TGF-β signals and a prepattern in Xenopus laevis endodermal development

Development

Volumn 122, Issue 3, 1996, Pages 1007-1015

  Henry, Gilbert L ^a   Brivanlou, Iman H ^a   Kessler, Daniel S ^a   Hemmati Brivanlou, Ali ^a,b   Melton, Douglas A ^a  

^a HARVARD UNIVERSITY   (United States)

^b ROCKEFELLER UNIVERSITY   (United States)

Author keywords

Cortical rotation; Endoderm; IFABP; TGF ; Xenopus; Xlhbox 8

Indexed keywords

CELL MARKER; FATTY ACID BINDING PROTEIN; FIBROBLAST GROWTH FACTOR; GENE PRODUCT; HOMEODOMAIN PROTEIN; TRANSCRIPTION FACTOR; TRANSFORMING GROWTH FACTOR BETA;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; EMBRYO; EMBRYO PATTERN FORMATION; ENDODERM; INTESTINE EPITHELIUM; NONHUMAN; PANCREAS; PRIORITY JOURNAL; PROTEIN EXPRESSION; SIGNAL TRANSDUCTION; XENOPUS LAEVIS;

ANIMALS; BASE SEQUENCE; CARRIER PROTEINS; CELL DIFFERENTIATION; DNA PRIMERS; DNA-BINDING PROTEINS; ECTODERM; EMBRYONIC INDUCTION; ENDODERM; FATTY ACID-BINDING PROTEINS; FEMALE; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HOMEODOMAIN PROTEINS; IN SITU HYBRIDIZATION; MALE; MOLECULAR SEQUENCE DATA; MORPHOGENESIS; MYELIN P2 PROTEIN; NEOPLASM PROTEINS; RNA, MESSENGER; TRANSFORMING GROWTH FACTOR BETA; XENOPUS LAEVIS; XENOPUS PROTEINS;

EID: 0029670111     PISSN: 09501991     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (69)

1. Amaya, E., Musci, T. J. and Kirschner, M. W. (1991). Expression of a dominant negative mutant of the FGF receptor disrupts mesoderm formation in Xenopus embryos. Cell 66, 257-270.
2. Asashima, M., Uchiyama, H., Nakano, H., Eto, Y., Ejima, D., Sugina, H., Davids, M., Plessow, S., Born, J., Hoppe, P., Tiedemann, H. and Tiedemann H. (1991a). The vegetalising factor from chicken embryos: its EDF (activin A)- like activity Mech Dev. 34, 135-141.
3. Asashima, M., Nakano, H., Uchiyama, H., Sugino, H., Nakamura, T., Eto, Y., Ejima, D., Davids, M., Plessow, S., Cichocka, I. and Kinoshita, K. (1991b). Follistatin inhibits the mesoderm-inducing activity of activin A and vegetalizing factor from chicken embryos. Roux's Arch Dev. Biol. 200, 4-7.
4. Banville, D. and Williams, J. G. (1985). The pattern of expression of the Xenopus laevis tadpole alpha-globin genes and the amino acid sequence of the three major tadpole alpha-globin polypeptides. Nucl. Acids Res 13, 5407-5421
5. Bass, N. M., Manning, J. A., Ockner, R. K., Gordon, J. I., Seetharam, S. and Alpers, D. H. (1985). Regulation of the biosynthesis of two distinct fatty acid-binding proteins in rat liver and intestine. Influences of sex difference and clofibrate. J. Biol. Chem. 260, 1432-1436.
6. Bienz, M. (1994) Homeotic genes and positional signaling in the Drosophila viscera. Trend. Genet. 10, 22-26.
7. Boterenbrood, E. C. and Nieuwkoop, P. D. (1973). The formation of the mesoderm in urodelean amphibians. V. Its regional induction by the endoderm. Roux's Arch. Dev. Biol. 173, 319-332.
8. Cai, H., Szeberenyi, J. and Cooper, G. M. (1990). Effect of a dominant inhibitory Ha-ras mutation on mitogenic signal transduction in NIH 3T3 cells. Mol. Cell. Biol. 10, 5314-5323.
9. Cooke, J. and Smith, J. C. (1987). The midblastula cell cycle transition and the character of mesoderm in u. v.-induced nonaxial Xenopus development. Development 99, 197-210.
10. Dale, L. and Slack, J. M. W. (1987). Fate map for the 32-cell stage of Xenopus laevis Development 99, 527-51
11. Dale, L., Matthews, G. and Colman, A. (1993). Secretion and mesoderm-inducing activity of the TGF-β-related domain of Xenopus Vg1. EMBO J. 12, 4471-4480.
12. Feig, L. A. and Cooper, G. M. (1988). Inhibition of NIH 3T3 cell proliferation by a mutant ras protein with preferential affinity for GDP. Mol. Cell. Biol. 8, 3235-3243.
13. Gamer, L. W. and Wright, C. V. E. (1995). Autonomous Endodermal Determination in Xenopus: Regulation of Expression of the Pancreatic Gene Xlhbox-8. Dev. Biol. 171, 240-251.
14. Gerhart, J. C., Danilchik, M., Doniach, T., Roberts, S., Rowning, B. and Stewart, R. (1989). Cortical rotation of the Xenopus egg: consequences for the antero-posterior pattern of embryonic dorsal development. Development 107 Supplement, 37-51.
15. Gittes, G. K. and Rutter, W. J. (1992). Onset of cell-specific gene expression in the developing mouse pancreas. Proc. Natl. Acad. Sci. USA 89, 1128-1132.
16. Graff, J. M., Thies, R. S., Song, J. J., Celeste, A. J. and Melton, D. A. (1994). Studies with a Xenopus BMP receptor suggest that ventral mesoderm-inducing signals override dorsal signals in vivo. Cell 79, 169-179.
17. Grunz, H. (1983). Change in differentiation pattern of Xenopus laevis ectoderm by variation of the incubation time and concentration of vegetalising factor. Roux's Arch. Dev. Biol. 192, 130-137.
18. Hemmati-Brivanlou, A. and Melton, D. A. (1992). A truncated activin receptor dominantly inhibits mesoderm induction and formation of axial structures in Xenopus embryos. Nature 359, 609-614.
19. Hemmati-Brivanlou, A. and Melton, D. A. (1994). Inhibition of activin signaling promotes neuralization in Xenopus laevis. Cell 77, 273-281
20. Hemmati-Brivanlou, A., Kelly, O. G. and Melton, D. A. (1994). Follistatin, an antagonist of activin, is expressed in the Spemann Organizer and displays direct neuralizing activity. Cell 77, 283-295.
21. Holtfreter, J. (1938a). Differenzierungspotenzen isolierter Teile der Urodelengastrula. Wilhelm Roux Arch. EntwMech. Org. 138, 522-656.
22. Holtfreter, J. (1938b). Differenzierungspotenzen isolierter Teile der Anurengastrula. Wilhelm Roux Arch. EntwMech. Org 138, 657-738.
23. Hopwood, N. D., Pluck, A. and Gurdon, J. B. (1989). A Xenopus mRNA related to Drosophila twist is expressed in response to induction in the mesoderm and the neural crest Cell 59, 893-903.
24. Isaacs, H. V., Pownall, M. E. and Slack, J. M. W. (1994). eFGF regulates Xbra expression during Xenopus gastrulation. EMBO J. 13, 4469-4481.
25. Jones, E. A., Snape, A. M. and Sargent, T. D. (1989). Transcriptional regulation of a Xenopus embryonic epidermal keratin gene. Development 106, 399-405.
26. Jones, E. A., Abel, M. H. and Woodland, H. R. (1993). The possible role of mesodermal growth factors in the formation of endoderm in Xenopus laevis. Roux's Arch. Dev. Biol. 202, 233-239.
27. Kao, K. R. and Elinson, R. P. (1988). The entire mesodermal mantle behaves as Spemann's organizer in dorsoanterior enhanced Xenopus laevis embryos. Dev. Biol. 127, 64-77.
28. Kessler, D. S. and Melton, D. A. (1994). Vertebrate embryonic induction: Mesodermal and neural patterning. Science 266, 596-604.
29. Kessler, D. S. and Melton, D. A. (1995). Induction of dorsal mesoderm by soluble mature Vg1 protein. Development 121, 2155-2164.
30. Kintner, C. R. and Melton, D. A. (1987). Expression of Xenopus N-CAM RNA in ectoderm as an early response to neural induction. Development 99, 311-325.
31. Klein, P. S. and Melton, D. A. (1994). Hormonal regulation of embryogenesis: The formation of mesoderm in Xenopus laevis. Endocrine Reviews 15, 326-341.
32. Kocher-Becker, U. and Tiedemann, H. (1971) Induction of mesodermal and endodermal structures and primordial germ cells in Triturus ectoderm by a vegetalising factor from chick embryos. Nature 233, 655-666.
33. Kogawa, K., Nakamura, T., Sugino, K., Takio, K., Titani, K. and Sugino, H. (1991). Activin-binding protein is present in pituitary. Endocrinology 128, 1434-1440.
34. Krieg, P. A. and Melton, D. A. (1984). Functional messenger RNAs are produced by SP6 in vitro transcription of cloned cDNAs. Nucl. Acids Res. 12, 7057-7070.
35. Kreig, P. A., Varnum, S., Wormington, M. and Melton, D. A. (1989). The mRNA encoding elongation factor 1α (EF1α) is a major transcript at the mid blastula transition in Xenopus laevis embryos. Dev. Biol. 133, 93-100.
36. Ku, M. and Melton, D. A. (1993). Xwnt-11: a maternally expressed Xenopus wnt gene. Development 119, 1161-1173.
37. Lamb, T. M., Knecht, A. K., Smith, W. C., Stachel, S. E., Economides, A. N., Stahl, N., Yancopolous, G. D. and Harland, R. M. (1992). Neural induction by the secreted polypeptide Noggin. Science 262, 713-718
38. Maeno, M., Ong, R. C., Suzuki, A., Ueno, N. and Kung, H. (1994). A truncated bone morphogenetic protein 4 receptor alters the fate of ventral mesoderm to dorsal mesoderm: Role of animal pole tissue in the development of ventral mesoderm. Proc. Natl. Acad. Sci. USA 91, 10260-10264
39. Minuth, M. and Grunz, H. (1980). The formation of mesodermal derivatives after induction with vegetalising factor depends on secondary cell interactions. Cell Differentiation 9, 229-238.
40. Moody, S. and Kline, M. (1990). Segregation of fate during cleavage of frog (Xenopus laevis) blastomeres Anat. Embryol. 182, 347-362.
41. Nakamura, O. and Kishiyama, K. (1971). Prospective fates of blastomeres at the 32 cell stage of Xenopus laevis embryos. Proc. Japan Acad. 47, 407-412
42. Nakamura, T., Takio, K., Eto, Y., Shibai, H., Titani, K. and Sugino, H. (1989). Activin-binding protein from rat ovary is follistatin. Science 247, 836-838.
43. Nieuwkoop, P. D. and Faber, J. (1967). Normal Table of Xenopus laevis. Amsterdam: Daudin.
44. Nieuwkoop, P. D. (1973). The 'organisation center' of the amphibian embryo: its origin, spatial organisation, and morphogenetic action. Adv. Morphogen. 10, 1-39.
45. Nieuwkoop, P. D. (1977). Origin and establishment of embryonic polar axes in amphibian development. Cur. Top. Dev. Biol. 11, 115-132.
46. Ogi, K.-I. (1967). Determination in the development of the amphibian embryo. Sci Rep. Tohoku Univ. Ser. IV (Biol.) 33, 239-247.
47. Ogi, K.-I. (1969). Regulative capacity in the early amphibian embryo. Res. Bull. Dept. Gen. Ed. Nagoya University 13, 31-40.
48. Ohlsson, H., Karlsson, K. and Edlund, T. (1993). IPF1, a homeodomain-containing transactivator of the insulin gene EMBO J. 12, 4251-4259.
49. Okada, T. S. (1953). On the role of the mesoderm in the differentiation of the presumptive endoderm. Mem. Coll Sci. Univ. Kyoto 20, 157-162.
50. Okada, T. S. (1954a). Experimental studies on the differentiation of the endodermal organs in Amphibia I. Significance of the mesencyhmatous tissue to the differentiation of the presumptive endoderm. Mem. Coll. Sci. Univ Kyoto 21, 1-6.
51. Okada, T. S. (1954b). Experimental studies on the differentiation of the endodermal organs in Amphibia. II. Differentiating potencies of the presumptive endoderm in the presence of the mesodermal tissues. Mem. Coll. Sci. Univ. Kyoto 21, 7-14
52. Ruiz i Altaba, A. (1993). Induction and axial patterning of the neural plate: planar and vertical signals. J. Neurobiol. 24, 1276-1304.
53. Saxen, L. (1989) Neural induction. Int. J. Dev. Biol. 33, 21-48.
54. Schulte-Merker, S., Smith, J. C. and Dale, L. (1994). Effects of truncated activin and FGF receptors and of follistatin on the inducing activities of BVg1 and activin: does activin play a role in mesoderm induction? EMBO J. 13, 3533-3541.
55. Shi, V. and Par Haves, W. (1994). Thyroid hormone-dependant regulation of the intestinal fatty acid-binding protein gene during amphibian metamorphosis. Dev. Biol. 161, 48-58.
56. Shuldiner, A. R., Phillips, S., Roberts, C. T., LeRoith, D. and Roth, J. (1989). Xenopus laevis contains two nonallelic preproinsulin genes. cDNA cloning and evolutionary perspective. J. Biol. Chem. 264, 9428-32.
57. Skaer, H. (1993). The alimentary canal. In The Development of Drosophila Melanogaster (ed. M. Bate and A. Martinez Arias), pp. 941-1012. New York: Cold Spring Harbor Laboratory Press.
58. Slack, J. M. W. (1993). Embryonic induction. Mech. Dev. 41, 91-107.
59. Smith, J. C., Price, B. M. J., Green, J. B. A., Weigel, D. and Herrmann, B. G. (1991) Expression of a Xenopus homolog of Brachyury (T) is an immediate-early response to mesoderm induction. Cell 71, 731-739.
60. Stutz, F. and Sphor, G. (1986). Isolation and characterization of sarcoplasmic actin genes expressed in Xenopus laevis embryogenesis J. Mol. Biol 187, 349-361.
61. Sweetser, D. A., Heuckeroth, R. O. and Gordon, J. I. (1987). The metabolic significance of mammalian fatty-acid-binding proteins: abundant proteins in search of a function. Annu. Rev. Nutr. 7, 337-359.
62. Takata, C. and Yamada, T. (1960). Endodermal tissues developed from the isolated newt ectoderm under the influence of guinea pig bone marrow. Embryologica 5, 8-20.
63. Takata, C. (1960). The differentiation in vivo of the isolated endoderm under the influence of the mesoderm in Triturus Pyrrhogaster. Embryologica 5, 38-70
64. Thomsen, G.,H. and Melton, D. A. (1993). Processed Vg1 protein is an axial mesoderm inducer in Xenopus. Cell 74, 433-441.
65. Weeks, D. L. and Melton, D. A. (1987). A maternal mRNA localized to the vegetal hemisphere in Xenopus eggs codes for a growth factor related to TGF-β. Cell 51, 861-867.
66. Wilson, P. A. and Melton, D. A. (1994). Mesodermal patterning by an inducer gradient depends on secondary cell-cell communication. Curr. Biol. 4, 676-686.
67. Wright C. V. E., Schnegelsberg, P. and De Robertis, E. M. (1988). Xlhbox8: a novel Xenopus homeoprotein restricted to a narrow band of endoderm. Development 105, 787-794.
68. Wu, M. and Gerhart, J. (1991) Raising Xenopus in the laboratory. Meth. Cell Biol. 36, 3-17.
69. Wylie, C. C., Snape, A., Heasman, J. and Smith, J. C. (1987). Vegetal pole cells and commitment to form endoderm in Xenopus laevis. Dev. Biol. 119, 496-502.