The mitochondrial genome of the hexactinellid sponge Aphrocallistes vastus: Evidence for programmed translational frameshifting
© Rosengarten et al; licensee BioMed Central Ltd. 2008
Received: 25 June 2007
Accepted: 23 January 2008
Published: 23 January 2008
Mitochondrial genomes (mtDNA) of numerous sponges have been sequenced as part of an ongoing effort to resolve the class-level phylogeny of the Porifera, as well as to place the various lower metazoan groups on the animal-kingdom tree. Most recently, the partial mtDNA of two glass sponges, class Hexactinellida, were reported. While previous phylogenetic estimations based on these data remain uncertain due to insufficient taxon sampling and accelerated rates of evolution, the mtDNA molecules themselves reveal interesting traits that may be unique to hexactinellids. Here we determined the first complete mitochondrial genome of a hexactinellid sponge, Aphrocallistes vastus, and compared it to published poriferan mtDNAs to further describe characteristics specific to hexactinellid and other sponge mitochondrial genomes.
The A. vastus mtDNA consisted of a 17,427 base pair circular molecule containing thirteen protein-coding genes, divergent large and small subunit ribosomal RNAs, and a reduced set of 18 tRNAs. The A. vastus mtDNA showed a typical hexactinellid nucleotide composition and shared a large synteny with the other sequenced glass sponge mtDNAs. It also contained an unidentified open reading frame and large intergenic space region. Two frameshifts, in the cox3 and nad6 genes, were not corrected by RNA editing, but rather possessed identical shift sites marked by the extremely rare tryptophan codon (UGG) followed by the common glycine codon (GGA) in the +1 frame.
Hexactinellid mtDNAs have shown similar trends in gene content, nucleotide composition, and codon usage, and have retained a large gene syntenty. Analysis of the mtDNA of A. vastus has provided evidence diagnostic for +1 programmed translational frameshifting, a phenomenon disparately reported throughout the animal kingdom, but present in the hexactinellid mtDNAs that have been sequenced to date.
The Phylum Porifera (sponges) is currently divided into three extant classes – the Hexactinellida, Demospongiae, and Calcarea – and one fossil class – the Archaeocyatha . Hexactinellids differ from the canonical sponge body plan in lacking discrete motile cells (see [1, 2] for a detailed review). The tissue of hexactinellids forms a continuous multinucleate syncytium. Cellular components exist, but all "cells" are connected by cytoplasmic bridges to one-another and to the syncytium. Choanocytes are branched; collar-flagella units ("collar bodies") form as enucleate buds, several arising from a single nucleated choanoblast [2–4]. The distinct tissue organization was considered important enough to warrant separation of hexactinellids from other Porifera at the subphylum level – Symplasma for the Hexactinellida and Cellularia for the Demospongiae and Calcarea . In no other animal is the tissue so inclusively connected in a giant syncytium, making the hexactinellid body construction unique among Porifera, as well as all Metazoa.
The Porifera has long been considered the earliest branching group of the metazoan crown, based on both morphological and molecular evidence, although the precise relationships of the lower metazoan phyla remains uncertain [6–11]. One on-going approach to resolve the overall metazoan phylogeny, as well as the problematic class-level relationships among the sponges, has been comparative analysis of mitochondrial genomes (mtDNA). To date, this effort has seen the sequencing and description of five complete demosponge mtDNAs [GenBank: NC_006894, NC_006990, NC_006991, NC_008944, NC_009090], and most recently, that of two partial hexactinellid sponge mtDNAs [GenBank: EF537576, EF537577]. Phylogenetic estimations based on concatenated mitochondrial protein sequences have been sensitive to taxon sampling, outgroup choice and algorithm implementation. These trees reveal artifacts likely due to variable rates of molecular evolution, such that placozoans, cnidarians, and demosponges are recovered as a monophyletic clade, with hexactinellids the sister group of bilaterians [12–16]. The tree topologies may become more stable, and consistent with plausible hypotheses of the evolution of morphological traits, as the mtDNA of additional taxa are added to the data set.
While sequence-based mtDNA comparisons of the lower metazoa have not been phylogenetically definitive, the efforts have dispelled some commonly held myths and revealed some general characteristics of animal mtDNA. Placozoan mtDNA, for example, is twice as large as most animal molecules, ranging from 32 to 43 kilobases, and retains various traits of the non-metazoan outgroups such as substantial intergenic space, introns and large open reading frames less commonly found in other animal mtDNA [12, 17]. On the other hand, demosponge mtDNA is more typical of other animals – compact molecules, between 18 and 25 kb, with few or no introns, little intergenic space, and coding for twelve to fourteen respiratory chain proteins and two ribosomal RNAs [13, 15, 16, 18, 19]. Two partial hexactinellid mitochondrial genomes, those of Sympagella nux (Order Lyssacinosida, Family Caulophacidae) and Iphiteon panicea (Order Hexactinosida, Family Dacylocalycidae), have recently been reported . These genomes were found to have similar protein-coding gene content as the published demosponges, but had several features such as tRNA structure and content more similar to that of bilaterians . The current paper reports on the complete mtDNA sequence of the hexactinellid sponge Aphrocallistes vastus (Order Hexactinosida, Family Aphrocallistidae), compares it to previously published poriferan mtDNAs, and highlights two translational frameshifts, a phenomenon that is unique to the hexactinellids among reported lower metazoan mitochondrial genomes.
Results and Discussion
Aphrocallistes vastus mtDNA gene content, size and overlap
nad2/58 trnF(gaa)/71# trnC(gca)/7
trnS1 (ucu) trnS2 (uga)
trnD, trnE, trnT
The beginnings and ends of the small and large rRNA subunits, 918 bp and 1718 bp, respectively, were approximated from alignment data as these genes retained little sequence similarity to the rRNAs from sequenced demosponge mtDNAs, or with those in the non-redundant BLAST database. Thus the complete rRNA sequences remain to be confirmed experimentally. The A. vastus rRNAs were similar to the predicted rRNAs of I. panicea and S. nux, and the rnl sequence was highly similar to the partial 16S rRNA from the hexactinellid Heterochone calyx [Genbank: AM183122], indicating that these genes are similar within the hexactinellids but divergent from those of other sponge classes. Whereas the first three published sponge mtDNAs, all of closely related demosponges, presented a picture of highly similar, conserved molecules [15, 19], additional demosponge and hexactinellid mtDNAs have since revealed that some sponge mtDNAs have unknown ORFs, genes on the complement strand (as in Oscarella carmela), and divergent gene sequences [13, 14, 16].
Genome organization, nucleotide composition and codon usage
The organization of the A. vastus mtDNA was quite compact, typical of sponges and most other animals. Nearly 72% of the mtDNA was predicted to encode proteins (including orf411), 22% to encode ribosomal and transfer RNAs, while only 6% was non-coding intergenic space. Almost 52% of the intergenic space was comprised of the predicted control region, is568 (Figure 1). Furthermore, there were eight examples of overlapping genes, including one remarkable instance in which the trnF gene was found entirely contained within the nad5 open reading frame (Table 1). Four of the eight gene overlaps involve the nad2-nad5 gene block, indicating that this region has experienced a higher rate of compaction than other parts of the mtDNA.
Exceptional mtDNA codon usage
Regions of synteny and unique transpositions among the hexactinellids
The largest block of genes shared between A. vastus and the previously published hexactinellid sponge mtDNAs consisted of atp6-cox3-nad2-nad5-trnF-trnC-nad1-trn(L, I, N, Y)-cob. Aphrocallistes contained trnI, N, and Y between nad1 and cob, while I. panicea had trnL and trnY, and S. nux retained the entire complement trnL, I, N, and Y. This region of synteny spanned 7,127 bp of the A. vastus mtDNA, or 41% of the genome (Figures 1 and 2). Aphrocallistes and I. panicea shared the cox2-rnl gene border, while in S. nux these genes were shuffled to rnl-cox2. With respect to hexactinellids, nad3 has transposed in the A. vastus mtDNA, adjacent to cox1, whereas it is adjacent to tRNAs and nad4L in I. panicea and S. nux. In A. vastus and I. panicea, nad4 and nad6 are adjacent but found in the opposite order. While nad6 has not been found in the sequenced portion of the S. nux mtDNA, the gap in the genome lies upstream of nad4. If nad6 is found in this gap upon completion of the S. nux mtDNA sequence, S. nux would share the nad4-nad6 boundary with A. vastus (Figure 2).
The mtDNA gene segment cox2-atp8-atp6-cox3 is a highly conserved syntenic region found in arthropods, echinoderms, chordates, and other higher animal groups . In the choanoflagellate Monosiga brevicollis the order of these four genes relative to one another is conserved, though the genes are not found as a contiguous block . Placozoan mtDNA does not contain this synteny [12, 17], but it is present in all known demosponges except O. carmela (Figure 2) [13, 15, 16, 19]. The synteny is also found in several described mtDNAs of octocorallians . Demosponges appear to be the most basal animal group to retain this plesiomorphy, as the hexactinellids have lost atp8 and translocated cox2 (Figure 2). All sponge mtDNAs sequenced to date revealed a highly conserved synteny between the nad2-nad5 gene block. Meanwhile, the cox1-tRNA(s)-nad1 region shared among the demosponges, including O. carmela, was not found in any of the hexactinellid mtDNAs (Figure 2). Recall that nad1 was part of the large hexactinellid-specific synteny described above.
Translational frameshifting in cox3 and nad6
One possibility is that the frameshift goes uncorrected and that functional proteins are encoded by nuclear copies of the genes. If this were the case, one would expect these mitochondrial genes to have diverged under relaxed selective pressure. The multiple alignment shows, however, that the amino acid sequences on both sides of the frameshift have retained strong similarity to closely and distantly related homologs (Figure 4). A second possibility is the frameshifts were corrected by RNA editing, as is commonly seen in the mtDNA of plants, fungi, and protists [24–27]. To test this possibility, a randomly primed cDNA pool was screened by PCR with cox3 and nad6 gene specific primers flanking the UGG codon. The amplified cDNA fragments from several independent PCR reactions were sequenced. The results (unpublished data) showed that all cDNA products contained the frameshift, (a) demonstrating that the mitochondrial genes are expressed, and (b) ruling out the possibility of an RNA editing mechanism to restore the cox3 and nad6 reading frames.
Yet another possibility is that the frameshift was corrected by translational frameshifting. A mechanism for +1 programmed translational frameshifting has been described in Saccharomyces cerevisaie [28–31] and reported in disparate bilaterian animal groups [32, 33]. The phenomenon occurs in three steps: first, the ribosomal P site-bound peptidyl-tRNA forms a "weak wobble interaction" with the gene transcript; second, translation halts because the next required tRNA is so rare that its codon is not readily recognized; and lastly, an abundant aminoacyl-tRNA of the +1 codon forces the ribosomal complex to shift frames . This scenario can be readily applied to the A. vastus cox3 and nad6 genes. We hypothesize that translation pauses due to poor recognition of the highly unusual UGG tryptophan codon, allowing an abundant tRNA Gly (GGA) to induce the +1 frameshift. This hypothesis begs many questions. For example: How efficient is the mechanism of frameshift correction? If the frameshift lowers the translation efficiency of the affected genes, why has selection allowed a frameshift to persist? Has this mechanism evolved convergently in each disparate taxa, or is it a shared but rarely employed tool available to any animal whenever a frameshift becomes fixed in the mitochondrial genome?
The few sequenced hexactinellid sponge mtDNAs contain a suite of shared traits, including the loss of the gene atp8, retention of the gene atp9, highly divergent ribosomal RNAs, and reduction of their tRNA complements. Hexactinellid nucleotide composition is distinct from that of demosponges, favoring adenine over thymine and cytosine over guanine on the coding strand. The hexactinellid mtDNAs share a large region of synteny spanning the atp6 to cob genes, but a syntenty putatively ancestral to the Metazoa, cox2-atp8-atp6-cox3, is not retained. Perhaps the most unique feature of hexactinellid mitochondrial genomes is the predicted +1 programmed translational frameshifting initiated by ribosomal pausing at the extremely rare UGG (tryptophan) codon. Future mtDNA sampling will reveal whether this phenomenon is common to yet more glass sponges or the other sponge classes.
Tissue preparation and DNA purification
The hexactinellid sponge Aphrocallistes vastus was collected using the manipulator arm of the remote operated vehicle ROPOS (Remote Operated Platform for Ocean Science; ropos.com) at San Jose Islets, Barkley Sound, Canada, and transferred without removal from seawater to tanks at the Bamfield Marine Sciences Centre. Tissue was cut into small pieces, and dissociated through Nitex mesh into cold seawater and allowed to reaggregate over 2 days to eliminate possible contamination by other taxa and to facilitate DNA preparation. Aggregates were cleaned twice daily with sea water and frozen directly at -80°C. The tissue was thawed and lysed simultaneously in 8 M urea buffer, incubated at 65°C for 20 min, and total DNA was prepared by phenol chloroform extraction and precipitation in isopropanol .
mtDNA PCR amplification, cloning and sequencing
A genome walker library was constructed from A. vastus genomic DNA using the GenomeWalker Kit (BD Biosciences) and restriction enzymes DraI, EcoRV, PvuII, SmaI, and StuI. This library was screened by PCR with universal 16S primers and adapter primers AP1 and nested AP2 to amplify a fragment of rnl. The initial contig was generated with primer P1313 (caattcaacatcgaggtcgcaaaca) and AP1(gtaatacgactcactatagggc). Genome-walking was continued until a 12 kb contig had been partially sequenced. Long-range primers designed against the ends of this contig were successful in amplifying the entire contig using TAKARA LA-Taq. This product was purified using the QiaQuick Gel Extraction kit (Qiagen), sheared by sonication, and end-repaired with the DNA Terminator kit (Lucigen). Two to four kilobase fragments were size-selected by gel electrophoresis, blunt-end cloned into the pSmart LC-Kan vector (Lucigen), and transformed into E. cloni Supreme cells (Lucigen) by electroporation. Colonies were screened by PCR for the presence of inserts using flanking vector primers SL1 and SR2 (Lucigen). Forty-eight PCR products were purified by poly-ethylene glycol-NaCl (PEG:NaCl)  and sequenced by BigDye® Terminator v3.1 cycle sequencing on ABI PRISM® 3700 DNA Analyzers (Applied Biosystems, Inc.) at the W.M. Keck facility at Yale University, New Haven, CT. Outward facing primers from the 12-kb contig were designed, and a 5.5 kb fragment was amplified also using TAKARA LA-Taq following manufacturers instructions. This product was gel-purified with the Qiagen kit, ligated into the PCR 2.1 Topo vector (Invitrogen) and transformed into Top10 cells. Four clones were recovered, grown overnight in LB and mini-prepped using Qiagen Qiaquick columns. All four clones were sequenced by primer walking.
Sequence assembly and annotation
Sequences were assembled from chromatography data using the Phred Phrap Consed software package, release 15.0 [36, 37]. Regions of lower quality data were sequenced by direct PCR on genomic DNA, or additional sequencing of select gap spanning clones. The complete contig had a minimum of 2× coverage with high phred values (40 or greater) at each position. The suite of tRNA genes were identified by tRNAscan-SE  using the program's default parameters for organellar DNA and the Mold and Protozoan mitochondrial translation code. BLASTN searches querying all published sponge mtDNA tRNAs against the A. vastus genome did not identify any additional tRNAs, nor did manual searching for missing anticodon-loop motifs. Protein-coding and ribosomal RNA genes were initially identified using the program DOGMA , and then aligned by Blast2  and ClustalW  with the mtDNA genes annotated in GenBank.
RNA extraction and cDNA preparation
One ml of frozen cell aggregate was pulverized under liquid nitrogen. Total RNA was extracted from half of the resulting ground tissue using the Illustra RNAspin Mini kit (GE Healthcare). The total RNA was treated with Dnase I for 1 hour, then cleaned by phenol chloroform extraction, precipitated in cold 100% ethanol, and resuspended in DEPC-dH2O with 1 μl RNase Inhibitor (Roche). 5 μg of RNA was reverse transcribed with Invitrogen SuperscriptII reverse transcriptase and random oligos, and the resulting cDNA treated with RNase H. As a control for subsequent PCRs, a sample of RNA was processed in parallel, receiving identical treatment except without reverse transcriptase enzyme ("no-RT control"). The cDNA and no-RT control were used as PCR templates with primers pairs P2775 (agcagaacaaagaccatgacc) and P2964 (tggaatcctgtggctacaaagaaag) for cox3 and P3182 (aacatcttcaagaagaacaatcaatagag) and P2962 (catggttattatggtgcgttggatt) for nad6, using Qiagen PCR reagents and manufacturer's instructions. PCR products, amplified from the cDNA template alone, were cleaned with the QiaQuick PCR Purification kit (Qiagen) and sequenced directly using the above primers.
List of Abbreviations
- (atp6, 8, 9):
ATP synthase F0 subunit #
cytochrome c oxidase #
- (nad1-6, 4L):
NADH dehydrogenase subunit #
small ribosomal RNA
large ribosomal RNA
open reading frame
We would like to thank Leo W. Buss, Derek E.G. Briggs and Kevin J. Peterson for helpful discussion, Elizabeth Kennard for technical assistance in the lab, and two anonymous reviewers for their insightful comments. This material is based upon work supported under a National Science Foundation Graduate Research Fellowship (R.D.R), and grants from the National Science Foundation GEN-EN program (S.L.D.), the Society of Systematic Biologists (E.A.S.) and the NSERC (S.P.L.). Computational assistance was provided by the Yale HPC Center, supported by Grant Number RR19895 from the National Center for Research Resources (NCRR), a component of the National Institutes of Health (NIH).
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