Structure of the zebrafish snail1 gene and its expression in wild-type, spadetail and no tail mutant embryos.

Mesoderm formation is critical for the establishment of the animal body plan and in Drosophila requires the snail gene. This report concerns the cloning and expression pattern of the structurally similar gene snail1 from zebrafish. In situ hybridization shows that the quantity of snail1 RNA increases at the margin of the blastoderm in cells that involute during gastrulation. As gastrulation begins, snail1 RNA disappears from the dorsal axial mesoderm and becomes restricted to the paraxial mesoderm and the tail bud. snail1 RNA increases in cells that define the posterior border of each somite and then disappears when somitic cells differentiate. Later in development, expression appears in cephalic neural crest derivatives. Many snail1-expressing cells were missing from mutant spadetail embryos and the quantity of snail1 RNA was greatly reduced in mutant no tail embryos. The work presented here suggests that snail1 is involved in morphogenetic events during gastrulation, somitogenesis and development of the cephalic neural crest, and that no tail may act as a positive regulator of snail1.

[1]  C. Kimmel,et al.  Cell lineages generating axial muscle in the zebrafish embryo , 1987, Nature.

[2]  M. Bennett,et al.  Cloning and developmental expression of Sna, a murine homologue of the Drosophila snail gene. , 1992, Development.

[3]  T. Gridley,et al.  Isolation of Sna, a mouse gene homologous to the Drosophila genes snail and escargot: its expression pattern suggests multiple roles during postimplantation development. , 1992, Development.

[4]  D. Wilkinson,et al.  Expression pattern of the mouse T gene and its role in mesoderm formation , 1990, Nature.

[5]  C. Nüsslein-Volhard,et al.  A gradient of nuclear localization of the dorsal protein determines dorsoventral pattern in the Drosophila embryo , 1989, Cell.

[6]  B. Thisse,et al.  Sequence-specific transactivation of the Drosophila twist gene by the dorsal gene product , 1991, Cell.

[7]  M. Frasch,et al.  Maternal regulation of zerknüllt: a homoeobox gene controlling differentiation of dorsal tissues in Drosophila , 1987, Nature.

[8]  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.

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

[10]  D Kosman,et al.  The dorsal morphogen gradient regulates the mesoderm determinant twist in early Drosophila embryos. , 1991, Genes & development.

[11]  M. Levine,et al.  The dorsal morphogen is a sequence-specific DNA-binding protein that interacts with a long-range repression element in drosophila , 1991, Cell.

[12]  R. Krumlauf,et al.  Molecular approaches to the segmentation of the hindbrain , 1990, Trends in Neurosciences.

[13]  C. Kimmel,et al.  The fub-1 mutation blocks initial myofibril formation in zebrafish muscle pioneer cells. , 1991, Developmental biology.

[14]  T. Jessell,et al.  Diffusible factors in vertebrate embryonic induction , 1992, Cell.

[15]  R. Harland,et al.  In situ hybridization: an improved whole-mount method for Xenopus embryos. , 1991, Methods in cell biology.

[16]  G. Streisinger,et al.  INDUCTION OF MUTATIONS BY γ-RAYS IN PREGONIAL GERM CELLS OF ZEBRAFISH EMBRYOS , 1983 .

[17]  P. Noguchi,et al.  The Drosophila gene escargot encodes a zinc finger motif found in snail-related genes , 1992, Mechanisms of Development.

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

[19]  S. Gluecksohn‐Schoenheimer The Development of Normal and Homozygous Brachy (T/T) Mouse Embryos in the Extraembryonic Coelom of the Chick. , 1944, Proceedings of the National Academy of Sciences of the United States of America.

[20]  J. Smith,et al.  Expression of a xenopus homolog of Brachyury (T) is an immediate-early response to mesoderm induction , 1991, Cell.

[21]  P. Chesley Development of the short‐tailed mutant in the house mouse , 1935 .

[22]  R. Steward Relocalization of the dorsal protein from the cytoplasm to the nucleus correlates with its function , 1989, Cell.

[23]  B. Thisse,et al.  Sequence of the twist gene and nuclear localization of its protein in endomesodermal cells of early Drosophila embryos. , 1988, The EMBO journal.

[24]  P. Lawrence,et al.  Parasegments and compartments in the Drosophila embryo , 1985, Nature.

[25]  N. Hopwood Cellular and genetic responses to mesoderm induction in Xenopus , 1990, BioEssays : news and reviews in molecular, cellular and developmental biology.

[26]  H. Lin,et al.  An improved DNA sequencing strategy. , 1985, Analytical biochemistry.

[27]  H. Urushihara,et al.  Effects of the brachyury (T) mutation on morphogenetic movement in the mouse embryo. , 1981, Developmental biology.

[28]  R. Ho,et al.  Cell-autonomous action of zebrafish spt-1 mutation in specific mesodermal precursors , 1990, Nature.

[29]  G. Streisinger,et al.  Production of clones of homozygous diploid zebra fish (Brachydanio rerio) , 1981, Nature.

[30]  R. Ho,et al.  Induction of muscle pioneers and floor plate is distinguished by the zebrafish no tail mutation , 1993, Cell.

[31]  J. Boulay,et al.  The snail gene required for mesoderm formation in Drosophila is expressed dynamically in derivatives of all three germ layers. , 1991, Development.

[32]  C. Nüsslein-Volhard,et al.  no tail (ntl) is the zebrafish homologue of the mouse T (Brachyury) gene. , 1994, Development.

[33]  C. Kimmel,et al.  Development of segmentation in zebrafish. , 1988, Development.

[34]  W. Gilbert,et al.  One-sided polymerase chain reaction: the amplification of cDNA. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[35]  B. Blumberg,et al.  Organizer-specific homeobox genes in Xenopus laevis embryos. , 1991, Science.

[36]  J. Gurdon,et al.  A Xenopus mRNA related to Drosophila twist is expressed in response to induction in the mesoderm and the neural crest , 1989, Cell.

[37]  R. Moon,et al.  Competence modifiers synergize with growth factors during mesoderm induction and patterning in xenopus , 1992, Cell.

[38]  P. Lawrence Cell lineage and cell states in the Drosophila embryo. , 1989, Ciba Foundation symposium.

[39]  J. Smith,et al.  Ectopic mesoderm formation in Xenopus embryos caused by widespread expression of a Brachyury homologue , 1992, Nature.

[40]  A. Poustka,et al.  Cloning of the T gene required in mesoderm formation in the mouse , 1990, Nature.

[41]  G. Streisinger,et al.  Segregation analyses and gene-centromere distances in zebrafish. , 1986, Genetics.

[42]  J. L. Boulay,et al.  The Drosophila developmental gene snail encodes a protein with nucleic acid binding fingers , 1987, Nature.

[43]  M. Bennett,et al.  Identification in Xenopus of a structural homologue of the Drosophila gene snail. , 1990, Development.

[44]  J. D. Huang,et al.  Functional analysis of the Drosophila twist promoter reveals a dorsal-binding ventral activator region. , 1991, Genes & development.

[45]  C. Kimmel,et al.  A mutation that changes cell movement and cell fate in the zebrafish embryo , 1989, Nature.

[46]  T. El-Baradi,et al.  Zinc finger proteins: what we know and what we would like to know , 1991, Mechanisms of Development.

[47]  P. Gerlinger,et al.  The M-twist gene of Mus is expressed in subsets of mesodermal cells and is closely related to the Xenopus X-twi and the Drosophila twist genes. , 1991, Developmental biology.

[48]  Ken W. Y. Cho,et al.  Molecular nature of Spemann's organizer: the role of the Xenopus homeobox gene goosecoid , 1991, Cell.