Tv-RIO1 – an atypical protein kinase from the parasitic nematode Trichostrongylus vitrinus
© Hu et al; licensee BioMed Central Ltd. 2008
Received: 31 July 2008
Accepted: 22 September 2008
Published: 22 September 2008
Protein kinases are key enzymes that regulate a wide range of cellular processes, including cell-cycle progression, transcription, DNA replication and metabolic functions. These enzymes catalyse the transfer of phosphates to serine, threonine and tyrosine residues, thus playing functional roles in reversible protein phosphorylation. There are two main groups, namely eukaryotic protein kinases (ePKs) and atypical protein kinases (aPKs); RIO kinases belong to the latter group. While there is some information about RIO kinases and their roles in animals, nothing is known about them in parasites. This is the first study to characterise a RIO1 kinase from any parasite.
A full-length cDNA (Tv-rio-1) encoding a RIO1 protein kinase (Tv-RIO1) was isolated from the economically important parasitic nematode Trichostrongylus vitrinus (Order Strongylida). The uninterrupted open reading frame (ORF) of 1476 nucleotides encoded a protein of 491 amino acids, containing the characteristic RIO1 motif LVHADLSEYNTL. Tv-rio-1 was transcribed at the highest level in the third-stage larva (L3), and a higher level in adult females than in males. Comparison with homologues from other organisms showed that protein Tv-RIO1 had significant homology to related proteins from a range of metazoans and plants. Amino acid sequence identity was most pronounced in the ATP-binding motif, active site and metal binding loop. Phylogenetic analyses of selected amino acid sequence data revealed Tv-RIO1 to be most closely related to the proteins in the species of Caenorhabditis. A structural model of Tv-RIO1 was constructed and compared with the published crystal structure of RIO1 of Archaeoglobus fulgidus (Af-Rio1).
This study provides the first insights into the RIO1 protein kinases of nematodes, and a foundation for further investigations into the biochemical and functional roles of this molecule in biological processes in parasitic nematodes.
Protein kinases are a group of enzymes essential for the regulation of a large variety of cellular processes, including cell-cycle progression, transcription, DNA replication and metabolic functions . These enzymes catalyse the transfer of phosphates to serine, threonine and tyrosine residues, thus playing functional roles in reversible protein phosphorylation. In organisms, such as Homo sapiens, Mus musculus, Drosophila melanogaster (vinegar fly), Caenorhabditis elegans (worm), Saccharomyces cerevisiae (yeast), Dictyostelium discoideum (slime mould) and Plasmodium falciparum (malaria parasite), the complete complement of protein kinases has been identified via the analysis of genome sequences . Based on their structure, protein kinases can be classified into two main groups, namely eukaryotic protein kinases (ePKs) and atypical protein kinases (aPKs) . The ePKs usually have 11 subdomains, including a nucleotide-binding loop (subdomain I), typically with the sequence GXGXXG, which binds and orients the phosphates of ATP; a hinge region which interacts with the adenine moiety of the ATP; a catalytic loop (subdomain VIb) which contains conserved catalytic Asn and Asp residues involved in phosphoryl transfer; a metal-binding or "DFG" loop (subdomain VII) for the positioning of metal ions; and an activation loop (subdomain VIII) . The aPKs are enzymes with protein kinase activity and limited sequence similarity to any known ePKs. Of the 518 kinases known to be encoded in the human genome, 40 have been identified as aPKs, which have been classified into 13 families or groups, one of which represents the RIO kinases . These serine kinases are conserved in sequence among a range of different organisms, yet are quite divergent from kinases of other families with known structures [5, 6].
Through sequence and structural analyses, RIO proteins have been found to contain the conserved signature residues, typifying protein kinases [7, 8]. RIO kinases are present in organisms from archaea to humans, suggesting key fundamental roles in the Metazoa. The function of RIO1 was first investigated in yeast . It was found that RIO1 is a non-ribosomal protein located in the cytoplasm and specifically required for 20S precursor ribosomal RNA (pre-rRNA) processing; the depletion of the protein RIO1 caused the inhibition of 18S rRNA production and an accumulation of the 20S pre-rRNA in the cytoplasm. Further sequence characterisation of RIO1 of Saccharomyces cerevisiae indicated that this protein was a serine kinase . Although the primary sequences of RIO1 proteins are quite divergent from those of members of other protein kinase families, their structural folding is similar to known canonical protein kinases. Also, they display protein kinase activity in vitro. Analysis by mutagenesis  showed that some of the conserved residues are crucial for enzymatic activity, and cytological study of RIO1 has revealed that it also plays an important role in cell-cycle progression (in G1 to S transition and in the control of the onset of anaphase) as well as the maintenance of mitotic chromosome stability . In contrast to RIO1, RIO2 kinase appears to be localized predominantly to the nucleus . The biological activities of these two proteins neither complement each other nor do they co-purify, although both are associated with the same fractions containing 20S precursor RNA in yeast .
Although not yet studied in detail in multicellular organisms, RIO1 kinases are encoded in the genome of the free-living nematode Caenorhabditis elegans . RNA interference (RNAi), which decreases messenger RNA (mRNA) levels of the targeted C. elegans gene, has been shown to affect predominantly embryonic and larval growth and/or development [13–17]. In spite of the functional importance of this molecule, there is no published information regarding its structure or function for any parasitic nematode. Clearly, the isolation and characterisation of RIO protein kinases from nematodes would provide a starting point for a better understanding of their roles in developmental processes. In a genomic study , we characterised an expressed sequence tag (EST), designated TVf09_H06, from an adult female-enriched cDNA library for Trichostrongylus vitrinus, an economically important parasitic nematode. The amino acid sequence inferred from this EST had the highest homology (e-value: 2e-37) to the protein encoded by predicted RIO1 kinase (M01B12.5; see http://www.wormbase.org/) from C. elegans (unpublished findings). Therefore, the aims of this study were to isolate and characterise the full-length complementary DNA (cDNA) of RIO1 of T.vitrinus corresponding to TVf09_H06 and carry out comparative analyses with related molecules encoded by other organisms, to explore transcription in different developmental stages and to predict its three-dimensional structure by comparison with known crystal structures of homologues.
Merino lambs (males; 8–12 weeks of age), maintained under helminth-free conditions, were inoculated intra-ruminally with 30,000 infective third-stage larvae (L3) of T. vitrinus. The patency of the infection (~24 days after inoculation) was established by the detection of strongylid eggs in the faeces using the McMaster flotation method . First- and second-stage larvae (L1 and L2) and L3 were collected after 1, 3 and 7 days of incubation of faeces at 28°C, respectively, and purified by repeated sedimentation and a migration through a nylon sieve (mesh size: 20 μm) for 16 h. For the collection of fourth-stage larvae (L4) and adults of T. vitrinus, infected lambs were euthanized by intravenous administration of an overdose of pentobarbitone sodium (Lethobarb, Virbac Pty. Ltd.) 8 and 30 days after intra-ruminal inoculation, respectively. Adult worms were collected (using fine forceps) from the chyme from the first 4 m of the small intestine, washed extensively in chilled (4°C) phosphate-buffered saline (PBS), and males and females (adults) separated prior to snap freezing in liquid nitrogen and subsequent storage at -70°C.
Isolation, purification, treatment and storage of nucleic acids
Total genomic DNA was extracted from ~0.5 g of single sex (male or female) adult worms using a small-scale sodium dodecyl-sulphate (SDS)/proteinase K extraction procedure , followed by mini-column (Wizard® Clean-Up, Promega) purification. The specific identity of the parasite material in each sample was confirmed by PCR amplification of the second internal transcribed spacer (ITS-2) of nuclear ribosomal DNA from genomic DNA and subsequent, automated sequencing [20, 21]. The sequences determined were required to be identical to the ITS-2 sequence with GenBank accession no. X78064.
Total RNA was extracted separately from different developmental stages (L1, L2, L3, L4 or adults) or sexes of T. vitrinus (homogenized under liquid nitrogen using a mortar and pestle) employing the TriPure isolation reagent® (Roche Molecular Biochemicals). RNA yields were estimated spectrophotometrically (ND-1000 UV-VIS spectrophotometer, v.3.2.1, NanoDrop Technologies), and the integrity of RNA was confirmed via the detection of discrete 18S and 28S ribosomal RNA bands on ethidium bromide-stained gels. Each RNA sample (~10 μg) was treated with 2 U of DNase I (Promega) and incubated at 37°C for 30 min prior to heat denaturation of the enzyme (75°C for 5 min). Both DNA and RNA samples were stored at -70°C.
Isolation of the full-length cDNA encoding RIO1 kinase from T. vitrinus
Using four gene-specific primers PK1F (forward: 5'-CGACTTCTCCAGCGTGGAACGTTAACC-3'); PK2R (reverse: 5'-GGAACCAGGGAGACCCGCTTGATGCT-3'); PK3F (forward: 5'-GAACCGGCTACTGCAAACACAACCCCCG-3'); PK4R (reverse: 5'-GCGGTGCACCCCAGCCATCACGACC-3') designed to the sequence of EST TVf09_H06 (accession no. NP_491102.2), two partially overlapping cDNA fragments were produced separately from total RNA from adult female worms using 5'- and 3'-rapid amplification of cDNA ends (RACE) (SMART™ RACE cDNA Amplification Kit, BD Biosciences). The cDNAs were ligated separately into the pGEM-T-Easy® vector (Promega); Escherichia coli (strain JM109) (108 colony forming units/μg) was transformed with recombinant plasmids via heat shock and then grown overnight at 37°C on Luria Bertani (LB) plates containing 10 mg/ml ampicillin, 0.5 mM isopropyl-β-d-thiogalactopyranoside (IPTG) and 80 μg/ml X-gal (5-bromo-4-chloro-3-indolyl-β-galactosidase). Plasmid DNA was isolated from recombinant clones and column-purified (Wizard®, Promega) from overnight cultures, and inserts sequenced in both directions using vector oligonucleotide primers (M13 and SP6), employing Big Dye Terminator v.3.1 chemistry in an automated ABI-PRISM sequencer (Applied Biosystems). Based on the resultant sequences, selected oligonucleotide primers were designed to amplify the full-length Tv-rio-1 cDNA from T. vitrinus adult females, which was subsequently cloned and sequenced.
Nucleotide sequences were assembled using the program EGassembler . The full-length cDNA sequence of Tv-rio-1 was conceptually translated (six different frames) into amino acid sequences using the Baylor College of Medicine (BCM) Search Launcher  and aligned using the program ClustalW . Sequences were compared with those available in public, non-redundant databases using BLASTn and BLASTx algorithms  available via the National Center for Biotechnology Information , the Sanger Centre  and the Parasite Genome database , in order to verify the identity of the molecules isolated. Protein motifs were identified by scanning the database PROSITE  and Pfam .
Phylogenetic analyses of inferred primary amino acid sequence data were conducted using the program PAUP*4.0b10 , as described previously . In brief, the neighbour-joining (NJ) method was used to construct trees from distance data. The maximum parsimony (MP) method, based on character state analysis, was also used. Characters were treated as unordered and were weighted equally; alignment gaps were treated as "missing" in all analysis. Exhaustive searches with tree-bisection-reconnection (TBR) branch swapping were used to infer the shortest trees. The length, consistency index, excluding uninformative characters, and the retention indices of each most parsimonious tree were recorded. Bootstrap analyses (1000 replicates) were conducted using heuristic searches and TBR branch swapping, with the MulTrees option, to determine the relative support for clades in the consensus trees.
The three-dimensional structure of the RIO1 kinase of Archaeoglobus fulgidus (Af-RIO1 kinase; PDB code 1ZTF; cf. [5, 6]) was used to create an homology model of the RIO domain of Tv-RIO1 using the program DeepView Swiss-PdbViewer and the SWISS-MODEL server . The energy of the resultant model was minimized in DeepView using Gromos 96 . The model did not include the C-terminal extension, characteristic of sequences of eukaryotic RIO1 proteins, including Tv-RIO1.
All comparative analyses with C. elegans were carried out using WormBase . Genetic interactions with the C. elegans orthologue (gene name M01B12.5) of Tv-RIO1 were predicted using the probabilistic functional gene network for C. elegans (see ); this computational network covers the majority (82%) of C. elegans genes and makes predictions regarding essentiality, spanning diverse cellular and developmental processes .
Reverse transcription real-time polymerase chain reaction (PCR)
Double-stranded cDNA was synthesized from total RNA separately from each stage and sex of T. vitrinus using reverse transcriptase (Superscript III, Invitrogen). Briefly, 5 μg of total RNA were added to 14 μl of H2O and 1 μl of oligo d(T)n = 12–18 primer (0.5 μg/μl), heated to 70°C for 10 min and chilled on ice. First- and second-strand cDNAs were synthesized via the addition of 4 μl of first-strand cDNA buffer (250 mM Tris-HCl, pH 8.3, 375 mM KCl and 15 mM MgCl2), 2 μl of 0.1 M dithiothreitol, and 1 μl of 10 mM of each dNTP, followed by an incubation at 25°C for 10 min, 42°C for 50 min and 70°C for 15 min. The transcripts (176 bp) representing Tv-rio-1 were amplified from individual cDNAs by real-time PCR using the primer pair PK3F-PK4R. The PCR amplification of a portion (187 bp) of the large subunit (28S) ribosomal RNA using primers 28S1/F (5'-GCATTAGCTCTCGCGTTACC-3') and 28S3/R (5'-GAGAGGGACAGCAGGTTCAC-3'), previously determined to be present equally in each developmental stage and sex in a related parasitic nematode, Oesophagostomum dentatum (see ), was used as a positive control. Samples without template (no-DNA controls) were included in each PCR run. For each sample, ~0.5 μg of cDNA was subjected to PCR (20 μl) using the SYBR® GreenER™ qPCR SuperMix Universal (Cat. no. 11762-100, Invitrogen) in a Rotor-Gene™ 3000 thermal cycler (Corbett Research) under the following conditions: one cycle of 50°C for 5 min and of 95°C for 10 min, followed by 40 cycles of 95°C for 15 s, 60°C for 30 s and 72°C for 30 s. Each sample was tested in triplicate, using a calibrator (28S) as well as positive and no-template controls. The specificity and identity of individual amplicons were verified by melting curve analysis and subsequent direct, automated sequencing using the same primers (individually) as employed for the PCR. Relative transcriptional differences were calculated from normalised values using method described by Livak and Schmittgen .
Results and discussion
Characterisation of Tv-RIO1 and relationship with selected homologues
Pairwise comparison of amino acid identity (%) among RIO1 protein kinase of Trichostrongylus vitrinus and other selected species for which full-length cDNA sequences encoding RIO1 protein kinases are predicted from publicly available data
Structural model for Tv-RIO1
Recently, crystal structures of the proteins RIO1 and RIO2 have been characterised from Archaeoglobus fulgidus [5, 6], allowing RIO kinases to be defined as a distinct, novel family of protein kinases. The structure of RIO2 was first investigated, revealing the presence of two domains . The N-terminal domain, conserved for the RIO2 family members and not present in the RIO1 protein kinase family, is structurally homologous to the winged helix (wHTH) domain, seen primarily in DNA-binding proteins. The C-terminal domain, the sequence of which is conserved between both proteins RIO1 and RIO2, is structurally homologous to known protein kinase (ePK) domains. The ePKs usually contain 11 conserved subdomains that form the catalytic core. Compared with ePKs, RIO kinase domains resemble a trimmed version of an ePK kinase domain, containing only eight of these subdomains, lacking the activation loop (subdomain VIII) and subdomains X and XI which are important for substrate binding . Detailed study of RIO1 and comparisons with RIO2 [39, 40] have defined the minimal consensus RIO-domain that, like ePKs, also contains an N-lobe, a hinge region, and a C-lobe. However, the RIO kinase domain contains only three α-helices (αE, αF and αI) in the C-lobe. All RIO domains contain an additional α-helix (αR) N-terminal to the canonical N-lobe and a loop inserted between αC and β3 called "flexible loop". Study of nucleotide binding by the RIO kinases and comparison with canonical protein kinases [5, 6] has identified specific phosphate-binding loops for subfamily RIO1 domains (with the sequence STGKEA) and RIO2 domains (with the sequence GxGKES), which are significantly different from their counterpart in ePKs. This finding indicates that the interaction of RIO kinases with the phosphate moiety and protein substrate is different from ePKs.
Transcription in different developmental stages and prediction of function based on comparisons with C. elegans
This study characterised an atypical protein kinase – RIO1 protein kinase – from an economically important parasitic nematode, Trichostrongylus vitrinus. The findings from the study provide the first insights into the RIO1 protein kinases of nematodes, and a foundation for further investigations into the biochemical and functional roles of this molecule in biological processes in parasitic nematodes.
This work was supported by the Australian Research Council (LP0667795 and LX0882231), Genetic Technologies Limited, Meat and Livestock Australia, the Australian Academy of Science, the Australian-American Fulbright Commission (RBG), and the Howard Hughes Medical Institute (PWS).
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