Formation of diploid and triploid hybrid groupers (hybridization of Epinephelus coioides ♀ × Epinephelus lanceolatus ♂) and their 5S gene analysis

Background Interspecies hybridization is widely used to achieve heterosis or hybrid vigor, which has been observed and harnessed by breeders for centuries. Natural allopolyploid hybrids generally exhibit more superior heterosis than both the diploid progenies and their parental species. However, polyploid formation processes have been long ignored, the genetic basis of heterosis in polyploids remains elusive. Results In the present study, triploid hybrids had been demonstrated to contain two sets of chromosomes from mother species and one set from father species. Cellular polyploidization process in the embryos had been traced. The triploid hybrids might be formed by failure formation of the second polarized genome during the second meiosis stage. Four spindle centers were observed in anaphase stage of the first cell division. Three spindle centers were observed in side of cell plate after the first cell division. The 5S rDNA genes of four types of groupers were cloned and analyzed. The diploid and triploid hybrids had been proved to contain the tandem chimera structures which were recombined by maternal and paternal monomer units. The results indicated that genome re-fusion had occurred in the hybrid progenies. To further elucidate the genetic patterns of diploid and triploid hybrids, fluorescence chromosome location had been carried out, maternal 5S gene (M-386) were used as the probe. The triploid hybrids contained fewer fluorescence loci numbers than the maternal species. The results indicated that participation of paternal 5S gene in the triploid hybrid genome had degraded the match rates of M-386 probe. Conclusions Our study is the first to investigate the cellular formation processes of natural allopolyploids in hybrid fish, the cellular polyploidization process may be caused by failure formation of the second polarized genome during the meiosis, and our results will provide the molecular basis of hybrid vigor in interspecies hybridization. Electronic supplementary material The online version of this article (doi:10.1186/s12863-016-0443-9) contains supplementary material, which is available to authorized users.


Background
Interspecies hybridization is a useful and important strategy for generating progeny with heterosis or hybrid vigor, which is a phenomenon that has been observed by naturalists, harnessed by breeders for centuries [1]. The utility of hybridization has tremendously increased the productivity in many species [2]. Preternaturally, through interspecies hybridization, natural polyploid hybrids are often produced.
The 5S ribosomal DNA (5S rDNA) gene is an important and useful resource for analyzing and tracing rapid evolutionary events. In vertebrates, the 5S rDNA unit is formed by 120-bp highly conserved coding sequence and highly variable non-transcribed spacer (NTS) [5]. The high level conservation of 5S coding sequence arises from their essential molecular function [12,13]. However, the NTS sequences show extensive variation, even between closely related species [13]. Many 5S rDNA studies had demonstrated the influence of polyploidy on intragenomic variation and gene expression [5,14].
Our previous study had reported the generation of natural triploid hybrid groupers from the crossing of female Epinephelus coioides (E. coioides) and male Epinephelus lanceolatus (E. lanceolatus) [15]. The triploid hybrids had been proved to possess superior growth performance to that of the diploid hybrids and the parent species [15]. In the present study, fine karyotype analyses were performed to investigate the chromosome filiation of diploid and triploid hybrids, triploidization processes were traced based on embryo images and sections. The genetic basis of the hybrids was evaluated by 5S rDNA gene sequences. Chromosome location was carried out to further investigate the 5S rDNA gene pattern.
The inheritance relationships of 'st' chromosome were displayed in Fig. 1-e; 'st' numbers of the groupers were 0, 6, 3, and 3 for E. coioides, E. lanceolatus, diploid hybrids, and triploid hybrids, respectively. The mother species, E. coioides, had no 'st' chromosome. The father species, E. lanceolatus, had 6 'st' chromosomes. Both the diploid and triploid hybrids had the same 'st' numbers of 3, half of the father species, which indicated that the father species supplied one set of chromosomes to diploid and triploid hybrids respectively. Therefore, the mother species might supply one set of chromosomes to the diploid hybrids and two sets of chromosomes to the triploid hybrids.
The assumption that mother species supplied two sets of chromosomes to triploid hybrids was supported by the results shown in Fig. 1-f. As shown in Fig. 1, the 2n mother species had 2 two-armed chromosomes ( Fig. 1-a), and the 2n father species had 8 two-armed chromosomes ( Fig. 1-b). The diploid hybrid had inherited 1 two-armed chromosome from the mother species (half of 2) and 4 two-armed chromosomes from the father species (half of 8), the number of two-armed chromosomes in diploid hybrid was 5 ( Fig. 1-c, f ). The number of two-armed chromosomes in triploid hybrids might be 6 (2 + 4, two sets of mother species chromosomes plus with one set of father species chromosomes) or 9 (1 + 8, one set of mother species plus with two sets of father species) ( Fig. 1-f ), as shown in Fig. 1-d, the triploid hybrids had 6 two-armed chromosomes. These results indicated that triploid hybrids had two sets of chromosomes inherited from the mother species plus with one set of chromosomes inherited from the father species.

Embryo development
To estimate the triploidization processes, embryo developments of the hybrids and E. coioides had been traced. The eggs were hatched in 27°C, 30 ‰ salt seawater with sufficient air supplement. Images of the related development processes were obtained with a Nikon 50i camera microscope. Time consuming points were recorded. Representative images of E. coioides were showed in Fig. 2 (left). No substantial differences were found between images of the hybrid and the E. coioides. The consuming time points were exhibited in Fig. 2 (right) and Additional file 3: Table S1. From the line chart in Fig. 2 (right), hybrid embryos hatched 2-3 h earlier than those of E. coioides.
To further survey the triploidization processes, histological sections of early embryo developments of the hybrid and E. coioides were carried out. Early embryo development processes of E. coioides were showed in Fig. 3. Spermaster was observed 30 s after fertilization (AF) (Fig. 3-a), the eggs remained in the second metaphase stage of meiosis at 1 min AF ( Fig. 3-b), the eggs excluded the second polar body at 2-4 min AF ( Fig. 3-c,d), the two pronuclei met and merged together at about 8 min AF (Fig. 3-e), the first cleavage took place at 24-28 min AF (Fig. 3-h-j).
Triploidization processes in hybrid embryos were showed in Fig. 4. In control group of E. coioides specimens, normal polarized meiosis took place ( Fig. 4-a), female and male pronuclei fused ( Fig. 4-b), two spindle centers were observed in the anaphase stage in the first cell division (Fig. 4-c), only a spindle center was observed in the side of the cell plate after the first cleavage ( Fig. 4-d). In the corresponding stages of hybrid embryos, abnormal phenomenon was observed during polarized meiosis ( Fig. 4-a), the female pronucleus might retain two sets of genomes, a pseudo polar body without genome might be extruded; tri-polarized nucleus was observed ( Fig. 4-b), two sets of maternal nuclei might fuse with the paternal pronucleus; four spindle centers were observed in the anaphase stage in the first cell division (Fig. 4-c); three spindle centers were observed in the side of the cell plate after the first cell cleavage ( Fig. 4-d). These results indicated that triploidization processes might be occurred during the second meiosis stage in hybrid eggs, the first mitoses in the triploid embryos were different from that of E. coioides.

5S gene sequence analysis
PCR amplifications of E. coioides, E. lanceolatus, diploid hybrids, and triploid hybrids were conducted and gel-separated. As showed in Fig. 5, all the lanes had two band patterns of approximately 400 bp (Class I) and 750 bp (Class II). To evaluate the 5S gene, a total of 160 clones were sequenced, including 15 clones of each band of each parental species and 25 clones of each band of each hybrid species. BLASTn was employed for sequence analyzing. Resulting data were summarized in Table 1. From Table 1, the Class I sequences contained the coding (120 bp) and NTS (266-284 bp) regions, which indicated that it was the monomeric structure of 5S gene. Compared with the Class I in parental species, the hybrids had no novel sequences. The Class II sequences were detected to contain the dimeric Class I structures, whereas, novel sequences were detected (781 bp, 790 bp) in diploid and triploid hybrids. The 781 bp sequences were the combination structure of 386 bp (maternal Class I) and 395 bp (paternal Class I), the 790 bp sequences were the combination structure of 386 bp (maternal Class I) and 404 bp (paternal Class I). These results indicated that the new sequences in the hybrids were combined with maternal and paternal monomeric sequences, the tandemly repeated units of the parental 5S rDNA genes might exchange with each other during the hybridization.
Multiple analysis of the 5S coding region had been conducted. The results were showed in Additional file 1: Figure

Chromosomal location of the 5S gene
Triploid hybrid groupers had two sets of maternal chromosomes. The M-386 sequence (GenBank Accession No. KR262163) was used as the probe. Results were listed in Table 2 and Fig. 7. Based on the information in Table 2, the chromosome loci numbers of E. coioides, E. lanceolatus, diploid hybrids, and triploid hybrids were mostly 5, 1, 2, and 3, respectively. Representative pictures of 5S gene chromosomal location were displayed in Fig. 7. There were fewer fluorescence loci in E. lanceolatus metaphase chromosomes ( Fig. 7-b) than that in E. coioides ( Fig. 7-a), and signal intensity of E. lanceolatus was weaker than that of E. coioides. More fluorescence loci numbers were detected in triploid hybrids than that in diploid hybrids and E. lanceolatus. Strong signals (in the white frames of Fig. 7-a, c, d) were found in E. coioides, diploid hybrids, and triploid hybrids. The strong signals were in the middle of chromosome in diploid hybrids,  2012) indicated that triploid hybrids had two sets of chromosomes from the mother species and one set from the father species, tetraploid hybrids had two sets of chromosomes from the mother and two sets from the father [8,9]. In this paper, triploid hybrid groupers were produced from E. coioides ♀ × E. lanceolatus ♂, karyotype results showed that triploid hybrids had two sets of chromosomes from the mother species and one set from the father species.
Natural polyploids were more and more commonly detected in many fish species in recent years. Tsuda et al. (2010) detected the occurring of triploid Rhamdia quelen [16]. Bai et al. (2011) reported the coexisting populations of diploid, triploid and polyploidy Carassius auratus individuals [17]. Triploid hybrids were generated from the interspecies hybridization of female Ctenopharyngodon idellus and male Megalobrama amblycephala [10]. However, the cellular formation processes of the polyploids were still unclear. In this study, embryo images and sections were conducted to investigate the triploidization processes. Results showed that the hybrid embryo images were not substantially different from the related of E. coioides, but the hybrid embryo had the abnormal polarized meiosis and cell division processes. The hybrid female pronucleus might retain two sets of chromosomes and  Analysis of genetic organization and variation may be helpful in evaluating the role of hybridization. The NTS of 5S rDNA gene is neutral and freely mutative, and it has been widely employed as a molecular marker to assess the organization of genomes and to trace recent evolutionary events [13,18]. Analysis of different ploidy hybrids of Carassius auratus red var. ♀ and Megalobrama amblycephala ♂ showed that the tetraploid hybrids partially inherited NTS classes from the female parent and obtained a novel NTS sequence [5]; similar results were obtained from tetraploid hybrids of Carassius auratus red var. ♀ and Erythroculter ilishaeformis ♂ [9]. In the present study, the 5S rDNA genes were cloned and analyzed, Class II sequences (781 bp, 790 bp) in diploid and triploid hybrids were composed of two monomer structures (Class I) which were originated from their parent species. The results indicated that the new sequences in the hybrids were recombined by the parental sequences. In this paper, the NTS sequences in diploid and triploid hybrids were slightly different, but not blocks of variant sequences, the results were similar to that of He et al. (2013) [10], the chimera sequences (except for a 10-bp poly A insertion in diploid hybrids) were found in the diploid and triploid hybrids [10]. The number of fluorescent loci in the triploid hybrids was less than that in mother species, which indicated that the recombination of 5S gene might enfeeble the efficiency of M-386 probe in triploid hybrid chromosomes.
However, despite this comprehensive investigation, a general and basic understanding of heterosis remains elusive. Single loci have a relatively small contribution to hybrid traits [2]. Heterosis or hybrid vigor may be shaped by different traits that are affected by multiple gene loci [19]. In our study, the new 5S gene sequences in diploid and triploid hybrids were composed of different parental monomer structures. The results indicated  Gene-exchange had occurred in the sequence that genome loci of parental species might be exchanged or recombined during the hybridization. Our results would provide the basic molecular evidence for explaining the heterosis phenomenon in hybrids.

Conclusions
In conclusion, triploidization processes and genetic patterns of 5S rDNA in hybrid groupers had been investigated in this paper. The extra sets of chromosomes in triploid hybrids had been demonstrated to come from the mother species. The failure exclusion of sister chromosomes might be occurred during the second meiosis stage, a pseudo polar body without genome might be excluded instead. Hybrid heterosis might be induced by interspecies genome re-fusion and gene exchanging. More evidence and further research are still needed to reveal the molecular mechanisms of natural polyploidization and hybrid vigor.

Karyotype analysis
Karyotype analyses of each five individuals of E. coioides (the female parent), E. lanceolatus (the male parent), diploid hybrids, and triploid hybrids were operated to infer the chromosomal origin. Karyotype slides were prepared from cultured peripheral blood cells. Detailed processes were conducted as described by Huang et al.
(2014) [15]; blood was collected and cultured in nutrient solution at 25.5°C with 5 % CO 2 for 68-72 h, and 0.1 ml colchicines solution was added 3 h before harvest. The cells were then treated with 0.075 M KCl at 37°C for 30 min. Blood cells were dropped on the cold slides and air-dried at room temperature. Chromosomes were stained by Giemsa solution (pH 6.8) for 30 min, washed in running water, air-dried. Good-quality metaphase spreads images were obtained by a Nikon 50i microscope (Nikon, Japan) for karyotype analyzing. Fine karyotype analysis was carried out as Qin et al. (2014) [8] had described. Long-arm to short-arm ratios of 1.0-1.7 were classified as metacentric (m), 1.7-3.0 as submetacentric (sm), 3.1-7.0 as subtelocentric (st), and > 7.1 as telocentric (t) chromosomes (Levan et al. 1964) [20].

Embryo development
Breeding of E. coioides and hybridization of E. coioides ♀ × E. lanceolatus ♂ were carried out. The methods were conducted as described in Huang et al. (2014) [15]. Good-quality eggs were hatched in seawater (nearly  30‰ salinity) at room temperature. The embryo development processes were imaged by a Nikon 50i microscope camera. The fry were reared to fingerlings in the same environment. Eggs were fixed in Bouin's solution after fertilization of 30 s, 1 min, 2 min, 3 min, 4 min, 6 min, and 8 min and then every 4 min until 40 min. The eggs were dehydrated in alcohol, embedded in paraffin wax, sectioned, and stained with hematoxylin and eosin. Photomicrographs were taken with a Nikon 50i microscope camera.

5S rDNA genetic analysis
Total genomic DNA of E. coioides (the female parent), E. lanceolatus (the male parent), diploid hybrids, and triploid hybrids were extracted from the caudal fin with a TIA-Namp Marine Animals DNA Kit (TIANGEN, China). The primers of 5S-F (5′-GCTTACGGCCATACCAACCTG-3′) and 5S-R (5′-AATACGCCCGATCTCGTCCGA-3′) were designed and synthesized to amplify the 5S rDNA gene. PCR conditions were the same as described by Qin et al. (2010) [5]. Amplification products were gel-separated and purified with an EZNA® Gel Extraction Kit (Omega, United States). The purified DNA products were ligated into the pMD18-T vector (TaKaRa, China) and transformed into E. coli DH5a. Monoclonal bacteria were obtained from culturing E. coli DH5a. Thirty monoclonal bacteria of parent grouper species and fifty monoclonal bacteria of each hybrid species were sequenced with an automated DNA sequence (ABI PRISM 3730, Applied Biosystems, United States). Sequences were analyzed with ClustalW 2.0 and Bioedit 7.2.

Chromosomal location of 5S rDNA
The chromosomal locations of the 5S rDNA gene were conducted in E. coioides (the female parent), E. lanceolatus (the male parent), diploid hybrids, and triploid hybrids. Probes labeled with DIG-11-dUTP (Roche, Germany) were made by purifying the PCR products of 5S rDNA. Fluorescence in situ hybridization was performed as described by He et al. (2012) [9]. Images were obtained and merged by the NIS-Elements software of Nikon 50i fluorescence microscope system (Nikon, Japan). For each type of grouper, 100 metaphase spreads (20 metaphase spreads per sample) of chromosomes were analyzed.