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. 2016 May 3;6:25471. doi: 10.1038/srep25471

Charactering the ZFAND3 gene mapped in the sex-determining locus in hybrid tilapia (Oreochromis spp.)

Keyi Ma 1, Minghui Liao 1, Feng Liu 1, Baoqing Ye 1, Fei Sun 1, Gen Hua Yue 1,2,3,a
PMCID: PMC4853787  PMID: 27137111

Abstract

Zinc finger AN1-type domain 3 (ZFAND3) is essential for spermatogenesis in mice. However, its function in teleosts remains unclear. In this study, we characterized the ZFAND3 gene (termed as OsZFAND3) in an important food fish, tilapia. The OsZFAND3 cDNA sequence is 1,050 bp in length, containing an ORF of 615 bp, which encodes a putative peptide of 204 amino acid residues. Quantitative real-time PCR revealed that the OsZFAND3 transcripts were exclusively expressed in the testis and ovary. In situ hybridization showed that the high expression of OsZFAND3 transcripts was predominantly localized in the spermatocyte and spermatid. These results suggest that OsZFAND3 is involved in male germ cell maturation. Three single nucleotide polymorphisms (SNPs) were detected in the introns of OsZFAND3. The OsZFAND3 gene was mapped in the sex-determining locus on linkage group 1 (LG1). The three SNPs in the OsZFAND3 gene were strictly associated with sex phenotype, suggesting that the OsZFAND3 gene is tightly linked to the sex-determining locus. Our study provides new insights into the functions of the OsZFAND3 gene in tilapia and a foundation for further detailed analysis of the OsZFAND3 gene in sex determination and differentiation.

Zinc fingers are extremely abundant in higher eukaryotes1. As a kind of protein motif with finger-like protrusions, zinc fingers were first identified in a study of transcription in the African clawed frog, which revealed that the binding strength of a small transcription factor (TFIIIA) was due to the presence of zinc finger structures2. Since the TFIIIA was reported, the DNA-binding properties of zinc fingers have been explored1. Also, it has been later reported that zinc fingers can mediate protein-protein interactions3. Until now, numerous genes with varying functions have been verified to encode zinc finger proteins, including sex-determining and differentiation genes. For example, transformer-1 (tra-1) in the nematode Caenorhabditis elegans, which activates sex differentiation genes downstream, encodes two zinc fingers4; steroidogenic factor-1 (SF-1) in humans, which can cause XY sex reversal, contains two zinc fingers5; and different isoforms of male-specific fruitless (fru) in Drosophila melanogaster have diverse regulatory roles conferred by zinc finger domains6.

Among the important zinc fingers, the A20/AN1-type zinc finger protein family is conserved in animals and plants7. However, only a few A20/AN1-type proteins have been found in fish and mammals7. A20, which contains seven Cys2/Cys2 zinc fingers at its C-terminal, is firstly identified as a cytokine-inducible gene with the function of primary response in humans8. As an ubiquitin-like fusion protein, the AN1 domain was originally found at the C-terminus of AN1 type and localized to the animal hemisphere of Xenopus laevis eggs or in early embryos9. However, the function of AN1 domain had been unclear until the characterization of zinc finger AN1-type 3 (ZFAND3) in mice in 199910. ZFAND3, also known as the testis-expressed sequence 27 (Tex27), was first isolated from the mouse testis and its expression is essential for spermatogenesis10. In humans, recent study showed that ZFAND3 is also involved in type II diabetes11. Although molecular cloning of ZFAND3 cDNA has been performed in vertebrates, such as reptiles12 and amphibians9, the function of ZFAND3 remains largely unclear in fish.

Tilapia is the common name for a group of cichlid fishes native to both fresh and salt water in Africa and the Middle East. As one of the most important food fish in the world13, tilapia could provide a good source of animal protein and high-quality meat with minimal inputs and efficient conversion from plant material to fish biomass14. In most tilapia species, there is a significant difference in growth performance between males and females. Males grow much faster than females and reach a larger size after reaching maturity14. The best way to obtain a male monosex population is through genetic control by developing YY “super males” which can sire more male progenies15. This technology is therefore, reliable and consistent, and more and more sex-associated markers were identified and utilized in various tilapiine species. For example, microsatellite markers on linkage group (LG) 3 and LG1 were linked or associated with sex phenotype in blue tilapia, respectively16. Sex-determining loci were mapped to LG1 and LG23 in Nile tilapia (Oreochromis niloticus)17,18, LG3 in hybrid population of O. niloticus × O. aureus19, and LG1 and LG22 in Mozambique tilapia and red tilapia13. By using RAD sequencing, a set of SNP markers highly associated with phenotypic sex were identified on LG1 in the O. niloticus families20. Recently, whole genome sequencing was performed in O. niloticus, in which a potential 8.8 Mb inversion was identified in a sex-determining locus on LG121. So far, one candidate sex-determining gene, amh on LG23, has been identified in O. niloticus22. Although our previous study showed that one sex-determining locus was mapped onto LG1 in a tilapia family13, no potential sex-determining gene has been identified on LG1 in this family yet.

The purpose of this study was to characterize the OsZFAND3 gene, which was mapped onto the sex-determining locus on LG1 in the family of hybrid tilapia (Oreochromis spp.) constructed by crossing a Mozambique tilapia male and a red tilapia female. We found that the gene was expressed exclusively in the testis and ovary. In situ hybridization showed that the high expression of OsZFAND3 transcripts was predominantly localized in the spermatocyte and spermatid. Additionally, three single nucleotide polymorphisms (SNPs), detected in the introns of OsZFAND3, were strictly associated with sex phenotypes. Our results suggest that OsZFAND3 is tightly linked to the sex-determining locus, and it may play an essential role in male germ cell maturation.

Results

Characterization of OsZFAND3 sequence and linkage mapping of the OsZFAND3 gene

Estimation of exon-intron boundaries by alignment of OsZFAND3 cDNA with the genomic sequence identified six exons and five introns in total (Supplementary Fig. S1A). All the observed splice acceptor and donor sites were in accordance with the consensus GT-AG rules. The OsZFAND3 cDNA sequence is 1,050 bp in length and contains an ORF of 615 bp, encoding a putative peptide of 204 amino acid residues (aa) (Supplementary Fig. S1B). The deduced amino acid sequence of OsZFAND3 has an A20-like zinc finger domain located from Pro19 to Ala41 at the N-terminal and a Serine-rich region from Ser102 to Ser164. After searching against the cNLS Mapper, potential nuclear localization signal (NLS) with consensus peptide sequences “RSRKRCHRC” was found in the OsZFAND3 protein. Targeted sequencing of the 279 tilapia F1 individuals of one family identified three SNPs (SNP1 T/C, SNP2 T/C and SNP3 A/G) in the OsZFAND3 gene (Supplementary Fig. S1A). SNP1 and SNP2 were located in the first intron, while SNP3 was found in the fifth intron. All the females (n = 151) were homozygous T/T for SNP1, T/T for SNP2 and A/A for SNP3, and the males (n = 128) were heterozygous C/T for SNP1, C/T for SNP2 and G/A for SNP3, respectively (Supplementary Table S1). This indicates that there is no recombination between the SNP genotypes and the sex phenotypes among the 279 individuals. In the following study, SNP1 was selected for linkage mapping (Fig. 1). Using this SNP, which has a logarithm of odds (LOD) value of 408, OsZFAND3 was mapped onto LG1, between microsatellite markers Onil_1-89 and Onil_19-15 (Fig. 1).

Figure 1. Locations of SNP1 and microsatellite markers on LG1 of hybrid tilapia and linkage mapping of OsZFAND3.

Figure 1

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Locations of the four markers (Onil_1-89, Onil_19-15, Onil_27-3 and SNP1) developed in this study are labelled in the genetic map in cM and anchored in the O. niloticus draft genome in bp.

Phylogenetic analysis of the OsZFAND3 gene

The deduced amino acid sequence of OsZFAND3 was compared with those of other vertebrates (Supplementary Table S2). OsZFAND3 showed a high identity (69–99%) with the ZFAND3 of fish (except Danio rerio) and relatively low identity (45–52%) with those of mammals, reptiles and birds. The data were further analyzed to construct the molecular phylogenetic tree using amino acid sequences of ZFAND3 of selected species (Supplementary Fig. S2). The sequences could be divided into two clades, one of which included ZFAND3 from the selected fish, and another one contained the ones from other vertebrates. As expected, the OsZFAND3 and O. niloticus ZFAND3 was clustered with each other, with a well-supported bootstrap value of 100%. In addition, the selected species were used to analyze the adaptive evolution of the ZFAND3 gene. Pairwise estimates revealed that the dN/dS values among these species were less than 1 (Supplementary Table S3), suggesting that purifying selection could be playing an essential role in the evolution of the ZFAND3 gene.

Tissue distribution of the OsZFAND3 transcripts and its expression patterns

The expression profiles of OsZFAND3 transcripts in 11 tissues were analyzed with qPCR. As shown in Fig. 2, OsZFAND3 transcriptional expression was observed exclusively in the testis and ovary. Moreover, the expression level of OsZFAND3 transcripts in the testis was approximately 90 times than that in the ovary (P < 0.01). No product was detected from the other examined tissues or the negative control using deionized water as a template.

Figure 2. Tissue distribution of OsZFAND3 mRNA in 11 tissues from three female and three male hybrid tilapia individuals using qPCR.

Figure 2

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Each bar indicates the mean + SE. ** Indicates that the difference is extremely significant.

Tilapia testis is composed of numerous seminiferous tubules which contain abundant germ cells at diverse developmental stages (Fig. 3). Each of the seminiferous tubules is surrounded by the epithelium where the sertoli cells are located (Fig. 3A). As the initial stage of spermatogenesis, the spermatogonium is the biggest in size of all the germ cells in the tilapia testis, located close to the inside edge of the seminiferous tubule (Fig. 3A). Through mitosis, the spermatogonium transforms into spermatocyte, which undergoes meiosis to produce spermatids, which in turn produce spermatozoa. In our study, the tilapia spermatozoa were found in the center of the seminiferous tubule (Fig. 3A). To examine the spatial expression pattern of OsZFAND3 transcripts in the gonads, in situ hybridization was performed on the testis and ovary of the hybrid tilapia. However, we failed to detect the OsZFAND3 transcripts in the ovary, possibly due to its low expression levels. At the beginning of spermatogenesis, the signal detected was very weak in most of the spermatogonia. At later stages of development, strong signals were detected in the spermatocytes and spermatids. Subsequently, weak signals could also appear in the spermatozoa (Fig. 3B). No signal was detected in the epithelia (Fig. 3B), and when using a sense RNA probe in the testis as a negative control (Fig. 3C).

Figure 3. Expression pattern of the hybrid tilapia OsZFAND3 transcripts as revealed by RNA in situ hybridization in the testis.

Figure 3

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(A) histological photograph of the testis development, and the section was stained with hematoxylin and eosin. (B) RNA in situ hybridization in the testis using the anti-sense probes, and (C) sense probes were used as the negative control. SE, sertoli cellls; ET, epithelia of the seminiferous tubule; SG, spermatogonium; SC, spermatocyte; SP, spermatid; SZ, spermatozoa.

Subcellular localization of the OsZFAND3 protein

To determine the subcellular localization of the OsZFAND3 in vitro, we detected the fluorescence using the inverted confocal after transient transfection of tilapia nerve fiber cells with recombinant plasmid pEGFP-OsZFAND3, and empty pEGFP-N1 vector was used as a control. As shown in Fig. 4, the green fluorescence was observed throughout the cytoplasm and nuclei in pEGFP-N1 transfected cells (lower row), while the green fluorescence of pEGFP-OsZFAND3 overlapped exactly with the blue fluorescence of nuclei stained by DAPI, indicating that the OsZFAND3 protein was only localized in the nuclei in the pEGFP-OsZFAND3 transfected cells (upper row).

Figure 4. Intracellular localization of OsZFAND3.

Figure 4

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Tilapia nerve fibers cells were transiently transfected with pEGFP-N1 control vector (below row) and pEGFP-OsZFAND3 (upper row). The localization of the nucleus was shown by DAPI staining.

Discussion

In the present study, we reported the identification and mapping of the OsZFAND3 gene in tilapiine species. Generally, ZFAND3 protein tends to contain two zinc-finger domains, the A20 zinc-finger domain and the AN1 zinc-finger domain12. However, the deduced OsZFAND3 protein has an A20-like zinc finger domain and a Serine-rich region located at N-terminal and C-terminal, but has lost the AN1 zinc-finger domain (Supplementary Fig. S1B). This could affect the three-dimensional structure and function of the OsZFAND3 protein. As a stable domain in protein structure, the Serine-rich region is often considered as a protein-interaction motif23. Furthermore, two (T/S) PXX sequences, existing in the Serine-rich region of the deduced OsZFAND3 protein, could mediate DNA-protein interaction12. Animals exhibit high diversity of domain organization in the A20/AN1 zinc finger gene during evolution24, and the gain and loss of entire zinc finger domains could enable the appearance of functional divergence in proteins25. Compared to the ZFAND3s of the Japanese quail and the leopard gecko12, the missing AN1 zinc-finger domain in OsZFAND3 leads to a large region of difference outside the zinc finger at N-terminal and may generate the function diversity of ZFAND3 gene.

Vertebrates exhibit diverse sex determination systems26, resulting in different sex-determining genes depending on the species26,27,28,29,30. The tilapiine sex determination system is relatively complex13,17,18,31,32, as both XX/XY and ZW/ZZ sex-determination systems are known to occur in tilapia, implying that tilapia with divergent genetic backgrounds could have different sex chromosomes. In this study, the three identified SNPs in the OsZFAND3 gene showed that our tilapia family might have an XX/XY sex determination system, which is consistent with the previous study in which the females were identified as homozygotes13,17. Due to prevalent interspecies crossing between the tilapiine species, the complexity of genetic backgrounds between families could be the main reason for this divergence of homozygosity or heterozygosity in both sexes. Additionally, various sex determination systems imply that different sex-determining genes may exist in tilapia families16.

One of the important characteristics of a sex-determining gene is its tight linkage with the non-recombinant part of the heterochromosome33. The three SNP loci of OsZFAND3 are strictly associated with the sex phenotype on LG1. Hence it implied that OsZFAND3 is tightly linked with the phenotype of sex in our tilapia family. However, to determine whether it is a potential sex-determining gene that plays an essential role in controlling testis differentiation, further work such as carrying out a transgene method should be performed. Additionally, the sex-determining region in the present study is very long (approximately 1.0 million bps), therefore, families of different genetic backgrounds and more offspring of tilapia are needed to fine map and detect whether recombination exists in this sex-determining locus in the future study.

According to the previous studies, ZFAND3 transcripts were expressed in various tissues in plants, and represented most of the expression profile of A20/AN1-type zinc-finger family genes7. The same result was also found in the mouse, where the ZFAND3 mRNA was expressed not only in the gonads, but also in the somatic tissues, such as kidney and liver10. In contrast to these studies, OsZFAND3 exhibits quite a distinct expression pattern, being exclusively expressed in the testis and ovary according to qPCR analysis (Fig. 2), suggesting that it could be essential for maintaining the function of testis and ovary. The determination of expression levels of OsZFAND3 transcripts in the testis was fully supported by the results of in situ hybridization. Although the hybridization signal was very weak in most of the spermatogonia, high expression of the transcripts was detected to be predominantly localized in the spermatocyte and spermatid germ cells. At the last stage of spermatogenesis, the weak signal then re-appeared in the spermatozoa (Fig. 3B). The best explanation of the differential distribution is that OsZFAND3 could be related to the meiosis from the stage of spermatocyte to spermatozoa, suggesting that OsZFAND3 could be involved in male germ cell maturation in tilapia.

Nuclear proteins typically contain NLS, directing nuclear import for the relative protein34. Unlike the classical NLS consensus isolated from nuclear import pathway35, other proteins with NLS consensus sequences have not been very clear so far. Although OsZFAND3 protein is exclusively localized in the nucleus, strongly suggesting that it is a nuclear protein, there was no NLS of OsZFAND3 found after running the NLS search against the PredictProtein server. Since the database in the PredictProtein must undergo experimental verification, novel NLS could be missed, which may lead to false-negative result. In contrast to the PredictProtein, potential NLS was found in the OsZFAND3 protein after searching against the cNLS Mapper, indicating that OsZFAND3 is a nuclear protein with a new probable NLS.

As a confirmed family of transcription factors, SOX proteins usually contain NLSs36. Among the family, SRY and Sox9 are critical regulators of the mammalian sex-determining pathway30,36. OsZFAND3 is a sex-linked gene in tilapia with probable existing NLS, implying that it could be a functional transcription factor like the members in Sox family. However, future research such as yeast two-hybrid system and electrophoretic mobility shift assay should be performed to confirm this point.

In summary, we characterized the OsZFAND3 cDNA sequence in the food fish tilapia. Although OsZFAND3 transcriptional expression was observed exclusively in the testis and ovary, the expression level in the testis was approximately 90 times than that in the ovary. In situ hybridization showed that the high expression of OsZFAND3 transcripts were predominantly localized in the spermatocyte and spermatid germ cells, and the weak signal appeared in the spermatozoa. Taken together, OsZFAND3 could be involved in male germ cell maturation in tilapia. In terms of the SNP genotype, the OsZFAND3 gene is tightly linked to the sex-determining locus on LG1 in our hybrid tilapia family constructed by crossing a Mozambique tilapia male and a red tilapia female. Our study sheds new insights on the function of OsZFAND3 in tilapia and provides the basis information for further detailed analysis of its function in sex determination and differentiation.

Materials and Methods

Ethics statement

All handling of fish was carried out in accordance with the guidelines on the care and use of animals for scientific purposes set up by the Institutional Animal Care and Use Committee (IACUC) of the Temasek Life Sciences Laboratory, Singapore. The IACUC approved this study with approval number, TLL (F)-12-004.

Fish rearing and tissue sampling

A total of 279 hybrid tilapia F1 offspring from crossing a Mozambique tilapia male and a red tilapia female, at the age of 140 days post-hatch (dph) with an average body weight of ~120.0 g, were used in this study. This tilapia family was used in our previous study, and one sex-determining locus was mapped on LG113. Tilapia individuals were reared in a three-ton tank in the animal house of the marine fish facility of Temasek Life Sciences Laboratory, and fed twice daily with commercial pellet feed (Biomar, Nersac, France). Brain, gill, spleen, liver, kidney, muscle, intestine, heart, skin, testis and ovary tissues were collected from three males and three females, respectively. The samples were immediately frozen in liquid nitrogen and stored at −80 °C until total RNA extraction. For histological observation and in situ hybridization, the ovarian and testis samples were fixed in 4% paraformaldehyde solution (PFA) overnight at 4 °C.

Sequence analyse of the ZFAND3 gene

The ZFAND3 gDNA (Genbank accession no. NC_022199.1) and cDNA (XP_005447615.1) sequences of Nile tilapia were obtained from the NCBI database. Primers were designed based on this gDNA sequence to confirm the OsZFAND3 cDNA sequence, and identify SNPs of the OsZFAND3 in the hybrid tilapia (Supplementary Table S4). All primers were designed by Primer3Plus (http://primer3plus.com/). The open reading frame (ORF) of OsZFAND3 was identified using the ORF Finder (http://www.ncbi.nlm.nih.gov/projects/gorf/). The NCBI alignment search tool, BlastN, was used to identify homologous sequences in GenBank (http://blast.ncbi.nlm.nih.gov/Blast.cgi). Sequences were aligned using CLUSTALW 2.037. Based on the deduced full-length ZFAND3 amino acid sequence alignments, a phylogenetic tree was constructed by the Neighbor-Joining (NJ) algorithm method embedded in the MEGA 6.0 software38. The reliability of the analysis was assessed by 1000 bootstrap searches. Maximum likelihood analysis was employed to detect adaptive evolution in the ZFAND3 gene using the YN00 program in the PAML X package39. The nuclear localization signal (NLS) of OsZFAND3 was identified using the PredictProtein server (https://www.predictprotein.org/) and cNLS Mapper (http://nls-mapper.iab.keio.ac.jp/).

Genotyping of microsatellite markers

In order to fine map the sex-determining locus on LG1, gDNA was extracted from the caudal fin of the 279 tilapia F1 individuals mentioned above, according to the protocol developed previously40, and primers of three microsatellite markers (Onil_1-89, Onil_19-15, Onil_27-3, see details in Supplementary Table S4) flanking the sex-determining locus were designed in this study. The PCR amplification for each individual sample was performed in a 25 μL volume, containing 10 ng gDNA, 1 × PCR buffer, 80 μM of each dNTPs, 0.2 μM forward and reverse primers and 1 U Taq DNA polymerase (Thermo Fisher Scientific, MA, USA). The reactions were carried out in a thermal cycler (MJ Research, CA, USA) using the following programme: one cycle of 3 min at 94 °C, 38 cycles of 30 sec at 94 °C, 30 sec at 55 °C and 30 sec at 72 °C, followed by a prolonged extension of 8 min at 72 °C. The PCR products were resolved on an ABI 3730XL DNA sequencer (Applied Biosystems, CA, USA) and genotyped against the internal size standard of GeneScan-500 ROX. Then the genotypes of the 279 individuals were analysed in GeneMapper 4.1 (Applied Biosystems).

Genotyping of SNPs in OsZFAND3 gene, linkage and QTL mapping

To map the OsZFAND3 gene on the previous linkage map13, all the 279 F1 individuals were used to genotype SNPs of OsZFAND3. Briefly, a targeted region of OsZFAND3 gDNA was amplified using two primer sets: x3 SNP1 and x3 SNP2 (Supplementary Table S4). PCR amplification and programme for each individual sample were similar to those for the genotyping, except that the annealing temperature was 50 °C. The genotyping of identified SNPs was carried out by directly sequencing the PCR products in both directions with ABI 3730XL DNA sequencer (Applied Biosystems). SNPs among the resultant sequences were detected by alignment. Microsatellites Onil_1-89, Onil_19-15 and Onil_27-3, together with five microsatellites (Om251, Om432, Om188, Om287 and Om293) from Liu et al.13 were used for linkage mapping using the previous methods41,42,43. In order to determine whether OsZFAND3 was localized on the reported sex-determing locus13, one of the identified SNPs was used to map OsZFAND3 onto the linkage map using the method as described by Xia et al.41, and a LOD threshold of 3.0 was used to generate the Linkage map. Quantitative trait loci (QTL) analysis was carried out under BP model and LOD scores were obtained by bootstrapping with 10,000 permutations. QTL with LOD threshold of more than 95% (P < 0.05) at chromosome level were considered as significant.

Analysis of tissue distribution of OsZFAND3 with quantitative real-time RT-PCR (qPCR)

To analyze the tissue distribution of OsZFAND3 mRNA, qPCR was used to determine the expression pattern. Total RNA from three males and three females was isolated using Trizol (Invitrogen, CA, USA), and treated with RNase-free DNase (Promega, WI, USA) for removal of contaminated gDNA. The A260/280 and A260/230 ratios of all the RNAs prepared were measured by Nanodrop 1000 spectrophotometer (Nanodrop Technologies, DE, USA), with the values within 1.80–2.00 and 2.00–2.50, respectively. The RNA quality was further accessed by electrophoresis on 2.0% agarose gel. The first strand of cDNA was synthesized using 5 μg of DNase-treated RNA by Reverse Transcriptase M-MLV Kit (Promega). The reactions in triplicates were performed using the KAPATM SYBR FAST qPCR Kit (KapaBiosystems, MA, USA) in an iQTM 5 Real Time PCR Detection System (Bio-Rad, CA, USA) according to the manufacturer’s instructions. The primers used for OsZFAND3 amplification are shown in Supplementary Table S4. Relative gene expression was analyzed using the 2−∆∆CT method44, and the housekeeping gene β-actin was selected to normalize the relative expression level of OsZFAND3 in different tissues. One-way analysis of variance (ANOVA) with Tukey’s HSD test was performed using the SPSS statistics software package (SPSS, IL, USA)45,46. All results were expressed as mean + SE. Significance was accepted at the level of P < 0.05.

Preparation of sense and anti-sense OsZFAND3 cRNA probes and in situ hybridization

A 136-bp fragment of OsZFAND3 transcript was amplified and sub-cloned into pGEM®-T Easy vector (Promega). The recombinant plasmid was linearized either with Sac II or Spe I (Promega). Anti-sense and sense RNA probes labelled were synthesized with a DIG RNA Labelling Kit (Roche Diagnostics, Germany) using the SP6 and T7 RNA polymerases (Roche), respectively. These probes were then treated with RNase-free DNase I (Promega) to remove the template DNA. In situ hybridization and histology was carried out as described previously44. Ovary and testis tissue sections (~5 μm) were hybridized with DIG-labeled antisense or sense RNA probes. Slides were mounted using Canada balsam (Sigma-Aldrich, MO, USA). The DIG was visualized using colorimetric substrate NBT/BCIP solutions (Roche) according to the manufacturer’s instructions and microscope images were captured through a light microscope (Lecia, Germany).

Plasmid construction and subcellular localization

A pair of primers, containing restriction enzyme cutting sites of Xho I and Hind III, were used to amplify the ORF of OsZFAND3. The PCR products were cloned into expression vector pEGFP-N1 (Clontech Laboratories, CA, USA) and the recombinant plasmid (namely pEGFP-OsZFAND3) was confirmed by sequencing. To examine the subcellular localization of OsZFAND3, 2.2 × 105 tilapia nerve fiber cells were transfected with 1 μg of plasmid pEGFP-OsZFAND3 or the control vector pEGFP-N1, using Turbofect transfection reagent (Thermo) according to the manufacturer’s protocol. After 24 h transfection, cells were washed with PBS (pH 7.4), fixed with chilled methanol, stained with 6-diamidino-2-pheny-lindole (DAPI) and observed through a LSM 510 META inverted confocal microscope (Zeiss, Germany).

Additional Information

How to cite this article: Ma, K. et al. Charactering the ZFAND3 gene mapped in the sex-determining locus in hybrid tilapia (Oreochromis spp.). Sci. Rep. 6, 25471; doi: 10.1038/srep25471 (2016).

Supplementary Material

Supplementary Information
srep25471-s1.pdf (526.9KB, pdf)
Supplementary Table S1
srep25471-s2.xls (68.5KB, xls)
Supplementary Table S3
srep25471-s3.xls (38KB, xls)

Acknowledgments

This material is based on research supported by the Singapore National Research Foundation under CRP Award No. NRF-CRP7-2010-01. We are grateful to our colleague Ms May Lee for English proofreading and our former colleague Ms Delia Quek for technical support.

Footnotes

Author Contributions G.H.Y. supervised the project. K.Y.M. designed the experiments. K.Y.M., M.H.L., F.L., B.Q.Y. and F.S. conducted the experiments. K.Y.M. conducted the data analyses and wrote the manuscript. G.H.Y. finalized the manuscript.

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Supplementary Materials

Supplementary Information
srep25471-s1.pdf (526.9KB, pdf)
Supplementary Table S1
srep25471-s2.xls (68.5KB, xls)
Supplementary Table S3
srep25471-s3.xls (38KB, xls)

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