dino and mercedes, two genes regulating dorsal development in the zebrafish embryo.

We describe two genes, dino and mercedes, which are required for the organization of the zebrafish body plan. In dino mutant embryos, the tail is enlarged at the expense of the head and the anterior region of the trunk. The altered expression patterns of various marker genes reveal that, with the exception of the dorsal most marginal zone, all regions of the early dino mutant embryo acquire more ventral fates. These alterations are already apparent before the onset of gastrulation. mercedes mutant embryos show a similar but weaker phenotype, suggesting a role in the same patterning processes. The phenotypes suggests that dino and mercedes are required for the establishment of dorsal fates in both the marginal and the animal zone of the early gastrula embryo. Their function in the patterning of the ventrolateral mesoderm and the induction of the neuroectoderm is similar to the function of the Spemann organizer in the amphibian embryo.

[1]  P. Ingham,et al.  A functionally conserved homolog of the Drosophila segment polarity gene hh is expressed in tissues with polarizing activity in zebrafish embryos , 1993, Cell.

[2]  D. Grunwald,et al.  Lithium perturbation and goosecoid expression identify a dorsal specification pathway in the pregastrula zebrafish. , 1993, Development.

[3]  H. Steller,et al.  Programmed cell death during Drosophila embryogenesis. , 1993, Development.

[4]  Stephen W. Wilson,et al.  The paired domain-containing nuclear factor pax[b] is expressed in specific commissural interneurons in zebrafish embryos. , 1992, Journal of neurobiology.

[5]  B. Hogan,et al.  DVR-4 (bone morphogenetic protein-4) as a posterior-ventralizing factor in Xenopus mesoderm induction. , 1992, Development.

[6]  D. Melton,et al.  Follistatin, an antagonist of activin, is expressed in the Spemann organizer and displays direct neuralizing activity , 1994, Cell.

[7]  D. Ransom,et al.  Intraembryonic hematopoietic cell migration during vertebrate development. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[8]  R. Moon,et al.  Synergistic principles of development: overlapping patterning systems in Xenopus mesoderm induction. , 1992, Development.

[9]  C. Nüsslein-Volhard,et al.  Large-scale mutagenesis in the zebrafish: in search of genes controlling development in a vertebrate , 1994, Current Biology.

[10]  C. Nüsslein-Volhard,et al.  The bicoid protein determines position in the Drosophila embryo in a concentration-dependent manner , 1988, Cell.

[11]  H. Sive,et al.  The frog prince-ss: a molecular formula for dorsoventral patterning in Xenopus. , 1993, Genes & development.

[12]  B. Blumberg,et al.  Disruption of BMP signals in embryonic Xenopus ectoderm leads to direct neural induction. , 1995, Genes & development.

[13]  J. Smith,et al.  Bone morphogenetic protein 4: a ventralizing factor in early Xenopus development. , 1992, Development.

[14]  J. Graff,et al.  Studies with a Xenopus BMP receptor suggest that ventral mesoderm-inducing signals override dorsal signals in vivo , 1994, Cell.

[15]  W. Knöchel,et al.  Bone morphogenetic protein 4 (BMP-4), a member of the TGF-β family, in early embryos of Xenopus laevis: analysis of mesoderm inducing activity , 1991, Mechanisms of Development.

[16]  P. Nieuwkoop The organization center of the amphibian embryo: its origin, spatial organization, and morphogenetic action. , 1973, Advances in morphogenesis.

[17]  Y. Sasai,et al.  Regulation of neural induction by the Chd and Bmp-4 antagonistic patterning signals in Xenopus , 1995, Nature.

[18]  J. Dodd,et al.  Hensen's node induces neural tissue in Xenopus ectoderm. Implications for the action of the organizer in neural induction. , 1991, Development.

[19]  C. Nüsslein-Volhard,et al.  The expression of a zebrafish gene homologous to Drosophila snail suggests a conserved function in invertebrate and vertebrate gastrulation. , 1993, Development.

[20]  D. Melton,et al.  Induction of dorsal mesoderm by soluble, mature Vg1 protein. , 1995, Development.

[21]  E M De Robertis,et al.  Expression of zebrafish goosecoid and no tail gene products in wild-type and mutant no tail embryos. , 1994, Development.

[22]  M. Allende,et al.  Developmental regulation of zebrafish MyoD in wild-type, no tail and spadetail embryos. , 1996, Development.

[23]  D. Kane,et al.  Domains of movement in the zebrafish gastrula , 1994 .

[24]  Terje Johansen,et al.  Expression pattern of zebrafish pax genes suggests a role in early brain regionalization , 1991, Nature.

[25]  C. Kimmel,et al.  Origin and organization of the zebrafish fate map. , 1990, Development.

[26]  N. Ueno,et al.  A truncated bone morphogenetic protein 4 receptor alters the fate of ventral mesoderm to dorsal mesoderm: roles of animal pole tissue in the development of ventral mesoderm. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[27]  C. Nüsslein-Volhard,et al.  Genetic analysis of fin formation in the zebrafish, Danio rerio. , 1996, Development.

[28]  R. Ho,et al.  The protein product of the zebrafish homologue of the mouse T gene is expressed in nuclei of the germ ring and the notochord of the early embryo. , 1992, Development.

[29]  Yoshiki Sasai,et al.  A conserved system for dorsal-ventral patterning in insects and vertebrates involving sog and chordin , 1995, Nature.

[30]  R. Beddington Induction of a second neural axis by the mouse node. , 1994, Development.

[31]  Y. Sasai,et al.  Xenopus chordin: A novel dorsalizing factor activated by organizer-specific homeobox genes , 1994, Cell.

[32]  J. Smith,et al.  Control of vertebrate gastrulation: inducing signals and responding genes. , 1993, Current opinion in genetics & development.

[33]  D A Kane,et al.  The identification of genes with unique and essential functions in the development of the zebrafish, Danio rerio. , 1996, Development.

[34]  William C. Smith,et al.  Expression cloning of noggin, a new dorsalizing factor localized to the Spemann organizer in Xenopus embryos , 1992, Cell.

[35]  J. Gerhart,et al.  Early cellular interactions promote embryonic axis formation in Xenopus laevis. , 1984, Developmental biology.

[36]  P. Wilson,et al.  Induction of epidermis and inhibition of neural fate by Bmp-4 , 1995, Nature.

[37]  P. Good,et al.  Dorsal-ventral patterning and differentiation of noggin-induced neural tissue in the absence of mesoderm. , 1995, Development.

[38]  J. Joly,et al.  The ventral and posterior expression of the zebrafish homeobox gene eve1 is perturbed in dorsalized and mutant embryos. , 1993, Development.

[39]  C. Kimmel,et al.  Stages of embryonic development of the zebrafish , 1995, Developmental dynamics : an official publication of the American Association of Anatomists.

[40]  M. Levine,et al.  Protein kinase A is a common negative regulator of Hedgehog signaling in the vertebrate embryo. , 1996, Genes & development.

[41]  E. Bier,et al.  Xenopus chordin and Drosophila short gastrulation genes encode homologous proteins functioning in dorsal-ventral axis formation , 1995, Cell.

[42]  N. Ueno,et al.  Localized BMP-4 mediates dorsal/ventral patterning in the early Xenopus embryo. , 1995, Developmental biology.

[43]  N. Ueno,et al.  A truncated bone morphogenetic protein receptor affects dorsal-ventral patterning in the early Xenopus embryo. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[44]  D A Kane,et al.  Genes establishing dorsoventral pattern formation in the zebrafish embryo: the ventral specifying genes. , 1996, Development.