An Application of Supertree Methods to Mammalian Mitogenomic Sequences

Abstract

Two different approaches can be used in phylogenomics: combined or separate analysis. In the first approach, different datasets are combined in a concatenated supermatrix. In the second, datasets are analyzed separately and the phylogenetic trees are then combined in a supertree. The supertree method is an interesting alternative to avoid missing data, since datasets that are analyzed separately do not need to represent identical taxa. However, the supertree approach and the corresponding consensus methods have been highly criticized for not providing valid phylogenetic hypotheses. In this study, congruence of trees estimated by consensus and supertree approaches were compared to model trees obtained from a combined analysis of complete mitochondrial sequences of 102 species representing 93 mammal families. The consensus methods produced poorly resolved consensus trees and did not perform well, except for the majority rule consensus with compatible groupings. The weighted supertree and matrix representation with parsimony methods performed equally well and were highly congruent with the model trees. The most similar supertree method was the least congruent with the model trees. We conclude that some of the methods tested are worth considering in a phylogenomic context.

Introduction

The phylogenomic era has brought a shift from single to multiple datasets (or genes) to study phylogenetic relationships.¹ While increasing the number of characters decreases stochastic errors, it also increases phylogenetic signal.^2–4 However, phylogenomic studies present numerous methodological challenges (see review by Delsuc et al).⁵ Two opposite views have been proposed as to how to incorporate the growing amount of data to infer evolutionary relationships. Whereas the combined approach (sensu de Queiroz)⁶ concatenates different datasets in a supermatrix,^7–10 the consensus approach (sensu de Queiroz)⁶ analyzes datasets separately and the resulting trees are combined with a consensus^11–13 or a supertree method.^14–16 The pros and cons of these competing approaches have been debated at length in the literature.^10,17–25 When the combined approach is used, the concatenation of numerous genes from different species often results in a supermatrix with missing data. Indeed, a taxon bias has been observed in genetic databases, with a large number of genes (or whole genome) sequenced for a few key species thus resulting in large supermatrices dominated by missing data.^{2,23,24,26,27}

An approach that can be applied to deal with incomplete matrices is the supertree method.^14–16,22 In the likely event that some gene sequences are not available for all species, it is possible to estimate a phylogenetic tree for each gene separately and then combine the resulting trees with a supertree approach. Whereas separate datasets may not contain identical sets of taxa (i.e. only overlapping sets), the resulting supertree includes all taxa. Numerous supertree methods have been developed, the most familiar being the matrix representation with parsimony (MRP).^28–30 They can be defined as a generalization of consensus methods, which only applies to trees defined on an identical set of taxa.^{6,11,12,20,31} Interestingly, it is possible to compare performances of classical consensus methods with that of supertree methods in a consensus setting, i.e. when all datasets have identical taxa.³² Since supertree methods are often developed from existing consensus methods, a setting that allows both types of methods to be directly compared is desirable to assess their relative accuracies.

The supertree strategy seems to be increasingly used in phylogenomics, where large amounts of data can be subdivided to facilitate phylogenetic analyses (i.e. divide-and-conquer strategy).^22,33 Furthermore, supertree methods have been proposed as representing the optimal solution to reconstruct the Tree of Life.^14,15,33,34 Consensus and supertree methods are similar in design, and both can be referred to as separate analyses, by opposition to a combined analysis (sensu de Queiroz)⁶ where sequence datasets are concatenated in a single supermatrix. A heated debate between those in favor and those opposed to the use of consensus has been raging for the last decade.^{18–20,35–37} The same debate has recently been extended to supermatrices and supertrees.^{7,10,14,16,17,23,25,38–40}

The mammalian phylogeny has been extensively studied and the analysis of different sources of data leads to congruent phylogenies (see review by Springer and Murphy,⁴¹ Springer et al⁴² and Wildman et al.)⁴³ Recent studies of mammal species have shown that mitochondrial phylogenies can be congruent to nuclear phylogenies when potential phylogenetic biases are removed. For example, additional taxa can be added to break long branches⁴⁴ and compositional bias and heterogeneity in substitution rates can be appropriately handle.^44–46 Another alternative is to use different substitution models depending on the codon position in order to account for a compositional bias of nucleotides among species.⁴⁷ Numerous mitogenomic sequences of mammalian species are available and this data availability combined to accurate phylogenetic hypotheses is an ideal setting to test different phylogenetic approaches.

In this study, three different approaches that are commonly used in phylogenomics to analyze DNA sequence matrices were studied in a consensus setting (sensu Bininda-Emonds³²): (1) topological consensus methods, (2) topological supertree methods, and (3) weighted supertree methods that account for branch lengths. Congruence among these competing approaches was compared with respect to model trees that were obtained from a complete matrix of mitogenomic mammalian sequences (i.e. a phylogenetic tree obtained from concatenated gene sequences) of 102 species representing 93 mammal families.

Methods

Model tree

DNA sequence alignments

In February 2009, 96 mammal families had at least one species with a complete mitochondrial (mt) sequence in GenBank. In this study, one taxon per family was chosen. When more than one taxon was available, only one species was selected per family (with a few exceptions, see below) and the entire mt sequence was downloaded (see Appendix 1 for Gen-Bank accession numbers). The twelve mitochondrial genes of the H-strand were aligned using ClustalX 2.0.10⁴⁸ and the alignment was further verified by eye in SeAl 2.0a11. Ambiguous sites and overlapping regions of the ATP6–ATP8 and NAD4-NAD4L were removed.

Stationarity of base frequencies across taxa was tested on the complete alignment using the chi-square test of homogeneity of base frequencies implemented in PAUP* 4.0.⁴⁹ A test of congruence among distance matrices (CADM)⁵⁰ was used to determine the congruence among the twelve mt genes using R 2.9.0,^51,52 and Ape 2.3 package,^53,54 with 9999 permutations for significance testing.

A well-supported tree, compatible with current consensus of mammal molecular phylogeny,^41,55 was required to represent interfamilial mitogenomic relationships. However, systematic errors, mainly caused by reconstruction artifacts, can produce a biased tree topology.⁵ Among potential systematic errors, heterogeneity in base composition^47,56–59 and different evolutionary rates among species^60–65 have often been cited as confounding factors affecting the inference of mammalian mitogenomic relationships. Indeed, preliminary analyses of our dataset revealed the presence of systematic biases and different strategies were used to reduce their effect.^46,58 For one, the third codon position was removed since it evolves more rapidly, especially in the mitochondrial genome,^56,66 and is often saturated for higher-level relationships.⁴⁷ Also, the first codon position of leucine (C and T) was recoded as pyrimidine (Y). Additionally, three problematic species were removed (Anomalurus sp., Anomaluridae, Erinaceus europaeus, Erinaceidae and Manis tetradactyla, Manidae). These species are known to be affected by either reduced or accelerated evolutionary rates which can lead to long-branch attraction or positional uncertainty due to short branches.^{46,62,66–68} Finally, nine extra species were added to break long branches⁴⁶ within the following six families: Chrysochloridae, Elephantidae, Macroscelidae, Procaviidae, Soricidae and Talpidae. Consequently, a total of 102 complete mt sequences, representing 93 mammalian families, were included (see Appendix 1).

Phylogenetic inference

Modeltest 3.7 was used to identify the best model of nucleotide substitution.⁶⁹ Both the hierarchical likelihood ratio tests (hLRTs) and Akaike information criterion (AIC) suggested a general time-reversible model (GTR)^70–72 following a gamma distribution (Γ)⁷³ with invariant sites (I). The equilibrium frequencies of nucleotides A, C, G, and T were: gA = 0.3452, gC = 0.2054, gG = 0.0901, gT = 0.3593, the relative substitution rates were: rAC = 1.1083, rAG = 6.7749, rAT = 1.1934, rCG = 1.3020, rCT = 3.9717, rGT = 1.0000, and parameters α and I were 0.6762 and 0.4437 respectively. Phylogenetic trees were estimated using two different methods: maximum likelihood (ML)^74,75 and Bayesian maximum likelihood (BML).^76,77 ML analysis was performed with PhyML 3.0,⁷⁸ with a GTR + Γ + I model, where base frequencies, proportion of invariable sites and gamma shape distribution parameters were estimated from the data. The number of categories for the gamma distribution was set to six. A subtree pruning and regrafting (SPR) algorithm was selected, starting from a BioNJ tree, and ten additional random starting trees. Non-parametric bootstrap support (BS) was assessed using identical settings in PhyML for 100 replicates. BML was performed with MRBAYES 3.1.2⁷⁶ on a shared-memory multiprocessor computer (Altix 4700). Two MCMC analyses were run for 5,000,000 generations each, using the same GTR + Γ + I model. The Metropolis coupling used eight chains, starting from a random tree and eight swaps with Markov chains sampled every 100th generation, and with a burn-in of 10%. The majority-rule consensus tree and Bayesian posterior probabilities (BPP) were obtained from the tree distribution.

Model tree topology

The ML and BML tree topologies were identical, except at two nodes. These incongruent clades were represented by polytomies in order to render the ML and BML trees completely congruent (Fig. 1). This topology was used as the first model tree (MT1). A second model tree (MT2) was then constructed by collapsing all branches that were not compatible to the current molecular consensus of mammal phylogeny. In this second tree (Fig. 2), eight extra polytomies were added to the first model tree to ensure that all clades were compatible with recent molecular studies.^{46,66,79–82}

Figure 1.

First model tree (MT1) representing mitogenomic relationships among 93 mammalian families. Bootstrap values (BS) and Bayesian posterior probabilities (BPP) are indicated on branches (BS/BPP). Branches without values correspond to BS/BPP = 100/100.

Figure 2.

Second model tree (MT2) representing mitogenomic relationships among mammalian families with eight extra polytomies added to MT1 to obtain a tree compatible with recent molecular studies. Bootstrap values (BS) and Bayesian posterior probabilities (BPP) are indicated on branches (BS/BPP). Branches without values correspond to BS/BPP = 100/100.

Consensus and Supertree Methods

Individual datasets

For the consensus and supertree methods, the twelve individual mt genes were analyzed separately. Stationarity of base frequencies across taxa was tested on each of the twelve datasets using the chi-square test of homogeneity of base frequencies implemented in PAUP* 4.0, with a Bonferroni correction for multiple tests.⁸³ Modeltest 3.7 was used to identify the best substitution model for each dataset. ML analyses were then performed on each dataset with PhyML 3.0, using the model suggested by the AIC criterion. Analytical parameters were identical to those described for the complete matrix analysis, except for the evolutionary model (listed in Table 1 for each gene). Individual gene trees are available upon request.

Table 1.

Statistical description of individual datasets (the twelve genes on the mitochondrial H-strand) and of concatenated datasets (AL). L (bp): length of the gene in base pairs. No cst: number of constant sites in the alignment. No info: number of informative sites in the alignment. AIC: Model selected according to AIC criterion in Modeltest, which always included parameters G (a gamma distribution of substitution rates) and I (a proportion of invariable sites). χ² (1, 2): chi square test for homogeneity of base frequencies across species on datasets with third codon position removed (P = 1.0 in every case). χ² (1, 2, 3): chi square test on datasets with codon positions 1, 2 and 3 included.

Datasets	L (bp)	No cst (%)	No info (%)	AIC	χ2 (1, 2)	χ2 (1, 2, 3)
ATP6	452	200 (44.2)	204 (45.1)	GTRa	78.25	419.99*
ATP8	60	10 (16.7)	47 (78.3)	TrNb	145.87	198.83
COX1	1022	780 (76.3)	157 (15.4)	GTR	15.85	573.75*
COX2	440	247 (56.1)	150 (34.1)	TVMc	28.26	290.95
COX3	522	339 (64.9)	137 (26.2)	TVM	33.42	320.19
CYTB	754	402 (53.3)	276 (36.6)	TIMd	80.04	525.82*
NAD1	618	312 (50.5)	239 (38.7)	GTR	69.18	484.12*
NAD2	690	173 (25.1)	463 (67.1)	GTR	129.20	623.00*
NAD3	230	109 (47.4)	100 (43.5)	TrN	78.92	251.49
NAD4	918	380 (41.4)	458 (49.9)	GTR	96.29	681.88*
NAD4 L	192	69 (35.9)	105 (54.7)	TVM	65.08	251.49
NAD5	1202	463 (38.5)	619 (51.5)	GTR	136.64	919.59*
ALL	7100	3484 (49.1)	2955 (41.6)	GTR	267.78	4107.63*

^*Identifies significant values after a Bonferroni correction, P < 0.004 (i.e. 0.05/12).

^aGTR: General time reversible mode.^l70–⁷²

^bTrN: Tamura-Nei model.¹¹¹

^cTVM: Tranversional model.⁶⁹

^dTIM: Transitional model.⁶⁹

Given that all twelve datasets included an identical number of taxa (n = 102), the comparison of consensus and supertree methods was performed in a consensus setting.³² Therefore, even though we will maintain the use of “supertree” for methods that have been developed in a supertree context, all methods can be considered as consensus methods and can be divided into three categories: (1) consensus techniques based on topological relationships (topological consensus methods), (2) supertree techniques based on topological relationships (topological supertree methods), and (3) supertree techniques that take into account branch lengths (branch-length supertree methods).

Topological consensus methods

Four consensus methods were applied to combine the twelve independent gene trees in PAUP* 4.0: (1) strict, (2) majority rule (MR), (3) majority rule with compatible groupings (MRC), and (4) Adams consensus. The strict consensus only retains groups that are identical among all input trees.^84,85 The majority rule consensus (MR) contains groups that are present in more than 50% of input trees,^11,86 such that groups found in seven or more trees were kept. The second type of majority rule consensus (MRC) retains all compatible groupings below 50% of occurrence in addition to those above 50%. The Adams consensus presents groups that are nested within another without necessarily including identical taxa.^87,88 Therefore, Adams consensus does not only propose monophyletic groups. A more complete description of these methods can be found in Swofford.¹¹

Topological supertree methods

Three different optimality criteria were used to construct supertrees (consensus) from the twelve independent gene trees in CLANN 3.0.2:⁸⁹ (1) matrix representation with parsimony (MRP), (2) most similar supertree (MSS), and (3) maximum splits fit (SFIT). In MRP, nodes present in each tree are coded into a binary matrix using the Baum and Ragan method.^28–30 The binary matrix is then analyzed with a parsimony algorithm⁹⁰ using ten TBR searches and a random starting tree. The MSS method calculates the symmetric differences between each gene tree and the supertree and sums these differences to obtain a supertree score.⁹¹ The optimal supertree is the one with the best score (smallest distance). For the SFIT method, the splits present in each gene tree and a candidate supertree are recorded and the supertree with the maximum split fit (sharing the greatest number of splits) is selected.⁸⁹ For MSS and SFIT, a SPR heuristic search using ten repetitions each starting with a different NJ tree was selected to search among all possible supertree topologies (default parameters in CLANN). For all of these methods, a strict consensus was used to combine equally optimal supertrees, if any.

Branch-length supertree methods

Three other optimality criteria, which take into account branch lengths of input trees, were also employed: (4) average consensus (AC), (5) unweighted super-distance matrix (SDM), and (6) weighted super-distance matrix (SDMw). These methods are implemented in the SDM program.⁹² The AC criterion optimizes the sum-of-squared distances between each source tree and the consensus tree, by averaging the path-length distance matrices computed from each gene tree and then applying a least-squares algorithm to this average matrix.⁹³ SDM applies the same criterion, except that pathlength distance matrices are first transformed so as to minimize the sum-of-squared distances among them.⁹² The weighted version (SDMw) assigns a weight to each tree prior to computing the average matrix, based on the sequence length of the corresponding gene. All supertrees (consensus) were estimated using an ordinary least squares algorithm⁹⁴ in PHYLIP 3.68⁹⁵ with the FITCH program, using the jumble option (J = 10) which randomizes the input order of species for each run, and with global rearrangements allowed (SPR algorithm).

Distance metrics

Two dissimilarity measures were computed in PAUP* 4.0 to quantify the congruence between model trees (MT1 and MT2) versus consensus and supertrees. The symmetric-difference or partition metric (PM) counts the number of different splits in the trees being compared.^96,97 PM was normalized by dividing each value by its maximal possible value (2n−6), where n is 102 taxa. The maximum agreement subtree index (D1) calculates the number of taxa that need to be pruned from the trees to obtain a congruent topology.^98–100 Here again, normalized D1 are obtained by dividing each value by its maximum possible value (n−3), where n is 102 taxa. Rohlf’s consensus information index (CII)¹⁰¹ was also calculated on the consensus trees to measure their relative resolution (this index ranges from 0 when the consensus is a bush to 1 when the tree is fully resolved).

Results

Individual datasets

The length (L) of each of the twelve aligned mitochondrial genes varied from 90 to 1803bp, when all three codon positions were included. The homogeneity test of base frequencies indicated that seven out of the twelve datasets were heterogeneous (Table 1). However, when only the two first codon positions were considered, all datasets were homogeneous. Consequently, subsequent analyses were performed using alignments with only the first and second codon positions. The two optimality criteria (hLRTs and AIC) implemented in Modeltest suggested different models for some datasets. Indeed, whereas the hLRTs criterion proposed a GTR model for all datasets, AIC suggested varying models depending on the dataset, as listed in Table 1. The congruence among distance matrix test (CADM) suggested that all twelve datasets were congruent (Friedman’s χ² = 44341.5, Kendall’s W = 0.7175, P = 0.0001).

Topological consensus methods

Important differences were observed between PM and D1 and among topological consensus methods (Table 2). These results may be explained by the fact that some consensus methods were poorly resolved, i.e. CII = 0.02 for strict consensus, 0.10 for MR and 0.18 for Adams, compared to CII ranging from 0.53 to 1.0 for all other methods. The resolution level affects the congruence indices. When comparing a fully resolved tree to a bush, PM will be of 0.5 because only the clades in the fully resolved tree are contributing to the distance. On the other hand, D1, which calculates the number of taxa that have to be pruned from both trees to obtain identical topologies, will exhibit a very big value given that n−2 taxa need to be deleted for both topologies to be compatible. Because the majority rule consensus that included all compatible groupings (MRC) is more resolved than other classical consensus methods (CII = 0.94), it provided the best results and was the closest to model tree topologies (PM = 0.22–0.23 for MT1–MT2). The majority rule consensus (MR) was the second most congruent consensus method (PM = 0.30–0.25 for MT1–MT2), although much less resolved (CII = 0.10), and thus D1 was considerably increased (0.79–0.73 for MT1–MT2, compared to 0.39–0.46 for MRC).

Table 2.

Congruence of phylogenetic trees inferred from consensus and supertree methods (that ignore or consider branch lengths). CI: Rohlf’s consensus information index (ranges from 0 to 1; 0 being a bush and 1 a fully resolved tree), PM: partition metric, D1: maximum agreement subtrees. Indices range from 0 to 1. MR: majority rule consensus, MRC: majority rule consensus with compatible groupings, MRP: matrix representation with parsimony, MSS: most similar supertree, SFIT: maximum splits fit, AC: average consensus, SDM: unweighted super-distance matrix, SDMw: weighted super-distance matrix.

		CII	Model tree 1 (MT1)		Model tree 1 (MT2)
			PM	D1	PM	D1
Topological consensus methods	Strict	0.02	0.46	0.94	0.39	0.94
	MR	0.10	0.30	0.79	0.25	0.73
	MRC	0.94	0.22	0.39	0.23	0.46
	Adams	0.18	0.42	0.78	0.36	0.75
Topological supertree methods	MRPa	0.98	0.23	0.47	0.23	0.43
	MSSb	0.91	0.54	0.62	0.56	0.60
	SFITc	0.53	0.24	0.51	0.22	0.50
Branch-length supertree methods	AC	1.00	0.25	0.43	0.22	0.49
	SDM	1.00	0.27	0.45	0.24	0.50
	SDMw	1.00	0.30	0.45	0.27	0.50

^aStrict consensus of five most parsimonious trees.

^bStrict consensus of two equally optimal supertrees.

^cStrict consensus of 184 equally optimal supertrees.

Supertree methods

The topological supertree techniques suggested more than one optimal supertree: 184 (SFIT), five (MRP), and two (MSS) optimal supertrees. These supertrees were combined using a strict consensus supertree, and thus, were not fully resolved (CII = 0.53 to 0.98, compared to a value of 1.0 for the branch-length supertree methods). The least congruent method was MSS (PM = 0.54–0.56 for MT1–MT2; D1 = 0.62–0.60 for MT1–MT2). MRP and SFIT performed well (for MRP: PM = 0.23 for MT1 and MT2 and D1 = 0.47–0.43; and for SFIT: PM = 0.24–0.22 and D1 = 0.51–0.50).

Weighted supertree methods that take branch lengths into account performed relatively well (PM range from 0.22 to 0.30, and D1 ranging from 0.43 to 0.50) and proposed one optimal, fully resolved supertree. AC was slightly more accurate than both SDM and SDMw. The weighted version of SDM (i.e. SDMw) did not improve phylogenetic performance (PM increased slightly while D1 remained the same).

Discussion

A method commonly used in large-scale studies is the construction of supertrees from individual source trees.¹⁴ Supertree methods combine trees that have overlapping taxon sets, whereas consensus methods summarize trees with identical taxon set. Both approaches have been extensively studied.^{6,18,32,92,102,103} They can be compared and tested in a consensus setting, where identical taxon sets are used.^32,103–108

Among the consensus methods, the majority rule with compatible groupings (MRC) was the most congruent to MT1 (and second most congruent to MT2), when compared to all other consensus and supertree methods tested. Criticisms of consensus methods emphasized the poor resolution of consensus trees.^9,18,36 However, MRC was well resolved (CII = 0.94), which may explain its performance relative to other topological consensus methods. Through simulations, Bininda-Emonds³² has also observed that MRC provided the highest accuracy amongst consensus methods.

In line with previous studies, we confirmed that supertree techniques based on topological relationships did not offer a fully resolved consensus tree. In general, most supertree methods gave similar results (except for MSS, see below). This result was surprising, given that numerous studies have proposed that methods accounting for branch lengths should provide more accurate supertrees.^106–108 However, Criscuolo et al⁹² have shown that MRP (that do not account for branch lengths) and SDM (that do account for branch lengths) were equally accurate at low levels of missing data (i.e. 25% of deleted taxa), and that the benefit of accounting for branch lengths was only revealed at higher levels of missing data (e.g. 75% of deleted taxa). The consensus setting used in this study did not allow the investigation of the effect of missing data and therefore the difference in performance could have been seen in a supertree setting.

MSS was the least accurate of all supertree methods. Creevey and McInerney⁸⁹ have compared their MSS approach to the AC technique, but without branch lengths (i.e. by setting all branch lengths equal to one). The better results obtained with AC (and SDM) with respect to MSS, might suggest that branch lengths contain information different from topological relationships, when supertree methods are used. A similar result was also observed by Criscuolo et al.⁹² As for the other supertree methods (SFIT and MRP), they provided similar results to techniques that use branch lengths. This result is consistent with studies that have shown that MRP is accurate under certain conditions.^{92,102,109,110} Through simulations, Bininda-Emonds and Sanderson¹⁰² have observed that MRP provided accuracy values comparable to those obtained from a supermatrix analysis (and that accuracy was slightly increased when a weighted MRP was used). Among the supertree methods that account for branch lengths, SDM outperformed slightly SDMw. The distance matrices are weighted according to sequence lengths in SDMw, with trees inferred from longer sequences contributing more to the “super” distance values. Thus, biases will be amplified if they are associated with longer sequence datasets. This might explain why SDMw might not always provide the optimal solution. Also, AC was slightly more accurate than SDM, in contrast with Criscuolo et al⁹² who showed the opposite under all conditions tested. Fitzpatrick et al¹⁰⁹ in a fungal study comparing AC, MRP and the supermatrix approach, reported that AC might be prone to long-branch attraction, but this was not the case here. Supertree methods that account for branch lengths may thus provide additional information, which could help resolve some least-resolved clades.

The results from this study demonstrate that most of the supertree methods tested were highly congruent with both model trees. Interestingly, the majority rule consensus with compatible clades was also highly congruent, which suggest that it represents an accurate and fast approach to summarize information obtained in separate analyses.

Supplementary data

Appendix 1.

GenBank accession numbers of complete mitochondrial DNA sequences from 102 species representing 93 mammalian families. Family and species taxonomy based on Wilson and Reeder.¹

Order	Family	Species	Complete
MONOTREMATA	Tachyglossidae	Tachyglossus aculeatus	NC_003321
	Ornithorhynchidae	Ornithorhynchus anatinus	NC_000891
DIDELPHIMORPHIA	Didelphidae	Didelphis virginiana	NC_001610
PAUCITUBERCULATA	Caenolestidae	Caenolestes fuliginosus	NC_005828
MICROBIOTHERIA	Microbiotheriidae	Dromiciops gliroides	NC_005826
DASYUROMORPHIA	Thylacinidae	Thylacinus cynocephalus	NC_011944
	Myrmecobiidae	Myrmecobius fasciatus	NC_011949
	Dasyuridae	Phascogale tapoatafa	NC_006523
PERAMELEMORPHIA	Thylacomyidae	Macrotis lagotis	NC_006520
	Peramelidae	Isoodon macrourus	NC_002746
NOTORYCTEMORPHIA	Notoryctidae	Notoryctes typhlops	NC_006522
DIPROTODONTIA	Phascolarctidae	Phascolarctos cinereus	NC_008133
	Vombatidae	Vombatus ursinus	NC_003322
	Phalangeridae	Trichosurus vulpecula	NC_003039
	Potoroidae	Potorous tridactylus	NC_006524
	Macropodidae	Macropus robustus	NC_001794
	Pseudocheiridae	Pseudocheirus peregrinus	NC_006519
	Petauridae	Petaurus breviceps	NC_008135
	Tarsipedidae	Tarsipes rostratus	NC_006518
	Acrobatidae	Distoechurus pennatus	NC_008145
XENARTHRA	Dasypodidae	Dasypus novemcinctus	NC_001821
	Bradypodidae	Bradypus tridactylus	NC_006923
	Megalonychidae	Choloepus didactylus	NC_006924
	Myrmecophagidae	Tamandua tetradactyla	NC_004032
PROBOSCIDEA	Elephantidae	Elephas maximus	NC_005129
		Loxodonta africana	NC_000934
SIRENIA	Dugongidae	Dugong dugon	NC_003314
	Trichechidae	Trichechus manatux	NC_010302
HYRACOIDEA	Procaviidae	Procavia capensis	NC_004919
		Dendrohyrax dorsalis	NC_010301
TUBULIDENTATA	Orycteropodidae	Orycteropus afer	NC_002078
MACROSCELIDEA	Macroscelididae	Macroscelides proboscideus	NC_004026
		Elephantulus sp.	NC_004921
AFROSORICIDA	Tenrecidae	Echinops telfairi	NC_002631
	Chrysochloridae	Chrysochloris asiatica	NC_004920
		Eremitalpa granti	NC_010304
CETACARTIODACTYLA	Balaenidae	Balaena mysticetus	NC_005268
	Balaenopteridae	Megaptera novaeangliae	NC_006927
	Eschrichtiidae	Eschrichtius robustus	NC_005270
	Neobalaenidae	Caperea marginata	NC-005269
	Delphinidae	Lagenorhynchus albirostris	NC_005278
	Monodontidae	Monodon monoceros	NC_005279
	Phocoenidae	Phocoena phocoena	NC_005280
	Physeteridae	Physeter catodon	NC_002503
	Iniidae	Inia geoffrensis	NC_005276
	Platanistidae	Platanista minor	NC_005275
	Ziphiidae	Berardius bairdii	NC_005274
	Suidae	Sus scrofa	NC_000845
	Tayassuidae	Pecari tajacu	NC_012103
	Hippopotamidae	Hippopotamus amphibius	NC_000889
	Camelidae	Lama pacos	NC_002504
	Giraffidae	Giraffa camelopardalis	NC_012100
	Cervidae	Cervus elaphus	NC_007704
	Bovidae	Bos taurus	NC_001567
PERISSODACTYLA	Equidae	Equus caballus	NC_001640
	Tapiridae	Tapirus terrestris	NC_005130
	Rhinocerotidae	Ceratotherium simum	NC_001808
CARNIVORA	Ailuridae	Ailurus fulgens	NC_011124
	Ursidae	Ursus americanus	NC_003426
	Canidae	Vulpes vulpes	NC_008434
	Felidae	Felis catus	NC_001700
	Herpestidae	Herpestes javanicus	NC_006835
	Mustelidae	Gulo gulo	NC_009685
	Otariidae	Eumetopias jubatus	NC_001050
	Odobenidae	Odobenus rosmarus	NC_004029
	Phocidae	Phoca vitulina	NC_001325
	Procyonidae	Procyon lotor	NC_009126
	Mephitidae	Mephitis mephitis	AY598529–AY598539, X94927
EULIPOTYPHLA	Soricidae	Crocidura russula	NC_006893
		Sorex unguiculatus	NC_005435
		Episoriculus fumidus	NC_003040
	Talpidae	Talpa europaea	NC_002391
		Galemys pyrenaicus	NC_008156
		Mogera wogura	NC_005035
		Urotrichus talpoides	NC_005034
CHIROPTERA	Pteropodidae	Pteropus dasymallus	NC_002612
	Vespertilionidae	Chalinolobus tuberculatus	NC_002626
	Mystacinidae	Mystacina tuberculata	NC_006925
	Rhinolophidae	Rhinolophus monoceros	NC_005433
	Phyllostomidae	Artibeus jamaicensis	NC_002009
RODENTIA	Thryonomyidae	Thryonomys swinderianus	NC_002658
	Caviidae	Cavia porcellus	NC_000884
	Gliridae	Myoxus glis	NC_001892
	Sciuridae	Sciurus vulgaris	NC_002369
	Dipodidae	Jaculus jaculus	NC_005314
	Spalacidae	Nannospalax ehrenbergi	NC_005315
	Cricetidae	Cricetulus griseus	NC_007936
	Muridae	Mus musculus	NC_005089
LAGOMORPHA	Ochotonidae	Ochotona princeps	NC_005358
	Leporidae	Oryctolagus cuniculus	NC_001913
PRIMATES	Lemuridae	Lemur catta	NC_004025
	Indriidae	Propithecus coquereli	NC_011053
	Daubentoniidae	Daubentonia madagascariensis	NC_010299
	Lorisidae	Nycticebus coucang	NC_002765
	Tarsiidae	Tarsius bancanus	NC_002811
	Cebidae	Cebus albifrons	NC_002763
	Aotidae	Aotus trivirgatus	AY250707
	Cercopithecidae	Macaca mulatta	NC_005943
	Hylobatidae	Hylobates lar	NC_002082
	Hominidae	Pan troglodytes	NC_001643
DERMOPTERA	Cynocephalidae	Cynocephalus variegatus	NC_004031
SCANDENTIA	Tupaiidae	Tupaia belangeri	NC_002521

¹Wilson DE, Reeder DM. Mammal Species of the World: A Taxonomic and Geographic Reference. 3rd ed. Baltimore, Maryland: The Johns Hopkins University Press; 2005.