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Putative SF2 helicases of the early-branching eukaryote Giardia lamblia are involved in antigenic variation and parasite differentiation into cysts

Pablo R Gargantini*, Marianela C Serradell, Alessandro Torri and Hugo D Lujan

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Laboratory of Biochemistry and Molecular Biology, School of Medicine, Catholic University of Córdoba, Córdoba, X5004ASK, Argentina

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Citation and License

BMC Microbiology 2012, 12:284  doi:10.1186/1471-2180-12-284

The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2180/12/284


Received:16 August 2012
Accepted:23 November 2012
Published:28 November 2012

© 2012 Gargantini et al.; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

Regulation of surface antigenic variation in Giardia lamblia is controlled post-transcriptionally by an RNA-interference (RNAi) pathway that includes a Dicer-like bidentate RNase III (gDicer). This enzyme, however, lacks the RNA helicase domain present in Dicer enzymes from higher eukaryotes. The participation of several RNA helicases in practically all organisms in which RNAi was studied suggests that RNA helicases are potentially involved in antigenic variation, as well as during Giardia differentiation into cysts.

Results

An extensive in silico analysis of the Giardia genome identified 32 putative Super Family 2 RNA helicases that contain almost all the conserved RNA helicase motifs. Phylogenetic studies and sequence analysis separated them into 22 DEAD-box, 6 DEAH-box and 4 Ski2p-box RNA helicases, some of which are homologs of well-characterized helicases from higher organisms. No Giardia putative helicase was found to have significant homology to the RNA helicase domain of Dicer enzymes. Additionally a series of up- and down-regulated putative RNA helicases were found during encystation and antigenic variation by qPCR experiments. Finally, we were able to recognize 14 additional putative helicases from three different families (RecQ family, Swi2/Snf2 and Rad3 family) that could be considered DNA helicases.

Conclusions

This is the first comprehensive analysis of the Super Family 2 helicases from the human intestinal parasite G. lamblia. The relative and variable expression of particular RNA helicases during both antigenic variation and encystation agrees with the proposed participation of these enzymes during both adaptive processes. The putatives RNA and DNA helicases identified in this early-branching eukaryote provide initial information regarding the biological role of these enzymes in cell adaptation and differentiation.

Keywords:
RNA/DNA helicases; Giardia lamblia; Encystation; Antigenic variation; Cell differentiation; Gene expression; RNAi; Dicer

Background

Helicases are encoded by a large fraction of prokaryotic and eukaryotic genomes and are found in all organisms –from bacteria to humans– and in many viruses. These nucleic acid-dependent NTPases (preferentially ATPases) have the ability to unwind DNA or RNA duplex substrates; to unwind/separate the helical structure of double-stranded nucleic acids and, in some cases, to disrupt protein-nucleic acid interactions [1,2].

DNA and RNA helicases are grouped into six superfamilies (SF). SF1 and SF2 do not form rings, whereas SF3 to SF6 comprise the ring-forming helicases [3]. All eukaryotic RNA helicases belong to SF1 and SF2, whereas the ring-shaped RNA helicases are found in viruses [4] and bacteria [5,6]. Functional groups for ATP binding and hydrolysis are highly conserved among SF1 and SF2 DNA and RNA helicases. In addition, these two superfamilies show high sequence similarity in their conserved regions, sharing eight conserved motifs; and variations within these conserved motifs are used to distinguish between these very closely related families.

The helicases from SF1 and SF2 are further divided into families, based on their sequence, structural, and mechanistic features [3,7]. According to an excellent classification proposed by Jankowsky’s group, these helicases can be grouped into three families in the SF1 and nine families and one group in the SF2 [8]. Although several helicase families contain both RNA and DNA helicases, six of these twelve families only contain RNA helicases (DEAD-box, DEAH-box, Ski2-like, RIG-I-like, NS3/NPH-II and Upf1-like families). As they are mainly composed by RNA helicases, these 6 families are termed “RNA helicase families”, and are often referred to as DExD/H proteins.

In the SF1 and SF2 helicases, the conserved motifs are clustered in a “central” core region that spans about 350 to 400 amino acids (named “Helicase Core Domain” - HCD). By contrast, the N- and C-terminal extensions of helicases are highly variable in size and composition. These regions are supposed to confer substrate specificity, comprising protein- and/or RNA-binding motifs that provide helicases with their capacity to be involved in multiple processes, and/or direct the helicases to their subcellular localization [9,10]. Within these extensions helicases also contain accessory domains that can confer specific functions, as in the case of the bidentate RNase III enzyme Dicer [11]. The conservation of these domains within a family is null; therefore, they are not used to define a typical group.

RNA is involved in virtually all aspects of gene expression, playing important regulatory roles in biological reactions and making RNAs biologically important molecules required by all living organisms. RNA helicases may act as a temporary clamp to prevent RNAs from re-associating, thereby allowing other RNA-RNA or RNA-protein interactions to occur. A recent report suggests that these proteins can also function as RNPases [12], which are enzymes that disrupt RNA-protein interactions.

Giardia lamblia is a single-celled eukaryotic microorganism that inhabits in the upper small intestine of humans and several other vertebrates. Phylogenetic studies have placed Giardia as one of the most early-branching eukaryotic cells [13-17]. In addition to its biological relevance, G. lamblia is one of the leading causes of human intestinal disease worldwide, the most frequent cause of defined waterborne outbreaks of diarrhea in developed countries and a common cause of diarrhea in daycare centers, institutionalized individuals, backpackers, and travelers [18]. The parasite has a simple life cycle, comprising the disease-causing trophozoites and the environmentally-resistant cysts, which are responsible for the transmission of the disease among susceptible hosts [18]. Giardia undergoes important adaptive mechanisms to survive both inside and outside the host’s intestine, such as “antigenic variation” and “encystation”, respectively [19]. Antigenic variation is characterized by the continuous switching of surface antigenic molecules, which allows the parasite to evade the immune response generated by the host [20]. In Giardia, antigenic variation involves variant-specific surface proteins (VSPs), cysteine-rich type 1a membrane proteins that cover the entire surface of the trophozoites [21]. Only one VSP, of approximately 200 VSP genes present in the parasite’s genome, is expressed on the surface of individual trophozoites at a given time, but switching to a different VSP occurs once every 6-18 generations. Antigenic variation in Giardia is regulated post-transcriptionally by a mechanism similar to RNA interference (RNAi) [22]. Notably, disruption of the RNAi pathway by knocking-down the expression of the dsRNA endonuclease Dicer promotes a change from single to multiple VSP expression on the surface of individual Giardia cells, indicating the direct involvement of this enzyme in controlling antigenic variation in this parasite [23]. Nonetheless, gDicer lacks the C-terminal RNA helicase domain, raising question about the function of this domain in Dicer enzymes of higher eukaryotes.

G. lamblia possesses functional RNAi machinery [22]. However, this early-branching eukaryote lacks Drosha and Exportin 5 molecules needed to process and export miRNA from the cell nucleus into the cytoplasm as well as other essential components of the RNAi machinery found in higher eukaryotes [24]. It was recently proposed, however, that lack of Drosha and Exportin 5 in Giardia could be bypassed by the use of snoRNAs as miRNAs precursors [25]. Interestingly, Giardia Dicer is still capable of robust dicing and of complementing the lack of a functional Dicer in Schizosaccharomyces pombe (which possesses the RNA helicase domain [26]) as well as ORF-derived miRNAs with gDicer apparently assuming the functions of both Drosha and Dicer [25]. Hence, two questions arise: (i) Are RNA helicases truly involved in the Giardia RNAi pathway? (ii) What is the minimal protein repertoire for post-transcriptional gene silencing in eukaryotic cells?

In the present study, we identified the complete set of SF2 helicases in this anaerobic flagellated protozoan by searching the G. lamblia genome database of the WB isolate, which allowed the identification of 22 DEAD-box, 6 DEAH-box and 4 Ski2p putative RNA helicases, along with seven helicases of family Swi2/Snf2, 3 helicases from family RecQ and 4 helicases from family Rad3. These sequences were used to analyze the relationship between the composition of the SF2 helicases in Giardia and their corresponding homologs in yeast and humans. In addition, the level of expression during antigenic variation and encystation was analyzed, demonstrating both differential and variable expression of individual RNA helicases in these processes. We also discuss the potential role of the RNA helicase domain in Dicer enzymes of higher eukaryotes.

Results

Identification of SF2 helicases in Giardia lamblia

By using the human eIF4A (Eukaryotic Initiation Factor 4A) amino acid sequence as the DEAD-box helicase prototype [27] and the human ATP-dependent RNA-helicase DHX8 amino acid sequence as the DEAH-box helicase prototype [27], we performed an extensive analysis of the Giardia assemblage A, isolate WB, genome database [28] and detected 22 and 6 orthologs, respectively. We were also able to obtain the sequences of 4 putative RNA helicases belonging to the Ski2 family, which is generally classified inside the DExH-box family; and a previously described UPF1 homolog from SF1 [29]. These helicases belong to three of the nine families described from SF2. Therefore, in an attempt to identify any other helicase from this superfamily we performed a PSI-BLASTP search within the Giardia genome using the sequences described from humans, yeast and Escherichia coli, following Fairman-Williams [8]. Using this approach, we were able to recognize 14 additional putative helicases from three different families, 3 helicases from the RecQ family, 7 helicases from the Swi2/Snf2 family, and 4 helicases from the Rad3 family. The sequences from the remaining three families of SF2 helicases present in humans, yeast and E. coli (RecG-like, RIG-I-like and NS3/NPH-II) do not have significant homology with any gene of G. lamblia.

The Giardia Database gene number, the Contig number and position, and the gene length and codified protein molecular weight for each one of the SF2 helicases studied in this work are summarized in Additional file 1: Table S1. The HCD is virtually conserved in length between the three RNA helicases families, ranging from 361 to 425 amino acids, whereas the greatest differences found, as expected, were in the N- and C-terminal regions of each helicase family (see Additional file 2: Table S2).

Additional file 1: Table S1. Putative SF2 Helicases from Giardia lamblia. The table indicates the Family, the gene number from the Assemblage A isolate WB (the number that is given should be preceded by the prefix GL50803_), the current Supercontig or positions where it is located, the number of nucleotides in base pairs (bp) and molecular mass of the putative protein in kDa, for each putative helicase. (DOCX 18 kb)

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Additional file 2: Table S2. Average lengths (amino acid) of SF2 helicase families from Giardia lamblia. The table indicates the average length (in number of amino acids) of each SF2 helicase family. The incompletes sequences were not considered in the computation.

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The presence of 8 to 10 motifs considered as “signature sequences” were useful for the classification of each putative RNA helicase within a specific family. This approach has already been used to identify DExD/H helicases in human, yeast, rice, Entamoeba histolytica, Plasmodium falciparum, Leishmania major, Trypanosoma cruzi and Trypanosoma brucei (Table 1). The relationship between the number of DEAD-box and DExH-box helicases supports our finding of 22 DEAD-box and 10 DExH-box (6 DEAH-box and 4 Ski2-like) in Giardia. Multiple sequence analysis generated a phylogenetic tree, showing the evolutionary separation of these six families (DEAD-box, DEAH-box, Ski2, RecQ, Rad3, and Swi2/Snf2) (see Additional file 3: Figure S1).

Additional file 3: Figure S1. Phylogenetic tree of the 46 putative SF2 helicase genes in Giardia lamblia. Phylogenetic tree derived from the alignment of the “Helicase Core Domain” amino acid sequences. Each helicase is named after its gene number, as in the GiardiaDB. The family groups are indicated as follows: DEAD-box (orange), DEAH-box (green), Ski2 (violet), RecQ (pink), Swi2/Snf2 (light orange) and Rad3 (light blue).

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Table 1. Number of putative DExD/H-box RNA helicases in other organisms

BLASTP analyses of the 46 G. lamblia SF2 helicases within the NCBI Human database presented the following ranges of identity and similarity, respectively: DEAD-box family (23–47% and 39–69%); DEAH-box family (26–39% and 42–54%); Ski2 family (28–43% and 47–63%); Swi2/Snf2 family (25–39% and 41–58%); RecQ family (25–32% and 41–50%); Rad3 family (27–35% and 47–51%). The unique UPF1 sequence presents 39% identity and 52% similarity to human UPF1. The yeast RNA helicase homologs, their predicted protein function and other features are also included in Additional file 4: Table S3 for each helicase identified in G. lamblia. The high sequence similarity between putatives RNA helicases from Giardia and the characterized homologous proteins suggest that they may have a similar function in RNA metabolism.

Additional file 4: Table S3. Giardia lamblia SF2 helicases homologues in human and yeast. The table indicates each putative Giardia helicase with its Accession Number and ORF, the protein length in aminoacid, its putative helicase homologue form human with the identity and similarity percentage, and its putative helicase homologue from yeast with their known functions.

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The DEAD-box family

The 22 sequences identified from this family were aligned for further analysis and the nine consensus motifs described in DEAD-box RNA helicases from other organisms were found. The Open Reading Frame (ORF) GL50803_34684 lacks the N-terminal region including the Q Motif; when we performed a new database search, we found that the homologous gene GL50581_3622 from Assemblage B, isolate GS, possesses the complete N-terminal region. Thus, we used this region to search the isolate WB genome database and found the missing region at the CH991776, location 21991–22645. The final gene location was at the CH991776, 21991 – 23994 (+), and the gene coded for a 667-amino acid protein with all the nine consensus motifs of the DEAD-box subfamily, including the Q motif. This motif contains nine amino acids, which is a distinctive and characteristic feature of the DEAD-box family of helicases, and can interact with Motif I and a bound ATP [36].

Another characteristic amino acid, the Phe (F) residue that is close to the Q Motif was also found in 13 of the 22 enzymes, whereas in other 7 helicases, Phe (F) was replaced by Trp (W), another aromatic amino acid, being absent only in GL50803_17239 and GL50803_34684 (see Additional file 5: Figure S2). To provide a schematic graphical overview of DEAD-box sequence motif conservation, we performed a multiple sequence alignment for each motif and then used the WebLogo software to obtain a precise description of sequence similarity [37,38] (Figure 1 - inset). Analysis of regions separating each pair of consecutive motifs was consistent with the reported low sequence but high length conservation (Figure 1) [33,34]. The DEAD-box family has an N-terminal length ranging from 2 to 233 amino acids and a C-terminal length from 29 to 507 amino acids, but lack any additional domain described in other DEAD-box proteins (Figure 1) [39]. In agreement with the analyses of Banroques [40], we found that almost 55% of Giardia putative DEAD-box helicases have an N-terminal length of 2-45 residues and a C-terminal length of 29-95 residues, whereas the size of the HCD containing the conserved motifs ranges between 331 and 403 residues in almost 70% of this family sequences.

Additional file 5: Figure S2. Alignment of conserved DEAD-box helicase motifs. The sequences were aligned using the “Multiple Align Show” software at “The Sequence Manipulation Suite” (http://www.bioinformatics.org/sms/index.html webcite). The residues conserved at 70% or more are highlighted in dark; other similar residues within each column are highlighted in grey.

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thumbnailFigure 1. Schematic diagram of the DEAD-box RNA helicase family in G. lamblia . Each motif is represented by a different color. The distances between the motifs, and the size of the N- and C- terminal extensions for each ORF, are indicated (number of aa). The red bars within the N- or C-terminal extensions represent the regions amplified with specific primers for the qPCR. The representation is to scale. Inset: sequence LOGO view of the consensus amino acids. The height of each amino acid represents the degree of conservation. Colors mark properties of the amino acids as follows: green (polar), blue (basic), red (acidic) and black (hydrophobic).

The DEAH-box family

The 6 putative RNA helicases belonging to the DEAH-box family were analyzed by multiple sequence alignment and subsequent manual scanning, in search of conserved motifs characteristic of this family. As shown in Additional file 6: Figure S3, the 5 helicases present the eight characteristic motifs, with the exception of GL50803_13200, which was incomplete in its N-terminal region, missing Motif I. As with the missing motif of DEAD-box helicase GL50803_34684, a new database search showed a homologous gene, GL50581_4549 from the isolate GS, with the complete N-terminal region that was used to search the isolate WB for the entire ORF. Surprisingly, this new putative 5´ DNA genomic region does not have a traditional ATG start codon; instead, there are two putative alternative initiation codons already described in rare cases for the fungus Candida albicans[41] or in mammalian NAT1 [42]. Studies in progress are analyzing this finding.

Additional file 6: Figure S3. Alignment of conserved DEAH-box helicase motifs. The sequences were aligned using the “Multiple Align Show” as before. The residues conserved at 70% or more are highlighted in dark; other similar residues within each column are highlighted in grey.

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The consensus sequence was obtained and was in agreement with the DEAH-box motifs published by Linder and Owttrim [43] (Figure 2 - inset). Within the C-terminal regions from five of these six putative DEAH-box RNA helicases, we found another domain called Helicase Associated Domain (HA2), of about 90-120 amino acid in length (Figure 2), whose function is unknown. The HA2 domain was found in more than 1,280 eukaryotic and 590 bacterial protein sequences according to the SMART (Simple Modular Architecture Research Tool) database [44], and was present only in this DEAH-box family, being absent in all other Giardia putative RNA helicases. For two of these DEAH-box proteins, there was an additional domain called DUF1605 (Domain of Unknown Function).

thumbnailFigure 2. Schematic diagram of the DEAH-box RNA helicase family in G. lamblia. Each HA2 domain is represented in gray and the DUF1605 domain is represented in brown, both inside the C-terminal region. Red lines within the C-terminal extensions represent the region amplified in the qPCR for each putative helicase. The representation is to scale. Inset: sequence LOGO view of the consensus amino acids. The height of each amino acid represents the degree of conservation. Colors indicate properties of the amino acids, as follows: green (polar), blue (basic), red (acidic) and black (hydrophobic).

The Ski2 family

Within this family, we found only four ORFs in the Giardia genome that were grouped according to the analysis of each sequence. The multiple sequence alignment (see Additional file 7: Figure S4) and the WebLogo graphic representation display the eight conserved motifs characteristic of this family [43] (Figure 3 - inset).

Additional file 7: Figure S4. Alignment of conserved Ski2 helicase motifs. The sequences were aligned using the “Multiple Align Show” as before. The residues conserved at 70% or more are highlighted in dark; other similar residues within each column are highlighted in grey.

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thumbnailFigure 3. Schematic diagram of the Ski2 RNA helicase family in G. lamblia. Each Sec63 domain is represented in pink, the DsHCT domain in brown, and the HhH1 domain in violet, all inside the C-terminal region of each ORF. Red lines within the N- or C-terminal extensions represent the region amplified in the qPCR for each putative helicase. The two overlap repeats of ~ 650 amino acids are indicated in blue under the ORF 87022. The representation is to scale. Inset: sequence LOGO view of the consensus amino acids. The height of each amino acid represents the degree of conservation. Colors mark properties of the amino acids, as follows: green (polar), blue (basic), red (acidic) and black (hydrophobic).

All of these Ski2 family members present C-terminal additional domains that can provide insights into their function (Figure 3). Two of them present a domain called Sec63, named after the yeast Sec63 protein (or NPL1) (also known as the Brl domain) where it was found, and that is required for assembly of functional endoplasmic reticulum translocons [45,46]. Another Giardia Ski2 protein exhibits a domain named HhH1, which is frequently found in prokaryotic and eukaryotic non-sequence-specific DNA-binding proteins [47]. The fourth Ski2 helicase presents a DSHCT domain, which is found in DOB1/SK12/helY-like helicases [48].

Interestingly, GL50803_87022 shows an internal repeat (red lines below 87022 design in Figure 3), as described for other RNA helicases [33]. This 2421-amino acid ORF consists of two RNA helicases joined together, presenting the eight Ski2 conserved motifs and an additional Sec63 motif of unknown function at the C-terminal region of each repeat. Marchat [33] detected the same patterns in several eukaryotic orthologs proteins and suggested horizontal gene transfer between bacteria and eukaryotes.

DNA helicases from other families

As mentioned above, only six of the twelve helicase families are supposed to comprise RNA helicases (DEAD-box, DEAH-box, Ski2-like, RIG-I-like, NS3/NPH-II and Upf1-like family) and the remaining families consist of DNA helicases. In Giardia we found 14 additional ORFs that could be considered DNA helicases and grouped them into the three following families:

Swi2/Snf2 family

Seven ORFs were linked to this family based on the sequence features and compared with members of this family belonging to other species. They present the eight characteristic motifs, with the sequence conservation being represented in the logos under the alignment (see Additional file 8: Figure S5). This family is one of the largest helicase families in G. lamblia SF2, with an average length of 1,560 amino acids (Table S2). The N- and C-terminal regions present characteristic domains; almost all of them show one or two SNF2N domains that were described as the ATPase component of the SNF2/SWI multi-subunit complex, disrupting histone-DNA interactions. Other domains found within these ORFs were the SANT domain, the BROMO domain and a CHROMO domain.

Additional file 8: Figure S5. Schematic diagram of the Swi2-Snf2 helicase family in G. lamblia. The SANT domain is represented in blue, the BROMO domain in brown, and the CHROMO domain in green. The SNF2N domains are represented in light grey, inside each one of them are the helicase motifs, when appropriate. The representation is to scale. Inset: sequence LOGO view of the consensus amino acids. The height of each amino acid represents the degree of conservation. Colors indicate properties of the amino acids, as follows: green (polar), blue (basic), red (acidic) and black (hydrophobic).

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RecQ family

This is the smallest family, with only three members found in the Giardia genome. These helicases also have one of the smallest average lengths, with only the central HCD. The eight characteristic motifs that defined this family are highly conserved, as shown in Additional file 9: Figure S6. The three ORFs share the greatest homology with the BLM (Bloom syndrome) gene from humans, which is believed to act by suppressing inappropriate recombination [49]. They are also homolog for the yeast SGS1 gene, a nucleolar DNA helicase of the RecQ family involved in genome integrity [50].

Additional file 9: Figure S6. Schematic diagram of the RecQ helicase family in G. lamblia. The representation is to scale. Inset: sequence LOGO view of the consensus amino acids. The height of each amino acid represents the degree of conservation. Colors mark properties of the amino acids as: green (polar); blue (basic); red (acidic) and black (hydrophobic).

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Rad3 family

This family is composed of four members in G. lamblia. It presents the largest HCD of all the SF2 helicases due to the presence of a differently large linker region between the DEXDc and the HELICc domains. They present homology in all the eight conserved motifs, except for ORF GL50803_5910, which lacks Motifs Ia and Ib (see Additional file 10: Figure S7). This ORF presents no significant similarity to human proteins; however, it was included in this family based on results of sequence and multiple alignment analyses (see Tree in Additional file 3: Figure S1).

Additional file 10: Figure S7. Schematic diagram of the Rad3 helicase family in G. lamblia. The representation is to scale. Inset: sequence LOGO view of the consensus amino acids. The height of each amino acid represents the degree of conservation. Colors indicate properties of the amino acids, as follows: green (polar), blue (basic), red (acidic) and black (hydrophobic).

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The helicase core domain within the dicer sequence

The HCD is an important component of higher eukaryotes’ Dicer enzymes, and is involved in some functions regarding the fundamental participation of this protein in RNAi [51-55]. As a deep-branching eukaryote, a database search using the entire Giardia Dicer amino acid sequence returned a list of Ribonuclease III (RIBOc) containing regions that belong to different species of bacteria with the highest alignment scores. Interestingly, these prokaryotic sequences of about 220-260 amino acids only possess one Ribonuclease III domain and one Double-stranded RNA binding motif (DSRM) (Figure 4–A).

thumbnailFigure 4. A) Graphical representation of Giardia lamblia Dicer homologs. Below the Giardia Dicer protein scheme are the two most homologous bacterial proteins found, and above it are the six protozoa most homologous proteins together with the human Dicer1 scheme. The representations are designed proportionally to their aa length, which is indicated below each organism’s name. The arrows alongside the figure indicate the degree of similarity to Giardia Dicer, divided into bacteria and protozoa. [Accession numbers: H. sapiens (Q9UPY3); N. gruberi (D2UZR2); T. thermophila (A4VD87); P. tetraurelia (Q3SE28); T. vaginalis (A2F201); D. discoideum (Q55FS1); P. pallidum (D3BF89); G. lamblia (A8BQJ3); R. marinus (D0MGH0); M. galactiae (D3VQS7)] B) Graphical representation of Arabidopsis thaliana DCL1 protozoa homologs: there are two N. gruberi represented in the diagram here indicated as (1) and (2). The representations are designed proportionally to their aa length, which are indicated below each name. The arrow alongside the figure indicates the degree of similarity to Arabidopsis Dicer. [Accession numbers: A. thaliana (Q9SP32); N. gruberi-1 (D2UZR2); E. siliculosus (GenBank: CBJ48587.1); T. thermophila (A4VD87); tetraurelia (Q3SD86); N. gruberi-2 (D2VEU9); P. marinus (C5LMV9)].

In the search of protozoa homologs containing the HCD within the Dicer sequence, we performed a BLASTP against the protozoa genomic database available at the NCBI with the entire Giardia Dicer sequence. We obtained the highest score with Polysphondylium pallidum, which contains only an amino-terminal DSRM domain and two C-terminal RIBOc domains. The other five protozoa with the highest scores against Giardia Dicer protein present different domains, as shown in Figure 4–A. The homologies were located only at the C-terminal region, spanning the two conserved RIBOc domains together with the PAZ domain. Interestingly, one of these homologs from Naegleria gruberi presents all the conserved domains, being also the protozoa protein with the highest sequence similarity to human Dicer1 (Figure 4–A). Remarkably, the HCD of this protozoan enzyme have low homology with any putative RNA helicases found in Giardia, as is also the case for the well-conserved helicase domain within other higher eukaryotes Dicer proteins used to search the Giardia genome database.

Using the Dicer-like 1 (DCL1) protein sequence from Arabidopsis thaliana, we searched the protozoan database for other Dicer-like proteins that could have the HCD together with the Ribonuclease III domains. Noticeably, besides the N. gruberi putative protein containing all the Dicer conserved domains, other protozoan homologs that have at least these two domains are Ectocarpus siliculosus, Tetrahymena thermophila, Paramecium tetraurelia, and Perkinsus marinus (Figure 4–B). These molecules do not present all Dicer domains and, in some cases, they only show one Ribonuclease III domain instead of two. Additionally, by taking only the HCD of these protozoa proteins and performing a BLASTP against the Giardia assemblage A isolate WB database, we did not find any significant homology with the described putative RNA helicases. Even when we generate a profile sequence from these five protozoan (the complete sequence or just the HCD sequence) and performed a more sensitive PSI-BLAST (iteration 5), the Giardia sequences presented low homology and corresponded to helicases already described in this work.

We also used eight Dicer sequences from higher eukaryotes (S. pombe; M. truncatula; H. sapiens; M. musculus; X. laevis; A. thaliana; D. melanogaster and C. elegans), all of them presenting a helicase domain and almost all the others Dicer specific domains (a PAZ domain, two Ribonuclease III domains and dsRNA binding motif). Considering only their HCD, we created a consensus sequence of 613 amino acids. A PSI-BLAST analysis (iteration 5) of the G. lamblia database using this consensus sequence give us 39 putative helicases already described and classified in this work. The best E-value was for the DEAD-box putative helicase GL50803_95898, with query coverage of only the 30%. To analyze the presence of patterns conserved in sets within this eight helicase domains, we performed a pattern matching using the Pratt software [56]. We obtained a series of best sets and subsets patterns that could be divided into four groups, two in the DEXDc domain, one in the HELICc domain and one in the region within this two. These four patterns were used again to search the Giardia database. First, we created a consensus sequence for each one of these patterns and used it to perform a PSI-BLAST analysis (iteration 5). Only with the best pattern, corresponding to the HELICc domain, our analysis gave a series of similar sequences, all of them already described as putative helicases. Again the putative DEAD-box helicase GL50803_95898 was at the top-five sequences with a 100% query coverage. The other patterns obtained provided no sequences producing significant alignments with E-value better than threshold.

RNA helicases relative expression during encystation

Based on in vitro experiments, the contribution of several DExD/H-box proteins in the accomplishment of crucial cellular functions has been revealed [30]. The fact that the entire life cycle of G. lamblia can be reproduced in vitro makes this species an attractive model to study cellular differentiation [57]. We analyzed the expression of all the DExD/H-box helicases genes by quantitative PCR (qPCR) (except for the ORF GL50803_11384 which presented very low efficiency in two pairs of primers tested), to explore the participation of these genes during the encystation process. The relative expression of these genes was determined in trophozoites under normal proliferating conditions, and in those induced to encyst after incubation for 16 hours in encystation medium, as described in Materials and Methods. Of a set of thirty one genes studied, we found eight whose expression did not change during encystation, five from the DEAD-box family, two from the DEAH-box family and one from the Ski2-like family. We also found down-regulation of one gene from the DEAH-box family after induction of trophozoites differentiation into cysts. In addition, we found twenty two genes that were up-regulated during encystation, seventeen from DEAD-box family, three from the DEAH-box family and two from the Ski2-like family (Figure 5). The encystation process was confirmed in these samples by analyzing the expression of a developmentally-regulated molecule [58] by Western blotting using a specific anti-CWP2 (Cyst Wall Protein 2) monoclonal antibody (see Additional file 11: Figure S8).

Additional file 11: Figure S8. Western blot of trophozoites grown under proliferating conditions and after induction to encyst. Total protein extracts from trophozoites grown under normal proliferating conditions (Normal) or after 16hs induction in encystation medium (Encyst) were separated using a 10% SDS-polyacrylamide gel and transferred to a PVDF membrane. The membrane was incubated with a monoclonal antibody against CWP2. The iqual loading of the samples is shown in the figure at the right with a Ponceau S staining. The numbers indicate the molecular weight of protein standards in kDa.

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thumbnailFigure 5. Real time quantitative PCR (qPCR) of RNA helicases from G. lamblia during encystation. The graph is a representative qPCR determination of three independent biological replicates. The ORFs are indicated at the bottom of the graph and separated in families. The up-regulated ORFs are represented in green bars, and the down-regulated ones, in red bars, each one with the corresponding relative expression ratio.

Comparing the up-regulated genes reported in the SAGE (Serial Analysis of Gene Expression) data [59] (sense tags) we found some correlation (11/21) with the DEAD-box family; (2/4) with the DEAH-box family and (1/3) with the Ski2-like family (see Additional file 12: Figure S9). The ORF GL50803_10255 was not included in the graph because the percentage of the sense tags was almost 10 times the percentage of the others ORFs in this study, but up-regulation of this gene correlated with the qPCR determination. This comparison between the qPCR results and the SAGE data should be taken with caution, as the induction protocols and the time points considered are not directly comparable. One explanation for the low agreement between the two methods is that encystation is poorly synchronic [59]. Another possible reason, as previously described for the validation process between two different methods of gene expression determination [60], is that these analyses have inherent pitfalls that may significantly influence the data obtained for each method and, in general, those genes showing small degrees of change also present lower correlations [61]. We were not able to determine the correlation of the down-regulated ORF GL50803_6616 or of the up-regulated ORF GL50803_17539 because there is no determination in the SAGE data, probably they are among the 7,256 unassigned SAGE tags [59]. We could not find also sense tag determination in the SAGE data for the ORF GL50803_113655. Taking in account the postulate that encystation genes can be divided into specific and up-regulated after induction [62], we assume that the twenty two putative RNA helicases genes with high relative expression described here would fall into the latter group.

Additional file 12: Figure S9. SAGE (Serial Analysis of Gene Expression) data. The graph represents the sense tag percentage from Giardia trophozoites (white bar) and four different encystation times (4, 12, 21 and 42 hours; grayscale bars). Under each ORF it is indicated if these ORFs were up-regulated (green up arrow), down-regulated (red down arrow) or remained unmodified (equal sign). A line graph is also provided for a better identification of the expression pattern. The colored boxes represent our RT-qPCR results (with the same color code), divided into families. The asterisk under each box stands for a correlation between the SAGE and the RT-qPCR data.

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RNA helicase relative expression during antigenic variation

Antigenic variation was induced on a unique VSP-expressing Giardia clone. The primers used for these determinations were the same as those used for the study of the encystation process. We also designed two additional pairs of primers to determine the relative expression of Giardia Dicer and Argonaute (Ago) transcripts. The relative expression from the thirty one Giardia putative RNA helicases was divided into earlier (30 min – 1 h) and later (3 – 4 h) up-regulated or down-regulated transcripts. Eight putative RNA helicases were up-regulated after antigenic variation induction, three of them earlier and five later. On the other hand, eight putative RNA helicases were down-regulated, five after early induction and three later (Figure 6).

thumbnailFigure 6. Real time quantitative PCR (qPCR) of RNA helicases from G. lamblia during antigenic variation. The relative expressions were calculated after induction of antigenic variation for 30 min – 1 hour (empty fill pattern) and for 3 to 4 hours (line fill pattern). The relative expression from different helicases was divided into up-regulated (upper panel) and down-regulated (lower panel). Green bars represent significant up-regulation and red bars represent significant down-regulation, gray bars represent no change in the relative expression. A. Helicases up-regulated during the first 30 min to 1 h. B. Helicases up-regulated at 3 to 4 h. C. Helicases down-regulated during the first 30 min to 1 h. D. Helicases down-regulated at 3 to 4 h. Center inset: relative expression for Giardia Dicer and Argonaute at earlier or later time points. The ORFs are indicated at the bottom of the graph. The graphs represent the mean of three different measures and the respective standard deviation.

A more detailed analysis of the relative expression of the eight putative RNA helicases that were up-regulated after antigenic variation induction showed a slight induction ranging from 1,189 to 1,729 times. In addition, two transcripts from the early up-regulation maintain induction after 3-4 hours. The eight down-regulated putative RNA helicases presented strong down-regulation earlier and significant down-regulation later during antigenic variation. Two of the five early down-regulated RNA helicases maintained low levels of expression after 3-4 h, while one of them was up regulated later. The three transcripts that were down-regulated later presented no significant variations at 30 min-1 h (Figure 6). The relative expression of gDicer presented an early up-regulation that is maintained at later times, while Giardia Ago presented a later up-regulation after 3-4 post induction of antigenic variation (Figure 6, inset).

Based on our results from the qPCR experiments, we searched the Giardia database for highly homologs to well known RNA helicases already described participating in the RNAi process in higher eukaryotes. We found that the human DEAH-box helicase RHA (DHX9), described in remodeling RISC to allow dsRNA loading onto this complex [52], has a high homology with the G. lamblia DEAH-box helicase GL50803_13200, which presents a later up-regulation during antigenic variation, in agreement with the Giardia Ago expression (3–4 h post induction). Another G. lamblia DEAH-box helicase found to have high homology with the HsRHA is GL50803_17387, which also presents a delayed up-regulation after induction of antigenic variation. Interestingly, a Giardia putative RNA helicase that presented an early up-regulation that was maintained for 3–4 h after antigenic variation induction is GL50803_2098, which has a great homology with the human DDX6 helicase (p54), a protein that interacts with Ago2 in affinity-purified RISC assemblies to facilitate formation of cytoplasmic P-bodies and that acts as a general translational repressor in human cells [63].

Other bona fide RNAi component in D. melanogaster S2 cells is the Belle (Bel) DEAD-box RNA helicase that seems to be important to both pathways (miRNA and siRNA). Our search found that the G. lamblia putative DEAD-box helicase GL50803_15048 present the highest homology with this Drosophila helicase described acting downstream of the dsRNA loading onto the RISC. Our qPCR data shows that even when the Giardia putative helicase GL50803_15048 presented an early down-regulation, their mRNA levels increased at 3–4 hs after the antigenic variation induction. The G. lamblia DEAD-box helicase GL50803_15048 was also found to have a high homology with two other RNA helicases described participating in the RNAi pathway. This two related DEAD-box RNA helicases (p68 and p72) were found to associate with a complex containing Drosha and required for processing of miRNA in mice [64].

Western blotting from total protein of the different samples and times analyzed by qPCR in the antigenic variation experiment showed that the level of the specific VSP protein do not change (see Additional file 13: Figure S10). Under these experiments conditions, a change in VSP protein expression was detected by immunofluorescence assays after 48 h. Since our intention was to determine the early participation of some putative helicases during this specific Giardia adaptation process, we performed qPCR reactions only at very short times (from 30 min to 4 h post- induction), where the changes at the protein level for VSPs cannot be detected. Although there was no VSP change at these times, we were able to detect specific up regulated expression of Dicer and Ago transcripts, two essential enzymes already related with this process [22]. Importantly, Dicer expression was up regulated at very short times and was maintained for hours, while gAgo expression raised at later times, in accordance with their roles in the RNAi process [65]. Although there is an incomplete understanding of how RNA helicases are regulated, it is possible that they operate at different steps of the RNAi pathway or performing different roles [66].

Additional file 13: Figure S10. Western blot during antigenic variation induction. Trophozoites were incubated for the indicated times with a 1:10.000 dilution of mAb 5C1directed against VSP-1267, mAb 7D2 against Cyst Wall Protein 2 or without antibody (Control). Total protein was electrophoresed, transferred to a PVDF membrane and incubated with a mAb against the VSP-1267. The molecular weights of standards are indicated in kDa.

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Discussion

As shown in several studies, RNA helicases are involved in a wide variety of processes, some of them being essential for survival, as demonstrated for the yeast putative RNA helicases, where their knockouts were lethal [32]. These results are essential for the correct annotation of the Giardia genome, since many of the helicases identified in this study were automatically annotated either as helicases without indicating any further information and others just as hypothetical proteins (http://www.giardiadb.org webcite).

The genome of a number of organisms contains a large number of putative helicases [34] and, as we found in this work, the relationship between the number of DEAD-box and DExH-box RNA helicases is conserved in Giardia as it is has been reported for other organisms (Table 1). Although Giardia is considered as an early-branching eukaryote and has a smaller and more compact genome [67], our findings regarding the type and number of RNA helicases in Giardia highlight the importance of these molecules in the biology of eukaryotic cells.

Since only a few DExD/H-box RNA helicases have been characterized biochemically, most of the reports assigning a putative function are based on the presence of the conserved and characteristic motifs that can define a putative RNA helicase and its family. Here we used the presence of those motifs for classification performing an in silico approach and then by manual identification of each motif. Then we confirmed and refined each motif at each position. Our results were in agreement with the phylogenetic tree obtained, because SF2 helicases were grouped specifically according to their sequence conservation as well as with the conservation of their motifs.

The particular finding within the Giardia Ski2 family regarding the internal duplication of the ORF GL50803_87022, having two helicases and Sec63 domains, probably indicates that the origin of this protein was by a fusion event of two ancestral prokaryotic genes, as proposed for the RNA helicases from Entamoeba histolytica EhDExH1 and EhDExH10 [33] and other homologous proteins from phylogenetically distant species. Unfortunately, the significance of this duplication found only in two early-branching parasitic intestinal protozoa is still unknown.

The DEAD-box protein family is present in many organisms, being the major RNA family of helicases, which seem to be involved in many, if not all, steps of RNA metabolism [68]. Although some DEAD-box helicases are closely related and have been described as paralogs [33], the comparison among amino acid sequences of all full-length sequences showed no paralogous DEAD-box helicases in Giardia because these proteins only share 14–29% identity and 24–43% similarity.

Regarding Giardia differentiation into cysts, it is known that encystation comprises the formation of a resistant cyst wall that allows the parasite to survive under hostile external environmental conditions and guarantees the transmission of the infection to susceptible hosts [69]. Several encystation-specific genes have been identified and characterized during the last decade, and have shown to be up-regulated with similar kinetics during encystation, suggesting that their regulation is at the transcriptional level [70]. Several reports also described putative transcription factors that regulate the expression of encystation-specific genes [71-74]. It was assumed that the encystation process is controlled at multiple levels (basic transcription, enhancement or de-repression) [62]. Moreover, it was hypothesized that epigenetic chromatin modifications via histone acetylation/deacetylation may participate in modulation of stage differentiation in this parasite [75]. In higher organisms, different RNA helicases have been described to interact with histone deacetylases (HDACs), such as the known transcriptional regulator DP103 (Ddx20, Gemin3), which was found to immunoprecipitate with histone deacetylases HDAC2 and HDAC5, suggesting a role in transcription repression through HDACs recruitment [76]. In addition, the role of the RNA helicases p68 (Ddx5) and p72 (Ddx17) as transcription repressors when interacting with HDAC1 [77], HDAC2 and HDAC3 has been reported [78]. Our findings regarding the levels of induction of the RNA helicase genes by qPCR were diverse, ranging from a smooth 2-4-fold induction in some DEAD-box genes to a high (20-31 times) relative expression in other genes. Two genes, DEAD-box GL50803_13791 and DEAH-box GL50803_13200, presented a marked induction of 554 and 228 times, respectively, under the encystation conditions. Notably, the up-regulation of the encystation-specific gene coding for CWP2 increased up to 2,187 times compared to its expression in trophozoites.

In Giardia, the RNAi machinery controlling antigenic variation has been found to involve a Dicer enzyme with unique characteristics when compared to Dicer enzymes from higher eukaryotes. Giardia Dicer lacks the DExD/H helicase domain as well as double-stranded RNA binding motifs present in other Dicer homologs. Because we are only starting to understand the different roles of RNA helicases in RNAi, there are still many unresolved questions. Since different RNA helicases might operate at different steps in the RNAi pathway or might play different roles, the presence of thirty two putative DExD/H-box helicases in the Giardia genome and their differential patterns of expression during antigenic variation support their importance for RNAi. It would be relevant to determine the role of particular Giardia RNA helicases for different subsets of miRNA or siRNAs. However, it is already clear that the presence of a RNA helicase activity (unwinding or as adaptor proteins) is necessary for the correct functioning at different steps of the RNAi pathway. As it was proposed in several reports, there are a number of potential roles for RNA helicases in RNAi [66]. Our findings in the qPCR experiments during antigenic variation suggest that RNA helicases may participate in RNAi. This could be the case of the G. lamblia putative DEAD-box helicase GL50803_15048, which was found to present high homology with the DmBel helicase and also with the DEAD-box RNA helicases p68 and p72. Taking into account that some studies pointed out extensive overlapping and interplay among small RNA directed silencing machineries [64] and different RNA helicases operate either at different steps or playing different roles in the RNAi pathway, the involvement of this G. lamblia RNA helicase (GL50803_15048) in post-transcriptional gene silencing deserve further analysis.

Although we did not find a putative helicase in Giardia with high similarity to the HCD of higher eukaryotes Dicer enzyme, it has been proposed that Dicer helicase domain is required for siRNA, but not miRNA, processing [79]. Point mutations within the helicase domain or Dicer lacking a functional HCD showed that pre-miRNA processing does not require helicase participation, but that it is necessary for long dsRNA (siRNA processing) [79].

In Giardia, we have demonstrated that purified RdRP generates high-molecular-weight VSP RNAs in vitro only when more than one VSP transcript is present in the reaction mixture [22] and proposed a mechanism where variations in either the general or local concentrations of different VSP transcripts may determine which transcript will circumvent the silencing system, as was suggested to occur in higher eukaryotes [53]. In addition, it has been proposed by others groups the presence in Giardia of a miRNA biogenesis pathway reminiscent of the canonical miRNA biogenesis pathway found in higher organisms [25,80], and they have identified conserved putative microRNA target site of several variant surface protein (VSP) mRNAs. Here Giardia Dicer apparently would assume the functions of both a Drosha and a Dicer, although no RNA-binding protein DAWDLE (DDL) homolog has yet been identified in this parasite. Furthermore Giardia Dicer must shuttle between the cytoplasm and the nucleus to process pri- and pre-miRNAs, although we determined its cellular localization by expressing a hemagglutinin-tagged version of the protein. Similar to that observed in other cells, Giardia Dicer localizes to the cytoplasm [22].

On one hand, the lack of the RNA helicase domain in Giardia Dicer is in agreement with the occurrence of a miRNA pathway. But, on the other hand, it was also proposed that a deletion or mutation of the helicase domain of human Dicer leads to a more active enzyme in vitro for cleavage of a perfectly matched 37-nt linear duplex RNA [51], allowing the enzyme to rapidly reinitiate cleavage on the long substrates. This last being the case for the generation of perfectly matched VSP dsRNAs by RdRP and subsequent degradation [22]. It is also important to highlight that the lack of the helicase domain was proposed to increase the effectiveness of long hairpins for intracellular applications in which multiple siRNAs are desired, as could be the case for VSP mRNA degradation. Interestingly, gDicer without the RNA helicase domain can complement the absence of the entire Dicer in S. pombe[26]. The lack of the RNA helicase domain in Giardia Dicer or, in other words, the inclusion of the RNA helicase domain in Dicer enzymes of higher eukaryotes, raises new questions about the function of this domain in Dicer activity and regulation.

Conclusions

The first in silico classification of SF2 G. lamblia helicases was achieved, describing some of their features, organization, structure, and homology to helicases from humans and yeast. A series of up- and down-regulated putative RNA helicases were found during encystation and antigenic variation, suggesting their participation in both adaptative processes. Most of them are assumed to be up-regulated after induction to encystation, while in the antigenic variation process we infer that the regulated RNA helicases studied may operate at different steps of the RNAi pathway, even when no putative helicase in Giardia presented high similarity to the HCD of higher eukaryotes Dicer enzymes.

Methods

Screening of databases

The G. lamblia complete genome sequence was screened at the Giardia Genome Resource [28] (strain ATCC 50803, Assemblage A, isolate WB) using the PSI-BLASTP program. The query used was the complete amino acid sequence of the human Eukaryotic Initiation Factor 4A-I (eIF4A) and the human ATP-dependent RNA helicase DHX8 as DEAD and DEAH-box prototypes, respectively. For the determination of identity/homology sequences within the human genome, we performed a BLASTP search at the NCBI Human database using the default parameters and the Build protein database. The yeast homologous proteins were obtained with the HomoloGene option from the NCBI database according to the human RNA helicase previously found, and the gene functions or characteristics are based on the literature. For the Helicase Core Domain analysis, we performed a BLASTP search using the entire Giardia Dicer amino acid sequence (ORF GL50803_103887). One search was conducted within the entire NCBI proteins database and the other only within the protozoa database available at the NCBI BLAST Assembled RefSeq Genomes. The search of protozoa proteins homologous to the Arabidopsis thaliana Dicer-like 1 was performed within the protozoa database at the NCBI website. The similarity between the Helicase Core Domain of the protozoa proteins found and the Giardia database was performed at the Giardia Genome Resource (strain ATCC 50803, Assemblage A, isolate WB) using the BLASTP program.

Sequence analysis

Multiple sequence alignment was performed with the ClustalW2 program at the European Bioinformatics Institute (EBI). For the alignments of each RNA helicase family shown in the figures we used the Multiple Align Show at The Sequence Manipulation Suite, specifying the fraction of residues that need to be identical or similar in a column of the alignment at 70% for highlighting. For the “Ident and Sim” analysis within the DEAD-box sequences, we first performed a MUSCLE alignment at the EBI website and then ran the program at “The Sequence Manipulation Suite”. The structural domains and sequence patterns were first predicted at the Eukaryotic Linear Motif resource (ELM) [81], getting the DEXDc and HELICc RNA helicase domains and the HA2 and Sec63 domains. After that, each specific family motif was checked manually and indicated using the putative consensus motifs described in the literature [43]. For the graphical representation of the amino acid conserved motifs within each family we used the web-based application WebLogo [38], where each logo consists of stacks of symbols, one stack for each position in the sequence. The overall height of the stack indicates the sequence conservation at that position, whereas the height of symbols within the stack indicates the relative frequency of each amino or nucleic acid at that position. The putative Dicer amino acid sequence analysis was performed using the Eukaryotic Linear Motif resource (ELM) and the ExPASy - PROSITE database [82].

Phylogenetic analysis

We used only the helicase domain from the RNA helicases selected to run a multiple alignment (MUSCLE) into the SeaView Version 4.2.12 [83-86]. Then we computed the tree using PhyML v3.0.1 as an external program [86].The design was edited using the Tree Figure Drawing Tool Version 1.3.1.

Cultures

G. lamblia trophozoites were cultured in TYI-S-33 medium at pH7.0 with 10% adult bovine serum and bovine bile (0.5 mg/ml) [87] in anaerobiosis at 37°C. For induction of encystation, the trophozoites were cultured until confluence and then the medium was replaced with encystation medium (porcine bile 0.45%, lactic acid 0.01% and pH 7.8) [88] and grown in anaerobiosis at 37°C during 16 h. For antigenic variation experiments, a Giardia clone expressing VSP-1267 was obtained by serial dilution and selection by immunofluorescence assays using specific monoclonal antibody that recognizes only this VSP, and then cultured until 90% confluence. Induction of antigenic variation was performed according to Torri et al. (manuscript in preparation).

RNA extraction and cDNA synthesis

Total RNA was extracted from each sample (trophozoites and encystation induction) using Trizol reagent (Invitrogen) according with manufacturer’s instructions. Total RNA was spectrophotometrically quantified and treated with DNase I (Roche) at 37°C for 1 h. After DNase inactivation total RNA was quantified again and several PCRs were performed to check for the presence of genomic DNA. If no DNA was detected after PCR, we performed the cDNA synthesis using SuperScript III Reverse Transcriptase (Invitrogen), following manufacturer’s instructions. All newly synthesized cDNA were collected together for the subsequently qPCR reactions.

Quantitative real time PCR (q-PCR) of RNA helicase mRNA

Quantitative PCR was performed using the QuantiTect SYBR Green PCR kit (Qiagen). We used 1 μl of cDNA in a final volume of 25 μl; a triplicate for each gene was performed. The primers used for this determination (0.6 μM each) were designed based on the N- or C-terminal extensions because they are highly variable in size and composition, and have no significant homology between them, making every pair of primers specific for each helicase as shown in Figures 2, 3 and 4 (red bars). Thermal conditions were as follow: initial incubation for 15 min at 95°C, 15 sec at 95°C, 30 sec at 50°C and 30 sec at 72°C for 35 cycles, with the plate read after each cycle, and a final incubation for 10 min at 72°C. The Melting Curve was performed from 50°C to 90°C, with a plate read at every 1°C. We used the Chromo4 system for Real-time PCR detection (BioRad) and the data collected was analyzed using the REST 2009 (Relative Expression Software Tool V2.0.13 – Qiagen) [89]. RNA was standardized by quantification of glutamate dehydrogenase (gdh) as a reference gene.

Protein isolation and Western blot analysis

Total protein extraction was performed from the same Trizol extraction procedure, as indicated by the manufacturer. Total protein content was determined with the BCA™ Protein Assay kit (Pierce). Fifty micrograms of total protein was loaded onto a 10% polyacrylamide gel (SDS-PAGE) and after running, it was transferred to a PVDF membrane (Immobilon–P, Millipore). The membrane was blocked with 5% milk in TBS-Tween20 for 1 hour and then incubated with a monoclonal antibody (mAbs 7D6) specific against G. lamblia CWP2 [1:2000]. After three washes with TBS-Tween20, the membrane was incubated with goat anti-mouse immunoglobulin serum conjugated with alkaline phosphatase [1:2000] (Southern Biotechnology) and revealed with alkaline phosphatase substrate (BCIP/NBT, Color Development Solution, BioRad).

Accession numbers

See Additional file 14: Table S4 for a complete list of proteins cited in the manuscript, organism it is derived and NCBI reference sequence number.

Additional file 14: Table S4. Accession numbers. The table indicates a complete list of proteins cited in the manuscript, the organism it is derived and the NCBI Reference Sequence Number.

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Abbreviations

SF: Superfamilies; HCD: Helicase Core Domain; VSP: Variant-specific Surface Protein; RNAi: RNA interference; RHA: RNA helicase A; Bel: Belle; Armi: Armitage; eIF4A: Eukaryotic Initiation Factor 4A; ORF: Open Reading Frame; HA2: Helicase-Associated Domain; SMART: Simple Modular Architecture Research Tool; DUF1605: Domain of Unknown Function; CHROMO: CHRromatin Organization Modifier; BLM: Bloom syndrome; RIBOc: Ribonuclease III; DSRM: Double-stranded RNA binding motif; DCL1: Dicer-like 1; CWP2: Cyst Wall Protein 2; qPCR: Quantitative PCR; SAGE: Serial Analysis of Gene Expression; ELM: Eukaryotic Linear Motif; gdh: Glutamate dehydrogenase.

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

PRG performed bioinformatics and sequence searching and comparison analysis, including motif and phylogenetic analyses, and assisted with manuscript writing. MCS performed the qPCR experiments, including the production of G. lamblia cultures. AT performed the induction of encystation and antigenic variation. HDL coordinated the project, writing process and analyses. All the authors read and approved the final manuscript. HDL is Guggenheim Fellow; PRG and HDL are Members of the Scientific Investigator’s Career of the National Research Council of Argentina (CONICET). All authors read and approved the final manuscript.

Acknowledgements

This work was supported by the Agencia Nacional para la Promoción de la Ciencia y la Tecnología (ANPCYT), the Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) and the Universidad Católica de Córdoba (UCC). The funding bodies had no role in data analysis, writing or decision for submission.

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