Evolution of Tubulin Gene Arrays in Trypanosomatid parasites: genomic restructuring in Leishmania
BMC Genomics volume 7, Article number: 261 (2006)
α- and β-tubulin are fundamental components of the eukaryotic cytoskeleton and cell division machinery. While overall tubulin expression is carefully controlled, most eukaryotes express multiple tubulin genes in specific regulatory or developmental contexts. The genomes of the human parasites Trypanosoma brucei and Leishmania major reveal that these unicellular kinetoplastids possess arrays of tandem-duplicated tubulin genes, but with differences in organisation. While L. major possesses monotypic α and β arrays in trans, an array of alternating α- and β tubulin genes occurs in T. brucei. Polycistronic transcription in these organisms makes the chromosomal arrangement of tubulin genes important with respect to gene expression.
We investigated the genomic architecture of tubulin tandem arrays among these parasites, establishing which character state is derived, and the timing of character transition. Tubulin loci in T. brucei and L. major were compared to examine the relationship between the two character states. Intergenic regions between tubulin genes were sequenced from several trypanosomatids and related, non-parasitic bodonids to identify the ancestral state. Evidence of alternating arrays was found among non-parasitic kinetoplastids and all Trypanosoma spp.; monotypic arrays were confirmed in all Leishmania spp. and close relatives.
Alternating and monotypic tubulin arrays were found to be mutually exclusive through comparison of genome sequences. The presence of alternating gene arrays in non-parasitic kinetoplastids confirmed that separate, monotypic arrays are the derived state and evolved through genomic restructuring in the lineage leading to Leishmania. This fundamental reorganisation accounted for the dissimilar genomic architectures of T. brucei and L. major tubulin repertoires.
Gene expression in kinetoplastids (Euglenozoa) takes a peculiar form, quite unlike the system of promoter and terminator signals typical of other eukaryotes. Expression of several, contiguous loci occurs simultaneously through polycistronic transcription [1–3] and regulation of individual genes is largely post-transcriptional . Within this context, an unusually large proportion of kinetoplastid genes is arranged in tandem gene arrays and includes transporter proteins , surface antigens  and the spliced-leader sequence responsible for cleavage of the polycistronic pre-mRNA . This study addresses the evolution of α- and β-tubulin arrays in the parasitic kinetoplastids, Trypanosoma spp. and Leishmania spp., with a comparative genomic approach. These unicellular flagellates are responsible for various human diseases around the world, namely African sleeping sickness, leishmaniasis and Chagas' disease.
Tubulin is a fundamental constituent of kinetoplastid cytoskeletons, cell division machinery and motile organelles . There is a large family of tubulin proteins but the α/β heterodimer is the essential building material for the microtubular cytoskeleton . Trypanosomatid parasites possess an extensive array of cytoplasmic, mitotic and flagellar microtubules and recent evidence suggests that tubulin expression varies greatly during the life cycles of Trypanosoma and Leishmania spp., possibly as the relative demand for these structures fluctuates [10–14]. Indeed, in certain species, different isoforms of tubulin may have specific expression profiles related to the parasitic life cycle; for example, L. mexicana has a β-tubulin isoform unique to the amastigote stage found within human macrophages .
Kinetoplastid gene expression is based on polycistronic transcription, followed by 5' trans-splicing of pre-mRNA and 3' poly-adenylation to form mature transcripts [16, 17]. A variety of structural motifs in untranscribed regions have been shown to regulate mRNA levels post-transcriptionally by affecting trans-splicing, RNA-binding capability and transcript stability [18–23]. Genes do not generally possess individual promoters and therefore, cannot be up-regulated through transcriptional initiation. Instead, where high transcript levels are required, genes may be duplicated to form tandem gene arrays, which are co-transcribed. Such dosage effects may explain why tubulin genes, and other genes, such as the paraflagellar rod proteins , are arrayed. However, it also seems possible for specific isoforms to be differentially expressed through regulation of particular repeats within the array, or of additional, non-arrayed (i.e., singleton) loci elsewhere in the genome [5, 15, 25, 26].
In yeast, equal concentrations of α and β tubulin are required for normal cellular function [27, 28]. Assuming that such coordination is desirable in trypanosomatids, the precise arrangement of tubulin genes could be crucial. Recently completed genome sequences have exposed the full extent of tandem gene arrays in Trypanosoma brucei  and Leishmania major  and these are illustrated in Figure 1. Tubulin gene arrays have long been known and used to understand gene regulation in these organisms. Trypanosoma spp. possess a single array of alternating α- and β-tubulin genes [31–35] (see Figure 1(a)), while Leishmania spp. possess separate α-tubulin and β-tubulin arrays on different chromosomes [36, 37] (see Figure 1(b)). The tandem repetition of these two character states suggests that they are independent solutions to a common need. Given that an alternating array is the more intuitive means of maintaining transcriptional parity between the α and β heterodimeric tubulins, quite how and why such a fundamental genomic rearrangement occurred in one or both lineages requires explanation.
This study examined the genomic architecture of tubulin tandem arrays in a range of kinetoplastids and combined this with bioinformatic analyses of various genome sequences to identify the origin of the two character states found in Trypanosoma spp. and Leishmania spp. It included representatives of the three non-parasitic clades within the Kinetoplastida, the 'bodonids', which together comprise the natural outgroup of trypanosomatids [38, 39]. A phylogeny for tubulin genomic architecture was created to ask several questions: first, can the relatedness of tubulin loci be traced through comparison of their genomic positions; second, what is the polarity of the character transition, i.e., is one alternating array or two monotypic arrays the derived state; and third, if one state is derived, what is the model for the genomic rearrangement.
The genomic arrangement of tubulin genes among kinetoplastids was examined in three stages. First, comparison of the completed genome sequences for T. brucei and L. major established the relationships between the distinct tubulin loci in these two organisms. Second, specific and degenerate polymerase chain reaction (PCR) primers, able to amplify the intergenic sequence (IGS) between any combination of α- and β-tubulin genes in tandem were designed from sequence alignments spanning the entire Kinetoplastida. These primers were used for molecular screening of various species, including the non-parasitic bodonids. Third, bioinformatic screening of draft genome sequences for tubulin loci in several other species allowed their character states to be confirmed. The characters identified by the second and third parts are described in Table 1 and were mapped on to an evolutionary tree to infer the ancestral state prior to the origins of Trypanosoma and Leishmania, and thereby, determine the phylogeny of tubulin tandem gene arrays.
Comparison of gene order in T. brucei and L. major genome sequences
The gene order surrounding the alternating array in T. brucei was conserved on chromosome 20 of L. major. A string of calpain-like genes, upstream in T. brucei, was contiguous with coatamer β-subunit and RNase-like genes, which were downstream in T. brucei (see Figure 2(b)). Thus, while there was a homoeologous position for the alternating array in L. major, there was no trace of tubulin, or the adjacent histone gene array found in T. brucei.
There was also colinearity around the location of the L. major arrays. The α-tubulin array on chromosome 13 was flanked by an N-acetyl transferase subunit gene and a long-chain fatty acid CoA ligase gene, as well as other hypothetical loci. These genes are adjacent on chromosome 11 in T. brucei (see Figure 2(a)), and hypothetical genes in syntenic positions showed sequence homology. Likewise for the β-tubulin array; two hypothetical genes that flank the array in L. major (LmjF33.0790 and LmjF33.0840) showed high BLAST scores to contiguous genes on chromsome10 in T. brucei: Tb10.26.0440 (7.9e-34) and Tb10.26.0430 (8.4e-141) respectively. The position of the singleton β-tubulin locus on chromosome 21 in L. major was partially conserved in T. brucei. The upstream gene order in L. major was recapitulated in the subtelomeric region of chromosome 10 in T. brucei; however, there was no tubulin locus and no conserved synteny downstream, suggesting that the tubulin locus corresponds to a strand break-point (see Figure 2(c)). No homoeologous position was identified in the T. brucei genome for the chromosome 8 β-tubulin locus in L. major.
Sequencing of tubulin arrays in further Kinetoplastida
Insect-parasitizing trypansomatids and non-parasitic bodonids were screened for tandem tubulin genes using specific and degenerate PCR, to provide outgroup comparisons to character states in Trypanosoma and Leishmania. Products that were amplified and sequenced from kinetoplastids without genome projects are shown in Table 1; these were non-coding IGS for the most part, although fragments of tubulin coding sequence (CDS) were present at either end to enable positive identification of gene order. L. mexicana, and C. fasciculata both possessed monotypic arrays and IGS from both α- and β-tubulin arrays were at least partially homologous with those from the existing Leishmania sequences. A monotypic α-tubulin gene array is also documented in Leptomonas seymouri, which is a close relative of Leishmania , (this information is included in Figure 4). There was no evidence of alternating arrays in any of these species. Three stercorarian trypanosomes, T. grayi, T. pestanai and T. cyclops, each possessed alternating arrays, with no evidence for monotypic arrays. While there are some gross similarities in base composition and polypurine strings, the IGSs from these species and T. cruzi did not align. Alternating arrays were also identified in the endosymbiont-bearing Crithidia deanei and another insect-parasitizing trypanosomatid, the aposymbiotic Herpetomonas megaseliae. Primers designed to amplify monotypic arrays produced bands for these two species when visualised on electrophoretic gels, but these were weak and inconsistent. Once sequenced, such bands from C. deanei were shown to result from mis-priming downstream from tubulin loci.
Table 1 includes many instances where a particular array could not be found or amplified (denoted by 'x'). This could reflect a genuine absence, as in the case of completed genome sequences, or it could reflect a failure of particular reactions, perhaps due to poor primer annealing. For instance, it was not possible to amplify the β-α IGS for T. pestanai, C. deanei, Neobodo designis or Bodo saltans; these sequences may or may not exist, for instance, Bodo may have only single β- and α-tubulin genes in tandem, nonetheless, their omission does not prevent the character states from being identified from the available evidence.
A variety of degenerate primer combinations generated products when applied to the non-trypanosomatid kinetoplastids, B. saltans, Parabodo caudatus and N. designis. When applied at relatively low annealing temperatures (around 52–58°C), this tended to permit priming at several sites, including on the wrong tubulin. However, this partial specificity was sufficient to amplify fragments of tubulin, which were then used to design secondary primers. These successfully generated specific products that confirmed the presence of alternating arrays in all three species. When sequenced, those products that had previously indicated monotypic arrays were shown to be IGS from the same alternating arrays and therefore, the result of mis-priming. IGSs from the three species could not be aligned.
The IGSs between tubulin repeats varied greatly in size and content, over relatively short evolutionary distances. IGSs within Leishmania aligned but showed substantial length variation, owing to repetitive DNA motifs. Beyond this, there was no sequence homology among IGSs of any array type. There were no obvious sequence motifs shared by IGSs, although Figure 4 shows that polypyrimidine and polypurine strings, as well as microsatellites, were very common.
Arrangement of tubulin genes in Trypanosoma genome sequences
Mining the T. congolense genome sequence produced two contigs that include alternating arrays of α- and β-tubulin genes, as in T. brucei; these can be retrieved from geneDB using the identifiers congo819f03.q1k and congo_endsN14h02.p1k respectively. The nucleotide sequence for the locus directly upstream of the array in T. brucei (Tb927.1.2320) was used to search T. congolense unassembled reads. Homologous sequences were identified and tiled together to complete the T. congolense homolog to the upstream locus; this showed 67% identity to the T. brucei gene. Tiling downstream from this gene showed that the homolog to Tb927.1.2320 is 234 bp upstream of an α-tubulin and then a further β-tubulin; it also demonstrated that IGSs following α- and β-tubulin copies are 353 bp and 443 bp in length respectively and do not align. Copies of each IGS were identical except for minor length differences in repetitive regions.
Two contigs confirmed that the situation is very similar in T. vivax. The first, retrievable from geneDB with the identifier tviv499h03.p1k, comprised an α-tubulin gene and homologs to loci directly upstream of the array in T. brucei, with conserved synteny. The second, identified by tviv1885f05.p1k, included six tubulin genes in an alternating array. The IGSs again formed two classes following α- and β-tubulin duplicates and were 332–339 bp and 492–497 bp in length respectively. There was some length variation between repeats due to repetitive elements within the IGSs.
No array is evident from the current release of the T. cruzi genome sequence . However, it is known that an alternating α-β array exists [40, 41], and sequence data independently deposited in GenBank comprises β- and α-tubulin genes in tandem (accessions [GenBank: AF091836] and [Genbank: M97956], among others). Otherwise, the genome sequence contained three contigs that include tubulin. The first (Tc00.1047053506563.40) showed a single β-tubulin and three other loci; together, they were colinear with chromosome 1 in T. brucei, and indicate that this single β-tubulin gene occupies a homoeologous position to the alternating array (shown in Figure 3). Given that an alternating arrangement is known to exist in T. cruzi, and is not represented elsewhere, this contig is interpreted as the location of the alternating array in T. cruzi. Since the array may start and end with a β-tubulin duplicate, the single β-tubulin locus could represent a 'collapsed' array. The second contig (Tc00.1047053509003.70) was a duplicate of the first, although the β-tubulin is annotated as a pseudogene and apparently lacks 700 bp from the 3' end. The third contig (Tc00.1047053411235.9) included a lone α-tubulin without any contextual information. In summary, these three Trypanosoma genome sequences concurred with the arrangement in T. brucei, showing an α-β alternating array, with conservation of surrounding gene order. IGSs following the two isotypes were always dissimilar, but each class of CDS and internal IGS were consistently concerted. There was no evidence for further tubulin loci.
Arrangement of tubulin genes in Leishmania genome sequences
The above analysis suggested that the Trypanosoma tubulin sequences were found only in a single alternating array. The situation in Leishmania spp. is more complex with multiple β-tubulin loci. The current release of the L. infantum genome sequence includes homologs to each L. major tubulin locus (shown in Figure 1). Searching with BLAST located two α-tubulin genes in tandem on contig 2963; comparison of the 958 bp IGS with L. major confirmed that it shows 95.5% homology to the α-array on chromosome 13. Similarly, tandem β-tubulin genes on contig 4336 had an IGS of 2217 bp, which were 94.2% homologous to those on chromosome 33 in L. major. Contig 4108 included a single β-tubulin and upstream loci that showed conserved synteny with chromosome 21. The 5' untranscribed region (UTR) of this single β-tubulin gene showed partial homology with the β-array (as in L. major) but the 3'UTR was unique. Finally, contig 4260 included a single β-tubulin gene with unique 5' and 3'UTRs that were 96% identical to those around the chromosome 8 locus in L. major.
At the time of writing, the draft genome sequence of L. braziliensis was available as a preliminary, automated assembly. This included partial α- and β-tubulin genes in approximately homoeologous positions to those in L. major. However, these genes did not comprise complete coding sequences and many of the surrounding loci present in L. major were not present in the draft assembly. In fact, the presence of homologs to each L. major locus was confirmed by manually assembling these loci in L. braziliensis by tiling reads together, using the last 100 bp of each read to locate the next. Three distinct 3' UTRs were identified by searching the read catalogue with the C-terminus of the L. major β-tubulin gene.
Tiling downstream from the first of these distinct sequences produced the N-terminus of another β-tubulin gene. This indicated the presence of (at least) a tandem pair of β-tubulin duplicates. It was not possible to confirm this by tiling inwards from flanking loci due to sequence gaps on both sides. The IGS between these duplicates was 1629 bp in length and showed sequence homology with the L. major β-β tubulin array IGS throughout its length (although its was substantially shorter due to indels).
The second distinct 3'UTR identified by BLAST also appeared to tile into another β-tubulin gene but, on closer inspection, this resulted from a section of repetitive DNA on either side of the tubulin that caused one to tile back into the N-terminus. In fact, this UTR corresponded to the chromosome 8 locus, which was confirmed by searching the read catalogue for the locus upstream of the chromosome 8 β-tubulin gene in L. major (LmjF08.1280). Tiling downstream from this identified a putative ortholog to LmjF08.1280 in L. braziliensis.
The third distinct UTR did not tile into another β-tubulin gene but a homolog to histone deacetylase gene, which was downstream of the chromosome 21 β-tubulin in L. major. After locating a homolog to the upstream locus in L. major (LmjF21.1855) and tiling downstream, the 5'UTR of a β-tubulin gene was identified; this confirmed the presence of an ortholog to the chromosome 21 locus. Tandem α-tubulin genes were identified with BLAST and shown to occupy a homoeologous position to the array in L. major, based on conserved synteny of surrounding loci. In summary, all three Leishmania genome sequences supported the presence of one α-tubulin locus on chromosome 13 and three distinct β-tubulin loci; two singletons are found on chromosomes 21 and 8, and an arrayed locus on chromosome 33. In all three species the three β-tubulin loci were flanked by distinct untranscribed regions, except the 5' UTRs of the chromosome 33 and 21 loci, which were partially homologous.
Phylogeny of tubulin genomic architecture
Phylogenetic estimation using 18S rRNA sequences produced a resolved and robust topology, with high bootstrap values at most nodes; the topology is consistent with previous reconstructions using this marker [38, 42–45]. The rRNA phylogeny is shown in Figure 4, the genomic architecture in each species is shown alongside, as well as sequence motifs identified in intergenic sequences. The figure demonstrates that the monotypic arrays in Leishmania spp., C. fasciculata and L. seymouri are the derived condition and have evolved from an ancestor bearing an alternating array. This derivation occurred once and has been maintained in all Leishmania species inspected here. Conversely, all Trypanosoma spp. have maintained an alternating arrangement. Alternating arrays in all three non-trypanosomatid clades (Bodo, Parabodo and Neobodo) suggests that this transition has only occurred once in the Kinetoplastida.
Through a combination of molecular screening of various kinetoplastid genomes and bioinformatic screening of trypanosomatid genome sequences, the genomic organisation of tubulin genes in these protists has been identified. The alternating tubulin array in T. brucei and the distinct, monotypic arrays in L. major are representative of their respective genera and mutually exclusive, i.e., they are not modified states of a common ancestral character. Rather, two results confirm that the monotypic arrays of Leishmania spp. and their close relatives (Crithidia fasciculata and Leptomonas seymouri) represent a fundamental rearrangement of tubulin genes, formed de novo in novel genomic locations. First, the presence of alternating arrays in all three clades of non-parasitic kinetoplastids indicates that this was the character state in the ancestral trypanosomatid. Second, gene order comparisons demonstrate that, while the chromosomal locations of tubulin arrays are reciprocally conserved, the alternating array has been entirely abolished in L. major and T. brucei has no orthologs to the monotypic arrays.
An important feature of this transition is that the alternating locus has been replaced by several novel loci without any obvious links, other than the tubulin sequence itself, between the ancestral and derived character states. Comparative genomics is beginning to generate a consensus on the evolution of genomic structure, with a distinction drawn between chromosomal rearrangements that cause disruptions in macrosynteny and may affect karyotype, and smaller, segmental duplications, inversions and transpositions, (often accompanied by differential gene loss), which all disrupt microsynteny . These events are taxonomically widespread and responsible for the creation of novel genes [47, 48]; segmental duplication and subsequent gene loss largely determines gene order evolution in comparisons of yeast genomes  and in primates , while gene order in Drosophila spp. is greatly affected by paracentric inversions . In addition to these mechanisms, selfish elements have been frequently implicated in the translocation of genomic DNA, for example in most plants  and in trypanosomes .
In this case coding sequences have moved to new locations that otherwise retain colinearity between T. brucei and L. major. The mechanism of translocation is unclear since nothing else that may have transposed simultaneously has survived, i.e., no neighbouring genes of the ancestral locus are seen at the derived loci to provide evidence for their source. The presence of 'calpain-like' proteins upstream of the alternating locus in T. brucei might suggest that this locus could 'hitch-hike' to new locations as a result of ectopic recombination between members of the calpain-like gene family; but the absence of calpain-like proteins adjacent to any derived loci precludes this. Breakpoints have been identified in otherwise excellent synteny between trypanosomatid genomes ; it emerged that breakpoints coincide with retrotransposon hotspots, suggesting that changes to gene order are mediated by selfish elements known from these organisms. A non-autonomous retroelement (RIME) sequence  does occur at the end of the alternating array in T. brucei, but this seemed to be associated with the movement of a contiguous array of histone H3 genes rather than the tubulin genes, as the RIME and histones were not found in other species where gene order was otherwise conserved. The two singleton loci in Leishmania did occur at the extreme 5' end of subtelomeric regions, where retrotransposons are frequently found [52–54], but beyond this there is no evidence for the role of selfish elements. The relationships of tubulin loci to strand-switches may provide evidence of previous chromosomal rearrangements, or place tubulin loci in regions of frequent rearrangement. The α-β array is 40 kb downstream of the nearest strand-switch. In L. major, the α-α array and chromosome 21 β-tubulin are only 25 Kb from a strand-switch, but for the β-β array and chromosome 8 β-tubulin, the distances are 75 Kb and 60 Kb respectively . Hence, the significance of chromosomal rearrangements may yet become clear, but the proximity of strand-switches does not currently look unusual, as they are relatively frequent in these genomes.
Hence, the physical mechanism responsible for new tubulin loci is unclear. Clearly, segmental duplications caused tubulin genes to be translocated from the ancestral locus around the genome; this must have created some kind of transitional structure in which both original and novel loci coexisted, before the ancestral locus was abolished. A future study should seek evidence in appropriate non-parasitic relatives of Leishmania, such as Herpetomonas spp.,Crithidia spp. and Phytomonas spp.; these organisms are the closest relatives to Leishmania still retaining alternating arrays; they could provide a transitional state between alternating and monotypic character states, if they possess other tubulin loci, perhaps additional arrays or lone genes, and if the gene order around these additional features could be related to loci in Trypanosoma. In other words, these organisms may retain elements of the ancestral, transitional character states in a manner expressly not seen in Leishmania. Genome structures diverge faster than genome sequences due to a higher rate of segmental duplication ; this suggests that most duplications are removed through purifying selection but also that there are regular opportunities for new loci. The issue here is, regardless of how tubulin loci were duplicated, why the selective environment changed from purifying to promoting their establishment.
Given the likely difficulties ensuing from a monomer production imbalance in a polymer/dimer polymerisation equation it is understandable that cells have developed transcriptional and post-transcriptional controls to regulate equivalent amounts of α and β tubulin . Coupled with the fact that the trypanosome requires large amounts of tubulin dimer, the T. brucei arrangement of a large number of alternating genes provides a very reasonable solution in an organism lacking transcriptional controls. Thus, what drivers might cause Leishmania to discard this structure? The first move appears to have been to separate the α and β tubulin loci into new sites. If large and essentially equivalent gene numbers are maintained at these sites and transcriptional passage is similar then this might appear to offer little disadvantage to the organism. At this time, we suggest that the alternating isoforms were separated to allow differential expression, and perhaps unilateral changes in regulation, of α- or β-tubulin or both. Within the context of polycistronic transcription, this would be the benefit of physical transposition, but the need that this transition fulfilled is not known.
Certainly, the evolution of differential expression cannot be related to the evolution of new life stages, since the major lifecycle difference influencing the cytoskeleton between T. brucei and L. major is that the latter produces an amastigote form that lacks a motile flagellum. However, an amastigote is also formed by T. cruzi, which has conserved the single array; furthermore, it is clear that the monotypic arrays evolved before the amastigote phase in Leishmania (as they are present in C. fasciculata and L. seymouri also). Equally, the derivation of monotypic arrays cannot be related to the evolution of additional, singleton loci on chromosomes 8 and 21 in Leishmania spp. , since these too evolved in Leishmania, after the monotypic arrays. Separation of the tubulin isoforms may have facilitated novel β-tubulin loci but it cannot have been derived from the same fundamental causes.
The restructuring of tubulin repertoire in trypanosomatids is an example of a very stable system being rapidly and entirely replaced by a novel derivation. The evolutionary causes of the replacement of an alternating α-β tubulin tandem array by separate, monotypic arrays probably reflects new expression regimes that became apparent in the lineage leading to Leishmania, and segmental transpositions that gave the opportunity to craft new loci. The role of transposition in the evolution of tubulin repertoire may itself reflect a ubiquitous constraint in kinetoplastids, and the reason why tubulin tandem arrays exist at all, the absence of individual gene promoters. The arrangement of tubulin genes in arrays ensures high expression levels in the context of polycistronic transcription, but prevents the divergence of non-coding regions and functional specialisation, probably due to repeated crossing-over between duplicate alleles and, consequentially, concerted evolution . Setting aside the exact reasons why new tubulin loci were established, transposition events in the ancestor of Leishmania may have been essential to overcome the historical constraint inherited from non-parasitic kinetoplastids, and facilitate the evolution of novel expression patterns. Furthermore, it was observed here that genomic environments around tubulin loci, past and present, are widely conserved across species while tubulin genes themselves are not. This suggests that, once transposed, these new loci supplanted the original locus, leading to its rapid eradication.
This study utilised the completed and draft genome sequences of various parasitic kinetoplastids: Trypanosoma brucei, T. cruzi, T. congolense, T. vivax, Leishmania major, L. infantum and L. braziliensis. These supplemented the molecular screening of related species that required cell culture (see references for culture details): T. pestanai, T. grayi and T. cyclops [45, 59],Herpetomonas megaseliae, Crithidia fasciculata, C. deanei, Bodo saltans (JC02 strain, ), Parabodo caudatus and Neobodo designis (Longstock strain, ). The completed genome sequences of T. brucei and L. major were first compared to establish the relationships (if any) of the genomic locations where tubulin loci now reside. Various other parasitic trypanosomatids and free-living bodonids were cultured and screened using specific and degenerate PCR to establish their character states. Draft genome sequences were interrogated for tubulin loci and to score each species for its character state (i.e., alternating or monotypic array).
Comparing genomic location and gene synteny
The genomic location of the T. brucei array is specified by gene order. This site was identified in L. major to establish if the location was conserved through time or, alternatively, if tubulin rearrangements had evolved in new chromosomal environments. DNA sequences of up- and downstream coding loci were used as queries for BLAST searches of the L. major genome in GeneDB. Similarly, the genomic locations of all four L. major tubulin genes were located in the T. brucei genome. Comparisons were also made between T. brucei and T. cruzi to establish if both species share a homologous alternating array, on the basis of chromosomal location. T. brucei sequences for flanking loci were used to search among the partially assembled T. cruzi contigs and locate their closest homologs as before.
Character scoring from genomic DNA
Where sequence data was gathered de novo, this required cell culture, genomic DNA extraction, amplification by PCR, molecular cloning and sequencing. Cell culture was carried out at room temperature for free-living species (B. saltans, P. caudatus and N. designis) in soil-extract solution, enriched with 0.25% beef extract. Parasitic species were cultured in standard media at 37°C: Warren medium (, for C. deanei and C. fasciculata), SDM-79 (, for T. cyclops, T. grayi and T. pestanai) and liver infusion tryptose (, for H. megaseliae). Genomic DNA was prepared from 50–100 ml of liquid culture (cell density: 1 × 106–107 ml-1) by phenol-chloroform extraction and resuspension in 10 mM Tris .
Both specific and degenerate primers were designed to anchor within the termini of tubulin CDSs at conserved points identified from alignments of kinetoplastid α- and β-tubulin genes, which included a natural outgroup Euglena gracilis , ([GenBank: AF182555, GenBank: AF182557]). Therefore, these primers could amplify across the IGS of any potential array. Specific primers were labelled: 'sensealpha' (GAGAAGGACTACGAGGAGGT); 'antialpha' (GAGTACCAGCAGTACCAG); 'sensebeta' (CA(TC)TGGTACGTCGGATGAGGG) and 'antibeta' (GGTGG(CT)ACTGGTCT(CT)). Degenerate primers were labelled: 'alphaF' (TCGA(CT)(CT)T(GCT)ATGTAC(AC)(GC)CAAGCG); 'alphaR' (TCCTTGCC(AG)(GC)(AT)(GC)A(CT)CAGCTGC); 'betaF' (AC(GCT)G(GCT)(GCT)ATGTTCCG(CT)CGCAAG) and 'betaR' (CCAG(AT)CTG(AGT)CCAAA(GT)A(CT)(AG)AAGTTG).
In combination, these primer pairs could amplify across the IGS of α-α, β-β, β-α and α-β tandem gene pairs in any of the cultured species. All combinations of specific and degenerate primers respectively were applied to each DNA preparation. 'Touchdown' PCR was performed under the following conditions: denaturation at 95°C, extension at 70°C and annealing at 58°C for 5 cycles, 56°C for 5 cycles and 52°C for 25 cycles (for specific primary primers) or 68°C for 5 cycles, 64°C for 5 cycles and 60°C for 25 cycles (for degenerate primary primers). Products were cloned into pGEM T-easy plasmid vectors (Promega), purified from bacterial culture and sequenced using an ABI 377 automated sequencer.
Character scoring from genome sequences: contig assembly and inspection
Tubulin genes were identified for Trypanosoma congolense and T. vivax by BLAST searching  within their draft genome sequences, available from the GeneDB website (Sanger Institute Pathogen Sequencing Unit ). T. brucei α- and β-tubulin DNA sequences were used as the search query. Positive contigs were then inspected using Artemis v5.0  to establish if arrayed tubulin genes could be found on a single contig. At this time, the Leishmania infantum and L. braziliensis genomes were available as first draft assemblies, without any manual annotation or checking of assembly. Prior to manual revision, a preliminary assembly can make errors, especially regarding duplicate gene loci. For this reason, it was necessary for these species to identify matches to tubulin by BLAST searching among read catalogues, then use these matches to search for overlapping reads and finally to assemble contigs by tiling together individual reads. L. major α- and β-tubulin DNA sequences were used as the search query.
Estimating species phylogenies
A comparative approach to the evolution of genomic characters requires a species phylogeny. This was obtained through phylogenetic analysis of small subunit ribosomal RNA sequences for the species concerned. These were selected from depositions to GenBank: T. cruzi [GenBank: AF232214], T. pestanai [GenBank: AJ009159], T. congolense [GenBank: AJ223563], T. brucei [GenBank: AJ009142], T. grayi [GenBank: AJ005278], T. cyclops [GenBank: AJ131958], T. vivax [GenBank: U22316], L. major [GenBank: X53915], L. mexicana [GenBank: X53912], H. megaseliae [GenBank: U01014], C. fasciculata [GenBank: Y00055], L. infantum [GenBank: X07773], L. braziliensis [GenBank: M80292], C. oncopelti [GenBank: AF038025], B. saltans [GenBank: AF208889], N. designis [GenBank: AY998646], P. caudatus [GenBank: AY490218] and L. seymouri [GenBank: AF153040]. Note that C. oncopelti, a close relative of C. deanei, was used as a surrogate in the rRNA alignment, given the absence of any SSU rRNA sequence for C. deanei. Sequences were aligned by eye and maximum likelihood phylogenetic estimation was carried out using PHYML [68, 69]. A general-time reversible (GTR, ) model was applied, with six rate categories estimated from the data. An initial tree topology was selected through neighbour-joining. Corrections were made for both invariant sites and rate heterogeneity by estimating the proportion of invariant sites and the gamma distribution parameter (α) from the data. 100 non-parametric bootstrapped data sets were estimated.
Polymerase chain reaction
Basic local alignment search tool
Imboden MA, Laird PW, Affolter M, Seebeck T: Transcription of the intergenic regions of the tubulin gene-cluster of Trypanosoma brucei – evidence for a polycistronic transcription unit in a eukaryote. Nucleic Acids Res. 1987, 15: 7357-7368.
Flinn HM, Smith DF: Genomic organization and expression of a differentially-regulated gene family from Leishmania major . Nucleic Acids Res. 1992, 20: 755-762.
Wong S, Morales TH, Neigel JE, Campbell DA: Genomic and transcriptional linkage of the genes for calmodulin, EF-hand 5-protein, and ubiquitin extension protein-52 in Trypanosoma brucei. Mol Cell Biol. 1993, 13: 207-216.
Campbell DA, Thomas S, Sturm NR: Transcription in kinetoplastid protozoa: why be normal?. Microb Infect. 2003, 5: 1231-1240. 10.1016/j.micinf.2003.09.005.
Bringaud F, Baltz T: African trypanosome glucose transporter genes: organization and evolution of a multigene family. Mol Biol Evol. 1994, 11: 220-30.
Rangarajan D, Harvey TI, Barry JD: Characterisation of the loci encoding the glutamic acid and alanine rich protein of Trypanosoma congolense. Mol Biochem Parasitol. 2000, 105: 281-90. 10.1016/S0166-6851(99)00190-5.
Roberts TG, Dungan JM, Watkins KP, Agabian N: The SLA RNA gene of Trypanosoma brucei is organized in a tandem array which encodes several small RNAs. Mol Biochem Parasitol. 1996, 83: 163-74. 10.1016/S0166-6851(96)02762-4.
Gull K: Protist tubulins: new arrivals, evolutionary relationships and insights to cytoskeletal function. Curr Opin Microbiol. 2001, 4: 427-432. 10.1016/S1369-5274(00)00230-7.
McKean PG, Vaughan S, Gull K: The extended tubulin superfamily. J Cell Sci. 2001, 114: 2723-2733.
Urmenyi TP, Decastro FT, Carvalho JFO, Desouza W, Rondinelli E: Transcriptional and posttranscriptional control of tubulin gene-expression in Trypanosoma cruzi. DNA Cell Biol. 1992, 11: 101-109.
Coulson RMR, Conner V, Chen TC, Ajioka JW: Differential expression of Leishmania major beta-tubulin genes during the acquisition of promastigote infectivity. Mol Biochem Parasitol. 1996, 82: 227-236. 10.1016/0166-6851(96)02739-9.
Gonzalez-Pino MJ, Rangel-Aldao R, Slezynger TC: Cloning and sequence analysis of a Trypanosoma cruzi alpha-tubulin cDNA. Biol Res. 1997, 30: 161-166.
Gonzalez-Pino MJ, Rangel-Aldao R, Slezynger TC: Expression of alpha- and beta-tubulin genes during growth of Trypanosoma cruzi epimastigotes. DNA Cell Biol. 1999, 18: 449-455. 10.1089/104454999315169.
Bartholomeu DC, Silva RA, Galvao LMC, El-Sayed NMA, Donelson JE, Teixeira SMR: Trypanosoma cruzi: RNA structure and post-transcriptional control of tubulin gene expression. Exp Parasitol. 2002, 102: 123-133.
Bellatin JA, Murray AS, Zhao M, McMaster WR: Leishmania mexicana: Identification of genes that are preferentially expressed in amastigotes. Exp Parasitol. 2002, 100: 44-53. 10.1006/expr.2001.4677.
Ullu E, Matthews KR, Tschudi C: Temporal-order of RNA-processing reactions in trypanosomes – rapid trans-splicing precedes polyadenylation of newly synthesized tubulin transcripts. Mol Cell Biol. 1993, 13: 720-725.
Shapira M, Zilka A, Garlapati S, Dahan E, Dahan I, Yavesky V: Post transcriptional control of gene expression in Leishmania. Med Microbiol Immunol. 2001, 190: 23-26.
Vassella E, Braun R, Roditi I: Control of polyadenylation and alternative splicing of transcripts from adjacent genes in a procyclin expression site – a dual role for polypyrimidine tracts in trypanosomes. Nucleic Acids Res. 1994, 22: 1359-1364.
Pays E, Vanhamme L, Berberof M: Genetic-controls for the expression of surface-antigens in African trypanosomes. Annu Rev Microbiol. 1994, 48: 25-52. 10.1146/annurev.mi.48.100194.000325.
Berberof M, Vanhamme L, Tebabi P, Pays A, Jefferies D, Welburn S, Pays E: The 3'-terminal region of the messenger-RNAs for VSG and procyclin can confer stage specificity to gene-expression in Trypanosoma brucei. EMBO J. 1995, 14: 2925-2934.
Hotz HR, Lorenz P, Fischer R, Krieger S, Clayton C: Role of 3'-untranslated regions in the regulation of hexose transporter mRNAs in Trypanosoma brucei. Mol Biochem Parasitol. 1995, 75: 1-14. 10.1016/0166-6851(95)02503-0.
Lopez-Estrano G, Tschudi CC, Ullu E: Exonic sequences in the 5 ' untranslated region of alpha-tubulin mRNA modulate trans-splicing in Trypanosoma brucei. Mol Cell Biol. 1998, 18: 4620-4628.
Duhagon MA, Dallagiovanna B, Garat B: Unusual features of poly[dT-dG]center dot[dC-dA] stretches in CDS-flanking regions of Trypanosoma cruzi genome. Biochem Biophys Res Comm. 2001, 287: 98-103. 10.1006/bbrc.2001.5545.
Deflorin J, Rudolf M, Seebeck T: The major components of the paraflagellar rod of Trypanosoma-brucei are 2 similar, but distinct proteins which are encoded by 2 different gene loci. J Biol Chem. 1994, 269: 28745-28751.
Blattner J, Clayton CE: The 3'-untranslated regions from the Trypanosoma brucei phosphoglycerate kinase-encoding genes mediate developmental regulation. Gene. 1995, 162: 153-6. 10.1016/0378-1119(95)00366-E.
Parker HL, Hill T, Alexander K, Murphy NB, Fish WR, Parsons M: Three genes and two isozymes: gene conversion and the compartmentalization and expression of the phosphoglycerate kinases of Trypanosoma (Nannomonas) congolense . Mol Biochem Parasitol. 1995, 69: 269-79. 10.1016/0166-6851(94)00208-5.
Burke D, Gasdaska P, Hartwell L: Dominant effects of tubulin overexpression in Saccharomyces cerevisiae . Mol Cell Biol. 1989, 9: 1049-1059.
Katz W, Weinstein B, Solomon F: Regulation of tubulin levels and microtubule assembly in Saccharomyces cerevisiae: consequences of altered tubulin gene copy number in yeast. Mol Cell Biol. 1990, 10: 2730-2736.
Berriman M, Ghedin E, Hertz-Fowler C, Blandin G, Renauld H, Bartholomeu DC, Lennard NJ, Caler E, Hamlin NE, Haas B, Bohme U, Hannick L, Aslett MA, Shallom J, Marcello L, Hou L, Wickstead B, Alsmark UC, Arrowsmith C, Atkin RJ, Barron AJ, Bringaud F, Brooks K, Carrington M, Cherevach I, Chillingworth TJ, Churcher C, Clark LN, Corton CH, Cronin A, Davies RM, Doggett J, Djikeng A, Feldblyum T, Field MC, Fraser A, Goodhead I, Hance Z, Harper D, Harris BR, Hauser H, Hostetler J, Ivens A, Jagels K, Johnson D, Johnson J, Jones K, Kerhornou AX, Koo H, Larke N, Landfear S, Larkin C, Leech V, Line A, Lord A, Macleod A, Mooney PJ, Moule S, Martin DM, Morgan GW, Mungall K, Norbertczak H, Ormond D, Pai G, Peacock CS, Peterson J, Quail MA, Rabbinowitsch E, Rajandream MA, Reitter C, Salzberg SL, Sanders M, Schobel S, Sharp S, Simmonds M, Simpson AJ, Tallon L, Turner CM, Tait A, Tivey AR, Van Aken S, Walker D, Wanless D, Wang S, White B, White O, Whitehead S, Woodward J, Wortman J, Adams MD, Embley TM, Gull K, Ullu E, Barry JD, Fairlamb AH, Opperdoes F, Barrell BG, Donelson JE, Hall N, Fraser CM, Melville SE, El-Sayed NM: The genome of the African trypanosome Trypanosoma brucei. Science. 2005, 309: 416-422. 10.1126/science.1112642.
El-Sayed NM, Myler PJ, Bartholomeu DC, Nilsson D, Aggarwal G, Tran AN, Ghedin E, Worthey EA, Delcher AL, Blandin G, Westenberger SJ, Caler E, Cerqueira GC, Branche C, Haas B, Anupama A, Arner E, Aslund L, Attipoe P, Bontempi E, Bringaud F, Burton P, Cadag E, Campbell DA, Carrington M, Crabtree J, Darban H, da Silveira JF, de Jong P, Edwards K, Englund PT, Fazelina G, Feldblyum T, Ferella M, Frasch AC, Gull K, Horn D, Hou L, Huang Y, Kindlund E, Klingbeil M, Kluge S, Koo H, Lacerda D, Levin MJ, Lorenzi H, Louie T, Machado CR, McCulloch R, McKenna A, Mizuno Y, Mottram JC, Nelson S, Ochaya S, Osoegawa K, Pai G, Parsons M, Pentony M, Pettersson U, Pop M, Ramirez JL, Rinta J, Robertson L, Salzberg SL, Sanchez DO, Seyler A, Sharma R, Shetty J, Simpson AJ, Sisk E, Tammi MT, Tarleton R, Teixeira S, Van Aken S, Vogt C, Ward PN, Wickstead B, Wortman J, White O, Fraser CM, Stuart KD, Andersson B: The genome sequence of Trypanosoma cruzi, etiologic agent of Chagas disease. Science. 2005, 309: 409-415. 10.1126/science.1112631.
Thomashow LS, Milhausen M, Rutter WJ, Agabian N: Tubulin genes are tandemly linked and clustered in the genome of Trypanosoma brucei. Cell. 1983, 32: 35-43. 10.1016/0092-8674(83)90494-4.
Seebeck T, Whittaker PA, Imboden MA, Hardman N, Braun R: Tubulin genes of Trypanosoma brucei: A tightly clustered family of alternating genes. Proc Natl Acad Sci Unit States Am. 1983, 80: 4634-4638. 10.1073/pnas.80.15.4634.
Maingon R, Gerke R, Rodriguez M, Urbina J, Hoenicka J, Negri S, Aguirre T, Nehlin J, Knapp T, Crampton J: The tubulin genes of Trypanosoma cruzi. Eur J Biochem. 1988, 71: 285-291. 10.1111/j.1432-1033.1988.tb13788.x.
Esquenazi D, Morel CM, Traub-Cseko YM: Characterisation of tubulin genes in Trypanosoma rangeli. Mol Biochem Parasitol. 1989, 34: 253-260. 10.1016/0166-6851(89)90054-6.
Ersfeld K, Asbeck K, Gull K: Direct visualisation of individual gene organisation in Trypanosoma brucei by high-resolution in situ hybridisation. Chromosoma. 1998, 107: 237-40. 10.1007/s004120050302.
Bellofatto V, Cross GA: Characterization of RNA transcripts from the alpha tubulin gene cluster of Leptomonas seymouri. Nucleic Acids Res. 1988, 16: 3455-3469.
Das S, Adhya S: Organization and chromosomal localization of beta-tubulin genes in Leishmania donovani. J Biosci. 1990, 15: 239-248.
Dolezel D, Jirku M, Maslov DA, Lukes J: Phylogeny of the Bodonid flagellates (Kinetoplastida) based on small-subunit rRNA gene sequences. Int J Syst Evol Microbiol. 2000, 50: 1943-1951.
Von der Heyden S, Chao EE, Vickerman K, Cavalier-Smith TJ: Ribosomal RNA phylogeny of bodonid and diplonemid flagellates and the evolution of euglenozoa. J Eukaryot Microbiol. 2004, 51: 402-16. 10.1111/j.1550-7408.2004.tb00387.x.
Weston D, La Flamme AC, Van Voorhis WC: Expression of Trypanosoma cruzi surface antigen FL-160 is controlled by elements in the 3' untranslated, the 3' intergenic, and the coding regions. Mol Biochem Parasitol. 1999, 102: 53-66. 10.1016/S0166-6851(99)00079-1.
Porcel BM, Tran AN, Tammi M, Nyarady Z, Rydaker M, Urmenyi TP, Rondinelli E, Pettersson U, Andersson B, Aslund L: Gene survey of the pathogenic protozoan Trypanosoma cruzi. Genome Res. 2000, 10: 1103-1107. 10.1101/gr.10.8.1103.
Lukes J, Jirku M, Dolezel D, Kral'ova I, Hollar L, Maslov DA: Analysis of ribosomal RNA genes suggests that trypanosomes are monophyletic. J Mol Evol. 1997, 44: 521-7. 10.1007/PL00006176.
Haag J, O'hUigin C, Overath P: The molecular phylogeny of trypanosomes: evidence for an early divergence of the Salivaria. Mol Biochem Parasitol. 1998, 91: 37-49. 10.1016/S0166-6851(97)00185-0.
Maslov DA, Podlipaev SA, Lukes J: Phylogeny of the kinetoplastida: taxonomic problems and insights into the evolution of parasitism. Mem Inst Oswaldo Cruz. 2001, 96: 397-402. 10.1590/S0074-02762001000300021.
Hamilton PB, Stevens JR, Gaunt MW, Gidley J, Gibson WC: Trypanosomes are monophyletic: evidence from genes for glyceraldehyde phosphate dehydrogenase and small subunit ribosomal RNA. Int J Parasitol. 2004, 34: 1393-404. 10.1016/j.ijpara.2004.08.011.
Taylor JS, Raes J: Duplication and divergence: the evolution of new genes and old ideas. Annu Rev Genet. 2004, 38: 615-43. 10.1146/annurev.genet.38.072902.092831.
Long M: Evolution of novel genes. Curr Opin Genet Dev. 2001, 11: 673-680. 10.1016/S0959-437X(00)00252-5.
Long M, Betran E, Thornton K, Wang W: The origin of new genes: glimpses from the young and old. Nat Rev Genet. 2003, 4: 865-875. 10.1038/nrg1204.
Fischer G, Neuveglise C, Durrens P, Gaillardin C, Dujon B: Evolution of gene order in the genomes of two related yeast species. Genome Res. 2001, 11: 2009-2019. 10.1101/gr.212701.
Cheng Z, Ventura M, She X, Khaitovich P, Graves T, Osoegawa K, Church D, DeJong P, Wilson RK, Paabo S, Rocchi M, Eichler EE: A genome-wide comparison of recent chimpanzee and human segmental duplications. Nature. 2005, 437: 88-93. 10.1038/nature04000.
Richards S, Liu Y, Bettencourt BR, Hradecky P, Letovsky S, Nielsen R, Thornton K, Hubiszz MJ, Chen R, Meisel RP, Couronne O, Hua S, Smith MA, Zhang P, Liu J, Bussemaker HJ, van Batenburg MF, Howells SL, Scherer SE, Sodergren E, Matthews BB, Crosby MA, Schroeder AJ, Ortiz-Barrientos D, Rives CM, Metzker ML, Muzny DM, Scott G, Steffen D, Wheeler DA, Worley KC, Havlak P, Durbin KJ, Egan A, Gill R, Hume J, Morgan MB, Miner G, Hamilton C, Huang Y, Waldron L, Verduzco D, Clerc-Blankenburg KP, Dubchak I, Noor MA, Anderson W, White KP, Clark AG, Schaeffer SW, Gelbart W, Weinstock GM, Gibbs RA: Comparative genome sequencing of Drosophila pseudoobscura: chromosomal, gene, and cis-element evolution. Genome Res. 2005, 15: 1-18. 10.1101/gr.3059305.
Bennetzen JL: Transposable elements, gene creation and genome rearrangement in flowering plants. Curr Opin Genet Dev. 2005, 15: 621-627. 10.1016/j.gde.2005.09.010.
Ghedin E, Bringaud F, Peterson J, Myler P, Berriman M, Ivens A, Andersson B, Bontempi E, Eisen J, Angiuoli S, Wanless D, Von Arx A, Murphy L, Lennard N, Salzberg S, Adams MD, White O, Hall N, Stuart K, Fraser CM, El-Sayed NM: Gene synteny and evolution of genome architecture in trypanosomatids. Mol Biochem Parasitol. 2004, 134: 183-91. 10.1016/j.molbiopara.2003.11.012.
Aksoy S: Site-specific retrotransposons of the trypanosomatid protozoa. Parasitol Today. 1991, 7: 281-5. 10.1016/0169-4758(91)90097-8.
Ivens AC, Peacock CS, Worthey EA, Murphy L, Aggarwal G, Berriman M, Sisk E, Rajandream MA, Adlem E, Aert R, Anupama A, Apostolou Z, Attipoe P, Bason N, Bauser C, Beck A, Beverley SM, Bianchettin G, Borzym K, Bothe G, Bruschi CV, Collins M, Cadag E, Ciarloni L, Clayton C, Coulson RMR, Cronin A, Cruz AK, Davies RM, De Gaudenzi J, Dobson DE, Duesterhoeft A, Fazelina G, Fosker N, Frasch AC, Fraser A, Fuchs M, Gabel C, Goble A, Goffeau A, Harris D, Hertz-Fowler C, Hilbert H, Horn D, Huang YT, Klages S, Knights A, Kube M, Larke N, Litvin L, Lord A, Louie T, Marra M, Masuy D, Matthews K, Michaeli S, Mottram JC, Muller-Auer S, Munden H, Norbertczak H, Oliver K, O'Neil S, Pentony M, Pohl TM, Price C, Purnelle B, Quail MA, Rabbinowitsch E, Reinhardt R, Rieger M, Rinta J, Robben J, Robertson L, Ruiz JC, Rutter S, Saunders D, Schafer M, Schein J, Schwartz DC, Seeger K, Seyler A, Sharp S, Shin H, Sivam D, Squares R, Squares S, Tosato V, Vogt C, Volckaert G, Wambutt R, Warren T, Wedler H, Woodward J, Zhou SG, Zimmermann W, Smith DF, Blackwell JM, Stuart KD, Barrell B, Myler PJ: The genome of the kinetoplastid parasite, Leishmania major . Science. 2005, 309: 436-442. 10.1126/science.1112680.
Cleveland DW, Sullivan KF: Molecular Biology and Genetics of Tubulin. Annu Rev Biochem. 1985, 54: 331-366. 10.1146/annurev.bi.54.070185.001555.
Jackson AP, Vaughan S, Gull K: Comparative genomics and concerted evolution of β-tubulin paralogs in Leishmania spp. BMC Genomics. 2006, 7: 137-10.1186/1471-2164-7-137.
Li W-H: Molecular Evolution. 1997, Sunderland MA: Sinauer
Stevens JR, Noyes HA, Schofield CJ, Gibson W: The molecular evolution of Trypanosomatidae. Adv Parasitol. 2001, 48: 1-56.
Warren LG: Metabolism of Schizotrypanum cruzi. Chagas. I. Effect of culture age and substrate concentration on respiratory rate. J Parasitol. 1960, 46: 529-539. 10.2307/3274932.
Brun R, Schonenberger M: Cultivation and in vitro cloning of procyclic culture forms of Trypanosoma brucei in a semi-defined medium. Acta Trop. 1979, 36: 289-292.
De Maio A, Urbina JA: Trypanosoma (Schizotrypanum) cruzi: terminal oxidases in two growth phases in vitro. Acta Cient Venez. 1984, 35: 136-141.
Sambrook J, Russell DW: Molecular cloning: a laboratory manual. 2001, Cold Spring Harbor, New York: Cold Spring Harbor Laboratory Press, 3
Canaday J, Tessier LH, Imbault P, Paulus F: Analysis of Euglena gracilis alpha-, beta- and gamma-tubulin genes: introns and pre-mRNA maturation. Mol Genet Genom. 2001, 265: 153-160. 10.1007/s004380000403.
Altschul S, Boguski MS, Gish W, Wootton JC: Issues in searching molecular sequence database. Nat Genet. 1994, 6: 119-129. 10.1038/ng0294-119.
Wellcome Trust Sanger Institute, Pathogen Sequencing Unit 'GeneDB' Interface. [http://www.genedb.org]
Rutherford K, Parkhill J, Crook J, Horsnell T, Rice P, Rajandream MA, Barrell B: Artemis: sequence visualisation and annotation. Bioinformatics. 2000, 16: 944-945. 10.1093/bioinformatics/16.10.944.
Guindon S, Gascuel O: A simple, fast and accurate method to estimate large phylogenies by maximum-likelihood. Syst Biol. 2003, 52: 696-704. 10.1080/10635150390235520.
Guindon S, Lethiec F, Duroux P, Gascuel O: PHYML Online: a web server for fast maximum likelihood-based phylogenetic inference. Nucleic Acid Res. 2005, 33: 557-559. 10.1093/nar/gki352.
Yang ZH: Maximum-likelihood phylogenetic estimation from DNA-sequences with variable rates over sites-approximate methods. J Mol Evol. 1994, 39: 306-314. 10.1007/BF00160154.
We gratefully acknowledge the donation of cell culture from Tom Cavalier-Smith (University of Oxford), Wendy Gibson (University of Bristol), Keith Vickerman (University of Glasgow) and Catarina Gadelha (University of Oxford). Genome sequence data was generated by the Pathogen Sequencing Unit at the Wellcome Trust Sanger Institute and funded by the Wellcome Trust. This work was funded by the Wellcome Trust. APJ is a Sanger Institute Postdoctoral Research Fellow. KG is a Wellcome Trust Principal Research Fellow.
APJ carried out cell culture, DNA preparation and molecular screening of kinetoplastids, as well as bioinformatic comparisons of genome sequences and drafting of the manuscript. SV produced preliminary bioinformatic analyses and gave assistance in experimental design and manuscript preparation. KG supervised the study design, concept and execution, and contributed to manuscript preparation. All authors read and approved the final manuscript.
About this article
Cite this article
Jackson, A.P., Vaughan, S. & Gull, K. Evolution of Tubulin Gene Arrays in Trypanosomatid parasites: genomic restructuring in Leishmania. BMC Genomics 7, 261 (2006). https://doi.org/10.1186/1471-2164-7-261
- Draft Genome Sequence
- Tubulin Gene
- Degenerate Polymerase Chain Reaction
- Selfish Element