr36, and Gr59c/d genes in different drosophilids were surveyed using the NCBI Genome Data Viewer (ncbi.nlm.nih.gov/genome/gdv/) (Rangwala et al., 2021). Gene intron-exon structures were manually surveyed using publicly available predictions available on RefSeq (via the Genome Data Viewer) and FlyBase, and visualized in SnapGene. The relative positions of introns were assessed via multiple sequence alignment of the protein sequences; for this analysis, we assumed that that entire sequences could be aligned (global alignment), and thus computed the alignment using the G-INS-i (Needleman-Wunsch) option in MAFFT.

H. sapiens PHTF1 and PHTF2 tissue-specific RNA expression data were obtained from the GTEx Portal (GTEx Analysis Release V8 [dbGaP Accession phs000424.v8.p2; https://gtexportal.org/home/datasets]). Tissue/life stage-specific RNA expression data of Phtf and Grl genes in D. melanogaster were downloaded from the Fly Atlas 2.0 (https://motif.mvls.gla.ac.uk/FlyAtlas2) (Krause et al., 2022) or, for the labellum, from Dweck et al., 2021. D. melanogaster scRNA-seq data was from the Fly Cell Atlas (Li et al., 2022): proboscis/maxillary palp (10× stringent dataset) and testis/seminal vesicle (10× relaxed dataset), visualized as HVG tSNE or UMAP plots, respectively, in the SCope interface (https://scope.aertslab.org/#/FlyCellAtlas) (Davie et al., 2018).