Ca2+ signaling and early embryonic patterning during the Blastula and Gastrula Periods of Zebrafish and Xenopus development

Biochimica et Biophysica Acta - Molecular Cell Research

Volumn 1763, Issue 11, 2006, Pages 1192-1208

  Webb, Sarah E ^a   Miller, Andrew L ^a  

^a HONG KONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Hong Kong)

Author keywords

Blastula Period; Ca2+; Gastrula Period; Xenopus; Zebrafish

Indexed keywords

CALCIUM CHANNEL; WNT PROTEIN;

BLASTULA; CALCIUM SIGNALING; CELL MOTION; EMBRYO DEVELOPMENT; EMBRYONIC STRUCTURES; GASTRULA; GASTRULATION; GERM LAYER; INVOLUTION; NONHUMAN; PRIORITY JOURNAL; REVIEW; XENOPUS; ZEBRA FISH; ANIMAL; CYTOLOGY; METABOLISM; PRENATAL DEVELOPMENT;

ANURA; DANIO RERIO; VERTEBRATA; XENOPUS LAEVIS;

ANIMALS; BLASTULA; CALCIUM SIGNALING; GASTRULA; XENOPUS; ZEBRAFISH;

EID: 33751174277     PISSN: 01674889     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbamcr.2006.08.004     Document Type: Review

References (94)

1. Jaffe L.F. Organization of early development by calcium patterns. BioEssays 21 (1999) 657-667
2. Berridge M.J., Lipp P., and Bootman M.D. The versatility and universality of calcium signaling. Nat. Rev., Mol. Cell Biol. 1 (2000) 11-21
3. Webb S.E., and Miller A.L. Calcium signalling during embryonic development. Nat. Rev., Mol. Cell Biol. 4 (2003) 539-551
4. Kimmel C.B., Ballard W.W., Kimmel S.R., Ullmann B., and Schilling T.F. Stages of embryonic development of the zebrafish. Dev. Dyn. 203 (1995) 253-310
5. Gilland E., Miller A.L., Karplus E., Baker R., and Webb S.E. Imaging of multicellular large-scale rhythmic calcium waves during zebrafish gastrulation. Proc. Natl. Acad. Sci. U. S. A. 96 (1999) 157-161
6. Wallingford J.B., Ewald A.J., Harland R.M., and Fraser S.E. Calcium signaling during convergent extension in Xenopus. Curr. Biol. 11 (2001) 652-661
7. Westfall T.A., Hjertos B., and Slusarski D.C. Requirement for intracellular calcium modulation in zebrafish dorsal-ventral patterning. Dev. Biol. 259 (2003) 380-391
8. Webb S.E., and Miller A.L. Calcium signalling during zebrafish embryonic development. BioEssays 22 (2000) 113-123
9. Créton R., Speksnijder J.E., and Jaffe L.F. Patterns of free calcium in zebrafish embryos. J. Cell Sci. 111 (1998) 1613-1622
10. Webb S.E., and Miller A.L. Imaging intercellular calcium waves during late epiboly in intact zebrafish embryos. Zygote 11 (2003) 175-182
11. Nieuwkoop P.D., and Faber J. Normal Table of Xenopus laevis (Daudin) (1967), Amsterdam, North Holland
12. In: Stern C.D. (Ed). Gastrulation: From Cells to Embryo (2004), Cold Spring Harbor Press, New York
13. Kane D.A., and Warga R.M. Teleost Gastrulation, In Gastrulation from Cells to Embryo. In: Stern C.D. (Ed) (2004), Cold Spring Harbor Press, New York 157-169
14. Newport J., and Kirschner M. A major developmental transition in early Xenopus embryos: I. Characterization and timing of cellular changes at the midblastula stage. Cell 30 (1982) 675-686
15. Newport J., and Kirschner M. A major developmental transition in early Xenopus embryos: II. Control of the onset of transcription. Cell 30 (1982) 687-696
16. Kane D.A., and Kimmel C.B. The zebrafish midblastula transition. Development 119 (1993) 447-456
17. Ober E.A., and Schulte-Merker S. Signals from the yolk cell induce mesoderm, neuroectoderm, the trunk organizer and the notochord in zebrafish. Dev. Biol. 215 (1999) 167-181
18. Kimmel C.B., Warga R.M., and Schilling T.F. Origin and organization of the zebrafish fate map. Development 108 (1990) 581-594
19. Schneider S., Steinbeisser H., Warga R.M., and Hausen P. Beta-catenin translocation into nuclei demarcates the dorsalizing centers in frog and fish embryos. Mech. Dev. 57 (1996) 191-198
20. Keller R., and Tibbetts P. Mediolateral cell intercalation in the dorsal, axial mesoderm of Xenopus laevis. Dev. Biol. 131 (1989) 539-549
21. Ibrahim H., and Winklbauer R. Mechanisms of mesendoderm internalization in the Xenopus gastrula: lessons from the ventral side. Dev. Biol. 240 (2001) 108-122
22. Warga R.M., and Nüsslein-Volhard C. Origin and development of the zebrafish endoderm. Development 126 (1999) 827-838
23. Cheng J.C., Miller A.L., and Webb S.E. Organization and function of microfilaments during late epiboly in zebrafish embryos. Dev. Dyn. 231 (2004) 313-323
24. Strähle U., and Jesuthasan S. Ultraviolet irradiation impairs epiboly in zebrafish embryos: evidence for a microtubule-dependent mechanism of epiboly. Development 119 (1993) 909-919
25. Solnica-Krezel L., and Driever W. Microtubule arrays of the zebrafish yolk cell: organization and function during epiboly. Development 120 (1994) 2443-2455
26. Keller R. The cellular basis of epiboly: an SEM study of deep-cell rearrangement during gastrulation in Xenopus laevis. J. Embryol. Exp. Morphol. 60 (1980) 201-234
27. Woo K., and Fraser S.E. Order and coherence in the fate map of the zebrafish nervous system. Development 121 (1995) 2595-2609
28. Concha M., and Adams R. Oriented cell divisions and cellular morphogenesis in the zebrafish gastrula and neurula: a time-lapse analysis. Development 125 (1995) 983-994
29. Agathon A., Thisse C., and Thisse B. The molecular nature of the zebrafish tail organizer. Nature 424 (2003) 448-452
30. Slack J.M.W. From Egg to Embryo, Chapter 4 (1991), Cambridge Univ. Press, UK 67-110
31. Keller R.E., Danilchik M., Gimlich R., and Shih J. The function and mechanism of convergent extension during gastrulation of Xenopus laevis. J. Embryol. Exp. Morphol. 89 (1985) 185-209
32. Keller R., and Danilchik M. Regional expression, pattern and timing of convergence and extension during gastrulation of Xenopus laevis. Development 103 (1988) 193-209
33. Chang D.C., and Meng C. A localized elevation of cytosolic free calcium is associated with cytokinesis in the zebrafish embryo. J. Cell Biol. 131 (1995) 1539-1545
34. Webb S.E., Lee K.W., Karplus E., and Miller A.L. Localized calcium transients accompany furrow positioning, propagation, and deepening during the early cleavage period of zebrafish embryos. Dev. Biol. 192 (1997) 78-92
35. Chang D.C., and Lu P. Multiple types of calcium signals are associated with cell division in zebrafish embryo. Micros. Res. Tech. 49 (2000) 111-122
36. 3 receptors is required for furrow deepening during cytokinesis in zebrafish embryos. Int. J. Dev. Biol. 47 (2003) 411-421
37. 2+ transient during the furrow positioning process in zebrafish zygotes. Zygote 14 (2006) 143-155
38. Reinhard E., Yokoe H., Niebling K.R., Allbritton N.L., Kuhn M.A., and Meyer T. Localized calcium signals in early zebrafish development. Dev. Biol. 170 (1995) 50-61
39. Winkel G.K., Ferguson J.E., Takeichi M., and Nuccitelli R. Activation of protein kinase C triggers premature compaction in the four-cell stage mouse embryo. Dev. Biol. 138 (1990) 1-15
40. Busa W.B., and Gimlich R.L. Lithium-induced teratogenesis in frog embryos prevented by a polyphosphoinositide cycle intermediate or a diacylglycerol analog. Dev. Biol. 132 (1989) 315-324
41. Maslanski J.A., Leshko L., and Busa W.B. Lithium-sensitive production of inositol phosphates during amphibian embryonic mesoderm induction. Science 256 (1992) 243-245
42. Kume S., Muto A., Inoue T., Suga K., Okano H., and Mikoshiba K. Role of inositol 1,4,5-trisphosphate receptor in ventral signaling in Xenopus embryos. Science 278 (1997) 1940-1943
43. 2+ signaling via Gβγ and transduce ventralizing signals in Xenopus. Dev. Biol. 226 (2000) 88-103
44. Dasgupta J.D., and Singh U.N. Spatio-temporal distribution of gap junctions in zebra fish embryo. Wilhelm Roux's Arch. 191 (1982) 378-380
45. Berridge M.J., Bootman M.D., and Roderick H.L. Calcium signaling: dynamics, homeostasis and remodeling. Nat. Rev. Mol. Cell Biol. 4 (2003) 517-530
46. 2+ signaling by Wnt-5A. Dev. Biol. 182 (1997) 114-120
47. Nusse R., and Varmus H.E. Wnt genes. Cell 69 (1992) 1073-1087
48. Yang-Snyder J., Miller J.R., Brown J.D., Lai C.J., and Moon R.T. A frizzled homolog functions in a vertebrate Wnt signaling pathway. Curr. Biol. 6 (1996) 1302-1306
49. Slusarski D.C., Corces V.G., and Moon R.T. Interaction of Wnt and a Frizzled homologue triggers G-protein-linked phosphatidylinositol signaling. Nature 390 (1997) 410-413
50. Sagerström C.G., Gammill L.S., Veale R., and Sive H. Specification of the enveloping layer and lack of autoneuralization in zebrafish embryonic explants. Dev. Dyn. 232 (2005) 85-97
51. Bozhkova V., and Voronov D. Spatial-temporal characteristics of intercellular junctions in early zebrafish and loach embryos before and during gastrulation. Dev. Genes Evol. 207 (1997) 115-126
52. Solnica-Krezel L. Pattern formation in zebrafish-fruitful liaisons between embryology and genetics. Curr. Top. Dev. Biol. 41 (1999) 1-35
53. Robertson A. Waves propagated during vertebrate development: observations and comments. J. Embryol. Exp. Morphol. 50 (1979) 155-167
54. Meyer T. Cell signaling by second messenger waves. Cell 64 (1991) 675-678
55. Betchaku T., and Trinkaus J.P. Contact relations, surface activity, and cortical microfilaments of marginal cells of the enveloping layer and of the yolk syncytial and yolk cytoplasmic layers of Fundulus before and during epiboly. J. Exp. Zool. 206 (1978) 381-426
56. Sharma D., Holets L., Zhang X., and Kinsey W.H. Role of fyn kinase in signaling associated with epiboly during zebrafish development. Dev. Biol. 285 (2005) 462-476
57. Fluck R.A., Killian C.E., Miller K., Dalpe J.N., and Shih T.M. Contraction of an embryonic epithelium, the enveloping layer of the medaka (Oryzias latipes), a teleost. J. Exp. Zool. 229 (1984) 127-142
58. Barber B., da Cruz M.J.B., DeLeon J., Fluck R.A., Hasenfeld M.P., and Unis L.A. Pacemaker region in a rhythmically contracting embryonic epithelium, the enveloping layer of Oryzias latipes, a teleost. J. Exp. Zool. 242 (1987) 35-42
59. Simon J.Z., and Cooper M.S. Calcium oscillations and calcium waves coordinate rhythmic contractile activity within the stellate cell layer of medaka fish embryos. J. Exp. Zool. 273 (1995) 118-129
60. Stableford L.T. A study of calcium in the early development of the amphibian embryo. Dev. Biol. 16 (1967) 303-314
61. Komazaki S. Calcium-containing, smooth-surfaced endoplasmic reticulum and vacuoles in cells of the blastopore-forming region during gastrulation of the newt, Cynops pyrrhogaster. Anat. Embryol. 191 (1995) 369-376
62. Muto A., Kume S., Inoue T., Okano H., and Mikoshiba K. Calcium waves along the cleavage furrows in cleavage-stage Xenopus embryos and its inhibition by heparin. J. Cell Biol. 135 (1996) 181-190
63. Leclerc C., Webb S.E., Daguzan C., Moreau M., and Miller A.L. Imaging patterns of calcium transients during neural induction in Xenopus laevis embryos. J. Cell Sci. 113 (2000) 3519-3529
64. Leclerc C., Lee M., Webb S.E., Moreau M., and Miller A.L. Calcium transients triggered by planar signals induce the expression of ZIC3 gene during neural induction in Xenopus. Dev. Biol. 261 (2003) 381-390
65. Palma V., Kukuljan M., and Mayor R. Calcium mediates dorsoventral patterning of mesoderm in Xenopus. Curr. Biol. 11 (2001) 1606-1610
66. Saneyoshi T., Kume S., Amasaki Y., and Mikoshiba K. The Wnt/calcium pathway activates NF-AT and promotes ventral cell fate in Xenopus. Nature 417 (2002) 295-299
67. Berridge M.J., Downes C.P., and Hanley M.R. Neural and developmental actions of lithium: a unifying hypothesis. Cell 59 (1989) 411-419
68. Cooke J., and Smith E.J. The restrictive effect of early exposure to lithium upon body pattern in Xenopus development, studied by quantitative anatomy and immunofluorescence. Development 102 (1988) 85-99
69. Kao K.R., and Elinson R.P. The entire mesodermal mantle behaves as Spemann's organizer in dorsoanterior enhanced Xenopus laevis embryos. Dev. Biol. 127 (1988) 64-77
70. Stachel S.E., Grunwald D.J., and Myers P.Z. Lithium perturbation and goosecoid expression identify a dorsal specification pathway in the pregastrula zebrafish. Development 117 (1993) 1261-1274
71. Kume S., Muto A., Okano H., and Mikoshiba K. Developmental expression of the inositol 1,4,5-trisphosphate receptor and localization of inositol 1,4,5-trisphosphate during early embryogenesis in Xenopus laevis. Mech. Dev. 66 (1997) 157-168
72. ras in Xenopus mesoderm induction. Nature 357 (1992) 252-254
73. Nutt S.L., Dingwell K.S., Holt C.E., and Amaya E. Xenopus Sprouty2 inhibits FGF-mediated gastrulation movements but does not affect mesoderm induction and patterning. Genes Dev. 15 (2001) 1152-1166
74. Sivak J.M., Petersen L.F., and Amaya E. FGF signal interpretation is directed by Sprouty and Spred proteins during mesoderm formation. Dev. Cell 8 (2005) 689-701
75. Moon R.T., Campbell R.M., Christian J.L., McGrew L.L., Shih J., and Fraser S. Xwnt5A: a maternal Wnt that affects morphogenetic movements after overexpression in embryos of Xenopus laevis. Development 119 (1993) 97-111
76. 2+ signaling. Mech. Dev. 106 (2001) 61-76
77. Winklbauer R., Medina A., Swain R.K., and Steinbeisser H. Frizzled-7 signalling controls tissue separation during Xenopus gastrulation. Nature 413 (2001) 856-860
78. Jones K.W., and Elsdale T.R. The culture of small aggregates of amphibian embryonic cells in vitro. J. Embryol. Exp. Morphol. 11 (1963) 135-154
79. 2+-dependent reaggregating activity in dissociated cells of Xenopus laevis embryos. Cell Differ. 13 (1983) 247-255
80. 2+ dependent and independent adhesion systems in adult and embryonic cells. Dev. Growth Differ. 28 (1986) 311-319
81. LeBlanc J., and Brick I. Calcium and spreading behaviour of amphibian blastula and gastrula cells. J. Embryol. Exp. Morphol. 64 (1981) 149-168
82. Brieher W.M., and Gumbiner B.M. Regulation of C-cadherin function during activin induced morphogenesis of Xenopus animal caps. J. Cell Biol. 126 (1994) 519-527
83. Kim S.H., Yamamoto A., Bouwmeester T., and Agius E. E.M. De Robertis, The role of paraxial protocadherin in selective adhesion and cell movements of the mesoderm during Xenopus gastrulation. Development 125 (1998) 4681-4690
84. Medina A., Swain R.K., Kuerner K.M., and Steinbeisser H. Xenopus paraxial protocadherin has signaling functions and is involved in tissue separation. EMBO J. 23 (2004) 3249-3258
85. Freyssenet D., Di Carlo M., and Hood D.A. Calcium-dependent regulation of cytochrome c gene expression in skeletal muscle cells. Identification of a protein kinase c-dependent pathway. J. Biol. Chem. 274 (1999) 9305-9311
86. Studzinski D.M., Callahan R.E., and Benjamins J.A. Increased intracellular calcium alters myelin gene expression in the N20.1 oligodendroglial cell line. J. Neurosci. Res. 57 (1999) 633-642
87. Dolmetsch R.E., Xu K., and Lewis R.S. Calcium oscillations increase the efficiency and specificity of gene expression. Nature 392 (1998) 933-936
88. 2+ spike frequency can optimize gene expression. Nature 392 (1998) 936-941
89. 2+-induced methyltransferase xPRMT1b controls neural fate in amphibian embryo. Proc. Natl. Acad. Sci. U. S. A. 102 (2005) 15128-15133
90. Cao Y., Zhao H., and Grunz H. XCL-2 is a novel m-type calpain and disrupts morphogenetic movements during embryogenesis in Xenopus laevis. Dev. Growth Differ. 43 (2001) 563-571
91. Manser E., Leung T., Salihuddin H., Zhao Z.S., and Lim L. A brain serine/threonine protein kinase activated by Cdc42 and Rac1. Nature 367 (1994) 40-46
92. 2+ signaling pathway. Dev. Biol. 244 (2002) 342-357
93. Cau J., Faure S., Comps M., Delsert C., and Morin N. A novel p21-activated kinase binds the actin and microtubule networks and induces microtubule stabilization. J. Cell Biol. 155 (2001) 1029-1042
94. Faure S., Cau J., de Santa Barbara P., Bigou S., Ge Q., Delsert C., and Morin N. Xenopus p21-activated kinase 5 regulates blastomeres adhesive properties during convergent extension movements. Dev. Biol. 277 (2005) 472-492