The Xenopus tadpole gut: Fate maps and morphogenetic movements

Development

Volumn 127, Issue 2, 2000, Pages 381-392

  Chalmers, Andrew D ^a   Slack, Jonathan M W ^a  

^a University of Bath ^*  (United Kingdom)

Author keywords

Endoderm; Epithelium; Fate map; Gut; Intestine; Liver; Mesoderm; Morphogenesis; Pancreas; Radial intercalation; Smooth muscle; Xenopus laevis

Indexed keywords

ANIMAL TISSUE; ARTICLE; EMBRYO; ENDODERM; INTESTINE; INTESTINE EPITHELIUM; MORPHOGENESIS; NONHUMAN; PRIORITY JOURNAL; SMOOTH MUSCLE; TADPOLE; XENOPUS LAEVIS;

ANIMALS; CARBOCYANINES; CELL LINEAGE; CELL MOVEMENT; DEXTRANS; ENDODERM; FLUORESCEINS; GASTRULA; GENE EXPRESSION REGULATION, DEVELOPMENTAL; INTESTINES; MICROSCOPY, FLUORESCENCE; MORPHOGENESIS; RESPIRATORY SYSTEM; XENOPUS LAEVIS;

ANIMALIA; VERTEBRATA; XENOPUS LAEVIS;

EID: 0033972450     PISSN: 09501991     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (51)

1. Ahlgren, U., Plaff, S. L., Jessell, T. M., Edlund, T. and Edlund, H. (1997). Independent requirement for ISL1 in Formation of pancreatic mesenchyme and islet cells. Nature 385, 257-260.
2. Andrew, A. and Rawdon, B. B. (1990). Intestinal mesenchyme provokes differentiation of intestinal endocrine cells in gizzard endoderm. Differentiation 43, 165-174.
3. Beck, C. W. and Slack, J. M. W. (1999). A developmental pathway controlling outgrowth of the Xenopus tail bud. Development 126, 1611-1620.
4. Bienz, M. (1994). Homeotic genes and positional signalling in the Drosophila viscera. Trends Genet. 10, 22-26.
5. Bouwmeester, T., Kim, S., Sasai, Y., Lu, B. and De Robertis, E. M. (1996) Cerberus is a head-inducing secreted factor expressed in the anterior endoderm of Spemann's organizer. Nature 382, 595-601.
6. Campione, M., Steinbeisser, H., Schweickert, A., Deissler, K., Bebber, F. V., Lowe, L. A., Nowotschin, S., Viebahn, C., Haffter, P., Kuehen, M. R. and Blum, M. (1999). The homeobox gene Pitx2: mediator of asymmetric left-right signalling in vertebrate heart and gut looping. Development 126, 1225-1234.
7. Chalmers, A. D. and Slack, J. M. W. (1998). Development of the gut in Xenopus laevis. Dev. Dynam. 212, 509-521.
8. Dale, L. and Slack, J. M. W. (1987). Fate map for the 32-cell stage of Xenopus laevis. Development 99, 527-51.
9. Gimlich, R. L. and Braun, J. (1985). Improved fluorescent compounds for tracing cell lineage. Dev. Biol. 109, 509-514.
10. Godsave, S. F., Isaacs, H. V. and Slack, J. M. W. (1988). Mesoderm-inducing factors: a small class of molecules. Development 102, 555-566.
11. Goette, A. (1875). Die Entwicklungsgeschichte der Unke. Leipzig: Leopold Voss.
12. Haffen, K., Kedinger, M. and Simon-Assmann, P. (1987). Mesenchyme-Dependent Differentiation of Epithelial Progenitor Cells in the Gut. J. Ped. Gastroenterol. Nutr. 6, 14-23.
13. Harrison, K. A., Thaler, J., Pfaff, S. L., Gu, H. and Kehrl, J. H. (1999) Pancreas dorsal lobe agenesis and abnormal islets of Langerhans in Hlxb9-deficient mice. Nature Genetics 23, 71-75.
14. Hebrok, M., Kim, S. K. and Melton, D. A. (1998). Notochord repression of endodermal sonic hedgehog permits pancreas development. Genes Dev. 12, 1705-1713.
15. Henry, G. L. and Melton, D. A. (1998). Mixer, a Homeobox Gene Required for Endoderm Development. Science 281, 91-96.
16. Hudson, C., Clements, D., Friday, R. V., Stott, D, and Woodland, H. R. (1997). Xsox17a and -B Mediate Endoderm Formation in Xenopus. Cell 91. 397-405.
17. Ishizuya-Oka, A. and Mizuno, T. (1984). Intestinal cytodifferentialion in vitro of chick stomach endoderm induced by the duodenal mesenchyme. J. Embryol. Exp. Morph. 82, 163-176.
18. Joseph, E. M. and Melton, D. A. (1998). Mutant Vg1 ligands disrupt endoderm and mesoderm formation in Xenopus embryos. Development 125, 2677-2685.
19. Keller, R. E. (1975). Vital dye mapping of the gastrula and neurula of Xenopus laevis. I. prospective areas and morphogenetic movements in the superficial layer. Dev. Biol. 42, 222-241.
20. Keller, R. E. (1976). Vital dye mapping of the gastrula and neurula of Xenopus luevis. II. Prospective areas and morphogenic movements of the deep layer. Der. Biol. 51, 118-137.
21. Keller, R. E. (1980). The cellular basis of epiboly: an SEM study of deep-cell rearrangement during gastrulation in Xenopus laevis. J. Embryol. Exp. Morph. 60, 201-234.
22. Keller, R. E. (1984). The cellular basis of gastrulation in Xenopus laevis: Active, postinvolution convergence and extension by mediolateral interdigitation. Am. Zool. 24, 589-603.
23. Keller, R. E. (1987). Cell Rearrangement in Morphogenesis. Zool. Sci. 4, 763-779.
24. Keller, R. E., Danilchik, M. and Gimlich, R. (1985). The function and mechanism of convergent extension during gastrulation of Xenopus laevis. J. Embryol. Exp. Morph. 89, 185-209.
25. Kordylewski, L. (1983). Light and Electron Microscope Observations of the Development of Intestinal Musculature in Xenopus. Z. Mikrosk.-anat. Forsh 97, 719-734.
26. Kim, S. K. and Melton, D. A. (1998). Pancreas development is promoted by cyclopamine, a hedgehog signaling inhibitior. Proc. Natl. Acad. Sci. USA 95, 13036-13041.
27. Lemaire, P., Darras, S., Caillol, D. and Kodjabachian, L. (1998) A role for the vegetally expressed Xenopus gene Mix. 1 in endoderm formation and in the restriction of mesoderm to the marginal zone. Development 125, 2371-2380.
28. Li, H., Arber, S., Jessell, T. M. and Edlund, H. (1999). Selective agenesis of the dorsal pancreas in mice lacking homeobox gene Hlxb9. Nature Genetics 23, 67-70.
29. Mathews, W. W. and Schoenwolf, G. C. (1998). Atlas of Descriptive Embryology. New Jersey: Prentice-Hall.
30. Matsushita, S. (1995). Fate mapping study of the splanchnopleural mesoderm of the 1.5-day-old chick embryo. Roux's Arch. Dev. Biol. 204, 392-399.
31. Matsushita, S. (1996). Fate mapping study of the endoderm of the 1.5 day-old chick embryo. Roux's Arch. Dev. Biol. 205, 225-231.
32. Minsuk, S. B. and Keller, R. E. (1997). Surface mesoderm in Xenopus: a revision of the stage 10 fate map. Dev. Genes Evol. 207, 389-401.
33. Muller, H. J. and Hausen, P. (1995). Epithelial cell polarity in early Xenopus development. Dev. Dynam. 202, 405-420.
34. Nieuwkoop, P. D. and Faber, J. (1967). Normal Table of Xenopus laevis (Daudin). Amsterdam: North-Holland.
35. Okada, T. S. (19571. The Pluripotency of the Pharyngeal Primordium in Urodelan Neurulae. J. Embryol. Exp. Morph. 5, 438-448.
36. Okada, T. S. (1960). Epithelio-Mesenchymal Relationships in the Regional Differentiation of the Digestive Tract in the Amphibian Embryo. Roux's Arch. Ent. Mech. 152, 1-21.
37. Rawdun, B. B. and Andrew, A. (1993). Origin and differentiation of gut endocrine cells. Histol. Histopath. 8, 567-580.
38. Roberts, D. J., Johnson, R. L., Burke, A. C., Nelson, C. E., Morgan, B. A. and Tabin, C. (1995). Sonic hedgehog is an endodermal signal inducing Bmp-4 and Hox genes during induction and regionalization of the chick hindgut. Development 121, 3163-3174.
39. Roberts, D. J., Smith, D. M., Goff, D. J. and Tabin, C. J. (1998) Epithelial-mesenchymal signaling during the regionalization of the chick gut. Development 125, 2791-2801.
40. Sasai, Y., Lu, B., Piccolo, S. and DeRobertis, E. (1996). Endoderm induction by the organiser-secreted factors chordin and noggin in Xenopus animal caps. EMBO J. 15, 4547-4555.
41. Shi, Y.-B. and Hayes, W. P. (1994). Thyroid Hormone-Dependent Regulation of the Intestinal Fatty Acid-Binding Protein Gene during Amphibian Metamorphosis. Dev. Biol. 161, 48-58.
42. Smith, J. C. and Malacinski, G. M. (1983). The origin of the mesoderm in an anuran. Xenopus laevis, and a urodele, Ambystoma mexicanum. Dev. Biol. 98, 250-4.
43. Tahara, Y. and Nakamura, O. (1961). Topography of the Presumptive Rudiments in the Endoderm of the Anuran Neurula. J. Embryol. Exp. Morph. 9, 138-158.
44. Warga, M. R. and Nusslein-Volhard, C. (1999). Origin and development of the Zebrafish endoderm. Development 126, 827-838.
45. Wolpert, L. (1998). Principles of Development. Oxford: Oxford University Press.
46. Wright, C. V., Schnegelsberg, P. and De Robertis, E. M. (1988). X1Hbox 8: a novel homeo protein restricted to a narrow band of endoderm. Development 104, 787-794.
47. Yasugi, S. and Mizuno, T. (1978). Differentiation of the digestive tract epithelium under the influence of the heterologous mesenchyme of the digestive tract in the bird embryos. Dev. Growth Diff. 20, 261-267.
48. Yasugi, S. and Mizuno, T. (1990). Mesenchymal-Epithelial Interactions in the Organogenesis of Digestive Tract. Zool. Sci. 7, 159-170.
49. Yokouchi, Y., Sakiyama, J. and Kuroiwa, A. (1995). Coordinated Expression of Abd-B Subfamily Genes of the HoxA Cluster in the Developing Digestive Tract of Chick Embryo. Dev. Biol. 169, 76-89.
50. Yost, H. J. (1998). Left-right development in Xenopus and Zebrafish. Sem. Cell Dev. Biol. 9, 61-66.
51. Zhang, J., Houston, D. W., King, M. L., Payne, C., Wylie, C. and Heasman, J. (1998). The role of maternal VegT in establishing the primary germ layers in Xenopus embryos. Cell 94, 515-524.