- Open Access
The minimal kinome of Giardia lamblia illuminates early kinase evolution and unique parasite biology
Genome Biology volume 12, Article number: R66 (2011)
The major human intestinal pathogen Giardia lamblia is a very early branching eukaryote with a minimal genome of broad evolutionary and biological interest.
To explore early kinase evolution and regulation of Giardia biology, we cataloged the kinomes of three sequenced strains. Comparison with published kinomes and those of the excavates Trichomonas vaginalis and Leishmania major shows that Giardia's 80 core kinases constitute the smallest known core kinome of any eukaryote that can be grown in pure culture, reflecting both its early origin and secondary gene loss. Kinase losses in DNA repair, mitochondrial function, transcription, splicing, and stress response reflect this reduced genome, while the presence of other kinases helps define the kinome of the last common eukaryotic ancestor. Immunofluorescence analysis shows abundant phospho-staining in trophozoites, with phosphotyrosine abundant in the nuclei and phosphothreonine and phosphoserine in distinct cytoskeletal organelles. The Nek kinase family has been massively expanded, accounting for 198 of the 278 protein kinases in Giardia. Most Neks are catalytically inactive, have very divergent sequences and undergo extensive duplication and loss between strains. Many Neks are highly induced during development. We localized four catalytically active Neks to distinct parts of the cytoskeleton and one inactive Nek to the cytoplasm.
The reduced kinome of Giardia sheds new light on early kinase evolution, and its highly divergent sequences add to the definition of individual kinase families as well as offering specific drug targets. Giardia's massive Nek expansion may reflect its distinctive lifestyle, biphasic life cycle and complex cytoskeleton.
Protein kinases modulate most cellular pathways, particularly in the co-ordination of complex cellular processes and in response to environmental signals. About 2% of genes in most eukaryotes encode kinases, and these kinases phosphorylate over 30% of the proteome . Kinases regulate the activity, localization and turnover of their substrates. Most kinases have dozens of substrates, and operate in complex, multi-kinase cascades. Hence, organisms with reduced kinomes can provide simple model systems to dissect kinase signaling.
The unicellular human gut parasite Giardia lamblia cycles between a dormant cyst stage and a virulent trophozoite, both of which are adapted to survival in different inhospitable environments . The life cycle starts with the ingestion of the cyst by a vertebrate host. Exposure to gastric acid during passage through the host stomach triggers excystation and the parasite emerges in the small intestine after stimulation by intestinal factors [3, 4]. The excyzoite  quickly divides into two equivalent binucleate trophozoites that attach to and colonize the small intestine. Trophozoites carried downstream by the flow of intestinal fluid differentiate into dormant quadrinucleate cysts. Cysts are passed in the feces, and can survive for months in cold water until they are ingested by a new host. Trophozoites are half-pear shaped and are characterized by four pairs of flagella, a ventral attachment disk and a median body (Figure 1). Each pair of flagella has a distinct beating pattern and likely has dedicated functions in swimming and attachment [6, 7].
The recent genome sequencing of strains from three assemblages (broadly equivalent to subspecies) of Giardia lamblia (syn. intestinalis) [8–10] revealed a compact genome of approximately 6,500 ORFs that is highly divergent in sequence from other eukaryotes. Many conserved pathways have substantially fewer components than in similarly sized genomes . Its minimal genome and the ability to culture and induce its complex life and cell cycle in vitro make Giardia an appealing model for studying the signaling underlying entry into and emergence from dormancy in a pathogen.
Few kinases and phosphorylation patterns have been studied in Giardia (Table 1) [11, 12]. Functional studies [13–16] suggest that regulation of protein phosphorylation by kinases and phosphatases plays a central role in modulating the dramatic remodeling of the parasite's morphology as it cycles between the dormant infectious cyst and the motile, virulent trophozoite (Table 1). Many of the known signaling proteins localize to cytoskeletal structures unique to Giardia, which may confer functional specificity (Figure 1).
Protein kinases are well-studied in other organisms, control most aspects of cellular functions, and are proven therapeutic targets. Hence, analysis of the Giardia kinome may give valuable insight into this parasite's biology and the evolution of signaling.
Results and discussion
We cataloged the Giardia kinome using hidden Markov model (HMM) profiles and Blast searches of genomic and EST sequences from three sequenced strains: two established human pathogens, WB (assemblage A)  and GS (assemblage B) , that appear to span the divergence of isolates infectious to humans, and a recently isolated porcine strain, P15 (assemblage E) . Despite their shared genus name, these genomes are quite divergent, with an average of 90% protein sequence identity between WB and P15, and approximately 79% between these two strains and GS .
We found 278 protein kinases in the WB strain (Table 2; Additional file 1), 272 in GS, and 286 in P15, using release 2.3 of the Giardia genomes . These include 46 new gene predictions and 86 sequences not previously annotated as kinases. We also extend 30 fragmentary gene predictions from WB to longer pseudogene sequences. Remarkably, over 70% of the kinome belongs to a huge expansion of one family, the Nek kinases. Since these have so many unusual characteristics, we will refer to the 80 non-Nek kinases as the core kinome and consider the Nek expansion separately.
The core kinome
The core kinome of 80 kinases is completely conserved between the three genomes. Sixty-one core kinases can be classified into 49 distinct classes (families or subfamilies) that are conserved in many other eukaryotes [18–23]; the remaining 19 include 5 in two small Giardia-specific families, and 14 with no close homologs (Table 2; Additional file 1). Giardia sequences are typically the most divergent of any within their families: comparison of a set of nine universally conserved kinase domain orthologs from human to various deep-branching lineages showed an average sequence identity of only 40% for Giardia, compared with 46% for the related excavate Trichomonas vaginalis, and 46 to 50% for other deep-branching lineages (ciliates, plants, fungi) (Additional file 2). This indicates that Giardia sequences are remarkably divergent, even for an early-branching lineage, and provides a useful resource to study the limits of how sequences can vary while still retaining their family-specific functions. Thus, Giardia encodes the smallest and most sequence-divergent of studied eukaryotic kinomes, other than those of parasites that have not been cultured axenically. No core kinome class has more than three members in Giardia, suggesting a lack of recent duplication and expansion into specialized functions.
Two previously predicted kinases could not be found: a protein kinase C (PKC) was inferred earlier by reactivity to antibodies against mammalian PKCs and by PKC-selective inhibitors , but no clear PKC homolog is seen in the genome sequence. Similarly, although an insulin-like growth factor receptor (IGFR) kinase was inferred by antibody binding and association with phosphotyrosine , we could not find an IGFR in the genomes of Giardia or any other protist.
Evolutionary origin and functional repertoire of the Giardiakinome
To probe the origin of the Giardia kinome, we annotated the kinomes of two other excavates, Trichomonas vaginalis  and Leishmania major  (Additional file 3). The excavates are one of about six anciently diverged 'supergroups' of eukaryotes, whose relationship to each other is uncertain . Excavates include free-living, symbiotic, and parasitic protists, many flagellated and often with reduced mitochondria. Comparison of the three excavate kinomes predicts a rich kinome of 68 distinct kinases in their common ancestor, with substantial losses of core kinases in extant species, possibly due to their reduced parasitic lifestyles  (Figure 2, Table 2). These losses provide a valuable model to explore the effect of gene deletion on pathway evolution and organismal biology. All three excavates lack 17 kinase classes found in at least two other major eukaryotic groups (unikonts, plants, chromalveolates), suggesting a very early divergence of the excavates  and/or even more losses across the entire clade. This suggests that the common ancestor of extant eukaryotes had 85 different kinase classes (or 68 if excavates are the earliest-diverging clade), substantially more than previous estimates [19, 20], and attesting to the many diverse conserved roles of kinases. Several noteworthy themes emerge from these losses (Table 2; see below).
Distinctive patterns of kinase losses in the Giardialineage
Five of the seven ancient kinases lost from Giardia and T. vaginalis, but found in L. major, are mitochondrial kinases (ABC1-A, -B, -C, PDHK, BCKDK), consistent with the degeneration of the mitochondrion to a mitosome or hydrogenosome in these largely anaerobic species . A separate degeneration occurred in some amoebozoa, and accordingly, these kinases are also secondarily lost from Entamoeba histolytica (GM, unpublished). The other two are likely involved in DNA repair and splicing (see below). The 17 kinases found in other early branching lineages but absent from excavates include IRE1 and PEK, which mediate endoplasmic reticulum stress responses, supporting the observed lack of a physiological unfolded protein response in Giardia  (see Additional file 4 for definitions of kinase classes discussed in the text). Giardia has unusual dual mitotic spindles , and all three excavates also lack the spindle-associated kinases BUB and cyclin-dependent kinase (CDK)11. They all also lack the mitosis-associated kinases SAK and Haspin, and their lack of a ribosomal S6 kinase (RSK) correlates with the lack of a regulatory substrate serine in the tail of ribosomal protein S6 in all excavates. Genes lost only from Giardia include three encoding DNA repair kinases (ATR, ATM, TLK) and two RNA polymerase kinases (CDK7, CDK12). Despite having an elaborate microtubule cytoskeleton, Giardia has lost the microtubule-associated kinases MAST and TTBK (Tau tubulin kinase), while microtubule affinity-regulating kinase (MARK) is missing from all excavates. Splicing and RNA-linked kinases DYRKP, YAK, PRP4, and SMG1, and basal transcription factor kinases TAF1 and CDK8 are also lost in different patterns within the excavates, suggesting gradual divergence or reduction in the regulation of these processes.
Losses of DNA repair kinases may explain sensitivity to radiation and chemical DNA damage
The PIKKs (phosphatidyl inositol 3' kinase-related kinases) ATM, ATR, and DNAPK are involved in recognition and repair of DNA breaks . Deletions of these in several organisms lead to increased radiation and mutagen sensitivity. Giardia is the only eukaryote known to lack all three, though it has one gene (GK009) with very weak similarity to the ATR and ATM kinase domains, yet lacks their conserved accessory domains. Giardia also lacks the Chk1 and Chk2 checkpoint kinases that are activated by ATM and ATR, and the downstream TLK kinases . ATM, ATR, and TLK are all found in T. vaginalis. Giardia does have homologs of other DNA break repair proteins, including MRE11 and RAD50 of the MRN complex, suggesting that aspects of DNA break repair may be functional, but perhaps recognized by a divergent mechanism. Giardia has a single histone H2A with a H2Ax-like ATM/ATR substrate site. Induction of double-stranded DNA breaks in trophozoites results in anti-phospho-H2A antibody staining . This suggests that some ATM/ATR-like kinase activity may be present, possibly acting through GK009. Giardia also lacks both DNAPK and its binding partners, Ku70 and Ku80, indicating that DNA break repair may be severely diminished or divergent in Giardia. This lack of DNA repair kinases correlates with the reported sensitivity of Giardia cysts to low doses of UV light and inability to repair DNA breaks .
Transcription and splicing kinases
Several CDK family members control RNA polymerase II by phosphorylation of a heptad repeat region in its carboxy-terminal domain (CTD) in plants and animals. These include CDK7, CDK8, CDK9  and CDK12 (CRK7) . Some protists, including ciliates and trypanosomes, lack both the heptad repeat of RNA polymerase II and CDK7/8/9, but retain CDK12, and several have many Ser-Pro (SP) motifs in the CTD, suggesting that CDK12 may phosphorylate this tail. T. vaginalis retains CDK7 and CDK12 and has 19 SP sites in the CTD, while Giardia has only two SP sites and has lost both kinases. CDK12 has also been associated with splicing, which is common in ciliates and trypanosomes, but very rare in Giardia. PRP4 is another splicing-associated kinase lost from Giardia, but other splicing kinases (SRPK, DYRK1, DYRK2) are retained, suggesting that these may have different functions, or be retained for use in the rare cases of Giardia splicing .
Giardia also lacks TAF1, an atypical kinase constituent of the general transcription factor TFIID that is known to phosphorylate Ser33 of histone H2B. Giardia H2B lacks this serine, and none of the other 13 subunits of TFIID have been identified . TAF1 and several other TFIID complex members are found in T. vaginalis, suggesting loss of this complex from Giardia.
Histidine and tyrosine phosphorylation
Unlike plants and most protists, Giardia lacks classical histidine kinases. Tyrosine phosphorylation in Giardia trophozoites can be seen by western blot (Figure 3), , proteomics (TL, FG, unpublished), and immunofluorescence (Figure 4). However, we found no classical tyrosine kinases (TK group) or members of the related tyrosine kinase-like (TKL) group. A number of other serine-threonine-like kinases have been reported to phosphorylate tyrosine, including Wee1 (cell cycle), MAP2K (though only acting on the MAPK activation loop), and TLK, while DYRK and glycogen synthase kinase (GSK) family kinases can autophosphorylate on tyrosine . Phosphoproteomic profiling of the excavate Trypanosoma brucei shows that more than half of the recorded phosphotyrosine (pTyr) phosphorylation events were found on these kinases . Giardia has one Wee, one MAP2K, one GSK, and four DYRK family kinases. Giardia has no SH2 or PTB phosphotyrosine-binding domains, supporting the lack of a phosphotyrosine signaling system as has been inferred in animals, plants, and Dictyostelium [20, 43]. By contrast, several proteins with putative phosphoserine or phosphothreonine binding domains are present: two clear forkhead-associated (FHA) domains, one 14-3-3, one WW and over 250 WD40 domains. Of these, only the 14-3-3 protein has been characterized and shown to bind phosphopeptides . Saccharomyces cerevisiae also lacks TK and TKL group kinases, but shows substantial tyrosine phosphorylation by phosphoproteomics . These data from both Saccharomyces and Giardia suggest that dual-specificity or undetected tyrosine kinases may be more important than previously thought.
Accessory domains are reduced or divergent
Most kinases from other genomes have additional domains that help in regulation, localization, or scaffolding. Many core Giardia kinases lack detectable accessory domains. However, the domains that are present correlate well with conserved family-characteristic domains : polo boxes in PLK family kinases; PBD/CRIB domains in PakA; HEAT, FAT and FATC domains in TOR; and pkinase_C in one PKA and one NDR kinase (Additional file 1; see Additional file 4 for definitions of domains). Cryptic PH domains are seen in Akt and PDK1, and the characteristic pkinase_C domain is absent from other AGC kinases, although this can be difficult to detect on such remote sequences. Several other kinases have regions of novel sequence outside of the kinase domain that may be orthologous domains too divergent in sequence to be detectable. No kinase has a clear signal peptide, and only four are predicted to have transmembrane domains. This is consistent with the observed false positive rate for predicting these regions, suggesting that Giardia has no receptor kinases. Other unrelated parasitic protists, including Entamoeba histolytica, have a rich complement of receptor kinases . The Nek kinases are highly enriched for ankyrin repeats and coiled-coil regions (see below).
Catalytically dead kinases
In most kinomes, about 10% of kinases lack critical catalytic residues (K72, D166, D184) and are likely to be catalytically inactive, yet may retain signaling functions as scaffolds or kinase substrates . In the WB strain, 10% (8 of 80) of the core kinome and 71% (139 of 195) of Neks lack one or more of these three key residues and are likely to be inactive (Additional file 1). The eight inactive core kinases include Scyl, whose orthologs are all inactive, and Ulk, which has some inactive homologs in other species. The functions of both families in any organism remain obscure. Four pseudokinases are highly divergent proteins specific to Giardia; some might have cryptic active sites that could not be found by alignment to other kinases.
The AGC kinase group (PKA/PKG/PKC kinases) mediates a wide variety of intracellular signals, including nutrient, phospholipid and extracellular signal responses. Giardia has seven AGC kinases, including a very divergent PDK1, Akt (GiPKB) , two PKAs (cyclic AMP-regulated kinases) [13, 14], a lipid flippase kinase (FPK) and two NDR kinases. The Akt and PDK1 genes are particularly divergent, but are partially validated by the presence of weakly predicted phospholipid-binding PH domains, and a likely PDK1 phosphorylation site that is seen in the activation loop of all Giardia AGC kinases. A possible PDK1-binding 'hydrophobic motif' is found in Akt (FKDF) and in one NDR kinase (YTYRA), but not in other AGC kinases, and no neighboring phosphorylation site is seen.
Cyclic AMP-dependent signaling is confirmed by the presence of two PKA catalytic subunits (Additional file 1), one regulatory subunit (Orf_9117 in GiardiaDB) , and one homolog (Orf_14367) of adenylate and guanylate cyclases. No clear AKAP (A kinase anchoring protein) was found. In many organisms, including Giardia, PKA localizes to the basal bodies/centrosomes . In addition, both the catalytic (PKAc) and regulatory (PKAr) subunits localize to the paraflagellar rods rather than the flagellar axonemes [13, 14] (Table 1, Figure 1). PKAc and PKAr localization to the basal bodies is constitutive, while their distribution to the paraflagellar rods is influenced by external stimuli, such as growth factors, encystation stimuli and cAMP levels . Inhibitor studies indicate that PKAc activity is also required for the cellular awakening of excystation .
The two Giardia phosphatidyl inositol kinases PI3K and one PI4K have been cloned and are expressed in trophozoites and encysting cells [48–50]. As in other species, PI3K likely relays signals from transmembrane receptors by activation of the protein kinase PDK1 to phosphorylate the survival kinase Akt and several other AGC group kinases, as well as the PI3K-like protein kinase TOR, which modulates energy level responses. This suggests that Giardia has intact phospholipid signaling pathways coupled to non-kinase receptors.
The MAPK cascade consists of a relay of up to four kinases that phosphorylate and activate each other, usually to transmit signals from the cell surface to the nucleus. The prototypical MAPK cascade involves the Erk MAPK, which is phosphorylated on both serine and tyrosine by a MAP2K (MEK, MKK, Ste7), which in turn is serine phosphorylated by a MAP3K (MEKK, Ste11), and that by a MAP4K. MAP2K, some MAP3Ks, and MAP4K make up the three families of the STE group of kinases, while Raf and MLK MAP3Ks are from the TKL group. All four kinase classes are found in all analyzed eukaryotic kinomes, apart from Plasmodium . Giardia has one canonical Erk (Erk1), and a member of the distinct Erk7 MAPK subfamily, called Erk2 . Both genes have the MAP2K dual phosphorylation motif (T[DE]Y sequence). We found a single MAP2K, along with three MAP3K and four MAP4K genes, one each from the primordial FRAY, MST, PAKA and YSK subfamilies. The single MAP2K indicates either that all the upstream kinases funnel though this single gene, or that there are alternative pathways that bypass MAP2K, for which Giardia may be a tractable model. Two of the three MAP3Ks are homologs of S. cerevisiae Cdc15, involved in the mitotic exit network and cytokinesis. These have orthologs in plants and other basal eukaryotes, but not in animals. The distinct functions of Erk1 and Erk2 are highlighted by their localization: in vegetative trophozoites, Erk1 was found in the disk and median body while Erk2 was in the nuclei and caudal flagella  (Figure 1). During encystation, their expression levels remained the same, but their phosphorylation and kinase activity were reduced and Erk2 became more cytoplasmic (Table 1).
Giardia has a full complement of basic cell cycle kinases (Table 2). These include three CDK1/CDC2 kinases, along with three mitotic (A/B) cyclins, a putative CDK5, three unclassifiable CDKs and two unclassifiable cyclin-like genes, as well as a Wee1 homolog. We also found single copies of the Aurora (AurK) and Polo (PLK) mitotic kinases, which are activated in M phase and involved in centrosome or kinetochore function, spindle assembly and cytokinesis. Giardia AurK is exclusively nuclear during interphase. During mitotic prophase, it is activated by phosphorylation and migrates to the mitotic spindle poles, as well as to the median bodies and anterior paraflagellar rods (PFRs; Figure 1) . Beginning in metaphase, pAurK localizes to the parental attachment disk, which persists until the daughter disks are developed. AurK inhibitors decreased growth and led to abnormal cytokinesis. Thus, AurK has a Giardia-specific localization and likely function in addition to its universal function and location in the mitotic spindle. In mammalian cells, Aur kinase is centrosomal, but interestingly, in Chlamydomonas gametes, it is localized to the flagellar tips or adhesion sites .
Expansion and divergence of the GiardiaNek kinase family
The Nek kinase family is universal in eukaryotes, and its members regulate entry to mitosis  and flagellum length [55, 56]. The Nek family is expanded in both ciliates and excavates, with 40 genes in Tetrahymena and 11 to 25 in trypanosomes [27, 57], compared with only 11 in humans and one in yeast. Giardia strain WB has a massive 198 Neks, making up 71% of its kinome and about 3.7% of the entire proteome. These have remarkably divergent sequences (Figure 5; Additional file 5); all but 56 have lost critical catalytic residues and are likely pseudokinases, and many show detectable sequence similarity only to other Neks but not to standard kinase domain models. Most retain a number of structural motifs (Additional files 6 and 7), but are so divergent in overall sequence that our count may not be precise.
The Neks are evolutionarily dynamic, accounting for all of the kinase gain and loss between Giardia strains. While 99.7% of all 4,570 'core' WB genes are found in strains GS and P15 , the Neks are one of four families (along with Protein 21.1, HCMP (high cysteine membrane protein) and VSP (variable/variant surface protein) genes) that are both highly expanded and polymorphic between strains, and may be responsible for strain-specific characteristics. Seventy-nine Neks (30%) are found in only one strain and a further 31 (12%) are found in two but are absent from the third, due to both gene duplication and loss (Additional file 8). Within the Neks, two patterns emerge: most are highly conserved and slowly evolving between strains, while a subset accounts for most of the gene gains and losses.
Of the Neks, 74% (147 of 198 genes in WB) have no close paralogs (labeled 'Nek-Unclassified'). Their average sequence identity to the next closest Nek is only 34% in the kinase domain, and for the most divergent 10% of Neks, this drops to only 20%. This is less than that of orthologous kinase domains between human and Giardia (40%), and even less than that of many kinases from different families, implying rapid diversification in sequence and function. However, they are well conserved between strains; 89% (131) have orthologs in all three strains, and their sequences are only slightly less conserved than those of core kinases (average kinase domain identity of 88% between WB and P15, 78% between WB and GS, compared with 92% and 84% for core kinase domains), indicating that these Neks may be quite ancient, rather than very rapidly evolving.
We classified 51 Neks (26% of Neks in WB) into 5 subfamilies, based on kinase domain sequence similarity: Nek1, which is conserved throughout eukaryotes, and GL1 to GL4, which are Giardia-specific. GL1 to GL3 are moderately sized subfamilies with 3 to 11 members each. GL4 is dramatically different. It has 32 members in WB, but only 5 of these genes are single copy in each strain. In total, 87 genes across the three strains are not three-way orthologs; 53 of these are found in 10 strain-specific clusters. The rapid turnover of GL4 Neks is further highlighted by our discovery of an additional 30 kinase pseudogenes in the WB strain (these are not counted in the overall kinome), of which 29 are from GL4. Moreover, five pairs of GL4 Neks are very recent duplicates, with over 98% identity within the pairs. In summary, the Giardia Nek expansion includes both highly divergent but evolutionarily stable members, small and largely stable families, and the GL4 family, which is turning over at a remarkable rate.
Of the Giardia Neks, 67% (133 of 198) have an amino-terminal kinase domain, followed by a variable array of ankyrin repeats (1 to 26 repeats, median of 8), which are not found in any core kinases. They are also evolutionarily mobile, with related members of most subfamilies having gained or lost these repeats. They are divergent in sequence but form a distinctive subclass, characterized by a four amino acid TALM motif at the start and a conserved E at the end (Additional file 9). Most other Giardia TALM-ankyrin (TA) repeats are found in members of the poorly described Protein 21.1 family, which have a similar structure to Neks but lack the amino-terminal kinase domain. Both families also have some members with coiled-coil regions and carboxy-terminal RING domains (Additional file 1, Text S1 in Additional file 2), and both are large and evolutionarily dynamic. Our examination of the amino-terminal regions of 21.1 proteins revealed very divergent kinase domains in 20, and cryptic kinase-like domains may exist in other 21.1 proteins that are beyond our limit of confident detection. The TA repeat is largely specific to Giardia: 59% of the 3,355 Giardia ankyrin repeats have an exact TALM motif, compared with just 2.6% (54 of 2,028) in human and 0.5% (24 of 4,602) in T. vaginalis. Curiously, the only other organism with many TA repeats is the mushroom Coprinopsis cinerea , which has 73 proteins containing 271 TA repeats, though none of them have kinase domains. Some are chromosomally clustered, but their functions are unknown (GM, unpublished).
Expression and localization of phosphorylated proteins in Giardia
Signaling proteins often gain specificity by localization close to their targets. This is especially relevant to Giardia with its unique cytoskeleton that is remodeled during differentiation. Moreover, the protein kinases characterized to date localize to distinct cytoskeletal structures that are specific to Giardia and whose functions remain unclear. We characterized major phosphoproteins by western blot and immunofluorescence, using antibodies against phosphoserine (pSer), phosphothreonine (pThr), and pTyr (Figures 3 and 4). Despite the lack of classical tyrosine kinases in Giardia, immunoblots showed strong staining of pTyr, along with pSer and pThr. This corroborates a previous study . Immunofluorescence of Giardia trophozoites with the same antibodies revealed distinct patterns for each phospho-amino acid (Figure 4). Consistent with the predicted absence of receptor kinases in Giardia, we did not observe staining at the plasma membrane. Strong pSer stain was seen in the intracellular and extracellular portions of three of the four pairs of flagellar axonemes (anterior, posterior-lateral, and caudal; Figure 1) as well as the nuclear envelope, with weaker nuclear and ventral flagellar staining. By contrast, pThr most strongly stained the remaining (ventral) pair of flagella, which beat in a sine wave pattern in both attached and swimming trophozoites . It also stained the rim of the ventral attachment disk and polar regions of the nuclei, possibly the nucleoli . In contrast to the largely cytoskeletal localization of pSer and pThr, pTyr staining was concentrated in the nuclei. It is noteworthy that pSer- and pThr-modified proteins tend to localize to the intracellular and extracellular portions of the flagellar axonemes. In contrast, the Ser/Thr kinases in published studies and two of the four Nek kinases tend to localize to intracellular flagellar-associated structures (Figures 1 and 6; see below). Thus, some of the actual phosphorylation may occur in the basal bodies, and the phosphorylated proteins are then incorporated into the flagella.
Expression and localization of individual kinases
Gene expression profiling by serial analysis of gene expression (SAGE)  confirms expression for 233 kinases, including 156 Neks (Additional file 1). Twenty-seven kinases are categorized as differentially expressed throughout the life cycle, of which 12 kinases, all Neks, were upregulated in trophozoites and encyzoites (encysting cells), and 9 Neks and 4 other kinases were selectively expressed in cysts and excyzoites (excysting cells) (Table 3). Overall, Neks are slightly less likely to be expressed than other genes or kinases, and slightly more likely to be differentially or highly expressed, although the differences are not statistically significant. These data suggest that most Neks are expressed and functional, despite their unusual evolution.
To begin to understand the roles of Neks in Giardia, we epitope-tagged five Neks under their own promoters. We observed a different localization pattern for each protein (Figure 6). Orf_5375 (Nek-GL2 subfamily) localized prominently to the PFRs of the anterior and posterior-lateral flagella and faintly to the caudal flagella. Orf_16279 (Nek-Unclassified) localized prominently to the outer half of the ventral attachment disk, to the region of the basal bodies and to the caudal and posterior-lateral flagella, but not to the PFRs. Similarly, Orf_92498 (Nek1) localized to the basal bodies/centrosome region in addition to three pairs of PFRs, as well as to the median bodies, disorganized stacks of microtubules unique to Giardia, whose functions are unknown  (Figure 1). Orf_101534 (Nek-GL4) localized to the posterior-lateral PFR and to the perinuclear regions and cytoplasm. In contrast, Orf_15409 (Nek-Unclassified), which has four ankyrin repeats and is catalytically inactive (Additional file 1), localized diffusely to much of the cytoplasm and to an anterior region that may be plasma membrane associated (Figure 6b). Deletion of the most conserved ankyrin repeat of Orf_15409 (amino acids 351 to 386) resulted in partial relocalization to the plasma membrane (Figure 6b).
The distinct localization of these five Neks likely mirrors their specific functions in the different subcellular compartments. Basal body/centrosomal localization of the conserved Nek1 and the Nek-Unclassified is similar to patterns seen in human (Nek2, Nek6, Nek7, and Nek9), Chlamydomonas (Fa2p), Trypanosoma brucei (TbNRKC), and Tetrahymena thermophila (NRK17p and NRK20p) [55, 57, 61]. The Giardia flagellar basal bodies become spindle poles during mitosis, suggesting that these Neks may be involved in regulating mitotic progression. In other organisms, Neks have also been localized to axonemes. For example, human Nek8 and Chlamydomonas Fa2p are found in the proximal region of primary cilia or flagella, respectively, and Tetrahymena thermophila NRK1 and NRK30p are located in various types of cilia, with the latter three being involved in regulating flagella/ciliary length [57, 62, 63]. All four active Neks (Orf_5375, Orf_16279, Orf_92498, and Orf_101534) localize to diverse Giardia cytoskeletal structures, and may be involved in regulating flagellar assembly, beat, or cellular attachment . In contrast, the inactive Nek (Orf_15409) is found in the cytoplasm, which may indicate a correlated loss of cytoskeletal association and catalytic activity.
Giardia encodes the simplest known kinome of any eukaryote that can be grown in axenic culture. Some obligate intracellular parasites have even more highly reduced genomes and kinomes (for example, the microsporidian Encephalitozoon cuniculi (29 kinases) , and Plasmodium falciparum (approximately 90) ), but are dependent on their hosts for many basic cellular functions, and their lost kinases may be functionally replaced by host kinases.
Protein kinases modulate the vast majority of biological pathways, and this minimal kinome still enables Giardia to carry out the broad repertoire of eukaryotic cellular functions needed for its complex life and cell cycles. Our comparison of the Giardia kinome to other early branching eukaryotes indicates that the last common ancestor of sequenced eukaryotes had a rich kinome of at least 67 kinase classes, from which Giardia has lost at least 18. These include kinases involved in central biological functions, such as DNA repair, transcription, splicing, and mitochondrial metabolism. Exploring how these pathways can function without individual components may help to understand the function of these pathways in more complex organisms.
Other missing kinases, such as those involved in endoplasmic reticulum stress response, are absent from all excavates, and may represent either early losses or reflect that excavates are the earliest branching of eukaryotic lineages. Conversely, Giardia retains many ancient kinases (Table 2) whose functions are still largely unexplored, despite their being essential for eukaryotic life.
The Giardia kinome is dominated by the expansion of the Nek kinases. The recurrent loss of kinase catalytic function coupled with the conservation of key structural and Nek-specific residues suggest that many Neks maintain a kinase-like fold and serve as scaffolds. The GL4 subfamily is highly dynamic, with most of its members being strain-specific, with loss of catalytic activity even within a single strain, and showing rampant gene duplication and pseudogenization. This high variation rate may underlie important strain differences. However, the rate of pseudogenization also suggests that the rate of duplication of this gene cluster may be enhanced and that at least some copies are under little purifying selection. By contrast, most other Neks are shared between strains and are likely to be anciently diverged, since their paralogs are more remote than orthologs between human and Giardia. While a homolog of the universal Nek1 was found, the vast majority of Neks are specific to Giardia, and the association with ankyrin repeats is not seen in any other species. The dual mitotic spindles and eight flagella of Giardia may explain some of the Nek expansion, but clearly not all of it. Ciliates are also binucleate and have expanded Neks, but no specific orthologs are found between the two clades, apart from Nek1.
We found long runs of a specific class of ankyrin repeat (TALM-Ankyrin: TA) in most Neks. These are likely important for their subcellular localization or protein interactions. While the four active Neks examined had very specific localization and did not contain ankyrin repeats, the deletion within the ankyrin region in Orf_15409 did alter its localization. Several genes annotated as Protein 21.1 are now found to be Neks, and the overall sequence and domain composition suggests that the Neks and Protein 21.1 genes may form a single family with related functions. The other two large, dynamic Giardia families (VSP and HCMP) are also related to each other and VSPs undergo antigenic variation . However, the roles and reasons for the expansion and variability of HCMP, 21.1 and Nek remain obscure. The arrays of divergent TA repeats and our results with non-ankyrin-containing Neks indicate that specific subcellular targeting is important for their function, and may allow Giardia to regulate complex processes within its single cell by targeting proteins to specific organelles. The Neks constitute a major target for exploration of Giardia-specific and strain-specific biology, and their extreme sequence divergence will be useful to explore the sequence limits of the protein kinase-like fold.
The few published studies and our current work on the first five Nek kinases suggest that several signaling proteins have distinct associations with the PFR, the different flagellar axonemes, or the unique ventral disk and median bodies. The latter, like the basal bodies and flagella, are microtubule-based. Several signaling proteins are shared between the caudal flagella with its associated structures and the disk - Neks 16279 and 92498, ERK1 and PP2Ac (protein phosphatase 2A) - suggesting that they may function in the same signaling pathway.
Understanding the replication and segregation of the two nuclei and complex cytoskeleton during the Giardia cell cycle and life cycle has been challenging . The flagellar basal bodies migrate laterally during mitosis to become spindle poles. Several of the Giardia kinases and phosphatases studied to date localize to the basal bodies during interphase, but most have not yet been studied in mitosis or differentiation (Table 1, Figure 1) and only AurK, PKA and PP2A phosphatase have been partially functionally analyzed. The strong pSer and pThr staining within the flagellar axonemes suggests that substrates may be phosphorylated in the basal bodies before incorporation into the axonemes. Analyses of flagellar-associated kinases and signaling may help better understand the roles of the four flagellar pairs in Giardia swimming, attachment, and detachment, which are central to disease , as well as to better understand the roles of this almost universal organelle.
Taken together, our data may help to prioritize future functional kinase studies, elucidate the signaling underlying the cell and life cycles and provide new drug targets to treat Giardia infections. Protein kinases are proven drug targets, and the high divergence of Giardia sequences suggests that specific inhibitors could be developed that have minimal activity against human kinases. Our findings help define the minimal kinase complement of a single-celled eukaryote with a complex life and cell cycle and add to our understanding of Giardia biology, pathogenesis, and evolution.
Materials and methods
Software, data sets and databases
The G lamblia genome assemblies for all three strains were from release 2.3 of GiardiaDB . Sequenced strains are from ATCC, accession numbers 50803 (assemblage A, WB clone C6), 50581 (assemblage B, clone GS) and GLP15 (assemblage E, clone p15). T. vaginalis sequences were from release 1.2 of TrichDB , and L. major from release 2.5 of TriTrypDB .
We constructed profile HMMs for the ePK, PIKK, RIO, ABC1, PDK, and alpha-kinase families with HMMer and used these to search the ORF, genomic, and EST sequences using Decypher hardware-accelerated HMMer implementation from Time Logic (Carlsbad, CA, USA). Divergent Neks were identified with several Nek-specific HMMs and Blast searches, followed by manual inspection for conserved kinase motifs. Final predicted kinase sequences were searched against the Pfam HMM profiles, using both local and glocal models. All matches with P scores < 0.01 were accepted and all matches with scores of 0.01 to 1.0 were evaluated in comparison with known, homologous sequences, inspection of the domain alignment, and reference to the literature. L. major sequences were classified in part using psi-blast with orthologous sequences from other kinetoplastids, and T. vaginalis expansions were also classified using psi-blast profiles built from paralogs. Signal peptides were detected using SignalP and transmembrane regions using TM-HMM  and coiled-coil domains according to Lupas et al. . Nek kinase domains were aligned with ClustalW  and HMMalign , and then extensively edited by hand using JalView . The Nek tree was built using the ClustalW neighbor-joining algorithm and colored by hand using Adobe Illustrator.
Cultivation of Giardia
Cells were washed with ice cold PBS and cell proteins were precipitated in 6% TCA (trichloroacetic acid) for 2 hours on ice. Protein pellets were resuspended in reducing SDS-PAGE sample buffer, neutralized with NaOH, boiled for 5 minutes and stored at -80°C until use. Protein concentrations were determined by the Bradford method (Biorad, Hercules, CA, USA). Proteins were separated by 4-20% SDS PAGE and transferred to PVDF filters. Filters were blocked with 1% milk in PBS supplemented with 0.1% Tween 20 (PBS-Tween) and incubated for 1 hour with the FITC-labeled mouse monoclonal antibodies against pSer, pThr or pTyr (Sigma, St. Louis, MO, USA) in 1% milk. Blots were then washed four times with PBS-Tween and incubated with secondary antibody (goat anti-mouse-horse radish peroxidase (HRP)) for 1 hour. The signal was developed with ECL-plus (GE Healthcare, Waukesha, WI, USA). As a protein loading control, blots were reprobed with the mouse monoclonal anti-taglin antibody  and goat anti-mouse-HRP. As a control for antibody specificity, antibodies were incubated with pSer, pThr or pTyr conjugated to bovine serum albumin (Sigma), respectively, prior to immunolabeling of filters. As an additional control, total Giardia lysates were dephosphorylated with protein phosphatase λ (New England Biolabs, Ipswich, MA, USA) according to the manufacturer's protocol. Both controls eliminated signal on western blot, confirming specificity of the antibodies (data not shown).
Epitope tagging of proteins
The region containing the promoter (> 100 base pairs upstream of the start codon) and coding sequences for Orf_5375 were amplified from G. lamblia strain WB clone C6 (ATCC 50803) genomic DNA with the primers 5'-taagggccccagcatctagctgaatgccga-3' and 5'-taagatatccatcttatacttgtaagcgcc-3', Orf_92498 with primers 5'-gggcccccggatgcgcgtctgttg-3' and 5'-gatatccctgacagtattgaacctgtcc-3', Orf_16279 with primers 5'-gggcccggatccgaggtcatgcgc-3' and 5'-gatatcagaaaggcgtctctgcgtcaaaac-3', Orf_101534 with primers 5'-gggcccggcctgactgcgcatgc-3' and 5'-gatatcctgtctgagcatctcgcacagc-3', and Orf_15409 with primers 5'-tttaagcttcccctgccgctgagtgaacat-3' and 5'-tttgggccccaggttcaggacctcacgcac-3'. The PCR products and the vector encoding the carboxy-terminal AU1 tag (Orf_15409)  or HA tag (all other Neks)  were digested with the respective restriction enzymes. Digested inserts and vectors were gel extracted using a QIAquick Gel Extraction Kit (Qiagen, Venlo, The Netherlands), and ligated overnight at 14°C. Plasmids were transformed into Escherichia coli JM109 (Promega, Fitchburg, WI, USA}). Bacteria were grown overnight in Luria broth and plasmid DNA was purified using a Maxiprep kit (Qiagen) and sequenced (Etonbio, San Diego, CA, USA}). Trophozoites were electroporated with 50 μg plasmid DNA and transfectants were maintained through puromycin selection . Base pairs 1.051 to 1,158 from the ankyrin repeat region of Orf_15409 were deleted by linking the upstream and downstream PCR products together with the internal primers 5'-agtccacatgtactggtctgtggaccctgcctggtg-3' and 5'-tccacagaccagtacatgtggactgcaaccatgtat-3'.
Trophozoites were harvested by chilling and allowed to adhere to coverslips at 37°C for 10 minutes. Whole trophozoites were fixed in situ with methanol (-20°C), permeabilized for 10 minutes with 0.5% Triton X-100 in PBS  and blocked for 1 hour in 5% goat serum, 1% glycerol, 0.1% bovine serum albumin, 0.1% fish gelatin and 0.04% sodium azide. Coverslips were subsequently incubated for 1 hour with the FITC-labeled mouse monoclonal antibodies against pSer, pThr or pTyr (Sigma) or with the rat anti-HA-FITC (Roche, Indianapolis, IN, USA). Cells that were expressing AU1-tagged Nek (Orf_15409) were incubated with the primary antibody mouse anti-AU1 for 1 hour, washed four times over 20 minutes, and incubated with the goat anti-mouse Alexa 488 secondary antibody (Invitrogen, Carlsbad, CA, USA). Coverslips were washed, postfixed with 4% paraformaldehyde, rinsed with PBS and mounted with Prolong Gold with DAPI (Molecular Probes, Eugene, OR, USA). As a control for antibody specificity, antibodies were incubated with pSer-, pThr- or pTyr-labeled albumin (Sigma), respectively, prior to immunolabeling. Staining was monitored and photographed on a Nikon Eclipse E800 microscope with an X-Cite™ 120 fluorescence lamp and 1,000 × magnification (Nikon Instruments Inc.). Confocal images were taken with the Leica TCS SP5 system attached to a DMI 6000 inverted microscope (Leica).
DNA protein kinase
expressed sequence tag
glycogen synthase kinase
high cysteine membrane protein
hidden Markov model
mitogen-activated protein kinase
open reading frame
phosphatidyl inositol kinase
phosphatidyl inositol 3' kinase-related kinase
serial analysis of gene expression
target of rapamycin
variant-specific surface protein.
Holt LJ, Tuch BB, Villen J, Johnson AD, Gygi SP, Morgan DO: Global analysis of Cdk1 substrate phosphorylation sites provides insights into evolution. Science. 2009, 325: 1682–1686. 10.1126/science.1172867.
Adam RD: Biology of Giardia lamblia. Clin Microbiol Rev. 2001, 14: 447–475. 10.1128/CMR.14.3.447-475.2001.
Bingham AK, Meyer EA: Giardia excystation can be induced in vitro in acidic solutions. Nature. 1979, 277: 301–302. 10.1038/277301a0.
Boucher SE, Gillin FD: Excystation of in vitro-derived Giardia lamblia cysts. Infec Immun. 1990, 58: 3516–3522.
Bernander R, Palm JE, Svard SG: Genome ploidy in different stages of the Giardia lamblia life cycle. Cell Microbiol. 2001, 3: 55–62. 10.1046/j.1462-5822.2001.00094.x.
Elmendorf HG, Dawson SC, McCaffery JM: The cytoskeleton of Giardia lamblia. Int J Parasitol. 2003, 33: 3–28. 10.1016/S0020-7519(02)00228-X.
Dawson SC, House SA: Life with eight flagella: flagellar assembly and division in Giardia. Curr Opin Microbiol. 2010, 13: 480–490. 10.1016/j.mib.2010.05.014.
Morrison HG, McArthur AG, Gillin FD, Aley SB, Adam RD, Olsen GJ, Best AA, Cande WZ, Chen F, Cipriano MJ, Davids BJ, Dawson SC, Elmendorf HG, Hehl AB, Holder ME, Huse SM, Kim UU, Lasek-Nesselquist E, Manning G, Nigam A, Nixon JE, Palm D, Passamaneck NE, Prabhu A, Reich CI, Reiner DS, Samuelson J, Svard SG, Sogin ML: Genomic minimalism in the early diverging intestinal parasite Giardia lamblia. Science. 2007, 317: 1921–1926. 10.1126/science.1143837.
Franzen O, Jerlstrom-Hultqvist J, Castro E, Sherwood E, Ankarklev J, Reiner DS, Palm D, Andersson JO, Andersson B, Svard SG: Draft genome sequencing of Giardia intestinalis assemblage B isolate GS: is human Giardiasis caused by two different species?. PLoS Pathog. 2009, 5: e1000560-10.1371/journal.ppat.1000560.
Jerlstrom-Hultqvist J, Franzen O, Ankarklev J, Xu F, Nohynkova E, Andersson JO, Svard SG, Andersson B: Genome analysis and comparative genomics of a Giardia intestinalis assemblage E isolate. BMC Genomics. 2010, 11: 543-10.1186/1471-2164-11-543.
Parsons M, Valentine M, Carter V: Protein kinases in divergent eukaryotes: identification of protein kinase activities regulated during trypanosome development. Proc Natl Acad Sci USA. 1993, 90: 2656–2660. 10.1073/pnas.90.7.2656.
Alvarado ME, Wasserman M: Analysis of phosphorylated proteins and inhibition of kinase activity during Giardia intestinalis excystation. Parasitol Int. 2010, 59: 54–61. 10.1016/j.parint.2009.10.005.
Abel ES, Davids BJ, Robles LD, Loflin CE, Gillin FD, Chakrabarti R: Possible roles of protein kinase A in cell motility and excystation of the early diverging eukaryote Giardia lamblia. J Biol Chem. 2001, 276: 10320–10329. 10.1074/jbc.M006589200.
Gibson C, Schanen B, Chakrabarti D, Chakrabarti R: Functional characterisation of the regulatory subunit of cyclic AMP-dependent protein kinase A homologue of Giardia lamblia: differential expression of the regulatory and catalytic subunits during encystation. Int J Parasitol. 2006, 36: 791–799. 10.1016/j.ijpara.2005.11.008.
Lauwaet T, Davids BJ, Torres-Escobar A, Birkeland SR, Cipriano MJ, Preheim SP, Palm D, Svard SG, McArthur AG, Gillin FD: Protein phosphatase 2A plays a crucial role in Giardia lamblia differentiation. Mol Biochem Parasitol. 2007, 152: 80–89. 10.1016/j.molbiopara.2006.12.001.
Ellis JGt, Davila M, Chakrabarti R: Potential involvement of extracellular signal-regulated kinase 1 and 2 in encystation of a primitive eukaryote, Giardia lamblia. Stage-specific activation and intracellular localization. J Biol Chem. 2003, 278: 1936–1945. 10.1074/jbc.M209274200.
Aurrecoechea C, Brestelli J, Brunk BP, Carlton JM, Dommer J, Fischer S, Gajria B, Gao X, Gingle A, Grant G, Harb OS, Heiges M, Innamorato F, Iodice J, Kissinger JC, Kraemer E, Li W, Miller JA, Morrison HG, Nayak V, Pennington C, Pinney DF, Roos DS, Ross C, Stoeckert CJ, Sullivan S, Treatman C, Wang H: GiardiaDB and TrichDB: integrated genomic resources for the eukaryotic protist pathogens Giardia lamblia and Trichomonas vaginalis. Nucleic Acids Res. 2009, 37: D526–530. 10.1093/nar/gkn631.
Eisen JA, Coyne RS, Wu M, Wu D, Thiagarajan M, Wortman JR, Badger JH, Ren Q, Amedeo P, Jones KM, Tallon LJ, Delcher AL, Salzberg SL, Silva JC, Haas BJ, Majoros WH, Farzad M, Carlton JM, Smith RK, Garg J, Pearlman RE, Karrer KM, Sun L, Manning G, Elde NC, Turkewitz AP, Asai DJ, Wilkes DE, Wang Y, Cai H, et al: Macronuclear genome sequence of the ciliate Tetrahymena thermophila, a model eukaryote. PLoS Biol. 2006, 4: e286-10.1371/journal.pbio.0040286.
Goldberg JM, Manning G, Liu A, Fey P, Pilcher KE, Xu Y, Smith JL: The Dictyostelium kinome--analysis of the protein kinases from a simple model organism. PLoS Genet. 2006, 2: e38-10.1371/journal.pgen.0020038.
Manning G, Plowman GD, Hunter T, Sudarsanam S: Evolution of protein kinase signaling from yeast to man. Trends Biochem Sci. 2002, 27: 514–520. 10.1016/S0968-0004(02)02179-5.
Manning G, Whyte DB, Martinez R, Hunter T, Sudarsanam S: The protein kinase complement of the human genome. Science. 2002, 298: 1912–1934. 10.1126/science.1075762.
Banks Jea: The compact Selaginella genome identifies changes in gene content associated with the evolution of vascular plants. Science. 2011, 332: 960–963. 10.1126/science.1203810.
Bazan-Tejeda ML, Arguello-Garcia R, Bermudez-Cruz RM, Robles-Flores M, Ortega-Pierres G: Protein kinase C isoforms from Giardia duodenalis: identification and functional characterization of a beta-like molecule during encystment. Arch Microbiol. 2007, 187: 55–66.
Lujan HD, Mowatt MR, Helman LJ, Nash TE: Insulin-like growth factors stimulate growth and L-cysteine uptake by the intestinal parasite Giardia lamblia. J Biol Chem. 1994, 269: 13069–13072.
Carlton JM, Hirt RP, Silva JC, Delcher AL, Schatz M, Zhao Q, Wortman JR, Bidwell SL, Alsmark UC, Besteiro S, Sicheritz-Ponten T, Noel CJ, Dacks JB, Foster PG, Simillion C, Van de Peer Y, Miranda-Saavedra D, Barton GJ, Westrop GD, Muller S, Dessi D, Fiori PL, Ren Q, Paulsen I, Zhang H, Bastida-Corcuera FD, Simoes-Barbosa A, Brown MT, Hayes RD, Mukherjee M, et al: Draft genome sequence of the sexually transmitted pathogen Trichomonas vaginalis. Science. 2007, 315: 207–212. 10.1126/science.1132894.
Naula C, Parsons M, Mottram JC: Protein kinases as drug targets in trypanosomes and Leishmania. Biochim Biophys Acta. 2005, 1754: 151–159.
Baldauf SL: The deep roots of eukaryotes. Science. 2003, 300: 1703–1706. 10.1126/science.1085544.
Ankarklev J, Jerlstrom-Hultqvist J, Ringqvist E, Troell K, Svard SG: Behind the smile: cell biology and disease mechanisms of Giardia species. Nat Rev. 2010, 8: 413–422.
Hampl V, Hug L, Leigh JW, Dacks JB, Lang BF, Simpson AG, Roger AJ: Phylogenomic analyses support the monophyly of Excavata and resolve relationships among eukaryotic "supergroups". Proc Natl Acad Sci USA. 2009, 106: 3859–3864. 10.1073/pnas.0807880106.
Regoes A, Zourmpanou D, Leon-Avila G, van der Giezen M, Tovar J, Hehl AB: Protein import, replication, and inheritance of a vestigial mitochondrion. J Biol Chem. 2005, 280: 30557–30563. 10.1074/jbc.M500787200.
Reiner DS, McCaffery JM, Gillin FD: Reversible interruption of Giardia lamblia cyst wall protein transport in a novel regulated secretory pathway. Cell Microbiol. 2001, 3: 459–472. 10.1046/j.1462-5822.2001.00129.x.
Sagolla MS, Dawson SC, Mancuso JJ, Cande WZ: Three-dimensional analysis of mitosis and cytokinesis in the binucleate parasite Giardia intestinalis. J Cell Sci. 2006, 119: 4889–4900. 10.1242/jcs.03276.
Yang J, Yu Y, Hamrick HE, Duerksen-Hughes PJ: ATM, ATR and DNA-PK: initiators of the cellular genotoxic stress responses. Carcinogenesis. 2003, 24: 1571–1580. 10.1093/carcin/bgg137.
Groth A, Lukas J, Nigg EA, Sillje HH, Wernstedt C, Bartek J, Hansen K: Human Tousled like kinases are targeted by an ATM- and Chk1-dependent DNA damage checkpoint. EMBO J. 2003, 22: 1676–1687. 10.1093/emboj/cdg151.
Hofstetrova K, Uzlikova M, Tumova P, Troell K, Svard SG, Nohynkova E: Giardia intestinalis: aphidicolin influence on the trophozoite cell cycle. Exp Parasitol. 2010, 124: 159–166. 10.1016/j.exppara.2009.09.004.
Linden KG, Shin GA, Faubert G, Cairns W, Sobsey MD: UV disinfection of Giardia lamblia cysts in water. Environ Sci Technol. 2002, 36: 2519–2522. 10.1021/es0113403.
Guo Z, Stiller JW: Comparative genomics and evolution of proteins associated with RNA polymerase II C-terminal domain. Mol Biol Evol. 2005, 22: 2166–2178. 10.1093/molbev/msi215.
Lee JM, Greenleaf AL: CTD kinase large subunit is encoded by CTK1, a gene required for normal growth of Saccharomyces cerevisiae. Gene Expression. 1991, 1: 149–167.
Best AA, Morrison HG, McArthur AG, Sogin ML, Olsen GJ: Evolution of eukaryotic transcription: insights from the genome of Giardia lamblia. Genome Res. 2004, 14: 1537–1547. 10.1101/gr.2256604.
Wikinome: Dual Specificity Kinases. [https://doi.org/kinase.com/wiki/index.php/Dual-Specificity_Kinases]
Nett IR, Martin DM, Miranda-Saavedra D, Lamont D, Barber JD, Mehlert A, Ferguson MA: The phosphoproteome of bloodstream form Trypanosoma brucei, causative agent of African sleeping sickness. Mol Cell Proteomics. 2009, 8: 1527–1538. 10.1074/mcp.M800556-MCP200.
Manning G, Young SL, Miller WT, Zhai Y: The protist, Monosiga brevicollis, has a tyrosine kinase signaling network more elaborate and diverse than found in any known metazoan. Proc Natl Acad Sci USA. 2008, 105: 9674–9679. 10.1073/pnas.0801314105.
Lalle M, Salzano AM, Crescenzi M, Pozio E: The Giardia duodenalis 14-3-3 protein is post-translationally modified by phosphorylation and polyglycylation of the C-terminal tail. J Biol Chem. 2006, 281: 5137–5148.
Anamika K, Bhattacharya A, Srinivasan N: Analysis of the protein kinome of Entamoeba histolytica. Proteins. 2008, 71: 995–1006. 10.1002/prot.21790.
Scheeff ED, Eswaran J, Bunkoczi G, Knapp S, Manning G: Structure of the pseudokinase VRK3 reveals a degraded catalytic site, a highly conserved kinase fold, and a putative regulatory binding site. Structure. 2009, 17: 128–138. 10.1016/j.str.2008.10.018.
Kim KT, Mok MT, Edwards MR: Protein kinase B from Giardia intestinalis. Biochem Biophys Res Commun. 2005, 334: 333–341. 10.1016/j.bbrc.2005.06.106.
Hernandez Y, Zamora G, Ray S, Chapoy J, Chavez E, Valvarde R, Williams E, Aley SB, Das S: Transcriptional analysis of three major putative phosphatidylinositol kinase genes in a parasitic protozoan, Giardia lamblia. J Eukaryot Microbiol. 2007, 54: 29–32. 10.1111/j.1550-7408.2006.00142.x.
Cox SS, van der Giezen M, Tarr SJ, Crompton MR, Tovar J: Evidence from bioinformatics, expression and inhibition studies of phosphoinositide-3 kinase signalling in Giardia intestinalis. BMC Microbiol. 2006, 6: 45-10.1186/1471-2180-6-45.
Morrison HG, Zamora G, Campbell RK, Sogin ML: Inferring protein function from genomic sequence: Giardia lamblia expresses a phosphatidylinositol kinase-related kinase similar to yeast and mammalian TOR. Comp Biochem Physiol B Biochem Mol Biol. 2002, 133: 477–491. 10.1016/S1096-4959(02)00218-X.
Ward P, Equinet L, Packer J, Doerig C: Protein kinases of the human malaria parasite Plasmodium falciparum: the kinome of a divergent eukaryote. BMC Genomics. 2004, 5: 79-10.1186/1471-2164-5-79.
Davids BJ, Williams S, Lauwaet T, Palanca T, Gillin FD: Giardia lamblia aurora kinase: a regulator of mitosis in a binucleate parasite. Int J Parasitol. 2008, 38: 353–369. 10.1016/j.ijpara.2007.08.012.
Pan J, Snell WJ: Regulated targeting of a protein kinase into an intact flagellum. An aurora/Ipl1p-like protein kinase translocates from the cell body into the flagella during gamete activation in chlamydomonas. J Biol Chem. 2000, 275: 24106–24114. 10.1074/jbc.M002686200.
O'Connell MJ, Krien MJ, Hunter T: Never say never. The NIMA-related protein kinases in mitotic control. Trends Cell Biol. 2003, 13: 221–228. 10.1016/S0962-8924(03)00056-4.
Mahjoub MR, Qasim Rasi M, Quarmby LM: A NIMA-related kinase, Fa2p, localizes to a novel site in the proximal cilia of Chlamydomonas and mouse kidney cells. Mol Biol Cell. 2004, 15: 5172–5186. 10.1091/mbc.E04-07-0571.
Liu S, Lu W, Obara T, Kuida S, Lehoczky J, Dewar K, Drummond IA, Beier DR: A defect in a novel Nek-family kinase causes cystic kidney disease in the mouse and in zebrafish. Development. 2002, 129: 5839–5846. 10.1242/dev.00173.
Wloga D, Camba A, Rogowski K, Manning G, Jerka-Dziadosz M, Gaertig J: Members of the NIMA-related kinase family promote disassembly of cilia by multiple mechanisms. Mol Biol Cell. 2006, 17: 2799–2810. 10.1091/mbc.E05-05-0450.
Stajich JE, Wilke SK, Ahren D, Au CH, Birren BW, Borodovsky M, Burns C, Canback B, Casselton LA, Cheng CK, Deng J, Dietrich FS, Fargo DC, Farman ML, Gathman AC, Goldberg J, Guigo R, Hoegger PJ, Hooker JB, Huggins A, James TY, Kamada T, Kilaru S, Kodira C, Kues U, Kupfer D, Kwan HS, Lomsadze A, Li W, Lilly WW, et al: Insights into evolution of multicellular fungi from the assembled chromosomes of the mushroom Coprinopsis cinerea (Coprinus cinereus). Proc Natl Acad Sci USA. 2010, 107: 11889–11894. 10.1073/pnas.1003391107.
Jimenez-Garcia LF, Zavala G, Chavez-Munguia B, Ramos-Godinez Mdel P, Lopez-Velazquez G, Segura-Valdez Mde L, Montanez C, Hehl AB, Arguello-Garcia R, Ortega-Pierres G: Identification of nucleoli in the early branching protist Giardia duodenalis. Int J Parasitol. 2008, 38: 1297–1304. 10.1016/j.ijpara.2008.04.012.
Birkeland SR, Preheim SP, Davids BJ, Cipriano MJ, Palm D, Reiner DS, Svard SG, Gillin FD, McArthur AG: Transcriptome analyses of the Giardia lamblia life cycle. Mol Biochem Parasitol. 2010, 174: 62–65. 10.1016/j.molbiopara.2010.05.010.
Pradel LC, Bonhivers M, Landrein N, Robinson DR: NIMA-related kinase TbNRKC is involved in basal body separation in Trypanosoma brucei. J Cell Sci. 2006, 119: 1852–1863. 10.1242/jcs.02900.
Shiba D, Manning DK, Koga H, Beier DR, Yokoyama T: Inv acts as a molecular anchor for Nphp3 and Nek8 in the proximal segment of primary cilia. Cytoskeleton. 2010, 67: 112–119.
Mahjoub MR, Montpetit B, Zhao L, Finst RJ, Goh B, Kim AC, Quarmby LM: The FA2 gene of Chlamydomonas encodes a NIMA family kinase with roles in cell cycle progression and microtubule severing during deflagellation. J Cell Sci. 2002, 115: 1759–1768.
Lauwaet T, Smith AJ, Reiner DS, Romijn EP, Wong CCL, Davids BJ, Shah SA, Yates JR, Gillin FD: Mining the Giardiagenome and proteome for conserved and unique basal body proteins. Int J Parasitol. 2011,
Miranda-Saavedra D, Stark MJ, Packer JC, Vivares CP, Doerig C, Barton GJ: The complement of protein kinases of the microsporidium Encephalitozoon cuniculi in relation to those of Saccharomyces cerevisiae and Schizosaccharomyces pombe. BMC Genomics. 2007, 8: 309-10.1186/1471-2164-8-309.
Kulakova L, Singer SM, Conrad J, Nash TE: Epigenetic mechanisms are involved in the control of Giardia lamblia antigenic variation. Mol Microbiol. 2006, 61: 1533–1542. 10.1111/j.1365-2958.2006.05345.x.
Nohynkova E, Tumova P, Kulda J: Cell division of Giardia intestinalis: flagellar developmental cycle involves transformation and exchange of flagella between mastigonts of a diplomonad cell. Eukaryotic cell. 2006, 5: 753–761. 10.1128/EC.5.4.753-761.2006.
Dawson SC: An insider's guide to the microtubule cytoskeleton of Giardia. Cell Microbiol. 2010, 12: 588–598. 10.1111/j.1462-5822.2010.01458.x.
Sonnhammer EL, von Heijne G, Krogh A: A hidden Markov model for predicting transmembrane helices in protein sequences. Proc Int Conf Intell Syst Mol Biol. 1998, 6: 175–182.
Lupas A, Van Dyke M, Stock J: Predicting coiled coils from protein sequences. Science. 1991, 252: 1162–1164. 10.1126/science.252.5009.1162.
Larkin MA, Blackshields G, Brown NP, Chenna R, McGettigan PA, McWilliam H, Valentin F, Wallace IM, Wilm A, Lopez R, Thompson JD, Gibson TJ, Higgins DG: Clustal W and Clustal × version 2.0. Bioinformatics. 2007, 23: 2947–2948. 10.1093/bioinformatics/btm404.
Eddy SR: A new generation of homology search tools based on probabilistic inference. Genome Informatics. 2009, 23: 205–211.
Waterhouse AM, Procter JB, Martin DM, Clamp M, Barton GJ: Jalview Version 2--a multiple sequence alignment editor and analysis workbench. Bioinformatics. 2009, 25: 1189–1191. 10.1093/bioinformatics/btp033.
Diamond LS, Harlow DR, Cunnick CC: A new medium for the axenic cultivation of Entamoeba histolytica and other Entamoeba. Trans R Soc Trop Med Hyg. 1978, 72: 431–432. 10.1016/0035-9203(78)90144-X.
Keister DB: Axenic culture of Giardia lamblia in TYI-S-33 medium supplemented with bile. Trans R Soc Trop Med Hyg. 1983, 77: 487–488. 10.1016/0035-9203(83)90120-7.
Ward HD, Lev BI, Kane AV, Keusch GT, Pereira ME: Identification and characterization of taglin, a mannose 6-phosphate binding, trypsin-activated lectin from Giardia lamblia. Biochemistry. 1987, 26: 8669–8675. 10.1021/bi00400a027.
Weiland ME, Palm JE, Griffiths WJ, McCaffery JM, Svard SG: Characterisation of alpha-1 giardin: an immunodominant Giardia lamblia annexin with glycosaminoglycan-binding activity. Int J Parasitol. 2003, 33: 1341–1351. 10.1016/S0020-7519(03)00201-7.
Touz MC, Lujan HD, Hayes SF, Nash TE: Sorting of encystation-specific cysteine protease to lysosome-like peripheral vacuoles in Giardia lamblia requires a conserved tyrosine-based motif. J Biol Chem. 2003, 278: 6420–6426. 10.1074/jbc.M208354200.
Knodler LA, Svard SG, Silberman JD, Davids BJ, Gillin FD: Developmental gene regulation in Giardia lamblia: first evidence for an encystation-specific promoter and differential 5' mRNA processing. Mol Microbiol. 1999, 34: 327–340. 10.1046/j.1365-2958.1999.01602.x.
This work was supported by NIH grants, AI42488, AI51687 and AI75527 (FG), and R01 HG004164 and P30 CA014195 (GM). AJS was supported by GI Training grant T32DK07202. We thank T Hunter and members of the Manning lab for critical reading of the manuscript. We are grateful to H Ward for the antibody to taglin. All sequence analysis presented here and additional supporting evidence are freely available at KinBase . Sequences and other annotations are from GiardiaDB .
FDG, GM, DSR, and SS conceived of the study, including its design and coordination. GM and FDG wrote the manuscript with contributions from TL, AS, and MD. DSR cataloged the initial WB kinome, and MD, GM, and YZ carried out extensive curation and computational and phylogenetic analysis of all five kinomes. TL performed the immunoblot identification and immunolocalization of phosphorylated proteins (Figures 3 and 4). TL and AS carried out the molecular genetic and cell biologic studies of the Nek kinases and prepared Figures 1 and 3 to 5 and Table 1. All authors contributed to the editing of the manuscript.
Electronic supplementary material
Authors’ original submitted files for images
About this article
Cite this article
Manning, G., Reiner, D.S., Lauwaet, T. et al. The minimal kinome of Giardia lamblia illuminates early kinase evolution and unique parasite biology. Genome Biol 12, R66 (2011) doi:10.1186/gb-2011-12-7-r66
- Basal Body
- Ankyrin Repeat
- Mitotic Exit Network
- Giardia Trophozoite
- Kinase Class