Literature DB >> 27767191

The first complete mitochondrial genome for the subfamily Limacodidae and implications for the higher phylogeny of Lepidoptera.

Qiu-Ning Liu1, Zhao-Zhe Xin1, Dan-Dan Bian1, Xin-Yue Chai1, Chun-Lin Zhou1, Bo-Ping Tang1.   

Abstract

The mitochondrial genome (mitogenome) provides important information for understanding molecular evolution and phylogeny. To determine the systematic status of the family Limacodidae within Lepidoptera, we infer a phylogenetic hypothesis based on the complete mitogenome of Monema flavescens (Lepidoptera: Limacodidae). The mitogenome of M. flavescens is 15,396 base pairs (bp), and includes 13 protein-coding genes (PCGs), two ribosomal RNA (rRNA) genes, 22 transfer RNA (tRNA) genes, and a control region (CR). The AT skew of this mitogenome is slightly negative and the nucleotide composition is also biased towards A + T nucleotides (80.5%). All PCGs are initiated by ATN codons, except for the cytochrome c oxidase subunit 1 (cox1) gene, which is initiated by CGA. All tRNAs display the typical clover-leaf structure characteristic of mitochondrial tRNAs, with the exception of trnS1 (AGN). The mitogenome CR is 401 bp and consists of several features common to Lepidoptera. Phylogenetic analysis using Bayesian Inference (BI) and Maximum Likelihood (ML) based on nucleotide and amino acid sequences of 13 mitochondrial PCGs indicates that M. flavescens belongs to Zygaenoidea. We obtain a well-supported phylogenetic tree consisting of Yponomeutoidea + (Tortricoidea + Zygaenoidea + (Papilionoidea + (Pyraloidea + (Noctuoidea + (Geometroidea + Bombycoidea))))).

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Year:  2016        PMID: 27767191      PMCID: PMC5073316          DOI: 10.1038/srep35878

Source DB:  PubMed          Journal:  Sci Rep        ISSN: 2045-2322            Impact factor:   4.379


The insect mitogenome is a circular molecule 14–19 kilobases in length. It contains 22 tRNAs, 13 PCGs, ATPase subunits 6 and 8 (atp6 and atp8), cox1-cox3, cytochrome B (cob), NADH dehydrogenase subunits 1–6 and 4L (nad1-6 and nad4L), the small and large subunit rRNAs (rrnL and rrnS), and a non-coding element termed the A + T-rich region (CR), which contains initiation sites for transcription and replication12. Because of their unique features, including coding content conservation, maternal inheritance, and rapid evolution, mitogenomes have been informative in diverse studies of molecular evolution, such as phylogenetics, population genetics, and comparative and evolutionary genomics34. Recent advances in sequencing technologies have led to the rapid increase in mitogenomic data in Genbank, including Lepidopteran mitogenomes. Lepidoptera is the second largest order of insects, accounting for more than 160,000 species5. Zygaenidae is a species-rich superfamily of predominantly diurnal moths with a worldwide distribution. This family is particularly diverse in tropical and subtropical Asia and the Palaearctic region6. Because of the broad geographical distribution of species, extensive variation in coloration patterns, and an intriguing chemical defence system, Zygaenidae is of great interest to lepidopterists and evolutionary biologists7. To date, more than 200 complete or near-complete Lepidopteran mitogenomes are available. However, only one mitogenome of Zygaenoidea has been sequenced8. Monema flavescens Walker, 1855 is a moth of the Limacodidae family found in Korea, Japan, China, and the Russian Far East. The mitogenome of M. flavescens has not been sequenced9. A better understanding of the Lepidopteran mitogenome requires an expansion of taxon and genome samplings. In this study, we sequence and describe the complete mitogenome of M. flavescens. We reconstruct a phylogenetic tree based on PCG sequences in order to analyse the evolutionary relationships among Lepidopteran insects. The assembly and annotation of the M. flavescens mitogenome will further the study of Zygaenidea mitochondrial genome architecture and phylogenetics. Furthermore, characterization of the M. flavescens mitogenome may provide novel insights into the mechanisms underlying mitogenome evolution.

Methods

DNA Extraction

The moths of M. flavescens were collected in Yancheng, Jiangsu Province. Total DNA was isolated using the Genomic DNA Extraction Kit (SangonBiotech, China) according to the manufacturer’s instructions. Extracted DNA was used to amplify the complete mitogenome by PCR.

PCR Amplification and Sequencing

For amplification of the M. flavescens mitogenome, primer sets were designed based upon mitogenomic sequences obtained from other Lepidopteran insects1011. PCR was performed under the following conditions: 3 min at 94 °C, followed by 35 cycles of 30 s at 94 °C, 1–3 min at 48–60 °C, and 10 min at 72 °C. All amplifications were performed on an Eppendorf Mastercycler and Mastercycler gradient in 50 μL reaction volumes. The PCR products were separated by agarose gel electrophoresis (1% w/v) and purified using a DNA gel extraction kit (Transgene, China). The purified PCR products were ligated into the T-vector (SangonBiotech, China) and sequenced at least three times.

Sequence Assembly and Gene Annotation

Sequence annotation was performed using NCBI BLAST (http://blast.ncbi.nlm.nih.gov/Blast) and the DNAStar package (DNAStar Inc. Madison, WI, USA). The identity of tRNA genes was verified using the tRNAscan-SE program (http://lowelab.ucsc.edu/tRNAscan-SE/)12. The nucleotide sequences of PCGs were translated with the invertebrate mitogenome genetic code. Alignments of M. flavescens PCGs with various Lepidopteran mitogenomes were performed using Clustal X13. Composition skewness was calculated according to the following formulas: AT skew = [A − T]/[A + T]; GC ske = [G−C]/[G + C]. Codon usage was calculated using MEGA version 6.06. Tandem repeats in the A + T-rich region were predicted using the Tandem Repeats Finder program (http://tandem.bu.edu/trf/trf.html)14.

Phylogenetic Analysis

To reconstruct the phylogenetic relationships among Lepidopteran insects, the complete mitogenomes of Lepidopteran species were obtained from GenBank (Table 1). The amino acid sequences for each of the 13 mitochondrial PCGs were aligned using default settings and concatenated. This concatenated set of amino acid and nucleotide sequences was used for phylogenetic analysis, which was performed with the Bayesian inference (BI) and Maximum Likelihood (ML) methods using MrBayes v 3.2.215 and raxmlGUI, respectively. Alignments of individual genes were performed using MAFFT16. Gblocks was used to identify conserved regions and remove unreliably aligned sequences within the datasets17. For the BI and ML analyses, GTR + I + G was the appropriate model for the nucleotide sequences using MrModeltest 2.3 based on Akaike’s information criterion (AIC)18. MtArt + I + G + F was the appropriate model for the amino acid sequence dataset according to ProtTest 3.4 based on AIC19. Four independent runs were conducted for 10,000,000 generations, and each was sampled every 1,000 generations. All analyses converged within 10,000,000 generations. We assessed the credibility of the results in two ways. First, the average standard deviation of split frequencies was less than 0.05 in the process of Bayesian. Second, we observed sufficient parameter sampling using software Tracer v1.6. The value of ESS was more than 200. This cumulatively suggested that our data was convergent. Posterior probabilities over 0.95 were interpreted as strongly supported. The mitogenomes of Hepialoidea insects were used as outgroups. The resulting phylogenetic trees were visualized in FigTree v1.4.2.
Table 1

List of the complete mitogenomes of Lepidopteran insects.

SuperfamilyFamilySubfamilySpeciesGenbank No.
ZygaenoideaLimacodidae Monema flavescensKU946971
ZygaenoideaZygaenidaeChalcosiinaeRhodopsona rubiginosaKM244668
BombycoideaBombycidaeBombycinaeBombyx mandarinaAB070263
BombycoideaBombycidaeBombycinaeBombyx moriAF149768
BombycoideaBombycidaeBombycinaeBombyx huttoniKP216766
BombycoideaBombycidaeBombycinaeRondotia mencianaKC881286
BombycoideaSaturniidaeSaturniinaeSamia cynthia riciniJN215366
BombycoideaSaturniidaeSaturniinaeActias seleneJX186589
BombycoideaSaturniidaeSaturniinaeAntheraea pernyiAY242996
BombycoideaSaturniidaeSaturniinaeAntheraea yamamaiEU726630
BombycoideaSaturniidaeSaturniinaeEriogyna pyretorumFJ685653
BombycoideaSaturniidaeSaturniinaeSaturnia boisduvaliiEF622227
BombycoideaSphingidaeSphinginaeManduca sextaEU286785
BombycoideaSphingidaeSphinginaeSphinx morioKC470083
BombycoideaSaturniidaeSaturniinaeAntheraea frithiKJ740437
BombycoideaSaturniidaeSaturniinaeAttacus atlasKF006326
BombycoideaSaturniidaeSaturniinaeActias artemis alienaKF927042
BombycoideaSaturniidaeSaturniinaeSamia canningiKJ159909
GeometroideaGeometridaeEnnominaeBiston panterinariaJX406146
GeometroideaGeometridaeEnnominaePhthonandria atrilineataEU569764
GeometroideaGeometridaeEnnominaeJankowskia athletaKR822683
GeometroideaGeometridaeEnnominaeApocheima cinerariumKF836545
GeometroideaGeometridaeLarentiinaeOperophtera brumataKP027400
HepialoideaHepialidae Ahamus yunnanensisHM744695
HepialoideaHepialidae Thitarodes renzhiensisHM744694
HepialoideaHepialidae Hepialus xiaojinensisKT834973
HepialoideaHepialidae Thitarodes puiKF908880
HepialoideaHepialidae Thitarodes gonggaensisKP718817
HepialoideaHepialidae Napialus hunanensisKJ632465
NoctuoideaErebidaeLymantriinaeLymantria disparFJ617240
NoctuoideaErebidaeArctiinaeHyphantria cuneaGU592049
NoctuoideaErebidaeAganainaeAsota plana lacteataKJ173908
NoctuoideaErebidaeErebinaeCatocala deuteronymphaKJ432280
NoctuoideaEuteliidaeEuteliinaeEutelia adulatricoidesKJ185131
NoctuoideaNolidaeChloephorinaeGabala argentataKJ410747
NoctuoideaNolidaeRisobinaeRisoba prominensKJ396197
NoctuoideaNoctuidaeAmphipyrinaeSesamia inferensJN039362
NoctuoideaNoctuidaeAmphipyrinaeSpodoptera frugiperdaKM362176
NoctuoideaNoctuidaeHeliothinaeHelicoverpa armigeraGU188273
NoctuoideaNotodontidaePhalerinaePhalera flavescensJF440342
NoctuoideaNotodontidaeThaumetopoeinaeOchrogaster luniferAM946601
PapilionoideaHesperiidaeHesperiinaeOchlodes venataHM243593
PapilionoideaLycaenidaeAphnaeinaeSpindasis takanonisHQ184266
PapilionoideaLycaenidaeTheclinaeProtantigius superansHQ184265
PapilionoideaNymphalidaeApaturinaeApatura metisJF801742
PapilionoideaNymphalidaeApaturinaeSasakia charondaAP011824
PapilionoideaNymphalidaeCalinaginaeCalinaga davidisHQ658143
PapilionoideaNymphalidaeDanainaeEuploea mulciberHQ378507
PapilionoideaNymphalidaeHeliconiinaeFabriciana nerippeJF504707
PapilionoideaNymphalidaeLibytheinaeLibythea celtisHQ378508
PapilionoideaNymphalidaeSatyrinaeHipparchia autonoeGQ868707
PapilionoideaPapilionidaePapilioninaeGraphium chironidesKP159289
PapilionoideaPapilionidaePapilioninaePapilio marahoFJ810212
PapilionoideaPapilionidaeParnassiinaeParnassius apolloKF746065
PapilionoideaPapilionidaeParnassiinaeParnassius cephalusKP100655
PapilionoideaPieridaePierinaeAporia crataegiJN796473
PapilionoideaPieridaePierinaePieris meleteEU597124
PapilionoideaPieridaeColiadinaeColias erateKP715146
PyraloideaCrambidaeSpilomelinaeMaruca vitrataKJ466365
PyraloideaCrambidaeCrambinaeDiatraea saccharalisFJ240227
PyraloideaCrambidaePyraustinaeCnaphalocrocis medinalisJN246082
PyraloideaPyralidaeGalleriinaeCorcyra cephalonicaHQ897685
PyraloideaPyralidaePhycitinaePlodia interpunctellaKP729178
PyraloideaPyralidaeEpipaschiinaeLista haraldusalisKF709449
TortricoideaTortricidaeOlethreutinaeRhyacionia leptotubulaJX028270
TortricoideaTortricidaeOlethreutinaeSpilonota lechriaspisHM204705
TortricoideaTortricidaeOlethreutinaeGrapholita molestaHQ392511
TortricoideaTortricidaeTortricinaeAdoxophyes oranaJX872403
TortricoideaTortricidaeTortricinaeAcleris fimbrianaHQ662522
TortricoideaTortricidaeTortricinaeAdoxophyes honmaiDQ073916
YponomeutoideaLyonetiidae Leucoptera malifoliellaJN790955
YponomeutoideaYponomeutidaePraydinaePrays oleaeKM874804
YponomeutoideaPlutellidae Plutella xylostellaJF911819

Results and Discussion

Genome Organization and Base Composition

The mitogenome of M. flavescens is a closed circular molecule 15,396 bp in size. The gene content is typical of other Lepidopteran insect mitogenomes, including 22 tRNA genes (one for each amino acid and two each for leucine and serine), 13 PCGs (cox1-3, nad1-6, nad4L, cob, atp6, and atp8), two mitochondrial rRNA genes (rrnS and rrnL), and a major non-coding region known as the CR. The majority strand (J strand) encodes 23 genes, while the opposite (N) strand encodes 14 genes (Fig. 1, Table 2). The arrangement of the genes within Lepidopteran mitogenomes is usually highly conserved. While the order and orientation of genes in the M. flavescens mitogenome are identical to the only other Zygaenoidea insect sequenced to date, this gene order differs from ancestral insects. Specifically, the placement of the trnM gene between the CR and trnI in the M. flavescens mitogenome (CR, trnM, trnI, trnQ, nad2) differs from ancestral insects in which trnM is located between trnQ and nad2 (CR, trnI, trnQ, trnM, nad2)20. However, the ancestral arrangement of the trnM gene cluster was also found in ghost moths21. This result in M. flavescens supports the hypothesis that the ancestral arrangement of the trnM gene cluster underwent rearrangement after Hepialoidea diverged from other Lepidopteran lineages. The tRNA gene rearrangements are commonly considered to be a consequence of tandem duplication in a portion of the mitogenome, followed by random or non-random loss of the duplicated copies22.
Figure 1

Circular map of the mitogenome of M. flavescens.

The tRNA genes are labelled according to the IUPAC-IUB. Single-letter amino acids above the bar indicate coding sequence on the major strand, whereas amino acids listed below the bar indicate coding sequence on the minor strand. The one-letter symbols S1, S2, L1, and L2 denote codons trnS1(AGN), trnS2(UCN), trnL1(CUN), and trnL2(UUR), respectively.

Table 2

Summary of the mitogenome of M. flavescens.

GeneDirectionLocationSizeAnticodonStart codonStop codonIntergenic nucleotides
trnMF1–6868CAT2
trnIF71–13565GAT−3
trnQR133–20169TTG50
nad2F252–12661015ATTT−3
trnWF1264–133269TCA−9
trnCR1324–138865GCA5
trnYR1394–146267GTA3
cox1F1466–29961531CGAT0
trnL2(UUR)F2997–306569TAA0
cox2F3066–3747682ATGT0
trnKF3748–382073CTT16
trnDF3837–389963GTC0
atp8F3900–4061162ATTTAA−7
atp6F4055–4728674ATGTAA3
cox3F4732–5517786ATGTAA2
trnGF5520–558869TCC0
nad3F5589–5942354ATTTAA6
trnAF5949–601870TGC36
trnRF6055–612167TCG1
trnNF6123–619674GTT1
trnS1(AGN)F6198–626366GCT10
trnEF6274–634370TTC−2
trnFR6342–641069GAA7
nad5R6418–81361719ATCTAA15
trnHR8152–821968GTG0
nad4R8220–95551336ATGT0
nad4LR9556–9839284ATAA24
trnTF9864–992764TGT0
trnPR9928–999366TGG8
nad6F10,002–10,520519ATATAA4
cobF10,525–11,6741150ATGT0
trnS2(UCN)F11,675–11,74470TGA−5
nad1R11,770–12,708939ATGTAA0
trnL1(CUN)R12,709–12,77971TAG0
rrnLR12,780–14,13813590
trnVR14,139–14,20365TAC0
rrnSR14,204–14,9957920
A + T-rich region 14,996–15,396401

Skewness, Overlapping, and Intergenic Spacer Regions

The mitogenome of M. flavescens has a 29 bp overlap between genes in six locations, with the longest 9 bp overlap located in between trnW and trnC. The mitogenome of M. flavescens contains 167 bp of intergenic spacer sequence spread over 17 regions, ranging in size from 1 to 50 bp (Table 2). The longest spacer sequence is 50 bp located between the trnQ and nad2 genes, and it is extremely A + T rich. The nucleotide composition of the M. flavescens mitogenome is as follows: A = 6,275 (40.8%), T = 6,115 (39.7%), G = 1,164 (7.5%), and C = 1,842 (12.0%). As observed in other Lepidopterans, the nucleotide composition of the M. flavescens mitogenome is A + T rich (80.5%). This enrichment is lower than in other species, such as D. punctiferalis (80.6%), M. vitrata (80.7%), M. testulalis (80.8%), L. haraldusalis (81.5%), and T. hypsalis and N. noctuella (both 81.4%). In contrast, this enrichment is slightly higher compared to S. incertulas (77.1%), C. suppressalis (79.7%), and D. saccharalis (80.0%). Additionally, the AT skew for the M. flavescens mitogenome is slightly positive, indicating a higher occurrence of A compared to T nucleotides. The GC skew values for the M. flavescens mitogenome are negative, indicating a higher content of C compared to G nucleotides. This is similar to GC skew values observed in all sequenced Lepidopteran mitogenomes to date.

Protein-Coding Genes

The start and stop codons of the 13 PCGs in the M. flavescens mitogenome are shown in Table 2. Like invertebrate mitogenomes, 12 of these PCGs begin with the standard ATN start codon, except for cox1. Sequence alignment revealed that the open reading frame of cox1 starts with a CGA codon, which encodes arginine. The putative start codon CGA is common in insects102324. An unusual start codon for the cox1 gene has also been described in various arthropods252627. In the M. flavescens mitogenome, the canonical termination codon, TAA, occurs in seven PCGs. However, the nad4L gene utilizes A and the cox1, cox2, nad2, nad4, and cob genes utilize T as a truncated stop codon instead. Similar results have also been found in other animal mitochondrial genes28293031. Relative synonymous codon usage values for the M. flavescens mitogenome are summarized in Table 3 and Fig. 2. The total number of codons in PCGs is 3,716, and the codons CUC, GUC, CCG, UGG, CGG, and AGG are not represented. The most common amino acids in mitochondrial proteins are leucine 2 (Leu 2, 484), isoleucine (Ile, 455), and phenylalanine (Phe, 393), which are likewise highly abundant in mitochondrial proteins in other animals323334. The average AT content of the 13 PCGs is 78.7%. Furthermore, the AT skew of these PCGs is slightly positive, while the GC skew is slightly negative (Table 4).
Table 3

Codon number and RSCU in M. flavescens mitochondrial PCGs.

CodonCountRSCUCodonCountRSCUCodonCountRSCUCodonCountRSCU
UUU(F)3701.88UCU(S2)992.39UAU(Y)1531.82UGU(C)291.76
UUC(F)230.12UCC(S2)140.34UAC(Y)150.18UGC(C)40.24
UUA(L2)4595.1UCA(S2)992.39UAA(*)82UGA(W)891.87
UUG(L2)250.28UCG(S2)40.1UAG(*)00UGG(W)60.13
CUU(L1)330.37CCU(P)571.81CAU(H)621.77CGU(R)181.38
CUC(L1)00CCC(P)130.41CAC(H)80.23CGC(R)20.15
CUA(L1)230.26CCA(P)561.78CAA(Q)601.88CGA(R)322.46
CUG(L1)00CCG(P)00CAG(Q)40.13CGG(R)00
AUU(I)4241.86ACU(T)762.14AAU(N)2251.75AGU(S1)180.43
AUC(I)310.14ACC(T)110.31AAC(N)320.25AGC(S1)10.02
AUA(M)2381.76ACA(T)531.49AAA(K)931.69AGA(S1)972.34
AUG(M)320.24ACG(T)20.06AAG(K)170.31AGG(S1)00
GUU(V)641.74GCU(A)722.44GAU(D)551.83GGU(G)551.11
GUC(V)00GCC(A)90.31GAC(D)50.17GGC(G)40.08
GUA(V)812.2GCA(A)341.15GAA(E)661.71GGA(G)1112.23
GUG(V)20.05GCG(A)30.1GAG(E)110.29GGG(G)290.58

A total of 3,716 codons were analysed, excluding the initiation and termination codons. Amino acids encoded by these codons are labelled according to the IUPAC-IUB single-letter amino acid codes.

Figure 2

The relative synonymous codon usage (RSCU) in the mitogenome of M. flavescens.

Table 4

Composition and skewness in the M. flavescens mitogenome.

M. flavescensSize (bp)A%G%T%C%A + T%AT skewnessGC skewness
mitogenome15,39640.87.539.712.080.50.014−0.231
PCGs11,14539.98.538.812.878.70.014−0.202
tRNAs151341.67.540.810.182.40.010−0.148
rRNAs215143.34.641.210.984.50.025−0.406
control region40143.72.0049.64.793.3−0.063−0.403

Transfer RNA Genes and Ribosomal RNA Genes

The tRNAscan-SE Search Server was used to predict the structure of the 22 tRNAs present in the M. flavescens mitogenome. Eight tRNAs are encoded by the L-strand and the remaining 14 are encoded by the H-strand. This tRNA genomic architecture is identical to that found in all Lepidopteran species examined to date. Furthermore, all M. flavescens tRNAs display the typical clover-leaf secondary structure observed in most mitochondrial tRNAs with the exception of the trnS1 (AGN) gene. Interestingly, trnS1 (AGN) lacking a stable dihydrouridine arm has been observed in several insects, including Lepidopteran species and metazoan mitogenomes35363738. A 7 bp amino acid acceptor stem, in addition to the anticodon stem and loop (7 bp), are both conserved in all tRNAs. While a total of 25 unmatched base pairs were detected in these tRNAs (Fig. 3), 18 of them are G-U pairs, which form a weak bond and are well-known non-canonical pairs in tRNA secondary structures. The remaining seven mismatches include one C-U and six U-U pairs. 22 tRNAs in the M. flavescens mitogenome are 1,513 bp long, each of which range in size from 63 to 73 bp. The A + T content is 82.4%. The AT skew for both tRNAs and rRNAs is slightly positive, indicating a higher occurrence of A compared to T nucleotides. The GC skew for both tRNAs and rRNAs is slightly negative, indicating a higher occurrence of C compared to G nucleotides. The two rRNA genes (rrnS and rrnL) present in M. flavescens mitogenome are located between trnL1 (CUN) and trnV or between trnV and the A + T-rich region, respectively. The sizes of rrnL and rrnS are 1,359 bp and 792 bp, respectively. The A + T content of the two rRNAs is 84.5% (Table 4).
Figure 3

Predicted secondary structures for the tRNA genes in the M. flavescens mitogenome.

Control Region

The CR possesses essential elements involved in the initiation of replication and transcription of the mitogenome39. The CR of the M. flavescens mitogenome extends over 401 bp and is located between rrnS and trnM. The CR contains the highest A + T content (93.3%) in the entire mitogenome. Both the AT skew and GC skew for the CR are slightly negative, indicating that T and C are more abundant than A and G, respectively. Several conserved structures found in other Lepidopteran mitogenomes are also observed in the A + T-rich region of M. flavescens. This includes the motif ‘ATAGA’ and a poly-T stretch downstream of rrnS, which is widely conserved in Lepidopteran mitogenomes and may represent the origin of minority or light strand replication40. A poly-A commonly observed in other Lepidopteran mitogenomes is also found immediately upstream of the trnM gene. We identified microsatellite (AT)10 elements in the A + T-rich region. Multiple tandem repeat elements are typically present in the A + T-rich region of most insects. However, only three tandem repeats are found in the CR of the M. flavescens mitogenome (Fig. 4).
Figure 4

Features present in the A + T-rich region of the M. flavescens mitogenome.

The reverse strand sequence is shown. Coloured nucleotides indicate the ATATG motif (red), the poly-T stretch (blue), two microsatellite T/A repeat sequences (green), and the poly-A stretch (pink). Two tandem repeats 51 bp in length are indicated in red and black single underline.

Phylogenetich Analyses

Phylogenetic relationships within the Zygaenoidea superfamily are highly debated. In the present study, concatenated amino acid and nucleotide sequences of the 13 PCGs from mitogenomes obtained from nine Lepidopteran superfamilies are used to reconstruct phylogenetic relationships by the BI and ML methods (Figs 5 and 6). The monophyly of each superfamily is generally well supported. The best-supported phylogenetic relationship found in this study is as follows: Yponomeutoidea + (Tortricoidea + Zygaenoidea + (Papilionoidea + (Pyraloidea + (Noctuoidea + (Geometroidea + Bombycoidea))))). The analyses show that M. flavescens belongs in the Zygaenoidea superfamily. Both Papilionoidea and Tortricoidea superfamilies are most closely related to Zygaenoidea. More mitogenomes from Zygaenoidea insects were required to resolve the position of Zygaenoidea and the relationships among these superfamilies. Our phylogeny clearly separates and demonstrates a similar topology as that derived from traditional classifications and other molecular data4142.
Figure 5

Phylogenetic trees inferred from amino acid (red) and nucleotide (black) sequences of 13 PCGs of the mitogenome using BI analysis.

Figure 6

Phylogenetic trees inferred from amino acid (blue) and nucleotide (black) sequences of 13 PCGs of the mitogenome using ML analysis.

Additional Information

The M. flavescens mitogenome was submitted under the accession number KU946971 to NCBI. How to cite this article: Liu, Q.-N. et al. The first complete mitochondrial genome for the subfamily Limacodidae and implications for the higher phylogeny of Lepidoptera. Sci. Rep. 6, 35878; doi: 10.1038/srep35878 (2016).
  33 in total

1.  Selection of conserved blocks from multiple alignments for their use in phylogenetic analysis.

Authors:  J Castresana
Journal:  Mol Biol Evol       Date:  2000-04       Impact factor: 16.240

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Authors:  Dennis V Lavrov; Walker Pett; Oliver Voigt; Gert Wörheide; Lise Forget; B Franz Lang; Ehsan Kayal
Journal:  Mol Biol Evol       Date:  2012-12-06       Impact factor: 16.240

3.  Characterization of mitochondrial genome of Chinese wild mulberry silkworm, Bomyx mandarina (Lepidoptera: Bombycidae).

Authors:  Minhui Pan; Quanyou Yu; Yuling Xia; Fangyin Dai; Yanqun Liu; Cheng Lu; Ze Zhang; Zhonghuai Xiang
Journal:  Sci China C Life Sci       Date:  2008-08-03

4.  The complete mitochondrial genome of the fall webworm, Hyphantria cunea (Lepidoptera: Arctiidae).

Authors:  Fang Liao; Lin Wang; Song Wu; Yu-Ping Li; Lei Zhao; Guo-Ming Huang; Chun-Jing Niu; Yan-Qun Liu; Ming-Gang Li
Journal:  Int J Biol Sci       Date:  2010-03-29       Impact factor: 6.580

5.  Characterization of the complete mitochondrial genome of Diaphania pyloalis (Lepidoptera: Pyralididae).

Authors:  Bao-Jian Zhu; Qiu-Ning Liu; Li-Shang Dai; Lei Wang; Yu Sun; Kun-Zhang Lin; Guo-Qing Wei; Chao-Liang Liu
Journal:  Gene       Date:  2013-06-26       Impact factor: 3.688

6.  The complete mitochondrial genomes of two ghost moths, Thitarodes renzhiensis and Thitarodes yunnanensis: the ancestral gene arrangement in Lepidoptera.

Authors:  Yong-Qiang Cao; Chuan Ma; Ji-Yue Chen; Da-Rong Yang
Journal:  BMC Genomics       Date:  2012-06-22       Impact factor: 3.969

7.  MrBayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space.

Authors:  Fredrik Ronquist; Maxim Teslenko; Paul van der Mark; Daniel L Ayres; Aaron Darling; Sebastian Höhna; Bret Larget; Liang Liu; Marc A Suchard; John P Huelsenbeck
Journal:  Syst Biol       Date:  2012-02-22       Impact factor: 15.683

8.  Improved systematic tRNA gene annotation allows new insights into the evolution of mitochondrial tRNA structures and into the mechanisms of mitochondrial genome rearrangements.

Authors:  Frank Jühling; Joern Pütz; Matthias Bernt; Alexander Donath; Martin Middendorf; Catherine Florentz; Peter F Stadler
Journal:  Nucleic Acids Res       Date:  2011-12-01       Impact factor: 16.971

9.  Comparative and phylogenetic analysis of the mitochondrial genomes in basal hymenopterans.

Authors:  Sheng-Nan Song; Pu Tang; Shu-Jun Wei; Xue-Xin Chen
Journal:  Sci Rep       Date:  2016-02-16       Impact factor: 4.379

10.  Complete mitochondrial genome of Bactrocera arecae (Insecta: Tephritidae) by next-generation sequencing and molecular phylogeny of Dacini tribe.

Authors:  Hoi-Sen Yong; Sze-Looi Song; Phaik-Eem Lim; Kok-Gan Chan; Wan-Loo Chow; Praphathip Eamsobhana
Journal:  Sci Rep       Date:  2015-10-16       Impact factor: 4.379

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  11 in total

1.  Mesozoic mitogenome rearrangements and freshwater mussel (Bivalvia: Unionoidea) macroevolution.

Authors:  Elsa Froufe; Ivan Bolotov; David C Aldridge; Arthur E Bogan; Sophie Breton; Han Ming Gan; Uthaiwan Kovitvadhi; Satit Kovitvadhi; Nicoletta Riccardi; Giulia Secci-Petretto; Ronaldo Sousa; Amilcar Teixeira; Simone Varandas; David Zanatta; Alexandra Zieritz; Miguel M Fonseca; Manuel Lopes-Lima
Journal:  Heredity (Edinb)       Date:  2019-06-14       Impact factor: 3.821

2.  The mitochondrial genome of Muga silkworm (Antheraea assamensis) and its comparative analysis with other lepidopteran insects.

Authors:  Deepika Singh; Debajyoti Kabiraj; Pragya Sharma; Hasnahana Chetia; Ponnala Vimal Mosahari; Kartik Neog; Utpal Bora
Journal:  PLoS One       Date:  2017-11-15       Impact factor: 3.240

3.  Mitochondrial Genomes of Two Bombycoidea Insects and Implications for Their Phylogeny.

Authors:  Zhao-Zhe Xin; Xiao-Yu Zhu; Ying Wang; Hua-Bin Zhang; Dai-Zhen Zhang; Chun-Lin Zhou; Bo-Ping Tang; Qiu-Ning Liu
Journal:  Sci Rep       Date:  2017-07-26       Impact factor: 4.379

4.  The first two complete mitochondrial genomes for the family Triglidae and implications for the higher phylogeny of Scorpaeniformes.

Authors:  Lei Cui; Yuelei Dong; Fenghua Liu; Xingchen Gao; Hua Zhang; Li Li; Jingyi Cen; Songhui Lu
Journal:  Sci Rep       Date:  2017-05-08       Impact factor: 4.379

5.  Complete mitochondrial genome of Clistocoeloma sinensis (Brachyura: Grapsoidea): Gene rearrangements and higher-level phylogeny of the Brachyura.

Authors:  Zhao-Zhe Xin; Yu Liu; Dai-Zhen Zhang; Xin-Yue Chai; Zheng-Fei Wang; Hua-Bin Zhang; Chun-Lin Zhou; Bo-Ping Tang; Qiu-Ning Liu
Journal:  Sci Rep       Date:  2017-06-23       Impact factor: 4.379

6.  Mitochondrial genome of the garfish Hyporhamphus quoyi (Beloniformes: Hemiramphidae) and phylogenetic relationships within Beloniformes based on whole mitogenomes.

Authors:  Lei Cui; Yuelei Dong; Rongbo Cao; Jian Gao; Jingyi Cen; Zhijia Zheng; Songhui Lu
Journal:  PLoS One       Date:  2018-11-15       Impact factor: 3.240

7.  Complete mitochondrial genomes of eight seahorses and pipefishes (Syngnathiformes: Syngnathidae): insight into the adaptive radiation of syngnathid fishes.

Authors:  Xin Wang; Yanhong Zhang; Huixian Zhang; Geng Qin; Qiang Lin
Journal:  BMC Evol Biol       Date:  2019-06-11       Impact factor: 3.260

8.  Complete mitochondrial genome of Zeuzera multistrigata Moore, 1881 (Lepidoptera: Cossidae).

Authors:  Iksoo Kim; Su Yeon Jeong; Min Jee Kim; Sei-Woong Choi
Journal:  Mitochondrial DNA B Resour       Date:  2017-08-02       Impact factor: 0.658

9.  Organization of the mitochondrial genome of Ramulus irregulatiter dentatus (Phasmatidae: Phasmatidae).

Authors:  Congfen Zhang; Xiaoqiang Guo
Journal:  Front Genet       Date:  2022-08-29       Impact factor: 4.772

10.  Comparative mitochondrial genome analysis of Eudocima salaminia (Cramer, 1777) (Lepidoptera: Noctuoidea), novel gene rearrangement and phylogenetic relationship within the superfamily Noctuoidea.

Authors:  Muzafar Riyaz; Rauf Ahmad Shah; Ignacimuthu Savarimuthu; Sivasankaran Kuppusamy
Journal:  Mol Biol Rep       Date:  2021-06-09       Impact factor: 2.316

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