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Computational Identification of Four Spliceosomal snRNAs from the Deep-Branching Eukaryote Giardia intestinalis

  • Xiaowei Sylvia Chen ,

    Affiliation Allan Wilson Centre for Molecular Ecology and Evolution, IMBS, Massey University, Palmerston North, New Zealand

  • W. Timothy J. White,

    Affiliation Allan Wilson Centre for Molecular Ecology and Evolution, IMBS, Massey University, Palmerston North, New Zealand

  • Lesley J. Collins,

    Affiliation Allan Wilson Centre for Molecular Ecology and Evolution, IMBS, Massey University, Palmerston North, New Zealand

  • David Penny

    Affiliation Allan Wilson Centre for Molecular Ecology and Evolution, IMBS, Massey University, Palmerston North, New Zealand

Computational Identification of Four Spliceosomal snRNAs from the Deep-Branching Eukaryote Giardia intestinalis

  • Xiaowei Sylvia Chen, 
  • W. Timothy J. White, 
  • Lesley J. Collins, 
  • David Penny


RNAs processing other RNAs is very general in eukaryotes, but is not clear to what extent it is ancestral to eukaryotes. Here we focus on pre-mRNA splicing, one of the most important RNA-processing mechanisms in eukaryotes. In most eukaryotes splicing is predominantly catalysed by the major spliceosome complex, which consists of five uridine-rich small nuclear RNAs (U-snRNAs) and over 200 proteins in humans. Three major spliceosomal introns have been found experimentally in Giardia; one Giardia U-snRNA (U5) and a number of spliceosomal proteins have also been identified. However, because of the low sequence similarity between the Giardia ncRNAs and those of other eukaryotes, the other U-snRNAs of Giardia had not been found. Using two computational methods, candidates for Giardia U1, U2, U4 and U6 snRNAs were identified in this study and shown by RT-PCR to be expressed. We found that identifying a U2 candidate helped identify U6 and U4 based on interactions between them. Secondary structural modelling of the Giardia U-snRNA candidates revealed typical features of eukaryotic U-snRNAs. We demonstrate a successful approach to combine computational and experimental methods to identify expected ncRNAs in a highly divergent protist genome. Our findings reinforce the conclusion that spliceosomal small-nuclear RNAs existed in the last common ancestor of eukaryotes.


Extant eukaryotes are marked by having RNA extensively processing other RNA molecules, whether it is RNase P on tRNAs, RNase MRP and snoRNAs on rRNAs, or snRNAs on mRNAs. In addition RNAi processes are known to inhibit or enhance mRNA expression. A major question in eukaryotic origin is the extent of RNA processing in the last common ancestor of eukaryotes. Perhaps the major question is whether much of the RNA processing traces back to the proposed RNA World [1] and how much is a later invention within eukaryotes [2]. Here we focus particularly on the major spliceosomal snRNAs involved in mRNA splicing, and address the question whether these small snRNAs occur in all deep eukaryotic lineages; in other words, whether the early splicing mechanism in eukaryotes involved both RNA and proteins, or was initially a protein mediated process, with RNAs added later. Here we use a combination of computational techniques with experimental evaluation of the results to help test these alternatives.

The spliceosome is one of the most important RNA-processing units in eukaryotes. The presence of some spliceosomal introns in deep-branching eukaryotes [3][5] is consistent with some form of the splicing mechanism having evolved very early during eukaryotic evolution [6]. Eukaryotes can be classified into five main groups [7], although the early branching order of these five groups is yet unknown. Giardia belongs to the deep-branching lineage of diplomonads; these are often considered one of the deepest branching lineages of eukaryotes, but little is known in diplomonads of RNA involvement in processing other RNAs. Therefore Giardia is particularly important for studying the evolution of major RNA-processing pathways. In general, we followed the approach of Collins and Penny [8] by searching for a feature in deep lineages of eukaryotes, to infer the ancestral state of modern eukaryotes.

To date only three introns have been experimentally confirmed in Giardia. The first is a short (35nt) non-canonical intron (5′-CT – AG-3′) located within the mitosomal [2Fe-2S] ferredoxin protein [5], the second a 109nt canonical intron (5′-GT – AG-3′) found in the ribosomal protein Rp17a [4] and the third a 220nt canonical intron found in an unassigned ORF [4]. Some additional introns have been predicted (SW Roy, pers. comm.), but they have not yet been confirmed experimentally. Introns can be both gained and lost during evolution [9] therefore we cannot just assume that the ancestral eukaryotes had very few introns. For example, there appears to be selection for the loss of introns in eukaryotes with a short life cycle [10].

Despite the common assumption that the spliceosome is responsible for the removal of introns in all eukaryotes, the existence and nature of a spliceosome in Giardia are at this stage still assumed. A desirable classical approach would be to biochemically extract whole spliceosomes, examine then test the individual components. However, this is an extremely non-trivial exercise even on model eukaryotic spliceosomes, for which a lot is known. Working with non-model organisms is even more difficult. Therefore, a more computational approach is necessary in order to identify good candidates.

Genomic surveys [5], [6] have inferred a number of spliceosomal proteins from the Giardia genome. These include homologues of Prp8, Prp11, Prp28 and Prp31; a number of DExH-box RNA-helicases which have homologues in bacteria but which also have important roles in eukaryotic intron splicing; 11 archaeal-like Sm and Lsm core peptides which coat the spliceosomal snRNAs; and a number of U-snRNA-specific peptides. It is therefore very likely that Giardia has a functional major spliceosome, but to date there have been no biochemical studies on the entire spliceosome or any of the snRNAs that comprise its catalytic core.

In humans, the major spliceosome is composed of over 200 proteins and five uridine-rich small nuclear RNAs (U1, U2, U4, U5 and U6) that form dynamic protein-RNA and RNA-RNA interactions [11]. Like other ribozymes, the RNA components of the spliceosome are the major catalysts of splicing. It has been shown that human protein-free spliceosomes are capable of catalysing reactions that resemble both the first [12] and second [13] steps of trans-esterification reactions during splicing. The U-snRNAs are found throughout much of the eukaryotic kingdom and have the characteristic Sm-protein binding site, which is a conserved 8–10nt uridine-rich sequence flanked by two stem-loops. The structures of these snRNAs are also highly conserved in eukaryotes where they have been found.

To date many studies have shown that the U-snRNAs from a wide range of organisms share the same stem-loop folds [13][19]. The stem-loops within these snRNAs are important for interactions with snRNA-specific proteins. Each of the five snRNAs has a number of specific interacting proteins ranging from 4 in human to 10 in yeast [20]. However in deep-branching eukaryotes, the protein components are usually reduced [21][23]. Bioinformatic studies have shown that Giardia is likely to have most of the more conserved snRNA-associated major spliceosomal proteins although the less conserved ones may not have existed or may have been lost [6].

In addition to the highly conserved stem-loop structures of individual U-snRNAs, functional interactions between U-snRNAs, and between U-snRNAs and intron sites, are also conserved in eukaryotes. The 5′ sequence of the U1 snRNA base-pairs with the intron at the 5′- intron site, but is released before the actual catalysis proceeds. U4 snRNA is required for bringing the U6-snRNA (through base-pairing) into the catalytic centre, and is released before the first step of the splicing reaction [24]. U2, U6 and U5 snRNAs remain at the catalytic core throughout the splicing reaction. U2-snRNA loosely binds to the branch site of the intron in the active spliceosome, leaving the unbound branch-site adenosine, which can then interact with the phosphate group on the guanosine at 5′ of the intron through its 2′-OH group, and form an intron lariat. Three interactions between U2 and U6 were identified from studies of mammalian and yeast systems, and were shown to be required for splicing [25][28]. U5 appears to act as a scaffold RNA to hold the two exon-intron junction sites at appropriate orientation by its invariant loop [29]. We show here that these interactions between U-snRNAs, or with mRNAs, can be used to identify U-snRNAs.

The Giardia U5-snRNA was identified by computational analysis [8], and it folds into a conserved U5 secondary structure, although the primary sequence itself does not show homology with U5-snRNAs from other species. The U5-snRNP is required for both steps of splicing [30] and is the only snRNP found in all three types of splicing: major-, minor- and trans-splicing. The U5-snRNP-specific proteins Prp8 and Brr2 are also found in other deep-branching eukaryotes including Trypanosoma brucei [31] and Trichomonas vaginalis [32]. The Prp8 protein, a large, unique and highly conserved protein which has no obvious homology to other proteins, has a central role within the spliceosome and makes extensive protein-protein interactions throughout the various stages of pre-mRNA splicing [33].

Therefore, given the likely presence of U5, Prp8 and many other spliceosomal protein components as well as a few spliceosomal introns, it seems highly likely that Giardia has a functional major spliceosome containing all five spliceosomal snRNAs. The aim here is to test these predictions. We found that using information from some candidates helped identifying others; e.g. U2 helped find U6, which then helped identify a good U4 candidate. This leads to the conclusion that Giardia spliceosome may contain the basic components seen in more highly researched eukaryotes such as human, yeast, and plants.


Prediction of a Giardia U1-snRNA candidate

Searching for U-snRNA candidates from Giardia based on primary sequence similarity failed, as expected, due to the observed low sequence similarity between Giardia and other well studied eukaryotes. However, the generally conserved structures of the U-snRNAs may allow a more advanced computational search for new U-snRNA candidates from the fully sequenced Giardia genome [34], [35]. Due to the reduced nature of the Giardia genome [21], [23], [35][37], it is not unlikely that some of the ncRNAs from Giardia also have been reduced in size and structure. For example, it has been shown that the U1 snRNA from Trypanosoma brucei is unusually reduced in that it only contains one stem-loop structure in contrast to the usual five stem-loops seen in other eukaryotes [38].

Besides structural information, sequence motifs of the U-snRNAs can also aid computational searches. It is known that U1-snRNA and U2-snRNA have direct interactions with introns through complementary nucleotide sequences; U1 binds to the 5′-intron splice site and U2 binds loosely at the branch site [39]. The three spliceosomal introns in Giardia [4], [5] share sequence similarities which indicate the presence of conserved 5′-, 3′- splice sites and the branch site [4]. Together with the conserved U-rich Sm-binding site, these sequence elements can be incorporated into a computational search for snRNAs from Giardia.

The computational prediction for U1-snRNA candidates was done using RNAbob (Materials and Methods). Since it was not known whether the U1-snRNA from Giardia was typical with conserved structure similar to human U1, or reduced like U1 from T. brucei [38], a relaxed model was set using the structural information from both the human and T. brucei U1-snRNA with human U1-snRNA as the upper limit of complexity and T. brucei U1-snRNA as the lower limit of complexity (Figure 1B). The stem-1 and stem-2 which were seen in both human and T. brucei are highly conserved at the loop sequence (Figure 1B). Therefore this loop sequence (conserved as “AUCACGAA”) is also incorporated into the search. Finally, a terminal stem which is present in both human and T. brucei was also used as a searching criterion. The descriptor file for U1 was written according to the proposed structure of the U1 candidate as shown in Figure 1A. This proposed structure is deduced based on known U1-snRNA structures together with information on the intron boundaries [4]. The descriptor file for searching U1 candidates is attached in supplementary information (Text S1).

Figure 1. Identification of a Giardia U1-snRNA candidate.

A. Proposed structure for writing the U1 descriptor file. The content in the U-1 descriptor cell can be visualized in this figure. “s” stands for strand and “h” stands for helix. The elements within the proposed U-1 structure are marked in order from the 5′-end to the 3′-end. The two stem-loops drawn as dotted lines are not compulsory in the proposed structure of Giardia U-1 candidate; therefore they are marked as a free-folding strand s4. B. The structures of Human, T. brucei and Giardia-candidate U1-snRNAs. The conserved loops among the human, Giardia and Trypanosome U1-snRNAs are indicated by the circles. The Sm-protein-binding sites are boxed. C. RT-PCR test showing high expression the of the Giardia U1-snRNA candidate. + control: PCR with genomic DNA. − control: PCR with total RNA without reverse transcription.

This search produced only one output sequence, which has two copies in the Giardia genome, differing by only one base (see later). Their secondary structure has four stem-loop structures, two more stem-loops (stem-loop 3 in Figure 1B) than T. brucei. Thus the Giardia candidate is intermediate between the standard eukaryotic pattern as found in human, and the reduced one in T. brucei. Structural modelling based on the conserved structural and sequence elements as highlighted in the figure (Figure 1B) shows that it is a good U1-snRNA candidate.Expression of this Giardia U1-snRNA candidate was confirmed by RT-PCR (Figure 1C).

Prediction of a Giardia U2-snRNA candidate

The same method was initially applied to search for U2 snRNAs from Giardia. However, this search did not give any results, probably due to the high degree of specificity required for constructing the descriptor file. Subsequently, a more general approach was tried. The new approach used the available sequences of U-snRNAs from Rfam [40] to search for the corresponding ncRNAs from the Giardia genome using the cmbuild and cmsearch programmes within the INFERNAL software package [41].

Two controls, one with U5 and the other with U1, were carried out to test the sensitivity of cmsearch. A control cmsearch using U5 snRNA was performed first. Using the model built from the alignment of 33 seed-sequences, the search resulted in 395 potential U5 sequences, including the previously reported U5 candidate [8]. This control strengthened the likelihood of obtaining a good candidate using cmsearch, but was clearly too general. A second control searching for U1 candidates was also performed. However, the putative U1 candidate found by RNAbob was not in the output which contains 29 sequences in total. This was not unexpected as the Giardia U1 candidate predicted by RNAbob has one stem-loop less than the conserved typical U1 structure (see Figure 1B), thus the search may have bypassed the Giardia sequence.

The cmsearch output for U2 produced only 5 hits. Blasting these hits against the Giardia genome database ( showed that 3 of the U2 hits lie within non-coding regions (including on the minus strand of protein-coding genes). Since the number of potential U2 candidates is small, RT-PCR analysis was carried out to test the expression of these hits, though the small number of hits may not cover all possible U2 candidates. Results (Figure 2A) clearly show that two of the three candidates (candidate-2 and candidate-3) are expressed and candidate-2 is highly expressed. Although candidate-3 is also shown to be expressed, it appears much less abundant than candidate-2. Structural modelling (Figure 2B) and sequence analysis show that candidate-2 is the most likely candidate for U2-snRNA.

Figure 2. Identification of a Giardia U2-snRNA candidate.

A. RT-PCR test for expression of the Giardia U2-snRNA candidates. The highly expressed candidate 2 was analysed further. − control: PCR with total RNA without reverse transcription. + control: PCR with genomic DNA. B. Structure of Giardia U2-snRNA candidate and its interaction with the branch-point intron region.

In the active spliceosome, the bulged branch-site adenosine is crucial for the function of the spliceosome. It is expected that any potential U2-candidate from Giardia must have a sequence motif complementary to the branch site. The likely U2-candidate shown in Figure 2B contains a “UAGUU” motif which complements the 5′ of intron branch site “AACUG (or AACUA)”, but does not have upstream bases that can bind to 3′ of the branch-site adenosine (coloured red), thus instead of leaving the branch-site adenosine bulged this interaction leaves an open-end at the branch site. However this alteration of branch-site recognition may not induce any functional difference because the branch-site adenosine is still free to attack the 5′-guanosine phosphate. The overall sequence of this U2-snRNA candidate can fold into a typical U2-snRNA structure with the presence of a putative Sm-binding site, suggesting it to be a good candidate for U2-snRNA. This U2 candidate was used subsequently in searching for U6 and U4 snRNA candidates.

Prediction of Giardia U6 and U4 snRNA candidates

Potential candidates for U6 and U4 snRNAs were first searched using INFERNAL. The outputs for U6 and U4 were large (1052 and 217 sequences respectively), and blasting the hits against the Giardia genome showed that 649 of the U6 hits and 114 of the U4 hits lie within non-coding regions. The large number of hits caused difficulty in further analysis; therefore an alternative method was used to search for U6 and U4 candidates based on the interactions between U2 and U6, and between U6 and U4.

It is known that conserved base pairings form between U2 and U6, and between U6 and U4 snRNAs during the dynamic process of splicing. These conserved base-pairings are shown in Figure 3A1-2. In the U2-U6 complex, the central region of U6-snRNA folds into an intramolecular-stem-loop (ISL) structure, which is highly conserved in the active spliceosome and juxtaposes the regions interacting with U2-snRNA [42]. The ISL has been shown to have important roles in the catalytic centre of the spliceosome with the uridine (indicated by * in the S. cerevisiae model shown in Figure 3A1) serving as a binding site for an Mg2+ ion during the catalytic step of splicing [43]. This uridine is seen in all but two U6-snRNAs from Rfam [44], and is usually situated below a “A·C” wobble base pair, which is readily protonated [43]. Mutation of the bulged uridine within U6-ISL has been shown to be lethal due to its resulted alteration of “A·C” wobble base pair which is important for melting the U6-ISL during structural rearrangement necessary for association with U4-snRNA [45]. It was later shown that base substitutions within the “A·C” wobble base pair disrupt Prp24 protein binding and reduce stability of the U4/U6 complex [46]. The structure of U6 ISL is highly similar to the catalytic stem-loop structure of Group-II ribozyme [13], [47] and it appears that this structure has been maintained through evolution of the splicing mechanism [48], [49].

Figure 3. Identification of Giardia U6 and U4 snRNA candidates.

A1. Structure of U2-U6-snRNA base pairing in S. cerevisiae. A2. Structure of U6-U4-snRNA base pairing in Human. B1. Visualization of the model for searching a U6-snRNA candidate. B2. RT-PCR test for expression of the U6 candidate. + control: PCR with genomic DNA. − control: PCR with total RNA without reverse transcription. B3. Interaction between Giardia U6 and U2 snRNA candidates. C1. RT-PCR test for expression of the U4 candidate. + control: PCR with genomic DNA. − control: PCR with total RNA without reverse transcription. C2. Interaction between Giardia U6 and U4 snRNA candidates.

In addition, two sequence motifs on the U6-snRNA are also conserved (coloured red in Figure 3A1). The “ACAGAG” is involved in base-pairing with the 5′-intron site and the branch site [47]. The invariant “AGC” tri-nucleotide is seen in all identified U6-snRNAs recorded in Rfam [44], and has both structural and functional roles during splicing [47]. A recent study also showed that the “ACAGAG” loop and “AGC” tri-nucleotide were binding sites of Mg2+ [50]. U6 and U4 also form extensive base-pairings [51] as shown in Figure 3A2. In this hybrid, the U6-snRNA has formed a 5′-stem-loop structure. Gathering all the sequence and structural features of U-snRNAs, Table 1 lists all the consensus properties used for searching U6 and U4 snRNA candidates.

A trial to search for a Giardia U6-snRNA candidate was carried out before U4 because there are more conserved features known for the U6-snRNA. A descriptor file (see supplementary information, Text S2) for the RNAbob programme was written based on the consensus features around the ISL, including the “AAC” motif which binds Giardia U2 at the 5′ end of the “ACAGAG” loop, and the “ACAGAG” motif and the “AGC” invariant tri-nucleotide which are two of the important characteristic features of U6-snRNA. The criteria used for writing the descriptor file can be visualized in Figure 3B1.

The descriptor file was then used to search against the whole genome sequence of Giardia. This gave 4 output sequences, of which two lie in non-coding regions. 40nt sequences upstream and downstream of the two output sequences were analysed. One of the two sequences has all the compulsory features of U6-snRNA (see Table 1), and was therefore identified as a candidate, even though this candidate is not found using INFERNAL-cmsearch. This is again possibly due to the low sequence conservation between Giardia U6 and those from most other organisms which were used as seeds for constructing the cmsearch model. Indeed low sequence conservation was the major problem in identifying Giardia ncRNAs and earlier trials to look for U6-candidates failed with sequence similarity search. RT-PCR testing has confirmed that this potential U6-snRNA candidate is highly expressed. Results are shown in Figure 3B2. Figure 3B3 shows the RNA complex formed by the U2 and U6 snRNA candidates from Giardia. Conserved sequence elements on the U6-snRNA candidate are coloured in blue.

Having used the U2 candidate to find U6, the U6 candidate was then used to search for a possible U4 candidate based on the conserved U6-U4 base-pairing feature shown in the human model in Figure 3A2. First, a potential U4-snRNA candidate was searched for from the 114 output sequences of INFERNAL-cmsearch. A few sequences from the cmsearch output contain a putative Sm-binding site but just one of them shows base-pairing with the U6-snRNA candidate. Expression of this sequence was tested by RT-PCR and the result (Figure 3C1) shows clear and high expression. The interaction between Giardia U6 and U4 snRNA candidates is shown in Figure 3C2. This structure (Figure 3C2) is consistent with the prediction that this is a good U4-candidate.

Transcriptional patterns of the Giardia U-snRNA candidates

All five Giardia U-snRNA candidates are found in transcriptionally intensive regions (rich in open reading frames) of the genome; most of them overlap with protein-coding genes on the antisense strands. Gene overlapping is very common in the reduced genome of Giardia, and the lengths between protein-coding genes are generally short (less than 200bp) [35]. Previously identified non-coding RNAs in Giardia [52][55] are all located either in intergenic regions or overlap with protein-coding genes on the antisense strands. Therefore the locations of the U-snRNA candidates identified here are as expected. Except for the U1 candidate which has two copies with just a single base substitution between them, the other candidates all have a single copy in the genome. The locations of Giardia U-snRNA candidates in relation to the positions of nearby protein-coding genes are shown in supplementary information (Figure S1).

The upstream 100nt sequence for each U-snRNA candidate was extracted from the genome and analysed. It is known that in most eukaryotes, the U6-snRNA is transcribed by RNA Pol III [56], and the other four snRNAs are transcribed by RNA Pol II. The Pol II promoter sequence in Giardia has been shown to be roughly conserved [34], but there has been no Pol III consensus sequence for Giardia published to date. Our studies on the potential promoter elements in Giardia (unpublished data) shows that two “A”-rich motifs are likely to be the upstream promoter elements of Pol III. This information provides the basis for further analysis of the upstream sequences of the Giardia snRNA candidates.

The general eukaryotic U6 promoter contains an upstream “TATA-box” and also upstream enhancer elements [56], [57]. The upstream sequence of Giardia U6-snRNA candidate does not show a “TATA-box” motif. The upstream sequences of the other four U-snRNA candidates do not show strong signals of either Pol II or Pol III promoter elements. Absence of significant promoter signals indicates that these candidates may be examples of ncRNA genes being co-transcribed with adjacent protein-coding genes. The same feature is seen in more than half of the new ncRNAs candidates expressed in Giardia [54].


This study has found four good candidates for Giardia snRNAs through computational methods, and confirmed by RT-PCR analysis that they are highly expressed. A U5 candidate was reported earlier [8]. The sequences and genomic locations of five (U1, U2, U4, U5 and U6) Giardia U-snRNA candidates are listed as supplementary information (Text S3). Previously, only one (U5) snRNA had been identified in Giardia, so it had appeared possible that the ancestral spliceosome was mainly protein based, and that the catalytic role of snRNAs had evolved later in eukaryotic evolution. Now it seems likely that the last common ancestor of modern eukaryotes had a full spliceosome that functioned in much the same way as in plants, animals and fungi – that is, with functional snRNAs. Apart from the primary tests of expression, the Giardia U-snRNA candidates found here have not been extensively verified by biochemical methods. Two types of tests could carry this work on further. Detailed biochemical tests are now possible based on the candidates we identified however this is not yet straightforward. On the other hand, computational tests can now be done to search for snRNAs in related genomes, although they do not replace biochemical studies. Trichomonas and Trypanosomes would be good candidates because their genomes are complete. A very recent study has found U-snRNAs in Trichomonas [58], supporting our prediction that major spliceosomal snRNAs are likely to be common in all eukaryotes.

Combining sequence and structural information (which summarises conserved features of characterised ncRNAs) appears to be an efficient way of searching for unknown homologues of these ncRNAs in phylogenetically distant lineages. The structures of non-coding RNAs are important for their functions. Like proteins, non-coding RNAs with similar functions need not share extensive sequence similarities; however they generally fold into similar structures. A number of computational methods have been developed to fold a single RNA sequence [59], [60]; however, computationally predicted structures are often different from the true structures in vivo, because the folding of RNAs in the cell is usually associated with protein-cofactor binding and different metal ion associations. These conditions are hard to simulate. The structures of non-coding RNAs can be determined more reliably from other phylogenetically or functionally related non-coding RNAs which have been previously characterised.

The primary results from this study show that homologues of spliceosomal snRNAs are found in Giardia. Although evolutionary divergence between Giardia and other eukaryotes causes difficulties, combining different computational approaches based on available biological information has proved to be an efficient strategy. The snRNA candidates found in this study can be used as examples of snRNAs in evolutionarily deep-branching eukaryotes and help understanding of the evolution of the major spliceosome.

In this study, two software packages with different approaches were applied to search for the U-snRNA candidates in Giardia. The INFERNAL software uses covariance models [61] which optimize the alignment of an RNA sequence to a conserved RNA structure. INFERNAL is comparable to the HMMER package, which builds profile Hidden Markov models for searching for homologous protein sequences from a database. Eukaryotic U-snRNAs from Rfam have been annotated with the INFERNAL package with multiple alignments and conserved secondary structures. These alignments were used in searching for potential U-snRNAs from the Giardia genome. In contrast, RNAbob uses a user-specified input descriptor file which specifies the expected sequence and structural motifs, and searches for matching motifs in a sequence database.

Although we are not comparing these software packages, it was clear that the searching algorithms have differing sensitivities. The RNAbob programme used here is highly sensitive for searching RNAs with known structures and conserved sequence motifs, but requires enough information to construct a descriptor file. On the other hand, the INFERNAL software applies to more general searches using alignments of both sequences and structures of seed RNAs; however successful searches using this method largely depend on the prerequisite that the candidate RNA is highly conserved at both sequence and structural levels with the seed RNAs used for the search. In this study of Giardia U-snRNAs, it was not clear as to what degree Giardia U-snRNAs may be conserved with other known U-snRNAs, therefore it was highly desirable to employ two search methods using different approaches to find candidates efficiently.

It is important to rely firstly on the biological information of the particular candidate before choosing a computational method. Using different computer programmes can increase the likelihood of finding the expected RNA candidate, although the outputs of different search methods do not always overlap. In all, our identification of Giardia snRNA candidates demonstrates an efficient way of searching for novel non-coding RNAs by combining biological information with computational methods. This approach is especially applicable where large scale biochemical isolation is not feasible. Results from this study also indicate that major spliceosomal snRNAs are highly likely to be present in ancestral eukaryotes, because they are found in all eukaryotes including the deep-branching lineages such as Giardia. This finding, if confirmed by future work, supports the highly distinctive nature of the eukaryotic cell [1].

Materials and Methods

Computational methods

The RNAbob source code was downloaded from, and modified to run under Windows. This programme uses a descriptor file which specifies the structure and sequence motifs of the RNA to be searched, and looks for matching candidates from a sequence database. The descriptor file for U1-snRNA was constructed using the information available for Giardia. The search model was set so that the expected output would have the 5′-intron site recognition sequence “AACAUA”, which complements the “UUGUAU” sequence at the 5′ end of the intron. The Sm-binding sequence was set to “AANUUUGN” where N indicates an uncertain nucleotide. All the “U”s are written as “T”s in the descriptor file for searching in a DNA genome.

In the descriptor file, lines starting with “#” are comments. The “strands” and “helices” elements within the proposed structure are listed in order, and each of them is then specified. “N” represents an uncertain nucleotide which is definitely present and “*” represents an optional nucleotide. [ ] indicates the maximum number of nucleotides present. Optional stems were replaced by long strands. The numbers immediately following an element (s1, h1 etc.) described indicate number of mismatches allowed. For example “h1 0:0” shows that no mismatches are allowed in the helix h1.

The INFERNAL software was downloaded from, and alignments of snRNAs from various species were downloaded in Stockholm format from the Rfam database [44]. The INFERNAL programmes were run under the Linux operating system with the default settings.

The alignments of U1, U2, U4, U5, and U6 were downloaded from Rfam [44] and covariance models for these alignments were built using the INFERNAL-cmbuild programme. Searching for potential U-snRNAs from the Giardia genome was done by the INFERNAL-cmsearch programme. An output hit from cmsearch consists of an alignment and a score. By default, scores above 0 are considered as hits.

Giardia total RNA preparation

Total RNA was extracted from Giardia WB strain Trophozoites grown in TY1-S-33 media. Cells were collected by centrifugation (10 min, 3000rpm, 4°C). RNA extraction was performed using Trizol reagent (Invitrogen, Cat# 15596-026) according to the manufacturer's instruction. The extracted RNA was dissolved in sterile double-distilled water. The purified RNA was treated with DNase-I (Roche Cat# 04 716 728 001) for 1 hour and purified by phenol/chloroform extraction and ethanol precipitation.


All the RT-PCR reactions were performed using the Thermoscript cDNA synthesis kit (Invitrogen, Cat# 11146024). Total RNA treated with DNase was mixed with the corresponding reverse primer and dNTPs. The mixture was heated to 85°C for 2 min and cooled gradually. Then a mixture of reaction buffer, RNaseOUT and reverse transcription enzyme was added. All RT reactions were carried out for 1 h at 55°C and then heated to 85°C to inactivate the enzyme. 2 µl RT reaction was taken out to serve as the template for the downstream PCR reaction. Results were analyzed on 2% agarose gels. Primers used for testing expression of the U2, U4 and U6 snRNA candidates are listed below:


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Supporting Information

Text S2.

U6 central region descriptor file

(0.00 MB TXT)

Text S3.

Sequences and genomic locations of Giardia snRNA candidates

(0.00 MB TXT)

Figure S1.

Locations of Giardia snRNA candidates In this figure, black arrows indicate the direction of protein-coding-gene transcription and grey arrows indicate the direction of Giardia U-snRNA candidates. The lengths of arrows are not proportional to the actual lengths of transcripts, because the mRNA transcripts are much longer than the snRNA candidates.

(0.78 MB TIF)


Thanks to Errol Kwan from MicroAquatech for supplying Giardia cell culture. This work was supported by the Marsden Fund New Zealand and the Allan Wilson Centre.

Author Contributions

Conceived and designed the experiments: XC LC DP. Performed the experiments: XC WTJW. Analyzed the data: XC. Contributed reagents/materials/analysis tools: XC WTJW. Wrote the paper: XC.


  1. 1. Kurland CG, Collins LJ, Penny D (2006) Genomics and the irreducible nature of eukaryote cells. Science 312: 1011–1014.
  2. 2. Martin W, Dagan T, Koonin EV, Dipippo JL, Gogarten JP, et al. (2007) The evolution of eukaryotes. Science 316: 542–543; author reply 542–543.
  3. 3. Vanacova S, Yan W, Carlton JM, Johnson PJ (2005) Spliceosomal introns in the deep-branching eukaryote Trichomonas vaginalis. Proc Natl Acad Sci U S A 102: 4430–4435.
  4. 4. Russell AG, Shutt TE, Watkins RF, Gray MW (2005) An ancient spliceosomal intron in the ribosomal protein L7a gene (Rpl7a) of Giardia lamblia. BMC Evol Biol 5: 45.
  5. 5. Nixon JE, Wang A, Morrison HG, McArthur AG, Sogin ML, et al. (2002) A spliceosomal intron in Giardia lamblia. Proc Natl Acad Sci U S A 99: 3701–3705.
  6. 6. Collins L, Penny D (2005) Complex spliceosomal organization ancestral to extant eukaryotes. Mol Biol Evol 22: 1053–1066.
  7. 7. Keeling PJ, Burger G, Durnford DG, Lang BF, Lee RW, et al. (2005) The tree of eukaryotes. Trends Ecol Evol 20: 670–676.
  8. 8. Collins LJ, Macke TJ, Penny D (2003) Searching for ncRNAs in eukaryotic genomes: Maximizing biological input with RNAmotif. Journal of Integrative Bioinformatics 0001:
  9. 9. Irimia M, Roy SW (2008) Spliceosomal introns as tools for genomic and evolutionary analysis. Nucleic Acids Res 36: 1703–1712.
  10. 10. Jeffares DC, Mourier T, Penny D (2006) The biology of intron gain and loss. Trends Genet 22: 16–22.
  11. 11. Nilsen TW (2003) The spliceosome: the most complex macromolecular machine in the cell? Bioessays 25: 1147–1149.
  12. 12. Valadkhan S, Mohammadi A, Wachtel C, Manley JL (2007) Protein-free spliceosomal snRNAs catalyze a reaction that resembles the first step of splicing. Rna 13: 2300–2311.
  13. 13. Valadkhan S (2005) snRNAs as the catalysts of pre-mRNA splicing. Curr Opin Chem Biol 9: 603–608.
  14. 14. Hinas A, Larsson P, Avesson L, Kirsebom LA, Virtanen A, et al. (2006) Identification of the major spliceosomal RNAs in Dictyostelium discoideum reveals developmentally regulated U2 variants and polyadenylated snRNAs. Eukaryot Cell 5: 924–934.
  15. 15. Ambrosio DL, Silva MT, Cicarelli RM (2007) Cloning and molecular characterization of Trypanosoma cruzi U2, U4, U5, and U6 small nuclear RNAs. Mem Inst Oswaldo Cruz 102: 97–105.
  16. 16. Miranda R, Salgado LM, Sanchez-Lopez R, Alagon A, Lizardi PM (1996) Identification and analysis of the u6 small nuclear RNA gene from Entamoeba histolytica. Gene 180: 37–42.
  17. 17. Vankan P, Edoh D, Filipowicz W (1988) Structure and expression of the U5 snRNA gene of Arabidopsis thaliana. Conserved upstream sequence elements in plant U-RNA genes. Nucleic Acids Res 16: 10425–10440.
  18. 18. Brown JW, Waugh R (1989) Maize U2 snRNAs: gene sequence and expression. Nucleic Acids Res 17: 8991–9001.
  19. 19. Hofmann CJ, Marshallsay C, Waibel F, Filipowicz W (1992) Characterization of the genes encoding U4 small nuclear RNAs in Arabidopsis thaliana. Mol Biol Rep 17: 21–28.
  20. 20. Jurica MS, Moore MJ (2003) Pre-mRNA splicing: awash in a sea of proteins. Mol Cell 12: 5–14.
  21. 21. Vanacova S, Liston DR, Tachezy J, Johnson PJ (2003) Molecular biology of the amitochondriate parasites, Giardia intestinalis, Entamoeba histolytica and Trichomonas vaginalis. Int J Parasitol 33: 235–255.
  22. 22. Dacks JB, Marinets A, Ford Doolittle W, Cavalier-Smith T, Logsdon JM Jr. (2002) Analyses of RNA Polymerase II genes from free-living protists: phylogeny, long branch attraction, and the eukaryotic big bang. Mol Biol Evol 19: 830–840.
  23. 23. Best AA, Morrison HG, McArthur AG, Sogin ML, Olsen GJ (2004) Evolution of eukaryotic transcription: insights from the genome of Giardia lamblia. Genome Res 14: 1537–1547.
  24. 24. Yean SL, Lin RJ (1991) U4 small nuclear RNA dissociates from a yeast spliceosome and does not participate in the subsequent splicing reaction. Mol Cell Biol 11: 5571–5577.
  25. 25. Hausner TP, Giglio LM, Weiner AM (1990) Evidence for base-pairing between mammalian U2 and U6 small nuclear ribonucleoprotein particles. Genes Dev 4: 2146–2156.
  26. 26. Datta B, Weiner AM (1991) Genetic evidence for base pairing between U2 and U6 snRNA in mammalian mRNA splicing. Nature 352: 821–824.
  27. 27. Madhani HD, Guthrie C (1992) A novel base-pairing interaction between U2 and U6 snRNAs suggests a mechanism for the catalytic activation of the spliceosome. Cell 71: 803–817.
  28. 28. Sun JS, Manley JL (1995) A novel U2-U6 snRNA structure is necessary for mammalian mRNA splicing. Genes Dev 9: 843–854.
  29. 29. Collins CA, Guthrie C (2000) The question remains: is the spliceosome a ribozyme? Nat Struct Biol 7: 850–854.
  30. 30. Dix I, Russell CS, O'Keefe RT, Newman AJ, Beggs JD (1998) Protein-RNA interactions in the U5 snRNP of Saccharomyces cerevisiae. Rna 4: 1675–1686.
  31. 31. Lucke S, Klockner T, Palfi Z, Boshart M, Bindereif A (1997) Trans mRNA splicing in trypanosomes: cloning and analysis of a PRP8-homologous gene from Trypanosoma brucei provides evidence for a U5-analogous RNP. Embo J 16: 4433–4440.
  32. 32. Fast NM, Doolittle WF (1999) Trichomonas vaginalis possesses a gene encoding the essential spliceosomal component, PRP8. Mol Biochem Parasitol 99: 275–278.
  33. 33. Grainger RJ, Beggs JD (2005) Prp8 protein: at the heart of the spliceosome. Rna 11: 533–557.
  34. 34. McArthur AG, Morrison HG, Nixon JE, Passamaneck NQ, Kim U, et al. (2000) The Giardia genome project database. FEMS Microbiol Lett 189: 271–273.
  35. 35. Morrison HG, McArthur AG, Gillin FD, Aley SB, Adam RD, et al. (2007) Genomic minimalism in the early diverging intestinal parasite Giardia lamblia. Science 317: 1921–1926.
  36. 36. Edlind TD, Chakraborty PR (1987) Unusual ribosomal RNA of the intestinal parasite Giardia lamblia. Nucleic Acids Res 15: 7889–7901.
  37. 37. Adam RD (2001) Biology of Giardia lamblia. Clin Microbiol Rev 14: 447–475.
  38. 38. Palfi Z, Schimanski B, Gunzl A, Lucke S, Bindereif A (2005) U1 small nuclear RNP from Trypanosoma brucei: a minimal U1 snRNA with unusual protein components. Nucleic Acids Res 33: 2493–2503.
  39. 39. Das R, Zhou Z, Reed R (2000) Functional association of U2 snRNP with the ATP-independent spliceosomal complex E. Mol Cell 5: 779–787.
  40. 40. Griffiths-Jones S, Bateman A, Marshall M, Khanna A, Eddy SR (2003) Rfam: an RNA family database. Nucleic Acids Res 31: 439–441.
  41. 41. Eddy SR (2006) Computational analysis of RNAs. Cold Spring Harb Symp Quant Biol 71: 117–128.
  42. 42. Fortner DM, Troy RG, Brow DA (1994) A stem/loop in U6 RNA defines a conformational switch required for pre-mRNA splicing. Genes Dev 8: 221–233.
  43. 43. Huppler A, Nikstad LJ, Allmann AM, Brow DA, Butcher SE (2002) Metal binding and base ionization in the U6 RNA intramolecular stem-loop structure. Nat Struct Biol 9: 431–435.
  44. 44. Griffiths-Jones S, Moxon S, Marshall M, Khanna A, Eddy SR, et al. (2005) Rfam: annotating non-coding RNAs in complete genomes. Nucleic Acids Res 33: D121–124.
  45. 45. Sashital DG, Allmann AM, Van Doren SR, Butcher SE (2003) Structural basis for a lethal mutation in U6 RNA. Biochemistry 42: 1470–1477.
  46. 46. McManus CJ, Schwartz ML, Butcher SE, Brow DA (2007) A dynamic bulge in the U6 RNA internal stem loop functions in spliceosome assembly and activation. Rna 13: 2252–2265.
  47. 47. Sashital DG, Cornilescu G, McManus CJ, Brow DA, Butcher SE (2004) U2-U6 RNA folding reveals a group II intron-like domain and a four-helix junction. Nat Struct Mol Biol 11: 1237–1242.
  48. 48. Seetharaman M, Eldho NV, Padgett RA, Dayie KT (2006) Structure of a self-splicing group II intron catalytic effector domain 5: parallels with spliceosomal U6 RNA. Rna 12: 235–247.
  49. 49. Lehmann K, Schmidt U (2003) Group II introns: structure and catalytic versatility of large natural ribozymes. Crit Rev Biochem Mol Biol 38: 249–303.
  50. 50. Yuan F, Griffin L, Phelps L, Buschmann V, Weston K, et al. (2007) Use of a novel Forster resonance energy transfer method to identify locations of site-bound metal ions in the U2-U6 snRNA complex. Nucleic Acids Res 35: 2833–2845.
  51. 51. Nottrott S, Urlaub H, Luhrmann R (2002) Hierarchical, clustered protein interactions with U4/U6 snRNA: a biochemical role for U4/U6 proteins. Embo J 21: 5527–5538.
  52. 52. Yang CY, Zhou H, Luo J, Qu LH (2005) Identification of 20 snoRNA-like RNAs from the primitive eukaryote, Giardia lamblia. Biochem Biophys Res Commun 328: 1224–1231.
  53. 53. Niu XH, Hartshorne T, He XY, Agabian N (1994) Characterization of putative small nuclear RNAs from Giardia lamblia. Mol Biochem Parasitol 66: 49–57.
  54. 54. Chen XS, Rozhdestvensky TS, Collins LJ, Schmitz J, Penny D (2007) Combined experimental and computational approach to identify non-protein-coding RNAs in the deep-branching eukaryote Giardia intestinalis. Nucleic Acids Res 35: 4619–4628.
  55. 55. Marquez SM, Harris JK, Kelley ST, Brown JW, Dawson SC, et al. (2005) Structural implications of novel diversity in eucaryal RNase P RNA. Rna 11: 739–751.
  56. 56. Kunkel GR, Pederson T (1988) Upstream elements required for efficient transcription of a human U6 RNA gene resemble those of U1 and U2 genes even though a different polymerase is used. Genes Dev 2: 196–204.
  57. 57. Jensen RC, Wang Y, Hardin SB, Stumph WE (1998) The proximal sequence element (PSE) plays a major role in establishing the RNA polymerase specificity of Drosophila U-snRNA genes. Nucleic Acids Res 26: 616–622.
  58. 58. Simoes-Barbosa A, Meloni D, Wohlschlegel JA, Konarska MM, Johnson PJ (2008) Spliceosomal snRNAs in the unicellular eukaryote Trichomonas vaginalis are structurally conserved but lack a 5′-cap structure. Rna 14: 1617–1631.
  59. 59. Hofacker IL (2003) Vienna RNA secondary structure server. Nucleic Acids Res 31: 3429–3431.
  60. 60. Mathews DH, Disney MD, Childs JL, Schroeder SJ, Zuker M, et al. (2004) Incorporating chemical modification constraints into a dynamic programming algorithm for prediction of RNA secondary structure. Proc Natl Acad Sci U S A 101: 7287–7292.
  61. 61. Eddy SR (2002) A memory-efficient dynamic programming algorithm for optimal alignment of a sequence to an RNA secondary structure. BMC Bioinformatics 3: 18.