- Research article
- Open Access
Mitogenomic evaluation of the historical biogeography of cichlids toward reliable dating of teleostean divergences
© Azuma et al; licensee BioMed Central Ltd. 2008
Received: 18 March 2008
Accepted: 23 July 2008
Published: 23 July 2008
Recent advances in DNA sequencing and computation offer the opportunity for reliable estimates of divergence times between organisms based on molecular data. Bayesian estimations of divergence times that do not assume the molecular clock use time constraints at multiple nodes, usually based on the fossil records, as major boundary conditions. However, the fossil records of bony fishes may not adequately provide effective time constraints at multiple nodes. We explored an alternative source of time constraints in teleostean phylogeny by evaluating a biogeographic hypothesis concerning freshwater fishes from the family Cichlidae (Perciformes: Labroidei).
We added new mitogenomic sequence data from six cichlid species and conducted phylogenetic analyses using a large mitogenomic data set. We found a reciprocal monophyly of African and Neotropical cichlids and their sister group relationship to some Malagasy taxa (Ptychochrominae sensu Sparks and Smith). All of these taxa clustered with a Malagasy + Indo/Sri Lankan clade (Etroplinae sensu Sparks and Smith). The results of the phylogenetic analyses and divergence time estimations between continental cichlid clades were much more congruent with Gondwanaland origin and Cretaceous vicariant divergences than with Cenozoic transmarine dispersal between major continents.
We propose to add the biogeographic assumption of cichlid divergences by continental fragmentation as effective time constraints in dating teleostean divergence times. We conducted divergence time estimations among teleosts by incorporating these additional time constraints and achieved a considerable reduction in credibility intervals in the estimated divergence times.
Recent technical advances in the molecular estimation of divergence times have provided molecular evolutionists with promising tools to introduce reliable time scales to molecular phylogenetic trees . One of the most significant advances common to these new methods is the departure from the molecular clock assumption, which in many cases does not strictly hold. Another advance is the use of time constraints at multiple nodes, rather than the assignment of a discrete time value to a particular node, for rate calibration. This is useful because of the various uncertainties in divergence time estimations based on fossil evidence. In general, the occurrence of the earliest fossil assignable to a particular branch can define the lower boundary of divergence time for the node at which this branch departed from its sister branch . However, when the corresponding fossil data are inadequate or sparse, the lower time boundary based on such data could considerably postdate the true divergence time, potentially leading to inaccurate or imprecise dating results [2, 3].
In general, fossils of bony fishes are not considered well preserved. Of the 425 teleostean families, 181 families do not have a fossil record. Of the remaining 244 that have fossil records, 58 have only otoliths . Thus, lower boundary values of divergence times based on teleostean fossil evidence could underestimate the true values [5–7]. Therefore, alternative methods that may provide effective time constraints in dating teleostean divergences should be explored, e.g., methods based on reasonable biogeographic assumptions. Because freshwater fishes do not disperse easily through saltwater, their evolution may be tightly linked to the geological history of the landmasses on which they evolved [8, 9]. Thus, evaluating the potential correlation of continental drift and lineage divergences in each of the freshwater fish groups that have multicontinental distributions is important .
Cichlids (order Perciformes: family Cichlidae) are freshwater fishes that are mainly distributed in landmasses of Gondwanaland origin (Africa, South and Central America, Madagascar, and Indo/Sri Lanka) . They have experienced an explosive radiation in the Great Lakes of East Africa, and they constitute one of the best-known model organisms for evolutionary biology . Phylogenetic studies based on morphological and molecular evidence have consistently recognized the monophyletic origin of the family, basal divergences of Malagasy and Indo/Sri Lankan taxa, and the sister-group relationship of African and South American clades [13–16]. These patterns of divergence among continental cichlid groups are entirely consistent with the geological history of continental drift, the proposed Gondwanan origin of Cichlidae, and subsequent vicariant divergences [5, 6, 13–18]. However, only a few molecular studies [7, 19] have attempted to evaluate this hypothesis by dating cichlid divergences; their different approaches led to opposite conclusions. Genner et al.  supported vicariant cichlid divergences during Cretaceous times (vicariant hypothesis), whereas Vences et al.  suggested a Cenozoic transmarine dispersal (dispersal hypothesis). The latter conclusion is more consistent with the Eocene occurrence of the oldest cichlid fossils .
We used molecular data obtained from complete mitochondrial DNA (mtDNA) sequences to investigate these hypotheses. Among the 54 fish taxa that we sampled, we newly determined the sequence data for six cichlid species. The two alternate hypotheses for cichlids, vicariant and dispersal ones, were evaluated by estimating the divergence times of the taxa using Bayesian analyses that incorporated extensive fossil-based time constraints for various divergences. Despite the relative paucity of fish fossil records, this set of time constraints allowed us to estimate cichlid divergence times with high enough resolution to discriminate between the two alternative hypotheses.
Cichlid taxa analyzed for mtDNAs
mtDNA size (bp)
DNA extraction, PCR, and sequencing
Fish samples were excised from live or dead specimens of each species and immediately preserved in 99.5% ethanol. Total genomic DNA was extracted from muscle, liver, and/or fin clips using a DNeasy tissue kit (Qiagen) or a DNAzol Reagent (Invitrogen), following manufacturer protocols. The mtDNA of each species was amplified using a long-PCR technique with LA-Taq (Takara). Seven fish-versatile primers for long PCR (S-LA-16S-L, L2508-16S, L12321-Leu, H12293-Leu, H15149-CYB, H1065-12S, and S-LA-16S-H [21–26]) and the two cichlid-specific primers cichlid-LA-16SH (5'-TTGCGCTACCTTTGCACGGTCAAAATACCG-3') and cichlid-LA-16SL (5'-CGGAGTAATCCAGGTCAGTTTCTATCTATG-3') were used in various combinations to amplify regions covering the entire mtDNA in one or two reactions. The long-PCR products were used as templates for subsequent short PCR.
Over 100 fish-versatile PCR primers [21–27] and 18 taxon-specific primers (Additional file 2) were used in various combinations to amplify contiguous, overlapping segments of the entire mtDNA for each of the six new cichlid species. The long PCR and subsequent short PCRs were performed as described previously [21, 28]. The short-PCR reactions were performed using the GeneAmp PCR System 9700 (Applied Biosystems) and Ex Taq DNA polymerase (Takara).
Double-stranded PCR products, treated with ExoSAP-IT (USB) to inactivate remaining primers and dNTPs, were directly used for the cycle sequencing reaction, using dye-labeled terminators (Applied Biosystems) with amplification primers and appropriate internal primers. Labeled fragments were analyzed on Model 3100 and Model 377 DNA sequencers (Applied Biosystems).
The DNA sequences obtained were edited and analyzed using EditView 1.0.1, AutoAssembler 2.1 (Applied Biosystems) and DNASIS 3.2 (Hitachi Software Engineering Co. Ltd.). Individual gene sequences were identified and aligned with their counterparts in 48 previously published mitogenomes. Amino acid sequences were used to align protein-coding genes, and standard secondary structure models for vertebrate mitochondrial tRNAs  were consulted for the alignment of tRNA genes. The 12S and 16S rRNA sequences were initially aligned using clustalX v. 1.83  with default gap penalties and subsequently adjusted by eye using MacClade 4.08 .
The ND6 gene was excluded from the phylogenetic analyses because of its heterogeneous base composition and consistently poor phylogenetic performance . The control region was also excluded because positional homology was not confidently established among such distantly-related species. The third codon positions of protein genes were excluded because of their extremely accelerated rates of change that may cause high levels of homoplasy. After the exclusion of unalignable parts in the loop regions of tRNA genes, as well as the 5' and/or 3' end regions of protein genes, all gene sequences were concatenated to produce 10,034-bp sites (6962, 1402, and 1670 positions for protein-coding, tRNA, and rRNA genes, respectively) for phylogenetic analyses.
Phylogenetic trees were reconstructed using partitioned Bayesian and maximum likelihood analyses. Partitioned Bayesian phylogenetic analyses were performed using MrBayes 3.1.2 . We set four partitions (first codon, second codon, tRNA, and rRNA positions). The general time-reversible model, with some sites assumed to be invariable and variable sites assumed to follow a discrete gamma distribution (GTR + I + Γ; ), was selected as the best-fit model of nucleotide substitution by MrModeltest 2.2 http://www.abc.se/~nylander/. The Markov chain Monte Carlo (MCMC) process was set so that four chains (three heated and one cold) ran simultaneously. We ran the program for 3,000,000 metropolis-coupled MCMC generations on each analysis, with tree sampling every 100 generations and burn-in after 10,000 trees.
Partitioned maximum likelihood (ML) analyses were performed with RAxML ver. 7.0.3 , a program implementing a novel, rapid-hill-climbing algorithm. For each dataset, a rapid bootstrap analysis and search for the best-scoring ML tree were conducted in one single program run, with the GTR + I + Γ nucleotide substitution model. The rapid bootstrap analyses were conducted with 1000 replications, with four threads running in parallel.
Statistical evaluation of alternative phylogenetic hypotheses was done using TREE- PUZZLE 5.2 , using the two-sided Kishino and Hasegawa (KH)  test, the Shimodaira and Hasegawa (SH)  test, and Bayes factors [39, 40]. We used the GTR + I + Γ model and its parameters optimized by MrModeltest 2.2.
Divergence time estimation
Maximum (U) and minimum (L) time constrains (MYA) used for dating at nodes in Fig. 2
Probable divergence time between chondrichthyans and osteichthyans (528 MYA), based on both fossils and molecules 
Stem-actinopterans known from the Givetian/Eifelian boundary 
Tournasian Cosmoptychius as the earliest stem-group neopterygian 
Estimated divergence time between polypterids and actinopterans 
Protosephuru (paddlefish) from Hauterivian (Cretaceous) 
Brachydegma from early Permian 
Stem-hiodontid Yambiania from the Lower Cretaceous 
Osteoglossoid fossil from the Aptian (Cretaceous) 
Stem-elopomorph Elopsomolos from the Kimmeridgian (Jurassic) 
Albuloid fossil from the Cenomanian (Cretaceous) 
Anguillid and congrid fossils from the Ypresian (Tertiary) 
Stem-ostariophysan Tischlingerichthys from Tithonian (Jurassic) 
Clupeid fossil from the Thanetian (Tertiary) 
Cyprinid fossil from the Ypresian (Tertiary) 
Esociform fossil from the Campanian (Cretaceous) 
Polymixiid fossil from the Cenomanian (Cretaceous) 
Pleuronectiform fossil from the Ypresian (Tertiary) 
Tetraodontiform fossil from the Cenomanian (Cretaceous) 
Estimated divergence time between Takifugu and Tetraodon 
Results and discussion
Mitochondrial genomes of cichlids
We determined complete or nearly complete mtDNA nucleotide sequences for six new cichlids from Africa, South America, Madagascar, and Indo/Sri Lanka (Table 1). The sizes of these genomes ranged from 16,457 to 16,556 bp, including approximately 800 bp in the control region. Tylochromis polylepis alone appears to have a somewhat longer control region (approximately 1200 bp) although the exact sequence of the region was unable to be determined because of the long poly-T sequences within the region. We also analyzed the previously published mitogenomic sequences of four cichlid species (Table 1). Oreochromis mossambicus (accession no. AY597335) was not included because a congeneric taxon (Oreochromis sp.) sequenced by Mabuchi et al.  had already been sampled.
All 37 genes encoding two rRNAs, 22 tRNAs, and 13 proteins were identified in these 10 cichlid mitogenomes, basically in the same order and orientation found for most other vertebrates. Transfer RNA genes could be folded into secondary structures typical of vertebrate mitochondrial tRNA . The base composition of cichlid mitogenomes was skewed (data not shown) similarly to those of other vertebrates .
Figure 1 shows the phylogenetic relationships inferred from the Bayesian analysis among the 52 bony fishes, estimated with two sharks as an outgroup. The tree topology was identical to that obtained by the partitioned ML analysis (data not shown). These bony fish taxa included two sarcopterygians (coelacanth and lungfish), nine basal actinopterygians (polypterids, acipenseriforms, lepisosteids, and amiid), and 41 teleosts, including 10 cichlids. The phylogenetic relationships obtained for non-cichlid taxa (Fig. 1) were largely consistent with those from previous mitogenomic studies [28, 43, 45], except for a difference in the sister group of holosteans (lepisosteids and amiid).
Comparison of divergence time estimates between different time constraints and studies
Yamanoue et al. 
Inoue et al. 
Cichlidae vs. Pomacentridae
127 (107 – 149)
144 (134 – 154)
137 (115 – 160)
Takifugu vs. Tetraodon
70 (55 – 86)
78 (65 – 93)
76 (60 – 94)
73 (57 – 94)
Tetraodontidae vs. Gasterosteus
154 (131 – 177)
170 (156 – 185)
161 (137 – 185)
192 (153 – 235)
Cichlidae vs. Oryzias
136 (115 – 159)
152 (141 – 165)
148 (125 – 171)
Cichlidae/Oryzias vs. Tetraodontidae
159 (136 – 183)
176 (163 – 191)
166 (142 – 191)
184 (154 – 221)
Percomorpha vs. Beryciformes
182 (157 – 206)
198 (183 – 215)
188 (162 – 214)
206 (174 – 245)
Acanthopterygii vs. Gadiformes
191 (166 – 216)
207 (190 – 224)
202 (176 – 229)
223 (191 – 264)
Acanthomorpha vs. Protacanthopterygii
249 (223 – 274)
262 (243 – 281)
270 (243 – 294)
280 (240 – 326)
232 (197 – 267)
Cyprinus vs. Danio
139 (111 – 169)
147 (120 – 174)
135 (107 – 164)
167 (131 – 208)
Euteleostei vs. Otocephala
276 (250 – 301)
288 (268 – 307)
291 (264 – 314)
315 (270 – 363)
278 (241 – 314)
Teleostei vs. Amiiformes
360 (339 – 376)
365 (348 – 378)
381 (363 – 392)
390 (340 – 442)
376 (337 – 413)
Sarcopterygii vs. Actinopterygii
428 (417 – 448)
429 (417 – 449)
428 (417 – 449)
470 (415 – 524)
451 (413 – 495)
Among the 10 cichlid taxa that we used, four were from Africa, two from South America, three from Madagascar, and one from Indo/Sri Lanka. The tree (Fig. 1) supports the monophyly of Cichlidae and two other continental groups from Africa and South America. Four basal taxa from Madagascar and Indo/Sri Lanka are not monophyletic, and two (Paretroplus from Madagascar and Etroplus from Indo/Sri Lanka) corresponding to Etroplinae sensu Sparks and Smith  form a sister group to all other cichlids. The other two Malagasy taxa (Paratilapia and Ptychochromoides), corresponding to Ptychochrominae sensu Sparks and Smith , form a sister group to the African + Neotropical clade. These results are consistent with previous molecular studies that used a few mitochondrial or nuclear gene sequences [14–16, 48], as well as morphological studies .
Test of alternative phylogenetic hypotheses for continental cichlid groups
2 ln Bayes factor
Best as in Fig. 1
Constraint 1: monophyly of Madagascar and Indo/Sri Lanka (Tree 1)
Constraint 2: monophyly of Africa, Madagascar and Indo/Sri Lanka (Tree 2)
Constraint 3: monophyly of Africa and Indo/Sri Lanka (Tree 3)
If Cichlidae originated in Cenozoic Africa and migrated into South America, Madagascar, and India via saltwater dispersal [19, 49], Malagasy/Indo Sri Lankan and/or Neotropical taxa would probably be nested in the African clade, and alternative relationships (e.g., those corresponding to constraints 2 and 3) would likely appear. However, these relationships were not found, thus supporting the vicariant divergence scenario [13, 14, 18], at least from a topological standpoint.
Timing of cichlid divergences
We then compared the estimated divergence times among cichlids and the probable times of continental fragmentation based on geological evidence. The divergence time between Malagasy and Indo/Sri Lankan taxa within Etroplinae (~87 MYA: 69–106 MYA) is very close to the time of separation between Madagascar and India (85–95 MYA) [50, 51]. The divergence time estimated between African and Neotropical clades (~89 MYA: 72–108 MYA) is also close to the time of separation between African and South American landmasses (~100 MYA) [50, 51]. The divergence time between African + Neotropical cichlids and Malagasy ptychochrominae cichlids (~96 MYA: 78–115 MYA) appears to be somewhat more recent than the time generally accepted for the complete separation of the Indo-Madagascar landmass from Gondwanaland (120–130 MYA) [50, 51]. However, some studies  have postulated an extended connection between India and Antarctica by approximately 112 MYA, which is within the 95% credibility range for the African/Neotropical vs. ptychochrominae cichlid divergence. Taken together, these results are consistent with the vicariant divergence of continental cichlid groups during Cretaceous times and argue against their Cenozoic dispersal.
Vences et al.  calibrated a molecular clock for cichlids that assumed that the divergence time of the most basal endemic lineages in East African Rift lakes (e.g., Tanganyika) corresponds to the geological estimate of the age of the lakes. These estimated divergence times between continental cichlid clades were all in the Cenozoic (rather than the Mesozoic, as we demonstrate in Fig. 2) and supported the hypothesis of long-distance Cenozoic transmarine dispersal of cichlids. This view of the Cenozoic (or latest Cretaceous) origin and transmarine dispersal of cichlids has also been supported by some biogeographers  because it is consistent with cichlid fossil records, which first occur in South America and Africa in the Eocene [20, 53]. However, the clock-based dating procedures of Vences et al.  present some problems. The strict molecular clock may not hold for all cichlid lineages , and the premise that the oldest endemic cichlid divergence is synchronized with the formation of the lakes may not be valid. Some lineages that had diverged outside the lake may have immigrated in parallel . In addition, there is no definitive, geologically based time estimate for the formation of the lakes.
More recently, Genner et al.  used two mitochondrial (cytochrome b and 16S rRNA) and one nuclear (TMO-4C4) gene fragments to estimate the divergence times among cichlids. When the cichlid divergence by Gondwanan vicariance was assumed, the resultant divergence times were more consistent with those estimated with time constraints from previous paleontological and molecular studies [2, 54–57] than when the Cenozoic cichlid divergence was assumed based on fossil records.
Although we concur on the Gondwanan origin and vicariant divergence of cichlids, Genner et al.  evaluated this biogeographic hypothesis somewhat indirectly, in that the fitness of estimated times of cichlid divergences to those obtained with time constraints from previous studies was qualitatively compared between alternative assumptions on cichlid biogeography. We evaluated cichlid divergence times more directly by using longer mitogenomic sequence data and dozens of non-cichlid taxa, allowing us to set many time constraints purely from the paleontological data and providing additional evidence for an ancient cichlid divergence on Gondwanaland, despite the general paucity of the Mesozoic and Cenozoic paleontological record on bony fishes.
Gondwana fragmentation as time constraints
Among the fossil data points, four data points in the Paleozoic show a fairly good 1:1 relationship, whereas other points mostly in the Mesozoic are considerably below the line of 1:1 relationship. This might mean that the Mesozoic fossils do not really represent the oldest fossil for the corresponding lineages whereas this is not the case for older Paleozoic lineages. This situation is somewhat reminiscent of the apparent relative paucity of Mesozoic fossil evidence of tetrapods (mammals and birds) .
Several papers have noticed that molecular time estimations are consistently older than paleontological ones [2, 3, 5–7, 59]. Benton and Ayala  have pointed out four pervasive biases that make molecular dates too old: i) too old calibration dates based on previous molecular studies; ii) undetected fast-evolving genes; iii) ancestral polymorphism that is maintained through long evolutionary period; and iv) asymmetric distributions of estimated times, with a constrained younger end but an unconstrained older end (this is caused because rates of evolution are constrained to be nonnegative, but the rates are unbounded above zero).
The first factor is not the case for the present study, because we did not use the calibration dates based on previous molecular studies, but used only those based on fossil records. The third factor would be the case when the used genomic regions are under the long-term balancing selection, but no mitochondrial gene has been reported to be under such selection. Regarding the second and fourth factors, we believe that they are also not the case for this study, because we used mitogenomic sequence data excluding peculiarly rapid evolving region (e.g., the control region), and because each mitochondrial gene used here was tested to perform well for dating vertebrate (tetrapod) divergences . According to Benton and Ayala , for reliable dating "careful choice of genes may be a more appropriate strategy (than the larger data strategy), with a focus on long and fast-evolving (yet alignable) sequences." Our present study based on nearly whole mitogenomic sequence data fairly accommodates such condition.
Improved dating of teleostean divergences
The addition of the cichlid constraints appears to shorten the 95% credibility intervals of the time estimates, especially for divergences occurring within Acanthomorpha 100–200 MYA. For example, our Figure 2 and Yamanoue et al.  estimated the divergence time of torafugu (Tetraodontiformes) and medaka (Beloniformes) to be approximately 159 (136–183) MYA and 184 (154–221) MYA, respectively. The cichlid constraints considerably narrowed the 95% credibility interval to 176 (163–191) MYA (Table 3), and also increased the precision of time estimates for other nodes. The use of ample molecular data from mitogenomic sequences also helped to narrow the credibility interval. For example, Kumazawa et al.  used two mitochondrial genes (NADH dehydrogenase subunit 2 and cytochrome b) and estimated the divergence between torafugu and zebrafish at 284 ± 28 (mean ± standard deviation) MYA, whereas our whole mitogenomic data set showed the divergence at 288 (268–307) MYA (Table 3).
We estimated the divergence times of major cichlid lineages as part of the longer evolutionary history of teleostean fishes. Our results and those of a recent molecular study based on both mitochondrial and nuclear data sets  support a vicariant history of cichlid divergences, while other researchers  have argued for the dispersal hypothesis. We presented additional strong evidence for the vicariant hypothesis and propose that the vicariant assumption can be used to generate time constraints to date other teleostean divergences in both deeper (100–300 MYA) and shallower (< 100 MYA) time ranges.
This could be a significant contribution toward the reliable dating of teleostean divergence times in light of the scarcity of teleostean fossil records in the Mesozoic and later (see above) and the probable deviation of molecular evolutionary rates of fishes from those of tetrapods [5, 62], for which molecular evolutionary rates are more reliably studied using ampler fossil records. A further exploration of biogeography-based time constraints for other groups of freshwater fishes that could be reasonably incorporated into the dating study (e.g. rainbowfishes ) would be expected to increase the accuracy and precision of teleostean divergence time estimates.
We thank J. G. Inoue and Y. Yamanoue for their helpful suggestions and technical assistance. We also thank J. G. Inoue for critically reading an earlier version of the manuscript and providing useful comments. This study was supported by grants from the Ministry of Education, Culture, Sports, Science, and Technology of Japan (grant No. 15380131, 17207007, 19207007 and 20405012).
- Yang Z: Computational Molecular Evolution. 2006, New York: Oxford University PressView ArticleGoogle Scholar
- Benton MJ, Donoghue PC: Paleontological evidence to date the tree of life. Mol Biol Evol. 2007, 24: 26-53. 10.1093/molbev/msl150.View ArticlePubMedGoogle Scholar
- Hedges SB, Kumar S: Precision of molecular time estimates. Trends Genet. 2004, 20: 242-247. 10.1016/j.tig.2004.03.004.View ArticlePubMedGoogle Scholar
- Benton MJ: The Fossil Record. 1993, London: Chapman & Hall, 2:Google Scholar
- Kumazawa Y, Yamaguchi M, Nishida M: Mitochondrial molecular clocks and the origin of euteleostean biodiversity: Familial radiation of perciforms may have predated the Cretaceous/Tertiary boundary. The biology of biodiversity. Edited by: Kato M. 1999, Tokyo: Springer, 35-52.Google Scholar
- Kumazawa Y, Nishida M: Molecular phylogeny of osteoglossoids: A new model for Gondwanian origin and plate tectonic transportation of the Asian arowana. Mol Biol Evol. 2000, 17: 1869-1878.View ArticlePubMedGoogle Scholar
- Genner MJ, Seehausen O, Lunt DH, Joyce DA, Shaw PW, Carvalho GR, Turner GF: Age of cichlids: new dates for ancient lake fish radiations. Mol Biol Evol. 2007, 24: 1269-1282. 10.1093/molbev/msm050.View ArticlePubMedGoogle Scholar
- Banarescu P: Zoogeography of fresh waters. 1990, Wiesbaden: AULA-VerlagGoogle Scholar
- Lundberg JG: African-South American freshwater fish clades and continental drift: Problems with a paradigm. Biological relationships between Africa and South America. Edited by: Goldblatt P. 1993, New Haven: Yale University Press, 156-198.Google Scholar
- Avise JC: Phylogeography: The History and Formation of Species. 2000, Cambridge: Harvard University PressGoogle Scholar
- Nelson JS: Fishes of the world. 2006, Hoboken: John Wiley & Sons, 4Google Scholar
- Kocher TD: Adaptive evolution and explosive speciation: the cichlid fish model. Nat Rev Genet. 2004, 5: 288-298. 10.1038/nrg1316.View ArticlePubMedGoogle Scholar
- Stiassny MLJ: Phylogenetic intrarelationships of the family Cichlidae: an overview. Cichlid Fishes: behaviour, ecology and evolution. Edited by: Keenleyside MHA. 1991, London: Chapman & Hall, 1-35.Google Scholar
- Zardoya R, Vollmer DM, Craddock C, Streelman JT, Karl S, Meyer A: Evolutionary conservation of microsatellite flanking regions and their use in resolving the phylogeny of cichlid fishes (Pisces: Perciformes). Proc R Soc Lond B. 1996, 263: 1589-1598. 10.1098/rspb.1996.0233.View ArticleGoogle Scholar
- Farias IP, Orti G, Meyer A: Total evidence: molecules, morphology, and the phylogenetics of cichlid fishes. J Exp Zool. 2000, 288: 76-92. 10.1002/(SICI)1097-010X(20000415)288:1<76::AID-JEZ8>3.0.CO;2-P.View ArticlePubMedGoogle Scholar
- Sparks JS, Smith WL: Phylogeny and biogeography of cichlid fishes (Teleostei: Perciformes: Cichlidae). Cladistics. 2004, 20: 501-517. 10.1111/j.1096-0031.2004.00038.x.View ArticleGoogle Scholar
- Chakrabarty P: Cichlid biogeography: comment and review. Fish Fish. 2004, 5: 97-119.View ArticleGoogle Scholar
- Sparks JS, Smith WL: Freshwater fishes, dispersal ability, and nonevidence: "Gondwana Life Rafts" to the rescue. Syst Biol. 2005, 54: 158-165. 10.1080/10635150590906019.View ArticlePubMedGoogle Scholar
- Vences M, Freyhof J, Sonnenberg R, Kosuch J, Veith M: Reconciling fossils and molecules: Cenozoic divergence of cichlid fishes and the biogeography of Madagascar. J Biogeogr. 2001, 28: 1091-1099. 10.1046/j.1365-2699.2001.00624.x.View ArticleGoogle Scholar
- Murray AM: The fossil record and biogeography of the Cichlidae (Actinopterygii : Labroidei). Biol J Linn Soc. 2001, 74: 517-532.View ArticleGoogle Scholar
- Miya M, Nishida M: Organization of the mitochondrial genome of a deep-sea fish, Gonostoma gracile (Teleostei : Stomiiformes): first example of transfer RNA gene rearrangements in bony fishes. Mar Biotechnol. 1999, 1: 416-426. 10.1007/PL00011798.View ArticlePubMedGoogle Scholar
- Miya M, Nishida M: Use of mitogenomic information in teleostean molecular phylogenetics: a tree-based exploration under the maximum-parsimony optimality criterion. Mol Phylogenet Evol. 2000, 17: 437-455. 10.1006/mpev.2000.0839.View ArticlePubMedGoogle Scholar
- Inoue JG, Miya M, Tsukamoto K, Nishida M: Complete mitochondrial DNA sequence of the Japanese sardine Sardinops melanostictus. Fish Sci. 2000, 66: 924-932. 10.1046/j.1444-2906.2000.00148.x.View ArticleGoogle Scholar
- Inoue JG, Miya M, Tsukamoto K, Nishida M: A mitogenomic perspective on the basal teleostean phylogeny: resolving higher-level relationships with longer DNA sequences. Mol Phylogenet Evol. 2001, 20: 275-285. 10.1006/mpev.2001.0970.View ArticlePubMedGoogle Scholar
- Ishiguro N, Miya M, Nishida M: Complete mitochondrial DNA sequence of ayu, Plecoglossus altivelis. Fish Sci. 2001, 67: 474-481. 10.1046/j.1444-2906.2001.00283.x.View ArticleGoogle Scholar
- Kawaguchi A, Miya M, Nishida M: Complete mitochondrial DNA sequence of Aulopus japonicus (Teleostei : Aulopiformes), a basal Eurypterygii: longer DNA sequences and higher-level relationships. Ichthyol Res. 2001, 48: 213-223. 10.1007/s10228-001-8139-0.View ArticleGoogle Scholar
- Inoue JG, Miya M, Aoyama J, Ishikawa S, Tsukamoto K, Nishida M: Complete mitochondrial DNA sequence of the Japanese eel Anguilla japonica. Fish Sci. 2001, 67: 118-125. 10.1046/j.1444-2906.2001.00207.x.View ArticleGoogle Scholar
- Inoue JG, Miya M, Tsukamoto K, Nishida M: Basal actinopterygian relationships: a mitogenomic perspective on the phylogeny of the "ancient fish". Mol Phylogenet Evol. 2003, 26: 110-120. 10.1016/S1055-7903(02)00331-7.View ArticlePubMedGoogle Scholar
- Kumazawa Y, Nishida M: Sequence evolution of mitochondrial tRNA genes and deep-branch animal phylogenetics. J Mol Evol. 1993, 37: 380-398. 10.1007/BF00178868.View ArticlePubMedGoogle Scholar
- Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG: The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res. 1997, 25: 4876-4882. 10.1093/nar/25.24.4876.PubMed CentralView ArticlePubMedGoogle Scholar
- Maddison WP, Maddison DR: MacClade 4.0: analysis of phylogeny and character evolution. 2000, Sunderland: Sinauer AssociatesGoogle Scholar
- Huelsenbeck JP, Ronquist F: MRBAYES: Bayesian inference of phylogenetic trees. Bioinformatics. 2001, 17: 754-755. 10.1093/bioinformatics/17.8.754.View ArticlePubMedGoogle Scholar
- Yang ZH: Maximum likelihood phylogenetic estimation from DNA sequences with variable rates over sites: approximate methods. J Mol Evol. 1994, 39: 306-314. 10.1007/BF00160154.View ArticlePubMedGoogle Scholar
- Nylander JA, Ronquist F, Huelsenbeck JP, Nieves-Aldrey JL: Bayesian phylogenetic analysis of combined data. Syst Biol. 2004, 53: 47-67. 10.1080/10635150490264699.View ArticlePubMedGoogle Scholar
- Stamatakis A: RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models. Bioinformatics. 2006, 22: 2688-2690. 10.1093/bioinformatics/btl446.View ArticlePubMedGoogle Scholar
- Schmidt HA, Strimmer K, Vingron M, von Haeseler A: TREE-PUZZLE: maximum likelihood phylogenetic analysis using quartets and parallel computing. Bioinformatics. 2002, 18: 502-504. 10.1093/bioinformatics/18.3.502.View ArticlePubMedGoogle Scholar
- Kishino H, Hasegawa M: Evaluation of the maximum likelihood estimate of the evolutionary tree topologies from DNA sequence data, and the branching order in Hominoidea. J Mol Evol. 1989, 29: 170-179. 10.1007/BF02100115.View ArticlePubMedGoogle Scholar
- Shimodaira H, Hasegawa M: Multiple comparisons of log-likelihoods with applications to phylogenetic inference. Mol Biol Evol. 1999, 16: 1114-1116.View ArticleGoogle Scholar
- Kass RE, Raftery AE: BAYES FACTORS. J Am Stat Assoc. 1995, 90: 773-795. 10.2307/2291091.View ArticleGoogle Scholar
- Brandley MC, Schmitz A, Reeder TW: Partitioned Bayesian analyses, partition choice, and the phylogenetic relationships of scincid lizards. Syst Biol. 2005, 54: 373-390. 10.1080/10635150590946808.View ArticlePubMedGoogle Scholar
- Thorne JL, Kishino H, Painter IS: Estimating the rate of evolution of the rate of molecular evolution. Mol Biol Evol. 1998, 15: 1647-1657.View ArticlePubMedGoogle Scholar
- Yang ZH: PAML: a program package for phylogenetic analysis by maximum likelihood. Comput Appl Biosci. 1997, 13: 555-556.PubMedGoogle Scholar
- Mabuchi K, Miya M, Azuma Y, Nishida M: Independent evolution of the specialized pharyngeal jaw apparatus in cichlid and labrid fishes. BMC Evol Biol. 2007, 7: 10-10.1186/1471-2148-7-10.PubMed CentralView ArticlePubMedGoogle Scholar
- Asakawa S, Kumazawa Y, Araki T, Himeno H, Miura K, Watanabe K: Strand-specific nucleotide composition bias in echinoderm and vertebrate mitochondrial genomes. J Mol Evol. 1991, 32: 511-520. 10.1007/BF02102653.View ArticlePubMedGoogle Scholar
- Miya M, Takeshima H, Endo H, Ishiguro NB, Inoue JG, Mukai T, Satoh TP, Yamaguchi M, Kawaguchi A, Mabuchi K, Shirai SM, Nishida M: Major patterns of higher teleostean phylogenies: a new perspective based on 100 complete mitochondrial DNA sequences. Mol Phylogenet Evol. 2003, 26: 121-138. 10.1016/S1055-7903(02)00332-9.View ArticlePubMedGoogle Scholar
- Kikugawa K, Katoh K, Kuraku S, Sakurai H, Ishida O, Iwabe N, Miyata T: Basal jawed vertebrate phylogeny inferred from multiple nuclear DNA-coded genes. BMC Biol. 2004, 2: 3-10.1186/1741-7007-2-3.PubMed CentralView ArticlePubMedGoogle Scholar
- Patterson C: Interrelationships of holosteans. Interrelationships of fishes. Edited by: Greenwood PH, Miles RS, Patterson C. 1973, London: Academic Press, 233-305.Google Scholar
- Streelman JT, Karl SA: Reconstructing labroid evolution with single-copy nuclear DNA. Proc R Soc Lond B. 1997, 264: 1011-1020. 10.1098/rspb.1997.0140.View ArticleGoogle Scholar
- Briggs JC: Fishes and birds: Gondwana life rafts reconsidered. Syst Biol. 2003, 52: 548-553.PubMedGoogle Scholar
- Smith AG, Smith DG, Funnell BM: Atlas of Mesozoic and Cenozoic coastlines. 1994, New York: Cambridge University PressGoogle Scholar
- Storey BC: The role of mantle plumes in continental breakup: case histories from Gondwanaland. Nature. 1995, 377: 301-308. 10.1038/377301a0.View ArticleGoogle Scholar
- Masters JC, de Wit MJ, Asher RJ: Reconciling the origins of Africa, India and Madagascar with vertebrate dispersal scenarios. Folia Primatol. 2006, 77: 399-418. 10.1159/000095388.View ArticlePubMedGoogle Scholar
- Malabarba MC, Zuleta O, Del Papa C: Proterocara argentina, a new fossil cichlid from the Lumbrera Formation, Eocene of Argentina. J Vertebr Paleontol. 2006, 26: 267-275. 10.1671/0272-4634(2006)26[267:PAANFC]2.0.CO;2.View ArticleGoogle Scholar
- Inoue JG, Miya M, Venkatesh B, Nishida M: The mitochondrial genome of Indonesian coelacanth Latimeria menadoensis (Sarcopterygii : Coelacanthiformes) and divergence time estimation between the two coelacanths. Gene. 2005, 349: 227-235. 10.1016/j.gene.2005.01.008.View ArticlePubMedGoogle Scholar
- Yamanoue Y, Miya M, Inoue JG, Matsuura K, Nishida M: The mitochondrial genome of spotted green pufferfish Tetraodon nigroviridis (Teleostei : Tetraodontiformes) and divergence time estimation among model organisms in fishes. Genes Genet Syst. 2006, 81: 29-39. 10.1266/ggs.81.29.View ArticlePubMedGoogle Scholar
- Steinke D, Salzburger W, Meyer A: Novel relationships among ten fish model species revealed based on a phylogenomic analysis using ESTs. J Mol Evol. 2006, 62: 772-784. 10.1007/s00239-005-0170-8.View ArticlePubMedGoogle Scholar
- Hurley IA, Mueller RL, Dunn KA, Schmidt EJ, Friedman M, Ho RK, Prince VE, Yang ZH, Thomas MG, Coates MI: A new time-scale for ray-finned fish evolution. Proc R Soc Lond B. 2007, 274: 489-498. 10.1098/rspb.2006.3749.View ArticleGoogle Scholar
- Kumar S, Hedges SB: A molecular timescale for vertebrate evolution. Nature. 1998, 392: 917-920. 10.1038/31927.View ArticlePubMedGoogle Scholar
- Wray GA, Levinton JS, Shapiro LH: Molecular evidence for deep precambrian divergences among metazoan phyla. Science. 1996, 274: 568-573. 10.1126/science.274.5287.568.View ArticleGoogle Scholar
- Benton MJ, Ayala FJ: Dating the tree of life. Science. 2003, 300: 1698-1700. 10.1126/science.1077795.View ArticlePubMedGoogle Scholar
- Kumazawa Y, Azuma Y, Nishida M: Tempo of mitochondrial gene evolution: Can mitochondrial DNA be used to date old divergences?. Endocytobiosis Cell Res. 2004, 15: 136-142.Google Scholar
- Martin AP, Palumbi SR: Body size, metabolic rate, generation time, and the molecular clock. Proc Natl Acad Sci USA. 1993, 90: 4087-4091. 10.1073/pnas.90.9.4087.PubMed CentralView ArticlePubMedGoogle Scholar
- Sparks JS, Smith WL: Phylogeny and biogeography of the Malagasy and Australasian rainbowfishes (Teleostei : Melanotaenioidei): Gondwanan vicariance and evolution in freshwater. Mol Phylogenet Evol. 2004, 33: 719-734. 10.1016/j.ympev.2004.07.002.View ArticlePubMedGoogle Scholar
- Botella H, Blom H, Dorka M, Ahlberg PE, Janvier P: Jaws and teeth of the earliest bony fishes. Nature. 2007, 448: 583-586. 10.1038/nature05989.View ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.