 Research article
 Open Access
 Published:
Improved mitochondrial amino acid substitution models for metazoan evolutionary studies
BMC Evolutionary Biology volume 17, Article number: 136 (2017)
Abstract
Background
Amino acid substitution models play an essential role in inferring phylogenies from mitochondrial protein data. However, only few empirical models have been estimated from restricted mitochondrial protein data of a hundred species. The existing models are unlikely to represent appropriately the amino acid substitutions from hundred thousands metazoan mitochondrial protein sequences.
Results
We selected 125,935 mitochondrial protein sequences from 34,448 species in the metazoan kingdom to estimate new amino acid substitution models targeting metazoa, vertebrates and invertebrate groups. The new models help to find significantly better likelihood phylogenies in comparison with the existing models. We noted remarkable distances from phylogenies with the existing models to the maximum likelihood phylogenies that indicate a considerable number of incorrect bipartitions in phylogenies with the existing models. Finally, we used the new models and mitochondrial protein data to certify that Testudines, Aves, and Crocodylia form one separated clade within amniotes.
Conclusions
We introduced new mitochondrial amino acid substitution models for metazoan mitochondrial proteins. The new models outperform the existing models in inferring phylogenies from metazoan mitochondrial protein data. We strongly recommend researchers to use the new models in analysing metazoan mitochondrial protein data.
Background
An amino acid substitution model (model for short) includes a 20 × 20 matrix and an amino acid frequency vector. The matrix represents the instantaneous substitution rates among amino acids while the amino acid frequency vector serves as the equilibrium frequencies of the 20 amino acids. The substitution rates characterise the biological, chemical, and physical correlations among amino acids [1]. Amino acid substitution models are the key to infer phylogenies from protein data. Distancebased methods use amino acid substitution models to estimate pairwise distances among sequences, while maximum likelihood or Bayesian methods require amino acid substitution models to calculate the likelihood of data [2].
Estimating amino acid substitution models is much more challenging than estimating nucleotide substitution models due to a large number of parameters to be optimised. For example, the general time reversible model for nucleotides contains 8 parameters in comparing to 208 parameters for models of amino acid substitutions. Thus, amino acid substitution models are typically estimated from large datasets.
It is well established that models of different species or protein types would be diverse [3,4,5]. For example, Dang et al. showed that the model for influenza proteins is highly different from general models [3]. Note that protein structures also contribute to amino acid evolution patterns [6, 7].
Mitochondria (mt) are energy factories and play an essential role in supplying cellular energy [8]. The mitochondrial genome encodes 13 proteins that are widely used to infer phylogenies [7, 9,10,11,12]. Few groups have estimated empirical models from mt protein data (mt models). Adachi and Hasegawa were the first to estimate an mt model, named mtREV, from 20 complete vertebrate sequences [13]. They argued that the difference between the universal code and the mitochondrial code might be partially responsible to the difference between amino acid substitution patterns from nuclear and mitochondrialencoded proteins. Abascal et al. built another mt model, mtArt, from 36 arthropod species to analyse the data of invertebrate species [14]. Note that although invertebrates are paraphyletic, the term invertebrates is widely used as a convenient shorthand in communication [5, 13,14,15]. Neither mtREV nor mtArt is appropriate for datasets consisting of diverse metazoan lineages, as they were specifically estimated from either vertebrate or invertebrate protein data. RotaStabelli et al. solved the problem by introducing an mt model (mtZoa) estimated from 117 general metazoan species [5]. They recommended to use mtZoa for analysing datasets from diverse or basal metazoan groups. The existing mt models (mtREV, mtArt, and mtZoa) outperform general models (e.g., LG [16] and WAG [17]) in inferring phylogenies from mt protein data, even though they were estimated from small datasets.
The main issue of the existing mt models comes from their small training datasets of at most 117 species. This was due to the limited mt protein data available and the capability of estimation methods at the time these studies were carried out. Consequently, the models might overfit to training data due to a large number of free parameters of the amino acid substitution model (precisely 208 free parameters). In other words, the existing models may fit too well to training sequences but poorly represent others. Above all, the existing mt models cannot appropriately represent nearly a million available mt protein sequences of more than 34 thousands metazoan species, as they were estimated from only a limited number of species.
In this paper, we introduce new mt models for metazoan and vertebrates. Although invertebrates are not monophyletic, their mitochondria have the same genetic codes. The genetic codes of invertebrate mitochondria are different from that of vertebrate mitochondria. The difference might result in different amino acid substitution patterns from invertebrate and vertebrate mitochondrialencoded proteins [5, 13, 14]. Therefore, we also introduce a new mt model for invertebrates. To this end, we created three datasets from 125,935 mt sequences of 13 proteins from 34,448 metazoan species. Then, we implemented the fast and accurate method, FastMG [18], to estimate three new mt models from these three datasets.
We validated the new models by assessing the likelihood of phylogenies with the new models for both training and testing data. We summarised the experimental results to show the advantage of the new models in inferring the maximum likelihood phylogenies (called the best phylogenies) in comparison to existing mt models. Experimental results revealed remarkable distances from the phylogenies with the existing models to the best phylogenies. We proved that the remarkable distances imply a considerable number of incorrect bipartitions in the phylogenies with the existing models. Although we could not evaluate the topological quality of phylogenies with the new models, as they were often the best phylogenies, we would expect significant topological improvement due to their large likelihood advantage over the phylogenies with the existing models.
Finally, we applied the new models to tackle a debated question about the location of Testudines within amniotes. We used IQTREE with the new models to build the maximum likelihood phylogeny of 993 amniotes from their mt protein data. We learned from the phylogeny that Testudines, Aves, and Crocodylia form one separated clade within amniotes.
Results and discussion
Data preparation
We downloaded all mt protein sequences of 34,448 species in the metazoan kingdom from NCBI (National Center for Biotechnology Information, 2016) and then mapped them onto 13 mt proteins. We selected one sequence per species to eliminate bias on intensively studied species (e.g., 30,000 human sequences). As the result, we obtained 125,935 sequences to form three datasets for metazoan, vertebrate, and invertebrate categories. We kept all sites, as removing sites with missing data would lead to worse phylogenies [19]. We divided each dataset into a training dataset and a testing dataset containing 90% and 10% of sequences, respectively.
We implemented the fast and accurate method, FastMG [18], to estimate three new mt models, mtMet, mtVer, and mtInv from metazoan, vertebrate, and invertebrate training datasets, respectively. As FastMG is infeasible for alignments of several thousands sequences, we split alignments based on the taxonomy tree to obtain subalignments of at most one thousand sequences. Then we divided these subalignments into smaller subalignments of at most 128 sequences using the treebased splitting algorithm in FastMG. In addition, we removed branches with lengths equal to zero or larger than two in order to eliminate data noise. The data are summarised in Tables 1 and 2. Note that the FastMG algorithm starts from an initial model and iteratively optimises the model until the likelihood improvement is insignificant.
The fit of new models to training datasets
We measured the fit of new models to the training datasets. Table 3 shows significant likelihood improvements of the new models over the initial model, mtZoa, for metazoan, vertebrate, and invertebrate training datasets. The first iteration contributed about 99% of the total likelihood improvement. The optimisation process was terminated after the third iteration, as the gain from the third iteration was insignificant.
The better Akaike and Bayesian information criterion scores [20, 21] of the new models in comparison to the initial model, mtZoa, confirm the better fit of the new models to the training data. The scores guarantee that the likelihood gain of the new models comes from their genuine fit and overwhelm the penalty of free parameters.
Model analysis
Figures 1 and 2 show significant differences in exchangeability patterns between amino acids among the four models: mtZoa, mtMet, mtVer, and mtInv (see). For example, the exchangeability rate between methionine and glutamine in mtMet is about 10 times greater than that in mtZoa (0.155 vs 0.0016). The exchangeability rate between these two amino acids in mtVer is a third of that in mtInv (0.075 vs 0.228). Figure 3 shows a clear variety of amino acid frequencies among the four models, especially between mtVer and mtInv). For instance, the frequency of Threonine in mtVer is about three times as much as that in mtInv (0.146 vs 0.0428).
The low pairwise correlations of exchangeability rate matrices (or frequency vectors) of the mt models confirm high varieties among the models (Table 4). The mtInv and mtVer models are the most diverse pair with the smallest correlation of exchangeability rates (0.775). Note that the correlation between the two popular general models LG and WAG is 0.912. As expected, mtMet is the closest model to mtZoa in terms of exchangeability rates, with a 0.929 correlation score, as both were trained from the metazoan data. Interestingly, mtMet is closer to mtInv than mtVer, although the metazoan training dataset consists of less invertebrate data than vertebrate data. The results indicate diverse evolutionary processes among lineages in the metazoan kingdom.
We observed remarkably low correlations between mt models and general models (e.g., the 0.46 correlation score between mtInv and LG). The low correlations imply considerably diverse evolutionary patterns between mt proteins and general proteins. Thus, general models are not an appropriate choice in inferring phylogenies from mt protein data.
Likelihood improvement on testing alignments
We assessed the performance of the new mt models (mtMet, mtVer, and mtInv) and the existing mt models (mtZoa, mtREV, and mtArt) on building maximum likelihood phylogenies. To this end, we used IQTREE [22] to build phylogenies with different models on the metazoan, vertebrate, and invertebrate testing datasets. For each testing alignment D and a model M, we optimised parameters of the rate heterogeneity model (i.e., proportion of invariable sites and shape of Gamma distribution with 4 categories), but fixed the exchangeability rates and base frequencies of the model M.
It is clear from Fig. 4 that the new models outperform the existing models for all three testing datasets. They are the bestfit models for their corresponding testing data (e.g., mtMet is the bestfit model for the metazoan testing data). Note that the secondbest fit model for a certain testing dataset is the existing model estimated from the training data of the same category as the testing dataset (e.g., mtZoa is the secondbest fit model for the metazoan testing data). The loglikelihoods of the phylogenies with the new models are significantly higher than those of the existing models. For example, the likelihood advantage of mtMet to the secondbest model, mtZoa, on the metazoan testing data is about 0.41 log points per site (or 1640 log points for a concatenated alignment of 4000 sites). This improvement is about four times as much as the improvements of LG from WAG [16]. In short, the three new models outperform the three existing models in their corresponding categories.
We analysed the performance of the mt models at the individual alignment level. We used the approximately unbiased SH test [23] to compute confidence levels for phylogenies with the models. Given a testing alignment D, we estimated the maximum likelihood tree T _{ i } according to model M _{i} where M _{i} is one of the six mt models. We computed the sitewise log likelihoods for every (T _{ i }, M _{ i }D), and subsequently used the CONSEL program [24] for assessing their confidence levels. The approximately unbiased SH test helps us to confirm whether the likelihood improvement comes from models and trees or from artefacts of numerical analyses in IQTREE. Figure 5 confirms the advantage of the new models in inferring phylogenies for all three testing datasets. The new models demonstrate a better fit for almost all testing alignments in comparison with the existing models (e.g., 85 out of 95 vertebrate alignments). The approximately unbiased SH test also confirms the superiority of the new models with high confidence levels (e.g., 67 out of 95 vertebrate alignments at the 0.9 confidence level). The existing models are still the bestfit models for some alignments, but only significantly better than the new models in a few cases. For example, the existing models are the bestfit models for 10 out of 95 vertebrate alignments, but only significantly better for one alignment at the 0.9 confidence level.
More specifically, we examined the performance of the six mt models individually (see Fig. 6). We highlight some following findings:

The bestfit model for a certain testing alignment is typically the one estimated from the training data of the same category as the testing alignment. For example, 85 out of 95 vertebrate testing alignments fit best with mtVer, which was estimated from the vertebrate training data.

The mtVer model outperforms the mtInv model for all vertebrate testing alignments and vice versa. This is explainable, as the two models are highly diverse. The mtMet model is usually the bestfit model for metazoan testing alignments. However, some metazoan testing alignments are biased on vertebrate or invertebrate species, therefore, mtVer or mtInv might fit better than mtMet for those diverse metazoan alignments.
Finally, we compared the performance of new mt models to LG4X, C60 (siteheterogeneous models) [25] and PHAT (a transmembranespecific amino acid substitution model) models [26]. Table 5 shows that the new mt models outperformed LG4X, C60 and PHAT models in terms of AIC and BIC.
Phylogeny topology differentiation on testing alignments
We investigated the topological quality of phylogenies with the six mt models by measuring their topological distances from the best phylogenies. Specifically, we used the RobinsonFoulds (RF) metric to measure the distance between two phylogenies, as it represents the number of unique bipartitions in two phylogenies [27]. We learn from Lemma 1 that the lowerbound number of incorrect bipartitions in a phylogeny can be approximated as a quarter of its RF distance from the best phylogeny.
Lemma 1.
Given two binary unrooted trees T and T ^{’} inferred from the same alignment of n taxa. The number of incorrect bipartitions in the worse likelihood phylogeny is at least a quarter of the RF distance between T and T ^{’}.
Proof:
Let T _{0} be the true binary unrooted tree. It is true that T, T ^{’}, and T _{0} have the same number of bipartitions, 2n − 3 [28].
Let p be the number of shared bipartions in both T and T’. Let x and y be the number of unique bipartitions in T and T ^{’}, respectively. As x = (2n − 3) − p and y = (2n − 3) − p, x must be equal to y.
The RF distance between T and T ^{’} is x + y or 2x.
Let S be the set of all bipartitions in T and T’, and S consists of (2n − 3) + x bipartitions. Since the true tree T _{0} has (2n − 3) bipartitions, S must consist of at least x (half of the RF distance) incorrect bipartitions.
Let T be the worse likelihood phylogeny. Then , T should include at least half of the incorrect bipartitions (x/2) as T is considered the worse phylogeny. In other words, T includes at least a quarter of RF distance between T and T ^{’}. Figure 7 illustrates an example with five taxa.
Table 6 discloses remarkable topological distances from the phylogenies with the three existing models to the best phylogenies. The distances imply a considerable number of incorrect bipartitions in the phylogenies. For example, the phylogenies with mtZoa for metazoan testing alignments contain at least 6.37% incorrect bipartitions (i.e., a quarter of their normalised RF distance from the best phylogenies, 0.255). The results reconfirm the essential role of model selections in inferring phylogenies as a poor model selection (i.e., model and testing data coming from different categories) would lead to low quality phylogenies. The lowerbound numbers of incorrect bipartitions of phylogenies with the new models are indeterminable as they are often the best phylogenies. However, the significant likelihood improvement would expectedly lead to better phylogenies with fewer incorrect bipartitions.
We also applied the approximately unbiased SH test to examine the tree topologies under the bestfit models. Given a testing alignment D and its bestfit model M _{ b }, we fixed tree topologies, but reoptimised other parameters (i.e., branch lengths, parameters of rate heterogeneity model) under the bestfit model M _{ b }. Then we used the CONSEL program for assessing their confidence levels. The test shows that the tree topologies built with the new models are better than that with the existing models in term of likelihood but with lower confidence (Fig. 8). The significant drop of confidence levels reveals that a large proportion of likelihood gain is due to the new models other than tree topologies.
Location of Testudines within amniotes
We applied the new models to tackle a question about the phylogenetic position of Testudines within amniotes. The question has a long history of debate with at least four hypothesises [29]. To this end, we built a concatenated alignment of 13 proteins for 993 amniotes and used IQTREE with all mt, LG4X, and C10 models to infer the best phylogeny, named T _{ a } (Fig. 9 ). As expected, mtVer resulted in a huge likelihood advantage over other models (i.e., 18,351 loglikelihood advantage over the secondbest model, mtMet). We also used a bootstrap method [30] to estimate the reliability of clades in T _{ a }.
In general, T _{ a } strongly supports the main clades of the NCBI taxonomy at the family, subfamily, and genus levels. However, the low bootstrap values of some clades at more high levels show the limitation of mt protein data in resolving ambiguous relationships among high level clades.
Specifically, T _{ a } shows strong support (100% bootstrap values) for the clades of the Testudines order, Crocodylia order, and Aves class. In other words, mt proteins contain sufficient phylogenetic signals to correctly place a Testudines, Crocodylia, or Aves species into its corresponding order or class. Moreover, T _{ a } also displays a strong support (100% bootstrap value) for the clade of all Testudines, Crocodylia, and Aves. This means that Testudines, Crocodylia, and Aves form one separated group within amniotes. We validated the finding by moving Testudines out of the clade of Crocodylia and Aves to other positions around. We found that T _{ a } was much better than other phylogenies examined (i.e., better than the secondbest phylogeny with 76 loglikelihood points). In other words, Testudines is unlikely to be located elsewhere, rather than within the clade of Crocodilian and Aves. The finding agrees with the conclusion by Crawford et al. [31].
Although T _{ a } shows a strong support for the position of Testudines within the clade of Crocodylia and Aves, unfortunately it cannot determine the exact relationships among them. The low bootstrap value of the clade including Testudines and Aves suggests the uncertainty of the ((Testudines,Aves),Crocodylia) topology. We examined this hypothesis by comparing the topology to two other possible topologies ((Crocodylia,Testudines),Aves) and ((Crocodylia, Aves), Testudines). The tiny likelihood difference among the three topologies implies that none of these topologies really outweighs the others (Table 7). For example, the 0.467 loglikelihood advantage of ((Testudines,Aves),Crocodylia) to ((Crocodylia,Aves),Testudines) is likely caused by the limits of numerical optimisation in IQTREE rather than by topological differentiation. The approximately unbiased SH test shows no evidence in favour of any topology (Table 7).
Conclusions
We introduced three new mt models estimated from large mt protein datasets of metazoan, vertebrate, and invertebrate species. Experimental results showed the advantage of the mt new models in inferring phylogenies for both training and testing data in comparison to the existing mt models. The significant likelihood improvement for almost all testing alignments suggests that the new mt models would help find better phylogenies. The phylogenies with the existing mt models may consist of a considerable number of incorrect bipartitions due to their large distances from the best phylogenies.
The low pairwise correlations among mt models for both amino acid frequency vectors and exchangeability rate matrices suggest remarkable varieties of evolutionary processes of different metazoan lineages. This is particularly true for vertebrates and invertebrates, where their models are the most diverse pair. The new mt models are highly specified to the category of the training data and significantly different from the general models. Note that we also applied the approach to estimate mtPro and mtDeu models for Protostomia and Deuterostomia clades, respectively.
Experimental results confirmed the essential role of model selections in inferring phylogenies from mt protein data. As a general rule, the bestfit model for a certain alignment is the new model estimated from the training data of the same category as the alignment. However, we recommend testing all three new mt models for the study of datasets containing diverse metazoan groups, as mtVer and mtInv might fit better than mtMet for the diverse metazoan alignments.
An alternative approach for model selection is to use model averaging method that allows the estimation of phylogenies and model parameters using all available mt models [32]. In addition, the new empirical mt models can be used as prior probability distribution of amino acid substitution rates in Bayesian analyses [33]. As the new empirical models do not explicitly encode sitespecific biological constrains, it is worth testing siteheterogeneous models (e.g., LG4X or C60). Finally, mitochondrially encoded proteins are transmembrane proteins with non stationary evolutions, researchers should consider to test transmembranespecific amino acid substitution models (e.g. PHAT [26]) and non stationary models (e.g. Coala [34]).
The phylogeny of 993 amniote species inferred from mt proteins with the new models shows strong support for the hypothesis that Testudines, Crocodylia, and Aves form one separated clade within amniotes. However, we could not determine precise relationships among Testudines, Crocodylia, and Aves.
Methods
Model
We assume the amino acid substitution process to be a general timereversible process and that the substitution processes of amino acid sites are independent [16]. The amino acid substitution model is characterised by a Markovian substitution matrix, Q = {q _{ x , y }}, that is unchanged during the evolution across all sites. The distribution of amino acid frequencies, π = {π _{ x }}, is also assumed to be stationary (or in equilibrium) and fixed across sites and evolution histories. Moreover, Q and π are dependent, where Q π = 0. Since the process is timereversible, Q = {q _{ x , y }} can be rewritten as:
where r _{ x , y } = r _{ y , x } is the exchangeability coefficient between amino acids x and y.
Since time and branch lengths are normally measured by the number of mutations, matrix Q is normalised such that a time unit is equivalent to one amino acid mutation as follows:
The normalisation of Q would not affect likelihood values or tree topologies but branch lengths only.
Given normalised matrix Q, the probability of amino acid substitutions over the course of time t is calculated as:
where the right term, e ^{Qt}, denotes the matrix exponential.
The likelihood of phylogeny T and matrix Q of a given alignment D is calculated as:
where D _{ i } is the data at site i of alignment D. In addition, LK(T, Q; D _{ i }) can be calculated using the pruning algorithm [35].
It is well known that evolution rates among sites are variant and are best described by a gamma distribution with parameter α [36]. The proportion of invariant sites also contributes to the likelihood of a phylogeny. The likelihood of phylogeny T, matrix Q, rate variants α,and the proportion of invariant sites, ν, with given alignment D can be calculated as follows:
where ρ _{ c } is the rate of category c of the gamma distribution with parameter α , and ρ _{ c } T is tree T with branch lengths multiplied by the factor ρ _{ c }.
Many software applications have been developed to estimate T , Q , α, and v for a given alignment D [22, 37, 38].
Given a set of alignments, D = {D ^{i}}, matrix Q can be estimated from D by maximising the likelihood function as follows:
Le and Gascuel [16] proposed a method to estimate matrix Q. First, T ^{i} , α ^{i}, and v ^{i} are estimated using an initial matrix Q, and subsequently matrix Q is estimated based on the newly estimated parameters T ^{i} , α ^{i}, and v ^{i}. The optimising process is repeated until the likelihood improvement is insignificant.
Abbreviations
 Mt.:

Mitochondrial
 NCBI:

National Center for Biotechnology Information
 RF:

RobinsonFoulds
References
Gray IC, Barnes MR. Amino acid properties and consequences of substitutions. Bioinforma. Genet. Chichester, UK: John Wiley & Sons. Ltd. 2003;4:289–304.
Benner S a, Cohen MA, Gonnet GH. Amino acid substitution during functionally constrained divergent evolution of protein sequences. Protein Eng. 1994, p. 1323–32.
Dang CC, Le QS, Gascuel O, Le VS. FLU, an amino acid substitution model for influenza proteins. BMC Evol Biol. 2010;10:99.
Nickle DC, Heath L, Jensen MA, Gilbert PB, Mullins JI, Kosakovsky Pond SL. HIVSpecific Probabilistic Models of Protein Evolution. Pybus O, editor. PLoS One 2007, 2:e503.
RotaStabelli O, Yang Z, Telford MJ. MtZoa: a general mitochondrial amino acid substitutions model for animal evolutionary studies. Mol Phylogenet Evol. 2009;52:268–72.
Le SQ, Gascuel O. Accounting for solvent accessibility and secondary structure in protein phylogenetics is clearly beneficial. Syst Biol. 2010;59:277–87.
Dunn KA, Jiang W, Field C, Bielawski JP. Improving Evolutionary Models for Mitochondrial Protein Data with SiteClass Specific Amino Acid Exchangeability Matrices. Salamin N, editor. PLoS One 2013, 8:e55816.
Taanman JW. The mitochondrial genome: structure, transcription, translation and replication. Biochim. Biophys. Acta  Bioenerg 1999, 1410:103–123.
Carapelli A, Liò P, Nardi F, van der Wath E, Frati F. Phylogenetic analysis of mitochondrial protein coding genes confirms the reciprocal paraphyly of Hexapoda and Crustacea. BMC Evol. Biol. 2007, 7 Suppl 2:S8.
Eo SH, DeWoody JA. Evolutionary rates of mitochondrial genomes correspond to diversification rates and to contemporary species richness in birds and reptiles. Proc Biol Sci. 2010;277:3587–92.
Cook CE, Yue Q, Akam M. Mitochondrial genomes suggest that hexapods and crustaceans are mutually paraphyletic. Proc Biol Sci. 2005;272:1295–304.
Spinks PQ, Shaffer HB, Iverson JB, McCord WP. Phylogenetic hypotheses for the turtle family Geoemydidae. Mol Phylogenet Evol. 2004;32:164–82.
Adachi J, Hasegawa M. Model of amino acid substitution in proteins encoded by mitochondrial DNA. J Mol Evol. 1996;42:459–68.
Abascal F, Posada D, Zardoya R. MtArt: a new model of amino acid replacement for Arthropoda. Mol Biol Evol. 2007;24:1–5.
Donoghue PCJ, Purnell MA. Genome duplication, extinction and vertebrate evolution. Trends Ecol. Evol. 2005, p. 312–9.
Le SQ, Gascuel O. An improved general amino acid replacement matrix. Mol Biol Evol. 2008;25:1307–20.
Whelan S, Goldman N. A general empirical model of protein evolution derived from multiple protein families using a maximumlikelihood approach. Mol Biol Evol. 2001;18:691–9.
Dang CC, Le VS, Gascuel O, Hazes B, Le QS. FastMG: a simple, fast, and accurate maximum likelihood procedure to estimate amino acid replacement rate matrices from large data sets. BMC Bioinformatics. 2014;15:341.
Tan G, Muffato M, Ledergerber C, Herrero J, Goldman N, Gil M, et al. Current methods for automated filtering of multiple sequence alignments frequently worsen singlegene phylogenetic inference. Syst Biol. 2015;64:778–91.
Akaike H. A new look at the statistical model identification. IEEE Trans Autom Control. 1974;19:716–23.
Schwarz G. Estimating the dimension of a model. Ann Stat. 1978;6:461–4.
Nguyen LT, Schmidt HA, Von Haeseler A, Minh BQ. IQTREE: a fast and effective stochastic algorithm for estimating maximumlikelihood phylogenies. Mol Biol Evol. 2015;32:268–74.
Shimodaira H. An approximately unbiased test of phylogenetic tree selection. Syst Biol. 2002;51:492–508.
Shimodaira H, Hasegawa M. CONSEL: for assessing the confidence of phylogenetic tree selection. Bioinformatics. 2001;17:1246–7.
Le SQ, Dang CC, Gascuel O. Modeling protein evolution with several amino acid replacement matrices depending on site rates. Mol Biol Evol. 2012;29:2921–36.
Ng PC, Henikoff JG, Henikoff S. PHAT: a transmembranespecific substitution matrix. Predicted hydrophobic and transmembrane. Bioinformatics. 2000;16:760–6.
Robinson DF, Foulds LR. Comparison of phylogenetic trees. Math Biosci. 1981;53:131–47.
Felsenstein J. The number of evolutionary trees. Syst Zool. 1978;27:27–33.
Fong JJ, Brown JM, Fujita MK, Boussau B. A Phylogenomic approach to vertebrate phylogeny supports a turtlearchosaur affinity and a possible paraphyletic Lissamphibia. PLoS One. 2012;7
Minh BQ, Nguyen MAT, Von Haeseler A. Ultrafast approximation for phylogenetic bootstrap. Mol Biol Evol. 2013;30:1188–95.
Crawford NG, Faircloth BC, McCormack JE, Brumfield RT, Winker K, Glenn TC. More than 1000 ultraconserved elements provide evidence that turtles are the sister group of archosaurs. Biol Lett. 2012;8:783–6.
Posada D, Buckley TR. Model selection and model averaging in phylogenetics: advantages of akaike information criterion and bayesian approaches over likelihood ratio tests. Syst Biol. 2004;53:793–808.
Huelsenbeck JP, Joyce P, Lakner C, Ronquist F. Bayesian analysis of amino acid substitution models. Philos. Trans. R. Soc. Lond. B. Biol. Sci 2008, 363:3941–3953.
Groussin M, Boussau B, Gouy M. A branchheterogeneous model of protein evolution for efficient inference of ancestral sequences. Syst Biol. 2013;62:523–38.
Felsenstein J. Evolutionary trees from DNA sequences: a maximum likelihood approach. J Mol Evol. 1981;17:368–76.
Yang Z. Maximumlikelihood estimation of phylogeny from DNA sequences when substitution rates differ over sites. Mol Biol Evol. 1993;10:1396–401.
Guindon S, Dufayard JF, Lefort V, Anisimova M, Hordijk W, Gascuel O. New algorithms and methods to estimate maximumlikelihood phylogenies: assessing the performance of PhyML 3.0. Syst Biol 2010, 59:307–321.
Yang Z. PAML 4: phylogenetic analysis by maximum likelihood. Mol Biol Evol. 2007;24:1586–91.
Acknowledgements
This work is financially supported by Vietnam National Foundation for Science and Technology Development (102.012013.04).
Funding
This work is financially supported by Vietnam National Foundation for Science and Technology Development (102.01–2013.04). The funding was used for the design of the study and collection, analysis, and interpretation of data and writing the manuscript.
Availability of data and materials
Data and new mt models are available at https://github.com/vinhbio/mt_metazoan_models
Authors’ contributions
VSL and QSL discussed ideas, conducted experiments, wrote the manuscript. All authors revised and approved the final manuscript. CCD participated in additional experiments for the revised version.
Competing interests
The authors declare that they have no competing interests.
Consent for publication
Not applicable
Ethics approval and consent to participate
Not applicable
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Author information
Authors and Affiliations
Corresponding authors
Rights and permissions
Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
About this article
Cite this article
Le, V.S., Dang, C.C. & Le, Q.S. Improved mitochondrial amino acid substitution models for metazoan evolutionary studies. BMC Evol Biol 17, 136 (2017). https://doi.org/10.1186/s128620170987y
Received:
Accepted:
Published:
DOI: https://doi.org/10.1186/s128620170987y
Keywords
 Mitochondrial amino acid substitution models
 Metazoa
 Vertebrates
 Invertebrates