The vasa gene encodes an ATP-dependent RNA helicase of the DEAD box protein family that functions in a broad range of molecular events involving duplex RNA. In most species, the germline specific expression of vasa becomes a molecular marker widely used in the visualization and labeling of primordial germ cells (PGCs) and a tool in surrogate broodstock production through PGC transplantation. The vasa gene from tongue sole (Cynoglossus semilaevis) was characterized to promote the development of genetic breeding techniques in this species. Three C. semilaevis vasa transcripts were isolated, namely vas-l, vas-m, and vas-s. Quantitative real-time PCR results showed that C. semilaevis vasa transcripts were prevalently expressed in gonads, with very weak expression of vas-s in other tissues. Embryonic development expression profiles revealed the onset of zygotic transcription of vasa mRNAs and the maternal deposit of the three transcripts. The genetic ZW female juvenile fish was discriminated from genetic ZZ males by a pair of female specific primers. Only the expression of vas-s can be observed in both sexes during early gonadal differentiation. Before PGCs started mitosis, there was sexually dimorphic expression of vas-s with the ovary showing higher levels and downward trend. The results demonstrated the benefits of vasa as a germline specific marker for PGCs during embryonic development and gonadal differentiation. This study lays the groundwork for further application of C. semilaevis PGCs in fish breeding.
Citation: Wang Z, Gao J, Song H, Wu X, Sun Y, Qi J, et al. (2014) Sexually Dimorphic Expression of vasa Isoforms in the Tongue Sole (Cynoglossus semilaevis). PLoS ONE 9(3): e93380. https://doi.org/10.1371/journal.pone.0093380
Editor: László Orbán, Temasek Life Sciences Laboratory, Singapore
Received: November 22, 2013; Accepted: March 3, 2014; Published: March 26, 2014
Copyright: © 2014 Wang et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by the National High-Tech Research and Development Program (2012AA10A402) and the National Natural Science Foundation of China (31172385). The URL is http://www.863.gov.cn and http://www.nsfc.gov.cn/Portal0/default152.htm, respectively. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
DEAD (Asp–Glu–Ala–Asp) box protein families are ATP-dependent RNA helicases present in almost all organisms. These proteins have significant functions in RNA metabolism and are associated with processes involving RNA from transcription to degradation . DEAD-box proteins comprised three subfamilies: VASA, PL10, and P68. The vasa gene was thought to arise from the duplication of a PL10-related gene prior to the appearance of sponges, but following the diversion of fungi and plants . Since the first isolation of the Drosophila vasa gene , vasa-like genes have been identified from invertebrates (e.g., hydra , planarian , nematode , and ascidian ) to vertebrates (e.g., Xenopus , chicken , mouse , and human ). With these observations, recent studies have revealed that the vasa gene and its products are restricted to the germ cell lineage in most species. Extragonadal vasa expression was also reported in teleosts, such as rainbow trout , European sea bass , and Senegalese sole .
Studies on teleosts have investigated on the vasa expression patterns during the embryogenesis and gonadal differentiation. Vasa isoforms were characterized in several teleosts such as zebrafish , , tilapia , rare minnow , Japanese flounder , and Senegalese sole . The expression profiles of different vasa transcripts were distinguished during sex differentiation in zebrafish , tilapia , and Senegalese sole . This distinction implies the functions of these isoforms in germline development and the significance of homolog characterizations.
The vasa gene is a molecular marker widely used in visualizing and labeling of primordial germ cells (PGCs). The stable labeling of these cells in teleosts is achieved through the specific expression of green fluorescence protein (GFP) driven by the vasa promoter. Transgenic fish lines have been reported only in model fish (e.g., zebrafish  and medaka ) and aquaculture species (e.g., rainbow trout ). PGCs are the progenitor cells of germ cell lineage responsible for genetic transmission to the next generation, which allow their applications in fish bioengineering, such as cryopreservation of the genetic resources ,  and transplantation for surrogate broodstock production –. These studies suggest the bioengineering potential of the vasa gene as a tool in fish breeding.
Tongue sole (Cynoglossus semilaevis) is an economically important marine fish in China. To date, only wild C. semilaevis broodstocks are used to produce robust eggs, thereby hampering the development of genetic breeding techniques. PGC transplantation provides a novel approach to generate viable offspring by surrogate breeding. We identified vasa transcripts in C. semilaevis to label and isolate their PGCs. We cloned and characterized the full length of three C. semilaevis vasa isoforms for the first time. We quantified the distribution patterns of each vasa transcript in adult tissues and the expression profiles during embryogenesis and gonadal differentiation. The results will facilitate further studies on labeling, isolation, and transplantation of PGCs as well as promote the progress of breeding techniques in this species.
Methods and Materials
C. semilaevis (Pleuronectiformes) samples were collected from local aquatic farms with permission from the local government of Yantai, Shandong, China. The samples were handled in accordance with the guidelines and regulations established by the Ocean University of China and the local government of Yantai.
All fish and embryos were collected from a commercial farm in Yantai, Shandong Province, China. All procedures complied with and were approved by the Institutional Animal Care and Use Committee of the Ocean University of China.
Six randomly selected healthy 2-year-old adults (three females and three males) were dissected. Tissues from the muscle, gill, heart, intestine, brain, kidney, liver, spleen, and gonad were collected.
Artificially fertilized eggs were incubated at 21±1°C in the hatching tanks with an open recirculation water system and sufficient air supply. Unfertilized eggs and embryos of different developmental stages (n = 50; 1-, 2-, 8-, and 16-cell, morula, high and low blastula, early and late gastrula, Kupffer's vesicle, neurula, somitogenesis, and hatching) were collected. Each sample was collected in triplicate.
Juvenile fish cultivated at 23°C during early gonadal differentiation [n = 10 per group; total length (TL) = 20±1, 25±1, 30±1, 35±1, 40±1, 45±1, 50±1, and 55±1 mm] were dissected. Isolating gonads from juveniles with TL≤60 mm is difficult, so we collected the whole abdomen that contained the gonadal anlagen by removing the head as well as most of the muscular dorsal and ventral parts of the fish. The muscle tissues of each fish were also collected.
Each sample was collected in triplicate. All samples were immediately frozen using liquid nitrogen and stored at −80°C for total RNA or genomic DNA preparation.
RNA and genomic DNA extraction
Total RNA was extracted using Trizol Reagent (Invitrogen, CA, USA) according to the manufacturer's protocol, treated with RNase-free DNase I (TaKaRa, Dalian, China) to degrade genomic DNA, and then frozen at −80°C. cDNA synthesis was performed with 1 μg total RNA and random hexamer primers using Reverse Transcriptase M-MLV (RNase H−) Kit (TaKaRa, Dalian, China) following the manufacturer's instructions. Genomic DNA was isolated from the muscle tissue using the traditional phenol/chloroform extraction method.
The quality and quantity of the RNA and DNA were evaluated by 1.5% agarose gel electrophoresis and spectrophotometry using NanoPhotometer Pearl (Implen, Munich, Germany).
Molecular cloning of vasa gene
De novo transcriptome sequencing and characterization for C. semilaevis were performed in our laboratory. The raw reads were submitted to SRA Databases in NCBI (Accession number: SRX257138). A total of 749,954 reads generated using a single 454 sequencing run in one full PicoTiter plate were assembled into 62,632 contigs with a ten-fold average sequencing coverage.
Two contigs were screened from the C. semilaevis transcriptome through sequence homology analysis. A pair of scaf-FW/RV primers (Table S1) was designed separately based on the contigs. PCR amplification was performed to link the two contig sequences under the following conditions: initial denaturation at 95°C for 5 min, followed by 30 cycles at 95°C for 30 s, at 60°C for 30 s, and at 72°C for 1 min; and a final extension at 72°C for 10 min.
The 5′ and 3′ RACE were performed to isolate the full-length cDNA of vasa from the ovary tissue using SMART RACE cDNA Amplification Kit (Clontech, CA, USA) according to manufacturer's protocol. Gene-specific primers (GSPs) were designed based on the known cDNA sequence. For the 5′ RACE, the GSPs were 5′ race1 and 5′ race2 (Table S1); for the 3′ RACE, the GSPs were 3′ race1 and 3′ race2 (Table S1). PCR was conducted according to the SMART RACE amplification methods. The full length of the vasa cDNA sequence was assembled with the sequenced PCR products using software suite Lasergene v7.0 (DNASTAR, WI, USA).
Genomic sequence of vasa was cloned through PCR amplification using LA Taq (TaKaRa, Dalian, China) with specific primers vasa-5′ FW and vasa-3′ RV (Table S1) designed based on the potential 5′ and 3′ UTR of the obtained vasa cDNA sequence. Subsequently, the genomic 5′ and 3′ vasa flanking sequences were amplified using the Genome Walking Kit (TaKaRa, Dalian, China); the primers 5′ GSP1/5′ GSP2/5′ GSP3 and 3′ GSP1/3′ GSP2/3′ GSP3 (Table S1) were designed according to the instructions. The PCR conditions likewise followed supplied instructions in the kit.
All PCR products were separated on 1.5% agarose gel electrophoresis, purified using the Zymoclean Gel DNA Recovery Kit (Zymo Research, CA, USA), cloned into pMD-18T Vector (TaKaRa, Dalian, China), and sequenced.
Phylogenetic analysis of vasa products
Homologous nucleotide and protein sequences were confirmed through the BLAST search at NCBI (http://www.ncbi.nlm.gov/blast). Multiple sequence alignments were conducted by ClustalX 2.1 (http://www.clustal.org/clustal2/). The phylogenetic tree was constructed using MEGA5  with neighbor-joining method . The branching reliability was tested via bootstrap resampling with 1,000 pseudoreplicates.
Tissue distribution pattern of vasa isoforms by quantitative real-time PCR (qRT–PCR)
Three specific primer pairs (vasaL-FW/RV, vasaM-FW/RV, vasaS-FW/RV; Table S1) were designed based on the characteristics of vas-l, vas-m, and vas-s. Pre-experiment was conducted to confirm a single cDNA PCR product and avoid the amplification of genomic DNA. Specific PCR products were verified through sequencing.
The evaluation of eight housekeeping genes as candidate references for gene expression analysis in C. semilaevis was assayed in our laboratory (unpublished). 18S rRNA was the most stable gene in the different tissues. Therefore, relative expression was determined using the 18S rRNA as the reference gene.
Total RNA was extracted from the adult tissues and cDNA synthesis was performed. Three biological replicates of each sample were analyzed, with each sample ran in triplicate.
qRT–PCR was performed in a 20 μl solution containing 20 ng template cDNA and SYBR Premix Ex Taq II (TaKaRa, Dalian, China) via LightCycler480 (Roche Applied Science, Mannheim, Germany) at 95°C (5 min) for pre-incubation, followed by 45 cycles at 95°C (15 s) and 60°C (45 s); finally, the melting curve was analyzed to detect single amplification. The accumulation of fluorescent signal from SYBR Green I was recorded at 60°C (45 s) phase during each cycle under the control of LightCycler480 Software 1.5. Negative control (no-template reaction) was always included.
Relative quantification for the target vasa gene that is expressed as fold variation over the reference gene 18S rRNA was calculated by the 2−ΔΔCt comparative Ct method.
Gonad samples (ovary and testis) for histological observation were fixed in Bouin's solution for 24 h and then stored in 70% ethanol at 4°C.
The fixed gonads were dehydrated in an ascending ethanol series, cleared with xylene, and embedded in paraffin wax. The 6 μm-thick sections were stained with hematoxylin and eosin (H&E) and observed under a Nikon Eclipse Ti-U microscope (Nikon, Tokyo, Japan).
In situ hybridization (ISH)
The gonad samples used for ISH were fixed immediately in 4% paraformaldehyde–PBS (4% PFA) overnight at 4°C, dehydrated in gradients of increasing methanol and stored in 100% methanol at −20°C.
ISH of vasa expression in the gonads was performed using a 364 bp probe spanning the 3′ UTR of the vasa cDNA (Table S1). DIG-labeled RNA sense and anti-sense probes were synthesized using the DIG RNA Labeling Kit (SP6/T7) (Roche, Mannheim, Germany) according to the manufacturer's instructions. ISH on paraffin sections of the gonads was performed , .
Ontogenic expression patterns of vasa isoforms by qRT–PCR
Expression patterns of vasa isoforms during embryogenesis was analyzed by relative qRT–PCR. Total RNA was prepared from the embryo samples collected at different developmental stages. Housekeeping gene B2M was the most stable gene during embryo development among the eight candidate reference genes and used as the reference gene.
Expression pattern of vasa isoforms during early gonadal differentiation by qRT–PCR
Genomic DNA was isolated from the juvenile fish muscle. Subsequently, the genetic sex of each fish was identified by PCR, which was conducted using control and female-specific primers developed by our laboratory . The PCR products were separated on 1.5% agarose gel. Female and male individuals were discriminated from each other by the existence of a female specific band. Then, 3 female and 3 male juvenile fish were selected from each group using the total length (TL), and the fish were used to analyze the expression pattern of vasa isoforms during early gonadal differentiation by relative qRT–PCR. Housekeeping gene RPL17 was the most stable during larval development among the eight candidate reference genes and used as the reference gene.
Molecular characterization of three vasa isoforms
A longer 1232 bp cDNA fragment containing the two contigs that was screened from the C. semilaevis transcriptome was obtained using scaf-FW/RV primers. The remaining parts of vasa were cloned through 5′ and 3′ RACE. Three types of 5′ extremities were identified from the sequenced 5′ RACE products. The three vasa isoforms were assembled with the cDNA fragments.
The longest isoform was the 2495-bp long vas-l (GenBank: KF856010), which contained an open reading frame (ORF) of 2046 bp and encoded 681 amino acid residues (Figure S1). The shortest was the 2441-bp long vas-s (GenBank: KF856012), which contained an ORF of 1992 bp and encoded 663 amino acid residues (Figure S1). The nucleotide sequence of the 2468-bp long vas-m (GenBank: KF856011) contained an ORF of 2019 bp ORF and encodes 672 amino acid residues (Figure S1).
Genomic and phylogenetic analysis of vasa
A 6388 bp genomic vasa fragment (GenBank: KF856013) was cloned based on the vasa cDNA sequence. Only the single genomic 5′ flanking sequence (GenBank: KF876914) or 3′ flanking sequence (GenBank: KF876915) of vasa was obtained through genome walking.
Comparison of the three vasa cDNA sequences with the genomic sequence revealed a possible genomic structure of vasa gene (Figure 1A). The vasa gene contained up to 23 exons, and the 5′ UTR was separated by the first and the longest intron.
(A) A graphical representation of vasa genomic structure was drawn. Exons were shown as boxes and numbered above the schematic (protein coding region in the black or grey box; UTR in the open box); introns were shown as fold lines. Exons 4 and 10a were shown as grey boxes. Scale bar = 200 bp. (B) Multiple sequence alignments of the three Vasa proteins were performed and the major motif locations were marked under the sequences. The motifs encoded by either exon 4 or 10a were boxed in red background. The motifs conserved among Vasa characteristic homologs of the DEAD-box proteins were boxed in yellow background. These motifs were encoded by exons 15 to 21. The RGG and RG repeats at the N-terminal regions were boxed in green and blue backgrounds and encoded by the exons 4 to 12. Given the sequence differences, Vas-l, Vas-m, and Vas-s had 11, 9 and 10 RG repeats, respectively. (C) The 5′ parts of the three vasa isoforms were graphically presented. The position of the specific primers used to clone the vasa isoforms was shown under the corresponding transcript. Exon 4 uniquely encoded the amino acids in vas-l transcript; exon 10a functioned as a part of CDS only in vas-m transcript. Scale bar = 10 bp.
The deduced amino acid sequence alignments of the three variants were conducted by ClustalX 2.1; the motif locations were shown in terms of the genomic structure of the vasa gene (Figure 1B). They shared significant similarities with the same highly conserved motifs characteristics of the DEAD box protein family. The three isoforms also contained the same five arginine–glycine–glycine (RGG) motifs and the different numbers of arginine–glycine (RG) motifs resulting from the sequence differences at N-terminal regions (Figure 1B).
Based on the genomic structure and the motif locations, we divided exon 10 into two parts, i.e., exons 10a and 10b (Figure 1B). Exon 10a was a part of coding sequence (CDS) only in vas-m transcript, but exon 10b was found in all three transcripts (Figure 1C). Exon 4 also uniquely functioned in encoding the amino acids in vas-l transcript (Figure 1C).
Phylogenetic analysis of the DEAD-box protein family revealed that Vas-l segregated with the VASA subfamily and did not cluster with the related proteins P68 and PL10 (Figure 2). Within the VASA clade of sequences, Vas-l clustered in the teleost branch with VASA homolog from another Soleoidei, Solea senegalensis.
The bootstrap consensus tree (1,000 replicates) represented the evolutionary history of the analyzed taxa. The evolutionary distances were computed using the Poisson correction method. The bootstrap value (%) of 1,000 replicates was shown next to the branches. Branches corresponding to partitions reproduced in less than 50% of the bootstrap replicates were collapsed. The GenBank accession numbers were shown in brackets after each species. Vas-l was clustered in the VASA subfamily in the teleost branch with the Vasa homologue from S. senegalensis (Soleoidei).
Tissue distribution pattern of vasa transcripts detected by qRT–PCR
Analyzing the expression of the three vasa isoforms in C. semilaevis by qRT–PCR revealed that only vas-s could be detected in the tissues, except in the gonads. Moreover, the expression level was about three orders of magnitude lower than those in the gonads (Figure 3A and 3B). The expression level of vas-s was predominant, whereas vas-m was almost undetected compared with that of vas-s. The expression level of vas-l was considerable at approximately 25% of that of vas-s. The relative expression level of vasa mRNA was much higher in the ovary compared with that in the testis (Figure 3C).
(A) The relative expression levels of vas-s in the adult tissues from males were analyzed. The relative expression level of vas-s in the testis was used as calibrator. (B) Relative expression levels of vas-s in the adult tissues from females were analyzed. The relative expression level of vas-s in the ovary was used as calibrator. (C) The relative expression levels of vasa transcripts in the testis were compared with that in the ovary. The relative expression level of vas-s in testis was used as calibrator. The variance in the relative expression was represented as a ratio (the amount of vasa mRNA normalized to the corresponding 18S rRNA values). Data were shown as mean±SEM (n = 3). Values with different superscripts indicated statistical significance (p<0.05), which were calculated via one-way ANOVA.
Localization of vasa mRNA-positive cells in the gonads by ISH
The expression and distribution of vasa during oogenesis and spermatogenesis were detected using ISH with DIG labeled anti-sense RNA probe. In the testis, histological observation revealed that the cells mainly comprised spermatocytes and spermatids. ISH results revealed that the vasa mRNA-positive signals were strong in the spermatocytes and were located at the peripheral region of the cysts. By contrast, the signals in spermatogonia were weaker than those in spermatocytes. No signal was detected in the spermatids and testicular somatic cells (Figure 4). The ovary mainly comprised stage II oocytes. The strong signal of vasa mRNA was uniformly distributed throughout the cytoplasm of the oocytes. No signal was likewise detected in the somatic cells.
The vasa mRNA-positive cells (A, B, E, and F) were stained as purple or blue, whereas the negative control with sense probe hybridization (C and G) was unstained. Others were stained with H&E (D and H). The box indicates the area magnified in the next frame (A, C, D, E, G, and H: 20×; B and F: 40×). The vasa mRNA transcripts were observed in the spermatogonia and spermatocytes, but no signals were detected in the spermatids in the testis (B). The black substance observed adjacent to the seminiferous lobules (arrow, A) was a sediment in the testis. Noticeable positive signals were exhibited in the cytoplasm of oocytes (F). Abbreviations: Sg, spermatogonia; Sc, spermatocytes; St, spermatids; Oc, oocytes; Nu, nucleus. Scale bars = 50 μm.
Expression pattern of vasa at different stages during embryonic development
The expression patterns of three vasa isoforms during embryonic development at 14 different stages were monitored by qRT–PCR. Three transcripts were detected in all stages, and their expression patterns were similar except for the expression levels relative to B2M. In all stages, vas-s expression level was also predominant similar to those in the gonads. The relative expression of all isoforms fluctuated in the first six stages with the highest level at the 8-cell stage. Following the high blastula stage, the expression levels of all isoforms increased, quickly reached the peak values at the early gastrula stage, and lowered sharply at the late gastrula stage. Thereafter, the expression was maintained at a low level until the hatching stage (Figure 5).
Relative expression levels of vas-l (A), vas-m (B), and vas-s (C) during embryonic development were examined. Abbreviations: uf-egg, unfertilized egg; MZT, maternal-to-zygotic transition. The relative expression level of vas-l in uf-egg was used as calibrator. The variance of this expression was represented as a ratio (the amount of vasa mRNA normalized to the corresponding B2M values). Data were shown as mean±SEM (n = 3). Values with different superscripts indicated statistical significance (p<0.05), which were calculated via one-way ANOVA.
Expression pattern of vasa isoforms during early gonadal differentiation by qRT–PCR
Only the expression of vas-s could be detected and showed sexually dimorphic during early gonadal differentiation. In female juveniles, the vas-s expression decreased with the TL from 20 mm to 25 mm. When gonadal differentiation started in the ovary, vas-s expression level continued to descend from TL = 30 mm to TL = 40 mm, at which it reached the lowest value. Then, vas-s expression level increased and quickly reached the peak at TL = 50 mm (Figure 6A). In male juveniles, the vas-s expression also declined from TL = 20 mm to TL = 25 mm. The expression increased steadily until TL = 50 mm, the point at which testis differentiation occurred (Figure 6B). The vas-s expression level in both sexes slightly decreased from TL = 50 mm to TL = 55 mm. In addition, the expression levels of vas-s in females were higher than those in males, except at TL = 40 mm.
Relative expression levels of vas-s during gonadal differentiation in females (A) and males (B) were shown. The relative expression level of vas-s at the initial stage in the ovary was used as calibrator. The stages were divided according to the histological observation of C. semilaevis gonadal differentiation . Primitive gonads appeared in juveniles having TL≤25 mm with the development of gonadal anlagen and the rapid proliferation of PGCs. The female juveniles entered into gonadal differentiation earlier than the males, and histological gonadal differentiation was first detected until females TL≥40 mm. This differentiation was signaled by the appearance of oogonia in the ovary. The testis remained undifferentiated until males TL≥50 mm with the rapid proliferation of spermatogonium and somatic cells forming seminiferous duct anlagen. The variance of this expression was represented as a ratio (the amount of vas-s mRNA normalized to the corresponding RPL17 values). Data were shown as mean±SEM (n = 3). Values with different superscripts indicated statistical significance (p<0.05), which were calculated via one-way ANOVA.
In this study, three isoforms of vasa homologs were identified in C. semilaevis. Multiple sequence alignments revealed that although slight sequence differences existed at the N-terminal regions, all deduced amino acid sequences of vasa variants contained the same conserved motifs characteristics of DEAD box proteins. Previous studies have implied that RG and RGG motifs functioned in RNA binding ,  and subcellular protein localization . Q motif, and Motifs I, II and VI were ATP binding and hydrolysis motifs –. Motifs Ia, Ib, Ic, IV, IVa, and V worked as RNA binding motifs , –. Motifs III and Va were intramolecular interactions motifs , , –. These motifs interact closely with each other to form an ATPase active site and a nucleic acid binding pocket so that the protein can catalyze hydrolysis of ATP and unwind RNA duplexes through non-processive, local strand separation , . The data strongly suggest that all the isolated isoforms encode DEAD-box proteins possessing ATP-dependent RNA helicase activities.
VASA, PL10 and P68 subfamilies are important DEAD-box protein family members. Phylogenetic analysis of vasa proteins involved other DEAD-box proteins from both vertebrates and invertebrates. The results revealed that the vasa proteins most closely resemble the VASA subfamily instead of the other DEAD-box protein family members, such as the P68 and PL10 subfamilies. The phylogenetic tree showed that the vasa proteins are clustered with the VASA homologue from S. senegalensis (Soleoidei; Euteleostei sub-branch). Therefore, it further confirmed that the sequences obtained in this study are C. semilaevis vasa-like genes.
Three vasa isoforms were currently cloned in C. semilaevis. In addition, two vasa isoforms have been isolated in tilapia , rare minnow , and zebrafish . In zebrafish, the long isoform contains one more exon 3 (length, 48 bp) resembling the exon 4 (length, 54 bp), which is uniquely located in vas-l. More than three isoforms are found in other flatfishes, such as Senegalese sole  and Japanese flounder . The three variants in this study are only different in the 5′ extremities at exons 4 and 10, similar to the ten isoforms detected in Japanese flounder that vary in the 5′ extremities from exons 1 to 10 with the same 3′ extremities. By contrast, the four vasa isoforms found in Senegalese sole vary in the 5′ and 3′extremities.
Comparing the genomic locus of vasa in C. semilaevis with those in Japanese flounder  and zebrafish  revealed that all vasa genes contain more than twenty exons with the 5′ UTR separated by the first intron. Meanwhile, the first intron in C. semilaevis was the longest (length, 1101 bp). The 5′ UTR is directly connected to the first exon and regulates gene expression. We conclude that the first intron regulates the vasa gene transcription. We can further focus on the potential transcription factor binding sites at the intron or the non-coding RNA produced by this intron.
Given that only one vasa gene locus exists in the zebrafish genome, the two vasa isoforms are attributed to the alternative splicing , , , . On the contrary, three vasa gene loci were found in the tilapia genome . In this case, further studies are necessary to determine how the tilapia vasa isoforms are produced. On the one hand, the genome walking results in this study revealed that no sequence polymorphism existed at the 5′ or 3′ flanking of the vasa gene. On the other hand, only one PCR product contained exon 4 or 10 in three males and three females (Figure S2). This result suggested that no sequence differences exist between the alleles at either exon 4 or 10. The three vasa transcripts are most probably alternative splice variants from a single vasa gene, and the alleles are not heterozygous. The C. semilaevis genome has been published . Comparison of our results with the published confirmed that only one vasa gene locus exists from which the three variants originate.
qRT–PCR analysis of the tissue distribution pattern of vasa implied that vas-l and vas-m were exclusively expressed in the gonads. The gonad-specific expression pattern of vasa is in agreement with the function of vasa as a germline marker and is similar to that found in other teleosts , –, –. The results show that despite the dominant vas-s expression in the gonads, a very weak expression of this gene was also detected in other tissues. A very low expression of vasa in the extragonadal tissues has also been reported in other teleosts, such as rainbow trout , European sea bass , and Senegalese sole . These expressions are attributed to the helicase activity of VASA protein. This protein is a possible translational regulator of certain mRNAs, which is essential to the specification and differentiation of germ cells and somatic cells –. The relative expression level of the vasa transcript was much higher in the ovary compared with that in the testis, especially the vas-s. Differential expression of vasa variants between males and females has also been described. In Senegalese sole, the long Ssvasa1 and Ssvasa2 are expressed in both sexes, whereas very low expression of Ssvasa3 and Ssvasa4 are detected in adult males . In tilapia, the expression of the short vas-s isoform is predominant compared with vas expression in the ovary. By contrast, the expression of the long vas isoform is predominant in the testis . Zebrafish only contain the short variant vas-δ4 in adult males, whereas both the long vas-l and vas-δ4 are expressed in adult females .
ISH during oogenesis and spermatogenesis revealed the strong signals of vasa mRNA in the spermatocytes as well as oocytes and weak signals in the spermatogonia. No signal was detected in somatic cells for both ovary and testis. The results suggested the expression and distribution patterns of vasa mRNA in male and female germ cells during gametogenesis. The vasa gene can thus be considered as a germline-specific marker in C. semilaevis.
The expression patterns of the three vasa transcripts during embryonic development were all similar and also had the same tendency variation on the whole. The relative expression levels of these transcripts also resemble those in the gonads. The three vasa transcripts were present in unfertilized eggs, strongly suggesting that these transcripts are maternally inherited. The relative expression of vasa mRNAs was kept stable during the first two stages compared with that in the unfertilized eggs. We inferred that no zygotic transcripts and decays exist in the early embryos and the amounts of the maternally inherited mRNAs (e.g., vasa) changed slightly. Recently, genome-wide analysis of the maternal-to-zygotic transition (MZT) has been conducted in Drosophila and zebrafish –. Based on these studies, the MZT in somatic cells and those in PGCs were marked in our results (Figure 5). The somatic MZT caused the massive degradation of maternal mRNAs and the zygotic genome activation in the soma. The MZT in PGCs was delayed relative to that in the soma. Studies on turbot (Scophthalmus maximus; Pleuronectiforme) have revealed that Smvas localized at cleavage furrows during embryogenesis resemble the pattern observed in zebrafish rather than medaka , , . Therefore, the PGCs of C. semilaevis are probably specified by the preformation mode and inherit maternal germ plasms (e.g., vasa, nanos, and piwi). Thus, we hypothesized that the amount of vasa mRNAs localized in PGCs continued its stability with the decay of other maternal mRNAs and the rapid zygotic transcription of somatic mRNAs during the somatic MZT. This hypothesis may explain the initial increase in the relative expression level, the reduction from 8-cell stage to 16-cell stage, and the continuous decrease until the morula stage. After the morula stage, vasa expression began to increase and quickly reached the peak value at early gastrula stage. The MZT occurred in the PGCs during these stages, which resulted in the decay of maternal mRNAs and activated the massive transcription of zygotic mRNAs in the PGCs along with the proliferation of PGCs. The amount of newly transcribed zygotic vasa transcripts probably increased much faster than the decay of maternal ones. This result facilitated the identification of a period of observing GFP if microinjection of the GFP expression vector driven by vasa promoter is performed. A sharp decrease in the vasa expression level was found in the following two stages, and vasa expression remained at this level during the last few stages. In zebrafish , gibel carp , and Japanese flounder , the high vasa expression level also dramatically declined following the early gastrula stage. This reduction is attributed to the dilution of the vasa mRNAs and the PGCs within a growing embryo.
The profiles of vasa expression levels during gonadal differentiation have been examined in European sea bass  and Senegalese sole . Discriminating females from males just based only on the phenotype with the indistinguishable primitive gonads during the early gonadal differentiation is difficult. Given this technical limit, the samples used during this stage were mixed groups in previous studies. In this study, heterogametic females (ZW) were identified by the female-specific PCR product from their primers . The juveniles were cultivated under 23°C to avoid sex reversal induced by high temperature. Considering that C. semilaevis females grow faster than males, we chose juveniles based on their size. Similar to the studies in European sea bass , Senegalese sole , and winter flounder , we proposed that the TL of the juveniles has more pronounced effect on gonadal differentiation than the teleost age. qRT–PCR results indicated that only the vas-s transcript can be detected during early gonadal differentiation. This result suggested a shift in the expression of vasa transcripts after the localization of PGCs to gonadal anlagen and the mediation by the interactions with the surrounding somatic cells during gonadal differentiation. The vas-s expression level in females decreased at TL = 40 mm. Histological observation revealed that a portion of the PGCs started to enter into mitosis and form clusters of germ cells at this stage . By contrast, the vas-s expression increased in males at TL = 50 mm, at which the testis entered into mitosis and gonadal differentiation . The sexual discrepancy are attributed to the opposite expression trends of vas-s expression before PGCs enter into mitosis. We speculate that the two stages have vital functions in the formation of germ cells and sexual differentiation. PGCs are probably more susceptible to the external environment during these stages, which sheds new light on the production of infertile or sterile fish. In our further studies, we will focus on the function of vasa in the gonadal differentiation or how this process regulates the expression patterns of vasa.
We reported the full length of three vasa cDNA sequences and genomic DNA sequence in C. semilaevis. The vasa genomic organization and structural differences between the three vasa transcripts were demonstrated. The expression profiles of vasa transcripts confirmed the use of vasa as a molecular marker for the germ cell linage in C. semilaevis. This study lays the foundation for constructing GFP expression vectors driven by the vasa to label, isolate, and transplant the PGCs of this species. This study also improves the development of a genetic breeding technique for C. semilaevis.
Sequence alignments of the three vasa isoforms. Nucleotides were numbered to the right. The nucleotides in light and dark grey backgrounds implied the vas-l and vas-m unique sequences. The polyadenylation signal and the poly-A tail were marked in boldface. The asterisk indicated stop codon.
PCR products containing exons 4 and 10. Using specific primers ex4-FW/RV and ex10-FW/RV as well as genomic DNA as templates, only a single PCR product contained exon 4 or 10 in males and females.
Conceived and designed the experiments: QZ. Performed the experiments: Zhongkai Wang JG HS XW YS. Analyzed the data: Zhongkai Wang JG HS XW YS. Contributed reagents/materials/analysis tools: JQ HY Zhigang Wang. Wrote the paper: Zhongkai Wang QZ.
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