Background

Recent genome-wide transcriptome analyses have documented the complexity of eukaryotic transcriptomes [1,2,3] and revealed that a substantial portion of the genome gives rise to non-protein coding RNAs (ncRNAs) [4, 5]. ncRNA species share common post-transcriptional modifications with protein-coding messenger-RNAs (mRNAs), including splicing and polyadenylation signals [6] but lack an open reading frame. These RNA types include ribosomal RNAs, transfer RNAs, microRNAs and long non-coding RNAs (lncRANs). In the past decade, particular attention was given to the ever-expanding class of lncRNAs, which are predicted to regulate important cellular processes, such as dosage compensation, imprinting, regulation of chromatin states [7,8,9,10], cell fate determination [11] and gene silencing [12, 13]. Nonetheless, the function of most lncRNAs remains uncharacterized.

One class of lncRNAs is natural antisense transcripts, which are transcribed from overlapping loci on the opposite strand of the DNA. They were found to regulate gene expression and thus provide an additional level of control by RNA-mediated mechanisms [14, 15]. Antisense RNAs may or may not code for proteins. They have been reported to exert their regulatory effects on the corresponding sense mRNAs via epigenetic regulation, chromatin remodeling [16,17,18], RNA-RNA interactions and post-transcriptional mechanisms, including regulation of mRNA processing and transport [19, 20]. The prevalence of lncRNAs has been reported in a wide range of eukaryotic organisms including plants [21], fungi [22, 23] and mammals [6, 14].

The 40-megabase genome of Neurospora crassa harbors 9730 protein-coding genes [24] and a broad spectrum of long intergenic ncRNAs (lincRNAs) as well as antisense transcripts [23]. In Neurospora, a well-documented example of an antisense lncRNA, qrf, was shown to regulate the core circadian clock gene frequency (frq) [25, 26]. Furthermore, the antisense transcript was found to be necessary to establish DNA methylation at the frq promoter [27].

Here we annotate and characterize 1478 lincRNAs and 1056 antisense transcripts in Neurospora crassa using published and new deep-sequencing data that includes RNA-seq, RNA polymerase II (RNAPII) ChIP-seq and polysome fractionation. Our data indicate that about 20% of the RNA polymerase II (RNAPII) transcripts of Neurospora are non-coding. We also confirmed annotated splice sites and identified new splice junctions and alternative splice sites, which are rare in Neurospora. In addition, we provide for the scientific community to access our webpage, which features a collection of genome-wide deep sequencing data for the model Neurospora crassa.

Methods

Unit detection pipeline and lincRNA detection

The N. crassa genome (NC10 genome model) was segmented into non-overlapping 50 base pair (bp) units (bins). αN-terminus RNAPII ChIP-seq [28] and pooled RNA-seq datasets [29,30,31] (accession numbers: SRX547956, SRX547981, SRR341283.4, SRR341284.2, SRR341429.4, SRR1578070, SRR1578069, SRR1636058; total RNA-seq read count of the pooled dataset is 174,462,581) were used to quantify the mapped reads per 50 bp unit. In order to detect continuous transcription units, logistic regression model (glm function, R [32]) was applied:

$$ logit\left({\pi}_i\right)=\log \left(\frac{\pi_i}{1-{\pi}_i}\right)={\beta}_0+{\beta}_1{x}_{i(rna)}+{\beta}_2{x}_{i(Pol)}+e $$

In the formula, π i denotes the coding indication, which assume to follow a binomial distribution (Binomial(n i , π i ) ), while x i(rna) and x i(Pol) denotes the i th unit coverage from RNA-seq and RNAPII ChIP-seq datasets, respectively. The training set was created by selecting 60% of the genome. Natural logarithm (ln) ratio of 1.5 was used as the cut-off value and continuous units with read counts higher than the cut-off were merged. The detected transcription units were compared to the NC10 genome model using bedtools [33]. The read counts were normalized to the length of the transcription units. The transcription units that overlapped with the annotated Neurospora genes were classified as coding genes and intergenic (at least 500 bp distant from a coding gene) non-overlapping transcription units were classified as possible lincRNA genes. The median read count of the polysomal RNA-seq of the detected coding regions was used to exclude intergenic transcripts present in polysomes (n = 434) (see text). Wt H3K4me2 ChIP-seq (accession number SRX550077) and wt H3K27me3 ChIP-seq datasets (accession number SRX1818756), which were used to characterize the presence of these histone marks on the novel intergenic transcripts (see Fig. 2a; Additional files 1 and 2: Figure S1d, e and S2b), were previously reported. The optimal averaging window size for the smoothening of the RNAPII ChIP-seq index analysis in Fig. 2a was determined based on the curve of the sum of absolute differences as the function of the window sizes.

Strand-specific RNA-seq and antisense RNA detection

The wild type Neurospora strain (FGSC#2489) used in this study was acquired from FGSC. The strain was grown in standard liquid growth medium that contains 2% glucose, 0.5% L-arginine, 1× Vogel’s medium and was cultured into mats. Mycelial discs were cut out from the mats, grown for 1 day in light under constant shaking at 115 rpm at 25 °C and transferred to darkness for 24 h before light exposure (100 μE). The discs were harvested at indicated time points (0, 30, 60, 120 min). Total RNA was prepared with peqGOLD TriFAST (peqLab, Erlangen, Germany). Sequencing libraries were prepared using NEBNext Ultra Directional RNA prep Kit for Illumina (E7420). RNAs were selected by purifying polyA+ transcripts. Total read counts are 12,294,480; 20,401,017; 24,757,383 and 12,114,415 for 0, 30, 60 and 120 min time points, respectively.

The raw reads were mapped to the Neurospora genome (NC10) using Bowtie 2.1.0 [34]. The parameters for mapping were set to allow up to three mismatches. The counts were normalized between samples by total count and to the length of the transcription units. Similarly to lincRNA detection analysis, the N. crassa genome (NC10 genome model) was segmented into non-overlapping 50 bp units (bins) and logistic regression (glm, R [32]) was fitted for Watson and Crick strands separately (see the above given formula). The antisense transcripts were identified from the fitted model using 1.5 ln-ratio as cut-off and having minimum 10 reads per 50 bp unit. Using bedtools [33], overlapping sense / antisense pairs (only if both sense and antisense units contained above cut-off read counts) were selected and the identified antisense fragments were merged if they were mapped to the same annotated protein-coding gene. The pairs were further filtered based on gene distance (distance < 500 bp), in order to eliminate false-positive hits due to overlapping protein-coding genes.

Detection of the coding genes which expressed an antisense RNA only

Sense and antisense read counts for all Neurospora protein coding genes were calculated with HTSeq [35] in the strand-specific RNA-seq datasets (wild type, in dark and in 30 min light). The counts were normalized between samples by total count. Loci with only antisense coverage were identified by selecting the genes, where the average sense coverage was below 1 (less than 1 sense read for every 50 bp bin) and the average antisense coverage was above 1 (more than 1 antisense read for every 50 bp bin), in both datasets. The overlapping protein-coding genes were filtered out from the outcome.

Polyribosome (polysome) fractionation analysis

The wild type Neurospora strain (FGSC#2489) was used for polysome fractionation. The cultures were grown in standard liquid growth medium (2% glucose, 0.5% L-arginine, 1× Vogel’s medium) in light (100 μE) for 1 day and released to constant darkness for 22 h and were harvested at 2 h intervals. The samples were pulverized in liquid nitrogen and approximately 0.25 g of the ground mycelia was used for each experiment, the powder was resuspended in 750 μl ice-cold polysome extraction buffer (20 mM TRIS-HCl, pH 8.0, 140 mM KCl, 10 mM MgCl2, 1% TritonX-100, 100 μg/ml cycloheximide, 0.5% DTT and 1 mM ribonuclease inhibitor). Cycloheximide was added to the cultures prior to harvesting. Gradients containing 10-50-60% sucrose were spun for 3.5 h at 38,000 x g at 4 °C in an ultracentrifuge tube (Beckman ID 331374). The fractions were collected from the top of the gradient and total RNA was prepared with peqGOLD TriFAST (peqLab, Erlangen, Germany). The raw reads were mapped to the Neurospora genome (NC10) using Bowtie 2.1.0 [34]. The counts were normalized between samples by total count and to the length of the transcription unit. For the bioinformatics analyses, all time points were pooled in order to obtain a deeper sequencing coverage. The read count of the pooled dataset is 174,777,343.

Splice junction detection

The splice junctions were predicted using TopHat2 (version 2.0.13 [36]) with the pooled RNA-seq datasets [29,30,31] (accession numbers: SRX547956, SRX547981, SRR341283.4, SRR341284.2, SRR341429.4, SRR1578070, SRR1578069, SRR1636058; total RNA-seq read count of the pooled dataset is 174,462,581). The reported intron lengths were set to minimum 50 bp and maximum 500,000 bp. The detected junctions were compared to the NC10 genome model and were divided into annotated and non-annotated junctions. The non-annotated junctions were filtered by a cut-off, defined as the quantile 25% coverage of the annotated introns. The junctions that match exactly to the annotated intron were classified as perfect matches, the junctions that varied from the annotated junction coordinates were classified as weak matches, junction pairs with shared donor or acceptor sites were classified as alternative splice isoforms and the remaining junctions were classified as novel junctions and were further analyzed (see text).

In order to detect the splice junctions in antisense transcripts, strand-specific RNA-seq datasets (wild type, in dark and in 30 min light) were mapped to Neurospora crassa genome with TopHat2 (version 2.0.14 [36]). 8502 splice sites with at least 10 spliced reads in either datasets were selected for the analysis (7883 had 10 or more spliced reads in both datasets). From this list of 8502 splicing sites 30 were found within the 1056 antisense RNA fragments identified (1224 sites were found within the corresponding 1056 sense transcript boundaries.)

NEUTRA setup

The normalized RNA-seq and ChIP-seq datasets for the selected genes were plotted with Charts Google [37]. The genome browser was set up by using JBrowse [38] based on the NC10 genome model and the Wiggle files were uploaded. Next-generation sequencing data are displayed using BigWig format while the binding sites are displayed using BED format.

Conversion of the data to NC12

The coordinates of the identified lincRNA genes, possibly coding genes, antisense transcripts and splicing junctions (Additional files 3, 4, 5, 6 and 7: Table S1,S2,S3,S4,S5) are provided in NC10 and the recently released NC12 version of the Neurospora crassa genome (http://fungi.ensembl.org/Neurospora_crassa) [39]. The difference between NC10 and NC12 is not substantial. Sequences of chromosomes 1 to 5 are identical. The NC12 version of chromosome 6 has the sequence from position 1,847,027 to position 2,788,223 reverse complemented while chromosome 7 has the whole sequence reverse complemented. NC10 coordinates were converted to NC12 coordinates by a custom R script [32], based on BLAT alignments [40] between the corresponding chromosomes.

Results and discussion

Neurospora transcriptome analysis

To catalogue distinct species of RNAs, such as mRNAs, lincRNAs and antisense RNAs; to investigate the structure of the annotated and novel genes in terms of their 5′ starts and 3′ ends, direction and splicing pattern; and to quantify the expression levels of the genes, we took advantage of various sequencing data. These data include published RNA-seq data from circadian, light induction and differential expression analyses of wild type (wt), Δsub1, Δff7 and Δcsp1 [29,30,31] strains and an unpublished strand-specific RNA-seq. ChIP-seq analyses of RNAPII [28] and a polyribosome (polysome) fractionation analysis were also included for the Neurospora transcriptome analysis.

The Neurospora crassa genome harbors 9730 annotated protein-coding genes. By using the above mentioned RNA-seq, ChIP-seq and polysome studies, our unit detection pipeline detected 92% of the annotated genes (8956 genes), validating our methodology. The remaining 774 annotated genes were not expressed under our conditions.

Long intergenic non-coding (linc) RNAs

To confidently determine the Neurospora repertoire of lincRNAs we pooled our available RNA-seq data, representing the polyadenylated transcriptome. In addition, we included an RNAPII ChIP-seq analysis [28] to confirm the boundaries of transcription units. Furthermore, to assess the non-protein-coding nature of transcripts we used RNA-seq analysis of a polysome fractionation. Non-annotated transcripts detected in the polysome fraction above the median read count of annotated coding genes (n = 434) were initially excluded as lincRNAs and analyzed in more detail (see below). Finally, considering that 95% of the Neurospora genes are more than 134 bp apart (Additional file 1: Figure S1a), and that the average intron length of Neurospora protein-coding genes comprises 69 bp (Additional file 1: Figure S1b), lincRNA segments that were less than 100 bp apart were merged.

With this approach, we identified 1060 lincRNA genes (Additional file 3: Table S1) that are scattered in the genome with a median distance of 19.5 kb (Additional file 1: Figure S1c). The lincRNA genes were transcribed at a lower rate than protein-coding genes (RNAPII ChIP-seq) and the transcripts accumulated at lower levels (RNA-seq) (Fig. 1a). The lincRNA genes (median length 551 bp) were considerably shorter than the transcription units of protein-coding genes (median length 1782 bp) (Fig. 1a). The mammalian long noncoding RNA (lncRNA) catalog GENCODE v7 shows that while lncRNAs have similar exon sizes to protein-coding genes, they exhibit a bias toward two-exon transcripts, resulting in processed transcript sizes of lncRNAs shorter than mRNAs [6].

Fig. 1
figure 1

Characterization of lincRNA genes. a Side by side comparison of lincRNA genes (n = 1060) with protein-coding genes (n = 9730). Boxplots of RNAPII ChIP-seq (αRNAPII N-terminus), RNA-seq and polysome fractionation datasets, and size distribution of protein-coding genes (median length 1782 bp) and lincRNA genes (median length 551 bp) are shown. b Correlation between transcription levels (RNAPII ChIP-seq) and RNA accumulation (RNA-seq). Sequence read counts are length normalized and shown in a scatter plot. R-square values were calculated by linear model fitting

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Overall, transcription (RNAPII ChIP-seq) and transcript levels (RNA-seq) correlated for coding genes and lincRNA genes (Fig. 1b). However, compared to protein-coding RNAs, lincRNA abundance was directly proportional to RNAPII occupancy, suggesting that turnover of lincRNAs may be more rapid and less variable than turnover of mRNAs.

We then ranked protein-coding genes and lincRNA genes by their corresponding RNAPII ChIP-seq coverage indices (Fig. 2a). Implementing this approach showed that increasing transcription levels of protein-coding genes correlated with the levels of total mRNA and polysome bound mRNA. The corresponding RNAPII ChIP-seq index analysis supported that lincRNAs were expressed at lower levels than the protein-coding genes and were indeed not present in polysomes. We verified that the lack of ribosome binding is not biased by the short length of lincRNAs by analyzing mRNAs that are shorter than 500 bp. These short mRNAs (n = 296) were significantly present in the polysome fractionation (Welch two sample t-test, p-value = 1.105e-07).

Fig. 2
figure 2

a RNAPII ChIP-seq index analysis. Exons of annotated protein coding genes (n = 25,246; left) and of the identified lincRNAs (n = 1068; right) were indexed according to their RNAPII ChIP-seq reads and plotted versus the read counts of RNAPII ChIP-seq, RNA-seq, polysomes RNA-seq, H3K4me2 ChIP-seq and H3K27me3 ChIP-seq, as indicated. Data are shown with a run-window averaging (see methods). Accession numbers of the H3K4me2 ChIP-seq and H3K27me3 ChIP-seq datasets are SRX550077 and SRX1818756, respectively. b Percentage of Neurospora protein-coding genes and lincRNA genes with homologies in Sordaria macrospora (S.m.), Chaetomium thermophilum (C.t.), Aspergillus niger (A.n.), Saccharomyces cerevisiae (S.c.) and Takifugu rubripes (T.r.). FASTA sequences of the 1478 lincRNA genes of Neurospora crassa were used for a discontiguous megablast (https://blast.ncbi.nlm.nih.gov) analysis. For control, 3 times 1478 protein-coding genes were randomly selected. The bars represent the percentage of input sequences that gave significant hits in each species, with + − SD for the control genes of the 3 measurement

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The presence of H3K4me2 modifications, which are associated with the transcribed regions of active genes [41], positively correlated with transcription (RNAPII ChIP-seq indices) of coding genes (Fig. 2a). However, H3K4me2 modifications were generally lower in lncRNA genes. This difference becomes in particular obvious in the fraction of highly expressed lincRNA genes, which carry considerably less H3K4me2 modifications than similarly transcribed protein-coding genes (Additional file 1: Figure S1d). In contrast, the presence of H3K27me3 modification, which is commonly associated with transcriptionally silent genes [42], negatively correlated with the transcriptional activity of both protein-coding mRNAs and lincRNAs (Fig. 2a, Additional file 1: Figure S1e).

Apart from the 1060 highly confident lincRNA genes, we detected 434 non-annotated intergenic transcripts that were, however, present above threshold in the polysome fractionation dataset. The coding potential of these transcripts was assessed by Coding Potential Calculator (CPC) [43]. Only 16 of these transcripts were predicted to have protein-coding potential (Additional file 4: Table S2). Using the BLASTX algorithm [44], the predicted protein products of only 3 of these genes were found to share homology with proteins of related species, such as Neurospora tetrasperma and Sordaria macrospora (Table 1). Taken together, our findings suggest that the list of these 16 genes may contain at least 3 novel protein-coding genes (Table 1). The remaining 418 genes with no significant coding potential were of similar length (median 451 bp) as lincRNAs and were expressed at low levels (Additional file 2: Figure S2a, b). They may therefore reflect false-positive hits of our polysome fractionation analysis (FDR = 0.05) and likely represent lincRNAs. It is also possible that some of these lincRNAs interact directly or indirectly with polysomes. Hence, these 418 intergenic transcripts with no coding potential were added to the list of 1060 lincRNAs, expanding the repertoire of Neurospora lincRNA genes to 1478 (see Additional file 3: Table S1).

Table 1 Un-annotated transcripts, which share homology with other species, with significant coding potential [43]
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We then studied the conservation patterns of the 9730 N. crassa protein-coding genes and the 1478 lincRNA genes by using BLAST (https://blast.ncbi.nlm.nih.gov) [44] and analyzed the sequence homologies in four Ascomycota species, Sordaria macrospora, Chaetomium thermophilum, Aspergillus niger and Saccharomyces cerevisiae, and a vertebrate with a small genome, the pufferfish Takifugu rubripes. In stark contrast to coding sequences, Neurospora lincRNAs are weakly conserved. While 87% of the Neurospora coding genes shared homologies in the phylogenetically closest relative Sordaria macrospora, only 3% of the lincRNA genes were conserved between these two species and less than 1% in other species (Fig. 2b). Despite this rapid evolution, we observed strong homologies between Neurospora crassa and Sordaria macrospora for 13 lincRNAs (Additional file 3: Table S1). On close inspection, we found that 9 of these Neurospora lincRNAs evolved from protein-coding into noncoding gene sequences by acquiring frame disruptions. Such a mechanism is reported for the human Xist gene involved in X-chromosome inactivation [45, 46]. In addition, in 4 cases open reading frames were detected on the opposite strand. These RNAs may be lncRNAs that are antisense to putative coding mRNAs and their sense partners might not be expressed in our experimental setup. These instances are further discussed in the following section. Low degree sequence conservation of lincRNAs is also reported between zebrafish and human [47] and between mouse and human [48, 49]. These studies along with ours suggest that evolution of lincRNA genes is distinct from protein-coding genes and they emerge within particular lineages or species. Despite the weak sequence constraint, large numbers of lincRNAs in many species imply unconventional functional contribution by these RNAs to gene regulation.

Identification of Neurospora antisense transcripts

Natural antisense transcripts are RNA products that are made from the opposite strand of a protein-coding (sense) transcript and overlap in part or completely with their sense partner. In our analysis, antisense transcription units overlapping the same protein-coding gene were merged and scored as a single antisense transcript. We found that 826 expressed protein-coding transcripts, representing 9% of the annotated genes, have overlapping antisense partners (Additional file 5: Table S3). The identified antisense transcripts were, for highly expressed antisense RNAs, verified by the ChIP-seq profiles of Ser5 phosphorylated RNAPII (Ser5-P) [28], which is enriched at transcription start sites and the 5′ region of transcription units (Fig. 3). The expression levels of the antisense transcripts were considerably lower than of protein-coding genes (Fig. 4a) and are not correlated with the expression levels of their sense partners (Pearson’s product-moment correlation, correlation = 0.22 in dark grown samples and correlation = 0.31 in light induced samples). Moreover, the antisense RNA genes were considerably shorter (median 251 bp) than their sense partners (median 1750 bp) (Fig. 4b). We also found that antisense transcripts initiate preferentially at the 3′ ends of coding genes (Fig. 4c, d). In mammalian genomes, antisense transcription was reported to be enriched at both ends of the protein-coding genes [50, 51]. Complementarity of antisense transcripts to the 3′ ends or 3’-UTRs of sense transcripts is evolutionary more conserved and has been suggested to have regulatory roles [50, 52, 53]. The finding that Neurospora sense-antisense pairs overlap at the 3′ end of the coding genes suggests similar regulatory roles in this organism.

Fig. 3
figure 3

Examples of Neurospora antisense transcripts. a NCU00551, which encodes for myosin type-2 heavy chain 2, and NCU02608, which encodes for a hypothetical protein, are presented. ChIP-seq of RNAPII Ser5-P [28] and strand-specific RNA-seq datasets are shown. Direction of the transcription is depicted with an arrow for both sense and antisense (a.s.) transcripts. b RNAPII Ser5-P and strand-specific RNA-seq of a coding gene without an antisense transcript. NCU04262 encodes for glycosylhydrolase family 76-2 protein. The data are visualized by IGV genome browser

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Fig. 4
figure 4

Characterization of the 826 antisense transcripts. a Expression levels (strand-specific RNA-seq) of antisense transcripts in comparison to their sense partners. b Length distribution of the antisense RNA genes (median length 251 bp) along with the corresponding sense protein-coding genes (median length 1750 bp). c-d Density diagram of antisense TSSs with respect to the corresponding sense transcription start site (TSS) or sense transcription termination site (TTS)

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In addition, we detected 230 annotated protein-coding genes, which expressed an antisense RNA but no sense RNA under our experimental conditions (Additional file 5: Table S3). For these genes ChIP-seq profiles of Ser5 phosphorylated RNAPII (Ser5-P), which accumulates around the transcription start site (TSS), and Ser2 phosphorylated RNAPII (Ser2-P), which accumulates in the transcribed region [54] were evaluated to confirm the antisense direction of transcription (Additional file 6: Figure S3).

Previously Arthanari et al. [23] identified 540 lincRNAs and 477 antisense transcripts in Neurospora crassa. In our study, more than twice as many lincRNAs and antisense RNAs were identified. 62.4% of the previously published lincRNAs are detected in our dataset of lincRNAs, and 50% of the published antisense transcripts were detected in our datasets of antisense RNAs with and without an expressed sense RNA (Additional file 8: Figure S4). The larger number of lincRNAs and antisense transcripts detected in our study is due to deeper sequence coverage and to the combination of RNA-seq and RNAPII ChIP-seq analyses that enabled a better detection of genes with unstable RNA products. The lncRNAs that were not detected in our study are due to different experimental and detection pipelines.

Light-induced expression of Neurospora lncRNAs

We investigated the light-dependent expression patterns of the Neurospora lncRNAs using the available RNA-seq datasets. We identified 687 light-inducible protein-coding genes in wt and 73% of the previously reported genes [30] are detected in our dataset. To detect light-induced lincRNAs, RNA-seq from this work and the published data [30] were used. We found that 181 of the identified 1478 lincRNAs are induced by light (>2× induction in either one of the time points) in both datasets (Additional file 9: Table S4). 58% (105 genes) of the light-induced lincRNAs accumulated within 30 min and the remainder of the transcripts peaked at later time points (60 min or 120 min).

Furthermore, we identified 179 light-inducible antisense transcripts (>2× induction in either one of the time points) out of the 1056 identified antisense RNAs in our analysis (Additional file 9: Table S4). 65% of these antisense RNAs were induced upon 30 min light exposure. Expression of only 35% (63 genes) of the corresponding sense transcripts was induced more than two fold at any time point, suggesting that a large fraction (65%) of light-induced antisense RNAs are regulated differently than their sense partners. In some cases light-induced antisense RNAs stem from neighboring light responsive bidirectional promoters.

Genome-wide splicing analysis

We then performed a genome-wide splicing analysis to detect novel splice site junctions and alternative splice isoforms. 73% of the annotated introns (12,251 of 16,708) were detected with 100% overlap and 199 annotated introns were detected with mismatches (Additional file 7: Table S5). In addition, we detected 328 introns with alternative acceptor or donor sites and 249 novel introns that were previously not annotated (Additional file 7: Table S5). Together the data show that alternative splicing in Neurospora is rare compare to human genes, of which 40-60% has alternative isoforms [55], and only 5% of Neurospora protein-coding genes have the potential of being alternatively spliced.

In the majority of cases alternative splicing events produce rare transcripts (Additional file 10: Figure S5A). For instance, NCU06661 and NCU03967 encode the 60S ribosomal protein L22 and VIVID (VVD), respectively. In both cases the alternative splicing variants are rare and lead to skipping of one and two amino acid residues, respectively (Additional file 10: Figure S5B). The alternative splice variant of L22 was expressed in other species such as Pseudogymnoascus pannorum and Colletotrichum gloeosporioides. In contrast, the splice variant of VVD was not detected in the annotated proteomes of other species.

In Neurospora, 80% of the protein-coding genes possess one or more introns (Fig. 5a), which have an average length of 69 bp (see Additional file 1: Figure S1a). Intriguingly, only 26 antisense RNA genes (2.5%) and 23 lincRNA genes (1.6%) were spliced (Fig. 5b, c). The absence of introns in the vast majority of lincRNAs (n = 1454) and antisense RNAs (n = 1030) is not due to their short length since protein-coding genes shorter than the median length of lincRNA genes (<551 bp) still contain introns (Fig. 5d). This finding is consistent with reports that mammalian lncRNAs exhibit inefficient splicing or remain unspliced [56, 57]. Many unspliced lncRNAs are shown to play cis-regulatory roles in the nucleus and are involved in genomic imprinting in mammalian genomes [58].

Fig. 5
figure 5

Majority of lncRNA genes do not contain introns. Fraction of (a) annotated Neurospora coding genes, (b) antisense RNA genes and (c) lincRNA genes with and without introns. d Fraction of intron containing genes in the subset of coding genes shorter than 551 bp (i.e. the median length of the Neurospora lincRNA genes)

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Neurospra crassa transcriptome (NEUTRA) tool

NEUTRA tool contains a collection of multiple RNA-seq [29,30,31] and ChIP-seq [28,29,30, 59] libraries from our research group. In addition to annotated gene models, the website presents the identified lincRNAs and several statistics for gene entries, including circadian gene expression profiles and a direct comparison of gene expression levels between the wild type and several knock-out strains, namely Δwc1, Δwc2, Δsub1, Δff7 and Δcsp1. This tool might be useful for the scientific community.

The NEUTRA tool is publicly available at http://neutra.bzh.uni-heidelberg.de. On the “Tools” dialog, users can access two main sections, which are “Search by Gene” and “Genome Browser” tools.

Clicking the “Search by Gene” tool directs the user to a query window and a list of published [28,29,30,31, 59] and unpublished RNA-seq and ChIP-seq datasets. After selecting the datasets of interest, querying is a matter of entering a gene ID (e.g. NCU02265). The NEUTRA tool will return a table that displays detailed information about the searched gene and graphs that depict the selected RNA-seq or ChIP-seq information and expression profiles of the same gene (Additional file 11: Figure S6a).

The “Genome Browser” tool directs the user to a genome browser that uses the NC10 version of the Neurospora crassa genome model by using the open source JBrowse (http://jbrowse.org/). A gene can be searched by entering the gene ID to the search box and requested datasets can be selected from the list that appears on the left side of the browser (Additional file 11: Figure S6b).

Conclusions

We provide a comprehensive genome-wide annotation and analysis of lincRNAs, antisense transcripts and alternative splice isoforms. We show that the prevalence of lincRNAs and antisense transcripts in Neurospora is higher than the previous report [23] and that 20% of the RNAPII transcripts are not coding for protein. The results provide novel insights into characteristics of Neurospora noncoding transcriptome. Given the large amount and diversity of these RNA species in many organisms combined with the findings that several examples of lncRNAs employ important biological functions, high-throughput identification of lncRNAs across a range of organisms is crucial to dissect their impact on gene regulation. We suggest that Neurospora can be a valuable model for studying functionality of non-coding RNAs.