Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Review Article
  • Published:

The ascidian tadpole larva: comparative molecular development and genomics

Key Points

  • Ascidians are sessile marine invertebrate chordates that, because of their phylogenetic position, have been invaluable in addressing the question of chordate origins and evolution.

  • Ciona intestinalis is a useful model for studying chordate origins and evolution because its tadpole larva is believed to represent the closest living form to the ancestral chordate. C. intestinalis is also an excellent model for studying gene function and regulation, because of its unduplicated compact genome — the sequence of which has recently been published — and its short gene-regulatory regions.

  • Analysis of notochord and neural tube development in Ciona, and comparison with the development of these structures in vertebrates, provides valuable information on how the vertebrate form has evolved. Such comparisons involve the identification of orthologues, and the temporal and spatial analysis of their expression.

  • Comparative studies of gene expression have also been helpful in unravelling the basic mechanisms that underlie notochord and neural-tube development; for example, they have shown the central importance of the T-box transcription factor Brachyury in these processes.

  • The recent sequencing of the Ciona genome — the smallest of the experimentally accessible chordates — provides new opportunities for evolutionary genomic studies of chordates. For example, studying gene families, such as that of the nuclear receptors, shows which genes are ancient and which represent recent evolutionary innovations.

Abstract

Evolution is of interest not only to developmental biology but also to genetics and genomics. We are witnessing a new era in which evolution, development, genetics and genomics are merging to form a new discipline, a good example of which is the study of the origin and evolution of the chordates. Recent studies on the formation of the notochord and the dorsal neural tube in the increasingly famous Ciona intestinalis tadpole larva, and the availability of its draft genome, show how the combination of comparative molecular development and evolutionary genomics might help us to better understand our chordate ancestor.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1: Tadpole-type larva of the ascidian Ciona intestinalis.
Figure 2: The evolution of the chordates.
Figure 3: A molecular phylogenetic tree of nuclear receptor (NR) proteins.

Similar content being viewed by others

References

  1. Gee, H. Before the Backbone: Views on the Origin of the Vertebrates (Chapman and Hall, London, 1996).

    Google Scholar 

  2. Nielsen, C. Animal Evolution: Interrelationships of the Living Phyla 2nd edn (Oxford Univ. Press, New York, 2001).

    Google Scholar 

  3. Kowalevsky, A. Entwicklungsgeschichte der Einfachen Ascidien. Mem. l'Acad. St. Petersbourg 7, 1–19 (1866).

    Google Scholar 

  4. Darwin, C. The Descent of Man, and Selection in Relation to Sex (Murray, London, 1871).

    Google Scholar 

  5. Schaeffer, B. Deuterostome monophyly and phylogeny. Evol. Biol. 21, 179–235 (1987).

    Google Scholar 

  6. Wada, H. & Satoh, N. Details of the evolutionary history from invertebrates to vertebrates, as deduced from the sequences of 18S rDNA. Proc. Natl Acad. Sci. USA 91, 1801–1804 (1994).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Wada, H. Evolutionary history of free-swimming and sessile lifestyles in urochordates as deduced from 18S rDNA molecular phylogeny. Mol. Biol. Evol. 15, 1189–1194 (1998).

    CAS  PubMed  Google Scholar 

  8. Cameron, C. B., Garey, J. R. & Swalla, B. J. Evolution of the chordate body plan: new insights from phylogenetic analyses of deuterostome phyla. Proc. Natl Acad. Sci. USA 97, 4469–4474 (2000). A careful and modern interpretation of the phylogenetic relationships of the deuterostomes, based on molecular and morphological data.

    CAS  PubMed  PubMed Central  Google Scholar 

  9. Peterson, K. J. & Eernisse, D. J. Animal phylogeny and the ancestry of bilaterians: inferences from morphology and 18S rDNA gene sequences. Evol. Dev. 3, 170–205 (2001).

    CAS  PubMed  Google Scholar 

  10. Stach, T. & Turbeville, J. M. Phylogeny of Tunicata inferred from molecular and morphological characters. Mol. Phylogenet. Evol. 25, 408–428 (2002).

    CAS  PubMed  Google Scholar 

  11. Winchell, C. J., Sullivan, J., Cameron, C. B., Swalla, B. J. & Mallatt, J. Evaluating hypotheses of deuterostome phylogeny and chordate evolution with new LSU and SSU ribosomal DNA data. Mol. Biol. Evol. 19, 762–776 (2002).

    CAS  PubMed  Google Scholar 

  12. Satoh, N. & Jeffery, W. R. Chasing tails in ascidians: developmental insights into the origin and evolution of chordates. Trends Genet. 11, 354–359 (1995).

    CAS  PubMed  Google Scholar 

  13. Satoh, N. Developmental Biology of Ascidians (Cambridge Univ. Press, New York, 1994). A general introduction to ascidian embryology as an interesting experimental system in developmental biology.

    Google Scholar 

  14. Satoh, N. Ascidian embryos as a model system to analyze expression and function of developmental genes. Differentiation 68, 1–12 (2001).

    CAS  PubMed  Google Scholar 

  15. Corbo, J. C., Di Gregorio, A. & Levine, M. The ascidian as a model organism in developmental and evolutionary biology. Cell 106, 535–538 (2001). A review of the recent studies on notochord formation in ascidian embryos, with an emphasis on their advantages as a model organism in the evo–devo field.

    CAS  PubMed  Google Scholar 

  16. Jeffery, W. R. Determinants of cell and positional fate in ascidian embryos. Int. Rev. Cytol. 203, 3–62 (2001).

    CAS  PubMed  Google Scholar 

  17. Nishida, H. Specification of developmental fates in ascidian embryos: molecular approach to maternal determinants and signaling molecules. Int. Rev. Cytol. 217, 227–276 (2002).

    CAS  PubMed  Google Scholar 

  18. Nishida, H. Patterning the marginal zone of early ascidian embryos: localized maternal mRNA and inductive interactions. Bioessays 24, 613–624 (2002).

    CAS  PubMed  Google Scholar 

  19. Conklin, E. G. The organization and cell lineage of the ascidian egg. J. Acad. Nat. Sci. 13, 1–119 (1905).

    Google Scholar 

  20. Nishida, H. Cell lineage analysis in ascidian embryos by intracellular injection of a tracer enzyme. III. Up to the tissue restricted stage. Dev. Biol. 121, 526–541 (1987).

    CAS  PubMed  Google Scholar 

  21. Nakatani, Y., Moody, R. & Smith, W. C. Mutations affecting tail and notochord development in the ascidian Ciona savignyi. Development 126, 3293–3301 (1999).

    CAS  PubMed  Google Scholar 

  22. Sordino, P., Belluzzi, L., De Santis, R. & Smith, W. C. Developmental genetics in primitive chordates. Phil. Trans. R. Soc. Lond. B 356, 1573–1582 (2001).

    CAS  Google Scholar 

  23. Takahashi, H. et al. Brachyury downstream notochord differentiation in the ascidian embryo. Genes Dev. 13, 1519–1523 (1999). With the aid of a subtractive hybridization method, the authors isolated nearly 40 genes that are candidates for Ciona Brachyury target genes (see also reference 55).

    CAS  PubMed  PubMed Central  Google Scholar 

  24. Imai, K. S., Satoh, N. & Satou, Y. Early embryonic expression of FGF4/6/9 gene and its role in the induction of mesenchyme and notochord in Ciona savignyi embryos. Development 129, 1729–1738 (2002).

    CAS  PubMed  Google Scholar 

  25. Satou, Y., Imai, K. S. & Satoh, N. Action of morpholinos in Ciona embryos. Genesis 30, 103–106 (2001).

    CAS  PubMed  Google Scholar 

  26. Corbo, J. C., Levine, M. & Zeller, R. W. Characterization of a notochord-specific enhancer from the Brachyury promoter region of the ascidian, Ciona intestinalis. Development 124, 589–602 (1997).

    CAS  PubMed  Google Scholar 

  27. Di Gregorio, A. & Levine, M. Analyzing gene regulation in ascidian embryos: new tools for new perspectives. Differentiation 70, 132–139 (2002).

    CAS  PubMed  Google Scholar 

  28. Holland, P. W. H., Garcia-Fernàndez, J., Williams, N. A. & Sidow, A. Gene duplications and the origins of vertebrate development. Dev. Suppl. 125–133 (1994).

  29. Dehal, P. et al. The draft genome of Ciona intestinalis: insights into chordate and vertebrate origins. Science 298, 2157–2167 (2002). A reading of the Ciona draft genome that shows that this 160 Mb genome contains 16,000 protein-coding genes. Comparison of the Ciona genome with invertebrate and vertebrate genomes indicates various biological events that might have led to the evolution of the chordates and the vertebrates.

    CAS  PubMed  Google Scholar 

  30. Satou, Y. & Satoh, N. Two cis-regulatory elements are essential for the muscle-specific expression of an actin gene in the ascidian embryo. Dev. Growth Differ. 38, 565–573 (1996).

    CAS  Google Scholar 

  31. Harafuji, N., Keys, D. N. & Levine, M. Genome-wide identification of tissue-specific enhancers in the Ciona tadpole. Proc. Natl Acad. Sci. USA 99, 6802–6805 (2002).

    CAS  PubMed  PubMed Central  Google Scholar 

  32. Brusca, R. C. & Brusca, G. J. Invertebrates (Sinauer Associates Inc., Sunderland, Massachusetts, 1990).

    Google Scholar 

  33. Munro, E. M. & Odell, G. M. Polarized basolateral cell motility underlies invagination and convergent extension of the ascidian notochord. Development 129, 13–24 (2002).

    CAS  PubMed  Google Scholar 

  34. Munro, E. M. & Odell, G. Morphogenetic pattern formation during ascidian notochord formation is regulative and highly robust. Development 129, 1–12 (2002).

    CAS  PubMed  Google Scholar 

  35. Nishino, A. & Satoh, N. The simple tail of chordates: phylogenetic significance of appendicularians. Genesis 29, 36–45 (2001).

    CAS  PubMed  Google Scholar 

  36. Nakatani, Y. & Nishida, H. Induction of notochord during ascidian embryogenesis. Dev. Biol. 166, 289–299 (1994).

    CAS  PubMed  Google Scholar 

  37. Nakatani, Y., Yasuo, H., Satoh, N. & Nishida, H. Basic fibroblast growth factor induces notochord formation and the expression of As-T, a Brachyury homolog, during ascidian embryogenesis. Development 122, 2023–2031 (1996).

    CAS  PubMed  Google Scholar 

  38. Yasuo, H. & Satoh, N. Function of vertebrate T gene. Nature 364, 582–583 (1993).

    CAS  PubMed  Google Scholar 

  39. Herrmann, B. G., Labeit, S., Poustka, A., King, T. R. & Lehrach, H. Cloning of the T gene required in mesoderm formation in the mouse. Nature 343, 617–622 (1990).

    CAS  PubMed  Google Scholar 

  40. Papaioannou, V. E. T-box genes in development: from hydra to humans. Int. Rev. Cytol. 207, 1–70 (2001).

    CAS  PubMed  Google Scholar 

  41. Yasuo, H. & Satoh, N. Conservation of the developmental role of Brachyury in notochord formation in a urochordate, the ascidian Halocynthia roretzi. Dev. Biol. 200, 158–170 (1998).

    CAS  PubMed  Google Scholar 

  42. Takahashi, H., Mitani, Y., Satoh, G. & Satoh, N. Evolutionary alterations of the minimal promoter for notochord-specific Brachyury expression in ascidian embryos. Development 126, 3725–3734 (1999).

    CAS  PubMed  Google Scholar 

  43. Corbo, J. C., Fujiwara, S., Levine, M. & Di Gregorio, A. Suppressor of Hairless activates Brachyury expression in the Ciona embryo. Dev. Biol. 203, 358–368 (1998).

    CAS  PubMed  Google Scholar 

  44. Cadigan, K. M. & Nusse, R. Wnt signaling: a common theme in animal development. Genes Dev. 11, 3286–3305 (1997).

    CAS  PubMed  Google Scholar 

  45. Moon, R. T. & Kimelman, D. From cortical rotation to organizer gene expression: toward a molecular explanation of axis specification in Xenopus. Bioessays 20, 536–545 (1998).

    CAS  PubMed  Google Scholar 

  46. Imai, K., Takada, N., Satoh, N. & Satou, Y. β-catenin mediates the specification of endoderm cells in ascidian embryos. Development 127, 3009–3020 (2000). Describes how the nuclear localization of β-catenin is the first step of endodermal-cell specification in ascidian embryos, which might activate various genes involved in endoderm differentiation or mesoderm induction.

    CAS  PubMed  Google Scholar 

  47. Satou, Y., Imai, K. S. & Satoh, N. Early embryonic expression of a LIM-homeobox gene Cs-lhx3 is downstream of β-catenin and responsible for the endoderm differentiation in Ciona savignyi embryos. Development 128, 3559–3570 (2001).

  48. Satou, Y., Imai, K. S. & Satoh, N. Fgf genes in the basal chordate Ciona intestinalis. Dev. Genes Evol. 212, 432–438 (2002).

    CAS  PubMed  Google Scholar 

  49. Imai, K. S., Satoh, N. & Satou, Y. An essential role of a FoxD gene in notochord induction in Ciona embryos. Development 129, 3441–3453 (2002).

    CAS  PubMed  Google Scholar 

  50. Imai, K. S., Satou, Y. & Satoh, N. Multiple functions of a Zic-like gene in the differentiation of notochord, central nervous system and muscle in Ciona savignyi embryos. Development 129, 2723–2732 (2002).

    CAS  PubMed  Google Scholar 

  51. Kim, G. J., Yamada, A. & Nishida, H. An FGF signal from endoderm and localized factors in the posterior–vegetal egg cytoplasm pattern the mesodermal tissues in the ascidian embryo. Development 127, 2853–2862 (2000).

    CAS  PubMed  Google Scholar 

  52. Minokawa, T., Yagi, K., Makabe, K. W. & Nishida, H. Binary specification of nerve cord and notochord cell fates in ascidian embryos. Development 128, 2007–2017 (2001).

    CAS  PubMed  Google Scholar 

  53. Shimauchi, Y., Murakami, S. D. & Satoh, N. FGF signals are involved in the differentiation of notochord cells and mesenchyme cells of the ascidian Halocynthia roretzi. Development 128, 2711–2721 (2001).

    CAS  PubMed  Google Scholar 

  54. Darras, S. & Nishida, H. The BMP signaling pathway is required together with the FGF pathway for notochord induction in the ascidian embryo. Development 128, 2629–2638 (2001).

    CAS  PubMed  Google Scholar 

  55. Hotta, K. et al. Characterization of Brachyury-downstream notochord genes in the Ciona intestinalis embryo. Dev. Biol. 224, 69–80 (2000). Following on from reference 23, the authors characterized 20 Ciona Brachyury target genes, which include an ascidian homologue of the Drosophila prickle gene.

    CAS  PubMed  Google Scholar 

  56. Di Gregorio, A. & Levine, M. Regulation of Ci-tropomyosin-like, a Brachyury target gene in the ascidian, Ciona intestinalis. Development 126, 5599–5609 (1999).

    CAS  PubMed  Google Scholar 

  57. Harada, Y., Yasuo, H. & Satoh, N. A sea urchin homologue of the chordate Brachyury (T) gene is expressed in the secondary mesenchyme founder cells. Development 121, 2747–2754 (1995).

    CAS  PubMed  Google Scholar 

  58. Shoguchi, E., Satoh, N. & Maruyama, Y. K. Pattern of Brachyury gene expression in starfish embryos resembles that of hemichordate embryos but not of sea urchin embryos. Mech. Dev. 82, 185–189 (1999).

    CAS  PubMed  Google Scholar 

  59. Croce, J., Lhomond, G. & Gache, C. Expression pattern of Brachyury in the embryo of the sea urchin Paracentrotus lividus. Dev. Genes Evol. 211, 617–619 (2001).

    CAS  PubMed  Google Scholar 

  60. Gross, J. M. & McClay, D. R. The role of Brachyury (T) during gastrulation movements in the sea urchin Lytechinus variegatus. Dev. Biol. 239, 132–147 (2001).

    CAS  PubMed  Google Scholar 

  61. Tagawa, K., Humphreys, T. & Satoh, N. Novel pattern of Brachyury gene expression in hemichordate embryos. Mech. Dev. 75, 139–143 (1998). Discusses how Brachyury is expressed in the archenteron invagination region and mouth invagination region in hemichordate embryos, indicating that a common expression pattern of this gene is shared by the protostomes and deuterostomes.

    CAS  PubMed  Google Scholar 

  62. Peterson, K. J., Cameron, R. A., Tagawa, K., Satoh, N. & Davidson, E. H. A comparative molecular approach to mesodermal patterning in basal deuterostomes: the expression pattern of Brachyury in the enteropneust hemichordate Ptychodera flava. Development 126, 85–95 (1999).

    CAS  PubMed  Google Scholar 

  63. Kispert, A., Herrmann, B. G., Leptin, M. & Reuter, R. Homologs of the mouse Brachyury gene are involved in the specification of posterior terminal structures in Drosophila, Tribolium, and Locusta. Genes Dev. 8, 2137–2150 (1994).

    CAS  PubMed  Google Scholar 

  64. Arendt, D., Technau, U. & Wittbrodt, J. Evolution of the bilaterian larval foregut. Nature 409, 81–85 (2001).

    CAS  PubMed  Google Scholar 

  65. Satoh, G., Harada, Y. & Satoh, N. The expression of nonchordate deuterostome Brachyury genes in the ascidian Ciona embryo can promote the differentiation of extra notochord cells. Mech. Dev. 96, 155–163 (2000).

    CAS  PubMed  Google Scholar 

  66. Davidson, E. H. et al. A genomic regulatory network for development. Science 295, 1669–1678 (2002).

    CAS  PubMed  Google Scholar 

  67. Rast, J. P., Cameron, R. A., Poustka, A. J. & Davidson, E. H. Brachyury target genes in the early sea urchin embryo isolated by differential macroarray screening. Dev. Biol. 246, 191–208 (2002). A characterization of the target genes of sea urchin Brachyury , which provides information to compare with Ciona Brachyury target genes.

    CAS  PubMed  Google Scholar 

  68. Ruppert, E. E. in Microscopic Anatomy of Invertebrates (ed. Harrison, F. W.) 349–504 (Willey-Liss, New York, 1997).

    Google Scholar 

  69. Suzuki, M. M. & Satoh, N. Genes expressed in the amphioxus notochord revealed by EST analysis. Dev. Biol. 224, 168–177 (2000).

    CAS  PubMed  Google Scholar 

  70. Smith, J. T-box genes: what they do and how they do it. Trends Genet. 15, 154–158 (1999).

    CAS  PubMed  Google Scholar 

  71. Smith, J. C. Making mesoderm — upstream and downstream of Xbra. Int. J. Dev. Biol. 45, 219–224 (2001).

    CAS  PubMed  Google Scholar 

  72. Tada, M. & Smith, J. C. T-targets: clues to understanding the functions of T-box proteins. Dev. Growth Differ. 43, 1–11 (2001).

    CAS  PubMed  Google Scholar 

  73. Mlodzik, M. Spiny legs and prickled bodies: new insights and complexities in planar polarity establishment. Bioessays 22, 311–315 (2000).

    CAS  PubMed  Google Scholar 

  74. Gubb, D. et al. The balance between isoforms of the prickle LIM domain protein is critical for planar polarity in Drosophila imaginal discs. Genes Dev. 13, 2315–2327 (1999).

    CAS  PubMed  PubMed Central  Google Scholar 

  75. Wallingford, J. B., Fraser, S. E. & Harland, R. M. Convergent extension: the molecular control of polarized cell movement during embryonic development. Dev. Cell 2, 695–706 (2002).

    CAS  PubMed  Google Scholar 

  76. Wallingford, J. B., Goto, T., Keller, R. & Harland, R. M. Cloning and expression of Xenopus Prickle, an orthologue of a Drosophila planar cell polarity gene. Mech. Dev. 116, 183–186 (2002).

    CAS  PubMed  Google Scholar 

  77. Keys, D. N., Levine, M., Harland, R. M. & Wallingford, J. B. Control of intercalation is cell-autonomous in the notochord of Ciona intestinalis. Dev. Biol. 246, 329–340 (2002).

    CAS  PubMed  Google Scholar 

  78. Lacalli, T. C. Apical organs, epithelial domains, and the origin of the chordate central nervous system. Amer. Zool. 34, 533–541 (1994).

    Google Scholar 

  79. Meinertzhagen, I. A. & Okamura, Y. The larval ascidian nervous system: the chordate brain from its small beginnings. Trends Neurosci. 24, 401–410 (2001). A comprehensive review of the structure, development and function of the nervous system of an ascidian tadpole larva.

    CAS  PubMed  Google Scholar 

  80. Wada, H. & Satoh, N. Patterning the protochordate neural tube. Curr. Opin. Neurobiol. 11, 16–21 (2001).

    CAS  PubMed  Google Scholar 

  81. Garstang, W. Preliminary note on a new theory of the phylogeny of the Chordata. Zool. Anz. 17, 122–125 (1894).

    Google Scholar 

  82. Garstang, W. The morphology of the Tunicata, and its bearings on the phylogeny of the Chordata. Q. J. Microsc. Sci. 72, 51–187 (1928).

    Google Scholar 

  83. Arenas-Mena, C., Martinez, P., Cameron, R. A. & Davidson, E. H. Expression of the Hox gene complex in the indirect development of a sea urchin. Proc. Natl Acad. Sci. USA 95, 13062–13067 (1998).

    CAS  PubMed  PubMed Central  Google Scholar 

  84. Mao, C. -A. et al. Altering cell fates in sea urchin embryos by overexpressing SpOtx, an orthodenticle-related protein. Development 122, 1489–1498 (1996).

    CAS  PubMed  Google Scholar 

  85. Takamura, K. Nervous network in larvae of the ascidian Ciona intestinalis. Dev. Genes Evol. 208, 1–8 (1998).

    CAS  PubMed  Google Scholar 

  86. Jiang, D. & Smith, W. C. An ascidian engrailed gene. Dev. Genes Evol. 212, 399–402 (2002).

    CAS  PubMed  Google Scholar 

  87. Imai, K. S., Satoh, N. & Satou, Y. Region specific gene expressions in the central nervous system of ascidian embryo. Gene Exp. Patt. 2, 319–321 (2002).

    CAS  Google Scholar 

  88. Holland, L. Z., Kene, M., Williams, N. A. & Holland, N. D. Sequence and embryonic expression of the amphioxus engrailed gene (AmphiEn): the metameric pattern of transcription resembles that of its segment-polarity homolog in Drosophila. Development 124, 1723–1732 (1997).

    CAS  PubMed  Google Scholar 

  89. Takatori, N., Satou, Y. & Satoh, N. Expression of hedgehog genes in Ciona intestinalis embryos. Mech. Dev. 116, 235–238 (2002).

    CAS  PubMed  Google Scholar 

  90. Harada, Y. et al. Developmental expression of the hemichordate otx ortholog. Mech. Dev. 91, 337–339 (2000).

    CAS  PubMed  Google Scholar 

  91. Shoguchi, E., Harada, Y., Numakunai, T. & Satoh, N. Expression of the Otx gene in the ciliary bands during sea cucumber embryogenesis. Genesis 27, 58–63 (2000).

    CAS  PubMed  Google Scholar 

  92. Tagawa, K., Humphreys, T. & Satoh, N. T-Brain expression in the apical organ of hemichordate tornaria larvae suggests its evolutionary link to the vertebrate forebrain. Mol. Dev. Evol. 288, 23–31 (2000).

    CAS  Google Scholar 

  93. Tagawa, K., Satoh, N. & Humphreys, T. Molecular studies of hemichordate development: a key to understanding the evolution of bilateral animals and chordates. Evol. Dev. 3, 443–454 (2001).

    CAS  PubMed  Google Scholar 

  94. Taguchi, S., Tagawa, K., Humphreys, T. & Satoh, N. Group B Sox genes that contribute to specification of the vertebrate brain are expressed in the apical organ and ciliary bands of hemichordate larvae. Zool. Sci. 19, 57–66 (2002).

    CAS  Google Scholar 

  95. The C. elegans Sequencing Consortium. Genome sequence of the nematode C. elegans: a platform for investigating biology. Science 282, 2012–2018 (1998).

  96. Adams, M. D. et al. The genome sequence of Drosophila melanogaster. Science 287, 2185–2195 (2000).

    PubMed  Google Scholar 

  97. International Human Genome Sequencing Consortium. Initial sequencing and analysis of the human genome. Nature 409, 860–921 (2001).

  98. Venter, J. C. et al. The sequence of the human genome. Science 291, 1304–1351 (2001).

    CAS  PubMed  Google Scholar 

  99. Aparicio, S. et al. Whole-genome shotgun assembly and analysis of the genome of Fugu rubripes. Science 297, 1301–1310 (2002).

    CAS  PubMed  Google Scholar 

  100. Holt, R. A. et al. The genome sequence of the malaria mosquito Anopheles gambiae. Science 298, 129–149 (2002).

    CAS  PubMed  Google Scholar 

  101. Mouse Genome Sequencing Consortium. Initial sequencing and comparative analysis of the mouse genome. Nature 420, 520–562 (2002).

  102. Zdobnov, E. M. et al. Comparative genome and proteome analysis of Anopheles gambiae and Drosophila melanogaster. Science 298, 149–159 (2002).

    CAS  PubMed  Google Scholar 

  103. Simmen, M. W., Leitgeb, S., Clark, V. H., Jones, S. J. M. & Bird, A. Gene number in an invertebrate chordate, Ciona intestinalis. Proc. Natl Acad. Sci. USA 95, 4437–4440 (1998).

    CAS  PubMed  PubMed Central  Google Scholar 

  104. Seo, H. -C. et al. Miniature genome in the marine chordate Oikopleura dioica. Science 294, 2506–2506 (2001).

    CAS  PubMed  Google Scholar 

Download references

Acknowledgements

I thank all my colleagues who have contributed to studies included in this review, and two anonymous referees for their helpful comments on the manuscript. The research of my laboratory is supported by Grants-in-Aid from the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan, by Human Frontier Science Programme Research Grants and by the Core Research for Evolutional Science and Technology (CREST) project of the Japan Science and Technology Corporation (JST).

Author information

Authors and Affiliations

Authors

Related links

Related links

DATABASES

LocusLink

Brachyury

prickle

FURTHER INFORMATION

Ghost Database

Glossary

CHORDATES

A phylum of animals (the Chordata) that is characterized by the possession of a notochord. It includes the urochordates (such as the ascidians), the cephalochordates (amphioxus) and the vertebrates.

DEUTEROSTOME

A bilaterian animal the mouth of which forms as a secondary opening that is separate from the blastopore. Deuterostomes include the chordates, the hemichordates and the echinoderms.

NOTOCHORD

A rod-like structure in the dorsal midline of the embryo that runs from the head to the tail beneath the future central nervous system.

CLADE

A lineage of organisms, or alleles, that comprises an ancestor and all of its descendants.

BLASTOMERE

An early embryonic cell that is derived from the cleavage of a fertilized egg.

MORPHOLINO

A chemically modified oligonucleotide that behaves as an antisense RNA analogue and is, therefore, used to interfere with gene function.

DIPLOBLAST

An animal with only two germ layers: the ectoderm and the endoderm. Diploblasts include the cnidarians, the ctenophorans and — according to some authors — the placozoans and the poriferans.

TRIPLOBLAST

An animal with three germ layers: the ectoderm, the mesoderm and the endoderm.

PROTOSTOME

A bilaterian animal, the mouth of which develops before the anus during embryogenesis. Protostomes include arthropods, molluscs and worms.

MONOPHYLETIC

A group that includes all of the descendants of a single common ancestor.

DIPLEURULA-TYPE LARVAE

A deuterostome larval type with a perforated ciliary band.

AURICULARIA LARVAE

A planktotrophic sea-cucumber larva with a continuous ciliary band.

TORNARIA LARVA

A hemichordate acorn-worm larva, with distinct ciliary bands.

PARAXIAL MESODERM

A subpopulation of the mesoderm that lies on both sides of the neural tube, which gives rise to the somites.

NEUROHYPOPHYSIS

A part of the hypophysis (along with the adenohypophysis), which is involved in neurohormone release.

APICAL ORGAN

The organ located at the anterior tip of the hemichordate tornaria larvae; a photoreceptor organ.

ARCHENTERON

The cavity formed inside the embryo when the endoderm and mesoderm invaginate during gastrulation, which forms the gut.

PRIMITIVE STREAK

A strip of cells that extends inwards from the posterior marginal zone. During gastrulation, cells move through the primitive streak into the interior of the blastoderm.

MARGINAL ZONE

The belt-like region surrounding the equator of the late blastula (found, in particular, in amphibians).

LIM DOMAIN

A repeat of 60 amino acids containing cysteine and histidine residues. It is thought to be involved in protein–protein interactions.

PLANAR-CELL POLARITY

The state in which epithelial cells are polarized in the apical–basolateral axis and in the horizontal plane of the epithelium.

CONVERGENT EXTENSION

The process by which a sheet of cells changes shape by extending in one direction and narrowing — converging —in a direction at right angles to the extension.

GASTRULATION

The process in animal embryos in which the endoderm and mesoderm move from the outer surface of the embryo to the inside, where they give rise to the internal organs.

NEURULATION

The process in which the ectoderm of the future brain and spinal cord develops folds and forms the neural tube.

NEIGHBOUR-JOINING METHOD

A distance-based molecular phylogenetic method that involves the sequential addition of taxa and the minimization of branch lengths, but does not assume a molecular clock.

BLASTOPORE

The slit-like or circular invagination on the surface of animal embryos, through which the mesoderm and endoderm move inside the embryo at gastrulation.

STOMODEUM

The invagination of the ectoderm that forms the mouth in animal embryos.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Satoh, N. The ascidian tadpole larva: comparative molecular development and genomics. Nat Rev Genet 4, 285–295 (2003). https://doi.org/10.1038/nrg1042

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1038/nrg1042

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing