- Research article
- Open Access
The central nervous system transcriptome of the weakly electric brown ghost knifefish (Apteronotus leptorhynchus): de novo assembly, annotation, and proteomics validation
© Salisbury et al.; licensee BioMed Central. 2015
- Received: 27 October 2014
- Accepted: 18 February 2015
- Published: 11 March 2015
The brown ghost knifefish (Apteronotus leptorhynchus) is a weakly electric teleost fish of particular interest as a versatile model system for a variety of research areas in neuroscience and biology. The comprehensive information available on the neurophysiology and neuroanatomy of this organism has enabled significant advances in such areas as the study of the neural basis of behavior, the development of adult-born neurons in the central nervous system and their involvement in the regeneration of nervous tissue, as well as brain aging and senescence. Despite substantial scientific interest in this species, no genomic resources are currently available.
Here, we report the de novo assembly and annotation of the A. leptorhynchus transcriptome. After evaluating several trimming and transcript reconstruction strategies, de novo assembly using Trinity uncovered 42,459 unique contigs containing at least a partial protein-coding sequence based on alignment to a reference set of known Actinopterygii sequences. As many as 11,847 of these contigs contained full or near-full length protein sequences, providing broad coverage of the proteome. A variety of non-coding RNA sequences were also identified and annotated, including conserved long intergenic non-coding RNA and other long non-coding RNA observed previously to be expressed in adult zebrafish (Danio rerio) brain, as well as a variety of miRNA, snRNA, and snoRNA. Shotgun proteomics confirmed translation of open reading frames from over 2,000 transcripts, including alternative splice variants. Assignment of tandem mass spectra was greatly improved by use of the assembly compared to databases of sequences from closely related organisms. The assembly and raw reads have been deposited at DDBJ/EMBL/GenBank under the accession number GBKR00000000. Tandem mass spectrometry data is available via ProteomeXchange with identifier PXD001285.
Presented here is the first release of an annotated de novo transcriptome assembly from Apteronotus leptorhynchus, providing a broad overview of RNA expressed in central nervous system tissue. The assembly, which includes substantial coverage of a wide variety of both protein coding and non-coding transcripts, will allow the development of better tools to understand the mechanisms underlying unique characteristics of the knifefish model system, such as their tremendous regenerative capacity and negligible brain senescence.
- De novo transcriptome
- Spinal cord
- Apteronotus leptorhynchus
- Brown ghost knifefish
- Non-coding RNA
- Splice-junction peptides
The brown ghost knifefish (Apteronotus leptorhynchus) is a weakly electric teleost fish belonging to the taxonomic order Gymnotiformes. This species has been widely studied over the past several decades as a model system in a variety of disciplines within biology and neuroscience, with particular focus on the ionic and neuromodulatory regulation of neural oscillations [1-6], neural control of communication via electric signals [7,8], and central nervous system (CNS) regeneration [9,10].
Most research involving this species has addressed diverse aspects of their nervous system. As all other species of the family Apteronotidae, A. leptorhynchus generates electric discharges using a neurogenic electric organ, formed by modified axonal terminals of spinal motoneurons . The electric organ discharge is used for orientation and object detection in close vicinity of the fish [12,13], and for communication with conspecifics [7,14-19]. Knifefish are able to sense both their own electric discharges and electric signals of other biological and non-biological sources through electroreceptors distributed on the skin [8,20,21]. The neural structures involved in the processing of behaviorally relevant electrosensory information, and in the motor control of the electric organ discharges, are among the best characterized brain and spinal cord systems of any non-mammalian vertebrate, thus establishing A. leptorhynchus as a significant model of neuroethology .
These neuroethological investigations have yielded an extensive body of information on the structure and function of the CNS of A. leptorhynchus, including the first neuroanatomical atlas of the brain of any teleost species . This knowledge base has, in turn, encouraged the use of the brown ghost knifefish as a model organism in several other biological disciplines, including developmental neurobiology and regenerative biology. For example, the availability of a brain atlas enabled the first comprehensive mapping of adult-born cells in the whole brain of any vertebrate species , establishing A. leptorhynchus as a major teleostean model system for the study of adult neurogenesis [9,10,25,26], and informing similar mappings of the stem cell niches in the adult brain of zebrafish (Danio rerio)  and the Mozambique tilapia (Oreochromis mossambicus) . Utilization of this model has provided substantial insight into the cellular mechanisms that underlie the generation, migration, and differentiation of adult-born cells in various regions of the CNS [29-33]. Recently, A. leptorhynchus has been introduced to the area of aging research as the first vertebrate model system exhibiting negligible brain senescence .
Like many other teleost fish studied thus far, apteronotids have a remarkable capacity for regeneration after CNS injury, a property which has been connected to the high levels of adult neurogenesis occurring throughout the life of fish . Adult neurogenesis and neuroregeneration have been studied extensively both in the brain and in the spinal cord of brown ghost knifefish. Studies using proteomic analysis in conjunction with brain lesion paradigms have contributed to a better understanding of the molecular dynamics triggered by injury and subsequent regeneration [35,36].
The unique neurogenic origin of the electric organ in apteronotids greatly facilitates the correlation of structural regeneration and functional recovery after spinal cord injuries, by allowing instantaneous non-invasive monitoring of the activity of newly formed spinal electromotor neurons. Thus, the spinal cord of brown ghost knifefish has proven to be a useful model both for understanding spontaneous regeneration of the CNS and for assessing the effectiveness of experimental manipulations aimed at improving natural recovery in regeneration-competent organisms [37-40].
Despite the extensive use of apteronotids as model systems, there are currently no large-scale genomic resources for any species of this family. Several studies have used molecular cloning and sequencing to determine partial or complete sequences of less than two dozen proteins, mostly transmembrane ion channels and receptors [41-54], but also synaptic scaffold proteins , enzymes , and homeobox genes . The addition of new, detailed sequence information on a large scale is required for the development of better tools to be used in the study of the CNS in knifefish.
The present investigation describes the de novo assembly and annotation of the A. leptorhynchus CNS transcriptome based on sequencing datasets derived from Illumina-based sequencing-by-synthesis. Results are presented for libraries prepared from both the brain and the spinal cord of ten adult male and female knifefish. Translation of a subset of transcript open reading frames was experimentally validated by shotgun proteomics.
De novo transcriptome assembly
Strand-specific cDNA libraries were prepared from CNS tissues (brain and spinal cord) of 10 adult male and female A. leptorhynchus. Final raw read counts included 24,164,311, 150 bp paired-end reads passing filter on an Illumina MiSeq platform, and 252,642,499 150 bp paired-end reads passing filter obtained using an Illumina HiSeq 2500 platform. These reads were combined and then assembled using Trinity . After optimizing parameters for trimming and transcript reconstruction (see below), an assembly with ~300,000 unique contigs, including ~1.2 M total isoforms, was produced. Of these, 42,459 contigs contained at least a partial protein-coding sequence based on alignment to a reference set of known Actinopterygii protein sequences. As many as 11,847 of these contigs contained full or near-full length (≥80%) unique protein sequences (based on significant sense alignments to the Actinopterygii reference set, described below), thus providing broad coverage of the A. leptorhynchus proteome. In general, we used BLAST alignment of transcripts (or translations of predicted ORFs from transcripts) to reference protein sets as a means of assessing coding transcript completeness. Transcripts with ≥ 80% sequence coverage (i.e. a significant alignment between a transcript sequence from our assembly and a target protein sequence, where the alignment covers at least 80% of the target protein sequence) are thus considered “full or near-full length”.
As part of optimizing our de novo assembly, we compared the effect of read trimming on de novo transcriptome assembly. Read trimming strategy affects assembly quality and can impact downstream analysis, with the best tradeoff between read loss and dataset quality dependent upon the dataset itself as well as research goals . For trimming reads prior to assembly, we evaluated no trimming, “soft” trimming, where 3’ adapter sequences present from insert read-through during sequencing were removed as well as leading and trailing bases that were uncalled (“N” bases) or with low quality (below 3), and “hard” trimming, where, in addition to the “soft” trimming criteria, a sliding window was used to eliminate bases that fall below a threshold quality (4-base wide sliding window, cutting when the average quality per base dropped below 15 [70,71]). In either of the trimmed read sets, trimmed sequences shorter than 35 bp were also removed before further analysis, as well as reads that became unpaired because of this. Prior to assembly, these trimmed read sets were pooled and normalized using the in silico normalization script packaged with Trinity, in order to remove highly redundant sequences and reduce assembly computational time. The trimmed, normalized read sets were then assembled with Trinity using the default settings for strand-specific, paired-end read sets, including a 200 bp minimum transcript length (additional parameters for transcript reconstruction were considered and are described below). Trinity produces transcripts that are assigned to ‘genes’ (previously referred to in Trinity as “components”), with each gene set potentially corresponding to multiple transcripts derived from the same genomic loci (i.e. transcripts within the same assembly gene are potential alternatively spliced variants). Here, we refer to unique Trinity “components” as “contigs”, where a single contig can include a set of multiple sequence variants.
In order to compare quality of assembly methods and permit further optimization, we BLASTx searched (E-value cut-off = 10−5) a D. rerio reference proteome (41,112 sequences) obtained from UniProtKB, which contained non-redundant sequences from both SwissProt and Trembl. Relative to the total number of protein sequences in this D. rerio reference proteome set, similar coverage was achieved regardless of trimming strategy, although the “soft” trimming strategy provided a minor advantage over “hard” trimming, recovering 2.44% more transcripts with at least 80% sequence coverage (12,446 sequences, including antisense alignments, for soft trimming compared with 12,149 sequences for hard trimming) (Additional file 1: Figure S1A). It has been reported that while the aggressive quality-based trimming strategy is common, a gentler strategy can favor increasing sensitivity of transcript reconstruction during de novo assembly .
Regardless of trimming strategy, each raw assembly was considerably large, with ~300,000 contigs and ~1.2 M total isoforms per assembly. Whereas these values were similar to the numbers observed using comparable methods [73,74], they are larger than more reasonable estimates of loci achieved with other datasets . This may be due to incomplete contiguous transcript reconstruction of low-expressed transcripts, resulting in multiple (non-overlapping) contigs per locus, as well as contamination and transcriptional noise. We attempted to determine whether the size of the assembly could be further limited, while retaining coverage of the D. rerio proteome, by evaluating different strategies for transcript reconstruction.
Transcript reconstruction optimization
With the goal of minimizing excessive alternative transcript reconstruction, we evaluated several reconstruction methods in Trinity. Aside from the default Trinity transcript reconstruction method, Butterfly , we considered Butterfly in “extended lock” mode, which favors more conservative transcript reconstruction resulting in fewer isoforms. In addition, CuffFly, an implementation of the Cufflinks assembly algorithm [74,77] that finds the minimum number of isoforms that capture the variation in the reads, and PasaFly, an implementation of the PASA (Program to Assemble Spliced Alignments) assembly algorithm  adapted for Butterfly transcript graphs, were also evaluated, as these methods generally tend to produce even more conservative isoform reconstructions. While the alternative transcript reconstruction methods reduced the overall number of transcripts in the assembly, they produced similar number of overall contigs (Additional file 1: Figure S1B). Despite similar number of contigs overall, the default (Butterfly) transcript reconstruction did provide some enhanced sensitivity, with 7.98% more sequences aligned than the next best reconstruction method (12,446 sequences, including antisense alignments, covered with Butterfly compared with 11,526 with PasaFly) (Additional file 1: Figure S1C).
Overall, while many contigs remained unassigned at this initial level of annotation, the identification of contigs with sense alignments covering ≥80% of 9901 D. rerio protein sequences indicated that the assembly was of substantial quality (Additional file 2: Table S1) despite being limited to libraries prepared from only the CNS of A. leptorhynchus. The large number of assembly contigs with only partial alignments suggested that higher coverage could be achieved with additional libraries from other tissues.
Full sequence coverage enrichment amongst highly expressed transcripts
From the assembly produced by the least stringent but most sensitive Butterfly method, the number of isoforms per contig followed a power law, with many contigs having few isoforms and a few contigs having many (100–1000) isoforms (Additional file 1: Figure S1D). However, after filtering for transcripts with number of fragments per kilobase of transcript per million mapped reads (FPKM) ≥ 1, the approximate equivalent of 1 transcript per cell , the number of transcripts per contig was reduced to a log distribution, where even though many contigs had multiple isoforms, the number of isoforms was on the order of 10’s (Additional file 1: Figure S1E). In terms of transcript length, the overall assembly had a N50 of 2539 bp (median transcript length = 1219 bp, average length = 1606 bp, total assembled bases = ~2.0Gb, Additional file 1: Figure S1F). However, when considering only the longest transcripts per assembly contig, the distribution shifted to an N50 of 940 bp (median transcript length = 377 bp, average length = 661 bp, total assembled bases = ~230 Mb, Additional file 1: Figure S1G), suggesting that the larger N50 calculated from the entire assembly (including every isoform per contig) was due to longer contigs having many long isoforms assembled by Trinity. After filtering for transcripts with FPKM ≥ 1, the N50 was 2093 bp (median transcript length = 1140 bp, average length = 1508 bp, total assembled bases = ~303 Mb Additional file 1: Figure S1H), with a more consistent (i.e. less biased) N50 of 1995 bp (median transcript length = 907 bp, average length = 1330 bp, total assembled bases = ~110 Mb) after considering only the longest transcript per contig (Additional file 1: Figure S1I). Thus, when considering only contigs with isoforms that had an FPKM ≥ 1, the overall distribution of transcript size was improved.
Out of all 766,261 transcripts from the assembly (including variant isoforms belonging to the same contig) with an alignment to a D. rerio reference protein, most transcripts aligned to <40% of the respective protein (Figure 1B). When filtering the assembly for transcripts with FPKM ≥ 1, the relative proportion of transcripts with less than complete alignments was reduced (Figure 1C). When selecting only the longest aligned transcript per contig, the relative proportion of shorter alignments was reduced (Figure 1D), suggesting many assembly transcripts within a contig group contained partial open reading frames (ORFs). This distribution was preserved when considering only the longest aligned transcript per contig that also had an FPKM ≥ 1 (Figure 1E). Out of the entire assembly, more than half of the transcripts had at least some alignment to a reference D. rerio sequence. Likewise, more than half of the sequences with FPKM ≥ 1 aligned to a D. rerio protein sequence (Figure 1F). Using only transcripts with FPKM ≥ 1, nearly 60% of the reference D. rerio proteome had at least one assembly transcript with an alignment (24,112 sequences), which represented ~80% of the D. rerio sequences that were hit by the entire assembly (30,121 unique sequences, Figure 1G).
Enrichment of sequences aligning to closely related fish species
Coverage of proteins for Actinopterygii species by relative number of entries in reference sets
Hits/Total (% of Total/% Relative)
Japanese rice fish
Takifugu rubripes (Fugu rubripes)
Spotted green pufferfish
Transcriptome coverage assessment and enrichment analysis
Anatomical enrichment of genes with high sequence coverage compared with genes having lower to no coverage
Significantly enriched anatomical terms sequences with high (≥80%) coverage
Significantly enriched anatomical terms sequences with < 80% or no coverage
Central nervous system
Cranial nerve II
Occipital lateral line neuromast
Extension of previously sequenced knifefish transcripts
Identification of non-coding RNA (ncRNA) expression and antisense transcripts
The importance and complexity of ncRNAs have attracted increasing attention over the last decade. Numerous classes of ncRNA are now known to be important modulators of gene expression, involved in the regulation of a wide variety of physiological and developmental processes [89,90]. In the CNS, ncRNAs are tightly regulated, and appear to play prominent roles in developmental processes such as neurogenesis and neuronal differentiation [89-91], which continue throughout adult life in A. leptorhynchus [9,10,26,92].
Summary of annotated transcripts/contigs by RNA types
# Transcripts (including contig isoforms)
Sense BlastX (D. rerio)
Sense BlastX (Actinopterygii)
rRNA (identified by RNAmmer)
rRNA (from D. rerio reference)
Mitochondrial rRNA (from D. rerio reference)
lncRNA (Kaushik et al.)
While our library preparation protocol was designed to limit the presence of rRNA, two contigs were found to align to D. rerio 5S and 5.8S rRNA, with two additional contigs corresponding to mitochondrial rRNA. Using an additional rRNA prediction tool, RNAmmer , four additional contigs were designated as 8 s rRNA (comp134303, comp138865, comp150483, and comp193485).
A total of 84 of the A. leptorhynchus assembly contigs were aligned to 81 miRNA transcripts from D. rerio. Out of these, 54 A. leptorhynchus assembly transcripts aligned to ≥80% of the corresponding D. rerio miRNA. Many of these alignments to miRNA sequences were included into longer assembly transcripts, which had portions that aligned to D. rerio protein sequences, suggesting that these transcripts likely included precursor miRNAs (pri-miRNAs), transcribed in conjunction with adjacent protein coding sequences .
Thirteen putative snRNA were identified, including all five snRNA components of the spliceosome (U1, U2, U4, U5, and U6), as well as U11 and U12 minor spliceosomal RNA. Also detected was 7SK small nuclear RNA (rn7sk), the RNA component of the 7SK snRNP involved in the control of transcription elongation and in the regulation of pre-mRNA splicing . The RNA component of the signal recognition particle (SRP), a universally conserved ribonucleoprotein that targets specific proteins to the endoplasmic reticulum in eukaryotes [96,97], was also detected, with 95.1% identity across 96.6% of the corresponding D. rerio transcript.
Seventeen transcripts aligned to snoRNA, a family of RNA which guide chemical modification (methylation and pseudouridylation) of nascent rRNA to generate mature rRNA . Amongst the snoRNA identified were 13 methylation-associated C/D-box class snoRNA and 4 pseudouridylation-associated H/ACA-box class snoRNA.
A total of 54 sequences of the A. leptorhynchus transcriptome showed significant alignment to known D. rerio long intergenic non-coding RNA (lincRNA), including two sequences that covered >90% of the corresponding D. rerio lincRNA. While sequence coverage was generally low, alignments to >1000 nucleotides with close to 80% identity were found.
To further investigate the presence and conservation of lncRNA expressed in adult CNS tissues of A. leptorhynchus, the assembly was searched against an additional set of lncRNAs expressed in adult D. rerio, including many with specific expression in the brain. LncRNAs have been shown to be expressed with high tissue specificity, in particular in the brain , where they have been associated with the control of neuronal diversification and specification . Kaushik et al. reported a set of 419 novel lncRNAs, including 47 specifically expressed in adult D. rerio brain when compared with heart, liver, muscle, and blood . Amongst these, we found evidence for at least one conserved lncRNA expressed exclusively in the brain (lncBr_002), as well as 10 additional lncRNAs found in adult D. rerio brain and other tissues examined, and finally 4 lncRNAs that were not observed in the brain previously, but were found in blood. It is possible that these transcripts could be novel, functional lncRNA. However, further investigation will be required to exclude the possibility of contamination from remaining blood vessels in the isolated brain tissue.
Antisense transcription contributes to the complexity of expression dynamics, and while antisense transcripts can play roles in regulating translation and splicing, separating functional antisense transcripts from transcriptional noise remains a challenge. Out of the 682 antisense sequences in the available D. rerio ncRNA reference set, only 25 had significant alignments (e-value < 10−10) to transcripts from 27 contigs in the A. leptorhynchus assembly, with significant alignments ranging from 46 bp to 930 bp. Expression of thousands of antisense transcripts was found to be conserved across humans, mice, and rats, although to a lesser degree than protein-coding genes . The relatively low coverage of antisense transcripts from D. rerio may be due to lack of sufficient sequencing depth or to the restriction of our analysis to RNA expressed in adult CNS tissue.
Detection of protein-coding ORFs and putative protein-coding gene duplications
To determine the overall protein-coding potential of transcripts in the A. leptorhynchus assembly, regardless of their alignment to known Actinopterygii protein sequences, protein-coding ORFs were predicted from the assembly using TransDecoder , both with and without biasing “best” ORF calling towards ORFs with a recognizable domain in the Pfam protein families database . When limiting the set of ORFs from each search to only those comprising at least 100 amino acids, the resulting distributions of ORF lengths were similar overall, regardless of whether or not Pfam domains were used for guiding ORF selection (Additional file 6: Figure S2A-B). Similarly, filtering for transcripts with FPKM ≥ 1 had little effect on ORF size distribution without Pfam (Additional file 6: Figure S2C-D), suggesting that resolution of the distribution of ORF lengths of 100 amino acids or greater was independent of expression levels. BLAST aligning ORFs with or without guidance from Pfam against the D. rerio reference sequence demonstrated that the Pfam option did slightly increase identification of ORFs with conserved protein coding sequences (Additional file 6: Figure S2E-F). Out of the approximately 202,000 A. leptorhynchus transcripts with FPKM ≥ 1, 87,945 transcripts with ORFs comprising at least 100 amino acids (as found with Pfam) aligned to D. rerio protein sequences. Transcripts with FPKM values ≥ 1 covered a total of 21,638 unique D. rerio proteins, or over 80% of the identifiable sequences (Additional file 6: Figure S2G). When transcripts with FPKM values < 1 were included, this coverage increased to 26,588 unique D. rerio sequences, indicating that even transcripts expressed at low levels could still provide recognizable sequences. An additional 6,090 transcripts with FPKM ≥ 1 contained ORFs of over 100 amino acids that did not align to a D. rerio protein in our reference sequence set. However, after BLAST aligning these ORFs against the entire NCBI non-redundant (nr) protein sequence database, 3,505 additional sequences had significant alignments -- 3,273 of these alignments were to sequences from Teleostei species (Additional file 6: Figure S2H) showing a similar trend to the results from the nt sequence set, including 2,079 A. mexicanus sequences and 425 D. rerio sequences absent from the UniProt reference set.
D. rerio proteins with ≥ 4 contigs aligning to ≥ 80% of the D. rerio sequence
D. rerio reference protein (UniProt ID)
# Contigs in assembly
# of D.rerio genes
Uncharacterized protein (fragment)
Phosphatidylinositol transfer protein, alpha b
Ubiquitin-conjugating enzyme E2D 2 (UBC4/5 homolog, yeast)
To exclude the possibility that contigs we assigned as putative duplicated genes (relative to D. rerio) are the result of artifactual contig splitting by Trinity, we compared at the nucleotide level the ORFs of the 491 contigs assigned as having a single duplication (i.e. two distinct contigs with full or near-full length ORFs that align to a single D. rerio protein sequence). Aligning the ORFs of these pairs of contigs, we observed substantially different sequences at the nucleotide level (sequence identity = 61 ± 8%, μ ± σ), with sequence identity ranging from a maximum of 87% and minimum of 34%. Such a high dissimilarity between two ORF sequences suggests these contigs derive from different genomic loci. That both sequences produce significant alignments covering > 80% of the same target protein sequence (from D. rerio) suggests that these contigs are both: 1) full or near-full length; and 2) encode related protein products.
Validation of putative protein coding regions via shotgun proteomics analysis of the A. leptorhynchus CNS
To analyze tandem mass spectrometry data, we used Mascot, which utilizes probability-based scoring in order to match tandem mass spectra to protease digest peptides predicted from a given sequence database . In Mascot, limiting the reference database size, as occurs when searching only the appropriate genus and species, increases probability-based scoring and leads to a greater percentage of statistically significant identifications. Alternatively, including more sequences, for example incomplete fragments, such as those found in our assembly, or proteins from other organisms that may not have been covered in the present assembly, could increase the total number of protein IDs, but may negatively impact scoring based on adjustments due to database size. We therefore considered several approaches when preparing our assembly as a sequence database for Mascot, including using only long ORFs (at least 100 amino acids), only ORFs from transcripts with FPKM values ≥ 1, or all ORFs regardless of size, and compared these results to results obtained using available sequences of D. rerio, as well as other Actinopterygii sequences, from NCBI.
Notably, any ORF set derived from the A. leptorhynchus assembly provided the most assignments at both the peptide and protein level when compared with the results from other existing databases. The results were compared using several different false discovery rates (FDR) (Figure 7B-D). As many as 2,813 proteins were identified (from 58,106 peptide assignments) with the conservative 1% FDR from the database containing all assembly ORFs (Additional file 9: Table S6). Within Mascot-assigned “protein families”, similar protein sequences identified from a given database are grouped together. These groups can include paralogous sequences (both known and unique) and alternatively spliced variants. When comparing the Mascot protein families with annotations from BLAST results, there was good agreement between the Mascot assigned protein families and known paralogues identified from alignment with D. rerio. For example, the first protein family assigned by Mascot included twelve ORFs from the A. leptorhynchus assembly that corresponded, after BLAST searching, to multiple isoforms of alpha tubulin, including tuba1a, tuba1c, tuba8l, tuba8l2, tuba8l3, and tuba8l4. Likewise, the second protein family assigned by Mascot included 15 ORFs from the A. leptorhynchus assembly that all aligned to beta tubulin isoforms. The 2,813 proteins identified (FDR < 1%) from the database containing all assembly ORFs were grouped by Mascot into 2,424 protein families.
Limiting the number of sequences in the database (by either filtering by FPKM or by ORF length) did not benefit the probabilistic assignment of tandem mass spectra, and including more sequences, such as partial and low-expression sequences, was not observed to be a limiting factor. Including shorter and less abundant transcripts from the A. leptorhynchus assembly helped in peptide assignment. In the present study, short ORFs identified through proteomics often represented terminal fragments of transcripts that were not fully assembled (these ORFs lacked 5’ and/or 3’ ends).
A powerful benefit of combined transcriptomics and proteomics is the ability to confirm translation of alternatively spliced transcripts through the detection of splice junction peptides . For example, within the spectrin family, which contained nine ORFs that were identified by proteomics, including spta2, sptb, sptbn1, sptbn2, there were two assembly ORFs derived from different transcript isoforms within the same contig, both aligned to D. rerio spta2. These two ORFs, with lengths of 1760 and 1780 amino acids, and both assigned as complete sequences based on TransDecoder, were identical except for the addition sequence TAVTKETCSVSVRMKQVEEL, present after amino acid Q352. Comparison of MS/MS sequence coverage confirmed the identification of unique splice junction peptides from each sequence (Figure 8C-E). Overall, there were 209 contigs identified in the proteomics results that had 2 or more isoforms with non-redundant ORFs identified (with two contigs each having 5 transcripts identified), although manual inspection of MS/MS for putative splice junction peptides is necessary to rule out false positives.
The present study represents the first major collection of transcriptomics data for a species of the order Gymnotiformes, weakly electric fish from South and Central America with great relevance for neurobiological research. Previously, only nineteen A. leptorhynchus mRNA sequences were publically available. With our de novo assembly of the adult A. leptorhynchus CNS transcriptome, broad coverage of protein-coding sequences was achieved, with as many as 11,847 contigs presenting full or near-full length ORFs. Our study provides the first survey of a broad variety of ncRNA in A. leptorhynchus, including miRNA, snRNA, snoRNA, and other ncRNA sequences. Shotgun proteomics confirmed translation of ORFs from over 2,000 transcripts, including alternative splice variants. Our de novo transcriptome-to-proteome analysis contributes to the growing trend of incorporating these two techniques for enhancing shotgun proteomics identifications while confirming ORF assignment from transcriptome assembly experiments.
A. leptorhynchus is an important model organism in particular for the study of fundamental neurobiological aspects, such as adult neurogenesis, neuronal regeneration, and the neural basis of behavior. The availability of a targeted CNS reference transcriptome will provide novel molecular tools to explore the underlying cellular mechanisms of such phenomena. In addition, the sequence information provided here can be employed to study phylogenetic relationships and various aspects of CNS evolution in vertebrates. Future studies, using libraries from different tissues and developmental stages, will further improve the quality and applicability of the A. leptorhynchus assembly.
Brown ghost knifefish (Apteronotus leptorhynchus) were supplied by tropical fish importers and maintained in the laboratory as described previously . A total of 10 individuals were used for sequencing, and 26 fish were used for the proteomics experiments. Both males and females were included, and all fish were adults in their second or third year of life. All animal experiments were approved by the Institutional Animal Care and Use Committee of Northeastern University. All efforts were made to reduce the number of animals used and to minimize animal suffering.
RNA-Seq library preparation and paired-end sequencing
Total RNA was extracted from brain samples collected individually from 3 adult females, as well as pooled spinal cord samples collected from 7 male and female individuals, using an Aurum Total RNA Fatty and Fibrous Tissue Kit (Bio-Rad, Hercules, CA). RNA quality was determined by calculating the RNA Integrity Number (RIN) after performing a Eukaryote Total RNA Pico assay on a Bioanalyzer 2100 (Agilent, Santa Clara, CA). A strand-specific cDNA library for Illumina-based sequencing-by-synthesis was created using the TruSeq Stranded mRNA Sample Prep kit (Illumina, San Diego, CA). Briefly, polyadenylated mRNA was purified using poly-dT oligo-attached magnetic beads. Following purification, the mRNA was fragmented into small pieces using divalent cations under elevated temperature. The cleaved RNA fragments were reverse transcribed into first strand cDNA using reverse transcriptase and random primers. This was followed by second strand cDNA synthesis using DNA Polymerase I and RNase H in the presence of dUTP, which is incorporated into the second strand to prevent its amplification during subsequent PCR . 3’ ends of double-stranded cDNA fragments were adenylated to permit ligation of barcoded adapters that allow for sorting of sequenced fragments that had been pooled prior to sequencing. The products were then purified and enriched with PCR to create the final strand-specific cDNA library. Concentration and quality of strand-specific cDNA libraries was assessed by NanoDrop (Thermo Scientific, Waltham, MA) and High Sensitivity DNA assay on a Bioanalyzer 2100, respectively. Paired-end sequencing (2 × 150 cycles) of pooled, strand-specific cDNA libraries derived from mRNA-enriched extracts was performed on MiSeq and HiSeq 2500 instruments (Illumina). After sequencing, reads were mapped to their respective samples based on ligated barcoded adapter sequences with CASAVA 1.8.2 (Illumina). Read quality was examined with FastQC and FastqScreen, which confirmed that read fidelity was maintained during sequencing and contamination from other organisms was negligible.
De novo transcriptome assembly and transcript annotation
Reads were trimmed with Trimmomatic . The “soft trimming” read set included reads trimmed to eliminate adapter sequences, leading and tailing bases with quality score less than 3 (including uncalled bases), and reads shorter than 35 bp after trimming. The “hard trimming” read set included reads trimmed with the “soft trimming” parameters as well as a 4-base wide sliding window, cutting when the average quality per base dropped below 15. Unpaired reads remaining after trimming were also removed in either case.
The trimmed read sets were then assembled using Trinity [68,76] (November 11, 2013 release) with default settings (which include minimum transcript length of 200 bp) for strand-specific, paired-end read sets. To reduce assembly time, trimmed reads were normalized prior to assembly using the in silico normalization script included with Trinity with default settings for strand-specific sequences. To evaluate the necessity of extensive alternative transcript reconstruction, additional Trinity assemblies were also performed using the extended lock feature of Butterfly. CuffFly and PasaFly were also examined as alternative transcript reconstruction methods.
To compare quality of Trinity assemblies based on trimming and transcript reconstruction strategies, sequences were blasted (BLASTx, version 2.2.28, E-value cut-off = 10−5) against a locally installed BLAST database containing the UniProtKB D. rerio complete proteome sequence set (41,102 sequences, retrieved April 2nd, 2014). The best assembly was further examined with BLASTx against two sequence sets (also retrieved April 2nd, 2014 from UniProtKB), including: an A. leptorhynchus protein set (18 sequences) and an Actinopterygii complete proteome set (211,131 sequences). The NCBI nt sequence set (retrieved August 17th, 2014) was used to BLASTn search the assembly. To identify ncRNA sequences, transcripts were blasted (BLASTn) against the Ensembl  D. rerio ncRNA database  (ftp://ftp.ensembl.org/pub/release-75/fasta/danio_rerio/ncrna/Danio_rerio.Zv9.75.ncrna.fa.gz), and an additional set of 417 lncRNA found in adult D. rerio . RNAmmer 1.2  was used to predict rRNA sequences in transcript assembly using scripts within Trinotate and HMMER 2.3.2 . Vector and primer contamination was identified by VecScreen (http://www.ncbi.nlm.nih.gov/tools/vecscreen/) and contaminants were removed prior to depositing with NCBI. FPKM (fragments per kilobase of exon per million fragments mapped) of transcripts was calculated by estimating transcript abundance using RSEM (RNA-Seq by Expectation Maximization) , followed by TMM (trimmed-mean of M-values) normalization within Trinity.
Gene ontology enrichment and KEGG pathway analysis
The WEB-based GEne SeT AnaLysis Toolkit (WebGestalt) [112,113] was used to map transcripts from blastX analysis of the D. rerio reference proteome to GO-slim categories and KEGG pathways. For this analysis, the corresponding D. rerio gene name for BLASTx-matched sequences with greater than 80% subject sequence coverage were used. For GO enrichment analysis, the same gene list was ranked by FPKM. In the case of multiple transcripts aligned to the same D. rerio protein, the FPKM of the highest expressed transcript corresponding to a given D. rerio protein was used to determine its rank in the list. The ranked list was analyzed with GOrilla [86,114] (Gene Ontology enRIchment anaLysis and visuaLizAtion tool). This process was performed similarly for proteomics results, using the D. rerio gene names from the BLASTp searches of the corresponding putative ORFs from TransDecoder (described below). Significant GO terms (Benjamini-Hochberg adjusted p-value < 0.001) were hard trimmed for redundancy using the GO Trimming tool . REVIGO  was then used to analyze the trimmed GO IDs and corresponding p-values to further combine GO categories (0.5 similarity) and visualize the results with a treemap scaled by -log10 p-values. For anatomical expression enrichment analysis, gene lists were analyzed with ZEOGS  using gene anatomical annotation from ZFIN and the adult stage filter (Benjamini-Hochberg adjusted hypergeometric p-value < 0.05).
Protein extraction and sample preparation for proteomics
Brain and spinal cord tissues were isolated rapidly on ice and stored at −80°C. To increase overall coverage of identified proteins, samples were prepared using both in-gel digestion and eFASP. In-gel digestion was performed as previously described . Tissue samples were homogenized for 3 min on ice in lysis buffer containing 50 mM Tris, 120 mM NaCl, 1 mM EDTA, 1% Triton X-100, 0.1% SDS, 10% glycerol (all from Fisher Scientific), pH 7.4, using a hand-held pestle homogenizer. The homogenate was placed in a rotating mixer for 40 min at 4°C, centrifuged for 10 min at 16,000×g, and the supernatant was collected and stored at −80°C. Protein concentration was determined using a BCA assay (Pierce). Samples were loaded onto 12% acrylamide gels (Bio-Rad) at 50 μg total protein per lane, and run at 120 V until the protein front was well focused at the beginning of the resolving gel, before band separation. The gels were transferred into fixative solution containing 10% acetic acid, 50% methanol (all from Fisher Scientific), and 40% water for 30 min, stained for a few seconds with Ponceau S (Boston Bioproducts, Inc.), then destained in fixative solution for 2–3 hours, until the protein band was clearly visible and the background minimal. The protein bands were excised, fragmented into 1-mm3-pieces, and stored in 1% acetic acid in water at 4°C overnight. The gel pieces were dried with 500 μl acetonitrile for 10 min, reduced with 10 mM DTT in 100 mM ammonium bicarbonate for 30 min at 56°C, dried with acetonitrile, alkylated with 55 mM iodoacetamide in 100 mM ammonium bicarbonate for 20 min at room temperature, and dried again with acetonitrile. The dried gel pieces were saturated with a solution of 13 ng/μl trypsin (Princeton Separations, Inc.) in 10 mM ammonium bicarbonate containing 10% acetonitrile, and incubated overnight in a thermo-mixer at 37°C and 400 rpm. Digests were extracted by adding a 1:2 solution of 5% formic acid in water and acetonitrile, followed by incubation at 37°C and 400 rpm for 15 min. Supernatant aliquots were collected and dried using a vacuum centrifuge.
eFASP was performed as previously described, with minor modifications . Tissue samples were fragmented and incubated in a thermo-mixer for 10 min at 95°C and 600 rpm, in lysis buffer containing 4% SDS, 0.2% sodium deoxycholate, 50 mM Tris(2-carboxyethyl)phosphine hydrochloride, 100 mM ammonium bicarbonate, pH 8. The sample was further homogenized on ice using a sonicator, centrifuged at 14,000×g, sonicated and pelleted again, and the supernatant was collected and stored at −80°C. For sample processing, 25 μl of tissue lysate were mixed with 200 μl exchange buffer, containing 8 M urea, 0.2% sodium deoxycholate, 100 mM ammonium bicarbonate, pH 8, and dispensed onto a Vivaspin 500 filter unit, 30 kDa MWCO (GE Healthcare), and centrifuged at 15,000×g. After two further washes with exchange buffer, the sample was alkylated by incubating for 1 hour at 37°C and 300 rpm with 100 μl buffer containing 8 M urea and 50 mM iodoacetamide in 100 mM ammonium bicarbonate, pH 8. After centrifugation for 10 min at 15,000×g, and two further washes with 200 μl exchange buffer each, the sample was washed three times with digestion buffer containing 0.2% sodium deoxycholate in 50 mM ammonium bicarbonate, pH 8. Trypsin was added in 100 μl digestion buffer at a ratio of 1:50 with the total protein in the sample, and the unit was incubated overnight at 37°C and 300 rpm. After centrifugation for 10 min at 15,000×g, the unit was washed twice with 50 μl of 50 mM ammonium bicarbonate, and all filtrate was collected. To remove residual detergent, 1 ml of ethyl acetate was added to the sample, sonicated for 10 seconds and centrifuged for 10 min at 16,000×g, and the upper organic layer removed. This process was repeated three times, then the aqueous samples were placed in a thermomixer at 60°C for 5 min, to remove residual ethyl acetate. The samples were then dried in a vacuum centrifuge and resuspended in 50% methanol several times to remove residual salts.
LC-MS/MS and data analysis for protein identification
Protein extract digests were analyzed on an impact HD Qq-Time-Of-Flight (Qq-TOF, Bruker Corporation, Billerica, MA) with a CaptiveSpray ion source (Bruker-Michrom, California, USA). The mass spectrometer was coupled to an Ultimate 3000 nano-LC system (Dionex, California, USA) fitted with an in-house packed C18 column (500 mm x 100 μm, 2.5 μm beads, XSelect, Waters Corp., Milford, MA). Solvent A was 0.1% formic acid in water, and solvent B was 0.1% formic acid in acetonitrile. The following gradient conditions were used: t = 0–5 min, 5% solvent B; t = 245 min, 40% solvent B; t = 248–262 min, 80% solvent B; t = 265 min, 5% solvent B. The flow rate was 1 μL/min. Tandem mass spectra were acquired at an intensity-dependent rate of 4-20Hz between precursor scans.
LC-MS/MS spectra were initially analyzed in DataAnalysis 4.2 (Bruker). Compounds were detected based on an AutoMSn intensity threshold of 104 and exported to a Mascot generic file (MGF) using the Protein Analysis function. The MGFs from individual runs were imported into ProteinScape 3.1 (Bruker), combined, and proteins were identified from LC-MS/MS runs by searching the MS/MS spectra using a local Mascot (Matrix Science Inc, Boston, MA) server. All Mascot searches were performed using trypsin as the enzyme, up to two missed cleavages allowed, carbamidomethyl cysteine as a fixed modification, oxidized methionine and deamidated asparagine/glutamine as variable modifications, 10-ppm tolerance on the precursor and 0.5-amu tolerance on the product ions, and charge states of +1, +2, and +3. Identifications were evaluated using MudPIT scoring, with a minimum peptide score of 20. A decoy database search was performed to allow correction of protein identifications by a FDR threshold of 1%, 2%, and 5% probability, as described in Results and discussion. For Mascot searches based on public data, the NCBI database searches were limited to either D. rerio sequences or the Actinopterygii taxon. To construct databases built around our A. leptorhynchus assembly, “mostly likely” longest-ORF peptides candidates were generated from the assembly using TransDecoder (http://transdecoder.sourceforge.net/), both with and without ORF calling being biased towards ORFs with a recognizable domain in the Pfam protein families database  determined by HMMER 3.1 [119,120]. Redundant ORFs within sets were removed prior to compiling the ORF sets as Mascot databases.
This Transcriptome Shotgun Assembly project (BioProject ID PRJNA259518) has been deposited at DDBJ/EMBL/GenBank under the accession GBKR00000000. The version described in this paper is the first version, GBKR01000000. The mass spectrometry proteomics data have been deposited at the ProteomeXchange Consortium  via the PRIDE partner repository  with the dataset identifier PXD001285 and DOI 10.6019/PXD001285.
The authors would like to thank Dr. Michele A. Busby for helpful discussions regarding experimental design and data analysis, Jessica Henderson for assisting with data analysis, and Dr. Iulian Ilieş for helpful discussions. We would like to thank the PRIDE Team in providing a resource for sharing proteomics data. This work was supported by intramural funds provided by Northeastern University to JNA and GKHZ.
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