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The Complete Maternally and Paternally Inherited Mitochondrial Genomes of the Endangered Freshwater Mussel Solenaia carinatus (Bivalvia: Unionidae) and Implications for Unionidae Taxonomy

  • Xiao-Chen Huang,

    Affiliations Center for Watershed Ecology, Institute of Life Science, Nanchang University, Nanchang, P. R. China, School of Life Sciences and Food Engineering, Nanchang University, Nanchang, P. R. China

  • Jun Rong,

    Affiliation Center for Watershed Ecology, Institute of Life Science, Nanchang University, Nanchang, P. R. China

  • Yong Liu,

    Affiliation School of Life Sciences and Food Engineering, Nanchang University, Nanchang, P. R. China

  • Ming-Hua Zhang,

    Affiliation School of Life Sciences and Food Engineering, Nanchang University, Nanchang, P. R. China

  • Yuan Wan,

    Affiliations Center for Watershed Ecology, Institute of Life Science, Nanchang University, Nanchang, P. R. China, School of Life Sciences and Food Engineering, Nanchang University, Nanchang, P. R. China

  • Shan Ouyang,

    Affiliation School of Life Sciences and Food Engineering, Nanchang University, Nanchang, P. R. China

  • Chun-Hua Zhou , (CHZ); (XPW)

    Affiliations Center for Watershed Ecology, Institute of Life Science, Nanchang University, Nanchang, P. R. China, School of Life Sciences and Food Engineering, Nanchang University, Nanchang, P. R. China

  • Xiao-Ping Wu (CHZ); (XPW)

    Affiliations Center for Watershed Ecology, Institute of Life Science, Nanchang University, Nanchang, P. R. China, School of Life Sciences and Food Engineering, Nanchang University, Nanchang, P. R. China

The Complete Maternally and Paternally Inherited Mitochondrial Genomes of the Endangered Freshwater Mussel Solenaia carinatus (Bivalvia: Unionidae) and Implications for Unionidae Taxonomy

  • Xiao-Chen Huang, 
  • Jun Rong, 
  • Yong Liu, 
  • Ming-Hua Zhang, 
  • Yuan Wan, 
  • Shan Ouyang, 
  • Chun-Hua Zhou, 
  • Xiao-Ping Wu


Doubly uniparental inheritance (DUI) is an exception to the typical maternal inheritance of mitochondrial (mt) DNA in Metazoa, and found only in some bivalves. In species with DUI, there are two highly divergent gender-associated mt genomes: maternal (F) and paternal (M), which transmit independently and show different tissue localization. Solenaia carinatus is an endangered freshwater mussel species exclusive to Poyang Lake basin, China. Anthropogenic events in the watershed greatly threaten the survival of this species. Nevertheless, the taxonomy of S. carinatus based on shell morphology is confusing, and the subfamilial placement of the genus Solenaia remains unclear. In order to clarify the taxonomic status and discuss the phylogenetic implications of family Unionidae, the entire F and M mt genomes of S. carinatus were sequenced and compared with the mt genomes of diverse freshwater mussel species. The complete F and M mt genomes of S. carinatus are 16716 bp and 17102 bp in size, respectively. The F and M mt genomes of S. carinatus diverge by about 40% in nucleotide sequence and 48% in amino acid sequence. Compared to F counterparts, the M genome shows a more compact structure. Different gene arrangements are found in these two gender-associated mt genomes. Among these, the F genome cox2-rrnS gene order is considered to be a genome-level synapomorphy for female lineage of the subfamily Gonideinae. From maternal and paternal mtDNA perspectives, the phylogenetic analyses of Unionoida indicate that S. carinatus belongs to Gonideinae. The F and M clades in freshwater mussels are reciprocal monophyly. The phylogenetic trees advocate the classification of sampled Unionidae species into four subfamilies: Gonideinae, Ambleminae, Anodontinae, and Unioninae, which is supported by the morphological characteristics of glochidia.


Unionoid bivalves, known as freshwater mussels (Bivalvia: Unionoida), are one of the most important faunas in freshwater ecosystems, for their potentials to enhance biodiversity and ecosystem functioning (e.g., 1,2). The family Unionidae is the most species-rich of the Unionoida and broadly distributed across North America and Eurasia as well as tropical Mesoamerica, Africa, and southeastern Asia [3]. The Unionidae is composed of six subfamilies: Parreysiinae (Afrotropic, Indomalaya), Modellnaiinae (Indomalaya), Rectidentinae (Indomalaya), Gonideinae (Indomalaya, Palearctic, western Nearctic), Ambleminae (Nearctic, Neotropic), and Unioninae (Palearctic, Nearctic, Indomalaya), in which the latter three subfamilies account for some 551 species (82%) [3-5]. Freshwater mussels have a distinct parasitic stage in the life cycle that involves a host-fish and a highly modified larva, the glochidium [6]. They are sensitive to environmental changes, especially in the post-parasitic phase [7-9].

The global decline of freshwater mussels makes them one of the most imperiled groups of animals [10]. In China, the middle and lower reaches of the Yangtze River have the most diverse freshwater mussel fauna [11]. However, more than 80% of the unionid species in these regions are considered to be threatened or near threatened, and the dominant taxa of bivalves have shifted from large-sized unionids to the small-sized clams [12].

For conservation purposes, we first need to accurately identify unionoid bivalves and estimate genetic diversity in wild populations. Identification and classification of unionoid bivalves are usually based on adult shell morphology. However, different environmental conditions may lead to a certain degree of phenotypic plasticity in conchology. In addition, morphological characteristics of the glochidium, especially the hook type (i.e., hooked, hookless, or axe-head larvae), are very useful to phylogenetic analyses, but only for higher taxonomic categories (e.g., 13,14). On the other hand, molecular data may provide more accurate estimates of the actual phylogenetic relationships and genetic diversity in unionoid bivalves. Owing to a relatively rapid evolutionary dynamics in bivalves, analyses of mitochondrial DNA (mtDNA) sequence data could lead to satisfactory resolution [15-17].

Freshwater mussels are the only freshwater animals that transmit their mtDNA both maternally and paternally; the two other bivalves are marine mussels (Mytiloida) and marine clams (Veneroida) [18,19]. These bivalves possess a peculiar system of mtDNA transmission, termed "doubly uniparental inheritance" (DUI; [20,21]; see 22,23 for reviews) and show two highly divergent gender-associated mitochondrial genomes [16] which still obey the rule of uniparental transmission. In lineages with DUI, both sons and daughters get the F mitogenome (female-transmitted mtDNA, F genome, F-type) from their mother bivalves, as standard maternal inheritance, whereas sons only inherit and transmit the M mitogenome (male-transmitted mtDNA, M genome, M-type) of the father through sperm (e.g., [22]; but see 24-26). The maternal and paternal mitogenomes have a peculiar pattern of tissue distribution: F genome predominates in somatic tissues of both sexes and female gonadal tissues, while M genome is predominant in male gonadal tissues [23,27,28]. In the light of the DUI system, migration rates via different sexes can easily be measured and compared. The M genome can be used as a new marker for the genetic diversity estimate to be compared with the results from the F genome. The combination of F and M genomes can offer new insights into the mitogenome evolutionary history and phylogeographic structure of the freshwater mussels. Additionally, the DUI system provides an excellent model for studying basic biological questions concerning with mtDNA inheritance and the evolution of mitochondrial genomes in general [17,18,23].

Poyang Lake Basin is one of the hotspots inhabiting biodiversity of freshwater mussels in the middle and lower reaches of the Yangtze River, with approximately 75% of the unionid species endemic to China [29-32], including the exclusive species Solenaia carinatus (Heude). In 1877, by virtue of a fossil fragment of S. carinatus collected in the middle reaches of the Yangtze River, Heude [33] thought they belonged to an additional new species, and considered it a fossil species. However, over the subsequent century, the validity of this new species had not been recognized by almost all mollusk taxonomists (e.g., Haas [34]) until Liu and Wu [35] collected live specimens in Wucheng Town, Poyang Lake region, and gave a further description in 1991. Fragmentary fossil specimens of S. carinatus were also collected from the Quaternary of conglomerate layer in the Yellow River bank [36], indicating it once lived in northern China. Currently, due to climate and environmental changes, it only persists at extremely low numbers in Poyang Lake basin [31,32]. Like other Solenaia species, S. carinatus is directly targeted by local people as food [35]. Meanwhile, other anthropogenic events in watersheds such as sand excavation, dam construction, pollution, agriculture runoff, and overfishing of its potential host-fish greatly threaten the survival of this species. With elongate shell lacking hinge teeth, the morphologically inferred taxonomy of genus Solenaia is confusing (e.g., 30,33) and challenged by phylogenetic studies based on partial 16S rRNA sequences of S. oleivora [37] and Chinese Unionidae cox1 sequences [38]. Consequently, prior to developing conservation recovery plans, the taxonomic status of S. carinatus needs to be resolved with more comprehensive analysis.

In this study, we described the first complete maternally and paternally inherited mitochondrial genomes of S. carinatus, and inferred the phylogenetic trees together with the published mitogenome data of unionoids, expecting the classification of unionids could reflect natural relationships with robust molecular evidence. The mitogenomes offer a number of genome-level features (e.g., gene orders, conserved gene clusters) that could be useful for phylogenetic purposes [17] and provide valuable tools for future ecological, population genetic assessments and conservation management of S. carinatus and the related unionoid species.

Materials and Methods

Ethics Statement

All necessary permits were obtained for the described field studies from the Poyang Lake Fishery Administration of Jiangxi Province, China. The handling of mussels was conducted in accordance with the guidelines on the care and use of animals for scientific purposes set by the Institutional Animal Care and Use Committee (IACUC) of Nanchang University, Jiangxi, China.

Sample collection and DNA extraction

Living specimens (N = 4) of Solenaia carinatus were obtained from Poyang Lake (Jiangxi province, China) in 2011-2013 and were sexed by microscopic examination of gonadal tissues. Dissected tissues (gonadal tissue for one male and adductor muscle for one female) were chosen for subsequent DNA extractions and preserved at −80 °C.

Total genomic DNA isolations were performed on the dissected tissues using Wizard® SV Genomic DNA Purification System (Promega) according to the manufacturer's instructions.

The DNA concentration and quality of the extract were measured on the Nanodrop 2000 spectrophotometer (Thermo Scientific) and examined on an agarose gel as well.

PCR amplification and mt genome sequencing

Universal primers were initially used to amplify and sequence short (ca. 500-1000 bp) regions of mtDNA. All obtained sequences of short fragments were BLAST against other unionoids in the GenBank to confirm the corresponding gender-associated mtDNA. Afterwards, specific primers were designed using Primer Premier 5.0 software (Premier Biosoft International).

To prepare the amplicons for primer-walking sequencing, amplification strategies were adjusted in these two mitogenomes due to the sequencing restriction of optimal amplicon length and complex structures (e.g., AT-rich, poly N, and repeated sequences).

For both female and male mtDNA, partial cox1 and rrnL gene sequences were obtained initially using the universal primers of LCO1490/HCO2198 [39] and 16SarL/16SbrH [40] respectively.

For F-type mtDNA, nad1 gene sequences were also obtained using the universal primers Leu-uurF/LoGlyR [41]. Three perfectly matching primers were then designed from these three gene sequences to amplify the F-type mitogenome in three long fragments (cox1-rrnL, rrnL-nad1 and nad1-cox1).

For M-type mtDNA, it was unable to amplify the nad1 gene sequence with universal primers, which could be explained by the rapid substitution rate of the M mtDNA [42,43]. Consequently, two long-range PCR products, approximately 11 kb long rrnL-cox1 and 5 kb long cox1-rrnL, were amplified but amplicons could not be sequenced or thoroughly sequenced. Subsequently, these two long fragments were used as the Sub-PCR templates to avoid coamplification of nuclear genes or contaminated F-type mitochondrial genes. Three pairs of Sub-PCR primers (to amplify the M5, M6 and M7 fragments, Table 1, Figure 1) were designed based on alignment and comparison of M-type mitogenome sequences of the Pyganodon grandis, Quadrula quadrula, and Venustaconcha ellipsiformis (Table 2). Five pairs of specific primers were designed according to Sub-PCR amplicon sequences and previously obtained sequences to amplify the remaining fragments from the M-type mt genome using long-range PCR or general PCR.

Fragment no.Primer namePrimer sequence (5' to 3')Length (bp)

Table 1. Primers used for PCR amplification of female and male Solenaia carinatus mitochondrial genomes.

Download CSV
Figure 1. Gene maps of the F and M mitochondrial genomes of Solenaia carinatus.

Genes illustrated on the outside of the main circle are encoded on the light (L) strand; genes on the inside of the circle are encoded on the heavy (H) strand. tRNA genes are abbreviated by one-letter code of the amino acid (S1 = tRNASer (ucu), S2 = tRNASer (uga), L1 = tRNALeu (uag), and L2 = tRNALeu (uaa)). The inner circle: solid lines represent the sizes and relative positions of amplified and sequenced fragments; the dotted lines represent the fragments that can be amplified but cannot be sequenced directly.

OrderFamilySpeciesGenderAccession numberReference
UnionoidaUnionidaeSolenaia carinatusFKC848654This study
MKC848655This study
Lampsilis ornataFNC_005335Serb & Lydeard, 2003
Unio pictorum FNC_015310Soroka et al., 2010
Cristaria plicataFNC_012716Jiang et al., 2010
Anodonta woodianaFHQ283346Soroka, 2010
Hyriopsis schlegeliiFNC_015110Lin et al. Unpublished
Hyriopsis cumingiiFNC_011763Zheng et al. Unpublished
Unio japanensisFAB055625Okazaki. Unpublished
MAB055624Okazaki. Unpublished
Pyganodon grandis FNC_013661Breton et al., 2009
MFJ809755Breton et al., 2009
Venustaconcha ellipsiformisFFJ809753Breton et al., 2009
MNC_013659Breton et al., 2009
Quadrula quadrulaFNC_013658Breton et al., 2009
MFJ809751Breton et al., 2009
Utterbackia peninsularisFHM856636Breton et al., 2011
MNC_015477Breton et al., 2011
Utterbackia imbecillisHNC_015479Breton et al., 2011
Toxolasma parvusHNC_015483Breton et al., 2011
Lasmigona compressaHNC_015481Breton et al., 2011
MargaritiferidaeMargaritifera falcataHNC_015476Breton et al., 2011
MytiloidaMytilidaeMytilus edulisFNC_006161Boore et al., 2004
MAY823624Breton et al., 2006

Table 2. Mitochondrial genomes used in analyses.

F-female, M-male, H-hermaphrodite (hermaphroditic F-like haplotype)
Download CSV

All the PCR and sequencing strategies were outlined in Figure 1. A full list of primers is presented in Table 1.

TaKaRa Ex Taq polymerase was used to amplify short fragments (<2 kb), and TaKaRa LA Taq polymerase was used to amplify long-range PCR products (>2 kb). PCR conditions were optimized for each reaction, with the annealing temperature adjusted to suit the used primers, extension time set to 1 min per kb of expected product size, and proper cycles adjusted depending upon the amplification efficiency of the primers.

General PCR conditions for Ex Taq were 98 °C for 10 s, followed by 35 cycles of 94 °C for 1 min, 50 °C for 1 min, 72 °C for 1-2 min, and a final extension of 72 °C for 7 min.

The long-range PCR was performed with the following amplification profile: 94 °C for 2 min, followed by 25-35 cycles of 94 °C for 30 s, 55 °C for 30 s, 68 °C for 5-11 min, and a final extension of 72 °C for 10 min.

Mitogenome data were generated using the primer-walking method. PCR products were purified with the SanPrep spin column DNA gel extraction kit or SanPrep spin column PCR product purification kit (Sangon Biotech), and directly sequenced using BigDye Terminator Sequencing Kit and ABI 3730xl DNA Analyzer (Applied Biosystems).

Gene annotation and mitogenome analysis

Sequences were assembled using SeqMan program (DNAstar). Protein-coding genes (PCGs) were initially identified using ORF Finder ( using the invertebrate mitochondrial code and confirmed by blastp and tblastn searches. Transfer RNA genes were inferred with ARWEN [44] and MITOS [45]. Ribosomal RNA genes were identified by homology to mitochondrial rRNA genes of other unionoids, and the ends of rrnL and rrnS genes were assumed to extend to the boundaries of their flanking genes.

The tandem repeats of the whole mitogenome were detected using mreps [46]. Secondary structures of CR regions were predicted in RNAfold WebServer [47] using minimum free energy (MFE) and partition function. Mitochondrial genomes were drawn using GenomeVx [48] followed by manual modification.

Nucleotide composition and codon usage were analyzed with MEGA 5.0 [49]. Strand asymmetry was measured using the formulas GC skew = (G - C)/(G + C) and AT skew = (A - T)/(A + T) [50]. To analyze nucleotide and amino acid sequence variability, pairwise p-Distances (pD) were used and computed with MEGA 5.0 [49]. The divergence of protein genes in synonymous (Ks) and non-synonymous (Ka) sites was calculated with PAML 4.7 [51] using Nei-Gojobori method [52].

Sequence alignment and phylogenetic analyses

In order to elucidate the phylogenetic positions of S. carinatus within Unionoida, all 20 currently available complete F and M mitochondrial genomes of 15 unionoid species were downloaded from the GenBank database (Last accession to databases was in May 2013) (Table 2) and combined with sequences from this study for phylogenetic analyses, using female and male marine mussel Mytilus edulis as outgroup taxa. Sequences of 12 PCGs except gender-specific ORFs and atp8 (due to its absence or constant annotation error in many bivalves [16,53]) were used in phylogenetic analyses. Each 12 PCGs was translated into amino acid sequence using the invertebrate mitochondrial genetic code in MEGA 5 [49], and aligned based on the amino acid sequence using the built-in MUSCLE [54] program with default settings, then the corresponding nucleotide sequences were retro-aligned. Alignments of sequences were manually checked and areas of ambiguous alignment as well as stop codons were excluded. The resulting alignments of trimmed nucleotides or amino acids were concatenated in SequenceMatrix [55] into two datasets with 10200 nucleotides or 3400 amino acids. To assess if the third codon position has saturation that's masking the signals required for a better resolution of the deep nodes, Mesquite 2.75 [56] was used to exclude the third codon positions and produced a new dataset with 6800 nucleotides. To sum up, three datasets were used for phylogenetic analyses: 1) amino acid sequences of 12 PCGs (AA); 2) nucleotide sequences of 12 PCGs (PCG123); 3) the first and the second codon positions of 12 PCGs (PCG12).

MrModeltest [57] and ProtTest [58] were used to select optimal substitution models for nucleotide sequence datasets and amino acid sequence alignment respectively, according to the Akaike Information Criterion (AIC).

The Bayesian phylogenetic analyses were performed using MrBayes 3.2.1 [59]. PCG123 and PCG12 were partitioned by codon sites using GTR+I+G model, while AA using JTT model. Two sets of four chains were conducted to run simultaneously for 1 million generations and trees were sampled every 1000 generations, with a burnin of 25%. Stationarity was considered to be reached when the average standard deviation of split frequencies was less than 0.01.

The codon site based partitioned ML analyses were performed for PCG123/PCG12 in RAxML [60] implemented in raxmlGUI v.1.3 [61], using GTRGAMMAI model of nucleotide substitution with the search strategy set to rapid bootstrapping. ML analysis for AA was performed using PhyML 3.0 online execution [62], with the best chosen amino acid model JTT+I+G+F. Bootstrap supports for ML trees were calculated using 1000 bootstrap replicates for all datasets.

Results and Discussion

General features of the mitochondrial genomes

The maternal and paternal mt genomes of S. carinatus are 16716 and 17102 bp in length, respectively (see Table 3). Sequences are available in GenBank (Accession Number: KC848654 and KC848655). Differences of the genome sizes are mainly due to unassigned regions and cox2. Both of the newly sequenced genomes consist of 13 protein-coding genes for subunits of the respiratory chain complexes, 1 novel gender-specific ORF (i.e., female-specific FORF and male-specific MORF), 2 rRNA genes and 22 tRNA genes. In both F and M mitogenomes, 11 out of typical 37 genes are encoded on the heavy strand, and the remaining 26 genes are on the light strand (Figure 1).

S. carinatus F mt genome   S. carinatus M mt genome
Total size1671617102
No. of gene overlapping26
Size range of gene overlapping1 to 81 to 168
Gender-specific ORF261435

Table 3. Main structural features of the female and male Solenaia carinatus mitochondrial genomes.

For each protein coding genes, start and stop codons are presented in parentheses. Gene lengths are in bp.
Download CSV

Overlapping adjacent genes are common in unionoid mt genomes. Comparing these two newly sequenced sex-linked mt genomes, the M genome shows a more compact structure than the F genome, having more overlapping genes (6 versus 2 overlapping genes), evidently longer PCGs (cox2 and nad6) and smaller CR (Figure 1, Table 3).

nad4L and nad4 overlap in both F and M mt genomes, which is the case for most sequenced unionoid mt genomes [16,43,63-66]. In addition, in S. carinatus M genome, protein-coding gene nad6 overlaps with nad4 and cox3 with cox1, sharing 168 and 8 bp sequences, respectively. The unusual overlap of nad6 and nad4 is also found in M genome of Unio japanesis, but only 4 bp were shared. However, the overlap of cox3 and cox1 has not been found in other unionoid mitogenomes so far. In F mitogenome, only one tRNA gene trnP overlaps with a protein-encoding gene cob. While in M mitogenome, not only tRNA genes overlap with PCG (trnM-nad2) but also different tRNA genes overlap with each other (trnN-trnP, trnQ-trnC).

Protein-coding genes

Gender-specific novel mitochondrial ORFs were already described and confirmed in DUI mtDNAs (Mytilidae: [67], Unionidae: [18], and Veneridae: [68]). In unionids, gender-specific ORFs are localized in the second largest unassigned region of F and M mtDNA [18]. In all the analyzed DUI Mytilus species, however, the novel FORF is found in the largest unassigned region (i.e., the control region) [67].

In S. carinatus mitogenomes, FORF is found in F trnE-trnW intergenic region on the light strand, while MORF is located in M nad4L-trnD unassigned region on the heavy strand. FORF sequence is 261 bp long (86 aa), while MORF is 435 bp (144 aa) (Table 3). Testcode [69] predictions of coding function for the S. carinatus FORF and MORF sequences are all very high. The testcode scores are 0.997 for FORF and 1.224 for MORF, which indicate that these ORFs are coding with the probability of 92% and 100% respectively. These sequences do not show homology with any known proteins using BLAST Tools; therefore, the precise function of these ORFs remains unclear.

In Venustaconcha ellipsiformis, the existence of FORF and MORF was shown by Western blot analysis [18], and the FORF protein was not only present in mitochondria but also in the nuclear membrane and in the nucleoplasm of eggs [43]. These gender-specific ORFs may have a role in the maintenance of sperm mitochondria during embryo development, possibly masking them from the degradation processes [70].

Mitochondrial genomes often contain a variety of nonstandard initiation codons. In the invertebrate mt genomes, there are three conventional start codons (ATG, ATA, and ATT) and three alternative start codons (ATC, TTG, and GTG) [71].

In the S. carinatus M genome, 9 out of 14 PCGs use conventional start codon (ATG, N = 5; ATA, N = 2; ATT, N = 2) and 5 with three alternative start codons (ATC, N = 1; TTG, N = 3; GTG, N = 1) (Table 3). In F genome, except for FORF (ATA), nad4 (ATT), cob (ATC), nad1 (ATC), nad6 (ATC), cox1 (TTG) and atp8 (GTG), 7 out of 14 PCGs start with orthodox ATG (Table 3).

Both F and M genome PCGs have complete termination codon TAG or TAA, with TAG occurs ten times in M and seven times in F mtDNA (Table 3). Being compared to the available bivalve mitogenomes from GenBank, S. carinatus M genome has the longest cox1 (1602 bp), nad2 (996 bp) in unionoid bivalves and the longest nad6 (681 bp) in bivalves, while F genome has the longest cob (1161 bp) in freshwater mussels.

Transfer RNA and ribosomal RNA genes

Both of the obtained S. carinatus F and M mt genomes contain 22 tRNA genes, including two serine tRNA and two leucine tRNA. Most of the tRNA genes are located on the light strand, except for the trnH and trnD. They vary from 61 (trnL1, trnG) to 74 (trnA) bp in F genome and 62 (trnY) to 71 (trnH) bp in M genome.

In both sexes, rrnS and rrnL are encoded on the light strand and are separated by trnK, trnT and trnY (Figure 1), as in all the unionoid mt genomes studied so far. For female and male mt genome of S. carinatus, respectively, the lengths of rrnS/rrnL are 857/1296 and 857/1313 bp (Table 3), and the AT contents are 60.2/61.6% and 60.9/60.7% (Table 4).

AT%GC%AT SkewGC Skew
Whole genome (L strand)60.961.
Protein-coding genes60.060.540.039.5-0.26-
1st codon position55.956.944.143.1-0.10-
2nd codon position59.960.540.139.5-0.46-0.41-0.030.03
3rd codon position64.
tRNA genes62.861.
Control region63.766.536.333.5-0.050-0.50-0.43

Table 4. Nucleotide composition of the female and male Solenaia carinatus mitochondrial genomes.

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Unassigned regions

Both F and M genomes have many unassigned regions (27 in F and 23 in M). Among these, F nad5-trnQ and M trnH-trnQ intergenic regions (Figure 1) are the most likely candidates for the control regions (CR).

Unlike vertebrates, the CR in invertebrates is not well characterized and lacks discrete, conserved sequence blocks used in identification [64], and can greatly vary in numbers, lengths and positions. Long and highly conserved motifs with tandem repeats are likely involved in controlling replication and transcription [17] (e.g., 72,73).

The putative control regions F nad5-trnQ and M trnH-trnQ are the largest unassigned regions (1049 and 848 bp respectively) and have relatively higher A+T content (F=63.7%, M=66.5%, Table 4) compared with other parts of the mt genome. Moreover, there are 8 tandem repeats of a 101 bp element in F nad5-trnQ region and 7 consecutive repeats of a 102 bp element in M trnH-trnQ region with both these elements have the potential to form stem-loop structures (Figure 2). Similar tandem repeat units were also found within the control regions of other unionoids [18] and other animals like nemerteans [74].

Figure 2. Stem-loop structures predicted for tandem repeat elements in putative control regions of female and male Solenaia carinatus mitochondrial genomes.

(A) Female S. carinatus mitochondrial genome. (B) Male S. carinatus mitochondrial genome.

Hence, F nad5-trnQ and M trnH-trnQ intergenic regions of S. carinatus match all three criteria used to identify mitochondrial control regions: length, AT content, and the presence of tandem repeats with stem-loop structure [18].

Base composition and codon usage

For the composition bias showing high values of C% over G%, the F and M coding strand can be considered as the light (L) strand. Though variable values of A+T content in mtDNA are common in the mollusks [53], the composition bias showing high values of A+T% over G+C%. As for S. carinatus, the A+T content of the L strand is also high (F = 60.9%, M = 61.0%, Table 4). The A+T content for PCGs in F and M is 60.0% and 60.5% respectively, and the third codon positions A+T composition is 64.0% and 64.1% in F and M genome respectively, consistent with the typical invertebrate bias favoring codons ending with an A or T [75]. The coding strand of PCGs displays the negative AT- and positive GC-skew, showing bias toward T over A and toward G over C, which is reflected further in the use of synonymous codons (Table S1).

UUU (F) is the most frequent codon in both F and M mt genomes, followed by AUU (I) in F genome and GUU (V) in M genome. UUU is also the most frequent codon in other invertebrate mtDNAs [16,53,76]. Except for the stop codons, CGC is the least used codon in F and M mt genomes, which is also among the least common codon in the mtDNA of other mollusks [53,76].

The extension of cox2 in male mtDNA

M genomes of unionoid bivalves possess a unique, rapidly evolving coding 3' extension of cox2 (Mcox2e) that typically yields an ~80% increase in gene length over that in the corresponding F genomes [77,78].

The male cox2 gene of S. carinatus shows a 543 bp extension, resulting in 79.7% 3' extension compared with the corresponding female cox2 gene, while in other DUI animals, an extra copy of the cox2 gene was found in the M genome of the marine mussel Musculista senhousia [53].

It is noteworthy that the unique extension of Mcox2 is functional. Seasonal expression of MCOX2e in testis suggests that it plays an important role in reproduction [24,79]. MCOX2e is localized to the inner and outer sperm mitochondrial membranes [24], and could be involved in segregation of male mitochondria to the gonad, preventing the M genome from degrading [77], which play a significant role in stability of the DUI system.

Sequence divergences of two gender-associated mitochondrial genomes

Among species with DUI, freshwater mussels exhibit the greatest nucleotide and amino acid divergences between their maternally and paternally inherited mtDNAs and the measured divergences considerably surpass intra- or inter-species values [16].

In S. carinatus, the amino acid divergence and the nucleotide divergence between the F and M genomes are 48% and 40% respectively (Table 5). The observed conspecific genome divergence is much higher than marine mussels in nucleotide (e.g., Musculista senhousia (23%) [53]; Mytilus edulis (23%) [80]), but relatively lower than other freshwater mussels both in amino acid and nucleotide divergence respectively (e.g., Unio japanensis (51%, 43%), Quadrula quadrula (52%, 42%), Pyganodon grandis (51%, 43%) and Venustaconcha ellipsiformis (50%, 41%) [16]).

GenepD ± SEntpD ± SEaaKaKsKa/Ks
rrnS0.291 ± 0.017NANANANA
rrnL0.289 ± 0.012NANANANA
cox10.299 ± 0.0120.311 ± 0.0190.2391 1.1643 0.2054
cox20.369 ± 0.0170.458 ± 0.0330.4031 1.0467 0.3851
cox30.351 ± 0.0190.397 ± 0.0300.3347 1.2319 0.2717
nad10.433 ± 0.0160.470 ± 0.0280.4418 2.3138 0.1909
nad20.496 ± 0.0150.631 ± 0.0260.6806 1.4316 0.4754
nad30.407 ± 0.0250.513 ± 0.0460.5059 0.9738 0.5195
nad40.408 ± 0.0120.500 ± 0.0220.4699 1.1809 0.3979
nad4L0.466 ± 0.0290.660 ± 0.0470.6874 0.9322 0.7374
nad50.432 ± 0.0110.556 ± 0.0200.5335 1.1510 0.4635
nad60.469 ± 0.0230.596 ± 0.0390.6197 1.1898 0.5209
cob0.385 ± 0.0130.411 ± 0.0240.3465 2.3282 0.1488
atp60.438 ± 0.0210.498 ± 0.0320.4962 1.5631 0.3175
atp80.508 ± 0.0370.638 ± 0.0620.7725 1.0234 0.7548
All proteins*0.404 ± 0.0040.481 ± 0.0080.4402 1.3230 0.3327

Table 5. Divergences in female and male Solenaia carinatus mitochondrial genomes.

pD = p-Distances.
SE = Standard Error.pD ± SEnt and pD ± SEaa are pD ± SE at nucleotide and amino acid level respectively.Ka and Ks = divergence of protein genes in non-synonymous (Ka) and synonymous (Ks) sites respectively.Ka/Ks = ratio values between Ka and Ks.NA = Not Available*: Female-specific FORF and male-specific MORF were excluded from the computation.
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Since existing universal primers were designed based on maternally inherited mitochondrial genomes, there are a limited number of universal primers (e.g., universal primers for cox1 and 16S rRNA) could apply to the M genome besides F genome in the freshwater mussels. Hence, knowing the sequence divergences among genes in these two sex-linked mitogenomes will help us select and develop suitable genetic markers, especially the M-specific marker, for population structure analysis and gene flow measurement.

Comparing these two mtDNAs, the most conserved protein-coding genes are cox1, cox3 and cob, while the least conserved are nad4L, atp8 and nad2 (amino acid divergence; Table 5). Synonymous (Ks) and non-synonymous (Ka) values between the two gender-associated mitogenomes vary among genes (Table 5). cox1 has lowest Ka (0.2391) and modest Ks (1.1643), suggesting this gene may be under higher selective pressure. In cob gene, Ka is lower than average but the Ks is the highest with the Ka/Ks value the lowest (0.1488). For nad1 gene, the Ks (2.3138) is the second highest, whereas Ka is modest (0.4418).

Phylogenetic relationships of Unionoida inferred from the mitochondrial genome sequences

The latest classification of Unionidae left out the hinge teeth as a higher-level taxonomic characteristic, and deemed that the subfamily Anodontinae should be demoted to a tribe within Unioninae owing to the shared hooked type and subtriangular external shape of the glochidia [81-83]. However, morphological characteristics of glochidia in these two subfamilies are not in complete consensus. According to Wu [13], the Anodontinae glochidia are elongated triangular (except for the non-parasitic Anodonta arcaeformis that is semicircular) in external shape and have pores on the shell surface, while the Unioninae glochidia are mostly wide triangular with pits on the shell. Therefore, we are more inclined to treat the tribe Anodontini as a subfamily paralleled to Unioninae, in accordance with traditional classifications.

We reconstructed the phylogenetic relationships of freshwater mussels using both F and M genomes of S. carinatus combined with all 20 currently available complete F and M mitochondrial genomes of 15 unionoid bivalves. Three datasets: 1) amino acid sequences of 12 protein-coding genes (AA); 2) nucleotide sequences of 12 protein-coding genes (PCG123); and 3) nucleotide sequences of the first and second codon positions of protein-coding genes (PCG12) were used. ML and BI trees based on all these three datasets have largely congruent topology and were statistically well supported by high bootstrap and posterior probability values in most nodes (Figure 3, Figure S1). Three datasets all have strong support (ML = 100, BI = 1.00) for the reciprocal monophyly of F and M clades, in accordance with the previous viewpoint [16]. Branch lengths indicate that unionoid M genomes have significantly higher substitution rate compared with the corresponding F genomes. The faster evolving nature of M genome may be due to higher rate of M mtDNA replication during spermatogenesis, smaller effective population size for the M genomes, positive selection for the M genomes, relaxed selective constrains for the M genomes, or a combination of these processes [84]. Adding M genome sequences to the traditional routine of F genome sequence phylogenetic analyses could often result in more robust evolutionary relationships than those provided by analyses of F sequences alone [42].

Figure 3. Phylogenetic trees of freshwater mussels inferred from 12 mitochondrial protein-coding gene sequences (except atp8 and gender-specific ORFs).

AA dataset have the best topology. Alternative M clade topology of PCG123 and PCG12 was correspondingly shown on the topside of the tree. Numbers from left to right are from AA, PCG123 and PCG12 alignments respectively. Numbers close to the branching points are ML bootstrap support values (above) and Bayesian posterior probabilities (below). An asterisk indicates that all three dataset-based nodal support values are 100%. The glochidium hook type and the comparison of F genome gene order were also annotated in the corresponding clades.

With currently available mitogenomes, all three datasets support the monophyly of four Unionidae subfamily (i.e., Unioninae, Anodontinae, Ambleminae, and Gonideinae) in both F and M (lack the only Unioninae species) clades by both ML and BI methods.

The AA dataset does not have strong ML support (ML = 59) but have robust BI support (BI = 1.00) for the monophyly of Gonideinae in F clade. The nucleotide sequence datasets (PCG123 and PCG12 datasets), however, do have high ML support and strong BI support (ML = 80, 81; BI = 1.00, 1.00). Additionally, the M genome sequences support the monophyly of Gonideinae with 100% by BI and ML analyses regardless of the dataset used.

The phylogenetic analyses of F genome sequences reveal: (Unioninae + Anodontinae) + (Ambleminae + Gonideinae) of Unionidae. Though the sister group relationship of Ambleminae and Gonideinae is not highly supported by ML in the F clade, it is consistent with the morphological taxonomy based on glochidial hook type [13,14,85,86] (Figure 3).

Amino acid sequences (AA dataset) of the M genome show the sister relationship between Ambleminae and Gonideinae congruent with F genome. However, nucleotide sequences (PCG123 and PCG12 datasets) place Ambleminae being sister to (Unioninae + Gonideinae) in the M clade, resulting from long-branch attraction artifacts, which could be solved by more representative and denser taxon availability of M-type mt genome sequences in the future.

Excluding third codon positions from the analysis (PCG12) significantly decreases support for the sister group relationship of Ambleminae and Gonideinae (ML = 66-50, BI = 1.00-0.61) in the F clade, and cannot solve the long-branch attraction due to the sparse M-type mt genome sampling in the present study.

S. carinatus belongs to the subfamily Gonideinae as revealed by all tree topologies obtained from both F and M genomes (ML = 100%, BI = 1.00), and shares closer relationships with the Asian unionid Unio japanensis, Hyriopsis cumingii and H. schlegelii (Figure 3). Analyses of partial 16S rRNA, however, indicated that Solenaia together with Lamprotula, Hyriopsis, and Ptychorhynchus were the Asian 'amblemines' [37]. It seems that the short sequence of partial 16S rRNA did not contain enough phylogenetic information to resolve the relationships correctly so that the Gonideinae was wrongly nested within Ambleminae. In the Gonideinae, another intriguing mussel is the western North American Gonidea angulata. Gonidea is a monotypic genus, and morphologically and anatomically more similar to freshwater mussels of Southeast Asia than that of North America [81]. We hypothesize that there is an affinity of Gonidea with East Asian Solenaia, especially the species S. triangularis, for the strikingly morphological and habitual similarities, which was also proposed by Simpson [87]. Further molecular phylogeny studies with denser representative taxa and more mitochondrial genomes are needed to test this hypothesis.

Gene order and its phylogenetic implications

Gene order of the animal mtDNA is particularly interesting for problems of deep-level phylogenetic relationships [88] as it is characterized by a large number of states and often remains unchanged over long evolutionary periods [15,89]. Bivalves show frequent and extensive mtDNA variability at intra-genus level, and the mtDNA plasticity is mainly due to variation in number and location of tRNA genes, which rarely concerns protein-coding and rRNA genes [15].

S. carinatus F and M genome gene arrangements are notably different from each other. The transposition of trnH and the gene order inversion of trnD-atp8 contribute to the differences of two gender-associated genomes (Figure 1), consistent with other freshwater mussels [18].

In addition, the rearrangement between cox2 and rrnS is also responsible for the remarkable structural differences between S. carinatus F and M genomes (Figure 1 and Figure 3). Most unionoid taxa (including both F and M mt genomes) have a congruent order and strand orientation of 13 typical PCGs and 2 rRNAs: cox1-cox2-nad3-nad2-rrnS-rrnL-cob-nad5-nad1-nad6-nad4-nad4L-atp8-atp6-cox3. However, the PCG order of F genome in S. carinatus differs substantially from corresponding M genome with the inversion of the relative position of nad2 and nad3.

This F genome cox2-rrnS gene arrangement is not unique for S. carinatus, but is also shown to exist in other available Gonideinae species (i.e., Unio japanensis, Hyriopsis cumingii, H. schlegelii (Table 2), and Lamprotula leai [90]), which suggests that this unique gene order is a synapomorphy for female lineage of the subfamily Gonideinae, and the unique apomorphic PCG arrangement supports its well-established monophyly (Figure 3).


The newly sequenced maternal and paternal mitochondrial genomes of the endangered freshwater mussel Solenaia carinatus diverge by about 48% in amino acid sequence and 40% in nucleotide sequence. Gene arrangements between these two gender-associated genomes are notably different, and the F genome cox2-rrnS gene arrangement is considered a genome-level synapomorphy for female lineage of Gonideinae. Combined with morphological characteristics of glochidia, phylogenetic analyses in the context of complete female and male mitochondrial genomes from 22 freshwater mussel mt genomes strongly indicate S. carinatus belongs to the subfamily Gonideinae and support the classification of the sampled Unionidae species into four subfamilies: Gonideinae, Ambleminae, Anodontinae, and Unioninae.

For phylogenetic analyses of freshwater mussel mt genome data, simply excluding the third codon positions of the protein-coding genes is detrimental to phylogenetic reconstruction, and the conservative amino acid sequences provide the best topologies in both F and M clades, given the underrepresentation in M genome of unionoids.

Glochidia, which transport both maternal and paternal mitochondrial genomes, have limited dispersal abilities mainly restricted to fish patterns; the M-type mitochondria, however, can move as sperm downstream, having greater gene mobility [91]. Furthermore, the M genome evolves much faster than the F genome resulting in higher polymorphism. Consequently, it is expected to be easier to deduce population structure using M instead of F mtDNA data. On the other hand, selective sweeps happen periodically and repeatedly in M lineages while less frequently in F lineages [19]. Therefore, the DUI system can be used as an ideal model to study the mitogenome evolution.

Supporting Information

Figure S1.

Six phylogenetic trees of freshwater mussels inferred from 12 mitochondrial protein-coding gene sequences (except atp8 and gender-specific ORFs).


Table S1.

Codon usage in female and male Solenaia carinatus mitochondrial genomes.


Author Contributions

Conceived and designed the experiments: XPW XCH CHZ. Performed the experiments: XCH YL. Analyzed the data: XCH JR. Contributed reagents/materials/analysis tools: XPW SOY CHZ MHZ YW. Wrote the manuscript: XCH JR.


  1. 1. Vaughn CC, Hakenkamp CC (2001) The functional role of burrowing bivalves in freshwater ecosystems. Freshwater Biology 46: 1431-1446. doi:10.1046/j.1365-2427.2001.00771.x.
  2. 2. Howard JK, Cuffey KM (2006) The functional role of native freshwater mussels in the fluvial benthic environment. Freshwater Biology 51: 460-474. doi:10.1111/j.1365-2427.2005.01507.x.
  3. 3. Graf DL, Cummings KS (2007) Review of the systematics and global diversity of freshwater mussel species (Bivalvia: Unionoida). Journal of Molluscan Studies 73: 291-314. doi:10.1093/mollus/eym029.
  4. 4. Whelan NV, Geneva AJ, Graf DL (2011) Molecular phylogenetic analysis of tropical freshwater mussels (Mollusca: Bivalvia: Unionoida) resolves the position of Coelatura and supports a monophyletic Unionidae. Mol Phylogenet Evol 61: 504-514. doi:10.1016/j.ympev.2011.07.016. PubMed: 21827862.
  5. 5. Bieler R, Carter JG, Coan EV (2010) Classification of bivalve families. In: P. BouchetJ-P Rocroi. Nomenclator of Bivalve Familes. Malacologia: 113-133.
  6. 6. Kat PW (1984) Parasitism and the Unionacea (Bivalvia). Biological Rev 59: 189-207. doi:10.1111/j.1469-185X.1984.tb00407.x.
  7. 7. Yeager MM, Cherry DS, Neves RJ (1994) Feeding and burrowing behaviors of juvenile rainbow mussels, Villosa iris (Bivalvia: Unionidae). Journal of the North American Benthological Society: 217-222.
  8. 8. Strayer DL (2008) Freshwater mussel ecology: a multifactor approach to distribution and abundance. University of California Press.
  9. 9. Geist J (2010) Strategies for the conservation of endangered freshwater pearl mussels (Margaritifera margaritifera L.): a synthesis of Conservation Genetics and Ecology. Hydrobiologia 644: 69-88. doi:10.1007/s10750-010-0190-2.
  10. 10. Lydeard C, Cowie RH, Ponder WF, Bogan AE, Bouchet P et al. (2004) The global decline of nonmarine mollusks. BioScience 54: 321-330.
  11. 11. Prozorova L, Sayenko E, Bogatov V, Wu M, Liu Y (2005) Bivalves of the Yangtze River drainage. The Bulletin of . the Russian Far East Malacological Society 9: 46-58.
  12. 12. Shu F-Y, Wang H-J, Pan B-Z, Liu X-Q, Wang H-Z (2009) Assessment of species status of mollusca in the mid-lower Yangtze lakes. Acta Hydrobiologica Sinica 33: 1051-1058.
  13. 13. Wu X, Liang Y, Wang H, Ouyang S (1999) Morphological characters of glochidia of Unionidae and the taxonomic significance. Acta Hydrobiologica Sinica 23 (supplement): 139-147.
  14. 14. Graf DL, Cummings KS (2006) Palaeoheterodont diversity (Mollusca: Trigonioida+ Unionoida): what we know and what we wish we knew about freshwater mussel evolution. Zoological Journal of the Linnean Society 148: 343-394. doi:10.1111/j.1096-3642.2006.00259.x.
  15. 15. Gissi C, Iannelli F, Pesole G (2008) Evolution of the mitochondrial genome of Metazoa as exemplified by comparison of congeneric species. Heredity (Edinb) 101: 301-320. doi:10.1038/hdy.2008.62. PubMed: 18612321.
  16. 16. Doucet-Beaupré H, Breton S, Chapman EG, Blier PU, Bogan AE et al. (2010) Mitochondrial phylogenomics of the Bivalvia (Mollusca): searching for the origin and mitogenomic correlates of doubly uniparental inheritance of mtDNA. BMC Evol Biol 10: 50. doi:10.1186/1471-2148-10-50. PubMed: 20167078.
  17. 17. Stöger I, Schrödl M (2012) Mitogenomics does not resolve deep molluscan relationships (yet?). Molecular phylogenetics and evolution: In press.
  18. 18. Breton S, Doucet-Beaupré H, Stewart DT, Piontkivska H, Karmakar M et al. (2009) Comparative mitochondrial genomics of freshwater mussels (Bivalvia: Unionoida) with doubly uniparental inheritance of mtDNA: gender-specific open reading frames and putative origins of replication. Genetics 183: 1575-1589. doi:10.1534/genetics.109.110700. PubMed: 19822725.
  19. 19. Doucet-Beaupré H, Blier PU, Chapman EG, Piontkivska H, Dufresne F et al. (2012) Pyganodon (Bivalvia: Unionoida: Unionidae) phylogenetics: a male-and female-transmitted mitochondrial DNA perspective. Mol Phylogenet Evol 63: 430-444. doi:10.1016/j.ympev.2012.01.017. PubMed: 22326838.
  20. 20. Zouros E, Ball AO, Saavedra C, Freeman KR (1994) Mitochondrial DNA inheritance. Nature 368: 818-818. doi:10.1038/368818a0. PubMed: 8159241.
  21. 21. Skibinski DO, Gallagher C, Beynon CM (1994) Mitochondrial DNA inheritance. Nature 368: 817-818. doi:10.1038/368817a0. PubMed: 8159240.
  22. 22. Breton S, Doucet-Beaupré H, Stewart DT, Hoeh WR, Blier PU (2007) The unusual system of doubly uniparental inheritance of mtDNA: isn't one enough? Trends Genet 23: 465-474. doi:10.1016/j.tig.2007.05.011. PubMed: 17681397.
  23. 23. Passamonti M, Ghiselli F (2009) Doubly uniparental inheritance: two mitochondrial genomes, one precious model for organelle DNA inheritance and evolution. DNA Cell Biol 28: 79-89. doi:10.1089/dna.2008.0807. PubMed: 19196051.
  24. 24. Chakrabarti R, Walker JM, Chapman EG, Shepardson SP, Trdan RJ et al. (2007) Reproductive function for a C-terminus extended, male-transmitted cytochrome c oxidase subunit II protein expressed in both spermatozoa and eggs. FEBS Lett 581: 5213-5219. doi:10.1016/j.febslet.2007.10.006. PubMed: 17950289.
  25. 25. Obata M, Sano N, Kawamura K, Komaru A (2007) Inheritance of two M type mitochondrial DNA from sperm and unfertilized eggs to offspring in Mytilus galloprovincialis. Dev Growth Differ 49: 335-344. doi:10.1111/j.1440-169X.2007.00930.x. PubMed: 17501909.
  26. 26. Obata M, Kamiya C, Kawamura K, Komaru A (2006) Sperm mitochondrial DNA transmission to both male and female offspring in the blue mussel Mytilus galloprovincialis. Dev Growth Differ 48: 253-261. doi:10.1111/j.1440-169X.2006.00863.x. PubMed: 16681650.
  27. 27. Garrido-Ramos MA, Stewart DT, Sutherland BW, Zouros E (1998) The distribution of male-transmitted and female-transmitted mitochondrial DNA types in somatic tissues of blue mussels: implications for the operation of doubly uniparental inheritance of mitochondrial DNA. Genome 41: 818-824. doi:10.1139/g98-081.
  28. 28. Venetis C, Theologidis I, Zouros E, Rodakis GC (2006) No evidence for presence of maternal mitochondrial DNA in the sperm of Mytilus galloprovincialis males. Proc Biol Sci 273: 2483-2489. doi:10.1098/rspb.2006.3607. PubMed: 16959639.
  29. 29. Tchang S, Li S-C (1965) Bivalves (Mollusca) of the Poyang Lake and surrounding waters, Kiangsi Province, China, with description of a new species. Acta Zoologica Sinica 3: 309-317.
  30. 30. Liu Y, Zhang W, Wang Y, Wang E (1979) Economic fauna of China: Freshwater mollusks. Science Press. pp. 116-117.
  31. 31. Wu X, Liang Y, Wang H, Xie Z, OuYang S (2000) Distribution and species diversity of freshwater mollusca of lakes along mid-lower reaches of the Yangtze river. Journal of Lake Sciences 12: 111-118.
  32. 32. Xiong L, OuYang S, Wu X (2012) Fauna and standing crop of freshwater mussels in Poyang Lake, China. Chin J Oceanol Limnol 30: 124-135. doi:10.1007/s00343-012-1070-6.
  33. 33. Heude RP (1875-1885) Conchyliologie fluviatile de la Province de Nanking. Paris: Librairie F Savy.
  34. 34. Haas F (1969). Superfamilia Unionacea das Tierreich 88: 1-663.
  35. 35. Liu Y, Wu X (1991) The further description of Solenaia carinatus (Lamellibranchia: Unionidae). Acta Zootaxonomica Sinica 16: 122-123.
  36. 36. Savazzi E, Yao P (1992) Some morphological adaptations in freshwater bivalves. Lethaia 25: 195-209. doi:10.1111/j.1502-3931.1992.tb01384.x.
  37. 37. Huang Y, Liu H, Wu X, OuYang S (2002) Testing the relationships of Chinese freshwater Unionidae (Bivalvia) based on analysis of partial mitochondrial 16S rRNA sequences. Journal of Molluscan Studies 68: 359-363. doi:10.1093/mollus/68.4.359.
  38. 38. Ouyang J, Wu X, Ouyang S, Li S, Zhao D (2011) Phylogenetic analysis of some Chinese freshwater Unionidae based on mitochondrial COI sequences. Journal of Conchology 40: 543.
  39. 39. Folmer O, Black M, Hoeh W, Lutz R, Vrijenhoek R (1994) DNA primers for amplification of mitochondrial cytochrome c oxidase subunit I from diverse metazoan invertebrates. Mol Mar Biol Biotechnol 3: 294-299. PubMed: 7881515.
  40. 40. Simon C, Frati F, Beckenbach A, Crespi B, Liu H et al. (1994) Evolution, weighting, and phylogenetic utility of mitochondrial gene sequences and a compilation of conserved polymerase chain reaction primers. Annals of the Entomological Society of America 87: 651-701.
  41. 41. Serb JM, Buhay JE, Lydeard C (2003) Molecular systematics of the North American freshwater bivalve genus Quadrula (Unionidae: Ambleminae) based on mitochondrial ND1 sequences. Mol Phylogenet Evol 28: 1-11. doi:10.1016/S1055-7903(03)00026-5. PubMed: 12801467.
  42. 42. Walker JM, Bogan AE, Bonfiglio EA, Campbell DC, Christian AD et al. (2007) Primers for amplifying the hypervariable, male-transmitted COII-COI junction region in amblemine freshwater mussels (Bivalvia: Unionoidea: Ambleminae). Molecular Ecology Notes 7: 489-491.
  43. 43. Breton S, Stewart DT, Shepardson S, Trdan RJ, Bogan AE et al. (2011) Novel protein genes in animal mtDNA: a new sex determination system in freshwater mussels (Bivalvia: Unionoida)? Mol Biol Evol 28: 1645-1659. doi:10.1093/molbev/msq345. PubMed: 21172831.
  44. 44. Laslett D, Canbäck B (2008) ARWEN: a program to detect tRNA genes in metazoan mitochondrial nucleotide sequences. Bioinformatics 24: 172-175. doi:10.1093/bioinformatics/btm573. PubMed: 18033792.
  45. 45. Bernt M, Donath A, Jühling F, Externbrink F, Florentz C et al. (2012) MITOS: Improved de novo Metazoan Mitochondrial Genome. Annotation - Molecular Phylogenetics and Evolution.
  46. 46. Kolpakov R, Bana G, Kucherov G (2003) mreps: efficient and flexible detection of tandem repeats in DNA. Nucleic Acids Res 31: 3672-3678. doi:10.1093/nar/gkg617. PubMed: 12824391.
  47. 47. Gruber AR, Lorenz R, Bernhart SH, Neuböck R, Hofacker IL (2008) The vienna RNA websuite. Nucleic Acids Res 36: W70-W74. doi:10.1093/nar/gkn188. PubMed: 18424795.
  48. 48. Conant GC, Wolfe KH (2008) GenomeVx: simple web-based creation of editable circular chromosome maps. Bioinformatics 24: 861-862. doi:10.1093/bioinformatics/btm598. PubMed: 18227121.
  49. 49. Tamura K, Peterson D, Peterson N, Stecher G, Nei M et al. (2011) MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol 28: 2731-2739. doi:10.1093/molbev/msr121. PubMed: 21546353.
  50. 50. Perna NT, Kocher TD (1995) Patterns of nucleotide composition at fourfold degenerate sites of animal mitochondrial genomes. J Mol Evol 41: 353-358. doi:10.1007/BF01215182. PubMed: 7563121.
  51. 51. Yang Z (2007) PAML 4: phylogenetic analysis by maximum likelihood. Mol Biol Evol 24: 1586-1591. doi:10.1093/molbev/msm088. PubMed: 17483113.
  52. 52. Nei M, Gojobori T (1986) Simple methods for estimating the numbers of synonymous and nonsynonymous nucleotide substitutions. Mol Biol Evol 3: 418-426. PubMed: 3444411.
  53. 53. Passamonti M, Ricci A, Milani L, Ghiselli F (2011) Mitochondrial genomes and Doubly Uniparental Inheritance: new insights from Musculista senhousia sex-linked mitochondrial DNAs (Bivalvia Mytilidae). BMC Genomics 12: 442. doi:10.1186/1471-2164-12-442. PubMed: 21896183.
  54. 54. Edgar RC (2004) MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res 32: 1792-1797. doi:10.1093/nar/gkh340. PubMed: 15034147.
  55. 55. Vaidya G, Lohman DJ, Meier R (2011) SequenceMatrix: concatenation software for the fast assembly of multi-gene datasets with character set and codon information. Cladistics 27: 171-180. doi:10.1111/j.1096-0031.2010.00329.x.
  56. 56. Maddison WP, Maddison DR (2011) Mesquite: a modular system for evolutionary analysis. version 2.75
  57. 57. Nylander J (2004) MrModeltest v2. Program distributed by the author. Evolutionary Biology Centre, Uppsala University.
  58. 58. Abascal F, Zardoya R, Posada D (2005) ProtTest: selection of best-fit models of protein evolution. Bioinformatics 21: 2104-2105. doi:10.1093/bioinformatics/bti263. PubMed: 15647292.
  59. 59. Ronquist F, Teslenko M, van der Mark P, Ayres DL, Darling A, et al. (2012) MrBayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space. Systematic Biology 61: 539-542.
  60. 60. Stamatakis A (2006) RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models. Bioinformatics 22: 2688-2690. doi:10.1093/bioinformatics/btl446. PubMed: 16928733.
  61. 61. Silvestro D, Michalak I (2012) raxmlGUI: a graphical front-end for RAxML. Organisms Diversity and Evolution 12: 335-337. doi:10.1007/s13127-011-0056-0.
  62. 62. Guindon S, Dufayard J-F, Lefort V, Anisimova M, Hordijk W, et al. (2010) New algorithms and methods to estimate maximum-likelihood phylogenies: assessing the performance of PhyML 3.0. Systematic biology 59: 307-321.
  63. 63. Jiang W-P, Li J-L, Zheng R-L, Wang GL (2010) Analysis of complete mitochondrial genome of Cristaria plicata. Hereditas 32: 153-162. PubMed: 20176560.
  64. 64. Serb JM, Lydeard C (2003) Complete mtDNA sequence of the North American freshwater mussel, Lampsilis ornata (Unionidae): an examination of the evolution and phylogenetic utility of mitochondrial genome organization in Bivalvia (Mollusca). Mol Biol Evol 20: 1854-1866. doi:10.1093/molbev/msg218. PubMed: 12949150.
  65. 65. Soroka M, Burzyński A (2010) Complete sequences of maternally inherited mitochondrial genomes in mussels Unio pictorum (Bivalvia, Unionidae). J Appl Genet 51: 469-476. doi:10.1007/BF03208876. PubMed: 21063064.
  66. 66. Soroka M (2010) Characteristics of mitochondrial DNA of unionid bivalves (Mollusca: Bivalvia: Unionidae). II. Comparison of complete sequences of maternally inherited mitochondrial genomes of Sinanodonta woodiana and Unio pictorum. Folia Malacologica 18: 189-209. doi:10.2478/v10125-010-0016-x.
  67. 67. Breton S, Ghiselli F, Passamonti M, Milani L, Stewart DT et al. (2011) Evidence for a fourteenth mtDNA-encoded protein in the female-transmitted mtDNA of marine mussels (Bivalvia: Mytilidae). PLOS ONE 6: e19365. doi:10.1371/journal.pone.0019365. PubMed: 21556327.
  68. 68. Ghiselli F, Milani L, Guerra D, Chang PL, Breton S et al. (2013) Structure, Transcription, and Variability of Metazoan Mitochondrial Genome: Perspectives from an Unusual Mitochondrial Inheritance System. Genome Biol Evol 5: 1535-1554. doi:10.1093/gbe/evt112. PubMed: 23882128.
  69. 69. Fickett JW (1982) Recognition of protein coding regions in DNA sequences. Nucleic Acids Res 10: 5303-5318. doi:10.1093/nar/10.17.5303. PubMed: 7145702.
  70. 70. Milani L, Ghiselli F, Guerra D, Breton S, Passamonti M (2013) A comparative analysis of mitochondrial ORFans: new clues on their origin and role in species with doubly uniparental inheritance of mitochondria. Genome Biol Evol 5: 1408-1434. doi:10.1093/gbe/evt101. PubMed: 23824218.
  71. 71. Wolstenholme DR (1992) Animal mitochondrial DNA: structure and evolution. Int Rev Cytol 141: 173-216. doi:10.1016/S0074-7696(08)62066-5. PubMed: 1452431.
  72. 72. Akasaki T, Nikaido M, Tsuchiya K, Segawa S, Hasegawa M et al. (2006) Extensive mitochondrial gene arrangements in coleoid Cephalopoda and their phylogenetic implications. Mol Phylogenet Evol 38: 648-658. doi:10.1016/j.ympev.2005.10.018. PubMed: 16442311.
  73. 73. Yuan Y, Li Q, Yu H, Kong L (2012) The Complete Mitochondrial Genomes of Six Heterodont Bivalves (Tellinoidea and Solenoidea): Variable Gene Arrangements and Phylogenetic Implications. PLOS ONE 7: e32353. doi:10.1371/journal.pone.0032353. PubMed: 22384227.
  74. 74. Chen H-X, Sun S-C, Sundberg P, Ren W-C, Norenburg JL (2012) A comparative study of nemertean complete mitochondrial genomes, including two new ones for Nectonemertes cf. mirabilis and Zygeupolia rubens, may elucidate the fundamental pattern for the phylum Nemertea. BMC Genomics 13: 139. doi:10.1186/1471-2164-13-139. PubMed: 22507536.
  75. 75. Brown W (1985) The mitochondrial genome of animals. Molecular evolutionary genetics. Plenum Press, New York. pp. 95-130.
  76. 76. Mizi A, Zouros E, Moschonas N, Rodakis GC (2005) The complete maternal and paternal mitochondrial genomes of the Mediterranean mussel Mytilus galloprovincialis: implications for the doubly uniparental inheritance mode of mtDNA. Mol Biol Evol 22: 952-967. doi:10.1093/molbev/msi079. PubMed: 15647523.
  77. 77. Curole JP, Kocher TD (2002) Ancient sex-specific extension of the cytochrome c oxidase II gene in bivalves and the fidelity of doubly-uniparental inheritance. Mol Biol Evol 19: 1323-1328. doi:10.1093/oxfordjournals.molbev.a004193. PubMed: 12140244.
  78. 78. Curole JP, Kocher TD (2005) Evolution of a unique mitotype-specific protein-coding extension of the cytochrome c oxidase II gene in freshwater mussels (Bivalvia: Unionoida). J Mol Evol 61: 381-389. doi:10.1007/s00239-004-0192-7. PubMed: 16082567.
  79. 79. Chapman EG, Piontkivska H, Walker JM, Stewart DT, Curole JP et al. (2008) Extreme primary and secondary protein structure variability in the chimeric male-transmitted cytochrome c oxidase subunit II protein in freshwater mussels: Evidence for an elevated amino acid substitution rate in the face of domain-specific purifying selection. BMC Evol Biol 8: 165. doi:10.1186/1471-2148-8-165. PubMed: 18513440.
  80. 80. Breton S, Burger G, Stewart DT, Blier PU (2006) Comparative analysis of gender-associated complete mitochondrial genomes in marine mussels (Mytilus spp.). Genetics 172: 1107-1119. PubMed: 16322521.
  81. 81. Graf DL (2002) Molecular phylogenetic analysis of two problematic freshwater mussel genera (Unio and Gonidea) and a re-evaluation of the classification of Nearctic Unionidae (Bivalvia: Palaeoheterodonta: Unionoida). Journal of Molluscan Studies 68: 65-71. doi:10.1093/mollus/68.1.65.
  82. 82. Campbell DC, Serb JM, Buhay JE, Roe KJ, Minton RL et al. (2005) Phylogeny of North American amblemines (Bivalvia, Unionoida): prodigious polyphyly proves pervasive across genera. Invertebrate Biology 124: 131-164. doi:10.1111/j.1744-7410.2005.00015.x.
  83. 83. Bouchet P, Rocroi J-P, Bieler R, Carter JG, Coan EV (2010) Nomenclator of bivalve families with a classification of bivalve families. Malacologia 52: 1-184. doi:10.4002/040.052.0101.
  84. 84. Stewart DT, Kenchington ER, Singh RK, Zouros E (1996) Degree of selective constraint as an explanation of the different rates of evolution of gender-specific mitochondrial DNA lineages in the mussel Mytilus. Genetics 143: 1349-1357. PubMed: 8807306.
  85. 85. Lefevre G, Curtis WC (1910) Reproduction and parasitism in the Unionidae. Journal of Experimental Zoology 9: 79-116. doi:10.1002/jez.1400090105.
  86. 86. Deein G, Pongsri C, Rattanadaeng P, Prateenpasen R (2008) Glochidium shell morphology of Solenaia khwaenoiensis Panha & Deeon, 2003 (Bivalvia: Unionidae). Natural History Journal of Chulalongkorn University 8: 61-64.
  87. 87. Simpson CT (1914) Descriptive Catalogue of the Naiades, Or Pearly Freshwater Mussels. Detroit, Michigan. Bryant Walker.
  88. 88. Boore JL (2006) The use of genome-level characters for phylogenetic reconstruction. Trends Ecol Evol 21: 439-446. doi:10.1016/j.tree.2006.05.009. PubMed: 16762445.
  89. 89. Lavrov DV, Lang BF (2005) Poriferan mtDNA and animal phylogeny based on mitochondrial gene arrangements. Syst Biol 54: 651-659. doi:10.1080/10635150500221044. PubMed: 16126659.
  90. 90. Chen L, Wang G, Li J (2012) Analysis on complete F type of mitochondrial genome in Lamprotula leai. Acta Ecologica Sinica 32: 2420-2429. doi:10.5846/stxb201109271418.
  91. 91. Krebs RA, Borden WC Evans NtM, Doerder FP (2013) Differences in population structure estimated within maternally- and paternally-inherited forms of mitochondria in Lampsilis siliquoidea (Bivalvia: Unionidae). Biological Journal of the Linnean Society 109: 229-240. doi:10.1111/bij.12025.