Many of true bugs are important insect pests to cultivated crops and some are important vectors of human diseases, but few cladistic analyses have addressed relationships among the seven infraorders of Heteroptera. The Enicocephalomorpha and Nepomorpha are consider the basal groups of Heteroptera, but the basal-most lineage remains unresolved. Here we report the mitochondrial genome of the unique-headed bug Stenopirates sp., the first mitochondrial genome sequenced from Enicocephalomorpha. The Stenopirates sp. mitochondrial genome is a typical circular DNA molecule of 15, 384 bp in length, and contains 37 genes and a large non-coding fragment. The gene order differs substantially from other known insect mitochondrial genomes, with rearrangements of both tRNA genes and protein-coding genes. The overall AT content (82.5%) of Stenopirates sp. is the highest among all the known heteropteran mitochondrial genomes. The strand bias is consistent with other true bugs with negative GC-skew and positive AT-skew for the J-strand. The heteropteran mitochondrial atp8 exhibits the highest evolutionary rate, whereas cox1 appears to have the lowest rate. Furthermore, a negative correlation was observed between the variation of nucleotide substitutions and the GC content of each protein-coding gene. A microsatellite was identified in the putative control region. Finally, phylogenetic reconstruction suggests that Enicocephalomorpha is the sister group to all the remaining Heteroptera.
Citation: Li H, Liu H, Shi A, Štys P, Zhou X, Cai W (2012) The Complete Mitochondrial Genome and Novel Gene Arrangement of the Unique-Headed Bug Stenopirates sp. (Hemiptera: Enicocephalidae). PLoS ONE 7(1): e29419. https://doi.org/10.1371/journal.pone.0029419
Editor: Nikolas Nikolaidis, California State University Fullerton, United States of America
Received: September 26, 2011; Accepted: November 28, 2011; Published: January 3, 2012
Copyright: © 2012 Li et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This study was supported by grants from the National Natural Science Foundation of China (Nos. 30825006, 30970394, 31061160186), Beijing Natural Science Foundation (No. 6112013), the Doctoral Program of Higher Education of China (No. 200800190015), the Key Laboratory of the Zoological Systematics and Evolution of the Chinese Academy of Sciences (No. O529YX5105) to Wanzhi Cai, the Innovation Program for Ph.D. Students of China Agricultural University (No. 15059211) to Hu Li and Grant Agency of Czech Academy of Sciences (IAA. 601110706) to Pavel Štys. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Mitochondrial (mt) genome sequences are becoming increasingly important for comprehensive evolutionary and population studies. Mt genome sequences are not only more informative than shorter sequences of individual genes, but also provide sets of genome-level characters, such as the relative position of different genes, RNA secondary structures and modes of control of replication and transcription –. For the past two decades, mtDNA has been widely regarded as the molecular marker of choice for the phylogenetic analysis in metazoans because of its abundance in animal tissues, the small genome size, faster rate of evolution, low or absence of sequence recombination, and evolutionary conserved gene products , , although the applicability of mt genomes as a marker of deeper divergences or highly divergent lineages is still controversial , . It is pertinent that the ideal molecular systematic approach would include both nuclear and organellar DNA such as mtDNA markers .
The suborder Heteroptera (true bugs) contains over 40,000 species, and majority of the agriculturally important true bugs are the group of phytophagous species attacking cultivated crops. The haematophagous assassin bug Triatoma dimidiata, a representative of Triatominae (a subfamily of Reduviidae), is the most important vector of Chagas disease in humans , . Relatively few cladistic analyses have addressed relationships among the seven infraorders of Heteroptera during the past 25 years and the hypotheses on infraordinal relationships conflict on crucial points . For example, what is the basal-most sister-group of the majority of Heteroptera - the Enicocephalomorpha (orthodoxy) or Nepomorpha ? Mt genome sequences provide a novel insight into the infraordinal relationships of Heteroptera, although the applicability remains to be elucidated. At present, the complete or nearly complete mt genomes of 32 species of heteropterans are available at NCBI (as of April 15, 2011; Table S1). Among these, 15 belong to Pentatomomorpha, nine belong to Nepomorpha, four belong to Cimicomorpha, two belong to Gerromorpha, and two belong to Leptopodomorpha , –. Most of the submitted sequences are typically a small double-stranded circular molecule of 14–18 kb in length and contain 13 protein-coding genes (PCGs), two rRNA genes, 22 tRNA genes and a control region (CR). The control region is mostly AT-rich and fulfils a role in the initiation of replication and transcription , . To date, mt genome sequences of Enicocephalomorpha and Dipsocoromorpha have not been reported. This lack of information impedes our ability to trace the evolution of the basal groups of Heteroptera based on mt genomes.
Enicocephalomorpha, or unique-headed bugs, are a relatively small group of true bugs –, the only ones that engage in nuptial swarming among Heteroptera. They comprise two families, Aenictopecheidae and Enicocephalidae, which include 22 and 322 valid species, respectively, although hundreds of species remain undescribed . Enicocephalomorpha was at one time placed in the Reduvioidea , but is now considered the putative sister group to all remaining Heteroptera , , –.
In this paper, we present the complete mt genome of a representative species from the unique-headed bug, Stenopirates sp. This is the first species from the Enicocephalomorpha for which the entire mt genome has been sequenced, and for the first time, we report the rearrangement of protein-coding genes in a Heteroptera mt genome. We also discuss architecture of Stenopirates sp. mt genome and analyze the RNA secondary structure across the heteropterans. Finally, results from phylogenomic analysis shed lights on the phylogenetic relationship of Enicocephalomorpha among heteropterans.
Results and Discussion
The complete mt genome of Stenopirates sp. is a typical circular DNA molecule of 15, 384 bp in length (GenBank accession no. JN100019; Figure 1). This genome is a medium level of true bug mt genome size, ranging from 14,935 bp to 17,191 bp . Within true bug mt genomes, the length variation was minimal in PCGs, tRNAs, the large and small rRNA subunits (rrnL and rrnS), but very different in the putative control region (Figure 2; Table S2). The mt genome of Stenopirates sp. contains 37 genes in total (13 PCGs, 22 tRNA genes, and two rRNA genes) which are typically present in metazoan mt genomes . Twenty-three genes were transcribed on the majority strand (J-strand), whereas the others were oriented on the minority strand (N-strand). Gene overlaps were found at 17 gene junctions and involved a total of 59 bp; the longest overlap (11 bp) existed between atp6 and cox3. In addition to the large non-coding region, several small non-coding intergenic spacers were present in the Stenopirates sp. mt genome and were spread over six positions, ranging in size from 1 to 67 bp (Table S3).
The tRNAs are denoted by the color blocks and are labelled according to the IUPACIUB single-letter amino acid codes. Gene name without underline indicates the direction of transcription from left to right, and with underline indicates right to left. Overlapping lines within the circle denote PCR fragments amplified used for cloning and sequencing.
Lower horizontal bar, non-outlier smallest observation; lower edge of rectangle, 25 percentile; central bar within rectangle, median; upper edge of rectangle, 75 percentile; upper horizontal bar, non-outlier largest observation; blue circle, outlier.
The gene order of the Stenopirates sp. mt genome differs largely from those of all other analyzed insect species. Compared to Drosophila yakuba, which is considered the representative ground pattern for insect mt genomes , 30 of the 38 gene boundaries in D. yakuba were conserved in Stenopirates sp. The most striking features were the inversion of two tRNA genes (trnT and trnP) and translocations of five gene clusters (trnT-trnP-nad6, cytB-trnS2, nad1-trnL2, rrnL-trnV-rrnS and CR) between nad4L and trnI (Figure 3).
Only protein-coding genes (blue), ribosomal RNA genes (yellow) and control region (green) are marked. Blue boxes represent protein-coding genes with the same relative position as in the insect ground pattern, Drosophila yakuba; purple boxes and horizontal lines represent gene clusters that changed positions relative to D. yakuba; red boxes represent inversions of tRNAs. tRNA genes are abbreviated using the one-letter amino acid code, with L1 = CUN; L2 = UUR; S1 = AGN; S2 = UCN. All genes are transcribed from left to right except those underlined to indicate an opposite transcriptional orientation.
The complete or nearly complete mt genomes of 32 species of Heteroptera have been sequenced and exhibit highly conserved gene order. The mt genomes of three Pentatomomorpha species present gene rearrangements in the inversion of tRNA genes . Two species in the superfamily Pyrrhocoroidea share the same gene order with the inversion of trnT and trnP. Two tRNA genes (trnI and trnQ) are inversed in the flat bug Neuroctenus parus. Rearrangements of the mt genome are relatively rare events at the evolutionary scale, and, therefore, provide a powerful tool to delimit deep divergences among some metazoan lineages . In comparison to Stenopirates sp., rearrangements in other true bugs seem to occur independently. These results suggest that mt gene orders might lack of resolution to deduce phylogenetic relationships among infraorders within Heteroptera, although it has been used extensively to elucidate phylogenetic relations at the superfamily level , .
Base composition and codon usage
As is the case in other heteropteran mt genome sequences, the nucleotide composition of the Stenopirates sp. mt genome was also biased toward A and T (J-strand: A = 43.9%, T = 38.6%, G = 7.5%, C = 10.0%; Table S4). The overall AT content (82.5%) of Stenopirates sp. was the highest and much higher than the average AT content of heteropteran mt genomes (Figure 4).
Measured in bp percentage (Y-axis) and level of nucleotide skew (X-axis). Values are calculated on J-strands for full length mt genomes. Green circle, Pentatomomorpha; blue circle, Nepomorpha; red circle, Cimicomorpha; yellow circle, Gerromorpha; purple circle, Leptopodomorpha; black circle, Enicocephalomorpha (Stenopirates sp.).
Metazoan mt genomes usually present a clear strand bias in nucleotide composition , , and the strand bias can be measured as AT- and GC-skews . A comparative analysis of A+T% vs AT-skew and G+C% vs GC-skew across all available mt genomes of true bugs is shown in Figure 4. The average AT-skew of true bug mt genomes was 0.15, ranging from 0.04 in Hydaropsis longirostris to 0.23 in Leptopus sp., whereas the Stenopirates sp. mt genome exhibited a slight AT-skew (0.06) (Table S4). The average GC-skew of true bug mt genomes was −0.18, ranging from −0.04 in Yemmalysus parallelus to −0.27 in Triatoma dimidiata, and the Stenopirates sp. mt genome exhibited a marked GC-skew (−0.14) (Table S4). AT- and GC-skews of true bug mt genomes are consistent compared to the usual strand biases of metazoan mtDNA (positive AT-skew and negative GC-skew for the J-strand).
The reversal of strand asymmetry over the entire mt genome was found to have accelerated gene rearrangement rates  and was caused by inversion of replication origin . However, species that have accelerated gene rearrangement rates do not always show a reversal of strand asymmetry, e.g., three Nasonia species (Insecta: Hymenoptera) , Thrips imagines (Insecta: Thysanoptera)  and Stenopirates sp. in this paper. Therefore, the mechanism of gene rearrangement also needs more in-depth study.
The genome-wide bias toward AT was well documented in the codon usage (Table S5). At the third codon position, A or T were overwhelmingly overrepresented compared to G or C. The overall pattern was very similar among the true bugs, with similar frequency of occurrences of various codons within a single codon family. There was a strong bias toward AT-rich codons with the six most prevalent codons in Stenopirates sp., as in order, TTA-Leu (12.76%), ATT-Ile (11.86%), ATA-Met (10.75%), TTT-Phe (9.93%), AAT-Asn (6.72%) and TAT-Tyr (4.49%) (Table S5).
The total length of all 13 PCGs was 11,056 bp, and accounted for 71.87% of the entire length of Stenopirates sp. mt genome. The overall AT content of PCGs was 82.05%, ranging from 74.0% (cox1) to 90.4% (atp8). Start and stop codons were determined based on alignments with the corresponding genes of other true bugs (Table S3). Five genes (atp6, cox3, nad4, cytB, nad1) used the standard ATG start codon, four genes (nad2, atp8, nad4L, nad6) started with ATA and three genes (cox2, nad3, nad5) initiated with ATT. Cox1 most likely started with codon TTG. Nine genes employ a complete translation termination codon, either TAG (nad3, cytB) or TAA (nad2, cox1, atp8, atp6, nad4L, nad1, nad6), whereas the remaining four have incomplete stop codons T. The presence of an incomplete stop codon is common in metazoan mt genomes  and these truncated stop codons are presumed to be completed via post-transcriptional polyadenylation .
The rate of non-synonymous substitutions (Ka), the rate of synonymous substitutions (Ks), and the ratio of Ka/Ks were calculated for each PCG, respectively. In this respect, atp8 showed the highest evolutionary rates, followed by nad2, while cox1 appeared to be the lowest (Figure 5). Notably, the ratio of Ka/Ks for each and every PCG was below 1, indicating that these genes are evolving under the purifying selection , . Furthermore, a negative correlation was observed between the Ka/Ks and the GC content of each PCG (R = −0.916, P<0.01) (Table S6), which indicate that the variation of GC content probably causes the different evolutionary patterns among genes .
The entire complement of 22 tRNAs typical of arthropod mt genomes was found in Stenopirates sp. and schematic drawings of their respective secondary structures are shown in Figure 6. Most of the tRNAs could be folded as classic clover-leaf structures, with the exception of trnS1, in which its DHU arm simply formed a loop. This phenomenon is a common theme in the true bug mt genomes. The aberrant tRNAs possess non-Watson-Crick matches, aberrant loops, or extremely short arms are common in metazoan mt genomes . Whether or not the aberrant tRNAs lose their respective functions is still unknown, however, a post-transcriptional RNA editing mechanism has been proposed to sustain functions for these modified tRNAs , .
The ends of rRNA genes are impossible to be precisely determined by DNA sequencing alone, so they are assumed to extend to the boundaries of flanking genes , . The srRNA was assumed to fill up the blanks between tRNA-V and nad1. For the boundary between the lrRNA gene and the non-coding putative control region, alignments with homologous sequences in other heteropteran mt genomes were applied to determine the 3′-end of the gene , –. The length of rrnL and rrnS of Stenopirates sp. was determined to be 1, 245 bp and 829 bp, respectively.
Both rrnL and rrnS are incongruent with the secondary structure models proposed for other insects –. The secondary structure of Stenopirates sp. rrnL consisted of six structural domains (domain III is absent in arthropods) (Figure 7). Among sequenced true bugs, the sequence variations were too high in some regions for meaningful structural comparisons. Overall, the 5′ and 3′ ends, some helices (H183, H589, H687, H736, H837, H991, H1196, H1648, H1792, H2077, H2520), and domain VI were the most variable regions. Domains IV and V were more conserved. The secondary structure of rrnS contained three domains (Figure 8). Conservative sites were mainly in domain III and some helices (loops of H673, H769 and H889) in domain II.
The nucleotides showing 100% identities among true bugs are marked with orange color, and more than or equal to 75% identities are marked with blue color. Roman numerals denote the conserved domain structure. Inferred Watson-Crick bonds are illustrated by lines, GU bonds by dots.
The nucleotides showing 100% identities among true bugs are marked with orange color, and ≥75% identities are marked with blue color. Roman numerals denote the conserved domain structure. Inferred Watson-Crick bonds are illustrated by lines, GU bonds by dots.
The largest non-coding region (765 bp) was flanked by trnS2 and rrnL in the Stenopirates sp. mt genome. It was highly enriched in AT (74.9%) and could form stable stem-loop secondary structures. Based on these features, it possibly functions as a control region , .
Based on the sequence pattern, the control region could be subdivided into five parts (Figure 9). The first region (10,779–10,807) was a 29 bp leading sequence enriched in AT. The second region (10,808–10,830) included the 9 bp poly-C and 14 bp poly-G. The poly-G has been reported in assassin bug Agriosphodrus dohrni (referred as G element) , and triatomine bugs Rhodnius prolixus and Triatoma dimidiata (referred as Gs) , and some dipterans (referred as G islands) . The possible involvement of this unique motif in insect replication and transcription initiation is one topic for the future research –. The third region (10,952–11,392) contained five (I–V) tandem repeats including two (I & III) 80 bp, one (V) 52 bp (a partial copy of the anterior repeat unit), and two (II & IV) repeats (with substitute of few nucleotides). The maximum size difference found in the control regions across all sequenced true bug mt genomes was 2,756 bp, indicating that strong size variation among true bug mt genomes is significantly correlated to the control regions (Figure 2). This result is consistent with previous findings from other insects , , . In fact, the control region has been identified as the source of size variation in the entire mt genome, usually due to the presence of a variable copy number of repetitive elements . Repeated sequences are common in the control region for most insects, and length variations due to the various numbers of repeats are not without precedent . Consequently, analysis of the repeat units among individuals from different geographical locations may shed light on the geographical structuring and phylogenetic relationships of species. The fact that tandem repeats are non-conserved among these heteropteran mt genomes indicates a lack of a functional role. Replication slippage is regarded as a dominant mechanism to account for the existence of tandem repeats , .
The control region flanking genes trnS2 (S2) and rrnL are represented in purple boxes. The blue and green boxes with roman numerals indicate the tandem repeat region; grey boxes represent the stem-loop region.
The fourth region (10,831–10,951 & 11,393–11,439) was near the tandem repeat region, and stem-loop structures which may be involved in the initiation of the replication of animal mtDNA  could be folded (Figure 10A), but none of these structures had flanking sequences similar to those that are conserved in the control region of the mt genomes of insects . The fifth region (11,440–11,543) contained five CTTT-repeats, 31 CT-repeats and 22 AT- repeats. This domain can be considered a microsatellite . In arthropod mtDNA such microsatellites are rare and only been reported for butterflies , the Asian arowana, Scleropages formosus , and a house dust mite, Dermatophagoides pteronyssinus . This is remarkable because a mt microsatellite has not been reported for any heteropteran species. As described previously, four other stretches of non-coding nucleotides were found outside the control region. These short sequences can fold into stable stem-loop structures (Figure 10B & C) which may function as splicing recognition sites during processing of the transcripts .
Phylogenetic analyses were carried out using nucleotide sequences of 13 mt PCGs from 31 heteropteran species and 4 outgroup hemipteran insect species (Pachypsylla venusta , Acyrthosiphon pisum , Sivaloka damnosa  and Lycorma delicatula ). BI and ML analyses generated identical tree topologies (Figure 11).
Phylogenetic analyses were carried out for the 31 true bugs based on all 13 protein-coding genes from their respective mt genomes. The tree was rooted with four outgroups (P. venusta, A. pisum, S. damnosa and L. delicatula). Numbers at the nodes are Bayesian posterior probabilities (left) and ML bootstrap values (right).
The seven-infraorder classification of Heteroptera has been accepted by most researchers , , however phylogenetic relationships among infraorders are still controversial , , , , –. The major problem is the basalmost sister-group of the majority of Heteroptera, the Enicocephalomorpha (orthodoxy) or Nepomorpha .
In the present study, the sister-relationship within the individual infraorders (as shown in Figure 11) are supported for the Pentatomomorpha (14 taxa), Nepomorpha (8 taxa), Leptopodomorpha (2 taxa) and Gerromorpha (2 taxa) by BI and ML analyses. In addition, both ML and BI analyses are highly supportive of the contention that Stenopirates sp. (Enicocephalomorpha) is the sister group to all the remaining Heteroptera , .
Within Cimicomorpha, Reduviidae was paraphyletic with respect to Anthocoridae and Miridae in our trees, and this is largely incongruent with previous phylogenetic works , , . The mt genome data in this study, however, may be limited to resolve the phylogeny of Cimicomorpha, and increased taxon sampling will be required to resolve this problem.
The ability of mt genome data to resolve infraordinal relationships of Heteroptera has not been fully evaluated. This study provides the initial evidence for the feasibility of using mt genome data to resolve infraordinal relationships of Heteroptera; however, the prerequisite is to ensure the integrity and representative of the infraorder-level taxa.
Future directions should focus on the following problems raised in the modern literature: (a) Are Dipsocoromorpha monophyletic and sister to the rest of Heteroptera (orthodoxy) or are they formed by two distinct clades with uncertain relationships (Štys, in prep.)? (b) Are Nepomorpha monophyletic (orthodoxy) or should the Pleomorpha be excluded and its origin seeked for elsewhere ? (c) Are some “Thaumastocoridae” pentatomomorphans and others cimicomorphans ? (d) Are the Pentatomomorpha monophyletic (orthodoxy) or should the Aradimorpha be excluded and its origin be seeked elsewhere ? and (e) What is the mutual relationship of Nepomorpha (s. lat.), Leptopodomorpha, and the truly terrestrial true bugs?
This is the first description of the complete mt genome of a species belonging to Enicocephalomorpha, an infraorder within Heteroptera. The overall AT content of Stenopirates sp. is the highest among sequenced heteropteran mt genomes. Although the gene order of the Stenopirates sp. mt genome is extremely rearranged and represents a new pattern, rearrangements exhibit relatively rare events and seem to occur independently within true bug mt genomes. Gene order comparison indicated that mt gene order seems less useful for deduction of phylogenetic relationships among infraorders of Heteroptera. Comparative analyses suggest that the gene size, gene content, and base composition are comparatively conserved among true bug mt genomes. PCGs exhibit a different nucleotide substitution pattern, negatively correlated with GC content. True bugs mt atp8 represents the highest evolutionary rate; whereas cox1 appears to be the lowest. Most of the tRNAs can be folded as classic clover-leaf structures, with the exception of trnS1, in which its DHU arm simply forms a loop. In addition to stem-loop structures in the control region, another common feature is the existence of tandem repeats. Phylogenetic analysis using concatenated PCG sequences succeeded in corroborating hypothesis on sister-group relationship of Enicocephalomorpha to other heteropterans. The present study demonstrates the great effectiveness of mt genome for inferring phylogenetic relationships at the infraorder level.
Materials and Methods
No specific permits were required for the insect collected for this study in Taiwan. The insect specimens were collected on the road side by sweeping. The field studies did not involve endangered or protected species. The species in the genus of Stenopirates are common small insects and are not included in the “List of Protected Animals in China”.
Samples and DNA extraction
The Oriental and East Palaearctic genus Stenopirates (Enicocephalinae: Enicocephalini) includes 8 described and about 20 undescribed species . Stenopirates sp. adult males were collected from Pingdong, Taiwan, China, in May 2009. All collections were initially preserved in 95% ethanol in the field, and transferred to −20°C for the long-term storage upon the arrival at the China Agricultural University (CAU). The genomic DNA was extracted from muscle tissues of a single Stenopirates sp. 's thorax using a CTAB-based protocol .
PCR amplification and sequencing
The mt genome of Stenopirates sp. was generated by amplification of overlapping PCR fragments (Figure 1 and Table S7). Initially, eleven fragments were amplified using the universal primer sets . Four perfectly matched primers (Table S7) were designed based on the read of these short fragments for the secondary PCRs.
Short PCRs (<1.5 kb) were carried out using Qiagen Taq DNA polymerase (Qiagen, Beijing, China) with the following cycling conditions: 5 min at 94°C, followed by 35 cycles of 50 s at 94°C, 50 s at 48–55°C, 1–2 min at 72°C depending on the size of amplicons, and the subsequent final elongation step at 72°C for 10 min. Long PCRs (>1.5 kb) were performed using NEB Long Taq DNA polymerase (New England BioLabs, Ipswich, MA) under the following cycling conditions: 30 s at 95°C, followed by 40 cycles of 10 s at 95°C, 50 s at 48–55°C, 3–6 min at 68°C depending on the size of amplicons, and the final elongation step at 68°C for 10 min . The quality of PCR products were evaluated by spectrophotometry and agarose gel electrophoresis.
The PCR fragments were ligated into the pGEM-T Easy Vector (Promega) and resulting plasmid DNAs were isolated using the TIANprp Midi Plasmid Kit (Qiagen, Beijing, China). All fragments were sequenced in both directions using the BigDye Terminator Sequencing Kit (Applied Bio Systems) and the ABI 3730XL Genetic Analyzer (PE Applied Biosystems, San Francisco, CA, USA) with two vector-specific primers and internal primers for primer walking.
Annotation and bioinformatic analysis
The complete mt genome of Stenopirates sp. has been deposited in GenBank under accession number JN100019. Mt DNA sequences were proof-read and aligned into contigs in BioEdit v.22.214.171.124 . PCGs and rRNA genes were identified based on sequence similarity with published insect mt sequences from public domains (e.g., GenBank).
The tRNA genes were identified by tRNAscan-SE Search Server v.1.21  with default settings. Some tRNA genes that could not be determined by tRNAscan-SE were determined in the unannotated regions by sequence similarity to tRNAs of other heteropterans. The base composition, codon usage, and nucleotide substitution were analyzed with Mega 4.0 .
The software packages DnaSP 5.0  was used to calculate the number of synonymous substitutions per synonymous site (Ks) and the number of nonsynonymous substitutions per nonsynonymous site (Ka) for each PCG.
Construction of secondary structures of rRNAs and non-coding Regions
Secondary structures of the small and large subunits of rRNAs were inferred using models predicted for Drosophila , Apis mellifera , Manduca sexta  and Ruspolia dubia . Stem-loops were named according to the convention of , as well as . Regions lacking significant homology and other non-coding regions were folded using Mfold .
Phylogenetic analyses were performed based on the 31 complete or nearly complete mt genomes of true bugs from GenBank (Table S1). Two species from Sternorrhyncha and two species from “Auchenorrhyncha”: Fulgoromorpha were selected as outgroups. Based on an analysis of mt genomes of nine Nepomorpha and five other hemipterans, Pleidae were recovered as the sister group to Geocorisae + Leptopodomorpha + remaining Nepomorpha, and were suggested to be raised from a superfamily to the infraorder Plemorpha . Similarly, the phylogenetic position of “Aradoidea” or “Aradimorpha” was also the problem . Since we didn't add samples to solve these problems, Paraplea frontalis (Nepomorpha: Pleidae) and Neuroctenus parus (Pentatomomorpha: Aradidae) were treated as incertae sedis. These two species were not included in the phylogenetic analyses to ensure the stability of the topology.
DNA alignment was inferred from the amino acid alignment of 13 PCGs using Clustal X  as implemented in the Mega 4.0 , which can translate between DNA and amino acid sequences within alignments. Alignments of individual genes were then concatenated excluding the stop codon. Model selection was based on Modeltest 3.7  for nucleotide sequences. According to the Akaike information criterion, the GTR+I+G model was optimal for analysis with nucleotide alignments. MrBayes v.3.1.2  and a PHYML online web server ,  were employed to reconstruct the phylogenetic trees. In Bayesian inference, two simultaneous runs of 3,000,000 generations were conducted. Each set was sampled every 200 generations with a burnin of 25% , , , . Trees inferred prior to stationarity were discarded as burnin, and the remaining trees were used to construct a 50% majority-rule consensus tree. In the ML analysis, the parameters were estimated during analysis and the node support values were assessed by bootstrap re-sampling (BP)  calculated using 100 replicates.
Summary of taxonomic groups used in this study.
The Size of PCGs, tRNAs, rrnL, rrnS, and CR, respectively, among sequenced true bug mt genomes.
Organization of Stenopirates sp. mt genome.
Base composition and strand bias in true bug mt genomes.
Codon usage of protein-coding genes in the Stenopirates sp. mt genome.
Different evolutionary patterns among protein-coding genes.
Special thanks go to Drs. John J. Obrycki, Eric G. Chapman (University of Kentucky) and Shujuan Li (Purdue University) for their comments on an earlier draft of the paper.
Conceived and designed the experiments: H. Li WZC. Performed the experiments: H. Li. Analyzed the data: H. Li. Contributed reagents/materials/analysis tools: H. Li H. Liu AMS. Wrote the paper: H. Li XZ. Contributed intellectually during the design and implementation of this study, and during the writing of the manuscript: WZC XZ PŠ.
- 1. Dowton M, Castro LR, Austin AD (2002) Mitochondrial gene rearrangements as phylogenetic characters in the invertebrates the examination of genome ‘morphology’. Invertebr Syst 16: 345–356.
- 2. Boore JL, Macey JR, Medina M (2005) Sequencing and comparing whole mitochondrial genomes of animals. Molecular Evolution: Producing the Biochemical Data, Part B Volume 395. San Diego: Elsevier Academic Press Inc. pp. 311–348.
- 3. Boore JL (2006) The use of genome-level characters for phylogenetic reconstruction. Trends Ecol Evol 21: 439–446.
- 4. Masta SE, Boore JL (2008) Parallel evolution of truncated transfer RNA genes in arachnid mitochondrial genomes. Mol Biol Evol 25: 949–959.
- 5. Lin CP, Danforth BN (2004) How do insect nuclear and mitochondrial gene substitution patterns differ? Insights from Bayesian analyses of combined datasets. Mol Phylogenet Evol 30: 686–702.
- 6. Gissi C, Iannelli F, Pesole G (2008) Evolution of the mitochondrial genome of Metazoa as exemplified by comparison of congeneric species. Heredity 101: 301–320.
- 7. Curole JP, Kocher TD (1999) Mitogenomics: digging deeper with complete mitochondrial genomes. Trends Ecol Evol 14: 394–398.
- 8. Cameron SL, Miller KB, D'Haese CA, Whiting MF, Barker SC (2004) Mitochondrial genome data alone are not enough to unambiguously resolve the relationships of Entognatha, Insecta and Crustacea sensu lato (Arthropoda). Cladistics 20: 534–557.
- 9. Rubinoff D, Holland BS (2005) Between two extremes: mitochondrial DNA is neither the Panacea nor the Nemesis of phylogenetic and taxonomic inference. Syst Biol 54: 952–961.
- 10. Lent H, Wygodzinsky P (1979) Revision of the Triatominae (Hemiptera, Reduviidae), and their significance as vectors of Chagas' disease. Bull Am Mus Nat Hist 163: 125–520.
- 11. Dotson EM, Beard CB (2001) Sequence and organization of the mitochondrial genome of the Chagas disease vector, Triatoma dimidiata. Insect Mol Biol 10: 205–215.
- 12. Weirauch C, Schuh RT (2011) Systematics and evolution of Heteroptera: 25 years of progress. Annu Rev Entomol 56: 487–510.
- 13. Mahner M (1993) Systema cryptoceratorum phylogeneticum (Insecta, Heteroptera). Zoologica 143: ix + 302.
- 14. Hua JM, Li M, Dong PZ, Cui Y, Xie Q, et al. (2008) Comparative and phylogenomic studies on the mitochondrial genomes of Pentatomomorpha (Insecta: Hemiptera: Heteroptera). BMC Genomics 9: 610.
- 15. Lee W, Kang J, Jung C, Hoelmer K, Lee SH, et al. (2009) Complete mitochondrial genome of brown marmorated stink bug Halyomorpha halys (Hemiptera: Pentatomidae), and phylogenetic relationships of hemipteran suborders. Mol Cells 28: 155–165.
- 16. Hua JM, Li M, Dong PZ, Cui Y, Xie Q, et al. (2009) Phylogenetic analysis of the true water bugs (Insecta: Hemiptera: Heteroptera: Nepomorpha): evidence from mitochondrial genomes. BMC Evol Biol 9: 134.
- 17. Wolstenholme DR (1992) Animal mitochondrial DNA: structure and evolution. Int Rev Cytol 141: 173–216.
- 18. Boore JL (1999) Animal mitochondrial genomes. Nucleic Acids Res 27: 1767–1780.
- 19. Štys P (1995) Enicocephalomorpha. In: Schuh RT, Slater JA, editors. True bugs of the world (Hemiptera: Heteroptera). Classification and natural history. Ithaca: Cornell University Press. pp. 67–73.
- 20. Schuh RT, Slater JA (1995) True bugs of the world (Hemiptera: Heteroptera). Classification and natural history. Ithaca: Cornell University Press. 336 p.
- 21. Štys P (1989) Phylogenetic systematics of the most primitive true bugs (Heteroptera, Enicocephalomorpha, Dipsocoromorpha). Práce Slovenská entomologická spolocnost' SAV, Bratislva 8: 69–85.
- 22. Štys P (2008) Zoogeography of Enicocephalomorpha (Heteroptera). Bull Insectol 61: 137–138.
- 23. Usinger RL (1943) A revised classification of the Reduvioidea with a new subfamily from South America (Hemiptera). Ann Entomol Soc Am 36: 602–617.
- 24. Štys P (1984) Phylogeny and classification of lower Heteroptera. Int Congr Entomol Proc 17: 12.
- 25. Štys P, Kerzhner I (1975) The rank and nomenclature of higher taxa in recent Heteroptera. Acta Entomol Bohemoslov 72: 65–79.
- 26. Wheeler WC, Schuh RT, Bang R (1993) Cladistic relationships among higher groups of Heteroptera: congruence between morphological and molecular data sets. Entomol Scand 24: 121–137.
- 27. Clary DO, Wolstenholme DR (1985) The mitochondrial DNA molecular of Drosophila yakuba: nucleotide sequence, gene organization and genetic code. J Mol Evol 22: 252–271.
- 28. Boore JL, Brown WM (1998) Big trees from little genomes: mitochondrial gene order as a phylogenetic tool. Curr Opin Genet Dev 8: 668–674.
- 29. Shao R, Campbell NJ, Schmidt ER, Barker SC (2001) Increased rate of gene rearrangement in the mitochondrial genomes of three orders of hemipteroid insects. Mol Biol Evol 18: 1828–1832.
- 30. Thao ML, Baumann L, Baumann P (2004) Organization of the mitochondrial genomes of whiteflies, aphids, and psyllids (Hemiptera: Sternorrhyncha). BMC Evol Biol 4: 25.
- 31. Hassanin A, Leger N, Deutsch J (2005) Evidence for multiple reversals of asymmetric mutational constraints during the evolution of the mitochondrial genome of Metazoa, and consequences for phylogenetic inferences. Syst Biol 54: 277–298.
- 32. Hassanin A (2006) Phylogeny of Arthropoda inferred from mitochondrial sequences: Strategies for limiting the misleading effects of multiple changes in pattern and rates of substitution. Mol Phylogenet Evol 38: 100–116.
- 33. Perna NT, Kocher TD (1995) Patterns of nucleotide composition at fourfold degenerate sites of animal mitochondrial genomes. J Mol Evol 41: 353–358.
- 34. Cameron SL, Johnson KP, Whiting MF (2007) The mitochondrial genome of the screamer louse Bothriometopus (Phthiraptera: Ischnocera): effects of extensive gene rearrangements on the evolution of the genome. J Mol Evol 65: 589–604.
- 35. Wei SJ, Shi M, Chen XX, Sharkey MJ, van Achterberg C, et al. (2010) New views on strand asymmetry in insect mitochondrial genomes. PLoS ONE 5: e12708.
- 36. Oliveira DCSG, Rhitoban R, Lavrov DV, Werren JH (2008) Rapidly evolving mitochondrial genome and directional selection in mitochondrial genes in the parasitic wasp Nasonia (Hymenoptera: Pteromalidae). Mol Biol Evol 25: 2167–2180.
- 37. Shao R, Barker SC (2003) The highly rearranged mitochondrial genome of the plague thrips, Thrips imaginis (Insecta: Thysanoptera): convergence of two novel gene boundaries and an extraordinary arrangement of rRNA genes. Mol Biol Evol 20: 362–370.
- 38. Ojala D, Montoya J, Attardi G (1981) tRNA punctuation model of RNA processing in human mitochondria. Nature 290: 470–474.
- 39. Roques S, Fox CJ, Villasana MI, Rico C (2006) The complete mitochondrial genome of the whiting, Merlangius merlangus and the haddock, Melanogrammus aeglefinus: a detailed genomic comparison among closely related species of the Gadidae family. Gene 383: 12–23.
- 40. Yuan ML, Wei DD, Wang BJ, Dou W, Wang JJ (2010) The complete mitochondrial genome of the citrus red mite Panonychus citri (Acari: Tetranychidae): high genome rearrangement and extremely truncated tRNAs. BMC Genomics 11: 597.
- 41. Masta SE, Boore JL (2004) The complete mitochondrial genome sequence of the spider Habronattus oregonensis reveals rearranged and extremely truncated tRNAs. Mol Biol Evol 21: 893.
- 42. Lavrov DV, Brown WM, Boore JL (2000) A novel type of RNA editing occurs in the mitochondrial tRNAs of the centipede Lithobius forficatus. Proc Natl Acad Sci USA 97: 13738–13742.
- 43. Boore JL (2001) Complete mitochondrial genome sequence of the polychaete annelid Platynereis dumerilii. Mol Biol Evol 18: 1413–1416.
- 44. Boore JL (2006) The complete sequence of the mitochondrial genome of Nautilus macromphalus (Mollusca: Cephalopoda). BMC Genomics 7: 182.
- 45. Cannone JJ, Subramanian S, Schnare MN, Collett JR, D'Souza LM, et al. (2002) The comparative RNA web (CRW) site: an An online database of comparative sequence and structure information for ribosomal, intron, and other RNAs. BMC Bioinformatics 3: 15.
- 46. Gillespie JJ, Johnston JS, Cannone JJ, Gutell RR (2006) Characteristics of the nuclear (18S, 5.8S, 28S and 5S) and mitochondrial (12S and 16S) rRNA genes of Apis mellifera (Insecta: Hymenoptera): Structure, organization and retrotransposable elements. Insect Mol Biol 15: 657–686.
- 47. Cameron SL, Whiting MF (2008) The complete mitochondrial genome of the tobacco hornworm, Manduca sexta (Insecta: Lepidoptera: Sphingidae), and an examination of mitochondrial gene variability within butterflies and moths. Gene 408: 112–123.
- 48. Zhou ZJ, Huang Y, Shi FM (2007) The mitochondrial genome of Ruspolia dubia (Orthoptera: Conocephalidae) contains a short A+T–rich region of 70 bp in length. Genome 50: 855–866.
- 49. Zhang DX, Hewitt GM (1997) Insect mitochondrial control region: A review of its structure, evolution and usefulness in evolutionary studies. Biochem Syst Ecol 25: 99–120.
- 50. Li H, Gao JY, Liu HY, Liu H, Liang AP, et al. (2011) The architecture and complete sequence of mitochondrial genome of an assassin bug Agriosphodrus dohrni (Hemiptera: Reduviidae). Int J Bio Sci 7: 792–804.
- 51. Oliveira MT, Barau JG, Junqueira AC, Feijão PC, Rosa AC, et al. (2008) Structure and evolution of the mitochondrial genomes of Haematobia irritans and Stomoxys calcitrans: The Muscidae (Diptera: Calyptratae) perspective. Mol Phylogenet Evol 48: 850–857.
- 52. Saito S, Tamura K, Aotsuka T (2005) Replication origin of mitochondrial DNA in insects. Genetics 171: 1695–1705.
- 53. Asin-Cayuela J, Dustafsson CM (2007) Mitochondrial transcription and its regulation in mammalian cells. Trends Biochem Sci 32: 111–117.
- 54. Ma C, Liu C, Yang P, Kang L (2009) The complete mitochondrial genomes of two band-winged grasshoppers, Gastrimargus marmoratus and Oedaleus asiaticus. BMC Genomics 10: 156.
- 55. Levinson G, Gutman GA (1987) Slipped-strand mispairing: a major mechanism for DNA sequence evolution. Mol Biol Evol 4: 203–221.
- 56. Fumagalli L, Taberlet P, Favre L, Hausser J (1996) Origin and evolution of homologous repeated sequences in the mitochondrial DNA control region of shrews. Mol Biol Evol 13: 31–46.
- 57. Crozier RH, Crozier YC (1993) The mitochondrial genome of the honeybee Apis mellifera: complete sequence and genome organization. Genetics 133: 97–117.
- 58. Wannes D, Thomas VL, Bartel V, Luc T (2009) The complete mitochondrial genome of the house dust mite Dermatophagoides pteronyssinus (Trouessart): a novel gene arrangement among arthropods. BMC Genomics 10: 107.
- 59. Goldstein DB, Schlotterer C (1999) Microsatellites: evolution and applications. USA: Oxford University Press. 352 p.
- 60. Yue GH, Liew WC, Orban L (2006) The complete mitochondrial genome of a basal teleost, the Asian arowana (Scleropages formosus, Osteoglossidae). BMC Genomics 7: 242.
- 61. He Y, Jones J, Armstrong M, Lamberti F, Moens M (2005) The mitochondrial genome of Xiphinema americanum sensu stricto (Nematoda: Enoplea): Considerable economization in the length and structural features of encoded genes. J Mol Evol 61: 819–833.
- 62. Barrett RJ, Crease TJ, Hebert PD, Via S (1994) Mitochondrial DNA diversity in the pea aphid Acyrthosiphon pisum. Genome 37: 858–65.
- 63. Song N, Liang AP, Ma C (2010) The complete mitochondrial genome sequence of the planthopper, Sivaloka damnosus. J Insect Sci 10: 76.
- 64. Schuh RT (1986) The influence of cladistics on the classification of the Heteroptera. Annu Rev Entomol 31: 67–93.
- 65. Schuh RT, Weirauch C, Wheeler WC (2009) Phylogenetic relationships within the Cimicomorpha (Hemiptera: Heteroptera): a total-evidence analysis. Syst Entomol 34: 15–48.
- 66. Sweet MH (2006) Justification for the Aradimorpha as an infraorder of the suborder Heteroptera (Hemiptera: Prosorrhyncha) with special reference to pregenital abdominal structure. Denisia 19: 225–248.
- 67. Xie Q, Tian Y, Zheng LY, Bu WJ (2008) 18S rRNA hyper-elongation and the phylogeny of Euhemiptera (Insecta: Hemiptera). Mol Phylogenet Evol 47: 463–471.
- 68. Schuh RT, Štys P (1991) Phylogenetic analysis of cimicomorphan family relationships (Heteroptera). J New York Entomol Soc 99: 98–350.
- 69. Tian Y, Zhu WB, Li M, Xie Q, Bu WJ (2008) Influence of data conflict and molecular phylogeny of major clades in cimicomorphan true bugs (Insecta: Hemiptera: Heteroptera). Mol Phylogenet Evol 47: 581–597.
- 70. Aljanabi SM, Martinez I (1997) Universal and rapid salt-extraction of high quality genomic DNA for PCR-based techniques. Nucleic Acids Res 25: 4692–4693.
- 71. Simon C, Buckley TR, Frati F, Stewart JB, Beckenbach AT (2006) Incorporating molecular evolution into phylogenetic analysis, and a new compilation of conserved polymerase chain reaction primers for animal mitochondrial DNA. Annu Rev Ecol Evol Syst 37: 545–579.
- 72. Hall TA (1999) BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp Ser 41: 95–98.
- 73. Lowe TM, Eddy SR (1997) tRNAscan–SE: a program for improved detection of transfer RNA genes in genomic sequence. Nucleic Acids Res 25: 955–964.
- 74. Tamura K, Dudley J, Nei M, Kumar S (2007) MEGA4: molecular evolutionary genetics analysis (MEGA) software version 4.0. Mol Biol Evol 24: 1596–1599.
- 75. Librado P, Rozas J (2009) DnaSP v5: a software for comprehensive analysis of DNA polymorphism data. Bioinformatics 25: 1451–1452.
- 76. Zuker M (2003) Mfold web server for nucleic acid folding and hybridization prediction. Nucleic Acids Res 31: 3406–3415.
- 77. Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG (1997) The CLUSTAL_X Windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res 25: 4876–4882.
- 78. Posada D, Crandall KA (1998) MODELTEST: testing the model of DNA substitution. Bioinformatics 14: 817–818.
- 79. Ronquist F, Huelsenbeck JP (2003) MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics 19: 1572–1574.
- 80. Guindon S, Gascuel O (2003) A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Syst Biol 52: 696–704.
- 81. Guindon S, Lethiec F, Duroux P, Gascuel O (2005) PHYML Online - a web server for fast maximum likelihood-based phylogenetic inference. Nucleic Acids Res 33: W557–559.
- 82. Wiegmann BW, MTrautwein MD, Winkler IS, Barr NB, Kim JW, et al. (2011) Episodic radiations in the fly tree of life. Proc Natl Acad Sci USA 108: 5690–5695.
- 83. Wei SJ, Shi M, Sharkey MJ, van Achterberg C, Chen XX (2010) Comparative mitogenomics of Braconidae (Insecta: Hymenoptera) and the phylogenetic utility of mitochondrial genomes with special reference to Holometabolous insects. BMC Genomics 11: 371.
- 84. Felsenstein J (1985) Confidence limits on phylogenies: an approach using the bootstrap. Evolution 39: 783–791.