Specification of cell fates at the dorsal margin of the zebrafish gastrula

Development

Volumn 122, Issue 7, 1996, Pages 2225-2237

  Melby, Anna E ^a,c   Warga, Rachel M ^a,b   Kimmel, Charles B ^a  

^a UNIVERSITY OF OREGON   (United States)

^b MAX PLANCK INSTITUTE FOR DEVELOPMENTAL BIOLOGY   (Germany)

^c UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

Author keywords

Axis; Brachyury; Fate map; floating head; no tail; Notochord; Organizer; Tail; Xnot; Zebrafish

Indexed keywords

ANIMAL TISSUE; ARTICLE; CELL CLONE; CONTROLLED STUDY; DEVELOPMENTAL GENETICS; EMBRYO; EMBRYO DEVELOPMENT; GASTRULA; HOMEOBOX; KUPFFER CELL; MESODERM; MUSCLE CELL; MUTANT; NONHUMAN; NOTOCHORD; PRIORITY JOURNAL; ZEBRA FISH;

ANIMALS; BLASTOMERES; CELL LINEAGE; CELL MOVEMENT; EMBRYO, NONMAMMALIAN; GASTRULA; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GENES, HOMEOBOX; HOMEODOMAIN PROTEINS; MESODERM; MORPHOGENESIS; MUTATION; NOTOCHORD; RNA; TAIL; TRANSCRIPTION FACTORS; ZEBRAFISH; ZEBRAFISH PROTEINS;

ANIMALIA; DANIO RERIO; TELEOSTEI;

EID: 0030056106     PISSN: 09501991     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (62)

1. Davidson, E. H. (1990). How embryos work: a comparative view of diverse modes of cell fate specification. Development 108, 365-389.
2. Davidson, E. H. (1993). Later embryogenesis: regulatory circuitry in morphogenetic fields. Development 118, 665-690.
3. Fan, C. M. and Tessier Lavigne, M. (1994). Patterning of mammalian somites by surface ectoderm and notochord: evidence for sclerotome induction by a hedgehog homolog. Cell 79, 1175-1186.
4. Garcia Martinez, V., Alvarez, I. S. and Schoenwolf, G. C. (1993). Locations of the ectodermal and nonectodermal subdivisions of the epiblast at stages 3 and 4 of avian gastrulation and neurulation. J. Exp. Zool. 267, 431-446.
5. Gont, L. K., Steinbeisser, H., Blumberg, B. and De Robertis, E. M. (1993). Tail formation as a continuation of gastrulation: the multiple cell populations of the Xenopus tailbud derive from the late blastopore lip. Development 119, 991-1004.
6. Halpern, M. E., Ho, R. K., Walker, C. and Kimmel, C. B. (1993). Induction of muscle pioneers and floor plate is distinguished by the zebrafish no tail mutation. Cell 75, 99-111.
7. Halpern, M. E., Thisse, C., Ho, R. K., Thisse, B., Riggleman, B., Trevarrow, B., Weinberg, E. S., Postlethwait, J. H. and Kimmel, C. B. (1995). Cell-autonomous shift from axial to paraxial mesodermal development in zebrafish floating head mutants. Development 121, 4257-4264.
8. Hammerschmidt, M. and Nüsslein-Volhard, C. (1993). The expression of a zebrafish gene homologous to Drosophila snail suggests a conserved function in invertebrate and vertebrate gastrulation. Development 119, 1107-1118.
9. Hashimoto, K., Fujimoto, H. and Nakatsuji, N. (1987). An ECM substratum allows mouse mesodermal cells isolated from the primitive streak to exhibit motility similar to that inside the mouse embryo and reveals a deficiency in the T/T mutant cells. Development 100, 587-598.
10. Hatta, K. and Kimmel, C. B. (1993). Midline structures and central nervous system coordinates in zebrafish. Perspect. Dev. Neurobiol. 1, 257-268.
11. Hatta, K., Kimmel, C. B., Ho, R. K. and Walker, C. (1991). The cyclops mutation blocks specification of the floor plate of the zebrafish central nervous system. Nature 350, 339-341.
12. Hauptmann, G. and Gerster, T. (1994). Two-color whole-mount in situ hybridization to vertebrate and Drosophila embryos. Trends Genet. 10, 266.
13. Ho, R. K. (1992). Axis formation in the embryo of the zebrafish. Brachydanio rerio. Sem. Dev. Biol. 3, 53-64.
14. Ho, R. K. and Kane, D. A. (1990). Cell-autonomous action of zebrafish spt-1 mutation in specific meosdermal precursors. Nature 348, 728-730.
15. Ho, R. K. and Kimmel, C. B. (1993). Commitment of cell fate in the early zebrafish embryo. Science 261, 109-111.
16. Joly, J. S., July, C., Schulte-Merker, S., Boulekbache, H. and Condamine, H. (1993). The ventral and posterior expression of the zebrafish homeobox gene eve I is perturbed in dorsalized and mutant embryos. Development 119, 1261-1275.
17. Jowett, T. and Lettice, L. (1994). Whole-mount in situ hybridizations on zebrafish embryos using a mixture of digoxigenin- and fluorescein-labeled probes. Trends Genet. 10, 73-74.
18. Keller, R. E. (1975). Vital dye mapping of the gastrula and neurula of Xenopus laevis. I. Prospective areas and morphogenetic movements of the superficial layer. Dev. Biol. 42, 222-241.
19. Keller, R.E. (1976). Vital dye mapping of the gastrula and neurula of Xenopus laevis. II. Prospective areas and morphogenetic movements of the deep layer. Dev. Biol. 51, 118-137.
20. Kimmel, C. B., Billiard, W. W., Kimmel, S. R., Ullmann, B. and Schilling, T. F. (1995). Stages of embryonic development of the zebrafish. Dev. Dyn. 203, 253-310.
21. Kimmel, C. B., Kane, D. A. and Ho, R. K. (1991). Lineage specification during early embryonic development of the zebrafish. In Cell-Cell Interactions in Early Development (J. Gerhart, Ed.). pp. 203-225. New York: Wiley-Liss, Inc.
22. Kimmel, C. B. and Warga, R. M. (1987). Cell lineages generating axial muscle in the zebrafish embryo. Nature 327, 234-237.
23. Kimmel, C. B., Warga, R. M. and Schilling, T. F. (1990). Origin and organization of the zebrafish fate map. Development 108, 581-594.
24. Kispert, A. and Hermann, B. G. (1993). The Brachyury gene encodes a novel DNA binding protein. EMBO J. 12, 4898-4899.
25. Koseki, H., Wallin, J., Wilting, J., Mizutani, Y., Kispert, A., Ebensperger, C., Herrmann, B. G., Christ, B. and Balling, R. (1993). A role for Pax-1 as a mediator of notochordal signals during the dorsoventral specification of vertebrae. Development 119, 649-660.
26. Krauss, S., Concordet, J. P. and Ingham, P. W. (1993). A functionally conserved homolog of the Drosophila segment polarity gene hh is expressed in tissues with polarizing activity in zebrafish embryos. Cell 75, 1431-1444.
27. Lawson, K. A., Meneses, J. J. and Pedersen, R. A. (1991). Clonal analysis of epiblast fate during germ layer formation in the mouse embryo. Development 113, 891-911.
28. Melby, A. E., Ho, R. K. and Kimmel, C. B. (1993). An identifiable domain of tail-forming cells in the zebrafish gastrula. Soc. Neurosci. Abs. 19, 445.
29. Myers, P. Z. and Bastiani, M. J. (1991). NeuroVideo: a program for capturing and processing time-lapse video. Comput. Methods Programs Biomed. 34, 27-33.
30. Nordahl, I. R. (1970). The development and morphology of Kupffer' s vesicle in the plaice Pleuronectes platessa (L.) and in the cod, Gadus morhua L. Sarsia 42, 41-62.
31. O'Reilly, M. A., Smith, J. C. and Cunliffe, V. (1995). Patterning of the mesoderm in Xenopus: dose-dependent and synergistic effects of Brachyury and Pintallavis. Development 121, 1351-1359.
32. Oppenheimer, J. M. (1936). Processes of localization in developing Fundulus. J. Exp. Biol. 73, 405-444.
33. Pasteels, J. (1943). Proliférations et croissance dans la gastrulation et la formation de la queue des Vertébrés. Arch. Biol. 54, 2-51.
34. Raible, D. W., Wood, A., Hodsdon, W., Henion, P. D., Weston, J. A. and Eisen, J. S. (1992). Segregation and early dispersal of neural crest cells in the embryonic zebrafish. Dev. Dyn. 195, 29-42.
35. Sasai, Y., Lu, B., Steinbeisser, H., Geissert, D., Gont, L. K. and De Robertis, E. M. (1994). Xenopus chordin: a novel dorsalizing factor activated by organizer-specific homeobox genes. Cell 79, 779-790.
36. Schilling, T. F. and Kimmel, C. B. (1994). Segment and cell type lineage restrictions during pharyngeal arch development in the zebrafish embryo. Development 120, 483-494.
37. Schoenwolf, G. C., Garcia Martinez, V. and Dias, M. S. (1992). Mesoderm movement and fate during avian gastrulation and neurulation. Dev. Dyn. 193, 235-248.
38. Schulte Merker, S., Ho, R. K., Herrmann, B. G. and Nüsslein-Volhard, C. (1992). 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. Development 116, 1021-1032.
39. Schulte-Merker, S., Hammerschmidt, M., Beuchle, D., Cho, K. W., De Robertas, E. M. and Nüsslein-Volhard, C. (1994a). Expression of zebrafish goosecoid and no tail gene products in wild-type and mutant no tail embryos. Development 120, 843-852.
40. Schulte-Merker, S., van Eeden, F. J., Halpern, M. E., Kimmel, C. B. and Nüsslein-Volhard, C. (1994b). no tail (ntl) is the zebrafish homologue of the mouse T(Brachyury) gene. Development 120, 1009-1015.
41. Selleck, M. A. and Stern, C. D. (1991). Fate mapping and cell lineage analysis of Hensen's node in the chick embryo. Development 112, 615-626.
42. Shih, J. and Fraser, S. E. (1995). Distribution of tissue progenitors within the shield region of the zebrafish gastrula. Development 121, 2755-2765.
43. Slack, J. M. W. (1991). From Egg to Embryo: Regional Specification in Early Development. Cambridge: Cambridge University Press.
44. Smith, J. L., Gesteland, K. M. and Schoenwolf, G. C. (1994). Prospective fate map of the mouse primitive streak at 7.5 days of gestation. Dev. Dyn. 201, 279-89.
45. Spemann, H. and Mangold, H. (1924). Über Induktion von Embryonalanlagen durch Implantation artfremder Organisatoren. Roux' Arch. Dev Biol. 100, 599-638.
46. Stachel, S. E., Grunwald, D. J. and Myers, P. Z. (1993). Lithium perturbation and goosecoid expression identify a dorsal specification pathway in the pregastrula zebrafish. Development 117, 1261-1274.
47. Strähle, U., Blader, P., Henrique, D. and Ingham, P. W. (1993). axial, a zebrafish gene expressed along the developing body axis, shows altered expression in cyclops mutant embryos. Genes Dev. 7, 1436-1446.
48. Streisinger, G., Singer, F., Walker, C., Knauber, D. and Dower, N. (1986). Segregation analysis and gene-centromere distances in zebrafish. Genetics 112, 311-319.
49. Talbot, W., Trevarrow, W., Halpern, M. E., Melby, A. E., Farr, H., Postlethwait, J. H., Jowett, T., Kimmel, C. B. and Kimelman, D. (1995). Requirement for the homeobox gene floating head in zebrafish notochord development. Nature 378, 150-157.
50. Thisse, C., Thisse, B., Halpern, M. E. and Postlethwait, J. H. (1994). goosecoid expression in neurectoderm and mesendoderm is disrupted in zebrafish cyclops gastrulas. Dev. Biol. 164, 420-429.
51. Thisse, C., Thisse, B., Schilling, T. F. and Postlethwait, J. H. (1993). Structure of the zebrafish snail1 gene and its expression in wild-type, spadetail and no tail mutant embryos. Development 119, 1203-1215.
52. Tucker, A. S. and Slack, J. M. W. (1995). The Xenopus laevis tail-forming region. Development 121, 249-262.
53. von Dassow, G., Schmidt, J. E. and Kimelman, D. (1993). Induction of the Xenopus organizer: expression and regulation of Xnot, a novel FGF and activin-regulated homeo box gene. Genes Dev. 7, 355-66.
54. Warga, R. M. (1996). Origin and specification of the endoderm in the zebrafish. Ph.D. Dissertation, University of Tubingen, Germany.
55. Warga, R. M. and Kimmel, C. B. (1990). Cell movements during epiboly and gastrulation in zebrafish. Development 108, 569-580.
56. Weinberg, E. S., Allende, M. L., Kelly, C. S., Abdelhamid, A., Murakami, T., Andermann, P., Doerre, O. G., Grunwald, D. J. and Riggleman, B. (1996). Developmental regulation of zebrafish MyoD in wild-type, no tail and spadetail embryos. Development 122, 271-280.
57. Weintraub, H. (1993). The MyoD family and myogenesis: redundancy, networks, and thresholds. Cell 75, 1241-4.
58. Westerfield, M. (1994). The Zebrafish Book. A guide for the laboratory use of zebrafish. Oregon: University of Oregon Press.
59. Wilson, V., Manson, L., Skarnes, W. C. and Beddington, R. S. (1995). The T gene is necessary for normal mesodermal morphogenetic cell movements during gastrulation. Development 121, 877-886.
60. Wilson, V., Rashbass, P. and Beddington, R. S. (1993). Chimeric analysis of T(Brachyury) gene function. Development 117, 1321-1331.
61. Wood, A. and Thorogood, P. (1984). An analysis of in vivo cell migration during teleost fin morphogenesis. J. Cell Sci. 66, 205-222.
62. Yamada, T., Placzek, M., Tanaka, H., Dodd, J. and Jessell, T. M. (1991). Control of cell pattern in the developing nervous system: polarizing activity of the floor plate and notochord. Cell 64, 635-647.