- Research article
- Open Access
Identification and analysis of serpin-family genes by homology and synteny across the 12 sequenced Drosophilid genomes
BMC Genomicsvolume 10, Article number: 489 (2009)
The Drosophila melanogaster genome contains 29 serpin genes, 12 as single transcripts and 17 within 6 gene clusters. Many of these serpins have a conserved "hinge" motif characteristic of active proteinase inhibitors. However, a substantial proportion (42%) lacks this motif and represents non-inhibitory serpin-fold proteins of unknown function. Currently, it is not known whether orthologous, inhibitory serpin genes retain the same target proteinase specificity within the Drosophilid lineage, nor whether they give rise to non-inhibitory serpin-fold proteins or other, more diverged, proteins.
We collated 188 orthologues to the D. melanogaster serpins from the other 11 Drosophilid genomes and used synteny to find further family members, raising the total to 226, or 71% of the number of orthologues expected assuming complete conservation across all 12 Drosophilid species. In general the sequence constraints on the serpin-fold itself are loose. The critical Reactive Centre Loop (RCL) sequence, including the target proteinase cleavage site, is strongly conserved in inhibitory serpins, although there are 3 exceptional sets of orthologues in which the evolutionary constraints are looser. Conversely, the RCL of non-inhibitory serpin orthologues is less conserved, with 3 exceptions that presumably bind to conserved partner molecules. We derive a consensus hinge motif, for Drosophilid inhibitory serpins, which differs somewhat from that of the vertebrate consensus. Three gene clusters appear to have originated in the melanogaster subgroup, Spn28D, Spn77B and Spn88E, each containing one inhibitory serpin orthologue that is present in all Drosophilids. In addition, the Spn100A transcript appears to represent a novel serpin-derived fold.
In general, inhibitory serpins rarely change their range of proteinase targets, except by a duplication/divergence mechanism. Non-inhibitory serpins appear to derive from inhibitory serpins, but not the reverse. The conservation of different family members varied widely across the 12 sequenced Drosophilid genomes. An approach considering synteny as well as homology was important to find the largest set of orthologues.
The serpins form a family of more than 1,000 proteins found in plants, animals and viruses, but only rarely in fungi, bacteria, or archaea . The majority are active SER ine P roteinase IN hibitors  with a unique cleavage mechanism. The serpin-fold consists of three β-pleated sheets with 8 or 9 short α-helical linkers. In the native state, serpins are in a metastable (stressed) configuration, which consists of a core structure with an exposed reactive centre loop (RCL) of 25-30 amino acids. The RCL presents an ideal bait to the target proteinase which cleaves between two residues known as P1 and P1'. Following cleavage, a covalent complex is formed with the target proteinase. The cut end of the RCL inserts between two β-strands within the serpin core and the molecule undergoes an extreme conformational transition to the stable (relaxed) configuration. The covalently attached proteinase is denatured by being crushed against the serpin core, which targets the complex for proteolytic degradation . Such a "suicide cleavage" mechanism gives rapid turnover of both inhibitor and proteinase, with the result that a reduction in inhibitor activity gives explosive activation of proteolytic cascades. The cleavage mechanism places particular constraints on the serpin-fold, which are common to all serpin inhibitors. In particular, the suicide inhibitory mechanism requires a run of small side-chain amino acids in the proximal "hinge" region [1, 4], seven residues N-terminal to the scissile bond, to allow RCL insertion into β-sheet A. This flexible hinge region is absent in the non-inhibitory serpin-fold proteins. Twelve of the 29 D. melanogaster serpin genes lack the critical short-side chain residues necessary for an active proteinase inhibitor [5, 6].
Serpins have been extensively studied in mammals where they regulate many extracellular proteolytic cascades. The coagulation, inflammatory and complement pathways are controlled by α1-Antithrombin, α1-Antitrypsin and C1-Inhibitor, respectively [2, 7, 8]; while Plasminogen Activator Inhibitor-1 modulates angiogenesis, affecting both wound-healing and tumour growth . There is also a related group of non-inhibitory serpin-fold proteins with diverse functions, including molecular chaperones [10, 11], hormone transport , chromosome condensation , tumour suppression  and storage proteins . In many cases, the functional requirement for the serpin-fold in the activity of these non-inhibitory molecules remains unclear.
In contrast to the mammals, insect serpins have been relatively little studied. In Drosophila, the Toll-mediated innate immune response is controlled by Spn43Ac (synonym, necrotic) [16, 17]. The phenol-oxidase cascade is inhibited, at two different steps, by Spn27A [18, 19] and Spn28Dc ; while tracheal melanization is regulated by Spn77Ba . Spn27A also controls dorso-ventral axis formation in the embryo . The alternatively spliced transcripts of the Spn42Da (synonym, Spn4) gene encode four separate RCL peptides. These protein isoforms inhibit furin-, chymotrypsin- and subtilase-like serine proteinases as well as papain-like cysteine proteinases [23–25]. Other than this, little is known about the Drosophila serpins, or the target proteinases that they inhibit. As there are 206 annotated chymotrypsin-fold serine proteinases in Drosophila, identification of target proteinases is difficult. It appears that individual serpins may inhibit proteinases in different proteolytic cascades; while particular physiological responses might be modulated by serpins targeting different steps in the same proteinase cascade.
Serpin specificity is determined by the amino acid sequence of the RCL, in particular the P1 and P1' sites, between which the peptide chain is cleaved . The identity of the P1 residue is critical, with a lesser contribution of the P1' site and adjacent residues [27, 28]. In general, this mechanism gives broad specificity, with each serpin inhibiting a range of related serine proteinases. This apparent "redundancy" has complicated studies of mammalian serpins, as most serpin null mutations give no discernable mutant phenotype. The lack of function of one serpin activity may be compensated by the activity of a related serpin. Furthermore, in a proteolytic cascade, the lack of inhibition of one proteinase could be compensated for by inhibition of another proteinase, by a serpin with a differing inhibitory profile. Such complex interactions are hard to analyse and are likely to have unpredictable effects on the evolutionary constraints acting on different serpin activities.
The vertebrate serpins have evolved through gene duplication and divergence, giving rise to a large number of transcripts encoding serpins with unique reactive centre loops and discrete physiological functions. These serpins have been divided into 9 clades of related proteins, based largely on sequence homology . The number of serpins varies widely between species, with the mouse genome containing 64, compared to 35 in the human. Fitting non-vertebrate serpins within this structure is difficult, although an expanded set of 16 clades, with a number of orphan sequences, has been proposed . The D. melanogaster serpins have been classified according to their chromosomal location, with many of them located in clusters of adjacent transcripts. This nomenclature is neutral with respect to functional similarities, but clusters of adjacent transcripts are immediately apparent. The serpins that map within polytene chromosome band 43A, for example, are identified as Spn43Aa, Spn43Ab, Spn43Ac and Spn43Ad. Of the 29 D. melanogaster serpin transcripts, 17 are located within 6 gene clusters. This aspect of genomic organisation has been given relatively little attention in vertebrates, but the mammalian Clade A and B serpins tend to be present in clusters and it is the relative expansion of these clusters that accounts largely for the increase of serpin transcripts in the mouse lineage [29–32]. In general, the D. melanogaster clusters contain widely diverged transcripts including inhibitory serpins and non-inhibitory serpin folds (Figure 1).
Although the tertiary structure of the core serpin-fold is strongly conserved, the primary sequence constraints are relatively loose . The major function of the serpin core is to deliver energy stored in its metastable, stressed configuration, following cleavage of the RCL . Relaxation of the serpin core distorts the active site of the proteinase and traps it in an inactive serpin/proteinase complex. This is quite different to the mechanism of action of Kunitz and Kazal-family inhibitors, which form a highly specific lock and key fit with their target proteinase. The loose sequence conservation of the serpin core presents particular problems when trying to identify the complete set of serpins in an organism. An initial homology search of the Drosophilid species available through FlyBase identifies 188 serpin genes, but even in the sibling-species, D. simulans, orthologues were identified for only 23 of the 29 D. melanogaster serpins. As the relative genomic location of putative orthologues was often conserved, we decided to use synteny as a way to check for other family members: the genes flanking annotated D. melanogaster serpins were used to identify the corresponding regions in the other species which were then closely examined for nearby serpin-like genes. This approach identified an additional 35 serpins. A final tBLASTx search of all 12 genomes with all 223 genes identified three further serpin genes. By analysing the sequence conservation of the serpin genes across the Drosophilidae, we address both evolutionary and structure-functional relationships within this protein super-family.
Results and Discussion
The tBLASTx search of the Drosophilid sequence-assemblies available through FlyBase identified 188 serpin orthologues. This number represents 59% (188/319) of the orthologues expected on the assumption that the different Drosophilid species average 29 serpin genes per genome, as in D. melanogaster. In general, fewer orthologues were found in the out-groups, than in species close to melanogaster (13 serpins in the Hawaiian D. grimshawi, compared to 23 in D. simulans), Table 1. The synteny search identified all the serpin genes annotated on FlyBase, plus an additional 36 genes, Table 1 (gene identifiers are given in Additional file 1). The further tBLASTx search, using all the previously identified genes, identified three additional serpins (Table 1). These additional genes bring our coverage up to 71% of the expected orthologues (with the least coverage being 16 serpins in D. grimshawi, compared to 28 in D. simulans). Following this, we trained a hidden Markov Model against the 16 D. grimshawi serpin genes and searched the 12 Drosophilid genomes. This search identified 139/255 (55%) of our set of D. melanogaster serpins plus Drosophilid orthologues, but no additional genes. A final search for homology to the consensus RCL hinge sequence of Drosophilid inhibitory serpins,
E [EKR]G [TSG] [ET] [AGS] [YAGS] [AGS] [VAGS] [TS] (see Additional File 2), identified 75/183 (41%) of the previous inhibitory serpins, but again no novel serpin genes.
Three genes identified as orthologues of Spn42Dd and also of either Spn28F, or Spn38F were assigned as Spn42Dd orthologues by synteny analysis: these three genes are so closely related in D. melanogaster (Figure 1), that distinguishing between their orthologues by homology alone is inconclusive. The structure of the orthologous Spn42D gene clusters in the 12 Drosophilid species is shown in Figure 2A. The synteny search strategy is illustrated in Figure 2B. The genes flanking D. sechellia show homology to genes adjacent to Spn42Dd in D. melanogaster, rather than those neighbouring Spn38F. Thus, GLEANR 3714 is syntenic to Spn42Dd, not Spn38F. Similarly, synteny analysis indicates that D. erecta GLEANR 8071 and D. pseudoobscura GLEANR 15081 are orthologous to Spn42Dd not Spn28F.
The distribution of serpin orthologues across the Drosophilidae
Orthologues of many of the inhibitory serpins were identified in all Drosophilid species, but five (out of 17) are restricted to the melanogaster group (Spn28B, Spn28Da, Spn28Db, Spn28 F and Spn88Eb) and one (Spn38F) has no identified orthologues in other species. In the case of the non-inhibitory serpin-fold proteins, five have identified orthologues across the Drosophilidae (Spn31A, Spn43Ab, Spn47C, Spn85F, Spn100A and Spn28B), while the other seven show a more restricted distribution (Spn28Db, Spn43Ad, Spn53F, Spn75F, Spn76A, Spn77Bb and Spn77B c) (Table 1).
Using synteny to find additional family members
Within multi-gene families, identifying the true orthologues of a particular gene becomes increasingly difficult in distantly related species. Here we have used conservation of gene order in the chromosome, both as a means to search for additional family members, and also as a way of assigning putative orthology in otherwise ambiguous cases. This approach is based on the finding that the order of the majority of the genes along the chromosome arms is conserved among the Drosophilid species [33–36]. This allows neighbouring transcripts to be used to identify putative serpin genes which may have been missed by homology-dependent searches. Using this approach, we identified 223 serpin genes in the Drosophilid lineage with conserved synteny to D. melanogaster, compared to 188 genes identified by sequence homology alone. A tBLASTx homology search using this expanded set of 223 genes as queries, identified 3 additional orthologues, bringing the total number of identified serpin genes to 226. The identity of candidate syntenic genes was confirmed by aligning their putative RCL sequences with that of the corresponding set of orthologues (Table 1 and see Additional file 2). By this criterion the synteny approach made no false assignments. In addition to increased identification of serpin transcripts, the method allows the assignment of putative orthology when considering closely-related genes.
There were three cases in which the tBLASTx and synteny searches failed to identify orthologues in a single species (D. sechellia Spn43Ab, D. willistoni Spn43Ad and D. erecta Spn85F). Examination of the sequence alignment of the syntenic genomic regions by eye identified the missing orthologues for D. sechellia Spn43Ab and D. erecta Spn85F, but the D. willistoni Spn43Ad transcript is deleted from the orthologous Spn43A gene complex.
If each of the Drosophilid species contained 29 serpin genes per genome, as in D. melanogaster, the synteny approach identifies 71% of the expected serpin genes. It is notable, however, that even in the sibling-species, D. simulans, only 23 orthologues were identified by sequence homology, with 5 more identified by synteny, Table 1. The number of identified serpin genes decreases uniformly with increasing evolutionary separation from D. melanogaster. Only 13 serpins are identified by sequence homology (and 16 by synteny) in D. grimshawi. While the exact number of serpins may vary among fruit-flies, it seems unlikely that this number should correlate with evolutionary separation from D. melanogaster. This progressive decrease implies that many of the "missing" serpin functions may be represented by transpositions of serpin genes to novel chromosome sites, followed by sequence divergence. Investigations aimed at identifying further serpin family members are described below.
Conservation of RCL sequences in serpin genes
Many of the RCL sequences are strongly conserved across the Drosophilid lineage, over 40 million years. This is particularly the case with putative inhibitory serpins, Additional file 2. The general RCL consensus hinge region sequence (P17-P9) for inhibitory serpins is E [EKR]G [TS].(AGS)4 , being the 17-9th residues N-terminal to the P1/P1'proteinase cleavage site. In the Drosophilid lineage the hinge consensus includes the P8 residue, which is constrained to [TS] and the P13 residue is predominantly [ET]. The presence, or absence, of the hinge-region consensus E [EKAQR]G [TSG] [ET] [AGS] [YAGS] [AGS] [VAGS] [TS] separates the Drosophilid serpins unambiguously into two classes (see Additional file 2), with the exception of Spn100A, see below.
The RCL sequences of the majority of inhibitory serpins are strongly conserved among species, with almost complete identity of the putative P1/P1' sites (Spn27A, Spn28B, Spn28Da, Spn28Dc, Spn42Dc, Spn43Aa, Spn43Ac, Spn55B, Spn77Ba, Spn88Ea and Spn100A), Table 1, Figure 3 and Additional file 2. There are three exceptions to this general rule, where the evolutionary constraints appear to be looser: Spn28F, Spn42Db and Spn42Dd. The orthologues of these three serpins show divergent RCL sequences, with variable P1/P1'sites affecting specificity for putative target proteinases. That these RCL sequences were able to diverge implies that their corresponding ancestral serpins were, at least partially, redundant genetic functions.
In general, the substrate specificity of many serpins is broad and loss of the activity of one serpin may be compensated by a related activity. Where this occurs, the constraints on RCL sequence divergence will be less stringent than for strictly non-redundant serpin functions. In addition, the loss of inhibition of a particular proteinase could be compensated by inhibition of a different proteinase within the same cascade, by a serpin with a different inhibitory spectrum. By the criterion that they have conserved P1/P1'sites, the majority of inhibitory serpins in the Drosophilid genomes are non-redundant. In D. melanogaster, visible or lethal phenotypes are associated with lack of function mutations (Spn27A [18, 19, 22], Spn28Dc Spn42Da [23–25, 37, 38], Spn43Ac [16, 17], Spn77Ba ). The Japanese collection of RNAi knockdown strains includes eight of the seventeen inhibitory serpins (Table 1). Of these, 5 give a lethal phenotype (Spn27A, Spn38F, Spn43Aa, Spn43Ac and Spn55B) and three (Spn28F, Spn42De and Spn55B) are viable http://www.shigen.nig.ac.jp/fly/nigfly/index.jsp. These data sets are incomplete, but again indicate that many of the inhibitory serpins represent non-redundant genetic functions. There is no evidence for a general expansion of transcripts within complex loci as occurred within the vertebrate A and B serpin clades [29, 30, 32, 39].
In contrast, the RCLs of non-inhibitory serpin-fold proteins (Spn28Db, Spn31A, Spn43Ab, Spn43Ad, Spn47C, Spn53F, Spn76A, Spn77Bb, Spn77Bc, Spn85F and Spn100A) are weakly conserved, implying relaxed sequence constraints, Additional file 2. There are three exceptions, in which the RCL is extremely conserved (Spn31A, Spn43Ab and Spn85F). The RCLs of these three serpin-folds presumably bind to strongly-conserved partner molecules. Four (out of 12) of the non-inhibitory melanogaster serpin-folds have orthologues restricted to the melanogaster group.
The serpin core structure, of 3 β-pleated sheets and 8 or 9 α-helical linkers would be expected to be relatively unconstrained within the Drosophilid lineage. We find that the alignment scores between D. melanogaster and D. grimshawi, separated by about 40 Myr, are higher for the RCL sequences of inhibitory serpins than for their serpin cores (Table 2). In the non-inhibitory serpin-fold proteins, the alignment scores of the core and RCL regions are similar, with three exceptions where the RCL sequence is strongly conserved (Spn31A, Spn43Ab and Spn85F) and one where both core and RCL are moderately conserved (Spn100A) (Table 2).
Structure of serpin gene clusters
The Spn42D gene cluster contains widely diverged transcripts in melanogaster (Figure 1) corresponding to ancient duplication events that are conserved across the most of the Drosophilidae. Within the Spn42D complex, the Spn42Db and Spn42Dd genes show particularly labile RCL sequences, however, the overall structure of the complex locus is maintained. The structure of the alternatively-spliced Spn42Da transcription unit is maintained within the 5 species of the melanogaster sub-group, but the RCL sequences diverge increasingly in the 7 outgroup species . Similarly, the structure of the Spn43A complex is conserved, apart from the loss of the Spn43Ab gene in D. sechellia and the Spn43Ad gene in D. willistoni. In general, there is little evidence of variation of number of genes within complex loci, such as occurs in the vertebrate Clade A and Clade B lineages [39, 30–32].
The Spn77B and Spn88E gene clusters, on the other hand, contain transcripts with closely related sequences in melanogaster (Figure 1). The duplication/divergence events which gave rise to these clusters apparently occurred within the last 5 Myr in the melanogaster subgroup [40, 41]. The ancestral gene for the Spn77B cluster appears to be the inhibitory serpin Spn77Ba, which has orthologues in all the Drosophilid species. The Spn77Bb gene is unique to D. melanogaster, while the closely homologous Spn77Bc gene is found in D. melanogaster, D. simulans and D. sechellia. The Spn77Bb and Spn77Bc genes, therefore, appear to have arisen from recent duplication events; they are both non-inhibitory serpin-fold proteins, one putatively cell-autonomous (lacking an export signal) and the other secreted (carrying an export signal). Similarly, with the inhibitory Spn88Ea and Spn88Eb serpins, the ancestral gene would be Spn88Ea, with an RCL loop that is extremely conserved across the 12 species. The Spn88Eb gene appears to have arisen as a tandem duplication within the melanogaster sub-group and retains the S/A P1/P1' sites of Spn88Ea, except in melanogaster, where it is S/S. We have here an example of duplication of a serpin gene, divergence of the RCL sequence and, finally, modification of the putative proteinase cleavage site in melanogaster itself.
Similarly, the inhibitory Spn28Da and non-inhibitory Spn28Db serpins, are adjacent, closely related genes (Figure 1). They appear to represent duplications in the melanogaster group. The most likely ancestral sequence is the inhibitory Spn28B, which has a single intron, like Spn28Db. The Spn28Da duplication event was associated with loss of an intron and divergence of the inhibitory RCL sequence. The Spn28Db duplication event retained the single intron, but lost the conserved flexible hinge-residues characteristic of inhibitory RCL sequences. In general, it should be more frequent for non-inhibitory serpin-fold to evolve from an active inhibitor than the reverse; a single substitution within the conserved hinge-region motif can inactivate the inhibitory mechanism ; while a series of changes in a non-inhibitory serpin-fold would be required to generate the hinge-region consensus. We did not identify any sets of orthologues that contained both inhibitory and non-inhibitory serpins, which ought to have been identified by the synteny approach. The absence of such mixed sets of inhibitory and non-inhibitory orthologues again implies that the evolution of serpin function is constrained, in the absence of duplication/divergence events.
Sporadic loss and gain of individual genes
The D. melanogaster minimum evolution tree (Figure 1) indicates that the Spn28F, Spn38F, Spn28B, Spn42D, Spn28Db and Spn28Da genes are related. Within this group, Spn28F and Spn38F are closely related and, like Spn42Dd, contain 3 introns. The transcripts of the Spn28 cluster, on the other hand, contain one, or no, introns and, on this basis, represent a separate sub-group. The identified orthologues of all six of these genes are restricted to the melanogaster species sub-group, with the exception of Spn42Dd, which also has identified orthologues in ananassae and the pseudobscura sub-group. The most parsimonious interpretation of the relationship of the Spn28F and Spn38F genes is that they represent recent duplication/divergence events within the melanogaster sub-group lineage. Similarly, we identified two orthologues for Spn28F in D. ananassae, which represent a presumptive duplication in this species, and failed to identify a Spn28F orthologue in D. sechellia, indicating a presumptive loss. As mentioned above, the putative P1/P1' sites of the Spn28F orthologues are variable within the melanogaster group implying a degree of functional redundancy; which is consistent with the loss of this orthologues in D. sechellia.
Apart from these instances there is little evidence of loss and gain of serpin genes. As discussed in the previous section, the Spn77B gene cluster in melanogaster, represents a set of recent duplication events, the Spn88Eb gene corresponds to a recent duplication in the melanogaster sub-group and the Spn43Ad gene is missing in D. willistoni. In general, loss and gain of serpin genes is rare in the Drosophilid lineage.
That said, we might have failed to detect additional transposition/divergence events in the more distant species to D. melanogaster. If such events had occurred, the loose sequence constraints on the serpin core would allow transposed genes to diverge rapidly, so that they would be difficult to identify by homology. Furthermore, single amino-acid substitutions in the RCL of an inhibitory serpin can completely alter its substrate specificity . The functions of the inhibitory serpins with orthologues restricted to the melanogaster sub-group could be replaced in the out-groups by serpins carrying similar P1/P1' residues in their RCLs attached to very distantly related serpin cores. Thus the melanogaster outgroups may well have additional serpin genes that we fail to identify by either homology or synteny.
A particular case of divergence/duplication of serpin inhibitory function can occur within the alternatively-spliced RCL-encoding exons of Spn42Da. Alternatively-spliced serpins were first identified in Bombyx mori , although the genetic mechanism was only later described in Manduca sexta [44, 45]. Similar alternative-exon cassettes have been described in Anopheles  and Caenorhabditis , although to date no mammalian examples are known. In the Drosophilid lineage, the furin-inhibitory RCL (exon 5) is maintained in all species as well as exons 6-8 in the melanogaster sub-group, but the corresponding exons duplicate and diverge in the 7 outgroup species . It might be expected that some of the inhibitory serpin orthologues that we failed to identify in the outgroup species were complemented by inhibitory functions on the alternative-exon cassettes of the Spn42Da orthologues. This appears not to be the case by the criterion that the putative P1/P1'sites of these melanogaster serpins (i.e: K/K, L/S, Y/S, K/S, R/A, E/S and S/S; corresponding to Spn28B, Spn28Da, Spn28Db, Spn38F, Spn42Dd, Spn42De and Spn88Eb) see Table 1, do not correspond to the P1/P1'sites on the novel alternative-exon cassettes in the outgroup species (i.e: D. ana S/R, C/S, L/S; D. per C/S, S/R; D. pse C/S, S/R; D. wil R/S, S/A, S/Y, C/S, R/I; D. moj L/T, E/M; D. vir R/T, E/M, D/S and D. gri G/M, E/M, M/L, D/M, R/A, L/M), information extracted from Figures 2, 3, 4 .
Conservation of N-terminal and serpin core sequences of Spn43Ac and Spn100A
The serpins are generally between 350 and 400 amino-acids in length, with very few having either N- or C-terminal extensions to the core serpin domain. One of the few human serpins with an N-terminal peptide, Heparin cofactor II, shows reduced substrate specificity after N-terminal cleavage . Similarly, the Drosophila melanogaster Spn43Ac (Nec) serpin has a long N-terminal extension, which is cleaved on immune challenge . In the case of Spn43Ac, both the full length protein and the cleaved core serpin are active proteinase inhibitors in vitro, but the core serpin shows increased substrate specificity for porcine pancreatic elastase (PPE) . Alignment of the Spn43Ac orthologues shows that the N-terminal extension is present throughout the Drosophilidae (see Additional file 3). This peptide varies in length between 69 amino acids (D. sechellia) and 145 amino acids in (D. grimshawi) with poor sequence conservation, other than the putative R/P scissile bond (see Additional file 3). A long, unstructured N-terminal extension appears to be critical for the function of the Spn43Ac orthologues, but its precise length and sequence are weakly constrained. Note the poor sequence conservation within Spn43Ac serpin core sequence, with the exception of the exposed RCL.
The Spn100A transcript encodes a putative 653 amino acid protein, which is outside the normal serpin size-range. The sequence shows two blocks of serpin homology: an N-terminal stretch of 44 amino acids and a C-terminal stretch of 235 amino acids, separated by an insertion of 294 amino-acids (Pfam alignment) (see Additional file 4). This structure is supported by comparison of genomic and cDNA sequences, which show a single intron of 87 bp in D. melanogaster. The novel internal segment of 294 amino acids can not, therefore, correspond to read-through of a nested transcript. The C-terminal of the Spn100 protein includes a putative RCL, including some of the flexible hinge region residues characteristic of inhibitory serpins. The alignment of the N- and C-terminal serpin domains is conserved in all 11 Drosophilid orthologues, and the amino-acid sequence conservation is similar across the whole length of the protein. The implication is that the Spn100A gene encodes a novel, serpin-derived, protein fold. Novel protein folds arise extremely infrequently and a mechanism involving chimeric transcripts formed from segments of pre-existing peptide-coding sequence has been proposed . Database searches identify Spn100A orthologues in mosquitoes and other insects, but not in other organisms.
Comparison of Drosophilid and vertebrate serpins
Vertebrate genomes contain a large, but variable number, of serpins and proteinases. The human complement of 35 serpins and 176 chymotrypsin-fold serine proteinases is increased to 64 and 227 in the mouse, with many of the differences being in genes involved in reproduction and immunity . Against this background, the D. melanogaster genome contains 29 serpins and 211 chymotrypsin-fold serine proteinases, with Spn42Da encoding 11 isoforms, with or without a signal peptide. A large proportion of these serpins have immune-related functions, or are expressed in the reproductive track. Comparison of human and mouse genomes shows that the serpins of nine of the vertebrate clades show conserved numbers and synteny, with the variations being restricted to clades A and B. In particular, the mouse clade A serpins have expanded, with human α1-antitrypsin being represented by a cluster of 5 genes in the mouse, and human α1-Antitrypsin being represented by a cluster of 14 genes. Similarly, 4 of the human clade B serpins are represented by clusters of 3 to 7 genes in the mouse [29, 31, 32]. A striking feature of this expansion in the mouse lineage, is that many of the RCL sequences are unique , novel sets of proteinases are being targeted. We find no evidence of a similar massive amplification of serpin genes in the Drosophilid lineage, although the melanogaster Spn77B and Spn88E clusters appear to represent recent tandem duplications. The one example of extensive duplication/divergence of serpin inhibitory functions that has been identified in the Drosophilid lineage is within the novel alternative-exon cassettes of the Spn42Da orthologues . As in the mouse clade A and B expansions, novel sets of proteinases are being targeted by the diverged alternative-exon cassettes (see above).
An essential component of the serpin suicide-inhibition mechanism, is that the cut RCL sequence inserts between two strands of β-sheetA, as the metastable serpin structure relaxes. As a consequence, it is possible for the RCL of one serpin to insert between β-sheetA of another in the absence of enzymatic cleavage, to form an inert, stable polymer [52, 53]. Under normal physiological conditions, this tendency is low, but it represents a constraint on serpin evolution and mutations which alter the stability of the serpin core can favour polymer formation. Such mutations underlie a set of human genetic diseases, including the Z-allele α1-antitrypsin serpinopathy  and conformational dementias . Similar constraints on the stability of the serpin core have been demonstrated in Drosophila, with the isolation of polymerogenic mutations of Spn43Ac (Necrotic) showing homologous amino acid substitutions to Z-allele α1-antitrypsin and other pathogenic serpin variants [56, 57].
We have developed a synteny search algorithm which is a powerful tool for identifying orthologous members of multi-gene families within related species. In the Drosophilid lineage, the majority of inhibitory serpin orthologues show a striking conservation of the critical the P1/P1' proteinase cleavage sites, indicating that these inhibitors do not readily change specificity for their target proteinases. Despite this, the distribution of orthologues is quite patchy: many D. melanogaster serpins have no identified orthologues in the more distant species. The balance between inhibitory serpins and the target proteinases that they control forms a strong evolutionary constraint. The majority of Drosophilid inhibitory serpin orthologues appear to represent non-redundant genetic functions, with strong constraints on the P1/P1'sites. Three complex loci in D. melanogaster appear to represent recent duplication/divergence events where the sequence constraints have been relaxed. Each complex contains a putative ancestral inhibitory serpin, with orthologues across the whole Drosophilid lineage, plus one or two genes restricted to the melanogaster group. Taken together our analyses imply that evolution within the Drosophilid serpin super-family has occurred predominantly by a gene duplication/divergence mechanism.
To assemble a curated set of serpin sequences within the Drosophilidae, we first compiled the orthologues from a tBLASTx search of the 12-species genes extracted from FlyBase http://flybase.bio.indiana.edu/. Additional serpins were identified using a synteny based approach, which relies on the conservation of the order of chromosomal transcripts between related species. The synteny search code is given in Additional file 5. Genes adjacent to serpin genes in Drosophila melanogaster were used to identify the corresponding region within the other Drosophilid genome sequence assemblies. Where the two adjacent genes on either side of a Drosophila melanogaster serpin could be uniquely resolved to orthologues in other species, the intervening sequence was examined for putative serpin genes. Where the adjacent gene orthologues could not be resolved in a given species, the process was repeated with more distant genes, up to a maximum of 3 genes from the original D. melanogaster serpin. Any putative matches were compared to the original serpin protein by tBLASTx alignment . High-scoring matches were considered to be likely orthologues on the basis of both synteny and sequence conservation. A final tBLASTx search was made using all the Drosophilid serpin genes identified in the previous searches as queries against all 12 Drosophilid genomes. The sets of serpin amino-acid sequences were aligned using CLUSTALW. Minimum evolution bootstraps were built using MEGA4  for each serpin within each Drosophilid species.
- Serpin (Spn):
Serine proteinase inhibitor
Reactive centre loop
proteinase cleavage site
Irving JA, Pike RN, Lesk AM, Whisstock JC: Phylogeny of the serpin superfamily: implications of patterns of amino acid conservation for structure and function. Genome Res. 2000, 10: 1845-1864. 10.1101/gr.GR-1478R.
Carrell RW, Travis J: alpha 1-Antitrypsin and the serpins: variation and countervariation. TIBS. 1986, 10: 20-24.
Huntington JA, Read RJ, Carrell RW: Structure of a serpin-protease complex shows inhibition by deformation. Nature. 2000, 407: 923-926. 10.1038/35038119.
Hopkins PC, Carrell RW, Stone SR: Effects of mutations in the hinge region of serpins. Biochemistry. 1993, 32: 7650-7657. 10.1021/bi00081a008.
Reichhart JM: Tip of another iceberg: Drosophila serpins. Trends Cell Biol. 2005, 15: 659-665. 10.1016/j.tcb.2005.10.001.
Gubb D, Dafforn T, Troxler L, Reichhart J-M: Drosophila serpins: regulatory cascades in innate immunity and morphogenesis. Molecular and cellular aspects of the serpinopathies and disorders of serpin activity. Edited by: Silverman G, Lomas D. 2007, Singapore: World Scientific Publishing, 207-227. full_text.
Bruce D, Perry DJ, Borg JY, Carrell RW, Wardell MR: Thromboembolic disease due to thermolabile conformational changes of antithrombin Rouen-VI (187 Asn-->Asp). J Clin Invest. 1994, 94: 2265-2274. 10.1172/JCI117589.
Cicardi M, Bergamaschini L, Cugno M, Beretta A, Zingale LC, Colombo M, Agostoni A: Pathogenetic and clinical aspects of C1 inhibitor deficiency. Immunobiology. 1998, 199: 366-376.
Providence KM, Higgins PJ: PAI-1 expression is required for epithelial cell migration in two distinct phases of in vitro wound repair. J Cell Physiol. 2004, 200: 297-308. 10.1002/jcp.20016.
Clarke EP, Cates GA, Ball EH, Sanwal BD: A collagen-binding protein in the endoplasmic reticulum of myoblasts exhibits relationship with serine protease inhibitors. J Biol Chem. 1991, 266: 17230-17235.
Dafforn TR, Della M, Miller AD: The molecular interactions of heat shock protein 47 (Hsp47) and their implications for collagen biosynthesis. J Biol Chem. 2001, 276: 49310-49319. 10.1074/jbc.M108896200.
Potempa J, Korzus E, Travis J: The serpin superfamily of proteinase inhibitors: structure, function, and regulation. J Biol Chem. 1994, 269: 15957-15960.
Grigoryev SA, Bednar J, Woodcock CL: MENT, a heterochromatin protein that mediates higher order chromatin folding, is a new serpin family member. J Biol Chem. 1999, 274: 5626-5636. 10.1074/jbc.274.9.5626.
Liu T, Pemberton PA, Robertson AD: Three-state unfolding and self-association of maspin, a tumor-suppressing serpin. J Biol Chem. 1999, 274: 29628-29632. 10.1074/jbc.274.42.29628.
Huntington JA, Pannu NS, Hazes B, Read RJ, Lomas DA, Carrell RW: A 2.6 A structure of a serpin polymer and implications for conformational disease. J Mol Biol. 1999, 293: 449-455. 10.1006/jmbi.1999.3184.
Green C, Levashina E, McKimmie C, Dafforn T, Reichhart JM, Gubb D: The necrotic gene in Drosophila corresponds to one of a cluster of three serpin transcripts mapping at 43A1.2. Genetics. 2000, 156: 1117-1127.
Levashina EA, Langley E, Green C, Gubb D, Ashburner M, Hoffmann JA, Reichhart JM: Constitutive activation of toll-mediated antifungal defense in serpin-deficient Drosophila. Science. 1999, 285: 1917-1919. 10.1126/science.285.5435.1917.
De Gregorio E, Han SJ, Lee WJ, Baek MJ, Osaki T, Kawabata S, Lee BL, Iwanaga S, Lemaitre B, Brey PT: An immune-responsive Serpin regulates the melanization cascade in Drosophila. Dev Cell. 2002, 3: 581-592. 10.1016/S1534-5807(02)00267-8.
Ligoxygakis P, Pelte N, Ji C, Leclerc V, Duvic B, Belvin M, Jiang H, Hoffmann JA, Reichhart JM: A serpin mutant links Toll activation to melanization in the host defence of Drosophila. Embo J. 2002, 21: 6330-6337. 10.1093/emboj/cdf661.
Scherfer C, Tang H, Kambris Z, Lhocine N, Hashimoto C, Lemaitre B: Drosophila Serpin-28D regulates hemolymph phenoloxidase activity and adult pigmentation. Dev Biol. 2008, 323: 189-196. 10.1016/j.ydbio.2008.08.030.
Tang H, Kambris Z, Lemaitre B, Hashimoto C: A serpin that regulates immune melanization in the respiratory system of Drosophila. Dev Cell. 2008, 15: 617-626. 10.1016/j.devcel.2008.08.017.
Ligoxygakis P, Roth S, Reichhart JM: A serpin regulates dorsal-ventral axis formation in the Drosophila embryo. Curr Biol. 2003, 13: 2097-2102. 10.1016/j.cub.2003.10.062.
Richer MJ, Keays CA, Waterhouse J, Minhas J, Hashimoto C, Jean F: The Spn4 gene of Drosophila encodes a potent furin-directed secretory pathway serpin. Proc Natl Acad Sci USA. 2004, 101: 10560-10565. 10.1073/pnas.0401406101.
Oley M, Letzel MC, Ragg H: Inhibition of furin by serpin Spn4A from Drosophila melanogaster. FEBS Lett. 2004, 577: 165-169. 10.1016/j.febslet.2004.10.003.
Osterwalder T, Kuhnen A, Leiserson WM, Kim YS, Keshishian H: Drosophila serpin 4 functions as a neuroserpin-like inhibitor of subtilisin-like proprotein convertases. J Neurosci. 2004, 24: 5482-5491. 10.1523/JNEUROSCI.5577-03.2004.
Gettins PG: Serpin structure, mechanism, and function. Chem Rev. 2002, 102: 4751-4804. 10.1021/cr010170+.
Bode W, Huber R: Natural protein proteinase inhibitors and their interaction with proteinases. Eur J Biochem. 1992, 204: 433-451. 10.1111/j.1432-1033.1992.tb16654.x.
Gettins PGW: Mechanisms of Serpin Inhibition. Molecular and cellular aspects of the serpinopathies and disorders of serpin activity. Edited by: Silverman G, Lomas D. 2007, Singapore: World Scientific Publishing, 207-227.
Askew DJ, Coughlin P, Bird PI: Mouse serpins and transgenic studies. Molecular and cellular aspects of the serpinopathies and disorders in serpin activity. Edited by: Silverman G, Lomas D. 2007, Singapore: World Scientific Publishing, 207-227.
Kaiserman D, Bird PI: Analysis of vertebrate genomes suggests a new model for clade B serpin evolution. BMC Genomics. 2005, 6: 167-10.1186/1471-2164-6-167.
Askew DJ, Askew YS, Kato Y, Luke CJ, Pak SC, Bromme D, Silverman GA: The amplified mouse squamous cell carcinoma antigen gene locus contains a serpin (Serpinb3b) that inhibits both papain-like cysteine and trypsin-like serine proteinases. Genomics. 2004, 84: 166-175. 10.1016/j.ygeno.2004.01.014.
Askew DJ, Askew YS, Kato Y, Turner RF, Dewar K, Lehoczky J, Silverman GA: Comparative genomic analysis of the clade B serpin cluster at human chromosome 18q21: amplification within the mouse squamous cell carcinoma antigen gene locus. Genomics. 2004, 84: 176-184. 10.1016/j.ygeno.2004.01.015.
Sturtevant AH, Tan CC: The comparative genetics of Drosophila pseudoobscura and Drosophila melanogaster. J Genet. 1937, 34: 415-432. 10.1007/BF02982303.
Sturtevant AH, Novitski E: The Homologies of the Chromosome Elements in the Genus Drosophila. Genetics. 1941, 26: 517-541.
Schaeffer SW, Bhutkar A, McAllister BF, Matsuda M, Matzkin LM, O'Grady PM, Rohde C, Valente VL, Aguade M, Anderson WW, et al: Polytene chromosomal maps of 11 Drosophila species: the order of genomic scaffolds inferred from genetic and physical maps. Genetics. 2008, 179: 1601-1655. 10.1534/genetics.107.086074.
Bhutkar A, Schaeffer SW, Russo SM, Xu M, Smith TF, Gelbart WM: Chromosomal rearrangement inferred from comparisons of 12 Drosophila genomes. Genetics. 2008, 179: 1657-1680. 10.1534/genetics.107.086108.
Bruning M, Lummer M, Bentele C, Smolenaars MM, Rodenburg KW, Ragg H: The Spn4 gene from Drosophila melanogaster is a multipurpose defence tool directed against proteases from three different peptidase families. Biochem J. 2007, 401: 325-331. 10.1042/BJ20060648.
Borner S, Ragg H: Functional diversification of a protease inhibitor gene in the genus Drosophila and its molecular basis. Gene. 2008, 415: 23-31. 10.1016/j.gene.2008.02.004.
Inglis JD, Hill RE: The murine Spi-2 proteinase inhibitor locus: a multigene family with a hypervariable reactive site domain. Embo J. 1991, 10: 255-261.
Lemeunier F, Ashburner M: Studies on the evolution of the melanogaster species subgroup of the genus Drosophila (Sophophora). II. Phylogenetic relationships of six species based upon polytene chromosome banding patterns. Proc R Soc Lond. 1976, 193: 275-294. 10.1098/rspb.1976.0046.
Lachaise D, Capy P, Cariou M-L, Joly D, Lemeunier F, David JR: Nine relatives from one African ancestor: population biology and evolution of the Drosophila melanogaster subgroup species. 2004, Cambridge University Press, UK
Hopkins PC, Crowther DC, Carrell RW, Stone SR: Development of a novel recombinant serpin with potential antithrombotic properties. J Biol Chem. 1995, 270: 11866-11871. 10.1074/jbc.270.20.11866.
Sasaki T: Patchwork-structure serpins from silkworm (Bombyx mori) larval hemolymph. Eur J Biochem. 1991, 202: 255-261. 10.1111/j.1432-1033.1991.tb16370.x.
Jiang H, Wang Y, Kanost MR: Mutually exclusive exon use and reactive center diversity in insect serpins. J Biol Chem. 1994, 269: 55-58.
Jiang H, Wang Y, Huang Y, Mulnix AB, Kadel J, Cole K, Kanost MR: Organization of serpin gene-1 from Manduca sexta. Evolution of a family of alternate exons encoding the reactive site loop. J Biol Chem. 1996, 271: 28017-28023. 10.1074/jbc.271.45.28017.
Danielli A, Kafatos FC, Loukeris TG: Cloning and characterization of four Anopheles gambiae serpin isoforms, differentially induced in the midgut by Plasmodium berghei invasion. J Biol Chem. 2003, 278: 4184-4193. 10.1074/jbc.M208187200.
Kruger O, Ladewig J, Koster K, Ragg H: Widespread occurrence of serpin genes with multiple reactive centre-containing exon cassettes in insects and nematodes. Gene. 2002, 293: 97-105. 10.1016/S0378-1119(02)00697-2.
Baglin TP, Carrell RW, Church FC, Esmon CT, Huntington JA: Crystal structures of native and thrombin-complexed heparin cofactor II reveal a multistep allosteric mechanism. Proc Natl Acad Sci USA. 2002, 99: 11079-11084. 10.1073/pnas.162232399.
Pelte N, Robertson AS, Zou Z, Belorgey D, Dafforn TR, Jiang H, Lomas D, Reichhart JM, Gubb D: Immune challenge induces N-terminal cleavage of the Drosophila serpin Necrotic. Insect Biochem Mol Biol. 2006, 36: 37-46. 10.1016/j.ibmb.2005.10.004.
Alva V, Koretke KK, Coles M, Lupas AN: Cradle-loop barrels and the concept of metafolds in protein classification by natural descent. Curr Opin Struct Biol. 2008, 18: 358-365. 10.1016/j.sbi.2008.02.006.
Puente XS, Sanchez LM, Overall CM, Lopez-Otin C: Human and mouse proteases: a comparative genomic approach. Nat Rev Genet. 2003, 4: 544-558. 10.1038/nrg1111.
Lomas DA, Evans DL, Finch JT, Carrell RW: The mechanism of Z alpha 1-antitrypsin accumulation in the liver. Nature. 1992, 357: 605-607. 10.1038/357605a0.
Yamasaki M, Li W, Johnson DJ, Huntington JA: Crystal structure of a stable dimer reveals the molecular basis of serpin polymerization. Nature. 2008, 455: 1255-1258. 10.1038/nature07394.
Lomas DA: Molecular mousetraps, alpha1-antitrypsin deficiency and the serpinopathies. Clin Med. 2005, 5: 249-257.
Lomas DA, Carrell RW: Serpinopathies and the conformational dementias. Nat Rev Genet. 2002, 3: 759-768. 10.1038/nrg907.
Green C, Brown G, Dafforn TR, Reichhart JM, Morley T, Lomas DA, Gubb D: Drosophila necrotic mutations mirror disease-associated variants of human serpins. Development. 2003, 130: 1473-1478. 10.1242/dev.00350.
Carrell R, Corral J: What can Drosophila tell us about serpins, thrombosis and dementia?. Bioessays. 2004, 26: 1-5. 10.1002/bies.10407.
Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ: Basic local alignment search tool. J Mol Biol. 1990, 215: 403-410.
Tamura K, Dudley J, Nei M, Kumar S: Molecular Evolutionary Genetics Analysis (MEGA) software version 4.0. Mol Biol Evol. 2007, 24: 1596-1599. 10.1093/molbev/msm092.
This work was supported by a Spanish Ministry of Education and Science grant and a Basque Government Department of Education, Universities and Research grant to D. Gubb. Additional support was provided from The Department of Industry, Tourism and Trade of the Government of the Autonomous Community of the Basque Country (Etortek Research Programs) and from the Innovation Technology Department of Bizkaia County. Matthew Garrett was supported by an MRC Ph.D. studentship and Ane Fullaondo was supported by a Basque Government Department of Education, Universities and Research Ph.D studentship.
MG wrote the synteny search code and extracted the orthologous genes from the genomic sequence databases. AF collated and analysed the sequence data. DG and AF wrote the manuscript. LT identified and corrected several alignment errors and incomplete gene sequences. GM participated in the design of search strategies and critically reviewed the manuscript.
Matthew Garrett, Ane Fullaondo contributed equally to this work.