Transcriptome analyses and differential gene expression in a non-model fish species with alternative mating tactics
© Schunter et al.; licensee BioMed Central Ltd. 2014
Received: 16 November 2013
Accepted: 20 February 2014
Published: 28 February 2014
Social dominance is important for the reproductive success of males in many species. In the black-faced blenny (Tripterygion delaisi) during the reproductive season, some males change color and invest in nest making and defending a territory, whereas others do not change color and ‘sneak’ reproductions when females lay their eggs. Using RNAseq, we profiled differential gene expression between the brains of territorial males, sneaker males, and females to study the molecular signatures of male dimorphism.
We found that more genes were differentially expressed between the two male phenotypes than between males and females, suggesting that during the reproductive period phenotypic plasticity is a more important factor in differential gene expression than sexual dimorphism. The territorial male overexpresses genes related to synaptic plasticity and the sneaker male overexpresses genes involved in differentiation and development.
Previously suggested candidate genes for social dominance in the context of alternative mating strategies seem to be predominantly species-specific. We present a list of novel genes which are differentially expressed in Tripterygion delaisi. This is the first genome-wide study for a molecular non-model species in the context of alternative mating strategies and provides essential information for further studies investigating the molecular basis of social dominance.
Polygamous mating systems are often defined by social dominance where territorial individuals top the social hierarchy. Alternative mating strategies in fish species are commonly associated with a dominance hierarchy including dominant or territorial males and secondary males or so-called sneaker males . Being the dominant individual comes at a cost, as the territorial male has to invest in defending the territory, attract the female and guard the nest . In some fish species those dominant individuals even do not feed during the reproductive period of several months . The sneaking individual on the other hand can obtain reproductive success by sneaking into nests or mimicking female behavior and phenotype .
The term ‘social dominance’ suggests that dominance depends on the social setting. The territorial male is often the largest male present in many fish species but there are exceptions [5, 6]. This is especially true for fish species where the change from sneaker to territorial male is not fixed for life, but temporary and therefore plastic. Here, the switch to becoming territorial could depend on the presence of plausible nest sites, the number of mature females or even the presence or absence of other males . For instance, in the goby Gobius niger  and the blenny Tripterygion delaisi [8, 9] a sneaker male can switch into a territorial male after the experimental removal of the previous territorial male.
Phenotypic plasticity, the ability of a genotype to respond to external conditions by changing its phenotype, has received considerable attention in evolutionary ecology . The assimilation of an initially plastic response to an altered environment and therefore the maintenance of the phenotype has long been understood as a fundamental component in selection and evolution [11, 12]. More recently, short-term and non-adaptive phenotypic changes have been the focus of several studies [13, 14]. In many species reproduction is a temporal or a short-term event, taking place for example only once a year in the reproductive period. This means that the alterations occurring during this period, being behavioral and/or phenotypic, are plastic and mostly reversible changes . In male alternative mating tactics, the different tactics are linked with differences in behavior often leading to phenotypic dimorphism with secondary sexual traits. Social interactions, in these cases, have been shown to trigger the behavioral and phenotypic change .
Social influences and behavioral changes lead to alterations in gene expression in the brain [17–19]. More specifically, social stimuli can lead to short term deviation from the baseline of gene expression in the brain . While it is unclear how these changes are transmitted to the other organs, clearly the brain plays a vital role . The neural basis of social status has been studied in the brain in Atlantic salmon (Salmo salar) where the plasticity in the development of alternative male phenotypes has been investigated [21, 22]. Aubin-Horth and coauthors  discovered that 15% of the analyzed genes were differentially expressed between brains of male morphs, but the investigations into alternative mating tactics in the Atlantic salmon were carried out on precocious males and lack the analysis of the large mature male. Alternative male mating strategies are also studied in cichlid fish species, due to their extreme diversity and the facility to be handled and kept in the laboratory (see  and references cited therein), whereas the non-dominant male is not reproductively active . Gene expression patterns related to phenotypic plasticity in different mating strategies have been analyzed either by targeting single genes or via microarray analyses [14, 19, 21]. To our knowledge up to now no attempt to characterize phenotypic plasticity in wild male phenotypes from the same population, both reproductively active, has been carried out using a genome-wide approach.
Our study species Tripterygion delaisi (Tripterygiidae), also called the black-faced blenny, is a common small rocky shore fish from the Mediterranean Sea and the east Atlantic coast [23, 24]. The black-faced blennies live camouflaged with the rock or algae they inhabit for most of the year. The sneaker males as well as the females exhibit the same camouflaged phenotype throughout the whole year, but in spring throughout the three months reproductive period, some males change their phenotype to a black head and a bright yellow coloring across the rest of the body. These males start protecting a small territory, which is referred to as their nest, against predators and other secondary males . This coloration and behavior is transitory and only observed during the reproductive period. If a territorial male is removed from its nest, in 20% of the cases, a sneaker male takes over and changes its coloration as well as its behavior and becomes territorial . This shows that territoriality is a plastic trait. After being courted by the territorial male, the female lays the eggs directly into the nest and leaves. The territorial male fertilizes the eggs by releasing the sperm directly on them and is left to protect the eggs until the larvae hatch. The sneaker male can dart by and ejaculate its sperm over the nest from a distance . Thus, in T. delaisi alternative mating tactics can be observed for two types of reproductively active males with different phenotypes.
In non-model species, it is often difficult to study molecular differentiation of plastic traits especially in absence of a reference genome . Here we used RNAseq to detect differentially expressed genes in the brain between males with alternative mating strategies in Tripterygion delaisi as well as between males and females. By sequencing and generating a de novo transcriptome assembly it is possible to look at a huge variety of expressed genes and demonstrate key genes which are expressed at a particular moment . By using RNAseq in this study we generate a genome-wide catalogue of genes expressed during the reproductive period of T. delaisi and analyze expression profile and differential expression to identify differences across the brain transcriptome of territorial males, sneaker males and females.
Results and discussion
De novo transcriptome assembly and annotation
In the absence of a reference genome for Tripterygion delaisi in this study we de novo assembled a transcriptome to use as a reference for read mapping and brain gene expression profiling. The de novo assembly of the reference brain transcriptome was performed with 50,360,654 trimmed reads (Phred score 35) of eight pooled individuals of normalized cDNA libraries and 38,056,381 trimmed reads of three separately sequenced not-normalized samples at 109 bp (Additional file 1: Table S1, Additional file 2: Figure S1). Normalizing libraries allowed for the detection of genes also expressed at low levels and therefore a more complete reference transcriptome. With the Trinity de novo assembler 328,565 contigs were produced, including different isoforms per contig, after removing contamination (see Methods section). The N50 of the reference transcriptome is 298 bp long, the N25 234 bp and the N75 is of 464 bp length. The longest contig has a length of 15,547 bp. On average 76% of the reads of the individual samples were mapped back onto the reference assembly. This is the first reference transcriptome for a fish belonging to the Perciforms Suborder Blennioidei (which includes more than 850 species and 151 genera ) and therefore provides a valuable resource and a first step towards a comprehensive understanding of genome-wide gene expression.
The de novo assembly includes differentially spliced isoforms . Most contigs in the reference assembly had one isoform, but many contigs combined differentially spliced isoforms, with the number of isoforms increasing with contig length (Additional file 3: Figure S2). However, given the lack of a reference genome, we cannot discard that some isoforms might result from paralogous genes or misassemblies. The few published genome-wide expression studies on non-model species primarily focus on differential expression at the gene level and de novo assemblies do not include alternatively spliced transcripts e.g. . However, alternative splicing has fundamental effects in the development and maintenance in eukaryotes with 92-94% of human genes undergoing alternative splicing [30, 31]. The products of alternatively spliced transcripts are shown to be responsible for a number of diseases by changing the biological function with differently spliced isoforms . Hence, it is likely that even social behavior or phenotypic expression patterns could be influenced or even dominated by alternative splicing.
Differential expression between phenotypes
Number of significantly expressed contigs and percentage of annotated genes between phenotypes and for a given phenotype with all comparisons combined
TM > SM
SM > TM
TM > F
F > TM
SM > F
F > SM
Annotation, meaning contigs with information on functional protein characteristics, was highest in sneaker males (55.5%, Table 1). For females and territorial males only about one third of the upregulated contigs could be annotated to known proteins (27% and 28% respectively). The enriched GO-terms for the sneaker male are predominantly involved in differentiation and development (Figure 4). This could suggest that the elevated annotation success for the upregulated genes in sneaker males might be related to the presence of more functional descriptions of these developmental genes in the databases. On the other hand, over 70% of differentially expressed genes are left unannotated to a known protein for the territorial male and the female and especially low annotation success was found for the upregulated genes in territorial males against sneaker males (Table 1). As stated above, general reasons for non-annotation of contigs could be lack of sequence conservation, non-coding RNA and orphan genes. However, here by comparing the annotation rate of the phenotypes directly, the results might indicate that the genes involved in social phenotypic plasticity are poorly studied and therefore lack information of the protein function in the databases.
Candidate genes in the context of social behavior
Several previous studies have proposed candidate genes for social behavior and dominance in other fish species with alternative mating tactics , for details please see Material and Methods]. All genes were present in all Tripterygion delaisi individuals and the expression levels of these selected genes were compared between phenotypes (Additional file 1: Table S7). The only candidate gene that showed significant differences in expression after correction for individual variation in T. delaisi was the Somatostatin receptor type 1 (sstr1) between territorial males and females. Somatostatin is a neuropeptide also known as a growth hormone-inhibiting hormone and therefore commonly studied in the context of growth. In the African cichlid (Astatotilapia burtoni) somatostatin and somatostatin receptors have been shown to play a role in social behavior [42–44]. Somatostatin prepropeptide and somatostatin receptor type 3 (sstr3) were elevated in the dominant cichlid males in comparison to the subordinate males. For T. delaisi, differential expression was found for sstr1, which was not measured in cichlids, with significant differential expression between territorial males and females (and intermediate expression levels for the sneaker male). It is probable that elevation in sstr1 levels for T. delaisi males and especially territorial males is correlated with aggression. For cichlids, somatostatin has been shown to have a significant effect on aggressive behavior and aggression levels were correlated with sstr (2 and 3) expression in the gonads . This is the first evidence for the role of sstr1 in association with different morph types demonstrating that the effects of somatostatin on the regulation of growth and behavior are complex .
No other previously suggested candidate genes for social dominance were differentially expressed at a significant level in Tripterygion delaisi with the exception of the brain aromatase enzyme (cyp19a1), which catalyzes the formation of aromatic estrogen. For this gene multiple isoforms were differentially expressed but only before adjustment for individual variation (Additional file 1: Table S7). Cyp19a1 was found at higher levels in territorial males in comparison to sneaker males in other fish species [e.g. . Aromatase is duplicated in fish and one form is expressed in the ovaries and the other one is expressed in the brain. Brain aromatase activity was found to be lower in castrated males than in non-castrated males of Salmo salar  and lower in individuals with developing gonads in comparison to individuals with fully developed gonads in Atlantic croaker (Micropogonias undulates; ). In peacock blennies aromatase activity was also suppressed in sneaker males and elevated in nesting males . Although this shows that brain aromatase clearly is an important enzyme involved in the regulation of social status between males in several fish species, individual variation of the expression of this gene was high in T. delaisi thus we don’t consider this gene differentially expressed (Additional file 1: Table S7). The five sneaker males all expressed the cyp19a1 isoforms at an equally low level, whereas two of the five territorial males show very high levels resulting in differential expression between the male types due to these outliers. This result could be attributed to slight differences in the reproductive phase of the territorial males (e.g. time since/until sperm ejaculation, female presence). Individual gene expression variation has previously been pointed out to be an important factor for phenotypic plasticity  and outlier expression might bias the outcome . Pairing careful behavioral studies with genome wide molecular analyses could therefore strengthen the conclusion, but this especially emphasizes the need of non-pooled biological replicates even in genome wide studies.
A commonly measured neuropeptide in relation to aggression, arginine vasotocin (avt), is differentially expressed between males in several fish species, but not in Tripterygion delaisi (Additional file 1: Table S7). In Atlantic salmon (Salmon salar) vasotocin is one of the key genes that is differentially expressed in the brain with down-regulation for the precocious male  as in the peacock blenny (Salaria pavo) where avt levels were detected to be higher in territorial nesting male in the forebrain . In the African cichlid (Astatotilapia burtoni) elevated expression of avt was found in the dominant male in the posterior preoptic area and in the anterior preoptic area avt mRNA levels were higher in the non-dominant male . Such regional expression differences were also observed in three-spined stickleback (Gasterosteus aculeatus) in relation to territoriality . The fact that whole brain expression was measured in T. delaisi might mask actual expression differences between different brain regions. Nonetheless, Santangelo & Bass point out that there might be a species and context dependency of avt regulation across teleost species as seen for tetrapods .
The fact that most of the previously mentioned candidate genes were not differentially expressed in Tripterygion delaisi could be due to slight differences in reproductive social system. In African cichlids, the subordinate males have undeveloped testes and need to become territorial to reproduce , which is distinct to the sneaker male in T. delaisi. Testes in T. delaisi sneaker males are significantly different in weight (Unpaired t-test: t = 5.089, p = 0.0002), on average they weighed 1.78 times more than those of the territorial males. This shows that the sneaker male has proportionally greater testes and is reproductively active. In Atlantic Salmon precocious males and adult males show differential expression in some of the candidate genes but the two male types reproduce at different ages and the adult males do not settle down and defend a nest . This suggests that the regulation of social and reproductive behaviors is complex, and consideration of expression patterns for candidate genes should take species-and context-specific differences into account.
Novel genes in the context of social behavior
It is important to not only focus on enrichments based on GO analyses, but to individually look at the genes of interest, as certain patterns could be drawn. The genes defining the sneaker male in T. delaisi mostly have functions related to transport. Rab33a, arf3 and mfsd3 are associated with protein transport, protein trafficking and vesicle transport. Klc1, kinesin light chain 1, is responsible for organelle transport along microtubules. For the territorial male some genes related to synaptic plasticity show elevated expression such as gpsm1, a G-protein signaling modulator and ncs1, a neuronal calcium sensor, both involved in the activation or deactivation of the G-protein cascade. The gpsm1 gene acts as a sink to regulate availability and stability of Gα in the G-protein pathway . This Gα component mediates signaling from vasoconstrictive hormone, such as vasopressin (homologue for vasotocin in fish) , a previously mentioned candidate gene for aggression in fish . The neuronal calcium sensor (ncs1), which is also upregulated in the territorial male, is sensitive to cytosolic Ca2+ changes and contributes to G-protein-coupled receptor desensitization and increases vesicle release in the presence of calcium. As ncs1 was found in the dendroids in mice it may allow for locally regulated protein synthesis, which is linked to long-term synaptic plasticity . Also upregulated in the territorial male is the protein kinase Cδ (prkcd) which is a recently-detected PKC isoform that plays critical roles in various cellular functions such as the control of growth, differentiation, and apoptosis . In rodents, though, prkcd is a gene involved in signal transduction that is correlated with behavior . The territorial male also expressed Aldh1l1 at elevated levels which encodes for an enzyme from the aldehyde dehydrogenase family. A gene from this family (aldh9) is one of the few genes that was associated with dominance of African cichlid males in a microarray study . Although in cichlids this gene was expressed in lower levels for the dominant male against the subordinate male, it might be interesting to study this gene family directly in relation to behavior.
Importance of alternative splicing in the context of social dominance
The importance of alternatively spliced gene isoforms has long been accepted  and with the development of RNAseq a more detailed understanding is possible. Although most studies using RNAseq focus on expression on the gene level, expression of differentially spliced isoforms might vary even though overall gene expression might not. For humans 10% of the protein coding genes reveal population-specific splicing . For Tripterygion delaisi nuclear mRNA splicing via the spliceosome is one of the three enriched biological functions differentially expressed for the territorial male, indicating the elevated importance of exon joining and possibly alternative splicing in territorial males (Figure 4). Nonetheless, for the differentially expressed genes in the context of social dominance, most alternatively spliced isoforms showed the same expression pattern (for details see gene tables in Additional file 1: Table S4, S5, and S6). However, five differentially expressed genes with functional annotations in the databases were expressed in an opposing manner in two isoforms between phenotypes. An isoform of phf20 was more highly expressed in the territorial male and a different isoform in the sneaker male. Two isoforms of the genes prkar2b and c7orf51 showed opposing expression patterns in the comparison between sneaker male and female, and different isoforms for the genes rap1gap and macf1 presented contrasting expression patterns between the territorial male and female. In the case of rap1gap evidence shows that differentially spliced isoform transcript variants encode distinct proteins leading to different functions e.g. . These genes would have been overlooked as not differentially expressed if only expression at the gene level was considered. However, due to the complexity and lack of complete understanding for the patterns of alternative splicing, it is still a major challenge to identify differential expression of isoforms and results need to be interpreted with caution. Nonetheless, advances in analysis methods for RNAseq, such as the assembly of clusters of full length alternative spliced isoforms  and models accommodating isoform expression estimates uncertainties , allow the estimation of differential gene expression for isoforms in our species. Even though more work is needed to fully understand the precision and accuracy as well as the possibilities and limitations of the methodologies used, this approach will allow for gene expression studies in non-model species of evolutionary and ecological importance.
Phenotypic plasticity was found to be a more important factor in differential gene expression during reproduction than sexual dimorphism as more genes were significantly expressed at different levels in the brain between the two male phenotypes than between males and females. Previously suggested candidate genes for social dominance in the context of alternative mating strategies seem to be mostly species-specific and here we present a list of novel genes which are differentially expressed in Tripterygion delaisi. Some genes that were differentially expressed for the territorial male were related to synaptic plasticity possibly indicating the drastic change in behavior and phenotype. The sneaker male expresses genes associated with differentiation and development. This result suggests that although this type of male is reproductively active it is largely expressing genes involved in development. This is the first study looking at transcriptome data and differential expression for a non-model species (T. delaisi) in the context of alternative mating strategies and provides essential information for further studies investigating the molecular basis of social dominance. Overall, RNAseq has proven to be a useful tool for the analysis of ecological and evolutionary questions for non-model species.
Territorial males, sneaker males and females of Tripterygion delaisi were collected in June 2010 on the rocky shore of the Costa Brava close to the town of Blanes (41°67’N, 2°30’E) in the northwest Mediterranean Sea. 15 individuals (five territorial males, five sneaker males and five females) were collected for individual expression analysis. Eight additional individuals (three territorial males, three females and two sneaker males) were collected and used as a pooled sample for the de novo transcriptome assembly. All specimens were caught on the same day with small nets and put into large containers for transport back to the laboratory under the same conditions. Territorial males were collected from their nests and females and sneaker males were collected in the surrounding area. Total body length and male gonad weight was measured. The territorial males were 6.52 cm (+/- 0.44 cm) long, whereas the sneaker males were 6.06 cm (+/-0.27 cm) long and the territorial males’ gonads weighed 0.037 g (+/-0.007 g) and the sneaker males’ gonads weighed 0.066 g (+/-0.015 g). Due to the small variation observed we can assume that individuals of each phenotype were in the same reproductive stage and can be considered biological replicates. About an hour elapsed between collecting and processing. Fish were euthanized immediately arriving to the laboratory, all individuals still showing the same phenotypic coloration, snap frozen in liquid nitrogen, and stored at ─80°C. The sex was double-checked especially for sneaker males and females, as they are phenotypically similar, by verifying the presence of ovaries or testes. The collection of fish samples was conducted in strict accordance with Spanish and European regulations. The method of euthanasia followed the Spanish Laws (Royal Executive Order, 53/2013) for Animal Experimentation and was done at the animal research facility of the Spanish National Research Council with the approval of the Directorate of Research of the Spanish Government. The study was found exempt from ethics approval by the ethics commission of the University of Barcelona since, according to article 3.1 of the European Union directive (2010/63/UE) from the 22/9/2010, no approval is needed for fish sacrification with the purpose of tissue or organ analyses. Furthermore, the study species Tripterygion delaisi is not listed in CITES.
Total RNA extraction and cDNA library construction
Fish brains were dissected out of the frozen heads, weighed and placed in TRI Reagent (Molecular Research Center). All Tripterygion delaisi brains weighed between seven and twenty milligrams. Tissues were homogenized in a Retsch homogenizer (MM200) at 25Hz for two intervals of 30 seconds. Phase separation was done with 1/10 volume of BCP Phase Separation Reagent (1-Bromo-3-Chloropropane, Molecular Research Center) and centrifuged for 15 minutes at 12.000 g. The RNA was precipitated with 1/2 volume of isopropanol and centrifuged at 12.000 g for 8 minutes. The total RNA pellet was washed twice with 75% ethanol by vortexing and centrifuging for 5 minutes at 7.500 g to then be dissolved in 50 ul of TE Buffer (pH 8.0).
Poly-A mRNA was purified using Dynabeads (Invitrogen) coated in Oligo(dT)25 following the manufacturer’s protocol, but adding a second wash-step. Random Hexamer Primers (Invitrogen) were added and incubated at 65°C for 5 minutes. First-strand cDNA was synthesized with SuperScript reverse transcriptase (Invitrogen) by incubating at 25°C for 10 minutes, followed by 50 minutes at 42°C and 15 minutes at 70°C. Second strand cDNA was synthesized using RNaseH (New England Biolabs (NEB)) and DNA Polymerase I (NEB), incubated for 2.5 hours at 16°C. cDNA was purified with the QIAquick PCR purification kit (Qiagen) and fragmented with dsDNA fragmentase (NEB) for 28 minutes at 37°C and purified with the same kit. Fragments were prepared for Illumina sequencing with NEB kits following the manufacturer’s instructions for each reagent module. Firstly, ends were repaired with the End Repair module using Escherichia coli ligase and End Repair enzyme mix. A single A-base was then added using the dA-Tailing module with Klenow DNA polymerase. Custom paired-end adapters with 4 bp barcodes (Integrated DNA Technologies) were added with the Quick T4 DNA ligase kit (Qiagen) to be able to multiplex the samples in the same Illumina lane. After each step the DNA was purified either with the PCR purification kit or the MiniElute PCR purification kit (Qiagen). Subsequently, 200-300 bp fragments were cut from a 2% ultra-pure agarose gel (Invitrogen), run for 60 minutes at 110 V, and cleaned with the QIAquick gel extraction kit (Qiagen). Finally, cDNA fragments were enriched using Phusion polymerase (NEB) and paired end PCR Primers (Integrated DNA Technologies). Enrichment PCR was performed as follows: initial denaturation at 98°C for 30 seconds, 15 cycles at 98°C for 10 seconds, 65°C for 30 seconds and 72°C for 30 seconds; and a final extension for 5 minutes at 72°C. PCR products were purified with the PCR purification kit (Qiagen) and resuspended with 30 μl of EB solution. Concentration and purity was measured several times throughout the process with the Agilent 2100 Bioanalyzer (Agilent RNA 6000 pico & DNA 1000 Kit).
Sequencing was conducted on an Illumina Hiseq 2000 using the Illumina 1.5 baseline calling pipeline. A duplex-specific nuclease (DSN) normalized pooled library of 8 mixed samples (three territorial males, three females and two sneaker males) were sequenced at the length of 109 bp, single-end, at DNAVision S.A. (Belgium). At the FAS Center for systems biology at Harvard University (USA) three individuals (one territorial male, one sneaker male and one female) were sequenced at the length of 109 bp and twelve individuals (four territorial males, four sneaker males and four females) were sequenced at a length of 52 bp, all single end. Reads sequenced at the length of 109 bp were used to assemble the reference transcriptome. The reason for the production of a normalized and pooled sample of 8 individuals was to increase the probability of sequencing rare genes. Reads sequenced from individual not-pooled samples, both at 109 bp and at 52 bp, were used for expression analysis.
Read processing, de novo transcriptome assembly and annotation
Reads were sorted and the four-mer barcodes were removed using custom Perl Scripts in the FASTX-Toolkit (http://hannonlab.cshl.edu/fastx_toolkit/). Read quality was checked and visualized with FastQC (Andrews 2010) and low quality reads were eliminated or trimmed in CLC Genomics Workbench 4.7 so that all base reads were superior to the Phred quality score of 35. Reads with the length below 20 bp were removed.
The de novo assembly was performed with Trinity , which allows for the detection of differentially spliced contig isoforms, using the default program settings. Contigs shorter than 200 bp were eliminated. Contamination was identified by blasting the contigs (BLASTn) against locally installed databases from November 2012 (NCBI UniVec database and NCBI fungal, bacterial and viral genomes). Contigs with successful hits (E-value cut-off of 1×10-25) were removed from the assembly before further analysis. The transcripts/contigs in the de-contaminated assembly were blasted against a locally installed UniProt protein database (release 2011_11) using BLASTx (version 2.2.22) with an E-value cut-off of 1x10-10, a word-size of 3 and the BLOSUM62 matrix. Transcripts were also compared to the annotated proteins available on the NCBI Unigene database of Danio rerio. The de novo assembly contigs were divided into two sets: ‘with BLAST’, which are the contigs that resulted in a successful BLAST hit and ‘without BLAST’, which are the contigs without homology in the protein databases. Both sets were then compared. Open reading frame presence and length was measured by using the getorf tool implemented in the program EMBOSS 188.8.131.52 . To detect the protein coding potential of the contigs we used the program CPAT v 1.2 , which is a coding potential assessment tool, and selected the Zebrafish (Zv9/danRer7) as the assembly database. We accepted contigs with a potential above 0.5 to be ‘more likely’ protein coding. Furthermore GC content and expression levels were compared between the two sets.
RNAseq analysis and differential expression
All transcriptome contigs (‘with BLAST’ and ‘without BLAST’) were used as the reference trancriptome for the evaluation of the expression values. The three individual samples of 109 bp length (one territorial male, one sneaker male and one female) were cut down to 48 bp to avoid a length bias in the expression value calculation, as the other 12 individual samples (four territorial males, four sneaker males and four females) were sequenced at a shorter length. On average 13 million quality trimmed reads for each of the 15 individuals (Additional file 1: Table S1) were mapped against the reference transcriptome with Bowtie, a short read aligner (specific parameters: -n 2, -l 25, -m 200 and-a) . RSEM v1.1.19  was then used to quantify mapped reads by using the standard settings. Unmapped reads were discarded. Differential expression values were computed with EBseq  by using a Bayesian approach to accurately estimate isoform expression. Three comparisons were performed to find the particular genes which distinguish each phenotype: territorial males versus sneaker males, territorial males versus females and sneaker males versus females. Count data were normalized by estimating a scaling factor for each contig in EBseq, which has been demonstrated to be a very robust method . We tested for differences between the normalized means with an empirical Bayes hierarchical model resulting in posterior probabilities of differential expression. Five iterations were run for each comparison. Comparisons were accepted to be significant at an FDR adjusted value of 0.05. To avoid outlier expression bias due to great individual variation, we accepted only contigs for which standard deviation was smaller than the mean expression value within phenotype (SD < Mean). For visualization of the significant comparisons, heatmaps of the significant genes after FDR adjustment were produced with the heatmaps2 package in R. Hierarchical clustering of individual samples with 1000 bootstrap replications was performed with the R package pvclust  and heatmaps were sorted accordingly. To visualize clusters of gene expression, we grouped the z-transformed expression ratios by using k-means in R.
The de novo assembled transcriptome was annotated with Blast2GO . We performed several enrichment analyses. Firstly, the top 1% contigs which were expressed at the highest level regardless of phenotype were compared in an enrichment analyses against the whole transcriptome by the means of a Fisher’s Exact test. Enriched GO-terms were then slimmed in REVIGO and treemaps produced . Secondly, enrichment analyses were performed for the differentially expressed genes for the three comparisons.
Genes previously reported to be of importance between phenotypes with alternative reproductive strategies in fish are here termed ‘candidate genes’ in the context of social dominance. The sequences of the candidate genes gnrh (gonadotropin releasing hormone receptor; [14, 19]), epd (ependymin; ), avp (arginine vasopressin; [22, 48, 55, 69]), somatostatin , egr1 (early growth response protein, ), galn (galanin, ) and cyp19a1 (brain aromatase enzyme, ) were blasted (BLASTn) against the de novo assembly contigs using BLAST 2 sequence in NCBI to confirm their presence in the reference transcriptome and evaluate its differential expression among phenotypes.
Availability of supporting data
This Transcriptome Shotgun Assembly project has been deposited at DDBJ/EMBL/GenBank under the accession GAJK00000000. The version described in this paper is the first version, GAJK01000000. Raw sequence reads can be found in the SRA database under BioProject PRJNA186408.
We would like to thank Brian Haas for his help with the de novo transcriptome assembly and Dan Barshis for very helpful input on the analysis of the RNA-seq data. Also, we are grateful to Cinta Pegueroles Queralt and anonymous reviewers for great input on the manuscript. Thank you to Enrique Ballersteros for the cover photo of T. delaisi. This work was partially funded by the Spanish Ministry of Science and Innovation (CTM2010-22218-C02) projects. The authors are part of the research groups 2009SGR-636 and 2009SGR-665 of the Generalitat de Catalunya and CS was funded by a JAE-Predoctoral Fellowship.
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