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Int J Mol Sci. 2017 November; 18(11): 2432.
Published online 2017 November 16. doi:  10.3390/ijms18112432
PMCID: PMC5713400

A Genomic Survey of SCPP Family Genes in Fishes Provides Novel Insights into the Evolution of Fish Scales


The family of secretory calcium-binding phosphoproteins (SCPPs) have been considered vital to skeletal tissue mineralization. However, most previous SCPP studies focused on phylogenetically distant animals but not on those closely related species. Here we provide novel insights into the coevolution of SCPP genes and fish scales in 10 species from Otophysi. According to their scale phenotypes, these fishes can be divided into three groups, i.e., scaled, sparsely scaled, and scaleless. We identified homologous SCPP genes in the genomes of these species and revealed an absence of some SCPP members in some genomes, suggesting an uneven evolutionary history of SCPP genes in fishes. In addition, most of these SCPP genes, with the exception of SPP1, individually form one or two gene cluster(s) on each corresponding genome. Furthermore, we constructed phylogenetic trees using maximum likelihood method to estimate their evolution. The phylogenetic topology mostly supports two subclasses in some species, such as Cyprinus carpio, Sinocyclocheilus anshuiensis, S. grahamin, and S. rhinocerous, but not in the other examined fishes. By comparing the gene structures of recently reported candidate genes, SCPP1 and SCPP5, for determining scale phenotypes, we found that the hypothesis is suitable for Astyanax mexicanus, but denied by S. anshuiensis, even though they are both sparsely scaled for cave adaptation. Thus, we conclude that, although different fish species display similar scale phenotypes, the underlying genetic changes however might be diverse. In summary, this paper accelerates the recognition of the SCPP family in teleosts for potential scale evolution.

Keywords: SCPP gene, evolution, scale, cavefish, mutation

1. Introduction

Phenotypic variations underlying the genetic differences between species are cryptic and attractive for biologists. The appearance of new gene(s) leading to innovative feature(s) can provide organisms with capacities to adapt to natural challenges [1]. The secretory calcium-binding phosphoprotein (SCPP) family have attracted special attention, mainly due to their crucial functions in the mineralization of bone, dentin, enamel, and enameloid, which are beneficial to vertebrates’ protection, predation, and locomotion [2,3,4]. These genes arose from gene duplication and originated from a common ancestor, SPARCL1 (the secreted protein, acidic, cysteine-rich like 1). According to their chemical constitutions, the SCPPs fall into two subclasses: acidic SCPPs containing >25% of Glu (E), Asp (A), and phospho-Ser (pS) residues and Pro/Gln (P/Q)-rich SCPPs consisting of >20% of Pro and Gln [5]. Acidic SCPPs are reported to participate in bone and dentin mineralization, whereas P/Q-rich SCPPs are involved in enamel mineralization [4].

Studies on fish genomes have paid attention to differences in the repertoire of SCPP genes that probably correlate with phenotypic transitions of mineralized tissues, and interesting and profound biological implications about the SCPP family have been reported. In elephant shark, a cartilaginous fish that diverged early from the bony fish lineage, only two SCPP-related ancestral genes (i.e., SPARC and SPARCL1) were identified in its genome, suggesting earlier origins compared to SCPP genes found in bony fishes [6]. The absence of SCPP genes in the elephant shark genome may account for the cartilaginous features of skeleton in chondrichthyes, which are in contrast to relatively higher degrees of mineralized skeleton in bony fish, including teleosts. Moreover, targeted mutagenesis of SPP1, an acidic protein in SCPPs, in zebrafish led to a reduction in bone formation [6]. This result suggests that the loss of SCPP genes would affect the process of skeletal mineralization, and corroborates the essential function of SPP1 in bone formation. In tiger tail seahorse, two acidic SCPP genes (SCPP1 and SPP1) were retained but P/Q-rich genes, associated with dentine and enameloid mineralization, were entirely missing in the genome, suggesting that P/Q-rich SCPP genes are presumably associated with their tooth loss [7].

In vertebrates, two SCPP genes, SPP1 and ODAM, and their common ancestor, SPARACL1, are conserved in jawed vertebrates with a significant similarity in encoded amino acid sequences between tetrapods and teleosts [8,9]. However, other members of the SCPP family are likely to be more specific between lineages, indicating that they arose with lineage specific duplications and deletions, which possibly results in the specialization of certain SCPP family genes in vertebrates. Although the specialization of SCPP family members existed between tetrapods and teleosts, the feature whereby the SCPP family forms a gene cluster is shared by genomes. In fishes such as fugu [10] and zebrafish [11], SPARCL1 and other SCPP genes (except for SPP1) constitute the SPARCL1-SCPP gene cluster (Figure 1). This cluster was also confirmed in coelacanth [9], spotted gar [8], and sunfish [12]. However, the knowledge of SPARCL1-SCPP gene cluster was limited to a few fishes as mentioned above, which hampers a deeper understanding of its evolution in teleosts.

Figure 1
The SPARCL1-SCPP cluster in fugu and zebrafish (modified from [10,11]).

A recent report showed the upregulation of SCPP genes during scale development in common carp, providing reliable evidence that SCPP genes are involved in the regulation of scale development in fishes [13]. The study further compared the existence of SCPP genes in scaled and scaleless fishes, and observed loss of SCPP1 and/or SCPP5 in scaleless fish, but the presence of them were exhibited in scaled fishes. Therefore, these two genes were regarded as candidates for determining scale phenotypes. Besides the strict scaled or scaleless phenotype in fishes, there is another pattern of phenotype called “sparsely scaled” feature, and it presents in fishes such as Mexican tetra (Astyanax mexicanus) [14] and Chinese golden-line fishes (Sinocyclocheilus rhinocerous and S. anshuiensis) [15]. A. mexicanus and S. anshuiensis are cave-restricted fishes, while S. rhinocerous is semi-cave-dwelling. These species exhibit sparse scales in their surface skin, whereas their relatives living in surface rivers present rich scales. Therefore, the functions of SCPP genes in determining scale phenotypes need to be further verified in sparsely scaled fishes. However, no such studies are available currently.

This present study focuses on the SCPP repertoire in 10 fishes, including A. mexicanus (abbreviated as AM), Ctenopharyngodon idellus (CI; grass carp), Cyprinus carpio (CC; common carp), Ictalurus punctatus (IP; Channel catfish), Leuciscus waleckii (LW; Amur ide), Pimephales promelas (PP; fathead minnow), Pygocentrus nattereri (PN; red-bellied piranha), Sinocyclocheilus anshuiensis (SA), Sinocyclocheilus grahamin (SG), and Sinocyclocheilus rhinocerous (SR). All species belong to the Series Otophysi and are classified as Cypriniformes, Characiformes, or Siluriformes. In terms of morphology, they present three scale phenotypes and can be categorized as scaled (including CI, CC, LW, PP, PN, and SG), scaleless (such as IP), or sparsely scaled (such as AM, SR and SA) fishes. The main purpose of our present research is to enrich the evolutionary studies of SPARCL1-SCPP cluster in certain fish lineages. We focused on sparsely scaled fishes to test the roles of SCPP1 and SCPP5 as candidate genes for scale phenotype determination. In this paper, we concentrate on SPARCL1 and SCPP genes, and attempt to answer three core questions: (1) Does the reported SPARCL1-SCPP cluster display a similar arrangement in the examined fishes? (2) How do the SPARCL1 and SCPP genes evolve among species? (3) Does the hypothesis of SCPP1 and SCPP5 serving as candidate genes for determining scale phenotypes work for the sparsely scaled species?

2. Results

2.1. Collection of SPARCL1 and SCPP Genes and Transcriptome Confirmation

We obtained a total of 115 nucleotide sequences for 14 SPARCL1 genes (Figure S1) and 101 SCPP family genes (including SPP1, SCPP1, ODAM, fa93e10, SCPP5, SCPP6, SCPP7, and SCPP9; Figures S2–S9). All these sequences were derived from 10 fish species, namely, AM, CI, CC, IP, LW, PP, PN, SA, SG, and SR, using the sequences from zebrafish (DR) as the queries (Figure 2). Multiple alignment of the nucleotide sequences for each gene displays high similarities among species (see more details in Figures S1–S9).

Figure 2
Phylogeny of SPARCL1 and eight SCPP family genes among 11 fish species. The sequences from zebrafish (Danio rerio; DR) were downloaded from NCBI (find detailed accession numbers in Table S1) for subsequent homology searching, and other sequences were ...

In Sinocyclocheilus species (SA, SG, SR) and CC, SPARCL1 and SCPP genes were found to be doubled, with an exception of only one copy of ODAM in SR. In contrast, only a single copy of SPARCL1 and SCPP genes was identified in other fishes (PP, LW, CI, IP, PN, and AM) as the same as spotted gar [8] and zebrafish [11]. Thus, double copies of SPARCL1 and SCPP genes in SA, SG, SR, and CC may imply that these genes had ever undergone a gene-duplication event. Our predicted SPARCL1 and SCPP genes in SG, SR, and SA were mostly supported by transcriptome assemblies [15] (see more details in Section 4.1), but with the exception for the SCPP5 gene.

Despite the success of collecting all genes in Cypriniformes, we failed to identify some of the SCPP genes from the genomes of species in Siluriformes and Characiformes, such as IP, AM, and PN. In IP, only SPARCL1, SCPP1, SPP1, and ODAM were identified, whereas more genes were identified in AM and PN, although SCPP6 and SCPP9 were still missing. It seems that the distribution of SCPP genes in the genomes of these teleost species is uneven, and certain SCPP genes may be evolved with lineage-specific activities.

2.2. Phylogenetic Topologies of SPARCL1 and SCPP Genes

The topology of evolutionary trees deduced from the alignments of SPARCL1, SCPP1, SPP1, fa93e10, ODAM, and SCPP9 commonly exhibits two major groups (Subclasses I and II in Figure 2) among SG, SA, SR, and CC, but with the exceptions of SCPP6, SCPP7, and SCPP5, suggesting that the evolution of these genes was not coincided.

In the phylogeny of SPARCL1, SCPP1, SPP1, fa93e10, ODAM, and SCPP9, Subclass I and Subclass II form sister groups (Figure 2a–f), indicating a closer relationship of these genes than the others. For SCPP6 and SCPP7, although two groups among SG, SA, SR, and CC were still presented, they did not form sister groups yet (Figure 2g,h). The different topologies of the Subclasses I and II may result from a higher nucleotide substitution rate of SCPP6 and SCPP7 in one subclass. In addition, the phylogenetic topology of SCPP5 (Figure 2i) is completely different from other SCPP genes, suggesting a more complex evolutionary history compared with other SCPP genes.

2.3. The Putative SPARCL1-SCPP Cluster and Pseudogenes

By mapping the SPARCL1 and SCPP sequences onto the 10 examined fish genomes, we observed that most of them are localized into a common region with the formation of a single or multiple gene cluster(s) (Figure 3). The single cluster includes fa93e10, SCPP5, SCPP7, SCPP6, ODAM, SCPP9, SPARCL1, and SCPP1 in CI and LW (Figure 3c), similar to the localization in the reported zebrafish genome [11]. While in IP, AM, PN, PP, CC, SG, SR, and SA, the SCPP genes were separated into two clusters, including a relatively long one and another short one. The long one includes fa93e10, SCPP5, SCPP7, SCPP6, SCPP9, and ODAM, and the short one consists of SPARCL1 and SCPP1 (Figure 3). These different genomic arrangements indicate that the SPARCL1-SCPP cluster within these fish species may be various in evolution.

Figure 3
The genomic arrangement of SPARCL1 and SCPP genes in the 10 examined fish genomes. (a,b,c,d) Siluriformes, Characiformes, and Cypriniformes fishes, respectively. The yellow, red, and blue colors represent the ancestral SPARCL1 gene, acidic SCPP-encoding ...

Interestingly, SPP1 is always separately distributed in the 10 examined genomes, suggesting its separation from the main gene cluster in the early evolution, which has been previously reported in fugu [10] and zebrafish [11].

By comparing the predicted gene structures of these collected genes, we considered those predicted genes with missing exons, codon frameshifts, or premature stop codons as possible pseudogenes (Figure 3b–d). Interestingly, we observed more possible pseudogenes in these sparsely scaled species (AM, SR, and SA). In AM, half of the SCPPs (SPARCL1, SCPP1, and fa93e10) were identified as possible pseudogenes (Figure 3b). Among the three Sinocyclocheilus fishes, only one possible pseudogene (SCPP9-C2) was identified in the surface-dwelling SG, but there are seven and five possible pseudogenes in the semi-cave-dwelling SR and cave-restricted SA, respectively (Figure 3d).

2.4. SCPP1 and SCPP5: Gene Structure Comparison between Cavefishes and Other Fishes

To test the hypothesis of SCPP1 and SCPP5 as candidate genes for determining scale phenotypes [13], we chose and compared fishes with scaled, sparsely scaled, and scaleless phenotypes (Figure 4). Interestingly, we found that the first five and three exons in SCPP1 of sparsely scaled AM and SR, respectively, were missing (Figure 4a), and the last five exons in SCPP1 of sparsely scaled AM were as well (Figure 4b). These structural changes suggest their pseudogene status. We did observe that SCPP1 and SCPP5 were quite normal in another sparsely scaled species SA, but no SCPP5 was identified in the scaleless IP.

Figure 4
Comparison of candidate genes for determining scale phenotype among scaled, sparsely scaled, and scaleless fishes. (a,b) Structural alignments of SCPP1 and SCPP5 genes, respectively, in six representative fishes, namely, scaled PN and SG, sparsely scaled ...

In the three Sinocyclocheilus fishes, an extra exon appeared (Figure 4b). Based on the pairwise alignment of SCPP1 between them and zebrafish, we evaluated that this additional exon was generated by a crack of the original Exon 9. We temporarily regard these SCPP5s as normal genes, although we cannot determine whether this crack causes pseudogenization.

3. Discussion

3.1. Comparison of the SPARCL1-SCPP Cluster in Teleosts

Since the report of SPARCL1-SCPP cluster in fugu [10], similar genomic arrangement was confirmed in zebrafish [11], coelacanth [9], spotted gar [8], and sunfish [12]. In our present work, this pattern was further corroborated (Figure 3c) in grass carp (CI) and Amur ide (LW). However, we observed a division of the putative SPARCL1-SCPP cluster into two segments in other examined fishes, with one portion consisting of SPARCL1 and SCPP1 and the other composed of fa93e10, SCPP5, SCPP7, SCPP6, ODAM, and SCPP9 (see more details in Figure 3). The crack of SPARCL1-SCPP cluster indicates chromosomal rearrangement in these fishes.

Furthermore, we compared a copy number of SPARCL1 and SCPP genes in fishes including Siluriformes, Characiformes and Cypriniformes. Siluriformes, such as IP, own the least number of such genes with only SPARCL1, ODAM, SCPP1, and SPP1 were identified (Figure 3a). Characiformes (such as AM and PN) have a medium number of SCPPs between Siluriformes and Cypriniformes (Figure 3b). The various amount of SCPP gene numbers among different groups suggests that some SCPP genes are lineage-specific and the evolutionary history of SCPPs in certain families of teleosts is uneven. Interestingly, among the eight SCPP genes, SCPP6 only existed in Cypriniformes, but disappeared in Siluriformes and Characiformes, implying a special role of SCPP6 in Cypriniformes. The loss of SCPP6 was also reported previously in fugu [10], sunfish [12], coelacanth [9], and spotted gar [8]. Taken together, it seems that SCPP6 is very unique with only existence in Cypriniformes. Thus, in addition to the previous report of the independent evolution of SCPP genes between teleosts and tetrapods [2], we also demonstrate that the evolution of the SPARCL1-SCPP cluster among lineages in teleosts are unparallel, with an independent history of certain SCPP genes.

3.2. Evolution of SPARCL1 and SCPP Genes during Whole Genome Duplication

In contrast to the richness of SCPP genes in teleosts, the SCPP family was absent in cartilaginous fishes (such as little skate, the small-spotted catshark, and elephant shark) and jawless vertebrates (such as sea lamprey) [6]. This indicates that the primary vertebrates had unevolved the SCPP family until the appearance of teleosts. Thus, SCPP genes existed in teleosts were thought to be evolved after the actinopterygian–sarcopterygian divergence [11]. In vertebrates, as we know, two rounds of whole-genome duplication (WGD) occurred in the common ancestor [16,17]. More specifically, the two rounds of WGD happened before the agnatha–gnatostoma and chrondrichthyes–osteichthyes split, respectively. The third round of WGD was specific to teleosts (TSGD) that occurred after the actinopterygian–sarcopterygian split [18,19]. Thereby, SCPP genes in teleosts are probably originated from TSGD and duplicated from the SPARCL1 gene. Subsequently, SCPP genes evolved along with the course of speciation and certain SCPP genes arose in lineage-specific ways.

Besides the above-mentioned three rounds of WGD, some fish lineages such as Acipenseridae, Catostomidae, Cobitidae, Cyprininae, and Salmonidae underwent a fourth round of WGD [20]. The genomic studies of common carp and Sinocyclocheilus species [15,20] indicate their tetraploid nature in Cyprininae. Thus, the double copies of SPARCL1 and SCPP genes in CC, SG, SR, and SA (Figure 3) were presented with a high possibility of yielding in the fourth Cyprininae-specific WGD. WGD was thought to provide raw genetic materials for new gene appearance, allowing organisms to acquire new traits to survive in the natural challenges [1]. TSGD-originated SCPP genes have proven to be crucial for tissue mineralization, such as the mineralizing process of tooth, bone, and scale formation [6,10,11,13]. These tissues help teleosts with predation, locomotion, digestion, and protection, which are the basic skills for survival. In contrast to the initially arisen SCPP genes, the newly yielded SCPP copies in the fourth WGD of Cypriniformes were reported for the first time in our present study. The exact functions of these new SCPP copies are still unknown, although SCPP7 and fa93e10 were reported to have much higher transcription during scale regeneration in common carp (CC) [13].

In general, the fate of WGD duplications can be either pseudogenization, subfunctionalization, or neofunctionalization. It has been reported that rapid gene loss did occur after the TSGD, and most genes were doubled in this event and were subsequently lost quickly in the initial 60 Ma after TSGD [21]. However, the fate of duplicated genes in the fourth round of WGD in Cyprininae has been unknown yet. From the perspective of SPARCL1 and SCPP genes, we found basically two copies in CC, SG, SR, and SA, despite the possibility that one copy of ODMA in SR was missing. This suggests the fate of duplicated SPARCL1 and SCPP genes in the fourth WGD may differ from the fast lost gene copies yielded in TSGD.

However, the structural changes displayed in some duplicated SCPP genes of CC, SG, SR, and SA (Figure 3d and Figure 4) suggest their possible transformation into pseudogenes. Thus, some duplicated SCPP genes faced fast functional loss after the fourth WGD. In contrast to the proportion of gene copies into pseudogenes, more SCPP gene copies were found as normal as those in zebrafish with similar gene structures (Figure 4). Therefore, this part of duplicated SCPP genes in the fourth WGD might be retained for neofunctionalization or subfunctionalization. Recently reported Atlantic salmon genome provides novel insights into gene fate after the fourth WGD in Salmonidae [22]. The fate of duplicates of salmonids in the fourth WGD likely prefers neofunctionalization to subfunctionalization, which provide salmonids with a wide range of ecological adaptions. According to this pattern, the newly predicated SCPP duplicates in Cyprininae may also generate outcomes of functional divergence and benefit their living in evolutionary history, but this needs further experimental verification.

3.3. Comparison of SCPP1 and SCPP5 in Scaled, Sparsely Scaled and Scaleless Fishes

Cavefishes are restricted to subterranean environments. Besides the blind eyes and albinism that are obviously different from the surface-dwelling counterparts, cavefishes also show a great decrease in the number of scales [14,15]. Previously, SCPP1 and/or SCPP5 have been reported to be candidate genes for determining scale phenotypes [13]. Our present study added two more cave-restricted fishes (AM and SA) and one semi-cave-dwelling SR to compare the gene changes of SCPP1 and SCPP5. Our results revealed structural changes in both SCPP1 and SCPP5 in AM but not in another cavefish SA; some exons in SCPP1 are missed in the semi-cave-dwelling SR, but not in the cave-restricted SA (Figure 4). These data suggest that the gene changes in AM and SA are not uniform, and even in phylogenetically closed species, SR and SA are also uneven, even though their scale phenotypes are similar.

It seems that the hypothesis of SCPP1 and SCPP5 regarded as candidate genes for determining scale phenotype is suitable for AM, but denied by SA. Consequently, we estimated that, in addition to SCPP1 and SCPP5, more genes are necessary for involvement in the process of scale development. Although both AM and SA are sparsely scaled, the underlying genetic mechanisms leading to this phenotype could be diverse.

Different changes between AM and SA were also revealed in melanogenesis-related gene Oca2. The albinism of AM might be generated because some exon regions of Oca2 are missed, resulting in the termination of upstream steps of the melanin synthesis pathway [23]. However, such changes were denied by albinotic SA [15]. Thus, given that the functions of SCPP1, SCPP5, and Oca2 are related to scales and albinism in AM and SA, we propose that, although fishes from different lineages present convergent evolution, molecular changes of similar phenotypes can be completely different.

4. Materials and Methods

4.1. Gene Collection and Transcriptome Confirmation

Firstly, the protein sequences (Table S1) of SPARCL1, SPP1, SCPP1, ODAM, fa93e10, SCPP5, SCPP6, SCPP7, and SCPP9 identified by Kawasaki (2009) were downloaded from the National Center for Biotechnology Information (NCBI). Secondly, whole genomes of nine fishes (AM, CC, IP, LW, PP, PN, SA, SG, and SR) were downloaded from NCBI, and the genome of grass carp (CI) retrieved from the official National Center for Gene Research website (, to construct a local database (Table S2). Nucleotide sequences of SPARCL1, SPP1, SCPP1, ODAM, fa93e10, SCPP5, SCPP6, SCPP7, and SCPP9 were extracted from these genomes using BLAST (version 2.2.28 [24]) and Exonerate (version 2.2.0 [25]). We also provided further confirmation of these extracted SPARCL1 and SCPP genes in skin transcriptome data among SG, SR, and SA. Related transcriptome assemblies were generated in our previous paper [15].

4.2. Sequence Alignment and Phylogenetic Reconstruction

The collected nucleotide sequence of SPARCL1, SPP1, SCPP1, ODAM, fa93e10, SCPP5, SCPP6, SCPP7, and SCPP9 were processed for phylogenetic analyses. Multiple codon-based alignments of the collected sequences were initially performed using MEGA (version 7.0 [26]) with the Muscle module. Each alignment of genes was subsequently adjusted manually. The final aligned nucleotide sequences were employed to predict their best nucleotide substitution model under the Akaike Information Criterion (AIC) [27], which was implemented in Jmodeltest (version 2.0 [28]). The parameters within the best nucleotide substitution models (GTR+G for SPARCL1, SPP1, SCPP1, ODAM, fa93e10, SCPP6, and SCPP7, HKY85+G for SCPP5, and GTR+I for SCPP9) were applied using PhyML (version 3.1 [29,30]) to construct phylogenetic topologies with the maximum likelihood (ML) method and 1000 replicates for the evaluation of their branch supports.

4.3. Genomic Location and Pseudogene Identification

By mapping the collected sequences onto their corresponding genomes, the genomic location of SPARCL1 and SCPP genes were determined, which was implemented in TBtools ( /CJ-Chen/TBtools). Pairwise alignment of SPARCL1, SPP1, SCPP1, ODAM, fa93e10, SCPP5, SCPP6, SCPP7, and SCPP9 between extracted species and zebrafish was also performed in Exonerate software (Figures S1–S9). Missing exon regions, codon frameshifts, or premature stop codon(s) within each gene were identified for the consideration of a possible pseudogene.

5. Conclusions

In this paper, we investigated and compared the SCPP repertoire from 10 fishes of Otophysi. We observed that the diversity of SCPP members among various fish lineages was uneven, and certain SCPP genes evolved specifically by lineages. After comparing the SCPP gene copies, we estimated that the fourth WGD in Cyprininae with a high possibility caused the duplication of SPARCL1 and SCPP genes. However, some duplicated SCPP genes changed into pseudogenes, whereas others were retained with structural normality. The previously reported hypothesis considering SCPP1 and/or SCPP5 as candidates for scale phenotype determination is suitable for AM, but denied by SA, even though they were both sparsely scaled cavefishes. Through these analyses and comparisons, we provide new insights into teleost SCPP family genes for potential scale evolution.


This work was supported by the National Natural Science Foundation of China (No. 31370047), the Shenzhen Special Program for Development of Emerging Strategic Industries (No. JSGG20170412153411369), and the Zhenjiang Leading Talent Program for Innovation and Entrepreneurship.


AMAstyanax mexicanus
CCCyprinus carpio
CICtenopharyngodon idellus
IPIctalurus punctatus
LWLeuciscus waleckii
Oca2Gene encoding oculocutaneous albinism II (melanocyte-specific transporter protein)
ODAMGene encoding odontogenic ameloblast-associated protein (Ameloblast-associated odontogenic protein)
PPPimephales promelas
PNPygocentrus nattereri
SASinocyclocheilus anshuiensis
SGSinocyclocheilus grahamin
SRSinocyclocheilus rhinocerous
SCPP1secretory calcium-binding phosphoprotein 1
SCPP5secretory calcium-binding phosphoprotein 5
SCPP6secretory calcium-binding phosphoprotein 6
SCPP7secretory calcium-binding phosphoprotein 7
SCPP9secretory calcium-binding phosphoprotein 9
SPARCsecreted protein acidic and rich in cysteine
SPARCL1Gene encoding SPARC-like protein 1
SPP1Gene encoding secreted phosphoprotein 1
TSGDteleosts-specific genome duplication
WGDwhole genome duplication

Supplementary Materials

Supplementary materials can be found at

Author Contributions

Author Contributions

Qiong Shi and Yunyun Lv conceived and designed the project. Yunyun Lv, Jia Li, Yanping Li, Chao Bian, Xinxin You, and Yu Huang participated in data analysis and figure preparation. Kazuhiko Kawasaki provided assistance to the SCPP classification. Yunyun Lv prepared the manuscript. Qiong Shi and Kazuhiko Kawasaki revised the manuscript.

Conflicts of Interest

Conflicts of Interest

The authors declare no conflict of interest.


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