- Open Access
The skeletal proteome of the sea star Patiria miniata and evolution of biomineralization in echinoderms
BMC Evolutionary Biology volume 17, Article number: 125 (2017)
Proteomic studies of skeletal proteins have revealed large, complex mixtures of proteins occluded within the mineral. Many skeletal proteomes contain rapidly evolving proteins with repetitive domains, further complicating our understanding. In echinoderms, proteomic analysis of the skeletal proteomes of mineralized tissues of the sea urchin Strongylocentrotus purpuratus prominently featured spicule matrix proteins with repetitive sequences linked to a C-type lectin domain. A comparative study of the brittle star Ophiocoma wendtii skeletal proteome revealed an order of magnitude fewer proteins containing C-type lectin domains. A number of other proteins conserved in the skeletons of the two groups were identified. Here we report the complete skeletal proteome of the sea star Patiria miniata and compare it to that of the other echinoderm groups.
We have identified eighty-five proteins in the P. miniata skeletal proteome. Forty-two percent of the proteins were determined to be homologous to proteins found in the S. purpuratus skeletal proteomes. An additional 34 % were from similar functional classes as proteins in the urchin proteomes. Thirteen percent of the P. miniata proteins had homologues in the O. wendtii skeletal proteome with an additional 29% showing similarity to brittle star skeletal proteins. The P. miniata skeletal proteome did not contain any proteins with C-lectin domains or with acidic repetitive regions similar to the sea urchin or brittle star spicule matrix proteins. MSP130 proteins were also not found. We did identify a number of proteins homologous between the three groups. Some of the highly conserved proteins found in echinoderm skeletons have also been identified in vertebrate skeletons.
The presence of proteins conserved in the skeleton in three different echinoderm groups indicates these proteins are important in skeleton formation. That a number of these proteins are involved in skeleton formation in vertebrates suggests a common origin for some of the fundamental processes co-opted for skeleton formation in deuterostomes. The proteins we identify suggest transport of proteins and calcium via endosomes was co-opted to this function in a convergent fashion. Our data also indicate that modifications to the process of skeleton formation can occur through independent co-option of proteins following species divergence as well as through domain shuffling.
Proteomic analysis of the matrices that mineral is deposited on during biomineralization has revealed complex mixtures of proteins. Among the more prominent proteins identified are groups of proteins that have evolved through gene duplication and concerted evolution of repetitive regions [1,2,3,4,5,6]. Although such proteins exist in disparate animal groups and share certain properties, they appear to have evolved independently [5, 6]. Also identified in skeletal proteomes have been proteins not previously thought to be involved in biomineralization or that have identified functions not previously associated with this process [7, 8]. In order to understand biomineralization we need to characterize what is necessary for it to occur and assign functional roles to the components that have been identified. Doing so may also shed light on how the process evolved. Comparative proteomics, as previously discussed by Degnan et al. , can provide information relevant to these questions.
Sea urchins have been a useful system to study skeleton formation during development. The cells that give rise to the skeleton appear early during cleavage and are easily studied both within the embryo and in culture. These cells produce an organic matrix upon which calcium carbonate is deposited to form the skeleton . Proteomic studies on this matrix has been carried out for both adult and embryonic tissues and have identified a large number of proteins [11,12,13]. Among the most prevalent proteins found are the spicule matrix proteins. These are secreted proteins characterized by a C-type lectin domain and a series of acidic amino acid repeats enriched in proline and glycine . Among other prevalent proteins are a membrane bound protein MSP-130 and carbonic anhydrase [11,12,13]. Studies of other sea urchins within the largest extant group, the euechinoids, shows these proteins to be conserved, although the exact sequence of the spicule matrix repeats varies . The functional importance of individual spicule matrix proteins has been called into question , perhaps indicating functional redundancy within this group of proteins.
We have recently carried out proteomic analysis of the skeletal proteome of two brittle stars [7, 8]. We found several C-type lectin proteins in the skeletal proteomes, but these lacked the repetitive domains seen in the sea urchin spicule matrix proteins. The sequences of the proteins found in the two brittle stars were highly conserved. The brittle star and sea urchin proteins formed separate groups, and it was unclear whether they were derived from a common ancestral protein, or if the C-type lectins evolved a mineralization function separately in the two echinoderm groups. Absent from the brittle star skeletal proteomes was MSP-130. We also found a number of proteins not previously implicated in echinoderm skeleton formation that were in common between the two brittle stars and sea urchins. The relevance of these proteins to biomineralization is not clear, but they are conserved. Interestingly, many of these proteins have also been found in vertebrate bone proteomes  and the proteomes of matrix vesicle [17, 18], which are involved in deposition of vertebrate bone.
The observed differences between sea urchins and brittle stars led us to examine a third echinoderm group. In this study we describe the skeletal proteome of the sea star Patiria miniata. Sea stars diverged from sea urchins some 500 mya and are thought to form a clade with brittle stars . The genome of P. miniata is available , allowing a comparison to an extensive list of gene models and computational predictions of peptide sequences. Surprisingly, we did not detect any C-type lectins in the P. miniata skeletal proteome, or MSP-130 like proteins. We did identify proteins that are conserved between all three echinoderm groups, as well as proteins unique to the sea star. Some of these proteins we identified have been determined to be present in vertebrate skeletal proteomes. We discuss the implications of our findings on the evolution of biomineralization in deuterostomes.
Results and discussion
Skeletal elements from entire Patiria miniata adults were isolated collectively. Skeletal proteins isolated from clean skeletal preparations were separated by SDS-PAGE and fractionated into twenty equal slices (Fig. 1). Following tryptic digestion and LC-MS-MS analysis the peptide sequences were compared to the complete set of proteins computationally identified from the Patiria miniata genome sequence, which includes 29,697 annotated genes [20, 21]. A total of 8654 spectra yielded 517 unique peptides (Additional file 1). Proteins with at least two peptide matches and a minimum protein value indicating 95% identification certainty were accepted. After removal of peptides with internal stop codons or short reading frames these peptides matched 85 proteins in the P. miniata genome (Additional file 2, 20). All of these matched sequences in the NCBI database, although nine proteins match proteins of unknown function (Tables 1, 2 and 3). Of the nine uncharacterized proteins, three were homologous to proteins found in the S. purpuratus skeleton; the other four had homologues in the S. purpuratus genome. The number of proteins identified is similar to what was found in the brittle star Ophiothrix spiculata , but fewer than what has been identified in S. purpuratus skeletal proteomes. The test and spine proteomes of S. purpuratus contained 103 proteins combined. Over 400 proteins were found cumulatively in the S. purpuratus mineralized tissues, test, spine, tooth and larval spicules [11,12,13]. It should be noted that the number of different functional classes of proteins found in the skeletal proteomes do not differ significantly. In S. purpuratus there are more versions of each of the proteins from any particular functional class.
A comparison with the proteins found in the S. purpuratus skeletal proteomes identified thirty six proteins (42%) in P. miniata that have orthologues in S. purpuratus (Table 1) as defined by proteins found in the skeletal proteomes that are the top hits in reciprocal best blasts. In addition, we found twenty nine P. miniata skeletal proteins (34%) that were most similar to S. purpuratus proteins that are of the same functional class as proteins in the S. purpuratus skeletal proteomes, but the top protein identified by BLAST was not the one found in the S. purpuratus skeletal proteome (Table 2). We also identified twenty proteins (24%) that are unique to the P. miniata skeletal proteome (Table 3). Comparison to the two brittle star total adult skeletal proteomes that have been characterized [7, 8] identified twenty-one proteins (28%) of the P. miniata skeletal proteins were similar to those found in Ophiocoma wendtii and thirty-one (44%) with Ophiothrix spiculata.
Notably absent from the P. miniata skeletal proteome were C-type lectin proteins which are abundant in the S. purpuratus skeletal proteomes [11,12,13] and are present in both brittle star skeletal proteomes as well [7, 8]. MSP-130, another protein prevalent in the S. purpuratus skeletal proteomes was also absent, as it was in the brittle star skeletal proteomes. In order to confirm that we did not miss any C-type lectins, with or without the spicule matrix protein repeats, we used the S. purpuratus spicule matrix protein sequences as well as those encoding the brittle star O. wendtii skeletal C-type lectins to performed a BLAST search against the P. miniata genome sequences and predicted peptides . We found that there are C-type lectins encoded in the genome, but nothing with repetitive domains resembling the sea urchin spicule matrix proteins. The C-type lectins identified in the P. miniata genome were most similar to the brittle star sequences. OwSM20 identified a group of proteins with an E-value high of e-22 and OwSM24 identified proteins with an E-value ranging up to e-20. Using the BLAST results, we examined proteins identified with single peptide hits and lowered the minimum protein value to 20%. We searched these proteins for the top 90 of the C-lectin proteins identified in the BLAST search. We identified two C-type lectin domain containing proteins in the P. miniata skeletal proteome. One, PMI_018577 had a single peptide hit and a 61% identification probability. It has two C-type lectin domains and very little similarity with spicule matrix proteins (e−19). The other, PMI_003522, had one peptide hit and a 41% identification probability. This protein also had additional Cub and FN3 domains not found in spicule matrix proteins. We also used S. purpuratus MSP-130 sequences to query the P. miniata genome and identified two proteins (PMI_017126 and PMI_019914) similar to MSP 130. We examined our LC/MS/MS data under relaxed stringency (one peptide match, <20% certainty) and could not find any matches to these two proteins. Computational analysis indicated trypsin digests would produce peptides that could be identified. MSP 130 is thought to be associated with the membrane and function in calcium transport. It is possible it is expressed in the skeleton forming cells in P. miniata, but is not incorporated into the skeleton in sea star adult skeletons. It is also possible that the gene annotations available missed the C-lectin and MSP 130 proteins in the skeletal proteome. 29,697 gene models were identified computationally ; however, the available genome is somewhat fragmented (N50 = 52 kb), which may overestimate the number of genes identified. Proteins similar to these are present in the Patiria miniata genome, but were not detected using LC/MS/MS analysis of the proteins we isolated from the skeleton. It is possible our methods failed to detect these proteins, however, at a minimum it suggests that C-type lectins and MSP 130 proteins are much reduced in the P. miniata skeletal proteome, if they are present at all.
The distribution of proteins into functional groups in members of sea stars and sea urchins are shown in Fig. 2. The types and distribution of proteins found in the skeleton are similar overall with some notable exceptions. Membrane, extracellular matrix, cytoskeletal proteins and proteins with enzymatic functions are present in similar proportions. The S. purpuratus skeletal proteome has more matrix metalloproteases, while the P. miniata skeletal proteome has more proteases and protease inhibitors, proteins with EGF domains, cub domain containing proteins and a large increase in scavenger receptor domain containing proteins. The greatest divergence is the presence of the large number of C-type lectin domain containing proteins in S. purpuratus that are missing in P. miniata, and the presence of Von Willebrand type C domain containing proteins in P. miniata that are missing in S. purpuratus.
S. purpuratus forms a skeleton in the embryo and during metamorphosis forms distinct test and spines. The proteomes of these skeletal elements in S. purpuratus have been studied separately. The types of proteins observed did not differ substantially between these tissues [11,12,13], although the spicule did contain some unique versions of protein families (e.g. SM30 and MMP’s) and there are similar differences between test and spine. In contrast, P. miniata does not form a skeleton in the embryo or larva. The skeleton formed at metamorphosis and in the adult has many smaller skeletal elements that are not as easily separated into classes. When comparing the proteins found in the P. miniata adult with the different proteomes of S. purpuratus, most of the homologous proteins in P. miniata were present in all of the S. purpuratus proteomes or in the adult skeleton (Table 1). There were a few exceptions to this. In some cases, multiple proteins from a functional group were found, and some of these were found in all of the S. purpuratus proteomes, while others were specific to the S. purpuratus spicule, for example Ldlr-like and scavenger receptors proteins. Two were uniquely found in the sea urchin spicule. One is the fibrinogen C-like -domain containing protein PMI_010282. In S. purpuratus this protein is only found in the larval skeleton and has been shown to be expressed at the growing ends of the spicule . The other is the MAM domain containing protein PMI_018059 similar to meprin. This is an extracellular domain thought to have an adhesive function. It is possible that activation of the gene regulatory network leading to skeleton formation in embryos in S. purpuratus has allowed some degree of specialization of skeletal proteins in the embryo versus the adult. This specialization of proteins would not be expected in sea stars, which only make an adult skeleton. The presence of proteins similar to both sea urchin adult and spicule skeletons in adult sea stars supports that.
Proteins conserved in echinoderm skeletal proteomes
Scavenger Receptor domain containing proteins
The protein with the highest spectral counts in the P. miniata skeletal proteome contained multiple scavenger receptor domains. The S. purpuratus protein with the highest similarity to this protein is not present in the skeletal proteome [11,12,13], however there are several proteins with scavenger receptor domains present in the S. purpuratus skeletal proteomes. Similar proteins were not detected in the brittle star skeletal proteomes [7, 8]. P. miniata has a large number of proteins with these domains in the skeletal proteome (Tables 1 and 2), some in combination with other domains such as IG domains (PMI_017807, Table 2). Scavenger receptor domains are cysteine rich and have been implicated in binding various ligands . The most prevalent protein with multiple scavenger receptors in the P.miniata skeletal proteome predicted to be 415 kd in size and was found in the fraction of the gel (Fig. 1) consistent with being of large molecular weight.
Fibrinogen C-like proteins
All three echinoderm groups studied have proteins related to fibrinogen in their skeletal proteomes. In the brittle stars [7, 8] and P. miniata, these proteins are among the most abundant in the skeleton as inferred from total spectral counts. In S. purpuratus a similar protein was less abundant and was detected only in the spicule and tooth. The sea urchin fibrinogen C-like gene(frp) has been shown to be expressed in the larval skeleton . The similarity to fibrinogen is found in the Fred domain that is found near the C-terminus of fibrinogen. These domains in vertebrate fibrinogen participate in lattice formation during blood clotting. The echinoderm proteins lack the collagen-like N-terminal domain of vertebrate fibrinogen C. The brittle star and sea urchin proteins contain a single Fred domain, while P. miniata has proteins with one and four Fred domains. The relationship between these proteins and the individual domains are shown in Fig. 3. The four FRED domains in the P. miniata protein PM 010282 were separated in silico and aligned with the other P. miniata Fic C protein found in the skeleton (PM 004711) and the S. purpuratus and O. wendtii skeletal fibrinogen C-like proteins, as well as some related S. purpuatus proteins not found in the skeleton. All but one of the Fibrinogen C proteins found in echinoderm skeletal proteomes clustered together, suggesting they are derived from an ancestral gene involved in skeleton formation. The larger, most prevalent P. miniata protein with four FRED domains is predicted to be 90 kd in size. It was detected in a gel fraction consistent with that, but was also found at lower molecular weights down to around 20 kd, which is consistent with a single domain and falls in fractions containing major bands on the gel (Fig. 1). This suggests the protein might be proteolytically processed.
Proteases and protease inhibitors
The S. purpuratus skeletal proteomes contain a large number of secreted proteases and protease inhibitors [11,12,13]. Prominent among these are matrix metalloproteinases, alpha-2-macroglobulins and agrin/kazal inhibitors. Several of these urchin matrix metalloproteinases have been shown to be specifically expressed in the skeleton forming cells during embryonic development . Representatives of these protein groups are also found in the brittle star skeletal proteomes [7, 8]. Two matrix metalloproteinases were found in the P. miniata skeletal proteome as well as four alpha-2-macroglobulin-like proteins (Tables 1 and 2). The most prevalent of these is homologous to MMP-14A and was found in the gel fraction where a major band of 28 kd was seen on the gel, consistent with the predicted molecular weight. A single protein with kazal inhibitor domains was detected. We also identified a novel protease that is present in all of the echinoderm skeletal proteomes examined. Our initial analysis using predicted peptides identified three P. miniata peptides similar to S. purpuratus LOC578177 (Table 1). A portion of this protein was identified in the S. purpuratus skeletal proteome using the original gene model that predicted it was a separate protein, but the current gene model has corrected that. A model of the domain structure is shown in Fig. 4. This figure also shows the relationship of this protein to the proteins it most closely resembles in Genbank databases. The only member of this group that has been characterized is human neurotrypsin, a secreted protease that cleaves proteoglycans and releases a signaling molecule . Proteoglycans play an important role in formation of sea urchin skeletons , suggesting a potential role for this conserved protease.
P. miniata has three gene models that were identified as encoding peptides present in the skeletal proteome (Table 1). These actually encode a single protein that is homologous to a protein detected in all of the S. purpuratus skeletal proteomes [11,12,13]. The S. purpuratus gene encoding this protein was originally annotated as three separate genes but is now corrected in the NCBI database. This protein was originally reported in separate studies as a component of the embryonic extracellular matrix in the sea urchin Lytechinus variegatus and was called ECM3 [28, 29]. The protein is expressed by ectodermal cells in the sea urchin embryo and forms an extracellular complex with the highest concentration in the vegetal pole. The mesenchyme cells that form the skeleton interact with this protein . These cells form an elongated syncytium, whose membrane surround a cylindrical, extracellular privileged space. The syncytial mesenchyme may engulf the ECM3 molecule as it forms the secluded space where the skeleton is formed. While ECM3 likely plays a role in skeletal patterning, its presence in the mineralized skeleton could be due to being trapped where mineralization occurs. In vertebrates the homologous protein (Fras or Frem) is found in the basal lamina and interacts with epithelial sheets . Defects in the Fras/Frem protein lead to a condition called Fraser syndrome where epithelial sheets form blebs instead of interacting smoothly with the basal lamina. This protein is highly conserved, with over 60% of the amino acids conserved across echinoderms and hemichordates and over 50% conserved with humans (Fig. 5). The distinguishing features of the protein are numerous chondroitin sulfate proteoglycan repeats and five Calx-beta domains that have been implicated in sodium/calcium exchange. These results suggest this protein plays a role in ECM-membrane interaction during skeleton formation in echinoderms.
Ldlr-like (Lrp) proteins
Proteins similar to low density lipoprotein-like receptors (Lrp) are found in the skeletal proteome of P. miniata, S. purpuratus [11,12,13] and both brittle stars [7, 8]. Similar proteins are found in vertebrate bone proteomes [16,17,18] and proteins with Lrp domains have now been identified in coral mineral proteomes . Genes encoding Lrp proteins have been implicated in human osteoporosis through genome-wide association studies [32, 33]. The P. miniata skeletal proteome has four Lrp proteins, while the S. purpuratus skeletal proteomes have six, four in the test and spine [11,12,13]. Figure 6 shows the domain structure of the P. miniata proteins as well as the two most prevalent S. purpuratus proteins. The proteins have similar domains, but the number and order of the domains varies, suggesting duplication and rearrangement within the proteins. The phylogenetic relationship between the proteins is also shown in Fig. 6. The S. purpuratus Lrp protein (Sp011678204) that is present in all of the skeletal proteomes and is the most prevalent in test and spine  groups with the P. miniata PM016447 protein and human Lrp 8. The other prevalent P. miniata Lrp proteins group together with two S. pupuratus proteins found only in the larval spicule . These proteins are also more similar to the human Lrp8 than to other human Lrp proteins involved in bone formation . The Lrp proteins in vertebrates have been shown to be wnt co-receptors , but we have not found wnts or wnt receptor proteins in the echinoderm skeletal proteomes. This suggests they also may play separate roles during mineralization.
A variety of other proteins associated with mineralization in echinoderms, vertebrates or other animals were detected in the P. miniata skeletal proteome. These include carbonic anhydrase, calmodulin, and a protein orthologous to the sea urchin p58 protein which has been shown to play a role in skeleton formation . The P. miniata skeletal proteome also contained a number of proteins that would not be expected to play a direct role in mineralization. These could be contaminants, although the stripping of organic material from the skeleton during isolation is extremely rigorous. It is also possible that these proteins are occluded within the mineral, but were trapped there because of involvement in cellular process involved with cell signaling, movement of materials into the extracellular space, membrane fusion, or proteolytic cleavage of ECM molecules, or are trapped in the organic matrix where mineralization occurs (e.g. ECM 3). When comparing different echinoderm skeletal proteomes, the presence of such proteins is not random; the same proteins are found in different classes of echinoderms. This includes cathepsin-like protein, alpha-2 macroglobulin, thrombospondin domain containing protein, actin and collagen (Table 1). Some proteins found in the echinoderm skeletal proteomes are not found occluded in vertebrate bone, but are associated with the process of mineralization, such as semaphorin, tetraspanin, a MAM domain containing membrane anchored protein related to meprin, a phospholipase and matrix metalloproteinases. In addition, there are a number of proteins that do not have exact homologues between the echinoderms and other metazoans examined, but that contain protein domains in various combinations that are prevalent in proteins found in all mineralized tissues. These include Cub, Egf, sushi, Ig, scavenger receptor and von willebrand factor type C (VWC) domains (Tables 1, 2 and 3). The P. miniata skeletal proteome has an expanded number of proteins with VWC and scavenger receptor domains.
Matrix proteins have been studied in a variety of systems [1,2,3,4,5,6,7,8,9]. Many of the prevalent proteins that have been identified have similar characteristics but have evolved independently. They tend to be elongated, somewhat unstructured or flexible, glycosylated, acidic proteins. Often they contain repetitive, rapidly evolving domains which can vary in amino acid sequence even among related groups. The sea urchin spicule matrix proteins fit this description, and there are many in the urchin skeletal proteome [11,12,13]. These spicule matrix proteins also have a C-type lectin domain that binds carbohydrates. The large number of spicule matrix proteins with extensive acidic repeat domains in the skeleton seems to be unique to sea urchins among echinoderms. Brittle stars have C-type lectin proteins in their skeleton, but these lack the repetitive domains [7, 8]. The data we present here suggest sea stars do not have similar proteins in their skeletons. It seems that a meshwork of proteins and carbohydrates with appropriate charge is necessary to provide an environment conducive to nucleation and/or propagation of calcium crystals. The exact sequence of the proteins seems less important than the overall structure, such that the proper conditions can be reached with different combinations. There is evidence the sea urchin spicule matrix proteins form such a lattice . The proteins in sea urchins [6, 11,12,13,14] molluscs [4, 5], and vertebrates [2, 3] that acquire repetitive domains seem well suited to biomineralization, such that they have been co-opted to this function numerous times and are highly prevalent in the skeleton. The appearance of the spicule matrix proteins in sea urchins likely supplanted proteins or reinforced proteins that formed an extracellular surface where mineral is deposited in ancestral echinoderms. A candidate for an ancestral protein that could also play this role is the fibrinogen C–like protein. This protein is one of the most abundant in the brittle star [7, 8] and sea star (ibid) skeletal proteome, but is much reduced in the sea urchin [11,12,13]. Similarly, the P. miniata proteome, which lacks C-type lectins, has a large number of proteins with VWC domains which are not found in the other echinoderm proteomes. These are extracellular proteins that could also play a similar role in forming a surface for mineral deposition.
While it is not unexpected to see proteins such as carbonic anhydrase or calmodulin conserved in skeletons among animals across a large phylogenetic distance, the conservation of a number of proteins seemingly unrelated to biomineralization is surprising. However, a number of these conserved proteins have been found in vertebrate matrix vesicles and are associated with formation and function of these exosomes in mineral deposition [17, 18, 38]. In vertebrates these matrix vesicles are released from the osteoblasts into the extracellular space where they contact collagen. Formation of the hydroxyapatite mineral is thought to begin within these vesicles . As the crystals grow the vesicles burst and the mineral formation continues in the extracellular space. This can explain the presence of proteins occluded in bone that are also found in the matrix vesicles. Sea urchin embryonic micromere descendants have been shown to be full of multivesicular bodies as they form the skeleton  which resemble the formation of matrix vesicles. This, along with our findings of multiple proteins associated with vertebrate matrix vesicles in echinoderm skeletal proteomes, suggests that the role of exosomes in mineral deposition is conserved among deuterostomes.
An interesting feature of the mineral proteomes is the number of conserved protein domains that are found in different numbers, combination and arrangements. Apparently non-homologous proteins containing cub, sushi, Egf, scavenger receptor, Ig and von Willebrand domains in varying combinations are found in vertebrates [16,17,18], echinoderms [7, 8, 11,12,13], corals  and molluscs [4, 40]. This supports the idea put forth by Kocot et al.  that rapid evolution of these proteins involves extensive domain shuffling and duplication.
Skeleton was isolated as described in Seaver and Livingston and Flores et al. [7, 8]. Whole animals were cut into small pieces and immersed in 6% sodium hypochlorite. Skeletal elements were allowed to settle. The sodium hypochlorite was changed three times and the skeletal elements were then washed three times with sterile water. Removal of material adhered to the skeleton was monitored with microscopy. The skeleton was then powdered with a mortar and pestle. The powder was added to 4% guanidine isothiocyanate containing beta-mercaptoethanol and buffered with sodium citrate. Following settling of the mineral, the solution was replaced twice followed by three washes with sterile water. Purified skeletal elements were de-mineralized with acid and dialyzed as described previously [7, 8]. The soluble fraction was concentrated using Amicon Ultra-15 centrifugal filter units, followed by Amicon Ultra-0.5 centrifugal filter units (3000 NMWL) (Millipore, Bellerica, MA). Samples were dissolved in NuPAGE LDS sample buffer under reducing conditions (Invitrogen, Carlsbad, CA) and the proteins separated by SDS-PAGE using NuPAGE 4–12% Bis-Tris Polyacrylamide gels 1.0 mm*10 well in the MES buffer system (Invitrogen, Carlsbad, CA). Running times, protocols, and reagents were used as described by the manufacturer (Invitrogen, Carlsbad, CA). Gels were stained with SYPRO RUBY Protein Gel Stain.
Protein quantitation was performed by Qubit Fluorometry (Invitrogen, Carlsbad, CA). 20 μg of material was separated on a 4–12% Bis Tris NuPage gel (Invitrogen, Carlsbad, CA) in the MOPS buffer system. The gel lane was excised into twenty equally sized segments. Using a robot (ProGest, DigiLab), gel pieces were reduced with 8 mM dithiothreitol at 60 °C followed by alkylation with 10 mM iodoacetamide at RT. Samples were then digested with sequencing grade trypsin (Promega, Madison, WI) at 37 °C for 4 h and quenched with formic acid. The supernatant was analyzed directly without further processing.
For each sample (n = 24; from 3 excised gel slices, 1 unfractioned liquid sample, and 20 fractioned gel slices), LC-MS/MS was performed identically. The digested sample was analyzed by nano LC/MS/MS with a Waters NanoAcquity HPLC system interfaced to a ThermoFisher LTQ Orbitrap Velos. Peptides were loaded on a trapping column and eluted over a 75 μm analytical column at 350 nL/min; both columns were packed with Jupiter Proteo resin (Phenomenex). The mass spectrometer was operated in data-dependent mode, with MS performed in the Orbitrap at 60,000 FWHM resolution and MS/MS performed in the LTQ. The fifteen most abundant ions from LC of each gel slice were selected for MS/MS in each round run in continuous mode.
Data were searched using a local copy of Mascot against the predicted peptides from the P. miniata genome in Echinobase . Trypsin was input as the digestive enzyme, mass values were monoisotopic, the peptide mass tolerance was 10 ppm, the fragment mass tolerance was 0.8 Da, and the maximum number of missed cleavages was 2. Carbamidomethylation (C) was set as a fixed modification and variable modifications included oxidation (M), acetyl (N-term), pyro-glu (N-term Q), and deamidation (N,Q). Mascot DAT files were parsed into the Scaffold software for validation, filtering and to create a non-redundant list per sample. The data were filtered using a minimum protein value of 95%, a minimum peptide value of 50% (Prophet scores) and requiring at least two unique peptide per protein.
Protein sequences were aligned in Clustal X and imported into Mega for refinement. Trees were constructed with maximum likelihood methods with 1000 bootstraps.
- O. wendtii :
- P. miniata :
Polyacrylamide Gel Electrophoresis
- S. pupuratus :
Wilt FH, Killian CE, Livingston BT. Development of calcareous skeletal elements in invertebrates. Differentiation. 2003;71:237–50.
Young MF. Skeletal biology: where matrix meets mineral. Matrix Biol. 2016; doi:10.1016/j.matbio.2016.04.003.
Kawasaki K, Weiss KM. Evolutionary genetics of vertebrate tissue mineralization: the origin and evolution of the secretory calcium-binding phosphoprotein family. J Exp Zool B Mol Dev Evol. 2006;15; 306(3):295–316.
Isowa Y, Sarashina I, Oshima K, Kito K, Hattori M, Endo K. Proteome analysis of shell matrix proteins in the brachiopod Laqueus rubellus. Proteome Sci. 2015;13:21.
Jackson DJ, McDougall C, Woodcroft B, Moase P, Rose RA, Kube M, et al. Degnan BM:parallel evolution of nacre building gene sets in molluscs. Mol Biol Evol. 2010;27(3):591–608.
Livingston BT, Killian CE, Wilt F, Cameron A, Landrum MJ, Ermolaeva O, et al. A genome-wide analysis of Biomineralization-related proteins in the sea urchin, Strongylocentrotus purpuratus. Dev Biol. 2006;300(1):335–48.
Seaver R, Livingston BT. Examination of the skeletal proteome of the brittle star Ophiocoma wendtii reveals overall conservation of proteins but variation in spicule matrix proteins. Proteome Sci. 2015;13:7.
Flores RL, Gonzales K, SEaver RW, Livingston BT. The skeletal proteome of the brittle star Ophiothrix spiculata identifies C-type lectins and other proteins conserved in echinoderm skeleton formation. AIMS Mol Sci. 2016;3(3):357–67.
Jackson DJ, Degnan BM. The importance of evo-devo to an understanding of molluscan biomineralization. J Struct Biol. 2016;196(2):67–74.
Benson SC, Benson NC, Wilt F. The organic matrix of the skeletal spicule of sea urchin embryos. J Cell Biol. 1986;102(5):1878–86.
Mann K, Poustka AJ, Mann M. The sea urchin [Strongylocentrotus purpuratus] test and spine proteomes. Proteome Sci. 2008;6:11.
Mann K, Poustka AJ, Mann M. In-depth, high-accuracy proteomics of sea urchin tooth organic matrix. Proteome Sci. 2008;6:33.
Mann K, Wilt FH, Poustka AJ. Proteomic analysis of sea urchin [Strongylocentrotus purpuratus] spicule matrix. Proteome Sci. 2010;8:33.
Meeds T, Lockard E, Livingston BT. Special evolutionary properties of genes encoding a protein with a simple amino acid repeat. J Mol Evol. 2001;53(3):180–90.
Wilt F, Killian CE, Croker L, Hamilton P. SM30 protein function during larval spicule formation. J Struct Biol. 2013;183(2):199–204.
Alves RD, Demmers JA, Bezstarosti K, van der Eerden BC, Verhaar JA, Eijken M, et al. Unraveling the human bone microenvironment beyond the classical extracellular matrix proteins: a human bone protein library. J Proteome Res. 2011;10(10):4725–33.
Thouverey C, Malinowska A, Balcerzak M, Strzelecka-Kiliszek A, Buchet R, Dadlez M, et al. Proteomic characterization of biogenesis and functions of matrix vesicles released from mineralizing human osteoblast-like cells. J Proteome. 2011;74:1123–34.
Balcerzak M, Malinowska A, Thouverey C, Sekrecka A, Dadlez M, Buchet R, et al. Proteome analysis of matrix vesicles isolated from femurs of chicken embryo. Proteomics. 2008;8:192–205.
Cannon JT, Kocot KM, Waits DS, Weese DA, Swalla BJ, Santos SR, et al. Phylogenomic resolution of the hemichordate and echinoderm clade. Curr Biol. 2014;24(23):2827–32.
Echinobase Genomic Database; http://echinobase.org
Cameron RA, Samanta M, Yuan A, He D, Davidson E. SpBase: the sea urchin genome database and web site. Nucleic Acid s Research pp. 2009:D750–4.
Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ. Basic local alignment search tool. J Mol Biol. 1990;15(3):403–10.
Sun, Z and Ettensohn, C.A. Signal-dependent regulation of the sea urchin skeletogenic gene regulatory network. Gene Expr Patterns 2014;16:93-103.
Zani IA, Stephen SL, Mughal NA, Russell D, Homer-Vanniasinkam S, Wheatcroft SB, et al. Scavenger receptor structure and function in health and disease. Cell. 2015;4(2):178–201.
Rafik K, Shashikant T, McManus J, Ettensohn CA. Genome-wide analysis of the skeletogenic gene regulatory network of sea urchins. Development. 2014;141:950–61.
Stephan A, Mateos JM, Kozlov SV, Cinelli P, Kistler AD, Hettwer S, et al. Sonderegger P Neurotrypsin cleaves agrin locally at the synapse. FASEB J. 2008;6:1861–73.
Piacentino ML, Zuch DT, Fishman J, Rose S, Speranza EE, Li C, et al. RNA-seq identifies SPGs as a ventral skeletal patterning cue in sea urchins. Development. 2016;143(4):703–14.
Wessel GM, Berg L. A spatially restricted molecule of the extracellular matrix is contributed both maternally and zygotically in the sea urchin embryo. Develop Growth Differ. 1995;37:517–27.
Hodor PG, Illies MR, Broadley S, Ettensohn CA. Cell-substrate interactions during sea urchin gastrulation: migrating primary mesenchyme cells interact with and align extracellular matrix fibers that contain ECM3, a molecule with NG2-like and multiple calcium-binding domains. Dev Biol. 2000;222(1):181–94.
Pavlakis E, Chiotaki R. Chalepakis GF the role of Fras1/Frem proteins in the structure and function of basement membrane. Int J Biochem Cell Biol. 2011;43(4):487–95.
Takeuchi T, Yamada L, Shinzato C, Sawada H, Satoh N. Stepwise evolution of coral Biomineralization revealed with genome-wide proteomics and Transcriptomics. PLoS One. 2016;11(6):e0156424.
Estrada K, Styrkarsdottir U, Evangelou E, Hsu YH, Duncan EL, Ntzani EE, Oei L, Albagha OM, Amin N, Kemp JP, Koller DL, Li G, Liu CT, Minster RL, Moayyeri A, Vandenput L, Willner D, Xiao SM, Yerges-Armstrong LM, Zheng HF, Alonso N, Eriksson J, Kammerer CM, Kaptoge SK, Leo PJ, Thorleifsson G, Wilson SG, Wilson JF, Aalto V, Alen M, Aragaki AK, Aspelund T, Center JR, Dailiana Z, Duggan DJ, Garcia M, Garcia-Giralt N, Giroux S, Hallmans G, Hocking LJ, Husted LB, Jameson KA, Khusainova R, Kim GS, Kooperberg C, Koromila T, Kruk M, Laaksonen M, Lacroix AZ, Lee SH, Leung PC, Lewis JR, Masi L, Mencej-Bedrac S, Nguyen TV, Nogues X, Patel MS, Prezelj J, Rose LM, Scollen S, Siggeirsdottir K, Smith AV, Svensson O, Trompet S, Trummer O, van Schoor NM, Woo J, Zhu K, Balcells S, Brandi ML, Buckley BM, Cheng S, Christiansen C, Cooper C, Dedoussis G, Ford I, Frost M, Goltzman D, González-Macías J, Kähönen M, Karlsson M, Khusnutdinova E, Koh JM, Kollia P, Langdahl BL, Leslie WD, Lips P, Ljunggren Ö, Lorenc RS, Marc J, Mellström D, Obermayer-Pietsch B, Olmos JM, Pettersson-Kymmer U, Reid DM, Riancho JA, Ridker PM, Rousseau F, Slagboom PE, Tang NL, Urreizti R, Van Hul W, Viikari J, Zarrabeitia MT, Aulchenko YS, Castano-Betancourt M, Grundberg E, Herrera L, Ingvarsson T, Johannsdottir H, Kwan T, Li R, Luben R, Medina-Gómez C, Palsson ST, Reppe S, Rotter JI, Sigurdsson G, van Meurs JB, Verlaan D, Williams FM, Wood AR, Zhou Y, Gautvik KM, Pastinen T, Raychaudhuri S, Cauley JA, Chasman DI, Clark GR, Cummings SR, Danoy P, Dennison EM, Eastell R, Eisman JA, Gudnason V, Hofman A, Jackson RD, Jones G, Jukema JW, Khaw KT, Lehtimäki T, Liu Y, Lorentzon M, Mc Closkey E, Mitchell BD, Nandakumar K, Nicholson GC, Oostra BA, Peacock M, Pols HA, Prince RL, Raitakari O, Reid IR, Robbins J, Sambrook PN, Sham PC, Shuldiner AR, Tylavsky FA, van Duijn CM, Wareham NJ, Cupples LA, Econs MJ, Evans DM, Harris TB, Kung AW, Psaty BM, Reeve J, Spector TD, Streeten EA, Zillikens MC, Thorsteinsdottir U, Ohlsson C, Karasik D, Richards JB, Brown MA, Stefansson K, Uitterlinden AG, Ralston SH, Ioannidis JP, Kiel DP, Rivadeneira F. Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. Nature Genet. 2012;44(5):491–501.
Zhao L, Cui B, Liu JM, Zhang MJ, Zhao HY, Sun LH, et al. Interactions of osteoporosis candidate genes for age at menarche, age at natural menopause, and maximal height in Han Chinese women. Menopause. 2011;18(9):1018–25.
Lara-Castillo N, Johnson ML. LRP receptor family member associated bone disease. Rev Endocr Metab Disord. 2015;16(2):141–8.
Kikuchi A, Yamamoto H, Kishida S. Multiplicity of the interactions of Wnt proteins and their receptors. Cell Signal. 2007;19(4):659–71.
Adomako-Ankomah A, Ettensohn CA. P58-a and P58-B: novel proteins that mediate skeletogenesis in the sea urchin embryo. Dev Biol. 2011;353:81–93.
Benson S, Jones EM, Crise-Benson N, Wilt F. Morphology of the organic matrix of the spicule of the sea urchin larva. Exp Cell Res. 1983;148(1):249–53.
Shapiro IM, Landis WJ, Risbud MV. Matrix vesicles: are they anchored exosomes? Bone. 2015;79:29–36.
Cui L, Houston DA, Farquharson C, MAcRae VE. Characterization of matris vesicles in skeletal and soft tissue mineralization. Bone. 2016;87:147–58.
Benson NC, Benson SC, Wilt F. Immunogold detection of glycoprotein antigens in sea urchin embryos. Am J Anat. 1989;185(2–3):177–82.
Kocot KM, Aguilera F, McDougall C, Jackson DJ, Degnan BM. Sea shell diversity and rapidly evolving secretomes: insights into the evolution of biomineralization. Front Zool. 2016;13:23.
We would like to thank Andy Cameron (CalTech) and the Echinobase genomic database (http://www.echinobase.org/Echinobase/) for providing genomic resources.
Availability of data and materials
This research was funded by a California State University CSUPERB award to BTL. RLF. was supported by NIH grant NIH/NIGMS T34GM008074.
RLF isolated the proteins examined, analyzed the LC/MS/MS data and participated in all evolutionary analyses and the construction of figures. BTL guided the project, assisted with the analysis and finalized the writing of the manuscript. Both authors read and approved the final manuscript.
The authors declare that they have no competing interest.
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Peptides identified by LC/MS/MS analysis. All MS/MS samples were analyzed using Mascot (Matrix Science, London, UK; version 2.4.0). Mascot was set up to search the P_Miniata_Custom_20130506 database  assuming the digestion enzyme stricttrypsin. (TXT 718 kb)
Proteins identified from MS/MS analysis. Scaffold (version Scaffold_4.6.1, Proteome Software Inc., Portland, OR) was used to validate MS/MS based peptide and protein identifications. Peptide identifications were accepted if they could be established at greater than 50.0% probability by the Peptide Prophet algorithm with Scaffold delta-mass correction. Protein identifications were accepted if they could be established at greater than 90.0% probability and contained at least 2 identified peptides. Protein probabilities were assigned by the Protein Prophet algorithm. Proteins that contained similar peptides and could not be differentiated based on MS/MS analysis alone were grouped to satisfy the principles of parsimony. (TXT 80 kb)
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Flores, R.L., Livingston, B.T. The skeletal proteome of the sea star Patiria miniata and evolution of biomineralization in echinoderms. BMC Evol Biol 17, 125 (2017). https://0-doi-org.brum.beds.ac.uk/10.1186/s12862-017-0978-z