Mutations affecting neurogenesis and brain morphology in the zebrafish, Danio rerio.

In a screen for embryonic mutants in the zebrafish a large number of mutants were isolated with abnormal brain morphology. We describe here 26 mutants in 13 complementation groups that show abnormal development of large regions of the brain. Early neurogenesis is affected in white tail (wit). During segmentation stages, homozygous wit embryos display an irregularly formed neural keel, particularly in the hindbrain. Using a variety of molecular markers, a severe increase in the number of various early differentiating neurons can be demonstrated. In contrast, late differentiating neurons, radial glial cells and some nonneural cell types, such as the neural crest-derived melanoblasts, are much reduced. Somitogenesis appears delayed. In addition, very reduced numbers of melanophores are present posterior to the mid-trunk. The wit phenotype is reminiscent of neurogenic mutants in Drosophila, such as Notch or Delta. In mutant parachute (pac) embryos the general organization of the hindbrain is disturbed and many rounded cells accumulate loosely in the hindbrain and midbrain ventricles. Mutants in a group of 6 genes, snakehead(snk), natter (nat), otter (ott), fullbrain (ful), viper (vip) and white snake (wis) develop collapsed brain ventricles, before showing signs of general degeneration. atlantis (atl), big head (bid), wicked brain (win), scabland (sbd) and eisspalte (ele) mutants have different malformation of the brain folds. Some of them have transient phenotypes, and mutant individuals may grow up to adults.

[1]  C. Nüsslein-Volhard,et al.  Zebrafish pigmentation mutations and the processes of neural crest development. , 1996, Development.

[2]  C. Nüsslein-Volhard,et al.  Mutations affecting the formation of the notochord in the zebrafish, Danio rerio. , 1996, Development.

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

[4]  D A Kane,et al.  Mutations in zebrafish genes affecting the formation of the boundary between midbrain and hindbrain. , 1996, Development.

[5]  C. Nüsslein-Volhard,et al.  Mutations affecting the cardiovascular system and other internal organs in zebrafish. , 1996, Development.

[6]  C. Nüsslein-Volhard,et al.  The zebrafish epiboly mutants. , 1996, Development.

[7]  C. Nüsslein-Volhard,et al.  Mutations affecting development of the zebrafish inner ear and lateral line. , 1996, Development.

[8]  C. Nüsslein-Volhard,et al.  Genes involved in forebrain development in the zebrafish, Danio rerio. , 1996, Development.

[9]  A. Schier,et al.  Mutations affecting the development of the embryonic zebrafish brain. , 1996, Development.

[10]  D A Kane,et al.  Mutations affecting somite formation and patterning in the zebrafish, Danio rerio. , 1996, Development.

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

[12]  H. Baier,et al.  Zebrafish mutations affecting retinotectal axon pathfinding. , 1996, Development.

[13]  C. Doe,et al.  A collection of cortical crescents: Asymmetric protein localization in CNS precursor cells , 1995, Neuron.

[14]  T. Mak,et al.  Disruption of the mouse RBP-J kappa gene results in early embryonic death. , 1995, Development.

[15]  S. Easter,et al.  Expression of glial fibrillary acidic protein and its relation to tract formation in embryonic zebrafish (Danio rerio) , 1995, The Journal of comparative neurology.

[16]  D. Simon,et al.  Transient and restricted expression during mouse embryogenesis of Dll1, a murine gene closely related to Drosophila Delta. , 1995, Development.

[17]  U. Lendahl,et al.  Expression of Notch 1, 2 and 3 is regulated by epithelial-mesenchymal interactions and retinoic acid in the developing mouse tooth and associated with determination of ameloblast cell fate , 1995, The Journal of cell biology.

[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]  David Ish-Horowicz,et al.  Expression of a Delta homologue in prospective neurons in the chick , 1995, Nature.

[20]  David Ish-Horowicz,et al.  Primary neurogenesis in Xenopus embryos regulated by a homologue of the Drosophila neurogenic gene Delta , 1995, Nature.

[21]  J. Rossant,et al.  Notch1 is required for the coordinate segmentation of somites. , 1995, Development.

[22]  J. Boulter,et al.  Jagged: A mammalian ligand that activates notch1 , 1995, Cell.

[23]  R. Kypta,et al.  Molecular genetics of neuronal adhesion , 1995, Current Opinion in Neurobiology.

[24]  V. Hartenstein,et al.  Neurogenic and proneural genes control cell fate specification in the Drosophila endoderm. , 1995, Development.

[25]  M. Bronner‐Fraser,et al.  Origins of the avian neural crest: the role of neural plate-epidermal interactions. , 1995, Development.

[26]  Kenji Matsuno,et al.  Notch signaling. , 1995, Science.

[27]  T. Mak,et al.  Disruption of the mouse RBP-Jκ gene results in early embryonic death , 1995 .

[28]  M. Allende,et al.  The expression pattern of two zebrafish achaete-scute homolog (ash) genes is altered in the embryonic brain of the cyclops mutant. , 1994, Developmental biology.

[29]  Stephen W. Wilson,et al.  Regulatory gene expression boundaries demarcate sites of neuronal differentiation in the embryonic zebrafish forebrain , 1994, Neuron.

[30]  M. Fortini,et al.  The suppressor of hairless protein participates in notch receptor signaling , 1994, Cell.

[31]  Raphael Kopan,et al.  An activated Notch suppresses neurogenesis and myogenesis but not gliogenesis in mammalian cells. , 1994, Development.

[32]  H. Weintraub,et al.  The intracellular domain of mouse Notch: a constitutively activated repressor of myogenesis directed at the basic helix-loop-helix region of MyoD. , 1994, Development.

[33]  D. E. Yorde,et al.  Barrier inhibition of a temporal neuraxial influence on early chick somitic myogenesis , 1994, Developmental dynamics : an official publication of the American Association of Anatomists.

[34]  G. Weinmaster,et al.  Notch1 is essential for postimplantation development in mice. , 1994, Genes & development.

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

[36]  C. Kimmel,et al.  Segment and cell type lineage restrictions during pharyngeal arch development in the zebrafish embryo. , 1994, Development.

[37]  D. E. Yorde,et al.  Analysis of chick somite myogenesis by in situ confocal microscopy of desmin expression. , 1994, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[38]  C. Kimmel,et al.  Cell cycles and clonal strings during formation of the zebrafish central nervous system. , 1994, Development.

[39]  H. Okamoto,et al.  Developmental regulation of Islet‐1 mRNA expression during neuronal differentiation in embryonic zebrafish , 1994, Developmental dynamics : an official publication of the American Association of Anatomists.

[40]  Y. Jan,et al.  Genetic control of cell fate specification in Drosophila peripheral nervous system. , 1994, Annual review of genetics.

[41]  M. Fortini,et al.  Notch: Neurogenesis is only part of the picture , 1993, Cell.

[42]  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.

[43]  J. Campos-Ortega Mechanisms of early neurogenesis in Drosophila melanogaster. , 1993, Journal of neurobiology.

[44]  J. Campos-Ortega,et al.  A zebrafish homologue of the Drosophila neurogenic gene Notch and its pattern of transcription during early embryogenesis , 1993, Mechanisms of Development.

[45]  J. Rossant,et al.  Defects in heart and lung development in compound heterozygotes for two different targeted mutations at the N-myc locus. , 1993, Development.

[46]  N. L. Le Douarin,et al.  Patterning of neural crest derivatives in the avian embryo: in vivo and in vitro studies. , 1993, Developmental biology.

[47]  P. Cochard,et al.  Lineage analysis of early neural plate cells: cells with purely neuronal fate coexist with bipotential neuroglial progenitors. , 1993, Developmental biology.

[48]  L. Reichardt,et al.  Extracellular Matrix 2: Role of extracellular matrix molecules and their receptors in the nervous system , 1993, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[49]  G. Struhl,et al.  Intrinsic activity of the lin-12 and Notch intracellular domains in vivo , 1993, Cell.

[50]  G. Technau,et al.  A common precursor for glia and neurons in the embryonic CNS of Drosophila gives rise to segment-specific lineage variants. , 1993, Development.

[51]  V. Korzh,et al.  Zebrafish primary neurons initiate expression of the LIM homeodomain protein Isl-1 at the end of gastrulation. , 1993, Development.

[52]  Y. Jan,et al.  Cell interactions and gene interactions in peripheral neurogenesis. , 1993, Genes & development.

[53]  E. Oxtoby,et al.  Cloning of the zebrafish krox-20 gene (krx-20) and its expression during hindbrain development. , 1993, Nucleic acids research.

[54]  U. Lendahl,et al.  Motch A and motch B--two mouse Notch homologues coexpressed in a wide variety of tissues. , 1993, Experimental cell research.

[55]  C. Kimmel,et al.  Patterning the brain of the zebrafish embryo. , 1993, Annual review of neuroscience.

[56]  C. Kimmel,et al.  Midline structures and central nervous system coordinates in zebrafish. , 1993, Perspectives on developmental neurobiology.

[57]  David J. Anderson,et al.  Isolation of a stem cell for neurons and glia from the mammalian neural crest , 1992, Cell.

[58]  Stephen W. Wilson,et al.  Axonal trajectories and distribution of GABAergic spinal neurons in wildtype and mutant zebrafish lacking floor plate cells , 1992, The Journal of comparative neurology.

[59]  J. Rossant,et al.  Expression analysis of a Notch homologue in the mouse embryo. , 1992, Developmental biology.

[60]  V. Hartenstein,et al.  The function of the neurogenic genes during epithelial development in the Drosophila embryo. , 1992, Development.

[61]  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.

[62]  K. Hatta Role of the floor plate in axonal patterning in the zebrafish CNS , 1992, Neuron.

[63]  M. Westerfield,et al.  Comparative analysis of Pax-2 protein distributions during neurulation in mice and zebrafish , 1992, Mechanisms of Development.

[64]  D. Raible,et al.  Segregation and early dispersal of neural crest cells in the embryonic zebrafish , 1992, Developmental dynamics : an official publication of the American Association of Anatomists.

[65]  R. Greenspan,et al.  Expression pattern of Motch, a mouse homolog of Drosophila Notch, suggests an important role in early postimplantation mouse development. , 1992, Development.

[66]  J. Eisen,et al.  Pathfinding by zebrafish motoneurons in the absence of normal pioneer axons. , 1992, Development.

[67]  R. Hynes,et al.  Contact and adhesive specificities in the associations, migrations, and targeting of cells and axons , 1992, Cell.

[68]  S. Krauss,et al.  Expression of the zebrafish paired box gene pax[zf-b] during early neurogenesis. , 1991, Development.

[69]  G. Weinmaster,et al.  A homolog of Drosophila Notch expressed during mammalian development. , 1991, Development.

[70]  J. Sklar,et al.  TAN-1, the human homolog of the Drosophila Notch gene, is broken by chromosomal translocations in T lymphoblastic neoplasms , 1991, Cell.

[71]  P. Simpson,et al.  The choice of cell fate in the epidermis of Drosophila , 1991, Cell.

[72]  W. Harris,et al.  Xotch, the Xenopus homolog of Drosophila notch. , 1990, Science.

[73]  J. Sanes,et al.  Lineage, arrangement, and death of clonally related motoneurons in chick spinal cord , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[74]  C. Kimmel,et al.  Organization of hindbrain segments in the zebrafish embryo , 1990, Neuron.

[75]  J. Palka,et al.  Neurogenic and antineurogenic effects from modifications at the Notch locus. , 1990, Development.

[76]  T. Jessell,et al.  The axonal glycoprotein TAG-1 is an immunoglobulin superfamily member with neurite outgrowth-promoting activity , 1990, Cell.

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

[78]  J. Sanes,et al.  Neurons and glia arise from a common progenitor in chicken optic tectum: demonstration with two retroviruses and cell type-specific antibodies. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[79]  V. Hartenstein Early neurogenesis in xenopus: The spatio-temporal pattern of proliferation and cell lineages in the embryonic spinal cord , 1989, Neuron.

[80]  Geraldine Seydoux,et al.  Cell autonomy of lin-12 function in a cell fate decision in C. elegans , 1989, Cell.

[81]  M. Westerfield,et al.  Early expression of acetylcholinesterase activity in functionally distinct neurons of the zebrafish , 1989, The Journal of comparative neurology.

[82]  A. Jacobson,et al.  Neural fold formation at newly created boundaries between neural plate and epidermis in the axolotl. , 1989, Developmental biology.

[83]  K. G. Coleman,et al.  Expression of engrailed proteins in arthropods, annelids, and chordates. , 1989, Cell.

[84]  L. Eng,et al.  Chapter 14 – GLIAL FIBRILLARY ACIDIC PROTEIN: A REVIEW OF STRUCTURE, FUNCTION, AND CLINICAL APPLICATION , 1988 .

[85]  Constance L. Cepko,et al.  A common progenitor for neurons and glia persists in rat retina late in development , 1987, Nature.

[86]  B. Mendelson Development of reticulospinal neurons of the zebrafish. I. Time of origin , 1986, The Journal of comparative neurology.

[87]  B. Mendelson Development of reticulospinal neurons of the zebrafish. II. Early axonal outgrowth and cell body position , 1986, The Journal of comparative neurology.

[88]  G. Piperno,et al.  Monoclonal antibodies specific for an acetylated form of alpha-tubulin recognize the antigen in cilia and flagella from a variety of organisms , 1985, The Journal of cell biology.

[89]  T. Nakao,et al.  Light- and electron-microscopic observations of the tail bud of the larval lamprey (Lampetra japonica), with special reference to neural tube formation. , 1984, The American journal of anatomy.

[90]  D. Fischman,et al.  Immunochemical analysis of myosin heavy chain during avian myogenesis in vivo and in vitro , 1982, The Journal of cell biology.

[91]  G. Schoenwolf,et al.  Ultrastructure of secondary neurulation in the chick embryo. , 1980, The American journal of anatomy.

[92]  Henri Korn,et al.  Neurobiology of the Mauthner cell , 1978 .

[93]  R. Freeman,et al.  Comparative remarks on the development of the tail cord among higher vertebrates. , 1974, Journal of embryology and experimental morphology.

[94]  P Karfunkel,et al.  The mechanisms of neural tube formation. , 1974, International review of cytology.