Identification of conserved proteins from diverse shell matrix proteome in Crassostrea gigas: characterization of genetic bases regulating shell formation

Abstract

The calcifying shell is an excellent model for studying biomineralization and evolution. However, the molecular mechanisms of shell formation are only beginning to be elucidated in Mollusca. It is known that shell matrix proteins (SMPs) play important roles in shell formation. With increasing data of shell matrix proteomes from various species, we carried out a BLASTp bioinformatics analysis using the shell matrix proteome from Crassostrea gigas against 443 SMPs from nine other species. The highly conserved tyrosinase and chitin related proteins were identified in bivalve. In addition, the relatively conserved proteins containing domains of carbonic anhydrase, Sushi, Von Willebrand factor type A, and chitin binding, were identified from all the ten species. Moreover, 25 genes encoding SMPs were annotated and characterized that are involved in CaCO3 crystallization and represent chitin related or ECM related proteins. Together, data from these analyses provide new knowledge underlying the molecular mechanism of shell formation in C.gigas, supporting a refined shell formation model including chitin and ECM-related proteins.

Introduction

An amazing diversity of mineralized structures to fulfill a host of biological functions have been constructed by animal life since the Phanerozoic Eon1. The products of these biomineralization processes range from individual functional elements, for example, shell, teeth, bone, to large scale geological structures, such as coral reefs2. Ever since the onset of metazoan biomineralization at the dawn of the Phanerozoic, their biomineralized structures have been mostly constructed from one of three minerals: Calcium carbonate (CaCO3), calcium phosphate (CaPO4), or silica (SiO2)3. CaCO3 products include in most brachiopod shells, molluscan shells, coral skeletons, echinoderm spines and tests, and sponge spicules2. The calcifying shell primarily consists of aragonite and/or calcite polymorphs, and exhibits prismatic, nacreous, foliate, cross-lamellar or homogenous microstructures4.

The calcifying shell serves as an excellent model for studying the process of biomineral formation and its evolution5. However, the molecular mechanisms by which shells are constructed are only beginning to be elucidated6,7. It has been shown that in addition to the major component of CaCO3, the shell is an extracellular ensemble of organic macromolecules including proteins, pigments, glycoproteins, lipid and polysaccharides. These organic materials are secreted by an evolutionarily homologous organ known as the mantle1,8. The mantle is divided into distinct morphogenetic regions consisting of highly specialized epithelial cell types9. The mantle produces shell matrix proteins (SMPs) that play important roles in crystal nucleation, polymorphism, morphology, and organization of CaCO3 crystallites during shell formation10.

In order to study the phylogenetic relationships among molluscs and refine the existing biomineralization models, it is necessary to understand the repertoire involved in shell formation. Many studies have been focused on the SMPs and genes expressed in the mantle, leading to the identification and characterization of several specific shell proteins11. Recently, high-throughput transcriptomics and proteomics analyses have been successively used to characterize shell matrix proteomes (SMPEs) in Haliotis asinina8, Pinctada margaritifera12, Pinctada maxima12, Crassostrea gigas13, Lottia gigantea14, Cepaea nemoralis6, Mytilus coruscus15, Pinctada. fucata10, Magellania venosa2, Mytilus galloprovincialis16, Mya truncata17, and C. gigas, Mytilus edulis, and Pecten maximus18. However, only two global SMPEs comparisons have been performed in C. nemoralis and M. venosa, revealing low similarities. Even in bivalves, two different models have been proposed for calcifying shell formation. The well-known matrix model of “chitin-silk fibroin gel proteins-acidic macromolecules” largely explained biomineralization in P. fucata from a crystal growth perspective10,19. While the cellular model shows that shell formation is orchestrated by cells and the extracellular matrix (ECM) and crystals are formed in haemocytes in eastern oyster, Crassostrea virginica20,21.

As sessile marine animal living in estuarine and intertidal regions, oysters must cope with harsh and dynamically changing environments under the protection of hard shell13. The Pacific oyster, C. gigas, is a potential model organism for marine molluscan due to extensive studies of biology and genetics and its economical, biological and ecological importance22. Up to date, only two genes related to shell formation have been cloned and characterized in C. gigas23,24. A previous study of SMPE consisting of 259 SMPs (SMPE-Cg1) suggested that the matrix model may not apply to C. gigas because the absence of silk-like proteins13. Recently, a SMPE of C. gigas consisting of 53 SMPs (SMPE-Cg2) was published18, providing new opportunities for comprehensive comparison and characterization of SMPs in marine molluscan.

Here, we compared two published SMPEs in C. gigas and chose SMPE consisting of 53 SMPs for global comparison against 443 SMPs from nine other species. A total of 58 SMPs were used to identify the homologous SMPs in C. gigas and analyze the molecular mechanisms of shell formation. Data from this study will assist our understanding of shell biomineralization and evolution.

Result and Discussion

C. gigas SMPE characterized by ID

With the SMPE-Cg2 published by Arivalagan et al., the integrated dataset with 76 SMPs from this work (SMPE-Cg3, refer to material and methods) and the SMPE-Cg1 from Zhang et al., in hand, we performed a global SMP comparison analysis. Comparing gene accession of SMPs, 39 proteins were found in both the dataset with 53 SMPs and 259 SMPs of which 31 SMPs were found in the integrated dataset with 76 SMPs. By BLASTp research, 45 proteins were identified from both the SMPE-Cg1 and the SMPE-Cg2 to have similar domains, of which 41 were found in the SMPE-Cg3. SMPE-Cg3 included in the majority of SMPs stably identified from both the SMPE-Cg1 and the SMPE-Cg2, suggesting that the majority of SMPs stably identified from the SMPE-Cg1 and the SMPE-Cg2 are specially or highly expressed in mantle. Considering that SMPE-Cg2 has more stably identified SMPs than the SMPE-Cg3 and is constructed using the same method as the other nine SMPEs, we conducted the subsequent comparison analysis using SMPE-Cg2.

It has been shown that proteins containing the repeated low-complexity domain (RLCD) are a prominent feature of all shell-forming proteomes, and most of which are found to be lineage-specific proteins7,14. The RLCDs are important implications for intrinsically unstructured/disordered (ID) proteins. ID proteins possess low binding affinity for other organic macromolecules, but weakly bind mineral surfaces and ions in aqueous phases, which is critical for matrix assembly14,25. In C. gigas SMPEs, 66 out of the SMPE-Cg3 and 47 out of the SMPE-Cg2 were predicted to have at least one region of ID (Supplementary Table S1). This is higher than that found in P. fucata which contained 22 ID proteins out of the 35 SMPs10. XSTREAM analysis predicted that 24 out of SMPE-Cg3 and 21 out of SMPE-Cg2 proteins to contain tandem repeats in C. gigas, which is higher than that reported in P. fucata (7 out of 35). Collectively, the SMPE-Cg2 contained more ID proteins than the SMPE-Cg3. Given that the SMPE is dominated by ID proteins within a wide range of molluscan shells, it is proposed that they might play crucial roles in shell formation or imparting to the shell certain physical properties such as fraction resistance.

Comparisons of shell matrix proteomes

Up to date, SMPEs of 13 species belonging to different taxons have been published and includes H. asinina 8, P. margaritifera12, P. maxima12, C. gigas13, L. gigantea14, C. nemoralis6, M. coruscus15, P. fucata10, M. venosa2, M. galloprovincialis16, M. truncata17, and M. edulis, and P. maximus18. In this work, SMPEs from nine species have been used to compare against that of C. gigas. SMPE in M. galloprovincialis was excluded for more than one EST mapped to each peptide. SMPEs in P. maximus and M. edulis were not published. These nine species belong to two phylums of Mollusca and Brachiopoda and two classes of Bivalve and Gastropod in Mollusca (Fig. S1). All ten datasets primarily consist of proteins isolated from the shells of the respective species, which are validated by transcriptomes or ESTs in shell-forming organs or genome databases.

Our data showed that in C. gigas, 29 out of 53 (54.7%) SMPs shared sequence similarity (at an e-value threshold of 10e-06) with one or more proteins derived from other nine SMPEs investigated here (Fig. 1). Interestingly, SMPs in C. nemoralis showed a poor similarity of 5.1% (3 out of 59) with SMPs in C. gigas, compared to 10.8% (7 out of 65) in M. venosa. Obviously, the C. gigas in Mollusc shared a more recent common ancestry in evolutionary history with C. nemoralis than with M. venosa in Brachiopoda. However, C. nemoralis living on land is differentiated from other all nine species living in the sea by habitation. Marine and terrestrial shell-forming Mollusca have adapted to different environments that would fundamentally affect the process of shell formation and the stability of the secreted composite biomineral6. Therefore, the proteins and genetic bases involved in shell formation could be expected to have evolved rapidly in response to different selective pressures from different living environment.

Figure 1: Comparisons of C. gigas shell proteome against nine other metazoan shell proteomes.
figure1

BLASTp based similarity comparison of the 53 C. gigas SMPs against 443 shell-forming proteins derived from nine other biocalcifying metazoans, P. fucata, P. margaritifera, P. maxima, M. truncata, M. coruscus, L. gigantea, H. asinina, C. nemoralis, M. venosa. Individual lines spanning the ideogram connect proteins that share significant similarity (e-value < 10e-06). Transparent red lines connect proteins with the lowest quartile of similarity (with a threshold of 10 e-6) and green lines with the highest quartile of similarity. The percentage of each shell proteome that shared similarity with the C. gigas proteome is provided.

Generally, the sequence similarity in Bivalve is greater than 30%, except M. truncata with a 20.9% similarity which was lower than L.gigantea with a 25.6% similarity in Gastropod. The mineralogy and shell microstructure of these species may account for that differences. The C. gigas shell is purely calcite: the outer shell layers are calcite prisms, the middle shell layers are chalky calcite and the inner shell layer are foliated calcite18. In contrast, M. truncata shell is composed only of aragonite. Other species in Mollusca are a combination of both calcitic and aragonitic layers. The imperfection of SMPE, speciation, and mineralogy might result in the relatively low similarity of 20.9–40.0% in Bivalve comparing with the 84.9% (45 SMPs in the SMPE-Cg2 have hits in the SMPE-Cg1 in C. gigas). It had been proposed that gastropod and bivalve nacre is the result of parallel evolution based on the large-scale differences in genes expression in nacre-forming cells of Pinctada and Haliotis26. Low and variable similarities of 5.1–25.6% in Gastropod imply the parallel evolution of shell between Gastropod and Bivalve. Collectively, comparison of the shell proteomes for sequence similarity gives some clues about the relationships between evolution and sequence conservation. However, it has been suggested that the similarity in SMPs depends not only on the evolutionary distance but is also influenced by mineralogy of shell, parallel evolution, adaptation to the environment etc18.

In order to identify the highly conserved SMPs, we ordered all 29 SMPs in C.gigas that were found in any other SMPEs according to the number of databases they were found in (Table S2). Four C. gigas SMPs were identified to have hits in all other five species in bivalve, which were annotated as Putative tyrosinase-like protein tyr-3 (Tyr-3), Histone-lysine N-methyltransferase MLL3 (MLL3), and Chitotriosidase-1. In molluscs, tyrosinase function has been implicated in seashell pigmentation and mineralization of seashell27,28. The tyrosinase family have gone through an expansion in bivalve. Chitotriosidase-1 consists of one region of glycohydro18_chitinase-like, which can hydrolyze chitin, the major non-protein component of mollusc shell29,30. The MLL3 proteins has a complex structure that consists of 16 domains. It was identified because of the tyrosinase region. These results emphasize the prominent role of tyrosinase and chitin related proteins in the shell formation of bivalve and many metazoan biominerals.

It should be noted that none of these proteins was found in all databases, suggesting that these SMPs are diverse or these databases are limited. Yet, ten proteins were found in at least five SMPEs, four of which are conserved genes in bivalve. Of that, Nacrein_like protein, whose homologue nacrein was the first shell matrix protein cloned from P. fucata, contains carbonic anhydrase (CA) domain. CA could control pH by converting CO2 to HCO3 and concentrate CO32+ to form amorphous CaCO3 in “chitin-silk fibroin gel proteins-acidic macromolecules” model10. Follistatin-related-protein was also identified, including chitin-binding 2 (CBD), immunoglobulin like (IG-like), and Lam-G. Lam-G is a Ca+2 mediated receptor, which has been implicated in cell adhesion and interaction. IG-like has been also implicated in cell adhesion and interaction. CBD can interact with chitin, which are usually found together with Von Willebrand factor type-A (VWA) in SMPs, like other three conservative proteins CGI_10009194, CGI_10028014, CGI_10012353. Both VWA and CBD are typically domains of collagen, the fundamental component of extracellular matrix (ECM). The identification of these conserved SMPs may help refine shell formation model, including the function of chitin and ECM related proteins in biomineralization framework and protein interactions.

Identification and characterization of shell proteins homologues

Since the first SMP gene Nacrein was cloned, many SMPs have been cloned and characterized. Besides the shell’s superior mechanical and remarkable biocompatibility properties, the high commercial value of pearl has made pearl oyster one of the best studied biomineralization models. Here, we used these SMPs mainly from P. fucata to identify the homologues in C. gigas and analyzed the structural domains underlying biomineralization. A total of 58 SMP sequences were used to perform BLAST (Supplementary Table S3) and 25 protein sequences were annotated and characterized (Table 1). Furthermore, theses SMPs were classified into four categories based on functions and domains: crystallization of CaCO3, chitin related proteins, ECM related proteins and other proteins.

Table 1 Identification and characterization of SMPs from C. gigas.

Crystallization of CaCO3: ACCBP, CaLP, Nacrein

Amorphous calcium carbonate-binding protein (ACCBP) is a member of the acetylcholine-binding protein family that was first isolated from the extrapallial fluid of P. fucata31. It has been reported that ACCBP inhibits undesired crystal growth and plays a key role in forming the exceedingly orderly microstructure of nacre31. ACCBP contains an ID region near the N-terminus (ACCN) that has been implicated in regulation of CaCO3 precipitation32. BLASTp search identified nine gene with sequence similarity to ACCBP (E-value < e-21, score > 100). Phylogenetic analysis of these nine genes formed two clades (Fig. 2), of which ACCBP, ACCBP-like, CGI_10024902, and CGI_10024903 were clustered into one clade. This suggests that CGI_10024902 and CGI_10024903 diverged from a common ancestral gene of ACCBP. These two genes are located on the same scaffold146, suggesting an intragenic duplication. Both proteins contain two neurotransmitter-gated ion-channel ligand-binding domains (NCLBD), as well as ACCBP and ACCBP-like. Sequence alignment showed that the conserved residues are different from those residues between ACCBP and the nAChR family (NCLBD-containing proteins in D. melanogaster)32, especially in the ACCN region (Fig. 2). There are significantly more conserved residues among ACCBP, ACCBP-like and the two proteins in ACCN sequence, which are assumed to play a role in mineralization activity.

Figure 2
figure2

(a). Molecular phylogenetic tree of the nine ACCBP hits in C. gigas and two ACCBP in P. fucata. A phylogenetic tree was inferred from the amino acid sequences using the neighbor-joining method. Bootstrap values from 1000 trials are indicated at each branch node. The scale bar indicates 0.1 amino acid replacements per site. b. Comparison of neurotransmitter-gated ion-channel ligand binding domains (NCLBD) of ACCBP. The ACCN sequence is underlined.

Calmodulin-like protein (CaLP) is a multifunctional calcium sensor that belongs to a new member of the CaM superfamily33,34. In bivalve, CaLP contains two Ca2+-binding EF hand domains, each of which contains a pair of EF-hand motifs. Immunostaining revealed that CaLP was localized in the organic layer sandwiched between nacre (aragonite) and the prismatic layer (calcite) and the prismatic layer in P. fucata35. These results suggested that CaLP might be involved in the growth of nacre layer and prismatic layer. We have identified three putative genes encoding CaLP using BLASTn search (E-value < E-05, score > 50). BLASTp search identified 26 gene models (E-value < E-05 and score > 100), which included the aforementioned three gene models in the best six hits. Using the best six protein sequences in BLASTp, the phylogenetic tree showed that CGI_10011294 and CaLP constitute a single clade, as well as CGI_10011293 and CaM (Supplementary Fig S2). Therefore, we annotated CGI_10011294 as CaLP, and CGI_10011293 as CaM.

Nacrein is the first identified molluscan organic matrix component36. Nacrein expressed throughout the entire mantle epithelium and it functions in the production of both prismatic and nacreous layer37,38. Nacrein contains two functional domains, a CA and a NG-repeat domain with a repeated sequence rich in Asn and Gly36. Nacrein-related proteins have been found in some congeneric species (P. maxima and P. margaritifera) and also one gastropod, Turbo marmoratus39. They have a similar primary structure as nacrein in P. fucata11. No nacrein-related genes could be identified using BLASTp search with E-value < E-21 and score > 100. However, four nacrein-related genes were identified with E-value < E-05 and score > 80. Sequence alignment showed that the four hits have no NG-repeat domain and corresponding active site39. Phylogenetic tree of the aforementioned protein sequences showed two different clusters of nacrein group and hits group (Supplementary Fig. S3). These four hits are not specifically or highly expressed in mantle. Taken together, we argue that the four hits as CA, but not nacrein, suggesting the NG-repeat domain in CA proteins was acquired independently in the lineages of bivalves and gastropods.

These three SMPs have been reported to participate in concentration of Ca2+ and CO32−, crystal nucleation, and inhibition of crystal growth.

Chitin Related Proteins: Chitin synthase, Clp

Chitin existing in both nacreous and prismatic organic matrix is thought to play important role in biomineralization40. Chitin synthases are expressed in mantle edge, contributing to the formation of the framework for shell calcification29. Chitin synthases characterized so far comprises three domains, A, B, and C29. It is noteworthy that the chitin synthase identified in Mollusca share a special feature-a myosin domain in the N-terminus29,41. We have identified two predicted gene models (CGI_10009438, CGI_10012656) that are homologous to chitin synthase using BLASTn search (E-value < E-63, score > 250). The two predicted gene models were located two different scaffolds. They encode two different predicted proteins that were also identified by BLASTp with E-value = 0, score > 1800.

We aligned the amino acid sequences of chitin synthases and discovered that these two proteins included all domains (a myosin domain and A, B, C domains) in PfCHY (Fig. 3). COILS analysis of CGI_10009438 showed a strong potential for coiled coil formation at four positions with PfCHS. Specifically, three positions showed a strong potential and one position showed a fairly weak potential. COILS analysis of CGI_10012656 showed strong potential for coiled coil formation at the same two relative positions with DmCHS. The phylogenetic tree strongly confirmed that the putative chitin synthase from C.gigas belongs to the chitin synthase family (Fig. 3). The mollusk chitin synthase group including PfCHS, ArCHS, MgCHS is separated from other chitin synthase groups by forming an independent cluster. This position of CgCHS in the phylogenetic tree is consistent with the evolutionary position in Mollusca. These data suggested that the chitin synthase of molluscan species gained the coiled-coil sequence in the N-terminal region during evolution.

Figure 3: Diagrams of domain structures and phylogenetic tree analyses.
figure3

(a). Diagrammatic representations of the domain structure of chitin synthase in different species. The myosin head domain is represented by a slashed box. Predicted coiled-coil regions are partially shaded. Asterisks represent the position of the chitin synthase active site (QRRRW), which is used to align the diagram. The three domains in these proteins are denoted A, B, and C. PfCHS, ArCHS and DmCHS are chitin synthases from Pinctada fucata, Atrina rigida and Drosophila melanogaster66. (b). A phylogenetic tree showing the evolutionary relationship of the predicted chitin synthases in C. gigas with known chitin synthases. The tree was constructed using maximum likelihood method. Sequences in the QRRRW catalytic domain were aligned to generate the tree. Numbers on the nodes indicate bootstrap values. ArCHS (AAY86556.1), PfCHS (BAF73720.1), MgCHS (ABQ08059.1), LaCHS (AHX26699.1), PdCHS (AHX26708.1), DmCHS (AAG09735.1) and CeCHS (NP_493682.2) are chitin synthases from A. rigida, P. fucata, Mytilus galloprovincialis, Leptochiton asellus, Platynereis dumerilii, Drosophila melanogaster, Caenorhabditis elegans.

Chitinase-like proteins (Clp) were first detected from P. margaritifera and P. maxima. Clp transcripts were localized in the mantle edge specifically implicated in the biomineralization of the prisms12. Clp3 in P. margaritifera includes in a region of GH18_chitinase-like, which can hydrolyze chitin. Using the Clp3 sequences, 14 gene models are identified by BLASTp with E-value < E-39, Score > 150. Of that, three hits CGI_10026599, CGI_10024867, CGI_10026605 are detected to specially express in mantle of C.gigas13, which strongly suggested that these gene models are related with shell formation. These three hits contain GH18 domain, showing hydrolysis of chitin activity.

Both of chitin synthase and chitinase play key roles in construction and reconstruction of chitin framework, just like “chitin-silk fibroin gel proteins-acidic macromolecules” model.

ECM related Proteins: Pif and BMSP, EGF-ZP, SPARC

Pif is an acidic matrix protein which regulates nacre formation. It was first identified in the pearl oyster P. fucata. The Pif gene encoded a precursor protein, which was posttranslationally cleaved to produce Pif 97 and Pif 80, respectively. Pif 97 has two conserved domains, a VWA domain for protein-protein interaction and chitin-binding domain. Pif 80 has aragonite-binding activity42. Sequence analysis revealed that blue mussel shell protein (BMSP) is a Pif homologous preproprotein in M. galloprovincialis. BMSP consisted of a signal peptide and two proteins, BMSP 120 and BMSP 100, respectively43. In addition, other Pif homologues from bivalves (P. margaritifera, P. maxima, and Pteria penguin) and gastropods (L. gigantea) have been identified, suggesting a common ancestral gene during evolution43.

We have identified six putative BMSP genes by BLASTp search (E-value < E-05 and score > 100), but no putative BMSP gene hits using BLASTn search (E-value < E-05, score > 50). Of that, the gene CGI_10009194 is homologous to BMSP with E-value = 0, score = 1415. Another two genes, CGI_10014497 and CGI_10017473, consist of the VWA domains and a CBD. We have identified ten putative Pif genes by BLASTp (E-value < E-05 and score > 100) using Pif177, but none using BLASTn search (E-value < E-05, score > 50). In addition to the former three genes (CGI_10014497, CGI_10017473, CGI_10009194), one more gene (CGI_10006697) with both VWA domains and a CBD is considered to be homologue of Pif, others have neither VWA domain no CBD. In phylogenetic analysis, the CGI 10009194 and BMSP formed a separate clade, suggesting that CGI 10009194 should be annotated as BMSP. The CGI 10014497 and CGI 10017473 clustered with Pif genes from L. gigantea with a low confidence value. CGI 10006697 formed a single clade with others and showed distant evolution, not being annotated as Pif (Fig. 4). Phylogenetic analysis of VWA domain showed that the former three VWA domains in CGI 10009194 formed a single clade consistently with the former three in BMSP that were evolved from BMSP-4 and CGI 10009194-4 (Fig. 4). These data indicated that BMSP and CGI 10009194 were likely evolved from an ancestral with four VWA domains. The phylogenetic tree showed that VWA domains in CGI 10014497 and CGI 10017473 have evolved from CGI 10009194-4 and Pif177, being annotated as Pif-like1 and Pif-like2. Schematic representation of Pif showed the common VWA domains, CBDs, chitin-binding like domains and various C-terminal aragonite-binding sequences (Fig. 4).

Figure 4: Phylogenetic tree of Pif and BMSP proteins in Mollusca.
figure4

The tree was constructed using the NJ method, and the number at each node shows the bootstrap value.

Epidermal growth factor (EGF) domain-containing SMPs were first identified from C. gigas44 and named as Cgigas-IMSP-2.They were subsequently discovered in P. maxima, P. margaritifera, and L. gigantea12,14. Generally, the SMP consists of both EGF-like domain and one zona pellucida (ZP) domain. The presence of both domains in one protein is uncommon12. EGF-like domains, which are characterized by six conserved cysteines linked in a characteristic pattern of disulfide bonds and two small β-sheets, are among the smallest but most widely distributed modules found in extracellular proteins. EGF-like domains occur in a variety of proteins associated with diverse biological functions such as cell adhesion, signaling, and Ca2+-binding45. The ZP domains are present in a range of extracellular filament or matrix proteins. The ZP domain is characterized by eight conserved cysteine residues, which are involved in protein polymerization. The specific function of the EGF- and ZP-containing SMPs in calcified shell biomineralization await validation. Three EGF-ZP genes were identified by BLASTp using the known IMSP-2 genes of C. gigas with (E-value < E-48, score > 100). CGI_10017543, CGI_10017544, and CGI_10017545 are located on the same scaffold 120. In combination with their relatively high degree of sequence identify (37.53%), it strongly suggests that they originated from a gene duplication event. A sequence alignment of these EGF-ZPs illustrated a strong conservation of each domain (signal peptide, EGF, ZP), suggesting a fundamental role in biomineralization (Fig. S4).

SPARC (secreted protein, acidic, rich in cysteine), also known as BM-40 or osteonectin, is a major noncollagenous matrix protein of bone and a common mineralization-related proteins of vertebrates and molluscs45. The primary structure of SPARC is characterized by the presence of three functional domains: the N-terminal acidic domain I; the follistatin-like domain II with 10 conserved cysteine residues; and the C-terminal domain III, which is involved in interactions with collagen molecules46. By searching the C. gigas genome, we could only identify a single SPARC gene (CGI_10005088). Thus, the C. gigas genome contains one SPARC gene as observed in most triploblastic organisms. The SPARC protein consists of a region Kazal type serine protease inhibitors, follistatin-like domains (KAZAL_FS), and a region extracellular Ca2+ binding domain (SPARC_EC). KAZAL_FS can inhibit serine proteases and play an important role in tissue specific regulation. SPARC_EC functions to regulate cell-matrix interactions and binds to proteins such as collagen and vitronectin. The EC domain interacts with a follistatin-like (FS) domain which appears to stabilize Ca2+ binding.

These ECM related proteins are involved in crystallization, chitin-binding, and interactions with macromolecules. Typically, Pif is modularly constructed with aragonite-binding domain, chitin-binding domain, and protein-protein interaction domain, strongly suggesting that each shell protein is able to perform different functions. ECM-related domains in the SMPs are generally related with mediating communication between cells and the extracellular matrix.

Other Proteins of Interest: Tyrosinase, Peroxidase

Tyrosinases belong to the type-3 copper protein superfamily that also include tyrosinase-related proteins, arthropod phenoloxidases, and widespread hemocyanins. These protein possess a conserved pair of copper-binding domains24,47. Tyrosinases can be classified into three subclasses of secreted (α), cytosolic (β), and membrane-bound (γ) based on domain architecture and conserved residues in the copper-binding sites48. Tyrosinase is a key enzyme that mediates the hydroxylation of monophenols and oxidation of o-diphenols. It is thus also classified as a phenoloxidase. Tyrosinase is well known for its key biological role in melanin biosynthesis via transformation of tyrosine to L-DOPA. Tyrosinase functions in pigmentation and innate immunity47. In addition, other products of the melanin pathway participate in cuticle sclerotization in insects49.

In Mollusca, tyrosinase have been suggested in pigmentation and biomineralization of seashell. Cephalopod tyrosinases are expressed in the ink sac, suggesting an important role in melanin production50. In P. fucata, three tyrosinase genes have been characterized, Pfty1 and Pfty2 are suggested to function in prismatic formation and OT47 is proposed to influence the periostracum formation51,52. In C. gigas, Cgtyr1 was cloned and proposed to specifically function in the initial phase of the larval shell biogenesis23. CgTyr2 was also cloned and showed high levels of expression in mantle edges. It has been suggested to play a role in the formation of periostracum/pigmentation24. These reports strongly suggest that tyrosinases play diverse roles in stages when seashell is constructed, pigmented, and covered with the periostracum.

Twenty six tyrosinase genes were identified from C. gigas genome. Two tyrosinase genes CGI_10007793 and CGI_10011913 were found to be identical to the reported Cgtyr1 and CgTyr2, respectively (Fig. 5). The tyrosinase gene family can be further classified into three types: secreted form with signal peptides (Type A), cytosolic form (Type B) and member-bound form (Type C). According to SignalP v4.0, and TMHMM Server v2.0, there are six TypeA tyrosinase genes, 15 Type B tyrosinase genes and five Type C tyrosinase genes. The phylogenetic tree of 26 tyrosinases showed that there are eight pairs of duplication genes. Among them, only two pairs of CGI_10021076 Type C and CGI_10021075 Type A, CGI_10009319 Type A and CGI_10009318 Type B are located in the same scaffold separately, belonging to intragenic duplication. The phylogenetic tree showed that the clusters of tyrosinase genes are influenced by not only position of genes, but also the type of genes. The phylogenetic tree consists of two major groups, one of which consists of eight Type B tyrosinase genes. In the other group, CGI_10011916 Type B, CGI_10011913 Type C, CGI_10011911 Type B and CGI_10011912 Type A are clustered, all of which are located in Scaffold 43702. Above all, it suggests that the tyrosinases have evolved through both intergenic duplication and intragenic duplication.

Figure 5: Tyrosinase genes diversity in C. gigas.
figure5

The phylogenetic tree of tyrosinases was constructed by the maximum likelihood method. Numbers on the nodes indicate bootstrap values. The tyrosinase genes are named by accession number and type.

Peroxidases are iron proteins that catalyse the oxidation of many aromatic amines and phenols by hydrogen peroxide. Inactivation experiments provide strong evidence that the DOPA reaction in the mantle of Lymnaea stagnalis is catalyzed by peroxidase, suggesting that peroxidase is involved in the quinone-tanning of periostracum proteins53. Peroxidase is exclusively expressed in the ink gland of Sepia officinalis, likely involved in melanin biosynthesis54. Typical peroxidase is characterized by a unique structural domain that contains two histidines (proximal and distal histidines) and one calcium-binding site, which was suggested to function in maintaining the protein structure in the heme environment54,55. Peroxidase has been retrieved from the shell matrix of P. margaritifera and L. gigantea. It was proposed to be involved in biomineral-hydrogel formation via protein matrix framework assembly12. We identified 26 peroxidase genes by BLASTp using the known peroxidase genes of P. margaritifera with (E-value < E-23, score > 100). The peroxidase genes have gone through an expansion as shown for tyrosinases in C. gigas. Nine out of the 26 peroxidase were specially or highly expressed in mantle of C. gigas. The two best hits (CGI_10023200 and CGI_10010240) are specifically expressed in mantle13. All nine peroxidases consist of two histidines and one calcium-binding site. Phylogenetic analysis showed that these peroxidases formed two clusters that could be identified as melanin biosynthesis group and the shell formation group (Fig. 6). Peroxidases from Drosophila melanogaster, Bombyx mori and Sepia officinalis have been implicated in melanin synthesis form melanin polymer54.

Figure 6: Peroxidase genes diversity in C. gigas.
figure6

The phylogenetic tree of peroxidases was constructed by the maximum likelihood method. Numbers on the nodes indicate bootstrap values. The peroxidase genes are named by accession number and species.

We noted in our bioinformatics analyses that in many cases, BLASTn gave no hits, however, BLASTp give hits (Table S2). This suggested that genes encoding SMPs have undergone more variation than SMPs protein sequences. Until now, literature on biomineralization is scattered with these identified SMPs. Obviously, SMPs do more than providing a framework for crystallization. They could be involved in interactions with other macromolecular components of the matrix and cells, giving subtle feedbacks between the shell and the calcifying mantle epithelium.

Materials and Method

Construction and characterization of SMPE in C. gigas

In C. gigas, a SMPE consisting of 53 proteins was recently published18. The SMPE was constructed from peptide fragments in shell, which can be mapped to the genome. In addition, a SMPE in C. gigas consisting of 259 proteins was also analyzed, which was constructed by Zhang and colleagues using the same method. Many house-keeping proteins, such as elongation factor 1α and ribosomal proteins, were found in these 259 SMPs, which are significantly more than SMPs identified from other molluscan shell proteome to date. Generally house-keeping proteins should not be found in shell matrix proteome and they do not play special role in biomineralization. Given that housekeeping genes are generally expressed at relatively constant levels in most non-pathological situations, we identified genes that are specifically or highly expressed in mantle to minimize the interference from housekeeping proteins. An integrated SMPE consisting of 76 SMPs was constructed. The revised SMPE was constructed from the intersection of two databases:1) 259 proteins isolated from oyster shells; 2) 492 genes that were specifically or highly expressed in mantle, of which, the highly expressed genes were defined as having RPFM values of at least 5 and at least five times of other organ average13. Intrinsically unstructured/disordered (ID) domains were predicted by IUPRED56 and XSTREAM57. IUPRED was used to recognize disordered regions from the amino acid sequences of SMPs based on the estimated pairwise energy content. XSTREAM was used to detect proteins with tandem-arranged repeat units in the default settings.

Comparisons of shell-forming proteomes

Based on BLASTp, the global similarity comparison of C. gigas SMPE was performed against 443 SMPs derived from nine other biocalcifying metazoans. These included 53 M. coruscus proteins15, 75 P. fucata proteins10, 45 P. margaritifera proteins12, 26 P. maxima proteins12, 39 L. gigantea proteins14, 14 H. asinina proteins8, 59 C. nemoralis proteins6, 67 M. truncata17, and 65 M. venosa2 proteins. All protein sequences are validated by mapping to the transcriptomes, ESTs in biocalcifying organs or genome assemblies. The e-value threshold was set to 1e-06. These comparisons were made using blast+ 58: blastp -query XX.fa -db XX.change.fasta -out XX.blp -outfmt 6 -evalue 10e-6 -num_threads 10. The *.blp files generated by blast+ were modified using custom Perl scripts and then passed to Circos in order to generate an ideogram59. The *.blp file with details of the BLASTp results is provided (Supplementary Table S4).

Identification of validated SMPs from C. gigas draft genome

The SMP searches in the C. gigas gene models (oyster_gene_v1) and induced protein sequences (oyster_peptides_v1) were performed using Oysterbase13. Shell formation complementary DNAs (cDNAs) in C.gigas were BLASTn and BLASTp searched. Identifies of the hit gene models associated with the original cDNAs were confirmed by sequence alignment. Similarly, SMPs identified from other molluscan species were BLAST searched, and the obtained gene models were reciprocally BLASTp searched against the NCBI nonredundant (nr) database to confirm the best-hit sequence.

Characterization of homologous SMPs in C.gigas

The conserved structural domains were examined using the SMART60 and InterproScan61. The amino acid sequences were aligned using MEGA562 or DNAMAN (Lynon Biosoft). For phylogenetic analysis, poorly aligned positions were checked and removed manually, the phylogenetic tree with bootstrap value was constructed using MEGA5. Protein sequences for the phylogenetic analysis were retrieved from GenBank, Swiss-Prot, or the Oysterbase. In the case of secretory proteins or peptides, the presence of a signal peptide was predicted by SignalP 4.063. COILS was used to detect coiled coil formation64. To identify membrane proteins, the TMHMM Server v2.0 prediction algorithm was used for transmembrane helices65.

Conclusion

We compared two different SMPEs of C. gigas consisting of 76 SMPs and 53 SMPs and chose the latter one to perform a broad level comparison by bioinformatic analysis. These SMPE were characterized by having a high proportion of ID proteins, especially RLCD proteins. We used a marine SMPE in C. gigas to perform a broad comparison against 443 SMPs from nine other species using BLASTp. Our data confirms the earlier findings that the SMPs similarity depends not only on the evolutionary distance but is influenced by mineralogy of shell, parallel evolution, adaptation to the environment etc. The highly conserved proteins tyrosinase and chitotriosidase are identified in bivalve, and the relatively conserved proteins with domains of CA, VWA, CBD, IG-like and LaG are identified from all ten species. 25 genes encoding SMPs were annotated and characterized that are chitin related or ECM related proteins involved in crystallization of CaCO3. These conserved SMPs and universal domains enrich the molecular knowledge of shell formation mechanism in C. gigas, urging for a refined shell formation model including both chitin and ECM-related proteins.

Additional Information

How to cite this article: Feng, D. et al. Identification of conserved proteins from diverse shell matrix proteome in Crassostrea gigas: characterization of genetic bases regulating shell formation. Sci. Rep. 7, 45754; doi: 10.1038/srep45754 (2017).

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Acknowledgements

This study was supported by the grants from National Natural Science Foundation of China (31372524), Shandong Seed Project, Shandong Province (2016ZDJS06A06), and Qingdao National Laboratory for Marine Science and Technology (2015ASKJ02).

Author information

D.D.F. and S.H.D. analyzed the data and wrote the paper. Q.L., H.Y. and L.F.K. conceived and designed the study.

Correspondence to Qi Li.

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Feng, D., Li, Q., Yu, H. et al. Identification of conserved proteins from diverse shell matrix proteome in Crassostrea gigas: characterization of genetic bases regulating shell formation. Sci Rep 7, 45754 (2017). https://doi.org/10.1038/srep45754

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