- Research article
- Open Access
The complete mitochondrial genome sequence of the hydrothermal vent galatheid crab Shinkaia crosnieri (Crustacea: Decapoda: Anomura): A novel arrangement and incomplete tRNA suite
BMC Genomics volume 9, Article number: 257 (2008)
- The Erratum to this article has been published in BMC Genomics 2008 9:504
Metazoan mitochondrial genomes usually consist of the same 37 genes. Such genes contain useful information for phylogenetic analyses and evolution modelling. Although complete mitochondrial genomes have been determined for over 1,000 animals to date, hydrothermal vent species have, thus far, remained excluded due to the scarcity of collected specimens.
The mitochondrial genome of the hydrothermal vent galatheid crab Shinkaia crosnieri is 15,182 bp in length, and is composed of 13 protein-coding genes, two ribosomal RNA genes and only 18 transfer RNA genes. The total AT content of the genome, as is typical for decapods, is 72.9%. We identified a non-coding control region of 327 bp according to its location and AT-richness. This is the smallest control region discovered in crustaceans so far. A mechanism of cytoplasmic tRNA import was addressed to compensate for the four missing tRNAs. The S. crosnieri mitogenome exhibits a novel arrangement of mitochondrial genes. We investigated the mitochondrial gene orders and found that at least six rearrangements from the ancestral pancrustacean (crustacean + hexapod) pattern have happened successively. The codon usage, nucleotide composition and bias show no substantial difference with other decapods. Phylogenetic analyses using the concatenated nucleotide and amino acid sequences of the 13 protein-coding genes prove consistent with the previous classification based upon their morphology.
The present study will supply considerable data of use for both genomic and evolutionary research on hydrothermal vent ecosystems. The mitochondrial genetic characteristics of decapods are sustained in this case of S. crosnieri despite the absence of several tRNAs and a number of dramatic rearrangements. Our results may provide evidence for the immigrating hypothesis about how vent species originate.
Since intraorganellar DNA characteristics were found in chick embryo mitochondria [1, 2], determination of mitochondrial genomes (mitogenomes) has become an important part of genome research. In 1981, Anderson et al reported the complete sequence of the human mitogenome . This was the first identified organellar genome. Until recently, 1,212 metazoan mitogenomes have now been determined (NCBI Organelle Genome Resource ). With a few exceptions [5–9], animal mitogenomes always consist of the same 37 genes which incorporate 13 subunits of proteins involved in the respiratory chain and oxidative phosphorylation, two ribosomal RNAs (rRNAs), and 22 transfer RNAs (tRNAs) (reviewed in ). These sequences can provide large datasets for phylogenetic analyses at different levels also serving as ideal models of gene rearrangement and genome evolution.
152 arthropod mitogenomes have been determined since Clary and Wolstenholme sequenced that of Drosophila yakuba in 1985 . Within the subphylum Crustacea, only 36 mitogenomes have been determined: one for each of the classes Cephalocarida, Ostracoda, Pentastomida and Remipedia, four for the Branchiopoda, eight for the Maxillopoda and 20 for the Malacostraca (including 14 decapods, see Table 1). Within the order Decapoda, the sampling is imbalanced: four for the suborder Dendrobranchiata and ten for the Pleocyemata (five for the infraorder Brachyura, two for the Caridea, and one for each of the Anomura, Astacidea and Palinura). Most decapod mitogenomes share the ancestral pancrustacean (crustacean + hexapod) gene order that shows only a trnL-UUR translocation from the ancestral arthropod arrangement depicted by the horseshoe crab Limulus polyphemus , or present only minor tRNA translocations. So far the anomuran mitogenome of the hermit crab Pagurus longicarpus has been determined to show dramatic gene rearrangements, including that of several large fragments .
Hydrothermal vents were first discovered along the Galápagos Rift in 1977 . Up to the present, their presence has been noted at mid-ocean spreading centers in the east Pacific, Atlantic, Arctic and Indian Oceans, and in the back-arc basins in the west Pacific (reviewed in ). These vent environments are considered as extreme given the high pressure, the high temperature (up to 390°C), the chemical toxicity of the fluids (H2S, CH4 and various heavy metals), and the total lack of photosynthetic production of animal nutrition. Nevertheless, with the exception of chemoautotrophic bacteria that oxidize hydrogen sulfide emitted from vents, surprisingly a number of specialized large faunas were also observed in these vents. Many invertebrates (e.g. vestimentiferan tube worms, vesicomyid and bathymodiolin bivalves, provannid gastropods, bythograeid and galatheid crabs, and bresiliid shrimps) often thrive with dramatically high densities, by utilizing (epi- or endo-)symbiotic chemoautotrophic bacteria or grazing on or filter feeding upon free-living chemoautotrophs . There are two main hypotheses about how vent faunas originate. The relic hypothesis derives principally from morphological analyses of extant vent taxa [16, 17], which considers the hydrothermal vent as a refugium for relic faunas during major historical extinction events. However, molecular studies of several vent-dominant taxa suggest that modern vent animals arose relatively recently . An immigrating hypothesis seems more reasonable, which speculates that vent species may immigrate either from the non-vent environments or with close shallow-water relatives (reviewed in ).
Thanks to the effective Crustacea-specific versatile primers [19, 20], mitochondrial DNA fragments can be used for studying the occurrence and dispersal of these vent species [21, 22]. However, no entire mitogenome data has been available for any vent species to date. Baba and Williams first identified Shinkaia crosnieri at the Bismarck Archipelago and in the Okinawa Trough in the west Pacific Ocean . The discoverers placed it into Decapoda: Anomura: Galatheidae according to its morphological features. Chan et al also mentioned this species as the first known hydrothermal crustacean in Taiwan . Gathering near the top of the vents, S. crosnieri probably feed on polychaetes and "culture" filamentous bacteria on their abdominal surface . No genetic data has been characterized for this species so far.
Here, we report the complete nucleotide sequence of the S. crosnieri mitogenome. It consists of the same 13 protein-coding genes, two rRNAs but only 18 tRNAs, with trnS-UCN, trnW, trnC and trnY missing from the usual structure. A mechanism of nuclear DNA-encoded tRNA import was addressed. Furthermore, the genes show surprising rearrangements from the ancestral pancrustacean order. Phylogenetic analyses indicate its close relationship with P. longicapus. No significant difference was found in the codon usage, nucleotide composition and bias. Our results may provide useful information on both genomics and the evolution of hydrothermal vent faunas.
Results and Discussion
The mitochondrial genome of the hydrothermal vent galatheid crab Shinkaia crosnieri is a 15,182-bp circular molecule (Figure 1). It is the smallest mitogenome found in the Malacostraca (15,289  to 18,197 ) to date. The genome contains the same 13 protein-coding genes and two ribosomal RNAs as in most metazoans. However, it exhibits incomplete transfer RNA encoding (18 instead of the usual 22, see below). 22 mitochondrial genes are transcribed from one strand (the plus strand) and the remaining 11 from the other (the minus strand). Totally 740 non-coding nucleotides exist intergenically, with the largest continuous region (327 bp, AT% = 83.5) between trnQ and rrnS. Due to its location and AT-richness, we considered this part of the genome as a non-coding control region in the similar manner as in the case of the Australian freshwater crayfish Cherax destructor . However, the control region is considerably smaller than those of any other decapods (Table 1) and shows no similarities with any previous decapod control region (data not shown). In the case of Pagurus longicarpus , approximately 300 bp of the control region remain unsequenced due to technical difficulties. Furthermore, as found in many mitogenomes, some genes overlap. atp8/atp6 and nad4L/nad4 each share seven nucleotides, although they are located on different reading frames. No further overlap of over two nucleotides was identified. Table 2 shows a summary of the S. crosnieri mitogenome organization.
Protein-coding genes and ribosomal RNAs
For the protein-coding genes, nine (atp8, atp6, cob, cox1—3, nad2—3 and nad6) are encoded in the plus strand while the remaining four (nad1, nad4–5 and nad4L) in the minus strand (Figure 1; Table 2). This orientation is shared by all decapod mitogenomes sequenced to date. 12 out of the 13 protein-coding genes appear to start with the codon ATN (Table 2), typical for metazoan mitogenomes . The cox1 initiates with GTT, in a case identical to Neocalanus cristatus . Eight genes possess TAA as their termination codons (Table 2). Truncated termination codons (TA or T) are observed in cox1—2, nad4—5 and cob. Post-transcriptional polyadenylation can subsequently generate mature TAA codons .
The rrnL and rrnS genes of S. crosnieri are 1,331 (AT% = 77.8) and 811 bp (AT% = 78.1) in length, respectively. The lengths are among values typical for crustaceans whereas the AT contents are slightly higher than those of other decapod counterparts (Table 1).
We analyzed the entire sequences of the genome and successfully identified 18 tRNA genes by their potential secondary structures (Figure 2). tRNAscan-SE determined 17 of them. The only manually folded trnS-AGN exhibits three mismatches on the acceptor stem while its DHU, TΨC and anticodon stems appear intact and well paired. The TΨC arm of trnS-AGN is often extremely short or completely missing in arthropods [32–35]. Besides trnS-AGN, each of trnI, trnK and trnL-CUN bears a mismatch on the acceptor stem. Usually tRNAs with a U in the wobble position (the first position) of the anticodons recognize either four-fold degenerate or NNR codons; those with a G in this position only recognize NNY codons. All tRNAs of S. crosnieri mitogenome obey this rule except for trnM, whose anticodon CAU recognizes both ATG and ATA. The C can be post-transcriptionally modified to 5-formylcytidine to pair with the ATA codon .
trnS-UCN, trnW, trnC and trnY are missing from the S. crosnieri mitogenome. We analyzed all fractions between protein-coding or ribosomal RNA genes [see Additional file 1], but no extra tRNAs or similar sequences were identified in the genome. This is not an exception in arthropods considering the absence of trnQ in the mitogenome of the whitefly Aleurodicus dugesii, trnS-AGN in the aphid Schizaphis graminum , and trnD in the scorpion Centruroides limpidus . Deficiencies of tRNA genes were often observed in protozoans, fungi, algae, plants and low metazoans (reviewed in ). In these cases, the mechanism of nuclear DNA-encoded tRNA import proves responsible for mitochondrial tRNA compensation. Furthermore, marsupial mitochondrial tRNAs show interesting patterns. Janke and Paabo identified a pseudogene-like trnD in Didelphis virginiana, as its anticodon is GCC instead of the usual GUC . They found that the cytosine is changed to uridine under a post-transcriptional RNA editing. Dorner et al discovered a trnK pseudogene in the same marsupial species by observing its non-functional secondary structure . Cytoplasmic tRNA import rather than RNA editing solves this problem. In our study, there seems no candidate template for RNA editing. The mechanism of tRNA import is therefore a plausible explanation.
Nucleotide composition and codon usage
The nucleotide composition of S. crosnieri mitogenome is as follows: A = 5,452 (35.9%), G = 1,415 (9.3%), T = 5,612 (37.0%) and C = 2,703 (17.8%). The genome has an overall AT content of 72.9%, which appears high for decapods (62.3–74.9%), but is a little lower than that of Geothelphusa dehaani . The composition is strongly skewed away from G in favor of C (the GC-skew is -0.313) while almost balanced for A and T (the AT-skew is -0.014). This feature is well conserved within decapods (Table 1). In mammals, the duration of single-stranded state of the "heavy-stranded" genes during mitochondrial DNA replication can explain this asymmetry . Whether or not the same explanation works on our results remains difficult to predict at this time due to the scarcity of information regarding DNA replication of invertebrate mitochondria.
The S. crosnieri mitogenome totally encodes 3,698 amino acids of protein-coding genes. Table 3 shows the codon usage. Although four tRNAs are absent, the corresponding codons 235 TCNs, 95 TGRs, 42 TGYs and 146 TAYs (for trnS-UCN, trnW, trnC and trnY, respectively) are used quite frequently (14% of total codons), evidently raising the need for tRNA compensation. We observed a strong AT-bias (AT% = 82.3) in the third codon positions, similar to those in the Anomura relative P. longicarpus, the Brachyura and the suborder Dendrobranchiata (73.9–84.0%). The values in the Caridea, Palinura and Astacidea are relatively lower (59.6–66.8%).
The S. crosnieri mitogenome shows a novel arrangement within arthropods. The gene order diverges in many positions from that of the ancestral pancrustacean pattern shared by lots of crustaceans and hexapods . Totally, we identified at least six rearrangements in this species (Figure 3). Two rearrangements involve protein-coding genes while the remainders are tRNA translocations. A major fragment containing nad1, trnL-CUN, rrnL, trnV, rrnS, control region and trnQ moves to upstream of nad3 from its ancestral position; trnI may translocate before or after this event. The fraction trnM-nad2 moves to upstream of trnD. This event, together with the trnG translocations, indicates potential synapomorphic characters for the Anomura. The location of trnR-trnN changes to downstream of cox3. The trnP moves to downstream of nad1. P. longicarpus  and Eriocheir sinesis  share this rearrangement. Finally, the trnI moves to the middle of nad3 and trnA. This translocation is novel within crustaceans. Rearrangements of trnI were observed in Speleonectes tulumensis  and Tigriopus japonicus , where trnI is translocated to different positions in both species. Morrison et al inferred parsimonious rearrangements of the crab-like form . They pointed out that the Galatheoidea diverged after the translocations of trnQ and trnI-trnM-nad2. Our results support their hypothesis.
We also analyzed data gathered thus far on rearrangements of both decapod (Figure 4) and all pancrustacean mitogenomes (Figure 5). For simplicity of analysis, all tRNAs and control regions (CRs) were excluded in the case of the pancrustaceans. The E. sinensis mitogenome shows the maximum 7 block interchanges within the Decapoda, and Shinkaia crosnieri exhibits 6 interchanges from the ancestral pancrustacean arrangement on its mitogenome (Figure 4). The ancestral pancrustacean pattern depicted by four dendrobranchiatans, two carideans and one palinuran, has only a trnL-UUR translocation from the ancestral arthropod order of Limulus polyphemus . In the analyses of large block (protein-coding genes plus rRNAs) rearrangements of all pancrustaceans, the class Maxillopoda shows maximum inversions (3–7) within crustaceans. In the case of the Hexapoda (81 mitogenomes determined to date), all large block rearrangements have happened within the class Insecta (Figure 5), where more rearrangements (both translocations and inversions) were observed within the orders Phthiraptera and Thysanoptera.
We used both nucleotide and amino acid sequences of protein-coding genes for the intraorder phylogenetic analyses. For each dataset, the maximum likelihood (ML) and Bayesian analysis gave the same tree topology (Figure 6) while the maximum parsimony (MP) analysis of the nucleotides showed a minor difference (Figure 6A). The nucleotide and amino acid trees are nearly the same except for the position of the Caridea clade (Halocaridina rubra + Macrobrachium rosenbergii) and the inner structure of the Dendrobranchiata clade. In the case of the nucleotides, the clade is placed together with other pleocyematans (Figure 6A), but not well supported (MP/ML/BPP = <50/60/0.59). However, in the amino acid tree, the Caridea shows a sister position of the Dendrobranchiata (Figure 6B), which also remains modestly statistically supported (MP/ML/BPP = 61/70/0.80). Therefore, according to our results, whether the Pleocyemata is monophyletic or paraphyletic appears ambiguous. The Dendrobranchiata clade was well reconstructed in the ML and Bayesian analyses of the nucleotide dataset (Figure 6A) but unresolved in the case of the MP analysis of the nucleotides and in all three analyses of the amino acids (Figure 6). The relationship (Marsupenaeus + (Litopenaeus + (Fenneropenaeus + Penaeus))) is more believable, as discussed in . In both trees, the two anomurans (S. crosnieri and P. longicarpus) form a separate clade, according with the relationship derived from the morphology . Whether or not the Anomura is monophyletic needs intensive sampling. In fact, phylogenetic relationships within this infraorder remain largely unsettled (reviewed in ). Furthermore, no unexpectedly long or short branch length of S. crosnieri was observed (Figure 6), indicating that the evolutionary acceleration/retardation is probably not evident for this vent species. Accurate calculation on evolutionary rates needs fossil records that remain absent for these vent taxa .
This is the first determination of the mitochondrial genome of a hydrothermal vent organism. It not only enlarges sampling with the Crustcean, but more importantly, provides useful information for understanding the evolutionary history of vent species.
The mitogenome of Shinkaia crosnieri exhibits almost the same characteristics with those of other metazoans with the exception of two differences. Firstly, four transfer RNAs are missing from the mitogenome. The codons recognized by these four tRNAs are frequently used (14%) for protein encoding. We proposed a mechanism of nuclear DNA-encoded tRNA import for this compensation. Secondly, the arrangement of the gene contents is significantly different from those of other pancrustacen mitogenomes. The changes are complicated and at least six rearrangements were observed. Some of them are shared by other crustaceans. However a novel trnI translocation was identified.
The codon usage, nucleotide composition and bias of S. crosnieri mitogenome are similar with other decapods. Phylogenetic analysis shows a close relationship with another anomuran Pagurus longicarpus, supporting for the taxonomic classification by the morphology . No trend of evolutionary acceleration or retardation was observed. An exterior origin may explain these conserved features found in S. crosnieri. In fact, one galatheid, Munidopsis subsquamosa, seems to be a non-vent species which can invade vent habitats for at least short periods of time . Our results may provide some evidence for the immigrating hypothesis about how hydrothermal vent species originate.
Samples and DNA preparation
One specimen of Shinkaia crosnieri was a generous gift from the Japan Agency for Marine-Earth Science and Technology (JAMSTEC). Sampling was done using manipulators and a slurp gun with single or six canisters set on the ROV Hype-dophin of JAMSTEC on Apr 24, 2005. The hydrothermal vent galatheid crab was collected at the Jade Site of the Izena Hole (27°16.307' N, 127°4.884' E, 1,309 m) in the Okinawa Trough.
150 mg of muscle was dissected in 1.2 ml of extraction buffer (60 mM Tris-HCl [pH 8.0], 100 mM EDTA and 0.5% SDS). Proteinase K was added to a final concentration of 500 μg/ml. Samples were digested thoroughly at 55°C. DNA was precipitated from the supernatant by the phenol/chloroform method  and dissolved in TE buffer (10 mM Tris-HCl [pH 7.4] and 1 mM EDTA).
Partial genic fragments of the genes cytochrome oxidase subunit 1 (cox1), large ribosomal RNA (rrnL) and NADH dehydrogenase subunit 5 (nad5) were amplified using the primers LCO1490/HCO2198 , 16Sar/16Sbr , and DEnad5F/DEnad5R, respectively [see Additional file 2]. The reactions were carried out with 1.25 units of Taq DNA polymerase (Promega, Madison, USA) and 125 ng of genomic DNA as templates, according to the manufacturer's instructions. The amplified fragments were cloned into pUCm-T vectors (Sangon, Shanghai, China) that were sequenced using the versatile primers M13F/R. After determination, the partial sequences were used for designing gene-specific primers. To facilitate the subsequent long PCR , we chose candidates with high melting temperatures. Long PCRs were performed with 1.25 units of LA Taq DNA polymerase (TaKaRa, Shiga, Japan) following the manufacturer's commendations. For each long fragment, we used nested primer pairs [see Additional file 2] and a two-step cycle (denaturation and annealing/extension). Considering the lack of available genome arrangement data for this species, all primer combinations were attempted. The long fragments were bidirectionally sequenced using a primer-walking strategy. All amplifications were done on a TGradient thermocycler (Whatman-Biometra, Goettingen, Germany). All sequencing was performed with ABI PRISM Big Dye terminator chemistry and analyzed on ABI 3730 automated sequencers (Applied Biosystems, Foster City, USA).
Gene annotation and sequence analysis
All sequences were edited using EditSeq version 5.00 (DNAStar, Madison, USA) and Vector NTI version 9.0.0 (InforMax, Frederick, USA). Protein-coding and ribosomal RNA genes were identified by aligning with other decapod mitochondrial genomes (Table 1). Borders of rRNA genes were determined by adjacent genes. Transfer RNAs were initially detected by tRNAscan-SE version 1.21  while the rest were identified by their potential secondary structures and anticodons. A circular display of S. crosnieri mitochondrial genome was depicted by OGDRAW version 1.1  and modified manually. All annotation information was imported to Sequin version 7.90 (NCBI) in which generated a standard output of submitted data [see Additional file 3]. The nucleotide sequences are deposited in GenBank/EMBL/DDBJ under the accession number EU420129. Codon usage and nucleotide composition were analyzed with MEGA 4 . Strand skew values were calculated according to the formulae by Perna and Kocher .
Block interchanges are defined as the minimum rearrangements from one genome to another. We used the ROBIN website  for calculating block interchanges of each mitogenome deviated from the ancestral pancrustacean (crustacean + decapod) arrangement. For decapod mitogenomes, we used all 37 genes plus the control region (CR). Considering the complication and inconstancy of their translocations, tRNAs and CR were omitted from the calculation on all pancrustacean rearrangements. Inversions were directly identified by gene orientations.
For phylogenetic analysis, we chose the 14 other decapod mitochondrial genomes determined to date (Table 1). The five stomatopods Gonodactylus chiragra [GenBank:NC_007442], Harpiosquilla harpax [NC_006916], Lysiosquilla harpax [NC_007443], Squilla empusa [NC_007444] and Squilla mantis [NC_006081] served as outgroups. Both nucleotides and amino acids of 13 protein-coding genes were subjected to concatenated alignments using ClustalX version 1.81 , with the opening/extension gap penalties 15/6.66 and 10/0.2, respectively. For the nucleotides, we omitted the third position of the codons before the alignment, according to the result of a saturation analysis  by DAMBE version 4.5.57 . Ambiguously aligned proportions of both alignments were excluded using Gblocks version 0.91b  with default block parameters. The final nucleotide and amino acid datasets consisted of 7,027 nt and 3,340 aa, respectively.
For the nucleotide dataset MODELTEST version 3.7  selected the model GTR+G+I for both the likelihood and Bayesian analyses. ProtTest version 1.4  chose the model MtArt+G+I for the amino acid dataset. Both selections were done following the Akaike information criterion (AIC) . As MtArt is so recent a model for the arthropod evolution , we could not implement it in the Bayesian analysis for the amino acids, where we used the best scoring alternative MtRev+G+I.
Maximum parsimony (MP) analyses with both datasets were done using a close-neighbor-interchange (CNI) with search level 1 method implemented in MEGA 4 , with 1,000 bootstrap replicates.
We performed maximum likelihood (ML) analyses of both nucleotide and amino acid alignments using TREEFINDER version of Mar, 2008  under the models GTR+G+I and MtArt+G+I, respectively. The alpha shape parameters were estimated from the datasets. The analyses started from BioNJ trees. Branch statistical supports were obtained after 100 bootstrap replicates each.
Bayesian analyses of both nucleotide and amino acid alignments were carried out using MRBAYES version 3.1.2 , under the models GTR+G+I and MtRev+G+I (see above), respectively. The Markov Chain Monte Carlo analyses were performed for 1,000,000 generations in two runs of eight chains each. The Bayesian posterior probability (BPP) of each tree partition was estimated by sampling the trees every 1,000 generations after discarding the first 10%.
- Mitochondrial genes: atp6 and atp8:
ATP synthase subunits 6 and 8
- cob :
- cox1–3 :
cytochrome c oxidase subunits 1–3
- nad1–6 and nad4L:
NADH dehydrogenase subunits 1–6 and 4L
- rrnS and rrnL:
small and large subunit ribosomal RNA (rRNA) genes
- trnX transfer RNA (tRNA) genes:
where X :is the one-letter abbreviation of the corresponding amino acid
putative control region
Bayesian posterior probability
Nass MM, Nass S: Intramitochondrial fibers with DNA characteristics. I. Fixation and electron staining reactions. J Cell Biol. 1963, 19 (3): 593-611. 10.1083/jcb.19.3.593.
Nass S, Nass MM: Intramitochondrial fibers with DNA characteristics. II. Enzymatic and other hydrolytic treatments. J Cell Biol. 1963, 19 (3): 613-629. 10.1083/jcb.19.3.613.
Anderson S, Bankier AT, Barrell BG, de Bruijn MH, Coulson AR, Drouin J, Eperon IC, Nierlich DP, Roe BA, Sanger F, Schreier PH, Smith AJ, Staden R, Young IG: Sequence and organization of the human mitochondrial genome. Nature. 1981, 290 (5806): 457-465. 10.1038/290457a0.
Wolfsberg TG, Schafer S, Tatusov RL, Tatusov TA: Organelle genome resource at NCBI. Trends Biochem Sci. 2001, 26 (3): 199-203. 10.1016/S0968-0004(00)01773-4.
Beagley CT, Okimoto R, Wolstenholme DR: The mitochondrial genome of the sea anemone Metridium senile (Cnidaria): introns, a paucity of tRNA genes, and a near-standard genetic code. Genetics. 1998, 148 (3): 1091-1108.
Helfenbein KG, Fourcade HM, Vanjani RG, Boore JL: The mitochondrial genome of Paraspadella gotoi is highly reduced and reveals that chaetognaths are a sister group to protostomes. Proc Natl Acad Sci U S A. 2004, 101 (29): 10639-10643. 10.1073/pnas.0400941101.
Davila S, Pinero D, Bustos P, Cevallos MA, Davila G: The mitochondrial genome sequence of the scorpion Centruroides limpidus (Karsch 1879) (Chelicerata; Arachnida). Gene. 2005, 360 (2): 92-102. 10.1016/j.gene.2005.06.008.
Papetti C, Lio P, Ruber L, Patarnello T, Zardoya R: Antarctic fish mitochondrial genomes lack ND6 gene. J Mol Evol. 2007, 65 (5): 519-528. 10.1007/s00239-007-9030-z.
Jeyaprakash A, Hoy MA: The mitochondrial genome of the predatory mite Metaseiulus occidentalis (Arthropoda: Chelicerata: Acari: Phytoseiidae) is unexpectedly large and contains several novel features. Gene. 2007, 391 (1-2): 264-274. 10.1016/j.gene.2007.01.012.
Boore JL: Animal mitochondrial genomes. Nucleic Acids Res. 1999, 27 (8): 1767-1780. 10.1093/nar/27.8.1767.
Clary DO, Wolstenholme DR: The mitochondrial DNA molecular of Drosophila yakuba: nucleotide sequence, gene organization, and genetic code. J Mol Evol. 1985, 22 (3): 252-271. 10.1007/BF02099755.
Lavrov DV, Boore JL, Brown WM: The complete mitochondrial DNA sequence of the horseshoe crab Limulus polyphemus. Mol Biol Evol. 2000, 17 (5): 813-824.
Hickerson MJ, Cunningham CW: Dramatic mitochondrial gene rearrangements in the hermit crab Pagurus longicarpus (Crustacea, anomura). Mol Biol Evol. 2000, 17 (4): 639-644.
Lonsdale P: Clustering of suspension-feeding macrobentos near hydrothermal vents at oceanic spreading centers. Deep-Sea Res. 1977, 24 (9): 857-863. 10.1016/0146-6291(77)90478-7.
Van Dover CL: The Ecology of Deep-Sea Hydrothermal Vents. 2000, Princeton University Press
McLean JH: Preliminary report on the limpets at hydrothermal vents. Biol Soc Wash Bull. 1985, 6: 159-166.
Newman WA: The abyssal hydrothermal vent invertebrate fauna. A glimpse of antiquity?. Biol Soc Wash Bull. 1985, 6: 231-242.
Van Dover CL: Evolution and biogeography of deep-sea vent and seep invertebrates. Science. 2002, 295 (5558): 1253-1257. 10.1126/science.1067361.
Folmer O, Black M, Hoeh W, Lutz R, Vrijenhoek R: DNA primers for amplification of mitochondrial cytochrome c oxidase subunit I from diverse metazoan invertebrates. Mol Mar Biol Biotechnol. 1994, 3 (5): 294-299.
Palumbi SR, Benzie J: Large mitochondrial DNA differences between morphologically similar Penaeid shrimp. Mol Mar Biol Biotechnol. 1991, 1 (1): 27-34.
Shank TM, Black MB, Halanych KM, Lutz RA, Vrijenhoek RC: Miocene radiation of deep-sea hydrothermal vent shrimp (Caridea: Bresiliidae): evidence from mitochondrial cytochrome oxidase subunit I. Mol Phylogenet Evol. 1999, 13 (2): 244-254. 10.1006/mpev.1999.0642.
Tokuda G, Yamada A, Nakano K, Arita N, Yamasaki H: Occurrence and recent long-distance dispersal of deep-sea hydrothermal vent shrimps. Biol Lett. 2006, 2 (2): 257-260. 10.1098/rsbl.2005.0420.
Baba K, Williams AB: New Galatheoidea (Crustacea, Decapoda, Anomura) from hydrothermal systems in the west Pacific Ocean: Bismarck Archipelago and Okinawa Trough. Zoosystema. 1998, 20 (2): 143-156.
Chan TY, Lee DA, Lee CS: The first deep-sea hydrothermal animal reported from Taiwan: Shinkaia crosnieri Baba and Williams, 1998 (Crustacea: Decapoda: Galatheidae). Bull Mar Sci. 2000, 67 (2): 799-804.
Ohta S, Kim D: Submersible observations of the hydrothermal vent communities on the Iheya Ridge, Mid Okinawa Trough, Japan. J Oceanogr. 2001, 57: 663-677. 10.1023/A:1021620023610.
Kilpert F, Podsiadlowski L: The complete mitochondrial genome of the common sea slater, Ligia oceanica (Crustacea, Isopoda) bears a novel gene order and unusual control region features. BMC Genomics. 2006, 7: 241-10.1186/1471-2164-7-241.
Segawa RD, Aotsuka T: The mitochondrial genome of the Japanese freshwater crab, Geothelphusa dehaani (Crustacea: Brachyura): evidence for its evolution via gene duplication. Gene. 2005, 355: 28-39. 10.1016/j.gene.2005.05.020.
Miller AD, Nguyen TT, Burridge CP, Austin CM: Complete mitochondrial DNA sequence of the Australian freshwater crayfish, Cherax destructor (Crustacea: Decapoda: Parastacidae): a novel gene order revealed. Gene. 2004, 331: 65-72. 10.1016/j.gene.2004.01.022.
Wolstenholme DR: Animal mitochondrial DNA: structure and evolution. Int Rev Cytol. 1992, 141: 173-216.
Machida RJ, Miya MU, Nishida M, Nishida S: Large-scale gene rearrangements in the mitochondrial genomes of two calanoid copepods Eucalanus bungii and Neocalanus cristatus (Crustacea), with notes on new versatile primers for the srRNA and COI genes. Gene. 2004, 332: 71-78. 10.1016/j.gene.2004.01.019.
Ojala D, Montoya J, Attardi G: tRNA punctuation model of RNA processing in human mitochondria. Nature. 1981, 290 (5806): 470-474. 10.1038/290470a0.
Lavrov DV, Brown WM, Boore JL: A novel type of RNA editing occurs in the mitochondrial tRNAs of the centipede Lithobius forficatus. Proc Natl Acad Sci U S A. 2000, 97 (25): 13738-13742. 10.1073/pnas.250402997.
Shao R, Campbell NJ, Barker SC: Numerous gene rearrangements in the mitochondrial genome of the wallaby louse, Heterodoxus macropus (Phthiraptera). Mol Biol Evol. 2001, 18 (5): 858-865.
Masta SE, Boore JL: The complete mitochondrial genome sequence of the spider Habronattus oregonensis reveals rearranged and extremely truncated tRNAs. Mol Biol Evol. 2004, 21 (5): 893-902. 10.1093/molbev/msh096.
Tjensvoll K, Hodneland K, Nilsen F, Nylund A: Genetic characterization of the mitochondrial DNA from Lepeophtheirus salmonis (Crustacea; Copepoda). A new gene organization revealed. Gene. 2005, 353 (2): 218-230. 10.1016/j.gene.2005.04.033.
Tomita K, Ueda T, Ishiwa S, Crain PF, McCloskey JA, Watanabe K: Codon reading patterns in Drosophila melanogaster mitochondria based on their tRNA sequences: a unique wobble rule in animal mitochondria. Nucleic Acids Res. 1999, 27 (21): 4291-4297. 10.1093/nar/27.21.4291.
Thao ML, Baumann L, Baumann P: Organization of the mitochondrial genomes of whiteflies, aphids, and psyllids (Hemiptera, Sternorrhyncha). BMC Evol Biol. 2004, 4: 25-10.1186/1471-2148-4-25.
Schneider A, Marechal-Drouard L: Mitochondrial tRNA import: are there distinct mechanisms?. Trends Cell Biol. 2000, 10 (12): 509-513. 10.1016/S0962-8924(00)01854-7.
Janke A, Paabo S: Editing of a tRNA anticodon in marsupial mitochondria changes its codon recognition. Nucleic Acids Res. 1993, 21 (7): 1523-1525. 10.1093/nar/21.7.1523.
Dorner M, Altmann M, Paabo S, Morl M: Evidence for import of a lysyl-tRNA into marsupial mitochondria. Mol Biol Cell. 2001, 12 (9): 2688-2698.
Reyes A, Gissi C, Pesole G, Saccone C: Asymmetrical directional mutation pressure in the mitochondrial genome of mammals. Mol Biol Evol. 1998, 15 (8): 957-966.
Boore JL, Lavrov DV, Brown WM: Gene translocation links insects and crustaceans. Nature. 1998, 392 (6677): 667-668. 10.1038/33577.
Sun H, Zhou K, Song D: Mitochondrial genome of the Chinese mitten crab Eriocheir japonica sinenesis (Brachyura: Thoracotremata: Grapsoidea) reveals a novel gene order and two target regions of gene rearrangements. Gene. 2005, 349: 207-217. 10.1016/j.gene.2004.12.036.
Lavrov DV, Brown WM, Boore JL: Phylogenetic position of the Pentastomida and (pan)crustacean relationships. Proc Biol Sci. 2004, 271 (1538): 537-544. 10.1098/rspb.2003.2631.
Machida RJ, Miya MU, Nishida M, Nishida S: Complete mitochondrial DNA sequence of Tigriopus japonicus (Crustacea: Copepoda). Mar Biotechnol (NY). 2002, 4 (4): 406-417. 10.1007/s10126-002-0033-x.
Morrison CL, Harvey AW, Lavery S, Tieu K, Huang Y, Cunningham CW: Mitochondrial gene rearrangements confirm the parallel evolution of the crab-like form. Proc Biol Sci. 2002, 269 (1489): 345-350. 10.1098/rspb.2001.1886.
Shen X, Ren J, Cui Z, Sha Z, Wang B, Xiang J, Liu B: The complete mitochondrial genomes of two common shrimps (Litopenaeus vannamei and Fenneropenaeus chinensis) and their phylogenomic considerations. Gene. 2007, 403 (1-2): 98-109. 10.1016/j.gene.2007.06.021.
Martin JW, Davis GE: An Updated Classification of the Recent Crustacea. Science Series. 2001, Natural History Museum of Los Angeles County
Little CTS, Vrijenhoek RC: Are hydrothermal vent animals living fossils?. Trends Ecol Evol. 2003, 18 (11): 582-588. 10.1016/j.tree.2003.08.009.
Van Dover CL: A comparison of stable isotope ratios (18O/16O and 13C/12C) between two species of hydrothermal vent decapods (Alvinocaris lusca and Munidopsis subsquamosa). Mar Ecol Prog Ser. 1986, 31: 295-299. 10.3354/meps031295.
Sambrook J, Russell D: Molecular Cloning: A Laboratory Manual. 2001, Cold Spring Harbor Laboratory Press, 2344-Third
Cheng S, Chang SY, Gravitt P, Respess R: Long PCR. Nature. 1994, 369 (6482): 684-685. 10.1038/369684a0.
Lowe TM, Eddy SR: tRNAscan-SE: a program for improved detection of transfer RNA genes in genomic sequence. Nucleic Acids Res. 1997, 25 (5): 955-964. 10.1093/nar/25.5.955.
Lohse M, Drechsel O, Bock R: OrganellarGenomeDRAW (OGDRAW): a tool for the easy generation of high-quality custom graphical maps of plastid and mitochondrial genomes. Curr Genet. 2007, 52 (5-6): 267-274. 10.1007/s00294-007-0161-y.
Tamura K, Dudley J, Nei M, Kumar S: MEGA4: molecular evolutionary genetics analysis (MEGA) software version 4.0. Mol Biol Evol. 2007, 24 (8): 1596-1599. 10.1093/molbev/msm092.
Perna NT, Kocher TD: Patterns of nucleotide composition at fourfold degenerate sites of animal mitochondrial genomes. J Mol Evol. 1995, 41 (3): 353-358. 10.1007/BF01215182.
Lu CL, Wang TC, Lin YC, Tang CY: ROBIN: a tool for genome rearrangement of block-interchanges. Bioinformatics. 2005, 21 (11): 2780-2782. 10.1093/bioinformatics/bti412.
Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG: The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res. 1997, 25 (24): 4876-4882. 10.1093/nar/25.24.4876.
Xia X, Xie Z, Salemi M, Chen L, Wang Y: An index of substitution saturation and its application. Mol Phylogenet Evol. 2003, 26 (1): 1-7. 10.1016/S1055-7903(02)00326-3.
Xia X, Xie Z: DAMBE: software package for data analysis in molecular biology and evolution. J Hered. 2001, 92 (4): 371-373. 10.1093/jhered/92.4.371.
Castresana J: Selection of conserved blocks from multiple alignments for their use in phylogenetic analysis. Mol Biol Evol. 2000, 17 (4): 540-552.
Posada D, Crandall KA: MODELTEST: testing the model of DNA substitution. Bioinformatics. 1998, 14 (9): 817-818. 10.1093/bioinformatics/14.9.817.
Abascal F, Zardoya R, Posada D: ProtTest: selection of best-fit models of protein evolution. Bioinformatics. 2005, 21 (9): 2104-2105. 10.1093/bioinformatics/bti263.
Akaike H: A new look at the statistical model identification. IEEE Trans Automat Control. 1974, 19 (6): 716-723. 10.1109/TAC.1974.1100705.
Abascal F, Posada D, Zardoya R: MtArt: a new model of amino acid replacement for Arthropoda. Mol Biol Evol. 2007, 24 (1): 1-5. 10.1093/molbev/msl136.
Jobb G, von Haeseler A, Strimmer K: TREEFINDER: a powerful graphical analysis environment for molecular phylogenetics. BMC Evol Biol. 2004, 4: 18-10.1186/1471-2148-4-18.
Huelsenbeck JP, Ronquist F: MRBAYES: Bayesian inference of phylogenetic trees. Bioinformatics. 2001, 17 (8): 754-755. 10.1093/bioinformatics/17.8.754.
Place AR, Feng X, Steven CR, Fourcade HM, Boore JL: Genetic markers in blue crabs (Callinectes sapidus). II. Complete mitochondrial genome sequence and characterization of genetic variation. J Exp Mar Biol Ecol. 2005, 319 (1-2): 15-27. 10.1016/j.jembe.2004.03.024.
Yamauchi MM, Miya MU, Nishida M: Complete mitochondrial DNA sequence of the swimming crab, Portunus trituberculatus (Crustacea: Decapoda: Brachyura). Gene. 2003, 311: 129-135. 10.1016/S0378-1119(03)00582-1.
Miller AD, Murphy NP, Burridge CP, Austin CM: Complete mitochondrial DNA sequences of the decapod crustaceans Pseudocarcinus gigas (Menippidae) and Macrobrachium rosenbergii (Palaemonidae). Mar Biotechnol (NY). 2005, 7 (4): 339-349. 10.1007/s10126-004-4077-8.
Yamauchi M, Miya M, Nishida M: Complete mitochondrial DNA sequence of the Japanese spiny lobster, Panulirus japonicus (Crustacea: Decapoda). Gene. 2002, 295 (1): 89-96. 10.1016/S0378-1119(02)00824-7.
Ivey JL, Santos SR: The complete mitochondrial genome of the Hawaiian anchialine shrimp Halocaridina rubra Holthuis, 1963 (Crustacea: Decapoda: Atyidae). Gene. 2007, 394 (1-2): 35-44. 10.1016/j.gene.2007.01.009.
Wilson K, Cahill V, Ballment E, Benzie J: The complete sequence of the mitochondrial genome of the crustacean Penaeus monodon: are malacostracan crustaceans more closely related to insects than to branchiopods?. Mol Biol Evol. 2000, 17 (6): 863-874.
Yamauchi MM, Miya MU, Machida RJ, Nishida M: PCR-based approach for sequencing mitochondrial genomes of decapod crustaceans, with a practical example from kuruma prawn (Marsupenaeus japonicus). Mar Biotechnol (NY). 2004, 6 (5): 419-429. 10.1007/s10126-003-0036-2.
We are grateful of Japan Agency for Marine-Earth Science and Technology (JAMSTEC) for the specimen. We thank Dr. Hiromichi Nagasawa of the University of Tokyo for many years of guidance and encouragement. We also thank Chris Wood of Zhejiang University for critical reading of this manuscript. This work was supported by the National Natural Sciences Foundation of China (40730212) and "863" program of China (2007AA09Z426).
J–SY designed and performed the experiments, analyzed the data, and wrote the paper. W–JY directed the research and in collaboration with J–SY performed the data analysis and paper writing.
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Yang, JS., Yang, WJ. The complete mitochondrial genome sequence of the hydrothermal vent galatheid crab Shinkaia crosnieri (Crustacea: Decapoda: Anomura): A novel arrangement and incomplete tRNA suite. BMC Genomics 9, 257 (2008). https://doi.org/10.1186/1471-2164-9-257
- Mitochondrial Genome
- Codon Usage
- Okinawa Trough
- Amino Acid Tree
- Potential Secondary Structure