Volume 7 Supplement 1
Comparative analysis of genome tiling array data reveals many novel primate-specific functional RNAs in human
© Zhang et al; licensee BioMed Central Ltd. 2007
Published: 8 February 2007
Widespread transcription activities in the human genome were recently observed in high-resolution tiling array experiments, which revealed many novel transcripts that are outside of the boundaries of known protein or RNA genes. Termed as "TARs" (Transcriptionally Active Regions), these novel transcribed regions represent "dark matter" in the genome, and their origin and functionality need to be explained. Many of these transcripts are thought to code for novel proteins or non-protein-coding RNAs. We have applied an integrated bioinformatics approach to investigate the properties of these TARs, including cross-species conservation, and the ability to form stable secondary structures. The goal of this study is to identify a list of potential candidate sequences that are likely to code for functional non-protein-coding RNAs. We are particularly interested in the discovery of those functional RNA candidates that are primate-specific, i.e. those that do not have homologs in the mouse or dog genomes but in rhesus.
Using sequence conservation and the probability of forming stable secondary structures, we have identified ~300 possible candidates for primate-specific noncoding RNAs. We are currently in the process of sequencing the orthologous regions of these candidate sequences in several other primate species. We will then be able to apply a "phylogenetic shadowing" approach to analyze the functionality of these ncRNA candidates.
The existence of potential primate-specific functional transcripts has demonstrated the limitation of previous genome comparison studies, which put too much emphasis on conservation between human and rodents. It also argues for the necessity of sequencing additional primate species to gain a better and more comprehensive understanding of the human genome.
Whole genome tiling array experiments
The human genome is the blueprint that encodes most of the functional components in the human body: proteins and RNAs. With the completion of sequencing of the human genome, the focus of the genomic research is shifting to identifying all the functional units encoded within the genome. A new technology, the maskless oligonucleotide tiling array, has recently emerged as a powerful tool to interrogate transcription activities on the whole genomic scale and at unprecedented high resolution [1, 2]. Using known genome sequence as blueprint, short oligonucleotides were synthesized to cover or "tile" each chromosome at regular intervals. Repetitive elements and regions of low complexity are usually avoided in such tiling experiments. Biological samples such as mRNAs or cDNAs are labelled with fluorescence and hybridized to the microarray spotted with the probes. Just like regular microarray experiments, the observed fluorescence intensities are interpreted as elevated transcription activity at specific genome locations. The tiling array experiments are most useful in verifying predicted exons and identify novel exons and other transcribed sequence elements.
A number of tiling array studies on the human and other genomes have been published since 2002 [3–6]. The major differences among these studies are the resolution of the tiles (length of the oligonucleotide probes and intervals between them), and the coverage of the genome. As of early 2006, the study by Bertone et al. (2005) is the only one that covers the entire human genome. These researchers designed ~51,000,000 probes of 36 mers, positioned at every 46 nucleotide interval on average, which cover ~1.5 GB of the non-repetitive genomic DNA sequence from both strands of the human genome . The biological sample used in this study was fluorescence-labelled cDNA, reverse-transcribed from triple-selected polyadenylated RNAs [poly(A)+] from liver tissue. In total, these researchers identified ~17,000 transcriptionally active regions (termed as TARs) in the entire genome. There are strong correlations between the TARs and the known gene annotations or predictions, e.g. 64% of the genes annotated in RefSeq and 57% in Ensembl and 70% in UniGene were observed in this study .
Widespread transcription activity in the human genome
Distribution of transcriptionally active regions (TARs), categorized by their distances from the nearest gene annotations
Annotation on the opposite strand
Annotation on the same strand as TAR4
Distribution of human genomic regions, categorized by annotations on both strands (Mb = megabases)
Annotation on the antisense strand (Mb)
Annotation on the sense strand 1
35 (1.2 %)
Total length and density of TARs in different types of genomic regions1
Annotation on the antisense strand
Annotation on the sense strand2
Such widespread transcription activities have also been observed in other human tiling array experiments as well [3–6]. There has not been a consensus opinion on the exact nature and origin of these TARs (or called "transfrags" as in ), however, it has been pointed out that many of these novel transcripts are not likely to code for proteins as they do not have open reading frames of longer than 300 nucleotides.
In addition to these microarray studies, widespread transcription activities outside of known human genes have also been observed in other types of experiments. Long serial analysis of gene expression experiments (LongSAGE) suggest that over 15,000 additional new exons exist in the human genome, and over half of these may be from new genes [7, 8]. Ota et al. analyzed full-length human cDNA library and discovered ~5,000 novel non-coding cDNA transcripts . A large number of noncoding transcripts has also been reported to exist in the mouse genome [10, 11]. In addition to the mammalian genomes, large number of intergenic transcripts were also observed in plants and fruit fly [12–14]. Taking all these pieces of evidences together, it was estimated that over half of the human genome could potentially be transcribed , or at least 90% of the transcription activity in the genome is outside of well-characterized protein-coding exons .
Possible functional roles of the novel transcripts
There have been many theories proposed to account for the origin, property, and possible functions of these novel transcripts. It was suggested that some of these TARs may be novel protein coding genes, novel RNA genes, anti-sense transcripts, alternative transcripts or just simply biological artefacts (please see  for a detailed discussion on the possible hypotheses). Because of the prevalence of such intergenic transcription activity (see above), it is unlikely that these novel transcripts are experimental artefact or false positives. It is also unlikely that any single mechanism can fully explain the observed novel transcripts, but perhaps the combination of explanations can account for the bulk of the observed novel transcripts. For example, it is possible that those TARs that are near the known genes could represent previously unidentified exons in the same gene structure, or represent alternative transcripts caused by alternative promoters. Depending on their degree of sequence conservation, some of the "distal" transcripts, i.e. those that are far away from known genes, are likely to be candidates for novel protein coding genes or noncoding RNAs. This notion has been suggested by many, including the researchers who conducted the tiling array experiments, as the most likely explanation for the bulk of the novel transcripts [9, 11, 16].
Some of the TARs may be functional noncoding RNAs
Noncoding RNAs that are known to have medical implications.
found in adult neural stem cells
Many of the known ncRNAs in human and mouse were discovered accidentally or from large-scale cloning experiments. The novel transcripts found in the tiling array experiments offer a new resource to identify novel non-coding RNA transcripts. Kampa and colleagues have screened the "transfrags" from Chromosomes 21 and 22 and identified 193 novel ncRNA candidates; they were able to verify 126 or 65% of these ncRNAs by RT-PCR. Remarkably, this extrapolates to ~4200 ncRNAs in the entire human genome . Several software tools have been developed to predict ncRNAs by computational approaches, especially on predicting miRNA, which have defined secondary structures. These programs mostly work by searching for conserved motifs, existence of secondary structure, cross-species conservation, or combination of above methods.
Large numbers of novel transcripts are conserved in other vertebrates
BLAST matches in the other genomes and databases (E-value < 0.01)
Genome or database
Number of hits
Human EST library
Human cDNA library
Chimpanzee (Pan troglodytes)
Macaque cDNA library
Mouse EST library
* Rodents: mouse ∪ rat
Dog (Canis familiaris,) partial genome
Chicken (Gallus gallus)
Frog (Xenopus tropicalis)
Japanese pufferfish (Takifugu rubripes)
Green spotted pufferfish (Tetraodon nigroviridis)
** Pufferfish: Takifugu rubripes ∪ Tetraodon nigroviridis
Sea squirt (Ciona intestinalis)
Noncoding RNA Databases
*** Rfam ∪ RNAdb ∪ mirBase ∪ NONCODE
Total number of TARs reported by Bertone et al.
Sequencing projects of two primates, Macaque (Macaca mulatta) and orangutan (Pongo pygmaeus), are currently under way. We downloaded the trace sequence files of these two primates and included them in the homology search as well. Because of the incompleteness of these genomes, the existence or absence of homologs in these libraries does not reflect the true level of conservation for each TAR. We also searched for TAR homologs in mammalian cDNA and EST libraries, including H-Invitational Database (H-InvDB) ), which contains 21,037 validated human full-length cDNA: mouse full-length cDNA library (FANTOM) [10, 23]); human and mouse EST libraries from NCBI; and a macaque cDNA library from .
Table 5 shows that 69% of the TARs have EST matches, and 43% of the TARs have matches in the human cDNA library, which further validated that the bulk of the novel transcripts identified from tiling arrays are real transcripts instead of experimental artefacts. As expected, more TARs are conserved in the chimpanzee genome than in the rodent genomes (90% vs. 50%), which is in line with what would be expected for random genomic regions. This is obviously the result of closer evolutionary relationship between the two primate species, but it also implies that there must be many primate-specific transcripts that are shared between human and chimpanzee but not between human and rodents. A significant number of TARs are also conserved in chicken (21%) and pufferfish (16%).
TARs in noncoding RNA databases
We also searched for homologs of the TARs in several sequence databases that contain known noncoding RNAs (Table 5, bottom). We found that there are ~2,637 non-protein-coding RNAs among the TARs, or about 15% of the entire novel transcripts, which also include 138 miRNAs. Note that some of these databases such as RNAdb also include hypothetical ncRNAs that are predicted from cDNA libraries.
Conservation profiles of TARs among vertebrates
Conservation profile *
# of hits
Human ∩ Chimp
Human ∩ Chimp ∩ rodents
Human ∩ Chimp ∩ rodents ∩ dog
Human ∩ Chimp ∩ rodents ∩ dog ∩ chicken
Human ∩ Chimp ∩ rodents ∩ dog ∩ chicken ∩ pufferfish
Human ∩ Chimp ∩ rodents ∩ dog ∩ chicken ∩ pufferfish ∩ sea squirt
Human ∩ macaque
Human ∩ macaque ∩ chimp
Human ∩ Rodent
Human ∩ Rodent ∩ dog
Human ∩ Rodents ∩ dog ∩ chicken
Human ∩ Rodent ∩ dog ∩ chicken ∩ pufferfish
Human ∩ Rodent ∩ dog ∩ chicken ∩ pufferfish ∩ sea squirt
Num. of TARs in human AND chimp, but NOT in rodents
Num. of TARs in human AND chimp, but NOT in any other vertebrates
Num. of TARs in human and chimp, but NOT in rodents, and NOT in databases (Rfam, RNAdb, mirBase, NONCODE)
Num. of TARs in human and chimp, but NOT in any other genomes, and NOT in databases (Rfam, RNAdb, mirBase, NONCODE)
Total # of TARs
Distal versus proximal TARs
Conservation of TARs in chimpanzee and rodents, categorized by their distance to known genes on both strands
Found in human AND chimp (15,757)
Found in human AND mouse (8,776)
Found in human AND chimp AND rodents (8,446)
Found in human AND in chimp NOT in rodents (7,311)
Many TARs are predicted to have stable secondary structures
It has been proposed that many of the transcripts identified in the tiling array or cloning experiments are novel non-protein-coding RNAs that have potential regulatory or catalytic functions. Okazaki and colleagues analyzed the mouse full-length cDNA library, and estimated 15,000 or about half of the library are non-protein-coding and functional RNA genes , but this number has been debated . A more thorough computational study of the mouse transcriptom by Numata et al revealed a set of ~4,200 functional non-protein-coding RNA candidates . Kampa and colleagues analyzed the tiling array data of human chromosome 21 and 22 . They identified 193 novel RNA candidates and experimentally verified 126 of them. These researchers only used evidence of transcription in their predictions, which is powerful as demonstrated by the respectable 65% verification rate, but the false-positive rates can be further reduced if additional lines of evidence are incorporated. In this study, we utilize 2 lines of evidence: sequence conservation and RNA secondary structure, to make prediction on conserved novel RNA transcripts hidden in the human genome.
Functional elements in the genomes are presumably under selective pressure to maintain their sequence, therefore sequence conservation in other organisms are generally a good indication of functionality. However, we have to be cautious when applying such principle onto RNA sequences. It has been observed that except for structural RNAs such as rRNAs, noncoding RNA genes are in general less conserved than protein coding genes. This is particular true for regulatory RNAs , as some of the non-protein-coding RNAs, which have identical functions in human and mouse, do not show obvious sequence homologies. In addition, as pointed out earlier, too much reliance on conservation can overlook lineage-specific transcripts. Given the limitations of using sequence conservation alone in detecting ncRNAs, it is obvious that additional approaches are needed to address these concerns, such as the probability of forming stable secondary structure.
RNA secondary structure and thermodynamic stability
Predictions of RNA secondary structures by RNAZ (p-value > 90%)
Found in human AND chimp (1436)
Found in human AND mouse (241)
Found in human AND chimp AND rodents (234)
Found in human AND in chimp NOT in rodents (1202)
Found in human AND in chimp NOT in rodents, and NOT present in databases (1073)
It is interesting and encouraging that our analysis has discovered a large number of potential noncoding RNAs that only exist in the primates. Conventional genome annotation efforts often limit the cross-species comparison to human and mouse, such strategy likely have overlooked many lineage-specific protein or RNA genes. As we discuss below, special strategies are needed to uncover these lineage-specific sequences.
Primate-specific noncoding RNAs in the human genome
It is important and fascinating to identify and characterize the genes that are responsible for the primate or human distinctiveness. In this paper, we discussed a bioinformatics analysis on the novel RNA transcripts discovered in our previous tiling array work . We are interested to identify those functional novel transcripts that are primate-specific, i.e. they emerged only recently in the primate lineage and thus have no obvious sequence homologs in other mammalian genomes. This is a novel research area that has been largely overlooked, and it potentially will have great impact in the field of non-protein-coding RNAs, comparative genomics, and also medicine.
Most of the current efforts in detecting novel coding or noncoding transcripts require the transcript to be conserved in at least another mammalian genome, mostly in rodent genomes since they were the only available mammalian genomes until the chimpanzee draft genome was finished in 2005. Rodents and human last shared common ancestor at about 75–80 million years ago; their evolutionary distance from human is considered sufficiently distant to be able to separate conserved functional sequence that are under selective (purifying) pressure from those background neutral DNA [29, 30]. A potential limitation of only using rodents as the yardstick in such comparative studies is that it overlooks those genes that have only emerged recently in the primate line-age, which likely determine primate-specific traits. Three-way comparisons between human-mouse-rat genomes have revealed 2302 rodent-specific exons, and similar number of human-specific genes [30–32]. These new genes were believed to have arisen through the following processes: (i) accelerated evolution in one lineage, (ii) arisen de novo from non-coding DNA, and (iii) derived from retroposition or recombinations . Similarly, lineage-specific ncRNAs must also be present in either rodents or primates, which remain to be discovered.
Comparison with other predictions
Pedersen and colleagues recently developed a computational method called EvoFold, which utilizes the algorithm of phylogenetic stochastic context-free grammar (Phylo-SCFG) to detect conserved structured RNAs in the genome . These researchers first aligned the whole genome sequences of eight vertebrates (human, chimpanzee, mouse, rat, dog, chicken, zebra-fish, and puffer-fish), and applied the EvoFold program to derive 48,479 sequences in the human genome that are predicted to have secondary structures. These predicted sequences can be accessed at the UCSC genome browser.
We are interested to analyze the overlap between the Evofold predictions and the TARs. For each TAR, we identified the closest ncRNA candidate as predicted by Evofold. Surprisingly these two datasets have very little overlap: 548 TARs overlap with an Evofold prediction, and 624 TARs (including the overlapping ones) are within 100 bp of a nearest Evofold prediction. Among the 548 TARs that overlap with Evofold, only 16 were predicted by RNAZ to be noncoding RNAs with P-value greater than 0.5. The lack of overlap between TARs and the Evolfold predictions is not really surprising, as the latter only looked at the genomic regions that are conserved in eight vertebrate species.
As discussed above, the conventional phylogenetic and comparative methods have their limitations in identification of lineage-specific transcripts. An alternative approach, "phylogenetic shadowing", has been recently used in a number of studies and is likely to be very useful in this area. Phylogenetic shadowing is an alternative method to phylogenetic footprinting, which is a more commonly used comparative technique . Both methods use comparative approach to identify functional elements hidden in a group of orthologous sequences, but they work in different ways and are most suited in different situations. Phylogenetic footprinting is most useful in searching for conserved elements that are present in organisms that are very distantly related. As at such great evolutionary distance, any conserved sequence would have been the result of selective pressure, therefore must be functionally important. In contrast, phylogenetic shadowing is best suited to study sequences from a group of closely related species. It analyzes patterns of sequence variations and mutations in a multiple sequence alignment, and separates the slowly evolving sites from the fast evolving sites. The sites that evolve slower are inferred as being under stronger selective pressure thus functionally important. In order to rigorously calculate the sequence variations without bias, phylogenetic relationships among the species is usually required. For closely related species, such phylogeny information is normally easy to obtain. Boffelli and Rubin were the first to employ phylogenetic shadowing, who used it on sequences from primates to discover regulatory elements and exon/intron boundaries . Phylogenetic shadowing was recently used among a group of 9 primate species to identify conserved miRNA sequences .
We have initiated a sequencing project to obtain orthologous sequences for the 353 candidate transcripts from several related primate species. Experimental details and analysis will be reported in the future.
Searching for homologs in other genomes
For each TAR, we used Blastn to search for homologous sequences in another fully sequenced genome or sequence library. It is important to select the most optimal Blastn e-value threshold, so that we will not miss any real homologs, and also avoid too many false positive hits. To select the e-value cut-off, we did the following control experiments. We selected the experimentally verified human miRNA hairpin sequences from the mirRegistry database  as query sequences, and BLASTed them against the mouse genome. We also included some negative sequences into the query set. All of these known human miRNAs have homologs in the mouse genome, so the resulted e-values from this Blastn search should be the optimal cutoff for selecting homologs in a different genome. The results confirmed that e-value = 0.01 is sufficient to identify the homologs and separate the real homologs from negative controls.
Predicting secondary structure in RNAs
Programs such as MiRscan, miRseeker and ProMiR are dedicated to search for miRNAs [38–40] and programs such as RNAZ, RNAFOLD, Mfold, ddbRNA, RANDFOLD, MSARI, QRNA, FOLDALIGN were written to detect stable RNA secondary structures [28, 41–46]. A track (EvoFold) was also implemented into the UCSC Genome Browser, which indicates the potential of forming secondary structures for any give genomics locus. A number of databases have been created to collect and categorize these ncRNA sequences, which include Rfam , NONCODE , microRNA Register , and RNAdb .
Among these RNA structure prediction tools, the RNAZ program has been evaluated as the most effective , and was used as the primary prediction tool . The effectiveness of the RNAZ program comes from its unique approach in combining the predicted thermodynamic stability with the structure and sequence conservation index . The program has been tested on positive and negative control sequences. At the P value cutoff at 0.9, the program has the sensitivity of 75% and specificity of 98% . We are currently also testing other prediction software such as QRNA, we will compare these two prediction results and investigate the possibility of using the intersection of the two predictions.
ZZ thanks Steve Scherer, Benjamin Blencowe, Timothy Hughes and Matthew Fagnani for helpful discussions. This work is partially supported by the Start-up fund from University of Toronto Faculty of Medicine and by a grant from Canadian Institutes of Health Research (CIHR) to ZZ. AP was partially funded by a summer research fellowship from Ontario Genomics Institute (OGI).
This article has been published as part of BMC Evolutionary Biology Volume 7 Supplement 1, 2007: First International Conference on Phylogenomics. The full contents of the supplement are available online at http://www.biomedcentral.com/bmcevolbiol/7?issue=S1.
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