Loss of ectodermal competence for lateral line placode formation in the direct developing frog Eleutherodactylus coqui

Developmental Biology

Volumn 213, Issue 2, 1999, Pages 354-369

  Schlosser, Gerhard ^a   Kintner, Chris ^b   Northcutt, R Glenn ^c  

^a Hanse Wissenschaftskolleg   (Germany)

^b SALK INSTITUTE FOR BIOLOGICAL STUDIES   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Competence; Direct development; Eleutherodactylus coqui; Evolution; Lateral line; NeuroD; Placodes; Xenopus laevis

Indexed keywords

AMBYSTOMA; ANIMAL CELL; ARTICLE; ECTODERM; EMBRYO; EMBRYO DEVELOPMENT; EVOLUTION; FROG; GENE EXPRESSION; LATERAL LINE SYSTEM; MOLECULAR CLONING; NERVE CELL; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; TISSUE INDUCTION; TRANSPLANTATION;

AMBYSTOMA; AMBYSTOMA MEXICANUM; ANIMALIA; ANURA; ELEUTHERODACTYLUS COQUI; XENOPUS LAEVIS;

EID: 0033568643     PISSN: 00121606     EISSN: None     Source Type: Journal    
DOI: 10.1006/dbio.1999.9404     Document Type: Article

References (72)

1. Adamson L., Harrison R. G., Bayley I. The development of the whistling frog Eleutherodactylus martinicensis of Barbados. Proc. Zool. Soc. London. 133:1949;453-469.
2. Andres G. Untersuchungen an Chimären von Triton und Bombinator. I. Entwicklung xenoplastischer Labyrinthe und Kopfganglien. Genetica. 24:1949;387-534.
3. Bock W. J., von Wahlert G. Adaptation and the form-function complex. Evolution. 19:1965;269-299.
4. Bordzilovskaya N. P., Dettlaff T. A., Duhon S. T., Malacinski G. M. Developmental-stage series of axolotl embryos. Armstrong J. B., Malacinski G. M. Developmental Biology of the Axolotl. 1989;201-219 Oxford Univ. Press, New York.
5. Chitnis A., Kintner C. Sensitivity of proneural genes to lateral inhibition affects the pattern of primary neurons in Xenopus embryos. Development. 122:1996;2295-2301.
6. Collazo A., Fraser S. E., Mabee P. M. A dual embryonic origin for vertebrate mechanoreceptors. Science. 264:1994;426-430.
7. Coombs S., Görner P., Münz H. The Mechanosensory Lateral Line: Neurobiology and Evolution. 1989;Springer, New York.
8. Dorsky R. I., Rapaport D. H., Harris W. A. Xotch inhibits cell differentiation in the Xenopus retina. Neuron. 14:1995;487-496.
9. Duellman W. E. Reproductive strategies of frogs. Sci. Am. 267:1992;80-87.
10. Duellman W. E., Trueb L. Biology of Amphibians. 1986;McGraw-Hill, New York.
11. Elinson R. P. Direct development in frogs: Wiping the recapitulationist slate clean. Semin. Dev. Biol. 1:1990;263-270.
12. Fang H., Elinson R. P. Patterns of distal-less gene expression and inductive interactions in the head of the direct developing frog Eleutherodactylus coqui. Dev. Biol. 179:1996;160-172.
13. Fang H., Elinson R. P. Evolutionary alteration in anterior patterning: otx2 expression in the direct developing frog Eleutherodactylus coqui. Dev. Biol. 205:1999;233-239.
14. Fritzsch B. The lateral-line and inner-ear afferents in larval and adult urodeles. Brain Behav. Evol. 31:1988;325-348.
15. Fritzsch B. Diversity and regression in the amphibian lateral line and electrosensory system. Coombs S., Görner P., Münz H. The Mechanosensory Lateral Line. 1989;99-114 Springer, New York.
16. Fritzsch B. The evolution of metamorphosis in amphibians. J. Neurobiol. 21:1990;1011-1021.
17. Fritzsch B., Wake M. The distribution of ampullary organs in Gymnophiona. J. Herpetol. 20:1986;90-93.
18. Gallagher B. C., Henry J. J., Grainger R. M. Inductive processes leading to inner ear formation during Xenopus development. Dev. Biol. 175:1996;95-107.
19. Gilbert S. F., Opitz J. M., Raff R. A. Resynthesizing evolutionary and developmental biology. Dev. Biol. 173:1996;357-372.
20. Hanken J., Klymkowsky M. W., Alley K. E., Jennings D. H. Jaw muscle development as evidence for embryonic repatterning in direct-developing frogs. Proc. R. Soc. London Ser. B. 264:1997;1349-1354.
21. Hanken J., Klymkowsky M. W., Summers C. H., Seufert D. W., Ingebrigtsen N. Cranial ontogeny in the direct-developing frog, Eleutherodactylus coqui (Anura, Leptodactylidae), analyzed using whole-mount immunohistochemistry. J. Morphol. 211:1992;95-118.
22. Harland R. G. In situ hybridization: An improved whole-mount method for Xenopus embryos. Methods Cell Biol. 36:1991;685-695.
23. Holtfreter J. Morphologische Beeinflussung von Urodelenektoderm bei xenoplastischer Transplantation. Roux Arch. Entw. Mech. 133:1935;367-426.
24. Jacobson M., Huang S. Neurite outgrowth traced by means of horseradish peroxidase inherited from neuronal ancestral cells in frog embryos. Dev. Biol. 110:1985;102-113.
25. Jeffery W. R. Evolution of ascidian development. Bioscience. 47:1997;417-425.
26. Knouff R. A. The developmental pattern of ectodermal placodes in Rana pipiens. J. Comp. Neurol. 62:1935;17-71.
27. Lee J. E. Basic helix-loop-helix genes in neural development. Curr. Opin. Neurobiol. 7:1997;13-20.
28. Lee J. E., Hollenberg S. M., Snider L., Turner D. L., Lipnick N., Weintraub H. Conversion of Xenopus ectoderm into neurons by NeuroD, a basic helix-loop-helix protein. Science. 268:1995;836-844.
29. Lutz B. Trends towards non-aquatic and direct development in frogs. Copeia. 1947:1947;242-252.
30. Lynn W. G. The embryology of Eleutherodactylus nubicola, an anuran which has no tadpole stage. Contrib. Embryol. Carnegie Inst. Washington. 190:1942;27-62.
31. Lynn W. G. Types of amphibian metamorphosis. Am. Zool. 1:1961;151-161.
32. Ma Q. F., Chen Z. F., Barrantes I. D., de la Pompa J. L., Anderson D. J. Neurogenin1 is essential for the determination of neuronal precursors for proximal cranial sensory ganglia. Neuron. 20:1998;469-482.
33. Metscher B. D., Northcutt R. G., Gardiner D. M., Bryant S. V. Homeobox genes in axolotl lateral line placodes and neuromasts. Dev. Genes Evol. 207:1997;287-295.
34. Moury J. D., Hanken J. Early cranial neural crest migration in the direct-developing frog, Eleutherodactylus coqui. Acta Anat. 153:1995;243-253.
35. Naya F. J., Huang H. P., Qiu Y. H., Mutoh H., DeMayo F. J., Leiter A. B., Tsai M. J. Diabetes, defective pancreatic morphogenesis, and abnormal enteroendocrine differentiation in Beta2/Neurod-deficient mice. Gene Develop. 11:1997;2323-2334.
36. Neave B., Holder N., Patient R. A graded response to BMP-4 spatially coordinates patterning of the mesoderm and ectoderm in the zebrafish. Mech. Dev. 62:1997;183-195.
37. Nguyen V. H., Schmid B., Trout J., Connors S. A., Ekker M., Mullins M. C. Ventral and lateral regions of the zebrafish gastrula, including the neural crest progenitors, are established by a bmp2b/swirl pathway of genes. Dev. Biol. 199:1998;93-110.
38. Nieuwkoop P. D., Faber J. Normal Table of Xenopus laevis (Daudin). 1967;North-Holland, Amsterdam.
39. Nieuwkoop P. D., Johnen A. G., Albers B. The Inductive Nature of Early Chordate Development. 1985;Cambridge Univ. Press, Cambridge.
40. Noble G. K. The value of life history data in the study of the evolution of the amphibia. Ann. N. Y. Acad. Sci. 30:1927;31-128.
41. Northcutt R. G. The phylogenetic distribution and innervation of craniate mechanoreceptive lateral lines. Coombs S., Görner P., Münz H. The Mechanosensory Lateral Line. 1989;17-78 Springer, New York.
42. Northcutt R. G. The phylogeny of octavolateralis ontogenies: A reaffirmation of Garstang's hypothesis. Webster D. B., Fay R. R., Popper A. N. The Evolutionary Biology of Hearing. 1992;21-47 Springer, New York.
43. Northcutt R. G. A reassessment of Goodrichs model of cranial nerve phylogeny. Acta Anat. 148:1993;71-80.
44. Northcutt R. G. The origin of craniates: Neural crest, neurogenic placodes, and homeobox genes. Isr. J. Zool. 42:1996;273-313.
45. Northcutt R. G. Evolution of gnathostome lateral line ontogenies. Brain Behav. Evol. 50:1997;25-37.
46. Northcutt R. G., Brändle K. Development of branchiomeric and lateral line nerves in the axolotl. J. Comp. Neurol. 355:1995;427-454.
47. Northcutt R. G., Brändle K., Fritzsch B. Electroreceptors and mechanosensory lateral line organs arise from single placodes in axolotls. Dev. Biol. 168:1995;358-373.
48. Northcutt R. G., Catania K. C., Criley B. B. Development of lateral line organs in the axolotl. J. Comp. Neurol. 340:1994;480-514.
49. Northcutt R. G., Gans C. The genesis of neural crest and epidermal placodes: A reinterpretation of vertebrate origins. Q. Rev. Biol. 58:1983;1-28.
50. Raff R. A. The Shape of Life. 1996;Univ. of Chicago Press, Chicago.
51. Roth G., Nishikawa K. C., Naujoks-Manteuffel C., Schmidt A., Wake D. B. Paedomorphosis and simplification in the nervous system of salamanders. Brain Behav. Evol. 42:1993;137-170.
52. Sadaghiani B., Thiébaud C. H. Neural crest development in the Xenopus laevis embryo, studied by interspecific transplantation and scanning electron microscopy. Dev. Biol. 124:1987;91-110.
53. Salthe S. N., Mecham J. S. Reproductive and courtship patterns. Lofts B. Physiology of the Amphibia II. 1974;309-521 Academic Press, New York.
54. Sasai Y., De Robertis E. M. Ectodermal patterning in vertebrate embryos. Dev. Biol. 182:1997;5-20.
55. Schlosser G., Roth G. Evolution of nerve development in frogs. II. Modified development of the peripheral nervous system in the direct-developing frog Eleutherodactylus coqui (Leptodactylidae). Brain Behav. Evol. 50:1997a;94-128.
56. Schlosser G., Roth G. Development of the retina is altered in the directly developing frog Eleutherodactylus coqui (Leptodactylidae). Neurosci. Lett. 224:1997b;153-156.
57. Servetnick M., Grainger R. M. Changes in neural and lens competence in Xenopus ectoderm: evidence for an autonomous developmental timer. Development. 112:1991;177-188.
58. Smith S. C., Lannoo M. J., Armstrong J. B. Development of the mechanorececeptive lateral-line system in the axolotl: Placode specification, guidance of migration, and the origin of neuromast polarity. Anat. Embryol. 182:1990;171-180.
59. Sommer L., Ma Q., Anderson D. J. Neurogenins, a novel family of atonal-related bHLH transcription factors, are putative mammalian neuronal determination genes that reveal progenitor heterogeneity in the developing CNS and PNS. Mol. Cell. Neurobiol. 8:1996;221-241.
60. Stephenson W. G. Observations on the development of the amphicoelus frogs, Leiopelma and Ascaphus. Zool. J. Linn. Soc. 42:1951;18-28.
61. Stone L. S. Experiments on the development of the cranial ganglia and the lateral line sense organs in Amblystoma punctatum. J. Exp. Zool. 35:1922;421-496.
62. Stone L. S. Experiments on the transplantation of placodes of the cranial ganglia in the amphibian embryo. IV. Heterotopic transplantation of the postauditory placodal material upon the head and body of Amblystoma punctatum. J. Comp. Neurol. 48:1929;311-330.
63. Stone L. S. The development of lateral-line sense organs in amphibians observed in living and vital-stained preparations. J. Comp. Neurol. 57:1933;507-540.
64. Townsend D. S., Stewart M. M. Direct development in Eleutherodactylus coqui (Anura: Leptodactylidae): A staging table. Copeia. 1985:1985;423-436.
65. Wagner G. P. Homologues, natural kinds and the evolution of modularity. Am. Zool. 36:1996;36-43.
66. Wake D. B., Hanken J. Direct development in the lungless salamanders - what are the consequences for developmental biology, evolution and phylogenesis. Int. J. Dev. Biol. 40:1996;859-869.
67. Wake M. H. Phylogenesis of direct development and viviparity in vertebrates. Wake D. B., Roth G. Complex Organismal Functions: Integration and Evolution in Vertebrates. 1989;235-250 Wiley, Chichester.
68. Wray G. A., Bely A. E. The evolution of echinoderm development is driven by several distinct factors. Development. 1994:1994;97-106.
69. Wilson P. A., Lagna G., Suzuki A., Hemmati-Brivanlou A. Concentration-dependent patterning of the Xenopus ectoderm by BMP4 and its signal transducer Smad1. Development. 124:1997;3177-3184.
70. Yntema C. L. Experiments on the determination of the ear ectoderm in the embryo of Amblystoma punctatum. J. Exp. Zool. 65:1933;317-357.
71. Yntema C. L. Self-differentiation of heterotopic ear ectoderm in the embryo of Amblystoma punctatum. J. Exp. Zool. 80:1939;1-17.
72. Yntema C. L. An analysis of induction of the ear from foreign ectoderm in the salamander embryo. J. Exp. Zool. 113:1950;211-244.