- Research article
- Open Access
Mitochondrial matR sequences help to resolve deep phylogenetic relationships in rosids
BMC Evolutionary Biology volume 7, Article number: 217 (2007)
Rosids are a major clade in the angiosperms containing 13 orders and about one-third of angiosperm species. Recent molecular analyses recognized two major groups (i.e., fabids with seven orders and malvids with three orders). However, phylogenetic relationships within the two groups and among fabids, malvids, and potentially basal rosids including Geraniales, Myrtales, and Crossosomatales remain to be resolved with more data and a broader taxon sampling. In this study, we obtained DNA sequences of the mitochondrial matR gene from 174 species representing 72 families of putative rosids and examined phylogenetic relationships and phylogenetic utility of matR in rosids. We also inferred phylogenetic relationships within the "rosid clade" based on a combined data set of 91 taxa and four genes including matR, two plastid genes (rbcL, atpB), and one nuclear gene (18S rDNA).
Comparison of mitochondrial matR and two plastid genes (rbcL and atpB) showed that the synonymous substitution rate in matR was approximately four times slower than those of rbcL and atpB; however, the nonsynonymous substitution rate in matR was relatively high, close to its synonymous substitution rate, indicating that the matR has experienced a relaxed evolutionary history. Analyses of our matR sequences supported the monophyly of malvids and most orders of the rosids. However, fabids did not form a clade; instead, the COM clade of fabids (Celastrales, Oxalidales, Malpighiales, and Huaceae) was sister to malvids. Analyses of the four-gene data set suggested that Geraniales and Myrtales were successively sister to other rosids, and that Crossosomatales were sister to malvids.
Compared to plastid genes such as rbcL and atpB, slowly evolving matR produced less homoplasious but not less informative substitutions. Thus, matR appears useful in higher-level angiosperm phylogenetics. Analysis of matR alone identified a novel deep relationship within rosids, the grouping of the COM clade of fabids and malvids, which was not resolved by any previous molecular analyses but recently suggested by floral structural features. Our four-gene analysis supported the placements of Geraniales, Myrtales at basal nodes of the rosid clade and placed Crossosomatales as sister to malvids. We also suggest that the core part of rosids should include fabids, malvids and Crossosomatales.
Rosids  comprise one-third of all angiosperm species. Their members are morphologically diverse without apparent universal synapomorphies. Nevertheless, rosids in general have a number of characters that are rare elsewhere in the angiosperms, including nuclear endosperm development, simple perforations in vessel end-walls, diplostemony, mucilaginous epidermis, and epicuticular wax rosettes [2–4]. Recent phylogenetic studies based on both morphology and DNA sequences have demonstrated that subclasses Dilleniidae, Hamamelidae, and Rosidae of Cronquist  and Takhtajan  are not monophyletic [[1–4, 7–15], and references therein]. Some orders, such as Malvales, Salicales, Violales, and Capparales of Dilleniidae and Fagales and Urticales of Hamamelidae have been shown to be rosids, whereas some families of Rosidae, such as Cornaceae, Apiaceae, and Icacinaceae, belong to the asterids [1–4, 9–18]. Delimiting the rosid clade and its subclades is therefore central to understanding the phylogeny of eudicots.
Several large-scale phylogenetic analyses of flowering plants at higher taxonomic levels have recently been published based on rbcL, atpB, 18S rDNA and matK sequences, either separately or combined [1–4, 9–15]. The results indicated that within the rosid clade there are 12–14 subclades that are well supported and thus recognized as orders. Most rosid orders have been assigned to two large assemblages, fabids (eurosids I) and malvids (eurosids II). Within fabids, there are two subclades, the nitrogen-fixing clade  including Cucurbitales, Fagales, Fabales and Rosales, and the COM clade  consisting of Celastrales, Oxalidales, and Malpighiales. Nevertheless, inter-ordinal relationships within fabids and malvids, and among fabids, malvids and other rosid orders unassigned to fabids or malvids are either poorly resolved or have low support as measured by jackknife or bootstrap percentages. For example, the placement of Crossosomatales, Myrtales and Geraniales with respect to other rosids still remains uncertain . Recent molecular analyses supported the family Huaceae as sister to Oxalidales in the COM clade [4, 21, 22], but it is desirable to further corroborate these relationships using a broader taxon sampling. A recent morphological study on supraordinal relationships within rosids [, and references therein] produced largely congruent results with DNA-based studies. However, a noteworthy relationship recognized by the morphological data  was the grouping of the COM clade of fabids and malvids, which was inconsistent with all previous molecular studies. Therefore, both comprehensive taxonomic sampling and more molecular characters from different genomes are needed to further clarify phylogenetic relationships within rosid clade.
In this study, we present new mitochondrial DNA (mtDNA) sequences, approximately 1,800 base pairs of the mitochondrial gene matR from 174 species to re-examine the phylogenetic relationships of rosids within the framework of eudicots . One advantage of mtDNA is the generally observed, reduced level of homoplasy among more distantly related taxa as a consequence of a slow rate of evolution [23–26]; another advantage is that mtDNA sequences belong to different linkage groups from plastid and nuclear genes, and, thus, provide the possibility of combining phylogenetic information from three genomes . Furthermore, this gene has been inherited vertically since it was inserted into nad1 group II intron in the common ancestor of non-liverwort land plants [28, 29], and no paralogue has been found so far. To date, few large-scale phylogenetic analyses of eudicots or rosids have included sequences from any mitochondrial gene, although their utility has been established in basal angiosperms and some orders and families of angiosperms [27, 30–33]. In addition to performing phylogenetic analysis based on matR alone, we also analyzed a smaller combined four-gene (matR, rbcL, atpB and 18S rDNA) 91-taxon matrix in an attempt to increase the resolution and internal support. To explore patterns of molecular evolution in matR and its contribution to resolving deep phylogenetic relationships, we also conducted a comparative analysis of matR and two plastid molecular makers (rbcL and atpB). The potential effect of RNA-editing in matR on phylogeny reconstruction is also evaluated. Our primary objectives are to resolve the deep relationships among orders of rosids and to evaluate the utility of matR in large-scale phylogenetic analyses by comparing the results of matR with those based on other widely used molecular markers.
Sequence variability and evolutionary analyses
For the 174-taxon matrix of matR, nucleotide compositions were not significantly different across the taxa as indicated by a χ2 test (χ2 = 59.804, df = 519, p = 1.0). A relatively high proportion of transversions was found, with an overall transition/transversion ratio of 1.241 under the GTR substitution model (Additional file 2). The overall uncorrected P distance was 0.04, and the largest distance occurred between Lobelia and Hypericum (11%) and the smallest between Leea and Yua (0%). Similar rates of change (steps/variable characters) were found among three-codon positions, with 2.56, 2.57 and 2.92 for the first, second, and third codon positions, respectively (Additional file 3). Saturation was not detected for either transitions or transversions at any codon position (data not shown). The selection-pressure plot revealed that both synonymous and nonsynonymous substitution correlate well with uncorrected P distances (Figure 1a), implying that there is no obvious lineage-specific selection pressure within the taxa sampled.
The extent of functional constraints among different domains of the matR gene was uneven (Figure 1b); the X domain was the most conserved (dN/dS = 0.43) as found in a previous study . Synonymous substitutions per synonymous site (dS) in the matR partition was approximately four times less than those in the plastid partition (atpB and rbcL) (Figure 1c), showing an extremely low rate of evolution in matR, as seen in other mitochondrial regions [23–26]. Nonsynonymous substitutions per nonsynonymous site (dN) in matR were near to synonymous substitutions per synonymous site (dS) (dN/dS = 0.81) (Figure 1c), indicating a relaxed evolutionary history of matR.
Based on the prediction of the C to U RNA-editing sites in 174 matR sequences, none of the sequences were found to belong to processed paralog, which is capable of adversely effecting the phylogeny estimation . A new data matrix, which excluded RNA-editing sites, was constructed on the basis of this prediction. The two data sets yielded nearly identical ML tree topologies except for some weakly supported interior branches (Additional file 8). In addition, we found that the ML tree from the predicted data received less bootstrap support on most branches than that based on original data, indicating that the exclusion of RNA-editing sites reduced phylogenetic signal. Therefore, we directly used genomic sequences for phylogenetic analysis as suggested by Bowe and dePamphilis .
Phylogenetic analysis of matR
Alignment of matR sequences resulted in a matrix of 1776 sites, of which 732 (41%) were potentially parsimony-informative. A parsimony analysis generated 34 most-parsimonious trees of 3168 steps with a consistency index (CI) of 0.53 and a retention index (RI) of 0.70. A maximum-likelihood (ML) analysis produced an optimal tree with an lnL score of -23390.64. The ML tree with bootstrap (BS) percentages above each branch and the maximum parsimony (MP) bootstrap (BS) percentages below each branch is presented in Figure 2 and 3. The ML and MP analyses recovered trees with virtually identical topologies; most of differences between ML and MP trees were distributed on extremely short branches. The ML-BS percentages on each of the branches were almost identical with the corresponding MP-BS percentages.
Relationships among the basal eudicots including Proteales, Tetracentraceae, Didymelaceae, Buxaceae, Sabiaceae were not resolved (Figure 2). The core eudicots were strongly supported (96% ML-BS and 97% MP-BS). Gunnera (Gunneraceae; Gunnerales) was sister to all other core eudicots (59% ML-BS and 56% MP-BS) as found in a previous study . Relationships among the major core eudicots including rosids, asterids, Caryophyllales, Santalales, Dilleniaceae and Saxifragales were also poorly resolved (Figure 2). The rosid clade was resolved with less than 50% BS.
Within the rosid clade (Figure 3), all orders with multiple representatives formed strongly supported groups except for Rosales and Geraniales. Rosaceae (97% ML-BS and 95% MP-BS) were separated from the remaining members of Rosales, but they were still retained in the nitrogen-fixing subclade of fabids. Fabids did not form a clade in the matR tree, and their monophyly [3, 12, 15] was also rejected by AU test (Additional file 4). The COM subclade of fabids was sister to malvids with 54% ML-BS support. Tribulus, the single representative of Zygophyllaceae, followed by Crossosomatales, was sister to the above large clade of the COM subclade of fabids plus malvids. Within the COM clade, Huaceae were sister to Oxalidales (76% ML-BS and 82% MP-BS), and alternative topologies without this relationship [3, 12] were rejected statistically by the Templeton and AU tests (Additional file 4). Malpighiales and Oxalidales/Huaceae were sisters (78% ML-BS and 69% MP-BS), and alternative topologies without this relationship were either rejected or close to the rejection threshold statistically by AU test (Additional file 4).
Monophyly of malvids was recovered (68% ML-BS and 65% MP-BS), including Malvales, Sapindales, Brassicales, Tapiscia (Tapisciaceae)/Dipentodon (Dipentodontaceae) (Figure 3). Brassicales were sister to Malvales with less than 50% BS, and this pair was in turn sister to Sapindales with less than 50% BS. Dipentodon plus Tapiscia (68% ML-BS and 72% MP-BS) were sister to all other malvids.
The four-gene matrix consisted of 6197 characters, of which 1637 (26%) were potentially parsimony-informative. A parsimony analysis produced 25 most parsimonious trees of 10591 steps with a CI of 0.36 and a RI of 0.49. ML analysis generated an optimal tree with an lnL score of -65288.16. The maximum likelihood (ML) tree with BS percentages above each branch and the maximum parsimony (MP) BS percentages below each branch is presented in Figure 4. Data partitions and tree statistics for all analyses are presented in Table 1. Comparison of supported supraordinal nodes within rosids is presented in Table 2. The topology of the ML-based analysis was virtually identical with that of the MP-based analysis. The ML-BS percentages were almost identical with those of the MP-analysis as in the analysis of the matR alone.
The topology of the four-gene analysis was largely congruent with that resulted from the analysis of matR alone (Figure 2 and 3), but with higher bootstrap percentages, especially on deeper nodes. The core eudicots were strongly supported (100% ML and MP BS). The rosid clade (excluding Vitaceae) was resolved with 66% BS support in the ML tree. Within rosids, Geranium was resolved as sister to a clade including all other rosid members (58% ML-BS and 61% MP-BS) in the ML tree, whereas the genus was excluded from rosids and nested within Saxifagales in the MP strict consensus tree. Myrtales (100% ML and MP BS) were sister to a combined clade (65% ML-BS) of fabids/malvids plus Crossosomatales. Crossosomatales (100% ML and MP BS) were sister to well-supported malvids with 69% ML-BS and 56% MP-BS support.
Monophyly of fabids was recovered (85% ML-BS and 70% MP-BS), and the sister relationship of the COM subclade of fabids with malvids found in the analysis of matR alone was rejected by all statistical tests (Additional file 4). All orders within fabids were monophyletic, including Oxalidales (100% ML and MP BS), Malpighiales (100% ML and MP BS), Celastrales (100% ML and MP BS), Fabales (100% ML-BS and 95% MP-BS), Fagales (100% ML and MP BS), Rosales (100% ML and MP BS), and Cucurbitales (100% ML and MP BS). Despite the typically high support of these orders, relationships among them were relatively weakly supported. There were two large subclades in fabids; one is the nitrogen-fixing clade with 93% ML-BS and 78% MP-BS support, and the other is the COM clade with 88% ML-BS and 74% MP-BS support (Figure 4). Huaceae were grouped with Oxalidales/Malpighiales with 60% BS support in ML tree, but alternative topologies without this relationship [3, 12] were not rejected statistically.
Monophyly of malvids was strongly supported (99% ML-BS and 96% MP-BS); they consisted of Malvales (100% ML and MP BS), Sapindales (100% ML and MP BS), Brassicales (100% ML and MP BS), and Tapiscia (Tapisciaceae). Malvales were sister to Sapindales with 82% ML-BS and 76% MP-BS support, but alternative topologies without this relationship [12, 15] were not rejected statistically. Tapiscia (Tapisciaceae) was resolved as sister to Brassicales with <50% ML-BS and 51% MP-BS support.
Phylogenetic relationships and their robustness
Both bootstrap and jackknife percentages have generally been considered as good indicators of the robustness of clades in phylogenetic trees. However, short internal branches, likely the result of rapid radiations that occurred during earlier periods of flowering plant evolution [4, 35], make phylogenetic reconstruction less accurate [36–38]. We noticed that, in our case, ML analyses resolved more inter-ordinal relationships with greater internal support than those with MP (Figure 2, 3 and 4), and most such cases involve clades with short internal branches (Additional file 6 and 7). In addition, most cases of contradictory resolution between ML and MP trees occur on those extremely short internal branches (Additional file 6 and 7). Several simulation studies have shown that model-based methods outperform parsimony in reconstructing short branches located deep in the tree if saturation does not occur [39–41]. Therefore, our discussion will be based on the ML tree although in general terms the two methods produced highly similar estimates of overall relationships and support.
The topology of the matR tree shows similar relationships among major eudicot lineages as those based on plastid genes rbcL, atpB and matK in previous separate or combined analyses [12–15]. Clades occurring at basal nodes include Proteales, Trochodendraceae, Buxaceae, and Sabiaceae. Core eudicots are strongly supported and consist of Gunnerales, Dilleniaceae, Caryophyllales, Santalales, Saxifragales, rosids, and asterids. The four-gene data set did not resolve relationships among major eudicot clades, including the rosids, asterids, caryophyllids, Santalales, and Saxifragales. Most rosid orders are well supported in both matR and four-gene trees. These orders, including their composition and phylogenetics have been discussed previously [4, 42]. Here we mainly focus on higher-level relationships that are different and compare them with other recent studies. Some clades do not receive strong support, but they nevertheless warrant attention in future studies.
The rosid clade (excluding Vitaceae) has been recovered with low to high bootstrap support in recent phylogenetic analyses of the angiosperms [3, 12, 15, 43, 44]. Low support for rosid clade was obtained in our four-gene analysis, and relatively short internal branch lengths were observed for the rosid node in both the matR and the four-gene trees (Additional file 6 and 7). Likewise, when we examine support for the rosid clade from the four single-gene matrices as well as various combinations of them we found that this clade was either not present or showed only low ML-BS support (Table 2), which is similar to some earlier studies [10, 12, 13]. Like three-gene analysis  and those of nearly complete plastid genomes [43, 44], our four-gene analysis also showed that Vitaceae are sister to rosids, but received less than 50% ML-BS support.
Geraniales, Myrtales and Crossosomatales
Previous analyses have produced several positions for the representatives of these three orders but they have never received more than 50% JK or BS support. Therefore, they are still among the major higher-level questions within the rosids . In this study, analysis of matR alone did not resolve their placements with greater than 50% bootstrap support, but the four-gene analysis did. In addition, it is also worth noting that Crossosomatales were resolved as a sister to a larger clade, including the COM subclade of fabids and malvids, with slightly less than 50% bootstrap support in the analysis of matR alone (results not shown). There are two morphological characters supporting the position obtained for Crossosomatales in this analysis: (1) arillate seeds are conspicuous in the COM clade of fabids, and they are also present in malvids and Crossosomatales although less prominent in the last two clades ; (2) free carpels in which the upper part is postgenitally united at anthesis, which appear to be restricted to Malvales and Sapindales of malvids, some Crossosomatales, and Saxifragales [20, 45, 46]. Therefore, we suggest that Crossosomatales may belong to malvids or a larger clade including the COM subclade of fabids and malvids.
This large clade includes Malpighiales, Oxalidales, Zygophyllaceae, Celastrales, Cucurbitales, Fagales, Fabales, and Rosales. Our four-gene analysis recovered this clade with moderate BS support, similar to the three-gene analysis of Soltis et al. . However, our analysis of matR alone did not recover fabids as a clade, and their monophyly is also rejected by the AU test. Instead, an additional sister relationship between the COM subclade of fabids and malvids was recognized, albeit with low ML-BS support. This conflicting resolution may arise from a different history or evolutionary phenomena for matR than the other partitions. Support for fabids primarily comes from the two plastid (rbcL and atpB) and nuclear genes (18S rDNA; Table 2), although addition of matR improved resolution within fabids. We note that a sister relationship of the COM subclade of fabids and malvids was moderately supported by floral structural features, but there was only weak support for the fabids from reproductive features , particularly an inner integument that is thicker than the outer at the time of fertilization. Other supporting characters  include: (1) contorted petals, (2) a tendency towards polystemony, (3) a tendency towards polycarpelly, and (4) integuments often free from each other and from the nucellus; none of these are particularly robust (most are tendencies). Thus, the deepest split within rosids might be between the nitrogen-fixing clade and a large clade including malvids, the COM subclade of fabids, Crossosomatales and Zygophyllaceae (Figure 3), as suggested by Endress and Matthews , not between fabids and malvids. It is obvious that more molecular data from all three genomes will be required to further assess whether this novel relationship is locus-specific or general. Our four-gene analysis also identified a larger assemblage of orders with low BS support including fabids, malvids and Crossosomatales, which constitutes the core part of rosids.
There are two major subclades within fabids, the nitrogen-fixing clade  and the COM clade . Our four-gene analysis is basically in agreement with those based on three genes  but obtains higher support for these two subclades. Within the nitrogen-fixing clade, the sister relationship of Cucurbitales and Fagales was supported in various analyses [3, 47]; however, our four-gene analysis does not recognize their sister relationship. In contrast, the sister relationship of Fagales and Rosales was weakly supported in the ML tree, and then they grouped with Cucurbitales to form a larger clade with moderate ML-BS support. These three orders each contain actinorhizal plants with roots nodulated by strains of Frankia . Previous molecular analyses have recognized these actinorhizal plants as a clade [47, 49], but the taxonomic sampling in these analyses seems to be inadequate for evaluating their relationships. Our results support the hypothesis that the actinorhizal plants originated separately from Fabaceae and Ulmaceae, which are nodulated by rhizobial bacteria [4, 19].
In the COM clade, Celastrales have been resolved as sister to Oxalidales in previous studies [9, 15, 31]. In a more recent multi-gene analysis, Celastrales were recognized as sister to Malpighiales with high JK support , consistent with the result of Chase et al. . In our analysis of the matR alone, Malpighiales and Oxalidales appeared as sister groups, consistent with several previous analyses [3, 12, 14], but with apparently higher support; in our four-gene ML tree, they were also resolved as sister groups, but with a decreasing BS support, indicating this signal is primarily derived from the matR gene (Table 2); alternatively, the weaker support could be the result of sparser sampling in the four-gene analysis. Analysis of the matR matrix placed Huaceae as sister to Oxalidales with moderate support, in agreement with other recent results [4, 21, 22], whereas our four-gene analysis demonstrates different resolutions between MP and ML trees: the MP analysis resolves Huaceae as sister to Celastrales with <50% BS support, whereas the ML analysis recognizes Huaceae as sister to Oxalidales plus Malpighiales with low BS support.
Malpighiales are a large order including more than 30 families , and they have received strong support in previous analyses [3, 12, 15]. Some families of Dilleniidae sensu Cronquist , such as Ochnaceae, Clusiaceae, Violaceae, Passifloraceae, Salicaceae and Flacourtiaceae are included in Malpighiales. In the matR tree, Salicaceae s.l. (including some former Flacourtiaceae ) form a strongly supported clade (BS 100%); Caryocar of Caryocaraceae and Drypetes of Putranjivaceae form a weakly supported clade (55% MP-BS). Balanops, the only genus of Balanopaceae, was previously supposed to be related to Fagales because of similar pollen and a cupule-like structure . The matR analyses support a position of Balanopaceae in Malpighiales, in agreement with the results of the three-gene analysis  and the recent morphology-based study .
Both matR alone and the four-gene combined analyses resolve malvids as a monophyletic clade, as has been found in other analyses [3, 12, 15, 30]. In our analysis of matR alone, Dipentodon (Dipentodontaceae), with uncertain position in APG (2003) , was resolved as sister to Tapiscia (Tapisciaceae) with low support, which is consistent with another recent analysis . Our analysis of matR alone did not resolve relationships of Malvales, Brassicales and Sapindales with greater than 50% BS support, but in our four-gene analysis, the sister-group relationship of Malvales and Sapindales received a moderate BS support, in agreement with the result (51% MP-JK) of three-gene analysis of Soltis et al.  and the result (89% MP-BS) of four-gene analysis of Nickrent et al. . Malvales and Sapindales share two morphological characters, i.e., "a tendency towards the presence of several (more than two) meiocytes in an ovule and elaborate apocarpy" .
Potential of matR in large-scale phylogenetic studies
Our analysis of matR alone produced a tree highly congruent with previous studies of single and multiple genes [3, 12, 15]. In particular, the main contribution of the matR data appears to be for estimating support of orders. When supraordinal relationships within the rosid clade are compared on the basis of individual genes, matR data resolves more nodes with ML-BS support >50% than rbcL, atpB or 18S rDNA (length corrected) and is similar to matK alone and rbcL-atpB combined (Table 2). In addition, when matR is combined with rbcL-atpB or rbcL-atpB-18S rDNA data, additional supraordinal relationships with BS support >50% occur (Table 2). This indicates that mitochondrial matR is suitable for reconstructing angiosperm phylogeny at higher levels.
The matR gene exhibits two outstanding evolutionary features, a slow rate of evolution and relaxed selection (Figure 1c). For phylogenetic analyses in general, genes that evolve relatively slowly are likely to contain fewer homoplasious substitutions, but then are also expected to have fewer informative sites. Obviously, slowly evolving matR should provide less phylogenetic information than plastid genes like rbcL and atpB, and this should affect its resolving power on short internal branches due to the reduction of phylogenetic signal [36, 52]. However, this reduction is at least partially offset by relaxed evolutionary constraints, which leads to more nonsynonymous substitution sites at otherwise conservative first and second codon positions. As a result, the matR data has more variable characters and parsimony-informative sites (Pi) compared to the other three genes (length corrected) (Table 1). Although both matR and plastid matK have experienced a relaxed evolutionary history , matR (Table 1) provides a significantly higher consistency index (CI) and slightly higher retention index (RI) than significantly more rapidly evolving matK [, and references therein].
Analyses of matR sequences alone or combined with atpB, rbcL, and 18S rDNA have provided new insights into several deep relationships among rosid lineages, albeit with low support, including the grouping of malvids and COM subclade of fabids from single matR gene analysis, and the placements of Geraniales, Myrtales and Crossosomatales from the combined four-gene analysis. At ordinal and deeper nodes, matR provides many informative sites with less homoplasy, which makes it suitable in higher-level angiosperm phylogenetics. Mitochondrial matR sequences have produced a different topology when combined with plastid and nuclear sequences, and therefore, more genes from the mitochondrial genome should be used in combination with plastid and nuclear genes to further investigate the results presented here, although there are major problems to be overcome with transfers of some gene to the nuclear genome and unusual patterns of molecular evolution for some mitochondrial genes, such as atp1 and coxI, used in monocot phylogenetics .
For this study, a total of 174 matR sequences representing 118 families of eudicots and 72 families of rosids, with representatives from 59% of fabid families and 41% of malvid families  were included. Of them, 93 matR sequences were newly generated. Vouchers are deposited in either the herbarium of the Institute of Botany, Chinese Academy of Sciences, Beijing, People's Republic of China (PE), or the Herbarium, Royal Botanic Gardens, Kew, UK (K). In addition to the 174-taxon matR matrix, we also analyzed a smaller four-gene combined matrix by combining the matR sequences with previously published sequences of rbcL, atpB, and 18S rDNA available from GenBank. The combined dataset consisted of 91 taxa. When possible, the same species was used for all four genes. The taxa and collection information have been listed in Additional file 1
DNA extraction and sequencing
For each of the 93 specimens newly sequenced for matR, fresh leaves were frozen or dried in silica gel . Total genomic DNAs were isolated following procedures described in . The primers matR 26F (5' GACCGCTNACAGTAGTTCT 3') and matR 1858R (5' TGCTTGTGGGCYRGGGTGAA 3') were used for both PCR amplification and sequencing. Two additional internal primers, matR 879F (5' ACTAGTTATCAGGTCAGAGA 3') and matR 1002R (5' CACCCACGATTCCCAGTAGT 3'), were also used in sequencing. These internal primers are not universal for all sampled taxa, and therefore, two additional sequencing primers were designed, matR-F3 (5' GGACACACCTGCGCGGATTA 3') and matR-R3 (5' ATCTAGGATAGGCRGCCAACC 3').
PCR was performed using a Perkin Elmer 9600 thermocycler (Norwalk, Connecticut, USA). PCR products were purified using Wizard PCR purification (Promega, Madison, Wisconsin, USA). Sequencing reactions were performed using the PRISM Dye Terminator Cycle Sequencing Ready Reaction Kit (Applied Biosystems, Inc., ABI, Foster City, California, USA), and the products were analyzed using an ABI 377 DNA sequencer, all following the manufacturer's protocols.
Alignment and Data matrix
The174 matR sequences were first aligned at the amino acid level using Clustal X , and then the corresponding DNA sequence alignment was constructed according to the protein sequence alignment using PAL2NAL program , followed by some manual adjustment. The smaller combined data matrix with 91 taxa was constructed by combining newly generated matR sequences with sequences of the three other genes from GenBank. The three protein-coding genes (matR, rbcL and atpB) used in combined matrix were aligned independently with the same procedure as described above. For 18S rDNA, some ambiguous regions were excluded because positional homology could not be established; a total of 61 ambiguously aligned positions were excluded. Autapomorphic insertions and ends of sequences were removed from each alignment. Alignments are available on TreeBASE  under M3533 and M3534.
The 174-taxon matR matrix and the four-gene combined matrix with 91 taxa were analyzed with maximum parsimony (MP) and maximum likelihood (ML) methods. Ranunculales were designed as outgroup based on topologies of the eudicots in previous large-scale angiosperm studies [3, 9, 12, 13, 59]. Equally weighted MP analysis was performed in PAUP* v4.0b10  using 1,000 random replicates of tree-bisection-reconnection (TBR) heuristic searches with a maximum of 1,000 trees held per TBR search. Robustness of clades under MP analysis was evaluated by non-parametric bootstrap using 500 pseudo-replicates with 100 random additions per replicate. For ML analyses, the optimal model and parameters were determined using the hierarchical likelihood ratio tests (hLRTs) as implemented in Modeltest v.3.6 , and analyses were implemented in PHYML v.2.4.4  under GTR+Γ model for 174-taxon matR matrix and GTR+I+Γ for four-gene combined matrix with all parameters for each data matrix (Additional file 2). Support was estimated by non-parametric bootstrap using 1000 replicates. We used the following descriptions and ranges in the text for describing bootstrap (BS) support in ML and MP analysis: low, up to 75%; moderate, 76–85%; high, 86–100% .
Several potential data partitions in the combined matrix were analyzed to compare their phylogenetic signal and contribution to results. These data partitions include each of the four genes, plastid genes (rbcL-atpB), plastid plus mitochondrial gene (rbcL-atpB-matR), plastid plus nuclear genes (rbcL-atpB-18S), and plastid plus mitochondrial plus nuclear genes (rbcL-atpB-18S-matR). The optimal models and parameters were derived from each partition (Additional file 2). In addition, analyses based on the three-codon positions in matR were also conducted on 174-taxon matR matrix to compare variation and phylogenetic signal.
To assess alternative phylogenetic hypotheses, we employed the Templeton  and winning-site  tests as implemented in PAUP* v4.0b10 under MP, and the Shimodaira-Hasegawa (SH)  and approximately unbiased (AU)  tests under ML as implemented in CONSEL . Constraint trees of alternative topologies were generated using MacClade v4.06 Additional file 5.
Sequence variability and pattern of molecular evolution
We used PAUP* v4.0b10  to analyze homogeneity of nucleotide composition, transition/transversion ratios and saturation. PAML v3.15  and MEGA v 3.1  were used to calculate synonymous substitutions per synonymous site (dS) and nonsynonymous substitutions per nonsynonymous site (dN) for each gene. We compared the dS and dN values among three protein-coding genes (matR, rbcL and atpB) to test for differences in rates and constraints. Such estimation was also performed for different domains in matR to evaluate the distribution of the variation. We plotted uncorrected pairwise sequence divergence distances against corresponding dS and dN values to test change in lineage-specific selection pressure. If some lineages experienced more relaxed or rigorous selection than others in the light of divergence distances, the dN value should reveal a poor linear fit than dS value. Use of nonsynonymous substitutions with lineage-specific selection pressure change could lead to incorrect phylogenetic inference .
Sites of C to U RNA-editing in matR have been identified experimentally in several angiosperm species [73–76]. Although previous small-scale studies revealed no significant differences in phylogenetic inference between including and excluding RNA-edited sites [34, 77], it may be necessary to test for this effect on phylogeny estimation when a large-scale analysis is conducted because these sites are not always conserved among species . In addition, processed paralogs, which may disrupt phylogeny estimation if they are jointly analyzed with vertically transferred DNA , can be also detected if a given sequence is relatively free from RNA editing. We used PREP-Mt program  with cutoff value of 0.6 for predicting RNA-editing sites in the 174-matR sequences. The resulting data matrix (TreeBASE: M3532) was analyzed and compared with original data matrix to examine effects of RNA editing.
- atpB – ATP synthase beta subunit:
Number of nonsynonymous substitutions per nonsynonymous site
Number of synonymous substitutions per synonymous site
general time reversible model (a model of DNA sequence evolution)
- I + Γ:
invariant sites plus gamma distribution
- matK :
plastid maturase K gene
- matR :
mitochondrial maturase R gene
- rbcL :
ribulose bisphosphate carboxylase/oxygenase, large subunit, plastid gene
tree bisection-reconnection branch swapping
APG: An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG II. Botanical Journal of the Linnean Society. 2003, 141: 399-436. 10.1046/j.1095-8339.2003.t01-1-00158.x.
Nandi OI, Chase MW, Endress PK: A combined cladistic analysis of angiosperms using rbcL and non-molecular data sets. Annals of the Missouri Botanical Garden. 1998, 85: 137-212. 10.2307/2992003.
Soltis DE, Soltis PS, Chase MW, Mort ME, Albach DC, Zanis M, Savolainen V, Hahn WH, Hoot SB, Fay MF, Axtell M, Swensen SM, Prince LM, Kress WJ, Nixon KC, Farris JS: Angiosperm phylogeny inferred from 18S rDNA, rbcL, and atpB sequences. Botanical Journal of the Linnean Society. 2000, 133: 381-461. 10.1006/bojl.2000.0380.
Soltis DE, Soltis PS, Endress PK, Chase MW: Phylogeny and evolution of angiosperms. 2005, Sunderland, Massachusetts: Sinauer Associates, Inc. Publishers
Cronquist A: The evolution and classification of flowering plants. 1988, New York: Columbia University Press, 2
Takhtajan A: Diversity and classification of flowering plants. 1997, New York: Columbia University Press
Crane PR, Blackmore S: Evolution, systematics, and fossil history of the Hamamelidae. Vol. 2: "Higher" Hamamelidae. Systematics Association Special Vol. No. 40B. 1989, Oxford, UK: Clarendon Press
Hufford L: Rosidae and their relationships to other nonmagnoliid dicotyledons: a phylogenetic analysis using morphological and chemical data. Annals of the Missouri Botanical Garden. 1992, 79: 218-248. 10.2307/2399767.
Chase MW, Soltis DE, Olmstead RG, Morgan D, Les DH, Mishler BD, Duvall MR, Price RA, Hills HG, Qiu YL, Kron KA, Rettig JH, Conti E, Palmer JD, Manhart JR, Sytsma KJ, Michaels HJ, Kress WJ, Karol KG, Clark WD, Hedren M, Gaut BS, Jansen RK, Kim KJ, Wimpee CF, Smith JF, Furnier GR, Strauss SH, Xiang QY, Plunkett GM, Soltis PS, Swensen SM, Williams SE, Gadek PA, Quinn CJ, Eguiarte LE, Golenberg E, Learn GH, Graham SW, Barrett SCH, Dayanandan S, Albert VA: Phylogenetics of seed plants: an analysis of nucleotide sequences from the plastid gene rbcL. Annals of the Missouri Botanical Garden. 1993, 80: 528-580. 10.2307/2399846.
Soltis DE, Soltis PS, Nickrent DL, Johnson LA, Hahn WJ, Hoot SB, Sweere JA, Kuzoff RK, Kron KA, Chase MW, Swensen SM, Zimmer EA, Chaw SM, Gillespie LJ, Kress WJ, Sytsma KJ: Angiosperm phylogeny inferred from 18S ribosomal DNA sequences. Annals of the Missouri Botanical Garden. 1997, 84: 1-49. 10.2307/2399952.
Magallón S, Crane PR, Herendeen PS: Phylogenetic pattern, diversity, and diversification of eudicots. Annals of the Missouri Botanical Garden. 1999, 86: 297-372. 10.2307/2666180.
Savolainen V, Chase MW, Hoot SB, Morton CM, Soltis DE, Bayer C, Fay MF, de Bruijn AY, Sullivan S, Qiu YL: Phylogenetics of flowering plants based on combined analysis of plastid atpB and rbcL gene sequences. Systematic Biology. 2000, 49: 306-362. 10.1080/10635159950173861.
Savolainen V, Fay MF, Albach DC, Backlund A, van der Bank M, Cameron KM, Johnson SA, Lledó MD, Pintaud JC, Powell M, Sheahan MC, Soltis DE, Soltis PS, Weston P, Whitten WM, Wurdack KJ, Chase MW: Phylogeny of the eudicots: A nearly complete familial analysis based on rbcL gene sequences. Kew Bulletin. 2000, 55: 257-309. 10.2307/4115644.
Soltis DE, Senters AE, Zanis MJ, Kim S, Thompson JD, Soltis PS, De Craene LPR, Endress PK, Farris JS: Gunnerales are sister to other core eudicots: Implications for the evolution of pentamery. American Journal of Botany. 2003, 90: 461-470. 10.3732/ajb.90.3.461.
Hilu KW, Borsch T, Muller K, Soltis DE, Soltis PS, Savolainen V, Chase MW, Powell MP, Alice LA, Evans R, Sauquet H, Neinhuis C, Slotta TAB, Rohwer JG, Campbell CS, Chatrou LW: Angiosperm phylogeny based on matK sequence information. American Journal of Botany. 2003, 90: 1758-1776. 10.3732/ajb.90.12.1758.
Albach DC, Soltis PS, Soltis DE, Olmstead RG: Phylogenetic analysis of the Asteridae based on sequences of four genes. Annals of the Missouri Botanical Garden. 2001, 88: 163-212. 10.2307/2666224.
Bremer B, Bremer K, Heidari N, Erixon P, Olmstead RG, Anderberg AA, Källersjö M, Barkhordarian E: Phylogenetics of asterids based on 3 coding and 3 non-coding chloroplast DNA markers and the utility of non-coding DNA at higher taxonomical levels. Molecular Phylogenetics and Evolution. 2002, 24: 274-301. 10.1016/S1055-7903(02)00240-3.
Olmstead R, Kim K-J, Jansen RK, Wagstaff SJ: The phylogeny of the Asteridae sensu lato based on chloroplast ndhF gene sequences. Molecular Phylogenetics and Evolution. 2000, 16: 96-112. 10.1006/mpev.1999.0769.
Soltis DE, Soltis PS, Morgan DR, Swensen SM, Mullin BC, Dowd JM, Martin PG: Chloroplast gene sequence data suggest a single origin of the predisposition for symbiotic nitrogen fixation in angiosperms. Proceedings of the National Academy of Sciences of the United States of America. 1995, 92: 2647-2651. 10.1073/pnas.92.7.2647.
Endress PK, Matthews ML: First steps towards a floral structural characterization of the major rosid subclades. Plant Systematics and Evolution. 2006, 260: 223-251.
Zhang LB, Simmons MP: Phylogeny and delimitation of the Celastrales inferred from nuclear and plastid genes. Systematic Botany. 2006, 31: 122-137. 10.1600/036364406775971778.
Davis CC, Wurdack KJ: Host-to-parasite gene transfer in flowering plants: phylogenetic evidence from Malpighiales. Science. 2004, 305: 676-678. 10.1126/science.1100671.
Wolfe KH, Li WH, Sharp PM: Rates of nucleotide substitution vary greatly among plant mitochondrial, chloroplast, and nuclear DNAs. Proceedings of the National Academy of Sciences of the United States of America. 1987, 84: 9054-9058. 10.1073/pnas.84.24.9054.
Palmer JD, Herbon LA: Plant mitochondrial DNA evolves rapidly in structure, but slowly in sequence. Journal of Molecular Evolution. 1988, 28: 87-97. 10.1007/BF02143500.
Gaut BS: Molecular clocks and nucleotide substitution rates in higher plants. Evolutionary Biology. Edited by: Hecht MK, MacIntyre RJ, Clegg MT. 1998, New York: Plenum Press, 30: 93-120.
Muse SV: Examining rates and patterns of nucleotide substitution in plants. Plant Molecular Biology. 2000, 42: 25-43. 10.1023/A:1006319803002.
Qiu YL, Lee J, Bernasconi-Quadroni F, Soltis DE, Soltis PS, Zanis M, Zimmer EA, Chen ZD, Savolainen V, Chase MW: The earliest angiosperms: evidence from mitochondrial, plastid and nuclear genomes. Nature. 1999, 402: 404-407. 10.1038/46536.
Dombrovska O, Qiu YL: Distribution of introns in the mitochondrial gene nad1 in land plants: phylogenetic and molecular evolutionary implications. Molecular Phylogenetics and Evolution. 2004, 32: 246-263. 10.1016/j.ympev.2003.12.013.
Zimmerly S, Hausner G, Wu X: Phylogenetic relationships among group II intron ORFs. Nucleic Acids Research. 2001, 29: 1238-1250. 10.1093/nar/29.5.1238.
Peng YL, Chen ZD, Gong X, Zhong Y, Shi SH: Phylogenetic position of Dipentodon sinicus: evidence from DNA sequences of chloroplast rbcL, nuclear ribosomal 18S, and mitochondrial matR genes. Botanical Bulletin of Academia Sinica. 2003, 44: 217-222.
Nickrent DL, Der JP, Anderson FE: Discovery of the photosynthetic relatives of the "Maltese mushroom" Cynomorium. BMC Evolutionary Biology. 2005, 5: 38-10.1186/1471-2148-5-38.
Qiu YL, Lee J, Bernasconi-Quadroni F, Soltis DE, Soltis PS, Zanis M, Zimmer EA, Chen ZD, Savolainen V, Chase MW: Phylogeny of basal angiosperms: Analyses of five genes from three genomes. International Journal of Plant Sciences. 2000, 161: S3-S27. 10.1086/317584.
Li RQ, Chen ZD, Lu AM, Soltis DE, Soltis PS, Manos PS: Phylogenetic relationships in Fagales based on DNA sequences from three genomes. International Journal of Plant Sciences. 2004, 165: 311-324. 10.1086/381920.
Bowe LM, dePamphilis CW: Effects of RNA editing and gene processing on phylogenetic reconstruction. Mol Biol Evol. 1996, 13 (9): 1159-1166.
Davis CC, Webb CO, Wurdack KJ, Jaramillo CA, Donoghue MJ: Explosive radiation of Malpighiales supports a mid-Cretaceous origin of modern tropical rain forests. The American Naturalist. 2005, 165: E36-E65. 10.1086/428296.
Fishbein M, Hibsch-Jetter C, Soltis DE, Hufford L: Phylogeny of Saxifragales (angiosperms, eudicots): analysis of a rapid, ancient radiation. Systematic Biology. 2001, 50: 817-847. 10.1080/106351501753462821.
Felsenstein JS: Cases in which parsimony or compatibility methods will be positively misleading. Systematic Zoology. 1978, 27: 401-410. 10.2307/2412923.
Huelsenbeck JP: Is the Felsenstein zone a fly trap?. Systematic Biology. 1997, 46: 69-74. 10.2307/2413636.
Hillis DM, Huelsenbeck JP, Cunningham CW: Application and accuracy of molecular phylogenies. Science. 1994, 264: 671-677. 10.1126/science.8171318.
Huelsenbeck JP: Performance of phylogenetic methods in simulation. Systematic Biology. 1995, 44: 17-48. 10.2307/2413481.
Weisrock DW, Harmon LJ, Larson A: Resolving deep phylogenetic relationships in salamanders: analyses of mitochondrial and nuclear genomic data. Systematic Biology. 2005, 54: 758-777. 10.1080/10635150500234641.
Judd WS, Olmstead RG: A survey of tricolpate (eudicot) phylogenetic relationships. American Journal of Botany. 2004, 91: 1627-1644. 10.3732/ajb.91.10.1627.
Jansen RK, Kaittanis C, Saski C, Lee SB, Tomkins J, Alverson AJ, Daniell H: Phylogenetic analyses of Vitis (Vitaceae) based on complete chloroplast genome sequences: effects of taxon sampling and phylogenetic methods on resolving relationships among rosids. BMC Evolutionary Biology. 2006, 6: 32-10.1186/1471-2148-6-32.
Ravi V, Khurana JP, Tyagi AK, Khurana P: Rosales sister to Fabales: towards resolving the rosid puzzle. Molecular Phylogenetics and Evolution. 2007, 44: 488-493. 10.1016/j.ympev.2006.11.014.
Matthews ML, Endress PK: Comparative floral structure and systematics in Celastrales (Celastraceae, Parnassiaceae, Lepidobotryaceae). Botanical Journal of the Linnean Society. 2005, 149: 129-194. 10.1111/j.1095-8339.2005.00445.x.
Hermsen EJ, Gandolfo MA, Nixon KC, Crepet WL: Divisestylus gen. nov. (aff. Iteaceae), a fossil saxifrage from the Late Cretaceous of New Jersey, USA. American Journal of Botany. 2003, 90: 1373-1388. 10.3732/ajb.90.9.1373.
Zhang LB, Simmons MP, Kocyan A, Renner SS: Phylogeny of the Cucurbitales based on DNA sequences of nine loci from three genomes: implications for morphological and sexual system evolution. Molecular Phylogenetics and Evolution. 2006, 39: 305-322. 10.1016/j.ympev.2005.10.002.
Torrey JG, Tjepkema JD: Symbiotic nitrogen fixation in actinomycete-nodulated plants. Botanical Gazette. 1979, 140 (Suppl): i-ii. 10.1086/337026.
Swensen SM: The evolution of actinorhizal symbiosis:evidence for multiple origins of the symbiotic association. American Journal of Botany. 1996, 83: 1503-1512. 10.2307/2446104.
Chase MW, Zmarzty S, Lledó MD, Wurdack KJ, Swensen SM, Fay MF: When in doubt, put it in Flacourtiaceae: a molecular phylogenetic analysis based on plastid rbcL DNA sequences. Kew Bulletin. 2002, 57: 141-181. 10.2307/4110825.
Sutter DM, Endress PK: Female flower and cupule structure in Balanopaceae, an enigmatic rosid family. Annals of Botany. 2003, 92: 459-469. 10.1093/aob/mcg158.
Donoghue MJ, Sanderson MJ: The suitability of molecular and morphological evidence in reconstructing plant phylogeny. Molecular systematics of plants. Edited by: Soltis PS, Soltis DE, Doyle JJ. 1992, New York: Chapman and Hall, 340-368.
Petersen G, Seberg O, Davis JI, Goldman DH, Stevenson DW, Campbell LM, Mihelangeli FA, Specht CD, Chase MW, Fay MF, Pires JC, Freudenstein JV, Hardy CR, Simmons MP: Mitochondrial data in monocot phylogenetics. Aliso. 2006, 22: 52-62.
Chase MW, Hills HG: Silica gel: an ideal material for field preservation of leaf samples for DNA studies. Taxon. 1991, 40: 215-220. 10.2307/1222975.
Bousquet J, Simon L, Lalonde M: DNA amplification from vegetative and sexual tissues of trees using polymerase chain reaction. Canadian Journal of Forest Research. 1990, 20: 254-257. 10.1139/x90-037.
Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG: The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Research. 1997, 25: 4876-4882. 10.1093/nar/25.24.4876.
Suyama M, Torrents D, Bork P: PAL2NAL: robust conversion of protein sequence alignments into the corresponding codon alignments. Nucleic Acids Research. 2006, 34 (Web Server issue): W609-612. 10.1093/nar/gkl315.
Hoot SB, Magallón S, Crane PR: Phylogeny of basal eudicots based on three molecular data sets: atpB, rbcL, and 18S nuclear ribosomal DNA sequences. Annals of the Missouri Botanical Garden. 1999, 86: 1-32. 10.2307/2666215.
Swofford DL: PAUP*: Phylogenetic analysis using parsimony (* and other methods). 2002, Sunderland, MA: Sinauer Associates, 4.0b10
Posada D, Crandall KA: MODELTEST: testing the model of DNA substitution. Bioinformatics. 1998, 14: 817-818. 10.1093/bioinformatics/14.9.817.
Guindon S, Gascuel O: A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Systematic Biology. 2003, 52: 696-704. 10.1080/10635150390235520.
Chase MW, Soltis DE, Soltis PS, Rudall PJ, Fay MF, Hahn W, Sullivan S, Joseph J, Givnish T, Sytsma KJ, Pires C: Higher-level systematics of the monocotyledons: an assessment of current knowledge and a new classification. 2000, Sydney, Australia: CSIRO Press
Templeton AR: Phylogenetic inference from restriction endonuclease cleavage site maps with particular reference to the evolution of humans and the apes. Evolution. 1983, 37: 221-244. 10.2307/2408332.
Templeton AR: Convergent evolution and nonparametric inferences from restriction data and DNA sequences. Statistical analysis of DNA sequence data. Edited by: WEIR BS. 1983, New York and Basel: Marcel Dekker, 151-179.
Shimodaira H, Hasegawa M: Multiple comparisons of log-likelihoods with applications to phylogenetic inference. Molecular Biology and Evolution. 1999, 16: 1114-1116.
Shimodaira H: An approximately unbiased test of phylogenetic tree selection. Systematic Biology. 2002, 51: 492-508. 10.1080/10635150290069913.
Shimodaira H, Hasegawa M: CONSEL: for assessing the confidence of phylogenetic tree selection. Bioinformatics. 2001, 17: 1246-1247. 10.1093/bioinformatics/17.12.1246.
Maddison DR, Maddison WP: MacClade 4: Analysis of phylogeny and character evolution, version 4.06. 2003, Sunderland, MA: Sinauer Associates
Yang Z: PAML: a program package for phylogenetic analysis by maximum likelihood. Computer Applications in the Biosciences. 1997, 13: 555-556.
Kumar S, Tamura K, Nei M: MEGA3: Integrated software for molecular evolutionary genetics analysis and sequence alignment. Briefings in Bioinformatics. 2004, 5: 150-163. 10.1093/bib/5.2.150.
Nei M, Kumar S: Molecular evolution and phylogenetics. 2000, New York: Oxford University Press
Begu D, Mercado A, Farre JC, Moenne A, Holuigue L, Araya A, Jordana X: Editing status of mat-r transcripts in mitochondria from two plant species: C-to-U changes occur in putative functional RT and maturase domains. Current Genetics. 1998, 33: 420-428. 10.1007/s002940050355.
Thomson MC, Macfarlane JL, Beagley CT, Wolstenholme DR: RNA editing of mat-r transcripts in maize and soybean increases similarity of the encoded protein to fungal and bryophyte group II intron maturases: evidence that mat-r encodes a functional protein. Nucleic Acids Research. 1994, 22: 5745-5752. 10.1093/nar/22.25.5745.
Giege P, Brennicke A: RNA editing in Arabidopsis mitochondria effects 441 C to U changes in ORFs. Proceedings of the National Academy of Sciences of the United States of America. 1999, 96: 15324-15329. 10.1073/pnas.96.26.15324.
Handa H: The complete nucleotide sequence and RNA editing content of the mitochondrial genome of rapeseed (Brassica napus L.): comparative analysis of the mitochondrial genomes of rapeseed and Arabidopsis thaliana. Nucleic Acids Research. 2003, 31: 5907-5916. 10.1093/nar/gkg795.
Qiu Y-L, Li L, Hendry T, Li R, Taylor DW, Issa MJ, Ronen AJ, Vekaria ML, White AM: Reconstructing the basal angiosperm phylogeny: evaluating information content of the mitochondrial genes. Taxon. 2006, 55: 837-856.
Mower JP: PREP-Mt: predictive RNA editor for plant mitochondrial genes. BMC Bioinformatics. 2005, 6: 96-10.1186/1471-2105-6-96.
The authors thank Min Feng, De-Yuan Hong, Ya-Ping Hong, Cha-Cha Huang, Xiao-Hua Jin, Qing-Jun Li, Zhen-Yu Li, Ya-Ling Peng, Qing-Feng Wang, Ke-Xue Xu, Jun-Bo Yang, Dao-Yuan Zhang, Shu-Ren Zhang, Cheng-Wu Zhou and Wei Wang for their help in the field work or providing plant tissue for this study; Cha-Cha Huang, and Jeffrey Joseph for their lab assistance. This research was supported by National Basic Research Program of China (973 Program no. 2007CB411600), Natural Science Foundation of China grant (30121003 and 39970057), Chinese Academy of Sciences (KSCX2-YW-R-136), Royal Botanic Gardens, Kew, and a Sino-U.K. international collaboration project.
XYZ carried out all data analyses, and wrote several sections of this manuscript; MWC, YLQ, DLD, and JHL revised several versions of this manuscript; HZK assisted with analyses and alignment of DNA sequences for phylogenetic analyses; ZDC designed the study, conducted field sampling, generated DNA sequences, and wrote several sections. All authors read and commented on drafts of the manuscript and approved the final manuscript.
Electronic supplementary material
Additional file 1: matR and combined data sets. The MS Excel file provides taxon sampling of the matR gene and GenBank accession numbers for matR alone and four-gene data sets. Entries in red denote the taxa newly sequenced for matR in this study. (XLS 368 KB)
Additional file 2: . An MS Excel file gives optimal models and parameters determined in ModelTest for matR-174-taxon and several data partitions in 91-taxon four-gene matrix using hierarchical likelihood ratio tests (hLRTs). (XLS 16 KB)
Additional file 3: matR. An MS Excel file gives statistics for the three-codon positions in matR. Values are based on the one of shortest trees found in 174-taxon matrix of matR. Pi, parsimony informative; CI, consistency index; RI, retention index; RC, rescaled consistency index. (XLS 15 KB)
Additional file 4: . An MS Excel file contains results of statistical tests, the Templeton and Winning-site tests for parsimony topologies, and the approximately unbiased (AU), and Shimodaira-Hasegawa (SH) tests for maximum likelihood topologies. Numbers in parentheses indicate the source of alternative topologies. Asterisks denote significance differences at P < 0.05 in column 4, 5, and 7. Alternative topologies are presented in Additional file 5. (XLS 16 KB)
Additional file 6: matR. A single tree with branch lengths proportional to the amount of change from the maximum likelihood (ML) analysis of the mitochondrial matR gene with 174 taxa using the GTR+Γ model, showing the pattern of long and short branches that occurs repeatedly in flowering plants. Asterisks denote contradictory resolutions between ML tree and MP strict consensus of all shortest trees. (PDF 39 KB)
Additional file 7: . A single tree with branch lengths proportional to the amount of change from the maximum likelihood (ML) analysis of the four-gene matrix of matR, rbcL, atpB and 18S rDNA using GTR+I+Γ model showing the pattern of long and short branches that occurs repeatedly in flowering plants. Asterisks denote contradictory resolutions between ML tree and MP strict consensus of all shortest trees. (PDF 23 KB)
Additional file 8: matR. The sites of C to U RNA-editing in matR are predicted using PREP-Mt program  with cutoff value of 0.6 for predicting RNA-editing sites in the 174-matR sequences. The resulting data matrix is analyzed using ML (GTR+Γ model). (PDF 31 KB)
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Zhu, XY., Chase, M.W., Qiu, YL. et al. Mitochondrial matR sequences help to resolve deep phylogenetic relationships in rosids. BMC Evol Biol 7, 217 (2007). https://doi.org/10.1186/1471-2148-7-217
- Maximum Parsimony
- Nonsynonymous Substitution
- Maximum Parsimony Analysis
- Plastid Gene