Expression pattern of Brachyury and Not in the sea urchin: comparative implications for the origins of mesoderm in the basal deuterostomes.

This work concerns the expression of two transcription factors during the development of the sea urchin Strongylocentrotus purpuratus: SpNot, the orthologue of the vertebrate Not gene, and SpBra, the orthologue of the vertebrate Brachyury gene. SpNot transcripts are detected by in situ hybridization in the vegetal plate at the mesenchyme-blastula stage. Later the gene is expressed in the secondary mesenchyme, but expression is no longer detectable after gastrulation. SpNot is upregulated during larval development, in the invaginating vestibule of the adult rudiment. Transcripts are also found in several larva-specific tissues, including the epaulets, blastocoelar cells, and pigment cells. SpBra also displays a discontinuous pattern of expression. Much like SpNot, this gene is expressed during embryogenesis in the embryonic vegetal plate and secondary mesenchyme founder cells, and expression is then extinguished. The gene is upregulated over a week later in the feeding larva, in the vestibule of the adult rudiment. In contrast to SpNot, SpBra is also expressed in the mesoderm of both left and right hydrocoels, and it is not expressed in any larva-specific tissues. We compare the spatial expression profile determined in this study with that of the orthologous Brachyury gene in an indirectly developing enteropneust hemichordate, a representative of the sister group to the echinoderms within the deuterostomes. These observations illuminate the genetic basis underlying the process of maximal indirect development in basal deuterostomes. Finally, Brachyury appears to be an excellent marker for the progeny of the set-aside cells of the sea urchin embryo.

[1]  E. Davidson,et al.  Specification of cell fate in the sea urchin embryo: summary and some proposed mechanisms. , 1998, Development.

[2]  C. Nielsen Origin and evolution of animal life cycles , 1998 .

[3]  E. Davidson,et al.  Cis-regulation downstream of cell type specification: a single compact element controls the complex expression of the CyIIa gene in sea urchin embryos. , 1998, Development.

[4]  A. Smith,et al.  Selectivity of extinction among sea urchins at the end of the Cretaceous period , 1998, Nature.

[5]  L. Silver,et al.  The T‐box gene family , 1998, BioEssays : news and reviews in molecular, cellular and developmental biology.

[6]  C. Jeffery Dawn of echinoid nonplanktotrophy: Coordinated shifts in development indicate environmental instability prior to the K-T boundary , 1997 .

[7]  A. Smith Echinoderm Larvae and Phylogeny , 1997 .

[8]  R. Raff,et al.  Homology and developmental genes. , 1997, Trends in genetics : TIG.

[9]  D. Melton,et al.  Notochord to endoderm signaling is required for pancreas development. , 1997, Development.

[10]  J. Green,et al.  Tales of tails: Brachyury and the T-box genes. , 1997, Biochimica et biophysica acta.

[11]  Christopher J. Lowe,et al.  Radical alterations in the roles of homeobox genes during echinoderm evolution , 1997, Nature.

[12]  J. Smith,et al.  Brachyury and the T-box genes. , 1997, Current opinion in genetics & development.

[13]  V. Papaioannou T-box family reunion. , 1997, Trends in genetics : TIG.

[14]  E. Davidson,et al.  The hardwiring of development: organization and function of genomic regulatory systems. , 1997, Development.

[15]  M. Kessel,et al.  Differential activation of the clustered homeobox genes CNOT2 and CNOT1 during notogenesis in the chick. , 1996, Developmental biology.

[16]  J. Singer,et al.  Drosophila brachyenteron regulates gene activity and morphogenesis in the gut. , 1996, Development.

[17]  R. Raff,et al.  Developmental genetics and traditional homology. , 1996, BioEssays : news and reviews in molecular, cellular and developmental biology.

[18]  A. Fainsod,et al.  Overexpression of the homeobox gene Xnot-2 leads to notochord formation in Xenopus. , 1996, Developmental biology.

[19]  B. Herrmann Introduction: The Brachyury gene , 1995 .

[20]  N. Satoh,et al.  A sea urchin homologue of the chordate Brachyury (T) gene is expressed in the secondary mesenchyme founder cells. , 1995, Development.

[21]  D. Melton,et al.  Induction and patterning of the vertebrate nervous system. , 1995, Trends in genetics : TIG.

[22]  B. Herrmann,et al.  Homologs of the mouse Brachyury gene are involved in the specification of posterior terminal structures in Drosophila, Tribolium, and Locusta. , 1994, Genes & development.

[23]  B. Herrmann,et al.  The T genes in embryogenesis. , 1994, Trends in genetics : TIG.

[24]  R. Raff,et al.  Deuterostome phylogeny and the sister group of the chordates: evidence from molecules and morphology. , 1994, Molecular biology and evolution.

[25]  G. Wray The Evolution of Cell Lineage in Echinoderms , 1994 .

[26]  H. Wada,et al.  Details of the evolutionary history from invertebrates to vertebrates, as deduced from the sequences of 18S rDNA. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[27]  B. Blumberg,et al.  Tail formation as a continuation of gastrulation: the multiple cell populations of the Xenopus tailbud derive from the late blastopore lip. , 1993, Development.

[28]  R. Britten,et al.  Whole mount in situ hybridization shows Endo 16 to be a marker for the vegetal plate territory in sea urchin embryos , 1993, Mechanisms of Development.

[29]  G. von Dassow,et al.  Induction of the Xenopus organizer: expression and regulation of Xnot, a novel FGF and activin-regulated homeo box gene. , 1993, Genes & development.

[30]  R. Britten,et al.  Macromere cell fates during sea urchin development. , 1991, Development.

[31]  E. Davidson Spatial mechanisms of gene regulation in metazoan embryos. , 1991, Development.

[32]  R. Emlet Larval Form and Metamorphosis of a "Primitive" Sea Urchin, Eucidaris thouarsi (Echinodermata: Echinoidea: Cidaroida), with Implications for Developmental and Phylogenetic Studies. , 1988, The Biological bulletin.

[33]  P. Chomczyński,et al.  Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. , 1987, Analytical biochemistry.

[34]  E. Ruppert,et al.  NEPHRIDIA IN THE LARVAE OF HEMICHORDATES AND ECHINODERMS , 1986 .

[35]  R. Emlet Crystal Axes in Recent and Fossil Adult Echinoids Indicate Trophic Mode in Larval Development , 1985, Science.

[36]  P. Hardin,et al.  Structure of the Spec1 gene encoding a major calcium-binding protein in the embryonic ectoderm of the sea urchin, Strongylocentrotus purpuratus. , 1985, Journal of molecular biology.

[37]  A. Smith,et al.  THE EARLY RADIATION AND PHYLOGENY OF ECHINODERMS , 1984 .

[38]  G. Church,et al.  Genomic sequencing. , 1993, Methods in molecular biology.

[39]  E. Davidson,et al.  A comparative molecular approach to mesodermal patterning in basal deuterostomes: the expression pattern of Brachyury in the enteropneust hemichordate Ptychodera flava. , 1999, Development.

[40]  B. David,et al.  Major events in the evolution of echinoderms viewed by the light of embryology , 1998 .

[41]  S. Ruffins,et al.  A fate map of the vegetal plate of the sea urchin (Lytechinus variegatus) mesenchyme blastula. , 1996, Development.

[42]  M. Kessel,et al.  A homeobox gene involved in node, notochord and neural plate formation of chick embryos , 1995, Mechanisms of Development.

[43]  M. Bienz Homeotic genes and positional signalling in the Drosophila viscera. , 1994, Trends in genetics : TIG.

[44]  William McGinnis,et al.  Drosophila Homeobox Genes , 1993 .

[45]  R. Britten,et al.  Expression of two actin genes during larval development in the sea urchin Strongylocentrotus purpuratus , 1989, Molecular reproduction and development.

[46]  P. Leahy Laboratory culture of Strongylocentrotus purpuratus adults, embryos, and larvae. , 1986, Methods in cell biology.