Expression of multiple cadherins and catenins in the chick optic tectum

Molecular and Cellular Neurosciences

Volumn 12, Issue 4-5, 1998, Pages 240-255

  Miskevich, Frank ^a   Zhu, Yan ^a   Ranscht, Barbara ^b   Sanes, Joshua R ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b BURNHAM INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CADHERIN; CATENIN;

ANIMAL EXPERIMENT; ARTICLE; CELLULAR DISTRIBUTION; CHICKEN; GROWTH REGULATION; NERVOUS SYSTEM DEVELOPMENT; NONHUMAN; OPTIC TECTUM; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; SYNAPTOGENESIS;

EID: 0031786281     PISSN: 10447431     EISSN: None     Source Type: Journal    
DOI: 10.1006/mcne.1998.0718     Document Type: Article

References (61)

1. Aberle H., Butz S., Stappert J., Weissig H., Kemler R., Hoschuetzky H. Assembly of the cadherin-catenin complex in vitro with recombinant proteins. J. Cell Sci. 107:1994;3655-3663.
2. Arndt K., Redies C. Restricted expression of R-cadherin by brain nuclei and neural circuits of the developing chicken brain. J. Comp. Neurol. 373:1996;373-399.
3. Arndt K., Nakagawa S., Takeichi M., Redies C. Cadherins and the formation of neural circuitry in the vertebrate CNS. Cell Tissue Res. 290:1997;405-413.
4. Arndt K., Nakagawa S., Takeichi M., Redies C. Cadherin-defined segments and parasagittal cell ribbons in the developing chicken cerebellum. Mol. and Cell. Neurosci. 10:1998;211-228.
5. Bagnoli P., Gigliola F., Alesci R., Erichsen J. T. Distribution of neuropeptide Y, substance P, and choline acetyltransferase in the developing visual system of the pigeon and effects of unilateral retina removal. J. Comp. Neurol. 318:1992;392-414.
6. Bixby J. L., Zhang R. Purified N-cadherin is a potent substrate for the rapid induction of neurite outgrowth. J. Cell Biol. 110:1990;1253-1260.
7. Bradley R. S., Espeseth A., Kintner C. NF-protocadherin, a novel member of the cadherin superfamily, is required forXenopus. Curr. Biol. 8:1998;325-334.
8. Buxton R. S., Magee A. I. Structure and interactions of desmosomal and other cadherins. Semin. Cell Biol. 3:1992;157-167.
9. Chomczynski P., Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal. Biochem. 162:1987;156-159.
10. Detrick R. J., Dickey D., Kintner C. R. The effects of N-cadherin misexpression on morphogenesis in Xenopus embryos. Neuron. 4:1990;493-506.
11. Drazba J., Lemmon V. The role of cell adhesion molecules in neurite outgrowth on Muller cells. Dev. Biol. 138:1990;82-93.
12. Dunne J., Hanby A. M., Poulsom R., Jones T. A., Sheer D., Chin W. G., Da S. M., Zhao Q., Beverley P. C., Owen M. J. Molecular cloning and tissue expression offat, Genomics. 30:1995;207-223.
13. Fannon A. M., Colman D. R. A model for central synaptic junctional complex formation based on the differential adhesive specificities of the cadherins. Neuron. 17:1996;423-434.
14. Fredette B. J., Ranscht B. T-cadherin expression delineates specific regions of the developing motor axon-hindlimb projection pathway. J. Neurosci. 14:1994;7331-7346.
15. Fredette B. J., Miller J., Ranscht B. Inhibition of motor axon growth by T-cadherin substrata. Development. 122:1996;3163-3171.
16. Fushimi D., Arndt K., Takeichi M., Redies C. Cloning and expression analysis of cadherin-10 in the CNS of the chicken embryo. Dev. Dynamics. 209:1997;269-285.
17. Ganzler S. I. I., Redies C. R-cadherin expression during nucleus formation in chicken forebrain neuromeres. J. Neurosci. 15:1995;4157-4172.
18. Hall Z. W., Sanes J. R. Synaptic structure and development: The neuromuscular junction. Cell. 72:1993;99-121.
19. Hamburger V., Hamilton H. L. A series of normal stages in the development of the chick embryo. J. Morphol. 88:1951;49-82.
20. Hatta K., Takeichi M. Expression of N-cadherin adhesion molecules associated with early morphogenetic events in chick development. Nature. 320:1986;447-449.
21. Hatta K., Nose A., Nagafuchi A., Takeichi M. Cloning and expression of cDNA encoding a neural calcium-dependent cell adhesion molecule: its identity in the cadherin gene family. J. Cell Biol. 106:1998;873-881.
22. Hirano S., Kimoto N., Shimoyama Y., Hirohashi S., Takeichi M. Identification of a neural α-catenin as a key regulator of cadherin function and multicellular organization. Cell. 70:1992;293-301.
23. Hunt S. P., Brecha N. The avian optic tectum: a synthesis of morphology and biochemistry. Comparative Neurology of the Optic Tectum. 1984;Plenum, New York. p. 619-648.
24. Inoue A., Sanes J. R. Lamina-specific connectivity in the brain: Roles for N-cadherin, neurotrophins, and glycoconjugates. Science. 276:1997;1428-1431.
25. Inoue T., Tanaka T., Suzuki S. C., Takeichi M. Cadherin-6 in the developing mouse brain: expression along restricted connection systems and synaptic localization suggest a potential role in neuronal circuitry. Dev. Dynamics. 211:1998;338-351.
26. Inuzuka H., Miyatani S., Takeichi M. R-cadherin: A novel Ca2+-dependent cell-cell adhesion molecule expressed in the retina. Neuron. 7:1991;69-79.
27. Itoh K., Ozaka M., Stevens B., Fields R. D. Activity-dependent regulation of N-cadherin in DRG neurons: Differential regulation of N-cadherin, NCAM, and L1 by distinct patterns of action potentials. J. Neurobiol. 33:1997;1-14.
28. Karten H. J., Cox K., Mpodozis J. Two distinct populations of tectal neurons have unique connections within the retinotectorotundal pathway of the pigeon (Columba livia). J. Comp. Neurol. 387:1997;449-465.
29. Kimura Y., Matsunami H., Takeichi M. Expression of cadherin-11 delineates boundaries, neuromeres, and nuclei in the developing mouse brain. Dev. Dynamics. 206:1996;455-462.
30. Kintner C. Regulation of embryonic cell adhesion by the cadherin cytoplasmic domain. Cell. 69:1992;225-236.
31. Kohmura N., Senzaki K., Hamada S., Kai N., Yasuda R., Watanabe M., Ishii H., Yasuda M., Mishina M., Yagi T. Diversity revealed by a novel family of cadherins expressed in neurons at a synaptic complex. Neuron. 20:1998;1137-1151.
32. Korematsu K., Nishi T., Okamura A., Goto S., Morioka M., Hamada J., Ushio Y. Cadherin-8 protein expression in gray matter structures and nerve fibers of the neonatal and adult mouse brain. Neuroscience. 87:1998;303-315.
33. Marrs J. A., Nelson W. J. Cadherin cell adhesion molecules in differentiation and embryogenesis. Int. Rev. Cytol. 165:1996;159-205.
34. Matsunaga M., Hatta K., Nagafuchi A., Takeichi M. Guidance of optic nerve fibres by N-cadherin adhesion molecules. Nature. 334:1988a;62-64.
35. Matsunaga M., Hatta K., Takeichi M. Role of N-cadherin cell adhesion molecules in the histogenesis of neural retina. Neuron. 1:1988b;289-295.
36. Miller J. R., Moon R. T. Signal transduction through β-catenin and specification of cell fate during embryogenesis. Genes Dev. 10:1996;2527-2539.
37. Miskevich F., Zhu Y., Tierney C., Ranscht B., Sanes J. R. Laminar distribution of cadherins in the chick optic tectum. Soc. Neurosci. Abstr. 23:1997;1975.
38. Nose A., Nagafuchi A., Takeichi M. Expressed recombinant cadherins mediate cell sorting in model systems. Cell. 54:1988;993-1001.
39. Obata S., Sago H., Mori N., Rochelle J. M., Seldin M. F., Davidson M., St. John T., Taketani S., Suzuki S. T. Protocadherin Pcdh2 shows properties similar to, but distinct from, those of classical cadherins. J. Cell Sci. 108:1995;3765-3773.
40. Ranscht B., Dours-Zimmermann M. T. T-cadherin, a novel cadherin cell adhesion molecule in the nervous system lacks the conserved cytoplasmic region. Neuron. 7:1991;391-402.
41. Redies C. Cadherins and the formation of neural circuitry in the vertebrate CNS. Cell Tissue Res. 290:1997;405-413.
42. Redies C., Inuzuka H., Takeichi M. Restricted expressions of N- and R-cadherin on neurites of the developing chicken CNS. J. Neurosci. 12:1992;3525-3534.
43. Redies C., Engelhart K., Takeichi M. Differential expression of N- and R-cadherin in functional neuronal systems and other structures of the developing chicken brain. J. Comp. Neurol. 333:1993;398-416.
44. Riehl R., Johnson K., Bradley R., Grunwald G. B., Cornel E., Lilienbaum A., Holt C. E. Cadherin function is required for axon outgrowth in retinal ganglion cells in vivo. Neuron. 17:1996;837-848.
45. Ruiz P., Brinkmann V., Ledermann B., Benzeno M., Grano C., Thalhammer C., Vogel F., Birchmeier C., Gunthert U., Franke W. W., Birchmeier W. Targeted mutation of plakoglobin in mice reveals essential functions of desmosomes in the embroyonic heart. J. Cell Biol. 135:1996;215-225.
46. Sanes J. R., Lichtman J. W. Development of the vertebrate neuromuscular junction. Ann. Rev. Neurosci. 22:1999;384-442.
47. Sano K., Tanihara H., Heimark R. L., Obata S., Davidson M., St. John T., Taketani S., Suzuki S. Protocadherins: A large family of cadherin-related molecules in central nervous system. EMBO J. 12:1993;2249-2256.
48. Schaeren-Wiemers N., Gerfin-Moser A. A single protocol to detect transcripts of various types and expression levels in neural tissue and cultured cells: In situ hybridization using digoxigenin-labelled cRNA probes. Histochemistry. 100:1993;431-440.
49. Simcha I., Shtutman M., Salomon D., Zhurinsky J., Sadot E., Geiger B., Ben-Zeev. A. differential nuclear translocation and transactivation potential of β-catenin and plakoglobin. J. Cell Biol. 141:1998;1433-1448.
50. Suzuki S., Sano K., Tanihara H. Diversity of the cadherin family: evidence for eight new cadherins in nervous tissue. Cell Regul. 2:1991;261-270.
51. Suzuki S. T. Structural and functional diversity of cadherin superfamily: Are new members of cadherin superfamily involved in signal transduction pathway. J. Cell. Biochem. 61:1996;531-542.
52. Suzuki S. C., Inoue T., Kimura Y., Tanaka T., Takeichi M. Neuronal circuits are subdivided by differential expression of type-II classic cadherins in postnatal mouse brains. Mol. Cell. Neurosci. 9:1997;433-437.
53. Takeichi M. The cadherins: Cell-cell adhesion molecules controlling animal morphogenesis. Development. 102:1988;639-655.
54. Uchida N., Honjo Y., Johnson K. R., Wheelock M. J., Takeichi M. The catenin/cadherin adhesion system is localized in synaptic junctions bordering transmitter release zones. J. Cell Biol. 135:1996;767-779.
55. Volk T., Cohen O., Geiger B. Formation of heterotypic adherins-type junctions between LCAM containing liver cells and ACAM containing lens cells. Cell. 50:1987;987-994.
56. Wong W. T., Sanes J. R., Wong R. O. L. Developmentally regulated spontaneous activity in the embryonic chick retina. J. Neurosci. 1998.
57. Wohrn J. C. P., Puelles L., Nakagawa S., Takeichi M., Redies C. Cadherin expression in the retina and retinofugal pathways of the chicken embryo. J. Comp. Neurol. 396:1998;20-38.
58. Yamagata M., Sanes J. R. Lamina-specific cues guide outgrowth and arborization of retinal axons in the optic tectum. Development. 121:1995a;189-200.
59. Yamagata M., Sanes J. R. Target-independent diversification and target-specific projection of chemically defined retinal ganglion cell subsets. Development. 121:1995b;3763-3776.
60. Yamagata M., Herman J. P., Sanes J. R. Lamina-specific expression of adhesion molecules in developing chick optic tectum. J. Neurosci. 15:1995;4556-4571.
61. Yap A. S., Brieher W. M., Gumbinder B. M. Molecular and functional analysis of cadherin-based cadherins junctions. Annu. Rev. Cell Biol. 13:1997;119-146.