A phylogenomic framework and timescale for comparative studies of tunicates

Transcriptome data collection

Live tunicate specimens were ordered from Gulf Specimen Marine Laboratories, Inc. (Panacea, FL, USA) and the Roscoff Biological Station (Roscoff, France) services and collected in Villefranche-sur-Mer (France) and Blanes (Spain). One single run of Roche 454 GS-FLX Titanium was conducted at GATC Biotech (Konstanz, Germany) on multiplexed total RNA libraries that were constructed for Clavelina lepadiformis, Cystodytes dellechiajei, Bostrichobranchus pilularis, Molgula manhattensis, Molgula occidentalis, Phallusia mammillata, Dendrodoa grossularia, Polyandrocarpa anguinea, and Styela plicata. Complementary RNA-seq data were acquired with paired-end 100-nt Illumina reads at Beijing Genome Institute (Shenzhen, China) for the thaliaceans Salpa fusiformis (mix of two blastozooids) and Doliolum nationalis (mix of 15 phorozooids), and with single-end 100-nt Illumina reads at GATC Biotech (Konstanz, Germany) for Clavelina lepadiformis and Cystodytes dellechiajei (mix of several individuals) [36]. Previously obtained 454 transcriptomic data for Microcosmus squamiger [16] were also considered. De novo assemblies were conducted with Trinity [37] for 454 reads and ABySS [38] for Illumina reads using the programs’ default parameters. For both kinds of libraries, we confirmed the sample taxonomic identifications by assembling the mitochondrial cytochrome c oxidase subunit 1 (CO1) and nuclear 18S rRNA barcoding genes and reconstructing maximum likelihood trees with available comparative data. Additional tunicate sequences were collected in public databases from various sequencing projects: Botryllus schlosseri, Halocynthia roretzi, and Diplosoma listerianum (expressed sequence tags (ESTs)), Molgula tectiformis (complementary DNAs), and Ciona robusta, Ciona savignyi, and Oikopleura dioica (genomes). Detailed information on biological specimens, basic statistics, and accession numbers of newly sequenced transcriptomes can be found in Additional file 1: Table S1.

Phylogenomic dataset assembly

We built upon a previous phylogenomic dataset [39] to select a curated set of 258 orthologous markers for deuterostomes. Alignments were complemented with sequences from the National Center for Biotechnology Information (NCBI) databases using a multiple best reciprocal hit approach implemented in the newly designed Forty-Two software [40]. Because 454 DNA sequence reads are characterized by sequencing errors typically disrupting the reading frame when translated into amino acids, alignments were verified by eye using the program ED from the MUST package [41]. Ambiguously aligned regions were excluded for each individual protein using Gblocks with medium default parameters [42] with a few subsequent manual refinements using NET from the MUST package to relax the fact that this automated approach is sometimes too conservative. This manual refinement step restored only 418 amino acid sites (i.e. 0.6% of the total alignment length). Potential environmental contaminations and cross-contaminations between our samples were also dealt with at the alignment stage by performing Basic Local Alignment Search Tool (BLAST) searches of each sequence against a taxon-rich reference database maintained for each curated gene alignment and were further sought by a visual examination of each individual gene phylogeny.

The concatenation of the resulting 258 amino acid alignments was constructed with SCaFoS [43] by defining 63 deuterostomian operational taxonomic units (OTUs) representing all major lineages. The taxon sampling included 18 tunicates, 34 vertebrates, and one cephalochordate, with seven echinoderms, two hemichordates, and one xenoturbellid as more distant outgroups. When several sequences were available for a given OTU, the slowest evolving one was selected by SCaFoS, according to maximum likelihood distances computed by TREE-PUZZLE [44] under a WAG+F model. The percentage of missing data per taxon was reduced by creating some chimerical sequences from closely related species (i.e. Eptatretus burgeri/ Myxine glutinosa, Petromyzon marinus/Lethenteron japonicum, Callorhinchus milii/ C. callorynchus, Latimeria menadoensis/L. chalumnae, Rana chensinensis/ R. catesbeiana, Alligator sinensis/ A. mississippiensis, Chrysemys picta/ Emys orbicularis/ Trachemys scripta, Patiria miniata/ P. pectinifera/ Solaster stimpsonii, Apostichopus japonicus/ Parastichopus parvimensis, Ophionotus victoriae/ Amphiura filiformis) and by retaining only proteins with at most 15 missing OTUs. The tunicate Microcosmus squamiger was excluded at this stage due to a high percentage of missing data resulting from the low number of contigs obtained in the assembly. The final alignment comprised 258 proteins and 63 taxa for 66,593 unambiguously aligned amino acid sites with 20% missing amino acid data.

Phylogenetic analyses

Bayesian cross-validation [45] implemented in PhyloBayes 3.3f [46] was used to compare the fit of site-homogeneous (LG and GTR) and site-heterogeneous (CAT-F81 and CAT-GTR) models coupled with a gamma distribution (Γ₄) of site-rate heterogeneity. Ten replicates were considered, each one consisting of a random subsample of 10,000 sites for training the model and 2000 sites for computing the cross-validation likelihood score. Under site-homogeneous LG + Γ₄ and GTR + Γ₄ models, 1100 sampling cycles were run and a burn-in of 100 samples was used, and under site-heterogeneous models CAT-F81 + Γ₄ and CAT-GTR + Γ₄, 3100 sampling cycles were run and the first 2100 samples were discarded as burn-in.

Bayesian phylogenetic reconstruction under the best-fitting CAT-GTR + Γ₄ mixture model [47] was conducted using PhyloBayes_MPI 1.5a [48]. Two independent Markov chain Monte Carlo (MCMC) simulations starting from a randomly generated tree were run for 6000 cycles with trees and associated model parameters being sampled every cycle. The initial 1000 trees sampled in each MCMC run were discarded as burn-in after checking for convergence in both likelihood and model parameters, as well as in clade posterior probabilities using bpcomp (max_diff < 0.3). The 50% majority-rule Bayesian consensus tree and the associated posterior probabilities (PPs) were then computed from the remaining combined 10,000 (2 × 5000) trees using bpcomp.

We further assessed the robustness of our phylogenomic inference by applying a gene jackknife resampling procedure [3]. A hundred jackknife replicates constituting 130 alignments drawn randomly out of the total 258 protein alignments were generated. The 100 resulting jackknife supermatrices were then analysed using PhyloBayes_MPI under the second best-fitting CAT-F81 + Γ₄ model instead of the best-fitting CAT-GTR + Γ₄ and for 2000 sampling cycles in order to reduce the computational burden. After removing the first 200 sampled trees of each chain as the burn-in, a majority-rule consensus tree was obtained for each replicate using the 1800 trees sampled from the posterior distribution. A consensus tree was then obtained from the 100 jackknife-resampled consensus trees. The support values displayed by this Bayesian consensus tree are thus gene jackknife support (JS) percentages. High values indicate nodes that have high posterior probability support in most jackknife replicates and are thus robust to gene sampling. We verified convergence of MCMCs in each jackknife replicate by checking that varying the burn-in value did not affect the JS percentages obtained in the final consensus.

Molecular dating

Molecular dating analyses were performed in a Bayesian relaxed molecular clock framework using PhyloBayes 3.3f [46]. In all dating calculations, the tree topology was fixed to the majority-rule consensus tree inferred in previous Bayesian analyses (Fig. 1). Dating analyses were conducted using the best-fitting site-heterogeneous CAT-GTR + Γ₄ mixture model and a relaxed clock model with a birth-death prior on divergence times combined with soft fossil calibrations following Lartillot et al. [46]. Given the lack of trustable fossils within tunicates, we used 12 calibration intervals defined within vertebrates [49, 50] and one within echinoderms [51]: (1) Chordata (Max. Age 581 Mya, Min. Age 519 Mya), (2) Olfactores (Max 581 Mya, Min 519), (3) Vertebrata (Max 581 Mya, Min 461), (4) Gnathostomata (Max 463 Mya, Min 422), (5) Osteichthyes (Max 422 Mya, Min 416), (6) Tetrapoda (Max 350 Mya, Min 330), (7) Amniota (Max 330 Mya, Min 312), (8) Diapsida (Max 300 Mya, Min 256), (9) Batrachia (Max 299 Mya, Min 200), (10) Clupeocephala (Max 165 Mya, Min 150), (11) Mammalia (Max 191 Mya, Min 163), (12) Theria (Max 171 Mya, Min 124), and (13) Echinoidea (Min 255 Mya). The prior on the root of the tree (Deuterostomia) was set to an exponential distribution of mean 540 Mya.

In order to select the best-fitting clock model, we compared the autocorrelated log-normal (LN) relaxed clock model [52] with the uncorrelated gamma (UGAM) model [53] and a strict molecular clock (CL) model. These three clock models were compared against each other using the same prior settings (see above) in a cross-validation procedure as implemented in PhyloBayes following Lepage et al. [54]. However, to reduce the computational burden, the CAT-F81 + Γ₄ mixture model was used instead of CAT-GTR + Γ₄. The cross-validation tests were performed by dividing the original alignment in two subsets with 90% of sites for the learning set (59,934 sites) and 10% of sites for the test set (6659 sites). The overall procedure was repeated over 10 random splits for which an MCMC simulation was run on the learning set for a total 4000 cycles sampling posterior rates and dates every cycle. The first 3000 samples of each MCMC were excluded as the burn-in for calculating the cross-validation scores averaged across the 10 replicates.

The final dating calculations were conducted under both LN and UGAM relaxed clock models and the CAT-GTR + Γ₄ mixture model of sequence evolution by running MCMCs for a total 25,000 cycles sampling posterior rates and dates every 10 cycles. The first 500 samples of each MCMC were excluded as the burn-in after checking for convergence in both likelihood and model parameters using readdiv. Posterior estimates of divergence dates and associated 95% credibility intervals were then computed from the remaining 2000 samples of each MCMC using readdiv. Additional dating calculations using the same sampling scheme were also conducted under the LN relaxed clock model but using the less computationally intensive CAT-F81 + Γ₄ mixture model.

A reference phylogenetic framework for model tunicates

The evolutionary relationships of tunicates have long been a matter of debate, mainly because tunicates are characterized by an overall accelerated rate of evolution in their nuclear and mitochondrial genomes compared to other deuterostome species. Moreover, the large lineage-specific variation in evolutionary rates among tunicates [16] could result in long-branch attraction (LBA) artefacts, which hamper the reliable reconstruction of their phylogenetic relationships [55–57]. Another contributing factor to our limited understanding of tunicate evolution is the uneven availability of genome data across different tunicate lineages. To address these limitations, we used: (1) a wider taxon sampling encompassing all major tunicate lineages including two divergent thaliaceans, (2) numerous nuclear genes to reduce stochastic error, and (3) powerful site-heterogeneous models that generally offer the best fit to phylogenomic data and have the advantage of being least sensitive to LBA and other potential phylogenetic artefacts [39, 58, 59]. Accordingly, the results of our Bayesian cross-validation tests showed that the CAT-GTR + Γ₄ mixture model offered the best statistical fit to the data (ΔlnL = 1506 ± 98 compared to LG + Γ₄), followed by the CAT-F81 + Γ₄ mixture model (ΔlnL = 817 ± 112 compared to LG + Γ₄) and the GTR + Γ₄ model (ΔlnL = 266 ± 41 compared to LG + Γ₄).

The majority-rule consensus tree obtained using Bayesian phylogenetic reconstruction under the best-fitting CAT-GTR + Γ₄ site-heterogeneous mixture model is thus presented in Fig. 1. This well-supported phylogenetic tree has been rooted between Xenambulacraria (Xenoturbellida + Ambulacraria) and Chordata following the results of Philippe et al. [39] showing that Xenacoelomorpha (acoelomorphs + xenoturbellids) were related to Ambulacraria (hemichordates + echinoderms) within Deuterostomia. These results have been recently challenged by two studies claiming support for a more external position of Xenacoelomorpha as a sister group to Nephrozoa (Protostomia + Deuterostomia) [60, 61]. However, this newly proposed position is still debated, as it might be the result of an LBA artefact caused by the very long branches of acoelomorphs in phylogenomic trees [62, 63]. Hence, we have chosen to root our trees according to Philippe et al. [39], which in any case does not affect the phylogenetic relationships of chordates.

The inferred topology unambiguously recovered the monophyly of chordates (PP = 1.0; JS = 100) and grouped the reciprocally monophyletic tunicates and vertebrates into Olfactores to the exclusion of cephalochordates (PP = 1.0; JS = 100) in accordance with the newly established chordate phylogeny [1, 3, 4]. Within tunicates, the appendicularian Oikopleura dioica was the sister group of all other included taxa (PP = 1.0; JS = 100). Within the latter, there was a well-supported split (PP = 1.0; JS = 100) between Stolidobranchia on one side, and Phlebobranchia, Aplousobranchia, and Thaliacea on the other side. The monophyletic Stolidobranchia included two main clades, the first corresponding to the family Molgulidae (PP = 1.0; JS = 100), and the second grouping the families Pyuridae and Styelidae (PP = 1.0; JS = 100). Within molgulids, Bostrichobranchus pilularis was the sister group of the three species within the genus Molgula (PP = 1.0; JS = 100), while M. occidentalis was the sister group of M. manhattensis + M. tectiformis (PP = 1.0; JS = 100). Lastly, the four styelids Styela plicata, Botryllus schlosseri, Polyandrocarpa anguinea, and Dendrodoa grossularia constituted a monophyletic group (PP = 1.0; JS = 100) with respect to the single species here representing pyurids (Halocynthia roretzi). Within styelids, S. plicata diverged first (PP = 1.0; JS = 98) followed by B. schlosseri as the sister group of P. anguinea + D. grossularia (PP = 1.0; JS = 100). On the other side of the tree, Thaliacea branched with maximum statistical support (PP = 1.0; JS = 100) as the sister group of the clade Phlebobranchia + Aplousobranchia. The traditional class-level taxon Ascidiacea — currently considered to embrace the orders Aplousobranchia, Phlebobranchia and Stolidobranchia [64] — therefore refers to a paraphyletic assemblage. An alternative classification scheme based on gonad position (not commonly used nowadays) recognized two orders within ascidians: Enterogona (corresponding to Phlebobranchia + Aplousobranchia) and Pleurogona (= Stolidobranchia) [30, 65]. These alternative order-level taxa are recovered as monophyletic in our analyses. The three aplousobranchs analysed here unambiguously formed a monophyletic clade (PP = 1.0; JS = 100) with Clavelina lepadiformis being the sister group of Diplosoma listerianum and Cystodytes dellechiajei (PP = 1.0; JS = 100). The phlebobranchs appeared as a paraphyletic group with the two Ciona species branching closer to the aplousobranchs than to the other phlebobranch species (Phallusia mammillata), although with no statistical support from the gene jackknife resampling analysis (PP = 100; JS = 42).

The results from this first phylogenomic study including all tunicate lineages were in line with recent studies [20, 25–28] demonstrating that ascidians (class Ascidiacea) form a paraphyletic group. Our results showed that phlebobranchs and aplousobranchs are undoubtedly closer to thaliaceans than to stolidobranchs (Fig. 1), and that a thorough taxonomic revision of the tunicate classes is necessary. It seems clear that the use of the Ascidiacea class should be abandoned in favour of more meaningful classification schemes. Even though the position of Thaliacea was not always statistically supported, it consistently appeared as the sister group of phlebobranchs + aplousobranchs in previous studies [20, 24–26, 28], except for a recent genome-scale study in which the positioning of Salpa thompsoni most likely suffered artefactual LBA attraction towards the fast-evolving appendicularians [66]. The robust phylogenetic position of thaliaceans found here indicates that they likely evolved from a sessile ancestor, and their study can provide valuable information on the morphological transformations associated with the transition to the pelagic lifestyle [29].

The monophyly of the clade uniting phlebobranchs and aplousobranchs has never been challenged, and thus we suggest to re-use the term Enterogona to define this group, as originally proposed by Perrier [65] and subsequently redefined by Garstang [67]. The close relationship between thaliaceans and enterogones has also been supported by all previous molecular studies, as well as by morphological observations. The gonad position and the shared paired ontogenetic rudiment of the atrial cavity and opening might constitute two of their anatomical synapomorphies [68]. Lastly, we also confirmed the previously reported monophyly of stolidobranchs (= Pleurogona), with molgulids being the sister group to styelids + pyurids.

Finally, our phylogenomic study casts new light on two recurring issues in tunicate phylogenetics. First, phlebobranchs have been repeatedly found to be paraphyletic, albeit usually with no statistical support [25–28, 69], and the phylogenetic affinities among its members remain unclear. Notably, the traditional position of Ciona as a phlebobranch ascidian was challenged by Kott [70], who placed the genus within aplousobranchs on the basis of morphological characters. More recently, Turon and López-Legentil [69] and Shenkar et al. [28] found that Ciona was closer to aplousobranchs than to other phlebobranchs using mitochondrial DNA. These results are in agreement with the tree topology obtained in the present study, although it was not statistically supported. The positioning of the model Ciona genus and the phylogenetic relationships of phlebobranchs need to be the focus of additional phylogenomic studies including a denser taxon sampling. Second, although the position of appendicularians as sister clade to all other tunicates was well supported here and in all previous tunicate phylogenomic studies [2, 3], the extremely long branch of Oikopleura dioica coupled with our current inability to completely alleviate a potential LBA artefact — even with complex site-heterogeneous mixture models (see [59]) — prevent us from considering this species phylogenetic position as conclusive. The long appendicularian branch should be subdivided with the inclusion of additional divergent species in future phylogenomic analyses to definitively settle this point.

Evolutionary rate variations and molecular clock models

As observed in previous phylogenomic studies of chordates [2–4], the Bayesian phylogram estimated under the best-fitting CAT-GTR + Γ₄ mixture model revealed marked branch length heterogeneity (Fig. 1). The tunicate branch lengths not only were much longer than those of all the other deuterostome clades, but they also displayed strong variations within tunicates. From the ancestral node of Olfactores, the tunicate median branch length was of 1.53 amino acid substitutions per site compared to the vertebrate median branch length, which was 0.65. From the ancestral vertebrate node, the average of branch lengths is 0.35 ± 0.05 amino acid replacements per site. In contrast, from the ancestral node of tunicates — excluding the super fast-evolving Oikopleura dioica — the average of branch lengths was 0.69 ± 0.19. For the proteins combined here for phylogenomic purposes, tunicates (with the exception of O. dioica) displayed on average a twice-higher number of amino acid substitutions than vertebrates.

Such substitution rate variation among lineages — within tunicates, and between tunicates and other deuterostomes — needs to be accounted for in molecular dating analyses by using models of clock relaxation [52]. The selection of the clock model is often arbitrary and appears mostly dependent on the software choice, with an overwhelming majority of studies relying on the BEAST software [71] using an uncorrelated gamma (UGAM, also known as UCLN) model of clock relaxation. However, it has been shown that autocorrelated rate models, such as the autocorrelated LN model, often provide a better fit with phylogenomic data [54, 72, 73]. Consequently, we compared the fit of both the UGAM and LN models to the fit of a strict CL model for our dataset using cross-validation tests under the CAT-GTR + Γ₄ model. As expected given the large lineage-specific rate variation, both relaxed clock models largely outperformed the strict clock model (UGAM vs. CL: ΔlnL = 4068 ± 125; LN vs. CL: ΔlnL = 4057 ± 118). Among relaxed clock models, UGAM and LN were statistically equivalent in offering a very similar fit to our data (UGAM vs. LN: ΔlnL = 11 ± 38).

The use of a relaxed clock model allowed us to perform evolutionary rate comparisons in terms of number of substitutions per site per million years for the 63 terminal taxa considered (Fig. 2). The box plots clearly showed that tunicates evolved faster than other groups, especially compared to vertebrates, which were the slowest evolving. On average, tunicates evolved 6.25 times faster than vertebrates (two-tailed t test; t = 4.542, p < 0.001), 2.08 times faster than cephalochordates (two-tailed t test not applicable with only one cephalochordate), and 2.45 times faster than the outgroups (two-tailed t test; t = 1.711, p = 0.099) included here. The evolutionary rate variation was also much more pronounced within tunicates than within other groups, even when the very fast evolver Oikopleura dioica was excluded. For instance, the colonial species Diplosoma listerianum and Salpa fusiformis evolved considerably faster than the solitary species Ciona spp. and Styela plicata. This confirmed earlier observations based on a reduced number of taxa and substitution rate estimations on 35 housekeeping genes [16], once again underlining the peculiar genomic evolution of tunicates that might find its root in elevated mutation rates and pervasive molecular adaptation [21, 22].

Even though the difference in fit between the two relaxed clock models was not significant for our dataset, in general LN provided more consistent dating estimates than UGAM with respect to the mean divergence dates of numerous vertebrate groups reported in the latest phylogenomic study of jawed vertebrates [35]. Notably, as observed in a previous phylogenomic study of tetrapods [74], the application of the UGAM relaxed clock model provided unrealistically recent estimates with respect to the maximum node age for the origin of turtles (LN mean age + SD: 180 ± 19 Mya [95% credibility interval 220–146]; UGAM: 59 ± 41 Mya [173–16]) (Table 1, Fig. 3, and Additional file 2: Figure S1). The UGAM model also tended to systematically provide much wider 95% credibility intervals than LN, with several of them actually spanning hundreds of millions of years (Table 1, Fig. 1, and Additional file 2: Figure S1). Given the uncertainty associated with the dating results obtained using the UGAM model of clock relaxation, we focused our discussion below on results obtained with the more robust autocorrelated LN model, which we considered as our currently most reliable dating estimates.

Nodes	LN CAT-GTR + Γ4		UGAM CAT-GTR + Γ4
	Mean ± SD	95% Cred. int.	Mean ± SD	95% Cred. int.
#63 Deuterostomia	599 ± 11	[621–579]	671 ± 108	[985–576]
#64 Xenambulacraria	588 ± 16	[616–555]	600 ± 89	[849–467]
#65 Ambulacraria	551 ± 16	[578–516]	517 ± 72	[677–403]
#66 Hemichordata	404 ± 34	[458–326]	206 ± 101	[427–63]
#67 Echinodermata	431 ± 21	[469–388]	403 ± 47	[507–323]
#68	406 ± 21	[442–363]	284 ± 83	[433–121]
#69	408 ± 20	[443–368]	360 ± 42	[450–287]
#70	158 ± 22	[210–112]	117 ± 51	[249–42]
#71 Echinoideaa	260 ± 18	[303–229]	266 ± 28	[342–222]
#72	89 ± 15	[121–61]	85 ± 49	[195–20]
#73 Chordataa	578 ± 6	[586–563]	575 ± 7	[586–558]
#74 Olfactoresa	547 ± 6	[557–532]	545 ± 11	[564–523]
#75 Tunicata	447 ± 20	[484–411]	450 ± 26	[495–398]
#76	389 ± 32	[449–333]	388 ± 30	[439–326]
#77	296 ± 44	[379–226]	311 ± 40	[380–228]
#78 Thaliacea	238 ± 44	[324–164]	218 ± 54	[318–118]
#79	274 ± 44	[356–203]	272 ± 43	[351–176]
#80	259 ± 43	[340–190]	246 ± 44	[330–154]
#81 Ciona	122 ± 33	[184–65]	97 ± 44	[196–32]
#82 Aplousobranchia	212 ± 39	[281–150]	196 ± 44	[282–120]
#83 Cystodytes /  Clavelina	117 ± 27	[168–73]	121 ± 32	[189–66]
#84 Stolidobranchia	350 ± 36	[416–292]	326 ± 39	[396–245]
#85 Mogulidae	219 ± 35	[285–156]	203 ± 48	[297–122]
#86 Molgula	176 ± 32	[233–118]	145 ± 40	[239–82]
#87 M. manhattensis  /  M. tectiformis	130 ± 26	[179–82]	94 ± 31	[162–44]
#88 Styelidae + Pyuridae	277 ± 35	[343–218]	228 ± 49	[323–139]
#89	197 ± 28	[252–145]	152 ± 41	[249–84]
#90	167 ± 25	[217–118]	113 ± 34	[187–59]
#91 Polyandrocarpa /  Dendrodoa	152 ± 24	[200–105]	84 ± 30	[156–37]
#92 Vertebrata	490 ± 7	[504–476]	481 ± 13	[510–460]
#93 Cyclostomata	434 ± 8	[449–418]	277 ± 94	[430–101]
#94 Gnathostomataa	443 ± 4	[452–435]	437 ± 9	[459–424]
#95 Chondrichthyes	363 ± 11	[380–338]	192 ± 96	[394–62]
#96	249 ± 22	[277–192]	88 ± 59	[261–23]
#97 Osteichthyesa	418 ± 2	[422–416]	419 ± 2	[422–416]
#98 Clupeocephalaa	159 ± 4	[165–150]	157 ± 5	[165–150]
#99	391 ± 3	[397–386]	393 ± 15	[415–360]
#100	377 ± 3	[383–371]	374 ± 16	[405–346]
#101 Tetrapodaa	349 ± 2	[351–345]	341 ± 6	[350–330]
#102 Amphibia	326 ± 3	[332–320]	246 ± 30	[299–200]
#103	180 ± 26	[232–132]	71 ± 51	[190–14]
#104 Batrachiaa	232 ± 21	[268–190]	123 ± 48	[225–47]
#105	118 ± 29	[174–68]	42 ± 32	[132–9]
#106	182 ± 25	[224–136]	71 ± 37	[160–21]
#107 Amniotaa	312 ± 1	[315–310]	319 ± 5	[329–312]
#108 Mammaliaa	186 ± 5	[192–172]	176 ± 8	[191–163]
#109 Theriaa	146 ± 9	[163–127]	143 ± 14	[170–123]
#110	69 ± 13	[96–47]	47 ± 35	[128–8]
#111	62 ± 11	[86–43]	55 ± 31	[127–15]
#112	52 ± 10	[]	35 ± 24	[100–9]
#113 Diapsidaa	271 ± 6	[282–259]	278 ± 14	[300–256]
#114 Lepidosauria	243 ± 10	[261–224]	166 ± 69	[283–57]
#115	168 ± 14	[189–138]	88 ± 47	[203–28]
#116	139 ± 14	[162–107]	55 ± 35	[152–16]
#117	252 ± 9	[269–233]	154 ± 69	[280–55]
#118 Testudines	180 ± 19	[220–146]	59 ± 41	[173–16]
#119	163 ± 19	[204–128]	38 ± 28	[120–11]
#120	96 ± 18	[136–62]	15 ± 14	[]
#121 Archosauria	218 ± 16	[249–186]	102 ± 51	[238–37]
#122	81 ± 29	[150–38]	23 ± 22	[85–4]
#123 Aves	111 ± 27	[170–67]	45 ± 28	[120–14]
#124 Crocodylia	86 ± 24	[142–46]	23 ± 18	[]

^aCalibration constraints

The reported values represent mean divergence dates and associated standard deviations and 95% credibility intervals obtained from a Bayesian relaxed molecular clock under the LN and UGAM models coupled with a CAT-GTR + Γ₄ mixture model. Values in bold refer to tunicates

A tentative timescale for tunicate evolution within chordates

The Bayesian chronogram obtained using the LN relaxed molecular clock model and the site-heterogeneous CAT-GTR + Γ₄ mixture model of amino acid sequence evolution is presented in Fig. 3. This phylogenomic timescale showed that major tunicate clades appeared early in chordate evolutionary history. The earliest split between appendicularians and all other tunicates was dated back to ca. 450 Mya (mean age + SD: 447 ± 20 Mya [95% credibility interval 484–411]), followed by the divergence between stolidobranchs and the clade grouping thaliaceans + phlebobranchs + aplousobranchs ca. 390 Mya (389 ± 32 Mya [449–333]) and the separation of stolidobranchs into Molgulidae and Styelidae + Pyuridae ca. 350 Mya (350 ± 36 Mya [416–292]) (Table 1 and Fig. 3). Even more recent divergences such as the ones between congeneric species within Ciona and Molgula occurred more than 100 Mya.

Given the relative uncertainty on the phylogenetic position of Xenoturbella, complementary LN relaxed molecular clock analyses were also conducted using Xenoturbella as an outgroup. As the dating results previously obtained with the CAT-F81 + Γ₄ and CAT-GTR + Γ₄ models with the original rooting were extremely similar (linear regression on mean dates R² = 0.99), we performed these additional analyses under the less computationally intensive CAT-F81 + Γ₄ model. With the new rooting configuration, the inferred mean divergence dates between the two alternative rooting schemes were globally highly correlated within chordates (linear regression R² = 0.89). An almost exact correspondence was found for vertebrates that contain most of the calibration points (linear regression R² = 1.00). For tunicates, within which there is unfortunately no available calibration constraint, the correlation remained very strong (linear regression R² = 0.95). The divergence dates within tunicates were on average older with the Xenoturbella rooting, while they remained in their vast majority within the original 95% credibility intervals (Additional file 3: Figure S2). An alternative rooting by Xenoturbella thus does not affect our main conclusions that divergence dates among the major tunicate lineages are ancient.

The relatively ancient origins of the different tunicate lineages revealed by our molecular dating estimates have two broader implications. First, there seems to be a larger gap than previously thought between tunicate and vertebrate taxonomic ranks, which exacerbates the inadequacy of their direct comparison. For example, when a vertebrate genus usually spans less than 40 million years [76], a tunicate genus (e.g. Molgula) can span up to two hundred million years (Fig. 3 and Table 1). The meaning of Linnean categorical ranks and their temporal inconsistencies among clades have been largely discussed [76], as recently illustrated by the debate around the taxonomic status of the main chordate lineages [77–79]. The parallel we draw here between tunicates and vertebrates should nevertheless help tunicate developmental biologists to interpret their results in light of the large divergences that might exist between tunicate model species despite their classification in the same genus. Second, the ancient age of their major divergence events can heavily complicate orthology assessment among tunicates, as well as between tunicates and vertebrates, thus reducing the quality of genome annotations. Indeed, the fast-paced molecular evolution of tunicates prevents the identification of some genes by simple similarity methods (e.g. BLAST), even when orthologs do exist in databases. For instance, in terms of evolutionary depth, a comparative study of the genus Molgula is roughly equivalent to a comparative study among turtles representing about 180 million years of evolution. In terms of amino acid sequence divergence, the differences are much more pronounced between Molgula occidentalis / M. tectiformis (88.1% similarity) than between Phrynops/ Chrysemys (98.0% similarity; see Fig. 3 and Table 1).

From an evo-devo perspective, the phylogenetic framework and tentative timescale presented here lead to an apparent paradox. Like most nematodes [80], the embryos of each ascidian species develop in a stereotyped manner, based on the use of invariant cell lineages [7]. Unlike nematodes however, ascidian stereotyped cell lineages are shared between evolutionarily distant species such as Ciona robusta (Enterogona) and Halocynthia roretzi (Pleurogona) [11]. The extreme morphological conservation of ascidian embryogenesis therefore contrasts with the high rates of protein divergence observed in their genomes. This paradox raises questions about the underlying mechanisms involved in developmental regulation of these animals with highly dynamic genomes. In this context, our reference phylogenetic tree and divergence date estimates among tunicate lineages could be used as an evolutionary framework to select model species sufficiently close to one another (i.e. retaining sufficient phylogenetic information) for future comparative genomic analyses assessing orthology by gene tree reconciliation and estimating evolutionary rate variations among genes belonging to different ontology categories.