The complete plastid genome sequence of the parasitic green alga Helicosporidium sp. is highly reduced and structured
© de Koning and Keeling; licensee BioMed Central Ltd. 2006
Received: 16 January 2006
Accepted: 21 April 2006
Published: 21 April 2006
Loss of photosynthesis has occurred independently in several plant and algal lineages, and represents a major metabolic shift with potential consequences for the content and structure of plastid genomes. To investigate such changes, we sequenced the complete plastid genome of the parasitic, non-photosynthetic green alga, Helicosporidium.
The Helicosporidium plastid genome is among the smallest known (37.5 kb), and like other plastids from non-photosynthetic organisms it lacks all genes for proteins that function in photosynthesis. Its reduced size results from more than just loss of genes, however; it has little non-coding DNA, with only one intron and tiny intergenic spaces, and no inverted repeat (no duplicated genes at all). It encodes precisely the minimal complement of tRNAs needed to translate the universal genetic code, and has eliminated all redundant isoacceptors. The Helicosporidium plastid genome is also highly structured, with each half of the circular genome containing nearly all genes on one strand. Helicosporidium is known to be related to trebouxiophyte green algae, but the genome is structured and compacted in a manner more reminiscent of the non-photosynthetic plastids of apicomplexan parasites.
Helicosporidium contributes significantly to our understanding of the evolution of plastid DNA because it illustrates the highly ordered reduction that occurred following the loss of a major metabolic function. The convergence of plastid genome structure in Helicosporidium and the Apicomplexa raises the interesting possibility that there are common forces that shape plastid genomes, subsequent to the loss of photosynthesis in an organism.
Plastids are organelles found in plants and algae. Plastids originated in the endosymbiotic uptake of a cyanobacterium, which was subsequently transformed from a complex free-living bacterium to the highly specialized organelle now integrated with its host. At the genomic level, this integration involved the loss of many genes and the transfer of many more to the host nuclear genome, the protein products of which are targeted back to the organelle . This process is not complete, however, as all known plastids have retained a residual genome that encodes a handful of RNA and protein-coding genes, which typically include many of the key components of photosystems I and II . Our concept of plastids is inexorably tied to photosynthesis, since this is the dominant metabolic process of most plastids. They are, however, metabolically diverse organelles that play a role in the biosynthesis of amino acids, fatty acids, isoprenoids and heme, as well as in other processes related to photosynthesis such as pigment biosynthesis, and radical detoxification. Indeed, in several lineages of plants and algae photosynthesis has been lost altogether, but the plastid has been retained for these and other purposes . Well-known examples of this include holoparasitic plants, many lineages of heterotrophic algae and parasitic apicomplexans (such as the malaria parasite). In most plastid genomes, the vast majority of genes encode products involved in either gene expression or photosynthesis. When photosynthesis is lost, so are most or all of the related genes, leading to dramatic changes in the plastid genome in size, coding capacity, and often also structure.
These genomes offer an opportunity to study the effects of massive genomic changes following a functional shift. Unfortunately, the number of fully-sequenced non-photosynthetic plastid genomes is small, limited to Epifagus virginiana (a holoparasitic angiosperm), Euglena longa (a heterotrophic euglenid), and several apicomplexan parasites bearing secondary plastids of red algal origin called apicoplasts (Plasmodium falciparum, Theileria parva, Eimeria tenella and Toxoplasma gondii). The E. virginiana plastid is about half the size of typical angiosperm plastids, having lost all its photosynthetic genes, but is otherwise similar to its relatives in many ways including non-coding DNA content, synteny of remaining genes and overall structure . Likewise, E. longa has lost most of the photosynthetic genes found in the plastid of its close relative Euglena gracilis, but they share many features that are unique to euglenids, such as three tandem repeats of the RNA operon and a multitude of distinctive introns . Apicomplexan plastid genomes, however, are quite different from those of other secondary red algal plastids found in photosynthetic lineages. They have undergone extensive rearrangments, are exceedingly small (~35 kb) and compact, and contain very little non-coding DNA [6–9]. The uniqueness of apicomplexan plastid genomes may simply be due to time: apicomplexan plastids probably lost photosynthesis long ago in the ancestor of this diverse group, whereas other sequenced non-photosynthetic plastid genomes come from organisms with close relatives that are photosynthetic.
To examine the process of genome reduction after the loss of a major metabolic function, we have completely sequenced the genome of the non-photosynthetic plastid of Helicosporidium sp., a parasitic green alga. Helicosporidia are obligate parasites of invertebrates with a unique morphology and infection strategy . Their evolutionary origin was disputed until recently, when molecular evidence surprisingly showed that they are highly adapted trebouxiophyte green algae, specifically related to the opportunistic vertebrate parasites, Prototheca [11, 12]. This led to the prediction that Helicosporidia contain plastids, and although they have not yet been visually identified, molecular evidence has confirmed their existence [13–15]. The function of this organelle has been investigated by examining nucleus-encoded plastid-targeted proteins, which cumulatively suggest the Helicosporidium plastid is functionally similar in many ways to that of apicomplexan parasites . Here, we show that the Helicosporidium plastid genome, while retaining many features confirming its phylogenetic affiliation, has been radically reduced in a non-random, structured fashion. The result is a genome that is highly ordered with regard to several characteristics such as coding strand and selective loss of tRNAs. Comparing the Helicosporidium plastid genome to that of other green algae and more distantly related non-photosynthetic plastids raises the interesting possibility that the 'structured-reduction' of Helicosporidium represents a common fate of such a genome.
Results and discussion
Genome size and density of coding regions
Plastid genome features compared between non-photosynthetic plastids and photosynthetic relatives
% non-coding DNA (including introns)
Mean intergenic distance (bp)
No. of genes (proteins & rRNAs)
No. of tRNAs
Containing secondarily acquired red algal plastids
Genome structure and organization
Unlike most plastid genomes, the Helicosporidium genome does not contain an inverted repeat (Figure 1). Although inverted repeats are probably an ancestral character state for all plastids, they have been independently lost in several lineages. Among the green algal plastids investigated so far, the inverted repeat is absent in charophytes (Staurastrum puctulatum and Zygnema circumcarinatum ), ulvophytes (Caulerpa sertularoides  and Codium fragile ) and the trebouxiophyte Chlorella vulgaris , but is present in Chlorella ellipsoidea . More interestingly, Helicosporidium has also lost the ribosomal RNA (rRNA) operon, which is a nearly universal feature of all genomes, including prokaryotes, eukaryotes and organelles. The plastid rRNA operon is normally part of the inverted repeat when it is present, and consists of the small and large subunit (SSU and LSU) rRNA genes separated by a spacer region containing the tRNA-Ile and tRNA-Ala genes. In Helicosporidium, the rRNA genes are separated by 22.6 kb of sequence, but tRNA-Ile and tRNA-Ala genes remain associated with the SSU and LSU genes, respectively, such that a typical rRNA operon has been broken in half and distributed at opposing ends of the circle (Figure 1). While the vast majority of plastids have the rRNA operon, it has been lost in C. ellipsoidea, S. punctulatum and the P. falciparum and coccidian apicoplasts, where the SSU and LSU rRNA genes are adjacent to each other but encoded on opposite strands [6, 7, 9, 19, 23]. It has also been disrupted in the charophytes, Z. circumcarinatum  and Spirogyra maxima , and the ulvophytes C. sertularoides  and C. fragile , where the two rRNA genes are located on the same strand but far apart, as in Helicosporidium. This genome rearrangement has therefore occurred in at least three independent lineages, and may be an outcome of loss of the inverted repeat.
The most striking feature of the Helicosporidium genome is the symmetry shown in strand bias of coding regions (Figure 1). The rRNA genes are nearly diametrically opposed, and all but two proteins and one tRNA on one side of them are on the same strand, while all but one tRNA on the other side are on the opposite strand. Similarly-organized coding strand biases are also found in some apicomplexan plastids and in the euglenid plastids, but the bias is not as strong. In P. falciparum, the coding strand switch occurs between the adjacent inverted repeats, each of which encodes LSU and SSU rRNA and nine tRNA genes  and contains the origin of replication . In Euglena, the coding strand symmetry is bound on one end by the origin of replication and on the other end by the replication termination site . In these organisms, the majority of genes are transcribed in each direction away from the bidirectional origin of replication, such that the leading strand of replication is largely the coding strand. Such bias is also widespread among bidirectional replicating prokaryote genomes, where it is hypothesized to be the result of selection to minimize collision between DNA and RNA polymerases moving in opposite directions .
The Helicosporidium genome encodes 26 proteins, 3 rRNAs and 25 tRNAs. The only intron is a group I intron in the tRNA Leu (UAA) gene. This particular intron is commonly found in cyanobacteria and plastids and may be an ancestral plastid feature, although lineage-specific losses have occurred among green algae . No unique ORFs of appreciable size were found and most of the protein-coding genes in Helicosporidium are identifiable as housekeeping proteins involved in transcription and translation (Figure 1). These include 16 ribosomal proteins, an elongation factor and components of an RNA polymerase (rpo). In plants, this polymerase is responsible mainly for transcription of genes associated with photosynthesis. In non-photosynthetic plants, algae and apicomplexans [4, 5, 9], some or all of the rpo subunits have been lost from the plastid genome, and it is thought that a separate nuclear-encoded polymerase is responsible for plastid transcription. In the Helicosporidium plastid, however, all 4 subunits of the RNA polymerase complex (rpoA, rpoB, rpoC1, and rpoC2) are present. The Helicosporidium plastid also encodes tRNA(Ile)-lysidine synthetase (tilS), which is responsible for modifying the CAU anticodon of a unique tRNA that is cognate for isoleucine. This CAU-reading tRNA is universally found among bacteria and plastids . In plastids, however, tilS is generally encoded in the nuclear genome and targeted to the organelle. In addition to Helicosporidium, tilS is also plastid-encoded in the rhodophyta, and in the green algae Nephroselmis olivacea, C. vulgaris, Chaetosphaeridium globosum and Mesostigma viride.
Only four protein coding genes encode products not involved in transcription or translation: FtsH protease, which degrades membrane-bound proteins [33, 34], ycf1, a poorly conserved gene of unknown function that has been shown to be essential [35, 36], Acetyl-CoA carboxylase beta subunit (accD), which is involved in fatty acid biosynthesis , and a sulfate transport protein (cysT) . These four genes have a scattered distribution among plastid genomes. FtsH protease is found in red algae, chromists (algae with plastids of secondary red algal origin) and green algae, but is nuclear-encoded in plants. AccD is found in plants, green algae and red algae. Ycf1 is only found in the plastid genomes of plants and green algae, while cysT is restricted to green algae, a few lower plants and one red alga. Other components of the metabolic pathways in which accD and cysT participate are known to be encoded in the nucleus of Helicosporidium and targeted to the plastid, confirming these as metabolic functions of the organelle . As expected, no genes involved in photosynthesis or bioenergetic processes were found.
As noted earlier, P. wickerhamii probably represents an intermediate form between autotrophic, Chlorella-like trebouxiophytes and the highly-reduced Helicosporidium. Over half the P. wickerhamii plastid genome is known, and no photosystem, electron transport or chlorophyll biosynthesis proteins have been found. However, the P. wickerhamii plastid does encode genes for six of the subunits of ATP synthase , which are not present in Helicosporidum or apicoplast genomes.
The Helicosporidiumplastid encodes a minimal set of tRNAs
In general, plastids use more than the minimal set: about 32 different tRNA species are usually found because more than one isoacceptor is often used to decode the 4-fold degenerate groups of serine, leucine, threonine, arginine and glycine and the 2-fold degenerate lysine (UAR) group. Helicosporidium minimizes the number of isoacceptors used, by complete utilization of 3rd position wobble. As Figure 4 shows, the complement of tRNAs encoded in the Helicosporidium genome are sufficient to decode all codons found in the mRNA, assuming that some known modifications [32, 39] are used. Furthermore, the GXX tRNA is present in every one of eight codon pairs ending in a pyrimidine, the UXX tRNA is present in every one of five codon pairs ending in a purine, and the UXX tRNA is present in seven out of eight 4-fold degenerate groups. The single exception to this uniformity is tRNA-Arg (ACG). The first anticodon position A is presumably modified to inosine and reads all four Arg codons, as happens in plant plastids [40, 41].
Once again, the closest comparison for this type of reduction lies in the non-photosynthetic plastids. P. falciparum takes near-complete advantage of the wobble rules but uses two anticodons for glycine. E. tenella, T. gondii and T. parva have dispensed with the extraneous tRNA-Gly and use the same suite of tRNAs as Helicosporidium. Curiously, however, all the apicomplexa appear to lack the modified tRNA-Ile (CAT reading ATA). The ATA codon frequently appears in these genomes, so either a unique and unknown modification system must exist , or they import a tRNA. In the holoparasitic plant E. virginiana, a number of tRNAs have been lost or exist as pseudogenes. Seven essential anticodons are missing, so it has been suggested that E. virginiana must import tRNAs . Helicosporidium is therefore unique in that it reduced its tRNA complement to a minimum without inventing new modifications, changing its genetic code or importing tRNAs from the cytoplasm; instead, it has simply done away with all redundant tRNAs to leave the perfect minimal set for the universal code.
Interestingly, there is a strong AT codon bias in Helicosporidium protein coding genes (the arginine codon CGG is used only once in the entire genome), and this bias is often counter to the tRNA complement (Figure 4). In some systems, there is a correlation between codon bias and what tRNA genes are present in the genome, and this is assumed to occur by selection for increased translation effieciency . However, in Helicosporidium, codon bias is clearly a result of an overall high AT bias, while the presence or absence of tRNAs is dictated by wobble rules.
When a major metabolic shift occurs, many genes may be lost. If photosynthesis disappears, this loss of genes can represent a large proportion of the plastid genome, so the effect is severe. By itself, however, this loss does not explain the nature of these reduced genomes, because there is no obvious reason that the resulting genome could not be similar in form to its photosynthetic ancestor, but reduced in content. Indeed, this is what we see in the holoparasitic plant E. virginiana and the heterotrophic euglenid E. longa. However, the genomes of the apicoplast and Helicosporidium are different; these genomes are highly reduced but more ordered than their ancestors. At least some aspects of this 'structured reduction' appears to be related to high coding density: the symmetrical coding strand bias probably developed to co-ordinate transcription and replication, and the elegant utilization of wobble rules is probably to reduce the complement of tRNA genes to a minimal functional set. The apicomplexa and Helicosporidium are not closely related; indeed, among plastid types they could hardly be more different: the apicoplast is a secondary plastid derived from a red alga whereas the Helicosporidium plastid is a primary green algal plastid. Their genomes have both retained characteristics that betray these origins, but they have also converged on a similar form in many ways. It is possible there are specific selective pressures operating here that are not important to other sequenced non-photosynthetic plastid genomes, or it could be that this is a predictable outcome for the evolution of these genomes, and less ordered examples are simply not there yet. Either way, the overall forms of apicomplexan and Helicosporidium plastid genomes have been shaped in parallel by common evolutionary forces. Comparing them raises interesting questions about whether there are selective pressures that lead genomes to compact, or if compaction is simply a by-product of reduction that occurs for neutral reasons.
Cell culture and genomic DNA isolation
Helicosporidium sp. (ATCC 50920, isolated from the blackfly Simulium jonesii) was cultured axenically in TNM-FH insect medium (Sigma-Aldrich) supplemented with 5% fetal bovine serum and 50 mg/ml of gentamycin at 25°C in the dark. Cells were harvested by centrifugation and ground under liquid nitrogen. Total genomic DNA was extracted from the ground cells using the Plant Dneasy Mini Kit (Qiagen).
Genes encoding accD and cysT were amplified by PCR using the degenerate primer pairs GGCGTGATGGACTTYCANTTYATGG/GCCGTCACCCCNCCNGTNGTNG and GACTACTATGTGGAYYTNCCNTTYGC/GCCCCGAAGTARTCRTAYTGYTC, respectively. In addition, a fragment containing a portion of the rpoC1 and rpoC2 genes was sequenced as part of an ongoing genomic sequence survey, and two sequences (a partial SSU rRNA [GenBank:AF538864] and rps12/rps7/tufA/rpl2 [GenBank:AY498714]) were characterized previously. These four sequences were used as anchors for long-range PCR containing 1 U Elongase polymerase mix (Invitrogen), 1.5 mM [Mg 2+] buffer, 100 ng template DNA, 200 μM dNTPs and 0.2 μM each of two primers, resulting in eight overlapping fragments of the plastid genome ranging in size from 867 to 8168 bp. These fragments were TOPO TA (Invitrogen) cloned and sequenced using BigDye terminator chemistry (ABI) on both strands by primer walking. Sequences were assembled using Sequencher (Gene Codes Corporation), yielding a circular molecule, with a total of about 2.4 kb of overlap between clones. The plastid genome sequence has been deposited in GenBank [DQ398104].
Annotation and analyses
Protein coding genes were initially identified by BLASTX  searches of NCBI protein databases. In cases of divergent sequence and/or length heterogeneity such that the Helicosporidium ORF could be defined by more than one initiation codon, the longest non-overlapping ORF was selected. Ultimately, 94.9% of the genome contained ORFs with detectable homologues in other plastid genomes, giving high confidence that all genes were identified and annotated. Ribosomal RNA (rRNA) genes were identified by BLASTN searches against the plastid genome database at NCBI. Endpoints of rRNA genes were determined by alignment with trebouxiophyte plastid rRNA genes [GenBank:AJ222802, GenBank:NC001865]. Transfer RNA (tRNA) genes were identified using tRNAscan-SE . All non-coding regions were re-analyzed with BLASTX and BLASTN searches, revealing no detectable matches. Mean intergenic distances were calculated from intergenic spaces between all genes, with overlapping genes given a value of 0.
This work was supported by a grant (MOP-42517) from the Canadian Institutes for Health Research (CIHR). We thank A. Tartar and D. Boucias for providing Helicosporidium cells in culture, and M. Rogers for helpful comments on the manuscript. APD is supported by scholarships from CIHR and the Michael Smith Foundation for Health Research (MSFHR), and PJK is a Fellow of the Canadian Institute for Advanced Research (CIAR) and a new investigator of the CIHR and MSFHR.
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