- Open Access
Lateral gene transfer and ancient paralogy of operons containing redundant copies of tryptophan-pathway genes in Xylellaspecies and in heterocystous cyanobacteria
© 2003 Xie et al.; licensee BioMed Central Ltd. 2003
- Received: 27 September 2002
- Accepted: 26 November 2002
- Published: 29 January 2003
Tryptophan-pathway genes that exist within an apparent operon-like organization were evaluated as examples of multi-genic genomic regions that contain phylogenetically incongruous genes and coexist with genes outside the operon that are congruous. A seven-gene cluster in Xylella fastidiosa includes genes encoding the two subunits of anthranilate synthase, an aryl-CoA synthetase, and trpR. A second gene block, present in the Anabaena/Nostoc lineage, but not in other cyanobacteria, contains a near-complete tryptophan operon nested within an apparent supraoperon containing other aromatic-pathway genes.
The gene block in X. fastidiosa exhibits a sharply delineated low-GC content. This, as well as bias of codon usage and 3:1 dinucleotide analysis, strongly implicates lateral gene transfer (LGT). In contrast, parametric studies and protein tree phylogenies did not support the origination of the Anabaena/Nostoc gene block by LGT.
Judging from the apparent minimal amelioration, the low-GC gene block in X. fastidiosa probably originated by LGT at a relatively recent time. The surprising inability to pinpoint a donor lineage still leaves room for alternative, albeit less likely, explanations other than LGT. On the other hand, the large Anabaena/Nostoc gene block does not seem to have arisen by LGT. We suggest that the contemporary Anabaena/Nostoc array of divergent paralogs represents an ancient ancestral state of paralog divergence, with extensive streamlining by gene loss occurring in the lineage of descent representing other (unicellular) cyanobacteria.
- Codon Usage
- Lateral Gene Transfer
- Gene Block
- Coxiella Burnetii
Lateral gene transfer
Lateral gene transfer (LGT) has been generally accepted for some time, as exemplified by the endosymbiotic hypothesis of organelle origin [1,2]. Nevertheless, a long-standing background of general conviction has held that LGT is rare, especially between distant organisms. However, the modern era of genomics has been accompanied by increasingly numerous claims that LGT is frequent [3,4,5,6], and there now seems little doubt that LGT exerts a significant influence upon evolutionary histories. Indeed, it has even been asserted that vertical evolutionary patterns of descent might be impossibly masked by rampant events of LGT and that, in fact, instead of bifurcating phylogenetic trees, a reticulate (net-like) pattern exists [7,8,9]. On the other hand, others urge a more balanced perspective, pointing out that alternative explanations for apparent cases of LGT have not always been considered [10,11,12,13,14]. The rationale for explanations other than LGT for genealogical incongruities (such as hidden paralogies and reconstruction artifacts) have been presented in comprehensive detail by Glansdorff .
Woese  contends that the rRNA tree is a valid representation of organismal genealogy, that LGT was rampant only before the initial bifurcation of the universal phylogenetic tree, and that LGT has become progressively more restricted as a function of elapsed evolutionary time. Using the aminoacyl-tRNA synthases as an example of the modular-type entities asserted to be most amenable to LGT, Woese concludes that the genealogical trace of vertical gene flow is readable, despite a significant jumbling influence of LGT. If correct, this allows the optimistic viewpoint that the complex interplay of vertical gene descent and LGT can be deciphered to yield correct evolutionary histories, provided that sufficiently detailed studies are done.
Approaches for detection of LGT events are either phylogenetic or parametric. Phylogenetic approaches depend on congruence of phylogenetic trees. Aside from technical difficulties of inferring high-quality trees, conflicts between trees under comparison are not necessarily due to LGT, but can arise from coincidental loss of divergent paralogs in different, widely spaced lineages or from convergent evolution. Parametric approaches for detection of LGT include (but are not limited to) the analysis of nucleotide composition, dinucleotide frequencies and codon usage biases. Lawrence and Ochman  used such parametric analysis to identify a set of Escherichia coli genes (17.5% of the genome) having putative origin by LGT, and this has stimulated much discussion. High rates of both false positives and false negatives have been asserted by others [18,19], but this is tempered by presentation of a rationale for why phylogenetic and different parametric methods detect different gene subsets [20,21,22]. A consensus seems to be emerging that the most proficient attempts to reconstruct evolutionary events will employ a multifaceted approach that combines tree inference with parametric analysis in a biological context [21,22]. Lawrence and Ochman  provide a number of examples of how the context of biological information can assist the analysis, and this approach is implemented herein.
If each member of a linked group of genes is already represented elsewhere in a genome, their origin by LGT is a distinct possibility, as their transfer en bloc as an operon unit would have required only a single evolutionary event. During an ongoing analysis of the genomic distribution of tryptophan-pathway genes, we observed two such cases, that is, where one set of genes was phylogenetically congruent, in contrast to the incongruence of redundant gene copies that were linked to one another. We have evaluated the evidence for the alternative possibilities of LGT or ancient paralogy, as reported here.
A block of Trp-pathway genes in Xylella
In Chlamydia trachomatis and Chlamydophila psittaci, trpR is positioned near structural genes of tryptophan biosynthesis, but no indication of recent origin by LGT of genes in this region was obtained . X. fastidiosa trpR is separated by three genes from two structural genes of tryptophan biosynthesis. These latter genes do not appear to be essential for the primary task of tryptophan biosynthesis as all seven genes of tryptophan biosynthesis are represented elsewhere in the genome within one of two operons. Thus, in X. fastidiosa the incongruous phylogenetic position of trpR, the redundancy of the trp-linked genes encoding trpAa and trpAb, and the distinct phylogenetic incongruence of the latter gene pair all supported a reasonable possibility of origin by LGT.
The tryptophan supraoperon of Anabaena/Nostoc
The tryptophan operons appear to be nested within what could be a larger unit of transcription that is reminiscent of what has been called a supraoperon in Bacillus subtilis . The genes comprising the supraoperon of B. subtilis are aroG → aroB → aroH → trpAaBDCEbEa → hisHb → tyrAp → aroF. A hierarchy of internal promoters and terminators exists for differential control of the B. subtilis supraoperon. The Anabaena/Nostoc linkage group is additionally reminiscent of the B. subtilis supraoperon in the presence of aroB and tyrA. Although B. subtilis does not have aroAIβ represented in its supraoperon (as do Anabaena and Nostoc), aroAIβ is the homology class (of three possible DAHP synthase homologs distributed in nature [25,26,27]) that is utilized by B. subtilis. A number of supraoperon gene insertions have occurred outside of the trp operon as well. These differ for Anabaena and Nostoc as depicted in Figure 2. Anabaena has genes encoding aph and a hypothetical gene (open reading frame (ORF)) inserted between aroB and the trpAa•trpAb fusion. The aph gene encodes an uncharacterized protein of the defined alkaline phosphatases (metalloenzyme superfamily) (group COG1524 in the COGS database). Among cyanobacteria, only Nostoc has homologs of these two Anabaena genes, although they are not inserted in the Nostoc supraoperon. Nostoc has frnE (encoding a thiol-disulfide isomerase) inserted between tyrA(p) and aroB. Four subclasses of tyrA are defined according to the substrate specificities of the TyrA gene product: tyrAp, specific for prephenate; tyrAa, specific for arogenate; tyrAc, accepts either prephenate or arogenate; and tyrA(p), has broad specificity but exhibits a distinct preference for prephenate. Among all cyanobacteria, only Nostoc possesses frnE.
In their genomes outside the supraoperon boundaries, Nostoc and Anabaena possess a full complement of genes for biosynthesis of tryptophan, tyrosine and phenylalanine. Even these extra-supraoperonic genes of the Anabaena/Nostoc lineage are represented by multiple paralogs in many cases (Figure 2). If one considers the single-copy assemblage of aromatic-pathway genes present in the Synechocystis/Synechococcus/Prochlorococcus lineage as a fundamental complement of genes common to all cyanobacteria, the Anabaena/Nostoc genomic repertoire contains substantial redundancy. Thus, Anabaena has two additional extra-operonic paralogs of aroAIβ and trpD. In addition to extra-operonic, free-standing copies of trpAa and trpAb, a second fused gene (trpAa•trpAb_2) encoding the two domains of anthranilate synthase is present in Anabaena. Nostoc has two extra-operonic copies of aroAIβ, aroB and trpD. All cyanobacteria possess AroA of the Iβ class (aroAIβ). While this is also true of the Anabaena/Nostoc lineage (in fact, having multiple copies), both Anabaena and Nostoc possess an additional gene encoding AroA of the Iα class (aroAIα). All cyanobacteria possess a tyrA gene of the arogenate-specificity class (tyrAa), but the Anabaena/Nostoc supraoperons also possess a tyrA gene deemed to be a cyclohexadienyl dehydrogenase  with a favored specificity for prephenate (tyrA(p)) (C.A.B., R.A.J., N.K. and McNally A., unpublished observation).
Since the basic single-copy repertoire of dispersed aromatic-pathway genes shown in Figure 2 for Synechocystis (Ssp) is representative of other cyanobacteria such as Synechococcus (Syn) and Prochlorococcus (Pmu) and is also present at dispersed extra-operonic loci of Anabaena and Nostoc, an obvious possibility would seem to be that the genes of the supraoperon originated by LGT in a common ancestor of Anabaena and Nostoc. If so, speciation was followed by different species-specific gene-insertion events. Because the divergence of Anabaena and Nostoc was relatively recent, evidence for LGT by analysis of GC content, codon usage, or dinucleotide frequency might be forthcoming. A number of distinctive properties of the supraoperon gene block represent items of biological context (as discussed by Lawrence and Ochman ) that potentially could provide excellent tracking clues about the identity of the putative donor in LGT. These include the overall gene organization of the trp operon, for which many microbial patterns are known; the extremely rare gene order of trpEa trpEb instead of the typical order trpEb trpEa; the fusion of genes encoding the alpha (trpAa) and beta (trpAb) subunits of anthranilate synthase, a fusion that exists in only a limited number of other taxa, and the presence of operonic genes exhibiting distinctive homology subtypes (aroAIβ and tyrA(p)).
Lateral gene transfer of a block of genes in Xylella
Statistical test of co-variation of 3:1 dinucleotide frequencies of trpR and its cognate genome
3:1 Dinucleotide frequencies
What is the origin of the LGT gene block?
Gene organization is subject to constant change. For precisely this reason, the overall gene organization within the low-GC gene block might implicate a donor organism because the LGT event is inferred to be recent. Because the enteric lineage is a reasonable source of the LGT gene block, it is pertinent that the gene organization around trpR is highly conserved in the enteric lineage. Without exception, trpR in the enteric lineage is preceded upstream by a gene encoding soluble lytic murein transglycosylase (slt). hemK is usually positioned directly downstream, except for the Haemophilus actinomycetemcomitans/H. influenzae/Pasteurella multocida grouping (where the downstream gene encodes a monofunctional biosynthetic peptidoglycan transglycosylase (mtgA)). No genomes of the enteric lineage were found to possess trpR in a context of flanking genes that resembled the X. fastidiosa gene organization.
The LGT-block of Xylella genes conceivably could have originated from a donor similar to a common ancestor of the chlamydiae before the massive gene reduction associated with the chlamydial lifestyle. This would be consistent with the low GC content of both the chlamydial genome and the LGT-block of genes, as well as with the observation that chlamydiae and Xylella are the only two known taxa where trpR is positioned near structural genes of the tryptophan pathway. Direct comparison of chlamydial trpAa and trpAb genes with those of the Xylella operon is not possible because all chlamydial genomes thus far mapped lack trpAa and trpAb . In this context, sequencing of genomes from closely related free-living relatives of the chlamydiae could be informative. The currently available chlamydial genomes also lack other genes of the low-GC block.
C. burnetii was also considered as a possible source of the low-GC gene block in X. fastidiosa because it possesses trpR. This potential LGT event seems ruled out because trpR is not near any structural genes encoding TrpAa and TrpAb in C. burnetti; C. burnetii TrpAa and TrpAb are not close to the corresponding X. fastidiosa enzymes on phylogenetic trees; and C. burnetii lacks the remaining genes in the low-GC gene block of X.fastidiosa.
If LGT accounts for the low-GC gene block in X. fastidiosa, how recent was this event? Presumably, it was sufficiently recent that significant amelioration to the genomic GC content has not yet occurred. The closest sequenced genome to Xylella is Xanthomonas. Genomes representing two species of the latter genus have been sequenced, and both lack the low-GC gene block. Therefore, the putative LGT event occurred some time after lineage divergence of Xylella and Xanthomonas. On the other hand, LGT presumably has predated speciation in the Xylella genus as all three strains of Xylella in the National Center for Biotechnology Information (NCBI) database possess the low-GC gene block. The T2 score of Hooper and Berg  measures the covariance of 3:1 dinucleotide signatures, and is designed to recognize very recent imports of alien genes by LGT. T2 scores calculated for the low-GC gene block of X. fastidiosa were not above the required threshold for very recent gene imports.
What is the function of the low-GC block of genes in Xyella?
Genes encoding the two anthranilate synthase subunits (trpAa and trpAb) and aryl-CoA ligase (acl) surely belong to an operon, as translational coupling is evident from the overlap of start and stop codons (Figure 4). Acl exhibits strong similarity to coenzyme F390 synthetase of methanogenic archaea, as well as to phenylacetate-CoA ligase of E. coli. As Xylella does not appear to make the F420 cofactor that is the substrate of F390 synthetase, the function of Acl is likely to be closer to phenylacetate-CoA ligase. The aromatic ring is highly stable, and CoA thioesterification can provide chemical activation, allowing cleavage of the aromatic ring, as exemplified by catabolism of benzoate, 4-hydroxybenzoate, and anthranilate . Because acl is tightly organized with trpAa and trpAb, it seems feasible that anthranilate might be the substrate of acl. An anthranilate-CoA ligase has been described recently in Azoarcus evansii by Schuhle et al. . The Xylella Acl exhibited greater identity with phenylacetate-CoA ligase of E. coli than with anthranilate-CoA ligase of A. evansii, but a given substrate specificity within homology groups often can be associated with different subgroupings [25,34].
If anthranilate is indeed the substrate of Acl in Xylella, it would be a futile cycle if anthranilate were formed biosynthetically, only to be subsequently catabolized. Therefore, it seems more likely that the activation of anthranilate could be a step in the formation of a siderophore or antibiotic compound that is assembled by a nonribosomal peptide synthetase mechanism (see Quadri et al.  and references therein for numerous examples). Pyochelin from Pseudomonas aeruginosa exemplifies an iron siderophore whose peptide-based synthesis depends on CoA-activated salicylate (closely related to anthranilate) as a starter unit .
While it appears likely that trpR, aryl-CoA ligase, trpAa and trpAb belong to a common functional unit, the possible roles of the remaining three genes downstream of acl are problematic at the present time.
The Anabaena/Nostocgene blocks
Did operonic genes originate by LGT?
First BLAST hit
Second BLAST hit
Analysis of protein trees
We evaluated whether the closest BLAST hits, using as queries the amino-acid sequences corresponding to the operonic genes of Anabaena or Nostoc, would be with other cyanobacteria (and therefore consistent with origin by gene duplication) or with another taxon grouping (consistent with LGT). In either case, one would expect that the sequences encoded by the operonic genes of Anabaena would be the best matches for the operonic genes of Nostoc, as was indeed the case. For all of the operonic Anabaena/Nostoc Trp-pathway proteins used as queries, homolog sequences from other cyanobacteria (Synechocystis, Synechococcus, Prochlorococcus) were the remaining top hits returned in the BLAST queue. As BLAST hits must be considered imperfect indicators of nearest-neighbor homologs , the conclusion that the operonic trp-pathway genes are of cyanobacterial lineage origin was confirmed more rigorously by examination of extensive trees (available upon request) constructed for each trp protein of Anabaena and Nostoc. For the Trp-pathway proteins, all the cyanobacterial proteins clustered together, regardless of whether they were Anabaena or Nostoc paralogs or whether they were the singly represented proteins of Synechocystis, Synechococcus, or Prochlorococcus. The same result was obtained for AroAIβ protein trees. All the redundant genes exhibited identity relationships that suggested their origin by one or more gene-duplication events in the common ancestor of Anabaena and Nostoc; that is, exactly as diagrammed in Figure 3.
A different result was obtained for genes encoding AroB and TyrA. AroB sequences in nature are rather divergent. All of the cyanobacterial AroB proteins form a compact cluster in the AroB tree (including the non-operonic Anabaena/Nostoc aroB genes), except for those encoded by the Anabaena/ Nostoc supraoperons. The supraoperonic AroB proteins occupy a tree position that is not particularly close to other AroB proteins (the closest matches being on the order of 30-35% identity with some enteric bacteria). A similar situation applies to TyrA(p). All cyanobacteria possess the arogenate dehydrogenase specificity class (denoted TyrAa) of the TyrA superfamily. The additional TyrA(p) present only in Anabaena and Nostoc and located as the carboxy-terminal gene of the supraoperon exhibits identities of 39-43% with the TyrA(p) proteins of some enteric bacteria. These results for supraoperonic aroB and tyrA(p) could be consistent with LGT, but with no clear donor candidates available. On the other hand, origin as ancient paralogs is also a possibility.
Gene fusions involving trpAa and or trpAb homologs
trpAa • trpAb
Brucella melitensis; Sinorhizobium meliloti; Agrobacterium tumefaciens; Azospirillum brasilense; Nostoc punctiforme; Thermomonospora fusca; Rhodopseudomonas palustris; Rhizobium loti; Legionella pneumophila; Anabaena sp._1; Anabaena sp._2
Pseudomonas aureofaciens; Pseudomonas aeruginosa; Pseudomonas chlororaphis; Pseudomonas fluorescens; Streptomyces venezuelae; Streptomyces coelicolor
trpAb • trpB
Escherichia coli; Salmonella typhi; Campylobacter jejuni; Thermotoga maritima
pabAa • pabAb †
pabAa • pabAc †
Neisseria meningitides; Neisseria gonorrhoeae; Chlorobium tepidum; Helicobacter pylori; Campylobacter jejuni; Streptococcus pneumoniae; Streptococcus pyogenes; Streptococcus equi; Streptococcus gordonii; Listeria innocua; Listeria monocytogenes; Geobacter sulfurreducens; Ralstonia solanacearum; Burkholderia fungorum; Novosphingobium aromaticivorans; Chlorobium tepidum; Ralstonia metallidurans; Lactococcus lactis; Burkholderia pseudomallei; Magnetococcus sp.
pabAb • pabAa †
Streptomyces griseus; Streptomyces venezuelae; Streptomyces pristinaespiralis; Thermomonospora fusca; Anabaena sp.; Nostoc punctiforme; Corynebacterium glutamicum; Saccharomyces cerevisiae; Aspergillus fumigatus; Plasmodium falciparum; Coprinus cinereus; Schizosaccharomyces pombe
A phylogenetic tree consisting of all free-standing TrpAa and TrpAb proteins was constructed, together with the corresponding two domains of the TrpAa•TrpAb fusions (available upon request). Surprisingly, each of the 10 fusion domains clustered tightly on the TrpAa and TrpAb trees, to the exclusion of the free-standing TrpAa and TrpAb domains. This is consistent with a single ancestral fusion event, but requires the assumption of multiple LGT events. However, it is surprising that no free-standing domains (that is, close homologs of the original fusion partners) cluster with either of the two sets of 10 fusion domains. This might suggest an alternative to LGT, namely that there has been extreme sequence convergence because of strong selection for appropriate residues mediating domain-domain interactions. If so, it is possible that trpAa•trpAb fusions occurred as a number of independent events, followed by strong convergence.
Figure 9 shows the individual genomic organization of trp-pathway genes in the 16S rRNA tree sector that is relevant to the trpAa•trpAb fusion. The Anabaena/Nostoc lineage is unique in having trpAa•trpAb linked to other trp-pathway genes and is further unique in having an additional set of freestanding genes encoding TrpAa and TrpAb. Although generally uncommon, complete dispersal of Trp-pathway genes is characteristic of the non-filamentous cyanobacteria, Aquifex aeolicus and Chlorobium tepidum. The ancestral state of trp gene organization has been asserted (G.X., C.B., N.K. and R.J., unpublished work) to be trpAa/Ab/B/D/C/Eb/Ea, an operon organization seen in contemporary Cytophaga hutchinsonii, Desulfovibrio vulgaris and Coxiella burnetii (Figure 9). Dynamic gene reorganization events that involve gene insertions, gene scrambling, gene duplications and gene dispersal are apparent from inspection of Figure 9.
It is expected that LGT would most easily be recognized if it occurred relatively recently before passage of sufficient time for amelioration of alien characteristics to those of the host genome, for example GC content. In the case of each of the known trpAa•trpAb gene fusions, the absence of the gene fusion in a closely related genome implies that the gene-fusion event (or the LGT event) occurred recently, that is, in the one lineage following the time of its separation from the other by speciation. Thus, the acquisition of trpAa•trpAb by Thermomonospora fusca must have occurred by fusion or by LGT relatively recently, that is, after the speciation event that generated the Streptomyces lineage (see Figure 9). In each of the remaining cases of trpAa•trpAb fusion, a relatively near time of fusion shown in Figure 9 origin can be identified. These are defined by points of speciation divergence between Anabaena/Nostoc and other cyanobacteria, between the Rhodopseudomonas/Sinorhizobium cluster (fusion) and Caulobacter (no fusion), between Azospirillum brasilense (fusion) and Magnetospirillum magnetotacticum (no fusion), and between Legionella pneumophila (fusion) and Coxiella burnetii (no fusion).
If any of the trpAa•trpAb fusions, other than the Nostoc/Anabaena pair, have a common origin, similar flanking regions of gene organization might be expected since all of the fusions are of relatively recent origin. On this criterion, only R. loti, B. melitensis, A. tumefaciens and S. meliloti exhibited similarities of flanking-gene organization, and this is phylogenetically congruent. These observations imply that within the span of phylogeny shown in Figure 9, the trpAa•trpAb fusion may have occurred independently as many as seven times.
Interdomain linker regions
Only the two operonic fusion proteins from Anabaena and Nostoc and the four rhizobial fusion proteins (Mlo, Bme, Rme and Atu) exhibit linker regions of identical length and obvious similarity. The paralog TrpAa•TrpAb protein of Anabaena sp (Asp_2) seems to have a distinctly different linker, and it maybe that the two fusions in Anabaena arose as two independent events. The partial sequences shown in Figure 10 are spaced to indicate the seven independent events of gene fusion that are suggested.
Function of the Anabaena/Nostocgene blocks?
The gene blocks shown in Figure 2 encode the entire tryptophan pathway (except for trpC), as well as the first two enzymes of the common aromatic pathway, and the key enzyme of tyrosine biosynthesis. Multiple enzymes catalyzing the same reaction have been described in developmental systems where differential regulation of isoenzymes are deployed in different temporal and spatial contexts. Filamentous cyanobacteria (such as Anabaena and Nostoc) subscribe to a developmental program of heterocyst formation that is widely considered the primitive state and that correlates with their exceedingly large genomes. Unicellular cyanobacteria such as Synechocystis, Synechococcus and Prochlorococcus have far smaller genomes and lack the ability to fix nitrogen (heterocyst formation). It, therefore, seems to be a distinct possibility that the gene blocks diagrammed in Figure 2 (as well as additional gene duplicates) are specifically involved in specialized capabilities of Nostoc/Anabaena that do not exist in other cyanobacteria. In terms of the evolutionary scenario, the Anabaena/Nostoc lineage may reflect the ancestral state, and modern unicellular cyanobacteria may be derived genomes that are smaller and more streamlined (reductive evolution).
Alien genes that may be subject to possible LGT can generally expect a hostile reception in that they lack a history of functional integration with the resident genome. Genes that offer immediate selective advantages (for example, antibiotic resistance) are likely to persist. The acquisition of a completely new functional capability will often require an entire suite of novel genes, and such recruitment is certainly easier to envision if all of the genes arrive en bloc (that is, as an operon). Once a primary biosynthetic pathway, such as that responsible for tryptophan formation, has been established and integrated with the individualistic metabolic circuitry of a given organism, one does not expect facile displacement of resident genes. This should apply even if the incoming genes all coexist as an operon. We have found only two examples of LGT of whole-Trp operons, that of trpAa/Ab/B/D•C/Eb/Ea from the enteric lineage to coryneform bacteria and to Helicobacter, as discussed earlier.
Has there been separate lateral gene transfer of individual genes?
According to the foregoing rationale, isolated genes that participate in multi-step processes would not generally be expected to have much success in LGT. In some cases analog genes encode enzymes that catalyze the same reaction in a multi-step pathway, and one analog gene might conceivably displace another. Lack of enough information about genomic representation of such analog genes can lead to incorrect inferences of LGT. For example, the initial discovery of "plant-type" AroAII in bacteria led to the assumption of LGT from plant to bacterium. Elucidation of the fuller genomic representation of aroA II ( and refs therein) demonstrated the origin of aroA II in Bacteria, and plants probably have received aroA II from the Bacteria via endosymbiosis. A similar outcome seems quite possible with respect to the "eukaryotic" fructose-1,6-bisphosphate aldolase in Xylella species. Phylogenetic incongruities that involve such analogs can pose great difficulties in distinguishing LGT from vertical progressions of differential analog losses in different lineages.
Specialized Trpgenes not required for primary biosynthesis
In this article we focus on a number of cases where at least several trp genes are linked, thus providing analytical advantages offered by the analysis of more than one gene. These genes are also redundant and phylogenetically incongruent, in contrast to coexisting homolog genes that are part of a full phylogenetically congruent set. Both of the latter are consistent with origin by LGT, but unrecognized ancient paralogy is also possible. In the first case, the homologs coexisting in one organism are xenologs, whereas in the latter case, they are paralogs. A relatively simple example is the trpAa/trpAb pair originally denoted phnA/phnB in Pseudomonas aeruginosa . This comprises an anthranilate synthase that is not strictly required for primary tryptophan biosynthesis and that is uniquely expressed during stationary-phase physiology . Why the generation of anthranilate under these conditions would be of value is unknown, but phylogenetic trees clearly show phnA/phnB to be xenologs originating from the enteric lineage via LGT (G.X. and R.A.J., unpublished data). In this case, genes that function for primary biosynthesis in the donor genome did not displace the corresponding genes in the recipient genome, but have instead been recruited to a specialized function. In Streptomyces coelicolor, trpAa/trpAb/trpB/trpD/aroAII are contained within a large cluster dedicated to antibiotic synthesis . Calcium-dependent antibiotic (CDC) contains tryptophan, and presumably the feedback-resistant variety of enzyme encoded by aroAII ensures enhanced precursor flow to tryptophan during antibiotic production. Detailed studies have not yet been done to see whether the CDC gene cluster originated via LGT or reflects ancient paralogy.
In this article, we have discussed at length the Xylella and cyanobacterial gene blocks that seem likely to have specialized functional roles other than primary biosynthesis. The Xylella genes are associated with other genes that presumably dictate a fate for anthranilate other than as a primary precursor of tryptophan. We suspect that selective advantages conferred by this specialized operon accommodated successful LGT to Xylella. The Anabaena/Nostoc supraoperon is reminiscent of the S. coelicolor system in the inclusion of AroAIβ, which might enhance precursor flow to chorismate. Although the Anabaena/Nostoc operon only lacks trpC, its features of gene fusion and gene organization are novel. It might perhaps have an unknown physiological function related to the complex developmental programs unique to heterocystous cyanobacteria. We conclude that in this case the operonic trp genes are ancient paralogs of a dispersed set of trp genes engaged in primary biosynthesis.
Against a backdrop where organisms generally possess highly efficient and integrated pathways of tryptophan biosynthesis, displacement of resident genes by LGT of the corresponding genes is relatively infrequent. Aside from the broadly distributed primary pathway, highly specialized pathways are known that utilize some or all tryptophan-pathway enzymes, and these pathways can originate by recruitment of paralog genes derived from the primary-pathway genes . The genes of such specialized operons may diverge considerably to meet the demands of a novel functional role. In a contemporary organism this might have the status of unrecognized (or recognized) paralogy, as we suggest for the Anabaena/Nostoc gene block. However, such an operon module also has strong potential for xenologous transfer because of its specialized functional potential.
The tryptophan pathway exemplifies the situation where paralogs can be engaged in primary amino-acid biosynthesis (widespread) or in a variety of specialized pathways (narrowly distributed). Aside from the extent to which the specialized pathways may be individually intriguing and important, this study illustrates that case-by-case analysis can distinguish paralogs (or xenologs) from their homologs engaged in primary biosynthesis. This conclusion is encouraging as it shows that both vertical and horizontal events of gene transfer can be deduced to track evolutionary history.
The CODONW program  was used to calculate 3:1 dinucleotide frequencies (third base of a given codon followed by the first base of the next codon). For whole-genome calculations, genome nucleotide sequences (.ffn file) were obtained from GenBank . Perl scripts were used to eliminate the defline and assemble all genomic ORFs together for CODONW calculation. The length (from UNIX wc command) divided by 3 was used to validate the absence of frameshift errors. Pairwise covariation of 3:1 dinucleotide frequencies was assessed by the Spearman rank correlation coefficient , a nonparametric rank statistic for testing monotonic relationships. T2 values were kindly provided by Hooper .
16S rRNA subtrees were derived from the Ribosomal Database site [49,50]. Unrooted phylogenetic protein trees were derived by input of the indicated homolog amino-acid sequences into the ClustalW program (Version 1.4) . Manual alignment adjustments were made as needed with the assistance of the BioEdit multiple alignment tool of Hall . The refined multiple alignment was used as input for generation of a phylogenetic tree using the program package PHYLIP . The neighbor-joining and Fitch programs  were used to obtain distance-based trees. The distance matrix was obtained using Protdist with a Dayhoff Pam matrix. The Seqboot and Consense programs were then used to assess the statistical strength of the tree using bootstrap resampling. Neighbor-joining and Fitch trees yielded similar clusters and arrangement of taxa within them. Bootstrap values indicate the number of times a node was supported in 1,000 resampling replications.
Identification of linker regions
Fusion proteins were aligned (ClustalW) with one another and with the assemblage of free-standing proteins corresponding to the amino-terminal and the carboxy-terminal domains of the fusion proteins. The boundaries of each domain were defined by the last highly conserved residues of the amino-terminal domain and the early highly conserved residues of the carboxy-terminal domain. The Conserved Domain Database was useful as a reference guide [54,55].
Comparative genome analysis
Most of the comparative genome analysis was carried out using the database and tools of ERGO .
G.X. was partially supported in this work through the STDGEN project at Los Alamos National Laboratory (NIH/NIAIDAGY1-A1-8228-05). We thank Sean Hooper (Department of Molecular Evolution, Uppsala University, Sweden) for assistance with dinucleotide frequency calculations. We are indebted to A. Osterman of Integrated Genomics, Inc. (Chicago, IL) for provision of access to ERGO . This is Florida Agricultural Experiment Station Journal series no. R-09159.
- Margulis L: Symbiosis in Cell Evolution. 1981, San Francisco: WH FreemanGoogle Scholar
- Gray MW: Evolution of organellar genomes. Curr Opin Genet Dev. 1999, 9: 678-687. 10.1016/S0959-437X(99)00030-1.PubMedView ArticleGoogle Scholar
- Aravind L, Tatusov RL, Wolf YI, Walker DR, Koonin EV: Evidence for massive gene exchange between archaeal and bacterial hyperthermophiles. Trends Genet. 1998, 14: 442-444. 10.1016/S0168-9525(98)01553-4.PubMedView ArticleGoogle Scholar
- Lawrence JG, Ochman H: Molecular archaeology of the Escherichia coli genome. Proc Natl Acad Sci USA. 1998, 95: 9413-9417. 10.1073/pnas.95.16.9413.PubMedPubMed CentralView ArticleGoogle Scholar
- Nelson KE, Clayton RA, Gill SR, Gwinn ML, Dodson RJ, Haft DH, Hickey EK, Peterson JD, Nelson WC, Ketchum KA, et al: Evidence for lateral gene transfer between archaea and bacteria from genome sequence of Thermotoga maritima. Nature. 1999, 399: 323-329. 10.1038/20601.PubMedView ArticleGoogle Scholar
- Ochman H, Lawrence JG, Groisman EA: Lateral gene transfer and the nature of bacterial innovation. Nature. 2000, 405: 299-304. 10.1038/35012500.PubMedView ArticleGoogle Scholar
- Doolittle WF: Phylogenetic classification and the universal tree. Science. 1999, 284: 2124-2129. 10.1126/science.284.5423.2124.PubMedView ArticleGoogle Scholar
- Martin W: Mosaic bacterial chromosomes: a challenge en route to a tree of genomes. BioEssays. 1999, 21: 99-104. 10.1002/(SICI)1521-1878(199902)21:2<99::AID-BIES3>3.3.CO;2-2.PubMedView ArticleGoogle Scholar
- Syvanen M: On the occurrence of horizontal gene transfer among an arbitrarily chosen group of 26 genes. J Mol Evol. 2002, 54: 258-266. 10.1007/s0023901-0007-z.PubMedView ArticleGoogle Scholar
- Kyrpides NC, Olsen GJ: Archaeal and bacterial hyperthermophiles: horizontal gene exchange or common ancestry?. Trends Genet. 1999, 15: 298-299. 10.1016/S0168-9525(99)01811-9.PubMedView ArticleGoogle Scholar
- Stiller JW, Hall BD: Lateral gene transfer, genome surveys, and the phylogeny of prokaryotes. Science. 1999, 286: 1443-10.1126/science.286.5444.1443a.View ArticleGoogle Scholar
- Kurland CG: Something for everyone: Horizontal gene transfer in evolution. EMBO Rep. 2000, 1: 92-95. 10.1093/embo-reports/kvd042.PubMedPubMed CentralView ArticleGoogle Scholar
- Salzberg SL, White O, Peterson J, Eisen JA: Microbial genes in the human genome: lateral transfer or gene loss?. Science. 2001, 292: 1903-1906. 10.1126/science.1061036.PubMedView ArticleGoogle Scholar
- Stanhope MJ, Lupas A, Italia MJ, Koretke KK, Volker C, Brown JR: Phylogenetic analyses do not support horizontal gene transfers from bacteria to vertebrates. Nature. 2001, 411: 940-944. 10.1038/35082058.PubMedView ArticleGoogle Scholar
- Glansdorff N: About the last common ancestor, the universal life-tree and lateral gene transfer: a reappraisal. Mol Microbiol. 2000, 38: 177-185. 10.1046/j.1365-2958.2000.02126.x.PubMedView ArticleGoogle Scholar
- Woese CR: Interpreting the universal phylogenetic tree. Proc Natl Acad Sci USA. 2000, 97: 8392-8396. 10.1073/pnas.97.15.8392.PubMedPubMed CentralView ArticleGoogle Scholar
- Lawrence JG, Ochman H: Molecular archaeology of the Escherichia coli genome. Proc Natl Acad Sci USA. 1998, 95: 9413-9417. 10.1073/pnas.95.16.9413.PubMedPubMed CentralView ArticleGoogle Scholar
- Wang B: Limitations of compositional approach to identifying horizontally transferred genes. J Mol Evol. 2001, 53: 244-250. 10.1007/s002390010214.PubMedView ArticleGoogle Scholar
- Koski LB, Morton RA, Golding GB: Codon bias and base composition are poor indicators of horizontally transferred genes. Mol Biol Evol. 2001, 18: 404-412.PubMedView ArticleGoogle Scholar
- Ragan MA: On surrogate methods for detecting lateral gene transfer. FEMS Microbiol Lett. 2001, 201: 187-191. 10.1016/S0378-1097(01)00262-2.PubMedView ArticleGoogle Scholar
- Lawrence JG, Ochman H: Reconciling the many facets of lateral gene transfer. Trends Microbiol. 2002, 10: 1-4. 10.1016/S0966-842X(01)02282-X.PubMedView ArticleGoogle Scholar
- Ragan M: Detection of lateral gene transfer among microbial genomes. Curr Opin Genet Dev. 2001, 11: 620-626. 10.1016/S0959-437X(00)00244-6.PubMedView ArticleGoogle Scholar
- Xie G, Bonner CA, Jensen RA: Dynamic diversity of the tryptophan pathway in the chlamydiae: reductive evolution and a novel operon for tryptophan recapture. Genome Biol. 2002, 3: research0005.1-0005.13. 10.1186/gb-2002-3-9-research0051.View ArticleGoogle Scholar
- Henner D, Yanofsky C: Biosynthesis of aromatic amino acids. In Bacillus subtilis and other Gram-positive Bacteria: Biochemistry, Physiology, and Molecular Genetics. Edited by: Sonenshein AL, Hoch J, Losick R. 1993, Washington, DC: ASM Press, 269-280.View ArticleGoogle Scholar
- Subramaniam PS, Xie G, Xia T, Jensen RA: Substrate ambiguity of 3-deoxy-D-manno-octulosonate 8-phosphate synthase from Neisseria gonorrhoeae in the context of its membership in a protein family containing a subset of 3-deoxy-D-arabino-heptulosonate 7-phosphate synthases. J Bacteriol. 1998, 180: 119-127.PubMedPubMed CentralGoogle Scholar
- Jensen RA, Xie G, Bonner CA: The correct phylogenetic relationship of KdsA (3-deoxy-D-manno-octulosonate 8-phosphate synthase) with one of two independently evolved classes of AroA (3-deoxy-D-arabino-heptulosonate 7-phosphate synthase. J Mol Evol. 2002, 54: 416-423.PubMedView ArticleGoogle Scholar
- Gosset G, Bonner CA, Jensen RA: Microbial origin of plant-type 2-keto-3-deoxy-D-arabino-heptulosonate 7-phosphate synthases, exemplified by the chorismate-and tryptophan-regulated enzyme from Xanthomonas campestris. J Bacteriol. 2001, 183: 4061-4070. 10.1128/JB.183.13.4061-4070.2001.PubMedPubMed CentralView ArticleGoogle Scholar
- Xie G, Bonner CA, Jensen RA: Cyclohexadienyl dehydrogenase from Pseudomonas stutzeri exemplifies a widespread type of tyrosine-pathway dehydrogenase in the TyrA protein family. Comp Biochem Physiol C Toxicol Pharmacol. 2000, 125: 65-83. 10.1016/S0742-8413(99)00090-0.PubMedGoogle Scholar
- Fitch WM: Homology: a personal view on some of the problems. Trends Genet. 2000, 16: 227-231. 10.1016/S0168-9525(00)02005-9.PubMedView ArticleGoogle Scholar
- Van Vliet F, Boyen A, Glansdorff N: On interspecies gene transfer: the case of the argF gene of Escherichia coli. Ann Inst Pasteur Microbiol. 1988, 139: 493-496. 10.1016/0769-2609(88)90111-1.PubMedView ArticleGoogle Scholar
- Hooper SD, Berg OG: Detection of genes with atypical nucleotide sequence in microbial genomes. J Mol Evol. 2002, 54: 365-375.PubMedView ArticleGoogle Scholar
- Mohamed MES, Zaar A, Ebenau-Jehle C, Fuchs G: Reinvestigation of a new type of aerobic benzoate metabolism in the proteobacterium Azoarcus evansii. J Bacteriol. 2001, 183: 1899-1908. 10.1128/JB.183.6.1899-1908.2001.PubMedPubMed CentralView ArticleGoogle Scholar
- Schühle K, Jahn M, Ghisla S, Fuchs G: Two similar gene clusters coding for enzymes of a new type of aerobic 2-aminobenzoate (anthranilate) metabolism in the bacterium Azoarcus evansii. J Bacteriol. 2001, 183: 5268-5278. 10.1128/JB.183.18.5268-5278.2001.PubMedPubMed CentralView ArticleGoogle Scholar
- Calhoun DH, Bonner CA, Gu W, Xie G, Jensen RA: The emerging periplasm-localized subclass of AroQ chorismate mutases, exemplified by those from Salmonella typhimurium and Pseudomonas aeruginosa. Genome Biol. 2001, 2: research0030.1-0030.16. 10.1186/gb-2001-2-8-research0030.View ArticleGoogle Scholar
- Quadri LEN, Keating TA, Patel HM, Walsh CT: Assembly of the Pseudomonas aeruginosa nonribosomal peptide siderophore pyochelin: In vitro reconstitution of aryl-4,2-bisthiazoline synthetase activity from PchD, PchE, and PchF. Biochemistry. 1999, 38: 14941-14954. 10.1021/bi991787c.PubMedView ArticleGoogle Scholar
- Patel HM, Walsh CT: In vitro reconstitution of the Pseudomonas aeruginosa nonribosomal peptide synthesis of pyochelin: characterization of backbone tailoring thiazoline reductase and N-methyltransferase activities. Biochemistry. 2001, 40: 9023-9031. 10.1021/bi010519n.PubMedView ArticleGoogle Scholar
- Guindon S, Perrière S: Intragenomic base content variation is a potential source of biases when searching for horizontally transferred genes. Mol Biol Evol. 2001, 18: 1838-1840.PubMedView ArticleGoogle Scholar
- Koski L, Golding GB: The closest BLAST hit is often not the nearest neighbor. J Mol Evol. 2001, 52: 540-542.PubMedView ArticleGoogle Scholar
- Essar DW, Eberly L, Hadero A, Crawford IP: Identification and characterization of genes for a second anthranilate synthase in Pseudomonas aeruginosa : interchangeability of the two anthranilate synthases and evolutionary implications. J Bacteriol. 1990, 172: 884-900.PubMedPubMed CentralGoogle Scholar
- Mavrodi DV, Bonsall RF, Delaney SM, Soule MJ, Phillips G, Thomashow LS: Functional analysis of genes for biosynthesis of pyocyanin and phenazine-1-carboxamide from Pseudomonas aeruginosa PA01. J Bacteriol. 2001, 183: 6454-6465. 10.1128/JB.183.21.6454-6465.2001.PubMedPubMed CentralView ArticleGoogle Scholar
- Ryding JJ, Anderson TB, Champness WC: Regulation of the Streptomyces coelicolor calcium-dependent antibiotic by absA, encoding a cluster-linked two-component system. J Bacteriol. 2002, 184: 794-805.PubMedPubMed CentralView ArticleGoogle Scholar
- Jensen RA: Enzyme recruitment in the evolution of new function. Annu Rev Microbiol. 1976, 30: 409-425. 10.1146/annurev.mi.30.100176.002205.PubMedView ArticleGoogle Scholar
- Peden J: CodonW as a freeware release for codon usage analysis. [http://www.molbiol.ox.ac.uk/cu/culong.html#Codonw]
- GenBank Database. [http://www.ncbi.nlm.nih.gov/Genbank/GenbankOverview.html]
- Lehmann EL, D'Abrera HJM: Nonparametrics: Statistical Methods Based on Ranks, Rev Edn. 1998, Englewood Cliffs, NJ: Prentice-Hall, 292-323.Google Scholar
- Pesole G, Attimonelli M, Liuni S: A backtranslation method based on codon usage strategy. Nucleic Acids Res. 1988, 16: 1715-1728.PubMedPubMed CentralView ArticleGoogle Scholar
- Nakamura Y, Gojobori T, Ikemura T: Codon usage tabulated from the international DNA sequence databases: status for the year 2000. Nucleic Acids Res. 2000, 28: 292-10.1093/nar/28.1.292.PubMedPubMed CentralView ArticleGoogle Scholar
- Codon Usage Database. [http://www.kazusa.or.jp/codon]
- Maidak BL, Cole JR, Lilburn TG, Parker CT, Saxman PR, Farris RJ, Garrity GM, Olsen GJ, Schmidt TM, Tiedje JM: The RDP-II (Ribosomal Database Project). Nucleic Acids Res. 2001, 29: 173-174. 10.1093/nar/29.1.173.PubMedPubMed CentralView ArticleGoogle Scholar
- Ribosomal Database Project II. [http://rdp.cme.msu.edu/html]
- Thompson JD, Higgins DG, Gibson TJ: CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res. 1994, 22: 4673-4680.PubMedPubMed CentralView ArticleGoogle Scholar
- Hall T: Biological Sequence Alignment Editor for Windows 95/98/NT, 5.0.9 Edn. Raleigh: North Carolina State University, [http://www.mbio.ncsu.edu/BioEdit/bioedit.html]
- Felsenstein J: PHYLIP - Phylogeny inference package (version 3.2). Cladistics. 1989, 5: 164-166.Google Scholar
- Marchler-Bauer A, Panchenko AR, Shoemaker BA, Thiessen PA, Geer LY, Bryant SH: CDD: a database of conserved domain alignments with links to domain three-dimensional structure. Nucleic Acid Res. 2002, 30: 281-283. 10.1093/nar/30.1.281.PubMedPubMed CentralView ArticleGoogle Scholar
- NCBI Conserved Domain Database. [http://www.ncbi.nlm.nih.gov/Structure/cdd/cdd.shtml]
- ERGO. [http://wit.integratedgenomics.com/ERGO]
- Xie G, Forst C, Bonner C, Jensen RA: Significance of two distinct types of tryptophan synthase beta chain in Bacteria, Archaea and higher plants. Genome Biol. 2002, 3: research0004.1-0004.13. 10.1186/gb-2001-3-1-research0004.View ArticleGoogle Scholar
- Mackenzie C, Simmons AE, Kaplan S: Multiple chromosomes in bacteria: The yin and yang of trp gene localization in Rhodobacter sphaeroides 2.4.1. Genetics. 1999, 153: 525-538.PubMedPubMed CentralGoogle Scholar
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