PMCCPMCCPMCC

Search tips
Search criteria 

Advanced

 
Logo of plosonePLoS OneView this ArticleSubmit to PLoSGet E-mail AlertsContact UsPublic Library of Science (PLoS)
 
PLoS One. 2012; 7(6): e38654.
Published online Jun 6, 2012. doi:  10.1371/journal.pone.0038654
PMCID: PMC3368884
Phylogenetic Analysis of the Complete Mitochondrial Genome of Madurella mycetomatis Confirms Its Taxonomic Position within the Order Sordariales
Wendy W. J. van de Sande*
Department of Medical Microbiology and Infectious Diseases, Erasmus MC, Rotterdam, The Netherlands
Vishnu Chaturvedi, Editor
New York State Health Department and University at Albany, United States of America
* E-mail: w.vandesande/at/erasmusmc.nl
Conceived and designed the experiments: WvdS. Performed the experiments: WvdS. Analyzed the data: WvdS. Contributed reagents/materials/analysis tools: WvdS. Wrote the paper: WvdS.
Received February 9, 2012; Accepted May 8, 2012.
Background
Madurella mycetomatis is the most common cause of human eumycetoma. The genus Madurella has been characterized by overall sterility on mycological media. Due to this sterility and the absence of other reliable morphological and ultrastructural characters, the taxonomic classification of Madurella has long been a challenge. Mitochondria are of monophyletic origin and mitochondrial genomes have been proven to be useful in phylogenetic analyses.
Results
The first complete mitochondrial DNA genome of a mycetoma-causative agent was sequenced using 454 sequencing. The mitochondrial genome of M. mycetomatis is a circular DNA molecule with a size of 45,590 bp, encoding for the small and the large subunit rRNAs, 27 tRNAs, 11 genes encoding subunits of respiratory chain complexes, 2 ATP synthase subunits, 5 hypothetical proteins, 6 intronic proteins including the ribosomal protein rps3. In phylogenetic analyses using amino acid sequences of the proteins involved in respiratory chain complexes and the 2 ATP synthases it appeared that M. mycetomatis clustered together with members of the order Sordariales and that it was most closely related to Chaetomium thermophilum. Analyses of the gene order showed that within the order Sordariales a similar gene order is found. Furthermore also the tRNA order seemed mostly conserved.
Conclusion
Phylogenetic analyses of fungal mitochondrial genomes confirmed that M. mycetomatis belongs to the order of Sordariales and that it was most closely related to Chaetomium thermophilum, with which it also shared a comparable gene and tRNA order.
Madurella mycetomatis is the most common causative agent of human mycetoma, a chronic inflammatory disease, which remains localized and involves subcutaneous tissues, fascia and bones [1]. The disease is characterised by tumefaction, discharging sinuses and the presence of fungal grains [1]. The generic criteria for Madurella are primarily based on tissue morphology and overall sterility on mycological media, as well as an invasive potential in human and animal hosts [2]. Since no sexual stage of M. mycetomatis has been discovered, the taxonomic classification of Madurella has long been a challenge. Especially, since there are also no asexual conidia produced nor other morphological and ultractructural characters which could be of aid in the taxonomic classification. With the development of molecular typing tools, such as sequencing of the nuclear sequences encoding for the internal transcribed spacer (ITS), the beta-tubulin gene and the ribosomal binding protein it became possible to establish the taxonomic place of Madurella among the ascomycetes [3], [4]. Based on these nuclear sequence data, it appeared that the genus Madurella, consisting of five species M. mycetomatis, M. grisea, M. pseudomycetomatis, M. fahalii and M. tropicana, could be taxonomically differentiated into two different orders, namely the orders Sordariales and Pleosporales [3], [4]. The generic type species M. mycetomatis belonged to the order of Sordariales together with M. pseudomycetomatis, M. fahalii and M. tropicana, and the genus Madurella appeared to be closely related to the genus Chaetomium [3], [4].
Next to nuclear sequences it is also possible to use mitochondrial sequences for phylogenetic analyses. Mitochondria are considered descendants of an endosymbiotic α-proteobacterium that was engulfed by a eukaryotic or archeabacteria-like cell more than one billion years ago [5]. The current mitochondrial data points to a single origin of mitochondria with no transfer of mitochondria between different eukaryotes [6]. The mitochondrial DNA present in all mitochondria examined to date is believed to be a remnant of the original endosymbiont’s DNA, with the number of genes contained greatly reduced [5]. In filamentous fungi, the mitochondria are uniparental inherited and their genomes evolve faster than the corresponding nuclear DNA of the fungus [7], [8], [9]. Fungal mitochondrial genomes encode 5 to 100 genes, with a typical fungal mitochondrial core genome containing 14 conserved protein-coding genes, 2 rRNA genes and a variable number of tRNAs [5], [10]. MtDNA divergence between different fungal species is predominantly associated with variation in intergenic regions, intronic sequences and gene order, but the core protein-coding genes are conserved [11]. These core conserved protein-coding genes are convincing tools for phylogenetic analysis as they provide not only a large gene-set for which the sequences can be compared directly, but also the opportunity to compare the position of these genes [11]. With the development of novel sequence methods, the number of mitochondrial genomes of fungi has been expanded in the recent past [10], [11], [12], [13], [14], [15]. This gives us an opportunity to study the phylogeny of fungi using not only nuclear DNA but also mitochondrial DNA. Here we present the mitochondrial genome sequence of M. mycetomatis. Its gene order and amino-acid sequences are used in phylogenetic analyses to determine the place of M. mycetomatis in the fungal kingdom.
Isolate
M. mycetomatis strain mm55, isolated from the lesion of a 22-year-old patient seen in the Mycetoma Research Centre, University of Khartoum, Sudan, was used in this study. Written informed consent was obtained from this patient and ethical clearance was obtained from Soba University Hospital Ethical Committee. This strain was isolated by direct culture of the black grains obtained by a deep biopsy and identified by morphology, PCR-RFLP and sequencing of the ITS region [16]. This strain is used in the only mouse model of eumycetoma in use today and considered the type strain in phylogenetic and antifungal susceptibility testing as well [17], [18], [19], [20]. The strain was maintained on Sabouraud Dextrose Agar (Difco Laboratories, Paris, France) at 37°C. Passage to fresh medium was done on a monthly basis.
DNA Extraction
Three-week-old Madurella cultures were scraped from Sabouraud agarplates, frozen in liquid nitrogen and ground with a mortar and pestle. DNA was extracted from the resulting pulp with the Promega Wizard Kit (Promega). To the grind mycelia, 300 µl lysis solution was added and mixed by pipetting gently. From this step onwards, the yeast protocol from the Promega Wizard Kit was used according to the manufacturer’s instructions.
Sequencing and Assembling of the Mitochondrial Genome
The genome of M. mycetomatis was sequenced using Roche GS junior titanium 454 sequencing according to the manufactures instructions. In short DNA was fragmented by nebulisation to an average fragment length of 600–900 bp after which the fragments were amplified and coupled to capture beads using the emPCR amplification kit Lib-L for the GS Junior Titatium Series (roche). In total 5×106 coupled beads were deposited on the GS junior titanium picotiterplates (Roche) and sequenced. To assemble the mitochondrial genome the GS de novo assembler of Roche was used. The two ends of the assembled sequence were amplified with primers mmmitofw (5′-TCATGGCTTAGATGTTGTGG-3′) and mmmitorv (5′-GAGCTATAGTGGCTCCTAGT-3′) and resequenced by sanger sequencing to confirm the circular nature of the mitochondrial genome.
Annotation of the Mitochondrial Genome
Open reading frames (ORFs) were searched with CLC sequence viewer version 6.5.1 (CLC bio, Aarhus, Denmark) and annotated manually using the published mitochondrial genomes of Podospora anserina, Sordaria macrospora and Neurospora crassa. For hypothetical proteins a cut off of 100 amino acids was used. Codon usage was determined by using the Sequence Manipulation Suite version 2 (www.bioinformatics.org/sms2/codon_usage.html). tRNAs were identified by using tRNAscan-SE 1.21 [21], [22], ARAGORN v1.2 [23], ARWEN [24] and RNAweasel [25] software programs. A tRNA was determined to be a true tRNA if it was found with at least 2 out of 4 software programs.
Phylogenetic Analysis
To compare the M. mycetomatis mitochondrial genome with the genome of other fungal mitochondrial genomes, the amino-acid sequences of the protein-encoding genes atp6, atp8, atp9, cob, cox1, cox2, cox3, nad1, nad2, nad3, nad4, nad4L, nad5 and nad6 were aligned by clustalW using the Mega 5.05 software package [26]. The sequences of the selected proteins were extracted from the fungal mitochondrial genomes deposited in the GenBank database. The aligned amino-acid sequences were used to construct a maximum likelihood tree with 1000 bootstrap replicates based on the cpREV model using Mega 5.05 [26].
Genbank Accession Number
The mtDNA sequence of M. mycetomatis strain mm55 was deposited in GenBank under accession number JQ015302.
Genome Organization
The mitochondrial genome of M. mycetomatis is a typical circular DNA molecule with a length of 45,590 bp. This mitochondrial genome size is small in comparison with the published mitochondrial genomes belonging to the order of the Sordariales. These genomes range from 64,840 nt (Neurospora crassa as stated by the Broad Institute)) to 127,206 nt (Chaetomium thermophilum) [14], [27], [28], [29]. This difference in genome size is due to the variation in intergenetic regions and the presence of hypothetical proteins. In overall, the mitochondrial genome of M. mycetomatis is highly compact, with 80% of the genome encoding for structural genes. The genome encodes for the small and the large subunit rRNAs, 27 tRNAs, 11 genes encoding subunits of respiratory chain complexes, 2 ATP synthase subunits, 5 hypothetical proteins and 6 intronic proteins including the ribosomal protein rps3 (Figure 1, table 1). All genes and tRNAs are found on the plus-strand of the mitochondrial genome, as was also found for mitochondria of most other ascomycetes although for some ascomycetes such as Mycosphaerella graminicola genes were located both strands of the mitochondrial genome. [11], [13], [14], [27], [30], [31]. The M. mycetomatis mitochondrial genome is AT-rich, with an overall G+C content of only 26.8%. The regions of the encoding RNA genes, have a slightly higher G+C content, namely 28.8%. This is in agreement with values found for other fungal mitochondria [10].
Figure 1
Figure 1
Physical map of the mitochondrial genome of M. mycetomatis.
Table 1
Table 1
Genome organization of M. mycetomatis.
Protein Coding Genes
The M. mycetomatis mitochondrial genome has the following genes encoding proteins involved in respiratory chain complexes: ATP synthase subunits 6 and 8 (atp6 and atp8), but not for subunit 9, apocytochrome b (cob), the cytochrome c oxidase subunits 1, 2, and 3 (cox1, cox2 and cox3) and NADH dehydrognease subunits 1, 2, 3, 4, 4 L, 5, and 6 (nad1, nad2, nad3, nad4L, nad5 and nad6) (table 1). Most of these proteins are highly conserved within fungal mitochondrial genomes [13], [27], [30], only for the nad genes and atp9 some variation is noted. No nad genes are present in most of the yeasts and in some fungi atp9 is located in the nuclear genome or on a different, independent circular molecule, rather than in the mitochondrial genome [12], [27], [32]. Next to the proteins involved in respiratory chain complexes, the mitochondrial DNA encodes for 5 hypothetical proteins and 6 intronic proteins including ribosomal protein S3 (rps3). Of the 5 hypothetical proteins only hypothetical proteins 1 and 3 do not show any homology with other known genes. For the other hypothetical genes some homology is found at the protein level. Hypothetical protein 2 shows homology with an unnamed protein product with accession number CAA38821, found in the mitochondrion of Podospora anserina (e-value: 3e-08, max identitiy 38%). Hypothetical protein 4 shows homology with YP_003127070, an GIY-YIG endonuclease found in an intronic protein in the cob gene of the yeast Dekkera bruxellensis (e-value: 5e-04, max identity 25%) [12]. Since no GIY-YIG motif is found in this hypothetical protein, it probably does not function as a GIY-YIG endonuclease. Hypothetical protein 5 shows homology with orf296 of P. anserina (Accesion number NP_074917, e-value:2e-19), UrfLM of Neurospora intermedia (Accession number AAU25928, e-value:3e-8) and an unnamed protein product of N. crassa (Accession number CAA31721.1, e-value: 5e-5). Orf 296 is in P. anserina a LAGLIDADG endonuclease found in an intronic sequence after exon3 of cox1 gene [27], [33]. Hypothetical protein 5 does not show a LAGLIDADG domain in its sequence and therefore probably does not function as a LAGLIDADG endonuclease. Hypothetical proteins 4 and 5 are probably remnants of endonucleases but do not function as endonucleases any more, there precise function, if any, remains unknown.
Introns
In the coding genes of the mitochondrial genome of M. mycetomatis, a total of 8 introns are found. All introns are group I introns (table 1). Two introns are found in both the large ribosomal subunit (intron IA) and in cox1 (both intron IB). Single introns are found in cob (intron ID), cox2 (intron IC2), nad3 (intron IC2) and nad5 (intron IA) (table 1). Group I introns are considered to be mobile genetic elements which interrupt protein-coding and structural RNA genes [34]. One of the features of group I introns is that they themselves are often invaded with smaller genes that encode mobility-promoting activities that enables the DNA element to move within and between genomes, usually so-called homing endonucleases [34]. In the M. mycetomatis mitochondrial DNA we find five intronic proteins, located in the introns of cob, cox1 (in each intron one), cox2 and nad3 which encode for such homing endonucleases and one intronic protein which encode for ribosomal protein S3 (rps3). Of the four families of homing endonuclease proteins only endonucleases with the conserved amino acid sequence motifs LAGLIDADG (intron proteins 1 2, and 4) and GIY-YIG (intron proteins 3 and 5) are found. The endonuclease assignment was supported by BLAST analysis and motif identification using PFAM. LAGLIDADG homing endonucleases are found in two forms: a single LAGLIDADG motif that dimerizes and double-motif forms derived form a gene fusion event between two monomeric forms [35]. The endonucleases found in the M. mycetomatis mitochondrial genome are all with double-motif forms.
Intergenic Regions
The presence of putative mitochondrial promoters are detected by comparison of the only promoter from the Sordariales, the Neurospora crassa sequence TTAG(A/T)RR(G/T)(G/C)N(A/T) [11], [36], [37]. Two putative promoter sequences are located within the intergenic regions and close to the 5′ end of coding genes, namely TTAGAATCTT (15885–15896) and TTAGTGGTCTA (36265–36276). Putative promoter sequence TTAGAATCTT is located 551 bp for the 5′ end of cox2, while putative promoter sequence TTAGAATCTT is located 899 bp for hypothetical protein 4. Both putative promoter sequences are preceded by a 15–23 bp long AT-rich region, as is also described for other fungal species, thus strengthening the hypothesis that these sequences may indeed be mitochondrial promoters [11], [37].
Genetic Code and Codon Usage
Using the genetic mould mitrochondrial code from NCBI (translation table 4), the codon usage of the M. mycetomatis mitochondrial ORFs is determined. Of the 23 ORFs, only the cox3 and hypothetical protein 3 starts with the ATT initiation codon, all other genes start with the ATG initiation codon (table 1). Most of the ORF end with the in preferred TAA stop-codon, only 5 ORFs (cox1, cox2, cox3, hypothetical protein 1 and intronprotein 3) end with the TAG stop-codon [38]. As is also found for other fungi, the most frequently used amino acid in the 23 protein genes is leucine followed by isoleucine (table 2) [11]. As seen in table 2, the codon usage in M. mycetomatis mitochondrial ORFs shows a strong bias towards codons ending with a U or A since 86.8% of the codons ends with these bases. The tendency for the A and U residues in the wobble position has also been observed in other fungal genomes [12], [39], [40], [41], [42]. As expected due to the high AU content of the mitochondrial genome, the preference of A and U residues is also noted in the overall codon use. The most frequently used codons consist only of Us and As and were UUA (9.04%), AUA (6.07%), AAU (5.68%), UUU (5.41%), AAA (5.17%), UAU (4.36%) and AUU (4.23%) (table 2). The least frequently used codons, CGC (0.02%), CGG (0.06%), CGG (0.06%), AGG (0.07%) and CCC (0.10%), are the codons which consist mainly of Cs and Gs (table 2).
Table 2
Table 2
Codon usage in protein coding genes of M. mycetomatis mitrochondrial genome.
tRNAs
In the M. mycetomatis mitochondrial genome 27 tRNAs are identified which clustered roughly in three groups (figure 1). Among the tRNAs all amino-acids are accounted for, but for some amino-acids multiple tRNAs are found (table 3). There are two tRNAs with different anticodons for arginine, four tRNAs with three different anticodons for leucine, three tRNAs with the same anticodon for methionine and two tRNAs with the same anticodon for tryptophane. All tRNAs have a cloverleaf structure except the tyrosine tRNA and the leucine tRNA with anticodon AAG, they have a TV-loop and D-loop structure respectively.
Table 3
Table 3
tRNAs identified in the genome of M. mycetomatis.
Phylogeny and Comparative Genomics
With the exception of the group of yeast that are lacking NADH genes, all other fungal mtDNAs contain the same essential functional genes [11]. Therefore, the sequences of these 14 conserved protein encoding genes, as well as the mitochondrial organization of these genes can be used tpone.0038654.g001.tifo determine the relations between different fungal species. Amino acid sequence of 14 protein coding genes in the mitochondrial genomes of M. mycetomatis and 20 other fungi are used for phylogenetic tree construction (figure 2). Most nodes in this tree have high bootstrap values which indicate the robustness of the tree computed. As found by others, the mitochondrial genomes of the yeast species cluster apart from the mitochondrial genomes obtained from filamentous fungi [10]. As is seen in figure 2, M. mycetomatis clusters amongst other species of the order Sordariales with high bootstrap support. Placing M. mycetomatis in the order Sordariales is in line with previous observations based on the nuclear sequences SSU, ITS, betatubulin 2 and ribosomal binding protein 2 [3], [4]. Based on an extensive phylogenetic comparison of the SSU rDNA sequence of M. mycetomatis with that of 157 other members of the Ascomycota belonging to the orders Chaetothyriales, Diaporthales, Dothideales, Eurotiales, Halosphaeriales, Hypocreales, Lecanorales, Leotiales, Microascales, Onygenales, Ophiostomatales, Pezizales, Pleosporales, Sordariales, Taphrinales and Tuberales it appeared that M. mycetomatis clustered among the members of the order Sordariales while M. grisea clustered among the members of the order Pleosporales [3]. In order to determine the phylogenetic place of M. mycetomatis within the order Sordariales, the ITS, betatubulin 2 and ribosomal binding protein 2 were also sequenced and compared to 39 members of the order Sordariales. In this latter study it appeared that M. mycetomatis was most closely related to M. tropicana, M. pseudomycetomatis and M. fahalli, but that the genus Madurella itself was most closely related to the genus Chaetomium [4]. This close relatedness to the genus Chaetomium is confirmed in this study. Based on the phylogenetic comparisons made with the mitochondrial sequence, it appears that the closest relative of M. mycetomatis is C. thermophilum.
Figure 2
Figure 2
Maximum likelihood phylogenetic tree based on amino acid sequences of conserved mitochondrial proteins of various fungal species.
The relatedness amongst the order Sordariales is further studied by comparing the mitochondrial organizatiopone.0038654.g002.tifn of M. mycetomatis to the 4 complete fungal mtDNA sequences belonging to the order Sordariales. Comparable to the high similarity in amino-acid sequence and the uniform mtDNA genome organization found for dermatophytes belonging to the order Onygenales [10], the mitochondrial genome organization found for the order Sordariales is apparently also uniform (figure 3). The only exception is the mitochondrial genome organization of P. anserina, which differs from the genome organization of the other members of the order Sordariales (figure 3). This marked difference has been noted in the past, and led to the conclusion that the mitochondrial gene order in the order Sordariales was apparently quite diverse [11]. Here it is shown, that for most mitochondrial genomes in the order Sordariales this is not the case. More mitochondrial genomes are needed for the order Sordariales to determine if the gene order is indeed similar and that P. anserina is the exception, or that the gene orders are in overall more diverse within this order. When comparing the different genome organizations it appears that the genome organization of M. mycetomatis is most closely related to that of C. thermophilum (figures 3), which only differed in the presence of the gene atp9 between nad3 and cox2 in C. thermophilum and its absence in M. mycetomatis. Next to having the same gene order, the tRNA clustering in the order Sordariales is similar. Again the tRNA order of M. mycetomatis resembles that of C. thermophilum the most (figure 3). Combining the phylogenetic data, the gene order and the tRNA order it appears that the mitochondrial genome of M. mycetomatis is most closely related to the mitochondrial genome of C. thermophilum. Fungi belonging to the order Sordariales are mostly soil-, wood- and dung-inhabiting fungi [43]. N. crassa is usually found in or on burned vegetation and the soil, while het natural habitat of S. macrospora P. anserina and C. thermophilum, is mainly the soil and herbivore dung [15], [44], [45], [46]. Although DNA of M. mycetomatis has been shown to be present in soil and on thorns in the endemic area, nobody has been able to culture M. mycetomatis directly from these niches [47]. Therefore the natural habitat of M. mycetomatis still needs to be confirmed. Based on this and other studies, it is demonstrated that M. mycetomatis clusters within the order Sordariales, therefore the natural habitat of M. mycetomatis might be sought on similar substrates. To discover the natural niche of this fungus could lead to strategies in the prevention of this mutilating disease.
Figure 3
Figure 3
Mitochondrial gene order of 5 members of the order Sordariales.
Conclusion
Comparative genomics provides a powerful tool for uncovering similarities and differences between species and placing them in their correct order. In order to gain insight in the evolutionary place of M. mycetomatis in the fungal kingdom, previous studies have used the nuclear ribosomal internal transcriped spacers (ITS) which showed that M. mycetomatis clusters amidst the order Sordariales. Here the complete mitochondrial genome of M. mycetomatis is reported. The composition and organization of the genes within this mtDNA are found to cluster amongst the Sordariales, and is found to be almost identical to that of C. thermophilum. Phylogenetic analyses of the whole protein-encoding gene content of M. mycetomatis confirm its position in the order of the Sordariales with C. thermophilum as its closest relative.
Footnotes
Competing Interests: The author has declared that no competing interests exist.
Funding: This research was financially supported by VENI grant 91611178 of the Netherlands Organisation of Scientific Research (NWO). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
1. Ahmed AO, van Leeuwen W, Fahal A, van de Sande WWJ, Verbrugh H, et al. Mycetoma caused by Madurella mycetomatis: a neglected infectious burden. Lancet Infect Dis. 2004;4:566–574. [PubMed]
2. van de Sande WWJ, Fahal AH, de Hoog GS, Van Belkum A. Madurella. In: Liu D, editor. Molecular detection of human fungal pathogens. Boca Raton: CRC Press, Taylor & Francis Group; 2011. pp. 117–128.
3. de Hoog GS, Adelmann D, Ahmed AO, van Belkum A. Phylogeny and typification of Madurella mycetomatis, with a comparison of other agents of eumycetoma. Mycoses. 2004;47:121–130. [PubMed]
4. de Hoog GS, van Diepeningen AD, Mahgoub el S, van de Sande WW. New species of madurella, causative agents of black-grain mycetoma. J Clin Microbiol. 2012;50:988–994. [PMC free article] [PubMed]
5. Bullerwell CE, Lang BF. Fungal evolution: the case of the vanishing mitochondrion. Curr Opin Microbiol. 2005;8:362–369. [PubMed]
6. Lang BF, Gray MW, Burger G. Mitochondrial genome evolution and the origin of eukaryotes. Annu Rev Genet. 1999;33:351–397. [PubMed]
7. Ballard JW, Whitlock MC. The incomplete natural history of mitochondria. Mol Ecol. 2004;13:729–744. [PubMed]
8. Basse CW. Mitochondrial inheritance in fungi. Curr Opin Microbiol. 2010;13:712–719. [PubMed]
9. van Diepeningen AD, Goedbloed DJ, Slakhorst SM, Koopmanschap AB, Maas MF, et al. Mitochondrial recombination increases with age in Podospora anserina. Mech Ageing Dev. 2010;131:315–322. [PubMed]
10. Wu Y, Yang J, Yang F, Liu T, Leng W, et al. Recent dermatophyte divergence revealed by comparative and phylogenetic analysis of mitochondrial genomes. BMC Genomics. 2009;10:238. [PMC free article] [PubMed]
11. Kouvelis VN, Ghikas DV, Typas MA. The analysis of the complete mitochondrial genome of Lecanicillium muscarium (synonym Verticillium lecanii) suggests a minimum common gene organization in mtDNAs of Sordariomycetes: phylogenetic implications. Fungal Genet Biol. 2004;41:930–940. [PubMed]
12. Prochazka E, Polakova S, Piskur J, Sulo P. Mitochondrial genome from the facultative anaerobe and petite-positive yeast Dekkera bruxellensis contains the NADH dehydrogenase subunit genes. FEMS Yeast Res. 2010;10:545–557. [PubMed]
13. Cardoso MA, Tambor JH, Nobrega FG. The mitochondrial genome from the thermal dimorphic fungus Paracoccidioides brasiliensis. Yeast. 2007;24:607–616. [PubMed]
14. Amlacher S, Sarges P, Flemming D, van Noort V, Kunze R, et al. Insight into structure and assembly of the nuclear pore complex by utilizing the genome of a eukaryotic thermophile. Cell. 2011;146:277–289. [PubMed]
15. Nowrousian M, Stajich JE, Chu M, Engh I, Espagne E, et al. De novo assembly of a 40 Mb eukaryotic genome from short sequence reads: Sordaria macrospora, a model organism for fungal morphogenesis. PLoS Genet. 2010;6:e1000891. [PMC free article] [PubMed]
16. Ahmed AO, Mukhtar MM, Kools-Sijmons M, Fahal AH, de Hoog S, et al. Development of a species-specific PCR-restriction fragment length polymorphism analysis procedure for identification of Madurella mycetomatis. J Clin Microbiol. 1999;37:3175–3178. [PMC free article] [PubMed]
17. van de Sande WWJ, Luijendijk A, Ahmed AO, Bakker-Woudenberg IA, van Belkum A. Testing of the in vitro susceptibilities of Madurella mycetomatis to six antifungal agents by using the sensititre system in comparison with a viability-based 2,3-bis(2-methoxy-4-nitro-5-sulfophenyl)-5- [(phenylamino)carbonyl]-2H-tetrazolium hydroxide (XTT) assay and a modified NCCLS method. Antimicrob Agents Chemother. 2005;49:1364–1368. [PMC free article] [PubMed]
18. Ahmed AO, van de Sande WWJ, van Vianen W, van Belkum A, Fahal AH, et al. In vitro susceptibilities of Madurella mycetomatis to itraconazole and amphotericin B assessed by a modified NCCLS method and a viability-based 2,3-Bis(2-methoxy-4-nitro-5- sulfophenyl)-5-[(phenylamino)carbonyl]-2H-tetrazolium hydroxide (XTT) assay. Antimicrob Agents Chemother. 2004;48:2742–2746. [PMC free article] [PubMed]
19. Ahmed A, van de Sande W, Verbrugh H, Fahal A, van Belkum A. Madurella mycetomatis strains from mycetoma lesions in Sudanese patients are clonal. J Clin Microbiol. 2003;41:4537–4541. [PMC free article] [PubMed]
20. Ahmed AO, van Vianen W, ten Kate MT, van de Sande WW, van Belkum A, et al. A murine model of Madurella mycetomatis eumycetoma. FEMS Immunol Med Microbiol. 2003;37:29–36. [PubMed]
21. Lowe TM, Eddy SR. tRNAscan-SE: a program for improved detection of transfer RNA genes in genomic sequence. Nucleic Acids Res. 1997;25:955–964. [PMC free article] [PubMed]
22. Schattner P, Brooks AN, Lowe TM. The tRNAscan-SE, snoscan and snoGPS web servers for the detection of tRNAs and snoRNAs. Nucleic Acids Res. 2005;33:W686–689. [PMC free article] [PubMed]
23. Laslett D, Canback B. ARAGORN, a program to detect tRNA genes and tmRNA genes in nucleotide sequences. Nucleic Acids Res. 2004;32:11–16. [PMC free article] [PubMed]
24. Laslett D, Canback B. ARWEN: a program to detect tRNA genes in metazoan mitochondrial nucleotide sequences. Bioinformatics. 2008;24:172–175. [PubMed]
25. Gautheret D, Lambert A. Direct RNA motif definition and identification from multiple sequence alignments using secondary structure profiles. J Mol Biol. 2001;313:1003–1011. [PubMed]
26. Tamura K, Peterson D, Peterson N, Stecher G, Nei M, et al. MEGA5: Molecular Evolutionary Genetics Analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol. 2011;28:2731–2739. [PMC free article] [PubMed]
27. Cummings DJ, McNally KL, Domenico JM, Matsuura ET. The complete DNA sequence of the mitochondrial genome of Podospora anserina. Curr Genet. 1990;17:375–402. [PubMed]
28. Collins RA, Lambowitz AM. Structural variations and optional introns in the mitochondrial DNAs of Neurospora strains isolated from nature. Plasmid. 1983;9:53–70. [PubMed]
29. Taylor JW, Smolich BD. Molecular cloning and physical mapping of the Neurospora crassa 74-OR23–1A mitochondrial genome. Curr Genet. 1985;9:597–603. [PubMed]
30. Woo PC, Zhen H, Cai JJ, Yu J, Lau SK, et al. The mitochondrial genome of the thermal dimorphic fungus Penicillium marneffei is more closely related to those of molds than yeasts. FEBS Lett. 2003;555:469–477. [PubMed]
31. Torriani SF, Goodwin SB, Kema GH, Pangilinan JL, McDonald BA. Intraspecific comparison and annotation of two complete mitochondrial genome sequences from the plant pathogenic fungus Mycosphaerella graminicola. Fungal Genet Biol. 2008;45:628–637. [PubMed]
32. Laforest MJ, Roewer I, Lang BF. Mitochondrial tRNAs in the lower fungus Spizellomyces punctatus: tRNA editing and UAG ‘stop’ codons recognized as leucine. Nucleic Acids Res. 1997;25:626–632. [PMC free article] [PubMed]
33. Cummings DJ, MacNeil IA, Domenico J, Matsuura ET. Excision-amplification of mitochondrial DNA during senescence in Podospora anserina. DNA sequence analysis of three unique "plasmids". J Mol Biol. 1985;185:659–680. [PubMed]
34. Edgell DR, Chalamcharla VR, Belfort M. Learning to live together: mutualism between self-splicing introns and their hosts. BMC Biol. 2011;9:22. [PMC free article] [PubMed]
35. Sethuraman J, Majer A, Friedrich NC, Edgell DR, Hausner G. Genes within genes: multiple LAGLIDADG homing endonucleases target the ribosomal protein S3 gene encoded within an rnl group I intron of Ophiostoma and related taxa. Mol Biol Evol. 2009;26:2299–2315. [PubMed]
36. Kleidon J, Plesofsky N, Brambl R. Transcripts and transcript-binding proteins in mitochondria of Neurospora crassa. Mitochondrion. 2003;2:345–360. [PubMed]
37. Kubelik AR, Kennell JC, Akins RA, Lambowitz AM. Identification of Neurospora mitochondrial promoters and analysis of synthesis of the mitochondrial small rRNA in wild-type and the promoter mutant [poky]. J Biol Chem. 1990;265:4515–4526. [PubMed]
38. Paquin B, Lang BF. The mitochondrial DNA of Allomyces macrogynus: the complete genomic sequence from an ancestral fungus. J Mol Biol. 1996;255:688–701. [PubMed]
39. Sekito T, Okamoto K, Kitano H, Yoshida K. The complete mitochondrial DNA sequence of Hansenula wingei reveals new characteristics of yeast mitochondria. Curr Genet. 1995;28:39–53. [PubMed]
40. Foury F, Roganti T, Lecrenier N, Purnelle B. The complete sequence of the mitochondrial genome of Saccharomyces cerevisiae. FEBS Lett. 1998;440:325–331. [PubMed]
41. Pramateftaki PV, Kouvelis VN, Lanaridis P, Typas MA. The mitochondrial genome of the wine yeast Hanseniaspora uvarum: a unique genome organization among yeast/fungal counterparts. FEMS Yeast Res. 2006;6:77–90. [PubMed]
42. Pramateftaki PV, Kouvelis VN, Lanaridis P, Typas MA. Complete mitochondrial genome sequence of the wine yeast Candida zemplinina: intraspecies distribution of a novel group-IIB1 intron with eubacterial affiliations. FEMS Yeast Res. 2008;8:311–327. [PubMed]
43. Zhang N, Castlebury LA, Miller AN, Huhndorf SM, Schoch CL, et al. An overview of the systematics of the Sordariomycetes based on a four-gene phylogeny. Mycologia. 2006;98:1076–1087. [PubMed]
44. Jacobson DJ, Dettman JR, Adams RI, Boesl C, Sultana S, et al. New findings of Neurospora in Europe and comparisons of diversity in temperate climates on continental scales. Mycologia. 2006;98:550–559. [PubMed]
45. Silliker ME, Cummings DJ. Genetic and molecular analysis of a long-lived strain of Podospora anserina. Genetics. 1990;125:775–781. [PubMed]
46. Paoletti M, Saupe SJ. The genome sequence of Podospora anserina, a classic model fungus. Genome Biol. 2008;9:223. [PMC free article] [PubMed]
47. Ahmed A, Adelmann D, Fahal A, Verbrugh H, van Belkum A, et al. Environmental occurrence of Madurella mycetomatis, the major agent of human eumycetoma in Sudan. J Clin Microbiol. 2002;40:1031–1036. [PMC free article] [PubMed]
48. Michel F, Westhof E. Modelling of the three-dimensional architecture of group I catalytic introns based on comparative sequence analysis. J Mol Biol. 1990;216:585–610. [PubMed]
Articles from PLoS ONE are provided here courtesy of
Public Library of Science