Tetraodon genome confirms Takifugu findings: most fish are ancient polyploids
© BioMed Central Ltd 2004
Published: 25 November 2004
An evolutionary hypothesis suggested by studies of the genome of the tiger pufferfish Takifugu rubripes has now been confirmed by comparison with the genome of a close relative, the spotted green pufferfish Tetraodon nigroviridis. Ray-finned fish underwent a whole-genome duplication some 350 million years ago that might explain their evolutionary success.
In 1993, Sydney Brenner and colleagues  proposed sequencing the pufferfish genome as a cost-effective way to identify and characterize human genes. The genome of the pufferfish is only about one-eighth of the size of that of human but was expected to contain a similar gene repertoire. Ten years later, not only has a draft genome sequence been released for Takifugu rubripes (Fugu, also known as the Japanese or tiger pufferfish) , but also for Tetraodon nigroviridis (green spotted pufferfish) , a close relative that diverged from Takifugu 18-30 million years ago (Mya). By comparing the two pufferfish genomes with that of human, several hundred novel human genes have already been uncovered, as was predicted by Brenner and colleagues . But the pufferfish genome sequencing projects have also yielded a surprising finding: ray-finned fish (Actinopterygii), such as pufferfish might have more genes than lobe-finned fish (coelacanths and lungfish) and land vertebrates, because of additional gene-duplication events . The recent release of the Tetraodon genome sequence  provides overwhelming evidence that a genome-duplication event did indeed occur early in the evolution of ray-finned fish.
A fish-specific genome duplication
Some of the first data pointing to a possible genome duplication in fish came from Hox genes and Hox gene clusters. Hox genes encode DNA-binding proteins that specify cell fate along the anterior-posterior axis of bilaterian animal embryos and occur in one or more clusters of up to 13 genes. Whereas lobe-finned fish, amphibians, reptiles, birds and mammals have four clusters, extra Hox gene clusters have been discovered in zebrafish, Medaka, Nile tilapia and pufferfish . The observation that such distantly related species  all have seven or eight Hox gene clusters suggested the occurrence of an additional genome-duplication event in the ray-finned fish lineage before the divergence of most teleost (bony fish) species. More recent comparative genomic studies have turned up many more genes and gene clusters for which there are two copies in fish but one in other vertebrates . The findings that different paralogous pairs seem to have originated at about the same time, that different fish species seem to share ancient gene duplications, and that different paralogs are found on different linkage groups in the same order as other duplicated genes, all support the hypothesis that these genes arose through a large-scale gene-duplication event. It is worth noting, however, that some authors have argued that an ancestral whole-genome-duplication event was not responsible for the abundance of duplicated fish genes .
A very similar approach was followed for the analysis of the Takifugu genome by Christoffels et al. , who obtained essentially the same result: by constructing linearized trees, the whole-genome-duplication event was estimated to have occurred approximately 350 Mya. To test whether the sudden increase in the number of duplicated genes in the Takifugu genome was the result of an entire-genome duplication rather than an increased rate of independent tandem-duplication events, both Vandepoele et al.  and Christoffels et al.  investigated the appearance of duplicated genes in duplicated blocks on chromosomes. Statistically significant regions of micro-colinearity were identified within the complete Takifugu genome, showing the same gene content and gene order. Indeed, both studies reported a large number of duplicated genes in so-called paralogons - homologous genomic segments that can be proved to have been created by duplication  - and concluded that most findings were congruent with a large-scale, probably whole-genome duplication event in a ray-finned ancestor that gave rise to the Takifugu and other fish lineages.
A comparative analysis between the human and Tetraodon genomes has also allowed inference of the basic structure of the ancestral bony vertebrate genome, and the reconstruction of much of the evolutionary history of ancient and recent chromosomal rearrangements leading to the modern human karyotype. By matching up the genes on the Tetraodon chromosomes with homologs on human chromosomes, Jaillon et al.  inferred that the ancestor of both fish and land vertebrates had no more than 12 chromosomes, a number that has been previously suggested on the basis of linkage relationships between zebrafish, Medaka, and human . Comparison of the genomes of Tetraodon and human also showed that chromosome evolution in both lineages differed considerably. Whereas all but one of the ancestral Tetraodon chromosomes had not undergone interchromosomal exchange for 450 Mya, only one human chromosome was similarly undisturbed. A possible explanation for the difference in genome evolution might be the massive integration of transposable elements in the human genome, with an increased overall frequency of chromosome breaks as a result .
As mentioned above, on the basis of previous analyses of the Takifugu genome, the whole-genome-duplication event in fish is thought to have occurred somewhere between 300 and 350 Mya [8, 9]. An interesting question is whether this date correlates with a decisive period in the evolution of the fish. For instance, if the genome duplication had been responsible for the biological diversification and large number of ray-finned fish, as suggested previously [4, 17], it must have occurred prior to the radiation of most fish lineages. The class Actinopterygii includes more than 23,500 species , of which the vast majority are teleosts or ray-finned fish. Interestingly, all older, more basal groups of ray-finned fish, namely Polypteriformes (bichirs), Acipenseriformes (sturgeons and paddlefish), Semionotiformes (gars), and Amiformes (bowfin), have only a few extant species (Figure 1). Most members of these basal actinopterygian lineages are considered to be 'living fossils', because their morphology has remained unchanged over very long evolutionary time periods.
In a recent study, Hoegg et al.  have tried to determine the timing of the duplication event in relation to the origin of lineages of teleost and 'nonteleost' fish by sequencing three nuclear genes - fzd8, sox11 and tyrosinase - from sturgeons, gars, bony tongues, and a tenpounder. For these three genes, two copies have been described previously in derived teleost model species, such as zebrafish and pufferfish, but only one orthologous copy has been found in tetrapods. The specific clustering of the genes in individual gene trees for these three genes and a dataset of concatenated genes support the hypothesis that the fish-specific genome-duplication event took place after the split of the Acipenseriformes and the Semionotiformes from the lineage leading to teleost fish, but before the divergence of Osteoglossiformes (bony tongues) and the other more derived groups of fish (Figure 1). This is in good agreement with the recent analyses of the Takifugu genome, as fossil data age the Semionotiformes at between 245 and 286 million years, whereas molecular estimates for the Amiiformes, which are of approximately the same age as the Semionotiformes, hint at a separation from the Teleostei stem lineage about 367-404 Mya. Likewise, molecular data suggest an age of 335 million years for the Osteoglossiformes . The inferred relative and absolute dates for the fish-specific genome duplication event seem to separate the species-poor branching lineages from the species-rich teleost lineages, providing evidence that the fish-specific genome duplication might be related causally to an increase in species and morphological diversity.
On the basis of isozyme studies, Werth and Windham  developed a model in which the 'reciprocal silencing' of genes in geographically separated populations would promote speciation. A few years ago, this idea was revived in a model called 'divergent resolution', in which the loss or silencing of gene duplicates was postulated to be more important for the evolution of species diversity than the acquisition of new functions by duplicated genes. Divergent resolution occurs when different copies of a duplicated gene are lost on different chromosomes in different populations, thereby creating genetic barriers for reproduction between them [21, 22]. Divergent resolution and lineage-specific subfunction partitioning  can promote incompatibility among populations within a species, and thus might facilitate evolutionary radiation. Gene duplications might, therefore, bring about rapid speciation in populations fixed for different copies of a duplicated locus. The fish-specific genome duplication has created many duplicates that could be divergently resolved. Potentially, such genes have played a prominent role in the radiation of the teleosts. Further studies of the genes encoded in these fish genomes may shed light on how important the fish-specific whole-genome duplication has been in the evolution of the ray-finned fish.
- Brenner S, Elgar G, Sandford R, Macrae A, Venkatesh B, Aparicio S: Characterization of the pufferfish (Fugu) genome as a compact model vertebrate genome. Nature. 1993, 366: 265-268. 10.1038/366265a0.PubMedView ArticleGoogle Scholar
- Aparicio S, Chapman J, Stupka E, Putnam N, Chia JM, Dehal P, Christoffels A, Rash S, Hoon S, Smit A, et al: Whole-genome shotgun assembly and analysis of the genome of Fugu rubripes. Science. 2002, 297: 1301-1310. 10.1126/science.1072104.PubMedView ArticleGoogle Scholar
- Jaillon O, Aury J-M, Brinet F, Petit J-L, Stange-Thomann N, Mauceli E, Bouneau L, Fischer C, Ozoef-Costaz C, Bernot A, et al: Genome duplication in the teleost fish Tetraodon nigroviridis reveals the early vertebrate proto-karyotype. Nature. 2004, 431: 946-957. 10.1038/nature03025.PubMedView ArticleGoogle Scholar
- Meyer A, Schartl M: Gene and genome duplications in verterbrates: the one-to-four (-to-eight in fish) rule and the evolution of novel gene functions. Curr Opin Cell Biol. 1999, 11: 699-704. 10.1016/S0955-0674(99)00039-3.PubMedView ArticleGoogle Scholar
- Chen W-J, Orti G, Meyer A: Novel evolutionary relationships among four fish model systems. Trends Genet. 2004, 20: 424-431. 10.1016/j.tig.2004.07.005.PubMedView ArticleGoogle Scholar
- Taylor JS, Braasch I, Frickey T, Meyer A, Van de Peer Y: Genome duplication, a trait shared by 22,000 species of ray-finned fish. Genome Res. 2003, 13: 382-390. 10.1101/gr.640303.PubMedPubMed CentralView ArticleGoogle Scholar
- Robinson-Rechavi M, Marchand O, Escriva H, Laudet V: An ancestral whole-genome duplication may not have been responsible for the abundance of duplicated fish genes. Curr Biol. 2001, 11: R458-R459. 10.1016/S0960-9822(01)00280-9.PubMedView ArticleGoogle Scholar
- Vandepoele K, De Vos W, Taylor JS, Meyer A, Van de Peer Y: Major events in the genome evolution of vertebrates: paranome age and size differs considerably between ray-finned fishes and land vertebrates. Proc Natl Acad Sci USA. 2004, 101: 1638-1643. 10.1073/pnas.0307968100.PubMedPubMed CentralView ArticleGoogle Scholar
- Christoffels A, Koh EG, Brenner S, Aparicio S, Venkatesh B: Fugu genome analysis provides evidence for a whole-genome duplication early during the evolution of ray-finned fishes. Mol Biol Evol. 2004, 21: 1146-1151. 10.1093/molbev/msh114.PubMedView ArticleGoogle Scholar
- Takezaki N, Rzhetsky A, Nei M: Phylogenetic test of the molecular clock and linearized trees. Mol Biol Evol. 1995, 12: 823-833.PubMedGoogle Scholar
- Van de Peer Y: Computational approaches to unveiling ancient genome duplications. Nat Rev Genet. 2004, 5: 752-763. 10.1038/nrg1449.PubMedView ArticleGoogle Scholar
- Wolfe KH, Shields DC: Molecular evidence for an ancient duplication of the entire yeast genome. Nature. 1997, 387: 708-713. 10.1038/42711.PubMedView ArticleGoogle Scholar
- Llorente B, Durrens P, Malpertuy A, Aigle M, Artiguenave F, Blandin G, Bolotin-Fukuhara M, Bon E, Brottier P, Casaregola S, et al: Genomic exploration of the hemiascomycetous yeasts: 20. Evolution of redundancy compared to Saccharomyces cerevisiae. FEBS Lett. 2000, 487: 122-133. 10.1016/S0014-5793(00)02291-2.PubMedView ArticleGoogle Scholar
- Dietrich FS, Voegeli S, Brachat S, Lerch A, Gates K, Steiner S, Mohr C, Pohlmann R, Luedi P, Choi S, et al: The Ashbya gossypii genome as a tool for mapping the ancient Saccharomyces cerevisiae genome. Science. 2004, 304: 304-307. 10.1126/science.1095781.PubMedView ArticleGoogle Scholar
- Kellis M, Birren BW, Lander ES: Proof and evolutionary analysis of ancient genome duplication in the yeast Saccharomyces cerevisiae. Nature. 2004, 428: 617-624. 10.1038/nature02424.PubMedView ArticleGoogle Scholar
- Naruse K, Tanaka M, Mita K, Shima A, Postlethwait J, Mitani H: A Medaka gene map: the trace of ancestral vertebrate proto-chromosomes revealed by comparative gene mapping. Genome Res. 2004, 14: 820-828. 10.1101/gr.2004004.PubMedPubMed CentralView ArticleGoogle Scholar
- Postlethwait P, Amores A, Cresco W, Singer A, Yan Y-L: Subfunction partitioning, the teleost radiation and the annotation of the human genome. Trends Genet. 2004, 20: 481-490. 10.1016/j.tig.2004.08.001.PubMedView ArticleGoogle Scholar
- Nelson J: Fishes of the World. 1994, New York: WileyGoogle Scholar
- Hoegg S, Brinkmann H, Taylor JS, Meyer A: Phylogenetic timing of the fish-specific genome duplication correlates with phenotypic and taxonomic diversification in fishes. J Mol Evol. 2004, 59: 190-203. 10.1007/s00239-004-2613-z.PubMedView ArticleGoogle Scholar
- Werth CR, Windham MD: A model for divergent allopatric speciation of polyploid pteridophytes resulting from silencing of duplicate gene expression. Am Nat. 1991, 137: 515-526. 10.1086/285180.View ArticleGoogle Scholar
- Lynch M, Force A: The origin of interspecific genomic incompatibility via gene duplication. Am Nat. 2000, 156: 590-605. 10.1086/316992.View ArticleGoogle Scholar
- Taylor JS, Van de Peer Y, Meyer A: Genome duplication, divergent resolution and speciation. Trends Genet. 2001, 17: 299-301. 10.1016/S0168-9525(01)02318-6.PubMedView ArticleGoogle Scholar