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Sequencing of multiple related species followed by comparative genomics analysis constitutes a powerful approach for the systematic understanding of any genome. Here, we use the genomes of 12 Drosophila species for the de novo discovery of functional elements in the fly. Each type of functional element shows characteristic patterns of change, or ‘evolutionary signatures’, dictated by its precise selective constraints. Such signatures enable recognition of new protein-coding genes and exons, spurious and incorrect gene annotations, and numerous unusual gene structures, including abundant stop-codon readthrough. Similarly, we predict non-protein-coding RNA genes and structures, and new microRNA (miRNA) genes. We provide evidence of miRNA processing and functionality from both hairpin arms and both DNA strands. We identify several classes of pre- and post-transcriptional regulatory motifs, and predict individual motif instances with high confidence. We also study how discovery power scales with the divergence and number of species compared, and we provide general guidelines for comparative studies.
The sequencing of the human genome and the genomes of dozens of other metazoan species has intensified the need for systematic methods to extract biological information directly from DNA sequence. Comparative genomics has emerged as a powerful methodology for this endeavour1,2. Comparison of few (two–four) closely related genomes has proven successful for the discovery of protein-coding genes3–5, RNA genes6,7, miRNA genes8–11 and catalogues of regulatory elements3,4,12–14. The resolution and discovery power of these studies should increase with the number of genomes15–20, in principle enabling the systematic discovery of all conserved functional elements.
The fruitfly Drosophila melanogaster is an ideal system for developing and evaluating comparative genomics methodologies. Over the past century, Drosophila has been a pioneering model in which many of the basic principles governing animal development and population biology were established21. In the past decade, the genome sequence of D. melanogaster provided one of the first systematic views of a metazoan genome22, and the ongoing effort by the FlyBase and Berkeley Drosophila Genome Project (BDGP) groups established a systematic high-quality genome annotation23–25. Moreover, the fruit-fly benefits from extensive experimental resources26–28, which enable novel functional elements to be systematically tested and used in the evaluation of genetic screens29,30.
The fly research community has sequenced, assembled and annotated the genomes of 12 Drosophila species22,31,32 at a range of evolutionary distances from D. melanogaster (Fig. 1a, b). The analysis of these genomes was organized around two complementary aims. The first, described in an accompanying paper32, was to understand the evolution of genes and chromosomes on the Drosophila phylogeny, and how it relates to speciation and adaptation. The second goal, described here, was to develop general comparative methodologies to discover and refine functional elements in D. melanogaster using the 12 genomes, and to investigate the scaling of discovery power and its implications for studies in vertebrates (Fig. 1c).
Here, we report genome-wide alignments of the 12 species (Supplementary Information 1), and the systematic discovery of euchromatic functional elements in the D. melanogaster genome. We predict and refine thousands of protein-coding exons, RNA genes and structures, miRNAs, pre- and post-transcriptional regulatory motifs and regulatory targets. We validate many of these elements using complementary DNA (cDNA) sequencing, human curation, small RNA sequencing, and correlation with experimentally supported transcription factor and miRNA targets. In addition, our analysis leads to several specific biological findings, listed below.
Although multiple closely related genomes provide sufficient neutral divergence for recognition of functional regions in stretches of highly conserved nucleotides16,17,33, measures of nucleotide conservation alone do not distinguish between different types of functional elements. Moreover, functional elements that tolerate abundant ‘silent’ mutations, such as protein-coding exons and many regulatory motifs, might not be detected when searching on the basis of strong nucleotide conservation.
Across many genomes spanning larger evolutionary distances, the information in the patterns of sequence change reveals evolutionary signatures (Fig. 2) that can be used for systematic genome annotation. Protein-coding regions show highly constrained codon substitution frequencies34 and insertions and deletions that are heavily biased to be multiples of three3 (Fig. 2a). RNA genes and structures tolerate substitutions that preserve base pairing35,36 (Fig. 2b). MicroRNA hairpins show a characteristic conservation profile with high conservation in the stem and mutations in loop regions10,11 (Fig. 2c). Finally, regulatory motifs are marked by high levels of genome-wide conservation3,4,12–14, and post-transcriptional motifs show strand-biased conservation12 (Fig. 2d, e).
We find that these signatures can be much more precise for genome annotation than the overall level of nucleotide conservation (for example, Fig. 3a).
The annotation of protein-coding genes remains difficult in metazoan genomes owing to short exons and complex gene structures with abundant alternative splicing. Comparative information has improved computational gene predictors5, but their accuracy still falls far short of well-studied gene catalogues such as the FlyBase annotation, which combines computational gene prediction37, high-throughput experimental data38–42 and extensive manual curation23. Recognizing this, we set out not only to produce an independent computational annotation of protein-coding genes in the fly genome, but also to assess and refine its already high-quality annotations43.
Our analyses of D. melanogaster coding genes are based on two independent evolutionary signatures unique to protein-coding regions (Fig. 2a): (1) reading frame conservation (RFC)3, which observes the tendency of nucleotide insertions and deletions to preserve the codon reading frame; and (2) codon substitution frequencies (CSF, see Supplementary Methods 2a), which observes mutational biases towards synonymous codon substitutions and conservative amino acid changes, similar to the non-synonymous/synonymous substitution ratio KA/KS34 and other methods44–46.
We first assessed the 13,733 euchromatic genes in FlyBase47 release 4.3. Using the above measures, we defined tests that ‘confirmed’ genes supported by the evolutionary evidence, ‘rejected’ genes inconsistent with protein-coding selection, or ‘abstained’ for genes that were not aligned or with ambiguous comparative evidence (Supplementary Methods 2a). Of the 4,711 genes with descriptive names, we confirmed 97%, rejected 1% and abstained for 2%, whereas the same criteria applied to 15,000 random non-coding regions ≥300 nucleotides rejected 99% of candidates and confirmed virtually none (Table 1). Together, these results illustrate the high sensitivity and specificity of our criteria.
Applying the same criteria to the 9,022 genes lacking a descriptive name (genes designated only by a CG identifier, referred to hereafter as CGid-only genes), our tests accepted 87%, rejected 5% (414 genes) and abstained for 8%. This provides strong evidence that most CGid-only genes encode proteins, but also suggests that they may be less constrained20,32 and/or may include incorrect annotations. Indeed, on manual review, 222 (54%) of the 414 rejected CGid-only genes were re-categorized as non-protein-coding or deleted (of which 55 were due to genomically primed clones), 73 (18%) were flagged as being of uncertain quality, and the remaining 119 (29%) were kept unchanged (Fig. 3b). Some of these are probably rapidly evolving protein-coding genes, but others may also prove to be non-protein-coding genes or spurious; in fact, none of these had any functional gene ontology (GO) annotation48.
In addition, we proposed specific corrections and adjustments to hundreds of existing transcript models, including translation start site adjustments (Supplementary Fig. 2b), alternative splice boundaries (Supplementary Fig. 2b), recent nonsense mutations (Supplementary Fig. 2c) and alternative translational reading frames43.
To predict new protein-coding exons, we integrated our metrics into a probabilistic algorithm that determines an optimal segmentation of the genome into protein-coding and non-coding regions (Fig. 3a) on the basis of whole-genome sequence alignments of the 12 fly species (Supplementary Methods 2a). Our genome-wide search predicted 1,193 new protein-coding exons, mostly in euchromatic regions annotated as intergenic (43%), intronic (26%), or 5′/3′ untranslated region (UTR; 23%) in FlyBase annotation release 4.3.
We manually reviewed 928 of these predictions according to FlyBase standards23 (Supplementary Methods 2a), leading to 142 new gene models (incorporating 192 predictions) and 438 revised gene models (incorporating 562 predictions) (Fig. 3b). In parallel, we tested 184 predictions (126 intergenic, 58 intronic) by directed cDNA sequencing using inverse polymerase chain reaction (inverse PCR) of circularized full-length clones49–51 (Fig. 3c), which validated 120 targeted predictions (65%) and an additional 42 predictions not directly targeted but contained within the recovered transcripts. Predictions in intergenic regions yielded 88 full-length cDNAs, providing evidence for 50 new genes and modification of 39 gene models. Predictions within introns of existing annotations yielded 32 full-length cDNAs, of which only 18 (56%) represent new splice variants of the surrounding gene, whereas the remaining 14 revealed nested or interleaved gene structures. This provides additional evidence that such complex gene structures are not rare in Drosophila23.
Overall, 83% of the 948 predicted exons that we assessed by manual curation or cDNA sequencing were incorporated into FlyBase, resulting in 150 new genes and modifications to hundreds of existing gene models. Finally, the 245 predictions that we did not assess were in non-coding regions of existing transcript models, or were already included in FlyBase independent of our study. In an independent analysis52, we predicted 98 new genes on the basis of inferred homology to predicted genes in the informant species32, of which 63% matched the above predictions.
Our analysis also predicted an abundance of unusual protein-coding genes that call for follow-up experimental investigation. First, we found open reading frames with clear protein-coding signatures and conserved start and stop sites on the transcribed strand of annotated UTRs, indicative of polycistronic transcripts23,53,54. These include 73% of 115 annotated dicistronic transcripts and 135 new candidate cistrons of 123 genes (Supplementary Fig. 2b).
Second, we predicted that 149 genes undergo stop codon readthrough, with protein-coding selection continuing past a deeply conserved stop codon (Fig. 3d), in some cases for hundreds of amino acids. It is unlikely that these genes are selenoproteins, as they appear to lack SECIS elements that direct selenocysteine recoding55–58. Other mechanisms may instead be at work, such as regulation of ribosomal release factors59, A-to-I editing39,60,61, alternative splicing, or other less-characterized mechanisms62. In fact, these genes are significantly enriched in neuronal proteins (P =10−4), which frequently undergo A-to-I editing63.
Third, we found four genes in which CSF signatures abruptly shift from one reading frame to another in the absence of nearby intron–exon boundaries or insertions and deletions (Fig. 3e). These are suggestive of conserved ‘programmed’ frameshifts64, which are thought to be rare in eukaryotes.
Overall, our results affected over 10% of protein-coding genes, and will be available in future releases of FlyBase. They also suggest that several types of unusual protein-coding gene structure may be more prevalent in the fly than previously appreciated.
Several comparative approaches to RNA gene identification have been developed6,7,65 that recognize their characteristic properties: compensatory double substitutions of paired nucleotides (for example, A•U↔C•G), structure-preserving single-nucleotide mutations involving G•U base pairs (G•U↔G•C and G•U↔A•U), and few nucleotide substitutions disrupting functional base pairs (Fig. 2b). To predict new structures, we applied EvoFold7 in highly conserved segments of the 12 Drosophila species and focused on high-stringency candidates with strong support by compensatory changes (Supplementary Methods 4).
Our search led to 394 predictions, recovering 68 known RNA structures (primarily transfer RNA genes) in 0.02% of the genome (570-fold enrichment). The novel candidates consisted of 177 structures in intergenic regions (54%), 103 in introns (32%), 36 in 3′ UTRs (11%) and 10 in 5′ UTRs (3%). In addition, we predicted 200 structures in protein-coding regions (Supplementary Methods 3). Notably, 75% of 3′ UTR structures and 80% of 5′ UTR structures were predicted on the transcribed strand, suggesting that they are frequently part of the messenger RNA. In contrast, only 47% of intronic structures are on the transcribed strand, suggesting that they are largely independent of the surrounding genes.
Of the 177 predicted intergenic structures, 30 were detected in a tiling-array expression study42. This fraction (17%) is significantly above that for all conserved intergenic regions (12%, P =0.007), but lower than that of known intergenic ncRNAs (21%), suggesting that these candidates may be of lower abundance, temporally or spatially constrained, or might include false positives. Two predictions were expressed throughout development, one extending the annotation of a previously reported but uncharacterized ncRNA66 and the other probably representing a novel type of ncRNA. The predictions also included nine novel H/ACA-box small nucleolar RNA candidates in introns of ribosomal genes, known to frequently contain small nucleolar RNAs that guide post-transcriptional base modifications of ncRNAs67.
Many of the 48 intronic candidates on the transcribed strand and many of the 200 hairpins in coding sequence are probably involved in A-to-I editing or post-transcriptional regulation (Fig. 4a). Hairpins in coding sequence were associated with 11 of the 157 known editing sites (120-fold enrichment) and both intronic and coding-sequence hairpins showed a strong enrichment for ion-channel genes (6%, P =0.007 and 10%, P =2×10−12, respectively), known to be frequent editing targets. Editing is known to occur at multiple sites in the same gene63, and we find an additional 10 hairpins in known editing targets, as well as 40 additional hairpins clustered in 18 genes not previously known to be edited (for example huntingtin68, which harbours four predicted hairpins, more than any other gene). Intronic predictions also showed the highest abundance of compensatory substitutions: for example, Resistant to dieldrin (Fig. 2b) contained a 26-base-pair (bp) intronic hairpin flanked by exons known to be edited69 with a striking 16 compensatory changes, lodestar showed one hairpin with 11 compensatory changes, and Inverted repeat-binding protein showed one hairpin with 10 compensatory substitutions (Fig. 4b).
We predicted 38 structures in 3′ UTRs, a density twofold higher than the genomic average, whereas fewer than 10 such examples are currently known70. A considerable fraction of these lies in regulatory genes (14 out of 38; P =10−4), including several transcriptional regulators (for example, cas, spen and Alh), the tyrosine phosphatase PTP-ER and the translation initiation factor eIF3-S8. This suggests that many regulatory genes may themselves be regulated post-transcriptionally through these structures.
3′ UTR structures were also enriched for genes involved in mRNA localization (3 out of 38, P =2.7 ×10−4), including oo18 RNA-binding protein (orb) and staufen (stau), both of which contain double-stranded RNA-binding domains, are involved in axis specification during oogenesis, and interact with the mRNA of maternal effect protein oskar. The hairpin in orb is known to be important for mRNA transport and localization71, whereas the highly similar stau hairpin has not been previously described to our knowledge.
The ten structures found in 5′ UTRs probably contain binding sites for factors that regulate translation. For example, the fly homologue of yeast ribosomal protein RPL24 contains a hairpin structure overlapping its start codon (Fig. 4c). This is interesting in light of high conservation upstream of the start codon in yeast ribosomal proteins3,4, and findings that ribosomal proteins bind to their mRNAs and control translation in prokaryotes72,73.
In an independent study74, we searched for conserved regions in the non-coding roX1 and roX2 (RNA on the X) genes to gain insights into their function. Both RNAs are components of the MSL (Male-specific lethal) complex and are crucial for dosage compensation in male flies, inducing lysine 16 acetylation of histone H4, leading to upregulation of hundreds of genes on the X chromosome75. We identified several stem-loop structures with repeated sequence motifs (for example, GUUNUACG), and found that tandem repeats of one of these were sufficient to recruit MSL complexes to the X chromosome and to induce acetylation of lysine 16 of histone H4. Although this structure could not fully rescue roX-deficient males, our results suggest that it mediates MSL recruitment during roX2-dependent chromatin modification and dosage compensation, illustrating the power of evolutionary evidence for directing experimental studies.
Focusing on specific classes of RNA genes markedly increases the accuracy of RNA gene prediction, reviewed in refs 35, 76 and illustrated here for Drosophila miRNA genes. The common biogenesis and function of miRNAs77 lead to evolutionary and structural signatures (Fig. 2c) that can be used for their systematic de novo discovery8–11. Using such signatures in the 12 fly genomes (Supplementary Methods 4a, b), we predicted 101 miRNAs78 (Supplementary Table 4d), which include 60 of the 74 verified Rfam miRNAs (81%), while spanning less than 0.006% of the fly genome (13,500-fold nucleotide enrichment).
Comparison of our predictions with high-throughput sequencing data of short RNA libraries from different stages and tissues of D. melanogaster78,79 revealed that 84 of the 101 predictions (83%), including 24 of the 41 novel predictions (59%), were authentic miRNA genes (Fig. 5a and Supplementary Table 4d). An independent computational method79 had 20 of its 45 novel predictions validated when used across six Drosophila species. Additional candidates may represent genuine miRNAs whose temporal or spatial expression pattern does not overlap with the surveyed libraries.
Several of the validated miRNAs were on the transcribed strand of introns or clustered with other miRNAs. For example, mir-11 and mir-998 (the vertebrate homologue of which, mir-29, has been implicated in cancer80) were both found in the last intron of E2f, and might be involved in cell-cycle regulation (Fig. 5b). Notably, two predictions overlapped exons of previously annotated protein-coding genes that were independently rejected above (Fig. 5c), providing an explanation for the previously observed transcripts of these annotations and highlighting the importance of specific signatures for genome annotation.
High-throughput sequencing data discovered an additional 50 miRNAs not found computationally79,81, thereby illustrating the limitations of purely computational approaches. Some of these had precursor structures not seen previously for animal miRNAs, including unusually long hairpins79 and hairpins corresponding to short introns (mirtrons)81,82. The remaining were often less broadly conserved or showed unusual conservation properties.
The exact position of 5′ cleavage of mature miRNAs is important, because it dictates the core of the target recognition sequence83–85. This leads to unique structural and evolutionary signatures, including direct signals, present at the 5′ cleavage site, and indirect signals, stemming from the relationship of miRNAs with their target genes (Supplementary Methods 4a, c). Combined into a computational framework78, these signatures predicted the exact start position in 47 of the 60 cloned Rfam miRNAs (78%), and were within 1 bp in 51 cases (85%). The method disagreed with the previous annotation in 9 of the 14 Rfam miRNAs that were not previously cloned, of which 6 were confirmed by sequencing reads78,79, leading to marked changes in the inferred target spectrum (Fig. 5d). Prediction accuracy was significantly lower (41% exact, 61% within 1 nucleotide) for novel miRNAs, which, however, also showed less accurate processing in vivo78,79.
We predicted targets for all conserved miRNAs identified by high-throughput sequencing79 searching for conserved matches to the seed region (similar to ref. 86) evaluated using the branch length score (Supplementary Methods 5a), a new scoring scheme described below. Whereas the resulting miRNA targeting network changed substantially79, we found that the novel and revised miRNAs shared many of their predicted targets with previously known miRNAs, resulting in a denser network with increased potential for combinatorial regulation78,79.
For ten miRNA hairpins, the mature miRNA and the corresponding miRNA star sequence (miRNA*, the small RNA from the opposite arm of the hairpin) both appeared to be functional: both reached high computational scores and were frequently sequenced78,79, often exceeding the abundance of many mature miRNAs (Supplementary Table 4e). The Hox miRNA mir-10 showed a particularly striking example of a functional star sequence (Fig. 5e): both arms showed abundant reads, high scores and highly conserved Hox gene targets78,79, suggesting a key role in Hox regulation.
In addition, for 20 miRNA loci, the anti-sense strand also folded into a high-scoring hairpin suggestive of a functional miRNA78 (Supplementary Table 4f). Indeed, sequencing reads confirmed that four of these anti-sense hairpins are processed into small RNAs in vivo79. Thus, a single genomic miRNA locus may produce up to four miRNAs, each with distinct targets.
Regulatory motifs recognized by proteins and RNAs to control gene expression have been difficult to identify due to their short length, their many weakly specified positions, and the varying distances at which they can act87,88. Recent studies have shown that comparative genomics of a small number of species can be used for motif discovery3,4,12–14, on the basis of hundreds of conserved instances across the genome (Fig. 2d). Many related genomes should lead to increased discovery power, but also pose new challenges, arising from sequencing, assembly, or alignment artefacts, and from movement or loss of motif instances in individual species.
To account for the unique properties of regulatory motifs, we developed a phylogenetic framework to assess the conservation of each motif instance across many genomes89. Briefly, we searched for motif instances in each of the aligned genomes, and based on the set of species that contained them, we evaluated the total branch length over which the D. melanogaster motif instance appears to be conserved (Supplementary Methods 5a, b), which we call the branch length score (BLS). We used BLS for the discovery of novel motifs (this section) and for the prediction of individual functional motif instances (next section).
To discover motifs, we estimated the conservation level of candidate sequence patterns with a motif excess conservation (MEC) score compared to overall conservation levels in promoters, UTRs, introns, protein-coding exons and intergenic regions (Supplementary Methods 5a).
Our search in regions with roles in pre-transcriptional regulation resulted in 145 distinct motifs (Table 2), obtained by collapsing variants across 83 motifs discovered in promoters, 35 in enhancers, 20 in 5′ UTRs, 35 in core promoters, 30 in introns and 84 in the remaining intergenic regions. Motifs discovered in each region showed similar properties and large overlap: 66 (46%) were discovered independently in at least two regions and 40 (28%) in at least three, consistent with shared regulatory elements in these regions90.
The 145 discovered motifs match 40 (46%) of the 87 known transcription factors in Drosophila (Supplementary Table 5c) compared to 8% expected at random (P =1 ×10−20). Several of the non-discovered known motifs are involved in early anterior–posterior segmentation of the embryo, consistent with reports that they are largely non-conserved91; indeed, 74% of these did not exceed the conservation expected by chance in promoter regions. Other non-discovered motifs often lacked characteristics expected for transcription factor motifs, suggesting that some may be spurious: 49% were unusually long (>10 nucleotides) compared to 23% of recovered ones, and showed only one or a few total instances genome-wide, suggestive of individual regulatory sites rather than motifs.
The discovered motifs showed strong signals with respect to embryonic expression patterns (Fig. 6a). Overall, 75 (52%) were either enriched or depleted in genes expressed in at least one tissue, compared to 59% of known motifs and 3% of random controls. Motif depletion may represent either specific repressors for individual tissues, or activators excluded from these tissues. Motif depletion was found more generally in ubiquitously expressed genes (30% of discovered and 34% of known motifs compared with 1% expected at random), similar to findings for in vivo binding sites92, and probably reflecting less complex regulation. We also found significant motif enrichment in groups of genetically interacting genes (collected by FlyBase) that often function in common developmental contexts or signalling pathways, genes of metabolic pathways (Kyoto Encyclopedia of Genes and Genomes, KEGG93), and genes with shared functions (GO).
In total, 68% of discovered and 70% of known motifs were enriched or depleted in one of the functional categories (14% random). Noteworthy examples include motif ME93 (GCAACA), which was more highly enriched in neuroblasts (P =4 ×10−12) than either of the two well-known regulators of neuroblast development, prospero and asense (P =4 ×10−5 and 2 ×10−7, respectively). Similarly, motifs ME89 (CACRCAC), ME11 (MATTAAWNATGCR) and ME117 (MAAMNNCAA) were highly enriched in malpighian tubule (P =4 ×10−7), trachea (P =4 ×10−5) and surface glia (6 ×10−7), respectively, in each case ranking above motifs for factors known to be important in these tissues (Supplementary Table 5c). These presumably correspond to as-yet-unknown regulators for these tissues.
A large number of motifs were depleted in coding sequence (57% of discovered versus 57% of known and 10% of random motifs, P =3 ×10−18) and in 3′ UTRs (30% versus 22% and 0%, P =4 ×10−11), suggesting specific exclusion similar to in vivo binding92.
Many of the intergenic or intronic instances occurred in clusters, a property of motifs that has been used to identify enhancer elements91,94–96. We assessed increased conservation of motifs when found near other instances of the same motif (whether conserved or not, to correct for regional conservation biases), and found significant multiplicity for 19% of the discovered motifs (compared to 24% of known and 4% of random motifs).
In addition, 15 of the discovered motifs (10%) were significantly enriched near transcription start sites (compared to 14% of known and 1% of random motifs). Several were enriched at precise positions and preferred orientations (Fig. 6b), including close matches to several known core promoter motifs involved in transcription initiation97. For example, ME5 (STATAWAWR), which matches the TATA-box motif, displayed a sharp peak on the transcribed strand, 27 nucleotides upstream of the transcription start site. Similarly, ME120 (TCAGTT), corresponding to the known initiator motif (Inr) strongly peaked directly on the transcription start site, and ME54 (RCGYRCGY), which matches a known downstream promoter element (DPE), peaked 30 nucleotides downstream of the transcription start site.
We also used BLS/MEC to discover motifs involved in post-transcriptional regulation, and developed methods to distinguish motifs acting at the DNA level, motifs acting at the RNA level and motifs stemming from protein-coding codon biases (Supplementary Methods 5a). Motifs acting post-transcriptionally at the RNA level generally showed highly asymmetric conservation12, as functional instances can only occur on the transcribed strand. Indeed, 71 of 90 motifs (79%) discovered in 3′ UTRs showed strand-specific conservation (compared with only 3% of 5′ UTR motifs and 5% of intron motifs, suggesting that these act primarily in pre-transcriptional regulation).
Overall, 33 motifs discovered in 3′ UTRs were complementary to the 5′ end of Rfam miRNAs, recovering 72% of known miRNAs (68% of 5′ unique miRNA families). An additional 21 motifs matched to 5′ ends of novel miRNAs predicted above, of which 12 were validated experimentally78,79, and 3 motifs matched uniquely to miRNA star sequences, all of which were abundantly expressed in vivo (Supplementary Table 4e).
We found 33 additional motifs in 3′ UTRs that were apparently not associated with miRNAs. MO40 (TGTANWTW) closely matches the Puf-family Pumilio motif98. MO32 (AATAAA) corresponds to the polyadenylation signal and displays both very strong conservation and a sharply defined distance preference with respect to the end of the annotated 3′ UTR (P =10−69). Finally, several motifs (for example, MO24 =TAATTTAT; MO94 =TTATTTT) are variants of known AU-rich elements, which are known to mediate mRNA instability and degradation99.
Protein-coding regions can also harbour functional regulatory motifs, such as exonic splicing regulatory elements100. However, motif conservation is difficult to assess within protein-coding regions because of the overlapping selective pressures. Indeed, the most highly conserved nucleotide sequence patterns of length seven (7mers) in coding sequence showed strong reading-frame-biased conservation, suggesting that they reflect protein-coding constraints rather than regulatory roles at the DNA or RNA level (Fig. 6c).
MicroRNA motifs, which function at the RNA level, instead showed high conservation in all three reading frames, suggesting that they are specifically selected within coding regions for their RNA-level function. Indeed, previous studies have shown that miRNA motifs in coding regions are preferentially conserved in vertebrates86, that they can lead to repression in experimental assays101,102, and that they are avoided in genes co-expressed with the miRNA103. Frame-invariant conservation allows us to demonstrate the coding-region targeting of individual miRNAs, and also enables the de novo discovery of miRNA motifs in coding regions. Using frame-invariant conservation, we recovered 11 miRNA motifs within the top 20 coding-region motifs (Supplementary Table 5g), whereas using overall conservation required several hundred candidates to recover 11 miRNA motifs.
Moreover, 7mers complementary to different positions in the mature miRNA show a distinctive conservation pattern indicative of functional targeting in coding regions (Fig. 6d) and similar to that found in 3′ UTRs12,83 (correlation coefficient 0.96). Finally, 6mers complementary to miRNA 5′ ends were depleted in coding exons of anti-target genes (Supplementary Fig. 5f), similar to findings for these genes’ 3′ UTRs103,104. Overall, these results, together with findings in vertebrates86,101–103, suggest that important miRNA targets have been overlooked by many target prediction methods105 that have traditionally focused exclusively on 3′ UTR sequences.
Previous methods for regulatory motif discovery3,4,12–14 integrated conservation information over hundreds of motif instances across the genome, leading to an exceedingly clear signal for motif discovery even if many of these instances are only marginally conserved. In contrast, the reliable identification of individual motif instances has been hampered by lack of neutral divergence and would require many related genomes15–19. In the absence of such data, previous studies have relied on motif clustering91,94–96 or other sequence characteristics106 to predict regulatory targets or regions.
With the availability of the 12 fly genomes, we inferred high-confidence instances of regulatory motifs by mapping the BLS of each motif instance to a confidence value (Supplementary Methods 5a). This value represents the probability that a motif instance is functional, on the basis of the conservation level of appropriate control motifs evaluated in the same type of region (promoter, 3′ UTR, coding, and so on). Because the number of conserved instances decreases much more rapidly for control motifs than for real motifs, the many genomes allowed us to reach high confidence values for many transcription factors and miRNAs, even at relatively modest BLS thresholds (Fig. 2e).
We found that increasing confidence levels selected for functional instances for both transcription factor and miRNA motifs: the normalized fraction of transcription factor motif instances within promoter regions rose from 20% to 90%; that of miRNA motif instances within 3′ UTRs rose from 20% to 90%; and the fraction of miRNA motif instances on the transcribed strand of 3′ UTRs rose from 50% (uniform) to 100% (Fig. 7a); in each case selecting the regions and strands where the motifs are known to be functional.
We further assessed how predicted motif instances compared with in vivo targets in promoter regions, defined experimentally (without comparative information). We used a set of high-confidence direct CrebA targets107 and three genome-wide chromatin immunoprecipitation (ChIP) data sets for Snail, Mef2 and Twist92,108,109, and in each case found that the enrichment between conserved motif instances and known in vivo regions increased sharply for increasing confidence values (Fig. 7b).
We also found that a large fraction of motif instances in experimentally determined target regions was conserved (Fig. 7c): 76% of motif instances in direct CrebA targets and 90% of motif instances in experimentally supported miRNA targets104,110 were recovered at 60% confidence. Although many of the miRNA targets stem from comparative predictions and are expected to be well conserved, their high recovery rate illustrates the increased sensitivity of the BLS measure compared to perfect conservation (Supplementary Fig. 7d). Similar results were found for motifs in known enhancers that were determined to be bound by ChIP (‘ChIP-bound’): 65% of Mef2 motifs, 65% of Snail motifs and 25% of Twist motifs were conserved (Fig. 7c).
To determine whether ChIP-bound motifs that lack conservation are biologically meaningful, we studied their enrichment in muscle gene promoters. We found that motifs that were both bound and evolutionarily conserved showed very strong correlation with muscle genes for all three factors: Mef2 showed eightfold enrichment, Twist showed sevenfold enrichment and Snail, a mesodermal repressor, showed threefold depletion for muscle genes. However, when only non-conserved sites were considered, the correlation dropped significantly to 1–2-fold for all three factors, suggesting that non-conserved ChIP-bound sites may be of decreased biological significance (Fig. 7d).
We also used the correlation with muscle genes to compare ChIP-on-chip and evolutionary conservation as two complementary methods for target identification (Fig. 7d). We found that the enrichment of conservation-inferred targets was consistently higher than the enrichment of ChIP-inferred targets for each of the three factors. Finally, we assessed the functional significance of motif instances that were only found by the conservation approach, specifically excluding those in ChIP-bound regions, and found that these were also enriched in the same functional categories as ChIP-bound sites with comparable or higher functional correlations (Fig. 7d). This suggests that the additional conserved instances are indeed functional, probably reflecting the higher coverage of conservation-based approaches, which are not restricted to the experimental conditions surveyed, or that they may be bound in vivo yet missed by ChIP-on-chip technology111,112.
In an independent study113 we compared several strategies for the prediction of motif instances and cis-regulatory modules and found that using the 12 fly genomes led to substantial improvements. In another study, we reported the recovery of conserved motifs for several known regulators, including Suppressor of Hairless, in genes of the Enhancer of split complex114.
Having established the accuracy of conserved motif instances, we present an initial regulatory network for D. melanogaster at 60% confidence (Supplementary Fig. 5i), containing 46,525 regulatory connections between 67 transcription factors and 8,287 genes, and 3,662 connections between 81 cloned miRNAs (clustered in 49 families with unique seed sequences) and 2,003 genes.
The distribution of predicted sites per target gene is highly nonuniform and indicative of varying levels of regulatory control. Genes with the highest number of sites appeared to be enriched in morphogenesis, organogenesis, neurogenesis and a variety of tissues, whereas ubiquitously expressed genes and maternal genes with housekeeping functions had the fewest sites104. Interestingly, transcription factors appeared to be more heavily targeted than other genes, both by transcription factors (10 sites versus 5.5 on average, P =10−15) and by miRNAs (2.3 versus 1.8 miRNAs, P =5 ×10−5). Moreover, genes with many transcription factor sites also had many miRNA sites, and conversely, genes with few transcription factor sites also had few miRNA sites (P =10−4 and P =7 ×10−3, respectively).
Several of the predicted regulatory connections have independent experimental support (Supplementary Table 5h), including direct regulation of achaete by Hairy115, of giant by Bicoid116, of Enhancer of split complex genes by Suppressor of Hairless117, and of bagpipe by Tinman (known to cooperate in mesoderm induction and heart specification118). More generally, when tissue-specific expression data were available, we found that on average 46% of all targets were co-expressed with their factor in at least one tissue (Supplementary Fig. 5i), which is significantly higher than expected by chance (P =2 ×10−3).
Theoretical considerations and pilot studies on selected genomic regions showed that the discovery power of comparative methods scales with the number and phylogenetic distance of the species compared16–20,46,119,120. We extended these analyses by investigating the scaling of genome-wide discovery power using evolutionary signatures for each class of functional elements (Fig. 8), on the basis of the recovery of known elements using different subsets of informant species (at a fixed stringency).
We found that recovery consistently increased with the total number of informant species, and that multi-species comparisons outperformed pairwise comparisons within the same phylogenetic clade. When we examined subsets of informants with similar total branch length (for example, several close species versus one distant species), multi-species comparisons sometimes performed better (protein-coding exons, ncRNAs), comparably (motifs), or worse (miRNAs) than pairwise comparisons. This complex relationship between total branch length and actual discovery power probably reflects imperfect genome assemblies/alignments, characteristics of each class of functional elements, and the specific methods we used. For example, ncRNA discovery probably benefits from observing more compensatory changes across more genomes, whereas miRNA discovery may be more sensitive to artefacts in low-coverage genomes, given the expected high conservation of miRNA arms.
As expected, longer elements were easier to discover than shorter elements. Long protein-coding exons (>300 nucleotides) were recovered at very high rates even with few species at close distances (leaving little room for improvement with additional species). In contrast, more informant species and larger distances were crucial for recovering short exons, miRNAs and regulatory motifs.
Notably, the optimal evolutionary distance for pairwise comparisons to D. melanogaster also seemed to depend on element length: for long protein-coding exons, the best pairwise informant was the closely related D. erecta, for exons of intermediate lengths D. ananassae, and for the shortest exons the distant D. willistoni (Supplementary Table 7a). Distant species were also optimal for other classes of short elements (ncRNAs, miRNAs and motifs, Fig. 8b–d). This suggests that a small number of species at close evolutionary distances may generally allow the discovery of long elements, possibly including clade-specific elements, whereas short clade-specific elements may not be reliably detectable without many genomes at close distances.
Finally, we investigated the effect of alignment choice on our results (Supplementary Fig. 8). We found high similarity between different alignment strategies for longer elements (>93% agreement for exons), whereas shorter elements showed larger discrepancies between alignments (81% and 59% agreement for miRNA and motif instances, respectively).
Although factors such as genome size, repeat density, pseudogene abundance and physiological differences might confound a simple analogy to the vertebrate phylogeny based on neutral branch length (Fig. 1c), our results suggest that comparisons spanning marsupials, birds and reptiles may prove surprisingly useful for biological signal discovery in the human genome.
Our results demonstrate the potential of comparative genomics for the systematic characterization of functional elements in a complete genome. Even in a species as intensely studied as D. melanogaster, our methods predicted several thousand new functional elements, including protein-coding genes and exons, novel RNA genes and structures, miRNA genes, regulatory motifs, and regulator targets. Our novel predictions have overwhelming statistical support, often surpassing that of known functional elements, and are additionally supported by experimental evidence in hundreds of cases. The common underlying methodology in this study has been the recognition of specific evolutionary signatures associated with each class of functional elements, which can be much more informative for genome annotation than overall measures of nucleotide conservation. These signatures are general and are immediately relevant to the analysis of the human genome and more generally of any species.
In addition to the many new elements, we gained specific biological insights and formulated hypotheses that we hope will guide follow-up experiments. We found 149 genes with potential translational readthrough, showing protein-like evolution downstream of a highly conserved stop codon, and possibly encoding additional protein domains or peptides specific to certain developmental contexts. We also found several candidate programmed frameshifts, which might be part of regulatory circuits (as for ODC/Oda 64) or help expand the diversity of protein products generated from one mRNA, similar to their role in prokaryotes121. We also presented evidence of miRNA processing from both arms of a miRNA hairpin and from both DNA strands of a miRNA locus in some cases, potentially leading to as many as four functional miRNAs per locus. As miRNA/miRNA* pairs are expressed from a single precursor and thus co-regulated, whereas sense/anti-sense pairs are expressed from distinct promoters, the use of both arms or both strands provides compelling general building blocks for higher-level miRNA-mediated regulation.
The newly discovered elements did not dramatically increase the total number of annotated nucleotides. Known and predicted elements explain 42% of nucleotides in phastCons elements33, compared to 35.5% for previous annotations (Supplementary Fig. 6), an 18% increase (mostly owing to conserved motif instances). The remaining phastCons elements and independent estimates based on transcriptional activity42 would suggest that a much higher fraction of the genome may be functional (Supplementary Fig. 6). Although it is possible that these estimates are artificially high and that we are in fact converging on a complete annotation of the fly genome, they might instead indicate that much remains to be discovered, which may require the recognition of as-yet-unknown classes of functional elements with distinct evolutionary signatures.
Our results also allowed us to compare and contrast evolutionary and experimental methods for the recovery of functional elements, particularly for the identification of regulator targets. We found that comparative genomics resulted in many functionally meaningful sites for transcription factors Mef2, Twist and Snail outside ChIP-bound regions, probably representing targets from diverse conditions not surveyed experimentally. Similarly, ChIP resulted in many additional sites outside those recovered by comparative genomics: some of these may have been replaced by functionally equivalent non-orthologous sequence, rendering them apparently non-conserved in sequence alignments122–124; others may have species- or lineage-specific roles, thus lacking sufficient signal for their comparative detection; finally, some bound sites may be biochemically active yet selectively neutral125. It is worth noting, however, that ChIP-bound motifs that were not conserved showed decreased enrichment in muscle/mesoderm development where the factors are known to act, suggesting that potential lineage-specific roles may lie outside the regulators’ conserved functions. To resolve these questions, comparative genomics studies would benefit greatly from experimental studies in several related species in parallel.
Overall, comparative genomics and species-specific experimental studies provide complementary approaches to biological signal discovery. Comparative studies help pinpoint evolutionarily selected functional elements across diverse conditions, whereas experimental studies reveal stage- and tissue-specific information, as well as species-specific sites. Ultimately, their integration is a necessary step towards a comprehensive understanding of animal genomes.
The Methods are described in Supplementary Information, with more details found in the cited companion papers for each section. The sections of the Supplementary Methods are arranged in the same order as the manuscript to facilitate cross-referencing, with an index on the first page to aid navigation.
We thank the National Human Genome Research Institute (NHGRI) for continued support. A.S. was supported in part by the Schering AG/Ernst Schering Foundation and in part by the Human Frontier Science Program Organization (HFSPO). P.K. was supported in part by a National Science Foundation Graduate Research Fellowship. J.S.P. thanks B. Raney and R. Baertsch, and the Danish Medical Research Council and the National Cancer Institute for support. J.B. thanks the Schering AG/Ernst Schering Foundation for a postdoctoral fellowship. L. Parts thanks J. Vilo. S.R. was supported by a HHMI-NIH/NIBIB Interfaces Training Grant and thanks T. Lane and M. Werner-Washburne. D.H., D.P.B., G.J.H. and T.C.K. are Investigators of the Howard Hughes Medical Institute, and B.P., J.G.R., E.H. and J.B. are affiliated with these investigators. J.W.C. and S.E.C. were supported by the NHGRI. M.K. was supported by start-up funds from the MIT Electrical Engineering and Computer Science Laboratory, the Broad Institute of MIT and Harvard, and the MIT Computer Science and Artificial Intelligence Laboratory, and by the Distinguished Alumnus (1964) Career Development Professorship.
Harvard FlyBase curators Madeline A. Crosby1, Beverley B. Matthews1, Andrew J. Schroeder1, L. Sian Gramates1, Susan E. St Pierre1, Margaret Roark1, Kenneth L. Wiley Jr1, Rob J. Kulathinal1, Peili Zhang1, Kyl V. Myrick1, Jerry V. Antone1 & William M. Gelbart1
1FlyBase, The Biological Laboratories, Harvard University, 16 Divinity Avenue, Cambridge, Massachusetts 02138, USA.
2BDGP, LBNL, 1 Cyclotron Road MS 64-0119, Berkeley, California 94720, USA.