Molecular co-evolution of a protease and its substrate elucidated by analysis of the activity of predicted ancestral hatching enzyme
© Kawaguchi et al.; licensee BioMed Central Ltd. 2013
Received: 31 May 2013
Accepted: 23 October 2013
Published: 25 October 2013
Hatching enzyme is a protease that digests the egg envelope, enabling hatching of the embryo. We have comprehensively studied the molecular mechanisms of the enzyme action to its substrate egg envelope, and determined the gene/protein structure and phylogenetic relationships. Because the hatching enzyme must have evolved while maintaining its ability to digest the egg envelope, the hatching enzyme-egg envelope protein pair is a good model for studying molecular co-evolution of a protease and its substrate.
Hatching enzymes from medaka (Oryzias latipes) and killifish (Fundulus heteroclitus) showed species-specific egg envelope digestion. We found that by introducing four medaka-type residue amino acid substitutions into recombinant killifish hatching enzyme, the mutant killifish hatching enzyme could digest medaka egg envelope. Further, we studied the participation of the cleavage site of the substrate in the species-specificity of hatching enzyme. A P2-site single amino acid substitution was responsible for the species-specificity. Estimation of the activity of the predicted ancestral enzymes towards various types of cleavage sites along with prediction of the evolutionary timing of substitutions allowed prediction of a possible evolutionary pathway, as follows: ancestral hatching enzyme, which had relatively strict substrate specificity, developed broader specificity as a result of four amino acid substitutions in the active site cleft of the enzyme. Subsequently, a single substitution occurred within the cleavage site of the substrate, and the recent feature of species-specificity was established in the hatching enzyme-egg envelope system.
The present study clearly provides an ideal model for protease-substrate co-evolution. The evolutionary process giving rise to species-specific egg envelope digestion of hatching enzyme was initiated by amino acid substitutions in the enzyme, resulting in altered substrate specificity, which later allowed an amino acid substitution in the substrate.
KeywordsCo-evolution Hatching enzyme Astacin family Egg envelope Chorion ZP domain Ancestral hatching enzyme
Many proteins co-evolve as a result of protein-protein interaction, and maintain or diversify their functions. This interaction is often complicated, so elucidation of the co-evolutionary process is difficult in many cases. The hatching enzyme of teleost species is secreted by the embryo to digest the egg envelope that surrounds the embryo and protects it from environmental, chemical, and mechanical stresses [1–4]. Considering that hatching enzyme would have evolved while maintaining the ability to digest the egg envelope, the hatching enzyme-egg envelope protein pair is a good model system for understanding molecular co-evolution of a protease and its substrate.
Both egg envelope protein and hatching enzyme have been studied in the model fish medaka (Oryzias latipes). The egg envelope consists of thick inner layers and a thin outer layer. The inner layers are composed of two groups of subunit proteins called ZI-1,2 and ZI-3 , which are classified into vertebrate-common egg envelope protein groups ZPB and ZPC, respectively [6, 7]. ZI-1,2 are heterogeneous glycoproteins derived from the precursors choriogenin H and H minor. ZI-3 is a homogenous glycoprotein derived from the precursor choriogenin L [8–10]. Both ZI-1,2 and ZI-3 have a zona pellucida (ZP) domain consisting of about 260 amino acids, with eight conserved cysteine residues . Additional characteristics of ZI-1,2 include a Pro-Xaa-Yaa repeat region and a trefoil domain upstream of the ZP domain.
Hatching enzyme is a member of the astacin metallo-protease family. Medaka possesses two types of hatching enzymes, high choriolytic enzyme (HCE; choriolysin H; EC 220.127.116.11) and low choriolytic enzyme (LCE; choriolysin L; EC 18.104.22.168) [12–14]. At hatching, both enzymes simultaneously act on the egg envelope and completely solubilize its inner layers . The thin filamentous outer layer remains undigested and is broken by embryo movement. Studies have shown that the molecular mechanism of the enzymes is as follows: HCE swells the envelope by cleaving the N-terminal region of egg envelope proteins, especially the Pro-Xaa-Yaa repeat region on ZI-1,2, into small pieces [15, 16]. LCE solubilizes the HCE-swollen envelope by cleaving only two sites, the N-terminal of the ZP domain of ZI-3, and the middle of the ZP domain of ZI-1,2 . Because ZP domains assemble each other to form a higher-order architecture as the egg envelope [17, 18], cleavage of the middle of the ZP domain by LCE may change the higher-order structure of the egg envelope and lead to its complete digestion . Indeed, our group recently uncovered the importance of the middle region of the ZP domain (mid-ZPd) for solubilization, as demonstrated by the following findings : the nine-spined stickleback possessed two types of LCE, LCEα and LCEβ, formed by gene duplication. LCEα cleaved the N-ZPd site but not the mid-ZPd site, while LCEβ cleaved only the mid-ZPd site but not the N-ZPd site. When only the N-ZPd site was cleaved by LCEα, the egg envelope was not solubilized, but remained swollen. The swollen egg envelope was solubilized only after the mid-ZPd site was cleaved by LCEβ. Thus, the mid-ZPd region is a key site for egg envelope solubilization.
Comparative studies have shown that the egg envelope digestion mechanism is conserved between medaka and Fundulus species. Fundulus possesses two isoforms of HCE, called FHCE1 and FHCE2, both of which swell the egg envelope . Fundulus LCE then solubilizes the swollen envelope completely [20, 21]. The positions of cleavage sites for Fundulus HCE (FHCE1/2) and LCE (FLCE) are similar to those of medaka HCE (MHCE) and LCE (MLCE) .
Recently, we identified both cross-species similarities and differences in the modes of action of hatching enzymes from medaka and Fundulus. When incubated with Fundulus hatching liquid containing both HCEs and LCE, the medaka egg envelope was swollen, but not solubilized . In addition, we found that isolated Fundulus HCEs swelled the medaka egg envelope, but that isolated Fundulus LCE did not digest the swollen medaka egg envelope. Therefore, mode of action of HCE is common to both Fundulus and medaka, but the action of LCE in egg envelope digestion is substrate-specific.
In the present study, we identified the amino acid residues of LCE responsible for conferring the specificity in egg envelope digestion, and discuss a molecular co-evolutionary pathway for hatching enzyme and egg envelope protein in a teleostean lineage, based on data obtained from the reconstruction and activities of probable ancestral forms of teleostean LCEs.
Species specificity of hatching enzyme from medaka and Fundulus
In contrast to HCE, LCE could only digest the swollen envelope of the species from which it originated (Figure 1A and 1D). Medaka LCE (MLCE) sharply increased solubilization of the swollen medaka egg envelope with incubation time, whereas MLCE only slightly solubilized that of Fundulus (Figure 1C). Similarly, Fundulus LCE (FLCE) efficiently solubilized the swollen envelope of Fundulus, but not that of medaka (Figure 1 F). These results suggested that LCE activity is substrate-specific in medaka and Fundulus.
Identification of key amino acid residues responsible for the species-specificity of LCE activity
(i) Egg envelope protein
FLCE cleaved the Fundulus mid-ZPd peptide (peptide 1), but not the medaka peptide (peptide 2) (Figure 2A), confirming the species-specificity of egg envelope digestion. MLCE digested the mid-ZPd peptides from both Fundulus and medaka (Figure 2B), suggesting that the species specificity of MLCE does not depend on the peptide sequence around the cleavage site. Because egg envelope has an insoluble macro-molecular structure, the species specificity of MLCE for cleavage of the intact swollen egg envelope may be due to the enzyme-to-substrate interaction in a higher-ordered conformation.
Next, we constructed mutant peptides of the mid-ZPd region whose residue(s) were substituted with either Fundulus- ormedaka-type residues (peptides 3–10). As shown in Figure 2A, FLCE only cleaved peptides 1, 3, and 6, all of which possess the common residue L at the P2 site . L to P substitution at the P2 site of the Fundulus peptide significantly reduced the activity of FLCE. In contrast, P to L substitution at the corresponding site of the medaka peptide enabled FLCE activity. These results suggested that the FLCE-specific digestion could be explained by the presence of L at the P2 site in the FLCE-cleavage site on the substrate.
(ii) Hatching enzyme
First, we focused on substitutions between amino acids with distinctly different properties, such as negative, positive, uncharged polar, and/or non-polar amino acids. Among the 20 substitutions, 10 sites showed such differences. These 10 residues in FLCE were substituted with medaka-type residues and named FLCE_mu10 (Figure 3A and C). FLCE_mu10 completely digested the swollen medaka egg envelope (Figure 4A). In addition, FLCE_mu10 had sufficient activity to cleave the medaka mid-ZPd peptide, and its Km value was similar to that of rMLCE (Figure 4E). Therefore, these 10 substitutions were sufficient to cause the FLCE-specific LCE activity.
The next strategy was as follows: two of the 10 mutations were returned to Fundulus-types, and named FLCE_mu10. If the returned residue(s) was an important site(s), the peptide cleavage activity of these mutant rFLCEs would decrease, and if not, the activity would not change. We generated five mutant rFLCEs, named FLCE_mu8a to 8e, whose returned sites are shown in Figure 3A. Only FLCE_mu8d did not change the peptide cleavage activity (Figure 4B). These observations suggested that some of the eight mutations (K3M, F74K, R79Y, P91F, N95K, K135H, K138D, and R183T) were important for the species specificity of FLCE.
Similar to the above strategy, one of the eight mutations was next returned to the Fundulus-type residue and named FLCE_mu8d. Eight separate mutant rFLCEs were generated, which were named FLCE_mu8d_“returned site”. As shown in Figure 4C, four of these eight mutant rFLCEs had decreased peptide cleavage activity, suggesting that F74K, P91F, K135H, and R183T were important substitutions for FLCE activity and species specificity.
Finally, we introduced these four mutations into FLCE and generated recombinant FLCE_mu4 (Figure 3A and B). As shown in Figure 4D, FLCE_mu4 completely solubilized the swollen medaka egg envelope, and its peptide cleavage activity was similar to that of rMLCE (Figure 4D). Therefore, the four residues at positions 74, 91, 135, and 183 were determined to be essential for the species specificity of FLCE.
To determine the contribution of the four FLCE sites to egg envelope digestion, we further individually returned one of the four sites of FLCE_mu4 to the Fundulus type, generating four new mutant rFLCEs, named FLCE_mu4_“returned site”. All the mutant rFLCEs decreased the peptide-cleaving activity (Figure 4D). FLCE_mu4_K74F and FLCE_mu4_T183R lost activity and, in addition, did not solubilize the swollen medaka egg envelope. The Km values of FLCE_mu4_K74F and FLCE_mu4_T183R toward the medaka peptide increased by 1.5- and 3.3-fold compared with that of FLCE_mu4, respectively, suggesting that the affinity of the mutant rFLCEs for the substrate was reduced due to the mutation at either position 74 or 183. Also, in terms of the egg envelope-solubilizing activity, residues at positions 74 and 183 appear to play a critical role in the species specificity of FLCE.
On the other hand, FLCE_mu4_F91P partially digested the swollen medaka egg envelope (Figure 4D and F), and its Km value was similar to that of rMLCE (Figure 4E). Although FLCE_mu4_H135K had the lowest activity toward the medaka mid-ZPd peptide among the four mutants, it completely solubilized the swollen medaka egg envelope. When positions 74 and 183 on rFLCE were substituted to the medaka types, mutant rFLCE (FLCE_F74K&R183T) could not solubilize the swollen medaka egg envelope. This result suggested that positions 91 and 135 are also necessary for the complete egg envelope solubilization. The cleavage of mid-ZPd may be dependent on more complicated enzyme-substrate interaction, in addition to recognition of primary sequence of the cleavage site. We conclude that these four residues are required for FLCE to maintain suitable activity towards the cleavage site peptide and to digest the swollen medaka egg envelope.
Substrate preference of LCEs
Next, we evaluated the P2 site preference of LCE by introducing four mutations at positions 74, 91, 135, and 183 that are important for the species specificity of LCE. When medaka-type residues were introduced into Fundulus FLCE (FLCE_mu4), its activity was similar to that of medaka rMLCE (Figure 5D). When Fundulus-type residues were introduced into medaka MLCE (MLCE_mu4), its activity was altered to that of the Fundulus type (Figure 5C). Therefore, we confirmed that the P2 site preference of LCEs was determined by the four amino acid residues in LCE.
A co-evolutionary pathway for hatching enzyme and egg envelope protein
The ancestral euteleostean LCE was predicted to have had 74 F, 91 F, 135Y, and 183R in its active site cleft. These essential residues were well conserved prior to Atherinomorpha. The ancestor of Atherinomorpha was characterized by a single substitution at position 135. Later, another substitution occurred at position 74 in the ancestor of Beloniformes. Finally, three further substitutions occurred in the ancestor of Oryziinae. These observations suggested that substitutions of the four essential residues in hatching enzyme LCE occurred prior to substitutions in the cleavage site on egg envelope protein.
Activity of ancestral recombinant LCE
Finally, we generated recombinant ancestral LCEs based on the predicted ancestral sequences (Additional file 2: Figure S2) and examined their P2 site preference (Figure 6). The ancestral LCE of Neoteleostei (ancNeotLCE) had strong P2 site preference, similar to that of FLCE. However, the P2 site preference of ancestral LCE of Acanthomorpha (ancAcmoLCE) was less stringent, and the ancestral LCE of Acanthopterygii (ancAcanLCE) had cleavage activity towards various substrates. Again, in the ancestor of Beloniformes (ancBeloLCE), high P2 site preference was revived, but was dramatically altered in the ancestor of Oryziinae, resulting in broader substrate preference. In summary, the MLCE-like activity had been established in the ancestor of Oryziinae, and this ancestral LCE (ancOryzLCE) acquired the ability to cleave the peptide containing P at the P2 site. Therefore, it is reasonable to conclude that the acquisition of this new ability would permit the substitution to P at the P2 site of the ancestor of the medaka egg envelope protein.
The present work demonstrated the molecular basis of species-specific egg envelope digestion by Fundulus hatching enzyme FLCE toward medaka egg envelope. The species specificity of FLCE depended on both the P2 site in the LCE-cleavage site on the egg envelope protein, and four sites in the active site cleft of LCE (positions 74, 91, 135, and 183). Generation of mutant recombinant enzymes suggested that positions 74 and 183 were indispensable for LCE activity. We further compared these residues among euteleosts (Additional file 1: Figure S1C). In most euteleosts, the residues at position 74 were hydrophobic; only medaka LCE contained a basic residue at this position. The residue at position 183 was well conserved, and was found to be R in most teleosts. However, the residue was occupied by S or T in beloniform LCEs, including medaka. The residue at position 91, which is the third important site for species specificity, has been substituted to P in Fundulus LCE (Additional file 1: Figure S1C). The site with the lowest contribution to specificity (position 135) was substituted to a basic residue in Fundulus (K) and medaka (H) (Additional file 1: Figure S1C).
We next examined how these substitutions were introduced into LCE during evolution, changing its specificity. We analyzed ancestral LCEs by reconstructing the proteins and examining their activities. As shown in Figure 6, the activity of the ancestral LCE of Beloniformes (ancBeloLCE) had a high P2 site preference. In the ancestor of Oryziinae, three substitutions (74 K, 135H, and 183 T) occurred in LCE, introducing a lower P2 site preference and high specific activity into LCE. The substitution from F (codon TTY) to K (codon AAR) at position 74 required a two-step nucleotide substitution. This two-step process was predicted by PAML to be a substitution from F (TTC) to I (ATC), and then to K (AAG). Such substitutions in LCE tolerated the substitution of V into the LCE cleavage site of the egg envelope, and then the substitution to P occurred during the evolution of Oryziinae.
We compared the species specificity of LCE in egg envelope digestion among several pairs of fishes. Three pairs (three-spined stickleback vs. medaka O. latipes, three-spined stickleback vs. nine-spined stickleback, and medaka O. latipes vs. saury) showed species-specificity, while two (O. latipes vs. O. javanicus, and Fundulus vs. saury) did not. The results suggested that the pairs within genus Oryzias and those within other euteleosts showed no species specificity, except the pair between three- and nine-spined sticklebacks, while those between Oryzias species and other euteleosts showed species specificity. Therefore, the manner of the establishment of the LCE species specificity found in Fundulus and medaka seems to be applicable to the other fish pairs, except the three- and nine-spined stickleback pair. As we only examined a few pairs of fishes, we cannot rule out the possibility that the LCE species specificity arose independently in different pairs of fishes in each co-evolutionary pathway.
The substitution in the substrate established the species specificity of FLCE. FLCE maintained the ancestral activity with high substrate specificity and was unable to digest medaka egg envelope (Figure 7C). Further substitutions in the enzyme and/or substrate conferred higher specificity on the interaction between enzyme and substrate, and thus MLCE could not digest Fundulus envelope (Figure 7C and 7D). In such a manner, the strict species specificity was established in Fundulus and medaka (Figure 7D). Determination of the substitution sites responsible for species specificity of medaka enzyme is in progress.
It is generally accepted that strategies such as mutation and subsequent production of a recombinant mutant protein, followed by the evaluation of its function, are required to understand the evolution of protein function at the molecular level . At present, such strategies have been extended to studies on reconstructed probable ancestors of the protein. One example is a study on hormone-receptor complexes, in which glucocorticoid and mineralocorticoid receptors switched their ligand preference following two amino acid substitutions . Another study showed that several sites are important for recognition of sugar by conger eel galectins . The former study suggested that several amino acid substitutions are required for switching the ligand preference or specificity, possibly accompanied with some conformational change of the 3D structure of the protein itself . In the present study we demonstrated that, in the hatching enzyme LCE-egg envelope protein pair, four substitutions in the LCEs allowed one amino acid substitution at the LCE-cleavage site on the substrate, egg envelope, during evolution. Interestingly, all four substitutions were located at the edge of the active site cleft, but not within the active site cleft itself, where some amino acid side chains might interact directly with those of the substrate around the cleavage site. These substitutions are likely to result in minor but not drastic changes in substrate specificity, suggesting that the enzyme activities have gradually been changed during evolution. A similar study reported that the substitutions responsible for environmental adaptation of fish lactate dehydrogenase are located outside of the active site cleft, and induced structural changes of the active site cleft .
In experiments to reconstruct ancestral LCE, ancNeotLCE showed strong P2 site preference. During evolution, the P2 site preference became less stringent in ancAcmoLCE, and then stronger again in ancBeloLCE, then lower in ancOryzLCE, i.e., P2 site preference seems to have fluctuated. These results imply that the enzyme has been continually changing during evolution while still maintaining its function in cleavage of the mid-ZPd site. When the substrate mutation fit with a change of enzyme specificity, the substrate mutation would be fixed, and then a new substrate-enzyme pair would be generated during later co-evolution. Therefore, the co-evolution of proteins is dependent on the evolution of protein-protein interaction, although this can sometimes be very complicated. The present study provides a molecular basis for understanding the mechanisms involved in protein-protein co-evolution.
The present study provides a molecular mechanism of co-evolution of a protease and its substrate using the interaction of hatching enzyme with egg envelope protein as a model. Four substitutions in LCE and a single substitution within egg envelope protein observed in medaka and Fundulus were responsible for the species-specific egg envelope digestion. We further observed how these residues were changed during the evolution of teleosts, and suggested that substitutions of the four essential residues on LCE occurred prior to substitutions in the cleavage site of egg envelope protein. The activities of predicted ancestral recombinant proteins were consistent with these proposed changes. Finally, we proposed a model for the protease-substrate co-evolution, whereby the evolutionary process leading to the species-specific action of LCE was initiated by amino acid substitutions in LCE, resulting in altered substrate specificity, which later allowed an amino acid substitution in the LCE-cleavage site of the egg envelope.
Fundulus heteroclitus embryos were supplied by the National Research Institute of Fisheries Science, Fisheries Research Agency, Japan. Saury (Cololabis saira) embryos and adults were obtained from Miyako Station, National Center for Stock Enhancement, Fisheries Research Agency, Japan. Oryzias species were supplied by the National BioResource Project (medaka) in Japan. O. luzonensis, O. mekongenesis, O. celebensis, and O. marmoratus were from Niigata University, while O. javanicus were from the National Institute for Basic Biology. Tissue samples of flying fish (Cypselurus agoo), halfbeak (Hyporhamphus sajori), and needlefish (Ablennes hians) were obtained from the National Museum of Nature and Science, Japan. Genomic DNA sequence from argentines (Glossanodon semifasciatus) was derived from Ishiguro et al., 2003 .
Estimation of egg envelope digestion activity of hatching enzymes
Hatching enzymes from medaka (MHCE and MLCE) and Fundulus (FHCE1/2 and FLCE) were purified from hatching liquids (culture medium of embryos immediately after hatching) according to a method described previously [13, 14, 21]. The egg envelope digestion activity of HCE was determined by turbidimetry, using fragments of fertilized egg envelope as substrate . The specific activity was expressed as ΔT610 · μg protein-1. For LCE activity, the amounts of peptides liberated from the swollen envelope were measured , and the specific activity was expressed as ΔA595 · μg protein-1.
The caseinolytic activity (CA) of hatching enzyme was measured in a 750 μL reaction mixture consisting of 83 mM Tris–HCl (pH 8.0) and 3.3 mg mL-1 of casein, according to a method described previously . CA was expressed in terms of ΔA280 · 30 min-1.
Synthetic peptide-cleaving activity
A 40-μL reaction mixture containing 100 μM of synthetic peptide in 50 mM Tris–HCl (pH 8) and an appropriate amount of enzyme was used to measure the activity according to a method described previously . To determine the Michaelis constant (Km), synthetic peptides were used as substrates in a concentration range from 10–1000 μM. Consumption of substrate was limited to 30 % of the starting concentration. The Km values were determined by Lineweaver-Burk plot.
The native nucleotide sequences of FLCE and MLCE were partially optimized for Escherichia coli codon preferences, without changing the deduced amino acid sequence. The mature enzyme region, containing suitable restriction enzyme sites (BamHI and NdeI) at both ends of the cDNA, was cloned into pET3c for expression in E. coli. Mutant FLCE or MLCE plasmids were constructed by PCR using mutagenic primers and codon-optimized FLCE or MLCE plasmids as a template. The recombinant proteins were synthesized using a protocol described previously . Because the refolding efficiencies of mutant recombinant proteins differed from sample to sample, the amount of active enzyme in the sample was estimated by CA. To compare the peptide-cleaving efficiency of the mutant recombinant proteins, the activities were normalized by CA, and expressed as nmol min-1 CA-1.
Cloning of hatching enzyme and choriogenin genes
Hatching enzyme cDNAs from saury, O. javanicus, and O. dancena were cloned by rapid amplification of cDNA ends (RACE) PCR, followed by RT-PCR, from RNA of pre-hatching embryos, according to a previously described method . LCE gene fragments from flying fish, needlefish, O. luzonensis, O. mekongenesis, O. celebensis, and O. marmoratus were amplified by PCR from genomic DNA using primers designed from MLCE. Gene fragments for the egg envelope precursor choriogenin H (ChgH) were amplified from genomic DNA of argentines, saury, flying fish, halfbeak, needlefish, O. luzonensis, O. mekongenesis, O. celebensis, and O. marmoratus using primers designed from conserved regions in ChgH genes, as described previously .
Ancestral sequence inference
Ancestral nucleotide sequences of LCE and ChgH were inferred by maximum likelihood using PAML 4.4 software , based on the molecular phylogeny of 33 euteleostean fish species for LCE, and 30 species for ChgH, according to Setiamarga et al.  and Takehana et al. . For ancestral reconstruction, the GTR model was assumed. Amino acid sequences were deduced from the inferred ancestral nucleotide sequences.
High choriolytic enzyme
Low choriolytic enzyme
Medaka high choriolytic enzyme
Medaka low choriolytic enzyme
Fundulus high choriolytic enzyme
Fundulus low choriolytic enzyme
We thank Dr. Akio Shimizu, National Research Institute of Fisheries Science, Fisheries Research Agency, for providing Fundulus embryos; the Medaka National BioResource Project (Niigata University and National Institute for Basic Biology) for providing medaka specimens; Mr. Yoshitomo Nagakura, Miyako Station, National Center for Stock Enhancement, Fisheries Research Agency, for providing adult fish and embryos of saury; and Dr. Takashi P. Satoh, Collection Center, National Museum of Nature and Science, Japan, for providing tissue samples of flying fish, halfbeak, and needlefish. The present study was supported in part by a Grant-in-Aid for JSPS Fellows to MK, by a Grant-in-Aid for Scientific Research (A) to MN, and by a Grant-in-Aid for Scientific Research (C) to SY. The nucleotide sequence data reported in this paper will appear in the DDBJ/EMBL/GenBank nucleotide sequence databases under accession numbers AB776785–AB776787.
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