Nodal/Bozozok-independent induction of the dorsal organizer by zebrafish cell lines

Developmental Biology

Volumn 321, Issue 2, 2008, Pages 387-396

  Hashiguchi, Megumi ^a,b   Shinya, Minori ^a,b   Tokumoto, Mika ^b   Sakai, Noriyoshi ^a,b  

^a GRADUATE UNIVERSITY FOR ADVANCED STUDIES   (Japan)

^b NATIONAL INSTITUTE OF GENETICS   (Japan)

Author keywords

Cultured cells; Dorsal axis formation; Dorsal organizer; Nodal; Zebrafish

Indexed keywords

ACTIVIN A; ALPHA TUBULIN; MYELOPID;

ANIMAL CELL; ARTICLE; BLASTULA; BOZ GENE; CELL DIFFERENTIATION; CELL LINE; CONTROLLED STUDY; DEVELOPMENTAL STAGE; EMBRYO; EMBRYO DEVELOPMENT; GASTRULA; GENE; MUTANT; NIDATION; NONHUMAN; NOTOCHORD; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; SQT GENE; ZEBRA FISH;

DANIO RERIO; VERTEBRATA;

EID: 51249100203     PISSN: 00121606     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ydbio.2008.06.035     Document Type: Article

References (65)

1. Asashima M., et al. Mesodermal induction in early amphibian embryos by activin A (erythroid differentiation factor). Rouxs Arch. Dev. Biol. 198 (1990) 330-335
2. Bisgrove B.W., et al. Regulation of midline development by antagonism of lefty and nodal signaling. Development 126 (1999) 3253-3262
3. Bormann P., et al. Target contact regulates GAP-43 and alpha-tubulin mRNA levels in regenerating retinal ganglion cells. J. Neurosci. Res. 52 (1998) 405-419
4. Chan A.P., and Etkin L.D. Patterning and lineage specification in the amphibian embryo. Curr. Top Dev. Biol. 51 (2001) 1-67
5. Cheng S.K., et al. Lefty blocks a subset of TGFbeta signals by antagonizing EGF-CFC coreceptors. PLOS Biol. 2 (2004) 215-226
6. De Robertis E.M., et al. The establishment of Spemann's organizer and patterning of the vertebrate embryo. Nat. Rev. Genet. 1 (2000) 171-181
7. De Robertis E.M., et al. Molecular mechanisms of cell-cell signaling by the Spemann-Mangold organizer. Int. J. Dev. Biol. 45 (2001) 189-197
8. Doniach T., et al. Planar induction of anteroposterior pattern in the developing central nervous system of Xenopus laevis. Science 257 (1992) 542-545
9. Dougan S.T., et al. The role of the zebrafish nodal-related genes squint and cyclopsin patterning of mesendoderm. Development 130 (2003) 1837-1851
10. Draper, B.W., et al., 2003. Zebrafish fgf24 functions with fgf8 to promote posterior mesodermal development. 130, 4639-4654.
11. Erter C.E., et al. Zebrafish nodal-related 2 encodes an early mesendodermal inducer signaling from the extraembryonic yolk syncytial layer. Dev. Biol. 204 (1998) 361-372
12. Fekany K., et al. The zebrafish bozozok locus encodes Dharma, a homeodomain protein essential for induction of gastrula organizer and dorsoanterior embryonic structures. Development 126 (1999) 1427-1438
13. Feldman B., et al. Zebrafish organizer development and germ-layer formation require nodal-related signals. Nature 395 (1998) 181-185
14. Fürthauer M., et al. Three different noggin genes antagonize the activity of bone morphogenetic proteins in the zebrafish embryos. Dev. Biol. 214 (1999) 181-196
15. Gritsman K., et al. The EGF-CFC protein one-eyed pinhead is essential for nodal signaling. Cell 97 (1999) 121-132
16. Gritsman K., et al. Nodal signaling patterns the organizer. Development 127 (2000) 921-932
17. Harland R., and Gerhart J. Formation and function of Spemann's organizer. Annu. Rev. Cell. Dev. Biol. 13 (1997) 611-667
18. Hashimoto H., et al. Zebrafish Dkk1 functions in forebrain specification and axial mesendoderm formation. Dev. Biol. 217 (2000) 138-152
19. Ho R.K., and Kimmel C.B. Commitment of cell fate in the early zebrafish embryo. Science 261 (1993) 109-111
20. Hatta K., and Takahashi Y. Secondary axis induction by heterospecific organizers in zebrafish. Dev. Dyn. 205 (1996) 183-195
21. Keller R., et al. Planar induction of convergence and extension of the neural plate by the organizer of Xenopus. Dev. Dyn. 193 (1992) 218-234
22. Kelly C., et al. Maternally controlled b-catenin-mediated signaling is required for organizer formation in the zebrafish. Development 127 (2000) 3899-3911
23. Kimmel C.B., and Warga R.M. Tissue-specific cell lineages originate in the gastrula ofthe zebrafish. Science 231 (1986) 365-368
24. Koos D.S., and Ho R.K. The nieuwkoid/dharma homeobox gene is essential for bmp2b repression in the zebrafish pregastrula. Dev. Biol. 215 (1999) 190-207
25. Koshida S., et al. Initial anteroposterior pattern of the zebrafish central nervous system is determined by differential competence of the epiblast. Development 125 (1998) 1957-1966
26. Krauss S., et al. A functionally conserved homolog of the Drosophila segment polarity gene hh is expressed in tissues with polarizing activity in zebrafish embryos. Cell 75 (1993) 1431-1444
27. Kurita K., and Sakai N. Functionally distinctive testicular cell lines of zebrafish to support male germ cell development. Mol. Reprod. Dev. 67 (2004) 430-438
28. Leung T., et al. bozozok directly represses bmp2b transcription and mediates the earliest dorsoventral asymmetry of bmp2b expression in zebrafish. Development 130 (2003) 3639-3649
29. Lin S., et al. Production of germ-line chimeras in zebrafish by cell transplants from genetically pigmented to albino embryos. Proc. Natl. Acad. Sci. USA 89 (1992) 4519-4523
30. Maegawa S., et al. FGF signaling is required for b-catenin-mediated induction of the zebrafish organizer. Development 133 (2006) 3265-3276
31. Meno C., et al. Mouse Lefty2 and zebrafish Antivin are feedback inhibitors of Nodal signaling during vertebrate gastrulation. Mol. Cell. 4 (1999) 287-298
32. Miller-Bertoglio V.E., et al. Differential regulation of chordin expression domains in mutant zebrafish. Dev. Biol. 192 (1997) 537-550
33. Mizuno T., et al. Mesoderm induction in zebrafish. Nature 383 (1996) 131-132
34. Morita T., et al. Differential expression of two zebrafish emx homeoprotein mRNAs in the developing brain. Neurosci. Lett. 198 (1995) 131-134
35. Nieuwkoop P.D. The formation of the mesoderm in urodelean amphibians. The origin of the dorso-ventral polarity of the mesoderm. Wilhelm Rouxs Arch. 163 (1969) 298-315
36. Nissen R.M., et al. Zebrafish foxi one modulates cellular responses to Fgf signaling required for the integrity of ear and jaw patterning. Development 130 (2003) 2543-2554
37. Oxtoby E., and Jowett T. Cloning of the zebrafish krox-20 gene (krx-20) and its expression during hindbrain development. Nucleic Acids Res. 21 (1993) 1087-1095
38. Piepenburg O., et al. Activin redux: specification of mesodermal pattern in Xenopus by graded concentrations of endogenous activin B. Development 131 (2004) 4977-4986
39. Rebagliati M.R., et al. cyclops encodes a nodal-related factor involved in midline signaling. Proc. Natl. Acad. Sci. USA 95 (1998) 9932-9937
40. Robertson E.J. Embryo-derived stem cell lines. In: Robertson E.J. (Ed). Teratocarcinoma and Embryonic Stem Cells: A Practical Approach (1987), IRL Press, Oxford 71-112
41. Rowning B.A., et al. Microtubule-mediated transport of organelles and localization of beta-catenin to the future dorsal side of Xenopus eggs. Proc. Natl. Acad. Sci. USA 94 (1997) 1224-1229
42. Sampath K., et al. Induction of the zebrafish ventral brain and floorplate requires cyclops/nodal signaling. Nature 395 (1998) 185-189
43. Saúde L., et al. Axis-inducing activities and cell fates of the zebrafish organizer. Development 127 (2000) 3407-3417
44. Schier A.F., and Talbot W.S. The zebrafish organizer. Curr. Opin. Genet. Dev. 8 (1998) 464-471
45. Schneider S., et al. b-catenin translocation into nuclei demarcates the dorsalizing centers in frog and fish embryos. Mech. Dev. 57 (1996) 191-198
46. Schulte-Merker S., et al. The zebrafish organizer requires chordino. Nature 387 (1997) 862-863
47. Shih J., and Fraser S.E. Characterizing the zebrafish organizer: microsurgical analysis at the early-shield stage. Development 122 (1996) 1313-1322
48. Shimizu T., et al. Cooperative roles of Bozozok/Dharma and Nodal-related proteins in the formation of the dorsal organizer in zebrafish. Mech. Dev. 91 (2000) 293-303
49. Shinya M., et al. Zebrafish Dkk1, induced by the pre-MBT Wnt signaling, is secreted from the prechordal plate and patterns the anterior neural plate. Mech. Dev. 98 (2000) 3-17
50. Sirotkin H.I., et al. bozozok and squint act in parallel to specify dorsal mesoderm and anterior neuroectoderm in zebrafish. Development 127 (2000) 2583-2592
51. Smith J.C. A mesoderm-inducing factor is produced by Xenopus cell line. Development 99 (1987) 3-14
52. Smith J.C., and Slack J.M. Dorsalization and neural induction: properties of the organizer in Xenopus laevis. J. Embryol. Exp. Morphol. 78 (1983) 299-317
53. Smith J.C., et al. Identification of a potent Xenopus mesoderm-inducing factor as a homologue of activin A. Nature. 345 (1990) 729-731
54. Spemann H., and Mangold H. Über Induktion von Embryonalanlagen durch Implantation Artfremder Organisatoren. Roux Arch. Entw. Mech. 100 (1924) 599-638
55. Stachel S.E., et al. Lithium perturbation and goosecoid expression identify a dorsal specification pathway in the pregastrula zebrafish. Development 117 (1993) 1261-1274
56. Talbot W.S., et al. A homeobox gene essential for zebrafish notochord development. Nature 378 (1995) 150-157
57. Thisse C., and Thisse B. Antivin, a novel and divergent member of the TGFb superfamily, negatively regulates mesoderm induction. Development 126 (1999) 229-240
58. Topczewska, et al. Embryonic and tumorigenic pathways converge via Nodal signaling: role in melanoma aggressiveness. Nat. Med. 12 (2006) 925-932
59. Tsang M., et al. A role for MKP3 in axial patterning of the zebrafish embryo. Development 131 (2004) 2769-2779
60. Vincent J.P., et al. Kinematics of gray crescent formation in Xenopus eggs: the displacement of subcortical cytoplasm relative to the egg surface. Dev Biol. 113 (1986) 484-500
61. Wang Y., and Ge W. Developmental profiles of activin betaA, betaB, and follistatin expression in the zebrafish ovary: evidence for their differential roles during sexual maturation and ovulatory cycle. Biol. Reprod. 71 (2004) 2056-2064
62. Weinberg E.S., et al. Developmental regulation of zebrafish MyoD in wild-type, no tail and spadetail embryos. Development 122 (1996) 271-280
63. Westerfield M. The Zebrafish Book: A Guide for the Laboratory Use of Zebrafish (1995), University of Oregon Press, Eugene
64. Yamanaka Y., et al. A novel homeobox gene, dharma, can induce the organizer in a non-cell-autonomous manner. Genes Dev. 12 (1998) 2345-2353
65. Zhang J., et al. Positional cloning identifies zebrafish one-eyed pinhead as a permissive EGF-related ligand required during gastrulation. Cell 92 (1998) 241-251